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NZ211550A - Liquid detergent composition containing acidic phosphorus compound and polyphosphate - Google Patents

Liquid detergent composition containing acidic phosphorus compound and polyphosphate

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Publication number
NZ211550A
NZ211550A NZ211550A NZ21155085A NZ211550A NZ 211550 A NZ211550 A NZ 211550A NZ 211550 A NZ211550 A NZ 211550A NZ 21155085 A NZ21155085 A NZ 21155085A NZ 211550 A NZ211550 A NZ 211550A
Authority
NZ
New Zealand
Prior art keywords
composition
phosphorus compound
alkanol
nonionic surfactant
microns
Prior art date
Application number
NZ211550A
Inventor
G Broze
T Ouhadi
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.)
Filing date
Publication date
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of NZ211550A publication Critical patent/NZ211550A/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
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • 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
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0013Liquid compositions with insoluble particles in suspension
    • 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
    • C11D3/062Special methods concerning phosphates
    • 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
    • C11D3/36Organic compounds containing phosphorus

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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

New Zealand Paient Spedficaiion for Paient Number £11 550 2 1 Priority Date(s) y • ■•■■•••< Complete Specification Filed: Class: Publication Date: P.O. Journal, No: 3:0JM .lacvi NO DRAWINGS Patents Form No. 5 .0 n. jr\r\ r* ;'•-o- :J ;u ;Number ;PATENTS ACT 1953 ;Dated ;COMPLETE SPECIFICATION ;LIQUID LAUNDRY DETERGENT COMPOSITION CONTAINING POLYPHOSPHATE ;#We COLGATE-PALMOLIVE COMPANY, 300 Park Avenue, New York, New York 10022, 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 #we pray that a Patent may be granted to me/us, and the method by which it is to be performed, to be particularly described in and by the following statement: ;1 ;This invention relates to liquid laundry detergent composition. ;Liquid nonaqueous heavy duty laundry detergent compositions are well known in the art. For instance, compositions of that type may comprise a liquid nonionic surfactant in which are dispersed particles of a builder, such as a polyphosphate builder, as shown for instance in U.S. patents Nos. 4,316,812; 3,630,929; 4,264,466, and British patents Nos. 1,205,711 and 1,270,040. ;It is known that such suspensions can be stabilized against settling by adding 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, or by including various clays, such as attapulgite, as disclosed in U.S. Patent 4,264,466. Grinding to very fine particle sizes also increases the stability. ;In accordance with one aspect of the invention, the stability of the suspension is increased by including therein an acidic organic phosphorus compound having an acidic - POH group. This may be, for instance, a partial ester of phosphoric acid and an alcohol such as an alkanol which has a lipophilic character, having, for instance, more than 5 carbon atoms, e.g. 8 to 20 carbon atoms. It is found that as a result of the inclusion of quite small amounts of the acidic organic phosphorus compound the suspension becomes significantly more ;J ;55 ;stable against settling on standing but remains pourable. Thus, as shown below, inclusion of the acidic phosphorus compound increases the yield value of the suspension, but decreases its plastic viscosity. ;It is believed that the use of the acidic phosphorus compound may result in the formation of a high energy physical bond between the -POH portion of the molecule and the surfaces of the inorganic polyphosphate builder so that these surfaces take on an organic character and become more compatible with the nonionic surfactant. ;The invention is particularly suitable for use with suspensions in which the particle size of the polyphosphate build-er is reduced to. below about 10 microns. ;The suspensions of the polyphosphate builder, such as sodium tripolyphosphate ("TPP") in the nonionic surfactant are found to behave, Theologically, substantially according to the Casson equation: ;£ 1/2 £o111 1/2 ^1/Z ;+ Y~\— oO ;^ is the shear rate, is the shear stress, is the yield stress (or yield value) and 7"V cyr> ^-s t^le shear rate plastic viscosity (which can be measured by determining the slope of the graph of the square root of the shear stress (as ordinate) vs. the square root of the shear rate) . The yield value is the minimum shear stress below which no flow occurs (i.e., it corresponds to the intercept at the ordinate, at zero ;- 3 - ;2 Hi 5 50 ;A ;shear rate, of the graph mentioned above). It i-s accordingly a criterion of stability. The plastic viscosity is a measure of the flowability once the yield value has been overcome. ;It is preferred that the yield value (measured at o ;25 C) be at least about 2 Paxcals and (for pourability and dispensability) not above about 8 Pascals, such as about 3 to 7 Pascals, more preferably about 4 Pascals. ;For studying this rheological behavior, one should use a uniform, well defined shear rate viscometer (with either coaxial cylinders or cone-plate geometry) such as a Rheometrics rheometer. ;The suspensions are preferably prepared by grinding a mixture of nonionic surfactant, particles of polyphosphate builder salt and the acidic organic phosphorus compound in a mill which will break down the builder particles to diameters below about 10 microns. The builder salt will generally be supplied as much larger particles of above about 40 microns diameter, such as 100, 200 or 400 microns. If desired, the builder salt may be premixed with the acidic organic phosphorus compound (e.g. by spraying the acidic compound, dispersed or dissolved in water or volatile organic solvent, onto the builder salt). ;During grinding it is preferred that the proportion of solid ingredients be high enough (e.g. at least about 40% such as about 50%) that the solid particles are in contact with each other and are not substantially shielded fto-m one another by the nonionic surfactant liquid. Mills which employ grinding balls (ball mills) or similar mobile grinding elements have given ;- 4 - ;-.■I 0 I:' ^ ;i1! il ^ ;tikam y £ ;5 C ;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 ;V; ;step of grinding to an average particle diameter below 10 microns in the continuous ball mill. ;The following Example is given to illustrate this invention further: ;EXAMPLE ;A nonaqueous heavy duty built liquid detergent composition is prepared by blending nonionic surfactant and sodium tripolyphosphate ("TPP") with other ingredients with and without an acidic organic phosphorus compound, as described below, and then grinding the blend in an attritor mill (to reduce the partic size of the suspended ingredients to less than 10 microns). The grinding conditions are identical in each case: grinding for *5 hour in an attritor mill containing 8 mm diameter steatite grinding balls. (Wieneroto W-l.S attritor, charged with 2.5Kg of mixture) . 2 115 A B C D Proportion of acidic organic phosphorus compound (%) 0 0-1 0.2 0.3 Yield stress (Pascals) 0 .3 1.6 3.2 5.6 Plastic viscosity (Pascal seconds) 1.1 1.0 1.0 0.9 The apparent viscosity at any shear rate can be calculated, using the Casson equation and the relationship: apparent viscosity equals shear stress divided by shear rate. ample is a partial ester of phosphoric acid an d a C16 to Clg alkanol (Empiphos 5632 from Marchon); it is made up of about 35% monoester and 65% diester.
The composition contains the following ingredients in the proportions specified. % nonionic surfactant comprising a mixture of equal parts of: (a) a relatively water soluble nonionic surfactant which forms a gel when mixed with water at 25°C specifically a C to alkanol which has been alkoxylated to introduce 10 ethylene oxide and 5 propylene oxide units per alkanol unit and Cb) a less water-soluble nonionic surfactant specifically a to C alkanol which has been alkoxylated to into duce 4 ethylene oxide and 7 propylene oxide units per alkanol unit.
The acidic organic phosphorus compound in this Ex- 12% of the reaction product prepared by mixing 100 g of succinic anhydride with 522 g. of the nonionic surfactant known as Dobanol 25-7 (the product of wthoxylation of a C^2 to alkanol, which product has about 7 ethyleneoxide units per molecule of alkanol) and 0.1 g. of pyridine (which acts as an esterification catalyst here); heating at 60°C for 2 hours; cooling and filtering to remove unreacted succinic • material (infrared analysis indicates that substantially all the free hydroxyls of the surfactant have reacted to form an acidic half ester in which the OH group of the nonionic surfactant has been esterified with one carboxyl group of the succinic anhydride). 31.5% TPP in formulation A; 31.4% in formulation B; 31.3% in C and 31.2% in D. 9% sodium perborate monohydrate, NaBOj'I^O. 4.5% tetraacetyl ethylene diamine; this 1b an activator for the sodium perborate 4% copolymer of about equal moles of methacrylic acid and maleic anhydride, completely neutralized to form the sodium salt theof (Sokalan CP5) ; this serves to inhibit incrustation (as from formation of dicalcium phosphate). 1% dlethylene diamine pentamethylene phosphonic acid sodium salt; this is a sequestering agent agent having a high stability constant for complexation. 1% proteolytic enzyme slurry (in nonionic surfactant) (Esperase) 1% mix of Na carboxymethylcellulose and hydroxymethyl-cellulose (an antiredepoition agent) (Relatin DM 4050) '£ % 15 5 0 0.5% perfume 0.5% optical brightener (of silbene 4 type) The TPP preferably is largely ahhydrous material containing a small amount of TPP hexahydrate (e.g. an amount such that the chemically bound water content is about 3%, which corresponds to about one H^O per pentasodium tripolyphosphate molecule). Such TPP may be produced by treating anhydrous TPP with a limited amount of water. The presence of the hexahydrate slows down the rapid rate of solution of the TPP in the wash bath and inhibits caking. One suitable grade of TPP is sold under the name Thermphos NW; the particle size of this TPP as supplied is in the neighborhood of 400 microns, iti phase 1 content is about 60%.
The mixture dispenses readily with cold water in the automatic washing machine. Its specific gravity is about 1.25 and it gives excellent washing when used at a dosage of about 100 grams per wash load (as compared with 170 grams per wash load for the usual heavy duty laundry detergent powders) in conventional European home laundry machines (which employ about 20 liters of water for the washing bath).
The partial esters of phosphoric acid are known to act as foam suppressants and are mentioned for that purpose in U.S. patent 4,264,466 (Column 33, lines 34-45). The compositions of this Example are, however, of the low-foaming type; when used to wash conventional wash loads in typical European, e.g., German, front—loading washing machines. They exhibit little foam even in the absence of the partial ester of phosphoric acid and thus do not require any foam suppressant. 2 115 5 0 The acidic organic phosphorus compound may be selected from a wide variety of materials, in addition to the partial esters of phosphoric acid and alkanols mentioned above. Thus, one may employ a partial ester of phosphoric or phosphorous acid with a mono or polyhydric alcohol such as hexylene glycol, ethylene glycol, di- or t'r i-e thylene glycol or higher polyethylene glycol, polypropylene glycol, glycerol, sorbitol, mono or di-glycerides of fatty acids, etc. in which one, two or more of the alcoholic OH groups of the molecule may be esterified with the phosphorus acid. The alcohol may be a nonionic surfactant such as an ethoxylated or ethoxylated-propoxylated higher alkanol, higher alkyl phenol, or higher alkyl amide. The -POH group need not be bonded to the organic portion of the molecule through an ester linkage; instead it may be directly bonded to carbon (as in a phosphonic acid, such as a polystyrene in which some of the aromatic rings carry phosphonic acid or phosphinic acid groups; or an alkylphosphonic acid, such as propyl or lauryl-phosphonic acid) or may be connected to the carbon through other intervening linkages (such as linkages through 0, S or N atoms). Preferably, the carbon:phosphorus atomic ratio in the organic phosphorus compound is at least 3:1, such as 5:1, 10:1, 20:1, 30:1 or 40:1. Among the suitable compounds are the Phosphate ester surfactants described and listed in Kirk-Othmer "Encyclopedia of Chemcial Technology", 3rd Edition, Vol. 22 (1983) Pages 359 to 361.
The particular partial alkyl ester of phosphoric acid and the Cl6 to Clg alkanol, described in the foregoing Example, is a solid which generally swells, but does not dissolve in the d. j 'i 5 5 nonionic surfactant. It is supplied as a powder. In a preferred method, used in that Example, the TPP is added last (after the other solid ingredients have been added to the liquid blend of nonionic surfactant and reaction product of succinic anhydride and nonionic surfactant) and the powder of partial alkyl ester of phosphoric acid is added just before the TPP. Acidic organic phosphorus compounds soluble in the nonionic surfactant may also be employed.
As is well known, the nonionic 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 alphatic 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 poly-hydration product thereof, polyethylene glycol, to form a nonionic detergent. The length of the hydrophilic or polyoxy-ethylene chain can be readily adjusted to achieve the desired balance between the hydrophobic and hydrophilic groups. Typical suitable nonionic surfactants are those disclosed in U.S. patents 4,316,812 and 3,630,929, 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.
Nonionic surfactants often tend to form gels with limited amounts of cold water; this can sometimes interfere with the £ 1 'i! 5 5 0 complete dispensing of the composition from the usual dispenser found in conventional automatic home laundry machines used in Europe. To lower the gelling temperature, and thus promote easier dispensing, there may be included in the composition a carboxylic acid anti-gelling agent. A preferred type of agent of this type is a compound having a carboxylic moiety joined to the residue of a nonionic surfactant, e.g., a half ester of succinic acid or other dicarboxylic acid in which the OH group of the nonionic surfactant has been esterified with one carboxyl group of the acid. This material is preferably in solution in nonionic surfactant.
The polyphosphate builder salt is preferably an alkali metal (e.g. Na or K) tripolyphosphate, pyrophosphate (e.g. tetra-sodium pyrophosphate) or hexamethaphosphate. It is preferred that these be largely in anhydrous form. Mixtures of two or more different polyphosphates may be used. The polyphosphate may also be used in admixture with one or more other water-soluble detergent builders.
Among the suitable builders are inorganic and organic builder salts such as the phosphates, carbonates, silicates, phosphonates, polyhydroxysulfonates, polycarboxylates and the like. Typical suitable builders are those disclosed in U.S. patents 4,316,812; 4,264,466; and 3,630,929.
Since, as indicated in the Example, the compositions of this invention may be used at relatively low dosages, it is desirable to supplement any phosphate or phosphate-forming builder (such as sodium tripolyphosphate) with an auxiliary builder such as polymeric carboxylic acid having high calcium binding capacity, in amount in the range, for instance, of about - li - X fe ij 3 <J 1 to 10% of the composition, to inhibit incrustation which could otherwise be caused by formation of an insoluble calcium phosphate. Such auxiliary builders are well known in the art.
The composition preferably comprises a peroxygen bleaching agent. This may be a peroxygen compound, such as an alkali metal perborate, percarbonate or perphosphate; a particularly suitable material is sodium perborate monohydrate. The peroxygen compound is preferably used in admixture with an activator therefor. Suitable activators are those disclsoed in U.S. patent A,264,466 or in column 1 of U.S. patent 4,430,244. Poly-acylated compounds are preferred activators; among these, compounds such as tetraacetyl ethylene diamine ("TAED") and glucose pentaacetate are particularly preferred.
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 complexing 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 compound Oj. 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/lite pK being conventionally defined by the formula: pK=-log K where K represent 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 2 1i 15 5 0 acid (NTA); ethylene diamine tetraacetic acid (EDTA); diethylene triamine pentaacetic acid (DETPA); diethylene triamine penta-methylene phosphonic acid (DTPMP); and ethylene diamine tetra-methylene phosphonic acid (EDITEMPA).
Other ingredients which may be included in the composition are enzymes (e.g. proteases, amylases or lipases or mixtures thereof), optical brighteners, antiredeposit ion agents, colorants (e.g. pigments or dyes) etc.
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%. For best results it is preferable, however, that compositions which form peroxyacids in the wash bath (e.g. compositions containing peroxygen compound and activator therefor) be substantially free of such compounds and of other silicates; it has been found, for instance, that silica and silicates promote the undesired decomposition of the peroxyacid. In addition, the use of these water-insoluble inorganic materials can present other problems in the system. No voluminous silica or chain structure type clay is needed in the practice of this invention and the composition is preferably substantially free os such materials. 2 1155 While in the preferred compositions the average particle size of the solids has been reduced to less than about 10 microns (e.g., typically only about 5-10% of the solids content has a particle size above 10 microns), the invention may also be applied to compositions which have not been so finely ground. It will be understood that finer grinding increases the stability of the composition against settling on standing; according to Stokes law the smaller the particle size the lower the rate of sedimentation. By raising the yield value obtained with a given degree of grinding, the use of the acidic phosphorus compound can make it possible to increase the stability of compositions in which the average particle diameter is say 15, 20, or 25 microns, as by using increased amounts of the acidic phosphorus compound to attain the desired yield value of at least about 2 Pascals.
In the compositions of the invention, typical proportions of the ingredients are as follows: Suspended detergent builder, within the range of about 10 to 60%, such as 20 to 50%, e.g., about 25 to 40%; Liquid phase comprising nonionic surfactant (and, optionally, dissolved carboxylic acid gel-Inhibitor) 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 glycol.
Carboxylic acid antigelling agent, an amount to supply in the range of about 0.5 to 10 parts (e.g., about 1 to 6 parts, such as about 2 to 5 parts) of -COOH (M.W.45) per 100 parts of - 14 - 21 iS the blend of such compound and the nonionic surfactant; typical ly the amount of this anti-gelling agent is in the range of about 0.01 to 1 part per part of nonionic surfactant, such a6 about 0.05 to 0.6 part, e.g. about 0.2 to 0.5 part; Peroxygen compound (such as sodium perborate mono-hydrate) in the range of about 2 to 15%, such as about 4 to 10% Activator, in the range of about 1 to 8%, such as about 3 to 62; Sequestering agent of high complexing power, in the range of about h to 3%, such as about h to 2%; Acidic organic -POH compound, in the range of OvOl to 5%, such as about 0.05 to 2%, e.g., about 0.1 to 1%.
In this application all proportions are by weight unless otherwise indicated. In the Exmples atmospheric pressure is used unless otherwise indicated.
It is understood that the foregoing detailed description is 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* - O aur^

Claims (15)

WHAT WE CLAIM IS!
1. A liquid heavy duty laundry detergent composition O o D comprising a suspension of an alkali metal polyphosphate builder salt in a liquid nonionic surfactant, said composition containing an organic phosphorus compound having an acidic -POH group which compound is present in a sufficient amount to raise the yield value of said composition.
2. A composition as in Claim 1 in which said composition is substantially nonaqueous and has a yield value in the range of 2 to 8.
3. A composition as in Claim 1 in which said composition is of the low-foaming type even in the absence of said organic phosphorus compound.
4. A composition as in Claim 1 in which said poly-phosphate salt is sodium tripolyphosphate.
5. A composition as in Claim 1 in which the particle size of said suspended builder salt is less than 10 microns.
6. A composition as in Claim 1 in which the C:P atomic ratio in said phosphorus compound is at least 3:1.
7. A composition as in Claim 1 in which said organic phosphorus compound is a partial ester of an alkanol and phosphoric acid. -16- 1 aus-s-o
8. A composition as in Claim 6 in which said alkanol is a higher alkanol.
9. A composition as in Claim 1 which has been prepared by grinding said suspension until the particle size of said suspended builder salt is less than 10 microns.
10. A composition as in Claim 1 in which said composition is substantially nonaqueous and contains a peroxygen bleach.
11. A composition as in Claim 10 in which said peroxygen bleach comprises sodium perborate and an activator therefor.
12. A composition as in Claim 11 in which said activator is tetraacetyl ethylene diamine.
13. A composition as in Claim 1 substantially free of silica and silicate thickening agent.
14. A composition as in Claim 1 substantially free of chain structure type clay.
15. A composition as in Claim 1 which contains a carboxylic acid anti-gelling agent. WEST-WALKER, McCABE por: ATTORNEY'S FOfl THE APPLICANT -17-
NZ211550A 1984-04-06 1985-03-22 Liquid detergent composition containing acidic phosphorus compound and polyphosphate NZ211550A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US59779384A 1984-04-06 1984-04-06

Publications (1)

Publication Number Publication Date
NZ211550A true NZ211550A (en) 1987-06-30

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AT (1) AT395433B (en)
AU (1) AU573324B2 (en)
BE (1) BE902131A (en)
BR (1) BR8501448A (en)
CA (1) CA1240228A (en)
CH (1) CH667668A5 (en)
DE (1) DE3511517A1 (en)
DK (1) DK162658C (en)
ES (1) ES8702482A1 (en)
FI (1) FI80292C (en)
FR (1) FR2568886B1 (en)
GB (1) GB2158453B (en)
GR (1) GR850880B (en)
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IT (1) IT1184272B (en)
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SE408714B (en) * 1974-11-25 1979-07-02 Berol Kemi Ab LIQUID AQUATIZED DETERGENT CONTAINING A SURFACTIVE PART AND COMPLEX MOLDERS
GB1569617A (en) * 1976-03-08 1980-06-18 Procter & Gamble Liquid detergent composition
GB1577120A (en) * 1976-05-24 1980-10-22 Unilever Ltd Liquid detergent compositions
US4137190A (en) * 1977-04-04 1979-01-30 Gaf Corporation Detergent composition comprising synergistic hydrotrope mixture of two classes of organic phosphate esters
GB1600981A (en) * 1977-06-09 1981-10-21 Ici Ltd Detergent composition
DE3065199D1 (en) * 1979-12-04 1983-11-10 Ici Plc Detergent composition
US4264466A (en) * 1980-02-14 1981-04-28 The Procter & Gamble Company Mulls containing chain structure clay suspension aids
EP0037184B1 (en) * 1980-04-01 1985-01-23 Interox Chemicals Limited Liquid detergent compositions, their manufacture and their use in washing processes
ZA852201B (en) * 1984-04-09 1986-11-26 Colgate Palmolive Co Liquid bleaching laundry detergent composition
ZA852200B (en) * 1984-04-09 1986-11-26 Colgate Palmolive Co Liquid laundry detergent composition

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CH667668A5 (en) 1988-10-31
KR920004794B1 (en) 1992-06-15
SE8501592D0 (en) 1985-04-01
JPS60231800A (en) 1985-11-18
MX164102B (en) 1992-07-07
AT395433B (en) 1992-12-28
ATA98485A (en) 1992-05-15
FI851383L (en) 1985-10-07
NL8501001A (en) 1985-11-01
SE466918B (en) 1992-04-27
FR2568886B1 (en) 1988-04-15
FI80292B (en) 1990-01-31
MY102604A (en) 1992-08-17
ES541940A0 (en) 1986-12-16
FR2568886A1 (en) 1986-02-14
DK150785A (en) 1985-10-07
FI80292C (en) 1990-05-10
GB8509083D0 (en) 1985-05-15
GB2158453B (en) 1987-11-18
IT8547929A0 (en) 1985-04-05
LU85838A1 (en)
DK162658B (en) 1991-11-25
GR850880B (en) 1985-11-25
FI851383A0 (en) 1985-04-04
HK91690A (en) 1990-11-16
DE3511517A1 (en) 1985-10-24
CA1240228A (en) 1988-08-09
DK162658C (en) 1992-04-13
ES8702482A1 (en) 1986-12-16
BE902131A (en) 1985-10-07
AU4077685A (en) 1985-10-10
PT80192B (en) 1986-11-10
SG76390G (en) 1990-11-23
DK150785D0 (en) 1985-04-02
IT1184272B (en) 1987-10-22
NO163627B (en) 1990-03-19
BR8501448A (en) 1985-11-26
NO851346L (en) 1985-10-07
GB2158453A (en) 1985-11-13
SE8501592L (en) 1985-10-07
ZA852197B (en) 1986-11-26
NO163627C (en) 1990-06-27
KR850007608A (en) 1985-12-07
PT80192A (en) 1985-04-01
AU573324B2 (en) 1988-06-02

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