EP0377807A1 - Détergent liquide hautement alcalin et sans phosphate - Google Patents

Détergent liquide hautement alcalin et sans phosphate Download PDF

Info

Publication number
EP0377807A1
EP0377807A1 EP89121135A EP89121135A EP0377807A1 EP 0377807 A1 EP0377807 A1 EP 0377807A1 EP 89121135 A EP89121135 A EP 89121135A EP 89121135 A EP89121135 A EP 89121135A EP 0377807 A1 EP0377807 A1 EP 0377807A1
Authority
EP
European Patent Office
Prior art keywords
weight
alkyl
composition according
component
sodium
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
EP89121135A
Other languages
German (de)
English (en)
Other versions
EP0377807B1 (fr
Inventor
Uwe Dr. Trabitzsch
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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
Priority claimed from DE3841129A external-priority patent/DE3841129A1/de
Priority claimed from DE19893906766 external-priority patent/DE3906766A1/de
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to AT89121135T priority Critical patent/ATE101412T1/de
Publication of EP0377807A1 publication Critical patent/EP0377807A1/fr
Application granted granted Critical
Publication of EP0377807B1 publication Critical patent/EP0377807B1/fr
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
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • Textile detergents to be used in commercial laundries differ considerably in their composition from those which are usually used in the household.
  • softened, ie Ca and Mg-free water is used regularly in commercial companies.
  • the commercially used agents often contain highly alkaline builder salts and alkalis, such as sodium metasilicate and sodium hydroxide, which can be handled safely by a person skilled in the art, but are unsuitable for safety reasons in the household.
  • These highly alkaline constituents can in turn interact with the surfactants usually present, in particular the nonionics from the class of the alkyl polyglycol ethers, and more or less decompose them if they are stored together for a long time.
  • Another aspect is the broadest possible use of surfactants that are derived from natural, i.e. raw materials are available and are characterized by their complete and rapid biodegradability in wastewater.
  • Component (A1) consists of alkyl glucosides or alkyl oligoglucosides, as are known, for example, from US Pat. Nos. 35 47 828, 37 72 269 and 38 39 318. They can be obtained by reacting glucose or depolymerized starch and alcohols with C8 ⁇ 14 alkyl radicals, without or in the presence of lower alcohols or glycols, such as butanol or propylene glycol, as well as acidic acetalization catalysts. Alcohols or alcohol mixtures obtained from native fats, such as coconut or palm kernel fat, are preferably used as fatty alcohols. Examples are octyl, decyl, lauryl and myristyl alcohol and their mixtures.
  • alkyl glucosides which are derived from oxo alcohols and which, in addition to linear alcohols, also contain methyl-branched alcohols in the mixture in the 2-position or have an even and / or odd number of C atoms in the alkyl chain.
  • R is preferably a C8 ⁇ 12 alkyl radical, in particular a C8 ⁇ 10 alkyl radical.
  • the alkyl glucosides can still contain small amounts of free fatty alcohol and glucose in their production. Those alkyl glucosides are preferably used whose content of fatty alcohols is less than 5% by weight, in particular less than 2% by weight (based on alkyl glucoside).
  • the agents can optionally also contain nonionic surfactants of the ethoxylated fatty alcohol and oxo alcohol type with 12 to 18 carbon atoms and 5 to 10 ethylene polyether groups (EO).
  • EO ethylene polyether groups
  • Suitable are e.g. Ethoxylates derived from coconut, tallow or palm kernel fatty alcohols with an HLB value of more than 12, for example from 13 to 18, and corresponding ethoxylates from oxo alcohols with 12 to 16 carbon atoms and 6 to 8 EO groups.
  • the builder component consists of sodium hydroxide (component B1), sodium silicate (component B2) and sequestering polyanionic salts derived from nitrilotriacetic acid (NTA) and possibly phosphonic acids (components B3 and B4).
  • the Na2O: SiO2 ratio can be 1: 1 (metasilicate) to 1: 3.4 (water glass).
  • metasilicate is preferably used in agents with lower proportions of sodium hydroxide, while in agents with higher sodium hydroxide contents the sodium silicate can consist predominantly or completely of water glass.
  • the NTA is in the form of the trisodium salt and is also used in this form of quantity calculation. In particular, its proportion is 5 to 10% by weight.
  • the sodium salt of 1-hydroxyethane-1,1-diphosphonic acid is primarily suitable as the phosphonate.
  • the quantity calculation is based on the tetrasodium salt.
  • the sodium salts of aminotrimethylenephosphonic acid (ATMP), ethylenediaminetetramethylenephosphonic acid (EDTMP), diethylenetriaminepentamethylenephosphonic acid (DTPMP) and their higher homologues are also usable. unexplained function in wastewater less preferred.
  • Your quantity calculation is based on neutral reacting sodium salts (Na3 salt with ATMP, Na5 salt with EDTMP, Na6 salt with DTPMP).
  • the sum of components B3 + B4 is 3 to 12% by weight, preferably 6 to 11% by weight.
  • the detergents can also contain conventional detergent constituents which do not act as surfactants and builders. These include optical brighteners in proportions of up to 1% by weight, preferably 0.05 to 0.3% by weight. Examples of these are derivatives of bis (triazinylamino) stilbene disulfonic acid for example, the sodium salt of 4,4'-bis (2-anilino-4-morpholino-1,3,5-triazin-6-yl-amino) -stilbene-2,2'-disulfonic acid and the chlorinated diphenyldistyrylsulfonic acids.
  • optical brighteners in proportions of up to 1% by weight, preferably 0.05 to 0.3% by weight. Examples of these are derivatives of bis (triazinylamino) stilbene disulfonic acid for example, the sodium salt of 4,4'-bis (2-anilino-4-morpholino-1,3,5-triazin-6-yl-amino) -stilbene-2,2'-disulfonic acid and the
  • hydrotropes are e.g. Toluene sulfonate, xylene sulfonate and cumene sulfonate, each in the form of the sodium salts.
  • Usable solvents are, for example, ethanol, propanol, isopropanol and ether alcohols, such as diglycol and C1 ⁇ 3 monoalkyl ethers of C2 ⁇ 4 diols.
  • the hydrotropes can be present in proportions up to 6% by weight, the alcohols or ether alcohols in proportions up to 10% by weight.
  • the agents may also contain neutral salts, such as sodium sulfate and sodium chloride, as minor substances in the raw materials used. The difference of up to 100% by weight is essentially water.
  • the agents are durable, pourable liquids that are suitable for automatic dosing as well as for preparing stock solutions (base liquors).
  • the concentrates are still liquid down to temperatures of -10 ° C and are resistant to segregation.
  • Their application concentration is generally 2 to 10, preferably 3 to 7 g / l.
  • the amount of laundry was 7.5 kg, the water hardness 0 ° dH, normal program (without prewash), detergent concentration 4 g / l, 5 minutes at 40 ° C and 15 minutes at 90 ° C, three rinses, low foaming.

Landscapes

  • 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)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Detergent Compositions (AREA)
EP89121135A 1988-12-07 1989-11-15 Détergent liquide hautement alcalin et sans phosphate Expired - Lifetime EP0377807B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT89121135T ATE101412T1 (de) 1988-12-07 1989-11-15 Phosphatfreies,fluessiges waschmittel mit hoher alkalitaet.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE3841129 1988-12-07
DE3841129A DE3841129A1 (de) 1988-12-07 1988-12-07 Phosphatfreies, fluessiges waschmittel mit hoher alkalitaet
DE19893906766 DE3906766A1 (de) 1989-03-03 1989-03-03 Phosphatfreies, fluessiges waschmittel mit hoher alkalitaet
DE3906766 1989-03-03

Publications (2)

Publication Number Publication Date
EP0377807A1 true EP0377807A1 (fr) 1990-07-18
EP0377807B1 EP0377807B1 (fr) 1994-02-09

Family

ID=25874879

Family Applications (2)

Application Number Title Priority Date Filing Date
EP89912958A Pending EP0447413A1 (fr) 1988-12-07 1989-11-15 Produit liquide de lavage sans phosphates a alcalinite elevee
EP89121135A Expired - Lifetime EP0377807B1 (fr) 1988-12-07 1989-11-15 Détergent liquide hautement alcalin et sans phosphate

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP89912958A Pending EP0447413A1 (fr) 1988-12-07 1989-11-15 Produit liquide de lavage sans phosphates a alcalinite elevee

Country Status (9)

Country Link
EP (2) EP0447413A1 (fr)
JP (1) JPH04502337A (fr)
AU (1) AU626954B2 (fr)
CA (1) CA2004895A1 (fr)
DE (1) DE58906948D1 (fr)
DK (1) DK101291A (fr)
ES (1) ES2061894T3 (fr)
PT (1) PT92396A (fr)
WO (1) WO1990006353A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994003569A1 (fr) * 1992-07-30 1994-02-17 Henkel Kommanditgesellschaft Auf Aktien Procede de fabrication d'agents tensioactifs non ioniques stables au stockage
EP0811052A1 (fr) * 1995-02-16 1997-12-10 Henkel Corporation Compositions liquides de nettoyage, a usage industriel et des collectivites, contenant des tensioactifs de polyglycoside d'alkyle

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4009533A1 (de) * 1990-03-24 1991-09-26 Henkel Kgaa Schwachschaeumendes nichtionisches tensidgemisch
US5503754A (en) * 1993-11-10 1996-04-02 Henkel Corporation Wet treatment of leather hides
US5542950A (en) * 1994-11-10 1996-08-06 Henkel Corporation Alkyl polyglycosides in textile scour/bleach processing
FR2744132B1 (fr) 1996-01-31 1998-04-24 Rhone Poulenc Chimie Systeme de base d'un agent tensioactif non-ionique et d'un silicate de metal alcalin, sous forme d'une dispersion ou de granules et son utilisation en detergence
US6194371B1 (en) 1998-05-01 2001-02-27 Ecolab Inc. Stable alkaline emulsion cleaners
US6369021B1 (en) * 1999-05-07 2002-04-09 Ecolab Inc. Detergent composition and method for removing soil
US7041177B2 (en) 2002-08-16 2006-05-09 Ecolab Inc. High temperature rapid soil removal method
US20170369819A1 (en) * 2016-06-27 2017-12-28 The Procter & Gamble Company Removal of hydrophilic body soils

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3721633A (en) * 1969-10-06 1973-03-20 Atlas Chem Ind Aqueous built liquid detergents containing alkyl glycosides
EP0075995A2 (fr) * 1981-09-28 1983-04-06 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant de mélanges d'alcylpolysaccharide et d'agents tensio-actifs non-ioniques
FR2540511A1 (fr) * 1983-02-04 1984-08-10 Henkel France Composition liquide de nettoyage, ainsi que procede de nettoyage a partir de cette composition
WO1987006949A1 (fr) * 1986-05-06 1987-11-19 A. E. Staley Manufacturing Company Detergent liquide pour lessive contenant un adjuvant et un agent tensio-actif a base d'alkyle glycoside

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3772259A (en) 1965-07-12 1973-11-13 American Cyanamid Co 2-vinyl-1-cycloamidinepropionamide polymers
US3547828A (en) 1968-09-03 1970-12-15 Rohm & Haas Alkyl oligosaccharides and their mixtures with alkyl glucosides and alkanols
US3839318A (en) 1970-09-27 1974-10-01 Rohm & Haas Process for preparation of alkyl glucosides and alkyl oligosaccharides
DE3518672A1 (de) * 1985-05-24 1986-11-27 Basf Ag, 6700 Ludwigshafen Fluessiges reinigungskonzentrat fuer stark alkalische reinigungsformulierungen
DE3708330A1 (de) * 1987-03-14 1988-09-22 Henkel Kgaa Fluessige, alkalische reinigerkonzentrate

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3721633A (en) * 1969-10-06 1973-03-20 Atlas Chem Ind Aqueous built liquid detergents containing alkyl glycosides
EP0075995A2 (fr) * 1981-09-28 1983-04-06 THE PROCTER & GAMBLE COMPANY Compositions détergentes contenant de mélanges d'alcylpolysaccharide et d'agents tensio-actifs non-ioniques
FR2540511A1 (fr) * 1983-02-04 1984-08-10 Henkel France Composition liquide de nettoyage, ainsi que procede de nettoyage a partir de cette composition
WO1987006949A1 (fr) * 1986-05-06 1987-11-19 A. E. Staley Manufacturing Company Detergent liquide pour lessive contenant un adjuvant et un agent tensio-actif a base d'alkyle glycoside

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994003569A1 (fr) * 1992-07-30 1994-02-17 Henkel Kommanditgesellschaft Auf Aktien Procede de fabrication d'agents tensioactifs non ioniques stables au stockage
US5556573A (en) * 1992-07-30 1996-09-17 Henkel Kommanditgesellschaft Auf Aktien Process for the production of storable nonionic surfactants
EP0811052A1 (fr) * 1995-02-16 1997-12-10 Henkel Corporation Compositions liquides de nettoyage, a usage industriel et des collectivites, contenant des tensioactifs de polyglycoside d'alkyle
EP0811052A4 (fr) * 1995-02-16 1999-10-27 Henkel Corp Compositions liquides de nettoyage, a usage industriel et des collectivites, contenant des tensioactifs de polyglycoside d'alkyle

Also Published As

Publication number Publication date
CA2004895A1 (fr) 1990-06-07
EP0377807B1 (fr) 1994-02-09
EP0447413A1 (fr) 1991-09-25
DK101291D0 (da) 1991-05-28
JPH04502337A (ja) 1992-04-23
ES2061894T3 (es) 1994-12-16
PT92396A (pt) 1990-06-29
AU626954B2 (en) 1992-08-13
DE58906948D1 (de) 1994-03-24
DK101291A (da) 1991-05-28
AU4626089A (en) 1990-06-26
WO1990006353A1 (fr) 1990-06-14

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