Title of Invention

AQUEOUS SUSPENSIONS OF GROUND MINERAL MATERIALS, WITH LOW ION LOAD AND GRINDING AID AGENT FOR THE SAME

Abstract

An aqueous suspension of refined mineral matter with dry matter concentration that can be high, with low Brookfield™ viscocity that remains stable over time, and having a pigmentary surface area with low ionic charge, characterized in that it contains, as a grinding aid agent, a copolymer consisting of: (a) at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof,

Full Text

FORM 2 THE PATENT ACT 197 0 (39 of 1970) The Patents Rules, 2003 PROVISIONAL / COMPLETE SPECIFICATION (See Section 10, and rule 13) TITLE OF INVENTION AQUEOUS SUSPENSIONS OF GROUND MINERAL MATERIALS, WITH LOW ION LOAD AND GRANTED AID AGENT FOR THE SAME APPLICANT(S) a) Name : OMYA AG b) Nationality : SWISS Company c) Address : BASLERSTRASSE 42, CH-4665 OFTRINGEN, SWITZERLAND PREAMBLE TO THE DESCRIPTION The following specification particularly describes the invention and the manner in which it is to be performed : - WEAKLY IONIC AQUEOUS SUSPENSIONS OF GROUND-MINERAL MATTER AND THEIR USES The present invention relates to the technical sector of suspensions of mineral matter and their applications in the fields of paper, paint and plastics, and more particularly their applications in the paper industry with a view to improving either the paper sheet manufacturing process, or the sheet treatment process, or the sheet properties. The invention firstly concerns aqueous suspensions or "slurries" of refined mineral matter, with a dry matter concentration that can be high, that are weakly ionic and have a low Brookfield™ viscosity that remains stable over time, that is to say it relates to aqueous suspensions of refined mineral matter, with a dry matter concentration that can be high, with a low Brookfield™ viscosity that remains stable over time and having a pigmentary surface area the ionic charge of which, as determined by ionic titration, is low. These aqueous suspensions are intended for pigmentary applications in the field of paper, paint and plastics and are used more particularly for paper applications such as paper coating and/or surface treatment of the paper, or such as the filler during the manufacture of the paper, board, or analogous sheets. This use as filler can be direct as composition of filler during manufacture of the paper, board, or analogous sheets, or indirect as recycling composition of coating brokes when the recycling compositions of coating brakes are used in the manufacture of the paper, board, or analogous sheets. The invention also relates to the use of a weakly ionic and water-soluble copolymer as a grinding aid agent for grinding mineral matter in aqueous suspension in order to obtain aqueous suspensions or "slurries' of said refined matter, with a dry matter concentration that can be high, with a low Brookfield™ viscosity that remains stable over time, and having the properly that it presents a pigmentary surface area the ionic charge of which, as determined by ionic titration, is low. The invention also relates to the use of same copolymer as dispersion agent of the filter cake obtained during an intermediate stage in the manufacture of refined mineral matter suspensions, with a dry matter concentration that can be high, with low Brookfield™ viscosity that remains stable over time and having a pigmentary surface area the ionic charge of which, as determined by ionic titration, is low, this intermediate stage taking place after grinding and before thermal reconcentration. The invention also relates to said grinding aid agent by means of which it is possible to obtain aqueous suspensions of said refined mineral matter, with a dry matter concentration that can be high, with low Brookfield™ viscosity that remains stable over time and having a pigmentary surface area the ionic charge of which, as determined by ionic titration, is low. The present invention moreover relates to the grinding process that implements said grinding aid agent. Moreover, the invention relates to the use of said aqueous suspensions of mineral matter before or after drying or re-dispersion after drying in the field of paper or paint, and after drying in the field of plastics, and more particularly in the field of paper for paper industry applications such as, in particular, paper coating and/or the surface treatment of paper, or such as the filler, whether the latter implements a direct composition of filler or a recycling composition of coating brokes. It also relates to the use of said aqueous suspensions of mineral matter in a drying process after grinding. Finally, it relates to paper, board or analogous products manufactured and/or coated according to the invention. In the manufacturing process of a sheet of paper, board or analogous product, the skilled man in the art increasingly tends to replace part of the expensive cellulose fibres by cheaper mineral matter in order to reduce the cost of the paper while improving its properties. This mineral matter, familiar to the skilled man in the art, comprises, for example, calcium carbonate and miscellaneous analogous fillers such as dolomite, gypsum, calcium hydroxide, satin white, titanium dioxide or mixed carbonate based fillers of various metals such as, in particular, calcium associated with magnesium and analogues, various matter such as talc or analogues, and mixtures of these fillers, such as, for example talc-calcium carbonate or calcium carbonate-kaolin mixtures, or mixtures of natural calcium carbonate with aluminium hydroxide, mica or with synthetic or natural fibres or co-structures of minerals such as talc-calcium carbonate or talc-titanium dioxide co-structures. For a long time now it has been quite common to use, as grinding aid agents, water-soluble polymers based on polyacrytic acid or its derivatives (FR 2 488 814, FR 2 603 042, EP 0 100 947, EP 0 100 948, EP 0 129 329, EP 0 542 643, EP 0 642 644) to provide aqueous mineral suspensions that meet the above-mentioned refinement and viscosity criteria, but these grinding aid agents are polymers and/or copolymers of the anionic type which have the disadvantage of requiring the addition of cationic compounds during the paper sheet manufacturing process when the aqueous mineral suspensions containing them are implemented in these sheet manufacturing operations. The end user therefore strives to minimise the polymer agent demand during paper manufacture, for every median diameter and/or for every point of the grain size curve of the particles of mineral matter implemented. To solve the problem, the skilled man in the art is currently familiar with the solution recommended in patent application FR 2 810 261, which has the disadvantage of not fully meeting the end user's needs because although this solution makes it possible to obtain aqueous suspensions of mineral matter with low ionic charge, it does not make it possible to have suspensions with a sufficiently low ionic charge to correspond to the end user's needs. 2 Moreover, the paper manufacturer who is the end user is faced with the problem of implementing coating colours which are not sufficiently stable during paper coating operations. The skilled man in the art, being familiar with this problem, also seeks to develop aqueous suspensions of mineral matter which make it possible to obtain coating colours which are highly stable even at low anionicity and for every median diameter and/or for every point of the grain size curve of the particles of mineral matter implemented. Faced with the above-mentioned problems, the Applicant took the surprising step of developing aqueous suspensions of refined minerals with dry matter concentration that can be high, with low Brookfieid™ that remains stable over time, and having a pigmentary surface area the ionic charge of which, determined by ionic titration, is very low, suspensions the implementation of which, both in the paper manufacturing processes and in the filler or in the paper sheet treatment processes such as coating, make it possible to solve the above-mentioned problems. These aqueous suspensions of refined minerals with dry matter concentration that can be high, with low Brookfieid™ that remains stable over time, and having a pigmentary surface area the ionic charge of which, determined by ionic titration, is low, are obtained by using a weakly charged polymer as a grinding agent of the mineral matter in aqueous suspension, or by using the same copolymer as dispersing agent of the filter cake obtained in an intermediary stage of the manufacture of the suspension, this intermediary stage taking place after grinding and possibly before a physical concentration process such as thermal concentration. The said aqueous suspensions of refined mineral matter with dry matter concentration that can be high, with low Brookfieid™ that remains stable over time, and having a pigmentary surface area the ionic charge of which, determined by ionic titration, is low, are characterized in that they contain, as a grinding aid agent, a copolymer consisting of: at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ct to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 I5£(m+n+p)q R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzyluretnane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (lie) or mixtures thereof: with formula (Ha) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 £ (m1+n1+p1)q1 s 150 and 0 £ (m2+n2+p2)q2 r represents a number such that 1 Ra represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinyiphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-oc' dimethyl-isopropenyl-benzyluretnane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, Rt, Rs, Rio and Rn represent hydrogen or the methyl or ethyl radical Re, R7, Rs and Rg represent straight or branched alkyl, aryl, alkylaryl or arylalkyi groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinyiphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, oc-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where: m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 r" represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinyiphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-cc' dimethyl-isopropenyl-benzyluretnane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, Ria and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyi groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, possibly at least one monomer of the acrylamide or methacrylamide type or their derivatives and mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acry!amido) propyl] trimethyl ammonium chloride or sulphate, dimethyl dialfyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof e) possibly at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others the total of the components a), b), c), d) and e) being equal to 100% and having an intrinsic viscosity less than or equal to 100 ml/g as determined in accordance with the method described in Vollmert publication "Outlines of macromolecular chemistry" volume III, Vollmert Veriag, Karlsruhe 1985 and by the implementation of a solution of demineralised water and a capillary tube defined in standard DIN 53101/0a, of constant 0.005 and diameter equal to 0.53 mm. This method will be referred to as the intrinsic viscosity method in this application. A second method that can be used to determine the intrinsic viscosity uses a 6% solution of NaCI and the same equipment as described above. In the examples where this second method is used in addition to the first method, the intrinsic viscosity values obtained using this second method correspond to the second value indicated. Thus, in order to minimise the cationic agent demand when manufacturing the paper, for every median diameter and/or for every point of the grain size curve of the particles of mineral matter implemented and in order to provide, when coating the paper, coating colours which are highly stable for every median diameter and/or for every point of the grain size curve of the particles of mineral matter implemented, the prime aim of the invention is to provide such aqueous suspensions of refined mineral substances containing the above-mentioned copolymers. Another aim of the invention is the use, as a grinding aid agent for mineral substances in aqueous suspensbn or as dispersing agent of the filter cake obtained in an intermediate stage of the manufacture of the suspension, said intermediate stage taking place after grinding and, if relevant, before a thermal concentration process, of a copolymer consisting of: at least one ethytenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 15 Ri represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, cc-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (He) or mixtures thereof: with formula (Ha) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allyjurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, R5, R10 and R11 represent hydrogen or the methyl or ethyl radical R6, Rr, R8 and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allyjurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 r' represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allyjurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, possibly at least one monomer of the acrylamide or methacryiamide type or their derivatives and mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacryiamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] tnmethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] tnmethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof possibly, at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methytene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others the total of the components a), b), c), d) and e) being equal to 100% and having an intrinsic viscosity less than or equal to 100 ml/g measured in accordance with the above-mentioned method. Another aim of the invention is to provide a grinding process in aqueous suspension of mineral particles implementing said selected copolymers as a grinding agent. Said copolymers implemented according to the invention furthermore present the advantage of reducing the formation of foam during the physical operation, such as grinding and/or pumping and/or stirring of mineral matter. Moreover, another aim of the invention is to use said refined mineral aqueous suspensions as is or after drying in the field of paper, paint and plastics. More particularly, another aim of the invention lies in using these refined mineral aqueous suspensions for paper filling, and more particularly in applications known as "wet-end" applications, i.e. applications in processes for manufacturing paper, board or analogous sheet where they are used as filler, whether directly or indirectly. Another aim also lies in the use of said refined mineral aqueous suspensions in the treatment of the paper, board or analogous sheet where they are used as coating colour filler. Another aim also lies in the use of said refined mineral aqueous suspensions in the field of plastic, such as low density (LLDPE) and high density (HMW-HDPE) polyolefines, or breathable membranes, or polyvinyl chlorides (PVC) and more particularly in the field of PVCs such as rigid or flexible PVCs. These goals are attained thanks to the use, as a grinding aid agent, of a copolymer consisting of: at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diackJs such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acryluretnane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (He) or mixtures thereof: with formula (Ha) where ml, p1, m2 and p2 represent a number of a Ikylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, oc-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Rs, Rio and R11 represent hydrogen or the methyl or ethyl radical Re, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, OKX' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, Ris and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, possibly at least one monomer of the acrylamide or methacrylamide type or their derivatives and mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof possibly at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriaciylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others the total of the components a), b), c), d) and e) being equal to 100%. and having an intrinsic viscosity less than or equal to 100 ml/g measured in accordance with the above-mentioned method. More particularly, the aqueous suspensions of refined mineral substances according to the invention are characterized in that said copolymer consists, by weight, of: from 2% to 95%, preferably from 3% to 25%, and even more preferably from 4% to 15%, of at least one ethylenicaily unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenicaily unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenicaily unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenicaily unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsuffonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenicaily unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acryiate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenicaily unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, From 97.9% to 4.9%, preferably from 95% to 65%, and even more preferably from 92% to 78%, of at least one non-ionic ethylenicaily unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 15£(m+n+p)q£l20, Ri represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, ce-a' dimethyl-isopropenyl-benzyluretnane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenicaily unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), from 0.1% to 50%, preferably from 0.2% to 10%, and even more preferably from 0.3% to 5%, of at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (He) or mixtures thereof: with formula (Ha) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, oc-oc' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenicaily unsaturated amides or imides, R», Rs, Rio and R11 represent hydrogen or the methyl or ethyl radical Re, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyi groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-cc' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 £ (m3+n3+p3)q3 £ 150 and 0 r" represents a number such that 1 f R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-ot' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof, D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, from 0% to 50%, preferably from 0% to 10%, and even more preferably from 0% to 5%, of at least one monomer of the acrylamide or methacrylamide type or their derivatives and mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one catJonic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyi ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof from 0% to 5%, preferably from 0% to 3%, of at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others the total of the components a), b), c), d) and e) being equal to 100%, and in that said copolymer has an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the above-mentioned method. More particularly, the aqueous suspensions of mineral matter according to the invention are characterized in that they contain from 0.05% to 10% of said co polymer by dry weight with respect to the dry weight of mineral substances. Equally particularly, the aqueous suspensions of mineral matter according to the invention are characterized in that said copolymer is in its acid form, or partially or fully neutralized by one or more neutralizing agents. These neutralizing agents are those that have a monovalent neutralizing function or a polyvalent neutralizing function such as, for example, for the monovalent function those selected from the group consisting of the alkaline cations, in particular sodium, potassium, lithium, ammonium or the primary, secondary or tertiary aliphatic and/or cyclic amines such as for example stearylamine, the ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methyteyclohexylamine, aminomethylpropanol, morpholine or, for the polyvalent function, those selected from the group consisting of alkaline earth divalent cations, in particular magnesium and calcium, or zinc, and of the trivalent cations, including in particular aluminium, or of certain cations of higher valency. Another variant of the invention consists in the fact that the aqueous suspensions of mineral matter according to the invention contain from 0.05% to 10% of said copolymer by dry weight with respect to the dry weight of mineral substances and at least one other dispersant or grinding aid agent. Said other dispersant or grinding aid agent is then selected from those other dispersants or grinding agents familiar to the skilled man in the art such as, in particular, homopolymers or copolymers of acrylic acid in their acid forms, or fully or partially neutralized by one or more neutralizing agents, said neutralizing agents being selected from the same list as that referred to above, or is selected from among the dispersants or grinding aid agents such as, in particular, H3O ion donors of which phosphoric acid and/or its salts with mono and/or divalent bases such as soda or lime are particularly worthy of mention. Specifically, the aqueous suspensions of mineral matter according to the invention contain from 0.05% to 1% by dry weight with respect to the dry weight of mineral substances of said other dispersants or grinding aid agents. Equally particularly, the aqueous suspensions of mineral matter according to the invention are characterized in that they have a dry matter content of between 15% and 85% by weight, and preferably between 40% and 80%, and even more preferably between 50% and 78%. In addition, the aqueous suspensions of mineral matter according to the invention are characterized in that the mineral matter is selected from among calcium carbonate and various analogous fillers such as dolomite, gypsum, calcium hydroxide, satin white, titanium dioxide, aluminium trihydroxide or mixed carbonate based fillers of various metals such as, in particular, calcium associated with magnesium and analogues, various matter such as talc or analogues, and mixtures of these fillers such as for example talc-calcium carbonate or calcium carbonate-kaolin mixtures, or mixtures of calcium carbonate with aluminium trihydroxide, the kaolins, calcine kaolins, mica or with synthetic or natural fibres or co-structures of minerals such as talc-calcium carbonate or talc-titanium dioxide co-structures. Preferably, the aqueous suspensions of mineral matter according to the invention are characterized in that the mineral matter consists of calcium carbonate such as natural calcium carbonate selected from among marble, calcite, chalk or mixtures thereof. These aqueous suspensions of mineral matter according to the invention are also characterized in that the mineral matter presents a median grain diameter, measured using the Sedigraph™ 5100, of between 50 u.m and 0.1 urn, preferably between 5 \im and 0.2 u,m and even more preferably between 2 u.m and 0.5 u.m. These aqueous suspensions of mineral matter according to the invention are also characterized in that they have a pH of between 7.5 and 13, preferably between 8 and 12, and even more preferably between 8.5 and 10. The use, according to the invention, of a copolymer as a grinding aid agent for mineral matter in aqueous suspension, is characterized in that said copolymer consists of: at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as C1 to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 <. and preferably represents an integer such that> 15^(m+n+p)q£l20, R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-o' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (He) or mixtures thereof: with formula (Ha) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 £ r £ 200 R3 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, OMX' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Rs, Rio and Rn represent hydrogen or the methyl or ethyl radical R6, R7, Ra and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) Si (OB)3 R-A-where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, oc-cc' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 £ (m3+n3+p3)q3 £ 150 and 0 r represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, oc-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, possibly at least one monomer of the acrylamide or methacrylamide type or their derivatives and mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or metnacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vmylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acry!amido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrytamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof possibly at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, ally! acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others the total of the components a), b), c), d) and e) being equal to 100%. and in that said copolymer has an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the above-mentioned method. More particularly, the use of the above-mentioned copolymer is characterized in that said copolymer consists, in terms of weight, of: from 2% to 95%, preferably from 3% to 25%, and even more preferably from 4% to 15%, of at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, From 97.9% to 4.9%, preferably from 95% to 65%, and even more preferably from 92% to 78%, of at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 15 R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acryhiretnane, methacrylurethane, a-a' dirnethyl-isopropenyl-benzyluretnane and allylurethane, and to the roup of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, :' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), from 0.1% to 50%, preferably from 0.2% to 10%, and even more preferably from 0.3% to 5%, of at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (lla) or (lib) or (He) or mixtures thereof: with formula (lla) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 Ri represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyi or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Ri, Rio and Rn represent hydrogen or the methyl or ethyl radical R6, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) q3 where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 r represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, preferably belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as for example acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, RM, Ris, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, Ru, Ris and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, from 0% to 50%, preferably from 0% to 10%, and even more preferably from 0% to 5%, of at least one monomer of the acrylamide or methacrylamide type or their derivatives or mixtures thereof such as N-[3-(dimethy!amino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acryfates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quatemary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, |3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof from 0% to 5%, preferably from 0% to 3%, of at least one crosslinking monomer selected, but not exclusively, from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-ois-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, sucrose or others. the total of the components a), b), c), d) and e) being equal to 100%, and in that said copolymer has an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the above-mentioned method. The copolymer used according to the invention is obtained by known radical copolymerization processes in solution, in direct or inverse emulsion, in suspension or precipitation in appropriate solvents, in the presence of known catalytic systems and transfer agents, or by means of controlled radical polymerization processes such as the method known as Reversible Addition Fragmentation Transfer (RAFT), the method known as Atom Transfer Radical Polymerization (ATRP), the method known as Nitroxide Mediated Polymerization (NMP), or the method known as Cobaloxime Mediated Free Radical Polymerization. This copolymer obtained in acid form and possibly distilled can also be fully or partially neutralized using one or more neutralizing agents having a monovalent neutralizing function or a polyvalent neutralizing function such as, for example, for the monovalent function those selected from the group consisting of the alkaline cations, in particular sodium, potassium, lithium, ammonium or the primary, secondary or tertiary aliphatic and/or cyclic amines such as for example stearylamine, the ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methylcyclohexylamine, aminomethylpropanol, morpholine or, for the polyvalent function those selected from the group consisting of alkaline-earth divalent cations, in particular magnesium and calcium, or zinc, and of the trivalent cations, including in particular aluminium, or of certain cations of higher valency. Each neutralizing agent then operates according to neutralization rates proper to each valency function. According to another variant, the copolymer obtained from the copolymerization reaction may, before or after the total or partial neutralization reaction, be treated and separated into several phases, according to statistical or dynamic processes known to the skilled man in the art, by one or more polar solvents belonging to the group consisting of water, methanol, ethanol, propanol, isopropanol, butanols, acetone, tetrahydrofurane or mixtures thereof. One of the phases then corresponds to the copolymer used according to the invention as dispersing agent or grinding aid agent of mineral matter in aqueous suspension. The invention also relates to said weakly ionic and water-soluble grinding aid agent of mineral substances in aqueous suspension having the property of being weakly charged. Said agent is characterized in that it is the above-described copolymer. The invention also relates to the grinding process that implements said grinding aid agent of mineral substances in aqueous suspension. In practice, according to the invention, grinding the mineral substance consists in refining said substance into very fine particles using a grinding body in an aqueous environment by means of the copolymer used as a grinding aid agent. A variant consists in forming, by introducing the total quantity of the copolymer, an aqueous suspension of the mineral substance to be ground, the particles of which have an initial dimension equal to no more than 50 micrometres. To the suspension of the mineral substance to be ground thus formed is added the grinding body of a grain size preferably between 0.20 millimetres and 4 millimetres. The grinding body is generally presented in the form of particles of materials as diverse as silicium oxide, aluminium oxide, zirconium oxide or mixtures thereof together with synthetic resins of great hardness, steels or others. The grinding body is preferably added to the suspension in a quantity such that the ratio by weight between this material and the mineral substance to be ground is at least 2/1, this ratio preferably being between the limits 3/1 and 5/1. The mixture of the suspension and the grinding body is then subjected to mechanical grinding action, such as that which occurs in a classical microelement grinder. The quantity of grinding aid agent introduced varies from 0.05% to 10% by dry weight of said copolymers with respect to the dry mass of the mineral substance to be refined. The time necessary to obtain a highly refined mineral substance after grinding varies according to the nature and quantity of the mineral substances to be refined and according to the stirring mode used and the temperature of the medium during the grinding operation. Another variant consists in using a part of the grinding aid agent before the grinding stage and implementing the rest of the quantity of the grinding agent during the grinding operation. Finally, another variant consists in not implementing the copolymer before the grinding stage and using the entire quantity necessary during the grinding operation, which takes place in one or more stages. Thus, according to the invention, the grinding process in aqueous suspension intended for pigmentary applications consisting in refining into very fine particles an aqueous suspension of said mineral materials is characterized in that use is made, as a grinding aid agent, of 0.05% to 10% by dry weight of the above-mentioned polymers with respect to the dry weight of mineral materials before and/or during the grinding stage. Another mode of implementing the invention also consists in implementing, in addition to said copolymer used as a grinding agent, at least one other grinding agent before and/or during the grinding stage. Thus, according to a variant, the grinding process according to the invention is characterized in that use is made, as a grinding aid agent, of 0.05% to 10% by dry weight of the above-mentioned polymers with respect to the dry weight of mineral materials and at least one other dispersant or grinding aid agent before and/or during the grinding stage. Said other dispersant or grinding aid agent is then selected from those other dispersants or grinding aid agents familiar to the skilled man in the art such as, in particular, homopolymers or copolymers of acrylic acid in their acid forms, or fully or partially neutralized by one or more neutralizing agents, said neutralizing agents being selected from the same list as that referred to above, or is selected from among the dispersants or grinding aid agents such as, in particular, H3O* ion donors of which phosphoric acid and/or its salts with mono and/or divalent bases such as soda or lime are particularly worthy of mention. Particularly, the grinding process according to the invention is characterized in that use is made of 005% to 1.0%, by dry weight with respect to the dry weight of mineral substances, of said other dispersant or grinding aid agent. The temperature during the course of the grinding stage and for all the variants of the grinding process according to the invention lies between 15°C and 150°C, preferably between 50°C and 105°C and especially preferably between 60°C and 98°C. For mineral matter containing carbonate, the pH during the course of the grinding stage and for all the variants of the grinding process according to the invention lies between 6 and 13, preferably between 7.5 and 12 and especially preferably Between 8 and 10. For mineral matter not containing carbonate, the pH during the course of the grinding stage and for all the variants of the grinding process according to the invention lies between 2 and 13, preferably between 7.5 and 12 and especially preferably between 8 and 10. When implementing these various grinding variants, apart from the problem that it resolves, the invention has the advantage that less foam is produced during grinding when using the copolymers than when using the polymers of the prior art. Another advantage of the invention consists in the fact that the aqueous suspensions of mineral matter refined according to the invention always have grains of mineral matter having, for an equivalent grain size, a specific surface area less than the grains of mineral matter of the aqueous suspensions of mineral matter refined according to the prior art by implementing polyacrylate. This advantage is perceptible when the end user uses latex in coating formulations. Thus the aqueous suspensions of mineral matter according to the invention are characterized in that the grains of mineral matter have, for an equivalent grain size, a BET specific surface area less than the grains of mineral matter of the aqueous suspensions of mineral matter refined using grinding aid agents such as polyacrylates, homopolymers or copolymers well known to the skilled man in the art. The mineral substances to be refined according to the process of the invention can be of highly diverse origin such as calcium carbonate, dolomites, kaolins, calcine kaolins, talc, gypsum, titanium oxide, or aluminium trihydroxide or any other filler and/or pigment that has to be ground in order to be used in applications such as the manufacture of papers, board or analogues and are preferably calcium carbonate such as natural calcium carbonate selected from among marble, calcite, chalk or mixtures thereof. The papers manufactured according to the invention are characterized in that they contain said aqueous suspensions of fillers and/or pigments according to the invention. The scope and interest of the invention will be better perceived thanks to the following examples, which are not of a comprehensive nature. EXAMPLE 1 This example illustrates, by comparison with comparable grain size, how to reduce the cationic polymer demand in the mass by implementing an aqueous suspension of calcium carbonate containing the copolymer used, according to the invention, as a grinding aid agent. Test No. 1 This test illustrates the prior art and implements 0.27% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 65.5% by weight and having a grain size such that 61% by weight of the particles have a diameter of less than 2 pm, and 30% by weight of the particles have a diameter of less than 1 (jm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 1.63 urn To do this, use is made of a Dyno-Mill™ type fixed-cylinder grinder with rotating impeller, the grinding body of which consists of zirconium based beads of a diameter between 0.6 millimetres and 1 millimetre. The total volume occupied by the grinding body is 1000 cubic centimetres while its weight is 2700 g. The grinding chamber has a volume of 1400 cubic centimetres. The circumferential speed of the grinder is 10 metres per second. The pigment suspension is recycled at a rate of 40 litres per hour. The output of the Dyno-Mill is fitted with a 200-micron grade separator by means of which it is possible to separate the suspension that results from the grinding and the grinding body. The temperature during each grinding test is maintained at approximately 60°C. One hour after grinding is completed, a sample of the pigmentary suspension, the grain size of which (% of particles less than 2 micrometres) is measured using a Sedigraph™ 5100 particle size analyzer, is recovered in a beaker. The Brookfield™ viscosity of the suspension is measured using a model RVT Brookfield™ viscometer, at a temperature of 23°C and a rotation speed of 100 rpm with the appropriate 3 spindle. Having left this sample lie in the beaker for 7 days, the Brookfield™ viscosity of the suspension is measured by introducing, into the unstitrred beaker, the appropriate spindle of the RVT model Brookfield™ viscometer, at a temperature of 23°C and a rotation speed of 100 rpm. (AVAG viscosity = viscosity before stirring). The same Brookfield™ viscosity measurements are also made once the beaker has been stirred for 5 minutes and constitute the APAG (after stirring) viscosity results. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained are as follows: S.C. = 65.5% Viscosity (To) = 115 mPa.s AVAG viscosity (TV days) = 620 mPa.s APAG viscosity (Tzdays) = 155 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined. The BET specific surface area, determined according to standard ISO 9277, is equal to 7.2 rrWg The PDDPC cationic polymer demand, measured using the Mettler DL77 titrator and the Miitec PCD 02 detector using the cationic titration method implementing 0.005 mole of a solution of 20% of poly(N,N-dimethyl-3,5-dimethylene-piperidinium chloride (PDDPC) sold by Acros Organics is equal to 12100 u. Val/kg, this value being the value corresponding to zero charge of the detector used. Test No. 2 This test illustrates the prior art and implements 0.47% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 urn, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 90% by weight of the particles have a diameter of less than 2 pm as measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.8% Viscosity (To) = 265 mPa.s AVAG viscosity (Todays) = 726 mPa.s APAG viscosity OW) = 278 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 12.0 m2/g and a PDDPC cationic polymer demand equal to 20220 u. Val/kg. Test No. 3 This test illustrates the prior art and implements 0.79% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 |im, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 76.5% by weight and having a grain size such that 78% by weight of the particles have a diameter of less than 1 pm as measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 77.1% Viscosity (To) = 371 mPa.s AVAG viscosity (TV days) = 886 mPa.s APAG viscosity (T7days) = 412 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 16.2 m2/g and a PDDPC cationic polymer demand equal to 33990 u. Val/kg. Test No. 4 This test illustrates the prior art and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: 14% acrylic acid 3% methacrylic acid 83% of polyethylene glycol methacrylate with a molecular weight of 2000 of intrinsic viscosity equal to 20.0 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 57% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 71.3% Viscosity (To) = 158 mPa.s AVAG viscosity (17 days ) = 677mPa.s APAG viscosity ) = 254 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 4.9 m2/g and a PDDPC cationic polymer demand equal to 3100 u, Val/kg. Test No. 5 This test illustrates the prior art and implements 1.17% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 4 to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under Ihe same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 87% by weight of the particles have a diameter of less than 2 |jm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 72.0% Viscosity (To) = 224 mPa.s AVAG viscosity OVM = 987 mPa.s APAG viscosity (Tntays) = 248 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 9.6 m2/g and a PDDPC cationic polymer demand equal to 10000 u, Val/kg. In this test, a measurement was made of the foam by measuring the time a certain height of foam (height h in cm) took to form and the time necessary for this foam to disappear (Up). -In this test, t = 90 seconds for h = 23 cm and tap = 5 minutes. Test No. 6 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: 3.0% acrylic acid and 2.0% maleic acid 94.0% of a monomer of formula (I) in which: Ri represents hydrogen R2 represents hydrogen R represents the vinyl group R' represents the methyl radical where m = p = 0; n = 114; q= 1 and (m+n+p)q = 114 1.0% of a monomer of formula (lib) in which R represents the methacrylate group A represents the propyl radical B represents the methyl radical of intrinsic viscosity equal to 39.5 ml/g according to the above-mentioned intrinsic viscosity method (and equal to 30.3 ml/g according to the second method), to obtain, from a calcium carbonate with a median diameter of 15 urn, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 59% by weight of the particles have a diameter of less than 2 |jm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 1.41 pm. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.2% Viscosity (To) = 125 mPa.s AVAG viscosity (Tzdays) = 338 mPa.s APAG viscosity (T7days) = 127 d™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are demPa.s Once these Brookfieltermined using the same method as in test No. 1. This gives a BET specific surface area equal to 4.8 m2/g and a PDDPC cationic polymer demand equal to 590 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 600 seconds for h = 6cm and tdisp = immediate. These results show that much less foam is created than in the test of the prior art. Test No. 7 This test illustrates the invention and implements 1.07% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 um, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 90% by weight of the particles have a diameter of less than 2 \im measured on the Sedigraph™ 5100, corresponding to a median diameter equal to 0.83 |jm. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.4% viscosity (To) = 241 mPa.s AVAG viscosity (Tzdays) ~ 359 mPa.s APAG viscosity (T7 Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 6.8 m2/g and a PDDPC cationic polymer demand equal to 2340 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 600 seconds for h = 6cm and tdisp = immediate. These results show that much less foam is created than in the test of the prior art. Test No. 8 This test illustrates the invention and implements 2.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 um, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 80% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100, corresponding to a median diameter equal to 0.55 \m\. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.0% Viscosity (To) = 717 mPa.s AVAG viscosity (Todays) = 1570 mPa.s APAG viscosity todays) = 697 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 8.4 m2/g and a PDDPC cationic polymer demand equal to 4590 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 600 seconds for h = 6cm and tdisp = immediate. These results show that much less foam is created than in the test of the prior art. Test No. 9 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: a) 8.7% acrylic acid and 1.5% methacrylic acid 89.4% of a monomer of formula (I) in which: Ri represents hydrogen ft2 represents hydrogen R represents the methacrylate group R' represents the methyl radical where m = p = 0; n = 114; q= 1 and (m+n+p)q = 114 v 0.4% of a monomer of formula (lib) in which R represents the methacrylate group A represents the propyl radical B represents the methyl radical of intrinsic viscosity equal to 20.7 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 58% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 71.9% Viscosity (To) = 138 rnPas AVAG viscosity (Tioays) = 486 mPa.s APAG viscosity (T7days) = 159 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 4.8 m2/g and a PDDPC cationic polymer demand equal to 340 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 510 seconds for h = 23 cm tdBp=2 minutes. These results show that much less foam is created than in the test of the prior art. Test No. 10 This test illustrates the invention and implements 1.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 9 to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 89% by weight of the particles have a diameter of less than 2 (jm measured on the Sedigraph™ 5100. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 73.5% Viscosity (To) = 164 mPa.s AVAG viscosity (T7 days) = 593 mPa.s APAG viscosity OVdays) = 175 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 7.8 m2/g and a PDDPC cationic polymer demand equal to 2770 \i Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 510 seconds for h = 23 cm and Up = 2 minutes. These results show that much less foam is created than in the test of the prior art. Test No. 11 This test illustrates the invention and implements 2.08% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 9 to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 81% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.7% Viscosity (To) = 712 mPa.s AVAG viscosity OW) = 2240 mPa.s APAG viscosity (Tzdays) = 686 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 4.8 m2/g and a PODPC cationic polymer demand equal to 7050 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 510 seconds for h = 23 cm and Up = 2 minutes. These results show that much less foam is created than in the test of the prior art. Test No. 12 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: a) 8.7% acrylic acid and 1.5% methacrylic acid 89.5% of a monomer of formula (I) in which: Ri represents hydrogen R2 represents hydrogen R represents the methacrylate group R' represents the methyl radical where m = p = 0; n = 114; q= 1 and (m+n+p)q = 114 0.3% of a monomer of formula (lib) in which R represents the vinyl group A is absent B represents the methyl radical of intrinsic viscosity equal to 20.4 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 58% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 73.0% Viscosity (To) = 144 mPa.s AVAG viscosity fT?*^) = 628 mPa.s APAG viscosity (T7days) = 171 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 4.8 m2/g and a PDDPC cationic polymer demand equal to 880 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 180 seconds for h = 23 cm and Usp = 3 minutes. These results show that less foam is created than in the test of the prior art. Test No. 13 This test illustrates the invention and implements 1.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 12 to obtain, from a calcium carbonate with a median diameter of 15 |xm, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 90% by weight of the particles have a diameter of less than 2 |jm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 73.1% Viscosity (To) = 195 mPa.s AVAG viscosity (J? days) = 731 mPa.s APAG viscosity fa days) = 185 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 8.1 rrvVg and a PDOPC cationic polymer demand equal to 3760 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 180 seconds for h = 23 cm and tap = 3 minutes. These results show that less foam is created than in the test of the prior art. Test No. 14 This test illustrates the invention and implements 2.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 12 to obtain, from a calcium carbonate with a median diameter of 15 urn, and orrater tfre* sams ojajrating- ewraWbror ams1 using tfle same equipment as fh tss{ iVo. f, an aqueous suspensfbn of groana" calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 83% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.3% Viscosity (To) = 613 mPa.s AVAG viscosity (T/days) = 3030 mPa.s APAG viscosity (Trdays) = 650 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 11.1 m2/g and a PDDPC cationic polymer demand equal to 7180 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 180 seconds for h = 23 cm and tap = 3 routes. These results show that less foam is created than in the test of the prior art. Test No. 15 This test illustrates the invention and implements 0,40% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: a) 8.5% acrylic acid and 1.5% methacrylic ;acid 87.0% of a monomer of formula (I) in which: Ri represents hydrogen R2 represents hydrogen R represents the methacrylate group R' represents the methyl radical where m = p = 0; n = 114; q= 1 and (m+n+p)q = 114 3.0% of a monomer of formula (lib) in which R represents the methacrylate group A represents the propyl radical B represents the methyl radical of intrinsic viscosity equal to 23.2 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 p.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 58% by weight of the particles have a diameter of less than 2 urn as measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S C - 73 7% viscosity (To) = 156 mPa.s AVAG viscosity fTVdays) = 733 mPa.s APAG viscosity (T7 days) = 197 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the. same method as in test No. 1. This gives a BET specific surface area equ^i to 4.9 m2/g and a PDDPC cationic polymer demand equal to 1280 p. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 150 seconds for h = 23 cm and Up = 4 minutes. These results show that less foam is created than in the test of the prior art. Test No. 16 This test illustrates the invention and implements 1.25% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 15 to obtain, from a calcium carbonate with a median diameter of 15 |im, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 87% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.9% Viscosity (To) = 196 mPa.s AVAG viscosity OW) = 642 mPa.s APAG viscosity (frdays) = 189 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 7.6 m2/g and a PDDPC cationic polymer demand equal to 4150 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 150 seconds for h = 23 cm and Up = 4 minutes. These results show that less foam is created than in the test of the prior art. Test No. 17 This test illustrates the invention and implements 2.08% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 15 to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 81% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 77.0% Viscosity (To) = 648 mPa.s AVAG viscosity QVdays) = 2840 mPa.s APAG viscosity (T7 days)= 747 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area equal to 9.3 m2/g and a PDDPC cationic polymer demand equal to 6900 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 150 seconds for h = 23 cm and Up= 4 minutes. These results show that less foam is created than in the test of the prior art. Test No. 18 This test illustrates the invention and implements 0.79% by dry weight, with respect to the dry weight of calcium carbonate, of a copolymer consisting, by weight, of: a) 8.5% acrylic acid and 1.5% methacrylic acid 87.0% of a monomer of formula (I) in which: R1 represents hydrogen R2 represents hydrogen R represents the methacrylate group R' represents the methyl radical where m = p = 0; n = 114; q= 1 and (m+n+p)q = 114 3.0% of a monomer of formula (lib) in which R represents the vinyl group A is absent j B represents the methyl radical i of intrinsic viscosity equal to 20.0 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 63% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.5% Viscosity (To) = 145 mPa.s AVAG viscosity [TV days) = 285 mPa.s APAG viscosity (T? nays) = 112 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 2500 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. Test No. 19 This test illustrates the invention and implements 1.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 18 to obtain, from a calcium carbonate with a median diameter of 15 u,m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 93% by weight of the particles have a diameter of less than 2 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.0% Viscosity (To) = 249 mPa.s AVAG viscosity 0W) = 1260 mPa.s APAG viscosity flVdays) = 279 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 4040 u, Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. Test No. 20 This test illustrates the invention and implements 2.10% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 18 to obtain, from a calcium carbonate with a median diameter of 15 urn, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75% by weight and having a grain size such that 83% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.3% Viscosity (To) = 808 mPas AVAG viscosity OW) = 3000 mPa.s APAG viscosity flVdays) = 802 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 7710 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. Test No. 21 This test illustrates the invention and implements 0.27% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 urn, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 65.1% by weight and having a grain size such that 60% by weight of the particles have a diameter of less than 2 (jm measured on the Sedigraph™, corresponding to a median diameter equal to 1.50 Mm. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 65.1% Viscosity (To) = 183 mPa.s AVAG viscosity (Jito*) = 354 mPa.s APAG viscosity fTVdays) = 205 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 410 ji Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 600 seconds for h = 6cm and tap = immediate. These results show that much less foam is created than in the test of the prior art. Test No. 22 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 urn, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 76.0% by weight and having a grain size such that 74% by weight of the particles have a diameter of less than 2 pm, and 39% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™, corresponding to a median diameter equal to 1.25 pm. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 76.0% Viscosity (To) = 295 mPa.s AVAG viscosity (T7days) = 505 mPa.s APAG viscosity (Trdays) = 195 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 550 u Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. In this test, a measurement was made of the foam using the same operating procedure as in test No. 5 and the result was: t = 600 seconds for h = 6cm and tap = immediate. These results show that much less foam is created than in the test of the prior art. EXAMPLE 2 This example illustrates the link between filler retention in filling and cationic polymer demand. Test No. 23 This test illustrates the prior art and implements 0.27% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 urn, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 65.5% by weight and having a grain size such that 61% by weight of the particles have a diameter of less than 2 pm and 30% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 1.63 urn. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 65.5% Viscosity (To) = 115 mPa.s AVAG viscosity (Trdays) = 620 mPa.s APAG viscosity (TVdays)= 155 mPa.s Filler retention in the filling is determined using the method described below and simulating prevalent conditions for a sheet of paper of a grammage equal to 80 g/m2 and charged to 20% by weight. The filler retention value then corresponds to the equation Filler retention = Turb. of incoming body - Turb. wire water x 100 Turb. of incoming body where Turb. = turbidity Turb. of incoming body = Turb. of fibre-filler mixture - Turb. of fibre To do this, it is therefore necessary to measure, on the one hand, the turbidity of the fibre-filter mixture and, on the other hand, the turbidity of the fibre alone and the turbidity of the water of the fabric. This latter is measured directly by reading the value of the turbidity indicated by the Nephelometer 155 from Defensor AG (Switzerland) in NTU (Nephelo Turbidity Unit) units, On the other hand, to determine the turbidity of the fibre-filler mixture, a fibre-filler mixture is made from a masterbateh formed by diluting 4 parts of fibres consisting of 80% birch and 20% pine in 10 litres of water. 18.2 dry grams of the fibre masterbateh and 9.8 grams of the dry filler to be tested are added to a device known as a distributor (Rapid-Kothen) and topped up with 5 litres of water. After 15 minutes of stirring and the addition of the quantities indicated in table 1 below, of a retaining agent of the polyacrylamide type marketed under the name Praestof™ PK 422, by Stockhausen, Krefeld, Germany, a mixture that simulates the prevalent conditions for a sheet of paper of grammage equal to 80 g/m2 and charged to 20% by weight is obtained. The mixture thus formed is dried in a vacuum of 0.2 bar for over 2 seconds. The values, at 700 rpm, of filler retentions in the filling, obtained by means of the above equation and as a function of the cationic retaining agent rate of the polyacrylamide type marketed under the name Praestof™ PK 422, by Stockhausen (Germany) are shown in table 1 below. Tabid 0.01% PK 422 0.02% PK 422 0.03% PK 422 0.04% PK 422 0.05% PK 422 5% filler retention 14% filler retention 26% filler retention 29% filler retention 31% filler retention Test No. 24 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 u.m, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 75.8% by weight and having a grain size such that 62% by weight of the particles have a diameter of less than 2 pm, and 32% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™, corresponding to a median diameter equal to 1.57 \im. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 75.8% Viscosity (To) = 175 mPa.s AVAG viscosity fTzdays) = 505 mPa.s APAG viscosity (T7day») = 195 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. The filler retention in the filling is determined using the same procedure and the same equipment as those used in the previous test. The values, at 700 rpm, of filler retentions in the filling, obtained by means of the above equation and as a function of the rate of cationic retaining agent of the polyacrylamide type marketed under the name Praestol™ PK 422, by Stockhausen (Germany) are shown in table 2 below. Table 2 0.01% PK 422 0.02% PK 422 0.03% PK 422 0.04% PK 422 0.05% PK 422 15% filler retention 26% filler retention 38% filler retention 47% filler retention 54% filler retention Tables 1 and 2 point to a better filler retention for the test according to the invention. EXAMPLE 3 This example illustrates, by means of a comparison with identical grain size, how to reduce the cationic polymer demand in the filling by implementing an aqueous suspension of calcium carbonate containing the copolymer used, according to the invention, as a grinding aid agent, for various grinding processes. Test No. 25 This test illustrates the invention and implements, as dispersant before the grinding stage, 0.1% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of an intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, and as a grinding aid agent during the grinding stage, 0.27% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 (im, with the same equipment as in test No. 1, a suspension of ground calcium carbonate having a dry matter concentration equal to 65.0% by weight and having a grain size such that 59% by weight of the particles have a diameter of less than 2 pm, and 34% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph 5100 corresponding to a median diameter equal to 1.58 u.m. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 65.0% Viscosity (To) = 163 mPa.s AVAG viscosity fT? days) = 319 mPa.s APAG viscosity (IVdays)= 185 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand of the calcium carbonate is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 1620 u. Val/kg. It can thus be seen that the cationic polymer demand is lower than that of the prior art for equivalent grain size. Test No. 26 This test illustrates the invention and implements, as a grinding aid agent, 1.8% by dry weight with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, via a two-stage grinding process, a 74.7% by dry matter weight suspension of calcium carbonate with grain size such that 98% by weight of the particles have a diameter of less than 2 pm and 78% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100. This two-stage grinding process consists in grinding, during the first stage, a suspension of calcium carbonate of initial average diameter equal to 5 urn measured using the Sedigraph™ 5100 particle size analyzer in an aqueous suspension of calcium carbonate to a grain size such that 62% by weight of the particles have a diameter of less than 2 pm and 37% by weight of the particles have a diameter of less than 1 pm measured using the Sedigraph™ 5100, then in grinding this suspension until the desired end grain size is obtained. The dry matter concentration (S.C.: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 74.7% Viscosity (To) = 750 mPa.s APAG viscosity (Todays) = 680 mPa.s Once these Brookfield™ viscosity measurements have been made, the specific surface area and the cationic demand of the calcium carbonate are determined using the same method as in test No. 1. This gives a BET specific surface area of the pigment obtained, determined according to standard ISO 9277, equal to 7.5 rtf/g and a PDDPC cationic polymer demand equal to 4140 p. Val/kg. EXAMPLE 4 This example illustrates, by means of a comparison with identical grain size, how to reduce the cationic polymer demand in the filling by implementing an aqueous suspension of various mineral matter containing the copolymer used, according to the invention, as a grinding aid agent. Test No. 27 This test illustrates the invention and implements 0.40% by dry weight, with respect to the dry weight of aluminium trihydroxide, of the copolymer implemented in test No. 6 to obtain, from an aluminium trihydroxide with a median diameter equal to 50 pm, and under the same operating conditions and using the same equipment as in test No. 1, an aqueous suspension of ground aluminium trihydroxide having a dry matter concentration equal to 51.4% by weight and having a grain size such that 48.8% by weight of the particles have a diameter of less than 2 |jm, and 29.4% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100, corresponding to a median diameter equal to 2.00 pm. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 48.8% Viscosity (To) = 62 mPa.s AVAG viscosity {T7 M = 115 mPa.s APAG viscosity (FVdaysj = 95 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 590 u, Val/kg. It can therefore be seen that the cationic polymer demand is low. Test No. 28 This test illustrates the invention and implements 0.40% by weight, with respect to the dry weight of talc, of the copolymer implemented in test No. 6 to obtain, from a talc of median diameter equal to 15.7 pm or with a grain size such that 14% by weight of the particles have a diameter of less than 5 pm, 4% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100 and under the same operating conditions and with the same equipment as in test No. 1, an aqueous suspension of ground talc having a dry matter concentration equal to 28.3% by weight and having a grain size such that 41% by weight of the particles have a diameter of less than 5 pm, and 12% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 6.3 urn The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C = 28.3% Viscosity (To) = 219 mPa.s AVAG viscosity fTVdays) = 415 mPa.s APAG viscosity (T7 days) = 134 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 520 u Val/kg. It can therefore be seen that the cationic polymer demand is low. Test No. 29 This test illustrates the invention and implements 0.40% by weight, with respect to the dry weight of kaolin, of the copolymer implemented in test No. 6 to obtain, from a kaolin of median diameter equal to 0.33 pm or with a grain size such that 92% by weight of the particles have a diameter of less than 0.5 pm, 4% by weight of the particles have a diameter of less than 0.2 m measured on the Sedigraph™ 5100 and under the same operating conditions and with the same equipment as in test N0.1, an aqueous suspension of ground kaolin having a dry matter concentration equal to 15% by weight and having a grain size such that 95% by weight of the particles have a diameter of less than 0.5 pm, and 7% by weight of the particles have a diameter of less than 0.2 pm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 0.30 u,m. The dry matter concentration (S.C: Solid Content) and Brookfield™ viscosity results obtained with the same measuring method as test No. 1 are as follows: S.C. = 15.0% Viscosity (To) = 244 mPa.s AVAG viscosity (T7da»s) = 212 mPa.s APAG viscosity 0W) = 199 mPa.s Once these Brookfield™ viscosity measurements have been made, the cationic demand is determined using the same method as in test No. 1. This gives a PDDPC cationic polymer demand equal to 420 u. Val/kg. It can therefore be seen that the cationic polymer demand is low. EXAMPLE 5 This example illustrates, via measurement of the gloss and by comparison at identical grain size, the stability of the coating colour obtained by implementing an aqueous suspension of calcium carbonate according to the invention. To do this in each of the tests of the example, it is necessary to prepare a coating colour with 68% concentration of dry matter, consisting of: 80 parts by dry weight of the calcium carbonate aqueous suspension to be tested, 5 parts by dry weight of a coarser calcium carbonate slurry, 15 parts of delaminated kaolin 9.5 parts of binder 0.32 parts of carboxymethyl cellulose, 0.6 parts of polyvinyl alcohol 0.15 parts of optical brightener, and 0.4 parts of calcium stearate Once the coating colour is prepared in this manner, its Brookfield™ viscosity is measured using a model DV-II+ Brookfield™ viscometer fitted with the corresponding spindle. The coating colour prepared is then applied to a wood based paper 53 u.m thick and with a grammage equal to 82, using a Combiblades pilot coater from Jagenberg GmbH fitted with a 0.457 mm thick blade. A long dwell time application head is used with a blade angle of 45°. The coating speed is 1000 m/s and the average coating deposited is 11 g/m2 on each surface of the paper. The relative humidity obtained for each paper is of the order of 4.2% to 4.6% weight for weight. The paper thus coated is then calendered using a supercalender with 9 contact zones between the two rollers, marketed by Kleinewefers. The iron calendering diameter is 180 mm and 270 mm with respect to the cotton. The measurement of the 75° TAPPI gloss (standard TAPPI T480 os-78 ) according to Lehmann of the coated and calendered paper, which consists in passing the coated and calendered paper sheet in the laboratory gloss meter (LGDL-05/2 from Lehmann Messtechnik AG, Switzerland) determines the supercalendering. Once this gloss measurement is made, the paper samples are cut into DIN A3 format and are conditioned in an air conditioned room as per standard DIN EN 20187 to determine the 75° DIN gloss values according to standard DIN 54 502, and the 45° DIN gloss values according to standard DIN 54 502. Test No. 30 This test illustrates the prior art and implements a suspension of calcium carbonate of the prior art. To do this, in order to prepare the coating colour to be tested the composition of which is as described above, 22.5 kg of an aqueous suspension, of 78.2% dry matter concentration, of coarser calcium carbonate marketed by Omya under the name Hydrocarb™ 60, and 356.5 kg of an aqueous suspension, with 78.5% dry matter concentration, of finer calcium carbonate marketed by Omya under the name Setacarb™ are mixed in a receptacle containing 20 kg of water and 0.125 kg of a sodium polyacrylate with dry matter concentration equal to 42% and intrinsic viscosity equal to 6.2 ml/g as per the above-mentioned intrinsic viscosity method. Once the calcium carbonates have been mixed, 52.5 kg of a delaminated kaolin marketed by Kaolin International B.V. under the name Amazon™ 88 are added while stirring at average speed. Stirring is continued at average speed for 15 minutes and, following visual verification of whether or not agglomerates are present, stirring is continued until the few agglomerates disappear, or is stopped if there are no agglomerates. 7.5 kg of a 15% aqueous solution of carboxymethyl cellulose previously dissolved for at least 20 minutes at least 90°C and marketed by Noviant under the name CMC Finnfix™ 10 are then added. 8.4 kg of a 25% aqueous solution of polyvinyl alcohol previously dissolved for at least 20 minutes at least 90°C and marketed by Clariant under the name Mowiol™ 4-98 are then added. 28 kg of an 50% by dry weight aqueous dispersion of styrene-butadiene marketed by Dow Europe under the name Dow Latex DL 940 and 38.5 kg of a 50% by dry weight aqueous dispersion of an acrylic ester copolymer marketed by BASF under the name Acronal™ S 360 D are then added as binder. Finally, 1.9 kg of optical brightener in the form of an aqueous derivative of 4,4-diaminostilbene-2,2-disulfonic acid marketed by Bayer under the name Blancophor™ P and 2.8 kg of a 50% concentration by dry weight aqueous dispersion of a calcium stearate sold by Henkel-Nopco AS under the name Nopcote™ C-104 are added. Once these additions are made, stirring is maintained for another 15 minutes. The pH of the coating colour is then checked and brought to a value of approximately 9 by means of a 10% soda solution. The dry matter content of the coating colour is also checked and brought to a value of approximately 68.5% by adding water if necessary. The Brookfield™ viscosity of the coating colour obtained as measured at 32°C using the Brookfield™ DV-II+ model viscometer fitted with the corresponding spindle is equal to 6100 mPa.s at 20 min-1 and 1800 mPa.s at 100 min1. The various gloss measurements are made in accordance with the above-mentioned method and are shown in table 3 following the next test. Test No. 31 This test illustrates the invention and implements the suspension of calcium carbonate of test No. 26 according to the invention. To do this, in order to prepare the coating colour to be tested the composition of which is as described above, 22.5 kg of an aqueous suspension, of 78.2% dry matter concentration, of coarser calcium carbonate marketed by Omya under the name Hydrocarb™ 60, and 375 kg of the aqueous suspension of calcium carbonate of test No. 26 according to the invention, with 74.7% dry matter concentration are mixed in a receptacle containing 20 kg of water and 0.125 kg of a sodium polyacrylate with dry matter concentration equal to 42% and intrinsic viscosity equal to 6.2 ml/g as per the above-mentioned intrinsic viscosity method. Once the calcium carbonates have been mixed, 52.5 kg of a delaminated kaolin marketed by Kaolin International B.V. under the name Amazon™ 88 are added while stirring at average speed. Stirring is continued at average speed for 15 minutes and, following visual verification of whether or not agglomerates are present, stirring is continued until the few agglomerates disappear, or is stopped if there are no agglomerates. 7.5 kg of a 15% aqueous solution of carboxymethyl cellulose previously dissolved for at least 20 minutes at least 90°C and marketed by Noviant under the name CMC Finnfix™ 10 are then added. 8.4 kg of a 25% aqueous solution of polyvinyl alcohol previously dissolved for at least 20 minutes at least 90"C and marketed by Clariant under the name Mowiol™ 4-98 are then added. 28 kg of an 50% by dry weight aqueous dispersion of styrene-butadiene marketed by Dow Europe under the name Dow Latex DL 940 and 38.5 kg of a 50% by dry weight aqueous dispersion of an acrylic ester copolymer marketed by BASF under the name Acronal™ S 360 D are then added as binder. Finally, 1.9 kg of optical brightener in the form of an aqueous derivative of 4,4-diaminostjlbene-2,2-disutfonic acid marketed by Bayer under the name Blancophor™ P and 2.8 kg of a 50% concentration by dry weight aqueous dispersion of a calcium stearate sold by Henkel-Nopco AS under the name Nopcote™ C-104 are added. Once these additions are made, stirring is maintained for another 15 minutes. The pH of the coating colour is then checked and brought to a value of approximately 9 by means of a 10% soda solution. The dry matter content of the coating colour is also checked and brought to a value of approximately 68.5% by adding water if necessary. The Brookfield™ viscosity of the coating colour obtained as measured at 32°C using the Brookfield™ DV-II+ model viscometer fitted with the corresponding spindle is equal to 3600 mPa.s at 20 min1 and 1200 mPa.s at 100 min1. The various gloss measurements are made in accordance with the above-mentioned method and are shown in table 3 below. TABLE 3 Standard Unit Prior art Test No. 32 Invention Test No. 33 ;oated paper 1301 ISO 536 g/m2 102 105 (75*TAPPI) OS gloss TAPPI y» 75 B0 J75°TAPPI)SS gloss TAPPI % 77 82 (75°DIN) OS gloss DIN 54 502 % 46 50 (75*DIN)SS gloss DIN 54 502 * 48 54 [45°DIN) OS gloss DIN 54 502 % 17 23 (45'DIN )SS gloss DIN 54 502 % 19 28 (PPS) 1.0 soft OS roughness ISO 8791-4 |jm 0.610 0.579 [PPS) 1.0 soft SS roughness ISO 8791-4 pm 0.608 D.530 OS = Upper surface (Oberseite) SS = Fabric side or rear side (Siebseite) The table shows that paper coated using coating colours containing aqueous suspensions of calcium carbonate according to the invention have a higher gloss irrespective of the viewing angle and a lower roughness than paper coated with standard coating colours of the prior art. EXAMPLE 6 This example illustrates the use of the aqueous suspension according to the invention in a drying process. Test No. 32 This test illustrates the prior art and implements 0.35% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 15 u.m, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 36.9% by weight and having a grain size such that 73% by weight of the particles have a diameter of lass than 2 pm and 46% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 1.17 u,m. The aqueous suspension obtained is then dried using a dryer such as the Media Slurry Drier MSD 100 from Nara Machinery CO., LTD (Japan). The drying capacity obtained is then equal to 1220 g/h of dry product. Test No. 3? This testrtefrates tfie invention and irnpternenfs G.45% by dry weight, wffh respect to the dry weight of cafci'um carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 15 u,m, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 36.9% by weight and having a grain size such that 74% by weight of the particles have a diameter of less than 2 pm, and 44% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™, corresponding to a median diameter equal to 1.18 pm. The aqueous suspension obtained is then dried using a dryer such as the Media Slurry Drier MSD 100 from Nara Machinery CO., LTD (Japan). The drying capacity obtained is then equal to 1542 g/h of dry product, thus bringing about an increase of 21% in the drying capacity. Test No. 34 This test illustrates the prior art and implements 0.45% by dry weight, with respect to the dry weight of calcium carbonate, of a sodium and magnesium polyacrylate of intrinsic viscosity equal to 7.8 ml/g according to the above-mentioned intrinsic viscosity method, to obtain, from a calcium carbonate with a median diameter of 0.72 u.m, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 33.3% by weight and having a grain size such that 98% by weight of the particles have a diameter of less than 2 pm and 84% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™ 5100 corresponding to a median diameter equal to 0.60 urn The aqueous suspension obtained is then dried using a dryer such as the Media Slurry Drier MSD 100 from Nara Machinery CO., LTD (Japan). The drying capacity obtained is then equal to 1,018 g/h of dry product. Test No. 35 This test illustrates the invention and implements 0.45% by dry weight, with respect to the dry weight of calcium carbonate, of the copolymer implemented in test No. 6 to obtain, from a calcium carbonate with a median diameter of 0.72 urn, an aqueous suspension of ground calcium carbonate having a dry matter concentration equal to 33.3% by weight and having a grain size such that 98% by weight of the particles have a diameter of less than 2 pm, and 81% by weight of the particles have a diameter of less than 1 pm measured on the Sedigraph™, corresponding to a median diameter equal to 0.67 pm. The aqueous suspension obtained is then dried using a dryer such as the Media Slurry Drier MSD 100 from Nara Machinery CO., LTD (Japan). The drying capacity obtained is then equal to 1,093 g/h of dry product, thus bringing about an increase of 7% in the drying capacity. EXAMPLE 7 This example illustrates the use of the dried slurry of calcium carbonate according to the invention in the field of plastics and more particularly in a PVC application, by comparing the dispersion, in a rigid PVC formulation, of a dried slurry of natural calcium carbonate according to the invention and according to the prior art by comparison of the theological behaviour obtained. To do this, for each of the tests of the example, the mixture corresponding to the following formulation, in parts, is prepared, with the exception of test No. 36 which does not contain calcium carbonate: PVC EVAPOLSH 6521 marketed by EVC (Germany) 100 tribasic lead sulphate 1.5 dibasic lead stearate 1.3 calcium stearate 0.6 WaxE 0.05 Calcium carbonate to be tested 30.0 This mixture is prepared in a Papenmeier mixer all 100°C for 10 minutes. The mixtures are then oelated on a rotarjna cylinder at 20 rpm at 170°C in a mixing chamber of the MP Gottfert extrusion meter Version 2.3.0. The theological behaviour is then evaluated by measuring the gelation time of the mixture. Test no. 36 - Control without filler This test is a control test which relates to the above-mentioned formulation but without calcium carbonate. The gelation time obtained is equal to 738 seconds. Test No. 37 This test illustrates the prior art and implements the dried product of test No. 32. The gelation time obtained is equal to 720 seconds for a formulation with 30 parts of filler, i.e. an increase of 2.5% with respect to the filler-free control. Test No. 38 This test illustrates the invention and implements the dried product of test No. 33. The gelation time obtained is equal to 562 seconds for a formulation with 30 parts of filler, i.e. an increase of 23.8% with respect to the filler-free control. These results show that a dry product of the invention can be favourably used in the field of plastics, and more particularly in rigid PVC formulations. We CLAIM 1- An aqueous suspension of refined mineral matter with dry matter concentration that can be high, with low Brookfield™ viscocity that remains stable over time, and having a pigmentary surface area with low ionic charge, characterized in that it contains, as a grinding aid agent, a copolymer consisting of: (a) at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, (b) at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 such that 15 R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of ally! or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), (c) at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (lie) or mixtures thereof: with formula (Ila) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 150, r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyMsopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, R5, R10 and R11 represent hydrogen or the methyl or ethyl radical R6, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lie) where m3, p3, m4 and p4 represent a number of alkylene Oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 150, r' represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, (d) possibly at least one monomer of the acrylamide or methacrylamide type or their derivatives or mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof (e) possibly at least one crosslinking monomer selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, or sucrose the total of the components a), b), c), d) and e) being equal to 100%, and having an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the method known as the intrinsic viscosity method. 2- An aqueous suspension of mineral substances refined as claimed in claim 1 wherein said copolymer consists, by weight, of: (a) from 2% to 95%, preferably from 3% to 25%, and even more preferably from 4% to 15%, of at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, (b) from 97.9% to 4.9%, preferably from 95% to 65%, and even more preferably from 92% to 78%, of at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 such that 15 R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), (c) from 0.1% to 50%, preferably from 0.2% to 10%, and even more preferably from 0.3% to 5%, of at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (Ha) or (lib) or (He) or mixtures thereof: with formula (Ha) qi where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 150, r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Rs, Rio and Rn represent hydrogen or the methyl or ethyl radical R6, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A ti a group m^ck may be p/sseni, ,i? Mfoijty case it represents a hydrocarbon radical having from 1 to 4 carton atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (He) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 150, r' represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, Itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, Ru, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, (d) from 0% to 50%, preferably from 0% to 10%, and even more preferably from 0% to 5%, of at least one monomer of the acrylamide or methacrylamide type or their derivatives or mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof (e) from 0% to 5%, and preferably from 0% to 3%, of at least one crosslinking monomer selected from the group consisting of ethylene glycol dimethacrylat^ trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylarnjde, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, or sucrose the total of the components a), b), c), d) and e) being equal to 100%, and in that said copolymer has an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the method known as the intrinsic viscosity method. 3- An aqueous suspension of mineral matter as claimed in claim 1 or 2, wherein said copolymer is in its acid form, fully neutralized or partially neutralized by one or more neutralizing agents having a monovalent neutralizing function or a polyvalent neutralizing function such as, for the monovalent function, those selected from among the group consisting of the alkaline cations, in particular sodium, potassium, lithium, ammonium or the primary, secondary or tertiary aliphatic and/or cyclic amines such as stearylamine, the ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methylcyclohexylamine, aminomethylpropanol, morpholine or, for the polyvalent function, those selected from among the group consisting of alkaline earth divalent cations, in particular magnesium and calcium, or zinc, and of the trivalent cations, including in particular aluminium, or of certain cations of higher valency. 4- An aqueous suspension of mineral matter as claimed in one of claims 1 to 3, wherein it contains from 0.05% to 10% of said copolymer by dry weight with respect to the dry weight of mineral substances. 5- An aqueous suspension of mineral matter as claimed in one of claims 1 to 3, wherein it contains from 0.05% to 10% of said copolymer by dry weight with respect to the dry weight of mineral substances and at least one other dispersant or grinding aid agent. 6- An aqueous suspension of mineral matter as claimed in claim 5, wherein the other dispersant or grinding aid agent is selected from among the dispersants or grinding aid agents such as the homopolymers or copolymers of acrylic acid in their acid form, or fully or partially neutralized by one or more neutralizing agents having a monovalent neutralizing function or a polyvalent neutralizing function such as, for the monovalent function, those selected from among the group consisting of the alkaline cations, in particular sodium, potassium, lithium, ammonium or the primary, secondary or tertiary aliphatic and/or cyclic amines such as stearylamine, the ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methylcyclohexylamine, aminomethylpropanol, morpholine or, for the polyvalent function, those selected from among the group consisting of alkaline earth divalent cations, in particular magnesium and calcium, or zinc, and of the trivalent cations, including in particular aluminium, or of certain cations of higher valency, or selected from among the dispersants or grinding aid agents such as the H3O ion donors preferably selected from among phosphoric acid and/or its salts with mono and/or divalent bases such as soda and lime. 7- An aqueous suspension of mineral matter as claimed in claim 5 or 6, wherein it contains from 0.05% to 1.0% by dry weight with respect to the dry weight of mineral substances of said other dispersant or grinding aid agent. 8- An aqueous suspension of mineral matter as claimed in one of claims 1 to 7, wherein that the mineral matter is selected from among calcium carbonate, dolomite, gypsum, calcium hydroxide, satin white, titanium dioxide, aluminium trihydroxide, mica, talc, kaolins, calcine kaolins, or mixed carbonate based fillers of various metals such as calcium associated with magnesium, and mixtures of said fillers such as talc-calcium carbonate or calcium carbonate-kaolin mixtures, or mixtures of calcium carbonate with aluminium trihydroxide, or mixtures with synthetic or natural fibres or co-structures of minerals such as talc-calcium carbonate or talc-titanium dioxide co-structures, and is preferably calcium carbonate such as natural calcium carbonate selected from among marble, calcite, chalk or mixtures thereof. 9- An aqueous suspension of mineral matter as claimed in one of claims 1 to 8, wherein the suspension has a dry matter concentration of between 15% and 85% by weight, preferably between 40% and 80%, and very preferably between 50% and 78%. 10- An aqueous suspension of mineral matter as claimed in one of claims 1 to 9, wherein the mineral matter presents a median grain diameter, as measured using the Sedigraph™ 5100, of between 50 u.m and 0.01 u.m, preferably between 5 urn and 02 \im and even more preferably between 2 |.tm and 0.3 urn. 11- An aqueous suspension of mineral matter as claimed in one of claims 1 to 10, wherein the mineral matter grains have, for equivalent grain size, a BET specific surface area determined according to standard ISO 9277 less than that of the mineral matter grains of the aqueous suspensions of mineral matter refined using grinding aid agents such as polyacrylates, homopolymers or copolymers. 12- An aqueous suspension of mineral matter as claimed in one of claims 1 to 11, wherein the pH of the final suspension is between 7.5 and 13, preferably between 8 and 12 and very preferably between 8.5 and 10. 13- A grinding aid agent for mineral matter in aqueous suspension as claimed in claims 1 to 12, characterised in that said agent is a copolymer consisting of: a) at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as C1 to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, (b) at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 such that 15 Ri represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), (c) at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (lla) or (lib) or (lie) or mixtures thereof: with formula (lla) where ml, p1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n 1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 150, r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Rs, R10 and Rn represent hydrogen or the methyl or ethyl radical R6, R7, Rs and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and lo the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, B represents a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lie) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 150, r' represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R14, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, Ri?p R18 and Ro represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, (d) possibly at least one monomer of the acrylamide or methacrylamide type or their derivatives or mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof (e) possibly at least one crosslinking monomer selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, or sucrose the total of the components a), b), c), d) and e) being equal to 100%, and having an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the method known as the intrinsic viscosity method. 14- A grinding aid agent for mineral matter in aqueous suspension as claimed in claim 13, wherein said agent is a copolymer consisting, by weight, of: (a) from 2% to 95%, preferably from 3% to 25%, and even more preferably from 4% to 15%, of at least one ethylenically unsaturated anionic monomer having a monocarboxyl function selected from among the ethylenically unsaturated monomers having a monocarboxyl function such as acrylic or methacrylic acid or hemiesters of diacids such as Ci to C4 monoesters of maleic or itaconic acid, or mixtures thereof, or having a dicarboxyl function selected from among the ethylenically unsaturated monomers having a dicarboxyl function such as crotonic, isocrotonic, cinnamic, itaconic, maleic acid, or anhydrides of carboxyl acids, such as maleic anhydride or having a sulfonic function selected from among the ethylenically unsaturated monomers having a sulfonic function such as acrylamido-methyl-propane-sulfonic acid, sodium methallylsulfonate, vinylsulfonic acid and styrenesulfonic acid or having a phosphoric function selected from among the ethylenically unsaturated monomers having a phosphoric function such as vinylphosphoric acid, ethylene glycol methacrylate phosphate, propylene glycol methacrylate phosphate, ethylene glycol acrylate phosphate, propylene glycol acrylate phosphate and their ethoxylates or having a phosphonic function selected from among the ethylenically unsaturated monomers having a phosphonic function such as vinylphosphonic acid, or mixtures thereof, (b) from 97.9% to 4.9%, preferably from 95% to 65%, and even more preferably from 92% to 78%, of at least one non-ionic ethylenically unsaturated monomer of formula (I): where m and p represent a number of alkylene oxide units less than or equal to 150 n represents a number of ethylene oxide units less than or equal to 150 q represents an integer equal to at least 1 and such that 5 such that 15 R1 represents hydrogen or the methyl or ethyl radical R2 represents hydrogen or the methyl or ethyl radical R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R' represents hydrogen or a hydrocarbon radical having from 1 to 40 carbon atoms, and preferably represents a hydrocarbon radical having from 1 to 12 carbon atoms and even more preferably a hydrocarbon radical having from 1 to 4 carbon atoms, or a mixture of several monomers of formula (I), (c) from 0.1% to 50%, preferably from 0.2% to 10%, and even more preferably from 0.3% to 5%, of at least one organofluorinated or organosilylated monomer, preferably selected from among the molecules of formulae (lla) or (lib) or (He) or mixtures thereof: with formula (lla) where m 1, p 1, m2 and p2 represent a number of alkylene oxide units less than or equal to 150 n1 and n2 represent a number of ethylene oxide units less than or equal to 150 q1 and q2 represent an integer equal to at least 1 and such that 0 150, r represents a number such that 1 R3 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, R4, Rs, R10 and Rn represent hydrogen or the methyl or ethyl radical R6, R?, R8 and R9 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof R12 represents a hydrocarbon radical having from 1 to 40 carbon atoms A and B are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms, with formula (lib) R-A-Si(OB)3 where R represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, A is a group which may be present, in which case it represents a hydrocarbon radical having from 1 to 4 carbon atoms, 8 represents a h^tfrQcarim radfcat ttsnwig from t to 4 carbon atoms, with formula (lie) where m3, p3, m4 and p4 represent a number of alkylene oxide units less than or equal to 150 n3 and n4 represent a number of ethylene Oxide units less than or equal to 150 q3 and q4 represent an integer equal to at least 1 and such that 0 150, r' represents a number such that 1 R13 represents a radical containing a polymerizable unsaturated function, belonging to the vinyl group and to the group of acrylic, methacrylic, maleic, itaconic, crotonic, and vinylphtalic esters and to the group of urethane unsaturates such as acrylurethane, methacrylurethane, a-a' dimethyl-isopropenyl-benzylurethane and allylurethane, and to the group of allyl or vinyl ethers, whether or not substituted, or to the group of ethylenically unsaturated amides or imides, Ru, R15, R20 and R21 represent hydrogen or the methyl or ethyl radical R16, R17, R18 and R19 represent straight or branched alkyl, aryl, alkylaryl or arylalkyl groups having from 1 to 20 carbon atoms, or a mixture thereof D and E are groups which may be present, in which case they represent a hydrocarbon radical having from 1 to 4 carbon atoms (d) from 0% to 50%, preferably from 0% to 10%, and even more preferably from 0% to 5%, of at least one monomer of the acrylamide or methacrylamide type or their derivatives or mixtures thereof such as N-[3-(dimethylamino) propyl] acrylamide or N-[3-(dimethylamino) propyl] methacrylamide, and mixtures thereof, or at least one non water-soluble monomer such as the alkyl acrylates or methacrylates or mixtures thereof, unsaturated esters such as N-[2-(dimethylamino) ethyl] methacrylate, or N-[2-(dimethylamino) ethyl] acrylate or mixtures thereof, vinyls such as vinyl acetate, vinylpyrrolidone, styrene, alphamethylstyrene and their derivatives or mixtures thereof, or at least one cationic monomer or quaternary ammonium such as [2-(methacryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [2-(acryloyloxy) ethyl] trimethyl ammonium chloride or sulphate, [3-(acrylamido) propyl] trimethyl ammonium chloride or sulphate, dimethyl diallyl ammonium chloride or sulphate, [3-(methacrylamido) propyl] trimethyl ammonium chloride or sulphate, or mixtures thereof (e) from 0% to 5%, and preferably from 0% to 3%, of at least one crosslinking monomer selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, allyl acrylate, the allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allyl ethers prepared from polyols such as pentaerythritol, sorbitol, or sucrose the total of the components a), b), c), d) ancj e) being equal to 100%, and having an intrinsic viscosity less than or equal to 100 ml/g determined in accordance with the method known as the intrinsic viscosity method. 15- A grinding aid agent for mineral matter in aqueous suspension as claimed in claims 13 or 14, wherein said agent is a copolymer in its acid form or fully neutralized or partially neutralized by one or more neutralizing agents having a monovalent neutralizing function or a polyvalent neutralizing function such as, for the monovalent function, those selected from among the group consisting of the alkaline cations, in particular sodium, potassium, lithium, ammonium or the primary, secondary or tertiary aliphatic and/or cyclic amines such as stearylamine, the ethanolamines (mono-, di-, triethanolamine), mono and diethylamine, cyclohexylamine, methylcyclohexylamine, aminomethylpropanol, morpholine or, for the polyvalent function, those selected from among the group consisting of alkaline earth divalent cations, in particular magnesium and calcium, or zinc, and of the trivalent cations, including in particular aluminium, or of certain cations of higher valency. 16- A grinding aid agent for mineral matter in aqueous suspension as claimed in claim 15, wherein said copolymer obtained from the copolymerization reaction may, before or after the total or partial neutralization reaction, be treated and separated into several phases, according to statistical or dynamic processes, by one or more polar solvents belonging to the group consisting of water, methanol, ethanol, propanol, isopropanol, butanols, acetone, tetrahydrofurane or mixtures thereof. J7- A process for grinding mineral metier in aqueous suspension as claimed in claim ) to 12 consisting of refining an aqueous suspension of said mineral materials into very fine particles characterized in that use is made, as a grinding aid agent before and/or during the grinding stage, of- 0.05% to 10% by dry weight, with respect to the dry weight of mineral matter, of the copolymer according to any one of claims 16 to 20, and in that use may be made of at least one other dispersant or grinding aid agent before and/or during the grinding stage. 18- A grinding process in aqueous suspension as claimed in claim 17, wherein said other dispersant or grinding aid agent is selected from among the dispersants or grinding aid agents such as homopolymers or copolymers of acrylic acid in their acid forms, or fully or partially neutralized by one or more neutralizing agents or selected from among the dispersants or grinding aid agents such as H30+ ion donors preferably selected from among phosphoric acid and/or its salts with mono and/or divalent bases such as soda or lime. 19- A grinding process in aqueous suspension as claimed in claim 18, wherein use is made of 0.05% to 1.0%, by dry weight with respect to the dry weight of mineral substances, of said other dispersant or grinding aid agent. 20- A grinding process in aqueous suspension as claimed in any of claims 17 to 19 , wherein the temperature during the course of the grinding stage and for all the variants of the grinding process according to the invention is between 15°C and 150°C, preferably between 50°C and 105°C and very preferably between 60°C and 98°C. 21- A grinding process in aqueous suspension as claimed in any one of claims 17 to 20 wherein for mineral matter containing carbonate, the pH during the course of the grinding stage lies between 6 and 13, preferably between 7.5 and 12 and very preferably between 8 and 10. 22- A grinding process in aqueous suspension as claimed in any one of claims 17 to 20, wherein, for mineral matter not containing carbonate, the pH during the course of the grinding stage lies between 2 and 13, preferably between 7.5 and 12 and very preferably between 8 and 10. Dated this 13th Day of April, 2005

Documents:

286-mumnp-2005-cancelled pages(29-09-2006)0064.pdf

286-mumnp-2005-claims(granted)-(29-09-2006).doc

286-mumnp-2005-claims(granted)-(29-09-2006).pdf

286-mumnp-2005-correspondence(21-01-2008).pdf

286-mumnp-2005-correspondence(ipo)-(16-08-2007).pdf

286-mumnp-2005-form 1(15-04-2005).pdf

286-mumnp-2005-form 18(15-04-2005).pdf

286-mumnp-2005-form 2(granted)-(29-09-2006).doc

286-mumnp-2005-form 2(granted)-(29-09-2006).pdf

286-mumnp-2005-form 3(13-04-2005).pdf

286-mumnp-2005-form 3(26-09-2006).pdf

286-mumnp-2005-form 5(13-04-2005).pdf

286-mumnp-2005-form-pct-isa-210(15-04-2005).pdf

286-mumnp-2005-power of attorney(15-04-2005).pdf