Title of Invention

"INDUSTRIAL POLUOLEFIN PIPES(SINGLE-OR MULTILAYER),FITTINGS,VALVES AND VESSELS"

Abstract

Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels with improved stiffness and impact strength for use at high service temperature, comprising single-or multilayer pipes, fittings, valves, chambers and vessels, consisting essentially of a propylene homopolymer with a melt index of 0.05 to 40 g/10 min at 230 °C/2.16 kg, wherein the propylene homopolymer is ß- nucleated and has an IRT ≥0.98, having a tensile modulus ≥1500 MPa, a Charpy impact strength at +23°C of ≥30 kJ/m2, using notched test specimens, a Vicat B temperature >90°C and a heat distortion temperature >100 °C.

Full Text

The present invention relates to industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels. Field of the invention The invention relates to an industrial polyolefin piping system with improved stiffness, impact strength for use at high service temperature, comprising single or multilayer pipes, fittings, valves, chambers and vessels, consisting of a propylene homopolymer, as well as a process for producing them. Background of the invention Pipes, injection molded parts and blow molded parts from propylene polymers are known (Moore, P., Polypropylene Handbook, Hanser Publishers Munich 1996, pp. 303-348). Of disadvantage of propylene polymer moldings from common propylene polymers are the insufficient impact properties of the moldings for industrial applications. Known methods for improving the impact properties are the use of blends comprising propylene polymers and butene polymers for producing pipes (EP 0 972 801), the use of blends comprising propylene polymers and hydrogenated butadiene-isoprene block copolymers for blow molded containers (JP 09,227,707) or the use of blends comprising propylene polymers and thermoplastic elastomers such as styrene-ethylene-butene-block copolymers or propylerie-ethylene-diene terpolymers for producing injection molded parts (DE 199 27 477). These molded articles have good impact properties, of disadvantage is however the reduced stiffness of the articles, Object of the invention It is the object of the present invention to provide an industrial polyolefin piping system with improved stiffness, impact strength for use at high service temperature, comprising pipes, fittings, valves and vessels from propylene polymers. Brief description of the invention According to the present invention, this object is achieved by an industrial polyolefin piping system with improved stiffness and impact strength for use at high service temperature, comprising single- or multilayer pipes, fittings, valves and vessels, consisting essentially of a propylene homopolymer with a melt index of 0.05 to 40 g/10 min at 230 C/2.16 kg, wherein the propylene homopolymer is p-nucleated and has an IRt ≥0.98, having a tensile modulus ≥1500 MPa, a Charpy impact strength at +23 °C of ≥30 kJ/m2, using notched test specimens, a Vicat B temperature ≥90 °C and a heat distortion temperature ≥100 °C. Detailed description of the invention p-nucleated propylene polymers are isotactic propylene polymers composed of chains in a 3i helical conformation having an internal microstructure of B-form spherulites being composed of radial arrays of parallel stacked lamellae. This microstructure can be realized by the addition of fi-nucleating agents to the melt and crystallization. The presence of the 6-form can be detected through the use of wide angle X-ray diffraction (Moore, J., Polypropylene Handbook, p. 134-135, Manser Publishers Munich 1996). The IRr of the propylene polymers is measured and calculated as described in EP 0 277 514 A2 on page 5 (column 7, line 53 to column 8, line 11). According to a preferred embodiment the p-nucleated propylene homopolymers have an IRt of SO.985. The difference of 0.005 in IR-c, IRt being a measure for isotacticity, encompasses a significant increase in mechanical polymer properties, especially in stiffness. According to a preferred embodiment of the invention the li-nucleated propylene polymers used for producing the industrial piping system have a melt index of 0.05 to 15 g/10min at 230 "C/2.16 kg, more preferably 0.1 to 8 g/10 min at 230 "C/2.16 kg, most preferably 0.2 to 5g/10minat230'C/2.16kg. For single- or multilayer pipe fabrication by extrusion propylene homopolymers with a melt index of 0.05 to 40 g/10 min at 230 "C/2.16 kg, preferably 0.05 to 15g/min at 230°C/216kg are particularly suitable. For producing fittings and valves by injection molding propylene homopolymers with a melt index of 0.05 to 40 g/10 min at 230 "C/2.16 kg are particularly suitable. For vessel fabrication by blow molding a propylene homopolymer with a melt index of 0.05 to 20 g/10 min at 230 "/2.16 kg are particularly suitable. The propylene homopolymers used for producing the industrial piping system show a Charpy impact strength of ≥30 kJ/m2, preferably >50 kJ/m2, most preferably ≥70 kJ/m2 at + 23 "C. According to an advantageous feature of the present invention, the fi-nucleated propylene polymers with an IRt so.98 of the industrial polyolefin piping system are propylene polymers obtained by polymerization with a Ziegler-Natta catalyst system comprising titanium-containing solid components, an organoalumina, magnesium or titanium compound as cocatalyst and an external donor according to the formula wherein R and R' are identical or different and are branched or cyclic aliphatic or aromatic hydrocarbon residues, and y and x independently from each other are 0 or 1, provided that x + y are 1 or 2. A preferred external donor in the Ziegler-Natta catalyst system for producing the propylene polymers for the industrial polyolefin piping system is dicyclopentyldimethoxysilane. According to a preferred embodiment of the present invention the fi-nucleated propylene polymers of the industrial polyolefin piping system contain 0.01 to 2.0 wt%, based on the polypropylene used, - dicarboxylic acid derivative type diamide compounds from C5-CB-cycloalkyl monoamines or C6-Cirarornatic monoamines and C5-C8-aliphatic, C5-C8- cycloaliphatic or C6-Ciraromatic dicarboxylic acids, and/or - diamine derivative type diamide compounds from C5-C8-cycloalkyl monocarboxylic acids or C6-C,2-aromatic monocarboxylic acids and C5-CB-cycloaliphatic or C6-C12- aromatic diamines, and/or amino acid derivative type diamide compounds from amidation reaction of C5-C8-alkyl, C6-C12--cycloalkyl- or C6-C12-arylamino acids, C5-C8-alkyl-, C5-C8-cycloalkyl- or C6-C12-aromatic monocarboxylic acid chlorides and C5-C8-alkyl-, C5-C8-cycloalkyl-or C6-Ci2-aromatic mono-amines, as B-nucleating agent. Examples of the dicarboxylic acid derivative type diamide compounds from C5-C8-cycloalkyl monoamines or C6-C12-raromatic monoamines and C5-C8-aliphatic, C5-C8-cycloaliphatic or C6-Ci2-aromatic dicarboxylic acids, optionally contained in the fi-nucleated propylene polymers of the industrial polyolefin piping system, are N,N'-di-C5-Ce-cycloalkyl-2,6-naphthalene dicarboxamide compounds such as N,N'-dicyclohexyi-2,6-naphthalene dicarboxamide and N,N'-dicyclooctyl-2,6-naphtha!ene dicarboxamide, - N,N'-di-C5-Crcycloalkyl-4,4-biphenyldicarboxarnide compounds such as N,N'-dicyclohexyl-4,4-biphenyldicarboxamide and N,N'-dicyclopentyl-4,4-biphenyldicarboxamide, N,N'-di-Cs-C8-cycloalkyl-terephthalamide compounds such as N,N'-dicydohexylterephthalamide and N.N'-dicyclopentylterephthalamide, - N, N'-di-Cs-Ce-cycloalkyl-1,4- cyclohexanedicarboxamide compounds such as N,N'-dicyclo-hexyl-1,4-cyclohexanedicarboxamide and N,N'-dicyclohexyl-1,4-cyclopentanedicarboxamide. Examples of the diamine derivative type diamide compounds from C5-C8-cycloalkyl-mono-carboxylic acids or C6-C12--aromatic monocarboxylic acids and C5-C8-cycloaliphatic or C6-Ci2-aromatic diamines, optionally contained in the industrial polyolefin piping system, are N,N'-C6-C12-arylerie-bis-benzamide compounds such as N,N'-p-phenylene-bis-benzamide and N,N'-1,5-naphthalene-bis-benzamide, N,N'-Cs-Ca-cycloalkyl-bis-benzamide compounds such as N,N'-1,4-cyclopentane-bis-benzamide and N,N'-1,4-cyclohexane-bis-benzamide, - N,N'-p-C6-C12-arylene-bis-C5-C8-cycloalkylcarboxamide compounds such as N,N'-1,5-naphthalene-bis-cyclohexanecarboxamide and N, N'-1,4-pheny!ene-bis-cyclohexanecarboxamide, and - N,N'-C5-Crcycloalkyl-bis-cyclohexanecarboxamide compounds such as N,N'-1,4-cyclopentane-bis-cyclohexanecarboxamide and N,N'-1,4-cyciohexane-bis-cyclohexanecarboxamide. Examples of the amino acid derivative type diamide compounds, optionally contained in the p-nucleated propylene polymers of the industrial polyolefin piping system, are N-phenyl-5-(N-benzoylamino)pentaneamide and/or N-cyclohexyl-4-(N-cyclohexyl-carbonylamino)benzamide. According to a further advantageous embodiment of the present invention the p-nucleated propylene polymers of the industrial polyolefin piping system contain 0.0001 to 2.0 wt%, based on the polypropylene used, quinacridone type compounds, preferably quinacridone, dimethylquinacridone and/or dimethoxyquinacridone; quinacridonequinone type compounds, preferably quinacridonequinone, a mixed crystal of 5,12-dihydro(2,3b)acridine-7,14-dione with quino(2,3b)acridine-6,7,13,14-(5H,12H)-tetrone as disclosed in EP-B0177961 and/or dimethoxyquinacridonequinone; and/or dihydroquinacridone type compounds, preferably dihydroquinacridone, dimethoxydihydroquinacridone and/or dibenzodihydroquinacridone, as p-nucleating agent. According to a further advantageous embodiment of the present invention the p-nucleated propyiene polymers of the industrial polyolefin piping system contain 0.01 to 2.0 wt%, based on the polypropylene used, dicarboxylic acid salts of metals from group Ha of periodic system, preferably pimelic acid calcium salt and/or suberic acid calcium salt; and/or mixtures of dicarboxylic acids and salts of metals from group Ha of periodic system, as p-nucleating agent. According to a further advantageous embodiment of the present invention the p-nucleated propylene polymers of the industrial polyolefin piping system contain 0.01 to 2.0 wt%, based on the polypropylene used, salts of metals from group lla of periodic system and imido acids of the formula wherein x = 1 to 4; R = H, -COOH, d-dz-alkyl, C5-C8-cycloalkyl or C6-C12-aryl, and Y = d-dz-alkyl, C5-Ce-cycloalkyl or C6-C12-aryl - substituted bivalent C6-d2-aromatic residues, preferably calcium salts of phthaloylglycine, hexahydrophthaloylglycine, N-phthaloylalanine and/or N-4-methylphthaloylglycine, as fi-nucleating agent. Preferably the fi-nucleated propylene polymers of the industrial piping system are propylene polymers produced by melt mixing propylene homopolymers with 0.0001 to 2.0 % by weight, based on the polypropylenes used, ft-nucleating agents at temperatures from 175 to 250 °C. The propylene polymers used for the inventive industrial polyolefm piping system articles may contain usual auxiliary materials, e.g. 0.01 to 2.5 wt% stabilizers and/or 0.01 to 1 wt% processing aids and/or 0.1 to 1 wt% antistatic agents and/or 0.2 to 3 wt% pigments, in each case based on the propylene polymers used. As stabilizers preferably mixtures of 0.01 to 0.6 wt% of phenolic antioxidants, 0.01 to 0.6 wt% of 3-arylbenzofuranones, 0.01 to 0.6 wt% of processing stabilizers based on phosphites, 0.01 to 0.6 wt% of high temperature stabilizers based on disulfides and thioethers and/or 0.01 to 0.8 wt% of sterically hindered amines (HALS) are suitable. A further object of the invention is a process for producing an industrial polyolefin piping system with improved stiffness, impact strength for use at high service temperature, comprising single- or multilayer pipe fabrication by extrusion of a propylene homopolymer with a melt index of 0.05 to 40 g/10 min at 230 "C/2.16 kg at a melt temperature of 195 to 250 °C, fitting and valve fabrication by injection molding of a propylene homopolymer with a melt index of 0.05 to 40 g/10 min at 230 "C/2.16 kg at a melt temperature of 220 to 290 "C, and vessel fabrication by blow molding of a propylene homopolymer with a melt index of 0.05 to 20 g/10 min at 230 "C/2.16 kg at a melt temperature of 185 to 230 "C, characterized in that the propylene homopolymers used are (3-nucleated propylene homopolymers with an IRt aO.98 having a tensile modulus >1500 MPa, a Charpy impact strength at +23 °C > 30 kJ/m2 using notched test specimens, a Vicat B temperature >90 °C and a heat distortion temperature >100 °C. In the inventive production of industrial polyolefin piping system articles, the extruders for producing the polyolefin pipes can be single screw extruders with an L/D of 20 to 40 or twin screw extruders or extruder cascades of homogenizing extruders (single screw or twin screw). Optionally, a melt pump and/or a static mixer can be used additionally between the extruder and the ring die head. Ring shaped dies with diameters ranging from approximately 16 to 2000 mm and even grater are possible. Advantageous die temperatures for discharging the melt are 180 to 240 °C. After leaving the ring-shaped die, the pipes are taken off over a calibrating sleeve and cooled. Preferably, for the production of injection molded parts of the inventive process for producing an industrial polyolefin piping system, injection molding machines with injection zones are used, which have three-zone screws with a screw length of 18 to 24 D. Preferred mass temperatures for the melt are 240 to 270 °C and temperatures for the injection molds are 20 to 50 "C. Suitable methods for producing the blow-molded articles of the industrial polyolefin piping system are extrusion blow molding, extrusion stretch blow molding, injection blow molding and injection stretch blow molding. The polyolefin mixtures are extruded through annular dies as a tubular parison, molded into a hollow object by being blown into a divided blowing mold, kept at a temperature of 10 to 55 °C and optionally to an additional longitudinal stretching by a stretching stamp and to further radial stretching by blown air. In a second variation, the mixture is injected into an injection mold, heated to 20 to 130 °C to produce the parison, and, after being removed and optionally preferably separate heating of the parison in a conditioning mold to temperatures of 80 to 160 °C, especially with a first premolding by blowing, transferred into a blowing mold, and by blowing molded into the hollow body, optionally preferably with additional longitudinal stretching by a stretching stamp. Preferred applications of industrial polyolefin piping system are chemical plant constructions comprising single- or multilayer pipes, fittings, valves, chambers and vessels with improved stiffness, impact strength and high service temperature for conveyance of fluids. The special benefits of the construction parts of the inventive industrial polyolefin piping system are tailor made parts depending on the requirements of service temperatures, conveyed chemical substances and safety aspects. Examples The following tests were made using injection molded test specimen prepared according to ISO 1873 Tensile modulus according to ISO 527 (cross head speed 1 mm/min) at +23 °C Charpy impact strength, using notched test specimens according to ISO 179/1eA at +23 °C Vicat B temperature according to ISO 306 Heat distortion temperature according to ISO 75 Method B Example 1 1.1 Preparation of the fi-nucleated propylene polymer A mixture of 94 wt% of a propylene homopolymer, obtained by bulk polymerization using a Ziegler- Natta catalyst system with dicyclopentyldimethoxysilane as external donor, having an IR-t of 0.985, and a melt index of 0.2 g/10 rnin at 230 "C/2.16 kg , 6 wt% of a master batch comprising 98.8 parts by weight of a propylene block copolymer having an ethylene content of 8.3 % by weight, an IRt of the propylene homopolymer block of 0.985, and a melt index of 0.30 g/10 min at 230 °C/2.16 kg, and 0.2 parts by weight of a mixed crystal of 5,12-dihydro(2,3b)acridine-7,14-dione with quino(2,3b)acridine-6,7,13,14-(5H,12H)-tetrone, and 0.05 wt% calcium stearate, 0.1 wt% tetrakis[methylene(3,5-di-t- butylhydroxyhydrocinnamate)] methane and 0.1 wt% tris-(2,4-di-t-butyl-phenyl)-phosphite, based on the sum of the propylene polymers used, is melted in a twin screw extruder with a temperature profile of 100/145/190/215/225/230/230/215/205/190 °C, homogenized, discharged and pelletized. The resulting polypropylene polymer has a melt index of 0.22 g/10 min at 230 "C/2.16 kg, a tensile modulus of 1600MPa and a Charpy impact strength, using notched test specimens, of 100 kJ/m2 at +23 °C. 1.2 Manufacture of the polyolefin pipe for the industrial polyolefin piping system For producing the propylene polymer pipe for the industrial polyolefin piping system, the p-nucleated propylene polymer of 1.1 is introduced in a single screw extruder (L/D=30, D=70mm, temperature profile 200/210/220/220/220/220/200 °C, 40 rpm), melted, extruded through a ring shaped die with a diameter of 110 mm, taken off over a vacuum calibrating sleeve as a pipe of a diameter of 110 mm and a wall thickness of 10 mm, and cooled in a 6 m water bath at 20 °C, the taking off velocity being 0.5 m/min. Milled test pieces have a Vicat B temperature of 92 °C and a Heat Distortion Temperature of 110°C. Example 2 2.1 Preparation of the p-nucleated propylene polymer A mixture of 94 wt% of a propylene homopolymer, obtained by bulk polymerization using a Ziegler-Natta catalyst system with dicyclopentyldimethoxysilane as external donor, having an IFh of 0.985, and a melt index of 8.0 g/10 min at 230 "C/2.16 kg, 6 wt% of a master batch comprising 98.8 parts by weight of a propylene homopolymer having an IRt of 0.987, a melt index of 8.0 g/10 min at 230 "C/2.16 kg, and 0.2 parts by weight of a mixed crystal of 5,12-dihydro(2,3b)acridine-7,14-dione with quino(2,3b)acridine-6,7,13,14-(5H,12H)-tetrone and 0.05 wt% calcium stearate, 0.1 wt% tetrakis[methylene(3,5-di-t-butylhydroxyhydrocinnamate)] methane and 0.1 wt% tris-(2,4-di-t-butyl-phenyl)-phosphite, based on the sum of the propylene polymers used, is melted in a twin screw extruder with a temperature profile of 100/145/190/215/225/230/230/215/205/190 °C, homogenized, discharged and pelletized. The resulting polypropylene polymer has a melt index of 8.2 g/10 min at 230 "C/2.16 kg, a tensile modulus of 1800MPa and a Charpy impact strength, notched, of 88 kJ/m2at +23 °C. 2.2 Manufacture of the injection molded polyolefin pipe fitting for the industrial polyolefin piping system The p-nucleated propylene polymer as described in 2.1 is processed in a injection molding machine, which has a three-zone screw with a screw length of 22 D, at a mass temperature of 220 °C and a mold temperature of 50 °C into a pipe fitting having a diameter of 60 mm, a wall thickness of 4 mm and a length of 92 mm . Milled test pieces have a Vicat B temperature of 91 °C and a heat distortion temperature of 102 °C. Example 3 3.1 Preparation of the p-nucleated propylene polymer A mixture of 75 wt% of a propylene homopolymer obtained by bulk polymerization using a Ziegler-Natta catalyst system with dicyclopentyldimethoxysilane as external donor, having an IRi of 0.985 and a melt index of 2.8 g/10 min at 230 "C/2.16 kg, 25 wt% of a master batch comprising 99.5 parts by weight of a propylene homopolymer obtained by bulk polymerization using a Ziegler-Natta catalyst system with dicyclopentyldimethoxysilane as external donor, having an IRt of 0.987 and a melt index of 13 g/10 min at 230 °C/2.16 kg, and 0.5 parts by weight of hexahydrophthaloylglycine calcium salt, and 0.1 wt% calcium stearate, 0.1 wt% tetrakis[methylene(3,5-di-t-butylhy-droxyhydrocinnamate)] methane and 0.1 wt% tris-(2,4-di-t-butylphenyl)phosphite, based on the sum of the propylene polymers used, is melted in a twin screw extruder with a temperature profile of 100/145/185/210/220/225/225/200/185 °C, homogenized, discharged and pelletized.The resulting polypropylene polymer has a melt index of 3.8 g/10 min at 230 °C/2.16 kg, a tensile modulus of 1700MPa and a Charpy impact strength, using notched test specimens, of 50 kJ/m2 at +23 CC. 3.2 Manufacture of the test container with rectangular base for the industrial polyolefin piping system An injection stretch blowing equipment comprising a plasticizing unit with a three-zone screw, a turning table with a quadruple injection mold, a conditioning mold with three heating zones, a blowing mold with a stretching stamp and ejection equipment, the p-nucleated propylene polymer of 3.1 is melted in the plasticizing unit at a temperature profile of 100/150/200/225/215 °C and injected into the quadruple injection mold, which had been heated to 110 °C. The parison, weighing 30 g and having a wall thickness of 4.6 to 5.5 mm and a height of 96 mm, is taken by the sleeve of the turning table from the injection mold and brought by a swiveling motion of 90° of the turning table into the electrically heated conditioning mold, the heating zones of which are adjusted to a temperature of 131 °C (bottom of the container parison), of 134 °C (center part of the container parison) and of 131 °C (upper part of the container parison). After a conditioning period of 85 seconds, preblow-molding by compressed air is followed by removal of the blow-molded preform and transfer by means of the sleeve of the turning table by the swiveling motion of the turning table through 90° into the blowing mold, where the blow-molded preform initially is subjected to longitudinal stretching by the stretching stamp and subsequently molded by compressed air at a pressure of 20 bar. The longitudinal stretching of the preform in the blowing mold is 2.8 : 1 and the radial stretching of the preform is 2.0 : 1. After 8.0 seconds, the blow-molded control container with rectangular base is removed from the open blowing mold, supplied by the swiveling motion of the turning table through 90° to the ejector and ejected. To determine Vicat B temperature, test pieces were milled after the container shell was cut open. Vicat test results in a Vicat B temperature of 93 °C. A heat distortion temperature of 104 °C was determined. Example 4 4.1 Preparation of the p-nucleated propylene polymer A mixture of 95 wt% of a propylene homopolymer, obtained by bulk polymerization using a Ziegler-Natta catalyst system with dicyclopentyldimethoxysilane as external donor, having an IRi of 0.986 and a melt index of 0.2 g/10 min at 230 °C/2.16 kg, 5 wt% of a master batch comprising 97.5 parts by weight of a propylene homopolymer having an IRi of 0.987 and a melt index of 4.2 g/10 min at 230 CC/2.16 kg , and 2.5 parts by weight of N,N'-dicyclohexyl-2,6-naphthalenedicarboxamide, and 0.05 wt% calcium stearate, 0.1 wt% tetrakis[methylene(3,5-di-t-butylhydroxyhydrocinnamate)]methane and 0.1 wt% tris-(2,4-di-t-buty!phenyl)-phosphite, based on the sum of the propylene polymers used, is melted in a twin screw extruder with a temperature profile of 100/145/190/215/225/225/225/205/190 °C, homogenized, discharged and pelletized. The resulting polypropylene polymer has a melt index of 0.28 g/10 min at 230 "C/2.16 kg , a tensile modulus of 1750MPa and a Charpy impact strength, using notched tes specimens, of 90 kJ/m2 4.2 Manufacture of the polyolefin pipe for the industrial polyolefin piping system For producing the propylene polymer pipe for the industrial polyolefin piping system, the p-nucleated propylene polymer of 4.1 is introduced in a single screw extruder (L/D=30, D=70mm, temperature profile 200/210/220/220/220/220/200 °C, 40 rpm), melted, extruded through a ring shaped die with a diameter of 110 mm, taken off over a vacuum calibrating sleeve as a pipe of a diameter of 110 mm and a wall thickness of 10 mm, and cooled in a 6 m water bath at 20 °C, the taking off velocity being 0.5 m/min. Vicat B temperature was 95 °C and Heat Distortion Temperature was 114 °C. WE CLAIM 1. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels with improved stiffness and impact strength for use at high service temperature, comprising single-or multilayer pipes, fittings, valves, chambers and vessels, consisting essentially of a propylene homopolymer with a melt index of 0.05 to 40 g/10 min at 230 "C/2.16 kg, wherein the propylene homopolymer is 6- nucleated and has an IRT ≥0.98, having a tensile modulus ≥1500 MPa, a Charpy impact strength at +23°C of ≥30 kJ/m2, using notched test specimens, a Vicat B temperature >90°C and a heat distortion temperature >100 °C. 2. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in claim 1, comprising a propylene homopolymer with a melt index of 0.05 to 15 g/10 min at 230 °C/2.16 kg. 3. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in one of the claims 1 or 2, wherein the ß-nucleated propylene polymers with an IRT ≥0.98 are propylene polymers obtained by polymerization with a Ziegler-Natta catalyst system comprising titanium-containing solid components, an organoaluminum, magnesium or titanium compound as catalyst and an external donor dicyclopentyldimethoxysilane. 4. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in one of claims 1 to 3, wherein the ß-nucleated propylene polymer contains 0.0001 to 2.0 wt%, based on the polypropylene used, -dicarboxylic acid derivative type diamide compounds from C5-C8-cycloalkyl monoamines or C6-C12-aromatic monoamines and C5-C8-aliphatic, C5-C8-cycloaliphatic or C6-C12 aromatic dicarboxylic acids, and/or - diamine derivative type diamide compounds from C5-C8-cycloalkyl monocarboxylic acids or C6-C12-aromatic monocarboxylic acids and Cs-Cs- cycloaliphatic or C6-C12-aromatic diamines, and/or - amino acid derivative type diamide compounds from amidation reaction of C5-C8-alkyl-, C5-C8-cycloalkyl- or C6-C12-arylamino acids, C5-C8-alkyl-, C5-C8-cycloalkyl-or C6-C12- aromatic monocarboxylic acid chlorides and C5-C8- alkyl-, C5-C8-cycloalkyl-or C6-C12- aromatic monoamines, as ß-nucleating agent. 5. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in one of the claims 1 to 3, wherein the ß-nucleated propylene polymer contains 0.0001 to 2.0 wt%, based on the polypropylene used, quinacridone type compounds, preferably quinacridone, dimethylquinacridone and/or dimethoxyquinacridone; quinacridonequinone type compounds, preferably quinacridonequinone, a mixed crystal of 5,12- dihydro (2,3b) acridine-7,14-dione with quino (2,3b) acridine-6,7,13,14- (5H, 12H)-tetrone and/or dimethoxyquinacridonequinone; and/or dihydroquinacridone type compounds, preferably dihydroquinacridone, dimethoxydihydroquinacridone and/or dibenzodihydroquinacridone, as ß- nucleating agent. 6. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in one of the claims 1 to 3, wherein the ß-nucleated propylene polymer contains 0.01 to 2.0 wt%, based on the polypropylene used, dicarboxylic acid salts of metals from group IIa of periodic system, preferably pimelic acid calcium salt and/or suberic acid calcium salt ; and/or mixtures of dicarboxylic acids and salts of metals from group Ila of periodic system, as ß-nucleating agent. 7. Industrial polyolefin pipes (single-or multilayer), fittings, valves and vessels as claimed in one of the claims 1 to 3, wherein the ß-nucleated propylene polymer contains 0.01 to 2.0 wt%, based on the polypropylene used, salts of metals from group IIa of periodic system and imido acids of the formula (Formula Removed) wherein x = 1 to 4; R = H, -COOH, C1-C12-alkyl, C5-C8-cycloalkyl or C6-C12- aryl, and Y= C6-C12-alkyl, C5-C8-cycloalkyl or C6-C12-aryl - substituted bivalent C6-C12 -aromatic residues, preferably calcium salts of phthaloylglycine, hexahydrophthaloylglycine, N-phthaloylalanine and/or N- 4-methylphthaloylglycine, as ß-nucleating agent.

Documents:

1966-DELNP-2003-Abstract (23-01-2009).pdf

1966-DELNP-2003-Abstract-(26-12-2008).pdf

1966-DELNP-2003-Abstract-02-05-2008.pdf

1966-delnp-2003-abstract.pdf

1966-DELNP-2003-Claims (23-01-2009).pdf

1966-DELNP-2003-Claims-(26-12-2008).pdf

1966-DELNP-2003-Claims-02-05-2008.pdf

1966-delnp-2003-claims.pdf

1966-delnp-2003-complete specification (granted).pdf

1966-DELNP-2003-Correspondence-Others-(26-12-2008).pdf

1966-DELNP-2003-Correspondence-Others-02-05-2008.pdf

1966-delnp-2003-correspondence-others.pdf

1966-delnp-2003-description (complete)-(23-01-2009).pdf

1966-delnp-2003-description (complete)-02-05-2008.pdf

1966-delnp-2003-description (complete).pdf

1966-DELNP-2003-Form-1-(23-01-2009).pdf

1966-delnp-2003-form-1.pdf

1966-delnp-2003-form-18.pdf

1966-DELNP-2003-Form-2-(23-01-2009).pdf

1966-DELNP-2003-Form-2-(26-12-2008).pdf

1966-delnp-2003-form-2.pdf

1966-DELNP-2003-Form-3-02-05-2008.pdf

1966-delnp-2003-form-3.pdf

1966-DELNP-2003-Form-5-(26-12-2008).pdf

1966-DELNP-2003-GPA-02-05-2008.pdf

1966-delnp-2003-gpa.pdf

1966-delnp-2003-pct-210..pdf

1966-delnp-2003-pct-409.pdf

1966-DELNP-2003-Petition-137-02-05-2008.pdf