AU628136B2 - Agglomerates for addition to detergent powders - Google Patents

Agglomerates for addition to detergent powders Download PDF

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Publication number
AU628136B2
AU628136B2 AU50542/90A AU5054290A AU628136B2 AU 628136 B2 AU628136 B2 AU 628136B2 AU 50542/90 A AU50542/90 A AU 50542/90A AU 5054290 A AU5054290 A AU 5054290A AU 628136 B2 AU628136 B2 AU 628136B2
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AU
Australia
Prior art keywords
agglomerate
agglomerates
particulate material
less
whitening
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Ceased
Application number
AU50542/90A
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AU5054290A (en
Inventor
Francois Delwel
William Derek Emery
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Unilever PLC
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Unilever PLC
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Filing date
Publication date
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Publication of AU5054290A publication Critical patent/AU5054290A/en
Application granted granted Critical
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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
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/1253Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/126Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/395Bleaching agents
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06Powder; Flakes; Free-flowing mixtures; Sheets

Description

I r
AUSTRALIA
PATENTS ACT 1952 Form COMPLETE SPECIFICATIO
(ORIGINAL)
FOR OFFICE USE Short Title: Int. Cl: SApplication Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: Priority: Related Art: TO BE COMPLETED BY APPLICANT p.
:Narr of Applicant: UNILEVER PLC Address of Applicant: UNILEVER HOUSE
BLACKFRIARS
LONDON EC4
ENGLAND
Actual Inventor: Address for SP-'-ice: GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
Complete Specification for the invention entitled: AGGLOMERATES FOR ADDITION TO DETERGENT POWDERS.
The following statement is a full description of this invention including the best method of performing it known to me:- IL_ s _C r i 1A- C3289 AGGLOMERATES FOR ADDITION TO DETERGENT POWDERS This invention relates to an agglomerated composition of improved colour and in particular to white agglomerates of clay fabric softener for addition to white or differently coloured detergent base powders.
Detergent powders without added colour are generally white or near-white in colour, but some ingredients especially certain classes of fabric softening clay, enzyme granules or bleach precursors may be brown, yellow or grey. The incidence of such discoloured particles in a finished detergent powder can give the whole product an off-white u ittractive appearance.
GB 2 199 338 (Unilever Plc) proposes the use of large vividly coloured particles ("speckles") in detergent powder to render the presence of slightly discoloured particles unnoticeable.
1~~-~111 2 C3289 33 9 3.
0 0 3e** 33* e 3 3*e* .3 3 3S GB 2 121 843 (Colgate-Palmolive Co) proposes incorporating dyes or pigments in a liquid agglomerating spray used in the manufacture of bentonite clay agglomerates to form clay speckles.
In some powders however the use ol speckles may not be desirable or may be ineffective in camouflaging the discoloured particles.
We have surprisingly found that agglomerates coated or granulated with a whitening particulate material of a certain average particle size, bulk density and reflectance value (measured as R infinity at 460 nm which represents the reflectance value of a layer so thick that a further increase in thickness of the layer fails to change the reflectance) are often especially white, bright and unnoticeable when added to a detergent base washing powder.
A first aspect of the present invention accordingly provides agglomerates comprising whitening particulate material of average particle size less than 20 microns, a bulk density of less than 400 grams per litre and a reflectance value (R infinity 460) of greater than A second aspect of the invention provides a fabric softener comprising clay agglomerates, said agglomerates comprising whitening particulate material of average particle size less than 20 microns, a bulk density of lesd than 400 grams per litre and a reflectance value (R infinity 460) of greater than A third aspect of the invention provides agglomerates comprising sufficient whitening particulate material to give the agglomerate an R infinity 460 value greater than 3 C3289 fe S 9000 0000 *5 *5*
S
*5 The agglomerates of improved colour can be formed either as a cogranulate with the whitening particulate material or as agglomerates coated with the whitening particulate material.
The cogranulated agglomerates preferably comprise from 30% to 60% by weight of the particulate material, more preferably from 40% to 50% by weight.
The average particle size of the particulate material is preferably less than 15 microns, more preferably less than 10 microns.
The bulk density of the particulate material is preferably less than 250 grams per litre.
The reflectance value measured as R infinity 460 is preferably greater than When the particulate material is present as a coating on the agglomerates it preferably comprises from 10 to 40% by weight of the total agglomerate composition.
More preferably the particulate material comprises from to 25% by weight of the total agglomerate composition.
The particulate material is preferably a precipitated calcium carbonate or a silica. ihe precipitated calcium carbonate employed can be in the form of particles of average particle size of the order of 4 microns, built up from trigonal or aragonite crystals.
The silica employed is in the form of a precipitated amorphous powder of particle size of the order of microns.
*r SS *9 5 5
S
S
0 5
S
1 "FI7-E~irY*n"rr- 4 C3289 ar a *a a ease *a C. C a
CO..
a
CC
C
a 4 A type of precipitated calcium carbonate which is most useful in whitening the agglomerates is that which is known as SOCAL U3 (ex Solvay). A type of silica which is most useful in whitening the agglomerates is that which is known as Microsil (ex Crosfields).
Clay softeners are well-known in the detergent patent literature. Included among such clay softeners are various heat-treated kaolins and various multi-layer smectites. GB 1 400 898 (Procter and Gamble) suggests the use of smectite clays having a relatively high exchange capacity. There is a desire to boost the performance of fabric softening clays in the wash and according to our copending patent application EP 287 344 it has been found that if certain nonionic surfactant materials are carried on the clay, at a specified level relative thereto, and the moisture content zf the composition is controlled, the fabric softening performance is enhanced. The examples of the invention included herein are directed towards clay carrying a nonionic surfactant but it should be understood that the invention is not limited to clays.
It has been found that the moisture content of clay agglomerates must be between 7.5% and 12% by weight, preferably from 8% to 10%. The term "moisture" in this context is not necessarily the total water content, but rather it is the water which is lost from the composition by drying in a static environment at 135 0 C to a constant weight. Usually, when freshly prepared, the clay/nonionic agglomerates will have a higher moisture content, such as, for example from 10% to 16% moisture, and will therefore be too sticky for use, so that some post, drying is necessary. When post-drying high moisture content clay/nonionic agglomerates, a drying air temperature of 85-90°C has been found to be suitable.
L- 5 C3289 Where the agglomerates are to be coated with precipitated calcium carbonate it may be desirable to "over-dry" the agglomerates so that moisture accommodated by the agglomerates as a result of the coating process leaves the agglomerates with a final moisture content in the desired range.
The nonionic surfactant system exists as a cloudy phase in the temperature range of 0 C to 80 0 C, preferably 0OC to 15 0 C in distilled water at 1% concentration. In .i practise this means that the system has a cloud point of e: not more than 80 0 C, preferably not more than 15°C. The I: cloud point correlates approximately to the hydrophiliclipophilic balance (HLB) of the surfactant system and it is therefore preferred that the HLB should be less than 13.5, such as not more than 12.0, ideally less than The HLB should be above 6.0, preferably -bove 8.0 to provide sufficient detergency.
Specific nonionic surfactants are alkyl (C 6
-C
2 2 Sphenols-ethylene oxide condensates, the condensation products of aliphatic (C8-Cla) primary or secondary linear or branched alcohols with ethylene oxides, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
S* The clay softener may be any such material capable of providing a softening benefit. The effectiveness of a clay material as a fabric softener will depend on the level of smectite clay. It is preferred that the rat.
of the clay to the nonionic surfactant in the agglomerate is from 3:1 to 20:1, most preferably 4:1 to 10:1.
Where the agglomerates are to be handled by conveyors, feeders, mixers, filling machinery or are to be subjected to shipping shocks it may be necessary to i~iik ~YI I a I I I 6 C3289
S.
*5 S. S SO S
SO
S
S
*5 0* S
SS
S
employ a binder, in addition to the nonionic if present, in the granulation process to improve the structural stability of the agglomerate. Suitable binders include copolymers of polyacrylate and maleic anhydride, polyacrylates, sugars, nonionic surfactrnts, polyethylene glycol, polyoxyethylene alkyl ether, fatty acid monoethanolamide, carboxymethyl cellulose, soap and latex.
The agglomerates can be made by known granulation processes typically by those described in GB 2 121 843B.
The cogranulated agglomerates can be made in any granulater where the binding material can be contacted with materials to be agglomerated; preferably a high shear, short residence time granulator, such as a Schugi Flexomix or a L 8dige Recycler, or a longer residence time, low shear granulater, such as a continuous drum granulater, Eirich pan granulater or a drum or cement mixer. The coated agglomerates can be made in any suitable device such as a rotary drum, pan or marumeriser mixer using agglomerates made by a known granulation process.
Where the agglomerates are to be coated with the particulate material, it may be desirable to include a binder in the coating solution (usually water) to aid adherence of the particulate material to the agglomerate and to form durable bonds within the coating layer.
A preferred process for forming coated agglomerates comprises granulating the agglomerates with an excess of nonionic surfactant in a drum mixer to form "sticky" granules followed by coating with the particulate material. The advantages of this process are that an improved coating adherence and colour is obtained. The especially improved colour is thought to be due to the -I UII- rwr 7 C3289 fact that no binder is present at the light scattering surface of the agglomerate.
A particularly preferred binder is Sokalan CP5 (ex BASF) a copolymer of maleic anhydride and polyacrylate supplied as a 40% aqueous solution.
In addition to the binder it may be necessary to employ a plasticiser to improve the friability resistance of the coating. For example the addition of 2% by weight sorbitol or glycerol to the binder spray greatly decreases the friability of the agglomerate, especially if the agglomerate is air dried.
When the agglomerates of the invention or the washing products containing them, contain a detergent active material, this may be selected from nonionic detergent active materials, anionic detergent active materials, zwitterionic or amphoteric detergent active materials or mixtures thereof.
The anionic detergent active materials are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to S. include the alkyl portion of higher acyl radicals.
Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C 8
-C
1 8 alcohols produced for example from tallow or coconut oil, sodium and potassium alkyl (C 9 20 benzene sulphonates, particularly sodium linear secondary alkyl (C 10 benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty 8 C3289 monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher
(C
8
-C
18 fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C -C 20 with sodium bisulphite and those derived from reacting paraffins with SO 2 and Cl2 and then hydrolysing with a base to produce a random sulphonate; and olefin Ssulphonates, which term is used to describe the material made by reacting olefins, particularly C 10
-C
20 alpha-olefins, with SO3 and then neutralising and hydrolysing the reaction product. The preferred anionic detergent compounds are sodium (C 11
-C
15 alkyl benzene sulphonates and sodium (C 16
-C
18 alkyl sulphates.
When the fabric washing products contain a detergency builder material this may be any material capable of reducing the level of free calcium ions in the wash l:quor and will preferably provide the composition with other beneficial properties such as the generation of an alkaline pH, the suspension of soil removed from the fabric and the dispersion of the fabric softening clay material.
Examples of phosphorus-containing inorganic detergency builders, when present, include the water-soluble salts, especially alkaline metal pyrophosphate, orthophosphates, polyphosphates and phosphonates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, phosphates and hexametaphosphates.
13L~liu*au~ ~1~---~-5---Ytyn.irZYli~iylXt 9 C3289 0 0 so 0 so .00 0.
0 00
S
0 0 0 .00.
a so 50 0 0 0@ a 0 Examples of non-phosphorus-containing inorganic detergency builders, when present, include water-soluble alkali metal carbonates, bicarbonates, silicates and crystalline and amorphous alumino silicates. Specific examples include sodium carbonate (with or without calicte seeds), potassium carbonate, sodium and potassium bicarbonates and silicates.
Examples of organic detergency builders, when present, include the alkaline metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxsulphonates. Specific examples include sodium, potassium lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid.
Apart from the ingredients already mentioned, a number of optional ingredients may also be present, either as part of the clay containing compositions or as part of the overall fabric washing product.
Examples of other ingredients which may be present in the composition include the lather boosters, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach percursors, chlorine-releasing bleaching agents such as tricloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases, lipalases, cellulases and amylases, germicides and colourants.
r 10 C3289 When the agglomerates are included in a detergent base powder they are typically present at a level from to 20% by weight.
A typical formulation is as follows: Parts by weight Lauryl alkyl sulphonate 6 Nonionic detergent active 3 Soap Zeolite 22 Sokalan CP5 3 Alkaline silicate Perborate Monohydrate TAED 1.8 Savinase 0.35 Carbonate 10.00 EDTA 0.15 SSulphate 24.39 SCMC 0.50 Clay agglomerates 10.00 Water, perfume, minors 9.31 *Examples The invention will now be illustrated by the following non-limiting examples.
Example 1A Clay/nonionic agglomerates were prepared by spraying 83 parts by weight of clay (KBU, clay of cec <50 meq/100g ex Colin Stewart Minerals) with !7 parts of Synperonic A3 (a nonionic surfactant ex ICI which is a C13-C15 alcohol ethoxylated with approximately 3 moles of ethylene oxide 11 C3289 per molecule and having a cloud point below 0 C) in a drum mixer.
The agglomerates were tumbled in a drum coater with by weight of Socal U3 (precipitated calcium carbonate ex SOLVAY having a bulk density of 230 g/1 a particle size of 4 microns, _nd an R infinity 460 of 96) and by weight of a 25% solution of Sokalan CP5. The moisture content of the agglomerates as made was 18%, these were dried to a moisture content of 8%.
Example 1B S* Example 1A was repeated excepting that the agglomerates were coated with 10% by wei,.it Microsil a silica (ex Crosfields) having a particle size of 10-15 microns, a bulk density of 130 g/l and a reflectance value (R infinity 460) of 98.4.
a 0 0* 0
S.
-YI~-YI i -s 12 C3289 Example 2 Example 1 was repeated excepting that the agglomerates were coated with 20% by weight Durcal, a calcite (ex Omya) having a bulk density of 670 g/l a particle size of 4 microns and a reflectance value (R infinity 460) of 93.
Example 3 Example 1 was repeated excepting that the agglomerates were coated with 20% by weight Speswhite, a S. kaolinite ex English China Clays Ltd (ECC).
siz Speswhite has a bulk density of 425 g/l, a particle size of 80% less than 2 microns and a reflectance value R infinity 460 of Example 4 Clay/nonionic/precipitated calcium carbonate S. agglomerates were prepared by co-granulating 83 ).oZz y weight of clay ('KBU) with 83 parts by weight Socai ti using 24 parts by weight of Synperonic A3 and 62 parts by weight of a 2% solution of Sokalan CP5 as a granulating spray.
C
The agglomerates were then dried to a moisture content of approximately 8% on a fluidised bed dryer using drying air having a temperature of 80 0
C.
13 C3289 Example Example 4 was repeated excepting that the agglomerates were cogranulated with 83 parts by weight Speswhite a kaolin ex ECC in place of the Socal U3.
The reflectance of the agglomerates was then determined and is quoted in Table I as an R460* (infinity) value which denotes, on a scale of 1 to 100 the amount of light reflected back from a sample. The *6 higher the reflectance value the whiter the sample.
R460* values presented here are an average of 5 with a least significant difference of u**
U
Table I Ue
*U
Examplr R460* iA 1B S2 58 S3 66 S4 62 9 6

Claims (9)

1. An agglomerate comprising whitening particulate material of average particle size less than 20 microns, a bulk density less than 400 grams per litre and a reflectance value (R infinity 460) of greater than
2. An agglomerate according to claim 1 comprising sufficient whitening particulate material to give the agglomerate an R infinity 460 value greater than
3. An agglomerate as claimed in claim 1 or claim 2, wherein the whitening particulate material is present as a coating on the agglomerate.
4. An agglomerate as claimed in claim 1 or claim 2 wherein the whitening particulate material is present throughout the agglomerate as a cogranulate.
5. An agglomerate as claimed in any preceding claim 20 wherein the bulk density of the whitening Larticulate material is less than 250 grams per litre.
6. An agglomerate as claimed in any preceding claim wherein the average particle size of the particulate material is less than 15 microns.
7. An agglomerate as claimed in any preceding claim wherein the average particle size of the particulate material is less than 10 microns.
8. An agglomerate as claimed in claim 3 wherein the particulate material comprises from 10 to 40% by weight of S a the total agglomerate composition. 15 C3289
9. A fabric softener comprising clay agglomerates, said agglomerates comprising whitening particulate material of average particle size less than 20 microns, a bulk density of less than 400 grams per litre and a reflectance value (R infinity 460) of greater than A detergent composition comprising from 5% to 20% by weight of agglomerates as claimed in claim 1. C e DATED TIS 28TH DAY OF FBRUARY 1990 UNILEVER PLC By its Patent Attorneys: GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia. u* *0 F iu mm f US
AU50542/90A 1989-03-02 1990-02-28 Agglomerates for addition to detergent powders Ceased AU628136B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8904750 1989-03-02
GB898904750A GB8904750D0 (en) 1989-03-02 1989-03-02 Agglomerates for addition to detergent powders

Publications (2)

Publication Number Publication Date
AU5054290A AU5054290A (en) 1990-09-06
AU628136B2 true AU628136B2 (en) 1992-09-10

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Country Status (9)

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EP (1) EP0385748B1 (en)
JP (1) JPH07122073B2 (en)
KR (1) KR950005383B1 (en)
AU (1) AU628136B2 (en)
BR (1) BR9000991A (en)
DE (1) DE69019399T2 (en)
ES (1) ES2074534T3 (en)
GB (1) GB8904750D0 (en)
ZA (1) ZA901608B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0579230B1 (en) * 1992-07-17 1998-12-09 Benckiser N.V. Gentle machine dishwashing compositions
DE4306665A1 (en) * 1993-03-03 1994-09-08 Sued Chemie Ag Detergent additive for fabric softening detergents
EP0627484A1 (en) * 1993-06-02 1994-12-07 The Procter & Gamble Company Coating clay agglomerates with finely divided particulate material
GB2348884A (en) * 1999-04-13 2000-10-18 Procter & Gamble Light reflecting particles
BRPI0401766A (en) * 2004-05-17 2006-08-01 Bentonit Uniao Nordeste Sa process for coating dry granulated powders, detergent and fabric softener

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2120293A (en) * 1982-04-08 1983-11-30 Colgate Palmolive Co Laundry softening detergent
GB2221457A (en) * 1988-08-01 1990-02-07 Ecc Int Ltd Coated clay granules

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4166039A (en) * 1973-10-15 1979-08-28 The Proctor & Gamble Company Detergent composition and process
JPS60262895A (en) * 1984-06-11 1985-12-26 ライオン株式会社 Manufacture of granular detergent
GB8711423D0 (en) * 1987-05-14 1987-06-17 Unilever Plc Detergent composition
JPH07122153B2 (en) * 1987-06-02 1995-12-25 第一工業製薬株式会社 Powder detergent composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2120293A (en) * 1982-04-08 1983-11-30 Colgate Palmolive Co Laundry softening detergent
GB2221457A (en) * 1988-08-01 1990-02-07 Ecc Int Ltd Coated clay granules

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DE69019399T2 (en) 1995-09-21
DE69019399D1 (en) 1995-06-22
GB8904750D0 (en) 1989-04-12
ES2074534T3 (en) 1995-09-16
JPH07122073B2 (en) 1995-12-25
EP0385748A2 (en) 1990-09-05
ZA901608B (en) 1991-11-27
AU5054290A (en) 1990-09-06
EP0385748A3 (en) 1991-06-05
KR900014575A (en) 1990-10-24
JPH02279797A (en) 1990-11-15
KR950005383B1 (en) 1995-05-23
EP0385748B1 (en) 1995-05-17
BR9000991A (en) 1991-02-19

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