EP0678572A1 - Waschmittelpulverzusammensetzungen - Google Patents

Waschmittelpulverzusammensetzungen Download PDF

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Publication number
EP0678572A1
EP0678572A1 EP94201092A EP94201092A EP0678572A1 EP 0678572 A1 EP0678572 A1 EP 0678572A1 EP 94201092 A EP94201092 A EP 94201092A EP 94201092 A EP94201092 A EP 94201092A EP 0678572 A1 EP0678572 A1 EP 0678572A1
Authority
EP
European Patent Office
Prior art keywords
acid
free
detergent powder
powder according
weight
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.)
Ceased
Application number
EP94201092A
Other languages
English (en)
French (fr)
Inventor
Achille Jules Edmond Doumen
Luc Goovaerts
Jose Luis Vega
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
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP94201092A priority Critical patent/EP0678572A1/de
Priority to PCT/US1995/004799 priority patent/WO1995029216A1/en
Priority to PE26682295A priority patent/PE996A1/es
Priority to JP7527734A priority patent/JPH09512300A/ja
Priority to CN 95193528 priority patent/CN1150450A/zh
Priority to BR9507326A priority patent/BR9507326A/pt
Priority to US08/722,090 priority patent/US5780419A/en
Priority to CA 2187517 priority patent/CA2187517A1/en
Priority to AU24602/95A priority patent/AU2460295A/en
Priority to TW084107455A priority patent/TW341597B/zh
Publication of EP0678572A1 publication Critical patent/EP0678572A1/de
Ceased 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
    • C11D3/046Salts
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium 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
    • 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
    • C11D3/168Organometallic compounds or orgometallic complexes
    • 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
    • C11D3/361Phosphonates, phosphinates or phosphonites
    • 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
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
    • 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

Definitions

  • the present invention relates to detergent powders which essentially comprise a complexed chelating agent and an anionic polymer.
  • the powders may be readily prepared by spray drying.
  • Detergent components and compositions have been made using various spray drying techniques for many years. Typically various detergent active materials are dissolved or dispersed in an aqueous solution which is then pumped under high pressure to an atomiser, such as a nozzle or a spinning disc.
  • an atomiser such as a nozzle or a spinning disc.
  • chelating agents are frequently precomplexed with magnesium in order to protect them from degradation in the presence of bleach.
  • molar ratios of magnesium : chelating agent of greater than 3:1 are difficult to prepare due to precipitation from aqueous solution. Precipitation in a spray drying process rapidly leads to blockage of the nozzle.
  • powders which essentially consist of chelating agent / magnesium complex have a very low rate of solubility.
  • anionic polymer also enables powders to be prepared which have a very high organic content, preferably greater than 80%. Such powders which are difficult to prepare by other means, provide a convenient method for handling and processing organic polymers.
  • the present invention relates to free-flowing detergent powder which is prepared by spray drying, the powder comprising :
  • the powder comprises less than 20%, more preferably less than 10% by weight (on anhydrous basis), of inorganic components other than the metal ion (a)(ii). Most preferably the total level of aluminosilicate and carbonate (on anhydrous basis) is less than 10% by weight.
  • the chelating agent is preferably selected from the group consisting of phosphonic acid, succinic acid, the salts of phosphonic or succinic acid, or mixtures thereof, even more preferred chelating agents are diethylene triamine penta (methylene phosphonic acid), or ethylenediamine-N-N'-disuccinic acid, or their salts, or mixtures thereof.
  • the preferred metal ion is magnesium.
  • the molar ratio of the metal ion to the chelating agent is preferably greater than 3:1.
  • the polymer may comprise carboxylate functional groups, especially the water-soluble salts of homo-and copolymers of aliphatic carboxylic acids such as acrylic acid, maleic acid, vinylic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid, methylenemalonic acid and mixtures thereof.
  • carboxylate functional groups especially the water-soluble salts of homo-and copolymers of aliphatic carboxylic acids such as acrylic acid, maleic acid, vinylic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid, methylenemalonic acid and mixtures thereof.
  • a preferred polymer is a copolymer of maleic and acrylic acid having a molecular weight of from 2000 to 100 000.
  • the free-flowing detergent powder may also comprise a cationic surfactant.
  • the cationic surfactant may be present at from 1% to 80% by weight , from 2% to 20% by weight of dimethyl ethoxy ammonium chloride being preferred.
  • the essential components of the present invention are a chelating agent and a polymer comprising anionic functional groups. Examples of these will now be given in more detail.
  • the chelating agents suitable for use in the present invention can be chosen from a wide range of chemicals which are known to the man skilled in the art.
  • suitable chelating agents are phosphonic and succinic acids and their salts.
  • the polyphosphonates are the sodium and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts of ethane 1-hydroxy-1,1-diphosphonic acid and the sodium and potassium salts of ethane, 1,1,2-triphosphonic acid.
  • particularly suitable chelating agents are ethylene diamine tetra (methylene phosphonic acid) and diethylene triamine penta (methylene phosphonic acid).
  • EDDS ethylenediamine-N,N'-disuccinic acid
  • Preferred EDDS compounds are the free acid form and the sodium or magnesium salt thereof.
  • Examples of such preferred sodium salts of EDDS include NaEDDS, Na2EDDS and Na4EDDS.
  • Examples of such preferred magnesium salts of EDDS include Mg EDDS and Mg2EDDS.
  • the magnesium salts are the most preferred for inclusion in compositions in accordance with the invention.
  • EDDS can be synthesised, for example, from readily available, inexpensive starting material such as maleic anhydride and ethylene diamine as follows : A more complete disclosure of methods for synthesising EDDS from commercially available starting materials can be found in US Patent 3,158,635, Kezerian and Ramsay, issued November 24, 1964.
  • the [S,S] isomer of EDDS can be synthesised from L-aspartic acid and 1,.2-dibromoethane, as follows : A more complete disclosure of the reaction of L-aspartic acid with 1,2-dibromoethane to form the [S,S] isomer of EDDS can be found in Neal and Rose, Stereospecific Ligands and Their Complexes of Ethylenediaminediscuccinic Acid, Inorganic Chemistry, Vol 7 (1968), pp. 2405-2412.
  • carboxylates and other chelanting agents which are suitable for use in the present invention are given below.
  • the polymers and co-polymers of the present invention may be chosen from a wide range of organic polymers, some of which also may function as builders to improve detergency. Included among such polymers may be mentioned sodium carboxy-lower alkyl celluloses, sodium lower alkyl celluloses and sodium hydroxy-lower alkyl celluloses, such as sodium carboxymethyl cellulose, sodium methyl cellulose and sodium hydroxypropyl cellulose, polyacrylates, polyaspartates and various copolymers, such as those of maleic and acrylic acids. Molecular weights for such polymers vary widely but most are within the range of 2,000 to 100,000.
  • Polymeric polycarboxyate builders are set forth in U.S. Patent 3,308,067, Diehl, issued March 7, 1967. Such materials include the water-soluble salts of homo-and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylenemalonic acid.
  • copolymers of maleic and acrylic acid having a molecular weight of from 2000 to 100000, carboxymethyl cellulose and mixtures thereof.
  • Optional ingredients in the spray dried powder of the present invention are cationic surfactants.
  • Useful cationic surfactants include water-soluble quaternary ammonium compounds of the form R4R5R6R7N+X ⁇ , wherein R4 is alkyl having from 10 to 20, preferably from 12-18 carbon atoms, and R5 is C1 to C20, R6 and R7 are each C1 to C7 alkyl preferably methyl; X ⁇ is an anion, e.g. chloride.
  • Examples of such trimethyl ammonium compounds include C12 ⁇ 14 alkyl trimethyl ammonium chloride, C12 ⁇ 14 alkyl dimethyl ethoxy ammonium chloride and C12 ⁇ 14 alkyl trimethyl ammonium methosulfate.
  • An essential step of the process of making the spray-dried powder of the present invention is the preparation of the complex of the chelating agent with the metal ion. Preferably this is done by dissolving a salt of the metal ion into a solution of the chelating agent in the required ratios.
  • the molar ratio of metal ion to chelating agent is preferably at least 1:1, the present invention allows molar ratios of greater than 3:1 to be prepared, most preferred is a molar ratio of about 5:1. Whilst any metal salt may be used, magnesium sulphate is most preferred.
  • the anionic polymer is added to the solution comprising the complex together with any other optional ingredients.
  • the resulting slurry or solution is then spray dried by conventional means.
  • the most preferred method for spray drying is the use of spinning disc atomiser.
  • the free-flowing spray-dried powder is admixed with other detergent powders to form a finished granular detergent product. It is an important advantage of the present invention that the spray-dried powder dissolves rapidly in water to release the chelating agent and polymer as early as possible into the washing process.
  • Components of the finished detergent composition may be chosen from a very wide range of detergent active materials. Common examples include surfactants, builders, bleach, bleach activator, enzymes, optical brighteners, soil release polymers, dye transfer inhibiting agents, softening clay, perfume, etc.
  • the spray-dried powder of the present invention may be further processed, for example by additional granulation, agglomeration, compaction steps.
  • a particularly preferred process is described in EP 508543, published on 14th October, 1992.
  • a process is disclosed for structuring or "conditioning" a high active surfactant paste and then granulating in the presence of detergent powder.
  • the spray-dried powder may be a component either of the conditioning step, or of the granulation step, or of both steps.
  • Using this process in combination with the spray-dried powder of the present invention enables free-flowing detergent granulates to be produced having a surfactant content of at least 40% by weight, and a bulk density of at least 600 g/l.
  • the composition was prepared by mixing a 40% active solution of the sodium salt of the copolymer, a 25% active solution of the phosphonic acid and the sulphate powder (MgSO4 . 7 H2O) to give a slurry.
  • the slurry was then processed through a continuous spray dryer with co-current air inlet and a rotating disc (15000 rpm) at the top of the tower. After the exit from the bottom of the tower, two fluid beds in series provide further drying and cooling of the spray dried product.
  • the resulting spray dried powder had a bulk density of 450 g/l (measured by the repour cup method).
  • the resulting powder is free flowing and has a bulk density of 460 g/l.
  • the resulting powder is free flowing and has a bulk density of 450 g/L.
  • the resulting powder is free flowing and has a bulk density of 430g/L.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP94201092A 1994-04-20 1994-04-20 Waschmittelpulverzusammensetzungen Ceased EP0678572A1 (de)

Priority Applications (10)

Application Number Priority Date Filing Date Title
EP94201092A EP0678572A1 (de) 1994-04-20 1994-04-20 Waschmittelpulverzusammensetzungen
PCT/US1995/004799 WO1995029216A1 (en) 1994-04-20 1995-04-20 Detergent powder compositions comprising metal ion-chelant complex and anionic functional polymer
PE26682295A PE996A1 (es) 1994-04-20 1995-04-20 Composiciones detergentes en forma de polvo
JP7527734A JPH09512300A (ja) 1994-04-20 1995-04-20 金属イオン−キレート化剤錯体および陰イオン官能重合体を含む洗剤粉末組成物
CN 95193528 CN1150450A (zh) 1994-04-20 1995-04-20 包含金属离子螯合配合物和阴离子官能聚合物的洗涤剂粉末组合物
BR9507326A BR9507326A (pt) 1994-04-20 1995-04-20 Composições em pó detergentes compreendendo complexo de quelante de íon de metal e polímero funcional aniônico
US08/722,090 US5780419A (en) 1994-04-20 1995-04-20 Detergent powder compositions comprising metal ion-chelant complex and anionic functional polymer
CA 2187517 CA2187517A1 (en) 1994-04-20 1995-04-20 Detergent powder compositions comprising metal ion-chelant complex and anionic functional polymer
AU24602/95A AU2460295A (en) 1994-04-20 1995-04-20 Detergent powder compositions comprising metal ion-chelant complex and anionic functional polymer
TW084107455A TW341597B (en) 1994-04-20 1995-07-19 Detergent powder compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP94201092A EP0678572A1 (de) 1994-04-20 1994-04-20 Waschmittelpulverzusammensetzungen

Publications (1)

Publication Number Publication Date
EP0678572A1 true EP0678572A1 (de) 1995-10-25

Family

ID=8216815

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94201092A Ceased EP0678572A1 (de) 1994-04-20 1994-04-20 Waschmittelpulverzusammensetzungen

Country Status (9)

Country Link
EP (1) EP0678572A1 (de)
JP (1) JPH09512300A (de)
CN (1) CN1150450A (de)
AU (1) AU2460295A (de)
BR (1) BR9507326A (de)
CA (1) CA2187517A1 (de)
PE (1) PE996A1 (de)
TW (1) TW341597B (de)
WO (1) WO1995029216A1 (de)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001044428A1 (en) * 1999-12-16 2001-06-21 Unilever Plc Detergent compositions
WO2001088077A1 (en) * 2000-05-15 2001-11-22 Unilever Plc Detergent compositions
WO2001092449A1 (en) * 2000-06-02 2001-12-06 Unilever Plc Detergent compositions
WO2011038078A1 (en) * 2009-09-23 2011-03-31 The Procter & Gamble Company Process for preparing spray-dried particles
WO2011075503A1 (en) * 2009-12-18 2011-06-23 The Procter & Gamble Company A spray-drying process
WO2011133462A1 (en) * 2010-04-23 2011-10-27 The Procter & Gamble Company Particle
US9096820B2 (en) 2009-12-24 2015-08-04 Akzo Nobel Chemicals International B.V. Coated particles of a glumatic acid N,N-diacetate chelating agent
WO2019162134A1 (en) * 2018-02-23 2019-08-29 Unilever N.V. Solid compositions comprising aminopolycarboxylate
WO2019211170A1 (en) * 2018-05-04 2019-11-07 Basf Se Granules or powders and methods for their manufacture

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE218611T1 (de) 1996-03-23 2002-06-15 Procter & Gamble Chelatbildner enthaltender sprühgetrockneter waschmittelbestandteil
US6599989B2 (en) 1998-03-03 2003-07-29 Nippon Skokubai Co., Ltd. Water-absorbent agents containing polycarboxylic amine chelating agents
DE19937345A1 (de) * 1999-08-11 2001-02-15 Basf Ag Mischpulver oder Mischgranulat auf Basis von Glycin-N,N-diessigsäure
EP1803801A1 (de) * 2006-01-03 2007-07-04 Basf Aktiengesellschaft Mischpulver oder Mischgranulat auf Basis von Glutaminsäure-N,N-diessigsäure und ihren Salzen
PL2380962T3 (pl) * 2010-04-23 2017-01-31 The Procter And Gamble Company Cząstka

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2453212A1 (fr) * 1979-04-06 1980-10-31 Unilever Nv Compositions de blanchiment et de nettoyage
US4846993A (en) * 1988-07-11 1989-07-11 Ecolab Inc. Zero phosphate warewashing detergent composition
WO1992009680A1 (en) * 1990-11-14 1992-06-11 The Procter & Gamble Company Nonphosphated dishwashing compositions with oxygen bleach systems
DE4213036A1 (de) * 1992-04-21 1993-10-28 Henkel Kgaa Granulares, alkalisches, phosphatfreies Reinigungsadditiv

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2493294A1 (fr) * 1980-11-04 1982-05-07 Air Liquide Compositions stabilisantes pour produits peroxydes
US4614646A (en) * 1984-12-24 1986-09-30 The Dow Chemical Company Stabilization of peroxide systems in the presence of alkaline earth metal ions
US4959409A (en) * 1988-01-14 1990-09-25 The Procter & Gamble Company Amino-functional compounds as builder/dispersants in detergent compositions
US5318728A (en) * 1992-11-30 1994-06-07 The Procter & Gamble Company Low sudsing polyhydroxy fatty acid amide detergents

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2453212A1 (fr) * 1979-04-06 1980-10-31 Unilever Nv Compositions de blanchiment et de nettoyage
US4259200A (en) * 1979-04-06 1981-03-31 Lever Brothers Company Bleaching and cleaning compositions
US4846993A (en) * 1988-07-11 1989-07-11 Ecolab Inc. Zero phosphate warewashing detergent composition
WO1992009680A1 (en) * 1990-11-14 1992-06-11 The Procter & Gamble Company Nonphosphated dishwashing compositions with oxygen bleach systems
DE4213036A1 (de) * 1992-04-21 1993-10-28 Henkel Kgaa Granulares, alkalisches, phosphatfreies Reinigungsadditiv

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001044428A1 (en) * 1999-12-16 2001-06-21 Unilever Plc Detergent compositions
AU760259B2 (en) * 1999-12-16 2003-05-08 Unilever Plc Detergent compositions
WO2001088077A1 (en) * 2000-05-15 2001-11-22 Unilever Plc Detergent compositions
WO2001092449A1 (en) * 2000-06-02 2001-12-06 Unilever Plc Detergent compositions
US6395696B2 (en) 2000-06-02 2002-05-28 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent compositions containing a cationic detergent and builder
CN100390258C (zh) * 2000-06-02 2008-05-28 荷兰联合利华有限公司 洗涤剂组合物
WO2011038078A1 (en) * 2009-09-23 2011-03-31 The Procter & Gamble Company Process for preparing spray-dried particles
EP2338970A1 (de) * 2009-12-18 2011-06-29 The Procter & Gamble Company Sprühtrockenverfahren
WO2011075503A1 (en) * 2009-12-18 2011-06-23 The Procter & Gamble Company A spray-drying process
US9096820B2 (en) 2009-12-24 2015-08-04 Akzo Nobel Chemicals International B.V. Coated particles of a glumatic acid N,N-diacetate chelating agent
WO2011133462A1 (en) * 2010-04-23 2011-10-27 The Procter & Gamble Company Particle
EP2383329A1 (de) * 2010-04-23 2011-11-02 The Procter & Gamble Company Partikel
WO2019162134A1 (en) * 2018-02-23 2019-08-29 Unilever N.V. Solid compositions comprising aminopolycarboxylate
CN111788290A (zh) * 2018-02-23 2020-10-16 荷兰联合利华有限公司 包含氨基多羧酸盐的固体组合物
CN111788290B (zh) * 2018-02-23 2021-08-27 联合利华知识产权控股有限公司 包含氨基多羧酸盐的固体组合物
WO2019211170A1 (en) * 2018-05-04 2019-11-07 Basf Se Granules or powders and methods for their manufacture

Also Published As

Publication number Publication date
TW341597B (en) 1998-10-01
CA2187517A1 (en) 1995-11-02
PE996A1 (es) 1996-02-21
JPH09512300A (ja) 1997-12-09
BR9507326A (pt) 1997-09-30
WO1995029216A1 (en) 1995-11-02
AU2460295A (en) 1995-11-16
CN1150450A (zh) 1997-05-21

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