Aqueous Alkaline, Silicate-Containing Composition for Bleaching Cellulosic Fibre Materials in the Presence of Per Compounds

The present invention relates to an aqueous alkaline, silicate-containing composition comprising a monomeric or oligomeric phosphonic acid ester, a polyhydroxy compound, a magnesium salt or magnesium oxide and an anionic dispersant, and to the use of said composition for bleaching cellulosic fibre materials in the presence of e.g. hydrogen peroxide.

An alkaline, peroxide-containing composition which may also contain silicate and which comprises an oligomeric phosphonic acid ester, a magnesium salt, a polyhydroxy compound and, as optional component, a nonionic or anionic wetting agent or dispersant, e.g. an alkylmonosulfonate, arylmonosulfonate or alkarylmonosulfonate, which composition is used for bleaching cellulosic fibre materials, is disclosed in U.S. Pat. No. 4,515,597. This known composition, which contains an alkylmonosulfonate, arylmonosulfonate or alkarylmonosulfonate as optional component, has an insufficient storage stability at high pH values of .gtoreq.14 and, in particular, at high alkali metal concentrations (e.g. from 9% of potassium hydroxide and/or sodium hydroxide, based on the total weight of the composition).

It has now been found that this shortcoming can be substantially overcome if the composition of the invention always contains an alkyldisulfonic, aryldisulfonic or alkaryldisulfonic acid, or a salt thereof, as anionic dispersant.

Accordingly, the present invention relates to an aqueous composition which comprises at least

(a) a mixture of monomeric and oligomeric compounds of the formula ##STR2## wherein Y.sub.1 is hydrogen or --CO--T.sub.1, R.sub.1, X.sub.1 and T.sub.1 are each independently C.sub.1 -C.sub.4 alkyl and m.sub.1 is an integer from 1 to 17,

(b) a polyhydroxy compound,

(c) an alkali metal silicate,

(d) an alkali metal hydroxide,

(e) a magnesium salt and

(f) an alkali metal salt of an alkyldisulfonic, aryldisulfonic or alkaryldisulfonic acid.

Further objects of the invention are:

a process for the preparation of the composition,

the use of said composition as bleaching activator and bleaching stabiliser in aqueous liquors that contain at least one per compound for pretreating cellulosic fibre materials,

a process for bleaching cellulosic fibre materials which comprises treating said materials with an aqueous liquor that contains at least one per compound and the composition of the invention,

an aqueous liquor for carrying out said process, which liquor contains at least one per compound and the composition of the invention, and

the cellulosic fibre material bleached by the process of the invention.

The monomeric compounds forming a constituent of the mixture of monomeric and oligomeric compounds of formula (1) correspond generally to the formula ##STR3## wherein Y.sub.1 is hydrogen or --CO--T.sub.1, and R.sub.1 and T.sub.1 are each independently of the other C.sub.1 -C.sub.4 alkyl.

Preferred monomeric compounds are those of the formula ##STR4## wherein Y.sub.2 is hydrogen or --CO--R.sub.1, where R.sub.1 is C.sub.1 -C.sub.4 alkyl, and R.sub.2 is methyl or ethyl; and especially those of the formula ##STR5## wherein R.sub.2 has the given meaning.

Particularly preferred monomeric compounds are those of the formula ##STR6## wherein Y.sub.3 is hydrogen or acetyl.

Preferred oligomeric compounds as constituent of the mixture of monomeric and oligomeric compounds of formula (1) are those of the formula ##STR7## wherein Y.sub.1 is hydrogen or --CO--T.sub.1, and R.sub.1, X.sub.1 and T.sub.1 are each independently C.sub.1 -C.sub.4 alkyl and n.sub.1 is an integer from 1 to 16; and, in particular, those of the formula ##STR8## wherein Y.sub.2 is hydrogen or --CO--R.sub.1, where R.sub.1 is C.sub.1 -C.sub.4 alkyl, and n.sub.2 is an integer from 1 to 14; and, most particularly, those of the formula ##STR9## wherein R.sub.2 is methyl or ethyl and n.sub.3 is an integer from 1 to 12. Such oligomeric phosphonic acid esters of formula (6) and their preferred embodiments of formulae (7) and (8) are disclosed e.g. in U.S. Pat. No. 4,515,597.

Particularly preferred oligomeric compounds are those of the formula ##STR10## wherein Y.sub.3 is hydrogen or acetyl and n.sub.4 is an integer from 1 to 3, preferably 2.

Preferred mixtures of monomeric and oligomeric compounds which may suitably be employed as component (a) of the composition of this invention are those of the formula ##STR11## wherein Y.sub.2 is hydrogen or --CO--R.sub.1, wherein R.sub.1 is C.sub.1 -C.sub.4 alkyl, and m.sub.2 is an integer from 1 to 15; and, in particular, those of the formula ##STR12## wherein R.sub.2 is methyl or ethyl and m.sub.3 is an integer from 1 to 13.

Component (a) is preferably a mixture of monomeric and oligomeric compounds of the formula ##STR13## wherein Y.sub.3 is hydrogen or acetyl and m is 1 to 4, preferably 1 and 3.

The mixtures of monomeric and oligomeric compounds of the aforementioned kind are known per se and are prepared by known methods. Thus, for example, the mixture of formula (12) is preferably obtained by reacting phosphorus trichloride, acetic acid and, optionally, acetic anhydride in aqueous medium.

As component (a) of the composition of this invention it is also possible to use oligomeric compounds of one of formulae (6) to (9) which form a basic constituent of the mixture of monomeric and oligomeric compounds. If such oligomeric compounds are used as component (a), they are at least partially hydrolysed to the corresponding monomeric compounds in the aqueous composition of this invention in the presence of an alkali metal hydroxide as component (d). Accordingly, monomeric compounds which may be suitably employed as component (a) of the composition of the invention are also preferably those of one of formulae (2) to (5).

Component (a) acts as complexing agent for alkaline earth metals and heavy metals when using the composition of this invention in aqueous liquors that contain a per compound, e.g. hydrogen peroxide, for pretreating, especially for bleaching, cellulosic fibre materials. In particular, component (a) inhibits the decomposition of the per compound in the bleaching liquor by free, i.e. non-complexed, heavy metals which may be present in the process water.

Component (a) is preferably added to the composition of this invention in the form of a 35 to 90% by weight, most preferably 40 to 60% by weight, aqueous solution. In addition to containing the monomeric and/or oligomeric compounds of the aforementioned kind, the aqueous solution of component (a) may contain e.g. phosphorus acid and acetic acid or the anhydride thereof.

The polyhydroxy compound employed as component (a) in the composition of this invention is in particular a compound that contains at least 2 hydroxyl groups. Such a compound preferably corresponds to the formula ##STR14## wherein each of Q.sub.1 and Q.sub.2 independently of the other is --CH.sub.2 OH, --CHO or --COOM, where M is hydrogen or an alkali metal, preferably potassium or, most preferably, sodium, and q is an integer from 2 to 5.

It is also preferred to use a hydroxycarboxylic acid of the formula ##STR15## wherein M and q have the given meanings, or a lactone of such a hydroxycarboxylic acid. Examples of specific representatives of such hydroxycarboxylic acids are: gluconic acid and the alkali metal salts thereof, preferably the potassium salt or, most preferably, sodium salt, as well as the .gamma.-lactone of gluconic acid.

Component (b) is also described in U.S. Pat. No. 4,515,597.

Component (b) acts as complexing agent when using the composition of the invention in bleaching liquors for pretreating cellulosic fibre materials. This action is ensured even in bleaching liquors with pH values above 11. Component (b) is usually added in the form of a solid.

The alkali metal silicate employed as component (c) is normally water-soluble. Sodium silicate, which as commercial product preferably has an SiO.sub.2 content of about 24 to 28% by weight, is particularly suitable. It is preferred to use a commercial aqueuos solution of sodium silicate of about 30 to 40% by weight as component (c).

Component (c) permits longer treatment times in bleaching liquors for pretreating cellulosic fibre materials.

An alkali metal hydroxide which may be suitably used as component (d) is preferably potassium hydroxide or, in particular, the cheaper sodium hydroxide. In view of the homogeneity of the composition, a mixture of potassium hydroxide and sodium hydroxide is especially suitable for use as component (d). Component (d) is preferably added undiluted and in an amount of not less than 9%, based on the total weight of the composition. Accordingly, component (d) will preferably be in the form of solid potassium hydroxide or, preferably, solid sodium hydroxide and, most preferably, of a mixture of solid potassium and sodium hydroxide, with the weight ratio of sodium hydroxide to potassium hydroxide being in general from 1:0.01 to 1:2, preferably 1:0.05 to 1:0.25. The addition of component (d) gives strongly alkaline compositions having a pH value of .gtoreq.14. The alkalinity of the compositions by addition of larger amounts of component (d) is determined by the concentration of alkali metal hydroxide.

The magnesium salt employed as component (e) is e.g. in the form of the acetate, preferably sulfate or heptahydrate thereof, and is in particular the chloride or hexahydrate thereof. Component (e) is normally added as solid, and is preferably in the form of solid magnesium chloride hexahydrate. As described in U.S. Pat. No. 4,515,597, component (e) forms with component (a) a water-soluble magnesium complex which acts as bleaching stabiliser. In particular, the presence of the magnesium complex formed by components (a) and (e) ensures that there is no loss, or at least a reduced loss, for some time in the original activity of the per compound, e.g. hydrogen peroxide, in the bleaching liquors containing the composition of the invention.

An anionic dispersant which may be suitably employed as component (f) is in particular the potassium or, preferably, sodium salt of an alkyldisulfonic acid, aryldisulfonic acid or alkaryldisulfonic acid which is used undiluted, e.g. as powder or paste or as an aqueous solution having a concentration of at least 40% by weight, preferably of 40 to 95% by weight. The alkyl moiety of the alkyldisulfonic acid in this case normally contains 8 to 20 carbon atoms. The disodium salt of pentadecane-1,8-disulfonic acid in the form of an aqueous 40 to 60% by weight solution is cited by way of example. An aryldisulfonic acid is preferably a derivative of naphthalenesulfonic acid which is preferably in the form of the condensate with formaldehyde, obtained by reacting 2 or 3 moles of naphthalenesulfonic acid with 1 or 2 moles of formaldehyde. Methylenebis(2,2'-naphthalene-7,7'-sodium sulfonate) in the form of an aqueous 80 to 95% by weight solution is cited by way of example. An alkaryldisulfonic acid which may also be suitably used as component (f) contains straight or branched alkyl chains of at least 4, preferably 4 to 22 and, most preferably, 4 to 18, carbon atoms. A preferred alkaryldisulfonic acid is e.g. a dodecylbenzenesulfonic acid or a 3,7-diisobutylnaphthalenedisulfonic acid or, most preferably, a disulfonated benzylalkylbenzimidazole which preferably contains 8 to 22 carbon atoms in the alkyl moiety. It is particularly preferred to use e.g. the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, preferably in powder form.

The alkali metal salt of the above disulfonic acids which is used as component (f) is an anionic dispersant that ensures the storage stability of the concentrated composition of this invention at high pH values of .gtoreq.14, especially at the higher concentrations of alkali (e.g. from 9% of potassium hydroxide and/or sodium hydroxide, based on the total weight of the composition).

The composition of this invention generally comprises

0.1 to 2.0, preferably 0.25 to 1.8% by weight of component (a),

0.4 to 8.0, preferably 1.50 to 5.0% by weight of component (b),

5.0 to 20.0, preferably 10.00 to 18.00% by weight of component (c),

9.0 to 21.0, preferably 10.00 to 16.0% by weight of component (d),

0.05 to 2.0, preferably 0.10 to 1.0% by weight of component (e),

0.5 to 3.0, preferably 0.75 to 2.5% by weight of component (f), and

44.0 to 84.95, preferably 55.7 to 77.40% by weight of water,

based on the total weight of said composition.

The method of preparing the composition of this invention normally comprises adding half the total amount of component (d) to an aqueous solution (A) of components (c) and (f), then adding an aqueous solution (B) containing components (a), (b) and (e) to solution (A), and finally adding the remaining half of component (d) to the mixture of solutions (A) and (B). In this method, the compounds of formulae (2) to (9) or their mixtures of formulae (1), (11) or (12) employed as component (a) of solution (B) are converted by the remainder of component (d) into the corresponding alkali metal salts, e.g. the potassium or, preferably, sodium salts. The addition of component (d) in portions causes the reaction mixture to exotherm, so that external cooling may be necessary, e.g. at temperatures above 80.degree. C. By controlling the rate of addition of component (d), the mixing of solution (A) with half the amount of component (d), then with solution (B) and, finally, with the remaining half of component (d) is preferably effected at a temperature not exceeding 80.degree. C., preferably in the range from 60.degree. to 70.degree. C.

The above described procedure affords the material advantage that the addition of component (d) in two portions does not give rise to any undesirable precipitations during the preparation of the composition of this invention. In addition, solution (A) containing components (c) and (f) and solution (B) containing components (a), (b) and (e), which solutions are normally in the form of aqueous solutions, can be kept in stock owing to their excellent storage stability and can be processed at any time, as required, by addition of component (d) as described above to give the composition of the invention.

The bleaching liquors mentioned at the outset for carrying out the method of treatment using the composition of this invention contain, as per compound, e.g. an alkali metal persulfate, preferably potassium persulfate or, most preferably, sodium persulfate (Na.sub.2 S.sub.2 O.sub.8), which is normally added undiluted, i.e. in solid form. However, the preferred per compound is hydrogen peroxide (H.sub.2 O.sub.2), which on account of its higher stability is normally used in the form of a concentrated solution (30 to 60% by weight).

Besides containing the composition of this invention and a per compound as mandatory components, the bleaching liquors may also contain wetting agents or dispersants, antifoams or deaerators and/or fluorescent whitening agents as optional components.

Wetting agents or dispersants are usually added to the bleaching liquors as optional components if the cellulosic fibre material to be treated is cellulose in the natural state or, in particular, consists of cotton in the natural state. Suitable wetting agents or dispersants are anionic or nonionic surfactants, but preferably mixtures thereof. Preferred anionic surfactants are e.g. alkarylmonosulfonates, fatty acid condensates, protein fission products or salts thereof and, most preferably, alkylmonosulfate salts and alkylbenzenemonosulfonic acids containing 12 to 22 carbon atoms in the alkyl moiety. Preferred nonionic surfactants are e.g. adducts of alkylene oxide, in particular propylene oxide and, most preferably, ethylene oxide, with alkylphenols containing e.g. 12 to 14 carbon atoms in the alkyl moiety, preferably with fatty acid amides and, most preferably, with fatty alcohols. Adducts of ethylene oxide and fatty alcohols are especially preferred, with mixtures of such adducts with the alkylmonosulfates of the indicated kind being most preferred. Further suitable components in these mixtures are silicone surfactants or silicone oils.

It is necessary to add an antifoam or deaerator to the bleaching liquor especially if a wetting agent and/or surfactant is present. Such antifoams or deaerators are e.g. higher alcohols, preferably isooctanol, but are preferably silicone-based antifoams and/or deaerators, especially silicone oil emulsions.

The fluorescent whitening agent added as optional component to the bleaching liquor to achieve a particularly high degree of whiteness on the materials to be treated will generally belong to the styryl or stilbene series, e.g. to the distyrylarylenes, diaminostilbenes, ditriazolylstilbenes, phenylbenzoxazolylstilbenes, stilbenenaphthotriazoles and dibenzoxazolylstilbenes. Preferred fluorescent whitening agents are those of the distyrylbiphenyl or bistriazinylaminostilbene types which contain sulfonic acid groups, e.g. sulfonated distyrylbiphenyl and distyrylbistriazinyl derivatives, preferably the bis(phenylaminomorpholino-s-triazinyl)stilbenedisulfonic acids in the form of alkali metal salts, especially potassium salts or, preferably, sodium salts. These are preferably added in the form of commercial aqueous 20 to 30% by weight liquid formulations.

In addition, especially if the treatment of the cellulosic fibre materials is not carried out by HT methods in the temperature range up to 150.degree. C. under pressure, it is expedient to add an alkali metal hydroxide, preferably potassium hydroxide or, most preferably, sodium hydroxide, conveniently in the form of an approximately 30% by weight solution or in the form of solid potassium hydroxide or, in particular, of solid sodium hydroxide.

The aqueous bleaching liquors generally contain

1 to 12.5% by weight of the novel aqueous composition,

0.2 to 5% by weight, preferably 0.7 to 3.5% by weight, of per compound,

0 to 1 or 0.1 to 1% by weight, preferably 0.1 to 0.5% by weight, of wetting agent or detergent,

0 to 0.5 to 0.05 to 0.5% by weight of antifoam or deaerator,

0 to 0.1 to 0.01 to 0.1% by weight of fluorescent whitening agent, and

0 to 1 or 0.1 to 1% by weight, preferably 0.2 to 0.7% by weight, of an alkali metal hydroxide,

based on the total weight of the bleaching liquor.

The process for bleaching cellulosic fibre materials with the composition of this invention generally comprises first applying the bleaching liquor to the fibre material, normally by immersion or, preferably, by padding, e.g. in the temperature range from 10.degree. to 60.degree. C., but preferably at room temperature (15.degree. to 25.degree. C.), to a pick-up of about 50 to 120% by weight, preferably 90 to 110% by weight, after pinching-off. After it has been impregnated, the fibre material is subjected, without drying, in the still wet state to a moist storage treatment in which the material is rolled up and packed airtight in plastic sheeting and stored at 80.degree. to 90.degree. C. for about 1 to 5 hours or, most preferably, at room temperature for about 10 to 30 hours.

The treatment of the fibre material may, however, also be carried out in a long liquor (exhaust method) at a liquor to goods ratio of e.g. 1:3 to 1:100, preferably of 1:8 to 1:25, in the temperature range from 20.degree. C. to 100.degree. C., preferably from 80.degree. to 98.degree. C., for about 1/4 hour to 3 hours under normal conditions, i.e. under atmospheric pressure in conventional apparatus, e.g. on a jigger or winch beck. If appropriate, however, exhaustion can also be effected in the temperature range up to 150.degree. C., preferably from 105.degree. to 140.degree. C., under pressure, in high temperature (HT) apparatus.

For industrial application, continuous methods are of particular interest.

It is best not to exceed treatment temperatures of 98.degree. C. so as to avoid damage to the fibre. However, in special HT apparatus the fibre material can also be treated in industrial continuous processes under pressure, e.g. up to 2.5 bar, at elevated temperature, e.g. up to 150.degree. C., provided the treatment time is sufficiently brief to rule out damage to the fibre.

Subsequently the fibre material is normally rinsed thoroughly first with hot water of about 90.degree. to 98.degree. C. and then with warm and, finally, with cold water, neutralised with e.g. acetic acid, if necessary, and then wrung out and dried at elevated temperature (e.g. up to 150.degree. C.).

The cellulosic material to be treated can be in a wide range of presentation, e.g. as loose material, yarn, wovens or knits. The material is thus normally always in the form of textile fibre materials which are made from pure textile cellulosic fibres or from blends of textile cellulosic fibres and textile synthetic fibres.

Suitable cellulosic fibres are for example those made from regenerated cellulose, e.g. viscous rayon and viscose, from natural cellulose such as hemp, linen, jute and, in particular, cotton, while suitable synthetic fibres are those made from polyacrylonitrile and, in particular, from polyester and polyamide.

Material made of cotton or regenerated cellulose, or cotton/polyester and cotton/polyamide blends are especially suitable for treatment according to the invention, with cotton wovens and knits being particularly preferred. Materials which have been prewashed with e.g. surfactants are also suitable. It is also possible to bleach sized cotton fibres, in which case bleaching is carried out after or before sizing.

The fibre materials treated with the composition of this invention are free from husks, they have good rewettability and a low ash content and, in particular, they have an excellent degree of whiteness. The cellulose or cellulosic component of the bleached material exhibits no damage and no appreciable diminution in the degree of cellulose polymerisation. The use of the composition of this invention effects a particularly high degree of stabilisation, especially in bleaching liquors with a pH above 11. The original content of available oxygen of the bleaching liquor is retained for some considerable time (e.g. up to 5 days) or decreases only insignificantly (e.g. by at most 10%). The bleaching effect is none the less excellent. The liquors are thus stable in respect of their content of available oxygen and can be used for some considerable time. Despite the fairly high content of component (c) (silicate, especially sodium silicate), the composition of this invention causes no, or scarcely any, incrustation of the bleaching apparatus and forms no deposits on the treated material.

A material advantage of the composition of the invention is its particularly good storage stability over several months.

In the following Examples, parts and percentages are by weight.

With stirring, 79 parts of sodium hydroxide flakes are added over 10 minutes to 667 parts of a solution (A) consisting of

70% of a 35% aqueous solution of sodium silicate (SiO.sub.2 content: 26%),

3% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid (in powder form), and

27% of water,

whereupon the reaction mixture exotherms to 55.degree. C.

With stirring, 208 parts of a solution (B) consisting of

10% of a 35% aqueous solution of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

15.5% of sodium gluconate,

5.5% of magnesium chloride hexahydrate, and

62.0% of water

are added at 55.degree. C. over 15 minutes to the above reaction mixture. After addition of solution (B), the temperature of the reaction mixture is 50.degree. C. To the reaction mixture are then added 79 parts of sodium hydroxide flakes over 10 minutes, whereupon the reaction mixture exotherms to 68.degree. C.

The reaction mixture is cooled to 20.degree. C., affording 1033 parts of a composition comprising

(a) 0.70% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

(b) 3.12% of sodium gluconate,

(c) 15.82% of sodium silicate,

(d) 15.30% of sodium hydroxide,

(e) 1.10% of magnesium chloride hexahydrate,

(f)

1.94% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

62.02% of water.

Even after 4 months storage the composition remains homogeneous.

The procedure of Example 1 is repeated, except for adding to solution (B) 10% of an aqueous solution containing, in addition to phosphorous acid and acetic acid, 44% of a mixture of phosphorus trichloride and acetic acid obtained in aqueous medium from monomeric and oligomeric compounds of formula (12), wherein Y.sub.3 is hydrogen, to give 1033 parts of a composition comprising

(a) 0.88% of a mixture of monomeric and oligomeric compounds of formula (2), wherein Y.sub.3 is hydrogen,

(b) 3.12% of sodium gluconate,

(c) 15.82% of sodium silicate,

(d) 15.30% of sodium hydroxide,

(e) 1.10% of magnesium chloride hexahydrate,

(f)

1.94% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

61.84% of water.

The composition remains homogeneous even after 4 months storage.

The procedure of Example 1 is repeated, except for adding to solution (B) 10% of an aqueous solution containing, in addition to phosphorous acid and acetic anhydride, 83% of a mixture of phosphorus trichloride, acetic acid and acetic anhydride obtained in aqueous medium from monomeric and oligomeric compounds of formula (12), wherein Y.sub.3 is acetyl, to give 1033 parts of a composition comprising

(a) 1.67% of a mixture of monomeric and oligomeric compounds of formula (12), wherein Y.sub.3 is acetyl,

(b) 3.12% of sodium gluconate,

(c) 15.82% of sodium silicate,

(d) 15.30% of sodium hydroxide,

(e) 1.10% of magnesium chloride hexahydrate,

(f)

1.94% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

61.05% of water.

The composition remains homogeneous even after 4 months storage.

With stirring, 12 parts of potassium hydroxide and then 50 parts of sodium hydroxide are dissolved over 10 minutes in 670 parts of a solution (A) consisting of

93 parts of water,

24 parts of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

553 parts of a 35% aqueous solution of sodium silicate (SiO.sub.2 content: 26%),

whereupon the temperature rises to 55.degree. C. To the reaction mixture are then added, with stirring, 208 parts of a solution (B) consisting of

5.8% of a 50% aqueous solution of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

15.5% of sodium gluconate,

5.5% of magnesium chloride hexahydrate, and

73.2% of water.

After the addition of solution (B), the temperature of the reaction mixture is 50.degree. C. Then 60 parts of sodium hydroxide are dissolved in the reaction mixture over 10 minutes, whereupon the temperature rises to 68.degree. C. The mixture is cooled to 20.degree. C., affording 1000 parts of a composition comprising

(a) 0.60% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl

(b) 3.22% of sodium gluconate,

(c) 19.36% of sodium silicate,

(d.sub.1) 1.20% of potassium hydroxide,

(d.sub.2) 11.00% of sodium hydroxide,

(e) 1.14% of magnesium chloride hexahydrate,

(f)

2.40% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

61.08% of water.

The composition is still homogeneous after 3 months storage at room temperature.

The procedure of Example 4 is repeated, except for using 1.2% of sodium hydroxide as component (d.sub.1) instead of 1.2% of potassium hydroxide, affording 1000 parts of a composition comprising

(a) 0.60% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

(b) 3.22% of sodium gluconate,

(c) 19.36% of sodium silicate,

(d) 12.20% of sodium hydroxide,

(e) 1.14% of magnesium chloride hexahydrate,

(f)

2.40% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

61.08% of water.

The composition has good storage stability.

The procedure of Example 4 is repeated, except for using the same amount of sodium glucoheptonate as component (b) instead of sodium gluconate, to give 1000 parts of a composition comprising

(a) 0.60% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

(b) 3.22% of sodium glucoheptonate

(c) 19.36% of sodium silicate,

(d.sub.1) 1.2% potassium hydroxide

(d.sub.2) 11.0% sodium hydroxide

(e) 1.14% of magnesium chloride hexahydrate,

(f)

2.40% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

61.08% of water.

The composition is still homogeneous after 2 months storage at room temperature.

A composition with comparably good storage stability is obtained by replacing sodium gluconate as component (b) in Examples 1 to 6 by sorbitol, mannitol or xylitol.

The procedure of Example 4 is repeated, except for replacing magnesium chloride heptahydrate as component (e) by magnesium acetate tetrahydrate or magnesium sulfate heptahydrate. Compositions of comparably good storage stability are obtained.

With stirring, 10 parts of potassium hydroxide and then 35 parts of sodium hydroxide are added over 10 minutes to 670 parts of a solution (A) consisting of

574 parts of water

5 parts of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

143 parts of a 35% aqueous solution of sodium silicate (SiO.sub.2 content: 26%).

whereupon the reaction mixture exotherms to 55.degree.-60.degree. C. To the reaction mixture are then added, with stirring, 208 parts of a solution (B) consisting of

0.97% of a 50% aqueous solution of the monomeric compound of formula (8), wherein R.sub.2 is methyl,

1.93% of sodium gluconate,

0.24% of magnesium chloride hexahydrate, and

96.86% of water.

After the addition of solution (B), the temperature of the reaction mixture is 50.degree. C. Then 45 parts of sodium hydroxide are dissolved over 10 minutes in the reaction mixture, whereupon the temperature rises to 68.degree.-70.degree. C. The reaction mixture is then cooled to 20.degree. C., affording 1000 parts of a clear, low-viscosity composition comprising

(a) 0.1% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

(b) 0.4% of sodium gluconate,

(c) 5.0% of sodium silicate,

(d.sub.1) 1.0% of potassium hydroxide,

(d.sub.2) 8.0% of sodium hydroxide,

(e) 0.05% of magnesium chloride hexahydrate,

(f)

2.4% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

94.85% of water.

The composition has good storage stability.

With stirring, 20 parts of potassium hydroxide and then 85 parts of sodium hydroxide are added over 10 minutes to 630 parts of a solution (A) consisting of

28 parts of water

30 parts of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

572 parts of a 35% aqueous solution of sodium silicate (SiO.sub.2 content: 26%),

whereupon the reaction mixture exotherms to 55.degree.-60.degree. C. To the reaction mixture are then added, with stirring, 208 parts of a solution (B) consisting of

19.23% of a 50% aqueous solution of the monomeric compound of formula (8), wherein R.sub.2 is methyl,

38.46% of sodium gluconate,

9.61% of magnesium chloride hexahydrate, and

32.7% of water.

After the addition of solution (B), the temperature of the reaction mixture is 55.degree. C. Then 105 parts of sodium hydroxide are dissolved over 10 minutes in the reaction mixture, whereupon the temperature rises to 70.degree. C. The reaction mixture is then cooled to 20.degree. C., affording 1048 parts of the following composition in the form of a pourable paste and comprising

(a) 2.00% of the oligomeric compound of formula (8), wherein R.sub.2 is methyl,

(b) 8.0% of sodium gluconate,

(c) 20.00% of sodium silicate,

(d.sub.1) 2.0% of potassium hydroxide,

(d.sub.2) 19.00% of sodium hydroxide,

(e) 2.00% of magnesium chloride hexahydrate,

(f)

3.00% of the disodium salt of a 1-benzyl-2-heptadecylbenzimidazoledisulfonic acid, and

44.00% of water.

Natural cotton fabric is padded with an aqueous bleaching liquor containing

25 g/l of the aqueous composition of Example 1,

1.6 g/l of sodium pentadecane-1-sulfonate,

0.5 g/l of an adduct of 4 moles of ethylene oxide and 1 mole of a mixture of decyl and lauryl alcohol, and

20 m/l of an aqueous 35% solution of hydrogen peroxide,

and pinched off to a pick-up 100%. The fabric is then steamed for 10 minutes at 100.degree. C. and immediately afterwards rinsed first with hot water (90.degree. to 98.degree. C.) and then with cold water. The fabric is then neutralised by washing off with a dilute aqueous solution of acetic acid, wrung out and finally dried at 100.degree. C.

The treated cotton fabric is free from husks and has an excellent rewettability of 2.5 s/l cm according to DIN 53924. The increase in whiteness of the bleached fabric compared with the untreated fabric before bleaching is determined by the CIBA-GEIGY whiteness scale [q.v. R. Griesser, "Tensile Detergents", Vol. 12, No. 2, pp. 93-100 (1975)]. The untreated fabric has a value of -38, compared with a value of +58 for the bleached fabric. The average degree of polymerisation of the bleached fabric is only insignificantly lower than that of the unbleached fabric. After treatment the residual peroxide content is still 29%. This bleaching liquor can be used for further bleaching treatments. The liquor can normally no longer be used if the concentration of hydrogen peroxide has fallen to below 20%. However, if a composition that does not contain a magnesium complex of components (a) and (e) is not added to the bleaching liquor, then the hydrogen peroxide present in the liquor will decompose almost completely. The residual peroxide content after bleaching will in this case be only 2%.

Similar results are also obtained by adding 25 g of the composition of Example 2 or 3 to the bleaching bath, or by padding desized, still moist cotton fabric wet in wet with an aqueous concentrated bleaching liquor to a pick-up of 20%, which liquor contains 125 g/l of the aqueous composition of Example 1, 2 or 3 and 100 ml/l of 35% aqueous solution of hydrogen peroxide, and subsequently steaming, rinsing, neutralising, wringing out and drying the fabric as described above.

Natural cotton fabric is treated on a winch beck by the exhaust method in a liquor to goods ratio of 1:40 for 15 minutes at 90.degree. C. in a bleaching liquor containing

12 g/l of the aqueous composition of Example 1,

2 g/l of sodium hydroxide,

0.3 g/l of sodium pentadecane-1-sulfonate,

0.1 g/l of an adduct of 4 moles of ethylene oxide and 1 mole of a mixture of decyl and lauryl alcohol, and

20 m/l of a 35% aqueous solution of hydrogen peroxide,

and subsequently rinsed, neutralised, wrung out and dried the fabric as described in Example 10.

The bleached fabric is free from husks. The degree of whiteness before bleaching is -40 and is +69 after treatment. The residual peroxide content after bleaching is 46%.

Comparable results are obtained by adding 12 g of the composition of Example 2 or 3 to the bleaching liquor.

Natural cotton fabric is padded to a pick-up of 100% with an aqueous bleaching liquor containing

25 g/l of the composition of Example 1,

7 g/l of sodium hydroxide,

1.6 g/l of sodium pentadecane-1-disulfonate,

0.5 g/l of an adduct of 4 moles of ethylene oxide and 1 mole of a mixture of decyl and lauryl alcohol, and

50 ml/l of a 35% aqueous solution of hydrogen peroxide.

The impregnated fabric is rolled up and packed airtight in plastic sheeting and stored for 24 hours at room temperature (15.degree.-25.degree. C.), and then rinsed, neutralised, wrung out and dried as described in Example 10.

The bleached fabric is free from husks. The degree of whiteness before bleaching is -77 and is +53 after treatment. The residual peroxide content after bleaching is 53%.

Comparable results are obtained by adding 25 g of the composition of Example 2 or 3 to the bleaching liquor.

An untreated cotton/polyester blend (35:65) is impregnated in a bleaching bath containing

25 g/l of the aqueous composition of Example 4,

20 ml/l of a 35% aqueous solution of hydrogen peroxide,

1.6 g/l of sodium pentadecane-1-sulfonate, and

0.5 g/l of an adduct of 4 moles of ethylene oxide and 1 mole of a mixture of decyl and lauryl alcohol,

and pinched off to a pick-up of 90%.

The impregnated fabric is then steamed for 5 minutes at 100.degree. C. and subsequently washed for 1 minute hot and 1 minute cold, neutralised and dried.

The degree of whiteness of the treated blend is increased by the bleaching process from 0 to 55 CIBA-GEIGY whiteness units. After treatment, the hydrogen peroxide content is still 58% of the original value.

The bleached fabric is virtually undamaged by the bleaching process. The average degree of polymerisation is 2760 before bleaching and 2690 after bleaching.