WO1995023205A1 - Granular detergent composition containing hydrotropes - Google Patents
Granular detergent composition containing hydrotropes Download PDFInfo
- Publication number
- WO1995023205A1 WO1995023205A1 PCT/US1995/002298 US9502298W WO9523205A1 WO 1995023205 A1 WO1995023205 A1 WO 1995023205A1 US 9502298 W US9502298 W US 9502298W WO 9523205 A1 WO9523205 A1 WO 9523205A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- detergent composition
- surfactant
- alkyl
- detergent
- composition according
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 126
- 239000003599 detergent Substances 0.000 title claims abstract description 123
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- GDJZZWYLFXAGFH-UHFFFAOYSA-M xylenesulfonate group Chemical group C1(C(C=CC=C1)C)(C)S(=O)(=O)[O-] GDJZZWYLFXAGFH-UHFFFAOYSA-M 0.000 claims abstract description 7
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical class CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 5
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- 239000004615 ingredient Substances 0.000 claims description 16
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
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- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 3
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- 239000003607 modifier Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical class CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- UQKAOOAFEFCDGT-UHFFFAOYSA-N n,n-dimethyloctan-1-amine Chemical compound CCCCCCCCN(C)C UQKAOOAFEFCDGT-UHFFFAOYSA-N 0.000 description 1
- PFPFHPHPGFCJND-UHFFFAOYSA-N n,n-dimethyltetracosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCN(C)C PFPFHPHPGFCJND-UHFFFAOYSA-N 0.000 description 1
- AJHTXGOGMRVJDS-UHFFFAOYSA-N n,n-dimethyltetradecan-1-amine;n-ethyl-n-methyltetradecan-1-amine Chemical compound CCCCCCCCCCCCCCN(C)C.CCCCCCCCCCCCCCN(C)CC AJHTXGOGMRVJDS-UHFFFAOYSA-N 0.000 description 1
- ONLRKTIYOMZEJM-UHFFFAOYSA-N n-methylmethanamine oxide Chemical compound C[NH+](C)[O-] ONLRKTIYOMZEJM-UHFFFAOYSA-N 0.000 description 1
- MERIVZAHHVOBCI-UHFFFAOYSA-N naphthalene-1-carboperoxoic acid Chemical class C1=CC=C2C(C(=O)OO)=CC=CC2=C1 MERIVZAHHVOBCI-UHFFFAOYSA-N 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000010951 particle size reduction Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000005029 sieve analysis Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 108010075550 termamyl Proteins 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
- C11D17/065—High-density particulate detergent compositions
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/37—Mixtures of compounds all of which are anionic
-
- 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
- C11D3/34—Organic compounds containing sulfur
- C11D3/3472—Organic compounds containing sulfur additionally containing -COOH groups or derivatives thereof
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/525—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
-
- 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
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
Definitions
- the present invention is generally directed to a granular detergent composition having improved solubility in cold temperature launde ⁇ ng solutions More particularh the invention is directed to a detergent composition containing high levels of a sulfated surfactant selected from the group consisting of alkyl sulfates (also referenced herein as "AS"), alkyl ethoxy sulfates (also referenced herein as “AES”), and secondary alkyl sulfates (also referenced herein as “SAS”) and mixtures thereof, and a hydrotrope selected from the group consisting of sulfyl succinates, xylene sulfonates, cumene sulfonates and mixtures thereof, together which improve solubilitv in cold temperature washing solutions (e g 5°C to 30°C) and high water hardness conditions (e g 7 grains/gallon)
- the detergent of the invention is in the form of detergent agglomerates rather than
- vanous anionic surfactants especially the alkyl benzene sulfonates
- vanous nonionic surfactants such as the alkyl ethoxylates and alkylphenol ethoxylates
- compact detergents have its difficulties.
- so ⁇ alled "inert" ingredients such as sodium sulfate are substantially eliminated
- such ingredients do play a role in enhancing solubility of conventional detergents.
- compact detergents often suffer from solubility problems, especially in cold temperature launde ⁇ ng solutions.
- conventional compact or low density detergent granules are usually prepared by spray drying processes which result in extremely porous detergent particles that are quite amenable to being dissolved in aqueous washing solutions.
- compact detergents are typically compnsed of less porous, high density detergent particles which are less soluble, e.g.
- Patent No 4,528, 144 is directed to a liquid detergent compositions containing terpene sulfonate hydrotropes and vanous other detergent ingredients in a similar fashion, Lamberti et al, U.S. Patent No 4.623.483 (Lever), is also directed to a liquid detergent composition comprising a hydrotrope and other conventional detergent ingredients
- Lamberti et al U.S. Patent No 4.623.483
- Gutierrez patents only suggest liquid compositions and are silent with respect to granular or agglomerated versions of the detergent disclosed therein Thus, these patents do not speak to the solubility problem associated with cold temperature laundering solutions, a problem particularly prevalent when using detergents which are not spray-dried.
- the present invention meets the needs identified above by prov iding a detergent composition in the form of agglomerates which exhibit improved solubility or dissolution of the anionic surfactants in cold temperature washing solutions as well as under high water hardness conditions
- the detergent composition compnses a surfactant system having a high level of a sulfated surfactant selected from the group of alkyl sulfates, alkyl ethoxy sulfates secondary alkyl sulfates and mixtures thereof, in combination with a hydrotrope selected from the group consisting of sulfyl succinates, xylene sulfonates, cu ene sulfonates and mixtures thereof
- Other adjunct detergent ingredients may also be included in the detergent agglomerates which form the detergent composition
- high active (high surfactant levels) particles may be optionally included to enhance cleaning
- biodegradabi high active (high surfactant levels) particles
- the phrase "improved solubility” means that the solubility of the anionic surfactants of the detergent composition is enhanced by at least 5% in the laundenng solution when employed in the manner of this invention, as compared to the solubility of the same anionic surfactants per se, under the same test conditions (i e water temperature and pH. stirring speed and Ume, particle size, water hardness, and the like)
- agglomerates refers to particles formed by agglomerating particles which typically have a smaller mean particle size than the formed agglomerates All percentages, ratios and proportions used herein are by weight, unless otherwise specified All documents including patents and publications cited herein are incorporated herein by reference
- a detergent composition in the form of agglomerates is provided herein
- the detergent composition compnses from about 1% to 50% by weight of a detersive surfactant system
- the surfactant system itself compnses by weight of the surfactant system, at least about 30% of a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates, secondary alkyl sulfates and mixtures thereof
- the detergent composition includes from about 1% to about 50% of a hydrotrope selected from the group consisting of sulfyl succinates.
- the detergent composition includes at least about 1% by weight of a detergency builder to enhance cleaning
- the surfactant system, hydrotrope, and builder are agglomerated to form detergent agglomerates which are substantially free of phosphates
- the anionic surfactants in the detergent composition have improved solubility in an aqueous launde ⁇ ng solution
- AS solubility of the sulfated surfactant
- AES and/or SAS is enhanced by at least 5%, preferably 10 to 50%, over those same surfactants alone under the same test conditions in aqueous washing solutions at cold temperatures, I e 5°C to 30°C
- a method for launde ⁇ ng soiled fab ⁇ cs is provided The method compnses the step of contacting soiled fab ⁇ cs with an effective amount of a detergent composition as desc ⁇ bed herein in an aqueous launde ⁇ ng solution An effective amount is typically on the order of 1000 to 1500 ppm
- the invention is directed to a granular detergent composition having improved solubility in cold temperature launde ⁇ ng solutions
- a multitude of consumers around the world launder soiled clothes in conventional washing machines unique to their particular geographic location Typically, these conventional washing machines launder the soiled clothes in water supplied at relatively cold temperatures, for example in range of 5°C to 30°C, and at high hardness concentrations, e g 7 grains/gallon (nch with Ca and Mg ions)
- Most of the modem day consumers also use compact or condensed laundry detergents to accomplish their launde ⁇ ng needs Under the aforementioned conditions, solubility of cunent detergents in aqueous launde ⁇ ng solutions has been a problem This problem is especially exacerbated when the detergent composition has high levels of alkyl sulfates, alkyl ethoxy sulfate and/or secondary alkyl sulfates which are not particularly amenable to dissolution in cold aqueous launde
- alkyl ethoxy sulfate and/or secondary alkyl sulfate (“sulfated" surfactant system) detergent composition
- a hydrotrope selected from the group consisting of sulfyl succinates, xylene sulfonates, cumene sulfonates and mixtures thereof To that end.
- the preferred detergent composition of the invention compnses from about 1% to about 50%, preferably from about 15% to about 40%, by weight of a hydrotrope
- the surfactant system of the detergent composition compnses at least 30%, preferably from about 35% to about 90%, of a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates, secondary alkyl sulfates and mixtures thereof
- the detergent composition is in the form of agglomerates and has an overall density of 650 g/1 or higher It has been found that such a detergent composition containing agglomerates having the aforementioned surfactant system and hydrotrope surp ⁇ singly has significantly improved solubility in cold temperature (5°C to 30°C) washing solutions as well as under high water hardness conditions
- the detergent composition of the invention also compnses at least about 1%. preferably from about 10% to about 40%, of a detergency builder
- the detergent composition mav also include one or more of adjunct detergent ingredients
- adjunct detergent ingredients Nonhmiting examples of the detergencv builder and such adjunct ingredients are desc ⁇ bed in detail hereinafter
- the detergent composition herein is formulated and processed to achie e a density of at least 650 g/1 for purposes of producing a "compact" detergent product
- the detergent agglomerates which form the detergent composition of the invention preferably do not contain phosphates
- the "improved solubility" achieved by the detergent com osition is concerned with enhanced solubility of the anionic surfactants contained in the sun-tant system, I e AS, AES, SAS or LAS if used
- the improvement represents at least a 5% increase in solubility of these anionics in the wash solution over the solubility of the same surfactants if they were dissolved alone or without being contained in a detergent composition as defined herein More preferably, the solubility improvement is from about 10% to about 50%
- any compa ⁇ son of anionic surfactant solubility should be completed under the same laundenng conditions, e g water temperature, hardness and pH, stimng speed and time, and particle size
- Typical anionic surfactant solubility improvements are set forth in the Examples hereinafter Those skilled in the art should also appreciate the numerous ways in which the amount of the surfactant system in the washing solution can be determined For example, in the so-called "catS03" titration technique
- the surfactant system in the detergent composition must include a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates, secondary alkyl sulfates. and mixtures thereof
- a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates, secondary alkyl sulfates. and mixtures thereof
- the anionic surfactants in the surfactant system of the invention i e AS, AES, and/or SAS
- the surfactant system may contain one or more of additional surfactants, nonlimiting examples of which are provided hereinafter
- the surfactant system preferably includes conventional pnmary alkyl sulfate surfactants have the general formula
- Branched-chain p ⁇ mary alkyl sulfate surfactants (1 e , branched-chain "PAS") having 10-20 carbon atoms can also be used herein, see, for example.
- alkyl is the alkyl portion of acyl groups
- AE X S especially EO 1-7 ethoxy sulfates
- mate ⁇ als which have the sulfate moiety dist ⁇ aded randomly along the hydrocarbyl "backbone" of the molecule
- Such mate ⁇ als may be depicted by the structure CH 3 (CH2) n (CHOS ⁇ 3-M + )(CH 2 ) rn CH3 wherein m and n are integers of 2 or greater and the sum of + n is typically about 9 to 17, and M is a water-solubihzing cation
- a selected secondary (2,3) alkyl sulfate surfactant is used herein which compnses structures of formulas A and B (A) CH 3 (CH 2 ) x (CHOS0 3 -M + ) CH 3 and
- x and (y+1) are, respectively, integers of at least about 6, and can range from about 7 to about 20, preferably about 10 to about 16 M is a cation, such as an alkali metal, ammonium, alkanolammonium, alkaline earth metal, or the like Sodium is typical for use as M to prepare the water-soluble (2,3) alkyl sulfates, but ethanolammomum, diethanolammonium, tnethanolammonium, potassium, ammonium, and the like, can also be used It is preferred that the secondary (2,3) alkyl sulfates be substantially free (1 e , contain less than about 20%. more preferably less than about 10%, most preferably less than about 5%) of such random secondary alkyl
- the granular detergent composition of the present invention preferably includes a hydrotrope such a those commonly used in liquid detergents It has been found that the inclusion of a hydrotrope into the agglomerated detergent composition desc ⁇ bed herein surprisingly aides in solubihzation of detergent agglomerates which are nch in sulfated surfactants (l e > 30% of the surfactant system)
- the hydrotrope regardless of form (I e solid, liquid or paste) is mixed with the surfactant paste p ⁇ or to, or dunng the agglomeration step
- the hydrotrope used herein is preferably selected from the group consisting of sulfyl succinates, xylene sulfonates, cumene sulfonates and mixtures thereof Most prefe ⁇ ed are the sodium salts of the aforementioned prefe ⁇ ed hydro
- the detergent composition of the invention also includes a detergency builder matenal to assist in controlling mineral hardness Inorganic as well as organic builders can be used
- Builders are typically used in fabnc laundenng compositions to assist in the removal of paniculate soils
- Inorganic detergent builders include, but are not limited to. the alkali metal, ammonium and alkanolammonium salts of phytic acid, silicates, carbonates (including bicarbonates and sesquicarbonates), sulphates, and aluminosilicates
- silicate builders are the alkali metal silicates, particularly those having a S1O2 Na2 ⁇ ratio in the range 1 6 1 to 3 2 1 and layered silicates, such as the layered sodium silicates desc ⁇ bed in U S Patent 4,664,839 issued May 12, 1987 to H P Rieck NaSKS-6 is the trademark for a crystalline layered silicate marketed by Hoechst (commonly abbreviated herein as "SKS-6")
- the Na SK.S-6 silicate builder does not contain aluminum NaSKS-6 has the delta-Na2S ⁇ 5 morphology form of layered silicate It can be prepared by methods such as those desc ⁇ bed in German DE-A-3,417,649 and DE-A-3,742,043
- SKS-6 is a highly prefe ⁇ ed layered silicate for use herein, but other such layered silicates, such as those having the general formula NaMS ⁇ ⁇ ⁇ 2 x + ⁇ -yH2 ⁇ wherein M is
- silicates may also be useful such as for example magnesium silicate, which can serve as a crisping agent in granular formulations, as a stabilizing agent for oxygen bleaches, and as a component of suds control systems.
- carbonate builders are the alkaline earth and alkali metal carbonates as disclosed in German Patent Application No 2.321,001 published on November 15, 1973
- Aluminosilicate builders are useful in the present invention Aluminosilicate builders are of great importance in most currently marketed heavy duty granular detergent compositions, and can also be a significant builder ingredient in liquid detergent formulations Aluminosilicate builders include those having the empirical formula M z (zA10 2 )y]-xH 2 0 wherein z and y are integers of at least 6, the molar ratio of z to y is in the range from 1 0 to about 0.5, and x is an integer from about 15 to about 264
- aluminosilicate ion exchange materials are commercially available These aluminosilicates can be crystalline or amorphous in structure and can be natural ly-occurnng aluminosilicates or synthetically denved
- a method for producing aluminosilicate ion exchange materials is disclosed in U.S. Patent 3,985,669, Krummel. et al, issued October 12, 1976
- Prefe ⁇ ed synthetic crystalline aluminosilicate ion exchange mate ⁇ als useful herein are available under the designations Zeolite A, Zeolite P (B), Zeolite MAP and Zeolite X.
- the crystalline aluminosilicate ion exchange material has the formula Na 1 2[(A10 2 ) 1 2(Si ⁇ 2)i2l H 2 0 wherein x is from about 20 to about 30, especially about 27
- the aluminosilicate has a particle size of about 0.1-10 microns in diameter.
- Organic detergent builders suitable for the purposes of the present invention include, but are not restricted to, a wide variety of polycarboxylate compounds
- poly- carboxylate refers to compounds having a plurality of carboxylate groups, preferably at least 3 carboxylates.
- Polycarboxylate builder can generally be added to the composition in acid form, but can also be added in the form of a neutralized salt When utilized in salt form, alkali metals, such as sodium, potassium, and lithium, or alkanolammonium salts are preferred
- alkali metals such as sodium, potassium, and lithium, or alkanolammonium salts are preferred
- Included among the polycarboxylate builders are a vanety of catego ⁇ es of useful materials
- polycarboxylate builders encompasses the ether polycarboxylates, including oxydisuccinate. as disclosed in Berg. U S Patent 3, 128,287, issued April 7, 1964. and Lamberti et al, U S Patent 3.635,830, issued January 18. 1972 See also "TMS/TDS" builders of U.S. Patent 4,663,071, issued to Bush et al, on May 5, 1987 Suitable ether polycarboxylates also include cyclic compounds, particularly alicyclic compounds, such as those desc ⁇ bed in U S Patents 3,923,679, 3,835, 163, 4,158,635, 4, 120,874 and 4, 102,903 Other useful detergency builders include the ether hydrovypolycarboxylates.
- polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid
- polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxyl ⁇ c acid, carb
- Citrate builders e g., citnc acid and soluble salts thereof (particularly sodium salt), are polycarboxylate builders of particular importance for heavy duty liquid detergent formulations due to their availability from renewable resources and their biodegradability Citrates can also be used, however, in granular compositions, especially in combination with zeolite and/or layered silicate builders. Oxydisuccinates are also especially useful in such compositions and combinations
- Laurylsuccinates are the prefe ⁇ ed builders of this group, and are desc ⁇ bed in European Patent Application 86200690.5/0,200,263, published November 5, 1986
- Other suitable polycarboxylates are disclosed in U.S. Patent 4,144,226, Crutchfield et al, issued March 13, 1979 and in U.S Patent 3,308,067, Diehl, issued March 7, 1967. See also Diehl U.S Patent 3,723,322
- Fatty acids e.g., C ⁇ 2 -C ⁇ monocarboxylic acids
- Such use of fatty acids will generally result in a diminution of sudsing, which should be taken into account by the formulator
- the surfactant system herein may include an optimum level, from about 0 1% to about 15% and more preferably from about 3% to about 8% by weight, for improving the overall solubility of the detergent composition without substantially decreasing the overall biodegradability of the present detergent composition
- the level of LAS may be included as from about 1% to about 40%. more preferably from about 10% to about 25%, by weight of the surfactant system in the detergent composition
- the surfactant system may also include an amine oxide surfactant
- an amine oxide surfactant Nonlimiting examples include C jQ .ig amine oxides, secondary amine oxides such as dimethyl amine oxide, and tertiary amine oxides having the general formula RR'R"NO in which R is a pnmary alkyl group containing 8 to 24 carbon atoms, R' is methyl, ethyl, or 2-hydroxyethyl, and R" is independently selected from methyl, ethyl, 2-hydroxyethly and pnmary alkyl groups containing 8 to 24 carbon atoms
- the tertiary amine oxide surfactant may be in hydrated form and have the general formula RR'R"NO 11H2O wherein R R' and R" are the same as above and n is 1 or 2
- tertiary amines suitable for use herein include those containing one or two short-chain groups independently selected from methyl, ethyl, and 2-hydroxyethyl groups, with the remaining valences of the amino nitrogen being satisfied with long-chain groups independently selected from pnmary alkyl groups containing 8-24 carbons, e g , octyl, decyl, dodecyl, tetradecyl, hexadecyl octadecyl, eicosyl, docosyl, and tetracosyl groups
- the pnmary alkyl groups may be branched-chain groups, but the prefe ⁇ ed amines are those in which at least most of the pnmary alkyl
- the detergent composition can also include any number of additional ingredients These include detergency builders, bleaches, bleach activators, suds boosters or suds suppressers, anti-tarnish and antico ⁇ osion agents, soil suspending agents, soil release agents, germicides, pH adjusting agents. non-builder alkalimty sources, chelating agents, smectite clays, enzymes, enzyme-stabilizing agents and perfumes See U S Patent 3,936,537, issued February 3, 1976 to Baskerville, Jr et al , incorporated herein by reference Also, fabnc conditioning agents may be included as an adjunct mate ⁇ al such as those descnbed in U S Patent 4,861,502, issued August 29, 1989 to Caswell. incorporated herein by reference Bleaching agents and activators are desc ⁇ bed in U S Patent 4,412,934. Chung et al , issued
- Suitable smectite clays for use herein are desc ⁇ bed in U S Patent 4,762,645, Tucker et al, issued August 9, 1988, Column 6, line 3 through Column 7, line 24, incorporated herein by reference Suitable additional detergency builders for use herein are enumerated in the Baskerville patent. Column 13, line 54 through Column 16, line 16, and in U S Patent 4,663,071, Bush et al, issued May 5, 19b both incorporated herein by reference
- Enzymes can be included in the formulations herein for a wide vanety of fabnc laundenng purposes, including removal of protein-based, carbohydrate-based, or t ⁇ glyce ⁇ de-based stains, for example, and for the prevention of refugee dye transfer, and for fabnc restoration
- the enzymes to be incorporated include proteases, amylases, Upases, cellulases, and peroxidases, as well as mixtures thereof
- Other types of enzymes may also be included They may be of any suitable o ⁇ gm, such as vegetable, animal, bacte ⁇ al, fungal and yeast o ⁇ gin However, their choice is governed by several factors such as pH-activity and/or stability optima, thermostability, stability versus active detergents. builders and so on In this respect bacte ⁇ al or fungal enzymes are prefe ⁇ ed, such as bacte ⁇ al amylases and proteases, and fungal cellulases
- proteases are the subtilisms which are obtained from particular strains of B subtilts and B lichemforms Another suitable protease is obtained from a strain of Bacillus having maximum activity throughout the pH range of 8-12 developed and sold bv Novo Indust ⁇ es A/S under the registered trade name ESPERASE
- proteases include Protease A (see European Patent Application 130,756, published January 9 1985) and Protease B (see European Patent Application Se ⁇ al No 87303761 8, filed Ap ⁇ l 28 1987 and European Patent Application 130,756, Bott et al, published January 9, 1985)
- Amylases include, for example, ⁇ -amylases desc ⁇ bed in Bntish Patent Specification No
- the cellulase usable in the present invention include both bacte ⁇ al or fungal cellulase Preferably, they will have a pH optimum of between 5 and 9 5 Suitable cellulases are disclosed in U S Patent 4,435,307, Barbesgoard et al, issued March 6, 1984, which discloses fungal cellulase produced from Humicola insolens and Humicola strain DSM1800 or a cellulase 212-producmg fungus belonging to the genus Aeromonas, and cellulase extracted from the hepatopancreas of a manne mollusk (Dolabella Au ⁇ cula Solander) suitable cellulases are also disclosed in GB-A- 2 075 028, GB-A-2 095 275 and DE-OS-2 247 832 Suitable l ⁇ ase enzymes for detergent usage include those produced by microorganisms of the Pseudomonas group, such as Pseudomona
- Peroxidase enzymes are used in combination with oxygen sources, e g , percarbonate, perborate, persulfate, hydrogen peroxide, etc They are used for "solution bleaching," I e to prevent transfer of dyes or pigments removed from substrates dunng wash operations to other substrates in the wash solution
- Peroxidase enzymes are known in the art, and include, for example, horseradish peroxidase, Ugninase, and haloperoxidase such as chloro- and bromo-peroxidase Peroxidase- containing detergent compositions are disclosed, for example, in PCT International Application WO 89/099813, published October 19, 1989, by O Kirk, assigned to Novo Industries
- a S A wide range of enzvme mate ⁇ als and means for their incorporation into synthetic detergent compositions are also disclosed in U S Patent 3 553 139 issued January 5 1971 to McCarty et al Enzymes are further disclosed in U S Patent 4 101 457 Place
- Step A Preparation of Surfactant Paste -
- the objective is to combine the surfactants and liquid in the compositions into a common mix in order to aid in surfactant soiubilization and agglomeration
- the surfactants and other liquid components including the hydrotrope are mixed together in a Sigma Mixer at 140°F (60°C) at about 40 rpm to about 75 rpm for a penod of from 15 minutes to about 30 minutes to provide a paste having the general consistency of 20 000- 40,000 centipoise
- the paste is stored at 140°F (60°C) until agglomeration Step (B) is ready to be conducted
- Step B Agglomeration of Powders with Surfactant Paste -
- the purpose of this Step is to transform the base formula ingredients into flowable detergent agglomerates having a mean particle size range of from about 800 microns to about 1600 microns
- the powders including mate ⁇ als such as zeolite, citrate, cit ⁇ c acid builder, layered silicate builder (as SKS-6) sodium carbonate, ethylenediaminedisuccinate, magnesium sulfate and optical b ⁇ ghtener
- the Ei ⁇ ch Mixer R-Senes
- the surfactant paste from Step A is then charged into the mixer and the mixing is continued at about 1500 rpm to about 3000 rpm for a penod from about 1 minute to about 10 minutes preferably 1-3 minutes, at ambient temperature
- the mixing is stopped when course agglomerates (average particle size
- Step D Coat Agglomerates and Add Free-Flow Aids -
- the objective in this Step is to achieve the final target agglomerate size range of from about 800 microns to about 1600 microns, and to admix materials which coat the agglomerates, reduce the caking/lumping tendency of the particles and help maintain acceptable flowability.
- the dried agglomerates from Step C are charged into the Eirich Mixer (R-Series) and mixed at a rate of about 1500 rpm to about 3000 rpm while adding 2-6% Zeolite A (median particle size 2-5 ⁇ m) during the mixing.
- the mixing is continued until the desired median particle size is achieved (typically from about 5 seconds to about 45 seconds). At this point, from about 0.1% to about 1.5% by weight of precipitated silica (average particle size 1-3 microns) is added as a flow aid and the mixing is stopped.
- compositions A-C are made in accordance with the agglomeration process described above.
- Compositions A and B are within the scope of the invention and composition C is outside of the invention and is presented for purposes of comparison as described in Example II hereinafter.
- the relative proportions of compositions A-C. in agglomerate form, are listed in Table I below.
- compositions A-C 1 170 ppm
- aqueous laundering solution having a water temperature of 10°C and a water hardness of 7 grains/gallon (Ca Mg ratio of 3 1)
- the launde ⁇ ng solution is continuously agitated at a rate of 75 rpm and samples of the wash solution were taken at vanous time intervals as shown in Table I below
- the amount of surfactant in the launde ⁇ ng solution is determined by conducting the well known "catS0 3 " titration technique on the samples taken from individual wash solutions containing one of the compositions A-C
- the amount of anionic surfactant in the launde ⁇ ng solution is determined by filte ⁇ ng the samples through 0 45 ny lon filter paper to remove the insolubles and thereafter, tit
- compositions A and B which are within the scope of the invention surpnsingly have improved solubility over composition C which is outside the scope of the invention
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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)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95911906A EP0748371A1 (en) | 1994-02-28 | 1995-02-24 | Granular detergent composition containing hydrotropes |
CA002183744A CA2183744C (en) | 1994-02-28 | 1995-02-24 | Granular detergent composition containing hydrotropes |
MX9603691A MX9603691A (en) | 1994-02-28 | 1995-02-24 | Granular detergent composition containing hydrotropes. |
JP7522474A JPH09509684A (en) | 1994-02-28 | 1995-02-24 | Granular detergent composition containing hydrotrope |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/203,287 | 1994-02-28 | ||
US08/203,287 US5478502A (en) | 1994-02-28 | 1994-02-28 | Granular detergent composition containing hydrotropes and optimum levels of anoionic surfactants for improved solubility in cold temperature laundering solutions |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995023205A1 true WO1995023205A1 (en) | 1995-08-31 |
Family
ID=22753321
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/002298 WO1995023205A1 (en) | 1994-02-28 | 1995-02-24 | Granular detergent composition containing hydrotropes |
Country Status (7)
Country | Link |
---|---|
US (1) | US5478502A (en) |
EP (1) | EP0748371A1 (en) |
JP (1) | JPH09509684A (en) |
CN (1) | CN1088747C (en) |
CA (1) | CA2183744C (en) |
MX (1) | MX9603691A (en) |
WO (1) | WO1995023205A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2323849A (en) * | 1997-04-02 | 1998-10-07 | Procter & Gamble | Detergent composition |
WO1998059024A1 (en) * | 1997-06-23 | 1998-12-30 | The Procter & Gamble Company | Granular detergent composition containing an optimum surfactant system for cold temperature laundering |
EP1352951A1 (en) * | 2002-04-11 | 2003-10-15 | The Procter & Gamble Company | Detergent granule comprising a nonionic surfactant and a hydrotrope |
Families Citing this family (18)
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US5858950A (en) * | 1993-06-28 | 1999-01-12 | The Procter & Gamble Company | Low sudsing liquid detergent compositions |
US5783547A (en) * | 1994-03-24 | 1998-07-21 | The Procter & Gamble Company | Enzyme granulates |
US5935922A (en) * | 1994-03-31 | 1999-08-10 | The Procter & Gamble Company | Detergent composition containing zeolite map for washing a mixture of white and colored fabrics |
US5849684A (en) * | 1994-04-14 | 1998-12-15 | The Procter & Gamble Company | Detergent additives comprising dye transfer inhibitors, and process for making them |
DE19538029A1 (en) * | 1995-10-12 | 1997-04-17 | Sued Chemie Ag | detergent additive |
CA2248160C (en) * | 1996-03-08 | 2002-08-06 | The Procter & Gamble Company | Preparation of secondary alkyl sulfate particles with improved solubility |
US6017873A (en) * | 1996-03-08 | 2000-01-25 | The Procter & Gamble Compnay | Processes for making agglomerated high density detergent composition containing secondary alkyl sulfate surfactant |
WO1998000489A1 (en) * | 1996-06-28 | 1998-01-08 | The Procter & Gamble Company | Detergent composition |
US6162784A (en) * | 1996-07-31 | 2000-12-19 | The Procter & Gamble Company | Process and composition for detergents |
GB2315763A (en) * | 1996-07-31 | 1998-02-11 | Procter & Gamble | Preparation of an agglomerated detergent composition comprising a surfactant a an acid source |
US6150322A (en) * | 1998-08-12 | 2000-11-21 | Shell Oil Company | Highly branched primary alcohol compositions and biodegradable detergents made therefrom |
US5955418A (en) * | 1997-02-26 | 1999-09-21 | The Procter & Gamble Company | Secondary alkyl sulfate surfactant with improved solubility by kneading/extruding process |
GB2323848A (en) * | 1997-04-02 | 1998-10-07 | Procter & Gamble | Detergent particle |
PL191310B1 (en) | 1999-03-30 | 2006-04-28 | Unilever Nv | Detergent powder composition |
US8063010B2 (en) * | 2004-08-02 | 2011-11-22 | Ecolab Usa Inc. | Solid detergent composition and methods for manufacturing and using |
US20110129610A1 (en) * | 2009-11-30 | 2011-06-02 | Patrick Fimin August Delplancke | Method for coating a hard surface with an anti-filming composition |
US20110126858A1 (en) * | 2009-11-30 | 2011-06-02 | Xinbei Song | Method for rinsing cleaned dishware |
US8685911B2 (en) | 2009-11-30 | 2014-04-01 | The Procter & Gamble Company | Rinse aid compositions |
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FR2206380A1 (en) * | 1972-11-13 | 1974-06-07 | Procter & Gamble | |
US4123395A (en) * | 1975-11-28 | 1978-10-31 | The Procter & Gamble Company | Compositions containing nonionic surfactant and sulfonated aromatic compatibilizing agent |
GB2116200A (en) * | 1982-03-01 | 1983-09-21 | Procter & Gamble | Granular detergent composition |
WO1993015180A1 (en) * | 1992-02-04 | 1993-08-05 | Henkel Kommanditgesellschaft Auf Aktien | Process for producing solid washing and cleaning agents with a high powder density and improved rates of dissolution |
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GB8900023D0 (en) * | 1989-01-03 | 1989-03-01 | Shell Int Research | Detergent composition |
US5244593A (en) * | 1992-01-10 | 1993-09-14 | The Procter & Gamble Company | Colorless detergent compositions with enhanced stability |
-
1994
- 1994-02-28 US US08/203,287 patent/US5478502A/en not_active Expired - Fee Related
-
1995
- 1995-02-24 JP JP7522474A patent/JPH09509684A/en not_active Ceased
- 1995-02-24 WO PCT/US1995/002298 patent/WO1995023205A1/en not_active Application Discontinuation
- 1995-02-24 CN CN95192618A patent/CN1088747C/en not_active Expired - Fee Related
- 1995-02-24 CA CA002183744A patent/CA2183744C/en not_active Expired - Fee Related
- 1995-02-24 MX MX9603691A patent/MX9603691A/en unknown
- 1995-02-24 EP EP95911906A patent/EP0748371A1/en not_active Ceased
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DE2333699A1 (en) * | 1972-07-03 | 1974-01-24 | Procter & Gamble | SPRAY DRIED DETERGENT AND METHOD FOR MANUFACTURING IT |
FR2206380A1 (en) * | 1972-11-13 | 1974-06-07 | Procter & Gamble | |
US4123395A (en) * | 1975-11-28 | 1978-10-31 | The Procter & Gamble Company | Compositions containing nonionic surfactant and sulfonated aromatic compatibilizing agent |
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WO1993015180A1 (en) * | 1992-02-04 | 1993-08-05 | Henkel Kommanditgesellschaft Auf Aktien | Process for producing solid washing and cleaning agents with a high powder density and improved rates of dissolution |
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GB2323849A (en) * | 1997-04-02 | 1998-10-07 | Procter & Gamble | Detergent composition |
WO1998059024A1 (en) * | 1997-06-23 | 1998-12-30 | The Procter & Gamble Company | Granular detergent composition containing an optimum surfactant system for cold temperature laundering |
US6207633B1 (en) | 1997-06-23 | 2001-03-27 | The Procter & Gamble Company | Granular detergent composition containing an optimum surfactant system for cold temperature laundering |
EP1352951A1 (en) * | 2002-04-11 | 2003-10-15 | The Procter & Gamble Company | Detergent granule comprising a nonionic surfactant and a hydrotrope |
WO2003087288A1 (en) * | 2002-04-11 | 2003-10-23 | The Procter & Gamble Company | Detergent granule comprising a nonionic surfactant and a hydrotrope |
Also Published As
Publication number | Publication date |
---|---|
EP0748371A1 (en) | 1996-12-18 |
MX9603691A (en) | 1997-06-28 |
CN1146214A (en) | 1997-03-26 |
JPH09509684A (en) | 1997-09-30 |
US5478502A (en) | 1995-12-26 |
CA2183744C (en) | 2000-04-18 |
CN1088747C (en) | 2002-08-07 |
CA2183744A1 (en) | 1995-08-31 |
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