US3130164A - Liquid bleaching and detergent composition - Google Patents

Liquid bleaching and detergent composition Download PDF

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Publication number
US3130164A
US3130164A US824800A US82480059A US3130164A US 3130164 A US3130164 A US 3130164A US 824800 A US824800 A US 824800A US 82480059 A US82480059 A US 82480059A US 3130164 A US3130164 A US 3130164A
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US
United States
Prior art keywords
sodium
weight
detergent
alkyl
composition
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
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US824800A
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English (en)
Inventor
Best Georg Peter
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.)
Lever Brothers Co
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Lever Brothers Co
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Filing date
Publication date
Application filed by Lever Brothers Co filed Critical Lever Brothers Co
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Publication of US3130164A publication Critical patent/US3130164A/en
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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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/225Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
    • 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
    • C11D3/3947Liquid compositions
    • 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

  • Concentrated liquid detergent compositions often suffer from the disadvantage that one or more of the components separate out during standing and/ or that a clear solution is not obtained on dilution to the lower concenration employed for actual use.
  • a bleaching agent in a concentrated liquid detergent composition to give a product which will retain its bleaching activity to an acceptable degree on storage and which will therefore compare with the well known solid bleaching detergent compositions, containing sodium perborate or sodium percarbonate, used in certain applications, particularly in the of a stable pourable emulsion, suspension, or coacervate' which contains (a) at least one anionic active detergent A of the general formula:
  • RO.(C,,H O) .SO M in which R is an alkyl radical containing from 6 to 18 carbon atoms or an alkylaryl radical containing from 6 to 18 carbon atoms in the alkyl radical; M is an alkalimetal, ammonium or substituted ammonium radical, preferably sodium; n is 2 or 3, and m is from 1 to 8, preferably 2 to 4; (b) a condensed phosphate; a soil-suspending agent; and (d) hydrogen peroxide.
  • the composition of the invention contains a mixture of detergents A of the general formula given, in which the average value of m is at least 2 and is preferably from 2 to 4.
  • Particularly suitable are the sodium salts of sulphated polyethyleneglycol mono-alkyl ethers of the general formula RO.(C H O) .SO Na, in which R is an alkyl radical with 6 to 12 carbon atoms and m is from 2 to 3, or R is an alkyl radical with 12 to 18 carbon atoms and m is from 3 to 4.
  • Preferred detergents of type A described above include the sodium salt of sulphated diethyleneglycol monolauryl ether, C H CH .O(C H O) .SO Na; the sodium salt of sulphated diethyleneglycol mono-alkyl ether RO.(C H O) SO Na, in which R denotes a mixture of alkyl radicals as these occur in coconut fatty alcohols, the
  • the amount of the condensed phosphates is desirably from 5 to 30%, preferably from 9 to 25%, by weight of the liquid composition.
  • the soil-suspending agent may be, for example a carboxymethylcellulose of any customary degree of substitution, such as 0.4-1.1 carboxymethyl groups per monosaccharide unit, in the conventional small amounts.
  • the composition preferably contains hydrogen peroxide in an amount of 0.5 to 3% by weight of the solution, preferably together with a small amount of a stabiliser for hydrogen peroxide, such as, for example, sodium p-hydroxybenzoate, sodium nitrilotriacetate or sodium ethylenediamine tetra-acetate.
  • a stabiliser for hydrogen peroxide such as, for example, sodium p-hydroxybenzoate, sodium nitrilotriacetate or sodium ethylenediamine tetra-acetate.
  • B may for example be a fatty alkyl sulphate salt with from 8 to 18, preferably about 12, carbon atoms in the molecule, or an alkylaryl sulphonate with from 8 to 16 carbon atoms in the alkyl group, preferably an alkylbenzene sulphonate with about 12 carbon atoms in the alkyl group. Salts of acylated hydroxy or amino sulfonic acids may also be used.
  • Preferred detergents of type B include sodium tetrapropylenebenzene sulphonate, sodium dodecylbenzene sulphonate, sodium pentapropylenebenzene sulphonate, sodium lauryl sulphate and sodium oleyl sulphate.
  • the expressions 5tetrapropylenebenzene and pentapropylenebenzene denote alkylbenzenes in which the alkyl groups are derived from propylene tetramer and propylene pentamer, respectively.
  • the weight ratio A:B is preferably from 1:1 to 1:6, most suitably from 1:2 to 1:4.
  • the active detergents A and B together suitably form from 5 to 25%, preferably from 6 to 20% by weight of the liquid composition.
  • compositions such as fatty acid monoor diethanolamides, optical brighteners and inorganic salts other than condensed phosphates, may be added, subject to the proviso that the compositions should not of course contain ingredients which will react with hydrogen peroxide or catalyse its decomposition on storage. , In particular, the compositions should not contain sodium silicate.
  • liquid bleaching and detergent compositions of the invention in order to ensure that they do not contain matter that is easily oxidised by hydrogen peroxide, all the ingredients may be subjected to an o-xidising pretreatment, preferably with hydrogen peroxide. It is, however, preferred to prepare the composition from untreated ingredients, using a slight excess of hydrogen peroxide. If the composition is then kept for a few weeks, the excess hydrogen peroxide becomes decomposed, but the remainder is surprisingly resistant to decomposition on prolonged storage.
  • the process of destroying easily oxidisable matter by oxidation with the excess hydrogen peroxide may be speeded up so as to o muao 7 L 1 Z 0 L0 0 1 1 F the same 5 1 6:0 n40 0 2 &
  • Example 3 The following compositions were prepared in the same way as in Example 1:
  • compositions of the invention can be effected by incorporating the ingredients (a), (b) and (c) in water, followed by addition of hydrogen peroxide.
  • a suitable procedure is as follows:
  • glycol mouo-lauryl other (A) Sodium salt of sulphated tetraethyleneglycol nonylphcnyl ether (AL. Salts of a protein-fatty acid condensate with bound su yl-hexyl sulphate (B).
  • Benzoyl ester of sodium phenol sul- Water Sodium oleyl sulphate (B) 35 Coconut-oil fatty acid monoethanolam1dc Sodium carboxymethy1cel1ulose Sodium pyrophosphate Sodium tripolyphosphate.
  • Optical brightencrr Hy *ogen per0xide p-Hydroxybenzoic acid Benzoyl ester of sodium 50 Sodium salt of sulphated diethylenc- Sodium eth 55 Why acid diethenolamide Sodium carboxymethyl cellulose.
  • Sodium tripolyphosphate Optical brightencrs.
  • compositions of the invention are general purpose detergent compositions in the form of stable pourable liquid emulsions, suspensions, or coacervates which have The invention will now be illustrated in more detail Water by the following examples:
  • Example 1 The following compositions were prepared by mixing together the ingredients in the proportions shown, the figlphated tetraethylcneglycol nonylphenyl other (A) Coconut-oil fatty acid mono-ethanolamide
  • Example 2 The following compositions were prepared in the same way as in Example 1.
  • compositions although clear to the eye, in fact show a Tyndall-elfect; that is, they are emulsions, suspensions or coacervates and not true solutions.
  • compositions are in the form of stable, pourable dispersions which have little tendency to separate out on standing.
  • composition according to claim 1 in which the value of m is from 2 to 4.
  • R is an alkyl radical with 6 to 12 carbon atoms
  • n 2 to 3.
  • composition according to claim 1 in which the anionic active detergent A, is the sodium salt of sulphated polyethylene glycol monalkyl ether, of the formula RO(C H O) SO Na, in which:
  • R is an alkyl radical with 13 to 18 carbon atoms, and m is from 3 to 4.
  • a composition according to claim 1 which contains a compound from the class consisting of sodium p-hydroxy benzoate, sodium nitrilotriacetate and sodium ethylene diamine tetra acetate, as stabilizer for hydrogen peroxide.
  • a composition according to claim 1 which contains, in addition to the anionic active detergent A, an anionic active detergent B, from the class consisting of alkyl sulphate salts containing 8 to 18 carbon atoms in the alkyl group, and alkylaryl sulphonates containing 8 to 16 carbon atoms in the alkyl group.
  • composition according to claim 6 in which the weight ratio of active detergent AzB is from 1:1 to 1:6.
  • composition according to claim 6 which contains the following constituents in the following percentages by weight of the liquid composition:
  • Detergent A 1.4-3.8 Detergent B 4.7-12.1 Fatty acid monoethanolamide 1.0-2.8 Sodium carboxymethyl cellulose 0.3-0.8 Sodium pyrophosphate 1.1-2.9 Sodium tripolyphosphate 8.0-18.1 Optical brightener 0.03-0.08 Hydrogen peroxide 1.0-2.6 Stabilizer for hydrogen peroxide 0.02-0.06 Water to 100.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
US824800A 1958-07-10 1959-07-03 Liquid bleaching and detergent composition Expired - Lifetime US3130164A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB22162/58A GB855679A (en) 1958-07-10 1958-07-10 Improvements in or relating to liquid detergent compositions

Publications (1)

Publication Number Publication Date
US3130164A true US3130164A (en) 1964-04-21

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Family Applications (1)

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US824800A Expired - Lifetime US3130164A (en) 1958-07-10 1959-07-03 Liquid bleaching and detergent composition

Country Status (8)

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US (1) US3130164A (da)
BE (1) BE580351A (da)
CH (1) CH387211A (da)
DE (1) DE1199422B (da)
ES (2) ES250871A1 (da)
FR (2) FR1229408A (da)
GB (2) GB855679A (da)
NL (2) NL113683C (da)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3407141A (en) * 1966-02-03 1968-10-22 Allied Chem Dissolution of metal with acidified hydrogen peroxide solutions
US3720621A (en) * 1969-06-17 1973-03-13 Citrex Sa Aquenous detergent compositions
US3852210A (en) * 1972-08-11 1974-12-03 Flow Pharma Inc Stable liquid detergent concentrates containing active oxygen
US4075116A (en) * 1975-09-15 1978-02-21 Produits Chimiques Ugine Kuhlmann Mixed persalts stable in detergent compositions
US4430236A (en) 1981-06-22 1984-02-07 Texize, Division Of Mortonthiokol Liquid detergent composition containing bleach
US4525291A (en) * 1980-04-01 1985-06-25 Interox Chemicals Limited Liquid detergent compositions
US4927627A (en) * 1987-09-24 1990-05-22 Henkel Kommanditgesellschaft Auf Aktien Emulsion-form hydrogen peroxide preparations for the bleaching and oxidative dyeing of hair
US20050096250A1 (en) * 2003-10-31 2005-05-05 Resource Development L.L.C. Cleaning and multifunctional coating composition containing an organosilane quaternary compound and methods of using
US20070227557A1 (en) * 2005-07-06 2007-10-04 Ohlhausen Howard G Thickened surfactant-free cleansing and multifunctional liquid coating compositions containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using
US20080161219A1 (en) * 2007-01-02 2008-07-03 Ohlhausen Howard G Clathrates of an organosilane quaternary ammonium compound and urea and methods of use
US8257780B2 (en) 2003-10-31 2012-09-04 Resource Development L.L.C. Therapeutic composition containing an organosilane quaternary compound and hydrogen peroxide for treating skin disorders and methods of using
US8735618B2 (en) 2010-05-07 2014-05-27 Resource Development L.L.C. Solvent-free organosilane quaternary ammonium compositions, method of making and use

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL259347A (da) * 1959-12-22
CA704966A (en) * 1961-02-03 1965-03-02 J. Devlin John Non-alcoholic liquid detergent composition containing anionic detergent surface active agents
BE614204A (da) * 1961-02-22
DE1277492C2 (de) * 1964-11-27 1975-11-20 Henkel & Cie. GmbH, 4000 Düsseldorf Fluessige suspensionsstabilisierte kochwaschmittel
US3468805A (en) * 1965-10-22 1969-09-23 Gaf Corp Detergent composition
DE2743607A1 (de) * 1977-09-28 1979-04-05 Huels Chemische Werke Ag Waessrige reinigungsmittelloesungen
IS1740B (is) * 1982-02-05 1999-12-31 Albright & Wilson Uk Limited Samsetning á hreinsivökva
GB8830296D0 (en) * 1988-12-28 1989-02-22 Unilever Plc Bleaching composition
LT3962B (en) 1993-12-21 1996-05-27 Albright & Wilson Funcional fluids
DE19623571C2 (de) * 1996-06-13 2000-06-08 Cognis Deutschland Gmbh Verdickungsmittel für wäßrige Wasserstoffperoxidlösungen

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2155899A (en) * 1932-10-31 1939-04-25 Colgate Palmolive Peet Co Sulphated aliphatic ethers
US2254434A (en) * 1937-09-07 1941-09-02 Procter & Gamble Stabilizing agent for oxygencontaining per-compounds
US2698302A (en) * 1951-05-02 1954-12-28 Colgate Palmolive Co Detergent compositions containing metal discoloration inhibitors
GB783585A (en) * 1954-11-18 1957-09-25 Armour & Co Improvements in or relating to liquid detergent compositions
US2903431A (en) * 1955-08-16 1959-09-08 Lever Brothers Ltd Nontarnishing detergent compositions containing stannous salts

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL178800C (nl) * 1952-06-02 Electricity Council Werkwijze en inrichting voor het galvanoplastisch vervaardigen van ijzer.
GB800706A (en) * 1955-09-06 1958-09-03 Colgate Palmolive Co Liquid detergent compositions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2155899A (en) * 1932-10-31 1939-04-25 Colgate Palmolive Peet Co Sulphated aliphatic ethers
US2254434A (en) * 1937-09-07 1941-09-02 Procter & Gamble Stabilizing agent for oxygencontaining per-compounds
US2698302A (en) * 1951-05-02 1954-12-28 Colgate Palmolive Co Detergent compositions containing metal discoloration inhibitors
GB783585A (en) * 1954-11-18 1957-09-25 Armour & Co Improvements in or relating to liquid detergent compositions
US2903431A (en) * 1955-08-16 1959-09-08 Lever Brothers Ltd Nontarnishing detergent compositions containing stannous salts

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3407141A (en) * 1966-02-03 1968-10-22 Allied Chem Dissolution of metal with acidified hydrogen peroxide solutions
US3720621A (en) * 1969-06-17 1973-03-13 Citrex Sa Aquenous detergent compositions
US3852210A (en) * 1972-08-11 1974-12-03 Flow Pharma Inc Stable liquid detergent concentrates containing active oxygen
US4075116A (en) * 1975-09-15 1978-02-21 Produits Chimiques Ugine Kuhlmann Mixed persalts stable in detergent compositions
US4525291A (en) * 1980-04-01 1985-06-25 Interox Chemicals Limited Liquid detergent compositions
US4430236A (en) 1981-06-22 1984-02-07 Texize, Division Of Mortonthiokol Liquid detergent composition containing bleach
US4927627A (en) * 1987-09-24 1990-05-22 Henkel Kommanditgesellschaft Auf Aktien Emulsion-form hydrogen peroxide preparations for the bleaching and oxidative dyeing of hair
US20050096250A1 (en) * 2003-10-31 2005-05-05 Resource Development L.L.C. Cleaning and multifunctional coating composition containing an organosilane quaternary compound and methods of using
US6994890B2 (en) 2003-10-31 2006-02-07 Resource Development L.L.C. Cleaning and multifunctional coating composition containing an organosilane quaternary compound and hydrogen peroxide
US8257780B2 (en) 2003-10-31 2012-09-04 Resource Development L.L.C. Therapeutic composition containing an organosilane quaternary compound and hydrogen peroxide for treating skin disorders and methods of using
US20070227557A1 (en) * 2005-07-06 2007-10-04 Ohlhausen Howard G Thickened surfactant-free cleansing and multifunctional liquid coating compositions containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using
US7754004B2 (en) 2005-07-06 2010-07-13 Resource Development, L.L.C. Thickened surfactant-free cleansing and multifunctional liquid coating compositions containing nonreactive abrasive solid particles and an organosilane quaternary compound and methods of using
US20080161219A1 (en) * 2007-01-02 2008-07-03 Ohlhausen Howard G Clathrates of an organosilane quaternary ammonium compound and urea and methods of use
US7589054B2 (en) 2007-01-02 2009-09-15 Resource Development L.L.C. Clathrates of an organosilane quaternary ammonium compound and urea and methods of use
US8735618B2 (en) 2010-05-07 2014-05-27 Resource Development L.L.C. Solvent-free organosilane quaternary ammonium compositions, method of making and use

Also Published As

Publication number Publication date
NL241165A (da)
ES250871A1 (es) 1960-04-16
CH387211A (de) 1965-01-31
FR1229408A (fr) 1960-09-07
ES250872A1 (es) 1960-04-16
DE1199422B (de) 1965-08-26
NL113683C (da)
FR1229521A (fr) 1960-09-07
BE580351A (da)
GB855893A (en) 1960-12-07
GB855679A (en) 1960-12-07

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