NZ211588A - Detergent composition containing sodium perborate monohydrate - Google Patents

Detergent composition containing sodium perborate monohydrate

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Publication number
NZ211588A
NZ211588A NZ211588A NZ21158885A NZ211588A NZ 211588 A NZ211588 A NZ 211588A NZ 211588 A NZ211588 A NZ 211588A NZ 21158885 A NZ21158885 A NZ 21158885A NZ 211588 A NZ211588 A NZ 211588A
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NZ
New Zealand
Prior art keywords
composition
grinding
weight
solids
particles
Prior art date
Application number
NZ211588A
Inventor
M Julement
M Marchal
L Laitem
Original Assignee
Colgate Palmolive 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.)
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Publication date
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Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of NZ211588A publication Critical patent/NZ211588A/en

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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
    • C11D3/395Bleaching 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
    • C11D17/0004Non aqueous liquid compositions comprising insoluble particles
    • 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
    • C11D3/3947Liquid compositions

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Description

<div class="application article clearfix" id="description"> <p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number £11 588 <br><br> 211581 <br><br> ' U 2'. P AT EHT OFFICE <br><br> ?6MAR i985 <br><br> • r- -.aw1 u- f* ~ -i. <br><br> J <br><br> NO DRAWINGS <br><br> 5.iority Dar-i(.•-■: J^rAfe-Al^s. <br><br> Complete S::...-;.;_.:;:;:i ; ;;orf. C:,"L • Gx\Ql.\6fe.cv\p3jQ^ <br><br> •Q&amp;.&amp;l.'i). ' <br><br> Publication C£to; ... 1987. P.O. Journal, No: t.7&gt;£jU, <br><br> Patents Form No. 5 Number <br><br> PATENTS ACT 1953 Dated <br><br> COMPLETE SPECIFICATION <br><br> LIQUID BLEACHING LAUNDRY DETERGENT COMPOSITION <br><br> xffWe COLGATE-PALMOLIVE COMPANY, 300 Park Avenue, New York, New York 1002 2, United States of America, a corporation organised under the laws of the State of Delaware, United States of America do hereby declare the invention for which ji/we pray that a Patent may be granted to bdk/us, and the method by which it is to be performed, to be particularly described in and by the following statement: <br><br> - 1 - <br><br> m <br><br> 21158 <br><br> This invention relates to nonaqueous liquid heavy duty laundry detergents. <br><br> In accordance with one aspect of this invention, a highly effective and stable nonaqueous liquid heavy duty laundry detergent is prepared by dispersing a solid builder salt, sodium perborate monohydrate and a solid activator for the perborate in a substantially anhydrous liquid nonionic surfactant and grinding the dispersion to reduce the particle w. size of those solids to less than about 10 microns, e.g., to an average particle size of 2 to 10 microns or even lower, such as 1 micron. Preferably, in the ground product, less than about 20% by weight (more preferably less than about 10% by weight) of the suspended particles have diameters above 10 microns. <br><br> It will be understood that as the particle size is decreased, by grinding, fresh reactive surfaces are exposed and the surface area available for reaction is increased. Also, the energy involved in the fine grinding operation necessarily i <br><br> causes localized rises in temperature within the mixture being ^ ground (even though the grinding mill is cooled, e.g. by cold water running through a jacket of the mill, during grinding). Despite this, the compositions of the invention are highly stable, showing little, if any, loss of bleaching activity during grinding or on storage. <br><br> - 2 - <br><br> 21158 <br><br> In the grinding operation it is preferred that the proportion of solid ingredients be high enough (e.g., at least about 40% such as about 50%) so that the solid particles are in contact vith each other and are not substantially shielded from one another by the nonionic surfactant liquid. <br><br> Mills which employ grinding balls (ball mills) or similar mobile grinding elements have given very good results. Thus, one may use a laboratory batch attritor having 8 mm diameter steatite grinding balls. For larger scale work a continuously operating mill in which there are 1 mm or 1.5 mm diameter grinding balls working in a very small gap between a stator and a rotor operating at a relatively high speed (e.g., a CoBall mill) may be employed; when using such a mill it is desirable to pass the blend of nonionic surfactant and solids first through a mill which does not effect such fine grinding (e.g., a colloid mill) to reduce the particle size to less than 100 microns (e.g., to about 40 microns), prior to the step of grinding to an average particle diameter below about 10 microns in the continuous ball mill. <br><br> It is preferred that the solid builder salt be an alkali metal polyphosphate such as sodium tripolyphosphate ("TPP") Other suitable polyphosphates include the pyrophoshates such as tetrasodium pyrophosphate and metaphosphates. In place of all or part of the polyphosphate one or more other detergent builder <br><br> - 3 - <br><br> 21158 <br><br> r&gt; <br><br> V J <br><br> salts may be used, such as alkali metal carbonates or bicarbon-ates, silicates, or organic builders such as polycarboxylates. Typical suitable builders are those disclosed in U.S. Patents 4,316,812; 4,264,466 and 3,630,929. <br><br> The preferred activator is tetraacetyl ethylene diamine ("TAED"). Another suitable activator is glucose pentaacetate. Other suitable activators are those disclosed in U.S. Patent 4,264,466 or in column 1 of U.S. Patent 4,430,244. Polyacylated compounds are preferred activators. <br><br> The following Examples are given to illustrate this invention further. All proportions in this application are by weight unless otherwise indicated. <br><br> Example 1 <br><br> The following compositions A and B are each ground for 30 minutes at room temperature in a Wieneroto W-l.S attritor with 8 mm diameter steatite 'balls, producing a liquid suspension in which the average particle size of the ground material is below about 10 microns in each case <br><br> Nonionic surfactant <br><br> Acid-converted nonionic surfactant TPP <br><br> • • <br><br> PROPORTIONS <br><br> A <br><br> B_ <br><br> 35 <br><br> 32.57 <br><br> 16 <br><br> 16 <br><br> 30 <br><br> 30 <br><br> - 4 - <br><br> A <br><br> 2115 <br><br> N <br><br> PROPORTIONS <br><br> Sodium salt of ethylenediamine tetramethy1ene phosphonic acid <br><br> (EDITEMPA) 1.5 1.5 <br><br> Copolymer of methacrylic acid and maleic anhydride completely converted to sodium salt form <br><br> (Sokalan CP5) 4 4 <br><br> Sodium carbonate 2.5 2.5 <br><br> Sodium perborate monohydrate <br><br> (NaBOjH 0) 4.5 <br><br> Sodium perborate tetrahydrate — 6.93 <br><br> TAED 5 5 <br><br> Optical brighteners of stilbene <br><br> 4 type 0.5 0.5 <br><br> Enzyme slurry (Protease slurried in nonionic surfactant) 1 1 <br><br> Each composition contains 0.72% active O2 and the content of unbound water of the ingredients is less than 1%. After 48 hour aging at 35°C, composition A is still liquid while composition B has become substantially solid (its yield stress has increased to a value greater than 20 Pascals). After 5 day aging at 35°C, analysis for available peracetic acid indicates that the effective loss of TAED on grinding and aging is 7% fox composition A and 45% for composition B. <br><br> The nonionic surfactant used in this Example comprises a mixture of equal parts of: <br><br> (a) a relatively water soluble nonionic surfactant <br><br> - 5 - <br><br> J <br><br> • 2115 <br><br> _v which forms a gel when mixed with water at 25°C, specifically a to alkanol which has been alkoxylated to introduce <br><br> 10 ethylene oxide and 5 propylene oxide units per alkanol unit and <br><br> (b) a less water-soluble nonionic surfactant, specifically a to alkanol which has been alkoxylated to introduce 4 ethylene oxide and 7 propylene oxide units per alkanol unit. <br><br> The acid-converted nonionic surfactant is a half ester of succinic acid and a nonionic surfactant (specifically ethoxy-lated to £^5 alkanol having about 5 ethylene oxide units per molecule of alkanol). This half ester can be produced by the reaction of succinic anhydride and the nonionic surfactant at elevated temperature (e.g., 60°C) preferably in the presence of a small amount of catalyst such as pyridine. The resulting acid-terminated product acts in the compositions as an antigelling agent. It reduces the temperature at which the nonionic surfactant forms a gel with cold water and thus aids in the dispensing of the compositions during operation of automatic home laundry machines at winter temperatures. Other carboxylic acid materials soluble in the nonionic surfactant may be used for this purpose. <br><br> The TPP is a blend of anhydrous TPP and a small amount of TPP hexahydrate such that the chemically bound water content is about 3%, which corresponds to about one H2O per pentasodium tripolyphosphate molecule. Such TPP may be produced by treating anhydrous TPP with a limited amount of water. The presence of <br><br> - 6 - <br><br> 21 1588 <br><br> the hexahydrate slows down the rapid rate of solution of the TPP in the wash bath and inhibits caking. One suitable TPP is sold under the name Thermphos NW; the particle size of this TPP as supplied is in the neighborhood of AOO microns; its phase I content is about 60%. <br><br> In preparing the mixture before grinding it is preferred to add the solid ingredients to the nonionic surfactant, <br><br> with the TPP being added last. <br><br> The mixture dispenses readily with cold water in the automatic washing machine. Its specific gravity is about 1.25. It gives excellent washing when used at a dosage of about 100 grams per wash load (as compared with 170 grams per wash load £or the usual heavy duty laundry detergent powders) in conventional European home laundry machines (which employ about 20 liters of water for the washing bath) in which the water is heated, during washing to about 60°C. <br><br> EXAMPLE 2 <br><br> A ground composition is prepared as in Example 1 from the following ingredients in the stated proportions: <br><br> nonionic surfactant 40.8 <br><br> TPP 49.8 <br><br> Ethylene diamine tetraacetic acid 1.2 <br><br> TAED 4 . 5 <br><br> Sodium perborate mono- <br><br> hydrate 3.6 <br><br> Hydroxylamine sulfate 0.1 <br><br> - 7 - <br><br> 211588 <br><br> The hydroxylamine sulfate acts to inhibit the undesirable bleach-decreasing action of the enzyme, catalase, present in soiled clothes. <br><br> As is well known, the nonionic synthetic surfactants are characterized by the presence of an organic hydrophobic group and an organic hydrophilic group and are typically produced by the condensation of an organic aliphatic or alkyl aromatic hydrophobic compound with ethylene oxide (hydrophilic in nature). Practically any hydrophobic compound having a carboxy, hydroxy, amido or amino group with a free hydrogen attached to the nitrogen can be condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a nonionic detergent. The length of the hydrophilic or polyoxyethylene chain can be readily adjusted to achieve the desired balance between the hydrophobic and hydrophilic groups. Typical suitable liquid nonionic surfactants are those disclosed in U.S. patents 4,316,812 and 3,630,9'29, as well as those described and listed in the discussion of nonionic surfactants in Kirk-Othmer "Encyclopedia of Chemical Technology", 3rd Edition, Vol. 22 (1983) pages 360 to 379. <br><br> The activator usually interacts with the peroxygen compound to form a peroxyacid bleaching agent in the wash water. It is preferred to include a sequestering agent of high com-plexing power to inhibit any undesired reaction between such peroxyacid and hydrogen peroxide in the wash solution in the presence of metal ions. Such a sequestering agent is an organic <br><br> - 8 <br><br> ? 11588 <br><br> 2 + <br><br> compound which is able to form a complex with Cu ions, such that the stability constant (pK) of the complexation is equal to or greater than 6, at 25°C, in water of an ionic strength of 0.1 mole/liter, pK being conventionally defined by the formula: pK=-log K where K represents the equilibrium constant. Thus, for example, the pK values for complexation of copper ion with NTA and EDTA at the stated conditions are 12.7 and 18.8, respectively. Suitable sequestering agents include the sodium salts of nitrilotriacetic acid (NTA); ethylene diamine tetraacetic acid (EDTA); diethylene triamine pentaacetic acid (DETPA); diethylene triamine pentamethylene phosphonic acid (DTPMP); and ethylene diamine tetramethylene phosphonic acid (EDITEMPA). <br><br> Other ingredients which may be included in the composition are enzymes (e.g. proteases, amylases or lipases or mixtures thereof); optical brighteners, antiredeposition agents (e.g. sodium carboxymethylcellulose), colorants (e.g. pigments or dyes) etc. <br><br> The composition may also contain an inorganic insoluble thickening agent or dispersant of very high surface area such as finely divided silica of extremely fine particle size (e.g. of 5-100 millimicrons diameter such as sold under the name Aerosil) or the other highly voluminous inorganic carrier materials disclosed in U.S. patent 3,630,929, in proportions of 0.1-10%, e.g. 1 to 5%. It is preferable, however, that the compositions <br><br> - 9 - <br><br> \ .Xr- <br><br> f- <br><br> 211588 <br><br> be substantially free of such compounds and of other silicates, it has been found, for instance, that silica and silicates promote an undesired decomposition of the peroxyacid formed in the wash bath. <br><br> In the compositions of the invention, typical pro-portions of the ingredients are as follows: <br><br> Suspended detergent builder, within the range of about 10 to 60%, such as about 20 to 50%, e.g., about 25 to 40%; <br><br> Liquid phase comprising nonionic surfactant (and, optionally, dissolved carboxylic acid material), within the range of about 30 to 70%, such as about 40 to 60%; this phase may also include a diluent such as a glycol, e.g., polyethylene glycol (e.g., "PEG 400") or hexylene gylcol. <br><br> Carboxylic acidic antigelling agent, in the range of about 0.01 to 1 part per part of nonionic surfactant, such as about 0.05 to 0.6 part, e.g. about 0.2 to 0.5 part; <br><br> Sodium perborate monohydrate, in the range of about <br><br> 2 to 15%, such as about 4 to 10%; <br><br> Activator in the range of about 1 to 8%, such as about <br><br> 3 to 6%. <br><br> The unbound moisture content of the composition should be less than about 2% preferably below about 1%, such as about Jj% or less . <br><br> While it is most convenient and effective to grind all the solid ingredients together it is within the broader scope of the invention to grind separate suspensions of individual ingredients or groups of ingredients and combine these together after such grinding. <br><br> - 10 - <br><br></p> </div>

Claims (7)

<div class="application article clearfix printTableText" id="claims"> <p lang="en"> ©<br><br> 211588<br><br> In this application all proportions are by weight unless otherwise indicated. In the Examples, atmospheric pressure is used unless otherwise indicated.<br><br> It is understood that the foregoing detailed description is given merely by way of illustration and that variations may be made therein without departing from the spirit of the invention as defined in the appended claims.<br><br> f<br><br> O '<br><br> J<br><br> 3<br><br> - 11 -<br><br> 211588<br><br> WHAT WE CLAIM IS :<br><br>
1. A substantially anhydrous liquid heavy duty laundry detergent composition comprising particles of solid sodium perborate monohydrate, particles of solid activator for the perborate, and particles of solid builder salt, all dispersed in a liquid nonionic surfactant, the sizes of said particles being less than 10 microns.<br><br>
2. A composition as in Claim 1 in which the activator comprises tetraacetyl ethylene diamine and the builder salt comprises pentasodium tripolyphosphate.<br><br>
3. A composition as in Claim 1 produced by grinding a suspension in said liquid of said solids, said solids having particle sizes of at least 40 microns before said grinding.<br><br>
4. A composition as in Claim 1 comprising 10<br><br> to 60% by weight of said builder salt, 2 to 15% by weight sodium perborate monohydrate and 1 to 8% by weight activator.<br><br>
5. A composition as in Claim 4 in which the amount of i<br><br> said builder /alt Is 25 to 40% by weight.<br><br>
6 A composition as in Claim 5 in which the activator comprises tetraacetyl ethylene diamine, the builder salt comprises pentasodium tripolyphosphate, said composition having been produced by grinding a suspension of said solids in said liquid, said solids having particle sizes of at least 40 microns before said grinding.<br><br>
7. A composition as in Claim 6 substantially free of silica or silicates.<br><br> WEST-WALKER, McCABE<br><br> j NX PATENT OFFICE per:<br><br> ATTORNEYS THE APPLICANT<br><br> j RECEIVED |<br><br> - 1 2 -<br><br> </p> </div>
NZ211588A 1984-04-09 1985-03-26 Detergent composition containing sodium perborate monohydrate NZ211588A (en)

Applications Claiming Priority (1)

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US59794984A 1984-04-09 1984-04-09

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Country Status (24)

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JP (1) JPS60230000A (en)
KR (1) KR920004793B1 (en)
AT (1) AT394864B (en)
AU (1) AU578671B2 (en)
BE (1) BE902144A (en)
BR (1) BR8501621A (en)
CA (1) CA1300465C (en)
CH (1) CH667669A5 (en)
DE (1) DE3511515A1 (en)
DK (1) DK158385A (en)
ES (1) ES8701221A1 (en)
FI (1) FI85601C (en)
FR (1) FR2562557B1 (en)
GR (1) GR850881B (en)
IT (1) IT1181629B (en)
LU (1) LU85845A1 (en)
MX (1) MX162806A (en)
NL (1) NL8501031A (en)
NO (1) NO851348L (en)
NZ (1) NZ211588A (en)
PH (1) PH21598A (en)
PT (1) PT80251B (en)
SE (1) SE8501590L (en)
ZA (1) ZA852201B (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ211550A (en) * 1984-04-06 1987-06-30 Colgate Palmolive Co Liquid detergent composition containing acidic phosphorus compound and polyphosphate
MX162823B (en) * 1985-03-29 1991-06-28 Colgate Palmolive Co IMPROVEMENTS TO LIQUID WHITENING DETERGENT COMPOSITION FOR LAUNDRY
NZ216987A (en) * 1985-08-20 1988-09-29 Colgate Palmolive Co Nonaqueous liquid low phosphate laundry detergent
US5250212A (en) * 1987-05-27 1993-10-05 The Procter & Gamble Company Liquid detergent containing solid peroxygen bleach and solvent system comprising water and lower aliphatic monoalcohol
GB8713756D0 (en) * 1987-06-12 1987-07-15 Procter & Gamble Liquid detergent
CA1323282C (en) * 1988-04-29 1993-10-19 John Stuart Galvin Liquid cleaning products
AU624634B2 (en) * 1989-08-18 1992-06-18 Colgate-Palmolive Company, The Non-aqueous, nonionic heavy duty laundry detergent
JPH10512601A (en) * 1994-11-18 1998-12-02 ザ、プロクター、エンド、ギャンブル、カンパニー Bleach detergent compositions containing bleach activators effective at low perhydroxyl concentrations
DE10105801B4 (en) * 2001-02-07 2004-07-08 Henkel Kgaa Detergents and cleaning agents comprising fine microparticles with detergent components
US8871807B2 (en) 2008-03-28 2014-10-28 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US20110257060A1 (en) * 2010-04-19 2011-10-20 Robert Richard Dykstra Laundry detergent composition comprising bleach particles that are suspended within a continuous liquid phase
US9321664B2 (en) 2011-12-20 2016-04-26 Ecolab Usa Inc. Stable percarboxylic acid compositions and uses thereof
BR112014020748B1 (en) 2012-03-30 2021-02-23 Ecolab Usa Inc. water treatment method, water source treatment method and aqueous water treatment composition with antimicrobial activity
US10165774B2 (en) 2013-03-05 2019-01-01 Ecolab Usa Inc. Defoamer useful in a peracid composition with anionic surfactants
US8822719B1 (en) 2013-03-05 2014-09-02 Ecolab Usa Inc. Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring
US20140256811A1 (en) 2013-03-05 2014-09-11 Ecolab Usa Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0030096B2 (en) * 1979-12-04 1993-07-14 Imperial Chemical Industries Plc Detergent composition
FI823446L (en) * 1981-10-16 1983-04-17 Unilever Nv FOERBAETTRAD KOMPOSITION FOER MASKINELL DISKNING OCH SKOELJNING
GB8308508D0 (en) * 1983-03-28 1983-05-05 Ici Plc Detergent compositions
GB8321923D0 (en) * 1983-08-15 1983-09-14 Unilever Plc Machine-dishwashing compositions

Also Published As

Publication number Publication date
MX162806A (en) 1991-06-26
AT394864B (en) 1992-07-10
BR8501621A (en) 1985-12-03
KR850007609A (en) 1985-12-07
FI85601B (en) 1992-01-31
FI851385L (en) 1985-10-10
FI851385A0 (en) 1985-04-04
IT1181629B (en) 1987-09-30
ZA852201B (en) 1986-11-26
ES542030A0 (en) 1986-11-16
IT8547931A1 (en) 1986-10-05
SE8501590D0 (en) 1985-04-01
FI85601C (en) 1992-05-11
FR2562557B1 (en) 1987-01-16
DK158385A (en) 1985-10-10
KR920004793B1 (en) 1992-06-15
LU85845A1 (en)
GR850881B (en) 1985-11-25
IT8547931A0 (en) 1985-04-05
BE902144A (en) 1985-10-09
PT80251B (en) 1987-02-06
DE3511515A1 (en) 1985-10-17
FR2562557A1 (en) 1985-10-11
CA1300465C (en) 1992-05-12
JPS60230000A (en) 1985-11-15
ATA98685A (en) 1991-12-15
DK158385D0 (en) 1985-04-09
NL8501031A (en) 1985-11-01
AU4086085A (en) 1985-10-17
CH667669A5 (en) 1988-10-31
PT80251A (en) 1985-05-01
NO851348L (en) 1985-10-10
PH21598A (en) 1987-12-11
AU578671B2 (en) 1988-11-03
SE8501590L (en) 1985-10-10
ES8701221A1 (en) 1986-11-16

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