US2730428A - Method and composition for washing and bleaching fibrous materials - Google Patents

Method and composition for washing and bleaching fibrous materials Download PDF

Info

Publication number
US2730428A
US2730428A US251623A US25162351A US2730428A US 2730428 A US2730428 A US 2730428A US 251623 A US251623 A US 251623A US 25162351 A US25162351 A US 25162351A US 2730428 A US2730428 A US 2730428A
Authority
US
United States
Prior art keywords
washing
bleaching
sodium
oxygen
fibrous materials
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US251623A
Inventor
Lindner Kurt
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
"tepha" Gesellschaft fur Pharmazeutische und Chemisch-Technische Erzeugnisse M B H
TEPHA GES fur PHARMAZEUTISCHE
Original Assignee
TEPHA GES fur PHARMAZEUTISCHE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by TEPHA GES fur PHARMAZEUTISCHE filed Critical TEPHA GES fur PHARMAZEUTISCHE
Application granted granted Critical
Publication of US2730428A publication Critical patent/US2730428A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/042Acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • C11D3/349Organic compounds containing sulfur additionally containing nitrogen atoms, e.g. nitro, nitroso, amino, imino, nitrilo, nitrile groups containing compounds or their derivatives or thio urea
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/30Organic compounds, e.g. vitamins containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/32Organic compounds, e.g. vitamins containing sulfur
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/40Proteins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06LDRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/10Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
    • D06L4/12Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives

Definitions

  • This invention relates to the manufacture of washing and bleaching materials containing active protecting agents whereby the S02 group is directly linked with a nitrogen atom of a basic nitrogen group.
  • the main object of the invention is to improve the quality of washing and 'bleac'hing materials containing active protecting agents selected from the class SOzN, SO2NH, SO2NH2.
  • a further object is the preparation of washing and bleaching materials for a careful treatment of artificial, animal or vegetable fibresor fabrics made therefrom.
  • Animal fibres as for instance silk, wool, crude skins or furs, feathers and artificial fibres, particularly those of the polyamide type, are also often subjected to washing and bleaching processes and tend to decay when treated with peroxygen compounds. These attacks are particularly harmful when alkaline Washing and bleaching materials are used because the generation of oxygen by hydrogen peroxide or other peroxygen compounds is irregular and violent in alkaline media.
  • alkali carbonates In alkaline washing materials ammonia, alkali carbonates, alkali hydroxides, alkali orthophosphates, alkali silicates may conventionally be used.
  • alkalis other bleaching and water softening agents such as anhydrous phosphates, for instance, sodium pyrophos- .phate, sodium tripolyphosphate, sodium tetrapolyphosphate, sodium hexametaphosphate or higher polymer alkali metaphosphates mayalso' be present in the conven- States Patent Cir tional washing and bleaching materials.
  • anhydrous phosphates for instance, sodium pyrophos- .phate, sodium tripolyphosphate, sodium tetrapolyphosphate, sodium hexametaphosphate or higher polymer alkali metaphosphates mayalso' be present in the conven- States Patent Cir tional washing and bleaching materials.
  • soap or other surface active substances is indispensable, for example, fatty alcohol sulfonates, alkyl sulfonates, alkyl aryl sulfonates, fatty acid condensation products or reaction products of ethylene oxide and alkyl phenoles, fatty acids, fatty alcohols or the like, It has been observed that even these surface active agents sometimes attack these fibres in alkaline Washing and bleaching solutions.
  • stabilizing and active protecting agents contain the group SOzN or SOzNI-I or SO2NH2. They may be of an inorganic or organic nature; the organic compounds belong to the aliphatic, cyclo aliphatic, aromatic or heterocyclic type. The majority of these agents are water soluble in an alkaline medium. The water solubility, however, is not indispensable because even water insoluble agents of the types according to the invention may exert a stabilizing and protecting effect when used in finely divided form.
  • the useful agents of the inorganic type are:
  • Nitrilo sulfonic acid Imido sulfonic acid Amido sulfonic acid Hydroxyl amin mono-sulfonic acid Hydroxylamin disulfonic acid Hydrazin monosulfonic acid or their respective salts; compositions of sulfamides or sulfimides are also suitable.
  • the useful organic agents are characterized by a S02 group directly linked with a nitrogen atom, for example, benzene sulfamide or other aliphatic, cyclo aliphatic or aromatic sulfamides, formed by a reaction of sulfonic acid chlorides with ammonia and primary or secondary amines respectively.
  • a nitrogen atom for example, benzene sulfamide or other aliphatic, cyclo aliphatic or aromatic sulfamides, formed by a reaction of sulfonic acid chlorides with ammonia and primary or secondary amines respectively.
  • the higher molecular alkyl aryl sulfamides as for instance, dodecyl benzene sulfamide.
  • Even the complex therapeutically valuable sulfonamides for instance, sulfam'l amidotbiazol, 2-sulfonamidopyridine or para-amino benzene sulfacetylamide may be used.
  • sulfochlorides with amino phenols, amino carhoxylic acids or other amino compounds have the same properties as the described active protecting agents and may be used according to this invention; for example, the reaction prod ucts of sulfonic acids chlorides with amino acids, i. e. glycocoll, alanine, lysine, sarcosine; or high molecular amino acids or polypeptides as albumin decomposition products. Condensation products of an albuminous matter may also be employed according to the invention. Low molecular as well as high molecular sulfochlorides may be used accordingly.
  • condensation products of an albuminous matter may be used together with higher molecular sulfonic or sulfinic acids, for instance, paraffine sulfonic acids or alkyl aryl sulfonic acids; the aliphatic hydrocarbon chains of the latter acids correspond to those of the soap forming fatty acids and contain about 8 to 20 C atoms.
  • These condensation products which may be used preferably in the form of their alkali salts are specially characterized bythe fact that they not only possess fibre protecting and stabilizing but also surface active and protective colloidal qualities. These products form soaplike aqueous strongly foaming solutions which have a considerable washing and dispersing effect.
  • one liter of the washing liquid contains about 3.5 grs. of soda, 1 g. of sodium metasilicate and 1 g. of an active substance in the form of the sodium salt of dodecylbenzenesulfonic acid or in the form of a fatty alcohol sulfonate.
  • the protection against the fibre weakening influence of oxygen is carried out by an addition of about 0.2 g. of paraarninobenzenesulfoneacetylamide per liter of the washing liquid.
  • the white linen goods which may also be mixed with staple fibre are then subjected to a boil washing process which may be repeated frequently, if desired, without leading to damages of the fibre.
  • the washing process may also be accomplished in the presence of 0.7 g. of sodium percarbonate or sodium perborate per liter of the washing liquid. No deleterious effect on the goods could be observed although even traces of copper were present in the washing liquid.
  • a washing powder is mixed which consists in about 56.0% of soda, of water glass, 1.5% of cellulose sodiumglycolate, 10% of sodium perborate and 28% of a neutralized condensation product of paraflinesulfochloride and a moderately decomposed skin albumin. 5 grs. of this washing powder are dissolved in a washing liquid. Steeped white linen was boiled as usually in this washing liquid. The cleansing and, bleaching eiicct was very good and a weakening of the strength of the fibre eventually caused by the attack of active oxygen could not be observed.
  • washing powder which contains about of calc. soda, 3.5% of water glass, 1.5% of cellulosesodiumglycolate, 24% of a neutralized condensation product of alkylarylsulfochloride- (12 to 16 C atoms) and a split off product of albumin of a moderate grade of cleavage, 9.0% of sodium percarbonate and 12.0% of sodium perpyrophosphate.
  • the thus manufactured washing powder was used according to Example 6 for the laundering of linen. The protection against a deteriorating attack on the fibres was increased as compared with the composition of the washing powder described in the foregoing example.
  • sodium pyrophosphate sodium tripolyphosphate or sodium hexametaphosphate may also be employed.
  • a mixture of 40 parts by weight of sodium pyrophosphate, 30 parts by weight of sodium percarbonate and 30 parts by weight of an albumine sulfonicacid condensate or an albumin sulfinic acid condensate is utilized in a concentration of 2 to 3 grs. per liter as a pre-cleansing, desizing or bleaching treatment of yarn, fabrics or tricot made from cotton, viscose rayon, copper rayon or acetate rayon.
  • the treatment starts with a temperature of about 30 C. and is gradually continued until a temperature of about to C. is obtained. Weakening of the fibres caused by oxidation is not to be feared.
  • a method for washing and bleaching fibrous materials susceptible to attack by oxygen in alkaline washing liquids which comprises washing and bleaching such materials in an alkaline washing liquid containing an active oxygen evolving compound and a protective compound containing an S02 radical connected directly with a nitrogen atom of a basic nitrogen group selected from the group consisting of sulfonamides of amino carboxylic acids, peptides and albumen cleavage products.
  • pro.- tective compound is a sulfonamide of an amino carboxylic acid.
  • said protective compound is an alkyl sulfonamide of an albumen cleavage product, the alkyl group of which contains 8 to 20 carbon atoms.

Description

lVIETI-IOD AND COMPOSITION FOR WASHING AND BLEACHING FIBROUS MATERIALS No Drawing. Application October 16, 1951,
' Serial No. 251,623
Claims priority, application Germany October 21, 1950 Claims. (Cl. 8-133) This invention relates to the manufacture of washing and bleaching materials containing active protecting agents whereby the S02 group is directly linked with a nitrogen atom of a basic nitrogen group.
The main object of the invention is to improve the quality of washing and 'bleac'hing materials containing active protecting agents selected from the class SOzN, SO2NH, SO2NH2. A further object is the preparation of washing and bleaching materials for a careful treatment of artificial, animal or vegetable fibresor fabrics made therefrom.
It is a further object of the invention to manufacture a washing and bleaching material having an alkaline reaction. Still other objects will-appear hereinafter.
.It has hitherto been proposed to subject textile fibres, yarns, fabrics or tricot of vegetable origin such as cotton, linen, jute fibre, ramie fibre or the like; or of artificial origin such as cellulosic material, staple fibre or rayon in wet processes to a treatment with active oxygen evolving compounds as, for instance, hydrogen peroxide, perborate, percarbonate or oxygen generating compounds such as bleaching powder, alkali hypochlorite or the like. Other oxygen evolving or generating compounds are sodium peroxide, perborates, percarbonates, perpyrophosphates but also chlorine bleaching agents, potassium permanganate or the like. The attack of the bleachingagent on the fibres results in the formation of oxycellulose or in a depolymerization of the cellulose leading to a loss of strength and Weight. In washing and bleaching processes of household linen where oxygen is evolved or generated in the washing liquid by means of the so-called automatid washing materials, the same damages will be observed, especially after repeated treatments with these washing materials.
Even the atmospheric oxygen contained in the washing and bleaching baths exerts a slight attack on the fibres. This is probably due to the presence of traces of catalytically active metal compounds, such as for instance, copper, iron and manganese which are contained in the water or in the chemicals used.
Animal fibres, as for instance silk, wool, crude skins or furs, feathers and artificial fibres, particularly those of the polyamide type, are also often subjected to washing and bleaching processes and tend to decay when treated with peroxygen compounds. These attacks are particularly harmful when alkaline Washing and bleaching materials are used because the generation of oxygen by hydrogen peroxide or other peroxygen compounds is irregular and violent in alkaline media.
In alkaline washing materials ammonia, alkali carbonates, alkali hydroxides, alkali orthophosphates, alkali silicates may conventionally be used. Besides these alkalis other bleaching and water softening agents such as anhydrous phosphates, for instance, sodium pyrophos- .phate, sodium tripolyphosphate, sodium tetrapolyphosphate, sodium hexametaphosphate or higher polymer alkali metaphosphates mayalso' be present in the conven- States Patent Cir tional washing and bleaching materials. In the washingprocess the presence of soap or other surface active substances is indispensable, for example, fatty alcohol sulfonates, alkyl sulfonates, alkyl aryl sulfonates, fatty acid condensation products or reaction products of ethylene oxide and alkyl phenoles, fatty acids, fatty alcohols or the like, It has been observed that even these surface active agents sometimes attack these fibres in alkaline Washing and bleaching solutions.
In accordance with the invention it was found that compounds containing the S02 group directly linked with a N- atom are of particular advantage when used in a combined operation with the conventional bleaching and washing agents because the undesired generation of oxygen is stopped and the washing and bleaching processes may easily be controlled without an attack on the fibre. Very small amounts of these compounds are already effective but acting as detergents themselves they may also be used in larger quantities.
These stabilizing and active protecting agents contain the group SOzN or SOzNI-I or SO2NH2. They may be of an inorganic or organic nature; the organic compounds belong to the aliphatic, cyclo aliphatic, aromatic or heterocyclic type. The majority of these agents are water soluble in an alkaline medium. The water solubility, however, is not indispensable because even water insoluble agents of the types according to the invention may exert a stabilizing and protecting effect when used in finely divided form.
The useful agents of the inorganic type are:
Nitrilo sulfonic acid Imido sulfonic acid Amido sulfonic acid Hydroxyl amin mono-sulfonic acid Hydroxylamin disulfonic acid Hydrazin monosulfonic acid or their respective salts; compositions of sulfamides or sulfimides are also suitable.
The useful organic agents are characterized by a S02 group directly linked with a nitrogen atom, for example, benzene sulfamide or other aliphatic, cyclo aliphatic or aromatic sulfamides, formed by a reaction of sulfonic acid chlorides with ammonia and primary or secondary amines respectively. Of particular interest are the higher molecular alkyl aryl sulfamides, as for instance, dodecyl benzene sulfamide. Even the complex therapeutically valuable sulfonamides, for instance, sulfam'l amidotbiazol, 2-sulfonamidopyridine or para-amino benzene sulfacetylamide may be used. Owing to the strongly negative character or" the R-S0z=group nearly al these sulfonamides are soluble in aqueous alkaline solutions.
It was also discovered that condensation products U1.
sulfochlorides with amino phenols, amino carhoxylic acids or other amino compounds have the same properties as the described active protecting agents and may be used according to this invention; for example, the reaction prod ucts of sulfonic acids chlorides with amino acids, i. e. glycocoll, alanine, lysine, sarcosine; or high molecular amino acids or polypeptides as albumin decomposition products. Condensation products of an albuminous matter may also be employed according to the invention. Low molecular as well as high molecular sulfochlorides may be used accordingly.
In a preferred embodiment of the present invention condensation products of an albuminous matter may be used together with higher molecular sulfonic or sulfinic acids, for instance, paraffine sulfonic acids or alkyl aryl sulfonic acids; the aliphatic hydrocarbon chains of the latter acids correspond to those of the soap forming fatty acids and contain about 8 to 20 C atoms. These condensation products which may be used preferably in the form of their alkali salts are specially characterized bythe fact that they not only possess fibre protecting and stabilizing but also surface active and protective colloidal qualities. These products form soaplike aqueous strongly foaming solutions which have a considerable washing and dispersing effect.
The following examples are illustrative of my invention:
1. 1 liter of a washing bath containing about 4.5 grs. of soda, 1.2 gm. of waterglass, 1.6 grs. of a 62% alkyl sulfonate preparation and about 0.07 g. of active oxygen in the form of hydrogen peroxide is efiiciently protected by an addition of about 0.1 g. of amidosulfonic acid. The washing liquid is therefore perfectly suited for a normal household boil washing process-whereby even mixed fabrics containing staple fibre may be laundered. Instead of amidosulfonic acid imidosulfonic acid or nitrilosulfonic acid and their sodium or ammonium salts may also be used.
2. In a laundry where the washing process is, for instance, carried out in a copper washing boiler one liter of the washing liquid contains about 3.5 grs. of soda, 1 g. of sodium metasilicate and 1 g. of an active substance in the form of the sodium salt of dodecylbenzenesulfonic acid or in the form of a fatty alcohol sulfonate. The protection against the fibre weakening influence of oxygen is carried out by an addition of about 0.2 g. of paraarninobenzenesulfoneacetylamide per liter of the washing liquid. The white linen goods which may also be mixed with staple fibre are then subjected to a boil washing process which may be repeated frequently, if desired, without leading to damages of the fibre. The washing process may also be accomplished in the presence of 0.7 g. of sodium percarbonate or sodium perborate per liter of the washing liquid. No deleterious effect on the goods could be observed although even traces of copper were present in the washing liquid.
3. After a normal boil Washing process the linen goods are rinsed and subjected to a mild bleaching aftertreatmerit in a warm solution containing about 0.8 g. of sodium perborate, 0.5 g. of sodium tetra polyphosphate and 0.1 g. of benzenesulfamide per liter of the washing liquid. Even delicate and fine fabrics withstood this treatment practically unharmed.
4. Mixed fabrics of staple fibre and cotton or staple fibre and wool or staple fibre and silk are subjected to a bleaching treatment with a solution containing about cc. of a hydrogen peroxide, 2 grs. of sodium pyrophosphate and 0.5 g. of a condensation product of an alkylsulfochloride with 12 to 16 C atoms in the alkyl rest and the sodium salt of methyl-aminoacetic acid. I The bleaching process is carried out within a period of 4 to 6 hours at a temperature of about 30 to C.
5. White or yellowish tinged goat skins are subjected to a clipping bleaching process whereby 60 cc. of hydrogen peroxide 30% per liter are used. This bleaching solutionv was buffered at a pH of 8 with ammonia. To this solution 1 g. per liter of a condensation product of an alkylated sulfochloridepeptide was added as a protective medium. After a treatment of 4 to 6 hours at a temperature of 30 to 35 C. the animal hairs are thoroughly bleached without involving a deterioration of the hair or the skin fibres. No carroting process is hereby necessary.
6. In a suitable mixer a washing powder is mixed which consists in about 56.0% of soda, of water glass, 1.5% of cellulose sodiumglycolate, 10% of sodium perborate and 28% of a neutralized condensation product of paraflinesulfochloride and a moderately decomposed skin albumin. 5 grs. of this washing powder are dissolved in a washing liquid. Steeped white linen was boiled as usually in this washing liquid. The cleansing and, bleaching eiicct was very good and a weakening of the strength of the fibre eventually caused by the attack of active oxygen could not be observed.
7. In a suitable mixera washing powder is manufactured which contains about of calc. soda, 3.5% of water glass, 1.5% of cellulosesodiumglycolate, 24% of a neutralized condensation product of alkylarylsulfochloride- (12 to 16 C atoms) and a split off product of albumin of a moderate grade of cleavage, 9.0% of sodium percarbonate and 12.0% of sodium perpyrophosphate. The thus manufactured washing powder was used according to Example 6 for the laundering of linen. The protection against a deteriorating attack on the fibres was increased as compared with the composition of the washing powder described in the foregoing example. Instead of sodium pyrophosphate sodium tripolyphosphate or sodium hexametaphosphate may also be employed.
8. A mixture of 40 parts by weight of sodium pyrophosphate, 30 parts by weight of sodium percarbonate and 30 parts by weight of an albumine sulfonicacid condensate or an albumin sulfinic acid condensate is utilized in a concentration of 2 to 3 grs. per liter as a pre-cleansing, desizing or bleaching treatment of yarn, fabrics or tricot made from cotton, viscose rayon, copper rayon or acetate rayon. The treatment starts with a temperature of about 30 C. and is gradually continued until a temperature of about to C. is obtained. Weakening of the fibres caused by oxidation is not to be feared.
9. Mixed textures of staple fibre and cotton or staple fibre and Wool or staple fibre and silk were bleached in a solution of hydrogen peroxide containing about 25 grs. of hydrogen peroxide 30%, 2 grs. of sodium pyrophosphate and l g. of sulfinic acid albumin condensate per liter. Instead of this condensation product a mixture of 50 parts by weight of this condensation product and 50 parts by weight of the sodium salt of dodecyl sulfonic acid may also be utilized.
It will be understood that wide latitude is permissible in the practice of the invention as special bleaching and oxidation processes according to the invention do not only take place in washing or color lightening but may also be combined with desizing processes, or dyeing and calico printing or with an aftertreatrnent of the fibres after dyeing and calico printing and the like. Following a bleaching process with chlorine oxygen containing solutions according to the invention may be used as an anti chlorine means. In all these cases the active protecting agents as described in the present invention have been found eminently suitable as to the desired purposes.
The terms and expressions used herein are to be regarded as terms of description and not of limitation.
What I claim is:
l. A method for washing and bleaching fibrous materials susceptible to attack by oxygen in alkaline washing liquids which comprises washing and bleaching such materials in an alkaline washing liquid containing an active oxygen evolving compound and a protective compound containing an S02 radical connected directly with a nitrogen atom of a basic nitrogen group selected from the group consisting of sulfonamides of amino carboxylic acids, peptides and albumen cleavage products.
2. A method according to claim 1, in which said active oxygen evolving compound is a peroxygen compound.
3. A method according to claim 2, in which said alkaline washing liquid contains an alkali metal phosphate.
4-. A method according to claim 1, in which said pro.- tective compound is a sulfonamide of an amino carboxylic acid.
5. A method according to claim 1, in which said protective compound is a sulfonamide of a peptide.
6. A method according to claim 1, in which said protective compound is a sulfonamide of an albumen cleavage product.
7. A method according to claim 1, in which said protective compound is an alkyl sulfonamide of an albumen cleavage product, the alkyl group of which contains 8 to 20 carbon atoms.
8. A method according to claim 1, in which said protective compound'is an alkyl aryl sulfonamide of an al- References Cited in the file of this patent UNITED STATES PATENTS 1,927,363 Freiberger -i Sept. 19, 1933 1,980,414 Lindner Nov. 13, 1934r by Alkalis." and 58.
6 Zabel Feb. 12, Zabel Mar. 10, Steindorff Sept. 3, Kamlet Sept. 9,
FOREIGN PATENTS Switzerland Aug. 16, Great Britain Sept. 12, Germany Dec. 29, Great Britain Aug. 28, Germany Oct. 5, France June 10,
OTHER REFERENCES Trotman: Protection of Woolen Goods From Damage Textile Recorder, June 15, 1928, pgs. 57

Claims (1)

1. THE METHOD FOR WASHING AND BLEACHING FIBROUS MATERIALS SUSCEPTIBLE TO ATTACK BY OXYGEN IN ALKALINE WASHING LIQUIDS WHICH COMPRISES WASHING AND BLEACHING SUCH MATERIALS IN AN ALKALINE WASHING LIQUID CONTAINING AN ACTIVE OXYGEN EVOLVING COMPOUND AND A PROTECTIVE COMPOUND CONTAINING AN SO2 RADICAL CONNECTED DIRECTLY WITH A NITROGEN ATOM OF A BASIC NITROGEN GROUP SELECTED FROM THE GROUP CONSISTING OF SULFONAMIDES OF AMINO CARBOXYLIC ACIDS, PEPTIDES AND ALBUMEN CLEAVAGE PRODUCTS.
US251623A 1950-10-21 1951-10-16 Method and composition for washing and bleaching fibrous materials Expired - Lifetime US2730428A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2730428X 1950-10-21

Publications (1)

Publication Number Publication Date
US2730428A true US2730428A (en) 1956-01-10

Family

ID=7997355

Family Applications (1)

Application Number Title Priority Date Filing Date
US251623A Expired - Lifetime US2730428A (en) 1950-10-21 1951-10-16 Method and composition for washing and bleaching fibrous materials

Country Status (1)

Country Link
US (1) US2730428A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2898181A (en) * 1953-05-20 1959-08-04 Degussa Process for washing and bleaching compositions therefor
US2909404A (en) * 1953-03-12 1959-10-20 Degussa Protection of polyamide fibers during treatment with peroxide containing bleaching or washing agents
US2927840A (en) * 1955-07-08 1960-03-08 Degussa Process for the treatment of fibrous materials
US3131991A (en) * 1960-07-07 1964-05-05 Henkel & Cie Gmbh Washing and bleaching
US3173749A (en) * 1957-07-05 1965-03-16 Bayer Ag Process for bleaching with chlorites
US3257324A (en) * 1955-04-20 1966-06-21 Colgate Palmolive Co Solid bleach composition and method of making and using same
US3671439A (en) * 1969-07-22 1972-06-20 American Home Prod Oxygen bleach-activator systems stabilized with puffed borax
US3751222A (en) * 1971-12-13 1973-08-07 Colgate Palmolive Co A process of cleaning cloth
US3990908A (en) * 1975-03-19 1976-11-09 Fmc Corporation Desizing glass fabric with sodium carbonate peroxide desizing solutions
US4073616A (en) * 1975-12-06 1978-02-14 Cassella Farbwerke Mainkur Aktiengesellschaft Oxidative after-treatment of materials dyed or printed with sulfur or vat dyestuffs
US20090092835A1 (en) * 2005-11-01 2009-04-09 Xu Meirong Bast fibers obtained from an extraction and preparation process

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR538492A (en) * 1920-08-04 1922-06-10 Anilin Fabrikation Ag Process for protecting animal fiber against the harmful influence of alkaline solutions
DE387594C (en) * 1922-06-02 1923-12-29 Anilin Fabrikation Ag Modification of the procedure for the protection of animal fibers when treated with alkaline liquids
DE434979C (en) * 1923-12-21 1926-10-05 J G Farbenindustrie Akt Ges Process for the protection of animal fibers when treated with alkaline liquids
GB380851A (en) * 1931-04-10 1932-09-12 James Yate Johnson Improvements in the manufacture and production of assistants in the textile and related industries and dispersing agents
US1927363A (en) * 1927-12-23 1933-09-19 Freiberger Moritz Process of treating vegetable or artificial fibers or fiber material
GB415718A (en) * 1932-02-29 1934-08-28 Ig Farbenindustrie Ag Process for the manufacture of acid amide derivatives
US1980414A (en) * 1934-11-13 Process for the production of sul
US1990852A (en) * 1935-02-12 Process of producing prints or dis
US2033219A (en) * 1933-03-25 1936-03-10 Gen Aniline Works Inc Treating cellulose esters
CH197839A (en) * 1937-05-10 1938-05-31 Chem Ind Basel Process for stabilizing alkaline superoxide baths.
US2213477A (en) * 1935-12-12 1940-09-03 Gen Aniline & Film Corp Glycol and polyglycol ethers of isocyclic hydroxyl compounds
US2427097A (en) * 1944-08-23 1947-09-09 Kamlet Jonas Shrinkproofing and feltproofing of keratinous textile fibers

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1980414A (en) * 1934-11-13 Process for the production of sul
US1990852A (en) * 1935-02-12 Process of producing prints or dis
FR538492A (en) * 1920-08-04 1922-06-10 Anilin Fabrikation Ag Process for protecting animal fiber against the harmful influence of alkaline solutions
DE387594C (en) * 1922-06-02 1923-12-29 Anilin Fabrikation Ag Modification of the procedure for the protection of animal fibers when treated with alkaline liquids
DE434979C (en) * 1923-12-21 1926-10-05 J G Farbenindustrie Akt Ges Process for the protection of animal fibers when treated with alkaline liquids
US1927363A (en) * 1927-12-23 1933-09-19 Freiberger Moritz Process of treating vegetable or artificial fibers or fiber material
GB380851A (en) * 1931-04-10 1932-09-12 James Yate Johnson Improvements in the manufacture and production of assistants in the textile and related industries and dispersing agents
GB415718A (en) * 1932-02-29 1934-08-28 Ig Farbenindustrie Ag Process for the manufacture of acid amide derivatives
US2033219A (en) * 1933-03-25 1936-03-10 Gen Aniline Works Inc Treating cellulose esters
US2213477A (en) * 1935-12-12 1940-09-03 Gen Aniline & Film Corp Glycol and polyglycol ethers of isocyclic hydroxyl compounds
CH197839A (en) * 1937-05-10 1938-05-31 Chem Ind Basel Process for stabilizing alkaline superoxide baths.
US2427097A (en) * 1944-08-23 1947-09-09 Kamlet Jonas Shrinkproofing and feltproofing of keratinous textile fibers

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2909404A (en) * 1953-03-12 1959-10-20 Degussa Protection of polyamide fibers during treatment with peroxide containing bleaching or washing agents
US3153565A (en) * 1953-03-12 1964-10-20 Degussa Process for the treatment of synthetic linear polycarbonamide textile fibers
US2898181A (en) * 1953-05-20 1959-08-04 Degussa Process for washing and bleaching compositions therefor
US3257324A (en) * 1955-04-20 1966-06-21 Colgate Palmolive Co Solid bleach composition and method of making and using same
US2927840A (en) * 1955-07-08 1960-03-08 Degussa Process for the treatment of fibrous materials
US3173749A (en) * 1957-07-05 1965-03-16 Bayer Ag Process for bleaching with chlorites
US3131991A (en) * 1960-07-07 1964-05-05 Henkel & Cie Gmbh Washing and bleaching
US3671439A (en) * 1969-07-22 1972-06-20 American Home Prod Oxygen bleach-activator systems stabilized with puffed borax
US3751222A (en) * 1971-12-13 1973-08-07 Colgate Palmolive Co A process of cleaning cloth
US3990908A (en) * 1975-03-19 1976-11-09 Fmc Corporation Desizing glass fabric with sodium carbonate peroxide desizing solutions
US4073616A (en) * 1975-12-06 1978-02-14 Cassella Farbwerke Mainkur Aktiengesellschaft Oxidative after-treatment of materials dyed or printed with sulfur or vat dyestuffs
US20090092835A1 (en) * 2005-11-01 2009-04-09 Xu Meirong Bast fibers obtained from an extraction and preparation process

Similar Documents

Publication Publication Date Title
US4025453A (en) Activated bleaching process and compositions therefor
US3795625A (en) Bleaching compositions
US2730428A (en) Method and composition for washing and bleaching fibrous materials
CA1105206A (en) Activated bleaching process and compositions therefor
US3211658A (en) Detergent composition with improved bleaching efficiency
US2141189A (en) Bleaching and cleansing compositions
CA1105658A (en) Activated bleaching process and compositions therefor
JPH0457719B2 (en)
US4880566A (en) Silicate-and magnesium-free stabilizer mixtures
DE1816348A1 (en) Washing, bleaching and cleaning agents
US2152520A (en) Bleaching, washing, cleansing, and rinsing agents
FR2463775A1 (en) N- (HYDROMETHYL) -AMINO-ALKANE-DIPHOSPHONIC ACIDS, THEIR USE AS STABILIZERS AND PROCESS FOR BLANCHING CELLULOSIC FIBERS
US3979312A (en) Detergent composition containing novel bleaching agent
US3556711A (en) Peroxymonosulfate compositions containing acylate oxidation promoters,and their use
BE1005650A3 (en) Method for pre-treating cellulosic fibre.
US2820690A (en) Process of bleaching cotton with hydrogen peroxide bleach stabilized with calcium ormagnesium orthophosphate
US4664837A (en) Bleaching and laundering composition containing magnesium monoperoxyphthalate a chelating agent, a peroxygen compound and phthalic anhydride
US2236617A (en) Treatment of textiles
DE1953519A1 (en) Textile treatment agents
US4775382A (en) Process for bleaching household laundry in a wash cycle
GB2110259A (en) Peroxyacid bleaching and laundering composition
US1522561A (en) Bleaching solution
US6605580B2 (en) Bleaching composition
US1075663A (en) Composition of matter.
US4014805A (en) Dry cleaning formulation