US3023168A - Heavy duty liquid detergent - Google Patents
Heavy duty liquid detergent Download PDFInfo
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- US3023168A US3023168A US776216A US77621658A US3023168A US 3023168 A US3023168 A US 3023168A US 776216 A US776216 A US 776216A US 77621658 A US77621658 A US 77621658A US 3023168 A US3023168 A US 3023168A
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- US
- United States
- Prior art keywords
- heavy duty
- triethanolamine
- composition
- liquid detergent
- sodium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003599 detergent Substances 0.000 title claims description 28
- 239000007788 liquid Substances 0.000 title claims description 13
- 239000000203 mixture Substances 0.000 claims description 74
- 239000004615 ingredient Substances 0.000 claims description 10
- 239000007900 aqueous suspension Substances 0.000 claims description 7
- 238000009472 formulation Methods 0.000 description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- 235000019832 sodium triphosphate Nutrition 0.000 description 21
- 229940077388 benzenesulfonate Drugs 0.000 description 20
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 17
- 239000001768 carboxy methyl cellulose Substances 0.000 description 17
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 17
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 16
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 16
- QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical compound CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 15
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- -1 triethanolamine alkyl benzene Chemical class 0.000 description 13
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 12
- 229910052700 potassium Inorganic materials 0.000 description 12
- 239000011591 potassium Substances 0.000 description 12
- 150000004996 alkyl benzenes Chemical class 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 150000001555 benzenes Chemical class 0.000 description 9
- 229940076134 benzene Drugs 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 239000000375 suspending agent Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 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 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
- 238000006277 sulfonation reaction Methods 0.000 description 3
- 150000003460 sulfonic acids Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000000271 synthetic detergent Substances 0.000 description 3
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 229920003064 carboxyethyl cellulose Polymers 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000019828 potassium polyphosphate Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 206010041232 sneezing Diseases 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229940023144 sodium glycolate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HIFJUMGIHIZEPX-UHFFFAOYSA-N sulfuric acid;sulfur trioxide Chemical compound O=S(=O)=O.OS(O)(=O)=O HIFJUMGIHIZEPX-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- JEJAMASKDTUEBZ-UHFFFAOYSA-N tris(1,1,3-tribromo-2,2-dimethylpropyl) phosphate Chemical compound BrCC(C)(C)C(Br)(Br)OP(=O)(OC(Br)(Br)C(C)(C)CBr)OC(Br)(Br)C(C)(C)CBr JEJAMASKDTUEBZ-UHFFFAOYSA-N 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
- C11D1/02—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
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
- C11D1/655—Mixtures of sulfonated products with alkylolamides of carboxylic acids
-
- 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
- This invention relates to heavy duty liquid detergent compositions and more particularly to heavy duty liquid detergent compositions containing sodium carboxymethylcellulose.
- an improved heavy duty liquid detergent composition can be produced if the triethanolamine salt of alkyl ben Zene sulfonic acids in which the alkyl group contains from 9 to 15 carbon atoms are combined with alkali metal tripolyphosphates in certain specific ratios and amounts and with sodium carboxymethylcellulose as a suspending agent.
- the improved heavy duty liquid detergent composition of this invention contains the following active ingredients in an aqueous medium with the range of amounts of each ingredient being expressed as weight percent based on the total weight of the composition including the water:
- the total quantity of potassium and sodium tripolyphosphate cannot exceed 25 weight percent of the total composition and that the sum of the quantities of triethanolamine alkyl benzene sulfonate and the laurylethanolarnide cannot exceed 25 weight percent of the composition.
- the ratio of the total quantity of the tripolyphosphate salts to the sum of the quantities of triethanolamine alkyl benzene sulfonate and laurylethanolamide should range between 0.8 to 1.0 and 1.25 to 1.0.
- compositions of this invention are suspensions instead of true solutions and thus have a cloudy appearance; however, when the concentrations and ratios of the ingredients are maintained Within the limits set forth, these formulations are completely homogeneous and stable, i.e. the ingredients do not settle and separate upon standing.
- tripolyphosphate may be the potassium salt because of the inherently greater solubility of this salt as compared with the sodium salt.
- the potassium tripolyphosphate may range from 10 to 25 weight percent.
- These tripolyphosphates have the general formula M P O wherein the M represents either sodium or potassium.
- the alkylated benzene sulfonic acids which are neutralized to produce the surface active agent of this composition contain from 9 to 15 carbon atoms in the alkyl group and may be produced by any one of a number of well known methods; for example, the alkylation may be accomplished by treating an excess of the benzene with a halogenated aliphatic hydrocarbon of 9 to 15 carbon atoms in the presence of a suitable alkylation catalyst of the Friedel-Crafts type, i.e. AlCl to obtain substantial yields of mono-alkylated benzenes.
- These monoalkylated benzenes may also be produced by alkylatiug benzene with an alcohol or mono-olefin of 9 to 15 carbon atoms using either sulfuric acid or a Friedel-Cnafts catalyst.
- a further method for producing the alkylated benzene or mixture of alkylated benzenes having 9 to 15 carbon atoms in the alkyl group is to polymerize an olefin such as propylene, or a gas stream containing propylene, with an acid catalyst such as a supported phosphoric acid catalyst or boron trifluoride catalyst at elevated temperatures and pressures according to well known methods thereby obtaining a mixture of propylene polymers which are fractionated to produce polymers of from 9 to 15 carbon atoms or intermediate fractions of a narrower molecular weight range.
- the benzene is then alkylated with the propylene polymer fraction in the presence of a Friedel-Crafts catalyst or with a sulfuric acid catalyst to produce the alkylated benzene or mixture of alkylated benzenes.
- alkylated benzene having an alkyl group of from 9 to 15 carbon atoms or a mixture of alkylated benzenes within this range is subjected to sulfonation with sulfuric not desirable.
- the benzene solution of the sulfonic acids is then extracted with a mixture of water and methanol or other lower alcohol to dissolve and remove the sulfonic acids from the benzene.
- the aqueous alcohol solution after separation from the benzene, is neutralized with triethanolamine and the resulting sulfonate solution evaporated to remove water and alcohol to produce a finished solution containing approximately 60 percent by weight of the triethanolamine alkyl benzene sulfonate. It is to be noted that in the foregoing composition the quantities of the triethanolamine alkyl benzene sulfonate are based on the anhydrous salt and not on the 60 percent solution which is produced commercially.
- a particularly preferred triethanolamine C -C alkyl benzene sulfonate has a major portion of the alkyl groups in the C -C range. More over, it has been found that only the triethanolamine salt is suitable for preparing the compositions of this invention.
- the alkali metal salts for example cannot be used since they are not sufliciently soluble to give a homogeneous composition.
- lau-rylethanolamide The function of the lau-rylethanolamide is that of a sudsing agent. Its use is not always required in certain applications of heavy duty detergents and accordingly it may be omitted entirely and replaced by an equal quantity of the triethanolamine alkyl benzene sulfonate. Laurylethanolamide is a commercially available material and it is this commercial material that is contemplated for use in this invention.
- the sodium carboxymethylcellulose suspending agent is the sodium salt of carboxymethylcellulose formed by the reaction of alkali cellulose with monochloroacetic acid.
- Sodium carboxymethylcellulose is available commercially in several viscosity types of the technical grade product and is generally a cream colored powder which dissolves readily in either hot or cold water to give a viscous colloidal solution.
- the viscosity types most suitable for use as suspending agents in the instant detergent formulation are the medium to high viscosity types particularly those which in 2 percent aqueous solution have a viscosity ranging between 50 and 2000 centipoises at C.
- Sodium carboxymethylcellulose viscosity types below the 50 centipoise lower limit do not produce suitable suspensions when combined with the other ingredients of the instant formulation since upon standing such formulations will stratify and settle. Viscosity types above the 2000 centipoise upper limit produce formulations which are too viscous for detergent formulations and hence are
- the commercial sodium carboxymethylcellulose product is from 65 to 70 percent pure. The remaining to percent of the product being various residual salts, principally sodium chloride with small amounts of sodium glycolate and sodium carbonate.
- the sodium carboxymethylcellulose to be used in this invention is the commercial product and the quantities set forth are based on the total commercial product containing the aforesaid impurities.
- quantities of the commercial sodium carboxymethylcellulose to be used in the compositions of this invention may range between 0.2 and 1.0 percent by weight based on the total weight of the composition, it has been found preferable to use about 0.5 weight percent since amounts in excess of this give very little added suspending action.
- naphtha or pine oils may be added to the formulation in amounts ranging up to 5 percent of the total solid content of the formulation. These materials are useful because of their solvent action.
- novel formulations of this invention may be prepared by a number of conventional methods; however, the preferred method is to add the tripolyphosphate salts to water and then heat the water to approximately 180 F. to 190 F. until they are dissolved.
- the solution is cooled to approximately F. and the triethanolamine alkyl benzene sulfonate and laurylethanolarnide are added.
- the powdered sodium carboxymethylcellulose is then added to the solution and put into colloidal suspension by means of high speed stirring with a propeller type mixer. If desired the sodium carboxymethylcellulose may be dissolved by adding the dry powder slowly to water heated to F. to F. and the resulting solution added to the aqueous polyphosphate-sulfonate-amide components.
- the preferred method is to add the dry powder by means of high speed mixing to the aqueous suspension of the other components of the formulation.
- Formulation E 95 so OOQQ 1 The triethanolamine salt at the mono-alkyl benzene sulfonic acids wherein the alkyl group contains between 9 and 15 carbon atoms with the major portion containing from 10 to 12 carbon atoms.
- EXAMPLE II A portion of formulation B of Example I was compared with a commercial standard alcohol sulfonate type built detergent composition by the same test methods as employed in Example I. The results of these tests are It will be seen from these data that the liquid detergent compositions of this invention are superior to commercial standard high detergency powdered formulations.
- EXAMPLE III Another detergent composition was prepared in accordance with the teachings of this invention to have the following composition in weight percent based on the total weight of the composition:
- the total quantity of the tripolyphosphate salts does not exceed 25.0 Weight percent
- the sum of the quantities of the triethanolarnine alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent
- the ratio of the total quantity of tripoly phosphate salts to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
- An improved heavy duty liquid detergent compostion consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
- the sum of the quantities of the triethanolamine C9-C15 alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent and the ratio of the quantity of potassium tripolyphosphate to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
- An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
- the total quantity of the tripolyphosphate salts does not exceed 25.0 weight percent
- the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent
- the ratio of the total quantity of tripolyphosphate salts to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
- An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
- An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
rte atent 3,023,168 Patented Feb. 27, 1962 This invention relates to heavy duty liquid detergent compositions and more particularly to heavy duty liquid detergent compositions containing sodium carboxymethylcellulose.
The development of heavy duty detergent compositions for cleaning heavily soiled cotton cloth materials has been marked by a number of successive improvements. One of the first and most important developments was the use of a class of surface active agents comprising the water soluble salts of the alkylated benzene sulfonic acids wherein the alkyl group contains from 9 to 15 carbon atoms and in particular the highly soluble triethanolamine salt of these sulfonic acids.
It was discovered subsequently that certain inorganic salts when combined with such synthetic detergents would improve their detergency properties and also effect savings in material costs. Some of the most important salts found suitable for this purpose were the alkali metal tripolyphosphates. The combination of the synthetic detergent and inorganic salts in the form of solid powders or flakes, termed built formulations, were found to be objectionable by the consumer, however, primarily for two reasons-one reason being that they were not readily soluble either in cold or hot water and required an appreciable time to go into solution, and the second reason being that the dust which arose from these flakes or powders was often times extremely irritating and caused violent sneezing by anyone standing nearby. In order to solve these problems aqueous solutions or suspensions of these built formulations were developed.
With the development of more accurate means of measuring detergency it was found that built detergent formulations were subject to another disadvantage-namely that after the dirt had been removed from the cloth by the detergent, frequently a portion of this dirt was redeposited in the cloth thus giving a gray appearance to the Washed cloth. It was found that when certain suspending agents were added to built detergent compositions that this redeposition of soil could be prevented in large measure thus eliminating the grayish appearance of the washed cloth.
A composition now has been found whereby a heavy duty built detergent formulation may be contained in an aqueous medium to avoid the disadvantages of the solid powdered formulations and which aqueous formulation also contains a suspending agent to provide the means of preventing redeposition of soil on the washing cloth.
It is an object of this invention to provide an improved heavy duty liquid detergent composition.
It is a further object of this invention to provide an improved heavy duty liquid detergent composition containing a built formulation of inorganic salts and a synthetic detergent together with a suspending agent.
Further objects of this invention will be apparent from the description and claims that follow.
In accordance with this invention it has been found that an improved heavy duty liquid detergent composition can be produced if the triethanolamine salt of alkyl ben Zene sulfonic acids in which the alkyl group contains from 9 to 15 carbon atoms are combined with alkali metal tripolyphosphates in certain specific ratios and amounts and with sodium carboxymethylcellulose as a suspending agent. The improved heavy duty liquid detergent composition of this invention contains the following active ingredients in an aqueous medium with the range of amounts of each ingredient being expressed as weight percent based on the total weight of the composition including the water:
Potassium tripolyphosphate 7.5-2.5 .0 Sodium tripolyphosphate 010.0 Triethanolamine C C alkyl benzene sulfonate 10.0-25.0 Laurylethanolamide 0- 5.0 Sodium carboxymethylcellulose 0.2- 1.0
It has also been found, however, that the total quantity of potassium and sodium tripolyphosphate cannot exceed 25 weight percent of the total composition and that the sum of the quantities of triethanolamine alkyl benzene sulfonate and the laurylethanolarnide cannot exceed 25 weight percent of the composition. Moreover, it has been found necessary to maintain the ratio of the total quantity of sodium and potassium tripolyphosphates to the sum of the quantities of sulfonate and amide within rather narrow limits in order to provide a stable homogeneous composition. The ratio of the total quantity of the tripolyphosphate salts to the sum of the quantities of triethanolamine alkyl benzene sulfonate and laurylethanolamide should range between 0.8 to 1.0 and 1.25 to 1.0.
The compositions of this invention are suspensions instead of true solutions and thus have a cloudy appearance; however, when the concentrations and ratios of the ingredients are maintained Within the limits set forth, these formulations are completely homogeneous and stable, i.e. the ingredients do not settle and separate upon standing.
It will be noted from the ranges which have been set forth that all of the tripolyphosphate may be the potassium salt because of the inherently greater solubility of this salt as compared with the sodium salt. In such compositions the potassium tripolyphosphate may range from 10 to 25 weight percent. These tripolyphosphates have the general formula M P O wherein the M represents either sodium or potassium.
The alkylated benzene sulfonic acids which are neutralized to produce the surface active agent of this composition contain from 9 to 15 carbon atoms in the alkyl group and may be produced by any one of a number of well known methods; for example, the alkylation may be accomplished by treating an excess of the benzene with a halogenated aliphatic hydrocarbon of 9 to 15 carbon atoms in the presence of a suitable alkylation catalyst of the Friedel-Crafts type, i.e. AlCl to obtain substantial yields of mono-alkylated benzenes. These monoalkylated benzenes may also be produced by alkylatiug benzene with an alcohol or mono-olefin of 9 to 15 carbon atoms using either sulfuric acid or a Friedel-Cnafts catalyst.
A further method for producing the alkylated benzene or mixture of alkylated benzenes having 9 to 15 carbon atoms in the alkyl group is to polymerize an olefin such as propylene, or a gas stream containing propylene, with an acid catalyst such as a supported phosphoric acid catalyst or boron trifluoride catalyst at elevated temperatures and pressures according to well known methods thereby obtaining a mixture of propylene polymers which are fractionated to produce polymers of from 9 to 15 carbon atoms or intermediate fractions of a narrower molecular weight range. The benzene is then alkylated with the propylene polymer fraction in the presence of a Friedel-Crafts catalyst or with a sulfuric acid catalyst to produce the alkylated benzene or mixture of alkylated benzenes.
The alkylated benzene having an alkyl group of from 9 to 15 carbon atoms or a mixture of alkylated benzenes within this range is subjected to sulfonation with sulfuric not desirable.
acid of 98 to 100 percent concentration at temperatures of 150 F. to 160 F. using about one volume of acid to one volume of the alkylated benzene mixture or more preferably it is subjected to sulfonation with percent fuming sulfuric acid at somewhat lower temperatures, i.e. 135 F. with about the same ratio of acid to hydro carbon. When the sulfonation reaction is completed the reaction mixture is diluted with a solvent such as benzene or hexane or mixtures thereof and the spent sulfuric acid is settled out leaving the alkylated benzene sulfonic acids in solution in the immiscible benzene layer. The benzene solution of the sulfonic acids is then extracted with a mixture of water and methanol or other lower alcohol to dissolve and remove the sulfonic acids from the benzene. The aqueous alcohol solution, after separation from the benzene, is neutralized with triethanolamine and the resulting sulfonate solution evaporated to remove water and alcohol to produce a finished solution containing approximately 60 percent by weight of the triethanolamine alkyl benzene sulfonate. It is to be noted that in the foregoing composition the quantities of the triethanolamine alkyl benzene sulfonate are based on the anhydrous salt and not on the 60 percent solution which is produced commercially. A particularly preferred triethanolamine C -C alkyl benzene sulfonate has a major portion of the alkyl groups in the C -C range. More over, it has been found that only the triethanolamine salt is suitable for preparing the compositions of this invention. The alkali metal salts for example cannot be used since they are not sufliciently soluble to give a homogeneous composition.
The function of the lau-rylethanolamide is that of a sudsing agent. Its use is not always required in certain applications of heavy duty detergents and accordingly it may be omitted entirely and replaced by an equal quantity of the triethanolamine alkyl benzene sulfonate. Laurylethanolamide is a commercially available material and it is this commercial material that is contemplated for use in this invention.
The sodium carboxymethylcellulose suspending agent is the sodium salt of carboxymethylcellulose formed by the reaction of alkali cellulose with monochloroacetic acid. Sodium carboxymethylcellulose is available commercially in several viscosity types of the technical grade product and is generally a cream colored powder which dissolves readily in either hot or cold water to give a viscous colloidal solution. The viscosity types most suitable for use as suspending agents in the instant detergent formulation are the medium to high viscosity types particularly those which in 2 percent aqueous solution have a viscosity ranging between 50 and 2000 centipoises at C. Sodium carboxymethylcellulose viscosity types below the 50 centipoise lower limit do not produce suitable suspensions when combined with the other ingredients of the instant formulation since upon standing such formulations will stratify and settle. Viscosity types above the 2000 centipoise upper limit produce formulations which are too viscous for detergent formulations and hence are The commercial sodium carboxymethylcellulose product is from 65 to 70 percent pure. The remaining to percent of the product being various residual salts, principally sodium chloride with small amounts of sodium glycolate and sodium carbonate. The sodium carboxymethylcellulose to be used in this invention is the commercial product and the quantities set forth are based on the total commercial product containing the aforesaid impurities. Although quantities of the commercial sodium carboxymethylcellulose to be used in the compositions of this invention may range between 0.2 and 1.0 percent by weight based on the total weight of the composition, it has been found preferable to use about 0.5 weight percent since amounts in excess of this give very little added suspending action.
In addition to the ingredients which have been set forth for this formulation, naphtha or pine oils may be added to the formulation in amounts ranging up to 5 percent of the total solid content of the formulation. These materials are useful because of their solvent action.
The novel formulations of this invention may be prepared by a number of conventional methods; however, the preferred method is to add the tripolyphosphate salts to water and then heat the water to approximately 180 F. to 190 F. until they are dissolved. The solution is cooled to approximately F. and the triethanolamine alkyl benzene sulfonate and laurylethanolarnide are added. The powdered sodium carboxymethylcellulose is then added to the solution and put into colloidal suspension by means of high speed stirring with a propeller type mixer. If desired the sodium carboxymethylcellulose may be dissolved by adding the dry powder slowly to water heated to F. to F. and the resulting solution added to the aqueous polyphosphate-sulfonate-amide components. This method is not preferred, however, since the quantity of water required for solution may be too great to permit producing a finished formulation having the desired concentrations. Accordingly, therefore, the preferred method is to add the dry powder by means of high speed mixing to the aqueous suspension of the other components of the formulation.
The following examples will serve to illustrate certain specific embodiments of the invention and to demonstrate the usefulness of the formulations of the invention as heavy duty detergents.
EXAMPLE 1 Two separate formulations were prepared having the composition shown in weight percent based on the total weight of the composition:
Formulation E 95 so OOQQ 1 The triethanolamine salt at the mono-alkyl benzene sulfonic acids wherein the alkyl group contains between 9 and 15 carbon atoms with the major portion containing from 10 to 12 carbon atoms.
The detergency and foam of these compositions were measured by the use of the Atlas Launderometer, in the manner described in Soap and Sanitary Chemicals, September 1948, page 42. This test procedure as described by S. Machlis and E. B. Michaels was modified by using cotton cloth in place of the glass fiber and maintaining a temperature of 120 F. during the washing cycle. Aqueous detergent concentrations of 0.2 percent, 0.3 percent and 0.5 percent of the total solids were employed in the test comparisons. A detailed description of the testing device is found in the Technical Manual and Yearbook of the American Association of Textile Chemists and Colorists for 1947-48 on page 98. In these tests detergencies are compared by means of the reflectance of washed cotton cloth, with a high reflectance (indicated by a large number of reflectometer units) corresponding to a high detergency value. The results are set forth in Table I below:
Table 1 Formula tion A B Detergent Reflect- Foam Reflect- Foam concentration ometer height ometer height in weight units in it units 111 as" percent solids umts units These data demonstrate the marked superiority of the sodium carboxymethylcellulose containing compositions of this invention as compared with the same detergent composition without the suspending agent.
EXAMPLE II A portion of formulation B of Example I was compared with a commercial standard alcohol sulfonate type built detergent composition by the same test methods as employed in Example I. The results of these tests are It will be seen from these data that the liquid detergent compositions of this invention are superior to commercial standard high detergency powdered formulations.
EXAMPLE III Another detergent composition was prepared in accordance with the teachings of this invention to have the following composition in weight percent based on the total weight of the composition:
Formulation, C:
Potassium tripolyphosphate 14.5 Sodium tripolyphosphate 10.0 Triethanolamine alkyl benzene sulfonate 20.0 Laurylethanolamide 5.0
Sodium carboxymethylcellulose Tl1e same material as employed in Example I.
Duplicate tests were made by the method of Example I to compare this formulation with the commercial standard of Example II. The results of these tests are set forth in Table III.
Table III Formulation Commercial 0 Standard Detergent con- Reflee- Foam Reflec- Foam eentration in tometer height tometer height weight percent units in 9% units in 3 8 solids units units 151: test 70 24 80 22 2nd test 70 24 78 20 Potassium tripolyphosphate 7.5-25.0 Sodium tripolyphosphate 0-10.0 Triethanolamine C -C alkyl benzene sulfonate 10.0-25.0 Laurylethanolamide 0-5.0 Sodium carboxymethylcellulose 0.2-1.0
wherein the total quantity of the tripolyphosphate salts does not exceed 25.0 Weight percent, the sum of the quantities of the triethanolarnine alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent and the ratio of the total quantity of tripoly phosphate salts to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
2. An improved heavy duty liquid detergent compostion consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
Potassium tripolyphosphate 10.0-25.0 Triethanolamine (I -C alkyl benzene sulfonate 10.0-25.0
Laurylethanolarnide 0-5.0 Sodium carboxyethylcellulose 0.2-1.0
wherein the sum of the quantities of the triethanolamine C9-C15 alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent and the ratio of the quantity of potassium tripolyphosphate to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
3. An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
Potassium tripolyphosphate -1 7.5-25.0 Sodium tripolyphosphate 0-10.0 Triethanolamine 0 -0 alkyl benzene sulfonate 10.0-25.0 Laurylethanolamide 0-5.0 Sodium carboxymethylcellulose 0.5
wherein the total quantity of the tripolyphosphate salts does not exceed 25.0 weight percent, the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide does not exceed 25.0 weight percent and the ratio of the total quantity of tripolyphosphate salts to the sum of the quantities of the triethanolamine alkyl benzene sulfonate and the laurylethanolamide ranges between 0.8 to 1.0 and 1.25 to 1.0.
4. An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
Potassium tripolyphosphate 19.5 Sodium tripolyphosphate 5.0 Triethanolamine C -C alkyl benzene sulfonate 20.0 Laurylethanolamide 5.0 Sodium carboxymethylcellulose 0.5
5. An improved heavy duty liquid detergent composition consisting essentially of a stable aqueous suspension of the following ingredients in weight percent based on the total weight of the composition:
Potassium tripolyphosphate 14.5 Sodium tripolyphosphate 10.0 Triethanolamine C -C alkyl benzene sulfonate 20.0 Laurylethanolamide 5.0 Sodium carboxyrnethylcellulose 0.5
References Cited in the file of this patent UNITED STATES PATENTS 2,560,839 Ayo et al July 17, 1951 2,581,677 Machlis et al Jan. 8, 1952 2,607,740 Vitale Aug. 19, 1952 2,859,182 Carroll Nov. 4, 1958 2,920,045 Hearn et al. Jan. 5, 1960 FOREIGN PATENTS 217,693 Australia Oct. 3, 1958 OTHER REFERENCES Properties and Uses of Hercules CMC pub. by Hercules Powder Co., recd. Jan. 25, 1952, page 12.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,023,,168 February 27 1962 Robert B. Doan It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 6, line 12, for "carboxyethylcellulose" read carboxymethylcellulose Signed and sealed this 12th day of June 1962.
(SEAL) Attest:
ERNEST w. SWIDER DAVID LADD Attesting Officer Commissioner of Patents
Claims (1)
1. AN IMPROVED HEAVY DUTY LIQUID DETERGENT COMPOSITION CONSISTING ESSENTIALLY OF A STABLE AQUEOUS SUSPENSION OF THE FOLLOWING INGREDIENTS IN WEIGHT PERCENT BASED ON THE TOTAL WEIGHT OF THE COMPOSITION:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US776216A US3023168A (en) | 1958-11-25 | 1958-11-25 | Heavy duty liquid detergent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US776216A US3023168A (en) | 1958-11-25 | 1958-11-25 | Heavy duty liquid detergent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3023168A true US3023168A (en) | 1962-02-27 |
Family
ID=25106785
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US776216A Expired - Lifetime US3023168A (en) | 1958-11-25 | 1958-11-25 | Heavy duty liquid detergent |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3023168A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3232878A (en) * | 1960-03-02 | 1966-02-01 | Lever Brothers Ltd | Liquid detergent compositions |
| US3236592A (en) * | 1961-07-24 | 1966-02-22 | Monsanto Co | Process for the production of alkali metal diimidotriphosphates |
| US3360476A (en) * | 1964-03-19 | 1967-12-26 | Fmc Corp | Liquid heavy duty cleaner and disinfectant |
| US3449430A (en) * | 1960-07-14 | 1969-06-10 | Henkel & Cie Gmbh | Amino oxides |
| DE1467704B1 (en) * | 1965-12-09 | 1971-01-21 | Witco Chemical Corp | Process for the production of aqueous high-performance detergents and cleaning agents |
| FR2390499A1 (en) * | 1977-05-10 | 1978-12-08 | Colgate Palmolive Co | CLEANING LIQUID COMPOSITION FOR HARD SURFACES |
| US4548727A (en) * | 1983-10-06 | 1985-10-22 | The Drackett Company | Aqueous compositions containing stabilized enzymes |
| US6631682B2 (en) * | 2001-06-13 | 2003-10-14 | Telluckram Maharaj | Non-aqueous cleaning system and method for a printing press recirculation system |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2560839A (en) * | 1947-07-24 | 1951-07-17 | Gen Aniline & Film Corp | Detergent composition |
| US2581677A (en) * | 1952-01-08 | Phosphate detergent composition in | ||
| US2607740A (en) * | 1950-05-03 | 1952-08-19 | Colgate Palmolive Peet Co | Liquid anionic-dialkylolamide detergent composition |
| US2859182A (en) * | 1956-11-02 | 1958-11-04 | Lever Brothers Ltd | Heavy duty liquid detergent composition |
| US2920045A (en) * | 1955-09-06 | 1960-01-05 | Colgate Palmolive Co | Heavy duty liquid detergent compositions |
-
1958
- 1958-11-25 US US776216A patent/US3023168A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2581677A (en) * | 1952-01-08 | Phosphate detergent composition in | ||
| US2560839A (en) * | 1947-07-24 | 1951-07-17 | Gen Aniline & Film Corp | Detergent composition |
| US2607740A (en) * | 1950-05-03 | 1952-08-19 | Colgate Palmolive Peet Co | Liquid anionic-dialkylolamide detergent composition |
| US2920045A (en) * | 1955-09-06 | 1960-01-05 | Colgate Palmolive Co | Heavy duty liquid detergent compositions |
| US2859182A (en) * | 1956-11-02 | 1958-11-04 | Lever Brothers Ltd | Heavy duty liquid detergent composition |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3232878A (en) * | 1960-03-02 | 1966-02-01 | Lever Brothers Ltd | Liquid detergent compositions |
| US3449430A (en) * | 1960-07-14 | 1969-06-10 | Henkel & Cie Gmbh | Amino oxides |
| US3236592A (en) * | 1961-07-24 | 1966-02-22 | Monsanto Co | Process for the production of alkali metal diimidotriphosphates |
| US3360476A (en) * | 1964-03-19 | 1967-12-26 | Fmc Corp | Liquid heavy duty cleaner and disinfectant |
| DE1467704B1 (en) * | 1965-12-09 | 1971-01-21 | Witco Chemical Corp | Process for the production of aqueous high-performance detergents and cleaning agents |
| FR2390499A1 (en) * | 1977-05-10 | 1978-12-08 | Colgate Palmolive Co | CLEANING LIQUID COMPOSITION FOR HARD SURFACES |
| US4548727A (en) * | 1983-10-06 | 1985-10-22 | The Drackett Company | Aqueous compositions containing stabilized enzymes |
| US6631682B2 (en) * | 2001-06-13 | 2003-10-14 | Telluckram Maharaj | Non-aqueous cleaning system and method for a printing press recirculation system |
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