CA2256892A1 - Detergent compositions - Google Patents

Abstract

There is provided a detergent composition suitable for use in laundry and dish washing methods comprising (a) a cationic ester surfactant; and (b) a grease dispersing agent.

Description

CA 022~6892 1998-11-26 W O 97/45512 PCT~US97/08235 Deter~ent compositions Technical field The present invention relates to detergent compositions cont~ining a cationic ester surfactant and a grease dispersing agent, which are suitable for use in laundry and dish w~hing methods.

Background -to the invention The satisfactory removal of greasy soils/stains, that is soils/stains having a high proportion of triglycerides or f.~tty acids, is a challenge faced by the form~ tor of detergent compositions for use in laundry and dish washing methods. Surfactant components ha~e traditionally been employed in detergent products to facilitate the removal of such greasy soils/stains. In particular, surfactant systems comprising cationic esters have been described for use in greasy soil/stain removal.

A challenge faced in laundry and dish washing is not just the removal of greasy soils and stains from the soiled/ stained substrate, but dispersion of the greasy stain/ soil components, thereby preventing their (re)deposition onto the substrates. Grease dispersing agents can be employed in detergents to achieve prevention of l re)deposition of greasy stains/soils.
Examples of grease dispersing agenls are polymers with hydrophobic side - chains and hydrophilic monomer units in the backbone.

EP-B-21,491 discloses detergent compositions cont~ining a nonionic/cationic surfactant mixture and a builder mixture comprising aluminosilicate and polycarboxylate builder. The cationic surfactant may CA 022~6892 1998-11-26 be a cationic ester. Improved particulate and greasy/oily soil removal is described.

US-A-4,228,042 discloses biodegradable cationic surfactants, including cationic ester surfactants for use in detergent compositions to provide greasy/oily soil removal. The combination of these cationic surfactants with nonionic surfactants in compositions designed for particulate soil removal is also described.

US-A-4,260,529 discloses laundry detergent compositions having a pH of no greater than 11 cont~ining cationic ester surfactant and nonionic surfactant at defined weight ratios.

WO 91/08281 discloses dispersing polymers for dispersion of detergent droplets, with a hydrophilic backbone and hydrophobic side chains.

It has now been found that the performance of certain grease dispersingagents in the traditional detergents is affected by the washing conditions, such as water hardness. Essential for the performance of grease dispersing agents is their affinity for and absorbance onto the (greasy) stain/ soil components on the fabric. However, absorbance onto the stained fabric can be problematic when 'limesoaps' (formed by the alkali and earth alkali metals of the water hardness with fatty acids) are present on the fabric. This problem is believed to cause the re~ ce~ performance of the dispersing agents.

The Applicants have now found that this problem can be ameliorated by the inclusion of cationic ester surfactants in detergents cont~inin~ grease dispersing agents, which are polymers with a hydrophilic backbone and hydrophobic side chain(s). Detergent compositions employing both components have shown to deliver a surprisingly better cleaning performance.

Two mechanisms are believed to be responsible for these benefits. Firstly, the cationic ester surfactant is can reduce deposition of 'lime soaps' on the fabric. The reduction of deposition will facilitate the absorbance of the grease dispersing agent onto the greasy soils or stains. Thereby, an CA 02256892 1998-ll-26 improvement of their dispersing performance is achieved. Secondly, it is believed that dle cationic ester surfactant can act to facilitate solubilisationof greasy soil/ st~in components. This will aid the grease dispersing agent's dispersal of the soil/ stain components. Thus, an overall improved cle~ning of the detergent is achieved.

All documents cited in the present description are, in relevant part, incol~orated herein by re~elellce.

S~mm~ry of the Invention The detergent coln~ ion of the ~rescll~ invention com~ises (a) a cationic ester surf~rt~nt; and (b) a grease dispersing agent.

Plefelably the grease dispersing agent is present at a level of from 0.1%
to 15 ~ by weight of the deterg~nt co.nl,osilion.

In a preferred aspect, the cationic ester surfactant is selected from those having the formula:

R
, +
Rl-- C~ (CH)no _ (X)u--( C H2 )m--(Y)v--(C H2 )t N- R3 M
-a wherein Rl is a Cs-C31 linear or branched alkyl, alkenyl or alkaryl chain or M-. N+(R6R7Rg)(CH2)S; X and Y, independently, are selected from the group conci~tin~ of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO, OCONH or NHCOO group; R2, R3, R4, R6, R7, and R8 are CA 022~6892 l998-ll-26 W O 97/45512 PCT~US97/08235 independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl, hydroxy-alkenyl and alkaryl groups having from 1 to 4 carbon atoms; and Rs is independently H or a C 1-C3 alkyl group;
wherein the values of m, n, s and t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v independently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter anion.

Detailed description of the invention Cationic ester surfactant An essential element of the detergent compositions of the invention is a cationic ester surfactant. The cationic ester surfactant is preferably present at a level from 0.1~ to 20.0~, more preferably from O.S% to 10%, most preferably from 1.0% to 5.0% by weight of the detergent composition.

The cationic ester surfactant of the present invention is a, preferablywater dispersible, compound having surfactant properties comprising at least one ester (i.e. -COO-) linkage and at least one cationically charged group.

Suitable cationic ester surfactants, including choline ester surfactants, have for example been disclosed in US Patents No.s 4228042, 4239660 and 4260529.

In one preferred aspect the ester linkage and cationically charged group are separated from each other in the surfactant molecule by a spacer group consisting of a chain comprising at least three atoms (i.e. of three atoms chain length), preferably from three to eight atoms, more preferably from three to five atoms, most preferably three atoms. The atoms forming the spacer group chain are selected from the group consisting of carbon, nitrogen and oxygen atoms and any mixtures thereof, with the proviso that any nitrogen or oxygen atom in said chain connects only with carbon atoms in the chain. Thus spacer groups having, for example, -O-O- (i.e. peroxide), -N-N-, and -N-O- linkages s are excluded, whilst spacer groups having, for example -CH2-O- CH2-and -CH2-NH-CH2- linkages are included. In a preferred aspect the spacer group chain comprises only carbon atoms, most preferably the chain is a hydrocarbyl chain.

Preferred cationic ester surf~ct~nt~e are those having the formula:

R5 1 +
Rl-- (3 (cH)no --(X)u--( C H 2 )m--(Y)v--(C H 2 )t--N--R3 M
- a R4 wherein Rl is a Cs-C31 linear or branched alkyl, alkenyl or alkaryl chain or M-. N+(~6R7R8)(CH2)S; X and Y, independently, are selected from the group con~ictin~ of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO, OCONH or NHCOO group; R2, R3, R4, R6, R7, and R8 are independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl and hydroxy-alkenyl groups having from 1 to 4 carbon atoms and alkaryl groups; and Rs is inde~elldently H or a Cl-C3 alkyl group; wherein the values of m, n, s and t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v in~ependently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter anion.

r~efe~ably M is selected from the group con.~i~tin~ of halide, methyl sulfate, sulf~te, and nitrate, more preferably methyl s~llf~te, chloride, bromide or iodide.

WO 97/45512 PCT/US97tO8235 In a preferred aspect, the cationic ester surfactant is selected from those having the formula:

R,2 R1 ~--(CH)nO (X) (CH2)m--N--R3 M-a wherein ~1 is a Cs-C31 linear or branched alkyl, alkenyl or alkaryl chain; X is seleceed from the group consisting of COO, OCO, OCOO, OCONH and NHCOO; R2, R3, and R4 are independently selected from the group con~ist~n~ of allyl and hydroxyalkyl groups having from 1 to 4 carbon atoms; and Rs is independently H or a Cl-C3 allyl group;
wherein the value of n lies in the range of from 0 to 8, the value of b lies in the range from 0 to 20, the value of a is ei~er 0 or 1, and ~e value of misfrom3to8.

More preferably R2, R3 and R4 are independently selected from a Cl-C4 alkyl group and a C1-C4 hydroxyalkyl group. In one preferred aspect at least one, preferably only one, of R2, R3 and R4 is a hydroxyalkyl group.
The hydroxyallyl ~refeldbly has from 1 to 4 carbon atoms, more plefel~bly 2 or 3 call,oll atoms, most preferably 2 carbon atoms. In al~otllcr preferred aspect at least one of R2, R3 and R4 is a C2-C3 alkyl group, more preferably two C2-C3 alkyl groups are present.

Highly p~felle~ water disl,ersible cationic ester surf~ct~nt~ are the esters having the formula:

1~
R1--C--O--(CH2)m--N+--CH3 M-where m is from 1 to 4, preferably 2 or 3 and wherein Rl is a C1 1-Clg linear or branched alkyl chain.

CA 022~6892 l998-ll-26 W O 97/45512 PCT~US97/08235 -Particularly preferred choline esters of this type include the stearoylcholine ester quaternary methylammonium halides (R1=C17 alkyl), palmitoyl choline ester quaternary methylammonium halides (R1=C1s alkyl), myristoyl choline ester quaternary methylammonium halides (Rl=C13 alkyl), lauroyl choline ester methylammonium halides (R1 =C1 1 alkyl), cocoyl choline ester quaternary methylammonium halides (Rl =Cl 1 C13 alkyl), tallowyl choline ester quaternary methylammonium halides (Rl =C 15 C 17 alkyl), and any mixtures thereof.

Other suitable cationic ester surfactants have the structural formulas below, wherein d may be from 0 to 20.

Rl- O - C -(CH2)d C - O - CH2CH2- 1 - CH3 M

M CH3- N - CH2 - CH2- O - C -(CH2)- C - O - CH2- CH2- N - CH3M

In a preferred aspect the cationic ester surfactant is hydrolysable under the conditions of a laundry wash method.

The particularly preferred choline esters, given above, may be preparedby the direct esterification of a fatty acid of the desired chain length with dimethylArninoethanol, in the presence of an acid catalyst. The reaction product is then quaternized with a methyl halide, preferably in the presence of a solvent such as ethanol, water, propylene glycol or preferably a fatty alcohol ethoxylate such as C1o-C1g fatty alcohol ethoxylate having a degree of ethoxylation of from 3 to 50 ethoxy groups per mole forming the desired cationic material. They may also be prepared by the direct esterification of a long chain fatty acid of the desired chain length together with 2-haloethanol, in the presence of an acid catalyst material. The reaction product is then quaternized with trimethyl~rnine, forming the desired cationic material.

CA 022~6892 1998-ll-26 W O 97/45512 PCT~US97/08235-Grease dispersin~ agent An essential element of the present invention is a grease dispersing agent.
By grease dispersing agent is meant herein a component capable of dispersing or suspending greasy stain/ soil components into the (wash) solution. The grease dispersing agents in accord with the present invention are typically polymers, which have a hydrophilic backbone and at least one hydrophobic side chain. The hydrophobic side chain acts functionally to provide affinity of the grease dispersing agent for greasy soil/stain components. The hydrophilic backbone acts functionally to provide affinity of the grease dispersing agent for a~ueous environments.

Generally the hydrophilic backbone of the polymer is predomin~ntly linear (the main chain of the backbone constitutes at least 50%, preferably more than 75 %, most preferred more than 90% by weight of the backbone), suitable monomer constituents of the hydrophilic backbone are for example ~ln~ rated C1-C6 acids, ethers, alcohols, aldehydes, ketones or esters, sugar units, alkoxy units, maleic anhydride and saturated polyalcohols such as glycerol. Examples of suitable monomer units are acrylic acid, methacrylic acid, maleic acid, vinyl acetic acid, glucosides, ethylene oxide and glycerol. The hydrophilic backbone made from the backbone constituents in the absence of hydrophobic side-groups is relatively water-soluble at ambient temperatures and a pH of between 6.5 and 14Ø
Preferably the solubility is more than 1 g/l, more preferably more than S
g/l, most preferably more than 10 g/l.

Preferably the hydrophobic sidegroups are composed of alkoxy groups forexample butylene oxide and/or propylene oxide and/or alkyl or alkenyl chains having from 5 to 24 carbon atoms. The hydrophobic groups may be connected to the hydrophilic backbone via relatively hydrophilic bonds for example a poly ethoxy linkage.

Preferred grease dispersing agents are the polymers of the formula:

H CH2 C C~2 C Q1 Q2 H

R10 R9 - r - - v q p - n Formula I
wherein:

Q2 is a molec~ r entity of formula (Ia):

j I R1 C02A1 C02A2 Co2A3 , R~ 1 2 - x - ~ Y L R3 , z Formula Ia wherein:

R1 represents -COO-O-, -O-, -O-CO-, -CH2-, CO-NH-, or is absent:

R2 represents from 1 to 50 independently selected alkyleneoxy groups preferably e~ylene oxide or propylene oxide groups, or is absent, provided that when R3 is absent and R4 represents hydrogen or contains CA 022~6892 1998-11-26 W O 97/45S12 PCT~US97/08235 -no more than 4 carbon atoms, then R2 must contain an alkyleneoxy group preferably more than S alkyleneoxy groups with at least 3 carbon atoms;

R3 represents a phenylene linkage, or is absent;

R4 represents hydrogen or a C 1-24 alkyl or C2 24 alkenyl group, with the provisos that (a) when Rl represents -O-CO-, R2 and R3 must be absent and R4 must contain at least 5 carbon atoms;
(b) when R2 is absent, then R4 is not hydrogen and when also R3 is absent, then R4 must contain at least 5 carbon atoms;

R5 represents hydrogen or a group of formula -CooA4;

R6 represents hydrogen or C1 4 alkyl; and A1, A2, A3 and A4 are independently selected from hydrogen, alkali metals, ~lk~line earth metals, ammonium and amine bases and C1=4, or (C2H4O)tH wherein t is from 1-50, and wherein the monomer units may be in random order.

Q1 is a multifunctional monomer, allowing the branching of the polymer,wherein the monomers of the polymer may be connected to Q1 in any direction, in any order, therewith possibly resulting in a branched polymer. Preferably Ql is trimethyl propane triacrylate (TMPTA), methylene bisacrylamide or divinyl glycol.

z and v are 1; n is at least 1; x is at least 1; (x + y + p + q + r): z is from 4: 1 to 1,000: 1, preferably from 6: 1 to 250: 1; in which the monomer units may be in random order; and preferably p and q are zero and/or r is zero; most preferably p, q, y and r are zero.

R7 and R8 represents -CH3 or is a hydrogen;
R9 and R10 represent substituent groups such as amino, amine, amide, sulphonate, sulphate, phosphonate, phosphate, hydroxy, carboxyl and CA 02256892 1998-ll-26 oxide groups, preferably they are selected from -SO3Na, -CO-O-C2H4-OSO3Na, -CO-O-NH-C(CH3)2-SO3Na, -CO-NH2, -O-CO-CH3, -OH;

It must be noted that the monomers of the polymer may be variable in direction and position along the polymer backbone and along the side chain(s).
P~eferably, polymeric grease dispersing agents for use in compositions of the invention which are of relatively high pH (say 10 or more) are subst~nti~lly free of hydrolysable groups such as carbonyl groups for increased polymer stability at high pH values. Particularly preferred polymeric grease dispersing agents for use in high pH compositions of the invention comprise hydrophilic backbones conctit~te~ by acid groups such as acrylic acid and at least one hydrophobic side chain which is con.~titl-ted of from S to 75 relatively water-insoluble alkoxy groups such as propoxy units optionally linked to the hydrophilic backbone via a poly-alkoxy linkage con~ti~lter~ of from 1-10 relatively water soluble alkoxy groups such as ethoxy units.

Especially preferred grease dispersing agents of this type are the polymers of the forrnula:-Ra R1 -- Z
Rb I' C
- -x - n Formula II
wherein: x, z and n are as above;

. _ . ~

CA 02256892 l998-ll-26 W O 97/4S512 PCTrUS97/08235 12 - R3 and R4 represent hydrogen or Cl 4 alkyl;
- R2 represents -CO-O-, -O-, -O-CO-, CH2-, -CO-NH-, or is absent;
- R 1 represents -C3H6-N + -(CH3)3 (C 1 ~), -C2H4-OSO3 -(Na + ), -SO3-(Na + ), -C2H4 N + (CH3)3 Cl-, -C2H4 N + (C2H6)3 Cl-~-CH2 N+ (CH3)3 Cl-, -CH2 N+ (C2H6)3 Cl- or benzyl-SO3- (Na+) or hydrogen;
- Ra is CH2, C2H4, C3H6 or is absent;
- Rb represents form 1 to 50 independently selected alkylene oxide groups, preferably ethylene oxide groups or is absent;
Rc represents -OH or -H; and wherein if R2, Ra and Rb are absent, then Rc is not -H.

Other preferred polymeric grease dispersing agents have the formula:

G~l CH ~H O CH CH
, HO---GH HC ~----CH HC~ 0- ~H HC --O--H
'~--O 6~- CH 6:~ o - -X1- _ x2_ _z - R2 - n Formula III

wherein:
-x = Xl + X2 - x, z and n are as defined above R1 represents -CH20- or -O-;
- R2 represents -CH2COO~Na+, -C3H60N+(CH3)3Cl- or -C3H3N+
(cH3)3cl-- R3 and R4 represents -OH, CH20H, -O(C3H60)p-H, CA 022~6892 1998-ll-26 WO 97/45512 PCTrUS97/08235--CH2-O(C3H6O)p-H or -OCH2COO-Na + or -O-C3H6ON + (CH3)3CI-or -O- C3H6N + (CH3)3Cl-- R5 represents -OH, ONH-CO-CH3 or -O(C3H6O)p-H
- R6 represents -OH, -CH2OH, -CH2-OCH3, -O(C3H6O)p-H or -CH2-0-(C3H60)p-H
- p is from 1 - 10.

Preferably grease dispersing agents for use in compositions have a molecular weight of between 500 and 100,000, more preferred from 1,000 to 20,000, especially preferred from 1,500 to 10,000 most preferred from 2,800 to 6,000. Grease dispersing agents for use in compositions of the invention may for example be prepared by using conventional aqueous polymerisation procedures, suitable methods are for example described in GB 89 24477, GB 89 24478 and GB 89 24479.

Generally the grease dispersing agent will be used at from 0.1 % to 15 ~, morepreferablyfromO.5% to8.0%, especiallypreferredfrom 1.0% to 5.0% by weight of the detergent composition.

Additional detergent components The detergent compositions of the invention may also contain additionaldetergent components. The precise nature of these additional components, and levels of incorporation thereof will depend on the physical form of the composition, and the precise nature of the washing operation for which it is to be used.

The compositions of the invention preferably contain one or more additional detergent components selected from additional surfactants, bleaches, builders, additional enzymes, suds suppressors, lime soap dispersants, and corrosion inhibitors.

, CA 022~6892 1998-11-26 Additional surfactant The detergent compositions of the invention preferably contain an additional surfactant selected from anionic, nonionic, non-ester cationic, ampholytic, amphoteric and zwitterionic surfactants and mixtures thereof.

A typical listing of anionic, nonionic, ampholytic, and zwitterionic classes, and species of these surfactants, is given in U.S.P. 3,929,678 issued to T ~lghlin and Heuring on December 30, 1975. Further examples are given in "Surface Active Agents and Detergents" (Vol. I and II by Schwartz, Perry and Berch). A list of suitable cationic surfactants is given in U.S.P. 4,259,217 issued to Murphy on March 31, 1981.

Where present, ampholytic, amphoteric and zwitteronic surfactants are generally used in combination with one or more anionic and/or nonionic surfactants.

Anionic surfactant The detergent compositions in accord with the present invention preferably comprise an additional anionic surfactant. Essentially any anionic surfactants useful for detersive purposes can be comprised in the detergent composition. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of the anionic sulfate, sulfonate, carboxylate and sarcosinate surfactants. Anionic sulfate surfactants are preferred.

Other anionic surfactants include the isethionates such as the acyl isethionates, N-acyl taurates, fatty acid amides of methyl tauride, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and ~lnc~hlrated C12-C18 monoesters) diesters of sulfosuccinate (especially saturated and lln~ lrated C6-C14 diesters), N-acyl sarcosinates. Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tallow oil.

CA 022~6892 1998-ll-26 W O 97/4S512 PCT~US97/08235 Anionic sulfate surfactant Anionic sulfate surfactants suitable for use herein include the linear and branched primary and secondary alkyl sulfates, alkyl ethoxysulfates, fatty oleoyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the Cs-C17 acyl-N-(Cl-C4 alkyl) and -N-(C1-C2 hydroxyalkyl) gll~c~min~
sulfates, and sulfates of alkylpolysaccharides such as the sulfates of alkylpolyglucoside (the nonionic nonsulfated compounds being described herein).

Alkyl sulfate surfactants are preferably selected from the linear and branched primary C1o-C1g alkyl sulfates, more preferably the Cl 1-C1s branched chain alkyl sulfates and the C12-C14 linear chain alkyl sulfates.

Alkyl ethoxysulfate surfactants are preferably selected from the group consisting of the C1o-C1g alkyl sulfates which have been ethoxylated with from 0.5 to 20 moles of ethylene oxide per molecule. More preferably, the alkyl ethoxysulfate surfactant is a C 1 1-C 18, most preferably C 1 1 -C 15 alkyl sulfate which has been ethoxylated with from 0.5 to 7, preferably from 1 to 5, moles of ethylene oxide per molecule.

A particularly preferred aspect of the invention employs mixtures of the preferred alkyl sulfate and alkyl ethoxysulfate surfactants. Such mixtures have been disclosed in PCT Patent Application No. WO 93/18124.

Anionic sulfonate surfactant Anionic sulfonate surf~ct~nt~ suitable for use herein include the salts of Cs-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerol sulfonates, and any mixtures thereof.

Anionic carboxylate surfactant .. . .. . .. ..

CA 022~6892 1998-11-26 W O 97/45512 PCTrUS9710823 Suitable anionic carboxylate surfactants include the alkyl ethoxy carboxylates, the alkyl polyethoxy polycarboxylate surfactants and the soaps ('alkyl carboxyls'), especially certain secondary soaps as described herem.

Suitable alkyl ethoxy carboxylates include those with the formula RO(CH2CH20)X CH2COO-M+ wherein R is a C6 to Clg alkyl group, x ranges from O to 10, and the ethoxylate distribution is such that, on a weight basis, the amount of material where x is 0 is less than 20 % and is a cation. Suitable alkyl polyethoxy polycarboxylate surfactants include those having the formula RO-(CHR1-CHR2-O)-R3 wherein R is a C6 to Clg alkyl group, x is from 1 to 25, R1 and R2 are selected from the group consisting of hydrogen, methyl acid radical, succinic acid radical, hydroxysuccinic acid radical, and mixtures thereof, and R3 is selected from the group consisting of hydrogen, substituted or unsubstituted hydrocarbon having between 1 and 8 carbon atoms, and mixtures thereof Suitable soap surfactants include the secondary soap surfactants which contain a carboxyl unit connected to a secondary carbon. Preferred secondary soap surfactants for use herein are water-soluble members selected from the group consisting of the water-soluble salts of 2-methyl-l-undecanoic acid, 2-ethyl-1-decanoic acid, 2-propyl-1-nonanoic acid, 2-butyl-1-octanoic acid and 2-pentyl-1-heptanoic acid. Certain soaps may also be included as suds suppressors.

Alkali metal sarcosinate surfactant Other suitable anionic surfactants are the alkali metal sarcosinates offormula R-CON (Rl) CH2 COOM, wherein R is a Cs-C17 linear or branched alkyl or alkenyl group, Rl is a C1-C4 alkyl group and M is an alkali metal ion. Preferred examples are the myristyl and oleoyl methyl sarcosinates in the form of their sodium salts.

Alkoxylated nonionic surfactant Essentially any alkoxylated nonionic surfactants are suitable herein. The ethoxylated and propoxylated nonionic surfactants are preferred.

CA 022~6892 1998-11-26 Preferred alkoxylated surfactants can be selected from the classes of the nonionic condensates of alkyl phenols, nonionic ethoxylated alcohols, nonionic ethoxylated/propoxylated fatty alcohols, nonionic ethoxylate/propoxylate condensates with propylene glycol, and the nonionic ethoxylate condensation products with propylene oxide/ethylene mine adducts.

Nonionic alkoxylated alcohol surfactant The condensation products of aliphatic alcohols with from 1 to 25 molesof alkylene oxide, particularly ethylene oxide and/or propylene oxide, are suitable for use herein. The alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from 6 to 22 carbon atoms. Particularly preferred are the condensation products of alcohols having an alkyl group cont~ining from 8 to 20 carbon atoms with from 2 to lO moles of ethylene oxide per mole of alcohol.

Nonionic polyhydroxy fatty acid amide surfactant Polyhydroxy fatty acid amides suitable for use herein are those having the structural formula R2CONR1Z wherein: R1 is H, C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, ethoxy, propoxy, or a mixture thereof, preferable C1-C4 alkyl, more preferably C1 or C2 alkyl, most preferably C1 alkyl (i.e., methyl); and R2 is a Cs-C31 hydrocarbyl, preferably straight-chain Cs-C1g alkyl or alkenyl, more preferably straight-chain Cg-C 1 7 alkyl or alkenyl, most preferably straight-chain C 1 1 -C 1 7 alkyl or alkenyl, or mixture thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z preferably will be derived from a reducing sugar in a reductive ~n~in~tion reaction; more preferably Z is a glycityl.

Nonionic fatty acid amide surfactant Suitable fatty acid amide surfactants include those having the formula:R6CoN(R7)2 wherein R6 is an alkyl group cont~ining from 7 to 21, CA 022~6892 1998-ll-26 W O 97/45512 PCTrUS97tO8235 preferably from 9 to 17 carbon atoms and each R7 is selected from the group consisting of hydrogen, Cl-C4 alkyl, Cl-C4 hydroxyalkyl, and -(C2H40)XH, where x is in the range of from 1 to 3.

Nonionic alkylpolysaccharide surfactant Suitable alkylpolysaccharides for use herein are disclosed in U.S. Patent 4,565,647, Llenado~ issued January 21, 1986, having a hydrophobic group cont~ining from 6 to 30 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group cont~ining from 1.3 to 10 saccharide units.

CA 02256892 1998-ll-26 O 97/45512 PCT~US97/08235-Preferred alkylpolyglycosides have the formula R~O(CnH2nO)t(glYC~sYl)x wherein R2 is selected from the group consisting of alkyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from 10 to 18 carbon atoms; n is 2 or 3; t is from O
to 10, and x is from 1.3 to 8. The glycosyl is preferably derived from glucose.

Amphoteric surfactant Suitable amphoteric surf~ct~nt.~ for use herein include the amine oxidesurfactants and the alkyl amphocarboxylic acids.

Suitable amine oxides include those compounds having the formula R3(0R4)XNO(R5)2 wherein R3 is selected from an alkyl, hydroxyallcyl, acylamidopropoyl and alkyl phenyl group, or mixtures thereof, containin~
from 8 to 26 carbon atoms; R4 is an alkylene or hydroxyalkylene group cont~inin~ from 2 to 3 carbon atoms, or mixtures thereof; x is from O to 5, preferably from O to 3; and each R5 is an alkyl or hydroxyalkyl group con~inin~ from l to 3, or a polyethylene oxide group con~inin~ from 1 to 3 ethylene oxide groups. Preferred are Clo-Clg alkyl dimethyl~mine oxide, and C10-l8 acylamido alkyl dimethylamine oxide.

A suitable example of an alkyl aphodicarboxylic acid is Miranol(TM) C2M Conc. manufactured by Miranol, Inc., Dayton, NJ.

Zwitterionic surfactant Zwitterionic surfactants can also be incorporated into the detergent compositions hereof. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. Betaine and sultaine surfactants are exemplary zwitterionic surfactants for use herein.

CA 022~6892 1998-ll-26 W O97/45512 PCTrUS97/08235 -Suitable betaines are those compounds having the formula R(R')2N+R2COO- wherein R is a C6-C1g hydrocarbyl group, each Rl is typically C1-C3 alkyl, and R2 is a C1-Cs hydrocarbyl group. Preferred betaines are C12 18 dimethyl-ammonio hexanoate and the C10-l8 acylamidopropane (or ethane) dimethyl (or diethyl) betaines. Complex betaine surfactants are also suitable for use herein.

Cationic surfactants Additional cationic surfactants can also be used in the detergent compositions herein. Suitable cationic surfactants include the quaternary ammonium surfactants selected from mono C6-C16, preferably C6-C1o N-alkyl or alkenyl ammonium surfactants wherein the rem~inin~ N
positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.

~lk~linity In the detergent compositions of the present invention preferably a alkalinity system is present to achieve optimal cationic ester surfactant performance. The ~lk~linity system comprises components capable of providing ~lk~linity species in solution. By alkalinity species it is meant herein: carbonate, bicarbonate, hydroxide, the various silicate anions, percarbonate, perborates, perphosphates, persulfate and persilicate.
Such ~lk~linity species can be formed for example, when ~lk~line salts selected from alkali metal or alkaline earth carbonate, bicarbonate, hydroxide or silicate, including crystalline layered silicate, salts and percarbonate, perborates, perphosphates, persulfate and persilicate salts and any mixtures thereof are dissolved in water.

Examples of carbonates are the ~lk~line earth and alkali metal carbonates, including sodium carbonate and sesqui-carbonate and any mixtures thereof with ultra-fine calcium carbonate such as are disclosed in Gerrnan Patent Application No. 2,321,001 published on November 15, 1973.

CA 022~6892 1998-ll-26 W O 97/45512 PCTrUS97tO8235-Suitable silicates include the water soluble sodium silicates with an SiO2:
Na20 ratio of from 1.0 to 2.8, with ratios of from 1.6 to 2.0 being preferred, and 2.0 ratio being most preferred. The silicates may be in the form of either the anhydrous salt or a hydrated salt. Sodium silicate with an SiO2: Na20 ratio of 2.0 is the most preferred silicate.

Preferred crystalline layered silicates for use herein have the generalformula NaMSix02x+1 YH20 wherein M is sodium or hydrogen, x is a number from 1.9 to 4 and y is a number from 0 to 20. Crystalline layered sodium silicates of this type are disclosed in EP-A-0164514 and methods for their preparation are disclosed in DE-A-3417649 and DE-A-3742043. Herein, x in the general formula above preferably has a value of 2, 3 or 4 and is preferably 2. The most preferred material is ~-Na2Si20s, available from Hoechst AG as NaSKS-6.

Water-soluble builder compound The detergent compositions of the present invention preferably contain a water-soluble builder compound, typically present at a level of from 1 %
to 80% by weight, preferably from 10% to 70% by weight, most preferably from 20% to 60% by weight of the composition.

Suitable water-soluble builder compounds include the water soluble monomeric polycarboxylates, or their acid forms, homo or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms, borates, phosphates, and mixtures of any of the foregoing.

The carboxylate or polycarboxylate builder can be momomeric or oligomeric in type although monomeric polycarboxylates are generally preferred for reasons of cost and performance.

CA 022~6892 1998-ll-26 W O 97/45512 PCTrUS97/08235 -Suitable carboxylates cont~inin~ one carboxy group include the water soluble salts of lactic acid, glycolic acid and ether derivatives thereof.
Polycarboxylates cont~ining two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycolic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates and the sulfinyl carboxylates. Polycarboxylates cont~ining three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No.
1,379,241, lactoxysuccinates described in British Patent No. 1,389,732, and aminosuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-1,1,3-propane tricarboxylates described in British Patent No. 1,387,447.

Polycarboxylates cor~t~ining four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1,1,2,2-ethane tetracarboxylates, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates. Polycarboxylates cont~ining sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1,398,421 and 1,398,422 and in U.S. Patent No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1,439,000. Preferred polycarboxylates are hydroxycarboxylates cont~ining up to three carboxy groups per molecule, more particularly citrates.

The parent acids of the monomeric or oligomeric polycarboxylate chelating agents or mixtures thereof with their salts, e.g. citric acid or citrate/citric acid mixtures are also contemplated as useful builder components.

Borate builders, as well as builders cont~ining borate-forrning materials that can produce borate under detergent storage or wash conditions are useful water-soluble builders herein.

Suitable examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the CA 022~6892 1998-11-26 W O 97/45512 PCTrUS97/08235 degree of polymerization ranges from about 6 to 21, and salts of phytic acld.

Partially soluble or insoluble builder compound The detergent compositions of the present invention may contain a partially soluble or insoluble builder compound, typically present at a level of from 1% to 80% by weight, preferably from 10% to 70% by weight, most preferably from 20% to 60% weight of the composition.

Examples of largely water insoluble builders include the sodium aluminosilicates .

Suitable aluminosilicate zeolites have the unit cell formula Nazl(AlO2)z(SiO2)y]. xH2O wherein z and y are at least 6; the molar ratio of z to y is from 1.0 to 0.5 and x is at least 5, preferably from 7.5 to 276, more preferably from 10 to 264. The aluminosilicate material are in hydrated form and are preferably crystalline, cont~ining from 10% to 28%, more preferably from 18% to 22% water in bound form.

The aluminosilicate zeolites can be naturally occurring materials, but are preferably synthetically derived. Synthetic crystalline aluminosilicate ion exchange materials are available under the designations Zeolite A, Zeolite B, Zeolite P, Zeolite X, Zeolite HS and mixtures thereof. Zeolite A has the formula Na 12 [Al~2) 12 (sio2)l2]. xH2O

wherein x is from 20 to 30, especially 27. Zeolite X has the formula Na86 [(Alo2)86(sio2)lo6]. 276 H2O.
Or~anic peroxyacid bleaching system A preferred feature of detergent compositions of the invention is an organic peroxyacid bleaching system. In one preferred execution the bleaching system contains a hydrogen peroxide source and an orgarlic peroxyacid bleach precursor compound. The production of the organic CA 022~6892 1998-11-26 peroxyacid occurs by an in situ reaction of the precursor with a source of hydrogen peroxide. Preferred sources of hydrogen peroxide include inorganic perhydrate bleaches. In an alternative preferred execution a preformed organic peroxyacid is incorporated directly into the composition. Compositions cont~inin~ mixtures of a hydrogen peroxide source and organic peroxyacid precursor in combination with a preformed organic peroxyacid are also envisaged.

Inor~anic perhydrate bleaches Inorganic perhydrate salts are a preferred source of hydrogen peroxide.These salts are normally incorporated in the form of the alkali metal, preferably sodium salt at a level of from 1 % to 40% by weight, more preferably from 2% to 30% by weight and most preferably from 5% to 25 % by weight of the compositions.

Examples of inorganic perhydrate salts include perborate, percarbonate,perphosphate, persulfate and persilicate salts. The inorganic perhydrate salts are normally the alkali metal salts. The inorganic perhydrate salt may be included as the cryst~lline solid without additional protection. For certain perhydrate salts however, the preferred executions of such granular compositions utilize a coated form of the material which provides better storage stability for the perhydrate salt in the granular product.
Suitable coatings comprise inorganic salts such as alkali metal silicate, carbonate or borate sa~ts or mixtures thereof, or organic materials such as waxes, oils, or fatty soaps.

Sodium perborate is a preferred perhydrate salt and can be in the form of the monohydrate of nominal formula NaB02H202 or the tetrahydrate NaB02H202 3H20 Alkali metal percarbonates, particularly sodium percarbonate are preferred perhydrates herein. Sodium percarbonate is an addition compound having a formula corresponding to 2Na2C03.3H202, and is available commercially as a crystalline solid.

CA 02256892 l998-ll-26 W O 97t45512 PCTAUS97/0823S .

Potassium peroxymonopersulfate is another inorganic perhydrate salt of use in the detergent compositions herein.

Peroxyacid bleach precursor Peroxyacid bleach precursors are compounds which react with hydrogen peroxide in a perhydrolysis reaction to produce a peroxyacid. Generally peroxyacid bleach precursors may be represented as i !
X-C-L

where L is a leaving group and X is essentially any functionality, such that on perhydroloysis the structure of the peroxyacid pro~h~ced is o X-C -OOH

Peroxyacid bleach precursor compounds are preferably incorporated at a level of from 0.5~ to 20% by weight, more prefelably from 1 % to 15%
by weight, most preferably from 1.5% to 10~ by weight of the detergent collll.ositions .

Suitable peroxyacid bleach precursor compounds typically contain one ormore N- or O-acyl groups, which precursors can be selected from a wide range of classes. Suitable classes include anhydrides, esters, imides, lart~mc and acylated derivatives of imidazoles and oximes. Examples of useful materials within these classes are disclosed in GB-A-1586789.
Suitable esters are disclosed in GB-A-836988, 864798, 1147871, 2143231 and EP-A-0170386.

Leavln~ groups The leaving group, hereinafter L group, must be sufficiently reactive for the perhydrolysis reaction to occur within the optimum time frame (e.g., a W O 97/45512 PCTrUS97/08235-wash cycle). However, if L is too reactive, this aetivator will be difficult to stabilize for use in a bleaching composition.

Preferred L groups are selected from the group consisting of:

--0~ --O~Y , and --~~

Il ~ 11 R3 r -O--C H=C--C H=C H2 --O--C H=C--C H=C H2 O ,CH~C, ,> C~NR4 Il 11 O O

--~C=CHR4 , and N--lv--CH--R4 R3 o and mixtures thereof, wherein R1 is an alkyl, aryl, or alkaryl group cont~ining from 1 to 14 carbon atoms, R3 is an alkyl chain cont~ining from 1 to 8 carbon atoms, R4 is H or R3, and Y is H or a solubilizing group. Any of R1, R3 and R4 may be substituted by essentially any functional group including, for example alkyl, hydroxy, alkoxy, halogen, amine, nitrosyl, amide and ammonium or alkyl ~mmmonium groups The preferred solubilizing groups are -S03-M+, -C02-M+, -S04-M+, -N +(R )4X- and O < --N(R )3 and most preferably -S03-M + and CA 02256892 1998-ll-26 W O 97/45512 PCTnJS97J08235 .

-CO2-M + wherein R3 is an alkyl chain cont~inin~ from 1 to 4 carbon atoms, M is a cation which provides solubility to the bleach activator and X is an anion which provides solubility to the bleach activator.
Preferably, M is an alkali metal, amrnonium or substituted ammonium cation, with sodium and potassium being most preferred, and X is a halide, hydroxide, methylsulfate or acet~te anion.

Alkyl percarboxylic acid bleach precursors Alkyl percarboxylic acid bleach precursors form percarboxylic acids on perhydrolysis. Preferred precursors of this type provide peracetic acid on perhydrolysis.

Preferred alkyl percarboxylic precursor compounds of ~e imide type include the N-,N,NlNl tetra acetylated alkylene diqminPs wherein the alkylene group contains from 1 to 6 carbon atoms, particularly those compounds in which the alkylene group contains l, 2 and 6 carbon atoms.
Tetraacetyl ethylene ~ mine (TAED) is particularly preferred.

Od~er preferred alkyl percarboxylic acid precursors include sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate (iso-NOBS), sodium nonanoyloxybenzene sulfonate tNOBS), sodium acetoxybenzene sulfonate (ABS) and pent~cetyl glucose.

Amide substitl~te~ allyl peroxyacid precursors Amide substi~te~l alkyl peroxyacid precursor compounds are suitable herein, including ~ose of ~e following gelleral formulae:

R1 C--N R2--C--L R1_--N C R2 C L
O R5 O or R5 O O

wherein Rl is an alkyl group with from 1 to 14 carbon atoms, R2 is an alkylene group cont~ining from 1 to 14 carbon atoms, and R5 is H or an alkyl group cont~ining 1 to 10 carbon atoms and L can be essentially any CA 022~6892 l998-ll-26 W O 97/45512 PCT~US97/08235 leaving group. Amide substituted bleach activator compounds of this type are described in EP-A-0170386.

Perbenzoic acid precursor Perbenzoic acid precursor compounds provide perbenzoic acid on perhydrolysis. Suitable O-acylated perbenzoic acid precursor compounds include the substituted and unsubstitl~te~l benzoyl oxybenzene sulfonates, and the benzoylation products of sorbitol, glucose, and all saccharides with benzoylating agents, and those of the imide type including N-benzoyl succinimide, tetrabenzoyl ethylene ~ min~ and the N-benzoyl substituted ureas. Suitable imidazole type perbenzoic acid precursors include N-benzoyl imidazole and N-benzoyl benzimidazole. Other useful N-acyl group-cont~inin~ perbenzoic acid precursors include N-benzoyl pyrrolidone, dibenzoyl taurine and benzoyl pyroglutamic acid.

Cationic peroxyacid precursors Cationic peroxyacid precursor compounds produce cationic peroxyacids on perhydrolysis.

Typically, cationic peroxyacid precursors are formed by substituting the peroxyacid part of a suitable peroxyacid precursor compound with a positively charged functional group, such as an ammonium or alkyl ~mmmonium group, preferably an ethyl or methyl ammonium group.
Cationic peroxyacid precursors are typically present in the solid detergent compositions as a salt with a suitable anion, such as a halide ion:

The peroxyacid precursor compound to be so cationically substituted maybe a perbenzoic acid, or substituted derivative thereof, precursor compound as described hereinbefore. Alternatively, the peroxyacid precursor compound may be an alkyl percarboxylic acid precursor compound or an amide substituted alkyl peroxyacid precursor as described hereinafter Cationic peroxyacid precursors are described in U.S. Patents 4,904,406;4,751,015; 4,988,451; 4,397,757; 5,269,962; 5,127,852; 5,093,022;

.

CA 022~6892 1998-11-26 5,106,528; U.K. 1,382,594; EP 475,512, 458,396 and 284,292; and in JP 87-318,332.

Examples of preferred cationic peroxyacid precursors are described in UK
Patent Application No. 9407944.9 and US Patent Application Nos.
08/298903, 08/298650, 08/298904 and 08/298906.

Suitable cationic peroxyacid precursors include any of the ammonium or alkyl ammonium substituted alkyl or benzoyl oxybenzene sulfonates, N-acylated caprolactams, and monobenzoyltetraacetyl glucose benzoyl peroxides. Preferred cationic peroxyacid precursors of the N-acylated caprol~t~m class include the trialkyl ammonium methylene benzoyl caprolactams and the trialkyl ammonium methylene alkyl caprol~ct~m~.

Benzoxazin organic peroxyacid precursors Also suitable are precursor compounds of the benzoxazin-type, as disclosed for example in EP-A-332,294 and EP-A-482,807, particularly those having the formula:

[~(N"C R~

wherein Rl is H, alkyl, alkaryl, aryl, or arylalkyl.

Preformed or~anic peroxyacid The organic peroxyacid bleaching system may contain, in addition to, oras an alternative to, an organic peroxyacid bleach precursor compound, a preformed organic peroxyacid, typically at a level of from 1 % to 15 % by weight, more preferably from 1 % to 10~ by weight of the composition.

CA 02256892 1998-ll-26 PCT~US97/08235 A preferred class of organic peroxyacid compounds are the amide substituted compounds of the following general formulae:

O R5 O or R5 O O

wherein Rl is an alkyl, aryl or alkaryl group with from 1 to 14 carbon atoms, R2 is an alkylene, arylene, and alkarylene group cont~inin~ from 1 to 14 carbon atoms, and R5 is H or an alkyl, aryl, or alkaryl group cont~inin~ 1 to 10 carbon atoms. Amide substituted organic peroxyacid co~ ,ounds of this type are described in EP-A-0170386.

Other organic p;eroxyacids include diacyl and tetraacylperoxides, especially diperoxy~lo(lec~n~lioc acid, diperoxytetr lec~n~ioc acid and diperoxyhex~ec~nç~lioc acid. Mono- and diper~ ic acid, mono- and diperbrassylic acid and N-phthaloyl~min~peroxicaproic acid are also suitable herein.

Bleach catalyst The compositions optionally contain a transition metal cont~inin~ bleach catalyst. One suitable type of bleach catalyst is a catalyst system comprising a heavy metal cation of defined bleach catalytic activity, such as copper, iron or .~ pn~~e cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or al~ nllm cations, and a se~ strant having defined stability conct~nts for the catalytic and ry metal cations, particularly ethylen~ min~tet~cetic acid, ethylell~li~min~tetra(methylenephosphonic acid) and water-soluble salts thereof. Such catalysts are disclosed in U.S. Pat. 4,430,243.

Other types of bleach catalysts include the ~ nPse-based complexes disclosed in U.S. Pat. 5,246,621 and U.S. Pat. 5,244,594. Plefel,~,d examples of these catalysts include MnIV2(u-O)3(1,4,7-trime~yl-1,4,7-triazacyclononane)2-(PF6)2, MnIII2(u-O) 1 (u-OAc)2( 1,4, 7-trimethyl-1,4,7-triazacyclononane)2-(C104)2, MnIV4(u-0)6(1,4,7-triazacyclononane)4-(ClO4)2, MnIIlMnIV4(u-o) 1 (u-OAc)2 ( 1 ,4, 7-CA 022~6892 1998-11-26 trimethyl-1,4,7-triazacyclononane)2-(Cl04)3, and mixtures thereof.
Others are described in European patent application publication no.
549,272. Other ligands suitable for use herein include 1,5,9-trimethyl-1,5,9-triazacyclodo~lec~ne, 2-methyl-1,4,7-triazacyclononane, 2-methyl-1,4,7-triazacyclononane, 1,2,4,7-tetramethyl-1,4,7-triazacyclononane, and mixtures thereof.

For examples of suitable bleach catalysts see U.S. Pat. 4,246,612 and U.S. Pat. 5,227,084. See also U.S. Pat. 5,194,416 which te~ches mononuclear m~n~n~ose (IV) complexes such as Mn(1,4,7-trimethyl-1,4,7-triazacyclononane)(OCH3)3 (PF6). Still another type of bleach catalyst, as disclosed in U.S. Pat. 5,114,606, is a water-soluble complex of m~n~nese (III), and/or (IV) with a ligand which is a non-carboxylate polyhydroxy compound having at least three consecutive C-OH groups.
Other examples include binuclear Mn complexed with tetra-N-dentate and bi-N-dentate ligands, including N4MnIII(u-O)2MnIVN4)+and [Bipy2MnIII(u-0)2MnIVbipy2]-(C104)3 .

Further suitable bleach catalysts are described, for example, in European patent application No. 408,131 (cobalt complex catalysts), European patent applications, publication nos. 384,503, and 306,089 (metallo-porphyrin catalysts), U.S. 4,728,455 (manganese/multidentate ligand catalyst), U.S. 4,711,748 and European patent application, publication no. 224,952, (absorbed m~n~nese on aluminosilicate catalyst), U.S.
4,601,845 (aluminosilicate support with m~n~nese and zinc or m~n~sium salt), U.S. 4,626,373 (m~np~nese/ligand catalyst), U.S.
4,119,557 (ferric complex catalyst), German Pat. specification 2,054,019 (cobaltchelantcatalyst) C~n~ n 866,191 (transitionmetal-cont~inin&
salts), U.S. 4,430,243 (chelants with m~n~nese cations and non-catalytic metal cations), and U.S. 4,728,455 (manganese gluconale catalysts).

Heavy metal ion sequestrant The detergent compositions of the invention preferably contain as an optional component a heavy metal ion sequestrant. By heavy metal ion sequestrant it is meant herein components which act to sequester (chelate) heavy metal ions. These components may also have calcium and CA 022~6892 1998-ll-26 W O 97/4S512 PCTrUS97/08235 - -m~nesium chelation capacity, but preferentially they show selectivity to binding heavy metal ions such as iron, m~n~nese and copper.

Heavy metal ion se~uestrants are generally present at a level of from 0.005% to 20%, preferably from 0.1% to 10%, more preferably from 0.25 % to 7.5 % and most preferably from 0.5 % to 5 % by weight of the compositions.

Suitable heavy metal ion sequestrants for use herein include organic phosphonates, such as the amino alkylene poly (alkylene phosphonates), alkali metal ethane l-hydroxy disphosphonates and nitrilo trimethylene phosphonates.

Preferred among the above species are diethylene tri~mine penta (methylene phosphonate), ethylene ~ mine tri (methylene phosphonate) hexamethylene cli~mine tetra (methylene phosphonate) and hydroxy-ethylene 1,1 diphosphonate.

Other suitable heavy metal ion sequestrant for use herein include nitrilotriacetic acid and polyaminocarboxylic acids such as ethylene~i~minotetracetic acid, ethylenetriamine pentacetic acid, ethylene~ mine disuccinic acid, ethylene~ mine diglutaric acid, 2-hydroxypropylen~ mine disuccinic acid or any salts thereof. Especially preferred is ethylene~ min~o-N,N'-disuccinic acid (EDDS) or the alkali metal, ~ lin-o earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.

Other suitable heavy metal ion sequestrants for use herein are iminodiacetic acid derivatives such as 2-hydroxyethyl diacetic acid or glyceryl imino diacetic acid, described in EP-A-317,542 and EP-A-399,133. The iminodiacetic acid-N-2-hydroxypropyl sulfonic acid and aspartic acid N-carboxymethyl N-2-hydroxypropyl-3-sulfonic acid sequestrants described in EP-A-516,102 are also suitable herein. The ~-~l~nin~?-N,N'-diacetic acid, aspartic acid-N,N'-diacetic acid, aspartic acid-N-monoacetic acid and iminodisuccinic acid sequestrants described in EP-A-509,382 are also suitable.

CA 022~6892 1998-11-26 W O 97/45512 PCT~US97/08235 EP-A-476,257 describes suitable amino based sequestrants. EP-A-510,331 describes suitable se~uestrants derived from collagen, keratin or casein.
EP-A-528,859 describes a suitable alkyl iminodiacetic acid sequestrant.
Dipicolinic acid and 2-phosphonobutane-1,2,4-tricarboxylic acid are alos suitable. Glycinamide-N,N'-disuccinic acid (GADS), ethylenedi~mine-N-N'-diglutaric acid ~EDDG) and 2-hydroxypropylene~ minç-N-N'-disuccinic acid (HPDDS) are also suitable.

Enzyme Another preferred ingredient useful in the detergent compositions is one or more additional enzymes.

Preferred additional enzymatic materials include the commercially available lipases, cutinases, amylases, neutral and ~lk~line proteases, cellulases, endolases, esterases, pectinases, lactases and peroxidases conventionally incorporated into detergent compositions. Suitable enzymes are discussed in US Patents 3,519,570 and 3,533,139.

Preferred commercially available protease enzymes include those sold under the tradenames Alcalase, Savinase, Primase, Durazym, and Esperase by Novo Industries A/S (Denmark), those sold under the tradename Maxatase, Maxacal and Maxapem by Gist-Brocades, those sold by Genencor International, and those sold under the tradename Opticlean and Optimase by Solvay Enzymes. Protease enzyme may be incorporated into the compositions in accordance with the invention at a level of from 0.0001% to 4% active enzyme by weight of the composition.

Preferred amylases include, for example, a-amylases obtained from a special strain of B licheniformis, described in more detail in GB-1,269,839 (Novo). Preferred commercially available amylases include for example, those sold under the tradename Rapidase by Gist-Brocades, and those sold under the tradename Termamyl and BAN by Novo Industries A/S. Amylase enzyme may be incorporated into the composition in accordance with the invention at a level of from 0.0001 to 2 % active enzyme by weight of the composition.

CA 022~6892 1998-11-26 Lipolytic enzyme may be present at levels of active lipolytic enzyme offrom 0.0001 % to 2% by weight, preferably 0.001 % to 1 % by weight, most preferably from 0.001 % to 0.5 % by weight of the compositions.

The lipase may be fungal or bacterial in origin being obt~ine~l~ for example, from a lipase producing strain of Humicola sp., Thermomyces sp. or Pseudomonas sp. including Pseudomonas pseudoalcali~enes or Pseudomas fluorescens. Lipase from chemically or genetically modified mutants of these strains are also useful herein A preferred lipase is derived from Pseudomonas pseudoalcali~enes, which is described in Granted European Patent, EP-B-0218272.

Another preferred lipase herein is obtained by cloning the gene from Humicola l~ inosa and expressing the gene in Aspergillus orvza, as host, as described in European Patent Application, EP-A-0258 068, which is commercially available from Novo Industri A/S, Bagsvaerd, Denmark, under the trade name Lipolase. This lipase is also described in U.S.
Patent 4,810,414, Huge-Jensen et al, issued March 7, 1989.

Non-grease-dispersing organic polymeric compound Non-grease-dispersing organic polymeric compounds are suitable additional components of the detergent compositions in accord with the invention, and are preferably present as components of any particulate components where they may act such as to bind the particulate component together.

By non-grease-dispersing organic polymeric compound it is meant herein essentially any polymeric organic compound which is not a grease dispersing agent in accord with the present invention and which is commonly used as dispersants, and anti-redeposition and non-greasy soil suspension agents in detergent compositions, including any of the high molecular weight organic polymeric compounds described as clay flocculating agents herein.

Non-grease-dispersing organic polymeric compound is typically incorporated in the detergent compositions of the invention at a level of CA 022~6892 l998-ll-26 W O 97/45512 PCTrUS97/08235 from 0.15~o to 30%, preferably from 0.5% to 15%, most preferably from 1 % to 10% by weight of the compositions.

Examples of suitable organic polymeric compounds for use herein are polyamino compounds, including those derived from aspartic acid such as those disclosed in EP-A-305282, EP-A-305283 and EP-A-351629.

Terpolymers cont~ining monomer units selected from maleic acid, acrylicacid, polyaspartic acid and vinyl alcohol, particularly those having an average molecular weight of from 5,000 to 10,000, are also suitable herein.

Further useful organic polymeric compounds are the polyethylene glycols, particularly those of molecular weight 1000-10000, more particularly 2000 to 8000 and most preferably about 4000.

Suds suppressing system The detergent compositions of the invention, when formulated for use inmachine washing compositions, preferably comprise a suds suppressing system present at a level of from 0.01 % to 15 ~, preferably from 0.05 % to lO ~, most preferably from 0.1 % to 5 % by weight of the composition.

Suitable suds suppressing systems for use herein may comprise essentially any known antifoam compound, including, for example silicone antifoam compounds and 2-alkyl alcanol antifoam compounds.

By antifoam compound it is meant herein any compound or mixtures of compounds which act such as to depress the foaming or sudsing produced by a solution of a detergent composition, particularly in the presence of agitation of that solution.

Particularly preferred antifoam compounds for use herein are silicone antifoam compounds defined herein as any antifoam compound including a silicone component. Such silicone antifoam compounds also typically contain a silica component. The term l'silicone" as used herein, and in general throughout the industry, encompasses a variety of relatively high molecular weight polymers cont~ining siloxane units and hydrocarbyl group CA 022~6892 1998-11-26 of various types. Preferred silicone antifoam compounds are the siloxanes, particularly the polydimethylsiloxanes having trimethylsilyl end blocking units.

Other suitable antifoam compounds include the monocarboxylic fatty acids and soluble salts thereof. These materials are described in US Patent 2,954,347, issued September 27, 1960 to Wayne St. John. The monocarboxylic fatty acids, and salts thereof, for use as suds suppressor typically have hydrocarbyl chains of 10 to 24 carbon atoms, preferably 12 to 18 carbon atoms. Suitable salts include the alkali metal salts such as sodium, potassium, and lithium salts, and ammonium and alkanolammonium salts.

Other suitable antifoam compounds include, for example, high molecular weight fatty esters (e.g. fatty acid triglycerides), fatty acid esters of monovalent alcohols, aliphatic C1g-C40 ketones (e.g. stearone) N-alkylated amino triazines such as tri- to hexa-alkylmelamines or di- to tetra alkyl~ mine chlortriazines forrned as products of cyanuric chloride with two or three moles of a primary or secondary amine cont~ining 1 to 24 carbon atoms, propylene oxide, bis stearic acid amide and monostearyl di-alkali metal (e.g. sodium, potassium, lithium) phosphates and phosphate esters.

A preferred suds suppressing system comprises (a) antifoam compound, preferably silicone antifoam compound, most preferably a silicone antifoam compound comprising in combination (i) polydimethyl siloxane, at a level of from 50% to 99%, preferably 75 % to 95 % by weight of the silicone antifoam compound; and (ii) silica, at a level of from 1 % to 50 %, preferably 5 % to 25 %
by weight of the silicone/silica antifoam compound;

CA 022~6892 1998-11-26 wherein said silica/silicone antifoam compound is incorporated at a level of from 5% to 505~, preferably 10% to 40% by weight;

(b) a dispersant compound, most preferably comprising a silicone glycol rake copolymer with a polyoxyalkylene content of 72-78 %
and an ethylene oxide to propylene oxide ratio of from 1:0.9 to 1:1.1, at a level of from 0.5% to 10%, preferably 1 ~ to 10% by weight; a particularly preferred silicone glycol rake copolymer of this type is DCO544, commercially available from DOW Corning under the tradename DCO544;

(c) an inert carrier fluid compound, most preferably comprising a C16-C1g ethoxylated alcohol with a degree of ethoxylation of from 5 to 50, preferably 8 to 15, at a level of from 5% to 80%, preferably 10% to 70%, by weight;

A highly preferred particulate suds suppressing system is described in EP-A-0210731 and comprises a silicone antifoam compound and an organic carrier material having a melting point in the range 50~C to 85~C, wherein the organic carrier material comprises a monoester of glycerol and a fatty acid having a carbon chain cont~inin~ from 12 to 20 carbon atoms. EP-A-0210721 discloses other preferred particulate suds suppressing systems wherein the organic carrier material is a fatty acid or alcohol having a carbon chain cont~ining from 12 to 20 carbon atoms, or a mixture thereof, with a melting point of from 45~C to 80~C.

Clay softening system The detergent compositions may contain a clay softening system comprising a clay mineral compound and optionally a clay flocc~ tin~
agent.

The clay mineral compound is preferably a smectite clay compound.
Smectite clays are disclosed in the US Patents No.s 3,862,058, 3,948,790, 3,954,632 and 4,062,647. European Patents No.s EP-A-299,575 and EP-A-313,146 in the name of the Procter and Gamble Company describe suitable organic polymeric clay flocculatin~ agents.

CA 022~6892 l998-ll-26 W O97/45512 PCTrUS97/08235 - -Polymeric dye transfer inhibitin~ a~ents The detergent compositions herein may additionally comprise from 0.01%
to 10 %, preferably from 0.05 % to 0.5 ~ by weight of polymeric dye transfer inhibiting agents.

The polymeric dye transfer inhibiting agents are preferably selected from copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof.
a) Copolymers of N-vinylpyrrolidone and N-vinylimidazole Suitable herein are copolymers of N-vinylimidazole and N-vinylpyrrolidone having an average molecular weight range of from 5,000 to 50,000. The preferred copolymers have a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1 to 0.2.
b) Polyvinylpyrrolidone The detergent compositions herein may also utilize polyvinylpyrrolidone("PVP") having an average molecular weight of from 2,500 to 400,000.
Suitable polyvinylpyrrolidones are commercially vailable from ISP
Corporation, New York, NY and Montreal, Canada under the product names PVP K-15 (viscosity molecular weight of 10,000), PVP K-30 (average molecular weight of 40,000), PVP K-60 (average molecular weight of 160,000), and PVP K-90 (average molecular weight of 360,000). PVP K-15 is also available from ~SP Corporation. Other suitable polyvinylpyrrolidones which are commercially available from BASF Cooperation include Sokalan HP 165 and Sokalan HP 12.

CA 022~6892 1998-ll-26 c) Polyvinyloxazolidone The detergent compositions herein may also utilize polyvinyloxazolidones as polymeric dye transfer inhibiting agents. Said polyvinyloxazolidones have an average molecular weight of from 2,500 to 400,000.

d) Polyvinylimidazole The detergent compositions herein may also utilize polyvinylimidazole as polymeric dye transfer inhibiting agent. Said polyvinylimidazoles preferably have an average molecular weight of from 2,500 to 400,000.

Optical bri~htener The detergent compositions herein also optionally contain from about 0.005% to 5 % by weight of certain types of hydrophilic optical brighteners.

Hydrophilic optical brighteners useful herein include those having the structural formula:

R, R2 N~O~ I ~C=C~ N

R2 So3M SO3M R~

wherein R1 is selected from anilino, N-2-bis-hydroxyethyl and NH-2-hydroxyethyl; R2 is selected from N-2-bis-hydroxyethyl, N-2-hydroxyethyl-N-methylamino, morphilino, chloro and amino; and M is a salt-forming cation such as sodium or potassium.

When in the above formula, Rl is anilino, R2 is N-2-bis-hydroxyethyl and M is a cation such as sodium, the brightener is 4,4',-bis[(4-anilino-6-(N-2-bis-hydroxyethyl)-s-triazine-2-yl)amino]-2,2'-stilbenedisulfonic acid and disodium salt. This particular brightener species is commercially CA 022~6892 1998-11-26 W O 97/4~512 PCTrUS97/08235 -marketed under the tradename Tinopal-UNPA-GX by Ciba-Geigy Corporation. Tinopal-UNPA-GX is the preferred hydrophilic optical brightener useful in the detergent compositions herein.

When in the above formula, Rl is anilino, R2 is N-2-hydroxyethyl-N-2-methylamino and M is a cation such as sodium, the brightener is 4,4'-bis[(4-~nilino-6-(N-2-hydroxyethyl-N-methylamino)-s-triazine-2-yl)amino]2,2'-stilbenedisulfonic acid disodium salt. This particular brightener species is commercially marketed under the tradename Tinopal SBM-GX by Ciba-Geigy Corporation.

When in the above forrnula, R1 is anilino, R2 is morphilino and M is a cation such as sodium, the brightener is 4,4'-bis[(4-anilino-6-morphilino-s-triazine-2-yl)amino]2,2'-stilbenedisulfonic acid, sodium salt. This particular brightener species is commercially marketed under the tradename Tinopal AMS-GX by Ciba Geigy Corporation.

Cationic fabric softening agents Cationic fabric softening agents can also be incorporated into compositions in accordance with the present invention. Suitable cationic fabric softening agents include the water insoluble tertiary amines or dilong chain amide materials as disclosed in GB-A-1 514 276 and EP-B-0 011 340.

Cationic fabric softening agents are typically incorporated at total levels of from 0.5% to 15% by weight, normally from 1% to 5% by weight.

Other optional in~redients Other optional ingredients suitable for inclusion in the compositions of the invention include perfumes, colours and filler salts, with sodium sulfate being a preferred filler salt.

CA 022~6892 1998-ll-26 W O 97/45512 PCTrUS97/08235 pH of the compositions The present compositions preferably have a pH measured as a 1%
solution in distilled water of at least 8.5, preferably from 9.0 to 12.5, most preferably from 9.S to 11Ø

Form of the compositions The compositions in accordance with the invention can take a variety ofphysical forms including granular, tablet, bar and liquid forms. The compositions are particularly the so-called concentrated granular detergent compositions adapted to be added to a washing machine by means of a dispensing device placed in the machine drum with the soiled fabric load.

In general, granular detergent compositions in accordance with the present invention can be made via a variety of methods including dry mixing, spray drying, agglomeration and granulation.

The mean particle size of the components of granular compositions in accordance with the invention should preferably be such that no more that 5 % of particles are greater than 1 .7mm in diameter and not more than 5 of particles are less than 0.15mm in diameter.

The term mean particle size as defined herein is calculated by sieving a sample of the composition into a number of fractions (typically 5 fractions) on a series of Tyler sieves. The weight fractions thereby obtained are plotted ~g~in~t the aperture size of the sieves. The mean particle size is taken to be the aperture size through which 50~ by weight of the sample would pass.

The bulk density of granular detergent compositions in accordance with the present invention typically have a bulk density of at least 600 g/litre, more preferably from 650 g/litre to 1200 g/litre. Bulk density is measured by means of a simple funnel and cup device consisting of a conical funnel moulded rigidly on a base and provided with a flap valve at its lower extremity to allow the contents of the funnel to be emptied into an axially aligned cylindrical cup disposed below the funnel. The funnel is 130 mm CA 022~6892 1998-11-26 high and has internal diameters of 130 mm and 40 mm at its respective upper and lower extremities. It is mounted so that the lower extremity is 140 mm above the upper surface of the base. The cup has an overall height of 90 mm, an internal height of 87 mm and an internal diameter of 84 mm. Its nominal volume is 500 ml.

To carry out a measurement, the funnel is filled with powder by hand pouring, the flap valve is opened and powder allowed to overfill the cup.
The filled cup is removed from the frame and excess powder removed from the cup by passing a straight edged implement eg; a knife, across its upper edge. The filled cup is then weighed and the value obtained for the weight of powder doubled to provide a bulk density in g/litre. Replicate measurements are made as required.

Surfactant a~glomerate particles The cationic ester surfactant herein, preferably with additional surfactants, is preferably present in granular compositions in the form of surfactant agglomerate particles, which may take the form of flakes, prills, marumes, noodles, ribbons, but preferably take the form of granules. The most preferred way to process the particles is by agglomerating powders (e.g. aluminosilicate, carbonate) with high active surfactant pastes and to control the particle size of the resultant agglomerates within specified limits. Such a process involves mixing an effective amount of powder with a high active surfactant paste in one or more agglomerators such as a pan agglomerator, a Z-blade mixer or more preferably an in-line mixer such as those manufactured by Schugi (Holland) BV, 29 Chroomstraat 8211 AS, Lelystad, Netherlands, and Gebruder Lodige Maschinenbau GmbH, D-4790 Paderborn 1, Elsenerstrasse 7-9, Postfach 2050, Germany. Most preferably a high shear mixer is used, such as a Lodige CB (Trade Name).

A high active surfactant paste comprising from 50% by weight to 95 % byweight, preferably 70% by weight to 85 % by weight of surfactant is typically used. The paste may be pumped into the agglomerator at a temperature high enough to m~i~t~in a pumpable viscosity, but low CA 022~6892 1998-11-26 enough to avoid degradation of the anionic surfactants used. An operating temperature of the paste of 50~C to 80~C is typical.

T.~lln-lry washing method Machine laundry methods herein typically comprise treating soiled laundry with an aqueous wash solution in a washing machine having dissolved or dispensed therein an effective amount of a machine laundry detergent composition in accord with the invention. By an effective amount of the detergent composition it is meant from 40g to 300g of product dissolved or dispersed in a wash solution of volume from 5 to 65 litres, as are typical product dosages and wash solution volumes commonly employed in conventional machine laundry methods.

In a preferred use aspect a dispensing device is employed in the washing method. The dispensing device is charged with the detergent product, and is used to introduce the product directly into the drum of the washing machine before the commencement of the wash cycle. Its volume capacity should be such as to be able to contain sufficient detergent product as would normally be used in the washing method.

Once the washing machine has been loaded with laundry the dispensing device cont~ining the detergent product is placed inside the drum. At the commencement of the wash cycle of the washing machine water is introduced into the drum and the drum periodically rotates. The design of the dispensing device should be such that it permits cont~inment of the dry detergent product but then allows release of this product during the wash cycle in response to its agitation as the drum rotates and also as a result of its contact with the wash water.

To allow for release of the detergent product during the wash the device may possess a number of openings through which the product may pass.
Alternatively, the device may be made of a material which is permeable to liquid but impermeable to the solid product, which will allow release of dissolved product. Preferably, the detergent product will be rapidly released at the start of the wash cycle thereby providing transient localised CA 022~6892 1998-11-26 W O 97/45512 PCT~US97/08235 high concentrations of product in the drum of the washing machine at this stage of the wash cycle.

Preferred dispensing devices are reusable and are designed in such a way that container integrity is m~int~ine-l in both the dry state and during the wash cycle. Especially preferred dispensing devices for use with the composition of the invention have been described in the following patents;
GB-B-2, 157, 717, GB-B-2, 157, 718, EP-A-0201376, EP-A-0288345 and EP-A-0288346. An article by J.Bland published in Manufacturing Chemist, November 1989, pages 41-46 also describes especially preferred dispensing devices for use with granular laundry products which are of a type commonly know as the "granulette". Another preferred dispensing device for use with the compositions of this invention is disclosed in PCT
Patent Application No. WO94/11562.

Especially preferred dispensing devices are disclosed in European Patent Application Publication Nos. 0343069 & 0343070. The latter Application discloses a device comprising a flexible sheath in the form of a bag extending from a support ring defining an orifice, the orifice being adapted to admit to the bag sufficient product for one washing cycle in a washing process. A portion of the washing medium flows through the orifice into the bag, dissolves the product, and the solution then passes outwardly through the orifice into the washing medium. The support ring is provided with a m~cking arrangemnt to prevent egress of wetted, undissolved, product, this arrangement typically comprising radially extending walls extending from a central boss in a spoked wheel configuration, or a similar structure in which the walls have a helical form.

Alternatively, the dispensing device may be a flexible container, such as a bag or pouch. The bag may be of fibrous construction coated with a water impermeable protective material so as to retain the contents, such as is disclosed in European published Patent Application No. 0018678.
Alternatively it may be formed of a water-insoluble synthetic polymeric material provided with an edge seal or closure designed to rupture in a~ueous media as disclosed in European published Patent Application Nos. 0011500, OOllS01, 0011502, and 0011968. A convenient for~n of CA 022~6892 1998-11-26 water frangible closure comprises a water soluble adhesive disposed along and sealing one edge of a pouch formed of a water impermeable polymeric film such as polyethylene or polypropylene.

Pack~in~ for the compositions Commercially marketed executions of the bleaching compositions can be packaged in any suitable container including those constructed from paper, cardboard, plastic materials and any suitable l~min~tes A
preferred pack~ging execution is described in European Application No.
94921505.7.

CA 02256892 l998-ll-26 W O 97/45512 PCT~US97/08235 Abbreviations used in Examples In the detergent compositions, the abbreviated component identifications have the following me~nin~s:

LAS : Sodium linear C12 alkyl benzene sulfonate TAS : Sodiumtallow alkyl sulfate C45AS : Sodium C 14-C 15 linear alkyl sulfate CxyEzS : Sodium C1x-Cly branched alkyl sulfate condensed with z moles of ethylene oxide C45E7 : A C14 15 predomin~ntly linear primary alcohol condensed with an average of 7 moles of ethylene oxide C25E3 : A C12 15 branched primary alcohol condensed with an average of 3 moles of ethylene oxide C25E5 : A C12 15 branched primary alcohol condensed with an average of 5 moles of ethylene oxide CEQ I : R1COOCH2CH2.N+(CH3)3 with Rl =
Cl l-C13 CEQ II : RlcoocH2cH2cH2N + (CH3)3 with ~1 =
Cl l-C13 CEQ III R1COO CH2CH2 N+(CH3)2(CH2CH2OH) with Rl=cll-cl3 CEQ IV : R1COOCH2CH2N+(CH3CH2)2(CH3) with Rl =Cl l-C13 QAS : R2.N+(CH3)2(C2H4OH) with R2 = C12 ~ C14 Soap : Sodium linear alkyl carboxylate derived from an 80/20 mixture of tallow and coconut oils.
TFAA : C16-Clg alkyl N-methyl glucamide TPKFA : C12-C14 topped whole cut fatty acids STPP : Anhydrous sodium tripolyphosphate Zeolite A : Hydrated Sodium Aluminosilicate of forrnula Na12(A102SiO2)12. 27H20 having a primary particle size in the range from 0.1 to 10 micrometers NaSKS-6 : Crystalline layered silicate of formula ~ -Na2Si205 CA 022~6892 l998-ll-26 W O 97/45512 PCT~US97/0823S -Citric acid : Anhydrous citric acid Carbonate : Anhydrous sodium carbonate with a particle size between 200~m and 900~1m Bicarbonate : Anhydrous sodium bicarbonate with a particle size distribution between 400~m and 1200,um Silicate : Amorphous Sodium Silicate (SiO2:Na2O; 2.0 ratio) Sodium sulfate: Anhydrous sodium sulfate Citrate : Tri-sodium citrate dihydrate of activity 86.4%
with a particle size distribution between 425,um and 850,um GDP : polymer of (CH2CHCOONa)25-CH(CH3)COOC12H2s, average molecular weight about 35,000 MA/AA : Copolymer of 1 :4 maleic/acrylic acid, average molecular weight about 70,000.
CMC : Sodium carboxymethyl cellulose Protease : Proteolytic enzyme of activity 4KNPU/g sold by NOVO Industries A/S under the tradename Savinase Alcalase : Proteolytic enzyme of activity 3AU/g sold by NOVO Industries A/S
Cellulase : Cellulytic enzyme of activity 1000 CEVU/g sold by NOVO Industries A/S under the tradename Carezyme Amylase : Amylolytic enzyme of activity 60KNU/g sold by NOVO Industries A/S under the tradename Termamyl 60T
Lipase : Lipolytic enzyme of activity 100kLU/g sold by NOVO Industries A/S under the tradename Lipolase Endolase : Endoglunase enzyme of activity 3000 CEVU/g sold by NOVO Industries A/S

CA 022~6892 1998-ll-26 PCTrUS97/08235-PB4 : Sodium perborate tetrahydrate of nominal formula NaBO2 .3H2o.H2o2 PB1 : Anhydrous sodium perborate bleach of nominal formula NaB~2-H2~2 Percarbonate : Sodium Percarbonate of nominal formula 2Na2C03 ~3H2~2 NOBS : Nonanoyloxybenzene sulfonate in the form of the sodium salt.
TAED : Tetraacetylethylen.odi~mine DTPMP : Diethylene tri~mine penta (methylene phosphonate), marketed by Monsanto under the Trade name Dequest 2060 Photoactivated: Sulfonated Zinc Phthlocyanine encapsulated in bleach dextrin soluble polymer Brightener 1 : Disodium 4,4'-bis(2-sulphostyryl)biphenyl Brightener 2 : Disodium 4,4'-bis(4-~nilino-6-morpholino-1.3.5-triazin-2-yl)amino) stilbene-2:2'-disulfonate.
HEDP : 1,1-hydroxyethane diphosphonic acid PVNO : Polyvinylpyridine N-oxide PVPVI : Copolymer of polyvinylpyrolidone and vinylimidazole SRP 1 : Sulfobenzoyl end capped esters with oxyethylene oxy and terephtaloyl backbone SRP 2 : Diethoxylated poly (1, 2 propylene terephtalate) short block polymer Silicone antifoam: Polydimethylsiloxane foam controller with siloxane-oxyalkylene copolymer as dispersing agent with a ratio of said foam controller to said dispersing agent of 10:1 to 100:1.

CA 022~6892 1998-ll-26 W O 97/45512 PCT~US97/08235-In the following Examples all levels are quoted as 5~ by weight of the composition:

Example 1 The following laundry detergent compositions A to F were prepared in accord with the invention:

A B C D E F
LAS 8.0 8.0 8.0 8.0 8.0 8.0 C25E3 3.4 3.4 3.4 3.4 3.4 3.4 CEQ I 0.8 0.8 2.0 2.0 1.0 0.7 CEQ II 0.2 0.5 0.5 0.7 2.0 0.8 QAS - - 0.8 - - 0.8 Zeolite A 18.1 18.1 18.1 18.1 18.1 18.1 Carbonate 13.0 13.0 13.0 27.0 27.0 27.0 Silicate 1.4 1.4 1.4 3.0 3.0 3.0 Sodium sulfate 26.1 26.1 26.1 26.1 26.1 26.1 PB4 9.0 9.0 9.0 9.0 9.0 9.0 TAED 1.5 1.5. 1.5 1.5 1.5 1.5 DETPMP 0.25 0.25 0.25 0.25 0.25 0.25 HEDP 0.3 0.3 0.3 0.3 0 3 0 3 Protease 0.26 0.26 0.26 0.26 0.26 0.26 WO 97/45512 PCT/US97/0823~ - -Amylase 0.1 0.1 0.1 0.1 0.1 0.1 GDP 0.5 0.8 2.0 1.0 3.0 3.0 MA/AA 0.3 0.3 0.3 0.3 0.3 0.3 CMC 0.2 0.2 0.2 0.2 0.2 0.2 Photoactivated 15 15 15 15 15 15 bleach (ppm) ppm ppm ppm ppm ppm ppm Brightener 1 0.09 0.09 0.09 0.09 0.09 0-09 Perfume 0.3 0.3 0.3 0.3 0.3 0.3 Silicone antifoam 0.5 0.5 0.5 0.5 0.5 0.5 Misc/minors to 100~

Density in g/litre 850 850 850 850 850 850 PCT~US97/08235-Example 2 The following granular laundry detergent compositions G to I of bulk density 750 g/litre were prepared in accord with the invention:

G H
LAS 5.25 5.61 4.76 TAS 1.25 1.86 1.57 C45AS - 2.24 3.89 C25AE3S - 0.76 1.18 C45E7 3.25 - 5.0 C25E3 - 5.5 CEQ II 0.8 2.0 2.0 CEQ III 0.4 1.0 0.5 STPP 19.7 - -Zeolite A - 19.5 19.5 NaSKS-6/citric acid - 10.6 10.6 (79:21) Carbonate 6.1 21.4 21.4 Bicarbonate - 2.0 2.0 Silicate 6.8 Sodium sulfate 39.8 - 14.3 CA 02256892 l998-ll-26 W O 97/45512 PCTrUS97/08235 -PB4 5.0 12.7 TAED 0.5 3.1 DETPMP 0.25 0.2 0.2 HEDP 0.3 0 3 Protease 0.26 0.85 0.85 Lipase 0.15 0.15 0.15 Cellulase 0.28 0.28 0.28 Amylase 0.1 0.1 0.1 GDP 0.8 2.0 0.2 MA/AA 0.8 1.6 1.6 CMC 0.2 0.4 0.4 Photoactivated bleach 15 ppm 27 ppm 27 ppm (ppm) Brightener 1 0.08 0.19 0.19 Brightener 2 - 0.04 0.04 Perfume 0.3 0.3 0.3 Silicone antifoam 0.5 2.4 2.4 Minors/misc to 1005~

CA 022~6892 1998-ll-26 W O 97/45512 PCT~US97/08235 -Example 3 The following detergent formulations, according to the present invention were prepared, where J is a phosphorus-cont~ining detergent composition, K is a zeolite-cont~ining detergent composition and L is a compact detergent composition:

J K L

Blown Powder STPP 24.0 - 24.0 Zeolite A - 24.0 C45AS 9.0 6.0 13.0 MA/AA 2.0 4.0 2.0 LAS 6.0 8.0 11.0 TAS 2.0 C E Q I - - 2.0 CEQ II - 2.0 C E Q III 2.0 Silicate 7.0 3.0 3.0 CMC 1.0 1.0 0.5 GDP 1.5 0.5 1.5 Brightener 2 0.2 0.2 0.2 Soap 1.0 1.0 1.0 DTPMP 0.4 0.4 0.2 Spray On C45E7 2.5 2.5 2.0 C25E3 2.5 2.5 2.0 Silicone antifoam 0.3 0.3 0.3 Perfume 0.3 0.3 0.3 Dry additives Carbonate 6.0 13 .0 15 .0 PB4 18.0 18.0 10.0 PB1 4.0 4.0 0 TAED 3.0 3.0 1.0 Photoactivated bleach 0.02 0.02 0.02 Protease 1.0 1.0 1.0 Lipase 0.4 0.4 0.4 CA 02256892 1998-ll-26 PCT~US97/08235 Amylase 0.25 0.30 0.15 Dry mixed sodium 3.0 3.0 5.0 sulfate Balance (Moisture ~ 100.0 100.0 100.0 Miscellaneous) Density (g/litre) 630 670 670 CA 022~6892 1998-11-26 W O 97/45512 PCT~US97/08235 -Example 4 The following nil bleach-cont~inin~ detergent formulations of particular use in the washing of colored clothing, according to the present invention were prepared:

M N O
Blown Powder Zeolite A 15.0 15.0 Sodium sulfate 0.0 5.0 LAS 3.0 3.0 CEQ I 0.5 CEQ II 1.0 3.0 CEQ IV 0.5 - 3.0 DTPMP 0.4 0.5 GDP 1.0 3.0 5.0 CMC 0.4 0.4 MA/AA 4.0 4.0 Agglomerates C45AS - - 11.0 LAS 6.0 5.0 TAS 3.0 2.0 Silicate 4.0 4.0 Zeolite A 10.0 15.0 13.0 CMC - - 0.5 MA/AA - - 2.0 Carbonate 9.0 7.0 7.0 Spray On Perfume 0.3 0.3 0.5 C45E7 4.0 4.0 4.0 C25E3 2.0 2.0 2.0 Dry additives MA/AA - - 3.0 NaSKS-6 - - 12.0 Citrate 10.0 - 8 .0 Bicarbonate 7.0 3.0 5.0 Carbonate 8.0 5.0 7.0 PVPVI/PVNO 0.5 0.5 0.5 CA 02256892 1998-ll-26 Alcalase 0.5 0.3 0.9 Lipase 0.4 0.4 0.4 Amylase 0.6 0.6 0.6 Cellulase 0.6 0.6 0.6 Silicone antifoam 5.0 5.0 5.0 Dry additives Sodium sulfate 0.0 9.0 0.0 R~l~n~e (Moisture and 100.0 100.0 100.0 Miscellaneous) Density (g/litre) 700 700 700 CA 022~6892 1998-11-26 WO 97t45512 PCT/US97/08235 -Examp~e 5 The following detergent formulations, according to the present invention were prepared:

P Q R S

LAS 20.0 14.0 24.0 22.0 QAS 0.7 1.0 - 0.7 CEQ III 0.4 0.4 3.8 CEQ IV 1.5 0.7 - 3.4 TFAA - 1.0 - -C25E5/C45E7 - 2.0 - 0.5 C45E3S - 2.5 - -STPP 30.0 18.0 30.0 22.0 Silicate 9.0 5.0 10.0 8.0 Carbonate 13 .0 7.5 - 5 .0 Bicarbonate - 7.5 DTPMP 0.7 1.0 SRP 1 0.3 0.2 - 0.1 GDP 0.8 2.2 3.4 5.1 MA/AA 2.0 1.5 2.0 1.0 CMC 0.8 0.4 0.4 0.2 Protease 0.8 1.0 0.5 0.5 Amylase 0.8 0.4 - 0.25 Lipase 0.2 0.1 0.2 0.1 Cellulase 0.15 0.05 Photoactivated 70ppm 45ppm - 10ppm bleach (ppm) Brightener 1 0.2 0.2 0.08 0.2 PB1 6.0 2.0 NOBS 2.0 1.0 B~l~nre 100 100 100 100 (Moisture and Miscellaneous) CA 02256892 1998-ll-26 W O 97/45512 PCT~US97/08235 - -Example 6 The following detergent formulations, according to the present invention were prepared:

T U V

Blown Powder Zeolite A 30.0 22.0 6.0 Sodium sulfate 19.0 5.0 7.0 M A/A A 3.0 3.0 6.0 G D P 1.0 2. 8 4.1 L A S 14.0 12.0 22.0 C45A S 8.0 7.0 7.0 C E Q II - 0.4 1.5 C E Q IV 1.5 1.5 1.5 Silicate - 1.0 5.0 Soap - - 2.0 Brightener 1 0.2 0.2 0.2 Carbonate 8.0 16.0 20.0 D TP M P - 0.4 0.4 Spray On C45E7 1.0 1.0 1.0 Dry additives P V P VI/P V N O 0.5 0.5 0.5 Protease 1.0 1.0 1.0 Lipase 0.4 0.4 0 4 Amylase 0.1 0.1 0.1 Cellulase 0.1 0.1 0.1 N O BS - 6.1 4.5 PBl 1.0 5.0 6.0 Sodium sulfate - 6.0 R~l~nce (Moisture 100 100 100 and Miscellaneous) CA 022~6892 1998-ll-26 W O 97/45512 PCTrUS97/08235 Example 7 The following high density and bleach-con~inin~ detergent formulations,according to the present invention were prepared:

W X Y

Blown Powder Zeolite A 15.0 15.0 15.0 Sodim sulfate 0.0 5.0 0.0 LAS 3.0 3.0 3.0 QAS - 1.5 1.5 CEQ II 0.5 0.5 1.2 CEQ III 0.9 1.2 0.5 DTPMP 0.4 0.4 0.4 GDP 3.2 1.4 5.8 CMC 0.4 0.4 0.4 MA/AA 4.0 2.0 2.0 Agglomerates LAS 5.0 5.0 5.0 TAS 2.0 2.0 1.0 Silicate 3.0 3.0 4.0 Zeolite A 8.0 8.0 8.0 Carbonate 8.0 8.0 4.0 Spray On Perfume 0.3 0.3 0.3 C45E7 2.0 2.0 2.0 C25E3 2.0 - -Dry additives Citrate 5.0 - 2.0 Bicarbonate - 3.0 Carbonate 8.0 15.0 10.0 TAED 6.0 2.0 5.0 PB1 14.0 7.0 10.0 Polyethylene oxide of MW - - 0.2 5,000,000 Bentonite clay - - 10.0 Protease 1.0 1.0 1.0 CA 02256892 l998-ll-26 W O 97/45512 PCT~US97/08235 -Lipase 0.4 0.4 0.4 Amylase 0.6 0.6 0.6 Cellulase 0.6 0.6 0.6 Silicone antifoam 5.0 5.0 5.0 Dry additives Sodium sulfate 0.0 3.0 0.0 Balance (Moisture and 100.0 100.0 100.0 Miscellaneous) Density (g/litre) 850 850 850 Example 8 The following high density detergent formulations, according to the present invention were prepared:

Z AA

Agglomerate C45AS 11.0 14.0 CEQ III 1.8 2.2 Zeolite A 15.0 6.0 Carbonate 4.0 8.0 GDP 2.8 3.3 MA/AA 4.0 2.0 CMC 0.5 0.5 DTPMP 0.4 0.4 Spray On C25E5 5.0 5.0 Perfume 0.5 0.5 Dry Adds HEDP 0.5 0.3 SKS 6 13.0 10.0 Citrate 3.0 1.0 TAED 5.0 7.0 Percarbonate 20.0 20.0 SRP 1 0.3 0.3 Protease 1.4 1.4 Lipase 0.4 0.4 Cellulase 0.6 0.6 Amylase 0. 6 0. 6 Silicone antifoam 5.0 5.0 Brightener 1 0.2 0.2 Brightener 2 0.2 Balance (Moisture and 100 100 Miscellaneous) Density (g/litre) 850 850 CA 022~6892 1998-11-26 Example 9 The following liquid detergent formulations, according to the present invention were prepared:

AB AC AD AE AF AG AH AI

LAS 10. 13.0 9.0 - 25.0 - - -o C25AS 4.0 1.0 2.0 10. - 13.0 18.0 15.0 o C25E3S 1.0 - - 3.0 - 2.0 2.0 4.0C25E7 6.0 8.0 13. 2.5 - - 4.0 4.0 o CEQ I 0.4 1.0 0.8 0.4 2.0 2.5 3.5 CEQ II 0.6 1.2 0.7 0.4 1.2 - - 3.5 TFAA - - - 4.5 - 6.0 8.0 8.0 QAS - - - - 3.0 1.0 TPKFA 2.0 - 13. 2.0 - 15.0 7.0 7.0 o Rapeseed fatty acids - - - 5.0 - - 4.0 4.0 Citricacid 2.0 3.0 1.0 1.5 1.0 1.0 1.0 1.0 Dodecenyl/tetradecenyl 12. 10.0 - - 15 .0 succinic acid 0 Oleic acid 4.0 2.0 1.0 - 1.0 Ethanol 4.0 4.0 7.0 2.0 7.0 2.0 3.0 2.0 1,2 Propanediol 4.0 4.0 2.0 7.0 6.0 8.0 10.0 13.-Mono Ethanol Amine - - - 5.0 - - 9.0 9.0 Tri Ethanol Amine - - 8 NaOH up to pH 8.0 8.0 7.6 7.7 8.0 7.5 8.0 8.2 Ethoxylated 0.5 - 0.5 0.2 - - 0.4 0.3tetraethylene pent~min~
DTPMP 1.0 1.0 0.5 1.0 2.0 1.2 1.0 GDP 0.4 0.6 0.9 1.6 2.2 3.1 2.8 1.8 SRP 2 0.3 - 0.3 0.1 - - 0.2 0.1PVNO

CA 02256892 1998-ll-26 W O 97/45512 PCTrUS97/08235-Protease 0.5 0.5 0.4 0.2 - 0.5 0.3 0.6 s Alcalase - - - - 1.5 Lipase - 0.10 - 0.0 - - 0.15 0.15 Amylase 0.2 0.25 0.6 0.5 0.25 0.9 0.6 0.6 Cellulase - - - 0.0 - - 0.15 0.15 s Endolase - - - 0.1 0 0.07 Boric acid 0.1 0.2 - 2.0 1.0 1.5 2.5 2.5 Na formate - - 1.0 - - - - -Ca chloride - 0.015 - 0.0 Bentonite clay - - - - 4.0 4.0 Suspending clay SD3 - - - - 0.6 0.3 Balance (Moisture and 100 100 100 100 100 100 100 100 Miscellaneous)

Claims (11)

WHAT IS CLAIMED IS:

1. A detergent composition comprising (a) a cationic ester surfactant; and (b) a grease dispersing agent.

2. A detergent composition according to Claim 1 wherein said cationic ester surfactant is present at a level from 0.5% to 10.0% by weight of said detergent composition.

3. A detergent composition according to either of Claims 1 or 2 wherein the cationic ester surfactant is selected from those having the formula:

wherein R1 is a C5-C31 linear or branched alkyl, alkenyl or alkaryl chain or M-. N+(R6R7R8)(CH2)s; X and Y, independently, are selected from the group consisting of COO, OCO, O, CO, OCOO, CONH, NHCO, OCONH and NHCOO wherein at least one of X or Y is a COO, OCO, OCOO, OCONH or NHCOO group; R2, R3, R4, R6, R7, and R8 are independently selected from the group consisting of alkyl, alkenyl, hydroxyalkyl, hydroxy-alkenyl and alkaryl groups having from 1 to 4 carbon atoms; and R5 is independently H or a C1-C3 alkyl group; wherein the values of m, n, s and t independently lie in the range of from 0 to 8, the value of b lies in the range from 0 to 20, and the values of a, u and v independently are either 0 or 1 with the proviso that at least one of u or v must be 1; and wherein M is a counter anion.

4. A detergent composition according to Claim 3 wherein R2,R3 and R4 are independently selected from the group consisting of -CH3 and -CH2CH2OH.

5. A detergent composition according to Claim 3 wherein both R2 and R3 are C2-C3 alkyl groups.

6. A detergent composition according to Claim 3 wherein the cationic ester is selected from the choline esters having the formula:

wherein m is from 1 to 4 and R1 is a C11-C19 linear or branched alkyl chain.

7. A detergent composition according to any of Claims 1 to 6 wherein said grease dispersing agent is present at a level of from 0.1% to 15% by weight of the detergent composition.

8. A detergent composition according to any of Claims 1 to 7 wherein the grease dispersing agent has the formula:

wherein:
- R3 and R4 represent hydrogen or C1-4 alkyl;
- R2 represents -CO-O-, -O-, -O-CO-, CH2-, -CO-NH-, or is absent;
- R1 represents -C3H6-N+-(CH3)3(C1-), -C2H4-OSO3-(Na+), -SO3-(Na+), -C2H4N+(CH3)3Cl-, -C2H4N+(C2H6)3Cl-, -CH2N+(CH3)3Cl-, -CH2N+(C2H6)3Cl- or benzyl -SO3-(Na+) or hydrogen;
- R a is CH2, C2H4, C3H6 or is absent;
- R b represents form 1 to 50 independently selected alkylene oxide groups, or is absent;
- R c represents -OH or -H; and wherein if R2, R a and R b are absent, then R c is not -H.
- x is at least 1; z is 1; and n is at least 1

9. A detergent composition according to Claim 8 wherein R2 is -CO-O- and R1 is a hydrogen.

10. A detergent composition according to any of Claims 1 to 7 wherein the grease dispersing agent has the formula:

wherein Q2 is a molecular entity of formula:

and wherein:
R1 represents -COO-O-, -O-, -O-CO-, -CH2-, CO-NH-, or is absent:

R2 represents from 1 to 50 independently selected alkyleneoxy groups, or is absent, provided that when R3 is absent and R4 represents hydrogen or contains no more than 4 carbon atoms, then R2 must contain an alkyleneoxy group preferably more than 5 alkyleneoxy groups with at least 3 carbon atoms;

R3 represents a phenylene linkage, or is absent;
R4 represents hydrogen or a C1-24 alkyl or C2-24 alkenyl group, with the provisos that (a) when R1 represents -O-CO-, R2 and R3 must be absent and R4 must contain at least 5 carbon atoms;
(b) when R2 is absent, then R4 is not hydrogen and when also R3 is absent, then R4 must contain at least 5 carbon atoms;

R5 represents hydrogen or a group of formula -COOA4;
R6 represents hydrogen or C1-4 alkyl; and A1, A2, A3 and A4 are independently selected from hydrogen, alkali metals, alkaline earth metals, ammonium and amine bases and C1=4, or (C2H4O)t H wherein t is from 1-50, and wherein the monomer units may be in random order.

Q1 is a multifunctional monomer, allowing the branching of the polymer,wherein the monomers of the polymer may be connected to Q1 in any direction, in any order, therewith possibly resulting in a branched polymer.

z and v are 1; n is at least 1; x is at least 1; (x + y + p + q + r): z is from 4 : 1 to 1,000 : 1; in which the monomer units may be in random order;

R7 and R8 represents -CH3 or is a hydrogen;

R9 and R10 represent substituent groups.

11. A method of washing laundry in a domestic washing machine in which a dispensing device containing an effective amount of a solid detergent composition according to any of Claims 1 to 10 is introduced into the drum of the washing machine before the commencement of the wash, wherein said dispensing device permits progressive release of said detergent composition into the wash liquor during the wash.