CA2305224C - A detergent composition - Google Patents

Abstract

The present invention relates to detergent compositions comprising anionic m id- branched surfactant compounds and a bleaching system comprising a hydrophobic and a hydrophilic bleach precursor. The compositions are particularly useful as solid laundry detergent compositions.

Description

A Detergent Composition Technical Field The present invention relates to detergent compositions comprising anionic mid-branched surfactant compounds and a bleaching system comprising a hydrophobic and a hydrophilic bleach precursor. The compositions are particularly useful as solid laundry detergent compositions.
Background to the Invention Recently, a certain new type of anionic mid-chain branched surfactants has been developed. These surfactants are described in Canadian Application Nos. 2,252,435; 2,252,362; 2,252,436; 2,252,424 and 2,252,437.
It has been determined that these mid-chain branched surfactants are excellent surfactants, in particular for use in laundry products, especially under cool or cold water washing conditions even as low as 20°C-5°C. It has also been found that combination of two or more of these mid-chain branched surfactants can provide a surfactant mixture that is even higher in surfactancy and has better low temperature water solubility.
A component traditionally present in most detergents is a bleach. Various bleaching systems have been developed over the past decades, such as bleaching systems, based on organic peroxyacids. The organic peroxyacids are often obtained by the in situ perhydrolysis of organic peroxyacid bleach precursor compounds (bleach activators).
However, it is generally known that a variety of other detergent ingredients, commonly used in detergent, are not always (fully) bleach compatible, for example certain surfactants, perfumes, enzymes. These ingredient can react with the bleach, which results in a reduction of the performance of both the bleach and these ingredients. It is thus desirable to formulate detergents which comprise as little bleach as necessary to obtain a excellent bleaching performance, and to formulate the detergents with bleach compatible ingredients It has now been found these mid-chain branched surfactants are very bleach compatible. Furthermore, it has been found that detergent compositions comprising these mid-chain branched surfactants and a mixed bleaching system, comprising hydrophobic and hydrophilic bleach precursors, an excellent bleaching and cleaning performance is achieved, even when low amounts of bleach are used. It has surprisingly been found that both hydrophilic and hydrophobic, bleachable and non-bleachable stains and soils are more effectively removed. Without being bound by theory, it is believed that this is due to the excellent stain and soil removal by the mid-chain branched surfactant, which facilitates the access to the remaining bleachable stains and soils by the hydrophobic and hydrophilic bleaches and allows these bleaches to bleach very effectively these remaining bleachable stains.
Another additional benefit is that by the reduction of the amount of bleach which is required for a good bleaching performance, the ease of formulation can be improved and the formulation costs can be reduced.
Summary of the invention The invention relates to detergent compositions comprising a) at least 0.5%, preferably at least 5%, more preferably at least 10% by weight of the composition a surfactant system, comprising one or more longer alkyl chain, mid-chain branched surfactant compounds of the formula:
Ab-X-B
wherein:
(I) Ab is a hydrophobic mid-chain branched alkyl moiety, having in total 9 to 22 carbons in the moiety,.preferably from 12 to about 18, having: (1) a longest linear carbon chain attached to the - X - B moiety in the range of from 8 to 21 carbon atoms; (2) one or more C 1 - C3 alkyl moieties branching from this longest linear carbon chain; (3) at least one of the branching alkyl moieties is attached directly to a carbon of the longest linear carbon chain at a position within the range of the position 2 carbon, counting from position 1 carbon (# 1 ) which is attached to the - X
- B moiety, to the position of the terminal carbon minus 2 carbons, (the (w -2) carbon); and (4) when more than one of these compounds is present, the average total number of carbon atoms in the Ab-X moieties in the above formula is within the range of greater than 14.5 to about 18, preferably from about 15 to about 17;
(II) B is a hydrophilic moiety selected from sulfates, sulfonates, amine oxides, polyoxyalkyiene, preferably polyoxyethylene and polyoxypropylene, alkoxylated sulfates, polyhydroxy moieties, phosphate esters, glycerol sulfonates, polygluconates, polyphosphate esters, phosphonates, sulfosuccinates, sulfosuccaminates, polyalkoxylated carboxylates, glucamides, taurinates, sarcosinates, glycinates, isethionates, dialkanolamides, monoalkanolamides, monoalkanolamide sulfates, diglycolamides, diglycolamide sulfates, glycerol esters, glycerol ester sulfates, glycerol ethers, glycerol ether sulfates, polyglycerol ethers, polyglycerol ether sulfates, sorbitan esters, polyalkoxylated sorbitan esters, ammonioalkanesulfonates, amidopropyl betaines, alkylated goats, alkyated/polyhydroxyalkylated goats, alkylated goats, alkylated/polyhydroxylated oxypropyl goats, imidazolines, 2-yl-succinates, sulfonated alkyl esters, and sulfonated fatty acids; and (III) X is selected from -CH2- and -C(O)-; and b) at least 0.5% by weight of the composition a bleaching system comprising (I) a hydrophobic bleach precursor; and (II) a hydrophilic bleach precursor.
Detailed description of the invention Mid-chain branched surfactant compounds-containing surfactant system The detergent compositions of the invention comprise at least 0.5%, preferably at least 5%, more preferably at least 10% by weight of the composition of a surfactant system, comprising longer alkyl chain, mid-chain branched surfactant compounds, selected from the group consisting of surfactant compounds having the formula as defined above.

Preferred surfactant systems herein comprise longer alkyl chain, mid-chain branched surfactant compounds of the above formula wherein the Ab moiety is a branched primary alkyl moiety having the formula:

CH3CH2(CH2)r,~,CH(CH2}xCH(CH2~CH(CH2)z-wherein the total number of carbon atoms in the branched primary alkyl moiety of this formula (including the R, R1, and R2 branching) is from 13 to 19; R, R1, and R2 are each independently selected from hydrogen and C1-C3 alkyl (preferably methyl), provided R, R1, and R2 are not all hydrogen and, when z is 0, at least R or R1 is not hydrogen; w is an integer from 0 to 13; x is an integer from 0 to 13; y is an integer from 0 to 13; z is an integer from 0 to 13; and w + x + y + z is from 7 to 13.
In general, for the mid-chain branched surfactant compounds of the surfactant system, certain points of branching (e.g., the location along the chain of the R, R1, andlor R2 moieties in the above formula) are preferred over other points of branching along the backbone of the surfactant. The formula below illustrates the mid-chain branching range (i.e., where points of branching occur), preferred mid-chain branching range, and more preferred mid-chain branching range for mono-methyl branched alkyl Ab moieties useful according to the present invention.
CH3CH2CH2CH2CH2CH2(CH2)1_~CH2CH2CH2CH2CH2 more referred ran p g preferred range mid-chain branching ran It should be noted that for the mono-methyl substituted surfactants these ranges exclude the two terminal carbon atoms of the chain and the carbon atom immediately adjacent to the -X - B group.
The formula below illustrates the mid-chain branching range, preferred mid-chain branching range, and more preferred mid-chain branching range for di-methyl substituted alkyl Ab moieties useful according to the present invention.

CH3CH2CH~CHZCH,CH2(CH2)o-6CH~CH~CH~CHZCH~ -more preferred rang preferred range mid-chain branching range Preferred are surfactant compounds wherein in the above formula the Ab moiety does not have any quaternary substituted carbon atoms (i.e., 4 carbon atoms directly attached to one carbon atom).
The most preferred mid-chain branched surfactants compounds for use in the detergent compositions herein are mid-chain branched primary alkyl sulfonate and, even more preferably, sulfate surfactants. It should be understood that for the purpose of the invention, it may be preferred that the surfactant system comprises a mixture of two or more mid-chain branched primary alkyl sulfate or sulphonate surfactants.
Preferred mid-chain branched primary alkyl sulfate surfactants are of the formula CH3CH2(CH2h,"CH(CH2~CH(CH2}yCH(CH2)ZOS03M
These surfactants have a linear primary alkyl sulfate chain backbone (i.e., the longest linear carbon chain which includes the sulfated carbon atom) which preferably comprises from 12 to 19 carbon atoms and their branched primary alkyl moieties comprise preferably a total of at least 14 and preferably no more than 20, carbon atoms. In the surfactant system comprising more than one of these sulfate surfactants, the average total number of carbon atoms for the branched primary alkyl moieties is preferably within the range of from greater than 14.5 to about 17.5.
Thus, the surfactant system preferably comprises at least one branched primary alkyl sulfate surfactant compound having a longest linear carbon chain of not less than 12 carbon atoms or not more than 19 carbon atoms, and the total number of carbon atoms including branching must be at least 14, and further the average total number of carbon atoms for the branched primary alkyl moiety is within the range of greater than 14.5 to about 17.5.

R, R1, and R2 are each independently selected from hydrogen and Cl-C; alkyl group (preferably hydrogen or C 1-C2 alkyl, more preferably hydrogen or methyl, and most preferably methyl), provided R, R1, and R2 are not all hydrogen.
Further, when z is 1, at least R or R1 is not hydrogen.
M is hydrogen or a salt forming cation depending upon the method of synthesis.
Examples of salt forming cations are lithium, sodium, potassium, calcium, magnesium, quaternary alkyl amines having the formula RS
wherein R3, R4, RS and R6 are independently hydrogen, C 1-C22 alkylene, C4-C22 branched alkylene, Cl-C6 alkanol, Cl-C22 alkenylene, C4-C22 branched alkenylene, and mixtures thereof. Preferred cations are ammonium (R3, R4, RS
and.
R6 equal hydrogen), sodium, potassium, mono-, di-, and trialkanol ammonium, and .
mixtures thereof. The monoalkanol ammonium compounds of the present invention have R3 equal to C 1-C6 alkanol, R4, RS and R6 equal to hydrogen; dialkanol ammonium compounds of the present invention have R3 and R4 equal to C 1-C6 alkanol, RS and R6 equal to hydrogen; trialkanol ammonium compounds of the present invention have R3, R4 and RS equal to Cl-C6 alkanol, R6 equal to hydrogen. Preferred alkanol ammonium salts of the present invention are the mono-, di- and tri- quaternary ammonium compounds having the formulas:
H3N+CH2CH20H, H2N+(CH2CH20H)2, HN+(CH2CH20H)3.
Preferred M is sodium, potassium and the C2 alkanol ammonium salts listed above;
most preferred is sodium.
Further regarding the above formula, w is an integer from 0 to 13; x is an integer from 0 to 13; y is an integer from 0 to 13; z is an integer of at least 1; and w + x + y + z is an integer from 8 to 14.
A preferred mid-chain branched primary alkyl sulfate surfactant is, a C 16 total carbon primary alkyl sulfate surfactant having 13 carbon atoms in the backbone and having l, 2, or 3 branching units (i.e., R, R1 and/or R2) of in total 3 carbon atoms, (whereby thus; the total number of carbon atoms is at least 16). Preferred branching units can be one propyl branching unit or three methyl branching units.
Another preferred surfactant :system of the pre;sent invention have one or more branched primary alkyl sulfates having the fomrrula R1 1~2 I f CH3CH~(CHZ)xCH(CHZ)y(~,H(CHz)zOSOaM
wherein the total number of carbon atoms. including branching, is from 15 to 18, and when more than one of these sulfates is present, the average total number of carbon atoms in the branched primary alkyl moieties having the above formula is within the range of greater than 14.5 to about 17.x; R1 and R2 are each independently hydrogen or C1-C3 alkyl; M is a water soluble canon; x is from 0 to I 1; y is from 0 to 11; z is at least 2; and x -+- y + z is liom 9 to 13;
provided R1 and R2 are not both hydrogen.
Preferably, the surfactant system comprises at least 20% by weight of the system, more preferably at least 60°,~° by weight , even mare preferably at least 90% by weight of the ;system, of a mid chain branched primary alkyl sulfates, preferably having R1 and R2 independently hydrogen or methyl, provided RI and R2 are not both hydrogen; x + y is equal to 8, 9, or 10 and z is at least 2, whereby the average total number of carbon atoms in these sulfate surfactants is preferably from I
S to 17, more preferably from 16-I i .
Furthermore, !referred surfactant systems are those, which comprise at least about' 20%, more pr~:ferably at least fi0%, even more preferably at least 95% by weight of the system, of one or more mid-chain branched alkyl sulfates having the formula:
CHI
(1) t:H3 (CHz)aCH (CHZ~CHZ OS03M or CH3 (CH~)dCH (C'.Hz)e CHCH~ OSQ3M
(!I) or mixtures thereof; wherein M represents one or mare canons; a, b, d, and a are integers, a+b is from 10 to l Cr, d+e is from 8 to 14 and wherein further when a + b = 10, a is an integer from 2 to 9 and b is an integer from 1 to 8;
when a + b -- 11, a is an integer from 2 to l 0 and b is an integer from 1 to 9:
when a + b = 12, a is an integer from 2 to i 1 .arrd b is an integer from I to 10;

when a + b = 13, a is an integer from 2 to 12 and b is an integer from I to 11;
when a + b = 14, a is an integer from 2 to 13 and b is an integer from 1 to 12;
when a + b = 15, a is an integer from 2 to 14 and b is an integer from I to 13;
when a + b = 16, a is an integer from 2 to 15 and b is an integer from 1 to 14;
when d + a = 8, d is an integer from 2 to 7 and a is an integer from 1 to 6;
when d + a = 9, d is an integer from 2 to 8 and a is an integer from 1 to 7;
when d + a = 10, d is an integer from 2 to 9 and a is an integer from 1 to 8;
when d + a = 11, d is an integer from 2 to 10 and a is an integer from 1 to 9;
when d + a = 12, d is an integer from 2 to 11 and a is an integer from 1 to 10;
when d + a = 13, d is an integer from 2 to 12 and a is an integer from 1 to 11;
when d + a = 14, d is an integer from 2 to 13 and a is an integer from 1 to 12;
whereby, when more than one of these sulfate surfactants is present in the surfactant system, the average total number of carbon atoms in the branched primary alkyl moieties having the above formulas is within the range of greater than 14.5 to about I7.5.
Preferred mono-methyl branched primary alkyl sulfates are selected from the group consisting of 3-methyl pentadecanol sulfate, 4-methyl pentadecanol sulfate, 5-methyl pentadecanol sulfate, 6-methyl pentadecanol sulfate, 7-methyl pentadecanol sulfate, 8-methyl pentadecanol sulfate, 9-methyl pentadecanol sulfate, 10-methyl pentadecanol sulfate, 11-methyl pentadecanol sulfate, 12-methyl pentadecanol sulfate, 13-methyl pentadecanol sulfate, 3-methyl hexadecanol sulfate, 4-methyl hexadecanol sulfate, 5-methyl hexadecanol sulfate, 6-methyl hexadecanol sulfate, 7-methyl hexadecanol sulfate, 8-methyl hexadecanol sulfate, 9-methyl hexadecanol sulfate, 10-methyl hexadecanol sulfate, 11-methyl hexadecanol sulfate, 12-methyl hexadecanol sulfate, 13-methyl hexadecanol sulfate, 14-methyl hexadecanol sulfate;
and mixtures thereof.
Preferred di-methyl branched primary alkyl sulfates are selected from the group consisting of: 2,3-methyl tetradecanol sulfate, 2,4-methyl tetradecanol sulfate, 2,5-methyl tetradecanol sulfate, 2,6-methyl tetradecanol sulfate, 2,7-methyl tetradecanol sulfate, 2,8-methyl tetradecanol sulfate, 2,9-methyl tetradecanol sulfate, 2,I0-methyl tetradecanol sulfate, 2,i 1-methyl tetradecanol sulfate, 2,12-methyl tetradecanol sulfate, 2,3-methyl pentadecanol sulfate, 2,4-methyl pentadecanol sulfate, 2,5-methyl pentadecanol sulfate, 2,6-methyl pentadecanol sulfate, 2,7-methyl pentadecanol sulfate, 2,8-methyl pentadecanol sulfate, 2,9-methyl pentadecanol sulfate, 2,10-methyl pentadecanol sulfate, 2,11-methyl pentadecanol sulfate, 2,12-methyl pentadecanol sulfate, 2,13-methyl pentadecanol sulfate, and mixtures thereof.
The following branched primary alkyl sulfates comprising 16 carbon atoms and having one branching unit are examples of preferred branched surfactants useful in the present invention compositions:
5-methylpentadecylsulfate having the formula:

6-methylpentadecylsulfate having the formula 7-methylpentadecylsulfate having the formula 8-methylpentadecylsulfate having the formula 9-methylpentadecylsulfate having the formula 10-methylpentadecylsulfate having the fonmula wherein M is preferably sodium.
The following branched primary alkyl sulfates comprising 17 carbon atoms and having two branching units are examples of preferred branched surfactants according to the present invention:
2,5-dimethylpentadecylsulfate having the formula:

2,6-dimethylpentadecylsulfate having the formula 2,7-dimethylpentadecylsulfate having the formula 2,8-dimethylpentadecylsulfate having the formula 2,9-dimethylpentadecylsulfate having the formula 2,10-dimethylpentadecylsulfate having the formula wherein M is preferably sodium.
Bleaching system The bleaching system of the invention comprises a hydrophobic and a hydrophilic bleach precursor.

The bleaching system is present at a level of at least 0.5% by weight of the composition, preferably from 0.5% to 45% by weight, more preferably from 1% to 30% by weight, most preferably from 1.5% to 25% by weight of the detergent compositions.
Preferably, the bleach precursors are peroxyacid bleach precursors which may be represented as X-C-L
where L is a leaving group and X is essentially any functionality, which determines for the present invention whether the precursor is hydrophobic or hydrophilic, and which is such that on perhydroloysis the structure of the peroxyacid produced is O
X-C-OOH
The hydrophobic bleach of the present invention comprises a group X which contain at least 6 carbon atoms. The hydrophilic bleach of the present invention comprises a group X which contain less than 6 carbon atoms.
Preferably, the bleaching system of the invention contains a hydrogen peroxide source and a hydrophilic and hydrophobic (organic peroxyacid) bleach precursor compound. The production of the organic peroxyacid occurs by an in situ reaction of the precursors with a source of hydrogen peroxide. Preferred sources of hydrogen peroxide include inorganic perhydrate bleaches. Preferred perhydrate bleaches are metal perborates, metal percarbonates, particularly the sodium salts.
Perborate can be mono or tetra hydrated. Sodium percarbonate has the formula corresponding to 2Na2C03.3H202, and is available commercially as a crystalline solid. Potassium or sodium peroxymonopersulfate is another optional inorganic perhydrate salt of use in the detergent compositions herein.
The inorganic perhydrate bleaches are preferably present at a level of from 1 % to 40% by weight, more preferably from 3% to 35% by weight, most preferably from 5% to 20% by weight of the detergent composition.

Leavine nrouQs The leaving group, hereinafter L group, must be sufficiently reactive for the perhydrolysis reaction to occur within the optimum time frame (e.g., a wash cycle).
However, if L is too reactive, this activator will be difficult to stabilize for use in a bleaching composition.
Preferred L groups are selected from the group consisting of:
Y R3 RsY
-O ~ , -O ~ Y , and -O
O
-N-C-R -N N , -N-C-CH-R4 , Y

-O-C H=C-C H=C H2 -O-C H=C-C H=C H2 O C H _O Y O
-O-C-R' -N~ ~NR4 , -Nw /NR4 C C

-O-C=CHR4 , and -N-S-CH-R4 and mixtures thereof, wherein R1 is an alkyl, aryl, or alkaryl group containing from 1 to 14 carbon atoms, R3 is an alkyl chain containing 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 ammmonium groups.
The preferred solubilizing groups are -S03 M+, -C02-M+, -S04-M+, -N+(R3)4X
and O<--N(R3)3 and most preferably -S03 M+ and -C02-M+ wherein R' is an alkyl chain containing 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, ammonium or substituted ammonium cation, with sodium and potassium being most preferred, and X is a halide, hydroxide, methylsulfate or acetate anion.
Preferred hydrophilic and hydrophobic precursors Suitable bleach precursors typically contain one or more N- or O-acyl groups, which precursors can be selected from a wide range of classes. Suitable classes include anhydrides, esters, imides, lactams 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, and EP-A-0170386.
Alk~Qercarboxvlic acid bleach precursors Alkyl percarboxylic acid bleach precursors are preferred precursors for use herein.
They form percarboxylic acids on perhydrolysis. Preferred precursors of this type provide peracetic acid on perhydrolysis.
Preferred can be phenyl esters of C ~4_zz - alkanoic or alkenoic acids, esters of hydroxylamine, geminal diesters of lower alkanoic acids and gem-idols, such as those described in EP-A-0125781 especiallyl,l,5-triacetoxypent-4-ene and 1,1,5,5-tetraacetoxypentane and the corresponding butene and butane compounds, ethylidene benzoate acetate and bis(ethylidene acetate) adipate and enol esters, for instance as described in EP-A-0140648 and EP-A-0092932.
Preferred alkyl percarboxylic precursor compounds of the imide type include the N-,N,N1N1 tetra acetylated alkylene diamines wherein the alkylene group contains from 1 to 6 carbon atoms, particularly those compounds in which the alkylene group contains 1, 2 and 6 carbon atoms. Tetraacetyl ethylene diamine (TAED, being a hydrophilic precursor) is particularly preferred.
Other highly preferred alkyl percarboxylic acid precursors include sodium acetoxybenzene sulfonate (ABS) and pentaacetyl glucose, dodecanolyloxy -benzenesulphonate sodium salt, decanoyloxy - benzenesulphonate sodium salt (DOBS) , benzoyloxy - benzenesulphonate sodium salt (BOBS), more preferred sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate (iso-NOBS) and even more preferred sodium nonanoyloxybenzene sulfonate (HOBS), (being hydrophobic precursors).
Amide substituted alkyl neroxyacid precursors Amide substituted alkyl peroxyacid precursors are preferred precursors herein.
They include those of the following general formulae:
R~--C-N-R2-C-L R~-N-C-R2--C-L
R5 O~ or R5 O[
wherein R1 is an alkyl group with from 1 to 14 carbon atoms, R2 is an alkylene group containing from 1 to 14 carbon atoms, and RS is H or an alkyl group containing 1 to 10 carbon atoms and L can be essentially any leaving group.
Amide substituted bleach activator compounds of this type are described in EP-A-O i 70386.
Perbenzoic acid precursor Perbenzoic acid precursors are other preferred precursors herein. They provide perbenzoic acid on perhydrolysis. Suitable 0-acylated perbenzoic acid precursor compounds include the substituted and unsubstituted 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 diamine and the N-benzoyl substituted areas.
Suitable imidazole type perbenzoic acid precursors include N-benzoyl imidazole and N-benzoyl benzimidazole. Other useful N-acyl group-containing perbenzoic acid precursors include N-benzoyl pyrrolidone, dibenzoyl taurine and benzoyl pyroglutamic acid.

Highly preferred hydrophobic precursors are (6-octanamido-caproyl)oxybenzenesulfonate, (6-decanamido-caproyl) oxybenzene- sulfonate, (6-nonanamidocaproyl)oxy benzene sulfonate, decanoyloxy - benzenesulphonate sodium salt and benzoyloxy - benzenesulphonate sodium salt.
Benzoxazin organic peroxyacid precursors Also suitable are precursors of the benzoxazin-type, as disclosed for example in EP-A-332,294 and EP-A-482,807, particularly those having the formula:
O
II
CEO
\.J , C-Rt 'N
wherein Rl is H, alkyl, alkaryl, aryl, or arylalkyl.
Additional deter~yent components The detergent compositions of the invention may also contain additional detergent 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, additional bleaches, bleach catalysts, alkalinity systems, builders, organic polymeric compounds, additional enzymes, suds suppressors, lime soap dispersants, soil suspension and anti-redeposition agents and corrosion inhibitors.
Additional surfactant The detergent compositions of the invention preferably contain an additional surfactant selected from additional anionic, nonionic, 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 Laughlin 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 of 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 succinate~ and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C 12-C 18 monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C6-C 14 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.
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-C 17 acyl-N-(C 1-alkyl) and -N-(C1-C2 hydroxyalkyl) glucamine 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 C I p-C I g alkyl sulfates, more preferably the C I I -C 15 branched chain alkyl sulfates and the C I2-C 14 linear chain alkyl sulfates.
Alkyl ethoxysulfate surfactants are preferably selected from the group consisting of the C I 0-C I g 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 I I -C I g, most preferably C I I -C I S 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 Publication No. WO 93/18124.
Anionic sulfonate surfactant Anionic sulfonate surfactants suitable for use herein include the salts of CS-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 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 herein.
Suitable alkyl ethoxy carboxylates include those with the formula RO(CH2CH20)x CH2C00-M+ wherein R is a C6 to CIg 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 M is a cation. Suitable alkyl polyethoxy polycarboxylate surfactants include those having the formula RO-(CHRI-CHR2-O)-R3 wherein R is a C6 to C I g alkyl group, x is from I to 25, RI 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-1-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 of formula R-CON (R1 ) CH2 COOM, wherein R is a CS-C 1 ~ linear or branched alkyl or alkenyl group, R1 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.
Alkoxvlated nonionic surfactant Essentially any alkoxylated nonionic surfactants are suitable herein. The ethoxylated and propoxylated nonionic surfactants are preferred.
The nonionic surfactant is preferably present at a ratio to the surfactant system a0, comprising the rnid-branched surfactants of the invention, of from 10:1 to 1;10, more preferably from 5:1 to 1:10, even more preferably from 1:1 to 1:10.
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 diamine adducts.
Nonionic alkoxylated alcohol surfactant The condensation products of aliphatic alcohols with from 1 to 25 moles of 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 containing from 8 to 20 carbon atoms, more preferably form 9 to 15 carbon atoms, with from 3 to 12 moles of ethylene oxide per mole of alcohol.
Nonionic nolyhydroxv 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 C 1-C4 alkyl, more preferably C 1 or C2 alkyl, most preferably C 1 alkyl (i.e., methyl); and R2 is a CS-C31 hydrocarbyl, preferably straight-chain CS-C 19 alkyl or alkenyI, more preferably straight-chain Cg-C 17 alkyl or alkenyl, most preferably straight-chain C 11-C

alkyl or aIkenyl, 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 amination 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 containing from 7 to 21, preferably from 9 to 17 carbon atoms and each R7 is selected from the group consisting of hydrogen, C 1-C4 alkyl, C 1-C4 hydroxyalkyl, and -(C2H4O)xH, where x is in the range of from 1 to 3.
Nonionic alkvlpolysaccharide surfactant Suitable alkylpolysaccharides for use herein are disclosed in U.S. Patent 4,565,647, Llenado, issued January 21, 1986, having a hydrophobic group containing from 6 to 30 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from 1.3 to 10 saccharide units.
Preferred alkylpolyglycosides have the formula R20(CnH2n0)t(glycosyl)x wherein R2 is selected from the group consisting of alkyl, alkyiphenyl, 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 0 to 10, and x is from 1.3 to 8. The glycosyl is preferably derived from glucose.
Amphoteric surfactant Suitable amphoteric surfactants for use herein include the amine oxide surfactants and the alkyl amphocarboxylic acids.
Suitable amine oxides include those compounds having the formula R3(OR4)xN0(RS)2 wherein R3 is selected from an alkyl, hydroxyalkyl, acylamidopropoyl and alkyl phenyl group, or mixtures thereof, containing from 8 to 26 carbon atoms; R4 is an alkylene or hydroxyalkylene group containing from 2 to 3 carbon atoms, or mixtures thereof; x is from 0 to 5, preferably from 0 to 3;
and each RS is an alkyl or hydroxyalkyl group containing from 1 to 3, or a polyethylene oxide group containing from l to 3 ethylene oxide groups. Preferred are C 10-C 1 g alkyl dimethylamine oxide, and C10_18 acylamido alkyl dimethyiamine 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.
Suitable betaines are those compounds having the formula R(R')2N+R2C00-wherein R is a C6-Clg hydrocarbyl group, each R1 is typically C1-C3 alkyl, and is a C 1-C~ hydrocarbyl group. Preferred betaines are C 12_1 g dimethyl-ammonio hexanoate and the C 1 U-18 acylamidopropane (or ethane) dimethyl (or diethyl) betaines. Complex betaine surfactants are also suitable for use herein.

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this page is blaric yon filing.

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-C I 6, preferably C6-C I O N-alkyl or alkenyl ammonium surfactants wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
Alkalinity In the detergent compositions of the present invention preferably an alkalinity system is present to achieve optimal cationic ester surfactant performance.
The alkalinity system comprises components capable of providing alkalinity species in solution. By alkalinity. species it is meant herein: carbonate, bicarbonate, hydroxide, the various silicate anions, percarbonate, perborates, perphosphates, persulfate and persilicate.
Such alkalinity species can be formed for example, when alkaline 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, as described above, and any mixtures thereof, are dissolved in water.
Examples of carbonates are the alkaline 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 German Patent Application No.
2,321,001 published on November 15, 1973.
Suitable silicates include the water soluble sodium silicates with an Si02:
Na20 ratio of from 1.0 to 2.8, with ratios of from 1.6 to 2.O 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 Si02: Na20 ratio of 2.0 is the most preferred silicate.
Preferred crystalline layered silicates for use herein have the general formula 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-3 742043. 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 8-Na2Si205, available from Hoechst AG as NaSKS-6 TM
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.
Suitable carboxylates containing one carboxy group include the water soluble salts of lactic acid, glycolic acid and ether derivatives thereof. Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, malefic acid, diglycolic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates and the sulfinyl carboxylates. Polycarboxylates containing 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 aminosuccintates described in Canadian Patent No. 973,771, and the oxypolycarboxylate materials such as 2-oxa-1,1,3-propane tricarboxylates described in British Patent No. 1,387,447.

Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1,1,2,2-ethane tetracarboxylafes, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates. Polycarboxylates containing 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 containing 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 containing borate-forming 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 degree of polymerization ranges from about 6 to 21, and salts of phytic acid.
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 Naz[(A102)z(Si02)y].
xH20 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, containing from I 0% to 28%, more preferably from 18% to 22% water in bound form.
The aluminositicate zeolites can be naturally occurring materials, but are preferably synthetically derived. Synthetic crystalline aluminosiiicate 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 (A102) 12 (Si02)12J. xH20 wherein x is from 20 to 30, especially 27. Zeolite X has the formula Nag6 [(A102)86(Si02)106~. 276 H20.
Preformed orsanic peroxyacid The detergent compositions or the bleaching system may contain, in addition to the bleach precursors, 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.
A preferred class of organic peroxyacid compounds are the amide substituted compounds of the following general formulae:
R~ -C-N-R2-C-OOH

R~ -N-C-R2-C-OOH
or R5 O O
wherein R1 is an alkyl, aryl or alkaryl group with from 1 to 14 carbon atoms, R2 is an alkylene, arylene, and alkarylene group containing from 1 to 14 carbon atoms, and RS is H or an alkyl, aryl, or alkaryl group containing 1 to 10 carbon atoms.
Amide substituted organic peroxyacid compounds of this type are described in EP-A-0170386.

Other organic peroxyacids include diacyl and tetraacylperoxides, especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid. Mono- and diperazelaic acid, mono- and diperbrassylic acid and N-phthaloylaminoperoxicaproic acid are also suitable herein.
Other suitable organic peroxyacids include diperoxyalkanedioc acids having more than 7 carbon atoms, such as diperoxydodecanedioc acid (DPDA), diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid. Mono- and diperazelaic acid, mono- and diperbrassylic acid and N-phthaloylaminoperoxicaproic acid (PAP), nonanoylamido peroxo-adipic acid (NAPAA) decanoyl- or dodecanoylamidoperoxy acids and hexane sulphenoyl peroxypropionic acid and are also suitable herein.
Other suitable organic peroxyacids include diamino peroxyacids, which are disclosed in WO 95/ 03275, with the following general formula:
MO~R-(R~N)ri C (NR2)n' -R3-~R2N)~,~--C (NR~)m-RCOOM
wherein:
R is selected from the group consisting of C1-C12 alkylene, CS-C12 cycloalkytene, C6-C12 arylene and radical combinations thereof;
R1 and R2 are independently selected from the group consisting of H, C1-C16 alkyl and C6-C12 aryl radicals and a radical that can form a C3-C12 ring together with R3 and both nitrogens; R3 is selected from the group consisting of C1-C12' alkylene, CS-C 12 cycloalkylene and C6-C 12 arylene ~ radicals; n and n' each are an integer chosen such that the sum thereof is 1; m and m' each are an integer chosen such that the sum thereof is 1; and M is selected from the group consisting of H, alkali metal, alkaline earth metal, ammonium, alkanolammonium cations and radicals and combinations thereof.
Other suitable organic peroxyacids are include the amido peroxyacids which are disclosed in WO 95I 16673, with the following general structure:
X-Ar-CO-NY-R(Z)-CO-OOH

in which X represents hydrogen or a compatible substituent, Ar is an aryl group, R represents (CH2)n in which n = 2 or 3, and Y and Z each represent independently a substituent selected from hydrogen or an alkyl or aryl or alkaryl group or an aryl group substituted by a compatible substituent provided that at least one of Y and Z is not hydrogen if n = 3. The substituent X on the' benzene nucleus is preferably a hydrogen or a meta or para substituent, selected from the group comprising halogen, typically chlorine atom, or some other non-released non-interfering species such as an alkyl group, conveniently up tv C6 for example a methyl, ethyl or propyl group. Alternatively, X can represent a second amido-percarboxylic acid substituent of formula:--CO-NY-R(Z)-CO-OOH
in which R, Y, Z and n are as defined above.

wherein Rlis selected from the group consisting of C1-C12 alkylene, CS-CI2 cycloalkylene, C6-C12 arylene and radical combinations thereof; R
It may be found to be particularly useful to mix the pre-formed peracid and cationic surfactant together prior to incorporation with any other components of the detergent composition.
Cationic peroxyacid~recursors Cationic peroxyacid precursors can be suitable additional components of the detergent compositions or bleaching systems herein. They 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 ammmonium group, preferably an ethyl or methyl ammonium group. Cationic peroxyacid precursors are typically present in the solid detergent compositions as a sait with a suitable anion, such as a halide ion.

The peroxyacid precursor compound to be so cationically substituted may be 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; 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 WO 95/29160 and US Patent Nos. 5,686,015; 5,460,747; 5,578,136 and 5,584,888.
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 caprolactam class include the trialkyl ammonium methylene benzoyl caprolactams and the trialkyl ammonium methylene alkyl caprolactams.
Bleach catalyst The compositions optionally contain a transition metal containing 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 manganese cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminum cations, and a sequestrant having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra(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 manganese-based complexes disclosed in U.S. Pat. 5,246,621 and U.S. Pat. 5,244,594. Preferred examples of these catalysts include MnIV2(u-O)3(1,4,7-trimethyl-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-O)6(1,4,7-triazacyclononane)4-(C104)2, MnIIIMnIV4(u-O)1(u-OAc)2_(1,4,7-trimethyl-1,4,7-triazacyclononane)2-(C104)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-triazacyclododecane, 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 teaches mononuclear manganese (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 manganese (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-O)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 manganese on aluminosilicate catalyst), U.S. 4,601,845 (aluminosilicate support with manganese and zinc or magnesium salt), U.S. 4,626,373 (manganese/ligand catalyst), U.S. 4,119,557 (ferric complex catalyst), German Pat. specification 2,054,019 (cobalt chelant catalyst) Canadian 866,191 (transition metal-containing salts), U.S. 4,430,243 {chelants with manganese cations and non-catalytic metal cations), and U.S. 4,728,455 (manganese gluconate catalysts).
Heaw 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 magnesium chelation capacity, but preferentially they show selectivity to binding heavy metal ions such as iron, manganese and copper.

Heavy metal ion sequestrants 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 1-hydroxy disphosphonates and nitrilo trimethylene phosphonates.
Preferred among the above species are diethylene triamine penta (methylene phosphonate), ethylene diamine tri (methylene phosphonate) hexamethylene diamine 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 ethylenediaminotetracetic acid, ethylenetriamine pentacetic acid, ethylenediamine disuccinic acid, ethylenediamine diglutaric acid, 2-hydroxypropylenediamine disuccinic acid or any salts thereof.
Especially preferred is ethylenediamine-N,N'-disuccinic acid (EDDS) or the alkali metal, alkaline 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 ~i-alanine-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.
EP-A-476,257 describes suitable amino based sequestrants. EP-A-510,331 describes suitable sequestrants 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), ethylenediamine-N-N'-diglutaric acid (EDDG) and 2-hydroxypropylenediamine-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 alkaline 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 trademarks Alcalase, Savinase, Primase, Durazym, and Esperase by Novo Industries A/S (Denmark), those sold under the trademarks Maxatase, Maxacal and Maxapem by Gist-Brocades, those sold by Genencor International, and those sold under the trademarks 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 trademark Rapidase by Gist-Brocades, and those sold under the trademarks 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.
Lipolytic enzyme may be present at levels of active lipolytic enzyme of from 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 obtained, 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 pseudoalcaligenes, which is described in Granted European Patent, EP-B-0218272.

Another preferred lipase herein is obtained by cloning the gene from Humicola lams ig'nosa 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 mark Lipolase. This lipase is also described in U.S. Patent 4,810,414, Huge-Jensen et al, issued March 7, 1989.
Organic polymeric compound Organic polymeric compounds are preferred 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 organic polymeric compound it is meant herein essentially any polymeric organic compound commonly used as dispersants, and anti-redeposition and soil suspension agents in detergent compositions, including any of the high molecular weight organic polymeric compounds described as clay flocculating agents herein.
Organic polymeric compound is typically incorporated in the detergent compositions of the invention at a level of from 0.1% to 30%, preferably from 0.5% to 15%, most preferably from 1 % to I 0% by weight of the compositions.
Examples of organic polymeric compounds include the water soluble organic homo-or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Polymers of the latter type are disclosed in GB-A-1,596,756.
Examples of such salts are polyacrylates of MWt 2000-5000 and their copolymers with malefic anhydride, such copolymers having a molecular weight of from 20,000 to 100,000, especially 40,000 to 80,000.
The polyamino compounds are useful herein including those derived from aspartic acid such as those disclosed in EP-A-305282, EP-A-305283 and EP-A-351629.
Terpolymers containing monomer units selected from malefic acid, acrylic acid, polyaspartic acid and vinyl alcohol, particularly those having an average molecular weight of from 5,000 to 10,000, are also suitable herein.

Other organic polymeric compounds suitable for incorporation in the detergent compositions herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose, hydroxypropylmethylcellulose and hydroxyethylcellulose.
Further useful organic polymeric compounds are the polyethylene glycols, particularly those of molecular weight 1000-10000, more particularly 2000 to and most preferably about 4000.
Suds suppressinyystem The detergent compositions of the invention, when formulated for use in machine washing compositions, preferably comprise a suds suppressing system present at a level of from 0.01% to 15%, preferably from 0.05% to 10%, 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 "silicone" as used herein, and in general throughout the industry, encompasses a variety of relatively high molecular weight polymers containing siloxane units and hydrocarbyl group 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 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 rnonovalent alcohols, aliphatic C 1 g-C4p ketones (e.g. stearone) N-alkylated amino triazines such as tri- to hexa-alkyimelamines or di- to tetra alkyldiamine chlortriazines formed as products of cyanuric chloride with two or three moles of a primary or secondary amine containing 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 SO% 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;
wherein said silica/silicone antifoam compound is incorporated at a level of from S%
to 50%, 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 DC0544, commercially available from DOW Corning under the trademark DC0544;
(c) an inert carrier fluid compound, most preferably comprising a C16-C18 ethoxylated alcohol with a degree of ethoxylation of from 5 to 50, preferably 8 to 15, at a level of from S% 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 containing 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 containing from I2 to 20 carbon atoms, or a mixture thereof, with a melting point of from 45°C to 80°C.
Clay softenin, s~ystem The detergent compositions may contain a clay softening system comprising a clay mineral compound and optionally a clay flocculating 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 flocculating agents.
Polymeric dye transfer inhibiting;.
The detergent compositions herein may also comprise from O.OI% to IO %, 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 polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof.
a) Polyamine N-oxide polymers Polyamine N-oxide polymers suitable for use herein contain units having the following structure formula P
(I) R
wherein P is a polymerisable unit, and II
A is NC, CO, C, -O-, -S-, -N-; x is O or 1;
R are aliphatic, ethoxylated aliphatics, aromatic, heterocyclic or alicyclic groups or any combination thereof whereto the nitrogen of the N-O group can be attached or wherein the nitrogen of the N-O group is part of these groups.
The N-O group can be represented by the following general structures O

(R1) x-N-(R2)Y t (R3)z or N_(R1 )x wherein R1, R2, and R3 are aliphatic groups, aromatic, heterocyclic or alicyclic groups or combinations thereof, x or/and y or/and z is 0 or 1 and wherein the nitrogen of the N-O group can be attached or wherein the nitrogen of the N-O
group forms part of these groups. The N-O group can be part of the polymerisable unit (P) or can be attached to the polymeric backbone or a combination of both.
Suitable polyamine N-oxides wherein the N-O group forms part of the polymerisable unit comprise polyamine N-oxides wherein R is selected from aliphatic, aromatic, alicyclic or heterocyclic groups. One class of said polyamine N-oxides comprises the group of polyamine N-oxides wherein the nitrogen of the N-O
group forms part of the R-group. Preferred polyamine N-oxides are those wherein R

is a heterocyclic group such as pyridine, pyrrole, imidazole, pyrrolidine, piperidine, quinoline, acridine and derivatives thereof.
Other suitable polyamine N-oxides are the polyamine oxides whereto the N-O
group is attached to the polymerisable unit. A preferred class of these polyamine N-oxides comprises the polyamine N-oxides having the general formula (I) wherein R is an aromatic,heterocyclic or alicyclic groups wherein the nitrogen of the N-O
functional group is part of said R group. Examples of these classes are polyamine oxides wherein R is a heterocyclic compound such as pyrridine, pyrrole, imidazole and derivatives thereof.
The polyamine N-oxides can be obtained in almost any degree of polymerisation.
The degree of polymerisation is not critical provided the material has the desired water-solubility and dye-suspending power. Typically, the aveFage molecular weight is within the range of 500 to 1000,000.
b) Copolymers of N-vinylpyrrolidone and N-vinylimidazole Suitable herein are coploymers 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.
c Polyvinylnyrrolidone 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), FVP 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 ISP Corporation. Other suitable polyvinylpyrroTM ones which are commercially available from BASF Cooperation include Sokalan HP 165 and Sokalan HP 12.
d) Polyvinyloxazolidone sa 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.
e) 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 htg ener 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:
Rl R2 N H H N
N N C C N N
~N H H N
R2/ S03M S03M Rt wherein Rl 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, R1 is anilino, R2 is N-2-bis-hydroxyethyl and M is a canon 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 marketed under the trademark Tinopal-LJNPA-GX by Ciba-Geigy Corporation. Tinopal-LJNPA-GX is the preferred hydrophilic optical brightener useful in the detergent compositions herein.

When in the above formula, RI 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-anilino-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 trademark Tinopal 5BM-GX by Ciba-Geigy Corporation.
When in the above formula, R1 is anilino, R2 is morphilino and M is a canon 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 trademark 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 ingredients Other optional ingredients suitable for inclusion in the compositions of the invention include colours and filler salts, with sodium sulfate being a preferred filler salt.
QH 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 9.5 to 11Ø
Form of the compositions The compositions in accordance with the invention can take a variety of physical preferably solid forms including granular, tablet, bar forms.
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 mid-chain branched surfactant system herein, preferably with additional surfactants, is preferably present in granular compositions in the form of surfactant agglomerate particles, preferably not comprising the bleach precursors, 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 l, Elsenerstrasse 7-9, Postfach 2050, Germany. Most preferably a high shear mixer is used, such as a Lodige CB (Trade Mark).
A high active surfactant paste comprising from 50% by weight to 95% by weight, preferably 70% by weight to 85% by weight of the surfactants, including the mid-chain branched surfactants, is typically used. The paste may be pumped into the agglomerator at a temperature high enough to maintain a pumpable viscosity, but low enough to avoid degradation of the anionic surfactants used. An operating temperature of the paste of 50°C to 80°C is typical.
The bleach precursors of the invention are preferably dry-added to the detergent base or the agglomerates.
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 0.1 Smm 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 against 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 300 g/litre, more preferably from 330 gllitre to 1200 g/litre, more preferably from 380g/litre to 850 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 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.
The compositions in accord with the present invention can also be used in or in combination with bleach additive compositions, for example comprising chlorine bleach, as mentioned above.
However, since preferred detergent compositions of the invention are solid, most liquid chlorine-based bleaching will not be suitable for these detergent compositions and only granular or powder chlorine-based bleaches will be suitable.
Alternatively, the detergent compositions can be formulated such that they are chlorine-based bleach-compatible, thus ensuring that a chlorine based bleach can be added to the detergent composition by the user at the beginning or during the washing process.

The chlorine-based bleach is such that a hypochlorite species is formed in aqueous solution. 'The hypochlorite ion is chemically represented by the formula OCh.
Those bleaching agents which yield a hypochlorite species in aqueous solution include alkali metal and alkaline earth metal hypochlorites, hyposchlorite addition products, chloramines, chlorimines, chloramides, and chlorimides. Specific examples of compounds of this type include sodium hypochlorite, potassium hypochlorite, monobasic calcium hypochlorite, dibasic magnesium hypochlorite, chlorinated trisodium phosphate dodecahydrate, potassium dichloroisocyanurate, sodium dichloroisocyanurate sodium dichloroisocyanurate dihydrate, trichlorocyanuric acid, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, Chloramine T, Dichloramine T, chloramine B and Dichloramine B. A preferred bleaching agent for use in the compositions of the instant invention is sodium hypochlorite, potassium hypochlorite, or a mixture thereof.. A preferred chlorine-based bleach can be Triclosan (Trade Mark).
Most of the above-described hypochlorite-yielding bleaching agents are available in solid or concentrated form and are dissolved in water during preparation of the compositions of the instant invention. Some of the above materials are available as aqueous solutions.
Laundry 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. The 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 containing 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 containment 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 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 maintained 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 Publication No. WO 94/11562.
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 i support ring is provided with a masking 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 aqueous media as disclosed in European published Patent Application Nos. 0011500, 0011501, 0011502, and 0011968. A convenient form of 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.
Packa~imP 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 laminates.
Abbreviations used in Examples In the detergent compositions,, the abbreviated component identifications have the following meanings:
LAS : Sodium linear C12 alkyl benzene sulfonate TAS : Sodium tallow alkyl sulfate C45AS . Sodium C14-C15 linear alkyl sulfate MES ~ : -sulpho methylester of C1g fatty acid CxyEzS : Sodium C 1 x-C 1 y branched alkyl sulfate condensed with z moles of ethylene oxide MBASx, y . Sodium mid-chain branched alkyl sulfate having an average of x carbon atoms, whereof an average of y carbon atoms are comprised in (a) branching) units) C.~g SAS : Sodium C,.~-C,g secondary alcohol sulfate SADE2S : Sodium C,4-Czz alkyl disulfate of formula 2-(R).C4 H~-1,4-(S04-)z where R = C,oOC,g, condensed with z moles of ethylene oxide C45E7 : A C14-15 Predominantly linear primary alcohol condensed with an average of 7 moles of ethylene oxide CxyEz : A C 1 x-1 y branched primary alcohol condensed with an average of z moles of ethylene oxide QAS II . R2.N'~'(CH3)2(C2H40H) with R2 = 50%-60% Cg;
40%-SO% C 11 QAS IV : RI.N+(CH3)(C2H40H)2 with RI = C12-C14 QAS V . R20(C2H40)x(giycosyl)2, wherein R2 is a Cg-C10 alkyl group ; t is from 2 to 8 Soap . Sodium linear alkyl carboxylate derived from an 80/20 mixture of tallow and coconut oils.
TFAA : C 16-C 1 g alkyl N-methyl glucamide TPKFA : C12-C14 topped whole cut fatty acids STPP : Anhydrous sodium tripolyphosphate Zeolite A : Hydrated Sodium Aluminosilicate of formula Nal2(A102Si02)12~ 27H20 having a primary particle size in the range from 0.1 to 10 micrometers NaSKS-6 : Crystalline layered silicate of formula 8 -Na2Si205 Citric acid : Anhydrous citric acid Carbonate : Anhydrous sodium carbonate with a particle size between 200~m and 900pm Bicarbonate : Anhydrous sodium bicarbonate with a particle size distribution between 400pm and 1200p,m Silicate : Amorphous Sodium Silicate (Si02:Na20;
2.0 ratio) Sodium sulfate : Anhydrous sodium sulfate Citrate : Tri-sodium citrate dihydrate of activity 86.4% with a particle size distribution between 425pm and q 850~m 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 ~'ademark Savinase i 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 trademark Carezyme Amylase . Amylolytic enzyme of activity 60KNU/g sold by NOVO Industries A/S under the trademark Termamyl Lipase : Lipolytic enzyme of activity I OOkLU/g sold by NOVO

Industries A/S under the trademark Lipolase Endolase : Endoglunase enzyme of activity 3000 CEVU/g sold by NOVO Industries A/S

PB4 . Sodium perborate tetrahydrate of nominal formula NaB02.3H20.H202 PB 1 . Anhydrous sodium perborate bleach of nominal formula NaB02.H202 Percarbonate . Sodium Percarbonate of nominal formula 2Na2C03.3H202 NAC-OBS . (Nonanamido caproyl) oxybenzene sulfonate in the form of the sodium salt.

NOBS . Nonanoyl oxybenzene sulfonate in the form of the sodium salt LOBS . Dodecanoyl oxybenzene sulfonate iri the form of the sodium salt DOBS . Decanoyl oxybenzene sulfonate in the form of the sodium salt DPDA . Diperoxydodecanedioic acid PAP . N-phthaloylamidoperoxicaproic acid NAPAA . Nonanoylamido peroxo-adipic acid NACA . 6 nonylamino - 6 oxo - capronic acid.

TAED . Tetraacetylethylenediamine DTPMP . Diethylene triamine penta (methylene phosphonate), marketed by Monsanto under the Trade mark bequest Phvtoactivated : Sulfonated Zinc or aluminium Phthlocyanine encapsulated .

Brightener 1 : Disodium 4,4'-bis(2-sulphostyryl)biphenyl Brightener 2 : Disodium 4,4'-bis(4-anilino-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 QEA : bis ({C2H50)(C2H4~)n) (CH3) -N+-C6H12-N+_ (CH3) bis ((C2HS0)-(C2H40)n), wherein n=from 20 to 30 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.

In the following Examples all levels are quoted as parts per weight of the composition or % by weight of the composition, as indicated:

Example 1 The following high density granular laundry detergent compositions A to F of particular utility under European machine wash conditions were prepared in accord with the invention:
A B C D E F

LAS 8.0 8.0 - 2.0 8.0 6.0 MES - - 5.0 - - 6.0 TAS - 0.5 - 0.5 1.00 1.5 C25E3 3.4 - - 3.4 5.4 2.4 C25E7 - 3.0 4.5 - - -C46AS 2.0 2.0 2.5 - - -C24AS - - - 7.0 4.0 5.0 SADS - - - - 1.0 -MBAS 165, 1.8 6.0 - 8.0 10 - 5.0 .

MBAS 16.5, 2.8 - 7.0 - - 8.0 5.0 QASII - - - -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 Citric acid 2.0 1.0 - - - -Silicate 1.4 1.4 1.4 3.0 3.0 3.0 Sulfate 26.1 26.1 26.1 26.1 26.1 26.1 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 PB4 9.0 9.0 ' 9.0 - - -Percarbonate - - - 18.0 15.0 20.0 TAED 0.5 1.0 4.0 1.5 1.0 1.0 NAC-OBS 4.0 2.5 0.5 1.0 2.0 5.0 DTPMP 0.25 0.25 0.25 0.25 0.25 0.25 EDDS - - 0.25 0.4 - -HEDP 0.3 0.3 0.3 0.3 0.3 0.3 QEA 0.5 1.0 - - 0.5 -Protease 0.26 0.26 0.26 0.26 0.26 0.26 Amylase 0.1 0.1 0.1 0.1 0.1 0.1 Photoactivated 15 ppm 1 S 15 ppm 15 ppm 15 ppm 15 ppm bleach (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 antifoam0.5 0.5 0.5 0.5 0.5 0.5 Density in g/litre850 850 850 850 850 850 Example 2 The following granular laundry detergent compositions G to I of bulk density g/litre are compositions according to the invention:
G H I

LAS 12.0 10.0 7.0 TAS 1.25 2.86 1.57 C45AS 3.5 3.24 2.0 C25AE3S - 0.76 1.0 C45E7 3.25 - -C25E3 - 3.5 . 3.5 QAS I 0.8 2.0 -MBAS 17, 1.7 7.0 - 5.0 MBAS 17, 2.5 - 2.0 -STPP 19.7 - -Zeolite A - 19.5 19.5 NaSKS-6/silicate (79:21 10.6 10.6 ) Citric acid/citrate 2.0 4.0 1.0 Carbonate 6.1 21.4 21.4 Bicarbonate - 2.0 2.0 Silicate 6.8 - -Sodium sulfate 39.8 - 7.0 PB4 5.0 12.7 -Percarbonate - - 16.0 TAED 0.5 0.7 2.0 NAC OBS 1.0 2.2 2.0 DTPMP 0.25 0.2 0.2 HEDP - 0.3 0.3 Protease 0.26 0.8 5 0.85 Lipase 0.15 0.15 0.15 Cellulase 0.28 0.28 0.28 Amylase 0.1 0.1 0.1 MA/AA 0.8 1.6 1.6 CMC 0.2 0.4 0.4 PVP - 0.8 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 Minorslmisc to 100% n.a. n.a.

Example 3 The following are detergent formulations, according to the present invention where J
is a phosphorus-containing detergent composition, K is a zeolite-containing detergent composition and L is a compact detergent composition:
J K L M

Blown Powder - _ , STPP 24.0 - 24.0 -Zeolite A - 24.0 - 24.0 C45AS 9.0 - 4.0 13.0 ___-QAS I - 1.0 - _ MBAS 17, 1.7 4.0 - 10.0 6.0 MBAS 17, 3.5 2.0 11.0 - -SADS 2.0 - - -C25AE3S - 1.0 - 1.0 _ _~~~ 2.0 4.0 2.0 4.0 LAS 6.0 12.0 13.0 5 TAS - 1.0 2.0 -Silicate 7.0 3.0 3.0 3.0 CMC 1.0 I.0 0.5 1.0 Brightener 2 0.2 0.2 0.2 0.2 Soap 1.0 - - 1.0 DTPMP 0.4 0.4 0.2 0.4 Spray On C45E7 - 2.5 - -C25E3 2.5 - - 1.5 Silicone antifoam 0.3 0.3 0.3 0.3 Perfume 0.3 0.3 0.3 0.3 Dry additives QEA - 0.5 1.0 -Carbonate 6.0 13.0 15.0 13.0 PB4 18.0 1$.0 5.0 -PB1 4.0 - - 14.0 NOBS 3.0 4.2 - 6.0 TAED I.0 1.0 5.0 1.0 LOBS - - 2.0 -Photoactivated bleach 0.02 0.02 0.02 0.02 Manganese catalyst - - 0.5 -Protease '1.0 1.0 1.0 1.0 Lipase 0.4 0.4 0.4 0.4 Amylase 0.25 0.30 0.15 0.3 Dry mixed sodium sulfate3.0 3.0 5.0 3.0 Balance (Moisture & 100.0 100.0 100.0 100.0 Miscellaneous) Density (g/litre) 630 670 6?0 670 Examgle 4 The following are detergent formulations according to the present invention:
N O P Q

LAS 20.0 14.0 13.0 20.0 .
_ TAS - 1.0 4.0 _ MBAS 16.5, 2.0 10.0 2.0 8.0 1.9 C45AS 4.0 4.0 6.0 6.0 MES 3.0 - -QAS II - 0.4 1.0 -TFAA - 1.0 - -C25ESIC45E7/C2- 2.0 - 1.0 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 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 - -Photoactivated70ppm 45ppm - lOppm bleach (ppm) Brightener 0.2 0.2 0.08 0.2 PB 1 6.0 ~~ 2.0 -Percarbonate - - 12.0 15.0 NACA - - - 3.0 NAC OBS 2.0 - - 3.1 TAED 2.0 4.0 2.0 1.0 DOBS - - 2.0 -LOBS - 3.0 - -Balance (Moisture100 100 100 100 and Miscellaneous) Example 5 The following are detergent formulations according to the present invention:
R S T

Blown Powder MBAS 16.5,1.7 6.0 10.0 -MBAS 17.5, 3.0 - - 12.0 Zeolite A 30.0 22.0 6.0 Sodium sulfate 19.0 5.0 7.0 MA/AA 3.0 3.0 6.0 LAS 3.0 9.0 3.5 C45AS 5.0 4.0 7.0 Silicate - 1.0 5.0 Soap - - 2.0 Brightener 1 0.2 0.2 0.2 Carbonate 8.0 16.0 20.0 Spray On C45E5 1.0 1.0 -Dry additives PVPVI/PVNO 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 TAED 6.4 2.0 2.0 NOBS - 6.1 -NAC OBS - - 4.5 Percarbonate - - 16.0 PB1 - 10.0 -PB4 8.0 - -Sodium sulfate - 6.0 Balance (Moisture 100 100 100 and Miscellaneous) Example 6 The following are high density and bleach-containing detergent formulations according to the present invention:
U V W _.__ Blown Powder _ Zeolite A 1 S.0 1 S.0 1 S.0 Sodium sulfate 0.0 S.0 0.0 LAS 3.0 - 3.0 C4SAS 3.0 2.0 4.0 QAS - - 1.5 DTPMP 0.4 0.4 0.4 CMC 0.4 0.4 0.4 MA/AA 4.0 2.0 2.0 Agglomerates LAS 6.0 4.0 1.0 MBAS 16.5, 1.6 2.0 S.0 10.0 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 Encapsulated Perfume 0.3 0.3 0.3 C2SE3 2.0 -Dry additives QEA - - O.S

Citrate S.0 - 2.0 Bicarbonate - 3.0 Carbonate 8.0 1 S.0 10.0 TAED 1.0 O.S 3.0 NACAOBS 6.0 - S.0 LOBS/ DOBS - I .0 -Manganese catalyst - - 0.3 NOBS - 2.0 PBI 14.0 7.0 10.0 Polyethylene oxide of MW - - 0.2 5,000,000 Bentonite clay - - 10.0 Citric acid - - 0.5 ~

Protease 1.0 1.0 1.0 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 7 The following are high density detergent formulations according to the present invention:
X Y

Agglomerate MES ~ - 8.0 LAS 12.0 TAS - 2.0 C45AS 6.0 4.0 MBAS 17.5, 1.6 4.0 3.0 MBAS 17.5, 2.8 4.0 -Zeolite A 15.0 6.0 Carbonate 4.0 8.0 M~~ 4 0 2.0 CMC 0.5 0.5 DTPMP 0.4 0.4 Spray On C25E3 1.0 1.0 Perfume 0.5 0.5 Dry Adds HEDP 0.5 0.3 SKS 6 13.0 10.0 Citrate - 1.0 Citric acid 2.0 -NAC OBS 4.1 -LOBS - 3.0 TAED 0.8 2.0 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 QEA 1.0 -Silicone antifoam S.0 5.0 Brightener 1 0.2 0.2 Brightener 2 0.2 -Density (g/litre) 850 850 Examgle 8 The following granular detergent formulations are examples of the present invention.
AH AI AJ

Blown powder MES - 6.0 -LAS 12.0 - 13.0 C45AS - 4.0 -C46AS 4.0 - -C45AE35 2.0 5.0 3.0 MBAS 17, 2.2 5.0 - 2-Zeolite A 16.0 19.0 16.0 MA/AA 3.0 - -AA 3.0 2.0 3.0 Sodium sulfate 3.3 24.0 13.3 Silicate 1.0 2.0 1.0 Carbonate 9.0 25.7 8.0 QEA 0.4 - 0.5 PEG 4000 - 1.0 1.5 Brightener 0.3 0.3 0.3 Spray on C25E5 0.5 1.0 -Perfume 0.3 1.0 0.3 Agglomerates C45AS 5.0 2.0 5.0 LAS 1.0 1.0 2.0 MBAS 17, 1.6 - 4.0 5.0 Zeolite A 7.5 - 7.5 HEDP 1.0 - 2.0 WO 99!19429 PCTIUS97/18842 Carbonate 4.0 - 4.0 PEG 4000 O.S - O.S

Misc (water etc) 2.0 - 2.0 Dry additives LOBS/DOBS/NOBS 4.0 4.0 -TAED ' - - 2.0 NACA-OBS - - 3.0 PB4 14.0 - 2.0 PB 1 - 7.0 -Carbonate S.3 - 2.S

Cumeme sulfonic acid 2.0 - 2.0 Lipase 0.4 0.1 O.OS

Cellulase 0.2 - 0.2 Amylase 0.3 - -Protease 1.6 - 1.6 PVPVI O.S - -PVNO O.S - -SRP1 O.S - -Silicone antifoam 0.2 - 0.2 Example 9 AK AL AM AN AO AP

C4SAS 11.0 S.1 4.0 8.S 4.1 9.8 C2SAES 1.3 1.0 - 1.3 1.0 -LAS 9.4 6.6 20.5 3.7 1.7 4.0 C2SE3/ C2SES 1.S 4.7 3.3 I.S 4.7 3.30 MBAS I6.S, 1.7 10.0 5.0 3.0 i2.2 S.9 14.1 QAS - I .1 0.4 - 1.7 S

Zeolite A 27.0 16.7 11.2 27.0 16.7 11.2 SKS-6 - 9.0 7.S - 9.0 7.S

Citric acid - 1.S - - I.S -MA/AA - 0.6 - - 0.6 -MAIAA 3 - - 7.0 - - 7.0 AA 2.2 - - 2.2 - -EDDS - 0.3 - - 0.3 -HEDP - O.S - - O.S -Carbonate 26.0 12.5 14.9 26.5 I2.S 14.9 Silicate O.S 0.8 I2 O.S 0.8 12 PB1 11.0 - 3.9 7.0 - 3.9 NOBS 3.0 2.7 4.0 - - 4.0 NACA-OBS - 2.7 - 4.0 2.75 -PC - 17.3 - - 17.3 -TAED 5.0 3.5 2.0 1.0 3.5 4.0 Protease 0.26 0.3 0.2 0.2 0.3 0.2 Lipase - - - - - -Carezyme IT 0.33 0.26 - 0.33 0.26 -Termamy1120T - 0.36 - - 0.36 -Brightener 0.17 0.06 0.30 0.17 0.06 0.30 SRP1 0.4 0.2 0.5 0.4 0.2 0.5 PEG 1.6 - 0.19 1.6 - 0.19 Sulfate 5.3 6.4 3.4 5.3 6.4 3.4 CMC - 0.5 - - 0.5 -MgS04 - 0.13 - - 0.13 -Photobleach - 0.0026 - - 0.0026-Silicone anti-foam - 0.21 0.17 0.02 0.21 0.17 Perfume 0.42 0.55 0.25 0.42 0.55 0.25 Example 10 The following laundry detergent compositions AQ to AT are prepared in accord with the invention:
AQ AR AS AT

MBAS 16.5, 1.8 22 16.5 11 5.5 C23E6.5 1.5 1.5 1.5 1.5 Zeolite A 17.8 20.8 20.8 27.8 AA 2.3 2.3 2.3 2.3 Carbonate 27.3 27.3 27.3 27.3 Silicate 0.6 0.6 0.6 0.6 Perborate 1.0 1.0 1.0 1.0 Protease 0.3 0.3 0.3 0.3 Cellulase 0.3 0.3 0.3 0.3 SRP1 0.4 0.4 0.4 0.4 WO 99/19429 PCTlUS97118842 Brightener 0.2 0.2 0.2 0.2 PEG 1.6 I .6 1.6 1.6 PB1 16.0 6.0 NOBS 2.4 4.5 0.8 3.5 PC 8.0 15.0 Sulfate 5.5 5.5 5.5 5.5 Silicone Antifoam0.42 0.42 0.42 0.42 TAED 0.5 4.5 8.0 2.0 Moisture & Minors---Balance---Density (g/L) 660 660 660 660 Example 11 The following laundry detergent compositions AU to AY are prepared in accord with the invention:
AU AV AW AX AY

MBAS 16.5, 1.7 14.8 16.4 12.3 8.2 4.1 TFAA 1.6 0 0 0 0 C24E3 4.9 4.9 4.9 4.9 4.9 Zeolite A I5 15 15 15 15 QAS 1.0 1.5 - - 1.0 NaSKS-6 11 11 11 11 11 Citratelcitric 1.0 2.0 3 3 -MAIAA 4.8 4.8 4.8 4.8 4.8 HEDP 0.5 0.5 0.5 0.5 0.5 Carbonate 8.5 8.5 8.5 8.5 8.5 Protease 0.9 0.9 0.9 0.9 0.9 Lipase 0.15 0.15 0.15 0.15 0.15 Cellulase 0.26 0.26 0.26 0.26 0.26 Amylase 0.36 0.36 0.36 0.36 0.36 NOBS - - - 4.0 5.0 NACA-OBS 4.0 2.0 6.0 - -TAED 4.0 5.0 2.0 1.0 0.5 PB1 - - 14.0 - 8.0 Percarbonate 20.0 14.0 - 22.0 -SRPI 0.2 0.2 0.2 0.2 0.2 QEA1 1.0 1.5 - -Brightener _ 0.2 0.2 0.2 0.2 0.2 ~

Sulfate 2.3 2.3 2.3 2.3 2.3 ~

Silicone Antifoam0.4 0.4 0.4 0.4 0.4 Moisture & Minors ---Balance---Density (g/L) 850 850 850 850 Example 12 The following laundry detergent compositions AZ to Ee are prepared in accord with the invention:
AZ Aa Bb Cc Dd Ee MBAS 16.5, 1.7 32 32 24 16 16 8 C23E6.5 3.6 3.6 3.6 3.6 3.6 3.6 QAS - 0.5 - - 0.5 -Zeolite A 9.0 9.0 9.0 9.0 9.0 9.0 Polycarboxylate 7.0 7.0 7.0 7.0 7.0 7.0 Carbonate 18.4 18.4 18.4 18.4 18.4 18.4 Silicate 11.3 11.3 11.3 11.3 11.3 11.3 PB 1 - - 3.9 10.0 3.9 15.0 TAED 2.0 5.0 1.0 0.5 6.0 2.0 Percarbonate 7.0 7.0 - - - -N()B S 4.1 4.1 4.1 4.1 4.1 4.1 Protease 0.9 0.9 0.9 0.9 0.9 0.9 SRP1 0.5 0.5 0.5 0.5 0.5 0.5 Brightener 0.3 0.3 0.3 0.3 0.3 0.3 PEG 0.2 0.2 0.2 0.2 0.2 0.2 Sulfate 5.1 5.1 5.1 5.1 5.1 5.1 Silicone Antifoam0.2 0.2 0.2 0.2 0.2 0.2 Moisture & Minors---Balance---Density (g/L) 810 810 810 810 810 810

Claims (16)

Claims:

1. A detergent composition comprising a) at least 0.5% by weight of the composition a surfactant system, wherein the surfactant system a) comprises at least about 20% by weight of the system of one or more mid-chain branched alkyl sulfates having the formula:
or mixtures thereof; wherein M represents one or more cations; a, b, d, and e are integers, a+b is from 10 to 16, d+e is from 8 to 14 and wherein further when a + b = 10, a is an integer from 2 to 9 and b is an integer from 1 to 8;
when a + b = 11, a is an integer from 2 to 10 and b is an integer from 1 to 9;
when a + b = 12, a is an integer from 2 to 11 and b is an integer from 1 to 10;
when a + b = 13, a is an integer from 2 to 12 and b is an integer from 1 to 11;
when a + b = 14, a is an integer from 2 to 13 and b is an integer from 1 to 12;
when a + b = 15, a is an integer from 2 to 14 and b is an integer from 1 to 13;
when a + b = 16, a is an integer from 2 to 15 and b is an integer from 1 to 14;
when d + e = 8, d is an integer from 2 to 7 and e is an integer from 1 to 6;
when d + e = 9, d is an integer from 2 to 8 and e is an integer from 1 to 7;
when d + e = 10, d is an integer from 2 to 9 and e is an integer from 1 to 8;
when d + e = 11, d is an integer from 2 to 10 and e is an integer from 1 to 9;
when d + e = 12, d is an integer from 2 to 11 and e is an integer from 1 to 10;
when d + e = 13, d is an integer from 2 to 12 and e is an integer from 1 to 11;
when d + e = 14, d is an integer from 2 to 13 and e is an integer from 1 to 12;
whereby, when more than one of these sulfate surfactants is present in the surfactant system, the average total number of carbon atoms in the branched primary alkyl moieties is from 14.5 to 17.5 ; and b) at least 0.5% by weight of the composition a bleaching system comprising (I) a hydrophobic bleach precursor; and (II) a hydrophilic bleach precursor.

2. A detergent composition according to claim 1 wherein the hydrophobic bleach precursor is of the formula:

wherein R1 is an aryl or alkaryl group with from about 1 to about 14 carbon atoms, R2 is an alkylene, arylene, and alkarylene group containing from about 1 to 14 carbon atoms, and R5 is H or an alkyl, aryl, or alkaryl group containing 1 to 10 carbon atoms and L can be essentially any leaving group.

3. A detergent composition according to claim 1 or 2 wherein the hydrophobic bleach precursor is selected from the group comprising (6-octanamido-caproyl)oxybenzene sulfonate, (6-decanamido-caproyl)oxybenzene sulfonate, (6,nonanamidocaproyl)oxybenzene sulfonate, decanoyloxy - benzene sulphonate sodium salt, benzoyloxy - benzenesulphonate sodium salt, sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate and sodium nonanoyl, decanoyl or dodecanoyloxybenzene sulfonate.

4. A detergent composition according to claim 1, or 3 wherein the hydrophilic bleach precursor is TAED.

5. A detergent composition according to any one of claims 1 to 4 wherein the bleaching system comprises an inorganic perhydrate salt.

6. A detergent composition according to any one of claims 1 to 5 wherein a nonionic surfactant is present at a ratio to the surfactant system a) of from 10:1 to 1:10.

7. A detergent composition according to claim 1 wherein the surfactant system is present in an amount of at least 5% by weight of the composition.

8. A detergent composition according to claim 1 wherein the surfactant system is present in an amount of at least 10% by weight of the composition.

9. A detergent composition according to claim 1 wherein the mid-chain branched alkyl moiety has from 12 to about 18 carbons in the moiety.

10. A detergent composition according to claim 1 wherein the average total number of carbon atoms in the mid-chain branched alkyl moiety is within the range of from about 15 to about 17.

11. A detergent composition according to claim 1 wherein the surfactant system a) comprises at least 90% by weight of one or more mid-chain branched alkyl sulfates as defined in claim 1.

12. A detergent composition according to claim 5 wherein the inorganic perhydrate salt is a perborate or percarbonate salt.

13. A detergent composition according to claim 5 wherein the inorganic perhydrate salt is present at a level of from 3% to 25% by weight of the composition.

14. A detergent composition according to claim 6 wherein the nonionic surfactant is a C9-15 primary alcohol ethoxylate containing from 3-12 moles of ethylene oxide per mole of alcohol.

15. A detergent composition according to claim 6 wherein the nonionic surfactant is present at a ratio to the surfactant system a) of from 1:1 to 1:10.

16. A detergent composition according to any one of claims 1 to 15 in the form of a solid laundry detergent composition.