US2543744A - Nonfoaming soap composition - Google Patents
Nonfoaming soap composition Download PDFInfo
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 - US2543744A US2543744A US659661A US65966146A US2543744A US 2543744 A US2543744 A US 2543744A US 659661 A US659661 A US 659661A US 65966146 A US65966146 A US 65966146A US 2543744 A US2543744 A US 2543744A
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 - US
 - United States
 - Prior art keywords
 - water
 - mixture
 - soap
 - glycol ether
 - carbon atoms
 - 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
 
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- 239000000203 mixture Substances 0.000 title claims description 38
 - 239000000344 soap Substances 0.000 title claims description 29
 - 239000003599 detergent Substances 0.000 claims description 11
 - 150000002989 phenols Chemical class 0.000 claims description 7
 - 229920001521 polyalkylene glycol ether Polymers 0.000 claims description 7
 - 229910052783 alkali metal Inorganic materials 0.000 claims description 6
 - 150000001340 alkali metals Chemical class 0.000 claims description 6
 - 238000005187 foaming Methods 0.000 claims description 6
 - 150000001875 compounds Chemical class 0.000 claims description 4
 - OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
 - 150000001298 alcohols Chemical class 0.000 claims description 3
 - 229920001515 polyalkylene glycol Polymers 0.000 claims 1
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
 - -1 mercapto compounds Chemical class 0.000 description 15
 - 239000006260 foam Substances 0.000 description 14
 - 229920000233 poly(alkylene oxides) Polymers 0.000 description 13
 - 239000002202 Polyethylene glycol Substances 0.000 description 11
 - 229920001223 polyethylene glycol Polymers 0.000 description 11
 - MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 10
 - 125000004432 carbon atom Chemical group C* 0.000 description 8
 - 125000005529 alkyleneoxy group Chemical group 0.000 description 5
 - 238000004851 dishwashing Methods 0.000 description 5
 - 239000000271 synthetic detergent Substances 0.000 description 5
 - ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
 - 150000001896 cresols Chemical class 0.000 description 4
 - 239000003921 oil Substances 0.000 description 4
 - 229910052700 potassium Inorganic materials 0.000 description 4
 - 239000011591 potassium Substances 0.000 description 4
 - 239000011734 sodium Substances 0.000 description 4
 - 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 3
 - ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
 - 239000002253 acid Substances 0.000 description 3
 - 150000007513 acids Chemical class 0.000 description 3
 - 125000000217 alkyl group Chemical group 0.000 description 3
 - 235000014113 dietary fatty acids Nutrition 0.000 description 3
 - 229930195729 fatty acid Natural products 0.000 description 3
 - 239000000194 fatty acid Substances 0.000 description 3
 - 150000004665 fatty acids Chemical class 0.000 description 3
 - 239000007788 liquid Substances 0.000 description 3
 - 235000019198 oils Nutrition 0.000 description 3
 - 229910052708 sodium Inorganic materials 0.000 description 3
 - DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
 - NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 2
 - PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
 - 150000001336 alkenes Chemical class 0.000 description 2
 - 125000002947 alkylene group Chemical group 0.000 description 2
 - 239000007864 aqueous solution Substances 0.000 description 2
 - 125000003438 dodecyl group Chemical group [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])* 0.000 description 2
 - 239000004088 foaming agent Substances 0.000 description 2
 - 125000005456 glyceride group Chemical group 0.000 description 2
 - 229910052751 metal Inorganic materials 0.000 description 2
 - 239000002184 metal Substances 0.000 description 2
 - 125000001117 oleyl 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])=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])[H] 0.000 description 2
 - 239000003208 petroleum Substances 0.000 description 2
 - 239000000243 solution Substances 0.000 description 2
 - 125000001424 substituent group Chemical group 0.000 description 2
 - 239000001993 wax Substances 0.000 description 2
 - ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
 - CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical group CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
 - QMLBSKYNWCPRQV-UHFFFAOYSA-N 2,3-bis(3-methylbutyl)phenol Chemical compound CC(C)CCC1=CC=CC(O)=C1CCC(C)C QMLBSKYNWCPRQV-UHFFFAOYSA-N 0.000 description 1
 - PTMRDOLOEDPHLB-UHFFFAOYSA-N 2,3-dipentylphenol Chemical class CCCCCC1=CC=CC(O)=C1CCCCC PTMRDOLOEDPHLB-UHFFFAOYSA-N 0.000 description 1
 - HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
 - BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
 - QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
 - RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
 - QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
 - 235000013162 Cocos nucifera Nutrition 0.000 description 1
 - 244000060011 Cocos nucifera Species 0.000 description 1
 - SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
 - GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
 - KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
 - BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
 - WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
 - 239000003513 alkali Substances 0.000 description 1
 - 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
 - 230000002152 alkylating effect Effects 0.000 description 1
 - 150000001412 amines Chemical class 0.000 description 1
 - 125000004429 atom Chemical group 0.000 description 1
 - 229910052799 carbon Inorganic materials 0.000 description 1
 - 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
 - 239000004359 castor oil Substances 0.000 description 1
 - 235000019438 castor oil Nutrition 0.000 description 1
 - 229930003836 cresol Natural products 0.000 description 1
 - 230000007423 decrease Effects 0.000 description 1
 - 125000002704 decyl group Chemical group [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])* 0.000 description 1
 - 230000001419 dependent effect Effects 0.000 description 1
 - ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
 - 239000012153 distilled water Substances 0.000 description 1
 - 238000002474 experimental method Methods 0.000 description 1
 - 239000003925 fat Substances 0.000 description 1
 - 235000019197 fats Nutrition 0.000 description 1
 - 239000007789 gas Substances 0.000 description 1
 - ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
 - 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
 - 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
 - 238000005984 hydrogenation reaction Methods 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
 - 125000005608 naphthenic acid group Chemical group 0.000 description 1
 - 125000001400 nonyl 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])[H] 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
 - ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 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
 - 150000002894 organic compounds Chemical class 0.000 description 1
 - IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
 - 125000000913 palmityl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
 - 238000005504 petroleum refining Methods 0.000 description 1
 - 229920001281 polyalkylene Polymers 0.000 description 1
 - 229940096992 potassium oleate Drugs 0.000 description 1
 - MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
 - 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
 - WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
 - 229960003656 ricinoleic acid Drugs 0.000 description 1
 - FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
 - 150000003839 salts Chemical class 0.000 description 1
 - 239000008234 soft water Substances 0.000 description 1
 - KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
 - 125000002948 undecyl 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])[H] 0.000 description 1
 - 235000015112 vegetable and seed oil Nutrition 0.000 description 1
 - 235000019871 vegetable fat Nutrition 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
 - C11D10/00—Compositions of detergents, not provided for by one single preceding group
 - C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
 - C11D10/045—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
 
 - 
        
- 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
 - C11D1/66—Non-ionic compounds
 - C11D1/72—Ethers of polyoxyalkylene glycols
 
 
Definitions
- the present invention relates to an improved detergent composition which, on mixing with water, produces little or no foam and is thus particularly adapted for use in mechanical dishwashing machines.
 - the present invention is directed to a novel detergent composition which comprises a mixture in suitable proportions of a non-ionic water-soluble synthetic detergent containing a polyalkylene oxide group with a soap.
 - non-ionic water-soluble synthetic detergents containing a polyalkylene oxide group which are employed as one component of the novel composition of the present invention are the derivatives of a water-insoluble organic compound selected from the group consisting of hvdroxyl, carboxyl, amino and mercapto compounds containing at least'fi carbon atoms and 1' reactive hydrogen atom andwhich derivatives contain a polyalkyleneoxy radical with a su'flicie'nt riumber of alkyleneoxy groups (at least 4) to impart water' solubility thereto.-
 - the compounds of this type which" are described in U. 8. Patents Nos.
 - 1,970,578 to Schoeller-et al., 2,174,761 to Schuette et al. and 2,213,477 to Steindorff et al. are broadly suitable for use in the present invention.
 - the polyalkylene oxide derivatives of -water-insoluble higher aliphatic alcohols and the 'polyalkylene oxide derivatives As examples of these preferred polyalkylene.
 - the polyalkylene oxide derivatives may be -mentioned the polyalkylene oxide derivatives of aliphatic alcohols containing from 12 to 18 carbon atomsfor example, the polyalkylene oxide derivativesof such alcohols as lauryl, oleyl, cetYL-octadecyl and the like, or mixtures of the same-for instance, ,the alcohols obtainable by hydrogenation of the fatty acids or glycerides present in animal and vegetable fats, oils and waxes such as cocoanut oil,
 - suitable phenolic compounds containing one or more alkyl substituents in which the total number of carbon atoms in the'alkyl substituents is between 6, and 18, may be mentioned isomeric, dibutyl and diamyl phenols and cresols, normal, secondaryor tertiary isomeric heptyl, octyl, nonyl, ,decyl, undecyl, dodecyl, tetradecyl, cetyl, oleyl, octodecyl, isooctyl and the like phenols and ,cresols.
 - products obtained by condensing oleflnes containing from 3 m5 carbon atoms, such as propylene, butylene and amylene it is desirable to produce the dialkyl substituted phenols while in the case of products obtained by condensing a phenol or cresol with an olefine containing 8 or more carbon atoms, the mono-substituted derivatives are preferred.
 - Particularly desirable derivatives can be obtained from the phenols and cresols containing a substituent derived from olefines containing 8 to 12 carbon atoms, such as di-isobutylene and other alkylenes, as nonylene, decylene, undecylene-and dodecylene.
 - the polyalkyleneoxy radical present in the substituent must contain a sufficient number of alkyleneoxy groups to impart water solubility to the polyalkylene oxide derivative employed in the invention. At least fouralkyleneoxy groups are necessary toimpart water solubilit and generally 10 to 30 or more such groups should be presentforbestresults-
 - ausual water -soluble soap such as the'a lkall metal, sodium "or potassium, ammonium 1 and amine, such as monoethanolamine,'diethanolamine and trlethanolamine, salts of such acids as .lauric, oleic, ,palmitic, steariailinoleic, ricinoleic acid, and the like, or mixtures of such acids such as may be obtained-from'animalorvegetable :glycerides; also soaps of; naphthenic acids.
 - the optimum proportion of soap to the polyalkylene oxide derivative depends on the derivative, itself and also on the type of soap employed. I have found that in general, compositions containing from 90% to 40% of the polyalkylene oxide derivative and from to 60% of soap are satisfactory and produce little foam and any foam which is produced is very quick-breaking. The optimum proportions within this range for any specific polyallgvlene oxide derivative and soap may readily be determined by those skilled in the art by simple experiment. My preferred range of proportions of polyalkylene oxide derivative to soap is within the range of 2:1 to 4:1.
 - the degree of foam produced is somewhat dependent on the character of the water employed. In distilled water the degree of foam reduction is somewhat less than in water of 50 to 300 P. P. M. hardness. It may therefore be advantageous, particularly in the case of compositions intended for use in areas having relatively soft water, to incorporate in the composition of the present invention a minor amount of an alkaline earth metal compound which imparts hardness to the water, for instance, in an amount of from 0.01% to 10%. It has also been found, as would be expected, that in the presence of small amounts of fats or oils such as would be washed off the dishes, the amount of foam formed decreases still further. The details of the present invention will be apparent to those skilled in the art after consideration of the following specific examples:
 - Example 1 66 parts of a water-soluble polyethylene glycol ether of diisoamyl phenol were mixed with 89 parts of an aqueous liquid potassium soap containing 38% soap (34 parts 100% soap) known as Hollingshead liquid soap. This mixture was employed in an electric dishwashing machine and performed satisfactorily as a good detergent.
 - Example 2 17.5 parts of the polyethylene glycol ether of isooctyl phenol in which the isooctyl group was the dilsobutyl radical were mixed with 7.5 parts of sodium oleate. The mixture was then diluted with 75 parts of water to give an aqueous solution having a 25% concentration of soap-polyethylene glycol ether. On using this mixture in an electric dishwasher, it performed satisfactorily and foamed very little.
 - Example 4 25 parts of the polyethylene glycol ether of oleyl alcohol were mixed with 7.5 parts of potassium oleate and 75 parts of water. This mixture was employed in an electric dishwasher in the usual manner and performed satisfactorily.
 - a non-foaming detergent composition consisting essentially of a mixture in proportions of from about 1:2 to about 1:4 of, respectively, an alkali metal soap and a water-soluble synthetic non-ionic surface active polyalkylene glycol ether of a compound selected from the group consisting of long chain aliphatic alcohols containing at least twelve carbon atoms and alkyl phenols containing at least six alkyl carbon atoms, said polyalkylene glycol ether radical containing at least four alkyleneoxy groups.
 - a non-foaming detergent composition consisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali metal soap and a water-soluble non-ionic synthetic surface active polyalkylene glycol ether of a long chain aliphatic alcohol said polyalkylene glycol ether radical containing at least 4 alkyleneoxy groups.
 - a non-foaming detergent composition consisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali metal soap and a water-soluble non-ionic surfact active polyethylene glycol ether of a long chain aliphatic alcohol said polyethylene glycol ether radical containing at least 4 ethanoxy groups.
 - a non-foaming detergent composition con- REFERENCES CITED sisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali' metal soap and a water-soluble synthetic nonionic surface active polyalkylene glycol ether of
 - the following references are of record in the file of this patent:
 
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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)
 
Description
Patented Mar. 6, 1951 NONFOAMING SOAP COMPOSITION Arthur L. Fox, Easton, Pa., assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application April 4, 1946, T 
Serial No. 659,661 1. 
g Claims. 
The present invention relates to an improved detergent composition which, on mixing with water, produces little or no foam and is thus particularly adapted for use in mechanical dishwashing machines. 
 The advent of commercial dishwashers has necessitated the use in them of detergents which produce little or no foam, as the presence of foam reduces very markedly the efficienc of these dishwashers. Thus, the amount of foam produced by the usual alkali metal soaps of higher fatty acids makes these soaps unsuitable for use in mechanical dishwashers. Also certain synthetic detergents such as the synthetic detergents containing a polyalkylene oxide group, produce too much foam to be satisfactory for use in dishwashing machines. 
 I have made the surprising discovery that if synthetic detergents containing a polyalkylene oxide group, which themselves are foaming agents, are mixed with water-soluble soaps of higher fatty acids, which are also foaming agents, the amount of foam produced by the mixture is far less than that produced by either component alone, while the detergent action of the mixture remains excellent, so that the novel mixture is suitable for use in dishwashing machines. 
 The present invention, therefore, is directed to a novel detergent composition which comprises a mixture in suitable proportions of a non-ionic water-soluble synthetic detergent containing a polyalkylene oxide group with a soap. 
 The types of non-ionic water-soluble synthetic detergents containing a polyalkylene oxide group which are employed as one component of the novel composition of the present invention are the derivatives of a water-insoluble organic compound selected from the group consisting of hvdroxyl, carboxyl, amino and mercapto compounds containing at least'fi carbon atoms and 1' reactive hydrogen atom andwhich derivatives contain a polyalkyleneoxy radical with a su'flicie'nt riumber of alkyleneoxy groups (at least 4) to impart water' solubility thereto.- The compounds of this type which" are described in U. 8. Patents Nos. 
1,970,578 to Schoeller-et al., 2,174,761 to Schuette et al. and 2,213,477 to Steindorff et al. are broadly suitable for use in the present invention. I particularlyprefer, however, the polyalkylene oxide derivatives of -water-insoluble higher aliphatic alcohols and the 'polyalkylene oxide derivatives As examples of these preferred polyalkylene. 
oxide derivatives may be -mentioned the polyalkylene oxide derivatives of aliphatic alcohols containing from 12 to 18 carbon atomsfor example, the polyalkylene oxide derivativesof such alcohols as lauryl, oleyl, cetYL-octadecyl and the like, or mixtures of the same-for instance, ,the alcohols obtainable by hydrogenation of the fatty acids or glycerides present in animal and vegetable fats, oils and waxes such as cocoanut oil, 
castor oil and the like. As examples of suitable phenolic compounds containing one or more alkyl substituents in which the total number of carbon atoms in the'alkyl substituents is between 6, and 18, may be mentioned isomeric, dibutyl and diamyl phenols and cresols, normal, secondaryor tertiary isomeric heptyl, octyl, nonyl, ,decyl, undecyl, dodecyl, tetradecyl, cetyl, oleyl, octodecyl, isooctyl and the like phenols and ,cresols. I particularly prefer the polyalkylene oxide derivatives of secondary and tertiary alkyl substituted phenols obtained by condensing oleflnesof the type obtained from petroleum refinery gases with phenols or cresols. In the case of products obtained by condensing oleflnes containing from 3 m5 carbon atoms, such as propylene, butylene and amylene, it is desirable to produce the dialkyl substituted phenols while in the case of products obtained by condensing a phenol or cresol with an olefine containing 8 or more carbon atoms, the mono-substituted derivatives are preferred. Particularly desirable derivatives can be obtained from the phenols and cresols containing a substituent derived from olefines containing 8 to 12 carbon atoms, such as di-isobutylene and other alkylenes, as nonylene, decylene, undecylene-and dodecylene. 
 The polyalkyleneoxy radical present in the substituent must contain a sufficient number of alkyleneoxy groups to impart water solubility to the polyalkylene oxide derivative employed in the invention. At least fouralkyleneoxy groups are necessary toimpart water solubilit and generally 10 to 30 or more such groups should be presentforbestresults- The other essential component of'the/novel composition of the present inventionisias stated, ausual water -soluble soap, such as the'a lkall metal, sodium "or potassium, ammonium 1 and amine, such as monoethanolamine,'diethanolamine and trlethanolamine, salts of such acids as .lauric, oleic, ,palmitic, steariailinoleic, ricinoleic acid, and the like, or mixtures of such acids such as may be obtained-from'animalorvegetable :glycerides; also soaps of; naphthenic acids. and synthetic acids obtained. byoxidation of -,petroleum oils and waxes or rosin soaps and the like. I have found that potassium soaps such as are sold in the form of liquid soaps generally give somewhat less foam. However. sodium soaps result in a very marked decrease-in the amount of foam and due to the fact that they are somewhat less expensive may be employed to good advantage in practicing the present invention. 
 The optimum proportion of soap to the polyalkylene oxide derivative depends on the derivative, itself and also on the type of soap employed. I have found that in general, compositions containing from 90% to 40% of the polyalkylene oxide derivative and from to 60% of soap are satisfactory and produce little foam and any foam which is produced is very quick-breaking. The optimum proportions within this range for any specific polyallgvlene oxide derivative and soap may readily be determined by those skilled in the art by simple experiment. My preferred range of proportions of polyalkylene oxide derivative to soap is within the range of 2:1 to 4:1. 
 I have also found that the degree of foam produced is somewhat dependent on the character of the water employed. In distilled water the degree of foam reduction is somewhat less than in water of 50 to 300 P. P. M. hardness. It may therefore be advantageous, particularly in the case of compositions intended for use in areas having relatively soft water, to incorporate in the composition of the present invention a minor amount of an alkaline earth metal compound which imparts hardness to the water, for instance, in an amount of from 0.01% to 10%. It has also been found, as would be expected, that in the presence of small amounts of fats or oils such as would be washed off the dishes, the amount of foam formed decreases still further. The details of the present invention will be apparent to those skilled in the art after consideration of the following specific examples: 
Example 1 66 parts of a water-soluble polyethylene glycol ether of diisoamyl phenol were mixed with 89 parts of an aqueous liquid potassium soap containing 38% soap (34 parts 100% soap) known as Hollingshead liquid soap. This mixture was employed in an electric dishwashing machine and performed satisfactorily as a good detergent. 
Only a small amount of foam was formed and this broke quickly. 
 A similar mixture was made up and diluted with 245 parts of water, making a concentration of the soap-polyethylene glycol ether. This aqueous solution was somewhat easier to handle and on using it in an electric dishwasher, it performed satisfactorily. 
Example 2 17.5 parts of the polyethylene glycol ether of isooctyl phenol in which the isooctyl group was the dilsobutyl radical were mixed with 7.5 parts of sodium oleate. The mixture was then diluted with 75 parts of water to give an aqueous solution having a 25% concentration of soap-polyethylene glycol ether. On using this mixture in an electric dishwasher, it performed satisfactorily and foamed very little. 
 Similar results were obtained when the polyethylene glycol ether of 3-methy1-4.6-dl-tertiary butyl phenol, nonvl phenol and a mixture of alkyl phenols obtained by alkylating phenol with an olefin fraction consisting of a mixture of olefins containing from 8 to 12 carbon atoms, obtained in petroleum refining, were employed in place of the polyethylene glycol ether of isooctyl phenol. 
Example 4 25 parts of the polyethylene glycol ether of oleyl alcohol were mixed with 7.5 parts of potassium oleate and 75 parts of water. This mixture was employed in an electric dishwasher in the usual manner and performed satisfactorily. 
 WhLe a substantial amount of water was present in each of the mixtures described in the foregoing examples, its purpose was principally to produce a solution which could be readily poured from a bottle into an electric dishwashing machine in economical amounts. If desired, however, the mixture of a polyethanoxy derivative or other polyalkyleneoxy derivative and soap need not be diluted with water before using, since sodium and potassium soaps are compatible with polyaikeneoxy derivatives and form solutions therewith The mixture is quite readily water soluble and, if desired, may be prepared in an anhydrous or substantially anhydrous condition and added to water only when used. 
 It will also be noted that in the foregoing specific examples the polyethanoxy derivatives of various organic hydrorw compounds have been specified as illustrative of one of the components of the composition of the present invention, since these. derivatives are at present commercially available. However, the corresponding derivatives of other alkylene oxides, such as propylene oxide, butylene oxide and the like, have similar properties and may be substituted for the specific derivatives mentioned as illustrations in these examples. 
I claim: 
 1. A non-foaming detergent composition consisting essentially of a mixture in proportions of from about 1:2 to about 1:4 of, respectively, an alkali metal soap and a water-soluble synthetic non-ionic surface active polyalkylene glycol ether of a compound selected from the group consisting of long chain aliphatic alcohols containing at least twelve carbon atoms and alkyl phenols containing at least six alkyl carbon atoms, said polyalkylene glycol ether radical containing at least four alkyleneoxy groups. 
 2. A non-foaming detergent composition consisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali metal soap and a water-soluble non-ionic synthetic surface active polyalkylene glycol ether of a long chain aliphatic alcohol said polyalkylene glycol ether radical containing at least 4 alkyleneoxy groups. 
 3. A non-foaming detergent composition consisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali metal soap and a water-soluble non-ionic surfact active polyethylene glycol ether of a long chain aliphatic alcohol said polyethylene glycol ether radical containing at least 4 ethanoxy groups. 
 5 2,643,744 6 4. A non-foaming detergent composition con- REFERENCES CITED sisting essentially of a mixture, in proportions of from 1:2 to 1:4, of, respectively, an alkali' metal soap and a water-soluble synthetic nonionic surface active polyalkylene glycol ether of The following references are of record in the file of this patent: 
5 UNITED STATES PATENTS an alkyl phenol containing at least six alkyl car- N b Na t bon atoms said polyalkylene glycol ether radical 1,970,573 s u Aug 21 9 containing at least 4 alkyleneoxy groups. 2,158,957 Coleman May 16, 1939 5. A non-foaming detergent composition con- 2,174,761 Schuette et a1. Oct. 31, 1939 sisting essentially of a mixture, in proportions '10 2,213,477 Steindorff et al. Sept. 3, 1940 of from 1:2 to 1:4, of, respectively, an alkali metal soap and a water-soluble synthetic non- FOREIGN PATENTS ionic surface active polyethylene glycol ether Number Country Date of an alkyl phenol containing .at least six alkyl 704,862 Germany April, 1941 carbon atoms said polyethylene glycol ether radi- 16 cal containing at least 4'ethanoxy groups. 
ARTHUR L. FOX. 
Claims (1)
1. A NON-FOAMING DETERGENT COMPOSITION CONSISTING ESSENTIALLY OF A MIXTURE IN PROPORTIONS OF FROM ABOUT 1:2 TO ABOUT 1:4 OF, RESPECTIVELY, AN. ALKALI METAL SOAP AND A WATER-SOLUBLE SYNTHETIC NON-IONIC SURFACE ACTIVE POLYALKYLENE GLYCOL CONSISTOF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF LONG CHAIN ALIPHATIC ALCOHOLS CONTAINING AT LEAST TWELVE CARBON ATOMS AND ALKYL PHENOLS CONTAINING AT LEAST SIX ALKYL CARBON ATOMS, SAID POLYALKYLENE GLYCOL ETHER RADICAL CONTAINING AT LEAST FOUR ALKYLENEOXY GROUPS.
    Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| US659661A US2543744A (en) | 1946-04-04 | 1946-04-04 | Nonfoaming soap composition | 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| US659661A US2543744A (en) | 1946-04-04 | 1946-04-04 | Nonfoaming soap composition | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| US2543744A true US2543744A (en) | 1951-03-06 | 
Family
ID=24646266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| US659661A Expired - Lifetime US2543744A (en) | 1946-04-04 | 1946-04-04 | Nonfoaming soap composition | 
Country Status (1)
| Country | Link | 
|---|---|
| US (1) | US2543744A (en) | 
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US2595300A (en) * | 1950-12-23 | 1952-05-06 | Wilson & Co Inc | Soap compositions and soap flakes | 
| US2702277A (en) * | 1955-02-15 | Detergent composition | ||
| US2875153A (en) * | 1955-04-27 | 1959-02-24 | Colgate Palmolive Co | Detergent compositions | 
| DE1058966B (en) * | 1953-09-15 | 1959-06-11 | Siemens Elektrogeraete Gmbh | Drum washing machine with a device for measuring the amount of foam | 
| US2913416A (en) * | 1955-03-04 | 1959-11-17 | Rohm & Haas | Liquid detergent composition | 
| US3010907A (en) * | 1957-04-09 | 1961-11-28 | Pennsalt Chemicals Corp | Alkaline cleaning compositions | 
| US3170915A (en) * | 1960-04-11 | 1965-02-23 | Monsanto Co | Sucrose ethers | 
| US3240819A (en) * | 1960-02-17 | 1966-03-15 | Monsanto Co | Ethenoxy-substituted alkanols | 
| US3304330A (en) * | 1961-03-17 | 1967-02-14 | Procter & Gamble | Tertiary phosphine oxide compounds | 
| US3907702A (en) * | 1971-07-29 | 1975-09-23 | Colgate Palmolive Co | Process for making a free flowing soap-nonionic detergent | 
| US4285826A (en) * | 1980-04-14 | 1981-08-25 | Armour-Dial, Inc. | Toilet soap bars imparting improved moisturing and skin feel characteristics | 
| US4695284A (en) * | 1984-06-15 | 1987-09-22 | Lever Brothers Company | Cool water fabric washing process using a particulate detergent containing a nonionic and a fatty acid builder salt | 
| US4975218A (en) * | 1988-04-29 | 1990-12-04 | Chesebrough-Ponds's USA Co. | Aqueous soap composition containing ethoxylated nonionic surfactants | 
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries | 
| US2158957A (en) * | 1937-02-20 | 1939-05-16 | Dow Chemical Co | Hydroxy-alkyl ethers of substituted phenols | 
| US2174761A (en) * | 1935-04-13 | 1939-10-03 | Ig Farbenindustrie Ag | Condensation products derived from hydroxy compounds and method of producing them | 
| US2213477A (en) * | 1935-12-12 | 1940-09-03 | Gen Aniline & Film Corp | Glycol and polyglycol ethers of isocyclic hydroxyl compounds | 
| DE704862C (en) * | 1938-12-18 | 1941-04-09 | I G Farbenindustrie Akt Ges | Anti-foam agent | 
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- 1946-04-04 US US659661A patent/US2543744A/en not_active Expired - Lifetime
 
 
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries | 
| US2174761A (en) * | 1935-04-13 | 1939-10-03 | Ig Farbenindustrie Ag | Condensation products derived from hydroxy compounds and method of producing them | 
| US2213477A (en) * | 1935-12-12 | 1940-09-03 | Gen Aniline & Film Corp | Glycol and polyglycol ethers of isocyclic hydroxyl compounds | 
| US2158957A (en) * | 1937-02-20 | 1939-05-16 | Dow Chemical Co | Hydroxy-alkyl ethers of substituted phenols | 
| DE704862C (en) * | 1938-12-18 | 1941-04-09 | I G Farbenindustrie Akt Ges | Anti-foam agent | 
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US2702277A (en) * | 1955-02-15 | Detergent composition | ||
| US2595300A (en) * | 1950-12-23 | 1952-05-06 | Wilson & Co Inc | Soap compositions and soap flakes | 
| DE1058966B (en) * | 1953-09-15 | 1959-06-11 | Siemens Elektrogeraete Gmbh | Drum washing machine with a device for measuring the amount of foam | 
| US2913416A (en) * | 1955-03-04 | 1959-11-17 | Rohm & Haas | Liquid detergent composition | 
| US2875153A (en) * | 1955-04-27 | 1959-02-24 | Colgate Palmolive Co | Detergent compositions | 
| US3010907A (en) * | 1957-04-09 | 1961-11-28 | Pennsalt Chemicals Corp | Alkaline cleaning compositions | 
| US3240819A (en) * | 1960-02-17 | 1966-03-15 | Monsanto Co | Ethenoxy-substituted alkanols | 
| US3170915A (en) * | 1960-04-11 | 1965-02-23 | Monsanto Co | Sucrose ethers | 
| US3304330A (en) * | 1961-03-17 | 1967-02-14 | Procter & Gamble | Tertiary phosphine oxide compounds | 
| US3907702A (en) * | 1971-07-29 | 1975-09-23 | Colgate Palmolive Co | Process for making a free flowing soap-nonionic detergent | 
| US4285826A (en) * | 1980-04-14 | 1981-08-25 | Armour-Dial, Inc. | Toilet soap bars imparting improved moisturing and skin feel characteristics | 
| US4695284A (en) * | 1984-06-15 | 1987-09-22 | Lever Brothers Company | Cool water fabric washing process using a particulate detergent containing a nonionic and a fatty acid builder salt | 
| US4975218A (en) * | 1988-04-29 | 1990-12-04 | Chesebrough-Ponds's USA Co. | Aqueous soap composition containing ethoxylated nonionic surfactants | 
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