EP0296813A1 - Compositions de poudre et compositions détergentes - Google Patents

Compositions de poudre et compositions détergentes Download PDF

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Publication number
EP0296813A1
EP0296813A1 EP88305669A EP88305669A EP0296813A1 EP 0296813 A1 EP0296813 A1 EP 0296813A1 EP 88305669 A EP88305669 A EP 88305669A EP 88305669 A EP88305669 A EP 88305669A EP 0296813 A1 EP0296813 A1 EP 0296813A1
Authority
EP
European Patent Office
Prior art keywords
powder
agglomerates
sodium
fines
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.)
Withdrawn
Application number
EP88305669A
Other languages
German (de)
English (en)
Inventor
J. E. Mole
J. J. Mackenzie
Sarah Thomson Galbraith
Alan Kenneth Cross
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 GB878714807A external-priority patent/GB8714807D0/en
Priority claimed from GB878714808A external-priority patent/GB8714808D0/en
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of EP0296813A1 publication Critical patent/EP0296813A1/fr
Withdrawn legal-status Critical Current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
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3942Inorganic per-compounds

Definitions

  • This invention relates to powder compositions for detergents and particularly to formulations which can be dry-blended into detergent powder compositions and comprising agglomerates of sodium perborate hydrate (usually tetrahydrate) fines.
  • the invention further relates to detergent compositions for dishwashers and to a method for the manufacture of agglomerates of sodium perborate (tetra)hydrate fines for use in detergent powder compositions.
  • Detergent powder compositions including dishwashing compositions are well known and comprise dry-blended mixtures of several ingredients selected typically from bleaching agents, surfactants, alkali water-softening agents, builders, bulking agents, binders and dyestuffs or pigments.
  • Standard sodium perborate tetrahydrate of particle size about 300 microns, dissolves only slowly in water and is generally deemed to be rather too slow dissolving to be satisfactory at low wash temperature.
  • Sodium perborate tetrahydrate in the form of fines dissolves rapidly in water but the fine particle size presents problems of handling since the material is 'dusty' and tends to segregate and cake in the detergent powder pack. Also, the fines tend to lack thermal in-pack stability in hot climates.
  • sodium perborate monohydrate is now being used to a significant extent in detergent powder compositions. The monohydrate comprises porous particles which dissolve rapidly in water at low temperatures to provide a rapid release of bleach in the washing process. However, the monohydrate is much more expensive than the tetrahydrate.
  • the present invention resides in the discovery that the valuable rapid-dissolving property of sodium perborate tetrahydrate fines can be utilized in detergent powder compositions whilst the handling and segregation problems associated with it are obviated, by agglomerating the fines into larger particles which contain one or more other ingredients of a detergent powder composition.
  • a powder composition for blending into detergent powder compositions which comprises agglomerates of sodium perborate hydrate,preferably tetrahydrate,fines together with one or more other ingredients of the detergent powder compositions.
  • a detergent powder composition containing agglomerates of sodium perborate hydrate,preferably tetrahydrate,fines together with one or more other ingredients of the detergent powder composition.
  • a particular detergent powder composition provided as a feature of the invention is a powder dishwashing composition.
  • sodium perborate tetrahydrate fines is meant a powder material in which the particles are of size from 6 microns to 160 microns.
  • Sodium perborate tetrahydrate fines are temperature sensitive and cannot be agglomerated by spray-drying agglomeration techniques which employ temperatures of above 100°C.
  • a further feature provided according to the invention is a process for producing agglomerates of sodium perborate tetrahydrate fines together with one or more other ingredients of detergent powder compositions, which comprises moistening the fines powder or powder mixture with water or an aqueous solution or dispersion of a substance to be incorporated in the agglomerates and agitating the moistened powder whilst removing water from it at a temperature of from about 20°C to about 60°C.
  • the other ingredient or ingredients of detergent powder compositions to be included in the agglomerates can be blended with the fines powder prior to moistening thereof and/or can be dissolved in the water with which the fines powder is moistened.
  • a preferred moistening solution is water glass solution.
  • a preferred process for producing the agglomerates comprises tumbling the fines powder or fines powder blends in a rotating inclined vessel to create a falling curtain of the particles, applying a predetermined amount of water, water glass solution or an aqueous solution in the form of a fine spray to the falling curtain of particles such that essentially all of the powder particles are moistened and tumbling the moistened powder particles until agglomerates of the desired size are produced.
  • An alternative process for forming agglomerates comprises moistening the powder mixture with water, water glass solution or an aqueous solution and extruding the moist powder through die plates to produce particles (agglomerates) of uniform size.
  • the agglomerates are then dried under conditions whereby they are prevented or at least inhibited from sticking together, for example by agitating them during drying or by laying them out in a thin layer in shallow trays. Fluid bed drying is preferred. Both the production and the drying of the agglomerates can be carried out at low temperatures at which the tetrahydrate fines are stable and in particular at temperatures below about 60°C. Agglomerate production and drying can be carried out at normal ambient temperature if desired although in general we prefer to heat the agglomerates at about 30°C to increase the rate of drying them. After drying, the agglomerates powder can be sieved to eliminate unwanted large or small particles.
  • the agglomerates may be dried at higher temperatures, e.g. above 60°C, such that the sodium perborate tetrahydrate is converted into sodium perborate monohydrate.
  • agglomerates are provided which in fact are novel particles of sodium perborate monohydrate or mixed tetrahydrate/monohydrate together with one or more other ingredients of detergent powder compositions.
  • Detergent powder compositions comprising these modified agglomerates are provided according to a further feature of the invention.
  • the agglomerates are in the form of a powder material, particle size say about 100 to 1000 microns, which can be dry-blended with other powders to form the final detergent powder compositions.
  • Detergent powder compositions containing the agglomerates are provided according to a further feature of the invention.
  • the other substances which may be incorporated in the agglomerated fines include any of the conventional ingredients of detergent powder compositions.
  • examples of such substances include the so-called precipitant builders, e.g. phosphates such as sodium tripolyphosphate, zeolites water-softeners (alkaline materials) e.g. sodium carbonate, the so-called bulking agents such as sodium sulphate, sodium silicate, active detergent surfactants and transition metal chelating agents such as EDTA and DTPA.
  • substances which presently are not commonly incorporated as ingredients of conventional detergent powder compositions may also be included in the agglomerated sodium perborate tetrahydrate fines, for example sodium bicarbonate and partially-calcined sodium sesquicarbonate and sodium bicarbonate or sesquicarbonate mother liquors.
  • some specific powder composition formulations according to the invention are agglomerates comprising: - sodium perborate tetrahydrate fines + partially-­calcined sodium sesquicarbonate (available under the trade name "Crex” from Imperial Chemical Industries plc) - sodium perborate tetrahydrate fines + partially-­calcined sodium sesquicarbonate (“Crex) + sodium sulphate - sodium perborate tetrahydrate fines + sodium silicate liquor optionally + partially calcined sodium sesquicarbonate ("Crex").
  • any of the above specific formulations may include other ingredients such as a surface active agent.
  • a preferred specific powder composition for dry-blending into a dishwashing powder are agglomerates comprising: - sodium perborate tetrahydrate fines + sodium carbonate + sodium sulphate + sodium silicate liquor
  • a preferred dishwashing composition incorporating this agglomerate formulation comprises the agglomerates dry-blended with a bulking agent such as sodium tripolyphosphate, a surfactant and sodium metasilicate.
  • This composition may also contain one or both of an amylolytic enzyme and a proteolytic enzyme.
  • the amount of the other additive in the agglomerated sodium perborate tetrahydrate fines may vary within wide limits but will usually be less than about 50% i.e. from 30% to 50% by weight of the agglomerates.
  • the amount of the agglomerates formulation incorporated in the final detergent powder composition will be such that the final composition contains the usual amount of sodium perborate bleaching additive and the amount of any other additive incorporated in the partial detergent composition will be such that the final composition contains the usual amount of said other additive.
  • a powder dishwashing composition for use in automatic dishwashing machines comprising -
  • the amounts of the ingredients in the agglomerate should be such as to provide in the dishwashing composition - - 1 to 10% by weight of sodium perborate tetrahydrate, - 10 to 40% by weight of sodium carbonate, - up to 40% by weight of bulking agent(s), and - 2 to 15% by weight of sodium silicate.
  • the composition is alkaline and in particular has a solution pH of about 12.0 to 13.0, this being the pH of a solution of 3 g/litre of the composition in water.
  • the alkalinity or solution pH of the composition which should generally be maintained above about 9 if an enzyme is included in order that the enzyme be effective, is largely established and maintained by components (a) and (b) and (c) which exhibit a builder/buffer effect on the solution and are used in sufficient amounts to provide the desired solution pH.
  • the composition will usually contain one or more bulking agents in an amount of from 20% to 40% by weight contained in the agglomerates. Any bulking agent may be used which does not appreciably inhibit the effectiveness of any enzymes present or adversely modify the alkalinity of the composition.
  • Sodium sulphate is a typical and preferred bulking agent and sodium chloride may also be used.
  • the compositions may contain both sodium sulphate and sodium chloride, for example in a ratio of about 1:0.5 by weight.
  • the preferred phosphate, component (b), is sodium tripolyphosphate.
  • the composition may contain a low-foaming surfactant and advantageously does contain a small amount, for example up to 5% by weight, of such a component.
  • a low-foaming surfactant may be employed but will usually be a non-ionic surfactant such as an alkylene oxide condensate in which the alkoxy moity is derived from ethylene oxide or propylene oxide or a mixture thereof.
  • suitable surfactants are the well-known ethoxylated straight-chain alcohols.
  • the surface active agent is biodegradable.
  • the composition may contain an amylolytic enzyme and a proteolytic enzyme.
  • an amylolytic enzyme and a proteolytic enzyme Preferably at least one of the enzymes and especially preferably both of the enzymes, if present, are in granular form.
  • the enzymes are used in mixtures in which the ratio by weight of amylolytic enzyme: proteolytic enzyme is from 1:4 to 4:1 and usually from 1:2 to 2:1. If present approximately equal amounts (by weight) of proteolytic enzyme and amylolytic enzyme may be used, typically from 0.5 to 1.5% by weight of each enzyme based on the weight of the composition.
  • amylolytic enzyme and any proteolytic enzyme may be used which at pH10 exhibits at least 50% and preferably at least 60% of its maximum activity.
  • the enzyme mixture is present in the composition in an amount such that the composition has an amylolytic activity of at least 150 KNU (Kilo Novo units), preferably at least 300 KNU, per kilogram and a proteolytic activity of at least 6 Anson units per kilogram.
  • Amylolytic activity in KNU is determined as described in United States Patent Specification No 3,931,034.
  • Proteolytic activity in Anson units is determined as the amount of enzyme which degrades haemaglobin under standard conditions as described in Journal of General Physiology, Vol 22 (1938), page 79.
  • compositions of the invention may if desired contain other ingredients known for use in automatic dishwasher compositions, for example sequestering agents, soil-suspending agents, corrosion inhibitors, drainage-promoting agents, crystal modifiers, dyes and perfumes.
  • compositions of the invention are presented as powders which can be produced by dry-mixing the powdered/granular materials and spraying any liquid components, e.g. a surfactant, on the the mixture during mixing.
  • PB4 fines Sodium perborate tetrahydrate fines (PB4 fines) of mean particle size 50 microns (210 g) were dry-blended with partially-calcined sodium sesquicarbonate of mean particle size 120 microns (90 g).
  • the partially-calcined sodium sesquicarbonate is available under the trade name "Crex" from ICI Chemicals & Polymers Ltd.
  • the blended powder mix was introduced into a pan-granulator of diameter 400 mm and depth 100 mm inclined at an angled of 30-40 degrees to the horizontal and rotating at 25-­30 rpm.
  • the mixture was tumbled for 2 minutes at ambient temperature using a wall scraper to remove particles adhering to the wall and create a falling curtain of the particles, whilst demineralised water (50 ml) was sprayed onto the falling curtain from a spray nozzle of diameter 0.2 mm.
  • the moistened powder mixture was then tumbled for a further 2 minutes to produce agglomerate granules which were then removed from the pan-granulator, placed in thin layers in shallow trays and dried overnight in an oven at 30°C.
  • the dry agglomerate granules were then removed from the trays and sieved to remove particles larger than 850 microns and particles smaller than 150 microns.
  • PB4 fines of mean particle size 50 microns (150 g) was dry-blended with "Crex" (64 g) and anhydrous sodium sulphate (86 g) and the mixture was agglomerated using 50 ml of demineralised water and the agglomerates dried as described in Example 1.
  • Example 2 The procedure described in Example 2 was repeated except that instead of 50 ml of demineralised water there was used 30 ml of a 50% by weight solution of water glass in demineralised water.
  • the water glass had the composition:- 18% Na20 : 29.5% Si02 : 52.4% water
  • Example 2 The procedure described in Example 1 was repeated except that instead of 50 ml of demineralised water there was employed 50 ml of a 5% aqueous solution of sodium sesquicarbonate.
  • PB4 fines of mean particle size 50 microns (220 g) were dry-blended with sodium carbonate of size 120 microns (40 g) and anhydrous sodium sulphate (140 g). The mixture was agglomerated as described in Example 1 using 50 ml of a water glass solution as described in Example 3.
  • a powder dishwashing composition was then blended to the following formulation:- % by weight Agglomerates (as above) 60 Sodium metasilicate powder 18 Sodium tripolyphosphate powder 20 Surfactant (“Ukanil” 2136) 2 100 "Ukanil” 2136 is an ethoxylated alcohol and is available from Imperial Chemical Industries plc.
  • the liquid surfactant was sprayed on to the sodium tripolyphosphate and then the three powders were dry-­blended together in a Kenwood food mixer.
  • a sample of the dishwashing composition was used to clean dirty plates in a domestic automatic dishwashing machine (Indesit 2260E).
  • the water softener reservoir in the machine was kept topped-up with sodium chloride and a rinse-aid was employed during the rinse cycle of the cleaning operation.
  • 15 g of the powder dishwashing composition was loaded into the machine in each trial.
  • the dirty plates being cleaned were soiled by coating them with both a greasy soil and a protein soil and baking them at 150°C in an oven. Some plates were baked for 5 minutes, some for 7.5 minutes and others for 10 minutes.
  • the greasy soil was a mixture of peanut butter (5), butter (2), lard (2.5) and mineral oil (2), the figures indicating parts by weight.
  • the protein soil was a mixture of raw egg (5) peanut butter (1), lard (1), butter (1) and milk (1), the figures being parts by weight.
  • the porosity of the agglomerates produced in Example 5 was determined by spraying a liquid non-ionic surfactant (known as A7) onto the agitated powder and measuring the amount of the surfactant which could be loaded onto the powder before its flow properties were adversely affected. An adverse effect on flow properties was quantified by measuring the change in the angle of repose of the powder.
  • A7 a liquid non-ionic surfactant
  • the storage stability at high ambient temperature of the agglomerates produced in Examples 1, 3 and 5 was assessed by placing 20 g samples of the agglomerates in sealed containers and maintaining them at 35°C for 50 days. For purposes of comparison, a Control test was carried out using standard sodium perborate tetrahydrate of mean particle size 300 microns.
  • results show the high in-pack stability of the agglomerates compared with standard sodium perborate tetrahydrate crystals at 35°C and the results for the agglomerates of Examples 3 and 5 compared with those for the agglomerates of Example 1 indicate the beneficial effect upon resistance to caking of incorporating sodium silicate in the agglomerates.
  • Example 1 The procedural steps described in Example 1 represent a general procedure for agglomerating fine powders and are illustrative of the process according to the invention for making agglomerates. The procedure has now been scaled up and operated with 1 tonne batches per hour on a number of commercially-available powders.
  • a powder dishwashing composition was blended to the following formulation:- % by weight Agglomerates (as in Example 5) 50 Sodium metasilicate 23 Sodium tripolyphosphate 25 Surfactant ("Ukanil” 2136) 2 100
  • composition was used to clean dishes as described in Example 5 and after the treatment all of the plates had a clean appearance.
  • PB4 fines of mean particle size 50 microns (200 gm) were sprayed with a solution of water glass and then dried.
  • the amount and type of water glass (sodium silicate solution) was varied (see attached table) and the properties measured.
  • Example 9 Sample 4 was further dried by heating the powder with hot air at 120°C till the powder temperature reached 60°C for a period of one hour.
  • the angle of repose was measured at various loadings of the surfactant. % Loading of surfactant w/w Angle of Repose (Degrees) 0 35 5 35 10 36 15 37 20 38
  • the agglomerate remained free flowing up to a substantial loading of the surfactant.
  • Drying of the agglomerate is not limited to Oxygen of 12.2% and covers all levels from 9.5% to 15% oxygen.
  • Example 9 The combination of PB4 fines and E 100 water glass sample 4 in Example 9 was extruded whilst in the damp state through a 2 mm dye plate. This formed extrudates of 2 mm in diameter and on average about 2 mm in length. These extrudates were dried in the normal manner by fluidising in hot air.
  • extrudates demonstrated the following properties: Mean particle size 200 ⁇ - uniform % Available oxygen 9.6 Dissolution time 32 seconds Friability hard, none dusty The needle shaped particles showed excellent dissolution rates for a large size particle together with uniform granulometry on handling.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP88305669A 1987-06-24 1988-06-21 Compositions de poudre et compositions détergentes Withdrawn EP0296813A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB8714807 1987-06-24
GB878714807A GB8714807D0 (en) 1987-06-24 1987-06-24 Powder compositions
GB878714808A GB8714808D0 (en) 1987-06-24 1987-06-24 Powder dishwashing compositions
GB8714808 1987-06-24

Publications (1)

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EP0296813A1 true EP0296813A1 (fr) 1988-12-28

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EP88305669A Withdrawn EP0296813A1 (fr) 1987-06-24 1988-06-21 Compositions de poudre et compositions détergentes

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EP (1) EP0296813A1 (fr)
JP (1) JPS6485300A (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990014412A1 (fr) * 1989-05-22 1990-11-29 Henkel Kommanditgesellschaft Auf Aktien Additif granulaire sans phosphates contenant des agents tensio-actifs non ioniques pour produit a lessive
US5395602A (en) * 1989-12-19 1995-03-07 Degussa Aktiengesellschaft Method for the production of sodium perborate hydrate granulates
EP0866118A2 (fr) * 1997-03-20 1998-09-23 The Procter & Gamble Company Particule de détergent
US7226899B2 (en) 2003-12-23 2007-06-05 Kimberly - Clark Worldwide, Inc. Fibrous matrix of synthetic detergents

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1129870A (fr) * 1954-08-20 1957-01-28 Unilever Nv Perfectionnements à des compositions sous forme de poudre
US2863385A (en) * 1956-08-24 1958-12-09 Master Addresser Company Printing machine
US2863835A (en) * 1957-10-08 1958-12-09 Theobald Ind Perborate composition
US2975142A (en) * 1955-06-11 1961-03-14 Henkel & Cie Gmbh Granular water-soluble perborate-containing salt mixture
US2979464A (en) * 1956-11-09 1961-04-11 Degussa Perborate granulation
US3154496A (en) * 1962-09-04 1964-10-27 Procter & Gamble Process for producing a quick dissolving agglomerated perborate
US3161597A (en) * 1961-11-14 1964-12-15 Du Pont Nonsegregating granular detergent-bleach products and their preparation
US3451935A (en) * 1966-04-25 1969-06-24 Procter & Gamble Granular enzyme-containing laundry composition
US3664961A (en) * 1970-03-31 1972-05-23 Procter & Gamble Enzyme detergent composition containing coagglomerated perborate bleaching agent

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1129870A (fr) * 1954-08-20 1957-01-28 Unilever Nv Perfectionnements à des compositions sous forme de poudre
US2975142A (en) * 1955-06-11 1961-03-14 Henkel & Cie Gmbh Granular water-soluble perborate-containing salt mixture
US2863385A (en) * 1956-08-24 1958-12-09 Master Addresser Company Printing machine
US2979464A (en) * 1956-11-09 1961-04-11 Degussa Perborate granulation
US2863835A (en) * 1957-10-08 1958-12-09 Theobald Ind Perborate composition
US3161597A (en) * 1961-11-14 1964-12-15 Du Pont Nonsegregating granular detergent-bleach products and their preparation
US3154496A (en) * 1962-09-04 1964-10-27 Procter & Gamble Process for producing a quick dissolving agglomerated perborate
US3451935A (en) * 1966-04-25 1969-06-24 Procter & Gamble Granular enzyme-containing laundry composition
US3664961A (en) * 1970-03-31 1972-05-23 Procter & Gamble Enzyme detergent composition containing coagglomerated perborate bleaching agent

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990014412A1 (fr) * 1989-05-22 1990-11-29 Henkel Kommanditgesellschaft Auf Aktien Additif granulaire sans phosphates contenant des agents tensio-actifs non ioniques pour produit a lessive
US5395602A (en) * 1989-12-19 1995-03-07 Degussa Aktiengesellschaft Method for the production of sodium perborate hydrate granulates
EP0866118A2 (fr) * 1997-03-20 1998-09-23 The Procter & Gamble Company Particule de détergent
EP0866118A3 (fr) * 1997-03-20 1998-12-16 The Procter & Gamble Company Particule de détergent
US7226899B2 (en) 2003-12-23 2007-06-05 Kimberly - Clark Worldwide, Inc. Fibrous matrix of synthetic detergents

Also Published As

Publication number Publication date
JPS6485300A (en) 1989-03-30

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