GB2141755A - Detergent bleach compositions - Google Patents

Abstract

Built detergent bleach compositions comprising a surface active agent, a peroxide compound/peracid precursor bleach system which forms peracids in solution, an alkali metal carbonate builder and from 0.005 to 0.1% by weight of manganese (II) ions. The detergent bleach compositions deliver an improved bleach performance and can be used for washing/cleaning of fabrics at temperatures of below 40 DEG C.

Description

SPECIFICATION Detergent bleach compositions This invention relates to detergent bleach compositions which are particularly, but not essentially, adapted for fabric washing, and more particularly to built detergent compositions including a bleach system.

It is known to incorporate peracid bleaches such as sodium perborate together with peracid bleach precursors i.e. an organic compound which in solution react with the sodium perborate or any hydrogen peroxide adduct forming peracids, in detergent compositions. Such detergent compositions conventionally include, in addition to a detergent active material, a phosphate detergency builder such as sodium triphosphate.

Though peracid bleach systems comprising a combination of a peroxide compound such as sodium perborate, and a peracid precursor which form peracid in situ, are more effective at lower temperatures e.g.

50-60"C than the peroxide compounds, they do not exhibit adequate bleaching at temperatures below 40etc.

With the increasing trend of saving energy, housewives are becoming more and more energy-conscious and have gradually changed their washing habit towards lower wash-temperatures. Today a major proportion of housewives are washing also their white laundry using the 60"C wash-cycle. A considerable saving of energy would be obtained if washing habits could be further shifted towards cooler and cold water washing e.g. below 40"C, also for whites. There is therefore a continuous desire from the part of investigators to find alternative and possibly simpler and cheaper ways of further activating peroxide peracid precursor bleaching systems so as to improve the bleaching action of said systems.

US Patent 3532 634 teaches the use of transition metals which must be used with special types of chelating agents to activate persalt/peracid precursor bleach systems.

There are several drawbacks of this teaching; firstly not all transition metals proposed in the US Patent are consistently effective in catalysing the bleaching action of the persalt/peracid precursor bleaching system; secondly the rather elaborate selection of the proper chelating agent to fit with the specific metal used, and thirdly the extra cost incurred for the special chelating agent being present.

It is an object of the present invention to avoid the use of such expensive chelating agents and by consequence overcome the above drawbacks.

It has now been found that the above object can be achieved if manganese is used as the transition metal in conjunction with a carbonate builder. This is quite surprising since only manganese is effective and other metals of the transition series having atomic number of from 24 to 29 i.e. Chromium, Iron, Cobalt, Nickel and Copper are ineffective or even cause a reduction in the bleaching effect. Only manganese exerts a catalysing effect on the peroxide compound/peracid precursor bleach system in the composition.

Thus, according to the invention there is provided a carbonate built detergent bleach composition comprising an alkalimetal carbonate, a peroxide compound bleach, a peracid precursor and trace levels of manganese (11) ions.

In terms of economy and simplicity the invention provides a substantial improvement over the US Patent 3532 634 teaching in that all drawbacks of the proposed system of the art have been removed.

In terms of economy and simplicity the invention provides a substantial improvement over the US Patent 3532 634 teaching in that all drawbacks of the proposed system of the art have been removed.

In some circumstances it is thought that the use of phosphates in detergent compositions can lead to environmental problems in waste waters. There is therefore a desire to reduce the level of phosphorus in detergent composition. Since carbonates, especially sodium carbonate have been suggested as alternative builders to phosphate, the present invention has the further advantage in that it uses less or no phosphate builder.

The ratio of peroxide compound to peracid precursor in the composition of the invention is not critical and can be varied widely from e.g. 1:1 to about 35:1. In addition thereto other sequestrant or non-sequestrant builders such as sodium triphosphate may be incorporated as desired in minor proportions to the carbonate builder e.g. up to 15% by weight of the composition.

In practice the composition of the invention will comprise from about 5 to 80% by weight preferably 10-60% by weight of the alkalimetal carbonate builder, preferably sodium carbonate, from 5 to about 50% by weight, preferably 5 to 35% by weight of the peroxide compound bleach, from about 0.1 to 25% by weight, preferably from 0.1 to 15% by weight of a peracid precursor, and from about 0.005 to 0.1% by weight of Manganese (II).

As already explained above the gist of the invention is that trace levels of manganese (II) ions is used in conjunction with a carbonate builder. Optimum effects are achieved if the manganese (II) ion concentration in the wash/bleach solution is within the range of from about 0.1 to 1 parts per million.

The Manganese (II) ions added for improving the bleach performance according to the invention can be derived from any water-soluble Manganese (II) salts or complexes, such as manganous sulphate or manganous chloride, or from any manganese compound in whatever form which delivers manganese (II) ions in aquous solution. Protection ofthe manganese (II) compound against contact with the bleaching agent may be necessary to avoid premature reaction prior to its point of use.

The detergent composition of the invention usually contains a surface active agent generally in an amount of from about 2 to about 50% by weight, preferably form 5-30% by weight. The surface active agent can be anionic, nonionic, zwitterionic or cationic in nature or mixtures thereof.

Preferred anionic non-soap surfactants are water soluble salts of alkylbenzene sulphonate, alkyl sulphate, alkylpolyethoxyether sulphate, paraffin sulphonate, alpha-olefin sulphonate, alpha-sulfocarboxylates and their esters, alkylglycerylethersulphonate, fatty acid monoglyceride-sulphates and-sulphonates, alkylphenolpolyethoxy ethersulphate, 2-acyloxy-alkane-1 -sulphonate, and beta-alkyloxy alkanesulphonate. Soaps are also preferred anionic surfactants.

Especially preferred are alkylbenzenesulphonates with about 9 to about 15 carbon atoms in a linear or branched alkyl chain, more especially about 11 to about 13 carbon atoms; alkylsulphates with about 8 to about 22 carbon atoms in the alkyl chain, more especially from about 12 to about 18 carbon atoms; alkylpolyethoxy ethersulphates with about 10 to about 18 carbon atoms in the alkyl chain and an average of about 1 to about 12 -CH2CH2O-groups per molecule, especially about 10 to about 16 carbon atoms in the alkyl chain and an average of about 1 to about 6 -CH2CH2O- groups per molecule; linear paraffin sulphonates with about 8 to about 24 carbon atoms, more especially from about 14to about 18 carbon atoms and alpha-olefin sulphonates with about 10 to about 24 carbons atoms, more especial-ly about 14 to about 16 carbon atoms; and soaps having from 8 to 24, especially 12 to 18 carbon atoms.

Water-solubility can be achieved by using alkali metal, ammonium, or alkanolamine cations; sodium is preferred.

Preferred nonionic surfactants are water-soluble compounds produced by the condensation of ethylene oxide with a hydrophobic compound such as an alcohol, alkyl phenol, polypropoxy glycol, or polypropoxy ethylene diamine.

Especially preferred polyethoxy alcohols are the condensation product of 1 to 30 moles of ethylene oxide with 1 mol of branched or straight chain, primary or secondary aliphatic alcohol having from about 8 to about 22 carbon atoms; more especially 1 to 6 moles of ethylene oxide condensed with 1 mol of straight or branched chain, primary or secondary aliphatic alcohol having from about 10 to about 16 carbon atoms; certain species of poly-ethoxy alcohol are commercially available under the trade-names of "Neodol"R, "Synperonic"R and "Tergitol"R, which are registered Trade Marks.

Preferred zwitterionic surfactants are water-soluble derivatives of aliphatic quaternary ammonium, phosphonium and sulphonium cationic compounds in which the aliphatic moieties can be straight or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water-solubilizing group, especially alkyldimethyl-propanesulphonates and alkyldimethyl-ammoniohydroxy-propane-sulphonates wherein the alkyl group in both types contains from about 1 to 18 carbon atoms.

Preferred cationic surface active agents include the quaternary ammonium compounds, e.g. cetyltrimethyl-ammonium-bromide or -chloride and distearyldimethyl-ammonium-bromide or-chloride, and the fatty alkyl amines.

Atypical listing of the classes and species of surfactants useful in this invention appear in the books "Surface Active Agents", Vol. l, by Schwartz & Perry (Interscience 1949) and "Surface Active Agents", Vol. II by Schwarz, Perry and Berch (Interscience 1958), the disclosures of which are incorporated herein by reference. The listing, and the foregoing recitation of specific surfactant compounds and mixtures which can be used in the specific surfactant compounds and mixtures which can be used in the instant compositions, are representative but are not intended to be limiting.

Typical examples of suitable peroxide compound bleaches are alkalimetal perborates, both tetrahydrates and monohydrates, alkali metal percarbonates, persilicates and perphosphates, of which sodium perborate is preferred.

Peracid bleach precursors, also called activators, have been amply described in the literature, including British patents 836,988,855,735, 907,356,907,358, 970,950, 1,003,310, 1,246,339, US patents 3,332,882 and 4,128,494, Canadian patent 844,481 and South African patent 68/6,344. Specific suitable activators include: (a) N-diacylated and N,N'-polyacylated amines, such as N,N,N',N'-tetraacetyl methylene diamine and N,N,N',N'-tetraacetyl ethylene diamine,N,N-diacetyl-aniline, N,N-diacetyl-p-toluidine; 1,3-diacylated hydantoins such as, for example, 1,3-diacetyl-5,5-dimethyl hydantoin and 1,3-dipropionyl hydantoin; -acetoxy-(NN,N')-poluacylmalonamide, for example -acetoxy-(N,N')-diacetylmalonamide; (b) N-alkyl-N-sulphonyl carbonamides, for example the compounds N-methyl-N-mesyl-acetamide, N methyl-N-mesylbenzamide, N-methyl-N-mesyl-p-nitrobenzamide, and N-methyl-N-mesyl-p methoxybenzamide; (c) N-acylated cyclic hydrazides, acylated triazones or urazoles, for example monoacetylmaleic acid hydrazide; (d) O,N,N-trisubstituted hydroxylamines, such as O-benzoyl-N,N-succinyl hydroxylamine, O-acetyl-N,N succinyl hydroxylamine, O-p-methoxybenzoyl-N,N-succinyl-hydroxylamine, O-p-nitrobenzoyl-N,N succinyl-hydroxylamine and O,N,N,-triacetyl hydroxylamine; ; (e) N,N'-diacyl-sulphurylamides, for example N,N'-dimethyl-N,N'-diacetyl-sulphurylamide and N,N' diethyl-N,N'-dipropionyl sulphurylamide; (f) Triacylcyanurates, for example triacetyl cyanurate and tribenzoyl cyanurate; (g) Carboxylic acid anhydrides, such as benzoicanhydride, m-chloro-benzoic anhydride, phthalic anydride, 4-chloro phthalic anhydride; (h) Eesters, for example glycose pentaacetate, xylose tetra acetate, sodium acetoxy benzene sulphonate and sodium benzoyloxy benzensulphonate; (i) 1 ,3-diacyl-4,5-diacyloxy-imidazolidine, for example, 1 ,3-difromyl-4,5-diacetoxy-imidazolidine, 1 ,3-diacetyl-4,5-diacetoxy-imidazolidine, 1 ,3-diacetyl-4,5-dipropionyloxy-imidazoline;; (j) Tetraacetylglycoluril and tetrapropionylglycoluril; (k) Diacylated 2,5-diketopiperazine, such as 1,4-diacetyl-2,5-diketopiperarize, 1,4-dipropionyl-2,5- diketopiperazine and 1,4-dipropionyl-3,6-dimethyl-2,5-diketopiperazine; (I) Acylation products of propylenendiurea or 2,2-dimethyl-propylenediurea (2,4,6,8-tetraaza-bicyclo- (3,3,1 )-nonane-3,7-dione or its 9,9-dimethyl derivative), especially the tetraacetyl- or the tetrapropionyl propylenediurea or their dimethyl derivatives; (m) Carbonic acid esters, for example the sodium salts of p-(eth oxyca rbonyloxy)-benzoic acid and p-(propoxycarbonyloxy)-benzenesulphonic acid.

(n) Acyloxy-(N,N1)polyacyl malonamides, such as alpha - acetoxy(N,N1)diacety malonamide.

The N-diacylated and N,N'-polyacylatedamines mentioned under (a) are of special interest, particularly N,N,N',N'-tetra-acetyl-ethylenediamine (TAED).

In addition thereto the compositions of the invention may contain any of the conventional components and/or adjuncts usable in fabric washing compositions.

As such can be named, for instance soil-suspending agents such as water-soluble salts of carboxymethylcellulose, carboxyhydroxymethylcellulose, copolymers of maleic hydride and vinyl ethers, and polyethylene glycols having a molecular weight of about 400 to 10.000. These can be used at levels of about 0.5% to about 10% by weight. Dyes, pigments, optical brighteners, perfumes, anti-caking agents, suds control agents, fabric softening agents, alkaline agents, fillers and ethylenediamine tetracetate can also be added in varying amounts as desired. Also stabilisers such as ethylene diamine tetra-(methylenephosphonates) and diethylene triamine penta-(methylene phosphonates) may be added as desired.

In the following Examples illustrating the invention manganous sulphate was used to deliver Mn2+.

Example I The following base detergent powder composition was used in the experiments.

Composition parts by weight C1415 fatty alcohol condensed with 13 ethylene oxide groups 1.5 Sodium coconut fatty acid soap 1.0 Sodium carbonate 33.0 Sodium silicate alkaline 1:2 7.6 Sodium carboxymethyl cellulose 0.33 Flurorescer 0.1 Sodium sulphate 44.0 Water 3.5.

The above base detergent powder composition was dosed at 4 g/l in water and 0.2 g/l TAED and 0.45 g/l sodium perborate tetrahydrate was added. A series of solutions with and without added metal ions were used for washing/bleaching of tea stained test cloths in a one hour isothermal wash at 25"C.

The bleaching effects achieved on tea-stained test cloths measured as At*460 (reflectance value) were as follows: TABLE I Metal ion ion concentration zppmJ AR*460 (reflectance value) None (control) - 3.3 Cobalt (Il) 1.0 -1.2 Chromium 1.0 3.1 Copper (II) 1.0 -1.0 Iron (III) 1.0 3.0 Nickel (II) 1.0 2.8 Manganese (II) 1.0 7.6 The above results clearly show that without the use of special chelating agents, Manganese (II) is the only metal which improves the bleaching performance of perborateiTAED system in a carbonate built detergent composition at 25"C.

All other metals of the above series were ineffective and Cobalt and Copper were even detrimental to the bleaching performance.

Example lI The following carbonate built detergent bleach powder composition was used in the experiments.

Composition Parts by weight C11-15 fatty alcohol condensed with 13 ethylene oxide groups 1.5 Sodium coconut fatty acid soap 1.0 Sodium carbonate 33.0 Sodium silicate alkaline 1:2 7.6 Sodium carboxymethyl cellulose 0.33 Flurorescer 0.1 Sodium sulphate 44.0 Water 3.5 Post dosed: TAED 2.0% Sodium perborate tetrahydrate 25.0% The above detergent bleach composition was dosed at 4 g/l in water and solutions with or without manganese or manganese/picolinic acid were used for washing and bleaching of tea-stained test clothes in a one hour isothermal wash test at 30"C and at PH 10.35.

The bleaching effects measured as AR*460 (reflectance value) were as follows: Solution AR*460 Without catalyst (control) 4.3 + Mn2+ (1 ppm) 9.6 + Mn2+ (1 ppm) + picolinicacid (1.7x10-4M) 8.7 The detrumental effect of picolinic acid on manganese catalysis of perborateiTAED bleach system is clearly demonstrated.

Example Ill The following detergent bleach powder compositions were prepared: Composition Parts by weight C14-15 fatty alcohol/13 ethylene oxide 1.5 1.5 Sodium coconut fatty acid soap 1.0 1.0 Sodium carbonate 33.0 33.0 Alkaline sodium silicate (1:2) 7.6 7.6 Sodium Carboxymethyl cellulose 0.33 0.33 Fluorescer 0.1 0.1 Sodium sulphate 44.0 44.0 Water 3.5 3.5 Post dosed: TAED (peroxy acid precursor) - 1.0% Sodium perboratetetrahydrate 40.0% 40.0% The compositions were used in a washing test at the same wash conditions as used in Example II.

The following results were obtained: Composition AR*460 freflectance value) A 1.3 A + Mn2+ (1 ppm in solution) 7.0 B 2.2 B + Mn2+ (1 ppm in solution) 11.4 The superior bleaching effect at 30"C of composition B + manganese according to the invention in the absence of any special chelating agent, over the other compositions is evident.

Claims (6)

1. A built detergent bleach composition comprising a surface active agent, a peroxide compound and a peracid precursor, characterized in that it contains an alkali metal carbonate builder and from 0.005 to 0.1% by weight of manganese (II) ions.

2. A composition according to Claim 1, characterized in that it comprises: (I) from about 2 to 50% by weight of said surface active agent, selected from the group consisting anionic, nonionic, zwitterionic and cationic detergents and mixtures thereof; (it ) from about 5 to 80% by weight of said alkali metal carbonate builder; (ill) from about 5 to 50% by weight of said peroxide compound; (IV) from about 0.1 to 25% by weight of said peracid precursor; and (V) from 0.005 to 0.1% by weight of manganese (II) ions.

3. A composition according to Claim 1 or 2, characterized in that said alkali metal carbonate builder is sodium carbonate.

4. A composition according to Claim 1 or 2, characterized in that said peroxide compound is sodium perborate.

5. A composition according to Claim 1 or 2, characterized in that said peracid precursor is N,N,N',N', tetra acetyl ethylene diamine.

6. A composition according to any of the above Claims, characterized in that it further comprises other sequestrant or non-sequestrant builders in an amount up to 15% by weight of the composition.