EP0356974A2 - Composition de nettoyage et de lavage - Google Patents

Composition de nettoyage et de lavage Download PDF

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Publication number
EP0356974A2
EP0356974A2 EP89115874A EP89115874A EP0356974A2 EP 0356974 A2 EP0356974 A2 EP 0356974A2 EP 89115874 A EP89115874 A EP 89115874A EP 89115874 A EP89115874 A EP 89115874A EP 0356974 A2 EP0356974 A2 EP 0356974A2
Authority
EP
European Patent Office
Prior art keywords
acid
weight
alanine
detergents
salts
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.)
Granted
Application number
EP89115874A
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German (de)
English (en)
Other versions
EP0356974B1 (fr
EP0356974A3 (en
Inventor
Richard Dr. Baur
Charalampos Dr. Gousetis
Wolfgang Dr. Trieselt
Werner Dr. Bochnitschek
Alfred Dr. Oftring
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.)
BASF SE
Original Assignee
BASF SE
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Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to AT89115874T priority Critical patent/ATE92952T1/de
Publication of EP0356974A2 publication Critical patent/EP0356974A2/fr
Publication of EP0356974A3 publication Critical patent/EP0356974A3/de
Application granted granted Critical
Publication of EP0356974B1 publication Critical patent/EP0356974B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines
    • 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
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids

Definitions

  • Detergents and cleaning agents for aqueous applications are generally composed of a combination of various surface-active substances and other auxiliaries.
  • softeners should be mentioned primarily, i.e. Substances that are able to bind the hardness constituents of water, especially Ca++ and Mg++ cations.
  • Nitrilotriacetic acid and its salts have recently been used as a replacement for the phosphates, but these compounds are also not fully satisfactory since they deposit deposits of hardness, e.g. on textile fabrics, not preventing them effectively enough.
  • the present invention was therefore based on detergents and cleaning agents for aqueous applications, which contain softeners which are even more effective than nitrilotriacetic acid.
  • detergents and cleaning agents for aqueous applications which contain 2 to 25% by weight, based on the total weight of the detergents, of ⁇ -alanine-N, N-diacetic acid or its alkali metal or ammonium salts.
  • ß-Alanine-N, N-diacetic acid like nitrilotriacetic acid, is biodegradable and can be produced particularly advantageously by reacting acrylic acid with iminodiacetic acid in an aqueous medium in large quantities (see our more recent application P 38 29 859.7 - OZ 0050/40154).
  • ß-alanine-N, N-diacetic acid is its lower binding capacity for heavy metal ions such as Cu2+ or Cd2+ compared to nitrilotriacetic acid, such as a comparison of the corresponding equilibrium constants on pages 564 and 565 in Organic Sequestering Agents, A.E. Martell, J. Wiley & Sons, Hew York (1959). This reduces the likelihood that traces of undegraded ß-alanine-N, N-diacetic acid in river sediments will release heavy metal ions.
  • the ⁇ -alanine-N, N-diacetic acid or its alkali metal or ammonium salts are used in amounts of 2 to 25, preferably in amounts of 5 to 15,% by weight.
  • Their alkali metal salts are used with particular advantage, the trisodium salt being particularly preferred.
  • the salts of ⁇ -alanine-N, N-diacetic acid with basic compounds such as potassium hydroxide, ammonia or primary, secondary or tertiary aliphatic organic amines having 1 to 4 carbon atoms in the aliphatic radicals such as methylamine, dimethylamine or trimethylamine can also be used .
  • Detergents generally also contain 5 to 50% by weight of other softeners 6 to 25% by weight of surface-active compounds as washing-active substances 5 to 35 wt% bleach 0 to 60% by weight of substances essential for the consistency of the preparation and in minor amounts other auxiliary substances such as bleach stabilizers, bleach activators, enzymes, graying inhibitors, foam regulators, corrosion inhibitors, optical brighteners, solubilizers, fragrances or dyes.
  • Cleaning agents generally contain other essential ingredients 30 to 80 wt .-% dirt-disrupting components 3 to 20% by weight of other agents which are able to bind hardening agents 2 to 10% by weight of surface-active substances 1 to 5% by weight of anti-corrosion agent 0 to 60% by weight of substances essential for the consistency of the preparation and in minor quantities other auxiliary substances such as enzymes, foam regulators, fragrances, solubilizers or disinfectants.
  • the washing and cleaning agents according to the invention can contain alkaline substances such as sodium carbonate, sodium silicate and sodium phosphate or complexing agents of an inorganic nature such as e.g.
  • Suitable phosphorus-containing organic complexing agents are methane diphosphonic acid, propane-1,2,3-triphosphonic acid, butane-1,2,3,4-tetraphosphonic acid, polyvinylphosphonic acid, 1-aminoethane-1,1-diphosphonic acid, 1-amino-1-phenyl -1,1-diphosphonic acid, aminotrimethylene triphosphonic acid, methylamino- or ethylaminodimethylene diphosphonic acid, ethylene diaminotetramethylene tetraphosphonic acid, 1-hydroxyethane-1,1-diphosphonic acid, phosphonoacetic acid, phosphonopropionic acid, 1-phosphonoethane-1,2-dicarboxylic acid, 2-phosphonopropane-2,3- dicarboxylic acid, 2-phosphonobutane-1,2,4-tricarboxylic acid, 2-phosphonobutane-2,3,4-tricarboxylic acid and copolymers of vinylphosphonic acid and
  • Suitable hydroxymono- or polycarboxylic acids are glycolic acid, lactic acid, malic acid, tartronic acid, methyltartronic acid, gluconic acid, glyceric acid, citric acid, tartaric acid and salicylic acid.
  • Zeolite 4A whose production is described in Ullmann's Encyclopedia of Industrial Chemistry, 4th Edition, Volume 24 on p. 120, is particularly suitable as an ion exchanger.
  • Suitable surfactants are those which contain at least one hydrophobic organic radical and one water-solubilizing ionic or nonionic group in the molecule.
  • the hydrophobic radical preferably consists of an aliphatic hydrocarbon radical with 8 to 26, preferably 10 to 22 and particularly preferably 12 to 18 C atoms or an alkyl aromatic radical with 6 to 18, preferably 8 to 16 C atoms in the alkyl group.
  • anionic surfactants are the sodium, potassium and ammonium salts of carboxylic acids, sulfonic acids and sulfuric acid monoesters with the specified number of carbon atoms.
  • the surfactants of the sulfonate type include, in particular, alkylbenzenesulfonates with 9 to 15 carbon atoms in the alkyl radical, alkene and hydroxyalkanesulfonates and disulfonates such as are obtained, for example, from monoolefins with terminal or internal double bonds by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation products receives.
  • alkanesulfonates which can be obtained from alkanes by sulfochlorination or sulfoxidation and subsequent hydrolysis or neutralization or by bisulfite addition to olefins.
  • More useful sulfonate type surfactants are the methyl or ethyl esters of ⁇ -sulfo fatty acids.
  • Suitable sulfate-type surfactants are the salts mentioned of the sulfuric acid monoesters of primary and secondary alcohols. Sulfated fatty acid monoglycerides and sulfated reaction products of 1 to 4 moles of ethylene oxide with primary or secondary fatty alcohols or alkylphenols are also suitable.
  • Preferred cationic surfactants are dialkyldimethylammonium chlorides such as distearyldimethylammonium chloride and imidazolinium salts of the 1-alkylamidoethyl-1-methyl-2-alkylimidazolinium methoxysulfate type.
  • Addition products of 4 to 40, preferably 4 to 20 moles of ethylene oxide with 1 mole of fatty alcohol, alkylphenol, fatty acid, fatty amine, fatty acid amide or alkanesulfonamide are advantageously used as nonionic surfactants.
  • the addition products of 5 to 16 moles of ethylene oxide with primary or secondary alcohols with 8 to 18, preferably 12 to 18 C atoms, and with mono- or dialkylphenols with 6 to 14 C atoms in the alkyl radicals are particularly preferred.
  • water-soluble stabilizers are the organic complexing agents suitable as auxiliaries for binding the hardeners Ca2+ and Mg2+.
  • Graying inhibitors are auxiliaries which keep the loosened dirt suspended in the aqueous solution.
  • Water-soluble colloids of an organic nature are suitable for this.
  • the water-soluble salts of polymeric carboxylic acids, salts of ether carboxylic acids or ether sulfonic acids of starch or of cellulose or salts of acidic sulfuric acid esters of cellulose or starch are preferred.
  • Water-soluble polyamides containing acidic groups and polyvinylpyrrolidone are also suitable.
  • the textile detergents often advantageously contain optical brighteners.
  • diaminostilbenedisulfonic acid or its alkali metal salts such as e.g. the alkali metal salts of 4,4'-bis (2-anilino-4-morpholino-1,3,5-triazin-6-yl-amino) -stilbene-2,2'-disulfonic acid, for polyamide fibers 1,3-diaryl- 2-pyrazolines such as 1- (p-sulfamoylphenyl) -3- (p-chlorophenyl) -2-pyrazoline, for polyester fibers 2,5-di- (2-benzoxazolyl) -thiophene and 1,2-di- (5-methyl-2-benzoxazolyl) ) -ethylene used.
  • Dirt-disrupting components for cleaning agents are, in particular, alkaline substances such as sodium or potassium hydroxide, sodium or potassium carbonate, alkaline salts of orthophosphoric acid as well as sodium and potassium silicates with a silicon dioxide / alkali metal oxide ratio of 0.7 to 1.5 and organic and inorganic cal acids such as hydrochloric acid, phosphoric acid, phosphoric acid ester, sulfuric acid, oxalic acid, citric acid, formic acid, amidosulfonic acid, adipic acid, glutaric acid or succinic acid are suitable.
  • alkaline substances such as sodium or potassium hydroxide, sodium or potassium carbonate, alkaline salts of orthophosphoric acid as well as sodium and potassium silicates with a silicon dioxide / alkali metal oxide ratio of 0.7 to 1.5
  • organic and inorganic cal acids such as hydrochloric acid, phosphoric acid, phosphoric acid ester, sulfuric acid, oxalic acid, citric acid, formic acid, amidos
  • the detergents and cleaning agents according to the invention can be in powder or liquid form.
  • inorganic salts in particular sodium sulfate, are generally added, while water is the basis of most liquid preparations.
  • the washing and cleaning agents according to the invention can be produced in a generally customary manner; e.g. the various constituents can be stirred into an aqueous slurry using water, which is then expediently dried in atomizing towers at 100.degree.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP89115874A 1988-09-02 1989-08-29 Composition de nettoyage et de lavage Expired - Lifetime EP0356974B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT89115874T ATE92952T1 (de) 1988-09-02 1989-08-29 Wasch- und reinigungsmittel.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3829847A DE3829847A1 (de) 1988-09-02 1988-09-02 Wasch- und reinigungsmittel
DE3829847 1988-09-02

Publications (3)

Publication Number Publication Date
EP0356974A2 true EP0356974A2 (fr) 1990-03-07
EP0356974A3 EP0356974A3 (en) 1990-04-11
EP0356974B1 EP0356974B1 (fr) 1993-08-11

Family

ID=6362150

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89115874A Expired - Lifetime EP0356974B1 (fr) 1988-09-02 1989-08-29 Composition de nettoyage et de lavage

Country Status (9)

Country Link
US (1) US4997587A (fr)
EP (1) EP0356974B1 (fr)
JP (1) JPH02163200A (fr)
KR (1) KR960015370B1 (fr)
AT (1) ATE92952T1 (fr)
AU (1) AU620640B2 (fr)
CA (1) CA1326427C (fr)
DE (2) DE3829847A1 (fr)
ES (1) ES2042913T3 (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0509382A3 (en) * 1991-04-17 1993-01-13 W.R. Grace & Co.-Conn. Biodegradable bleach stabilizers for detergents
EP0513948A3 (en) * 1991-05-15 1993-04-21 W.R. Grace & Co.-Conn. (A Connecticut Corp.) Hard-surface cleaning compositions containing biodegradable chelants
WO1994029420A1 (fr) * 1993-06-15 1994-12-22 Henkel Kommanditgesellschaft Auf Aktien Detergents pour lave-vaisselle formant peu de depot
EP0846753A1 (fr) * 1993-06-16 1998-06-10 Basf Aktiengesellschaft Utilisation de Alanine-N,N-acide et leurs sels comme agents complexants biodégradables pour des ions de métaux lourds et alcaline-terreux en alcalino composition détergentes et procédés de lavage en industrie des boissons et industrie des denrées alimentaires

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221496A (en) * 1992-06-02 1993-06-22 Basf Corp. Aqueous prewash stain remover compositions with efficacy on tenacious oily stains
US5186856A (en) * 1992-06-02 1993-02-16 Basf Corp. Aqueous prewash stain remover compositions with efficacy on tenacious oily stains
CZ285638B6 (cs) * 1994-10-07 1999-10-13 Eka Chemicals Ab Částice obsahující peroxysloučeninu a prostředek, který je obsahuje
SK281152B6 (sk) * 1994-10-07 2000-12-11 Eka Chemicals Ab Častica obsahujúca peroxyzlúčeninu a prostriedok, ktorý ju obsahuje
DE4445820A1 (de) * 1994-12-21 1996-06-27 Hoechst Ag Verfahren zum Entwickeln bestrahlter, strahlungsempfindlicher Aufzeichnungsmaterialien
DE19543162A1 (de) * 1995-11-18 1997-05-22 Basf Ag Feste Textilwaschmittel-Formulierung aus anorganischen Buildern, Glycin-N,N-diessigsäure-Derivaten als organische Cobuilder sowie anionischen und nichtionischen Tensiden
JP3810854B2 (ja) * 1996-01-22 2006-08-16 花王株式会社 高密度粉末洗剤組成物
JP3810847B2 (ja) * 1996-01-22 2006-08-16 花王株式会社 高密度粉末洗剤組成物
GB2311535A (en) * 1996-03-29 1997-10-01 Procter & Gamble Detergent compositions
GB2311536A (en) * 1996-03-29 1997-10-01 Procter & Gamble Dishwashing and laundry detergents
GB2311538A (en) * 1996-03-29 1997-10-01 Procter & Gamble Detergent compositions
GB2311537A (en) * 1996-03-29 1997-10-01 Procter & Gamble Rinse composition for dishwashers
EP0834549A1 (fr) * 1996-10-07 1998-04-08 The Procter & Gamble Company Compositions de nettoyage
JP3290382B2 (ja) * 1997-07-18 2002-06-10 花王株式会社 粉末洗剤組成物
GB0522658D0 (en) 2005-11-07 2005-12-14 Reckitt Benckiser Nv Composition
GB0611206D0 (en) 2006-06-07 2006-07-19 Reckitt Benckiser Nv Detergent composition

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2371623A (en) * 1943-02-06 1945-03-20 Lever Brothers Ltd Method of preserving soap and resulting product
DE2125249A1 (de) * 1971-05-21 1972-11-30 Chemische Werke Hüls AG, 4370 Mari Gerüstsubstanzen für Wasch- und Reinigungsmittel
CH621999A5 (fr) * 1976-06-24 1981-03-13 Ciba Geigy Ag
US4265777A (en) * 1980-04-17 1981-05-05 The Procter & Gamble Company Detergent compositions containing an aluminosilicate detergency builder and an unsaturated fatty acid soap
US4404128A (en) * 1981-05-29 1983-09-13 The Procter & Gamble Company Enzyme detergent composition
US4440663A (en) * 1981-09-14 1984-04-03 The Procter & Gamble Company Alkaline aqueous liquid detergent compositions containing normally unstable ester perfumes
EP0089136A3 (fr) * 1982-03-10 1984-05-30 The Procter & Gamble Company Produits d'hygiène orale
US4690771A (en) * 1985-08-05 1987-09-01 Colgate-Palmolive Company Phosphate free nonaqueous liquid nonionic laundry detergent composition and method of use
DE3829859A1 (de) * 1988-09-02 1990-03-22 Basf Ag Verfahren zur herstellung von ss-alanindiessigsaeure oder ihren alkalimetall- oder ammoniumsalzen

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0509382A3 (en) * 1991-04-17 1993-01-13 W.R. Grace & Co.-Conn. Biodegradable bleach stabilizers for detergents
EP0513948A3 (en) * 1991-05-15 1993-04-21 W.R. Grace & Co.-Conn. (A Connecticut Corp.) Hard-surface cleaning compositions containing biodegradable chelants
WO1994029420A1 (fr) * 1993-06-15 1994-12-22 Henkel Kommanditgesellschaft Auf Aktien Detergents pour lave-vaisselle formant peu de depot
EP0846753A1 (fr) * 1993-06-16 1998-06-10 Basf Aktiengesellschaft Utilisation de Alanine-N,N-acide et leurs sels comme agents complexants biodégradables pour des ions de métaux lourds et alcaline-terreux en alcalino composition détergentes et procédés de lavage en industrie des boissons et industrie des denrées alimentaires

Also Published As

Publication number Publication date
ES2042913T3 (es) 1993-12-16
AU620640B2 (en) 1992-02-20
US4997587A (en) 1991-03-05
ATE92952T1 (de) 1993-08-15
DE58905235D1 (de) 1993-09-16
JPH02163200A (ja) 1990-06-22
CA1326427C (fr) 1994-01-25
KR960015370B1 (ko) 1996-11-11
EP0356974B1 (fr) 1993-08-11
KR900004924A (ko) 1990-04-13
AU4095689A (en) 1990-03-08
DE3829847A1 (de) 1990-03-15
EP0356974A3 (en) 1990-04-11

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