EP0796911A1 - Spray-dried detergent component comprising chelant - Google Patents

Spray-dried detergent component comprising chelant Download PDF

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Publication number
EP0796911A1
EP0796911A1 EP96200801A EP96200801A EP0796911A1 EP 0796911 A1 EP0796911 A1 EP 0796911A1 EP 96200801 A EP96200801 A EP 96200801A EP 96200801 A EP96200801 A EP 96200801A EP 0796911 A1 EP0796911 A1 EP 0796911A1
Authority
EP
European Patent Office
Prior art keywords
spray
chelant
weight
dried component
component according
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
EP96200801A
Other languages
German (de)
French (fr)
Other versions
EP0796911B2 (en
EP0796911B1 (en
Inventor
Scott John Donoghue
Achille Jules Edmond Doumen
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.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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
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Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP96200801A priority Critical patent/EP0796911B2/en
Priority to DE69621584T priority patent/DE69621584T3/en
Priority to PT96200801T priority patent/PT796911E/en
Priority to ES96200801T priority patent/ES2177718T5/en
Priority to AT96200801T priority patent/ATE218611T1/en
Priority to DK96200801T priority patent/DK0796911T3/en
Priority to CA002249268A priority patent/CA2249268C/en
Priority to CN97194764A priority patent/CN1119403C/en
Priority to PCT/US1997/004651 priority patent/WO1997035953A1/en
Priority to JP09534515A priority patent/JP3093283B2/en
Priority to US09/155,161 priority patent/US5958866A/en
Priority to BR9708333A priority patent/BR9708333A/en
Priority to ARP970101151A priority patent/AR006349A1/en
Publication of EP0796911A1 publication Critical patent/EP0796911A1/en
Publication of EP0796911B1 publication Critical patent/EP0796911B1/en
Application granted granted Critical
Publication of EP0796911B2 publication Critical patent/EP0796911B2/en
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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
    • 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
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • C11D11/02Preparation in the form of powder by spray drying
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • C11D3/364Organic compounds containing phosphorus 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/10Salts
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/32Organic compounds containing nitrogen
    • C11D7/3245Aminoacids
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/36Organic compounds containing phosphorus

Definitions

  • the present invention relates to a spray-dried component comprising a chelant, in particular diethylene triamine penta(methylene phosphonic acid) or its salts.
  • a chelant in particular diethylene triamine penta(methylene phosphonic acid) or its salts.
  • Such components are useful in granular detergent products, and also as intermediate products in the manufacture of bar soap, detergent tablets and other detergent forms such as extrudates, agglomerates and the like.
  • US-A-4 259 200 discloses phosphonates complexed with calcium, magnesium, zinc or aluminium ions, the molar ratio of metal ion to phosphonate being at least 1:1. It is disclosed that the magnesium and the phosphonate can be premixed in any suitable solvent, including water, optionally mixed with other detergent components and spray-dried. Improved storage stability in bleaching compositions is sought.
  • EP-A-0 225 309 discloses the addition of salts of alkali or alkaline earth metals into particles comprising diethylene triamine penta(methylene phosphonic acid) for the purpose of improving free-flow and storage properties.
  • the amount of sulphate is 60% to 200% of the dry weight of the chelant, corresponding to a weight ratio of metal ion salt to chelant of from 0.6:1 to 2:1.
  • Preferred water content after spray-drying is less than 10% by weight of the particle.
  • spray-dried components may be prepared having a high chelant content (at least 50% by weight) and which still maintain good free-flowing properties.
  • the object of the present invention is to provide a spray-dried component which is in the form of a free-flowing particle with high chelant activity
  • a spray-dried component comprising:
  • the chelant is preferably a phosphonic or succinic acid, or salt of phosphonic or succinic acid, more preferably the chelant is selected form the group consisting of diethylene triamine penta(methylene phosphonic acid), ethylene diamine-N,N'-disuccinic acid, or mixtures, or salts thereof.
  • the alkaline earth metal is preferably magnesium.
  • the spray-dried component of the present invention comprises a chelant.
  • Chelants are used, for example in detergent compositions, for their ability to complex with metal irons such as iron and/or manganese forming soluble chelates.
  • Suitable chelants can be selected from the group consisting of amino carboxylates, amino phosphonates, polyfunctionally-substituted aromatic chelants and mixtures thereof.
  • Useful amino carboxylates include ethylenediaminetetracetates (“EDTA”), N-hydroxyethylethylene diaminetriacetates, nitrilotriacetates, ethylene diamine tetraproprionates, triethylene tetraaminehexacetates, diethylenetriaminepentaacetates, and ethanoldiglycines, alkali metal, ammonium, and substituted ammonium salts thereof, and mixtures thereof.
  • EDTA ethylenediaminetetracetates
  • N-hydroxyethylethylene diaminetriacetates N-hydroxyethylethylene diaminetriacetates
  • nitrilotriacetates nitrilotriacetates
  • ethylene diamine tetraproprionates triethylene tetraaminehexacetates
  • diethylenetriaminepentaacetates diethylenetriaminepentaacetates
  • ethanoldiglycines alkali metal, ammonium, and substituted ammonium
  • Useful amino phosphonates include ethylenediaminetetrakis (methylenephosphonates), sold as DEQUEST®. Preferably these amino phosphonates do not contain alkyl or alkenyl groups with more than about 6 carbon atoms.
  • Particularly preferred chelants are diethylene triamine penta(methylene phosphonic acid) (“DTPMP”) and ethylene diamine tetra(methylene phosphonic acid) (EDTMP).
  • DTPMP diethylene triamine penta(methylene phosphonic acid)
  • ETMP ethylene diamine tetra(methylene phosphonic acid)
  • Polyfunctionally-substituted aromatic chelants are also useful in the components herein. See US-A-3 812 044, issued May 21, 1974, to Connor et al.
  • Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2-dihydroxy-3,5-disulfobenzene.
  • a preferred biodegradable chelant for use herein is ethylene diamine-N,N'-disuccinate ("EDDS"), especially the [S,S] isomer as described in US-A-4 704 233, issued on November 3, 1987, to Hartman and Perkins.
  • EDDS ethylene diamine-N,N'-disuccinate
  • magnesium sulphate is preferred for use in the present invention, magnesium sulphate being the most preferred.
  • Epsom salts; MgSO4 . 7H2O, i.e. the hydrated, crystalline form of magnesium sulphate with seven moles of water is particularly preferred.
  • the chelants used in the present invention may be conveniently provided from commercially available sources in aqueous solution. Typical commercially available solutions have a chelant activity of from about 40% to about 60% by weight.
  • the spray-dried component may be produced by mixing such an aqueous solution with the required amount of the sulphate, with the addition of more water if necessary to reduce total solids content, and then forming granules by spraying the solution into a conventional counter-current or co-current spray-drying tower. In the tower water is evaporated by hot gas, usually hot air, preferably to a level of less than 10% by weight of free moisture in the finished spray-dried component.
  • the spray-dried granules may pass through further drying and/or cooling steps in conventional process equipment, such as a fluid bed. Oversize and fines fractions are normally removed, for example, by passing the granules over vibrating screen.
  • Further processing including additional granulation steps, agglomeration or compaction, as well as dry mixing with other components may be to provide finished products such as detergent powders, bar soaps and tablets.
  • Example 1 Example 2 DTPMP 80 84 MgSO4 . 7H2O 10 5 Sodium chloride 5 6 Free moisture 5 5 DTPMP is hepta sodium salt of diethylene triamine penta(methylene phosphonic acid) MgSO4 . 7H2O is Epsom salts All levels are % by weight unless otherwise specified
  • the spray-dried component produced in these examples have a bulk density of from 500 g/l to 700 g/l.
  • the component absorbs very little moisture after manufacture (e.g. from atmospheric humidity) and hence flowability and caking problems are minimsed or eliminated even in environments of high temperature and high humidity.

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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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

The present invention relates to a spray-dried component which is in the form of a free-flowing particle with high chelant activity comprising:
  • i) at least 50%, preferably at least 60%, by weight of a chelant;
  • ii) from 1% to 25%, preferably from 5% to 10%, by weight of a alkali metal, or alkaline earth metal sulphate; and
  • iii) preferably less than 10% by weight free moisture.

Description

  • The present invention relates to a spray-dried component comprising a chelant, in particular diethylene triamine penta(methylene phosphonic acid) or its salts. Such components are useful in granular detergent products, and also as intermediate products in the manufacture of bar soap, detergent tablets and other detergent forms such as extrudates, agglomerates and the like.
  • US-A-4 259 200, issued on March 31, 1981, discloses phosphonates complexed with calcium, magnesium, zinc or aluminium ions, the molar ratio of metal ion to phosphonate being at least 1:1. It is disclosed that the magnesium and the phosphonate can be premixed in any suitable solvent, including water, optionally mixed with other detergent components and spray-dried. Improved storage stability in bleaching compositions is sought.
  • EP-A-0 225 309, published on June 10th, 1987, discloses the addition of salts of alkali or alkaline earth metals into particles comprising diethylene triamine penta(methylene phosphonic acid) for the purpose of improving free-flow and storage properties. The amount of sulphate is 60% to 200% of the dry weight of the chelant, corresponding to a weight ratio of metal ion salt to chelant of from 0.6:1 to 2:1. Preferred water content after spray-drying is less than 10% by weight of the particle.
  • The prior art does not suggest that spray-dried components may be prepared having a high chelant content (at least 50% by weight) and which still maintain good free-flowing properties.
  • The object of the present invention is to provide a spray-dried component which is in the form of a free-flowing particle with high chelant activity
  • Summary of the Invention
  • This object is achieved by a spray-dried component comprising:
    • i) at least 50%, preferably at least 60%, by weight of a chelant;
    • ii) from 1% to 25%, preferably from 5% to 10%, by weight of a alkali metal, or alkaline earth metal sulphate; and
    • iii) preferably less than 10% by weight free moisture.
  • The chelant is preferably a phosphonic or succinic acid, or salt of phosphonic or succinic acid, more preferably the chelant is selected form the group consisting of diethylene triamine penta(methylene phosphonic acid), ethylene diamine-N,N'-disuccinic acid, or mixtures, or salts thereof.
  • The alkaline earth metal is preferably magnesium.
  • Detailed Description of the Invention
  • The spray-dried component of the present invention comprises a chelant. Chelants are used, for example in detergent compositions, for their ability to complex with metal irons such as iron and/or manganese forming soluble chelates. Suitable chelants can be selected from the group consisting of amino carboxylates, amino phosphonates, polyfunctionally-substituted aromatic chelants and mixtures thereof.
  • Useful amino carboxylates include ethylenediaminetetracetates ("EDTA"), N-hydroxyethylethylene diaminetriacetates, nitrilotriacetates, ethylene diamine tetraproprionates, triethylene tetraaminehexacetates, diethylenetriaminepentaacetates, and ethanoldiglycines, alkali metal, ammonium, and substituted ammonium salts thereof, and mixtures thereof.
  • Useful amino phosphonates include ethylenediaminetetrakis (methylenephosphonates), sold as DEQUEST®. Preferably these amino phosphonates do not contain alkyl or alkenyl groups with more than about 6 carbon atoms.
  • Particularly preferred chelants are diethylene triamine penta(methylene phosphonic acid) ("DTPMP") and ethylene diamine tetra(methylene phosphonic acid) (EDTMP).
  • Polyfunctionally-substituted aromatic chelants are also useful in the components herein. See US-A-3 812 044, issued May 21, 1974, to Connor et al. Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2-dihydroxy-3,5-disulfobenzene.
  • A preferred biodegradable chelant for use herein is ethylene diamine-N,N'-disuccinate ("EDDS"), especially the [S,S] isomer as described in US-A-4 704 233, issued on November 3, 1987, to Hartman and Perkins.
  • Magnesium, aluminium or zinc sulphates are preferred for use in the present invention, magnesium sulphate being the most preferred. Epsom salts; MgSO4 . 7H2O, i.e. the hydrated, crystalline form of magnesium sulphate with seven moles of water is particularly preferred.
  • The chelants used in the present invention may be conveniently provided from commercially available sources in aqueous solution. Typical commercially available solutions have a chelant activity of from about 40% to about 60% by weight. The spray-dried component may be produced by mixing such an aqueous solution with the required amount of the sulphate, with the addition of more water if necessary to reduce total solids content, and then forming granules by spraying the solution into a conventional counter-current or co-current spray-drying tower. In the tower water is evaporated by hot gas, usually hot air, preferably to a level of less than 10% by weight of free moisture in the finished spray-dried component.
  • Optionally the spray-dried granules may pass through further drying and/or cooling steps in conventional process equipment, such as a fluid bed. Oversize and fines fractions are normally removed, for example, by passing the granules over vibrating screen.
  • Further processing including additional granulation steps, agglomeration or compaction, as well as dry mixing with other components may be to provide finished products such as detergent powders, bar soaps and tablets.
  • Examples
  • Example 1 Example 2
    DTPMP 80 84
    MgSO4 . 7H2O 10 5
    Sodium chloride 5 6
    Free moisture 5 5
    DTPMP is hepta sodium salt of diethylene triamine penta(methylene phosphonic acid)
    MgSO4 . 7H2O is Epsom salts
    All levels are % by weight unless otherwise specified
  • The spray-dried component produced in these examples have a bulk density of from 500 g/l to 700 g/l. The component absorbs very little moisture after manufacture (e.g. from atmospheric humidity) and hence flowability and caking problems are minimsed or eliminated even in environments of high temperature and high humidity.

Claims (6)

  1. A spray-dried component comprising:
    i) chelant;
    ii) from 1% to 25% by weight of a alkali metal, or alkaline earth metal sulphate; and
    iii) free moisture
    characterised in that the spray dried component comprises at least 50% by weight of a chelant.
  2. A spray-dried component according to claim 1 comprising:
    i) at least 60% by weight of chelant;
    ii) from 5% to 10% by weight of a alkali metal, or alkaline earth metal sulphate; and
    iii) less than 10% by weight free moisture.
  3. A spray-dried component according to either claim 1 or claim 2 wherein the chelant is a phosphonic or succinic acid, or salt of phosphonic or succinic acid, or mixtures thereof.
  4. A spray-dried component according to claim 3 wherein the chelant is selected form the group consisting of diethylene triamine penta(methylene phosphonic acid), ethylene diamine-N,N'-disuccinic acid, salts of diethylene triamine penta(methylene phosphonic acid), salts of ethylene diamine-N,N'-disuccinic acid, or mixtures thereof.
  5. A spray-dried component according to any of the previous claims wherein the alkaline earth metal is magnesium.
  6. A spray-dried component according to claim 5 wherein the alkaline erth metal sulphate is in the hydrated, crystalline form of MgSO4 . 7H2O.
EP96200801A 1996-03-23 1996-03-23 Spray-dried detergent component comprising chelant Expired - Lifetime EP0796911B2 (en)

Priority Applications (13)

Application Number Priority Date Filing Date Title
EP96200801A EP0796911B2 (en) 1996-03-23 1996-03-23 Spray-dried detergent component comprising chelant
DE69621584T DE69621584T3 (en) 1996-03-23 1996-03-23 Chelating agent-containing spray-dried detergent ingredient
PT96200801T PT796911E (en) 1996-03-23 1996-03-23 A DETERGENT DRY DETERGENT COMPONENT FOR SPRAY SPRAY CONTAINING A QUELATING AGENT
ES96200801T ES2177718T5 (en) 1996-03-23 1996-03-23 DETERGENT DRYING COMPONENT BY SPRAYING THAT INCLUDES COMPLAINANT.
AT96200801T ATE218611T1 (en) 1996-03-23 1996-03-23 SPRAY DRIED DETERGENT INGREDIENTS CONTAINING CHELATING GENERS
DK96200801T DK0796911T3 (en) 1996-03-23 1996-03-23 Spray-dried detergent component comprising chelating agent
PCT/US1997/004651 WO1997035953A1 (en) 1996-03-23 1997-03-21 Spray-dried component comprising chelant
CN97194764A CN1119403C (en) 1996-03-23 1997-03-21 Spray-dried component comprising chelant
CA002249268A CA2249268C (en) 1996-03-23 1997-03-21 Spray-dried component comprising chelant
JP09534515A JP3093283B2 (en) 1996-03-23 1997-03-21 Spray-dried ingredients containing chelating agents
US09/155,161 US5958866A (en) 1996-03-23 1997-03-21 Spray-dried component comprising chelant
BR9708333A BR9708333A (en) 1996-03-23 1997-03-21 Spray-dried component comprising chelator
ARP970101151A AR006349A1 (en) 1996-03-23 1997-03-21 DETERGENT COMPONENT, DRYED BY ASPERSION, INCLUDING CHEATING AGENT.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP96200801A EP0796911B2 (en) 1996-03-23 1996-03-23 Spray-dried detergent component comprising chelant

Publications (3)

Publication Number Publication Date
EP0796911A1 true EP0796911A1 (en) 1997-09-24
EP0796911B1 EP0796911B1 (en) 2002-06-05
EP0796911B2 EP0796911B2 (en) 2005-07-13

Family

ID=8223811

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96200801A Expired - Lifetime EP0796911B2 (en) 1996-03-23 1996-03-23 Spray-dried detergent component comprising chelant

Country Status (12)

Country Link
EP (1) EP0796911B2 (en)
JP (1) JP3093283B2 (en)
CN (1) CN1119403C (en)
AR (1) AR006349A1 (en)
AT (1) ATE218611T1 (en)
BR (1) BR9708333A (en)
CA (1) CA2249268C (en)
DE (1) DE69621584T3 (en)
DK (1) DK0796911T3 (en)
ES (1) ES2177718T5 (en)
PT (1) PT796911E (en)
WO (1) WO1997035953A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999013040A1 (en) * 1997-09-11 1999-03-18 The Procter & Gamble Company Detergent compositions
WO2000012463A1 (en) * 1998-08-27 2000-03-09 The Dow Chemical Company Stable free-flowing solid chelants
WO2000020550A1 (en) * 1998-10-05 2000-04-13 The Procter & Gamble Company Process for delivering chelant agglomerate into detergent composition for improving its storage stability, flowability and scoopability
US6451224B1 (en) 1999-07-21 2002-09-17 The Dow Chemical Company Stable free-flowing solid chelants
EP1281676A1 (en) * 2001-08-01 2003-02-05 NV Solutia Europe S.A. Solid free-flowing phosphonate composition and method of use
US6635612B1 (en) 1999-10-01 2003-10-21 The Procter & Gamble Company Process for delivering chelant agglomerate into detergent composition for improving its storage stability, flowability and scoopability
US7423005B2 (en) * 2003-11-20 2008-09-09 Ecolab Inc. Binding agent for solidification matrix

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2380962B1 (en) * 2010-04-23 2016-03-30 The Procter and Gamble Company Particle

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EP0040038A2 (en) * 1980-05-10 1981-11-18 THE PROCTER & GAMBLE COMPANY Granular detergent compositions
EP0225309A2 (en) * 1985-11-29 1987-06-10 Monsanto Europe S.A./N.V. Aminomethylenephosphonate compositions
FR2677370A1 (en) * 1991-06-05 1992-12-11 Nln Sa Sequestering agent for liquid detergent compositions; liquid detergent compositions containing the said sequestering agent

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GB1513550A (en) † 1975-05-05 1978-06-07 Unilever Ltd Hard surface cleaning compositions
US4105573A (en) † 1976-10-01 1978-08-08 The Procter & Gamble Company Dishwasher detergent composition
CH642678A5 (en) * 1979-04-06 1984-04-30 Unilever Nv Bleach and detergent.
GB8504489D0 (en) † 1985-02-21 1985-03-27 Monsanto Europe Sa Aminomethylenephosphonate compositions
CA2096255C (en) * 1990-11-14 1998-01-20 Jeffrey D. Painter Nonphosphated automatic dishwashing compositions with oxygen bleach systems and process for their preparation
EP0678572A1 (en) † 1994-04-20 1995-10-25 The Procter & Gamble Company Detergent powder compositions

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Publication number Priority date Publication date Assignee Title
FR2289603A1 (en) * 1974-11-04 1976-05-28 Witco Chemical Corp DETERGENT COMPOSITION BASED ON LINEAR ALKYL-ARYL-SULPHONATE AND A NON-AGGLUTINING AGENT
EP0040038A2 (en) * 1980-05-10 1981-11-18 THE PROCTER & GAMBLE COMPANY Granular detergent compositions
EP0225309A2 (en) * 1985-11-29 1987-06-10 Monsanto Europe S.A./N.V. Aminomethylenephosphonate compositions
FR2677370A1 (en) * 1991-06-05 1992-12-11 Nln Sa Sequestering agent for liquid detergent compositions; liquid detergent compositions containing the said sequestering agent

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999013040A1 (en) * 1997-09-11 1999-03-18 The Procter & Gamble Company Detergent compositions
WO2000012463A1 (en) * 1998-08-27 2000-03-09 The Dow Chemical Company Stable free-flowing solid chelants
WO2000020550A1 (en) * 1998-10-05 2000-04-13 The Procter & Gamble Company Process for delivering chelant agglomerate into detergent composition for improving its storage stability, flowability and scoopability
US6451224B1 (en) 1999-07-21 2002-09-17 The Dow Chemical Company Stable free-flowing solid chelants
US6635612B1 (en) 1999-10-01 2003-10-21 The Procter & Gamble Company Process for delivering chelant agglomerate into detergent composition for improving its storage stability, flowability and scoopability
EP1281676A1 (en) * 2001-08-01 2003-02-05 NV Solutia Europe S.A. Solid free-flowing phosphonate composition and method of use
US7423005B2 (en) * 2003-11-20 2008-09-09 Ecolab Inc. Binding agent for solidification matrix

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JP3093283B2 (en) 2000-10-03
BR9708333A (en) 1999-08-03
CA2249268A1 (en) 1997-10-02
CN1219197A (en) 1999-06-09
ATE218611T1 (en) 2002-06-15
AR006349A1 (en) 1999-08-25
EP0796911B2 (en) 2005-07-13
ES2177718T5 (en) 2005-12-01
DE69621584D1 (en) 2002-07-11
JPH11507098A (en) 1999-06-22
CA2249268C (en) 2002-02-05
WO1997035953A1 (en) 1997-10-02
PT796911E (en) 2002-10-31
DE69621584T3 (en) 2006-06-01
DE69621584T2 (en) 2003-01-16
CN1119403C (en) 2003-08-27
ES2177718T3 (en) 2002-12-16
DK0796911T3 (en) 2002-09-30
EP0796911B1 (en) 2002-06-05

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