US3624006A - Stable opacified liquid detergent compositions - Google Patents
Stable opacified liquid detergent compositions Download PDFInfo
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- US3624006A US3624006A US839670A US3624006DA US3624006A US 3624006 A US3624006 A US 3624006A US 839670 A US839670 A US 839670A US 3624006D A US3624006D A US 3624006DA US 3624006 A US3624006 A US 3624006A
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- detergent compositions
- liquid detergent
- stable
- alcohol
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- 239000000203 mixture Substances 0.000 title abstract description 41
- 239000003599 detergent Substances 0.000 title abstract description 31
- 239000007788 liquid Substances 0.000 title description 23
- -1 alkylbenzene sulfonate Chemical class 0.000 abstract description 25
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 15
- 239000000194 fatty acid Substances 0.000 abstract description 15
- 229930195729 fatty acid Natural products 0.000 abstract description 15
- 150000004665 fatty acids Chemical class 0.000 abstract description 14
- 229910019142 PO4 Inorganic materials 0.000 abstract description 8
- 239000010452 phosphate Substances 0.000 abstract description 8
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 abstract description 5
- 229920000388 Polyphosphate Polymers 0.000 abstract description 5
- 239000001205 polyphosphate Substances 0.000 abstract description 5
- 235000011176 polyphosphates Nutrition 0.000 abstract description 5
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 4
- 150000001340 alkali metals Chemical class 0.000 abstract description 4
- 150000003014 phosphoric acid esters Chemical class 0.000 description 17
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 239000003605 opacifier Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical group [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 229940031957 lauric acid diethanolamide Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- 229920000847 nonoxynol Polymers 0.000 description 2
- REIUXOLGHVXAEO-UHFFFAOYSA-N pentadecan-1-ol Chemical compound CCCCCCCCCCCCCCCO REIUXOLGHVXAEO-UHFFFAOYSA-N 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 230000000153 supplemental effect Effects 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- CKNOIIXFUKKRIC-HZJYTTRNSA-N (9z,12z)-n,n-bis(2-hydroxyethyl)octadeca-9,12-dienamide Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)N(CCO)CCO CKNOIIXFUKKRIC-HZJYTTRNSA-N 0.000 description 1
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 1
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 1
- KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- HTRVTKUOKQWGMO-UHFFFAOYSA-N 2-ethyloctan-1-ol Chemical compound CCCCCCC(CC)CO HTRVTKUOKQWGMO-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- 150000002028 dodecanols Chemical class 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- SQEDZTDNVYVPQL-UHFFFAOYSA-N dodecylbenzene;sodium Chemical compound [Na].CCCCCCCCCCCCC1=CC=CC=C1 SQEDZTDNVYVPQL-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D1/65—Mixtures of anionic with cationic compounds
- C11D1/652—Mixtures of anionic compounds with carboxylic amides or alkylol amides
-
- 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
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- 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
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
Definitions
- Opacified liquid detergent compositions as opposed to clear or light colored solutions, have been found to be commercially advantageous because of their milk-white appearance, creamy consistency and relatively higher viscosity.
- a polymeric latex opacifier to the composition.
- These conventional opacifiers are generally polymers and copolymers of styrene and other'substances. Representatives of such polystyrene opacifiers are the materials described in US. Pat. Nos. 3,326,807 and 3,382,177. While these polymers contribute to opacity, they have no influence upon the detergent properties of the liquid system.
- stable, opaque liquid detergent compositions can be prepared by combining, as essential ingredients, from about 1 percent to 4 percent by weight of a phosphate ester of (a) an ethoxylated linear aliphatic alcohol having from eight to 18 carbon atoms, or of (b) ari ethoxylated branched chain aliphatic alcohol having from to carbon atoms, the aforesaid alcohols being ethoxylated with from about 2 to
- the aforesaid phosphate esters which are used to produce the stable opacified liquid detergent compositions of the present invention have been found to be essential to produce said compositions and to enable the higher molecular weight alkanolamides to coact in the compositions to function as opacifiers.
- the quantity of phosphate ester may vary from about 1 percent to 4 percent by weight. If the concentration is increased substantially about the 4 percent level, opacity is not obtained, while use of less than about 1 percent by weight phosphate ester will generally render the composition unstable.
- the liquid detergent compositions of the present invention will contain from L5 percent to 2.5 percent, on the average about 2 percent, by weight phosphate ester.
- alkylbenzene or alkyltoluene sulfonates useful in preparing the compositions of the present invention are well about 20 mols of ethylene oxide prior to being converted into their phosphate esters, from about 3 percent to 6 percent by weight of an alkylbenzene or alkyl toluene sulfonate, wherein the alkyl group contains from eight to 18 carbon atoms from about l percent to 6 percent by weight higher molecular weight fatty acid alkanolamide, from about 1 percent to 10 percent by weight alkali metal polyphosphate, and the balance water.
- compositions are characterized by excellent stability and the ingredients utilized, which react to produce opacity, are not inactive, as are the polymer or copolymer opacifiers but, instead, contribute to the desired detergent properties of the liquid detergent compositions.
- the phosphate esters of the ethoxylated linear C to C aliphatic alcohols and the phosphate esters of the ethoxylated branched chain C to C aliphatic alcohols, in which said alcohols have been adducted with from about 2 to about 20, particularly from 2 to 8 mols, of ethylene oxide per mol of said alcohol prior to being converted into their phosphate esters, are well known to the art and have found widespread use in various detergent compositions and other related applications such as are disclosed in many patents, among which are US. Pat. Nos. 3,004,056; 3,042,697; 3,033,889; 3,088,917 and 3,1 12,508.
- the phosphate esters used in preparing the detergent compositions of the present invention are preferably prepared by reacting 1 mol of P 0 with from 2 to 4.5 mols of the ethylene oxide adducts of the linear or branched chain aliphatic alcohol at a temperature in range of up to about l00 C., most advantageously in the range of about 50 to 65 C.
- Such phosphating procedures are disclosed for instance, in U.S. Pat. Nos. 2,441,295; 2,676,975; 2,701,958 and 3,004,056; Chemical Industries, Oct. 1942, pp. 516-521, 557; and Organo Phosphorus Compounds, John Wiley & Sons, New York, [950, pp. 220-223.
- the phosphate esters are advantageously used in the form of their water-soluble salts, preferably the sodium slats and the alkanolamine salts such as the diethanolamine and triethanolamine salts.
- Illustrative of the linear and branched chain aliphatic alcohols used in the production of the phosphate esters are noctyl alcohol, n-nonyl alcohol, n-decyl alcohol, n-dodecyl alcohol, n-tridecyl alcohol, n-tetradecyl alcohol, n-pentadecyl alcohol, n-hexadecyl alcohol, oleyl alcohol, n-stearyl alcohol, Oxo alcohols such as Oxo-hexadecyl alcohol and Oxo-pentadecyl alcohol (and others as shown in U.S. Pat. No.
- the at may be generally described as those containing from eight to 18 carbon atoms in the alkyl group. For economical reasons they will generally be present as the sodium salt. They may also be present as the monovalent metal, ammonium or organic amine salt. Especially suitable is sodium dodecylbenzene sulfonate.
- the concentration may range from 3 percent to 6 percent by weight, preferably about 4 percent to 5 percent by weight, of the liquid detergent compositron.
- the higher molecular weight fatty acid alkanolamide opacifier as used herein also acts, in its known manner, as a viscosity builder and foam stabilizer.
- the acyl radical of the alkanolamide is selected from the class of fatty acids having 10 to 18 carbon atoms, preferably 12 to 14 carbon atoms, and the alkanol group may have up to four carbon atoms in the case of monoalkanoamine derivatives and eight carbon atoms in the case of dialkanolamine derivatives.
- diethanolamides of C to C fatty acids such as lauric acid diethanolamide.
- alkanolaides are oleic diethanolamide, tall oil fatty acid diethanolamide, linoleic acid diethanolamide, and the corresponding fatty acid amides of glycerol monoand di-amines, diisopropanolamine, aminoethylethanolamine, dibutanolamine and diisobutanolamine.
- fatty acid alkanolamides may be prepared by various well-known techniques such as by condensing equimolar quantities of fatty acid with alkanolamine, or by condensing a molar excess of alkanolamine with fatty acid, or by reacting a fatty acid ester with alkanolamine, or by oxyalkylating, such as oxyethylating, the amide of the fatty acid.
- the fatty acid alkanolamide should be employed in amounts of about 1 percent to 4 percent and preferably about 2 percent to 3 percent, by weight of the liquid detergent composition.
- alkali metal polyphosphates useful in preparing the compositions of the present invention serve primarily as builders and concentration may vary from about I to l0 percent, preferably about 6 percent, by weight of the liquid detergent composition.
- Illustrative polyphosphates are sodium tripolyphosphate, tetrasodium pyrophosphate, trisodium phosphate and tetrapotassium pyrophosphate, tetrapotassium pyrophosphate being preferred.
- aqueous liquid detergent compositions of the present invention are prepared simply by combining the aforementioned ingredients with water at room temperature. No particular order of addition is necessary.
- the fmal preferred products exhibit a viscosity of approximately centipoises, which is most advantageous from a commercial standpoint for opalescent liquids.
- Certain supplemental ingredients for obtaining particular properties can, of course, be added to the stable opacified liquid detergent compositions of the present invention. Those which are used must, of course, be of such character and/or employed in such amounts as not adversely to affect the stability and opacity of the liquid detergent compositions of the present invention.
- Illustrative supplemental ingredients are perfumes, colors, chelating agents, corrosion inhibitors, deodorants, disinfectants, and the like.
- 3,l22,508 discloses detergent compositions which contain phosphate esters, which may be those which are used in accordance with the present invention or which may be phosphate esters of ethoxylated higher alkyl phenols such as phosphated ethoxylated nonyl phenol, in admixture with dodecylbenzene sulfonates, higher fatty acid alkanolamides, and alkali metal polyphosphates.
- the said patent has as one of its objective, however, the preparation of heavy duty detergent compositions which are clear, homogeneous liquids. While said patent discloses opaque, very viscous compositions, they involve the utilization in the detergent compositions of large proportions of such ingredients as tall oil fatty acids and mineral oil.
- EXAMPLE [I] A mixture was prepared consisting of 5 percent phosphate ester ofa 9 mol ethylene oxide adduct of nonyl phenol, 5 percent sodium dodecylbenzene sulfonate, 1 percent lauroyl diethanolamide, 10 percent sodium tripolyphosphate and the balance water. The resulting composition was unstable and immediately broke down upon standing.
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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)
Abstract
Stable, opaque aqueous detergent compositions comprising alkali metal polyphosphate, alkylbenzene sulfonate, higher molecular weight fatty acid alkanolamide and a phosphate ester of an ethoxylated linear or branched chain aliphatic alcohol in the ranges of proportions as set forth hereafter.
Description
United States Patent Inventor Gerhart Karg Pompton Lakes, NJ. Appl. No. 839,670 Filed July 7, 1969 Patented Nov. 30, 1971 Assignee Witco Chemical Corporation New York, N.Y.
STABLE OPACIFIED LIQUID DETERGENT COMPOSITIONS 1 Claim, No Drawings U.S. Cl 252/529, 252/89, 252/539. 252/DlG. 14,252/DIG. 17 Int. Cl C1 1d 1/34, C 1 1d 3/066 Field of Search 252/89,
[52, I37, DIG. l7,DlGr 14 [56] References Cited UNITED STATES PATENTS 3,122,508 2/1964 Grifo etal 252/137X OTHER REFERENCES General Aniline Technical Bulletinl960#7543094 Mayhew et aL- Soap & Chemical Specialties- April 1962- p. 55- 58. 93. 95
Mayhew- Soap & Chemical Specialties- May 1962- p. 80. 81, I67, I96
Primary Examiner-Leon D. Rosdol Assistant Examiner-Dennis L. Albrecht A!rorne \'Wallenstein, Spangenberg. Hattis & Strampel STABLE OPACIFIED, LIQUID DETERGENT COMPOSITIONS This invention relates to opaque, stable liquid detergent compositions.
Opacified liquid detergent compositions, as opposed to clear or light colored solutions, have been found to be commercially advantageous because of their milk-white appearance, creamy consistency and relatively higher viscosity. In order to impart these characteristics to an aqueous solution of detergent ingredients, it has heretofore been the practice, generally, to add a polymeric latex opacifier to the composition. These conventional opacifiers are generally polymers and copolymers of styrene and other'substances. Representatives of such polystyrene opacifiers are the materials described in US. Pat. Nos. 3,326,807 and 3,382,177. While these polymers contribute to opacity, they have no influence upon the detergent properties of the liquid system.
In accordance with this invention, it has been discovered that stable, opaque liquid detergent compositions can be prepared by combining, as essential ingredients, from about 1 percent to 4 percent by weight of a phosphate ester of (a) an ethoxylated linear aliphatic alcohol having from eight to 18 carbon atoms, or of (b) ari ethoxylated branched chain aliphatic alcohol having from to carbon atoms, the aforesaid alcohols being ethoxylated with from about 2 to The aforesaid phosphate esters which are used to produce the stable opacified liquid detergent compositions of the present invention have been found to be essential to produce said compositions and to enable the higher molecular weight alkanolamides to coact in the compositions to function as opacifiers. Said alkanolamides also contribute significantly their heretofore known properties of surfactancy. Broadly speaking, the quantity of phosphate ester may vary from about 1 percent to 4 percent by weight. If the concentration is increased substantially about the 4 percent level, opacity is not obtained, while use of less than about 1 percent by weight phosphate ester will generally render the composition unstable. Particularly advantageously, the liquid detergent compositions of the present invention will contain from L5 percent to 2.5 percent, on the average about 2 percent, by weight phosphate ester.
The alkylbenzene or alkyltoluene sulfonates useful in preparing the compositions of the present invention are well about 20 mols of ethylene oxide prior to being converted into their phosphate esters, from about 3 percent to 6 percent by weight of an alkylbenzene or alkyl toluene sulfonate, wherein the alkyl group contains from eight to 18 carbon atoms from about l percent to 6 percent by weight higher molecular weight fatty acid alkanolamide, from about 1 percent to 10 percent by weight alkali metal polyphosphate, and the balance water. The aforesaid compositions are characterized by excellent stability and the ingredients utilized, which react to produce opacity, are not inactive, as are the polymer or copolymer opacifiers but, instead, contribute to the desired detergent properties of the liquid detergent compositions.
The phosphate esters of the ethoxylated linear C to C aliphatic alcohols and the phosphate esters of the ethoxylated branched chain C to C aliphatic alcohols, in which said alcohols have been adducted with from about 2 to about 20, particularly from 2 to 8 mols, of ethylene oxide per mol of said alcohol prior to being converted into their phosphate esters, are well known to the art and have found widespread use in various detergent compositions and other related applications such as are disclosed in many patents, among which are US. Pat. Nos. 3,004,056; 3,042,697; 3,033,889; 3,088,917 and 3,1 12,508. The phosphate esters used in preparing the detergent compositions of the present invention are preferably prepared by reacting 1 mol of P 0 with from 2 to 4.5 mols of the ethylene oxide adducts of the linear or branched chain aliphatic alcohol at a temperature in range of up to about l00 C., most advantageously in the range of about 50 to 65 C. Such phosphating procedures are disclosed for instance, in U.S. Pat. Nos. 2,441,295; 2,676,975; 2,701,958 and 3,004,056; Chemical Industries, Oct. 1942, pp. 516-521, 557; and Organo Phosphorus Compounds, John Wiley & Sons, New York, [950, pp. 220-223. The phosphate esters are advantageously used in the form of their water-soluble salts, preferably the sodium slats and the alkanolamine salts such as the diethanolamine and triethanolamine salts.
Illustrative of the linear and branched chain aliphatic alcohols used in the production of the phosphate esters are noctyl alcohol, n-nonyl alcohol, n-decyl alcohol, n-dodecyl alcohol, n-tridecyl alcohol, n-tetradecyl alcohol, n-pentadecyl alcohol, n-hexadecyl alcohol, oleyl alcohol, n-stearyl alcohol, Oxo alcohols such as Oxo-hexadecyl alcohol and Oxo-pentadecyl alcohol (and others as shown in U.S. Pat. No. 2,965,078), 2-ethyl octanol, and branched chain dodecanols, tetradecanols, hexadecanols, and octadecanols. Of especial usefulness are the phosphate esters of the 2 to 8 mol ethylene oxide adducts of Cm to C linear aliphatic alcohols and mixtures of two or more of said alcohols, in the form of their sodium and alkanolamine salts.
known to the at and may be generally described as those containing from eight to 18 carbon atoms in the alkyl group. For economical reasons they will generally be present as the sodium salt. They may also be present as the monovalent metal, ammonium or organic amine salt. Especially suitable is sodium dodecylbenzene sulfonate. The concentration may range from 3 percent to 6 percent by weight, preferably about 4 percent to 5 percent by weight, of the liquid detergent compositron.
The higher molecular weight fatty acid alkanolamide opacifier as used herein also acts, in its known manner, as a viscosity builder and foam stabilizer. The acyl radical of the alkanolamide is selected from the class of fatty acids having 10 to 18 carbon atoms, preferably 12 to 14 carbon atoms, and the alkanol group may have up to four carbon atoms in the case of monoalkanoamine derivatives and eight carbon atoms in the case of dialkanolamine derivatives. Especially suitable are the diethanolamides of C to C fatty acids such as lauric acid diethanolamide. Also illustrative of the said alkanolaides are oleic diethanolamide, tall oil fatty acid diethanolamide, linoleic acid diethanolamide, and the corresponding fatty acid amides of glycerol monoand di-amines, diisopropanolamine, aminoethylethanolamine, dibutanolamine and diisobutanolamine. These fatty acid alkanolamides may be prepared by various well-known techniques such as by condensing equimolar quantities of fatty acid with alkanolamine, or by condensing a molar excess of alkanolamine with fatty acid, or by reacting a fatty acid ester with alkanolamine, or by oxyalkylating, such as oxyethylating, the amide of the fatty acid. In general the fatty acid alkanolamide should be employed in amounts of about 1 percent to 4 percent and preferably about 2 percent to 3 percent, by weight of the liquid detergent composition.
The alkali metal polyphosphates useful in preparing the compositions of the present invention serve primarily as builders and concentration may vary from about I to l0 percent, preferably about 6 percent, by weight of the liquid detergent composition. Illustrative polyphosphates are sodium tripolyphosphate, tetrasodium pyrophosphate, trisodium phosphate and tetrapotassium pyrophosphate, tetrapotassium pyrophosphate being preferred.
The aqueous liquid detergent compositions of the present invention are prepared simply by combining the aforementioned ingredients with water at room temperature. No particular order of addition is necessary. The fmal preferred products exhibit a viscosity of approximately centipoises, which is most advantageous from a commercial standpoint for opalescent liquids.
The following examples are illustrative of the practice of the present invention but are not to be considered as limitative of its scope. All percentages stated are by weight.
EXAMPLE I An opaque system having a viscosity of approximately I00 centipoises was prepared by combining the following:
a. Phosphate ester oflincar aliphatic alcohol (mixture of about 80% C and about C alkyl radicals) adductcd with 6 mols ofcthylene oxide per mol of alcohol (sodium salt) 2.0% b. Sodium dodecylbenzene sulfonatc 4.5% c. Lauric acid diethanolamide 2.5% d. Tclrapotassium pyrophosphatc 6.0% c. Water 850% Samples observed over a 2-week period showed no loss of stability or opacity.
EXAMPLE ll Example I was repeated except that 1.5 percent of (a), 3.3 percent of(b), 1.8 percent of (c), 4.5 percent of(d) and 89.9 percent of (e) were combined, and again a stable, opaque composition resulted.
Certain supplemental ingredients for obtaining particular properties can, of course, be added to the stable opacified liquid detergent compositions of the present invention. Those which are used must, of course, be of such character and/or employed in such amounts as not adversely to affect the stability and opacity of the liquid detergent compositions of the present invention. Illustrative supplemental ingredients are perfumes, colors, chelating agents, corrosion inhibitors, deodorants, disinfectants, and the like.
It is important to the achievement of a stable, opacified liquid detergent composition pursuant to the present invention to utilize, in the manner and in the proportions described above, phosphate esters of ethoxylated linear C to C aliphatic alcohols and/or phosphate esters of ethoxylated branched chain C to C aliphatic alcohols. US. Pat. No. 3,l22,508, referred to above, discloses detergent compositions which contain phosphate esters, which may be those which are used in accordance with the present invention or which may be phosphate esters of ethoxylated higher alkyl phenols such as phosphated ethoxylated nonyl phenol, in admixture with dodecylbenzene sulfonates, higher fatty acid alkanolamides, and alkali metal polyphosphates. The said patent has as one of its objective, however, the preparation of heavy duty detergent compositions which are clear, homogeneous liquids. While said patent discloses opaque, very viscous compositions, they involve the utilization in the detergent compositions of large proportions of such ingredients as tall oil fatty acids and mineral oil. Such latter compositions are sharply distinguished from those made in accordance with the present invention. The said patent fails to provide any guide to or teaching of the production of the stable, opacified liquid detergent compositions of the present invention. In further regard thereto, it may be noted that, while US. Pat. No. 3,122,508 makes no distinction between the various phosphate esters of nonionic ethoxylated compounds so far as their functioning in the heavy duty detergent composition of said patent is concerned, it has been found that in order to obtain the stable, opacified liquid detergent compositions of the present invention, it is necessary to employ phosphate esters of ethoxylated linear C C aliphatic alcohols and/or phosphate esters of branched chain C -C aliphatic alcohols and proportions of the various ingredients specified above. If phosphate esters of ethoxylated higher alkyl phenols are used, such as ethoxylated nonyl phenols, in proportions of about 5 percent of the detergent composition, the resulting liquid detergent compositions are unstable. This is demonstrated by the following example III which was based upon example 77 of said patent, utilizing 5 percent of a phosphate ester of a 9 mol ethylene oxide adduct of nonyl phenol as the surfactant.
EXAMPLE [I] A mixture was prepared consisting of 5 percent phosphate ester ofa 9 mol ethylene oxide adduct of nonyl phenol, 5 percent sodium dodecylbenzene sulfonate, 1 percent lauroyl diethanolamide, 10 percent sodium tripolyphosphate and the balance water. The resulting composition was unstable and immediately broke down upon standing.
What is claimed is: I l. A stable, opacified liquid detergent composition having a
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83967069A | 1969-07-07 | 1969-07-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3624006A true US3624006A (en) | 1971-11-30 |
Family
ID=25280366
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US839670A Expired - Lifetime US3624006A (en) | 1969-07-07 | 1969-07-07 | Stable opacified liquid detergent compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3624006A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3951826A (en) * | 1972-07-25 | 1976-04-20 | Colgate-Palmolive Company | All purpose liquid detergent |
| US4070309A (en) * | 1976-07-27 | 1978-01-24 | The Procter & Gamble Company | Detergent composition |
| US4493782A (en) * | 1983-07-07 | 1985-01-15 | Amchem Products, Inc. | Cleansing compositions comprising ethoxylated alcohol monoesters of phosphoric acid |
| US4752411A (en) * | 1984-05-28 | 1988-06-21 | Cotelle, S.A. | Liquid composition for cleaning hard surfaces |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3122508A (en) * | 1960-07-28 | 1964-02-25 | Gen Aniline & Film Corp | Heavy duty detergent compositions |
-
1969
- 1969-07-07 US US839670A patent/US3624006A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3122508A (en) * | 1960-07-28 | 1964-02-25 | Gen Aniline & Film Corp | Heavy duty detergent compositions |
Non-Patent Citations (3)
| Title |
|---|
| General Aniline Technical Bulletin 1960 -7543 094 * |
| Mayhew et al. Soap & Chemical Specialties April 1962 p. 55 58, 93, 95 * |
| Mayhew Soap & Chemical Specialties May 1962 p. 80, 81, 167, 196 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3951826A (en) * | 1972-07-25 | 1976-04-20 | Colgate-Palmolive Company | All purpose liquid detergent |
| US4070309A (en) * | 1976-07-27 | 1978-01-24 | The Procter & Gamble Company | Detergent composition |
| FR2359893A1 (en) * | 1976-07-27 | 1978-02-24 | Procter & Gamble | LIQUID DETERGENT COMPOSITION FOR DELICATE WASHES |
| US4493782A (en) * | 1983-07-07 | 1985-01-15 | Amchem Products, Inc. | Cleansing compositions comprising ethoxylated alcohol monoesters of phosphoric acid |
| US4752411A (en) * | 1984-05-28 | 1988-06-21 | Cotelle, S.A. | Liquid composition for cleaning hard surfaces |
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