AU703720B2

AU703720B2 - Bleaching compositions

Info

Publication number: AU703720B2
Application number: AU25934/95A
Authority: AU
Inventors: Gianmarco Polotti; Stefano Scialla; Raffaele Scoccianti
Original assignee: Procter and Gamble Co
Current assignee: Procter and Gamble Co
Priority date: 1994-06-17
Filing date: 1995-05-18
Publication date: 1999-04-01
Anticipated expiration: 2015-05-18
Also published as: JPH10503162A; AU2593495A; DE69426597T2; DE69426597D1; CA2191572A1; ES2152974T3; EP0687727A1; WO1995035256A1; EP0687727B1; MX9606568A; GR3035270T3

Description

WO 95/35256 PCTI/US95/06224 1 BLEACHING COMPOSITIONS Technical Field The present invention relates to bleaching compositions. The compositions herein are particularly useful for the bleaching of fabrics.

Background Compositions for the bleaching of laundry have been extensively described in the art. Bleaching compositions can be classified into peroxide bleaching compositions and hypochlorite bleaching compositions. Peroxide bleaching compositions have the advantage over hypochlorite bleaching compositions that they are generally considered as being somewhat safer to fabrics, specifically to colored fabrics. Peroxide compositions however have the inconveniency that they are often chemically unstabie, which makes it difficult to formulate peroxide bleaching compositions which are sufficiently stable to be commercialized. A possible solution to this problem consists in formulating compositions with a high level of peroxide, to extend the "effective" period of the composition. A possible drawback of this solution is that compositions may reach the user which still comprise a high amount of peroxide, whereby possible skin itching may occur if the user's skin comes in contact with the peroxide composition, before or during use. This itching phenomenon is quite moderate and fully reversible, but is does constitute potential discomfort for the user.

It would therefore be desirable to formulate a composition comprising a peroxygen bleach in lower amounts, i.e. in amounts where substantially no itching occurs, and which yet remain effective in bleaching fabrics.

It has now been found that some of the problems of the prior art can be overcome or at least ameliorated by formulating an aqueous composition comprising, in addition to lower amounts of peroxygen bleach, a water-soluble cationic surfactant in combination with a hydrophilic nonionic surfactant.

Summary of the invention The compositions of the present invention comprise hydrogen peroxide or a source thereof, a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H40)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, 15 or (C2H40)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion, said composition further comprising a hydrophilic nonionic surfactant having an HLB above 13.

In one aspect, the present invention provides an aqueous bleaching composition comprising water, from 1% to 10% of hydrogen peroxide or a source thereof; from 0.1% to 20% of at least one cationic surfactant of formula

R

1

R

2

R

3

R

4 N+X wherein R 1 is C8-C16 alkyl or is R-T-CO-R 6 wherein T is O, NH or N-C1-C4 alkyl; R 5 is a divalent C1-C3 alkylene or -(C 2

H

4 0)m- R 6 is a C8-C16 Salkyl; m is from 1-8; wherein each of R 2

R

3 and R 4 is independently C1 to C4 alkyl or hydroxyalkyl, benzyl or -(C 2

H

4 0)x-H, where x is from 2 to 5, not more than one of R 2

R

3 -'nd R 4 being benzyl; and X is an anion; said composition further comprising at least one hydrophilic nonionic surfactant having a HLB above 13 in an amount from 0.1% to 20% by weight of the total composition.

IC C:\WINWORDILONA\MLHMLHSPECI'SP25934 DOC 2a Detailed description of the invention The compositions according to the present invention are peroxide bleaching compositions. Thus the compositions herein comprise hydrogen peroxide or a source thereof. As discussed hereinbefore, a problem which may occur with compositions comprising hydrogen peroxide above a certain level, is that the skin of the user which comes in contact with the composition may itch.

This itching phenomenon is harmless and quickly tully reversible, but it may nevertheless cause discomfort to the user. This problem will not occur directly if the composition comprises a hydrogen peroxide source instead of hydrogen peroxide per so, but it may occur upon use, when the composition is diluted in water before use and hydrogen peroxide is then formed. The compositions herein thus comprise hydrogen peroxide or a source thereof in amounts not causing any skin itching, 0 0 CC '.WINWORDIJLONAWLHMLHSPECSP25934 DOC

I

WO 95/35256 PCT/US95/06224 3 Suitable sources of hydrogen peroxyde for use herein include perborates, percarbonates, persulfates and the like. It is preferred however to use hydrogen peroxide per se, and the compositions herein will comprise from 1% to 10% by weight of the total composition of hydrogen peroxide, preferably from 2% to Indeed, we have found that, when used in higher amounts, skin itching phenomenon start to appear.

Because the level of hydrogen peroxide, or source thereof, is reduced, there would result a poorer bleaching performance, compared to compositions with higher amounts of peroxygen bleach which in turn might cause skin itching.

We have found that the bleaching performance at higher temperatures, e.g.

as from 50 0 C could be maintained, even with lower amounts of peroxygen bleach, by formulating a specific surfactant system comprising a narrowlydefined cationic surfactant as well as a narrowly-defined hydrophilic nonionic surfaptant.

Accordingly, the compositions herein comprise a cationic surfactant according to the formula R1R2R3R4N+X-, where R1 is C8-C16 alkyl or is R5-T-CO-R6, wherein T is O, NH or N-C1-C4 alkyl, R5 is a divalent C1-C3 alkylene group or (C2H40)m, wherein m is from 1 to 8, wherein each of R2,R3,R4 is independently C1-C4 alkyl or hydroxy alkyl, benzyl, or (C2H40)xH where x is from 2 to 5, not more than one of R2,R3,R4 being benzyl, and X is an anion. It is of course possible to use herein mixtures of different cationic surfactants according to the formula hereinabove.

Preferred alkyl chain length for R1 is C12-15, particularly where the alkyl group is a mixture of chain length derived from coconut or palm kernel fat or is derived synthetically by olefin build up or OXO alcohol synthesis.

Preferred groups for R2,R3 and R4 are methyl and hydroxyethyl groups and suitable anion X include halide, methosulfate, acetate and phosphate ions.

Examples of suitable cationic surfactant for use herein are: coconut trimethyl ammonium chloride, preferred for use herein, or bromide as Cequartyl from Rhone Poulenc and Empigen 5141 from Albright Wilson, coconut methyl dihydroxyethyl ammonium chloride or bromide, II- -I WO 95/35256 PICT/US95/16224 4 decyl triethyl ammonium chloride, decyl dimethyl hydroxyethyl ammonium chloride or bromide, C12-15 dimethyl hydroxyethyl ammonium chloride or bromide, coconut dimethyl hydroxyethyl ammonium chloride or bromide, myristyl trimethyl ammonium methyl sulfate, lauryl dimethyl benzyl ammonium chloride or bromide as Bacforbl 80 from Sidobre, Sinove and Bardac 205 M from Lonza.

lauryl dimethyl (ethenoxy)4 ammonium chloride or bromide.

The compositions herein comprise from 0.1% to 20% by weight of the total composition of said cationic surfactants, or mixtures thereof, preferably from 1% to As a further essential ingredient, the compositions herein comprise a hydrophilic nonionic surfactant. We have found that the suitable nonionic surfactants for use herein are those having an HLB above 13. It is of course possible to use mixtures of said nonionic surfactants. A wide variety of nonionic surfactants are commercially available. Typically, nonionic surfactants are alkoxylated fatty alcohols. And the HLB of a given nonionic surfactant depends on the chain length of the fatty alcohol, the nature of the alkoxylating group as well as the degree of alkoxylation. Surfactant catalogs are available which list nonionic surfactants with their corresponding HLBs.

Suitable for use herein are those which have an HLB of above 13. Such nonionic surfactants are commercially available for instance under the trade name Dobanol 91-8, 91-9, 91-10 and 91-12, all from Shell.

The compositions herein should comprise from 0.1% to 20% by weight of the total composition, preferably from 2% to 10% of said hydrophilic nonionic surfactant or mixtures thereof. In a preferred embodiment of the present invention, said cationic surfactant and said hydrophilic nonionic surfactant should be present in a weight ratio of cationic to nonionic of about 1:3.

The compositions herein can be advantageously formulated as emulsions comprising two nonionic surfactants with different HLBs. Indeed, by WO 95135256 PCTIl!S95/06224 formulating in an aqueous medium at least two different nonionic surfactants having different HLBs, a stable emulsion can be obtained. This emulsion can then be used to formulate, in a single composition, different ingredients which are otherwise poorly compatible, e.g. a bleach activator with hydrogen peroxide. In this embodiment of the invention the compositions herein comprise at least one hydrophilic nonionic surfactant, which can be the nonionic surfactant described herein before, and a more hydrophobic nonionic surfactant. Suitable hydrophobic surfactants to form the hydrophobic phase of the emulsion typically have an HLB of less than about 9. The compositions of this embodiment can be made by mixing together all the hydrophilic ingredients, i.e. water, said hydrophilic nonionic surfactant, said cationic surfactant and all other hydrophilic ingredients such as dyes, optical brighten:r;s. Separately, all hydrophobic ingredients are mixed, i.e.

said hydrophobic nonionic surfactant together with other, optional, hydrophobic ingredients which are to be formulated in the composition, such.

as perfumes, solvents, enzymes, bleach activators and polymers. Then, both mixtures are mixed together. If the composition comprises a bleach activator, i.e. a peracid precursor, it is preferable to choose a hydrophobic bleach activator which can be formulated in said hydrophobic mixture, and thus remains separated from the hydrophilic peroxygen bleach. This adds to the chemical stability of the compositions, thus its performance as more oxygen remains available throughout time. A suitable hydrophobic bleach activator for use herein includes acetyl triethyl citrate, as described in WO 93/12067, as well as compounds according to the formula R-O-O-R' where R and R' are independently alkyl, alkenyl, alkanoyl, aryl, aroyl, alkylaryl or alkylaroyl radicals.

We have observed that the pH of the compositions herein plays a role in the chemical stability of the composition. Accordingly, the compositions herein are preferably formulated at a pH of from 1 to 7, preferably 3 to 5. A variety of suitable means can be used for adjusting the pH of the compositions, including organic or inorganic acids, alkanolamines and the like. It may be desirable to use alkanolamines herein, as we have found that alkanolamines have an effect on the viscosity of the product, and thus can be used as viscosity regulators, if necessary.

The compositions herein may comprise a variety of optional ingredients. A preferred optional feature of the compositions herein is the presence of radical scavengers, which are beneficial to the stability of the compositions herein. Suitable radical scavengers for use herein include the well known substituted mono and di hydroxy benzenes and their analogs, alkyl and aryl carboxylates, and mixtures thereof. Preferred radical scavengers for use herein include butyl hydroxy toluene, mono-tert-butyl hydroquinone, benzoic lo acid, toluic acid, t-butyl catechol, benzylamine, 1,1,3-tris(2-methyl-4-hydroxybutane, commercially available under the trade name Topanol CA ex ICI, as well as n-propyl-gallate. Radical scavengers, when used, are typically present herein in amounts ranging from 0.01% to 2% by weight of the total composition, preferably 0.01% to 0.2%.

Tha compositions herein may further comprise other optionals, including anionic and cationic surfactants, to be formulated in the hydrophilic phase herein, builders and chelants, as well as aesthetics, including dyes and *aooaa *ole ~1.

6a perfumes and the like. Accordingly throughout the description and claims of this specification, the word "comprise" and variations of the word, such as "comprising" and "comprises", is not intended to exclude other additives or components or integers.

The compositions according to the present invention are useful as laundry bleaches, including for the pretreatment of stains on laundry items prior washing.

Indeed, pretreatr .ent of fabrics before washing allows a close contact of the product with the stains, and the bleaching mechanism described herein occurs at a later stage, when the pretreated fabrics are contacted with warm water. The compositions herein can also be formulated as detergent compositions per se, or as detergency additives, to be used in addition to a detergent. Compositions herein can further be used as dishwashing compositions, or as hard surface cleaners, provided that contact with warm water occurs at some point in time in the washing process.

The present invention further encompasses a process of bleaching fabrics, dishes or hard surfaces wherein said fabrics, dishes or hard surfaces are contacted with a bleaching liquor comprising a composition according to any

*Z

IC C \WINWORD'JLONAMLHNLHSPECISP25934 DOC WO 95/35256 PCT/US95/06224 7 of the preceding claims in an aqueous medium at a temperature of from to 90°C, and said bleaching liquor is subsequently rinsed off of said fabrics, dishes or hard surfaces. In one embodiment of this process, the composition described herein is first applied to fabrics, as a so-called pretreater, preferably to the stained portions of said fabrics, and said pretreated fabrics are subsequently contacted with an aqueous medium at a temperature of from 30"C tc 70"C, for a period of time sufficient to bleach said fabrics. In this embodiment, said bleaching liquor is formed at the time the fabrics are introduced in said aqueous medium. Subsequently, said bleaching liquor is rinsed off of said fabrics, The present invention is further illustrated by the following examples and data.

Examples Experimental Part The following formulations according to the present invention are made by mixing the listed ingredients in the listed proportions (in weight Composition 1 Dobanol 91-8 Coconut trimethyl ammonium chloride H202 Sodium Coconut Alkyl Sulfate Dobanol 23-3 Water ana minors pH 3% 1% 4% to balance WO 95/35256 PCTIJS95/06224 Composition 2 Dobanol 91-8 Coconut trimethyl ammonium chloride H202 Sodium Coconut Alkyl Sulfate Dobanol 23-3 Water and minors pH 3% 1% 4% 4% to balance 4 Composition 3 Dobanol 91-10 Coconut trimethyl ammonium chloride H202 Sodium Coconut Alkyl Sulfate Dobanol 23-3 Water and minors pH 3% 1% 4% 2% 7% to balance 4 Composition 4 Dobanol 91-8 Bardac 205M H202 Sodium Coconut Alkyl Sulfate Dobanol 23-3 Water and minors pH 3% 1% 4% 2% to balance 4 The present invention concerns the incorporation of a specific cationic/nonionic surfactant system in a liquid peroxygen bleaching composition which allows to reduce the amount of peroxygen bleach without losing performance. The technical data below illustrate the present invention.

The tests are made with the following conditions. The tests are performed on WO 95/35256 PCT/US '6224 9 cotton fabrics, with 6 replicates per test. The fabriL are stained as indicated hereinabove, and 0.2g of prototype is applied to the stains, prior to washing.

Then the fabrics are washed in a Launder-O-meter, with 5 g of Dash Ultra Powder in 500 ml water. There is no waiting period between application of the prototype on the stains, and the subsequent washing.

Prototype A is a composition as composition 1 hereinabove, but without Dobanol 91-8 and without cationic surfactant. Prototype B is the same as Prototype A, but with 7% level instead of The results are listed in the table below.

Stains Prototype 1 Comp. 1 Prototype A Comp. 1 vs. vs. vs. vs.

Prototype B Prototype B Prototype B Prototype B C 40 C 60 C 60 C Grass -0.8s -0.2 -1.0s -0.3 Cocoa +0.1 +0.3 -0.9 0.0 Tea -0.4 -0.4 -0.7 -0.2 Wine -0.8 -0.3 -0.7 s 0.0 Vegetal Oil -1.0s +0.1 -1.0s 0.0 Blood -3.2s -1.7s -4.0s -0.8s The results are expressed as panel score units as evaluated by expert judges. Comparing Prototype A vs Prototype B shows that a decrease in H202 leads to a loss of performance. Comparing Composition 1 vs Composition B shows that Composition 1 is as gozd as prototype B, even though it has about half less H202.

Another test is performed as in the previous experiment. In this test, composition 2 exemplified hereinbefore is compared to a reference composition. The reference is an activated bleaching composition comprising hydrogen peroxide and acetyl triethyl citrate. More specifically, the formulation comprises 6% H202, 3.5% acetyl triethyl citrate, 6% Lutensol T03, 8% Dobanol 45-7, 1.5% Sodium Alkyl Sulfate, 0.3% Citric Acid, water to balance, pH=4).

WO 95/35256 P C''/)S95/06224 Prototype 2 vs. reference 0 C 600 C Grass 0.2 0.0 Cocoa +0.0 +0.2 Tea -0.6 -0.2 Wine -0.1 0.0 Vegetal Oil -0.5 Mineral Oil +0.3 +0.3 Make Up +0.92s +0.9s Tomato +0.92s +0.4 Sebum -0.67 Blood -1.0s -4.0 s This comparison shows that a composition according to the present invention performs better than an activated bleaching composition comprising a higher amount of hydrogen peroxide.

Claims

1. An aqueous bleaching composition comprising water, from 1% to 10% of hydrogen peroxide or a source thereof; from 0,1% to 20% of at least one cationic surfactant of formula R 1 R 2 R 3 R 4 NX wherein R 1 is C8-C16 alkyl or is R 5 -T-CO-R 6 wherein T is O, NH or N-C1-C4 alkyl; R 5 is a divalent C1-C3 alkylene or (C 2 H 4 R 6 is a C8-C16 alkyl; m is from 1-8; wherein each of R 2 R 3 and R 4 is independently C1 to C4 alkyl or hydroxyalkyl, benzyl or -(C 2 H40)x-H, where x is from 2 to 5, not more than one of R 2 R 3 and R 4 being benzyl; and X is an anion; said composition further comprising at least one hydrophilic nonionic surfactant having a HLB above 13 in an amount from 0.1% to 20% by weight of the total composition.

2. A composition according to claim 1 wherein the amount of hydrogen peroxide is in the range of from 2% to 4%.

3. A composition according to any one of the preceding claims which comprises from 1% to 5% by weight of the total composition of said cationic surfactants, or mixtures thereof.

4. A composition according to any one of the preceding claims wherein sa cationic surfactant is coconut trimethyl ammonium chloride. A composition according to any one of the preceding claims which comprises from 0.1% to 20% by weight of the total composition of said nonionic surfactant, or mixtures thereof. S IC C NWORDlLONAVMLH\MLHSPECIlSP25934 DOC CMs~C''r 12

6. A composition according to claim 5 which compri'ns from 2 to 10% by weight of the total composition of said nonionic surfactan or mixtures thereof.

7. A composition according to any one of the preceding claims where said cationic surfactant and said hydrophilic nonionic surfactant are present in a weight ratio of said cationic surfactant to said hydrophilic nonionic surfactant of about 1:3.

8. A composition according to any one of the preceding claims which is formulated as an emulsion comprising at least two nonionic surfactants having different HLBs, S: 9. A composition according to any one of the preceding claims which further comprises a bleach .ctivator. A process of bleaching fabrics, dishes or hard surfaces wherein said fabrics, dishes or hard surfaces are contacted with a bleaching liquor comprising a composition according to any of the preceding claims in an aqueous medium at a temperature of from 300C to 900C, and said bleaching liquor is subsequently rinsed off of said fabrics, dishes or hard surfaces. 9 9 S: 11. A process according to claim 10, wherein said fabrics are pretreated by applying thereon a composition according to claims 1 to 9, and said pretreated fabrics are subsequently contacted with an aqueous medium at a temperature of from 300C to 700C, thereby forming said bleaching liquor, for a period of time sufficient to bleach said fabrics, and said bleaching liquor is subsequently rinsed off of said fabrics.

12. A process according to claim 11, wherein the composition according to any one of claims 1 to 9 is applied to at least the stained portion of said fabrics. IC C %WIORD LONAWLHJ.LHSPECI$P25934 DC 13

13. A composition according to claim 1 substantially as herein described with reference to any one of the examples. DATED: 11 February, 1999 PHILLPS ORMVONDE FITZPATRICK Attorneys for:Od~e/ THE PROCTER GAMBLE CO PANY a. a a 4 a. a a. *a a a a. a a a a a *0a~~a a L) IC AWINOROJLONAWLHV\ALHSPECM\P25914 DC 4.1