IE840262L - Granular detergent compositions containing mixed polymer¹additive system. - Google Patents
Granular detergent compositions containing mixed polymer¹additive system.Info
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- IE840262L IE840262L IE840262A IE26284A IE840262L IE 840262 L IE840262 L IE 840262L IE 840262 A IE840262 A IE 840262A IE 26284 A IE26284 A IE 26284A IE 840262 L IE840262 L IE 840262L
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- homopolymeric
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3761—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Granular detergent compositions with no or reduced levels of phosphorus -containing builders containing a mixture of homopolymeric and copolymeric carboxylates. Preferred homopolymeric carboxylates are polyacrylates having a molecular weight below 3000, most preferably a mixture of polymer species having molecular weights of 1000 and 2000 respectively. The preferred copolymeric ingredient contains maleic acid and (meth)-acrylic acid monomers.
Description
This invention relates to granular detergent compositions which are free of or with reduced levels of phosphorus -containing builders containing a mixed polymer additive system. The polymer system comprises specific homo-polymeric polyacrylates and copolymeric carboxylates whereby the homopolymeric species are characterized by a molecular weight below 3000. The preferred copolymeric component is prepared from an ethylenically unsaturated carboxylic acid, most preferably maleic acid, and (meth)-acrylic acid monomers. Particularly preferred polyacrylates herein are represented by substantially equiponderant mixtures of polyacrylates having molecular weights of around 1000 and 2000 respectively.
The polymer additive system provides unpredictable and significant textile cleaning benefits expressed, for example, in terms of whiteness and whiteness maintenance after multiple washes as compared to identical granular detergents containing same total level of either the individual polymers or mixtures of various conventional detergent polymers. The claimed technology is especially beneficial in granular detergent compositions containing reduced levels of polyphosphate builders such as from 8% to 20% by weight of the composition. As is well-known, the polyphosphate builder level reduction leads to performance deficiencies which cannot be cured in a fully acceptable manner with the sole aid of a conventional detergent additive such as a polymeric carboxylate.
The individual components of the polymer additive system are well-known in detergent technology and may have found commercial application.
The copolymeric ingredient is known from European Patent 0 025 551, BASF AG, which discloses such material in an incrustation inhibitor functionality in detergent compositions.
The deterqent art is also possessed of combinations of the copolymeric ingredient and conventional detergent additives. FR-A- 2 308 04 5, The PROCTER & GAMBLE Company, is representative of this general knowledge. It discloses detergent compositions containing surface-active agents, builders, and a binary system of additive levels of a polyphosphonate and a polymeric ingredient which latter ingredient can be represented by copolymers of (meth)-acrylic acid and maleic anhydride.
The detergent utilization of the copolymeric ingredient is also known from European Patent Application 0 066 915. In detail, this reference discloses the utilization of the copolymeric ingredient in combination with detergent performance additives inclusive of hydrocarbon detergent suds regulants, photoactivators, amine or oxidized amine soil release agents, silicone detergent suds regulants and bleach activators/peracids.
The detergent utilization of polyacrylates, having a molecular weight in the range of from 1000 to 5000, is known from U.K. Patent Application 2.097.419, Colgate-Palmolive. Detergent compositions are disclosed containing high levels of difficultly processable components inclusive of sodium carbonate, sodium bi-carbonate, detergent zeolites, and bentonites. It is said that the polyacrylates are added 4 in a processing aid functionality to ensure uniform mixing of the crutcher mix component. Comparable disclosures are known from U.K. Patent Application 2 095 274, Colgate-Palmolive. Detergent compositions containing substantial 5 levels of water-insoluble ingredients inclusive of zeolite m builders, and bentonites, carbonates and bi-carbonates are processed into beads whereby physical and detergent properties are controlled with the aid of polyacrylates having & molecular weight e.g. in the range from 1000 to 5000. 10 The detergent utilization of mixed polymer systems is known from German Patent Application 29 10 133, BASF AG; German Patent Application 26 25 444, CIBA-GEIGY AG; and Belgian Patent 881 488, SENZORA B.V. The BASF '133 reference relates to the utilization of detergent builder mixtures 15 consisting of a copolymeric ingredient and polymaleic acid.
The CIBA-GEIGY *444 citation refers to the use of low molecular weight polymer mixtures, namely combinations of hydroli-zed polymaleic anhydride, having a molecular weight in the range from 300 to 5000, in combination with a hydrolized co-20 polymer of maleic anhydride and an ethylenically unsaturated monomer whereby the molecular weight of the copolymeric species is below 1000. The SENZORA '488 reference refers to the partial or total replacement of polyphosphate detergent builders by a ternary combination consisting of polyvalent 25 substituted carboxylic acids, a copolymer of methyl vinyl ether and maleic anhydride; and a polyacrylic acid having a molecular weight in the range of from 12,000 to 20,000.
The total prior art is consistently and unequivocally confirmatory of a standing desire for improving and enhancing 30 textile laundry performance of granular detergent compositions containing no or reduced levels of conventional polyphosphate builders with the aid of carboxylates. While prior art attempts for solving the problem have yielded some benefits, frequently processing advantages, the claimed sys-35 tern procures significant textile laundry benefits and can * constitute basis for superior commercial detergent executions.
It is a major object of this invention to formulate granular detergent compositions having no or reduced level of phosphorus-containing builders capable of providing textile cleaning performance ccsnparable to phosphate built compositions.
It is a further object of this invention to formulate granular detergent compositions capable of providing superior textile cleaning benefits over a broad range of laundry conditions particularly in up to the boil washing operations.
It has now been discovered that significantly enhanced 10 textile cleaning can be obtained from the use of granular detergent compositions which do not contain or contain reduced level of conventional phosphorus (P)-containing detergent builders. In more detail, it has been discovered that such benefits are derived from the utilization of granular 15 detergent compositions containing no or reduced levels of P-containing builders and further containing surface-active agents, polymeric carboxylates and, if desired, conventional detergent additives including non-phospliorus detergent builders, the compositions further containing: 20 a) from 0.5% to 15% by weight of a polyacrylate homopolymer having a molecular weight below 3000; and b) from 0.5% to 15% by weight of a copolymer which consists of an ethylenically unsaturated monocarboxylic acid monomer having not more than 5 carbon atoms, and an 25 ethylenically unsaturated dicarboxylic acid monomer having not more than 6 carbon atoms, whereby the molar ratio of the monomers is from 1:4 to 4:1; and whereby the weight ratio of the homopolymeric ingredient to 30 the copolymeric ingredient is in the range from 4;l to 1;4.
In a preferred aspect of this invention, the compositions herein comprise reduced (vs. current practice) levels of 6 polyphosphate bui Iders ;;uch as corresponding to phosphorus levels in the range of from 2?, to 5% by weight. The latter P-levels, if e.g. calculated on basis of sodiumtripolyphos-phate amount to from 8?. to 201 by weight.
» The invention herein comprises a scries of essential components, namely: a granular detergent composition containing conventional matrix components; and a binary polymer system containing a homopolymeric polyacrylate having a low molecular weight and a copolymeric polycarboxylate with a 10 given monomers ratio and whereby further the weight ratio of homopolymer to copolymer can be varied within narrowly set conditions. The major parameters of the invention are described in more detail hereinafter.
Unless indicated to the contrary, the "percent" indications 15 represent "percent by weight" indications.
The detergent matrix comprises a surface-active agent, a detergent builder, preferably reduced level of tripolyphos-phate, and a series of optional, but frequently desirable, components such as an oxygen-bleach component, possibly an 20 activator therefore, a suds regulant frequently based on silicones, and further usual additives in the art established level for their known functionality.
Qualitatively and quantitatively suitable surface-active agents for use herein are disclosed in U.S.-PS 4,192,761, 25 column 3, line 49 to column 5, line 42.
Qualitative and quantitative indications concerning suitable detergent builder materials for use herein are found in U.S.-PS 4,192,761, column 8, line 56 to column 9, line 68.
The compositions herein unexpectedly provide superior laundry cleaning performance, as compared to commercial phos phate built detergent compositions, in the absence of or with reduced levoL of phosphate builder, especially detergent compositions containing phosphate builder levels representing from 2-5% of phosphorus. The latter limit, in terms of sodium tripolyphosphate, amounts to from 8% to 20%. The detergent builder can be represented by non-phosphorus containing builders, by mixtures of such non-phosphorus containing builders and phosphorus-containing builders, or by reduced levels (vs. current levels) of P-containing builders alone, such as sodium tripolyphosphate. The total level of the detergent builder ingredients can vary within broad limits well-known in the detergent art. Importantly, the inventive technology is particularly adapted for use in combination with a detergent composition containing a phosphorus-containing detergent builder in a level, calculated as phosphorus, from 2% to 5%.
Suitable non-phosphorus containing detergent builders can be represented by conventional species inclusive of but not limited to detergent zeolites such as zeolite A, zeolite X and zeolite P, most preferably zeolite A, having a particle size in the range from 1-10 um as e.g. described in DE-B 24 22 655. Additional builders for use herein include nitrilotriacetic acids or the water-soluble alkali salts thereof, sodium carbonate, sodium citrate, sodium silicates and fatty acid soaps e.g. sodium or potassium soaps.
The total level of the detergent builder can vary within broad ranges. The builder usually represents from 5% to 70%, but frequently, and depending upon the selection of the builder, is in the range from 10% to 503.
The compositions herein contain as an essential detergent component a mixture of a polyacrylic homopolymer and a copolymeric ingredient.
The polyacrylate homopolymer has a molecular weight below 3000 and is utilized in levels of from 0. 58 to 15%. In a preferred execution, the homopolymeric polyacrylate is 8 represented by a mixture of two different polyacrylates, one having a molecular weight of about 2000 and a second one having a molecular weight of about 1000, whereby these species are used in a weight ratio of 2:1 to 1:2, most prefe-5 rably 1:1. The polyacrylate component is well-known in de- tergent technology. The molecular weight of the polyacrylate polymer is determined with the aid of known techniques inclusive of intrinsic viscosity measurements.
The level of the polyacrylate homopolymer can vary as 10 pointed out above and depending upon the nature of the detergent matrix components. Particularly relevant in this respect are variations in the qualitative and quantitative parameters of the builder system. Reduced levels of polyphosphate e.g. between 8-12% by weight will require a rela-15 tively higher level of the homopolymer as compared to what is needed for levels of sodium tripolyphosphate in the range of from e.g. 15%-18%.
A further essential component for use herein is a copolymer of an unsaturated monocarboxylic acid and an unsatura-20 ted di-carboxylic acid. This copolymeric ingredient is used in levels from 0.5% to 15%. The copolymeric ingredient consists of an ethylenically unsaturated monocarboxylic acid monomer having not more than 5, preferably 3 or 4, carbon atoms, and an ethylenically unsaturated dicarboxylic acid 25 monomer having not more than 6, preferably 4 carbon atoms, whereby the molar ratio of the monomers is in the range from 1:4 to 4:1, most preferably 1:1. Suitable examples of the monocarboxylic acid monomer are : acrylic acid, methacrylic acid and vinyl acetic acid. Acrylic and methacrylic acids 30 are preferred. Suitable examples of the dicarboxylic acid monomers are : maleic acid; fumaric acid; cltraconlc acid; itaconic acid; and mesaconic acid. Preferred dicarboxylic acids are maleic acid, citraconic acid, and itaconic acid.
The copolymeric ingredient can be further defined with 35 the aid of the calcium sequestration value. These values can * be measured by nephelometric titration methods (as described in literature - S. Chaberek. and A.E. Martell, Organic Sequestering Agents, Wiley, New York, 1959; - R.L. Smith, The Sequestration of Metals, Chapman and Hall, London, 1959): a calcium nitrate solution is added to a solution containing sequcstrant and sodium oxalate until turbidity is produced; the titration is being carried out at constant pH = 10 and room temperature.
The sequestration value is expressed in mgCaCO^/gram of copolymeric ingredient.
The calcium sequestration value of the copolymeric ingredient is preferably higher than 200 mg CaC03/g.
The weight ratio of the homopolymeric ingredient to the copolymeric ingredient is normally in the range from 1:4 to 4:1 and preferably from 2:1 to 1:2. While the quantitative levels of the individual homopolymer and the individual copolymer can vary from 0.5% to 15% provided their weight ratio is from 4:1 to 1:4, the level selection of these individual polymers will vary depending upon the major detergent matrix ingredients, particularly the detergent builder. The homopolymer and copolymer are preferably used in levels of 0.5% to 4% each when incorporated in built detergent compositions containing from 2% to 5% phosphorus In another embodiment the detergent compositions herein preferably contain from 2% to 8% of the homopolymeric ingredient and from 2% to 8% of the copolymeric ingredient if the phosphorous based builder/sequestrant is present in a level, expressed as phosphorus of below 2%.
The detergent compositions herein can comprise, in addition to the essential components, a series of supplementary substances to perfect and augment the performance benefits. The additional components are represented by known ingredients which have already found application in deter-gency, for their known functionality in the art established levels. Examples of the like components include peroxygen 1 « bleaches, such as perborate mono-or tetrahydrate and percar-bonate, oxygen bleach activators such as tetraacetyl ethylene diamine, oxygen bleach regulants such as a copolymer of maleic anhydride and methylvinylether, detergent enzymes such as proteases, amylases, lipases and mixtures thereof, and stabilizing agents for the like enzymes. Other optional components include soil suspending agents such as the sodium salt of carboxymethylcellulose and the sodium salt of methyl-hydroxypropyl cellulose; through-the-wash softening smectite clays such as alkali montmorillonites, saponites and hecto-rites, having an ion-exchange capacity of at least 50m.eq./ 100 g, and photoactivators, for example, sulfonated metal phthalocyanines such as zinc and aluminium phthalocyanines.
The subject compositions further can comprise suds regulants e.g. those of U.S. Patent 4,192,761 and more in general suds regulants based on silicones, silica, water-insoluble hydrocarbons, either individually or optimized mixtures thereof, and renewable textile soil release agents such as described in European Patent Applications 0 042 187 and 0 042 188. Preferred soil release agents include N-hy-drogenated tallow CJ6-C^g-N,N',N"-tri-(2-hydroxyethyl)-propylene-1, 3-diamine and N-C12-C14-coconutalkyl-N,N-dinie-thyl-N-amine oxide and can be utilized in levels of from 0.1%-1,5%. The claimed compositions also can contain brighteners, perfumes, dyes, bactericidal agents, antioxidants and fillers. A preferred additive system is comprised of a combination of a tertiary amine and an impalpable smectite clay as described in European Patent Application 0 011 340.
The following Examples illustrate the invention and highlight the benefits derivable therefrom.
The abbreviations for the individual ingredients have the . following meaning; I, LAS : Sodium salt of linear dodecyl benzene sulfonate TAS : Sodium salt of tallow alcohol sulfate oC-OS : Sodium salt of o<-olefin (C12_1g) sulfonate FAE-jS : Sodium salt of fatty alcohol (c12-i8' (ethoxy)3 sulfate AO : C12_14 alkyl dimethylamine oxide TAE11 : Tallow alcohol ethoxylated with about 11 moles of ethylene oxide FAjjEjj : Fatty alcohol ethoxylated with X moles of ethylene oxide DTMA : Ditallow icethyl amine CFA : Ci2-14 coconut fatty acid HFA : Hydrogenated c^g_22 ^attV acid STPP : Sodium tripolyphosphate Zeolite A : Sodium salt of zeolite 4A (average particle size between 2-6 microns) NTA : Sodium salt of nitrilotriacetate Copolymer : = copolymer of acrylic acid 40* mol.% and maleic acid 60S mol.% CMC : Sodium salt of carboxymethyl cellulose Clay : Sodium montmorillonite Silicate 1.6 : Sodium silicate SiO^NajO = 1.6 Silicate 1.0 : Sodium metasilicate STS : Sodium salt of toluene sulfonate EDTA : Sodium salt of ethylene diamine tetra-acetate Perborate : NaBOj.HjOj.3H20 P.A. : Photoactivator sulfonated Zn phthalocyanine Antioxidant : 4,4'-thiobis(6-tertiary butyl-3-m-cresol) The following granular detergent compositions were prepared by conventional spray-drying of a slurry of most of the individual ingredients and subsequent dry-mixing of the 1 ■■} spray-dried powder with spray-drying sensitive ingredients, namely perborate enzyme photoactivator and suds regulant.
COMPOSITIONS (% by weight) EXAMPLES I A B II C LAS .0 .0 .0 .0 .0 TAS 3.0 3.0 3.0 3.0 3.0 TAE 1.0 1.0 1.0 1.0 1.0 HFA 1.0 1.0 1.0 1.0 1.0 STPP 18.0 18.0 18.0 18.0 18.0 Copolymer MA^/AA^" 2.0 2.0 4.0 1.0 1.0 Polyacrylate MW 1000 1.0 - - - - " m 2000 1.0 - - 2.0 - MW 4500 - 2.0 - - - ffli 200 000 - - - - 2.0 P. A 0.004 0.004 0.004 0,004 0.004 QfC 1.0 1.0 1.0 1.0 1.0 Silicate 1.6 8.0 8.0 8.0 8.0 8.0 MgS04 0.5 0.5 0.5 0.5 0.5 Eom 0.2 0.2 0.2 0.2 0.2 Perborate 24.0 24.0 24.0 24.0 24.0 Enzyme 0.6 0.6 0.6 0.6 0.6 Suds regulant (1) 1.0 1.0 1.0 1.0 1.0 Brightener/Perfume/Water/ Sodium Sulfate balance to 100 (1) Prilled suds regulant system consisting of: 77.5% sodiumtripolyphosphate and 22.5% active consisting of: 13.5% paraffin oil; 6% paraffin wax (m.p. 70°C); and 3% amorphous hydrophobic silica.
The compositions of Examples I (invention), A and B (prior art) were compared under the following conditions. The variations were expressed as whiteness maintenance: - minidrums testing apparatus; i 3 - 0-6% product concentration in wash liquor; - 0.3 g/1 (18 grains/US gallon) water hardness (3:1 Ca/Mg ratio); - healing up from 15°C to 90°C; +20' at 90°C; - fabrics : terry tracers; - 4 cumulative cycles; - whiteness readings under standard daylight: visual grading by two judges working independently. O to 4 scale (0 = no difference, 1 = probable difference, 2 = consistent small difference, 3 - clear difference, 4 = big differen- ce> • The testing results were as follows: Composition I vs. Composition A standard - 1.7 Composition I vs. Composition B standard - 0.4 These results show the significant performance benefits derivable from inventive Composition I vs. closely related prior art compositions A and B.
The compositions of Examples II and C were compared as 20 described hereinbefore except for the following conditions. - commercial washing machine; - 1% product concentration; - 0.2 g/1 (12 grains/US gallon) water hardness (3:1 Ca/Mg ratio); - 90°C prewash + mainwash cycle; - 8 cumulative washes.
The whiteness maintenance results were as follows: Composition II vs. Composition C standard - 1.1 4 1 4 The performance superiority of the claimed technology vs. identical compositions containing high molecular weight polyacryiatcs is confirmed.
An additional composition of this invention --ill— and closely related prior art compositions were spray-dried/dry-mixed as described above, the sole difference being the levels of polymers as follows: EXAMPLES III D E F Copolymer MA60/AA40 1.5 1.0 3.0 Polyacrylate MW 1000 0.75 - - 1.5 MW 2000 0.75 - - 1.5 MW 4500 - 2.0 - The compositions of Examples III, D, and E were compared for whiteness maintenance under the conditions recited for Examples II and C, except that the water hardness was 0.3 g/1 (18 grains/US gallon).
The results were as follows: Composition III vs. Composition D standard - 2.8 Composition III vs. Composition E standard - 2.1 The inventive composition is again markedly superior over the art.
Compositions III and F were compared for soil anti-redeposition, measured as whiteness, thereby using the following testing conditions: - tubes testing apparatus; - 0.3% to 1.0% product concentrations; - 0.4 g/1 (25 grains/US gallon) water hardness (3:1 Ca/Mg ratio); t 5 - heating up from 15°C to 90°C +30* at 90°C; - fabrics : terry tracers.
The whiteness readings were done with a Zeiss-spectrophotometer. The results were as follows: EXAMPLE III F % of soil deposition avoided at: 0.3% prod, concentration 70.3 70.4 0.4% " 71.1 71.0 0.5% " 71.2 63.9 0.6% " 72.3 61.2 0.7% " 71.9 70.9 0.8% " 72.5 72.3 0.9% " 72.6 72.7 1.0% " 73.0 72.9 These results show that the combined utilization of the copolymeric and the homopolymeric ingredients is a requisite for obtaining the inventive benefits. 1 6 Additional detergents of this invention are prepared having the following composition.
INGREDIENT IV EXAMPLES (% by weight) VI VII LAS TAS <-OS Coconut-trimethyl-quaternary ammonium chloride TAE^ FA25E7 DTMA CFA HFA STPP Zeolite A NTA Na^Citrate Copolymer AA^®/MA®" Polyacrylate MW 1000 Polyacrylate MW 2000 CMC Montmorillonite Silicate 1.6 MgS04 NaOH EDTA Perborate Suds regulant (1) Enzyme (proteolytic) Brightener, perfume, water/ sodium sulfate .0 3.0 1.0 .0 6.0 1.5 1.0 1.0 0.8 6.0 0.5 0.8 0.2 32.0 1.0 0.2 .0 2.0 2.5 .5 0.5 20.0 .0 2.0 1.5 1.5 8.0 6.0 1.3 0.2 2.7 0.6 2.5 5.0 4.0 4.0 .0 3.0 1.0 16.0 28.0 16.0 2.0 1.0 1.0 1.0 2.0 0.5 0.95 0.3 28.0 1.5 0.3 1.0 0.5 0.5 0.8 6.0 1.0 0.75 0.2 28.0 1.2 0.2 balance t o 100 (1) See Example I S 7 EXAMPLES (% by weight) INGKKDIENTS VIII IX X LAS o o 1 .0 7.0 TAS - 3.0 - FAEjS 3.0 - - TAE11 1.0 1.0 2.7 HFA - 4.0 3.5 STPP - 24.0 .0 NTA 6.0 - 4.0 Na2C03 Copolymer MAA50/MA50 .0 7.7 1.4 .0 3.3 CMC 1.0 1.0 0.8 Polyacrylates 1:1(MW1000/2000) 7.7 1.0 3.3 Silicate solids 1.6 4.0 3.0 8.0 MgS04 1.0 - 0.5 NaOH 1.1 0.9 0.2 STS 1.4 - - EDTA 0.2 0.3 0.3 Perborate .0 - .0 P.A. 0.007 0.003 0.0G Enzyme (proteolytic) 0.3 0.6 0.2 Brightener, perfume, H,0/ sulfate balance to 100 i 1 8 EXAMPLES (% by weight) INGREDIENT XI XII XIII XIV LAS 7.0 4.5 7.0 4.5 TAS - 2.5 - 2.5 A.O. 0.5 0.3 0.8 1.0 TAE11 2.7 - 2.7 - FA25E7 CFA 2.0 2.0 : 2.0 2.0 HFA 3.5 4.0 3.5 4.0 STPP 4.0 24.0 16.0 8.0 Zeolite A - - 16.0 - NTA - 4.0 - 6.0 Copolymer AA60/MA40 .0 1.0 2.0 3.0 Polyacrylate MW 1000 2.0 1.0 1.5 1.0 Polyacrylate MW 2000 2.0 0.5 1.5 2.0 CMC 0.8 0.8 1.0 1.0 Silicate 1.6 .0 .0 2.0 2.0 MgS04 Na2c°3 Ethylenediamine tetramethyl-phosphonate Na-salt .0 1.3 0.5 0.5 6.0 0.8 1.0 10.0 EDTA 0.2 0.3 0.3 0.2 Perborate 32.0 28.0 .0 28.0 Enzyme (proteolytic) 0.2 0.2 0.3 0.2 Brightener, perfume, water, sulfate balance to 100 EXAMPLES (% by weight) INGREDIENTS XV XVI XVII LAS 4.0 4.0 - <<- OS - - 4.5 FA25E7 12.0 .0 6.0 CFA - 2.0 6.0 HFA 0.5 - 0.5 STPP 12.0 .0 18.0 Zeolite A - - .0 Na^ Citrate Copolymer AA'^/MA^ 2.0 .0 1.0 1.3 Polyacrylates 1:1 mix (MW 1000 and 2000) 4.0 1.0 2.5 CMC 0.8 1.0 0.8 Silicate 1.6 6.0 6.0 2.0 MgSO^. 0.5 - 1.0 Sodium carbonate .0 ..0 - NaOH 1.3 0.8 0.8 EDTA 0.2 0.2 0.3 Perborate 24.0 .0 28.0 Antioxidant 0.01 0.01 0.01 Silicone suds regulant of Example I 1.6 2.1 1.3 Brightener, perfume, H-O, sulfate balance to 100 EXAMPLES (% by weight) ingredient XVIII XIX XX XXI LAS 7.0 .0 .0 4.0 TAS TAEX1 FA25E7 CFA 2.7 3.0 2.0 2.0 2.5 12.0 HFA 3.5 - 0.5 0.5 STPP Zeolite A .0 16.0 16.0 .0 24.0 Copolymer AA®®/MA4® 2.0 2.0 1.0 1.0 Polyacrylate MW 1000 1.0 1.5 0.5 1.0 Polyacrylate MW 3000 1.0 1.5 0.5 0.5 CMC 0.8 1.2 1.0 1.0 Silicate solids 1.6 .0 2.0 .0 6.0 Silicate solids 1.0 1.0 - - - MgS04 0.5 1.0 0.5 1.0 Sodium carbonate 6.0 - 6.0 6.0 NaOH 0.75 0.50 0.95 1.1 TAED 3.0 2.5 4.0 2.5 Perborate 24.0 .0 8.0 2.0 Antioxidant - - - 0.01 Enzyme (proteolytic) 0.3 0.6 0.6 0.3 Suds regulant silicone - 0.5 1.3 0.16 Brightener, perfume, water, sulfate balance to 100 a
Claims (8)
1. A granular detergent composition containing no or reduced levels of P-containing builders, and further containing surface-active agents, polymeric earboxylates and, if desired, conventional detergent additives including non-phosphorus detergent builders, the composition further containing a) from 0.5% to 15% by weight of a polyacrylate homopolymer having a molecular weight below 3000; b) from 0.5% to 15% by weight of a copolymer which consists of an ethylenically unsaturated monocarboxylic acid monomer having not more than 5 carbon atoms, and an ethylenically unsaturated dicarboxylic acid monomer having not more than 6 carbon atoms, whereby the molar ratio of the monomers is from 1:4 to 4:1, and, whereby the weight ratio of the homopolymeric ingredient to the copolymeric ingredient is in the range from 4:1 to 1:4.
2. A composition in accordance with Claim 1 wherein the copolymeric ingredient is comprised of (meth)-acrylic acid and maleic acid monomers.
3. A composition in accordance with Claim 1 wherein, for a detergent composition containing P-builders in a level, expressed as phosphorus, of from 2% to 5% by weight/ the homopolymeric ingredient represents from 0.5 to 4% by weight and the copolymeric ingredient represent from 0.5% to 4% by weight.
4. A composition in accordance with Claim 1 wherein, for a detergent composition containing P-builders in a level, expressed as phosphorus , below 2% by weight, the homopolymeric ingredient represents from 2% to 8% by weight and the copolymeric ingredient from 2% to 8% by weight.
5. a composition in accordance with Claims 1,3 and 4 wherein the weight ratio of the copolymeric ingredient to the homopolymeric ingredient is from 2:1 to 1:2.
6. A composition in accordancc with Claim 1 wherein the homopolymeric ingredient is comprised of a polyacrylate having a molecular weight of 2000 and a polyacrylate of a molecular weight of 1000 in a weight ratio of 2:1 to 1:2.
7. A detergent composition in accordance with Claims 1 and 6 wherein the homopolymer is represented by a 1:1 weight ratio mixture of polyacrylates having molecular weights of 1000 and 2000 respectively.
8. A detergent composition according to claim 1, substantially as hereinbefore described with particular reference to Examples I - XXI of the accompanying Examples. Dated this the 3rd day of February, 1984 F. R. KELLY & CO. BY : I EXECUTIVE 27 Clyde Road, Ballsbridge, Dublin 4 AGENTS FOR THE APPLICANTS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8309610 | 1983-04-08 |
Publications (2)
Publication Number | Publication Date |
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IE840262L true IE840262L (en) | 1984-10-08 |
IE56762B1 IE56762B1 (en) | 1991-12-04 |
Family
ID=10540835
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE262/84A IE56762B1 (en) | 1983-04-08 | 1984-02-03 | Granular detergent compositions containing mixed polymer additive system |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0124913B1 (en) |
JP (1) | JPS6018595A (en) |
AT (1) | ATE20476T1 (en) |
CA (1) | CA1220998A (en) |
DE (1) | DE3460228D1 (en) |
GR (1) | GR81656B (en) |
IE (1) | IE56762B1 (en) |
MX (1) | MX159427A (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3444960A1 (en) * | 1984-12-10 | 1986-06-12 | Henkel KGaA, 4000 Düsseldorf | GRAINY ADSORPTION |
IN165509B (en) * | 1984-12-24 | 1989-11-04 | Colgate Palmolive Co | |
GB8504733D0 (en) * | 1985-02-23 | 1985-03-27 | Procter & Gamble Ltd | Detergent compositions |
DE3720806C2 (en) * | 1986-07-03 | 1997-08-21 | Clariant Finance Bvi Ltd | Use of a stabilizer in peroxide bleaching processes |
DE3717227A1 (en) * | 1987-05-21 | 1988-12-01 | Henkel Kgaa | PHOSPHATE-FREE DETERGENT WITH REDUCED INCRUSTING TENDENCY |
AU4211889A (en) * | 1989-05-02 | 1990-11-29 | Ecolab Inc. | Zero phosphorus heavy duty laundry detergent composition |
GB8928320D0 (en) * | 1989-12-14 | 1990-02-21 | Unilever Plc | Polymers and detergent compositions containing them |
US5273675A (en) * | 1990-02-16 | 1993-12-28 | Rohm And Haas Company | Phosphate-free liquid cleaning compositions containing polymer |
US5401807A (en) * | 1992-10-08 | 1995-03-28 | Rohm And Haas Company | Process of increasing the molecular weight of water soluble acrylate polymers by chain combination |
DE4239076A1 (en) * | 1992-11-20 | 1994-05-26 | Basf Ag | Mixtures of polymers of monoethylenically unsaturated dicarboxylic acids and polymers of ethylenically unsaturated monocarboxylic acids and / or polyaminocarboxylic acids and their use |
WO2010125154A1 (en) | 2009-04-30 | 2010-11-04 | Sanofi-Aventis Deutschland Gmbh | Pen-type injector with ergonomic button arrangement |
EP2689001B1 (en) * | 2011-05-20 | 2017-09-27 | Dow Global Technologies LLC | Method of promoting soil release from fabrics |
GB2502558A (en) * | 2012-05-30 | 2013-12-04 | Reckitt Benckiser Nv | Water softening composition |
EP2855371B1 (en) * | 2012-05-30 | 2021-12-01 | Reckitt Benckiser Calgon BV | A water softening composition |
JP2017149936A (en) * | 2016-02-23 | 2017-08-31 | ライオン株式会社 | Powder detergent composition for clothing |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3922230A (en) * | 1971-08-04 | 1975-11-25 | Lever Brothers Ltd | Oligomeric polyacrylates as builders in detergent compositions |
JPS5827320B2 (en) * | 1975-06-30 | 1983-06-08 | 株式会社日本触媒 | Senzai Sosabutsu |
NL7900849A (en) * | 1979-02-02 | 1980-08-05 | Senzora B V | DETERGENTS. |
DE2936984A1 (en) * | 1979-09-13 | 1981-04-02 | Basf Ag, 6700 Ludwigshafen | USE OF (METH) ACRYLIC ACID-MALEIC ACID COPOLYMERISATES AS INCREDIBLE INHIBITORS IN DETERGENTS |
IN161821B (en) * | 1981-02-26 | 1988-02-06 | Colgate Palmolive Co | |
AU549000B2 (en) * | 1981-02-26 | 1986-01-09 | Colgate-Palmolive Pty. Ltd. | Base beads for detergent compositions |
DE3277630D1 (en) * | 1981-05-30 | 1987-12-17 | Procter & Gamble | Detergent composition containing performance additive and copolymeric compatibilizing agent therefor |
-
1984
- 1984-01-30 EP EP84200104A patent/EP0124913B1/en not_active Expired
- 1984-01-30 AT AT84200104T patent/ATE20476T1/en not_active IP Right Cessation
- 1984-01-30 DE DE8484200104T patent/DE3460228D1/en not_active Expired
- 1984-02-03 IE IE262/84A patent/IE56762B1/en not_active IP Right Cessation
- 1984-02-16 CA CA000447604A patent/CA1220998A/en not_active Expired
- 1984-02-20 GR GR73845A patent/GR81656B/el unknown
- 1984-02-27 MX MX200467A patent/MX159427A/en unknown
- 1984-03-13 JP JP59048006A patent/JPS6018595A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
EP0124913B1 (en) | 1986-06-18 |
DE3460228D1 (en) | 1986-07-24 |
JPS6018595A (en) | 1985-01-30 |
ATE20476T1 (en) | 1986-07-15 |
MX159427A (en) | 1989-05-29 |
GR81656B (en) | 1984-12-12 |
CA1220998A (en) | 1987-04-28 |
EP0124913A1 (en) | 1984-11-14 |
JPH0522757B2 (en) | 1993-03-30 |
IE56762B1 (en) | 1991-12-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed |