Title of Invention	"A BLEACH DETERGENT COMPOSITION"
Abstract	A bleach detergent composition comprising a bleach agent, and a complexed polyamine which comprises a modified polyamine and an anionic species capable of forming a complex with the modified polyamine. The modified polyamine is especially useful as a cotton soil release and dispersant agent. The complexed polyamine is substantially non-reactive with the bleach agent in a wash solution containing the bleach detergent composition. The invention also relates to a process for preparing a bleach detergent composition that contains a bleach agent and a complexed polyamine which is substantially non-reactive with the bleach agent in the wash solution.

Title of Invention

"A BLEACH DETERGENT COMPOSITION"

Abstract

A bleach detergent composition comprising a bleach agent, and a complexed polyamine which comprises a modified polyamine and an anionic species capable of forming a complex with the modified polyamine. The modified polyamine is especially useful as a cotton soil release and dispersant agent. The complexed polyamine is substantially non-reactive with the bleach agent in a wash solution containing the bleach detergent composition. The invention also relates to a process for preparing a bleach detergent composition that contains a bleach agent and a complexed polyamine which is substantially non-reactive with the bleach agent in the wash solution.

Full Text	BLEACH DETERGENT COMPOSITIONS CONTAINING MODIFIED POLYAMINE POLYMERS FIELD OF THE INVENTION The present invention relates to a bleach detergent composition that contains a modified polyamine especially useful as a cotton soil release and dispersant agent, and to processes for making. BACKGROUND OF THE INVENTION Various fabric surface modifying agents have been commercialized and are currently used in detergent compositions and fabric softener/antistatic articles and compositions. Examples of surface modifying agents are soil release polymers. Soil release polymers typically comprise an oligomeric or polymeric ester "backbone" and are generally very effective on polyester or other synthetic fabrics where the grease or similar hydrophobic stains form an attached film and are not easily removed in an aqueous laundering process. The soil release polymers have a less dramatic effect on "blended" fabrics, that is, on fabrics that comprise a mixture of cotton and synthetic material, and have little or no effect on cotton articles. Alkoxylated polyamines are heretofore known and have been shown to provide specific cleaning benefits. Examples of alkoxylated polyamines are disclosed in U.S. Patent 4,548,744, Connor, issued October 22, 1985. However, it has been surprisingly discovered that effective soil release agents for cotton articles and dispersants can be prepared from certain modified polyamines. This unexpected result has yielded compositions that can provide soil release benefits for cotton articles that were once available only on synthetic and synthetic-cotton blended fabric. Typically, if bleaching agents are present, especially peroxygen bleaches which are formulated into both liquid and granular laundry detergent compositions, the formulator must consider the instability of a particular soil dispersant toward the bleach. Many successful dispersents have polyalkyleneamine or polyalkyleneimine backbones which are susceptible to oxidation at the amine functionalities and potentially to breakdown or fragmentation by bleaching agents which may be present. From another view, the interaction of bleaching agents with these polyalkyleneimine-based dispersents depletes the amount of bleach present, therefore affecting the bleaching performance. Accordingly, there remains a need in the art for bleach compatible, highly effective hydrophobic soil dispersents. Surprisingly, it has been found that certain higher molecular weight polyalkyleneimines when complexed with an anionic species, particularly when complexed at a pH of from about pH 5 to about pH 10, are compatible with a bleach agent in the bleach detergent composition, and additionally provide hydrophobic soil dispersion. SUMMARY OF THE INVENTION The present invention is a bleach detergent composition that comprises a bleach agent, and a complexed polyamine which comprises a modified polyamine and an anionic species capable of forming a complex with the modified polyamine. The modified polyamine is especially useful as a cotton soil release and dispersant agent. The complexed polyamine is less reactive with the bleach agent in a wash solution containing the bleach detergent composition. The invention also relates to a process for preparing a bleach detergent composition that contains a bleach agent and a complexed polyamine which is substantially non-reactive with the bleach agent in the wash solution. The bleach detergent composition more particularly comprises a peroxygen bleach agent, a complexed polyamine comprising a modified polyamine and an anionic agent capable of forming a complex with the modified polyamine, and adjunct detergent ingredients. The process of the present invention more particularly comprises the steps of pre-mixing a modified polyamine with an anionic agent, preferably an anionic detersive surfactant, to form a complexed polyamine, and thereafter, adding adjunct detergent ingredients, such as builders and water to form the bleach detergent composition. All documents cited herein are incorporated herein by reference. All percentages and proportions are on a weight basis unless otherwise indicated. DETAILED DESCRIPTION OF THE INVENTION The bleach detergent composition preferably comprises: a) at least about 0.01 % to about 95%, preferably from about 0.1% to about 60%, more preferably from about 0.1% to about 30% by weight, of a detergent surfactant selected from the group consisting of anionic, nonionic, cationic, zwitterionic, and ampholytic surfactants, and mixtures thereof; b) from about 0.05% to about 30%, more preferably from about 0.5% to about 30%, most preferably from about 1% to about 20%, by weight, of a bleach agent; c) from about 0.01 to about 10% by weight, of a complexed polyamine, the complexed polyamine comprising a water-soluble alkoxylated polyamine and an anionic detersive surfactant; and d) adjunct ingredients selected from the group consisting of builders, optical brighteners, soil release polymers, dye transfer agents, dispersents, enzymes, suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes, enzymes, photoactivators, fluorescers, fabric conditioners, hydrolyzable surfactants, preservatives, anti-oxidants, chelants, stabilizers, anti-shrinkage agents, anti-wrinkle agents, germicides, fungicides, and corrosion agents, and mixtures thereof. The Bleach Agent The bleaching agent preferably is a peroxygen bleaching compound which is capable of yielding hydrogen peroxide in an aqueous liquor. These compounds are well known in the art and include hydrogen peroxide and the alkali metal peroxides, organic peroxide bleaching compounds such as urea peroxide, and inorganic persalt bleaching compounds, such as the alkali metal perborates, percarbonates, perphosphates, and the like. Mixtures of two or more such bleaching compounds can also be used, if desired. Preferred peroxygen bleaching compounds include sodium perborate, commercially available in the form of mono-, tri-, and tetra-hydrate, sodium pyrophosphate peroxyhydrate, urea peroxy-hydrate, sodium peroxide, peroxyphthalate and sodium percarbonate. Particularly preferred are sodium perborate tetrahydrate, sodium perborate monohydrate and sodium percarbonate. Sodium percarbonate is especially preferred because it is very stable during storage and yet still dissolves very quickly in the bleaching liquor. It is believed that such rapid dissolution results in the formation of higher levels of percarboxylic acid and, thus, enhanced surface bleaching performance. Another category of bleaching agent that can be used without restriction encompasses percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of meta-chloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid. Such bleaching agents are disclosed in U.S. Patent 4,483,781, Hartman, issued November 20, 1984, U.S. Patent Application 740,446, Burns et al, filed June 3, 1985, European Patent Application 0,133,354, Banks et al, published February 20, 1985, and U.S. Patent 4,412,934, Chung et al, issued November 1, 1983. Highly preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid as described in U.S. Patent 4,634,551, issued January 6, 1987 to Bums et al. A preferred percarbonate bleach comprises dry particles having an average particle size in the range from about 500 micrometers to about 1,000 micrometers, not more than about 10% by weight of said particles being smaller than about 200 micrometers and not more than about 10% by weight of said particles being larger than about 1,250 micrometers. Optionally, the percarbonate can be coated with silicate, borate or water-soluble surfactants. Percarbonate is available from various commercial sources such as FMC, Solvay and Tokai Denka. Mixtures of bleaching agents can also be used. Bleach activators can also be added to the bleach detergent composition in addition to the peroxygen bleaching agents. The peroxygen bleaching agents, the perborates, the percarbonates, etc., are preferably combined with bleach activators, which lead to the in situ production in aqueous solution (i.e., during the washing process) of the peroxy acid corresponding to the bleach activator. Various nonlimiting examples of activators are disclosed in U.S. Patent 4,915,854, issued April 10, 1990 to Mao et al, and U.S. Patent 4,412,934. The nonanoyloxybenzene sulfonate (NOBS) and tetraacetyl ethylene diamine (TAED) activators are typical, and mixtures thereof can also be used. See also U.S. 4,634,551 for other typical bleaches and activators useful herein. If present, the amount of bleach activators will typically be from about 0.1% to about 60%, more typically from about 0.5% to about 40% of the bleaching composition comprising the bleaching agent-plus-bleach activator. Another class of bleach activators comprises the benzoxazin-type activators disclosed by Hodge et al in U.S. Patent 4,966,723, issued October 30, 1990, incorporated herein by reference. A highly preferred activator of the benzoxazin-type is: (Formula Removed) Still another class of preferred bleach activators includes the acyl lactam activators, especially acyl caprolactams and acyl valerolactams of the formulae: (Formula Removed) wherein R^ is H or an alkyl, aryl, alkoxyaryl, or alkaryl group containing from 1 to about 12 carbon atoms. Highly preferred lactam activators include benzoyl caprolactam, octanoyl caprolactam, 3,5,5-trimethylhexanoyl caprolactam, nonanoyl caprolactam, decanoyl caprolactam, undecenoyl caprolactam, benzoyl valerolactam, octanoyl valerolactam, decanoyl valerolactam, undecenoyl valerolactam, nonanoyl valerolactam, 3,5,5-trimethylhexanoyl valerolactam and mixtures thereof. See also U.S. Patent 4,545,784, issued to Sanderson, October 8, 1985, incorporated herein by reference, which discloses acyl caprolactams, including benzoyl caprolactam, adsorbed into sodium perborate. Another preferred bleach agent is a peroxyacid bleaching agent, of which an amide substituted peroxyacid precursor compound is more preferred, including one having the formula: (Formula Removed) wherein R1 is C1-C14 alkyl, aryl, alkylaryl, and mixtures thereof; R2 is C1-C14 alkylene, arylene, alkylarylene, and mixtures thereof; R5 is hydrogen, C1-C10 alkyl, aryl, alkylaryl, and mixtures thereof; L is any suitable leaving group (a preferred leaving group is phenyl sulfonate). R1 preferably contains from 6 to 12 carbon atoms. R2 preferably contains from 4 to 8 carbon atoms. R1 may contain, where applicable, branching, substitution, or both and may be sourced from either synthetic sources or natural sources including for example, tallow fat. Analogous structural variations are permissible for R2. The substitution can include alkyl, halogen, nitrogen, sulfur and other typical substituent groups or organic compounds. R5 is preferably H or methyl. R1 and R5 should not contain more than 18 carbon atoms in total. Amide substituted bleach activator compounds of this type are described in EP-A-0170386. Preferred examples of bleach activators of the above formulae include (6-octanamido-caproyl)oxybenzenesulfonate, (6-nonanamidocaproyl)oxybenzenesulfonate, (6-decanamido-caproyl)oxybenzenesulfonate, and mixtures thereof as described in U.S. Patent 4,634,551, incorporated herein by reference. Bleaching agents other than oxygen bleaching agents are also known in the art and can be utilized herein. One type of non-oxygen bleaching agent of particular interest includes photoactivated bleaching agents such as the sulfonated zinc and/or aluminum phthalo-cyanines. See U.S. Patent 4,033,718, issued July 5, 1977 to Holcombe et al. If used, detergent compositions will typically contain from about 0.025% to about 1.25%, by weight, of such bleaches, especially sulfonate zinc phthalocyanine. If desired, the bleaching compounds can be catalyzed by means of a manganese compound. Such compounds are well known in the art and include, for example, the manganese-based catalysts disclosed in U.S. Pat. 5,246,621, U.S. Pat. 5,244,594; U.S. Pat. 5,194,416; U.S. Pat. 5,1 14,606; and European Pat. App. Pub. Nos. 549.271A1, 549.272A1, 544,440A2, and 544,490A1; Preferred examples of these catalysts include MnIV2(u-0)3(1 ,4,7-trimethyl- 1 ,4, 7-triazacyclononane)2(PF6)2, MnIII2(u-0) 1 (u-OAc)22( 1 ,4,7-trimethyl-l,4,7-triazacyclononane)2.(ClO4)2, MnIV4(u-O)6( 1,4,7-triazacyclononane)4(C104)4, MnIIIMnIV4(u-0) \ (u-OAc)2_( 1 ,4,7-trimethyl- 1 ,4,7-triazacyclononane)2(CI04)3, MnIV(l,4,7-trimethyl-l,4,7-triazacyclononane)-(OCH3)3(PF6), and mixtures thereof. Other metal-based bleach catalysts include those disclosed in U.S. Pat. 4,430,243 and U.S. Pat. 5,1 14,61 1. The use of manganese with various complex ligands to enhance bleaching is also reported in the following United States Patents: 4,728,455; 5,284,944; 5,246,612; 5,256,779; 5,280,117; 5,274,147; 5,153,161; and 5,227,084. As a practical matter, and not by way of limitation, the compositions and processes herein can be adjusted to provide on the order of at least one part per ten million of the active bleach catalyst species in the aqueous washing liquor, and will preferably provide from about 0.1 ppm to about 700 ppm, more preferably from about 1 ppm to about 500 ppm, of the catalyst species in the laundry liquor. The Modified Polvamine The modified polyamines used in the process invention are water-soluble or water-dispersible, especially useful for cleaning cotton-containing fabrics or as a dispersant. These polyamines comprise backbones that can be either linear or cyclic. The polyamine backbones can also comprise polyamine branching chains to a greater or lesser degree. In general, the polyamine backbones described herein are modified in such a manner that each nitrogen of the polyamine chain is thereafter described in terms of a unit that is substitutedt quatemized, oxidized, or combinations thereof. For the purposes of the present invention the term "modification" is defined as replacing a backbone -NH hydrogen atom by an E unit (substitution), quatemizing a backbone nitrogen (quatemized) or oxidizing a backbone nitrogen to the N-oxide (oxidized). The terms "modification" and "substitution" are used interchangeably when referring to the process of replacing a hydrogen atom attached to a backbone nitrogen with an E unit. Quaternization or oxidation may take place in some circumstances without substitution, but preferably substitution is accompanied by oxidation or quaternization of at least one backbone nitrogen. The linear or non-cyclic polyamine backbones that comprise the modified polyamines have the general formula: (Formula Removed) where the backbones prior to subsequent modification comprise primary, secondary and tertiary amine nitrogens connected by R "linking" units. The cyclic polyamine backbones comprising the modified polyamines used in the present invention have the general formula: (Formula Removed) where the backbones prior to subsequent modification comprise primary, secondary and tertiary amine nitrogens connected by R "linking" units. For the purpose of the present invention, primary amine nitrogens comprising the backbone or branching chain once modified are defined as V or Z "terminal" units. For example, when a primary amine moiety, located at the end of the main polyamine backbone or branching chain having the structure (Formula Removed) is modified according to the present invention, it is thereafter defined as a V "terminal" unit, or simply a V unit. However, for the purposes of the present invention, some or all of the primary amine moieties can remain unmodified subject to the restrictions further described herein below. These unmodified primary amine moieties by virtue of their position in the backbone chain remain "terminal" units. Likewise, when a primary amine moiety, located at the end of the main polyamine backbone having the structure (Formula Removed) is modified according to the present invention, it is thereafter defined as a Z "terminal" unit, or simply a Z unit. This unit can remain unmodified subject to the restrictions further described herein below. In a similar manner, secondary amine nitrogens comprising the backbone or branching chain once modified are defined as W "backbone" units. For example, when a secondary amine moiety, the major constituent of the backbones and branching chains of the present invention, having the structure (Formula Removed) is modified according to the present invention, it is thereafter defined as a W "backbone" unit, or simply a W unit. However, for the purposes of the present invention, some or all of the secondary amine moieties can remain unmodified. These unmodified secondary amine moieties by virtue of their position in the backbone chain remain "backbone" units. In a further similar manner, tertiary amine nitrogens comprising the backbone or branching chain once modified are further referred to as Y "branching" units. For example, when a tertiary amine moiety, which is a chain branch point of either the polyamine backbone or other branching chains or rings, having the structure (Formula Removed) is modified according to the present invention, it is thereafter defined as a Y "branching" unit, or simply a Y unit. However, for the purposes of the present invention, some or all or the tertiary amine moieties can remain unmodified. These unmodified tertiary amine moieties by virtue of their position in the backbone chain remain "branching" units. The R units associated with the V, W and Y unit nitrogens which serve to connect the polyamine nitrogens, are described herein below. The final modified structure of the polyamines of the present invention can be therefore represented by the general formula (Formula Removed) for linear polyamine polymers and by the general formula (Formula Removed) for cyclic polyamine polymers. For the case of polyamines comprising rings, a Y' unit of the formula (Formula Removed) serves as a branch point for a backbone or branch ring. For every Y1 unit there is a Y unit having the formula (Formula Removed) that will form the connection point of the ring to the main polymer chain or branch. In the unique case where the backbone is a complete ring, the polyamine backbone has the formula (Formula Removed) therefore comprising no Z terminal unit and having the formula (Formula Removed) wherein k is the number of ring forming branching units. Preferably the polyamine backbones of the present invention comprise no rings. In the case of non-cyclic polyamines, the ratio of the index n to the index m relates to the relative degree of branching. A fully non-branched linear modified polyamine according to the present invention has the formula (Formula Removed) that is, n is equal to 0. The greater the value of n (the lower the ratio of m to n), the greater the degree of branching in the molecule. Typically the value for m ranges from a minimum value of 4 to about 400, however larger values of m, especially when the value of the index n is very low or nearly 0, are also preferred. Each polyamine nitrogen whether primary, secondary or tertiary, once modified according to the present invention, is further defined as being a member of one of three general classes; simple substituted, quaternized or oxidized. Those polyamine nitrogen units not modified are classed into V, W, Y, or Z units depending on whether they are primary, secondary or tertiary nitrogens. That is unmodified primary amine nitrogens are V or Z units, unmodified secondary amine nitrogens are W units and unmodified tertiary amine nitrogens are Y units for the purposes of the present invention. Modified primary amine moieties are defined as V "terminal" units having one of three forms: a) simple substituted units having the structure: (Formula Removed) b) quatemized units having the structure: (Formula Removed) wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure: (Formula Removed) Modified secondary amine moieties are defined as W "backbone" units having one of three forms: a) simple substituted units having the structure: (Formula Removed) b) quatemized units having the structure: (Formula Removed) wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure: (Formula Removed) Modified tertiary amine moieties are defined as Y "branching" units having one of three forms: a) unmodified units having the structure: (Formula Removed) b) quaternized units having the structure: (Formula Removed) wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure: (Formula Removed) Certain modified primary amine moieties are defined as Z "terminal" units having one of three forms: a) simple substituted units having the structure: (Formula Removed) b) quaternized units having the structure: (Formula Removed) wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure: (Formula Removed) When any position on a nitrogen is unsubstituted of unmodified, it is understood that hydrogen will substitute for E. For example, a primary amine unit comprising one E unit in the form of a hydroxyethyl moiety is a V terminal unit having the formula (HOCH2CH2)HN- For the purposes of the present invention there are two types of chain terminating units, the V and Z units. The Z "terminal" unit derives from a terminal primary amino moiety of the structure -NH2- Non-cyclic polyamine backbones according to the present invention comprise only one Z unit whereas cyclic polyamines can comprise no Z units. The Z "terminal" unit can be substituted with any of the E units described further herein below, except when the Z unit is modified to form an N-oxide. In the case where the Z unit nitrogen is oxidized to an N-oxide, the nitrogen must be modified and therefore E cannot be a hydrogen. The polyamines of the present invention comprise backbone R "linking" units that serve to connect the nitrogen atoms of the backbone. R units comprise units that for the purposes of the present invention are referred to as "hydrocarbyl R" units and "oxy R" units. The "hydrocarbyr R units are C2-C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene wherein the hydroxyl moiety may take any position on the R unit chain except the carbon atoms directly connected to the polyamine backbone nitrogens; C4-C12 dihydroxyalkylene wherein the hydroxyl moieties may occupy any two of the carbon atoms of the R unit chain except those carbon atoms directly connected to the polyamine backbone nitrogens; C8-C12 dialkylarylene which for the purpose of the present invention are arylene moieties having two alkyl substituent groups as part of the linking chain. For example, a dialkylarylene unit has the formula (Formula Removed) although the unit need not be 1,4-substituted, but can also be 1,2 or 1,3 substituted C2-C12 alkylene, preferably ethylene, 1,2-propylene, and mixtures thereof, more preferably ethylene. The "oxy" R units comprise -(R1O)XR5(ORI)X-, -CH2CH(OR2)CH20)z(R10)yR1 (OCH2CH(OR2)CH2)W-, -CH2CH(OR2)CH2-, -(R'O)xRl-, and mixtures thereof. Preferred R units are C2~C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxyalkylene, C8-C12 dialkylarylene, -(R 10)XR 1 -,-CH2CH(OR2)CH2-, -(CH2CH(OH)CH20)z(R10)yR1(OCH2CH-(OH)CH2)w-, -(R10)XR5(OR1)X-, more preferred R units are C2-C12 alkylene, C3-C12 hydroxy-alkylene, C4-C12 dihydroxyalkylene, -{R1O)xR1-, -(R10)xR5(ORi)x-, -(CH2CH(OH)CH20)z(R10)yR1(OCH2CH-(OH)CH2)w-. and mixtures thereof, even more preferred R units are C2-C12 alkylene, C3 hydroxyalkylene, and mixtures thereof, most preferred are C2-C6 alkylene. The most preferred backbones of the present invention comprise at least 50% R units that are ethylene. R1 units are C2-C6 alkylene, and mixtures thereof, preferably ethylene. R2 is hydrogen, and -{R1O)XB, preferably hydrogen. R3 is C1-C18 alkyl, C1-C12 arylalkylene, C1-C12 alkyl substituted aryl, C6-C12 aryl, and mixtures thereof, preferably C1-C12 alkyl, C7-C12 arylalkylene, more preferably C1-C12 alkyl, most preferably methyl. R3 units serve as part of E units described herein below. R4 is C1-C12 alkylene, C4-C12 alkenylene, C8-C12 arylalkylene, C6-C10 arylene, preferably C1-C10 alkylene, C8-C12 arylalkylene, more preferably C2-C8alkylene, most preferably ethylene or butylene. R5 is C1-C12 alkylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxyalkylene, C8-C12 dialkylarylene, -C(O)-, -C(O)NHR6NHC(O)-, -C(0)(R4)rC(O)-, -R1(OR1)-, -CH2CH(OH)CH2O(R1O)yR1OCH2CH(OH)CH2-, -C(0)(R4)rC(0)-, -CH2CH(OH)CH2-, R5 is preferably ethylene, -C(O)-, -C(O)NHR6NHC(0)-, -R1(OR1)-, -CH2CH(OH)CH2-, -CH2CH(OH)CH20(R10)yR1OCH2CH-(OH)CH2-, more preferably -CH2CH(OH)CH2-. R6 is C2-C12 alkylene or C6-C12 arylene. The preferred "oxy" R units are further defined in terms of the R1, R2, and R5 units. Preferred "oxy" R units comprise the preferred R1, R2, and R5 units. The preferred modified polyamines comprise at least 50% R1 units that are ethylene. Preferred R1, R2, and R5 units are combined with the "oxy" R units to yield the preferred "oxy" R units in the following manner. i) Substituting more preferred R5 into -(CH2CH2O)XR5(OCH2CH2)X- yields -(CH2CH2O)XCH2CHOHCH2(OCH2CH2)X-. ii) Substituting preferred R1 and R2 into -(CH2CH(OR2)CH20)Z- (R10)yRI0(CH2CH(OR2)CH2)w- yields -{CH2CH(OH)CH20)Z-(CH2CH20)yCH2CH20(CH2CH(OH)CH2)w-. iii) Substituting preferred R2 into -CH2CH(OR2)CH2- yields -CH2CH(OH)CH2-. E units are selected from the group consisting of hydrogen, C1-C22 alkyl, C3-C22 alkenyl, C7-C22 arylalkyl, C2-C22 hydroxyalkyl, -{CH2)pC02M, -(CH2)qS03M, -CH(CH2C02M)C02M, -{CH2)pPO3M, -(R1O)mB, -C(0)R3, preferably hydrogen, C2-C22 hydroxyalkylene, benzyl, C1-C22 alkylene, -(R1O)mB, -C(0)R3, -(CH2)pC02M, -{CH2)qS03M, -CH(CH2CO2M)CO2M, more preferably C1-C22 alkylene, -(R1O)xB, -C(0)R3, -(CH2)pC02M, -{CH2)qS03M, -CH(CH2C02M)C02M, most preferably C1-C22 alkylene, -(R1O)xB, and -C(0)R3. When no modification or substitution is made on a nitrogen then hydrogen atom will remain as the moiety representing E. E units do not comprise hydrogen atom when the V, W or Z units are oxidized, that is the nitrogens are N-oxides. For example, the backbone chain or branching chains do not comprise units of the following structure: (Formula Removed) Additionally, E units do not comprise carbonyl moieties directly bonded to a nitrogen atom when the V, W or Z units are oxidized, that is, the nitrogens are N-oxides. According to the present invention, the E unit -C(0)R3 moiety is not bonded to an N-oxide modified nitrogen, that is, there are no N-oxide amides having the structure (Formula Removed) or combinations thereof. B is hydrogen, C1-C6 alkyl, -(CH2)qS03M, -(CH2)pCO2M, -(CH2)q-(CHS03M)CH2S03M, -(CH2)q(CHS02M)CH2S03M, -(CH2)pP03M, -P03M, preferably hydrogen, -(CH2)qS03M, -(CH2)q(CHS03M)CH2S03M, -(CH2)q-(CHSO2M)CH2S03M, more preferably hydrogen or -(CH2)qS03M. M is hydrogen or a water soluble cation in sufficient amount to satisfy charge balance. For example, a sodium cation equally satisfies -{CH2)pC02M, and -{CH2)qS03M, thereby resulting in -{CH2)pC02Na, and -(CH2)qS03Na moieties. More than one monovalent cation, (sodium, potassium, etc.) can be combined to satisfy the required chemical charge balance. However, more than one anionic group may be charge balanced by a divalent cation, or more than one mono-valent cation may be necessary to satisfy the charge requirements of a poly-anionic radical. For example, a -(CH2)pP03M moiety substituted with sodium atoms has the formula -(CH2)pP03Na3. Divalent cations such as calcium (Ca2+) or magnesium (Mg2+) may be substituted for or combined with other suitable mono-valent water soluble cations. Preferred cations are sodium and potassium, more preferred is sodium. X is a water soluble anion such as chlorine (Cl~), bromine (Br) and iodine (I-) or X can be any negatively charged radical such as sulfate (SO42-) and methosulfate (CH3S03-). The formula indices have the following values: p has the value from 1 to 6, q has the value from 0 to 6; r has the value 0 or 1; w has the value 0 or 1, x has the value from 1 to 100; y has the value from 0 to 100; z has the value 0 or 1; k is less than or equal to the value of n; m has the value from 4 to about 400, n has the value from 0 to about 200; m + n has the value of at least 5. The preferred modified polyamines used in the present invention comprise polyamine backbones wherein less than about 50% of the R groups comprise "oxy" R units, preferably less than about 20% , more preferably less than 5%, most preferably the R units comprise no "oxy" R units. The most preferred polyamines which comprise no "oxy" R units comprise polyamine backbones wherein less than 50% of the R groups comprise more than 3 carbon atoms. For example, ethylene, 1,2-propylene, and 1,3-propylene comprise 3 or less carbon atoms and are the preferred "hydrocarbyl" R units. That is when backbone R units are C2-C12 alkylene, preferred is C2-C3 alkylene, most preferred is ethylene. The polyamines of the present invention comprise modified homogeneous and non-homogeneous polyamine backbones, wherein 100% or less of the -NH units are modified. For the purpose of the present invention the term "homogeneous polyamine backbone" is defined as a polyamine backbone having R units that are the same (i.e., all ethylene). However, this sameness definition does not exclude polyamines that comprise other extraneous units comprising the polymer backbone which are present due to an artifact of the chosen method of chemical synthesis. For example, it is known to those skilled in the art that ethanolamine may be used as an "initiator" in the synthesis of polyethyleneimines, therefore a sample of polyethyleneimine that comprises one hydroxyethyl moiety resulting from the polymerization "initiator" would be considered to comprise a homogeneous polyamine backbone for the purposes of the present invention. A polyamine backbone comprising all ethylene R units wherein no branching Y units are present is a homogeneous backbone. A polyamine backbone comprising all ethylene R units is a homogeneous backbone regardless of the degree of branching or the number of cyclic branches present. For the purposes of the present invention the term "non-homogeneous polymer backbone" refers to polyamine backbones that are a composite of various R unit lengths and R unit types. For example, a non-homogeneous backbone comprises R units that are a mixture of ethylene and 1,2-propylene units. For the purposes of the present invention a mixture of "hydrocarbyl" and "oxy" R units is not necessary to provide a non-homogeneous backbone. The proper manipulation of these "R unit chain lengths" provides the formulator with the ability to modify the solubility and fabric substantivity of the modified polyamines. Preferred polyamines of the present invention comprise homogeneous polyamine backbones that are totally or partially substituted by polyethyleneoxy moieties, totally or partially quaternized amines, nitrogens totally or partially oxidized to N-oxides, and mixtures thereof. However, not all backbone amine nitrogens must be modified in the same manner, the choice of modification being left to the specific needs of the formulator. The degree of ethoxylation is also determined by the specific requirements of the formulator. The preferred polyamines that comprise the backbone of the compounds of the present invention are generally polyalkyleneamines (PAA's), polyalkyleneimines (PAI's), preferably polyethyleneamine (PEA's), polyethyleneimines (PEI's), or PEA's or PEI's connected by moieties having longer R units than the parent PAA's, PAI's, PEA's or PEI's. A common polyalkyleneamine (PAA) is tetrabutylenepentamine. PEA's are obtained by reactions involving ammonia and ethylene dichlonde, followed by fractional distillation. The common PEA's obtained are triethylenetetramine (TETA) and teraethylenepentamine (TEPA). Above the pentamines, i.e., the hexamines, heptamines, octamines and possibly nonamines, the cogenerically derived mixture does not appear to separate by distillation and can include other materials such as cyclic amines and particularly piperazines. There can also be present cyclic amines with side chains in which nitrogen atoms appear. See U.S. Patent 2,792,372, Dickinson, issued May 14, 1957, which describes the preparation of PEA's. Preferred amine polymer backbones comprise R units that are C2 alkylene (ethylene) units, also known as polyethylenimines (PEI's). Preferred PEI's have at least moderate branching, that is the ratio of m to n is less than 4:1, however PEI's having a ratio of m to n of about 2:1 are most preferred. Preferred backbones, prior to modification have the general formula: (Formula Removed) wherein m and n are the same as defined herein above. Preferred PEI's, prior to modification, will have a molecular weight greater than about 200 daltons. The relative proportions of primary, secondary and tertiary amine units in the polyamine backbone, especially in the case of PEI's, will vary, depending on the manner of preparation. Each hydrogen atom attached to each nitrogen atom of the polyamine backbone chain represents a potential site for subsequent substitution, quaternization or oxidation. These polyamines can be prepared, for example, by polymerizing ethyleneimine in the presence of a catalyst such as carbon dioxide, sodium bisulfite, sulfuric acid, hydrogen peroxide, hydrochloric acid, acetic acid, etc. Specific methods for preparing these polyamine backbones are disclosed in U.S. Patent 2,182,306, Ulrich et al., issued December 5, 1939; U.S. Patent 3,033,746, Mayle et al., issued May 8, 1962; U.S. Patent 2,208,095, Esselmann et al., issued July 16, 1940; U.S. Patent 2,806,839, Crowther, issued September 17, 1957; and U.S. Patent 2,553,696, Wilson, issued May 21, 195 1; all herein incorporated by reference. Examples of modified polyamines of the present invention comprising PEI's, are illustrated in Formulas I - IV: Formula I depicts a polymer comprising a PEI backbone wherein all substitutable nitrogens are modified by replacement of hydrogen with a polyoxyalkyleneoxy unit, -(CH2CH2O)7H,having the formula (Formula Removed) This is an example of a polymer that is fully modified by one type of moiety. Formula II depicts a polymer comprising a PEI backbone wherein all substitutable primary amine nitrogens are modified by replacement of hydrogen with a polyoxyalkyleneoxy unit, -(CH2CH2O)7H, the molecule is then modified by subsequent oxidation of all oxidizable primary and secondary nitrogens to N-oxides, wherein the polymer has the formula (Formula Removed) Formula III depicts a polymer comprising a PEI backbone wherein all backbone hydrogen atoms are substituted and some backbone amine units are quaternized. The substituents are polyoxyalkyleneoxy units, -(CH2CH2O)7H, or methyl groups. The modified PEI polymer has the formula (Formula Removed) Formula IV depicts a polymer comprising a PEI backbone wherein the backbone nitrogens are modified by substitution (i.e. by -(CH2CH2O)7H or methyl), quatemized, oxidized to N-oxides or combinations thereof. The resulting polymer has the formula (Formula Removed) In the above examples, not all nitrogens of a unit class comprise the same modification. The present invention allows the formulator to have a portion of the secondary amine nitrogens ethoxylated while having other secondary amine nitrogens oxidized to N-oxides. This also applies to the primary amine nitrogens, in that the formulator may choose to modify all or a portion of the primary amine nitrogens with one or more substiruents prior to oxidation or quatemization. Any possible combination of E groups can be substituted on the primary and secondary amine nitrogens, except for the restrictions described herein above. The Anionic Agent The anionic agent can form an ionic complex with the nitrogens of the modified polyamine. Preferably this ion complex can be formed and is stable at a pH value in the range from about 5, up to about 10. The anionic agent has anionic functionality within this pH range, whereby when mixed with the modified polyamine under conditions where the pH of the mixture is from about 5 to about 10, the anionic agent and the polyamine can complex to form a stable, complexed polyamine. The complexation occurs at the nitrogen sites of the polyamine, where the unshared pairs of electrons are available to complex with the anionic species of the anionic agent. Preferred anionic agents are detergent ingredients that are typically used in detergent products and which are capable of forming the anionic species within the pH range of about 5 to about 10. Nonlimiting examples of such anionic agents include anionic detersive surfactants and inorganic salts having a buffering pH of between 7 and 10, and include polyphosphate builders, such as alkali tripolyphosphate and alkali pyrophosphate. Other common detergent ingredients such as sodium carbonate and sodium silicate are generally not suitable as an anionic agent, since they either do not form a suitable anionic species at such pH, or their alkalinity is sufficiently high that solutions containing these materials have a pH generally above 10. At a pH above about 10, the modified polyamine will resist forming any kind of an ionic complex. Therefore, when mixed with agents that have high alkalinity, or when mixed with an anionic agent of the present invention but at solution conditions where the pH is above about 10, the desired complexed polyamine will not be formed. Consequently, then the mixture is processed into a bleach detergent composition, and subsequently added into a wash solution, the uncomplexed nitrogen sites of the modified polyamine can react with and destroy the bleach agent. Nonlimiting examples of an anionic detersive surfactant useful as an anionic agent include the conventional C11-C18 alkyl benzene sulfonates ("LAS") and primary, branched-chain and random C10-C20 alkyl sulfates ("AS"), the C10-C18 secondary (2,3) alkyl sulfates of the formula CH3(CH2)X(CHOS03~M+) CH3 and CH3 (CH2)y(CHOS03~M+) CH2CH3 where x and (y + 1) are integers of at least about 7, preferably at least about 9, and M is a water-solubilizing cation, especially sodium, unsaturated sulfates such as oleyl sulfate, the C10-C18 alkyl alkoxy sulfates ("AExS"; especially EO 1-7 ethoxy sulfates),C10-C18 alky! alkoxy carboxylates (especially the EO 1-5 ethoxycarboxylates), the C10-18 glycerol ethers, and C12-C18 alpha-sulfonated fatty acid esters. Adjunct Detergent Ingredients One or more adjunct detergent ingredients can be incorporated in the detergent composition during subsequent steps of the present process invention. These adjunct ingredients include other surfactants such as cationic surfactants, other detergency builders, suds boosters or suds suppressors, anti-tarnish and anticorrosion agents, soil suspending agents, soil release agents, germicides, pH adjusting agents, non-builder alkalinity sources, dictating agents such as diethylene triamine penta acetic acid (DTPA) and diethylene triamine penta(methylene phosphonic acid), smectite clays, enzymes, enzyme-stabilizing agents, dye transfer inhibitors and perfumes. See U.S. Patent 3,936,537, issued February 3, 1976 to Baskerville, Jr. et al., incorporated herein by reference. Other builders can be generally selected from the various water-soluble, alkali metal, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, borates, polyhydroxy sulfonates, polyacetates, carboxylates, and polycarboxylates. Preferred are the alkali metal, especially sodium, salts of the above. Preferred for use herein are the phosphates, carbonates, C10-18 fatty acids, polycarboxylates, and mixtures thereof. More preferred are sodium tripolyphosphate, tetrasodium pyrophosphate, citrate, tartrate mono- and di-succinates, and mixtures thereof (see below). In comparison with amorphous sodium silicates, crystalline layered sodium silicates exhibit a clearly increased calcium and magnesium ion exchange capacity. In addition, the layered sodium silicates prefer magnesium ions over calcium ions, a feature necessary to insure that substantially all of the "hardness" is removed from the wash water. These crystalline layered sodium silicates, however, are generally more expensive than amorphous silicates as well as other builders. Accordingly, in order to provide an economically feasible laundry detergent, the proportion of crystalline layered sodium silicates used must be determined judiciously. The crystalline layered sodium silicates suitable for use herein preferably have the formula (Formula Removed) wherein M is sodium or hydrogen, x is from about 1.9 to about 4 and y is from about 0 to about 20. More preferably, the crystalline layered sodium silicate has the formula (Formula Removed) wherein M is sodium or hydrogen, and y is from about 0 to about 20. These and other crystalline layered sodium silicates are discussed in Corkill et al, U.S. Patent No. 4,605,509, previously incorporated herein by reference. Specific examples of inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphates. Examples of polyphosphonate builders are the sodium and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts of ethane I-hydroxy-1, 1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid. Other phosphorus builder compounds are disclosed in U.S. Patents 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148, all of which are incorporated herein by reference. Examples of nonphosphorus, inorganic builders are tetraborate decahydrate and silicates having a weight ratio of SiO2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4. Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates. Examples of polyacetate and polycarboxylate builders are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylene diamine tetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid. Polymeric polycarboxylate builders are set forth in U.S. Patent 3,308,067, Diehl, issued March 7, 1967, the disclosure of which is incorporated herein by reference. Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itacomc acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylene malonic acid. Some of these materials are useful as the water-soluble anionic polymer as hereinafter described, but only if in intimate admixture with the non-soap anionic surfactant. Other suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al, and U.S. Patent 4,246,495, issued March 27, 1979 to Crutchfield et al, both of which are incorporated herein by reference. These polyacetal carboxylates can be prepared by bringing together under polymerization conditions an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a detergent composition. Particularly preferred polycarboxylate builders are the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al., issued May 5, 1987, the disclosure of which is incorporated herein by reference. Suitable smectite clays for use herein are described in U.S. Patent 4,762,645, Tucker et al, issued August 9, 1988, Column 6, line 3 through Column 7, line 24, incorporated herein by reference. Suitable additional detergency builders for use herein are enumerated in the Baskerville patent, Column 13, line 54 through Column 16, line 16, and in U.S. Patent 4,663,071, Bush et al, issued May 5, 1987, both incorporated herein by reference. In order to make the present invention more readily understood, reference is made to the following examples, which are intended to be illustrative only and not intended to be limiting in scope. Process for Preparing Complexed Polvamines and Detergent Products therefrom The process of the instant invention involves premixing a selected modified polyamine and an anionic agent to form the complexed polyamine. A preferred anionic agent is an anionic detersive surfactant, preferably in the form of a neutralized sulfate or sulfonate detersive surfactant paste. The surfactant paste can comprise the anionic detersive surfactant, and optionally a nonionic surfactant, but preferably will not contain a cationic surfactant. In addition to the improved stability to bleach agents, the polyamine/surfactant complex typically has a higher oxidative degradation temperature as compared to the degradation temperature of the modified polyamines by themselves. In a preferred process, the modified polyamine and anionic surfactant are mixed in an in-line static mixer or a conventional mixer (e.g., crutcher) for at least about 1 minute. The temperature at which the premixing step using the surfactant paste is performed typically is at a temperature of from about 25°C to about 80°C. Also, it is preferred to maintain the pH of the premix at from about 5 to about 10, more preferably at from about 8 to about 10, and most preferably at about 8 to 9. While the mixture will typically comprise only the anionic surfactant and the modified polyamine, other detergent adjuncts can be added with or to the mixture; such adjuncts can include, by example, sodium tripolyphosphate, water, and other detersive surfactants The modified polyamine is preferably present in an amount of from about 0.01% to about 10%, more preferably from about 0.05% to about 5%, and most preferably from about 0.1% to about 1.0%, by weight of the overall detergent composition. Further, in the premixing step, the detersive surfactant paste preferably comprises from about 1% to about 70%, more preferably from about 20% to about 60%, and most preferably from about 25% to about 50%, by weight of surfactant, and the balance water and other minor ingredients. The surfactant paste comprising the complexed polyamine can then be made into detergents products, including both granular detergent products and liquid detergent products, by processes well known to those skilled in the art. The premixed complexed polyamine is then further processed into detergent compositions by known methods, which include slurrying and spray drying, and agglomeration, as discussed herein below. The bleach detergent compositions made using the complexed polyamine, when placed into wash solutions, with or without soil loads, exhibit less loss of the bleach agent present in a washing solution compared to comparable compositions made by similar processes, except that the modified polyamine is either sprayed-on to or admixed as a particle into the detergent. In a preferred process, the surfactant paste containing the complexed polyamine is made into a granular detergent process via a spray drying method. After the surfactant paste is processed into a detergent slurry along with other detergent adjuncts (including, by example, zeolite, inorganic salts such as sodium tripolyphosphate, carbonate and sulfate, silicates, optional detergent surfactants, polymeric polycarboxylate builders, silicates, optical brighteners, colorants, antiredeposition agents, fillers, and other compatible detergent ingredients, and mixtures thereof), the slurry is spray dried to form a spray-dried granular detergent composition. This step can be completed in a conventional spray drying tower operated at an inlet temperature range of from about 180°C to about 420°C. Such known apparatus operates by spraying the slurry via nozzles into a counter-current (or co-current) stream of hot air which ultimately forms porous spray-dried granules. An alternative process comprises a) premixing an anionic surfactant paste and a modified polyamine, b) agglomerating the surfactant paste comprising the complexed polyamine with other dry detergent ingredients i) initially in a high speed mixer/densifier, and ii) subsequently in a moderate speed mixer/densifier, to form agglomerates. The modified polyamine and surfactant paste are mixed for at least about 5 seconds, preferably from about 5 seconds to about 1 minute in any acceptable known mixing apparatus such as an in-line static mixer, twin-screw extruder, stirred mixing tanks and the like. The temperature at which the premixing step using the surfactant paste is performed typically is at a temperature of from about 25°C to about 80°C. The pH of the premix should be maintained between a pH of about 5 to about 10, preferably at from about 8 to about 10, and preferably without other detergent ingredients present. The modified polyamine is preferably present in an amount of from about 0.01% to about 10%, more preferably from about 0.05% to about 5%, and most preferably from about 0.1% to about 1.0%, by weight of the overall detergent composition. Further, in the premixing step, the detersive surfactant paste preferably comprises from about 1 % to about 70%, more preferably from about 20% to about 60%, and most preferably from about 25% to about 50%, by weight of a detersive surfactant the balance water and other minor ingredients. The premix of modified polyamine and surfactant paste is initially agglomerated in a high speed mixer/densifier followed by a moderate speed mixer/densifier. The high speed mixer/densifier is a Lodige CB 30 mixer or similar brand mixer. These types of mixers essentially consist of a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached. Preferably, the shaft rotates at a speed of from about 100 rpm to about 2500 rpm, more preferably from about 300 rpm to about 1600 rpm. Preferably, the mean residence time of the detergent ingredients in the high speed mixer/densifier is preferably in range from about 2 seconds to about 45 seconds, and most preferably from about 5 seconds to about 15 seconds. Preferably, the resulting detergent agglomerates formed in the high speed mixer/densifier are then fed into a lower or moderate speed mixer/densifier during which further agglomeration and densification is carried forth. This particular moderate speed mixer/densifier used in the present process should include liquid distribution and agglomeration tools so that both techniques can occur simultaneously. It is preferable to have the moderate speed mixer/densifier be, for example, a Lodige KM 600 (Ploughshare) mixer, Drais® K-T 160 mixer or similar brand mixer. The residence time in the moderate speed mixer/densifier is preferably from about 0.5 minutes to about 15 minutes, most preferably the residence time is about 1 to about 10 minutes. The liquid distribution can be accomplished by cutters, generally smaller in size than the rotating shaft, which preferably operate at about 3600 rpm. It should be understood that while the processing described herein is relative to formation of high density agglomerates, the same equipment and processing steps may be used to produce less or moderately dense agglomerates. Of course, agglomerates produced by the process regardless of the density can be admixed with less dense spray-dried granules in the final detergent product, if desired. The detergent agglomerates produced by the process preferably have a surfactant level of from about 25% to about 55%, more preferably from about 35% to about 55% and, most preferably from about 45% to about 55%. The particle porosity of the resulting detergent agglomerates produced according to the process of the invention is preferably in a range from about 5% to about 20%, more preferably at about 10%. In addition, an attribute of dense or densified agglomerates is the relative particle size. The present process typically provides detergent agglomerates having a median particle size of from about 400 microns to about 700 microns, and more preferably from about 400 microns to about 600 microns. As used herein, the phrase "median particle size" refers to individual agglomerates and not individual particles or detergent granules. The combination of the above-referenced porosity and particle size results in agglomerates having density values of 650 g/1 and higher. Alternatively, the particle size and porosity can be adjusted to produce agglomerates having lower densities, as well (e.g., 300 g/1 to 500 g/l). Such features are especially useful in the production of low as well as high or conventional dosage laundry detergents as well as other granular compositions such as dishwashing compositions. The detergent agglomerates formed by the above process are then optionally dried in a fluid bed dryer and/or further conditioned by cooling the agglomerates in a fluid bed cooler or similar apparatus as are well known in the art. Another optional process step involves adding a coating agent to improve flowability and/or minimize over agglomeration of the detergent composition in one or more of the following locations of the instant process: (1) the coating agent can be added directly after the fluid bed cooler or dryer; (2) the coating agent may be added between the fluid bed dryer and the fluid bed cooler; (3) the coating agent may be added between the fluid bed dryer and the mixer/densifier(s); and/or (4) the coating agent may be added directly to one or more of the mixer/densifiers. The coating agent is preferably selected from the group consisting of aluminosilicates, silicates, carbonates and mixtures thereof. The coating agent not only enhances the free flowability of the resulting detergent composition which is desirable by consumers in that it permits easy scooping of detergent during use, but also serves to control agglomeration by preventing or minimizing over agglomeration, especially when added directly to the mixer/densifier(s). As those skilled in the art are well aware, over agglomeration can lead to very undesirable flow properties and aesthetics of the final detergent product. Other optional steps in the present process involve recycling oversized and undersized agglomerates as described in Capeci et al, U.S. Patent Nos. 5,489,392 and 5,516,448 (Procter & Gamble). Also, the step of including an anhydrous material at selected points in the process can be incorporated as described by Capeci et al, U.S. Patent No. 5,366,652 and 5,486,303 (Procter & Gamble). Optionally, the agglomerates exiting the moderate speed mixer/densifier can be dried in a spray drying tower as described in Capeci et al, U.S. Patent 5,496,487 (Procter & Gamble). Optionally, the process can comprises the step of spraying an additional binder in the mixer/densifier(s). A binder is added for purposes of enhancing agglomeration by providing a "binding" or "sticking" agent for the detergent components. The binder is preferably selected from the group consisting of water, anionic surfactants, nonionic surfactants, polyethylene glycol, polyvinyl pyrrolidone polyacrylates, citric acid and mixtures thereof. Other suitable binder materials including those listed herein are described in Beerse et al, U.S. Patent No. 5,108,646 (Procter & Gamble), the disclosure of which is incorporated herein by reference. Another optional step of the instant process entails finishing the resulting detergent agglomerates by a variety of processes including spraying and/or admixing other conventional detergent ingredients. For example, the finishing step encompasses spraying on perfumes, and the addition of brighteners and enzymes to the finished agglomerates to provide a more complete detergent composition. Such techniques and ingredients are well known in the art. EXAMPLE I Preparation of PEI 1800 E7 This Example illustrates a method by which one of the selected modified polyamines is made. The ethoxylation is conducted in a 2 gallon stirred stainless steel autoclave equipped for temperature measurement and control, pressure measurement, vacuum and inert gas purging, sampling, and for introduction of ethylene oxide as a liquid. A -20 Ib. net cylinder of ethylene oxide (ARC) is set up to deliver ethylene oxide as a liquid by a pump to the autoclave with the cylinder placed on a scale so that the weight change of the cylinder could be monitored. A 750 g portion of polyethyleneimine (PEI) (Nippon Shokubai, Epomin SP-018 having a listed average molecular weight of 1800 equating to about 0.417 moles of polymer and 17.4 moles of nitrogen functions) is added to the autoclave. The autoclave is then sealed and purged of air (by applying vacuum to minus 28" Hg followed by pressurization with nitrogen to 250 psia, then venting to atmospheric pressure). The autoclave contents are heated to 130 °C while applying vacuum. After about one hour, the autoclave is charged with nitrogen to about 250 psia while cooling the autoclave to about 105 °C. Ethylene oxide is then added to the autoclave incrementally over time while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate. The ethylene oxide pump is turned off and cooling is applied to limit any temperature increase resulting from any reaction exotherm. The temperature is maintained between 100 and 110 °C while the total pressure is allowed to gradually increase during the course of the reaction. After a total of 750 grams of ethylene oxide has been charged to the autoclave (roughly equivalent to one mole ethylene oxide per PEI nitrogen function), the temperature is increased to 110 °C and the autoclave is allowed to stir for an additional hour. At this point, vacuum is applied to remove any residual unreacted ethylene oxide. Next, vacuum is continuously applied while the autoclave is cooled to about 50 °C while introducing 376 g of a 25% sodium methoxide in methanol solution (1.74 moles, to achieve a 10% catalyst loading based upon PEI nitrogen functions). The methoxide solution is sucked into the autoclave under vacuum and then the autoclave temperature controller setpoint is increased to 130 °C. A device is used to monitor the power consumed by the agitator. The agitator power is monitored along with the temperature and pressure. Agitator power and temperature values gradually increase as methanol is removed from the autoclave and the viscosity of the mixture increases and stabilizes in about 1 hour indicating that most of the methanol has been removed. The mixture is further heated and agitated under vacuum for an additional 30 minutes. Vacuum is removed and the autoclave is cooled to 105 °C while it is being charged with nitrogen to 250 psia and then vented to ambient pressure. The autoclave is charged to 200 psia with nitrogen. Ethylene oxide is again added to the autoclave incrementally as before while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate while maintaining the temperature between 100 and 110 °C and limiting any temperature increases due to reaction exotherm. After the addition of 4500 g of ethylene oxide (resulting in a total of 7 moles of ethylene oxide per mole of PEI nitrogen function) is achieved over several hours, the temperature is increased to 110 °C and the mixture stirred for an additional hour. The reaction mixture is then collected in nitrogen purged containers and eventually transferred into a 22 L three neck round bottomed flask equipped with heating and agitation. The strong alkali catalyst is neutralized by adding 167 g methanesulfonic acid (1.74 moles). The reaction mixture is then deodorized by passing about 100 cu. ft. of inert gas (argon or nitrogen) through a gas dispersion frit and through the reaction mixture while agitating and heating the mixture to 130 °C. The final reaction product is cooled slightly and collected in glass containers purged with nitrogen. In other preparations the neutralization and deodorization is accomplished in the reactor before discharging the product. EXAMPLE II Formation of amine oxide of PEI 1800 E7 This Example illustrates another method by which one of the selected modified polyamines is made. To a 500 mL Erlenmeyer flask equipped with a magnetic stirring bar is added polyethyleneimine having a molecular weight of 1800 and ethoxylated to a degree of about 7 ethoxy groups per nitrogen (PEI-1800, E7) (209 g, 0.595 mole nitrogen, prepared as in Example I), and hydrogen peroxide (120 g of a 30 wt % solution in water, 1.06 mole). The flask is stopped, and after an initial exotherm the solution is stirred at room temperature overnight. 1H-NMR (D20) spectrum obtained on a sample of the reaction mixture indicates complete conversion. The resonances ascribed to methylene protons adjacent to unoxidized nitrogens have shifted from the original position at ~2.5 ppm to ~3.5 ppm. To the reaction solution is added approximately 5 g of 0.5% Pd on alumina pellets, and the solution is allowed to stand at room temperature for approximately 3 days. The solution is tested and found to be negative for peroxide by indicator paper. The material as obtained is suitably stored as a 51.1 % active solution in water. EXAMPLE III Preparation of PEI 1200 E7 This Example illustrates yet another method by which one of the selected modified polyamines is made. The ethoxylation is conducted in a 2 gallon stirred stainless steel autoclave equipped for temperature measurement and control, pressure measurement, vacuum and inert gas purging, sampling, and for introduction of ethylene oxide as a liquid. A -20 Ib. net cylinder of ethylene oxide (ARC) is set up to deliver ethylene oxide as a liquid by a pump to the autoclave with the cylinder placed on a scale so that the weight change of the cylinder could be monitored. A 750 g portion of polyethyleneimine (PEI) (having a listed average molecular weight of 1200 equating to about 0.625 moles of polymer and 17.4 moles of nitrogen functions) is added to the autoclave. The autoclave is then sealed and purged of air (by applying vacuum to minus 28" Hg followed by pressurization with nitrogen to 250 psia, then venting to atmospheric pressure). The autoclave contents are heated to 130 °C while applying vacuum. After about one hour, the autoclave is charged with nitrogen to about 250 psia while cooling the autoclave to about 105 °C. Ethylene oxide is then added to the autoclave incrementally over time while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate. The ethylene oxide pump is turned off and cooling is applied to limit any temperature increase resulting from any reaction exotherm. The temperature is maintained between 100 and 110 °C while the total pressure is allowed to gradually increase during the course of the reaction. After a total of 750 grams of ethylene oxide has been charged to the autoclave (roughly equivalent to one mole ethylene oxide per PEI nitrogen function), the temperature is increased to 110 °C and the autoclave is allowed to stir for an additional hour. At this point, vacuum is applied to remove any residual unreacted ethylene oxide. Next, vacuum is continuously applied while the autoclave is cooled to about 50 °C while introducing 376 g of a 25% sodium methoxide in methanol solution (1.74 moles, to achieve a 10% catalyst loading based upon PEI nitrogen functions). The methoxide solution is sucked into the autoclave under vacuum and then the autoclave temperature controller setpoint is increased to 130 °C. A device is used to monitor the power consumed by the agitator. The agitator power is monitored along with the temperature and pressure. Agitator power and temperature values gradually increase as methanol is removed from the autoclave and the viscosity of the mixture increases and stabilizes in about 1 hour indicating that most of the methanol has been removed. The mixture is further heated and agitated under vacuum for an additional 30 minutes. Vacuum is removed and the autoclave is cooled to 105 °C while it is being charged with nitrogen to 250 psia and then vented to ambient pressure. The autoclave is charged to 200 psia with nitrogen. Ethylene oxide is again added to the autoclave incrementally as before while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate while maintaining the temperature between 100 and 110 °C and limiting any temperature increases due to reaction exotherm. After the addition of 4500 g of ethylene oxide (resulting in a total of 7 moles of ethylene oxide per mole of PEI nitrogen function) is achieved over several hours, the temperature is increased to 110 °C and the mixture stirred for an additional hour. The reaction mixture is then collected in nitrogen purged containers and eventually transferred into a 22 L three neck round bottomed flask equipped with heating and agitation. The strong alkali catalyst is neutralized by adding 167 g methanesulfonic acid (1.74 moles). The reaction mixture is then deodorized by passing about 100 cu. ft. of inert gas (argon or nitrogen) through a gas dispersion frit and through the reaction mixture while agitating and heating the mixture to 130 °C. The final reaction product is cooled slightly and collected in glass containers purged with nitrogen. In other preparations the neutralization and deodorization is accomplished in the reactor before discharging the product. EXAMPLE IV A modified polyamine is made in accordance with Example I ("PEI1800 E7") and used in the process of the current invention to form spray dried laundry granules for a bleach detergent composition. For purposes of comparison, a bleach-containing spray-dried detergent composition is made into which the PEI 1800 E7 is not premixed, but is instead added after other adjunct detergent ingredients in the detergent slurry. Tthe detergent-making process illustrated herein is executed in a conventional pilot scale system. The system contains a batch mixer (called a "crutcher") in which the premixing and slurry mixing steps are completed, followed by a conventional spray drying tower ("tower"). The PEI1800 E7 is added to the crutcher along with a sodium linear alkylbenzene sulfonate ("LAS") surfactant paste (30% LAS and balance water) and is premixed at 25°C for about 5 minutes, wherein the pH of the premix is maintained at about 8 to 10. Thereafter, silicate, optical brightener, carboxymethyl cellulose ("CMC"), sodium carbonate, and water are added to the crutcher which is then mixed. Steam at a temperature of about 120°C, sodium sulfate and sodium tripolyphosphate are added to the crutcher as the contents are continuously mixed. The crutcher is operated in a batch mode, and contains 180 kg of wet crutcher mix per batch. In the tower, the wet crutcher mix is pumped under high pressure through atomizing nozzles to form a finely divided mist. A counter-current flow of hot air (210°C) is impinged upon the atomized mist, causing the drying of the mixture ultimately resulting in spray dried granules which are collected at the exit of the tower. Continuous operation of the spray drying tower is accomplished by using an intermediate tank which accumulates multiple batches from the crutcher and feeds in a continuous manner the spray drying tower. The spray-dried granules may be further processed, by adding additional detergent ingredients, if desired, to form a fully formulated laundry detergent composition. The following spray-dried bleach-containing granular detergent compositions are made in accordance with the process invention (i.e. Compositions Band C) and processes outside the scope of the invention (i.e. Compositions A). PEI1800E7 PEI1800E7 Composition Weight % in finished granules Order of Addition A 1.0 % Last wet Ingredient B 1.0% Premix with LAS First C 0.5 % Premix with LAS First Composition A is made via a process in which PEI1800 E7 is added as the last wet ingredient into the crutcher, without a premixing step with LAS. At this stage, the pH of the crutcher slurry is substantially higher than 10 (about 10.5-11.0). The order of addition to the crutcher is LAS paste / Silicate / Optical brightener / CMC / PEI 1800 E7 / Sodium Carbonate / Water; Steam / Sodium Sulphate / Sodium Tripolyphosphate ("STPP"). Sodium tripolyphosphate and other minors are admixed to the blown powder resulting in finished granular compositions A-C for which the relative proportions of the ingredients are set forth below: Detergent Ingredient A B C LAS 18.0 18.0 18.0 PEI1800E7 1.0 1.0 0.5 Bleach agent* 4.0 4.0 4.0 Sodium silicate (2.0R) 5.8 5.8 5.8 Optical brightener** 0.2 0.2 0.2 CMC 0.3 0.3 0.3 Sodium carbonate 10.0 10.0 10.0 Sodium sulfate 31.9 31.9 32.4 STPP 22.0 22.0 22.0 Water and minors 6.8 6.8 6.8 100.0 100.0 100.0 * The bleach agent is a 2:1 weight ratio of sodium perborate monohydrate and sodium nonanoyloxybenzene sulfonate bleach activator. ** Optical brightener slurried in 0.2% C45E7 Nonionic to ensure presence in organic phase. The bleach detergent compositions B and C, made by premixing the PEI1800 E7 with LAS, exhibits less loss of the bleach agent in a wash solution compared to composition A made by same process, except wherein the PEI1800 E7 is the last wet ingredient added to the slurry. EXAMPLE V A modified polyamine is made in accordance with Example I ("PEI1800 E7") and used in the process of the current invention to form an agglomerated detergent composition. An in-line static mixer is used into which the PEI1800 E7 is added continuously along with a sodium linear alkylbenzene sulfonate ("LAS") surfactant paste (60% LAS and balance water) at about 60°C in order to completely mix the ingredients, wherein the pH of the premix is maintained at about 7 to 10. Thereafter, the premix are continuously fed to a high speed mixer/densifier (Lodige CB-30, commercially available from Lodige) along with sodium aluminosilicate (zeolite) and sodium carbonate. The rotational speed of the shaft in the Lodige CB-30 mixer/densifier is about 1400 rpm and the mean residence time is about 10 seconds. The contents from the Lodige CB-30 mixer/densifer are continuously fed into a Lodige KM 600 mixer/densifer for further agglomeration during which the mean residence time is about 6 minutes. The detergent agglomerates are then screened with conventional screening apparatus resulting in a uniform particle size distribution. A bleach agent is then admixed with the detergent agglomerates to form the bleach detergent product, having the set forth below: Component % Weight C12-13 linear alkylbenzene sulfonate 27.1 Sodium aluminosilicate 34.4 Sodium carbonate 17.5 Polyethylene glycol (MW 4000) 1.3 PEI1800E7 1.0 Bleach agent* 3.0 Misc. (water, etc.) 15.7 100.0 ** The bleach agent is a 2:1 weight ratio of sodium perborate monohydrate and sodium nonanoyloxybenzene sulfonate bleach activator. The agglomerated detergent composition made by premixing the PEI1800 E7 with LAS in the premixer exhibits less loss of the bleach agent in a wash solution, compared to a composition made by same process, except wherein the PEI1800 E7 is sprayed-on to the detergent agglomerates after agglomeration. Having thus described the invention in detail, it will be clear to those skilled in the art that various changes may be made without departing from the scope of the invention and the invention is not to be considered limited to what is described in the specification. We Claim:- 1. A bleach detergent composition comprising: a) a bleach agent, and b) a complexed polyamine, comprising i) a modified polyamine useful as a cotton soil release and dispersant agent, and ii) an anionic species capable of forming a complex with the modified polyamine. 2. The bleach detergent composition according to Claim 1 wherein the modified polyamine has a polyamine backbone corresponding to the formula: (Formula Removed) having a modified polyamine formula V(n+1)WmYnZ or a polyamine backbone corresponding to the formula: (Formula Removed) having a modified polyamine formula V(n-k+1)WmYnY'kZ, wherein k is less than or equal to n, said polyamine backbone prior to modification has a molecular weight greater than about 200 daltons, wherein i) V units are terminal units having the formula: (Formula Removed) ii) W units are backbone units having the formula: (Formula Removed) iii) Y units are branching units having the formula: (Formula Removed) ; and iv) Z units are terminal units having the formula: (Formula Removed) wherein backbone linking R units are selected from the group consisting of C2-C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxy-alkyiene, C8-C12 dialkylarylene, -(R10)XR1-, -(R10)xR5(OR1)x-, -(CH2CH(OR2)CH20)Z(R10)yR1 (OCH2CH(OR2)CH2)W-, -C(0)(R4)rC(0)-, -CH2CH(OR2)CH2-, and mixtures thereof; wherein R1 is C2-C6 alkylene and mixtures thereof; R2 is hydrogen, -(R10)XB, and mixtures thereof; R3 is C1-C18 alkyl, C7-C12 arylalkyl, C7-C12 alkyl substituted aryl, C6-C12 aryl, and mixtures thereof; R4 is C1-C12 alkylene, C4-C12 alkenylene, C8-C12 arylalkylene, C6-C10 arylene, and mixtures thereof; R5 is C1-C12 alkylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxy-alkyiene, C8-CI2 dialkylarylene, -C(0)-, -C(0)NHR6NHC(0)-, -R1(OR1)-, -C(0)(R4)rC(0)-, -CH2CH(OH)CH2-, - CH2CH(OH)CH20(R10)yR1OCH2CH(OH)CH2-, and mixtures thereof; R6 is C2-C12 alkylene or C6-C12 arylene; E units are selected from the group consisting of hydrogen, C1-C22 alkyl, C22 alkenyl, C7-C22 arylalkyl, C2-C22 hydroxyalkyl, -(CH2)pC02M, -(CH2)qS03M, -CH(CH2C02M)C02M, -(CH2)pPO3M, -(R10)XB, -C(0)R3, and mixtures thereof; oxide; B is hydrogen, C1-C6 alkyl, -(CH2)qS03M, -(CH2)pC02M, -(CH2)q(CHS03M)CH2S03M,-(CH2)q-(CHSO2M)CH2S03M, -(CH2)pp03M- -PO3M, and mixtures thereof; M is hydrogen or a water soluble cation in sufficient amount to satisfy charge balance; X is a water soluble anion; m has the value from 4 to about 400; n has the value from 0 to about 200; p has the value from 1 to 6, q has the value from 0 to 6; r has the value of 0 or 1; w has the value 0 or 1; x has the value from 1 to 100; y has the value from 0 to 100; z has the value 0 or 1. 3. The bleach detergent composition according to Claim 2 wherein the anionic agent is selected from an anionic detersive surfactant, and inorganic salt having a buffering pH of between 7 and 10, and mixtures thereof. 4. The bleach detergent composition according to Claim 3 wherein the anionic agent is an anionic detersive surfactant selected from the group consisting of C11-C18 alkyl benzene sulfonate, C10-C20 alkyl sulfate, C10-C18 secondary (2,3) alkyl sulfate of the formula CH3(CH2)x(CHOS03-M+) CH3 and CH3 (CH2)y(CHOSO3-M+) CH2CH3 where x and (y + 1} are integers of at least about 7, and M is a water-solubilizing cation, especially sodium, alkenyl sulfate, C10-C18 alkyl alkoxy sulfate, C10-C18 alky! alkoxy carboxylate, C10-C18 glycerol ether, C12-C18 alpha-sulfonated fatty acid ester, and mixtures thereof. 5. The bleach detergent composition of Claim 2 wherein the bleach agent is selected from the group consisting of sodium perborate tetrahydrate, sodium perborate monohydrate, sodium percarbonate, and mixtures thereof. 6. The bleach detergent composition according to Claim 5 further comprising a bleach activator which can combine with a peroxygen bleaching agents in situ in an aqueous solution to form a peroxy acid bleaching agent corresponding to the bleach activator. 7. The bleach detergent composition according to Claim 6 wherein the bleach activator is selected from nonanoyloxybenzene sulfonate, tetraacetyl ethylene diamine, and mixtures thereof. 8. A bleach detergent composition comprising: a) from about 0.1 % to about 30% by weight a detersive surfactant selected from the group consisting of anionic, nonionic, cationic, zwitterionic, and ampholytic surfactants, and mixtures thereof; b) from about 0.5% to about 30% by weight a bleach agent; c) from about 0.01 to about 10% by weight a complexed polyamine comprising a water-soluble alkoxylated polyamine and an anionic detersive surfactant; and d) adjunct ingredients selected from the group consisting of builders, optical brighteners, soil release polymers, dye transfer agents, dispersents, enzymes, suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes, enzymes, photoactivators, fluorescers, fabric conditioners, hydrolyzable surfactants, preservatives, anti-oxidants, chelants, stabilizers, anti-shrinkage agents, anti-wrinkle agents, germicides, fungicides, anti corrosion agents, and mixtures thereof. 9. A process for preparing a bleach detergent composition comprising the steps of: a) premixing a modified polyamine which is useful as a cotton soil release and dispersant agent, with an anionic agent capable of forming a complex with the modified polyamine, to form a complexed polyamine; b) combining the premix with other detergent ingredients; and c) adding to the combination a bleach agent. 10. The process according to Claim 9 wherein the anionic agent is an anionic detersive surfactant, in the form of a surfactant paste. 11. A process for prepaing a bleach detergent composition, substantially as hereinbefor described in any of the Examples. 12. A bleach detergent composition, substantially as herein before described in any of the Examples.

Full Text

BLEACH DETERGENT COMPOSITIONS CONTAINING MODIFIED POLYAMINE POLYMERS
FIELD OF THE INVENTION
The present invention relates to a bleach detergent composition that contains a modified polyamine especially useful as a cotton soil release and dispersant agent, and to processes for making.
BACKGROUND OF THE INVENTION
Various fabric surface modifying agents have been commercialized and are currently used in detergent compositions and fabric softener/antistatic articles and compositions. Examples of surface modifying agents are soil release polymers. Soil release polymers typically comprise an oligomeric or polymeric ester "backbone" and are generally very effective on polyester or other synthetic fabrics where the grease or similar hydrophobic stains form an attached film and are not easily removed in an aqueous laundering process. The soil release polymers have a less dramatic effect on "blended" fabrics, that is, on fabrics that comprise a mixture of cotton and synthetic material, and have little or no effect on cotton articles. Alkoxylated polyamines are heretofore known and have been shown to provide specific cleaning benefits. Examples of alkoxylated polyamines are disclosed in U.S. Patent 4,548,744, Connor, issued October 22, 1985. However, it has been surprisingly discovered that effective soil release agents for cotton articles and dispersants can be prepared from certain modified polyamines. This unexpected result has yielded compositions that can provide soil release benefits for cotton articles that were once available only on synthetic and synthetic-cotton blended fabric.
Typically, if bleaching agents are present, especially peroxygen bleaches which are formulated into both liquid and granular laundry detergent compositions, the formulator must consider the instability of a particular soil dispersant toward the bleach. Many successful dispersents have polyalkyleneamine or polyalkyleneimine backbones which are susceptible to oxidation at the amine functionalities and potentially to breakdown or fragmentation by bleaching agents which may be present. From another view, the interaction of bleaching agents with these polyalkyleneimine-based dispersents depletes the amount of bleach present, therefore affecting the bleaching performance.
Accordingly, there remains a need in the art for bleach compatible, highly effective hydrophobic soil dispersents. Surprisingly, it has been found that certain higher molecular weight polyalkyleneimines when complexed with an anionic species, particularly when

complexed at a pH of from about pH 5 to about pH 10, are compatible with a bleach agent in the bleach detergent composition, and additionally provide hydrophobic soil dispersion.
SUMMARY OF THE INVENTION
The present invention is a bleach detergent composition that comprises a bleach agent, and a complexed polyamine which comprises a modified polyamine and an anionic species capable of forming a complex with the modified polyamine. The modified polyamine is especially useful as a cotton soil release and dispersant agent. The complexed polyamine is less reactive with the bleach agent in a wash solution containing the bleach detergent composition. The invention also relates to a process for preparing a bleach detergent composition that contains a bleach agent and a complexed polyamine which is substantially non-reactive with the bleach agent in the wash solution.
The bleach detergent composition more particularly comprises a peroxygen bleach agent, a complexed polyamine comprising a modified polyamine and an anionic agent capable of forming a complex with the modified polyamine, and adjunct detergent ingredients.
The process of the present invention more particularly comprises the steps of pre-mixing a modified polyamine with an anionic agent, preferably an anionic detersive surfactant, to form a complexed polyamine, and thereafter, adding adjunct detergent ingredients, such as builders and water to form the bleach detergent composition.
All documents cited herein are incorporated herein by reference. All percentages and proportions are on a weight basis unless otherwise indicated.
DETAILED DESCRIPTION OF THE INVENTION
The bleach detergent composition preferably comprises:
a) at least about 0.01 % to about 95%, preferably from about 0.1% to about
60%, more preferably from about 0.1% to about 30% by weight, of a
detergent surfactant selected from the group consisting of anionic, nonionic,
cationic, zwitterionic, and ampholytic surfactants, and mixtures thereof;
b) from about 0.05% to about 30%, more preferably from about 0.5% to about
30%, most preferably from about 1% to about 20%, by weight, of a bleach
agent;
c) from about 0.01 to about 10% by weight, of a complexed polyamine, the
complexed polyamine comprising a water-soluble alkoxylated polyamine and
an anionic detersive surfactant; and
d) adjunct ingredients selected from the group consisting of builders, optical
brighteners, soil release polymers, dye transfer agents, dispersents, enzymes,
suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes,
enzymes, photoactivators, fluorescers, fabric conditioners, hydrolyzable
surfactants, preservatives, anti-oxidants, chelants, stabilizers, anti-shrinkage

agents, anti-wrinkle agents, germicides, fungicides, and corrosion agents, and mixtures thereof. The Bleach Agent
The bleaching agent preferably is a peroxygen bleaching compound which is capable of yielding hydrogen peroxide in an aqueous liquor. These compounds are well known in the art and include hydrogen peroxide and the alkali metal peroxides, organic peroxide bleaching compounds such as urea peroxide, and inorganic persalt bleaching compounds, such as the alkali metal perborates, percarbonates, perphosphates, and the like. Mixtures of two or more such bleaching compounds can also be used, if desired. Preferred peroxygen bleaching compounds include sodium perborate, commercially available in the form of mono-, tri-, and tetra-hydrate, sodium pyrophosphate peroxyhydrate, urea peroxy-hydrate, sodium peroxide, peroxyphthalate and sodium percarbonate. Particularly preferred are sodium perborate tetrahydrate, sodium perborate monohydrate and sodium percarbonate. Sodium percarbonate is especially preferred because it is very stable during storage and yet still dissolves very quickly in the bleaching liquor. It is believed that such rapid dissolution results in the formation of higher levels of percarboxylic acid and, thus, enhanced surface bleaching performance.
Another category of bleaching agent that can be used without restriction encompasses percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of meta-chloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid. Such bleaching agents are disclosed in U.S. Patent 4,483,781, Hartman, issued November 20, 1984, U.S. Patent Application 740,446, Burns et al, filed June 3, 1985, European Patent Application 0,133,354, Banks et al, published February 20, 1985, and U.S. Patent 4,412,934, Chung et al, issued November 1, 1983. Highly preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid as described in U.S. Patent 4,634,551, issued January 6, 1987 to Bums et al.
A preferred percarbonate bleach comprises dry particles having an average particle size in the range from about 500 micrometers to about 1,000 micrometers, not more than about 10% by weight of said particles being smaller than about 200 micrometers and not more than about 10% by weight of said particles being larger than about 1,250 micrometers. Optionally, the percarbonate can be coated with silicate, borate or water-soluble surfactants. Percarbonate is available from various commercial sources such as FMC, Solvay and Tokai Denka.
Mixtures of bleaching agents can also be used.
Bleach activators can also be added to the bleach detergent composition in addition to the peroxygen bleaching agents. The peroxygen bleaching agents, the perborates, the

percarbonates, etc., are preferably combined with bleach activators, which lead to the in situ production in aqueous solution (i.e., during the washing process) of the peroxy acid corresponding to the bleach activator. Various nonlimiting examples of activators are disclosed in U.S. Patent 4,915,854, issued April 10, 1990 to Mao et al, and U.S. Patent 4,412,934. The nonanoyloxybenzene sulfonate (NOBS) and tetraacetyl ethylene diamine (TAED) activators are typical, and mixtures thereof can also be used. See also U.S. 4,634,551 for other typical bleaches and activators useful herein. If present, the amount of bleach activators will typically be from about 0.1% to about 60%, more typically from about 0.5% to about 40% of the bleaching composition comprising the bleaching agent-plus-bleach activator.
Another class of bleach activators comprises the benzoxazin-type activators disclosed by Hodge et al in U.S. Patent 4,966,723, issued October 30, 1990, incorporated herein by reference. A highly preferred activator of the benzoxazin-type is:
(Formula Removed)
Still another class of preferred bleach activators includes the acyl lactam activators, especially acyl caprolactams and acyl valerolactams of the formulae:
(Formula Removed)
wherein R^ is H or an alkyl, aryl, alkoxyaryl, or alkaryl group containing from 1 to about 12 carbon atoms. Highly preferred lactam activators include benzoyl caprolactam, octanoyl caprolactam, 3,5,5-trimethylhexanoyl caprolactam, nonanoyl caprolactam, decanoyl caprolactam, undecenoyl caprolactam, benzoyl valerolactam, octanoyl valerolactam, decanoyl valerolactam, undecenoyl valerolactam, nonanoyl valerolactam, 3,5,5-trimethylhexanoyl valerolactam and mixtures thereof. See also U.S. Patent 4,545,784, issued to Sanderson, October 8, 1985, incorporated herein by reference, which discloses acyl caprolactams, including benzoyl caprolactam, adsorbed into sodium perborate.
Another preferred bleach agent is a peroxyacid bleaching agent, of which an amide substituted peroxyacid precursor compound is more preferred, including one having the formula:

(Formula Removed)
wherein R1 is C1-C14 alkyl, aryl, alkylaryl, and mixtures thereof; R2 is C1-C14 alkylene, arylene, alkylarylene, and mixtures thereof; R5 is hydrogen, C1-C10 alkyl, aryl, alkylaryl, and mixtures thereof; L is any suitable leaving group (a preferred leaving group is phenyl sulfonate). R1 preferably contains from 6 to 12 carbon atoms. R2 preferably contains from 4 to 8 carbon atoms. R1 may contain, where applicable, branching, substitution, or both and may be sourced from either synthetic sources or natural sources including for example, tallow fat. Analogous structural variations are permissible for R2. The substitution can include alkyl, halogen, nitrogen, sulfur and other typical substituent groups or organic compounds. R5 is preferably H or methyl. R1 and R5 should not contain more than 18 carbon atoms in total. Amide substituted bleach activator compounds of this type are described in EP-A-0170386.
Preferred examples of bleach activators of the above formulae include (6-octanamido-caproyl)oxybenzenesulfonate, (6-nonanamidocaproyl)oxybenzenesulfonate, (6-decanamido-caproyl)oxybenzenesulfonate, and mixtures thereof as described in U.S. Patent 4,634,551, incorporated herein by reference.
Bleaching agents other than oxygen bleaching agents are also known in the art and can be utilized herein. One type of non-oxygen bleaching agent of particular interest includes photoactivated bleaching agents such as the sulfonated zinc and/or aluminum phthalo-cyanines. See U.S. Patent 4,033,718, issued July 5, 1977 to Holcombe et al. If used, detergent compositions will typically contain from about 0.025% to about 1.25%, by weight, of such bleaches, especially sulfonate zinc phthalocyanine.
If desired, the bleaching compounds can be catalyzed by means of a manganese compound. Such compounds are well known in the art and include, for example, the manganese-based catalysts disclosed in U.S. Pat. 5,246,621, U.S. Pat. 5,244,594; U.S. Pat. 5,194,416; U.S. Pat. 5,1 14,606; and European Pat. App. Pub. Nos. 549.271A1, 549.272A1, 544,440A2, and 544,490A1; Preferred examples of these catalysts include MnIV2(u-0)3(1 ,4,7-trimethyl- 1 ,4, 7-triazacyclononane)2(PF6)2, MnIII2(u-0) 1 (u-OAc)22( 1 ,4,7-trimethyl-l,4,7-triazacyclononane)2.(ClO4)2, MnIV4(u-O)6( 1,4,7-triazacyclononane)4(C104)4, MnIIIMnIV4(u-0) \ (u-OAc)2_( 1 ,4,7-trimethyl- 1 ,4,7-triazacyclononane)2(CI04)3, MnIV(l,4,7-trimethyl-l,4,7-triazacyclononane)-(OCH3)3(PF6), and mixtures thereof. Other metal-based bleach catalysts include those disclosed in U.S. Pat. 4,430,243 and U.S. Pat. 5,1 14,61 1. The use of manganese with various complex ligands to enhance bleaching is also reported in the following United States

Patents: 4,728,455; 5,284,944; 5,246,612; 5,256,779; 5,280,117; 5,274,147; 5,153,161; and 5,227,084.
As a practical matter, and not by way of limitation, the compositions and processes herein can be adjusted to provide on the order of at least one part per ten million of the active bleach catalyst species in the aqueous washing liquor, and will preferably provide from about 0.1 ppm to about 700 ppm, more preferably from about 1 ppm to about 500 ppm, of the catalyst species in the laundry liquor. The Modified Polvamine
The modified polyamines used in the process invention are water-soluble or water-dispersible, especially useful for cleaning cotton-containing fabrics or as a dispersant. These polyamines comprise backbones that can be either linear or cyclic. The polyamine backbones can also comprise polyamine branching chains to a greater or lesser degree. In general, the polyamine backbones described herein are modified in such a manner that each nitrogen of the polyamine chain is thereafter described in terms of a unit that is substitutedt quatemized, oxidized, or combinations thereof.
For the purposes of the present invention the term "modification" is defined as replacing a backbone -NH hydrogen atom by an E unit (substitution), quatemizing a backbone nitrogen (quatemized) or oxidizing a backbone nitrogen to the N-oxide (oxidized). The terms "modification" and "substitution" are used interchangeably when referring to the process of replacing a hydrogen atom attached to a backbone nitrogen with an E unit. Quaternization or oxidation may take place in some circumstances without substitution, but preferably substitution is accompanied by oxidation or quaternization of at least one backbone nitrogen.
The linear or non-cyclic polyamine backbones that comprise the modified polyamines have the general formula:
(Formula Removed)
where the backbones prior to subsequent modification comprise primary, secondary and tertiary amine nitrogens connected by R "linking" units. The cyclic polyamine backbones comprising the modified polyamines used in the present invention have the general formula:
(Formula Removed)
where the backbones prior to subsequent modification comprise primary, secondary and tertiary amine nitrogens connected by R "linking" units.
For the purpose of the present invention, primary amine nitrogens comprising the backbone or branching chain once modified are defined as V or Z "terminal" units. For

example, when a primary amine moiety, located at the end of the main polyamine backbone or branching chain having the structure
(Formula Removed)
is modified according to the present invention, it is thereafter defined as a V "terminal" unit, or simply a V unit. However, for the purposes of the present invention, some or all of the primary amine moieties can remain unmodified subject to the restrictions further described herein below. These unmodified primary amine moieties by virtue of their position in the backbone chain remain "terminal" units. Likewise, when a primary amine moiety, located at the end of the main polyamine backbone having the structure
(Formula Removed)
is modified according to the present invention, it is thereafter defined as a Z "terminal" unit, or simply a Z unit. This unit can remain unmodified subject to the restrictions further described herein below.
In a similar manner, secondary amine nitrogens comprising the backbone or branching chain once modified are defined as W "backbone" units. For example, when a secondary amine moiety, the major constituent of the backbones and branching chains of the present invention, having the structure
(Formula Removed)
is modified according to the present invention, it is thereafter defined as a W "backbone" unit, or simply a W unit. However, for the purposes of the present invention, some or all of the secondary amine moieties can remain unmodified. These unmodified secondary amine moieties by virtue of their position in the backbone chain remain "backbone" units.
In a further similar manner, tertiary amine nitrogens comprising the backbone or branching chain once modified are further referred to as Y "branching" units. For example, when a tertiary amine moiety, which is a chain branch point of either the polyamine backbone or other branching chains or rings, having the structure
(Formula Removed)
is modified according to the present invention, it is thereafter defined as a Y "branching" unit, or simply a Y unit. However, for the purposes of the present invention, some or all or the tertiary amine moieties can remain unmodified. These unmodified tertiary amine moieties by virtue of their position in the backbone chain remain "branching" units. The R units associated with the V, W and Y unit nitrogens which serve to connect the polyamine nitrogens, are described herein below.
The final modified structure of the polyamines of the present invention can be therefore represented by the general formula

(Formula Removed)
for linear polyamine polymers and by the general formula
(Formula Removed)
for cyclic polyamine polymers. For the case of polyamines comprising rings, a Y' unit of the formula
(Formula Removed)
serves as a branch point for a backbone or branch ring. For every Y1 unit there is a Y unit having the formula
(Formula Removed)
that will form the connection point of the ring to the main polymer chain or branch. In the unique case where the backbone is a complete ring, the polyamine backbone has the formula
(Formula Removed)
therefore comprising no Z terminal unit and having the formula
(Formula Removed)
wherein k is the number of ring forming branching units. Preferably the polyamine backbones of the present invention comprise no rings.
In the case of non-cyclic polyamines, the ratio of the index n to the index m relates to the relative degree of branching. A fully non-branched linear modified polyamine according to the present invention has the formula
(Formula Removed)
that is, n is equal to 0. The greater the value of n (the lower the ratio of m to n), the greater the degree of branching in the molecule. Typically the value for m ranges from a minimum value of 4 to about 400, however larger values of m, especially when the value of the index n is very low or nearly 0, are also preferred.
Each polyamine nitrogen whether primary, secondary or tertiary, once modified according to the present invention, is further defined as being a member of one of three general classes; simple substituted, quaternized or oxidized. Those polyamine nitrogen units not modified are classed into V, W, Y, or Z units depending on whether they are primary, secondary or tertiary nitrogens. That is unmodified primary amine nitrogens are V or Z units, unmodified secondary amine nitrogens are W units and unmodified tertiary amine nitrogens are Y units for the purposes of the present invention.

Modified primary amine moieties are defined as V "terminal" units having one of three forms:
a) simple substituted units having the structure:
(Formula Removed)
b) quatemized units having the structure:
(Formula Removed)
wherein X is a suitable counter ion providing charge balance; and
c) oxidized units having the structure:
(Formula Removed)
Modified secondary amine moieties are defined as W "backbone" units having one of three forms:
a) simple substituted units having the structure:
(Formula Removed)
b) quatemized units having the structure:
(Formula Removed)
wherein X is a suitable counter ion providing charge balance; and
c) oxidized units having the structure:
(Formula Removed)
Modified tertiary amine moieties are defined as Y "branching" units having one of three forms:
a) unmodified units having the structure:
(Formula Removed)
b) quaternized units having the structure:

(Formula Removed)
wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure:
(Formula Removed)
Certain modified primary amine moieties are defined as Z "terminal" units having one of three forms:
a) simple substituted units having the structure:
(Formula Removed)
b) quaternized units having the structure:
(Formula Removed)
wherein X is a suitable counter ion providing charge balance; and c) oxidized units having the structure:
(Formula Removed)
When any position on a nitrogen is unsubstituted of unmodified, it is understood that hydrogen will substitute for E. For example, a primary amine unit comprising one E unit in the form of a hydroxyethyl moiety is a V terminal unit having the formula (HOCH2CH2)HN-
For the purposes of the present invention there are two types of chain terminating units, the V and Z units. The Z "terminal" unit derives from a terminal primary amino moiety of the structure -NH2- Non-cyclic polyamine backbones according to the present invention comprise only one Z unit whereas cyclic polyamines can comprise no Z units. The Z "terminal" unit can be substituted with any of the E units described further herein below, except when the Z unit is modified to form an N-oxide. In the case where the Z unit nitrogen is oxidized to an N-oxide, the nitrogen must be modified and therefore E cannot be a hydrogen.

The polyamines of the present invention comprise backbone R "linking" units that serve to connect the nitrogen atoms of the backbone. R units comprise units that for the purposes of the present invention are referred to as "hydrocarbyl R" units and "oxy R" units. The "hydrocarbyr R units are C2-C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene wherein the hydroxyl moiety may take any position on the R unit chain except the carbon atoms directly connected to the polyamine backbone nitrogens; C4-C12 dihydroxyalkylene wherein the hydroxyl moieties may occupy any two of the carbon atoms of the R unit chain except those carbon atoms directly connected to the polyamine backbone nitrogens; C8-C12 dialkylarylene which for the purpose of the present invention are arylene moieties having two alkyl substituent groups as part of the linking chain. For example, a dialkylarylene unit has the formula

(Formula Removed)
although the unit need not be 1,4-substituted, but can also be 1,2 or 1,3 substituted C2-C12 alkylene, preferably ethylene, 1,2-propylene, and mixtures thereof, more preferably ethylene. The "oxy" R units comprise -(R1O)XR5(ORI)X-,
-CH2CH(OR2)CH20)z(R10)yR1 (OCH2CH(OR2)CH2)W-, -CH2CH(OR2)CH2-, -(R'O)xRl-, and mixtures thereof. Preferred R units are C2~C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxyalkylene, C8-C12 dialkylarylene, -(R 10)XR 1 -,-CH2CH(OR2)CH2-, -(CH2CH(OH)CH20)z(R10)yR1(OCH2CH-(OH)CH2)w-, -(R10)XR5(OR1)X-, more preferred R units are C2-C12 alkylene, C3-C12 hydroxy-alkylene, C4-C12 dihydroxyalkylene, -{R1O)xR1-, -(R10)xR5(ORi)x-,
-(CH2CH(OH)CH20)z(R10)yR1(OCH2CH-(OH)CH2)w-. and mixtures thereof, even more preferred R units are C2-C12 alkylene, C3 hydroxyalkylene, and mixtures thereof, most preferred are C2-C6 alkylene. The most preferred backbones of the present invention comprise at least 50% R units that are ethylene.
R1 units are C2-C6 alkylene, and mixtures thereof, preferably ethylene. R2 is hydrogen, and -{R1O)XB, preferably hydrogen.
R3 is C1-C18 alkyl, C1-C12 arylalkylene, C1-C12 alkyl substituted aryl, C6-C12 aryl, and mixtures thereof, preferably C1-C12 alkyl, C7-C12 arylalkylene, more preferably C1-C12 alkyl, most preferably methyl. R3 units serve as part of E units described herein below.
R4 is C1-C12 alkylene, C4-C12 alkenylene, C8-C12 arylalkylene, C6-C10 arylene, preferably C1-C10 alkylene, C8-C12 arylalkylene, more preferably C2-C8alkylene, most preferably ethylene or butylene.

R5 is C1-C12 alkylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxyalkylene, C8-C12 dialkylarylene, -C(O)-, -C(O)NHR6NHC(O)-, -C(0)(R4)rC(O)-, -R1(OR1)-, -CH2CH(OH)CH2O(R1O)yR1OCH2CH(OH)CH2-, -C(0)(R4)rC(0)-, -CH2CH(OH)CH2-, R5 is preferably ethylene, -C(O)-, -C(O)NHR6NHC(0)-, -R1(OR1)-, -CH2CH(OH)CH2-, -CH2CH(OH)CH20(R10)yR1OCH2CH-(OH)CH2-, more preferably -CH2CH(OH)CH2-.
R6 is C2-C12 alkylene or C6-C12 arylene.
The preferred "oxy" R units are further defined in terms of the R1, R2, and R5 units. Preferred "oxy" R units comprise the preferred R1, R2, and R5 units. The preferred modified polyamines comprise at least 50% R1 units that are ethylene. Preferred R1, R2, and R5 units are combined with the "oxy" R units to yield the preferred "oxy" R units in the following manner.
i) Substituting more preferred R5 into -(CH2CH2O)XR5(OCH2CH2)X- yields
-(CH2CH2O)XCH2CHOHCH2(OCH2CH2)X-.
ii) Substituting preferred R1 and R2 into -(CH2CH(OR2)CH20)Z-
(R10)yRI0(CH2CH(OR2)CH2)w- yields -{CH2CH(OH)CH20)Z-(CH2CH20)yCH2CH20(CH2CH(OH)CH2)w-.
iii) Substituting preferred R2 into -CH2CH(OR2)CH2- yields -CH2CH(OH)CH2-.
E units are selected from the group consisting of hydrogen, C1-C22 alkyl, C3-C22 alkenyl, C7-C22 arylalkyl, C2-C22 hydroxyalkyl, -{CH2)pC02M, -(CH2)qS03M, -CH(CH2C02M)C02M, -{CH2)pPO3M, -(R1O)mB, -C(0)R3, preferably hydrogen, C2-C22 hydroxyalkylene, benzyl, C1-C22 alkylene, -(R1O)mB, -C(0)R3, -(CH2)pC02M, -{CH2)qS03M, -CH(CH2CO2M)CO2M, more preferably C1-C22 alkylene, -(R1O)xB, -C(0)R3, -(CH2)pC02M, -{CH2)qS03M, -CH(CH2C02M)C02M, most preferably C1-C22 alkylene, -(R1O)xB, and -C(0)R3. When no modification or substitution is made on a nitrogen then hydrogen atom will remain as the moiety representing E.
E units do not comprise hydrogen atom when the V, W or Z units are oxidized, that is the nitrogens are N-oxides. For example, the backbone chain or branching chains do not comprise units of the following structure:
(Formula Removed)
Additionally, E units do not comprise carbonyl moieties directly bonded to a nitrogen atom when the V, W or Z units are oxidized, that is, the nitrogens are N-oxides. According

to the present invention, the E unit -C(0)R3 moiety is not bonded to an N-oxide modified nitrogen, that is, there are no N-oxide amides having the structure
(Formula Removed)
or combinations thereof.
B is hydrogen, C1-C6 alkyl, -(CH2)qS03M, -(CH2)pCO2M, -(CH2)q-(CHS03M)CH2S03M, -(CH2)q(CHS02M)CH2S03M, -(CH2)pP03M, -P03M, preferably hydrogen, -(CH2)qS03M, -(CH2)q(CHS03M)CH2S03M, -(CH2)q-(CHSO2M)CH2S03M, more preferably hydrogen or -(CH2)qS03M.
M is hydrogen or a water soluble cation in sufficient amount to satisfy charge balance. For example, a sodium cation equally satisfies -{CH2)pC02M, and -{CH2)qS03M, thereby resulting in -{CH2)pC02Na, and -(CH2)qS03Na moieties. More than one monovalent cation, (sodium, potassium, etc.) can be combined to satisfy the required chemical charge balance. However, more than one anionic group may be charge balanced by a divalent cation, or more than one mono-valent cation may be necessary to satisfy the charge requirements of a poly-anionic radical. For example, a -(CH2)pP03M moiety substituted with sodium atoms has the formula -(CH2)pP03Na3. Divalent cations such as calcium (Ca2+) or magnesium (Mg2+) may be substituted for or combined with other suitable mono-valent water soluble cations. Preferred cations are sodium and potassium, more preferred is sodium.
X is a water soluble anion such as chlorine (Cl~), bromine (Br) and iodine (I-) or X can be any negatively charged radical such as sulfate (SO42-) and methosulfate (CH3S03-).
The formula indices have the following values: p has the value from 1 to 6, q has the value from 0 to 6; r has the value 0 or 1; w has the value 0 or 1, x has the value from 1 to 100; y has the value from 0 to 100; z has the value 0 or 1; k is less than or equal to the value of n; m has the value from 4 to about 400, n has the value from 0 to about 200; m + n has the value of at least 5.
The preferred modified polyamines used in the present invention comprise polyamine backbones wherein less than about 50% of the R groups comprise "oxy" R units, preferably less than about 20% , more preferably less than 5%, most preferably the R units comprise no "oxy" R units.
The most preferred polyamines which comprise no "oxy" R units comprise polyamine backbones wherein less than 50% of the R groups comprise more than 3 carbon atoms. For

example, ethylene, 1,2-propylene, and 1,3-propylene comprise 3 or less carbon atoms and are the preferred "hydrocarbyl" R units. That is when backbone R units are C2-C12 alkylene, preferred is C2-C3 alkylene, most preferred is ethylene.
The polyamines of the present invention comprise modified homogeneous and non-homogeneous polyamine backbones, wherein 100% or less of the -NH units are modified. For the purpose of the present invention the term "homogeneous polyamine backbone" is defined as a polyamine backbone having R units that are the same (i.e., all ethylene). However, this sameness definition does not exclude polyamines that comprise other extraneous units comprising the polymer backbone which are present due to an artifact of the chosen method of chemical synthesis. For example, it is known to those skilled in the art that ethanolamine may be used as an "initiator" in the synthesis of polyethyleneimines, therefore a sample of polyethyleneimine that comprises one hydroxyethyl moiety resulting from the polymerization "initiator" would be considered to comprise a homogeneous polyamine backbone for the purposes of the present invention. A polyamine backbone comprising all ethylene R units wherein no branching Y units are present is a homogeneous backbone. A polyamine backbone comprising all ethylene R units is a homogeneous backbone regardless of the degree of branching or the number of cyclic branches present.
For the purposes of the present invention the term "non-homogeneous polymer backbone" refers to polyamine backbones that are a composite of various R unit lengths and R unit types. For example, a non-homogeneous backbone comprises R units that are a mixture of ethylene and 1,2-propylene units. For the purposes of the present invention a mixture of "hydrocarbyl" and "oxy" R units is not necessary to provide a non-homogeneous backbone. The proper manipulation of these "R unit chain lengths" provides the formulator with the ability to modify the solubility and fabric substantivity of the modified polyamines.
Preferred polyamines of the present invention comprise homogeneous polyamine backbones that are totally or partially substituted by polyethyleneoxy moieties, totally or partially quaternized amines, nitrogens totally or partially oxidized to N-oxides, and mixtures thereof. However, not all backbone amine nitrogens must be modified in the same manner, the choice of modification being left to the specific needs of the formulator. The degree of ethoxylation is also determined by the specific requirements of the formulator.
The preferred polyamines that comprise the backbone of the compounds of the present invention are generally polyalkyleneamines (PAA's), polyalkyleneimines (PAI's), preferably polyethyleneamine (PEA's), polyethyleneimines (PEI's), or PEA's or PEI's connected by moieties having longer R units than the parent PAA's, PAI's, PEA's or PEI's. A common polyalkyleneamine (PAA) is tetrabutylenepentamine. PEA's are obtained by reactions involving ammonia and ethylene dichlonde, followed by fractional distillation. The common PEA's obtained are triethylenetetramine (TETA) and teraethylenepentamine

(TEPA). Above the pentamines, i.e., the hexamines, heptamines, octamines and possibly nonamines, the cogenerically derived mixture does not appear to separate by distillation and can include other materials such as cyclic amines and particularly piperazines. There can also be present cyclic amines with side chains in which nitrogen atoms appear. See U.S. Patent 2,792,372, Dickinson, issued May 14, 1957, which describes the preparation of PEA's.
Preferred amine polymer backbones comprise R units that are C2 alkylene (ethylene) units, also known as polyethylenimines (PEI's). Preferred PEI's have at least moderate branching, that is the ratio of m to n is less than 4:1, however PEI's having a ratio of m to n of about 2:1 are most preferred. Preferred backbones, prior to modification have the general formula:
(Formula Removed)
wherein m and n are the same as defined herein above. Preferred PEI's, prior to modification, will have a molecular weight greater than about 200 daltons.
The relative proportions of primary, secondary and tertiary amine units in the polyamine backbone, especially in the case of PEI's, will vary, depending on the manner of preparation. Each hydrogen atom attached to each nitrogen atom of the polyamine backbone chain represents a potential site for subsequent substitution, quaternization or oxidation.
These polyamines can be prepared, for example, by polymerizing ethyleneimine in the presence of a catalyst such as carbon dioxide, sodium bisulfite, sulfuric acid, hydrogen peroxide, hydrochloric acid, acetic acid, etc. Specific methods for preparing these polyamine backbones are disclosed in U.S. Patent 2,182,306, Ulrich et al., issued December 5, 1939; U.S. Patent 3,033,746, Mayle et al., issued May 8, 1962; U.S. Patent 2,208,095, Esselmann et al., issued July 16, 1940; U.S. Patent 2,806,839, Crowther, issued September 17, 1957; and U.S. Patent 2,553,696, Wilson, issued May 21, 195 1; all herein incorporated by reference.
Examples of modified polyamines of the present invention comprising PEI's, are illustrated in Formulas I - IV:
Formula I depicts a polymer comprising a PEI backbone wherein all substitutable nitrogens are modified by replacement of hydrogen with a polyoxyalkyleneoxy unit, -(CH2CH2O)7H,having the formula

(Formula Removed)
This is an example of a polymer that is fully modified by one type of moiety.
Formula II depicts a polymer comprising a PEI backbone wherein all substitutable primary amine nitrogens are modified by replacement of hydrogen with a polyoxyalkyleneoxy unit, -(CH2CH2O)7H, the molecule is then modified by subsequent oxidation of all oxidizable primary and secondary nitrogens to N-oxides, wherein the polymer has the formula
(Formula Removed)
Formula III depicts a polymer comprising a PEI backbone wherein all backbone hydrogen atoms are substituted and some backbone amine units are quaternized. The substituents are polyoxyalkyleneoxy units, -(CH2CH2O)7H, or methyl groups. The modified PEI polymer has the formula
(Formula Removed)
Formula IV depicts a polymer comprising a PEI backbone wherein the backbone nitrogens are modified by substitution (i.e. by -(CH2CH2O)7H or methyl), quatemized, oxidized to N-oxides or combinations thereof. The resulting polymer has the formula
(Formula Removed)
In the above examples, not all nitrogens of a unit class comprise the same modification. The present invention allows the formulator to have a portion of the secondary amine nitrogens ethoxylated while having other secondary amine nitrogens oxidized to N-oxides. This also applies to the primary amine nitrogens, in that the formulator may choose to modify all or a portion of the primary amine nitrogens with one or more substiruents prior to oxidation or quatemization. Any possible combination of E groups can be substituted on the primary and secondary amine nitrogens, except for the restrictions described herein above. The Anionic Agent
The anionic agent can form an ionic complex with the nitrogens of the modified polyamine. Preferably this ion complex can be formed and is stable at a pH value in the range from about 5, up to about 10. The anionic agent has anionic functionality within this pH range, whereby when mixed with the modified polyamine under conditions where the pH of the mixture is from about 5 to about 10, the anionic agent and the polyamine can complex

to form a stable, complexed polyamine. The complexation occurs at the nitrogen sites of the polyamine, where the unshared pairs of electrons are available to complex with the anionic species of the anionic agent.
Preferred anionic agents are detergent ingredients that are typically used in detergent products and which are capable of forming the anionic species within the pH range of about 5 to about 10. Nonlimiting examples of such anionic agents include anionic detersive surfactants and inorganic salts having a buffering pH of between 7 and 10, and include polyphosphate builders, such as alkali tripolyphosphate and alkali pyrophosphate. Other common detergent ingredients such as sodium carbonate and sodium silicate are generally not suitable as an anionic agent, since they either do not form a suitable anionic species at such pH, or their alkalinity is sufficiently high that solutions containing these materials have a pH generally above 10.
At a pH above about 10, the modified polyamine will resist forming any kind of an ionic complex. Therefore, when mixed with agents that have high alkalinity, or when mixed with an anionic agent of the present invention but at solution conditions where the pH is above about 10, the desired complexed polyamine will not be formed. Consequently, then the mixture is processed into a bleach detergent composition, and subsequently added into a wash solution, the uncomplexed nitrogen sites of the modified polyamine can react with and destroy the bleach agent.
Nonlimiting examples of an anionic detersive surfactant useful as an anionic agent include the conventional C11-C18 alkyl benzene sulfonates ("LAS") and primary, branched-chain and random C10-C20 alkyl sulfates ("AS"), the C10-C18 secondary (2,3) alkyl sulfates of the formula CH3(CH2)X(CHOS03~M+) CH3 and CH3 (CH2)y(CHOS03~M+) CH2CH3 where x and (y + 1) are integers of at least about 7, preferably at least about 9, and M is a water-solubilizing cation, especially sodium, unsaturated sulfates such as oleyl sulfate, the C10-C18 alkyl alkoxy sulfates ("AExS"; especially EO 1-7 ethoxy sulfates),C10-C18 alky! alkoxy carboxylates (especially the EO 1-5 ethoxycarboxylates), the C10-18 glycerol ethers, and C12-C18 alpha-sulfonated fatty acid esters. Adjunct Detergent Ingredients
One or more adjunct detergent ingredients can be incorporated in the detergent composition during subsequent steps of the present process invention. These adjunct ingredients include other surfactants such as cationic surfactants, other detergency builders, suds boosters or suds suppressors, anti-tarnish and anticorrosion agents, soil suspending agents, soil release agents, germicides, pH adjusting agents, non-builder alkalinity sources, dictating agents such as diethylene triamine penta acetic acid (DTPA) and diethylene triamine penta(methylene phosphonic acid), smectite clays, enzymes, enzyme-stabilizing agents, dye transfer inhibitors and

perfumes. See U.S. Patent 3,936,537, issued February 3, 1976 to Baskerville, Jr. et al., incorporated herein by reference.
Other builders can be generally selected from the various water-soluble, alkali metal, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, borates, polyhydroxy sulfonates, polyacetates, carboxylates, and polycarboxylates. Preferred are the alkali metal, especially sodium, salts of the above. Preferred for use herein are the phosphates, carbonates, C10-18 fatty acids, polycarboxylates, and mixtures thereof. More preferred are sodium tripolyphosphate, tetrasodium pyrophosphate, citrate, tartrate mono- and di-succinates, and mixtures thereof (see below).
In comparison with amorphous sodium silicates, crystalline layered sodium silicates exhibit a clearly increased calcium and magnesium ion exchange capacity. In addition, the layered sodium silicates prefer magnesium ions over calcium ions, a feature necessary to insure that substantially all of the "hardness" is removed from the wash water. These crystalline layered sodium silicates, however, are generally more expensive than amorphous silicates as well as other builders. Accordingly, in order to provide an economically feasible laundry detergent, the proportion of crystalline layered sodium silicates used must be determined judiciously.
The crystalline layered sodium silicates suitable for use herein preferably have the formula
(Formula Removed)
wherein M is sodium or hydrogen, x is from about 1.9 to about 4 and y is from about 0 to about 20. More preferably, the crystalline layered sodium silicate has the formula
(Formula Removed)
wherein M is sodium or hydrogen, and y is from about 0 to about 20. These and other crystalline layered sodium silicates are discussed in Corkill et al, U.S. Patent No. 4,605,509, previously incorporated herein by reference.
Specific examples of inorganic phosphate builders are sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphates. Examples of polyphosphonate builders are the sodium and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts of ethane I-hydroxy-1, 1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid. Other phosphorus builder compounds are disclosed in U.S. Patents 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148, all of which are incorporated herein by reference.
Examples of nonphosphorus, inorganic builders are tetraborate decahydrate and silicates having a weight ratio of SiO2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4. Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, ammonium and substituted ammonium

polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates. Examples of polyacetate and polycarboxylate builders are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylene diamine tetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid.
Polymeric polycarboxylate builders are set forth in U.S. Patent 3,308,067, Diehl, issued March 7, 1967, the disclosure of which is incorporated herein by reference. Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itacomc acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylene malonic acid. Some of these materials are useful as the water-soluble anionic polymer as hereinafter described, but only if in intimate admixture with the non-soap anionic surfactant.
Other suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S. Patent 4,144,226, issued March 13, 1979 to Crutchfield et al, and U.S. Patent 4,246,495, issued March 27, 1979 to Crutchfield et al, both of which are incorporated herein by reference. These polyacetal carboxylates can be prepared by bringing together under polymerization conditions an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a detergent composition. Particularly preferred polycarboxylate builders are the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al., issued May 5, 1987, the disclosure of which is incorporated herein by reference.
Suitable smectite clays for use herein are described in U.S. Patent 4,762,645, Tucker et al, issued August 9, 1988, Column 6, line 3 through Column 7, line 24, incorporated herein by reference. Suitable additional detergency builders for use herein are enumerated in the Baskerville patent, Column 13, line 54 through Column 16, line 16, and in U.S. Patent 4,663,071, Bush et al, issued May 5, 1987, both incorporated herein by reference.
In order to make the present invention more readily understood, reference is made to the following examples, which are intended to be illustrative only and not intended to be limiting in scope. Process for Preparing Complexed Polvamines and Detergent Products therefrom
The process of the instant invention involves premixing a selected modified polyamine and an anionic agent to form the complexed polyamine. A preferred anionic agent is an anionic detersive surfactant, preferably in the form of a neutralized sulfate or sulfonate detersive surfactant paste. The surfactant paste can comprise the anionic detersive surfactant, and optionally a nonionic surfactant, but preferably will not contain a cationic

surfactant. In addition to the improved stability to bleach agents, the polyamine/surfactant complex typically has a higher oxidative degradation temperature as compared to the degradation temperature of the modified polyamines by themselves.
In a preferred process, the modified polyamine and anionic surfactant are mixed in an in-line static mixer or a conventional mixer (e.g., crutcher) for at least about 1 minute. The temperature at which the premixing step using the surfactant paste is performed typically is at a temperature of from about 25°C to about 80°C. Also, it is preferred to maintain the pH of the premix at from about 5 to about 10, more preferably at from about 8 to about 10, and most preferably at about 8 to 9. While the mixture will typically comprise only the anionic surfactant and the modified polyamine, other detergent adjuncts can be added with or to the mixture; such adjuncts can include, by example, sodium tripolyphosphate, water, and other detersive surfactants
The modified polyamine is preferably present in an amount of from about 0.01% to about 10%, more preferably from about 0.05% to about 5%, and most preferably from about 0.1% to about 1.0%, by weight of the overall detergent composition. Further, in the premixing step, the detersive surfactant paste preferably comprises from about 1% to about 70%, more preferably from about 20% to about 60%, and most preferably from about 25% to about 50%, by weight of surfactant, and the balance water and other minor ingredients. The surfactant paste comprising the complexed polyamine can then be made into detergents products, including both granular detergent products and liquid detergent products, by processes well known to those skilled in the art.
The premixed complexed polyamine is then further processed into detergent compositions by known methods, which include slurrying and spray drying, and agglomeration, as discussed herein below. The bleach detergent compositions made using the complexed polyamine, when placed into wash solutions, with or without soil loads, exhibit less loss of the bleach agent present in a washing solution compared to comparable compositions made by similar processes, except that the modified polyamine is either sprayed-on to or admixed as a particle into the detergent.
In a preferred process, the surfactant paste containing the complexed polyamine is made into a granular detergent process via a spray drying method. After the surfactant paste is processed into a detergent slurry along with other detergent adjuncts (including, by example, zeolite, inorganic salts such as sodium tripolyphosphate, carbonate and sulfate, silicates, optional detergent surfactants, polymeric polycarboxylate builders, silicates, optical brighteners, colorants, antiredeposition agents, fillers, and other compatible detergent ingredients, and mixtures thereof), the slurry is spray dried to form a spray-dried granular detergent composition. This step can be completed in a conventional spray drying tower operated at an inlet temperature range of from about 180°C to about 420°C. Such known

apparatus operates by spraying the slurry via nozzles into a counter-current (or co-current) stream of hot air which ultimately forms porous spray-dried granules.
An alternative process comprises a) premixing an anionic surfactant paste and a modified polyamine, b) agglomerating the surfactant paste comprising the complexed polyamine with other dry detergent ingredients i) initially in a high speed mixer/densifier, and ii) subsequently in a moderate speed mixer/densifier, to form agglomerates. The modified polyamine and surfactant paste are mixed for at least about 5 seconds, preferably from about 5 seconds to about 1 minute in any acceptable known mixing apparatus such as an in-line static mixer, twin-screw extruder, stirred mixing tanks and the like. The temperature at which the premixing step using the surfactant paste is performed typically is at a temperature of from about 25°C to about 80°C. The pH of the premix should be maintained between a pH of about 5 to about 10, preferably at from about 8 to about 10, and preferably without other detergent ingredients present. The modified polyamine is preferably present in an amount of from about 0.01% to about 10%, more preferably from about 0.05% to about 5%, and most preferably from about 0.1% to about 1.0%, by weight of the overall detergent composition. Further, in the premixing step, the detersive surfactant paste preferably comprises from about 1 % to about 70%, more preferably from about 20% to about 60%, and most preferably from about 25% to about 50%, by weight of a detersive surfactant the balance water and other minor ingredients.
The premix of modified polyamine and surfactant paste is initially agglomerated in a high speed mixer/densifier followed by a moderate speed mixer/densifier. The high speed mixer/densifier is a Lodige CB 30 mixer or similar brand mixer. These types of mixers essentially consist of a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached. Preferably, the shaft rotates at a speed of from about 100 rpm to about 2500 rpm, more preferably from about 300 rpm to about 1600 rpm. Preferably, the mean residence time of the detergent ingredients in the high speed mixer/densifier is preferably in range from about 2 seconds to about 45 seconds, and most preferably from about 5 seconds to about 15 seconds.
Preferably, the resulting detergent agglomerates formed in the high speed mixer/densifier are then fed into a lower or moderate speed mixer/densifier during which further agglomeration and densification is carried forth. This particular moderate speed mixer/densifier used in the present process should include liquid distribution and agglomeration tools so that both techniques can occur simultaneously. It is preferable to have the moderate speed mixer/densifier be, for example, a Lodige KM 600 (Ploughshare) mixer, Drais® K-T 160 mixer or similar brand mixer. The residence time in the moderate speed mixer/densifier is preferably from about 0.5 minutes to about 15 minutes, most preferably the residence time is about 1 to about 10 minutes. The liquid distribution can be accomplished

by cutters, generally smaller in size than the rotating shaft, which preferably operate at about 3600 rpm. It should be understood that while the processing described herein is relative to formation of high density agglomerates, the same equipment and processing steps may be used to produce less or moderately dense agglomerates. Of course, agglomerates produced by the process regardless of the density can be admixed with less dense spray-dried granules in the final detergent product, if desired.
The detergent agglomerates produced by the process preferably have a surfactant level of from about 25% to about 55%, more preferably from about 35% to about 55% and, most preferably from about 45% to about 55%. The particle porosity of the resulting detergent agglomerates produced according to the process of the invention is preferably in a range from about 5% to about 20%, more preferably at about 10%. In addition, an attribute of dense or densified agglomerates is the relative particle size. The present process typically provides detergent agglomerates having a median particle size of from about 400 microns to about 700 microns, and more preferably from about 400 microns to about 600 microns. As used herein, the phrase "median particle size" refers to individual agglomerates and not individual particles or detergent granules. The combination of the above-referenced porosity and particle size results in agglomerates having density values of 650 g/1 and higher. Alternatively, the particle size and porosity can be adjusted to produce agglomerates having lower densities, as well (e.g., 300 g/1 to 500 g/l). Such features are especially useful in the production of low as well as high or conventional dosage laundry detergents as well as other granular compositions such as dishwashing compositions.
The detergent agglomerates formed by the above process are then optionally dried in a fluid bed dryer and/or further conditioned by cooling the agglomerates in a fluid bed cooler or similar apparatus as are well known in the art. Another optional process step involves adding a coating agent to improve flowability and/or minimize over agglomeration of the detergent composition in one or more of the following locations of the instant process: (1) the coating agent can be added directly after the fluid bed cooler or dryer; (2) the coating agent may be added between the fluid bed dryer and the fluid bed cooler; (3) the coating agent may be added between the fluid bed dryer and the mixer/densifier(s); and/or (4) the coating agent may be added directly to one or more of the mixer/densifiers. The coating agent is preferably selected from the group consisting of aluminosilicates, silicates, carbonates and mixtures thereof. The coating agent not only enhances the free flowability of the resulting detergent composition which is desirable by consumers in that it permits easy scooping of detergent during use, but also serves to control agglomeration by preventing or minimizing over agglomeration, especially when added directly to the mixer/densifier(s). As those skilled in the art are well aware, over agglomeration can lead to very undesirable flow properties and aesthetics of the final detergent product.

Other optional steps in the present process involve recycling oversized and undersized agglomerates as described in Capeci et al, U.S. Patent Nos. 5,489,392 and 5,516,448 (Procter & Gamble). Also, the step of including an anhydrous material at selected points in the process can be incorporated as described by Capeci et al, U.S. Patent No. 5,366,652 and 5,486,303 (Procter & Gamble). Optionally, the agglomerates exiting the moderate speed mixer/densifier can be dried in a spray drying tower as described in Capeci et al, U.S. Patent 5,496,487 (Procter & Gamble).
Optionally, the process can comprises the step of spraying an additional binder in the mixer/densifier(s). A binder is added for purposes of enhancing agglomeration by providing a "binding" or "sticking" agent for the detergent components. The binder is preferably selected from the group consisting of water, anionic surfactants, nonionic surfactants, polyethylene glycol, polyvinyl pyrrolidone polyacrylates, citric acid and mixtures thereof. Other suitable binder materials including those listed herein are described in Beerse et al, U.S. Patent No. 5,108,646 (Procter & Gamble), the disclosure of which is incorporated herein by reference.
Another optional step of the instant process entails finishing the resulting detergent agglomerates by a variety of processes including spraying and/or admixing other conventional detergent ingredients. For example, the finishing step encompasses spraying on perfumes, and the addition of brighteners and enzymes to the finished agglomerates to provide a more complete detergent composition. Such techniques and ingredients are well known in the art.
EXAMPLE I Preparation of PEI 1800 E7
This Example illustrates a method by which one of the selected modified polyamines is made. The ethoxylation is conducted in a 2 gallon stirred stainless steel autoclave equipped for temperature measurement and control, pressure measurement, vacuum and inert gas purging, sampling, and for introduction of ethylene oxide as a liquid. A -20 Ib. net cylinder of ethylene oxide (ARC) is set up to deliver ethylene oxide as a liquid by a pump to the autoclave with the cylinder placed on a scale so that the weight change of the cylinder could be monitored.
A 750 g portion of polyethyleneimine (PEI) (Nippon Shokubai, Epomin SP-018 having a listed average molecular weight of 1800 equating to about 0.417 moles of polymer and 17.4 moles of nitrogen functions) is added to the autoclave. The autoclave is then sealed and purged of air (by applying vacuum to minus 28" Hg followed by pressurization with nitrogen to 250 psia, then venting to atmospheric pressure). The autoclave contents are heated to 130 °C while applying vacuum. After about one hour, the autoclave is charged with nitrogen to about 250 psia while cooling the autoclave to about 105 °C. Ethylene oxide is then added to the autoclave incrementally over time while closely monitoring the autoclave

pressure, temperature, and ethylene oxide flow rate. The ethylene oxide pump is turned off and cooling is applied to limit any temperature increase resulting from any reaction exotherm. The temperature is maintained between 100 and 110 °C while the total pressure is allowed to gradually increase during the course of the reaction. After a total of 750 grams of ethylene oxide has been charged to the autoclave (roughly equivalent to one mole ethylene oxide per PEI nitrogen function), the temperature is increased to 110 °C and the autoclave is allowed to stir for an additional hour. At this point, vacuum is applied to remove any residual unreacted ethylene oxide.
Next, vacuum is continuously applied while the autoclave is cooled to about 50 °C while introducing 376 g of a 25% sodium methoxide in methanol solution (1.74 moles, to achieve a 10% catalyst loading based upon PEI nitrogen functions). The methoxide solution is sucked into the autoclave under vacuum and then the autoclave temperature controller setpoint is increased to 130 °C. A device is used to monitor the power consumed by the agitator. The agitator power is monitored along with the temperature and pressure. Agitator power and temperature values gradually increase as methanol is removed from the autoclave and the viscosity of the mixture increases and stabilizes in about 1 hour indicating that most of the methanol has been removed. The mixture is further heated and agitated under vacuum for an additional 30 minutes.
Vacuum is removed and the autoclave is cooled to 105 °C while it is being charged with nitrogen to 250 psia and then vented to ambient pressure. The autoclave is charged to 200 psia with nitrogen. Ethylene oxide is again added to the autoclave incrementally as before while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate while maintaining the temperature between 100 and 110 °C and limiting any temperature increases due to reaction exotherm. After the addition of 4500 g of ethylene oxide (resulting in a total of 7 moles of ethylene oxide per mole of PEI nitrogen function) is achieved over several hours, the temperature is increased to 110 °C and the mixture stirred for an additional hour.
The reaction mixture is then collected in nitrogen purged containers and eventually transferred into a 22 L three neck round bottomed flask equipped with heating and agitation. The strong alkali catalyst is neutralized by adding 167 g methanesulfonic acid (1.74 moles). The reaction mixture is then deodorized by passing about 100 cu. ft. of inert gas (argon or nitrogen) through a gas dispersion frit and through the reaction mixture while agitating and heating the mixture to 130 °C. The final reaction product is cooled slightly and collected in glass containers purged with nitrogen. In other preparations the neutralization and deodorization is accomplished in the reactor before discharging the product.
EXAMPLE II Formation of amine oxide of PEI 1800 E7

This Example illustrates another method by which one of the selected modified polyamines is made. To a 500 mL Erlenmeyer flask equipped with a magnetic stirring bar is added polyethyleneimine having a molecular weight of 1800 and ethoxylated to a degree of about 7 ethoxy groups per nitrogen (PEI-1800, E7) (209 g, 0.595 mole nitrogen, prepared as in Example I), and hydrogen peroxide (120 g of a 30 wt % solution in water, 1.06 mole). The flask is stopped, and after an initial exotherm the solution is stirred at room temperature overnight. 1H-NMR (D20) spectrum obtained on a sample of the reaction mixture indicates complete conversion. The resonances ascribed to methylene protons adjacent to unoxidized nitrogens have shifted from the original position at ~2.5 ppm to ~3.5 ppm. To the reaction solution is added approximately 5 g of 0.5% Pd on alumina pellets, and the solution is allowed to stand at room temperature for approximately 3 days. The solution is tested and found to be negative for peroxide by indicator paper. The material as obtained is suitably stored as a 51.1 % active solution in water.
EXAMPLE III Preparation of PEI 1200 E7
This Example illustrates yet another method by which one of the selected modified polyamines is made. The ethoxylation is conducted in a 2 gallon stirred stainless steel autoclave equipped for temperature measurement and control, pressure measurement, vacuum and inert gas purging, sampling, and for introduction of ethylene oxide as a liquid. A -20 Ib. net cylinder of ethylene oxide (ARC) is set up to deliver ethylene oxide as a liquid by a pump to the autoclave with the cylinder placed on a scale so that the weight change of the cylinder could be monitored. A 750 g portion of polyethyleneimine (PEI) (having a listed average molecular weight of 1200 equating to about 0.625 moles of polymer and 17.4 moles of nitrogen functions) is added to the autoclave. The autoclave is then sealed and purged of air (by applying vacuum to minus 28" Hg followed by pressurization with nitrogen to 250 psia, then venting to atmospheric pressure). The autoclave contents are heated to 130 °C while applying vacuum. After about one hour, the autoclave is charged with nitrogen to about 250 psia while cooling the autoclave to about 105 °C. Ethylene oxide is then added to the autoclave incrementally over time while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate. The ethylene oxide pump is turned off and cooling is applied to limit any temperature increase resulting from any reaction exotherm. The temperature is maintained between 100 and 110 °C while the total pressure is allowed to gradually increase during the course of the reaction. After a total of 750 grams of ethylene oxide has been charged to the autoclave (roughly equivalent to one mole ethylene oxide per PEI nitrogen function), the temperature is increased to 110 °C and the autoclave is allowed to stir for an additional hour. At this point, vacuum is applied to remove any residual unreacted ethylene oxide.

Next, vacuum is continuously applied while the autoclave is cooled to about 50 °C while introducing 376 g of a 25% sodium methoxide in methanol solution (1.74 moles, to achieve a 10% catalyst loading based upon PEI nitrogen functions). The methoxide solution is sucked into the autoclave under vacuum and then the autoclave temperature controller setpoint is increased to 130 °C. A device is used to monitor the power consumed by the agitator. The agitator power is monitored along with the temperature and pressure. Agitator power and temperature values gradually increase as methanol is removed from the autoclave and the viscosity of the mixture increases and stabilizes in about 1 hour indicating that most of the methanol has been removed. The mixture is further heated and agitated under vacuum for an additional 30 minutes.
Vacuum is removed and the autoclave is cooled to 105 °C while it is being charged with nitrogen to 250 psia and then vented to ambient pressure. The autoclave is charged to 200 psia with nitrogen. Ethylene oxide is again added to the autoclave incrementally as before while closely monitoring the autoclave pressure, temperature, and ethylene oxide flow rate while maintaining the temperature between 100 and 110 °C and limiting any temperature increases due to reaction exotherm. After the addition of 4500 g of ethylene oxide (resulting in a total of 7 moles of ethylene oxide per mole of PEI nitrogen function) is achieved over several hours, the temperature is increased to 110 °C and the mixture stirred for an additional hour. The reaction mixture is then collected in nitrogen purged containers and eventually transferred into a 22 L three neck round bottomed flask equipped with heating and agitation. The strong alkali catalyst is neutralized by adding 167 g methanesulfonic acid (1.74 moles). The reaction mixture is then deodorized by passing about 100 cu. ft. of inert gas (argon or nitrogen) through a gas dispersion frit and through the reaction mixture while agitating and heating the mixture to 130 °C. The final reaction product is cooled slightly and collected in glass containers purged with nitrogen. In other preparations the neutralization and deodorization is accomplished in the reactor before discharging the product.

EXAMPLE IV
A modified polyamine is made in accordance with Example I ("PEI1800 E7") and used in the process of the current invention to form spray dried laundry granules for a bleach detergent composition. For purposes of comparison, a bleach-containing spray-dried detergent composition is made into which the PEI 1800 E7 is not premixed, but is instead added after other adjunct detergent ingredients in the detergent slurry. Tthe detergent-making process illustrated herein is executed in a conventional pilot scale system. The system contains a batch mixer (called a "crutcher") in which the premixing and slurry mixing steps are completed, followed by a conventional spray drying tower ("tower"). The PEI1800 E7 is added to the crutcher along with a sodium linear alkylbenzene sulfonate ("LAS") surfactant paste (30% LAS and balance water) and is premixed at 25°C for about 5 minutes, wherein the pH of the premix is maintained at about 8 to 10. Thereafter, silicate, optical brightener, carboxymethyl cellulose ("CMC"), sodium carbonate, and water are added to the crutcher which is then mixed. Steam at a temperature of about 120°C, sodium sulfate and sodium tripolyphosphate are added to the crutcher as the contents are continuously mixed. The crutcher is operated in a batch mode, and contains 180 kg of wet crutcher mix per batch. In the tower, the wet crutcher mix is pumped under high pressure through atomizing nozzles to form a finely divided mist. A counter-current flow of hot air (210°C) is impinged upon the atomized mist, causing the drying of the mixture ultimately resulting in spray dried granules which are collected at the exit of the tower. Continuous operation of the spray drying tower is accomplished by using an intermediate tank which accumulates multiple batches from the crutcher and feeds in a continuous manner the spray drying tower. The spray-dried granules may be further processed, by adding additional detergent ingredients, if desired, to form a fully formulated laundry detergent composition.
The following spray-dried bleach-containing granular detergent compositions are made in accordance with the process invention (i.e. Compositions Band C) and processes outside the scope of the invention (i.e. Compositions A).
PEI1800E7 PEI1800E7
Composition Weight % in finished granules Order of Addition
A 1.0 % Last wet Ingredient
B 1.0% Premix with LAS First
C 0.5 % Premix with LAS First
Composition A is made via a process in which PEI1800 E7 is added as the last wet ingredient into the crutcher, without a premixing step with LAS. At this stage, the pH of the crutcher slurry is substantially higher than 10 (about 10.5-11.0). The order of addition to the crutcher is LAS paste / Silicate / Optical brightener / CMC / PEI 1800 E7 / Sodium Carbonate / Water; Steam / Sodium Sulphate / Sodium Tripolyphosphate ("STPP").

Sodium tripolyphosphate and other minors are admixed to the blown powder resulting in finished granular compositions A-C for which the relative proportions of the ingredients are set forth below: Detergent Ingredient
A B C
LAS 18.0 18.0 18.0
PEI1800E7 1.0 1.0 0.5
Bleach agent* 4.0 4.0 4.0
Sodium silicate (2.0R) 5.8 5.8 5.8
Optical brightener** 0.2 0.2 0.2
CMC 0.3 0.3 0.3
Sodium carbonate 10.0 10.0 10.0
Sodium sulfate 31.9 31.9 32.4
STPP 22.0 22.0 22.0
Water and minors 6.8 6.8 6.8
100.0 100.0 100.0
* The bleach agent is a 2:1 weight ratio of sodium perborate monohydrate and sodium nonanoyloxybenzene sulfonate bleach activator.
** Optical brightener slurried in 0.2% C45E7 Nonionic to ensure presence in organic phase.
The bleach detergent compositions B and C, made by premixing the PEI1800 E7 with LAS, exhibits less loss of the bleach agent in a wash solution compared to composition A made by same process, except wherein the PEI1800 E7 is the last wet ingredient added to the slurry.
EXAMPLE V
A modified polyamine is made in accordance with Example I ("PEI1800 E7") and used in the process of the current invention to form an agglomerated detergent composition. An in-line static mixer is used into which the PEI1800 E7 is added continuously along with a sodium linear alkylbenzene sulfonate ("LAS") surfactant paste (60% LAS and balance water) at about 60°C in order to completely mix the ingredients, wherein the pH of the premix is maintained at about 7 to 10. Thereafter, the premix are continuously fed to a high speed mixer/densifier (Lodige CB-30, commercially available from Lodige) along with sodium aluminosilicate (zeolite) and sodium carbonate. The rotational speed of the shaft in the Lodige CB-30 mixer/densifier is about 1400 rpm and the mean residence time is about 10 seconds. The contents from the Lodige CB-30 mixer/densifer are continuously fed into a Lodige KM 600 mixer/densifer for further agglomeration during which the mean residence time is about 6 minutes. The detergent agglomerates are then screened with conventional screening apparatus

resulting in a uniform particle size distribution. A bleach agent is then admixed with the
detergent agglomerates to form the bleach detergent product, having the set forth below:
Component % Weight
C12-13 linear alkylbenzene sulfonate 27.1
Sodium aluminosilicate 34.4
Sodium carbonate 17.5
Polyethylene glycol (MW 4000) 1.3
PEI1800E7 1.0
Bleach agent* 3.0
Misc. (water, etc.) 15.7
100.0
** The bleach agent is a 2:1 weight ratio of sodium perborate monohydrate and sodium nonanoyloxybenzene sulfonate bleach activator.
The agglomerated detergent composition made by premixing the PEI1800 E7 with LAS in the premixer exhibits less loss of the bleach agent in a wash solution, compared to a composition made by same process, except wherein the PEI1800 E7 is sprayed-on to the detergent agglomerates after agglomeration.
Having thus described the invention in detail, it will be clear to those skilled in the art that various changes may be made without departing from the scope of the invention and the invention is not to be considered limited to what is described in the specification.

We Claim:-
1. A bleach detergent composition comprising:
a) a bleach agent, and
b) a complexed polyamine, comprising
i) a modified polyamine useful as a cotton soil release and dispersant agent, and
ii) an anionic species capable of forming a complex with the modified polyamine.
2. The bleach detergent composition according to Claim 1 wherein the
modified polyamine has a polyamine backbone corresponding to the
formula:
(Formula Removed)
having a modified polyamine formula V(n+1)WmYnZ or a polyamine backbone corresponding to the formula:
(Formula Removed)
having a modified polyamine formula V(n-k+1)WmYnY'kZ,
wherein k is less than or equal to n, said polyamine backbone prior to modification has a molecular weight greater than about 200 daltons, wherein
i) V units are terminal units having the formula:
(Formula Removed)
ii) W units are backbone units having the formula:
(Formula Removed)
iii) Y units are branching units having the formula:
(Formula Removed)

; and

iv) Z units are terminal units having the formula:
(Formula Removed)
wherein backbone linking R units are selected from the group consisting of C2-C12 alkylene, C4-C12 alkenylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxy-alkyiene, C8-C12
dialkylarylene, -(R10)XR1-, -(R10)xR5(OR1)x-, -(CH2CH(OR2)CH20)Z(R10)yR1 (OCH2CH(OR2)CH2)W-, -C(0)(R4)rC(0)-, -CH2CH(OR2)CH2-, and mixtures thereof; wherein R1 is C2-C6 alkylene and mixtures thereof; R2 is hydrogen, -(R10)XB, and mixtures thereof; R3 is C1-C18 alkyl, C7-C12 arylalkyl, C7-C12 alkyl substituted aryl, C6-C12 aryl, and mixtures thereof; R4 is C1-C12 alkylene, C4-C12 alkenylene, C8-C12 arylalkylene, C6-C10 arylene, and mixtures thereof; R5 is C1-C12 alkylene, C3-C12 hydroxyalkylene, C4-C12 dihydroxy-alkyiene, C8-CI2 dialkylarylene, -C(0)-, -C(0)NHR6NHC(0)-, -R1(OR1)-, -C(0)(R4)rC(0)-, -CH2CH(OH)CH2-, -
CH2CH(OH)CH20(R10)yR1OCH2CH(OH)CH2-, and mixtures thereof; R6 is C2-C12 alkylene or C6-C12 arylene; E units are selected from the group consisting of hydrogen, C1-C22 alkyl, C22 alkenyl, C7-C22 arylalkyl, C2-C22 hydroxyalkyl, -(CH2)pC02M, -(CH2)qS03M,
-CH(CH2C02M)C02M, -(CH2)pPO3M, -(R10)XB, -C(0)R3, and mixtures thereof; oxide; B is hydrogen, C1-C6 alkyl, -(CH2)qS03M, -(CH2)pC02M,
-(CH2)q(CHS03M)CH2S03M,-(CH2)q-(CHSO2M)CH2S03M, -(CH2)pp03M- -PO3M, and mixtures thereof; M is hydrogen or a water soluble cation in sufficient amount to satisfy charge balance; X is a water soluble anion; m has the value from 4 to about 400; n has the value from 0 to about 200; p has the value from 1 to 6, q has the value from 0 to 6; r has the value of 0 or 1; w has the value 0 or 1; x has the value from 1 to 100; y has the value from 0 to 100; z has the value 0 or 1.

3. The bleach detergent composition according to Claim 2 wherein the
anionic agent is selected from an anionic detersive surfactant, and inorganic
salt having a buffering pH of between 7 and 10, and mixtures thereof.
4. The bleach detergent composition according to Claim 3 wherein the
anionic agent is an anionic detersive surfactant selected from the group
consisting of C11-C18 alkyl benzene sulfonate, C10-C20 alkyl sulfate,
C10-C18 secondary (2,3) alkyl sulfate of the formula
CH3(CH2)x(CHOS03-M+) CH3 and CH3 (CH2)y(CHOSO3-M+) CH2CH3
where x and (y + 1} are integers of at least about 7, and M is a water-solubilizing cation, especially sodium, alkenyl sulfate, C10-C18 alkyl alkoxy sulfate, C10-C18 alky! alkoxy carboxylate, C10-C18 glycerol ether, C12-C18 alpha-sulfonated fatty acid ester, and mixtures thereof.
5. The bleach detergent composition of Claim 2 wherein the bleach
agent is selected from the group consisting of sodium perborate
tetrahydrate, sodium perborate monohydrate, sodium percarbonate, and
mixtures thereof.
6. The bleach detergent composition according to Claim 5 further
comprising a bleach activator which can combine with a peroxygen
bleaching agents in situ in an aqueous solution to form a peroxy acid
bleaching agent corresponding to the bleach activator.
7. The bleach detergent composition according to Claim 6 wherein the
bleach activator is selected from nonanoyloxybenzene sulfonate, tetraacetyl
ethylene diamine, and mixtures thereof.
8. A bleach detergent composition comprising:

a) from about 0.1 % to about 30% by weight a detersive surfactant
selected from the group consisting of anionic, nonionic,
cationic, zwitterionic, and ampholytic surfactants, and mixtures
thereof;
b) from about 0.5% to about 30% by weight a bleach agent;

c) from about 0.01 to about 10% by weight a complexed
polyamine comprising a water-soluble alkoxylated polyamine
and an anionic detersive surfactant; and
d) adjunct ingredients selected from the group consisting of
builders, optical brighteners, soil release polymers, dye
transfer agents, dispersents, enzymes, suds suppressors,
dyes, perfumes, colorants, filler salts, hydrotropes, enzymes,
photoactivators, fluorescers, fabric conditioners, hydrolyzable
surfactants, preservatives, anti-oxidants, chelants, stabilizers,
anti-shrinkage agents, anti-wrinkle agents, germicides,
fungicides, anti corrosion agents, and mixtures thereof.
9. A process for preparing a bleach detergent composition comprising
the steps of:
a) premixing a modified polyamine which is useful as a cotton soil
release and dispersant agent, with an anionic agent capable of forming a
complex with the modified polyamine, to form a complexed polyamine;
b) combining the premix with other detergent ingredients; and
c) adding to the combination a bleach agent.
10. The process according to Claim 9 wherein the anionic agent is an
anionic detersive surfactant, in the form of a surfactant paste.
11. A process for prepaing a bleach detergent composition, substantially as hereinbefor described in any of the Examples.
12. A bleach detergent composition, substantially as herein before described in any of the Examples.

Documents:

in-pct-2000-123-del-abstract.pdf

in-pct-2000-123-del-assignment.pdf

in-pct-2000-123-del-claims.pdf

in-pct-2000-123-del-correspondence-others.pdf

in-pct-2000-123-del-correspondence-po.pdf

in-pct-2000-123-del-description (complete).pdf

in-pct-2000-123-del-form-1.pdf

in-pct-2000-123-del-form-19.pdf

in-pct-2000-123-del-form-2.pdf

in-pct-2000-123-del-form-26.pdf

in-pct-2000-123-del-form-3.pdf

in-pct-2000-123-del-form-5.pdf

in-pct-2000-123-del-gpa.pdf

in-pct-2000-123-del-pct-210.pdf

in-pct-2000-123-del-pct-331.pdf

in-pct-2000-123-del-pct-409.pdf

in-pct-2000-123-del-pct-416.pdf

in-pct-2000-123-del-petition-137.pdf

in-pct-2000-123-del-petition-138.pdf

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Patent Number

215645

Indian Patent Application Number

IN/PCT/2000/00123/DEL

PG Journal Number

11/2008

Publication Date

14-Mar-2008

Grant Date

28-Feb-2008

Date of Filing

07-Aug-2000

Name of Patentee

THE PROCTER & GAMBLE COMPANY,

Applicant Address

ONE PROCTER & GAMBLE PLAZA, CINCINNATI, OHIO 45202, UNITED STATES OF AMERICA.

Inventors:

#	Inventor's Name	Inventor's Address
1	CHAPMAN, BENJAMIN, EDGAR	9469 GALECREST DRIVE, CINCINNATI, OH, 45231, U.S.A.

PCT International Classification Number

C11D 1/02

PCT International Application Number

PCT/US99/02394

PCT International Filing date

1999-02-03

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	60/075383	1998-02-20	U.S.A.