WO1994003580A1 - Detergent compositions - Google Patents

Detergent compositions Download PDF

Info

Publication number
WO1994003580A1
WO1994003580A1 PCT/GB1993/001636 GB9301636W WO9403580A1 WO 1994003580 A1 WO1994003580 A1 WO 1994003580A1 GB 9301636 W GB9301636 W GB 9301636W WO 9403580 A1 WO9403580 A1 WO 9403580A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
weight
condensed phosphate
salt
phosphate builder
Prior art date
Application number
PCT/GB1993/001636
Other languages
English (en)
French (fr)
Inventor
James Swales
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Plc filed Critical Imperial Chemical Industries Plc
Priority to EP93917976A priority Critical patent/EP0652940B1/en
Priority to DE69308856T priority patent/DE69308856T2/de
Priority to AU47204/93A priority patent/AU678378B2/en
Priority to JP6505116A priority patent/JPH07509520A/ja
Publication of WO1994003580A1 publication Critical patent/WO1994003580A1/en
Priority to NO950391A priority patent/NO950391L/no

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
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2086Hydroxy carboxylic acids-salts thereof
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates

Definitions

  • This invention relates to detergent compositions and in particular to non-aqueous laundry liquid detergent compositions.
  • Detergent compositions which comprise a suspension of a builder and optionally other solids in an organic liquid which comprises a surfactant.
  • Non-aqueous compositions of this type are described in European Patent Specifications Nos EP 0030096 B and EP 0120659 B.
  • Such compositions may contain phosphate builders, for example alkali metal condensed phosphates, for example sodium tripolyphosphate.
  • detergents are placed in containers which are introduced into the washing zone. If the container has restricted access solid deposits may be left in it especially if it was not dry when detergent was placed in it.
  • This invention accordingly provides a substantially non-aqueous liquid laundry detergent composition which comprises a surfactant, a condensed phosphate builder and a water soluble salt of a hydroxy ⁇ carboxylic acid containing 1 to 6 -C00H groups and 1 to 5 -OH groups, or a water soluble salt of such an acid.
  • substantially non-aqueous we mean that the amount of water in the composition is sufficiently small that the tendency of the condensed phosphate builder to hydrolyse and thus to cause the viscosity of the detergent formulation to increase or the formulation to gel during storage prior to use is overcome.
  • it is free water i.e. water that is not chemically bound as in water of crystallisation, in the formulation that is problematical and the amount of free water will usually be kept to less than 21 , and very desirably less than 12, by weight of the composition.
  • Small quantities of free water are typically present in various components of the formulation e.g. non-ionic surfactants and polyethylene glycol, and it is the concentration of water from such sources that should be kept suitably low. Water of crystallisation in materials such as the hydroxycarboxylic acid salt(s), as in sodium citrate dihydrate, is not usually a problem.
  • the hydroxycarboxylic acid salt is desirably a salt of an acid which contains a total of at least 3 hydroxyl and carboxyl groups. Salts of tartaric and citric acids are particularly useful materials. Mixtures of salts of these acids can be used if desired. The use of salts of either or both of these acids forms a particularly advantageous feature of this invention.
  • the salt cation is desirably an ammonium, substituted ammonium or alkali metal, particularly sodium, salt.
  • the salt is desirably present in an amount to give a weight ratio of the condensed phosphate builder to the hydroxy ⁇ carboxylic acid salt of 60:1 to 5:1, and particularly 30:1 to 7:1, especially about 20:1.
  • the amount of hydroxycarboxylic acid salt used in compositions of this invention is relatively small. At relatively high concentrations, hydroxycarboxylic acid salts can act as builders in detergent formulations. In this invention, the amount used is typically sufficiently small that the hydroxycarboxylic acid salt does not provide significant effect as a builder over and above that provided by the condensed phosphate builder.
  • the composition is preferably alkaline in reaction i.e. when added to water, as in use, the laundry water is rendered alkaline. It is preferred that normally acidic substances when present in the composition are in a form neutralised with alkali, particularly containing one or more of ammonium, substituted ammonium or, and preferably, alkali metal ions. Specific additives can be included to control the alkalinity of the laundry water in use, such as sodium disiiicate or, especially if somewhat less alkaline conditions are desired, sodium bicarbonate.
  • the condensed phosphate builder may be an alkali metal, preferably a potassium or sodium salt of a condensed phosphate.
  • Linear condensed phosphates are better builders than cyclic materials and are thus preferred—
  • the condensed phosphate will be a di-phosphate (pyrophosphate) for example sodium pyrophosphate Na4P2 ⁇ 7 , or tri-phosphate (tripolyphosphate) , for example potassium tripolyphosphate, or, and particularly desirably, sodium tripolyphosphate.
  • the total builder content of the composition (including the condensed phosphate builder) will generally be from 25 to 602 by weight.
  • Other builders e.g. sodium carbonate and sodium bicarbonate, can be included if desired, but the amounts of such builders, when present, are usually relatively small for example from 1 to 10Z by weight of the composition.
  • the composition can include a bleach such as a perborate or percarbonate e.g. as an alkali metal, particularly sodium, salt.
  • a bleach such as a perborate or percarbonate e.g. as an alkali metal, particularly sodium, salt.
  • the amount of the bleach will typically be from 1 to 252, particularly 2 to 20Z, more particularly 5 to 202, and especially about 10 to about 152, by weight of the composition.
  • a bleach activator such as tetra-acetyl ethylene diamine, can also be included in the composition.
  • the surfactant will typically include at least one non-ionic surfactant.
  • Suitable non-ionic surfactants include alkylene oxide derivatives, particularly where the alkylene oxide is ethylene and/or propylene oxide, especially ethylene oxide.
  • Particularly suitably materials include reaction products of an amine, alkyl phenol or alkanol with ethylene and/or propylene oxide, especially ethylene oxide.
  • the amine will usually be an alkyl amine in which the alkyl group can be straight or branched chain and can contain from 6 to 20, particularly 10 to 16, carbon atoms.
  • alkyl phenol reaction products are used, the alkyl group can be straight or branched chain and can contain from 6 to 20, particularly 6 to 12, carbon atoms.
  • the alkanol is preferably a primary or secondary alkanol having a linear or mono branched alkyl chain and the alkanol can contain 6 to 20, preferably 10 to 16, carbon atoms.
  • the (poly)oxyalkylene chain in the ncn-ionic surfactant has from 1 to 10, preferably 3 to 8, alkylene oxide residues. Of course, the number of alkylene oxide residues given is an average value.
  • the amount of non-ionic surfactant is typically from 5 to 252, particularly 7 to 202, by weight of the composition.
  • non-ionic surfactants are generally the preferred surfactants in this invention, the surfactant may alternatively be or include one or more anionic or cationic surfactants.
  • anionic or cationic surfactants may be of known type for example the anionic detergents may be soaps, alkylbenzene or olefin sulphonates, alcohol sulphates or alcohol alkoxylate sulphates; the cationic surfactants are suitably di-C ⁇ o-22 and preferably di-Ci5_i8 alkyl, di-lower alkyl ammonium salts or hydroxides for example chlorides or sulphates or for example fabric softeners of the CIQ-16 alkyl, di-lower alkyl (for example methyl), substituted ethyl ammonium salts.
  • the substituent on the ethyl group may be an -00CR group where R is a C ⁇ s-22 alkyl group, and the anion of the salt may be a RSO4- group where R is lower alkyl for example methyl.
  • the lower alkyl groups are suitably methyl groups.
  • the composition desirably also includes a polyalkylene glycol, for example a polyethylene/polypropylene glycol or and particularly advantageously a polyethylene glycol. This enhances the fluidity of the compositions and, particularly where the polyalkylene glycol is a polyethylene glycol, is readily biodegradable.
  • the polyalkylene glycol desirably has a molecular weight of 100 to 1500 D, especially 100 to 500, and for example 150 to 400, D.
  • Polyalkylene glycols, particularly polyethylene glycols, of average molecular weight 100 to 400 and preferably 150 to 300 are especially useful as they can act to reduce the pour point of the liquid laundry detergent compositions thus making them more easily usable in a cold environment.
  • the polyalkylene glycol, particularly polyethylene glycol is typically present as 5 to 552, particularly 10 to 502 and especially 25 to 452, by weight of the composition.
  • composition may also contain additives conventionally found in detergent compositions, for example fabric conditioners, anti- redeposition aids such as carboxymethyl cellulose (see below), pH adjusters (see above), anti-corrosion additives e.g. sodium disilicate
  • the liquid composition will generally take the form of a dispersion of solid particles in a liquid medium.
  • the solids will include the condensed phosphate builder, other inorganic builders, when present, the hydroxycarboxylic acid salt(s), the bleach, when present, and other solid minor components not soluble in the liquid medium.
  • the laundry liquid composition will comprise 25 to 702 and particularly 30 to 652, for example 40 to 652, by weight of total solids.
  • the solids will be finely divided solids and in particularly the solids have an average particle size of at most 10 ⁇ m and very particularly from 1.2 to 8 ⁇ .
  • the proportion of relatively large particles will usually be kept small and, thus, it is very desirable that at least 902 of the solid particles have a size of less than 10 ⁇ m.
  • Stated particle sizes are the diameters of particles of equal volume. Desirably, the particle size distribution is relatively narrow so that average particle sizes expressed as number average or weight average sizes are similar. Particle sizes can be measured, for example, using Coulter counters or laser particle size measuring equipment such as that sold under the Malvern name.
  • the liquid medium will include the liquid surfactant such as non-ionic surfactant(s) , when present, the polyoxyalkylene glycol, when present, other minor liquid components and solid components soluble in the liquid medium.
  • the liquid medium will comprise 75 to 302 and particularly 70 to 352, for example 60 to 352, by weight of the composition.
  • Cationic and anionic surfactants when present will, depending on their properties either form part of the solids or will be wholly or partly liquid or dissolved in the liquid medium.
  • the formulation can include anti-redeposition aids. These include polycarboxylic acids having at least 10, usually at least 100, particulalry 150 to 2000 and especially 200 to 1000, COOH groups. Carboxymethyl cellulose is a suitable anti-redeposition aid.
  • the composition suitably has a pour point (ASTM D 97-66, 1971) of less than 10°C and particularly less than 5°C.
  • the pour point may be adjusted by- varying the liquid phase composition, for example, by including surfactants and/or polyethylene glycol of low pour point.
  • compositions according to the invention the dispersion of the solids in the non-ionic surfactant is remarkably stable especially if the particle size of the solids is at most 10 ⁇ m. If the solids separate at all then the resulting phase is usually loosely flocculated and is readily redispersible while if the relative amounts of the solids, polyethylene glycol and surfactant in the composition are correctly chosen there is little phase separation as the liquid fills the space between the loosely packed solid particles.
  • An especially useful substantially non-aqueous liquid laundry detergent composition which forms a particular feature of the invention is one which comprises: from 25 to 602 by weight of condensed phosphate builder; from 5 to 252 by weight of at least one non-ionic surfactant; from 5 to 552 by weight of polyethylene glycol having a molecular weight of from 100 to 500; optionally from 1 to 252 by weight of sodium perborate or percarbonate bleach; and a water soluble ammonium, substituted ammonium and/or alkali metal salt of tartaric and/or citric acid in an amount to give a weight ratio of condensed phosphate builder to acid or salt of from 60:1 to 10:1, and wherein the composition comprises from 65 to 402 by weight of solid particles having an average size of less than 10 ⁇ m dispersed in a liquid medium which is correspondingly from 35 to
  • compositions according to the invention may suitably be made by a process which comprises milling ingredients together for example by bead milling.
  • the invention is illustrated by the following Examples. All parts and percentages are by weight and in the Examples weight percentages are based on the total weight of the composition unless otherwise specified.
  • Tripolyphosphate is sodium tripolyphosphate.
  • Sodium EDTAte is the tetrasodium salt of ethylene diamine tetra-acetic acid.
  • Optical brightener is "Leucophor DUK” optical brightener from Sandoz.
  • CMC is carboxymethyl cellulose sold as “Courlose” A610, degree of substitution 0.5 to 0.7, molecular weight believed to be 60000 to 100000.
  • A3 is "Synperonic" A3 which is the product of condensing an average of 3 moles ethylene oxide with a mixture of two parts C13 primary alkanol to one part C15 primary alkanol, both having some 2-methyl branching.
  • 87K is "Synperonic” 87K which is the product of condensing an average of 7 moles of a mixture of 922 ethylene oxide and 82 propylene oxide with a mixture of two parts C13 primary alkanol to one part C]_5 primary alkanol, both having some 2-methyl branching.
  • PEG 200 is Polyethylene glycol of average molecular weight 200 D
  • Liquid formulations A - H (Control sample Cl - formulation A and Examples 1 to 7 - formulations B - H) were produced by mixing together the components in the amounts given in Table 1 below in a homogeniser and then bead milling the mixtures until the solids had an average particle size of 3 ⁇ m. TABLE 1
  • each formulation was assessed by weighing 60g of the laundry liquid into a commercially available rectangular plastic dosing device measuring ca. 6.5 x 5 x 3.5 cm which was placed in the drum of a Philips 036 washing machine on top of 3.5 kg of laundry (laboratory coats and towels). The machine was started on programme No 5 which has a 27 minute wash cycle with cold water fill, taking 10 minutes to reach the 40°C wash temperature. 10 minutes after the drum had started to roll the machine was stopped, drained and the dosing device removed. The amount of any residues left in the dosing device was recorded. This procedure was carried out at least 3 times for each formulation. The test results are set out in Table 2 below.

Landscapes

  • 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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
PCT/GB1993/001636 1992-08-03 1993-08-03 Detergent compositions WO1994003580A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
EP93917976A EP0652940B1 (en) 1992-08-03 1993-08-03 Detergent compositions
DE69308856T DE69308856T2 (de) 1992-08-03 1993-08-03 Waschmittelzusammensetzungen
AU47204/93A AU678378B2 (en) 1992-08-03 1993-08-03 Condensed phosphate built non-aqueous liquid laundry detergent including a hydroxycarboxylic acid or salt
JP6505116A JPH07509520A (ja) 1992-08-03 1993-08-03 洗剤配合物
NO950391A NO950391L (no) 1992-08-03 1995-02-02 Vaskemiddelblandinger

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB929216454A GB9216454D0 (en) 1992-08-03 1992-08-03 Detergent compositions
GB9216454.0 1992-08-03

Publications (1)

Publication Number Publication Date
WO1994003580A1 true WO1994003580A1 (en) 1994-02-17

Family

ID=10719741

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1993/001636 WO1994003580A1 (en) 1992-08-03 1993-08-03 Detergent compositions

Country Status (12)

Country Link
EP (1) EP0652940B1 (es)
JP (1) JPH07509520A (es)
AT (1) ATE150082T1 (es)
AU (1) AU678378B2 (es)
CA (1) CA2141452A1 (es)
DE (1) DE69308856T2 (es)
DK (1) DK0652940T3 (es)
ES (1) ES2098767T3 (es)
GB (1) GB9216454D0 (es)
NZ (1) NZ254900A (es)
WO (1) WO1994003580A1 (es)
ZA (1) ZA935578B (es)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0752466A1 (en) * 1995-07-05 1997-01-08 The Procter & Gamble Company Nonaqueous detergent compositions comprising effervescent systems
WO1997049616A1 (en) * 1996-06-26 1997-12-31 The Procter & Gamble Company Vented container containing a liquid product with particulate solids
WO1998000507A2 (en) * 1996-06-28 1998-01-08 The Procter & Gamble Company Nonaqueous detergent compositions containing bleach precursors
US6548134B1 (en) 1996-06-26 2003-04-15 The Procter & Gamble Company Vented container containing a liquid product with particulate solids
US8871807B2 (en) 2008-03-28 2014-10-28 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US9242879B2 (en) 2012-03-30 2016-01-26 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US9253978B2 (en) 2008-03-28 2016-02-09 Ecolab USA, Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9288992B2 (en) 2013-03-05 2016-03-22 Ecolab USA, Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
US9290448B2 (en) 2008-03-28 2016-03-22 Ecolab USA, Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9585397B2 (en) 2013-03-05 2017-03-07 Ecolab Usa Inc. Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring
US9902627B2 (en) 2011-12-20 2018-02-27 Ecolab Usa Inc. Stable percarboxylic acid compositions and uses thereof
US10165774B2 (en) 2013-03-05 2019-01-01 Ecolab Usa Inc. Defoamer useful in a peracid composition with anionic surfactants

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5394635B2 (ja) * 2007-12-07 2014-01-22 正一 中村 洗浄添加剤及びその製造方法

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3850831A (en) * 1971-07-15 1974-11-26 Mo Och Domsjoe Ab Liquid detergent compositions containing surfactants and peroxide bleaching agents
EP0030096A1 (en) * 1979-12-04 1981-06-10 Imperial Chemical Industries Plc Detergent composition
EP0120659A2 (en) * 1983-03-28 1984-10-03 Imperial Chemical Industries Plc Detergent compositions
FR2585720A1 (fr) * 1985-08-05 1987-02-06 Colgate Palmolive Co Compositions detergentes liquides non aqueuses non ioniques de blanchissage a teneur faible ou nulle en phosphate et procedes pour nettoyer des tissus salis les utilisant
EP0256343A1 (en) * 1986-08-12 1988-02-24 MIRA LANZA S.p.a. Non aqueous liquid detergent product consisting of two separate base compositions
GB2196981A (en) * 1986-10-29 1988-05-11 Colgate Palmolive Co Liquid built detergent compositions
FR2619823A1 (fr) * 1987-08-31 1989-03-03 Colgate Palmolive Co Compositions detergentes liquides non aqueuses pour le blanchissage a temperatures elevees, et leurs applications
EP0339999A2 (en) * 1988-04-29 1989-11-02 Unilever Plc Liquid cleaning products
EP0413616A1 (en) * 1989-08-18 1991-02-20 Colgate-Palmolive Company Non-aqueous, nonionic heavy duty laundry detergent
EP0423014A2 (en) * 1989-10-10 1991-04-17 Colgate-Palmolive Company Nonaqueous liquid automatic dishwasher detergent composition containing a dual bleach system
WO1992009678A1 (en) * 1990-11-26 1992-06-11 S.B. Chemicals Limited Liquid built detergent compositions
WO1992020772A1 (en) * 1991-05-24 1992-11-26 Imperial Chemical Industries Plc Detergent compositions

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3850831A (en) * 1971-07-15 1974-11-26 Mo Och Domsjoe Ab Liquid detergent compositions containing surfactants and peroxide bleaching agents
EP0030096A1 (en) * 1979-12-04 1981-06-10 Imperial Chemical Industries Plc Detergent composition
EP0120659A2 (en) * 1983-03-28 1984-10-03 Imperial Chemical Industries Plc Detergent compositions
FR2585720A1 (fr) * 1985-08-05 1987-02-06 Colgate Palmolive Co Compositions detergentes liquides non aqueuses non ioniques de blanchissage a teneur faible ou nulle en phosphate et procedes pour nettoyer des tissus salis les utilisant
EP0256343A1 (en) * 1986-08-12 1988-02-24 MIRA LANZA S.p.a. Non aqueous liquid detergent product consisting of two separate base compositions
GB2196981A (en) * 1986-10-29 1988-05-11 Colgate Palmolive Co Liquid built detergent compositions
FR2619823A1 (fr) * 1987-08-31 1989-03-03 Colgate Palmolive Co Compositions detergentes liquides non aqueuses pour le blanchissage a temperatures elevees, et leurs applications
EP0339999A2 (en) * 1988-04-29 1989-11-02 Unilever Plc Liquid cleaning products
EP0413616A1 (en) * 1989-08-18 1991-02-20 Colgate-Palmolive Company Non-aqueous, nonionic heavy duty laundry detergent
EP0423014A2 (en) * 1989-10-10 1991-04-17 Colgate-Palmolive Company Nonaqueous liquid automatic dishwasher detergent composition containing a dual bleach system
WO1992009678A1 (en) * 1990-11-26 1992-06-11 S.B. Chemicals Limited Liquid built detergent compositions
WO1992020772A1 (en) * 1991-05-24 1992-11-26 Imperial Chemical Industries Plc Detergent compositions

Cited By (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0752466A1 (en) * 1995-07-05 1997-01-08 The Procter & Gamble Company Nonaqueous detergent compositions comprising effervescent systems
WO1997049616A1 (en) * 1996-06-26 1997-12-31 The Procter & Gamble Company Vented container containing a liquid product with particulate solids
EP0816247A1 (en) * 1996-06-26 1998-01-07 The Procter & Gamble Company Venting container containing a liquid product with particulate solids
US6548134B1 (en) 1996-06-26 2003-04-15 The Procter & Gamble Company Vented container containing a liquid product with particulate solids
WO1998000507A2 (en) * 1996-06-28 1998-01-08 The Procter & Gamble Company Nonaqueous detergent compositions containing bleach precursors
WO1998000507A3 (en) * 1996-06-28 1998-05-28 Procter & Gamble Nonaqueous detergent compositions containing bleach precursors
US6165959A (en) * 1996-06-28 2000-12-26 The Procter & Gamble Company Nonaqueous detergent compositions containing bleach precursors
US11827867B2 (en) 2008-03-28 2023-11-28 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US10017720B2 (en) 2008-03-28 2018-07-10 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9253978B2 (en) 2008-03-28 2016-02-09 Ecolab USA, Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US11015151B2 (en) 2008-03-28 2021-05-25 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9290448B2 (en) 2008-03-28 2016-03-22 Ecolab USA, Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9359295B2 (en) 2008-03-28 2016-06-07 Ecolab USA, Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9540598B2 (en) 2008-03-28 2017-01-10 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US10669512B2 (en) 2008-03-28 2020-06-02 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US9676711B2 (en) 2008-03-28 2017-06-13 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US8871807B2 (en) 2008-03-28 2014-10-28 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US10323218B2 (en) 2008-03-28 2019-06-18 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
US10077415B2 (en) 2008-03-28 2018-09-18 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US9902627B2 (en) 2011-12-20 2018-02-27 Ecolab Usa Inc. Stable percarboxylic acid compositions and uses thereof
US10023484B2 (en) 2012-03-30 2018-07-17 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US10017403B2 (en) 2012-03-30 2018-07-10 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing enzymes for treatment of drilling fluids, frac fluids, flowback water and disposal water
US9926214B2 (en) 2012-03-30 2018-03-27 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US9242879B2 (en) 2012-03-30 2016-01-26 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US11180385B2 (en) 2012-10-05 2021-11-23 Ecolab USA, Inc. Stable percarboxylic acid compositions and uses thereof
US11939241B2 (en) 2012-10-05 2024-03-26 Ecolab Usa Inc. Stable percarboxylic acid compositions and uses thereof
US10165774B2 (en) 2013-03-05 2019-01-01 Ecolab Usa Inc. Defoamer useful in a peracid composition with anionic surfactants
US9585397B2 (en) 2013-03-05 2017-03-07 Ecolab Usa Inc. Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring
US10893674B2 (en) 2013-03-05 2021-01-19 Ecolab Usa Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
US9288992B2 (en) 2013-03-05 2016-03-22 Ecolab USA, Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
US11026421B2 (en) 2013-03-05 2021-06-08 Ecolab Usa Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
US11206826B2 (en) 2013-03-05 2021-12-28 Ecolab Usa Inc. Defoamer useful in a peracid composition with anionic surfactants

Also Published As

Publication number Publication date
AU4720493A (en) 1994-03-03
DK0652940T3 (da) 1997-09-01
NZ254900A (en) 1997-02-24
DE69308856T2 (de) 1997-07-10
EP0652940B1 (en) 1997-03-12
AU678378B2 (en) 1997-05-29
GB9216454D0 (en) 1992-09-16
ES2098767T3 (es) 1997-05-01
ZA935578B (en) 1994-03-14
JPH07509520A (ja) 1995-10-19
ATE150082T1 (de) 1997-03-15
CA2141452A1 (en) 1994-02-17
EP0652940A1 (en) 1995-05-17
DE69308856D1 (de) 1997-04-17

Similar Documents

Publication Publication Date Title
EP0120659B1 (en) Detergent compositions
US4316812A (en) Detergent composition
CA2078718C (en) Detergent powders and process for preparing them
US6008174A (en) Powder detergent composition having improved solubility
KR960012274B1 (ko) 개선된 세정작용의 과립형 흡착제
EP0652940B1 (en) Detergent compositions
JPH0726290A (ja) 洗 剤
JP2849041B2 (ja) 洗剤組成物
CA1109762A (en) Agglomeration process for making granular detergents
JPH09500410A (ja) 低使用量洗剤組成物
EP0678119B2 (en) Use of ethoxylated diphatic alcohols as dissolution aids
US5514295A (en) Dispensable powder detergent
CA1229021A (en) Granular detergent compositions containing sodium aluminosilicate or other phosphorus-free detergency builders
CA1306166C (en) Machine dishwashing compositions
JP2693827B2 (ja) 液体洗剤組成物
JP3268597B2 (ja) 洗浄剤組成物
JP2672814B2 (ja) 高密度粒状洗剤組成物
EP1085080B1 (en) Surfactant composition
EP0710717B1 (en) Dispensable powder detergent
JP5132860B2 (ja) 粉末洗剤組成物及びその製造方法
JP2000192096A (ja) 高嵩密度洗剤粒子群
JP2001164288A (ja) ランドリー用洗浄剤組成物
SK130393A3 (sk) Kvapalná dctcrgcntná kompozícia

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA JP NO NZ US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 1993917976

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2141452

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 254900

Country of ref document: NZ

ENP Entry into the national phase

Ref document number: 1995 379635

Country of ref document: US

Date of ref document: 19950328

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 1993917976

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 1993917976

Country of ref document: EP