WO1997020020A1 - Detergent builder granule - Google Patents

Detergent builder granule Download PDF

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Publication number
WO1997020020A1
WO1997020020A1 PCT/EP1996/004886 EP9604886W WO9720020A1 WO 1997020020 A1 WO1997020020 A1 WO 1997020020A1 EP 9604886 W EP9604886 W EP 9604886W WO 9720020 A1 WO9720020 A1 WO 9720020A1
Authority
WO
WIPO (PCT)
Prior art keywords
weight
zeolite
builder
granules
builder granule
Prior art date
Application number
PCT/EP1996/004886
Other languages
English (en)
French (fr)
Inventor
Theodorus Johannes Cornelis Arts
Govert Johannes Augustijn
Hendrik Johannes J. Connotte
Theo Jan Osinga
Original Assignee
Unilever N.V.
Unilever Plc
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 Unilever N.V., Unilever Plc filed Critical Unilever N.V.
Priority to AU75679/96A priority Critical patent/AU701161B2/en
Priority to DE69626302T priority patent/DE69626302T2/de
Priority to CA002237575A priority patent/CA2237575C/en
Priority to EP96938147A priority patent/EP0863974B1/en
Priority to JP9520103A priority patent/JP2000500799A/ja
Priority to BR9611645A priority patent/BR9611645A/pt
Publication of WO1997020020A1 publication Critical patent/WO1997020020A1/en

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
    • C11D3/20Organic 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites

Definitions

  • the present invention relates to detergent builder granules, more particularly zeolite builder granules.
  • the invention also relates to detergent compositions including such granules.
  • Zeolites of the molecular sieve type have commonly been employed in cleansers, particularly in laundry detergent compositions, as a builder to provide a water softening function, when the detergent or cleanser is placed in an aqueous solution. Zeolites have more recently been employed to replace phosphate builders.
  • zeolites have been found to be relatively difficult to employ in dry-mixed detergent compositions, for a number of reasons. Difficulties arising during manufacture of detergent compositions with zeolite have often been related to the fine particle size of the crystalline zeolites. Typically, zeolites have a particle size of approximately 1-20 microns. Thus, if the zeolite is used in its normal state with such a particle size, it commonly presents problems with dusting and segregation in the detergent composition.
  • EP-A-403,084 discloses a method of forming a zeolite agglomerate, including the steps of blending zeolite particles with a filler and a surfactant, and then agglomerating the thus formed blend in a rotary agglomerator with a zeolite binder.
  • the zeolite agglomerate is subsequently combined with other detergent constituents in a second agglomeration step to form a granular detergent product with minimal segregation and dusting.
  • Silicate and polyacrylate are mentioned as preferred binding agents.
  • EP-A-368,364 and EP-A-279,038 disclose other types of zeolite granules comprising crystalline zeolite material and relatively small amounts of nonionic surfactant and carboxymethyl cellulose.
  • the present invention provides a builder granule suitable for use in a particulate detergent composition, comprising:
  • alkalimetal carboxymethyl cellulose having a purity of more than 80% by weight, up to 20% by weight, preferably 5-12% by weight, of water.
  • the present invention provides a particulate detergent composition, comprising one or more nonionic and/or anionic surfactants and builder granules according to the present invention.
  • the builder granule of the present invention has an average particle size which is generally in the range of 180-2000 microns, an average particle size of 200-800 microns being preferred.
  • the binding agent is the binding agent
  • Alkalimetal carboxymethyl cellulose preferably sodium carboxymethyl cellulose
  • the CMC in the builder granule should have a purity of at least 80% by weight, preferably at least 85% by weight. A purity of at least 90% by weight is more preferred, the remainder of the CMC being mainly salts and absorbed water.
  • the level at which the CMC is present in the builder granule of the invention is generally 1-10% by weight, whereas a level of 3-5% by weight is preferred.
  • the builder granule of the invention further contains a level of up to 25% by weight of a nonionic surfactant. If the builder granule is applied as such, for instance as water softener, then it preferably does not contain any nonionic surfactant.
  • the builder granule of the invention is applied as a constituent of a particulate detergent formulation, then it contains nonionic surfactant material at a level of preferably 5-25%, more preferably 10-20% by weight.
  • a low meso-phase forming surfactant is defined as a type of surfactant which does not show substantial gel-formation when diluted with water, whereas a non meso-phase forming surfactant does not show substantial viscosity increase when diluted with water.
  • Suitable types of nonionic surfactants for use in the builder granule of the invention are fatty alcohol ethoxylates having an average of 3 - 8 ethylene oxide groups per molecule.
  • Preferred fatty alcohol ethoxylates are non or low meso-phase forming.
  • the zeolite material which is present in the builder granule of the invention at a level of 50-90%, preferably 60-90%, more preferably 70-80% by weight, can be a crystalline sodium aluminosilicate detergency builder, as described, for example, in GB 1 429 143 (Procter & Gamble) .
  • Suitable sodium aluminosilicates of this type are the well- known commercially available zeolites A and X, and mixtures thereof.
  • the zeolite may be the commercially available zeolite 4A now widely used in laundry detergent powders.
  • the zeolite material incorporated in the builder granule of the invention is maximum aluminium zeolite P (zeolite MAP) , as described and claimed in EP-A-384,070 (Unilever) .
  • Zeolite MAP is defined as an alkalimetal aluminosilicate of the zeolite P type having a silicon to aluminium ratio not exceeding 1.33, preferably within the range of from 0.90 to 1.33, and more preferably within the range of from 0.90 to 1.20.
  • zeolite MAP having a silicon to aluminium ratio not exceeding 1.07, more preferably about 1.00.
  • the calcium binding capacity of zeolite MAP is generally at least 150 mg CaO per gram of anhydrous material, as measured according to method 1 as disclosed in EP-A-384,070.
  • zeolite MAP is most preferred for use in the builder granules of the present invention.
  • zeolite MAP has a lower water content than commercially available zeolite 4A; zeolite MAP has a water level below 18%, whereas zeolite 4A has a water level above 18%. Moreover, the water vapour pressure of zeolite MAP is clearly lower than of zeolite 4A.
  • Zeolite MAP granules have lower friability values than zeolite 4A granules, indicating that zeolite MAP is a stronger type of zeolite. Therefore, detergent formulations including builder granules of the invention containing zeolite MAP have improved properties such as dynamic flow rate and compressibility. Furthermore, the particle size distribution of said formulations may be more uniform and therefore less sensitive to powder segregation, than with builder granules containing zeolite 4A.
  • the liquid carrying capacity of builder granules including zeolite MAP is relatively high, as compared to builder granules including zeolite 4A. Therefore, detergent formulations with high liquid surfactant percentages can be made via simple dry-mixing, when applying zeolite MAP in the builder granules of the invention.
  • the builder granules of the invention are effectively produced by granulating zeolite material with the other constituents of the granules in a low speed mixer/granulator such as a V-blender, a PK Niro Zigzag granulator or a rotating drum.
  • a low speed mixer/granulator such as a V-blender, a PK Niro Zigzag granulator or a rotating drum.
  • this granulation process is carried out in a high speed mixer/granulator such as a FUKAE mixer, a VOMM turbo granulator, a Schugi Flexomix or a L ⁇ dige ploughshare mixer.
  • the thus formed granules are dried in a fluid bed and sieved to obtain the required particle size distribution.
  • the bulk density of the builder granules of the invention is typically in the range of 300-800 g/l, more preferably in the range of 400-700 g/l.
  • the bulk density of the produced builder granules could be effectively controlled by incorporating therein a spray-dried amorphous alkalimetal silicate (desirably having a density of 50-600 g/l) at a level of 0.5-25%, more preferably 0,5-10% by weight.
  • Preferred spraydried amorphous alkalimetal silicates are sodium silicates having a Si0 2 to Na 2 0 mol ratio being in the range of 1.7 - 3.4, sodium silicates having a Si0 2 to Na0 mol ratio in the range of 1.7 to 2.4 being most preferred.
  • the builder granules may be used for producing a wide range of particulate detergent formulations, via the dry-mixing route.
  • the detergent formulation of the invention desirably comprises a peroxy bleach and one or more anionic and/or nonionic surfactants, in addition to the builder granules of the invention. These builder granules are preferably present in said formulation at a level of 20-80% by weight.
  • the total amount of anionic and/or nonionic surfactant present in the detergent composition of the invention will preferably range from 5 to 40% by weight, more preferably from 10 to 30% by weight and especially from 10 to 20% by weight. These figures are typical for fully formulated detergent compositions.
  • the detergent composition of the invention preferably contains one or more nonionic surfactants.
  • Nonionic surfactants that may be used include the primary and secondary alcohol ethoxylates, especially the C -C .. primary and secondary alcohols ethoxylated with an average of from 3 to 20 moles of ethylene oxide per mole of alcohol.
  • Primary and secondary alcohol alkoxylates also containing propylene oxide groups and/or butylene oxide groups as well as end-capped alkoxylates may also be used as a constituent of the detergent composition of the invention.
  • anionic surfactants may be present at a level of up to 20% by weight, said level being desirably in the range of from 1 to 10% by weight, these figures being based on a fully formulated detergent composition.
  • Anionic surfactants are well known to those skilled in the art. Examples include alkylbenzene sulphonates, particularly sodium linear alkylbenzene sulphonates having an alkyl chain length of C 8 -C 1 C- ; primary and secondary alkyl sulphates, particularly sodium C -C primary alcohol sulphates; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
  • the detergent composition of the invention may also comprise a bleach component, encapsulated or not, in an amount of up to 30% by weight.
  • Said bleach component may be a hypohalite bleach such as NaDCCA, or a peroxygen compound, i.e. a compound capable of yielding hydrogen peroxide in aqueous solution.
  • a peroxygen compound selected from alkali metal peroxides, organic peroxides, such as urea peroxide, and inorganic persalts such as the alkali metal perborates, percarbonates, perphosphates, per- silicates and persulphates, is preferably used. Mixtures of two or more of such compounds may also be suitable.
  • Particularly preferred are sodium perborate tetrahydrate and, especially, sodium perborate monohydrate.
  • Sodium perborate monohydrate is preferred because of its high active oxygen content.
  • Sodium percarbonate may also be preferred for environmental reasons.
  • the peroxygen bleach compound is suitably present in the detergent composition of the invention at a level of up to 25% by weight, preferably of from 5 to 20% by weight.
  • the hypohalite bleach may be suitably used in an amount of up to 10%, preferably 1-5% by weight, as active chlorine.
  • Organic peroxyacids may also be suitable as peroxygen bleaching agent.
  • Such materials normally have the general formula:
  • R is an alkylene or substituted alkylene group containing from 1 to about 20 carbon atoms, optionally having an internal amide linkage; or a phenylene or substituted phenylene group; and Y is hydrogen, halogen, alkyl, aryl, an i ido-aromatic or non-aromatic group, a COOH or 0
  • Typical monoperoxy acids useful herein include, for example:
  • peroxybenzoic acid and ring-substituted peroxybenzoic acids e.g. peroxy- ⁇ -naphthoic acid
  • aliphatic, substituted aliphatic and arylalkyl monoperoxyacids e.g. peroxylauric acid, peroxystearic acid and N,N-phthaloylaminoperoxy caproic acid (PAP)
  • PAP N,N-phthaloylaminoperoxy caproic acid
  • 6-octylamino-6-oxo-peroxyhexanoic acid 6-octylamino-6-oxo-peroxyhexanoic acid.
  • Typical diperoxyacids useful herein include, for example:
  • inorganic peroxyacid compounds are suitable, such as for example potassium monopersulphate (MPS) . If organic or inorganic peroxyacids are used as the peroxygen compound, the amount thereof will normally be within the range of about 2-10 % by weight, preferably from 4-8 % by weight.
  • MPS potassium monopersulphate
  • All these peroxide compounds may be utilized alone or in conjunction with a peroxyacid bleach precursor.
  • Peroxyacid bleach precursors are known and amply described in literature, such as in the British Patents 836988; 864,798; 907,356; 1,003,310 and 1,519,351; German Patent 3,337,921; EP-A-0185522; EP-A-0174132; EP-A-0120591; and US Patents 1,246,339; 3,332,882; 4,128,494; 4,412,934 and 4,675,393.
  • peroxyacid bleach precursors are that of the cationic i.e. quaternary ammonium substituted peroxyacid precursors as disclosed in US Patent 4,751,015 and 4,397,757, in EP-A0284292 and EP-A-331,229.
  • peroxyacid bleach precursors of this class are: 2- (N,N,N-trimethyl ammonium) ethyl sodium-4-sulphonphenyl carbonate chloride (SPCC) ;
  • a further special class of bleach precursors is formed by the cationic nitriles as disclosed in EP-A-303, 520 and in European Patent Specification No.'s 458,396 and 464,880.
  • any one of these peroxyacid bleach precursors can be used in the present invention, though some may be more preferred than others.
  • the preferred classes are the esters, including acyl phenol sulphonates and acyl alkyl phenol sulphonates; the acyl-amides; and the quaternary ammonium substituted peroxyacid precursors including the cationic nitriles.
  • Examples of said preferred peroxyacid bleach precursors or activators are sodium-4-benzoyloxy benzene sulphonate (SBOBS) ; N,N,N'N' -tetraacetyl ethylene diamine (TAED) ; sodium-1-methyl-2-benzoyloxy benzene-4-sulphonate; sodium- 4-methyl-3-benzoloxy benzoate; SPCC; trimethyl ammonium toluyloxy-benzene sulphonate; sodium nonanoyloxybenzene sulphonate (SNOBS) ; sodium 3, 5, 5-trimethyl hexanoyloxyben- zene sulphonate (STHOBS) ; and the substituted cationic nitriles .
  • SBOBS sodium-4-benzoyloxy benzene sulphonate
  • TAED N,N,N'N' -tetraacetyl ethylene diamine
  • TAED sodium-1-methyl-2-benz
  • the precursors may be used in an amount of up to 12 %, preferably from 2-10 % by weight, of the composition.
  • Other ingredients may be used in an amount of up to 12 %, preferably from 2-10 % by weight, of the composition.
  • the detergent composition of the invention can contain any of the ingredients conventionally present in compositions intended for the washing of fabrics.
  • examples of such components include inorganic and organic detergency builders, other inorganic salts such as sodium sulphate, fluorescers, polymers, lather control agents, enzymes and perfumes .
  • anti-redeposition agents include anti-redeposition agents, bleach stabilisers, and photobleaches.
  • Dobanol 25-7 c i 2 "Ci 5 ethoxylated alcohol containing an average of 7 ethylene oxide groups per molecule, ex Shell;
  • Example 1 Comparative Example A Two types of builder granules were obtained by granulating zeolite MAP material (as herein defined) with different types of nonionic surfactant and sodium carboxymethyl cellulose (SCMC) , in a Patterson-Kelley blendmaster. For carrying out this granulation process, the SCMC is added as a solution in water.
  • SCMC sodium carboxymethyl cellulose
  • composition of the thus-formed zeolite MAP granules is as follows:
  • Example No. 1 A (%wt) (%wt) zeolite MAP 72.7 72.7
  • Example 1 contains a CMC compound having a purity according to the present invention whereas the granules of Example A contain a different SCMC compound having a purity below the lower limit of 80% by weight, as specified in the present patent application.
  • Example 2 Comparative Example B
  • the zeolite MAP granules of Examples 1 and A were used to prepare particulate detergent formulations, by spraying a surfactant mixture onto said granules and postdosing the other constituents of the formulations.
  • compositions which only differ in respect of the composition of the zeolite MAP granules present therein, have the following composition:
  • a wascator dispenser bank with automatic powder dosing was used.
  • the water intake temperature was set at a constant temperature of 10°C.
  • the water hardness was 6°GH, and the pressure was adjusted at 1.5 bar.
  • the automatic feeding unit was adjusted such that it doses 100 gr of the particulate detergent composition in 8 seconds in a wet dispenser.
  • a pre-wetting time of 1 minute was applied; subsequently, 8 litre water was dosed in 1 minute (at a pressure of 1.5 bar) to flush the detergent formulation out of the dispenser. After 7 minutes powder dosing was started again. This was repeated 10 times.
  • Dispenser residues were assessed by weighing the detergent residues remaining in the dispenser after the test. These residues were collected in the wet state.
  • Builder granules according to the invention were prepared using the granulation process according to the invention.
  • Commercially available builder granules ex Degussa (tradename: Wessalith) was used
  • composition of these zeolite granules is as follows: Example No. 3 C
  • the so-called black spot test was carried out as follows. 10 grams of the builder granule was added inside a small black cotton wash-rag.
  • a Siemens Siwamat Plus 3803 washing machine was operated with water having a hardness of 9.4°GH.
  • the wash load being l kg of fabric, consisted of 2 kitchen towels, 1 wash towel, 2 pillow cases, and underwear.
  • the black cotton wash rag containing the 10 grams of builder granules was placed on a wash towel inside the machine.
  • the wash load was washed using the wool-wash programme.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
PCT/EP1996/004886 1995-11-29 1996-11-07 Detergent builder granule WO1997020020A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
AU75679/96A AU701161B2 (en) 1995-11-29 1996-11-07 Detergent builder granule
DE69626302T DE69626302T2 (de) 1995-11-29 1996-11-07 Waschmittelbuildergranulat
CA002237575A CA2237575C (en) 1995-11-29 1996-11-07 Detergent builder granule
EP96938147A EP0863974B1 (en) 1995-11-29 1996-11-07 Detergent builder granule
JP9520103A JP2000500799A (ja) 1995-11-29 1996-11-07 顆粒状洗剤ビルダー
BR9611645A BR9611645A (pt) 1995-11-29 1996-11-07 Gránulos reforçador adequado para uso numa composição detergente particulada e composição detergente particulada

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP95203280.3 1995-11-29
EP95203280 1995-11-29

Publications (1)

Publication Number Publication Date
WO1997020020A1 true WO1997020020A1 (en) 1997-06-05

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ID=8220885

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1996/004886 WO1997020020A1 (en) 1995-11-29 1996-11-07 Detergent builder granule

Country Status (10)

Country Link
EP (1) EP0863974B1 (es)
JP (1) JP2000500799A (es)
AU (1) AU701161B2 (es)
BR (1) BR9611645A (es)
CA (1) CA2237575C (es)
DE (1) DE69626302T2 (es)
ES (1) ES2192233T3 (es)
TR (1) TR199800973T2 (es)
WO (1) WO1997020020A1 (es)
ZA (1) ZA969640B (es)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998029528A2 (en) * 1996-12-26 1998-07-09 The Procter & Gamble Company Laundry detergent compositions with cellulosic polymers
EP0926232A2 (de) * 1997-12-22 1999-06-30 Henkel KGaA Teilchenförmiges Wasch- und Reinigungsmittel
US6833347B1 (en) 1997-12-23 2004-12-21 The Proctor & Gamble Company Laundry detergent compositions with cellulosic polymers to provide appearance and integrity benefits to fabrics laundered therewith

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5470022B2 (ja) * 2008-12-25 2014-04-16 ライオン株式会社 高嵩密度粒状洗剤組成物

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0260971A2 (en) * 1986-09-19 1988-03-23 Unilever Plc Detergent composition and process for its production
EP0279038A1 (de) * 1987-01-30 1988-08-24 Degussa Aktiengesellschaft Waschmittelbuilder
EP0552054A1 (en) * 1992-01-17 1993-07-21 Unilever Plc Detergent compositions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0260971A2 (en) * 1986-09-19 1988-03-23 Unilever Plc Detergent composition and process for its production
EP0279038A1 (de) * 1987-01-30 1988-08-24 Degussa Aktiengesellschaft Waschmittelbuilder
EP0552054A1 (en) * 1992-01-17 1993-07-21 Unilever Plc Detergent compositions

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998029528A2 (en) * 1996-12-26 1998-07-09 The Procter & Gamble Company Laundry detergent compositions with cellulosic polymers
WO1998029528A3 (en) * 1996-12-26 1998-09-17 Procter & Gamble Laundry detergent compositions with cellulosic polymers
EP0926232A2 (de) * 1997-12-22 1999-06-30 Henkel KGaA Teilchenförmiges Wasch- und Reinigungsmittel
EP0926232A3 (de) * 1997-12-22 1999-08-25 Henkel KGaA Teilchenförmiges Wasch- und Reinigungsmittel
US6833347B1 (en) 1997-12-23 2004-12-21 The Proctor & Gamble Company Laundry detergent compositions with cellulosic polymers to provide appearance and integrity benefits to fabrics laundered therewith

Also Published As

Publication number Publication date
EP0863974A1 (en) 1998-09-16
JP2000500799A (ja) 2000-01-25
ZA969640B (en) 1998-05-18
BR9611645A (pt) 1999-02-23
DE69626302T2 (de) 2003-07-24
TR199800973T2 (xx) 1998-08-21
CA2237575C (en) 2005-06-28
EP0863974B1 (en) 2003-02-19
ES2192233T3 (es) 2003-10-01
DE69626302D1 (de) 2003-03-27
CA2237575A1 (en) 1997-06-05
AU701161B2 (en) 1999-01-21
AU7567996A (en) 1997-06-19

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