US2793132A - Metallic soaps of fatty acids and alphahydroxy alkanoic acids - Google Patents
Metallic soaps of fatty acids and alphahydroxy alkanoic acids Download PDFInfo
- Publication number
- US2793132A US2793132A US419611A US41961154A US2793132A US 2793132 A US2793132 A US 2793132A US 419611 A US419611 A US 419611A US 41961154 A US41961154 A US 41961154A US 2793132 A US2793132 A US 2793132A
- Authority
- US
- United States
- Prior art keywords
- grams
- solution
- soap
- acid
- hydroxy
- 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
- 239000000344 soap Substances 0.000 title claims description 48
- 239000002253 acid Substances 0.000 title claims description 29
- 235000014113 dietary fatty acids Nutrition 0.000 title claims description 16
- 229930195729 fatty acid Natural products 0.000 title claims description 16
- 239000000194 fatty acid Substances 0.000 title claims description 16
- 150000004665 fatty acids Chemical class 0.000 title claims description 15
- 150000007513 acids Chemical class 0.000 title description 8
- 239000000203 mixture Substances 0.000 claims description 23
- 229910052751 metal Inorganic materials 0.000 claims description 21
- 239000002184 metal Substances 0.000 claims description 21
- 229910052782 aluminium Inorganic materials 0.000 claims description 17
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 17
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 239000000243 solution Substances 0.000 description 39
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- GHPVDCPCKSNJDR-UHFFFAOYSA-N 2-hydroxydecanoic acid Chemical compound CCCCCCCCC(O)C(O)=O GHPVDCPCKSNJDR-UHFFFAOYSA-N 0.000 description 17
- 238000004078 waterproofing Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 239000008149 soap solution Substances 0.000 description 11
- 239000012530 fluid Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229940037003 alum Drugs 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 229940116226 behenic acid Drugs 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000002023 wood Substances 0.000 description 5
- 239000004566 building material Substances 0.000 description 4
- 239000004567 concrete Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 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
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004568 cement Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- YDZIJQXINJLRLL-UHFFFAOYSA-N 2-hydroxydodecanoic acid Chemical compound CCCCCCCCCCC(O)C(O)=O YDZIJQXINJLRLL-UHFFFAOYSA-N 0.000 description 2
- DJDGGSPGQFGVMX-UHFFFAOYSA-N 3-ethyl-2-hydroxyheptanoic acid Chemical compound CCCCC(CC)C(O)C(O)=O DJDGGSPGQFGVMX-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229940061720 alpha hydroxy acid Drugs 0.000 description 2
- 150000001280 alpha hydroxy acids Chemical class 0.000 description 2
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 2
- 229940063655 aluminum stearate Drugs 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 150000002169 ethanolamines Chemical class 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- 229960001763 zinc sulfate Drugs 0.000 description 2
- 229910000368 zinc sulfate Inorganic materials 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- ZQWVBNYTPYVDQZ-UHFFFAOYSA-N 2-ethyl-3-hydroxyhexanoic acid Chemical compound CCCC(O)C(CC)C(O)=O ZQWVBNYTPYVDQZ-UHFFFAOYSA-N 0.000 description 1
- WTJGBZUNSVJMNV-UHFFFAOYSA-N 2-hydroxy-4,6,6-trimethylheptanoic acid Chemical compound CC(C)(C)CC(C)CC(O)C(O)=O WTJGBZUNSVJMNV-UHFFFAOYSA-N 0.000 description 1
- JKRDADVRIYVCCY-UHFFFAOYSA-N 2-hydroxyoctanoic acid Chemical compound CCCCCCC(O)C(O)=O JKRDADVRIYVCCY-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- VSYMNDBTCKIDLT-UHFFFAOYSA-N [2-(carbamoyloxymethyl)-2-ethylbutyl] carbamate Chemical compound NC(=O)OCC(CC)(CC)COC(N)=O VSYMNDBTCKIDLT-UHFFFAOYSA-N 0.000 description 1
- 238000003811 acetone extraction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- -1 greases Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N hexane carboxylic acid Natural products CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- 239000010514 hydrogenated cottonseed oil Substances 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-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
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/01—Saturated compounds having only one carboxyl group and containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
Definitions
- This invention relates to polyvalent metal soaps capable of forming fluid solutions in organic solvents when dissolved therein in amounts up to 30% and to coating, impregnating, sealing and water-proofing compositions containing them. More particularly, the invention is directed to mixed polyvalent metal salts wherein both an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and a higher fatty acid of about to 22 carbon atoms are combined into an aluminum, zinc, calcium or magnesium soap composition possessing the property of forming low viscosity solutions in volatile hydrocarbon and chlorinated hydrocarbon solvents. The invention includes the soaps themselves and impregnating and water-proofing compositions containing them.
- the coating and waterproofing properties of the polyvalent metal soaps has been well recognized and their application of these and similar uses is now firmly established.
- the most convenient method of applying such polyvalent metal soaps to various surfaces such as wood, paper, cloth, leather, masonry, wall-board, and the like, has been to make up a solution thereof in an organic solvent and to spray the same on the surface to be treated.
- Various volatile organic solvents have been used in the preparation of the polyvalent metal soap solutions, the more common ones including the aliphatic and aromatic hydrocarbons and their halogenated derivatives.
- a principal object of the present invention is to overcome the foregoing defects and other disadvantages.
- Another principal'object of the present invention is to provide an improved, relatively highly concentrated polyvalent metal soap solution of low viscosity.
- a further principal object of the'present invention is to provide an improved coating and waterproofing composition.
- a still further principal object of the invention is to provide fluid polyvalent metal soap solutions containing up to 30% polyvalent metal soap concentrations.
- an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms in conjunction with the fatty acid, or equivalent acid, used in the formation of the polyvalent metal soap. It has been found that the use of the alpha-hydroxy alkanoic acid remarkably reduces the viscosity of the resulting commercial compositions whereby readily sprayable solutions containing high percentages of metallic soaps can be prepared.
- alkanoic acids of the present invention would include as illustrative, but not as limitative, the following: alpha-hydroxy octanoic acid; alpha-hydroxy decanoic acid; alpha-hydroxy dodecanoic acid; 2-hydroxy- 4-methyl-6,6'-dimethyl heptanoic acid; 3-ethyl-2-hydroxy heptanoic acid; 6-niethyl-2-hydroxy heptanoic acid; etc. It is to be particularly noted that in all these acids, the hydroxy group'is 'attacii'ed to the carbon atom adjacent the carboxyl group.
- any suitable water-insoluble polyvalent metal soap of a higher fatty acid or 'similar' acid'rnay be'e'm'ployed examples include the polyvalent metal soaps of fatty acidscoirtainin'g'fromfl0 to 22 or more carbon atoms, su cha's for 'xa'mple, the aluminum, calcium, magnesium, zinc, etc., soapsfof capric, lauric, myristic, palmitic, stearic, ara'chidic, behenic, oleic, palmitoleic, lauroleic, myristoleic, linoleic, ricinoleic, and the like acids?" Mixtures of acids such as hydrogenated fish oil fatty acids, hydrogenated cottonseed oil fatty acids, hydrogenated tallow fatty acids, hydrogenated soya bean fatty acids, and the like, are similarly usable. While any suitable polyvalent metal soap may be used in accordance with the
- Example 1 A soap solution was prepared from grams of 2- hydroxy-4-methyl-6,6-dimethyl heptanoic acid, 400 grams of Hydrofol 51 (having the approximate composition: 7.5% C14; 33.3% C16; 27.2% C13; 17.2% C20; 14.8% C22; 4.3% unsaturated acids); 'grarns of 98% sodium hydroxide and 1500 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 270 grams of alum and 2000 grams of water was added thereto. The aluminum soap precipitate which formed was filtered, washed on a laboratory crock and dried overnight at a temperature of approximately 75 C. The dried material was ground in a 3 inicropulverizer at a speed of approximately 4000 R. P. M. through a V8 inch r. p. screen.
- a 20% solution in commercial toluene was found to be very fluid at room temperature and could be easily sprayed on fabrics, paper, wood shingles, concrete and other building materials as a waterproofing agent therefor.
- a 20% solution in Stoddard solvent was very fluid and could be readily sprayed on textile materials, masonry, wall-board, asbestos, rockwool, and the like.
- the material was also readily soluble in benzene, xylene, carbon tetrachloride and similar aliphatic and aromatic hydrocarbons and their halogenated derivatives.
- Example 2 A soap solution was prepared from 200 grams of alpha hydroxy decanoic acid; 800 grams of Hydrofol 45 (1.5% C14; 28.0% C15; 70.5% Cm; 6.0% unsaturated acids), 175 grams of 98% sodium hydroxide and 15,000 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 400 grams of zinc sulfate and 500 grams of water was added thereto. The zinc soap precipitate which formed was filtered, washed on a laboratory c'i'ock and dried overnight at a temperature of approximately 75 C. The dried product was ground in a micro-pulverizer at 4000 R. P. M. through a $43 inch r. p. screen. A laboratory analysis of the zinc soap indicated the following:
- Example 3 A soap solution was prepared from 200 grams of alphahydroxy decanoic acid, 800 grams of Hydrofol 51, 212
- the solubility of the aluminum soap was investigated further as follows: It was found to be clear, thin and readily sprayable in 15 solutions of petroleum ether, carbon tetrachloride, trichlorobenzene, cyclohexane, and other similar solvents.
- Example 4 A soap solution was prepared from 100 grams of alpha-hydroxy decanoic acid, 17 grams of 98% sodium hydroxide and 4000 grams of water. This solution was heated to a temperature of approximately C. and to it was added a second solution comprising 45 grams of zinc sulfate and 2500 grams of water. The zinc soap precipitate which formed was filtered, washed and dried overnight in an oven maintained at a temperature of approximately 75 C. A laboratory analysis of the zinc soap indicated the following: 14.95% ash; 13.37% washed ash; 1.58% water-soluble ash; and 1.6 mgm. KOH acid value.
- Example 5 The following materials were employed to prepare the aluminum soap of alpha-hydroxy decanoic acid and mixed fatty acids:
- the alum solution was added to the sodium soap.
- the sodium soap solution was added to the alum solution; and in the third method; the sodium soap solution and the alum solution were added simultaneously to the precipitation tank.
- Example 6 The procedures set forth in Example 1 were followed substantially as set forth therein with the exception that a single pressed stearic acid was substituted for the mixed fatty acids used therein The resulting aluminum soap was very similar to that derived from Example 1.
- a soap solution was prepared from 100 grams of alphahydroxy capric acid, 400 grams of Hydrofol 405, 100 grams of 98% sodium hydroxide and 16,000 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 540 grams of alum and 500 grams of water was added thereto. The aluminum soap precipitate which formed was filtered and washed and then dried overnight at a temperature of about 70 C. A laboratory analysis of the dried material indicated the following: 9.13% ash; 8.8% washed ash; 0.33% water-soluble ash; and 18.7 mgm. KOH acid value. A 10% solution in commercial toluene was used as a waterproofing agent and was sprayed on cotton, wool, asbestos, and like textile materials. A 15% solution in commercial toluene was applied to wood shingles, concrete, cement, masonry, and like building materials.
- Example 8 A soap solution was prepared from 400 grams of Emersol 110 (a mixture of C12 to C18 fatty acids), 100 grams of 2-ethyl-3-hydroxy hexanoic acid, 100 grams of 98% sodium hydroxide and 16,000 grams of water. This solution was heated to a temperature of approximately 75 C. and to it was added a second solution comprising 270 grams of alum and 1000 grams of water. The aluminum soap which precipitated was filtered and Washed and then dried overnight in an oven at a temperature of approximately 80 C. Laboratory analysis indicated the following: 9.57% ash; 8.71% washed ash; 0.86% watersoluble ash; 2.26% moisture and volatile matter at C. and 28.6 mgm. KOH acid value. 10% waterproofing solutions in commercial toluene were applied to concrete, cement, masonry, and like building materials.
- Emersol 110 a mixture of C12 to C18 fatty acids
- 2-ethyl-3-hydroxy hexanoic acid 100 grams of 98% sodium hydroxide and 16,000 grams of
- the quantity by weight of alpha-hydroxy alkanoic acids used in proportion to the total acid in the preparation of the soap may be varied within wide As little as 1% or less by weight of the alpha-hydroxy acid may be used and as high as up to 100% may be used, although the higher cost of such compositions renders them commercially and economically impracticable as coating, impregnating, sealing, or waterproofing agents. In general, it may be stated that compositions containing from about 5% to about 30% by weight of the alpha-hydroxy alkanoic acid, are economically and industrially most desirable.
- these metallic soaps are soluble up to as high as 30% in a very wide range of solvents without becoming too thick or gelatinous to use readily. It was observed that in many cases, aluminum stearate, when used without the addition of the alpha-hydroxy acid, could not form the thin and clear concentrated solutions which were sprayable, which solutions were made possible by the addition of the hydroxy acids during the soap formation.
- This viscosity reducing characteristic created by the use of such an acid is also of value in decreasing the viscosity, when desired, of other compounded compositions such as greases, waxes, soaps, paints, varnishes, plastics, cosmetics, adhesives, rubber and the like.
- a soap composition comprising metal soaps of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and 95% to 70% by weight of a fatty acid containing from to 22 carbon atoms, said metal being selected from the group consisting of aluminum, zinc, calcium and magnesium.
- composition according to claim 1 wherein the alpha-hydroxy alkanoic acid is alpha-hydroxy decanoic acid.
- composition according to claim 1 wherein the alpha-hydroxy alkanoic acid is 2-hydroxy-3-ethyl heptanoic acid.
- a soap composition comprising an aluminum soap of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and 95% to by weight of a fatty acid containing from 10 to 22 carbon atoms.
- a water-proofing composition comprising a volatile hydrocarbon solvent containing up to 30% of a metal soap of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and to 70% by weight of a fatty acid containing from 10 to 22 carbon atoms, said metal being selected from the group consisting of aluminum, zinc, calcium and magnesium.
- a water-proofing composition according to claim 5 wherein the alpha-hydroxy alkanoic acid is alpha-hydroxy decanoic acid.
- a water-proofing composition according to claim 5 wherein the alpha-hydroxy alkanoic acid is Z-hydroxy- 3-ethyl-heptanoic acid.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
United States Patent lVIETALLIC SOAPS 0F FATTY ACIDS AND ALPHA- HY DROXY ALKANOIC A'CIDS Gerald M. Davis, Clark, Arthur L. Fowler, Jr., Metuchen, and Maynard B. Winston, Woodbridge, N. J., assignors to American Cyanamid Company, New York, N. Y., a corporation of Maine No Drawing. Application March 29, 1954, Serial No. 419,611
7 Claims. (Cl. 106-243) This invention relates to polyvalent metal soaps capable of forming fluid solutions in organic solvents when dissolved therein in amounts up to 30% and to coating, impregnating, sealing and water-proofing compositions containing them. More particularly, the invention is directed to mixed polyvalent metal salts wherein both an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and a higher fatty acid of about to 22 carbon atoms are combined into an aluminum, zinc, calcium or magnesium soap composition possessing the property of forming low viscosity solutions in volatile hydrocarbon and chlorinated hydrocarbon solvents. The invention includes the soaps themselves and impregnating and water-proofing compositions containing them.
The coating and waterproofing properties of the polyvalent metal soaps, better known in the art as metallic soaps, has been well recognized and their application of these and similar uses is now firmly established. The most convenient method of applying such polyvalent metal soaps to various surfaces such as wood, paper, cloth, leather, masonry, wall-board, and the like, has been to make up a solution thereof in an organic solvent and to spray the same on the surface to be treated. Various volatile organic solvents have been used in the preparation of the polyvalent metal soap solutions, the more common ones including the aliphatic and aromatic hydrocarbons and their halogenated derivatives.
While the foregoing practice has found some success in the art, many difficulties have been encountered, inasmuch as when more than about 2% or 3% of some soaps are dissolved in some organic solvents, the resulting mass either thickens to such an extent or actually forms a solidified gel, as to render it substantially useless as a sprayable coating or waterproofing composition. While the thickened mass or solidified gel can be heated to render it less viscous, the application thereof in a heated state is occasionally dangerous due to the volatile and inflammable solvents used and is usually unsatisfactory for most purposes. Furthermore, the application of solutions containing only from 2% to 3% of the polyvalent metal soap is also highly commercially im practical in view of the low concentration of the solids in the solution, which factor additionally increases the cost of the product due to the large amounts of solvent necessary.
Various efforts have been made to solve the foregoing problems by increasing the soap concentration without undesirably decreasing the fluidity of the resulting solution. Peptizing agents having an acidic nature, such as acetic acid, phenol, tartaric acid, oxalic acid, and the like, have been used to increase the soap concentration in a solvent mixture without affecting the fluidity thereof. This proposal has proven to be undesirable commercially in view of the corrosive character imparted to the composition by such acidic agents. Another elfort has involved the use of the ethanolamines, or the ethanolamine salts of the higher fatty acids, for the purpose of increasing the concentration of polyvalent metal soap 2,793,132 Patented May 21, 1957 solution. A solutionproduced according to this teaching has not found toowidespread success.
A principal object of the present invention is to overcome the foregoing defects and other disadvantages.
Another principal'object of the present invention is to provide an improved, relatively highly concentrated polyvalent metal soap solution of low viscosity.
A further principal object of the'present invention is to provide an improved coating and waterproofing composition.
A still further principal object of the invention is to provide fluid polyvalent metal soap solutions containing up to 30% polyvalent metal soap concentrations.
It has now been found that the foregoing and other objects of the present invention may be achieved by the use of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms, in conjunction with the fatty acid, or equivalent acid, used in the formation of the polyvalent metal soap. It has been found that the use of the alpha-hydroxy alkanoic acid remarkably reduces the viscosity of the resulting commercial compositions whereby readily sprayable solutions containing high percentages of metallic soaps can be prepared.
Representative alkanoic acids of the present invention would include as illustrative, but not as limitative, the following: alpha-hydroxy octanoic acid; alpha-hydroxy decanoic acid; alpha-hydroxy dodecanoic acid; 2-hydroxy- 4-methyl-6,6'-dimethyl heptanoic acid; 3-ethyl-2-hydroxy heptanoic acid; 6-niethyl-2-hydroxy heptanoic acid; etc. It is to be particularly noted that in all these acids, the hydroxy group'is 'attacii'ed to the carbon atom adjacent the carboxyl group.
In the preparation of the composition of the invention, any suitable water-insoluble polyvalent metal soap of a higher fatty acid or 'similar' acid'rnay be'e'm'ployed. Examples ar ues soaps include the polyvalent metal soaps of fatty acidscoirtainin'g'fromfl0 to 22 or more carbon atoms, su cha's for 'xa'mple, the aluminum, calcium, magnesium, zinc, etc., soapsfof capric, lauric, myristic, palmitic, stearic, ara'chidic, behenic, oleic, palmitoleic, lauroleic, myristoleic, linoleic, ricinoleic, and the like acids?" Mixtures of acids such as hydrogenated fish oil fatty acids, hydrogenated cottonseed oil fatty acids, hydrogenated tallow fatty acids, hydrogenated soya bean fatty acids, and the like, are similarly usable. While any suitable polyvalent metal soap may be used in accordance with the invention, the aluminum soaps are preferred, and particularly aluminumstearate, palmitate or other saturated soaps of this'metal.
The invention will be further described in greater detail by the following specific examples. It should be understood, however, that although these examples may set forth in particular detail some of the more specific features of the invention, they are given primarily for purposes of illustration of preferred preparations and evaluations and the invention in its broader aspects is I not to be construed as limited thereto.
Example 1 A soap solution was prepared from grams of 2- hydroxy-4-methyl-6,6-dimethyl heptanoic acid, 400 grams of Hydrofol 51 (having the approximate composition: 7.5% C14; 33.3% C16; 27.2% C13; 17.2% C20; 14.8% C22; 4.3% unsaturated acids); 'grarns of 98% sodium hydroxide and 1500 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 270 grams of alum and 2000 grams of water was added thereto. The aluminum soap precipitate which formed was filtered, washed on a laboratory crock and dried overnight at a temperature of approximately 75 C. The dried material was ground in a 3 inicropulverizer at a speed of approximately 4000 R. P. M. through a V8 inch r. p. screen.
A 20% solution in commercial toluene was found to be very fluid at room temperature and could be easily sprayed on fabrics, paper, wood shingles, concrete and other building materials as a waterproofing agent therefor.
A 20% solution in Stoddard solvent was very fluid and could be readily sprayed on textile materials, masonry, wall-board, asbestos, rockwool, and the like. The material was also readily soluble in benzene, xylene, carbon tetrachloride and similar aliphatic and aromatic hydrocarbons and their halogenated derivatives.
A laboratory analysis of the aluminum soap indicated the following: 10.10% ash, 9.22% washed ash; 0.88% water-soluble ash; 5.9 mgm. KOH acid value (hot acetone extraction method).
Example 2 A soap solution was prepared from 200 grams of alpha hydroxy decanoic acid; 800 grams of Hydrofol 45 (1.5% C14; 28.0% C15; 70.5% Cm; 6.0% unsaturated acids), 175 grams of 98% sodium hydroxide and 15,000 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 400 grams of zinc sulfate and 500 grams of water was added thereto. The zinc soap precipitate which formed was filtered, washed on a laboratory c'i'ock and dried overnight at a temperature of approximately 75 C. The dried product was ground in a micro-pulverizer at 4000 R. P. M. through a $43 inch r. p. screen. A laboratory analysis of the zinc soap indicated the following:
16.65% ash, 14.7% washed ash and 1.9% water-solubles. A 15% solution in commercial toluene was applied as a waterproofing agent to wood shingles, concrete, cement, and similar building materials.
Example 3 A soap solution was prepared from 200 grams of alphahydroxy decanoic acid, 800 grams of Hydrofol 51, 212
grams of 98% sodium hydroxide and 15,000 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 540 grams of alum and 2500 grams of water was added thereto. The aluminum soap precipitate which formed was filtered, washed, and dried overnight in an oven maintained at a temperature of approximately 75 C. A laboratory analysis of the aluminum soap indicated: 10.05% ash; 9.18% washed ash; 0.87% water-soluble ash and 20.7 mgm. KOH acid value. A 30% solution in alpha-pinene was heated to 67 C. and was very thin and clear while hot. It was a readily sprayable waterproofing solution and could be sprayed on various surfaces such as wood, masonry, and the like. A solution in Stoddard solvent was fluid and could be easily sprayed. A solution in commercial toluene was similarly fluid and could also be readily sprayed. A solution in commercial toluene was slightly thicker but still fluid.
The solubility of the aluminum soap was investigated further as follows: It was found to be clear, thin and readily sprayable in 15 solutions of petroleum ether, carbon tetrachloride, trichlorobenzene, cyclohexane, and other similar solvents.
Example 4 A soap solution was prepared from 100 grams of alpha-hydroxy decanoic acid, 17 grams of 98% sodium hydroxide and 4000 grams of water. This solution was heated to a temperature of approximately C. and to it was added a second solution comprising 45 grams of zinc sulfate and 2500 grams of water. The zinc soap precipitate which formed was filtered, washed and dried overnight in an oven maintained at a temperature of approximately 75 C. A laboratory analysis of the zinc soap indicated the following: 14.95% ash; 13.37% washed ash; 1.58% water-soluble ash; and 1.6 mgm. KOH acid value.
A 15 solution in commercial toluene was heated to C., was very fluid and could be readily sprayed as a waterproofing agent. On cooling, the solution remained very thin and fluid and retained its sprayable characteristics.
Example 5 r The following materials were employed to prepare the aluminum soap of alpha-hydroxy decanoic acid and mixed fatty acids:
800 grams of Hydrofol 55 200 grams of alpha-hydroxy decanoic acid 212 grams of 98% sodium hydroxide 540 grams of alum 18,500 grams of water.
Various methods of precipitation were used to form the aluminum soap. In the first method, the alum solution was added to the sodium soap. In the second method, the sodium soap solution was added to the alum solution; and in the third method; the sodium soap solution and the alum solution were added simultaneously to the precipitation tank.
All three methods were found to be satisfactory but the second method was found to produce a filter cake which was not too grainy and a smoother resulting product. The temperatures of precipitation were varied from about 50 to about 80 and all temperatures were found satisfactory although it was noted that a lower temperature occasionally prevented the formation of a precipitate which was too grainy.
Example 6 The procedures set forth in Example 1 were followed substantially as set forth therein with the exception that a single pressed stearic acid was substituted for the mixed fatty acids used therein The resulting aluminum soap was very similar to that derived from Example 1.
Example] A soap solution was prepared from 100 grams of alphahydroxy capric acid, 400 grams of Hydrofol 405, 100 grams of 98% sodium hydroxide and 16,000 grams of water. This solution was heated to a temperature of approximately 65 C. and a second solution comprising 540 grams of alum and 500 grams of water was added thereto. The aluminum soap precipitate which formed was filtered and washed and then dried overnight at a temperature of about 70 C. A laboratory analysis of the dried material indicated the following: 9.13% ash; 8.8% washed ash; 0.33% water-soluble ash; and 18.7 mgm. KOH acid value. A 10% solution in commercial toluene was used as a waterproofing agent and was sprayed on cotton, wool, asbestos, and like textile materials. A 15% solution in commercial toluene was applied to wood shingles, concrete, cement, masonry, and like building materials.
Example 8 A soap solution was prepared from 400 grams of Emersol 110 (a mixture of C12 to C18 fatty acids), 100 grams of 2-ethyl-3-hydroxy hexanoic acid, 100 grams of 98% sodium hydroxide and 16,000 grams of water. This solution was heated to a temperature of approximately 75 C. and to it was added a second solution comprising 270 grams of alum and 1000 grams of water. The aluminum soap which precipitated was filtered and Washed and then dried overnight in an oven at a temperature of approximately 80 C. Laboratory analysis indicated the following: 9.57% ash; 8.71% washed ash; 0.86% watersoluble ash; 2.26% moisture and volatile matter at C. and 28.6 mgm. KOH acid value. 10% waterproofing solutions in commercial toluene were applied to concrete, cement, masonry, and like building materials.
The quantity by weight of alpha-hydroxy alkanoic acids used in proportion to the total acid in the preparation of the soap may be varied within wide As little as 1% or less by weight of the alpha-hydroxy acid may be used and as high as up to 100% may be used, although the higher cost of such compositions renders them commercially and economically impracticable as coating, impregnating, sealing, or waterproofing agents. In general, it may be stated that compositions containing from about 5% to about 30% by weight of the alpha-hydroxy alkanoic acid, are economically and industrially most desirable.
As shown primarily in the examples, these metallic soaps are soluble up to as high as 30% in a very wide range of solvents without becoming too thick or gelatinous to use readily. It was observed that in many cases, aluminum stearate, when used without the addition of the alpha-hydroxy acid, could not form the thin and clear concentrated solutions which were sprayable, which solutions were made possible by the addition of the hydroxy acids during the soap formation.
This viscosity reducing characteristic created by the use of such an acid is also of value in decreasing the viscosity, when desired, of other compounded compositions such as greases, waxes, soaps, paints, varnishes, plastics, cosmetics, adhesives, rubber and the like.
Although we have described several specific embodiments of our inventive concept, we consider the same not to be limited thereto nor to the specific substances and compounds mentioned therein, but to include various other compounds and compositions of equivalent constitution as set forth in the claims appended hereto. It is understood, of course, that any suitable changes, modifications and variations may be made without departing from the spirit and scope of the invention.
What we claim is:
1. A soap composition comprising metal soaps of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and 95% to 70% by weight of a fatty acid containing from to 22 carbon atoms, said metal being selected from the group consisting of aluminum, zinc, calcium and magnesium.
2. A composition according to claim 1 wherein the alpha-hydroxy alkanoic acid is alpha-hydroxy decanoic acid.
3. A composition according to claim 1 wherein the alpha-hydroxy alkanoic acid is 2-hydroxy-3-ethyl heptanoic acid.
4. A soap composition comprising an aluminum soap of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and 95% to by weight of a fatty acid containing from 10 to 22 carbon atoms.
5. A water-proofing composition comprising a volatile hydrocarbon solvent containing up to 30% of a metal soap of about 5% to 30% by weight of an alpha-hydroxy alkanoic acid containing from 8 to 12 carbon atoms and to 70% by weight of a fatty acid containing from 10 to 22 carbon atoms, said metal being selected from the group consisting of aluminum, zinc, calcium and magnesium.
6. A water-proofing composition according to claim 5 wherein the alpha-hydroxy alkanoic acid is alpha-hydroxy decanoic acid.
7. A water-proofing composition according to claim 5 wherein the alpha-hydroxy alkanoic acid is Z-hydroxy- 3-ethyl-heptanoic acid.
References Cited in the file of this patent UNITED STATES PATENTS 2,081,407 Minich May 25, 1937 2,223,158 Licata et a1. Nov. 26, 1940 2,350,688 Licata et a1. June 6, 1944 2,453,520 Lang Kammerer Nov. 9, 1948 2,618,596 Minich et a1. Nov. 18, 1952 2,626,897 Young et a1. Jan. 27, 1953 2,628,202 Allison et al. Feb. 10, 1953
Claims (1)
1. A SOAP COMPOSITION COMPRISING METAL SOAPS OF ABOUT 5% TO 30% BY WEIGHT OF AN ALPHA-HYDROXY ALKANOIC ACID CONTAINING FROM 8 TO 12 CARBON ATOMS AND 95% TO 70% BY WEIGHT OF A FATTY ACID CONTAINING FROM 10 TO 22 CARBON ATOMS, SAID METAL BEING SELECTED FROM THE GROUP CONSISTING OF ALUMINUM, ZINC, CALCIUM AND MAGNESIUM.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US419611A US2793132A (en) | 1954-03-29 | 1954-03-29 | Metallic soaps of fatty acids and alphahydroxy alkanoic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US419611A US2793132A (en) | 1954-03-29 | 1954-03-29 | Metallic soaps of fatty acids and alphahydroxy alkanoic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
US2793132A true US2793132A (en) | 1957-05-21 |
Family
ID=23662994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US419611A Expired - Lifetime US2793132A (en) | 1954-03-29 | 1954-03-29 | Metallic soaps of fatty acids and alphahydroxy alkanoic acids |
Country Status (1)
Country | Link |
---|---|
US (1) | US2793132A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3124934A (en) * | 1964-03-17 | Method of reducing seepage from | ||
US3305488A (en) * | 1963-05-10 | 1967-02-21 | Lloyd I Osipow | Detergent compositions |
US4526816A (en) * | 1982-01-07 | 1985-07-02 | Brockway, Inc., (Ny) | Fatty acid emulsion and coating of glassware therewith |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2081407A (en) * | 1937-05-25 | Drier | ||
US2223158A (en) * | 1938-07-22 | 1940-11-26 | Nat Oil Prod Co | Metallic soap solution |
US2350688A (en) * | 1940-08-03 | 1944-06-06 | Nat Oil Prod Co | Metallic soap composition |
US2453520A (en) * | 1946-09-28 | 1948-11-09 | Du Pont | Organic titanium compound and method of making same |
US2618596A (en) * | 1950-06-07 | 1952-11-18 | Nuodex Products Co Inc | Oil soluble gelling agent |
US2626897A (en) * | 1951-03-28 | 1953-01-27 | Sun Chemical Corp | Aluminum soaps |
US2628202A (en) * | 1949-09-23 | 1953-02-10 | Leffingwell Chemical Company | Soap useful for making lubricating greases |
-
1954
- 1954-03-29 US US419611A patent/US2793132A/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2081407A (en) * | 1937-05-25 | Drier | ||
US2223158A (en) * | 1938-07-22 | 1940-11-26 | Nat Oil Prod Co | Metallic soap solution |
US2350688A (en) * | 1940-08-03 | 1944-06-06 | Nat Oil Prod Co | Metallic soap composition |
US2453520A (en) * | 1946-09-28 | 1948-11-09 | Du Pont | Organic titanium compound and method of making same |
US2628202A (en) * | 1949-09-23 | 1953-02-10 | Leffingwell Chemical Company | Soap useful for making lubricating greases |
US2618596A (en) * | 1950-06-07 | 1952-11-18 | Nuodex Products Co Inc | Oil soluble gelling agent |
US2626897A (en) * | 1951-03-28 | 1953-01-27 | Sun Chemical Corp | Aluminum soaps |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3124934A (en) * | 1964-03-17 | Method of reducing seepage from | ||
US3305488A (en) * | 1963-05-10 | 1967-02-21 | Lloyd I Osipow | Detergent compositions |
US4526816A (en) * | 1982-01-07 | 1985-07-02 | Brockway, Inc., (Ny) | Fatty acid emulsion and coating of glassware therewith |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2417071A (en) | Preparation of water-insoluble organic salts | |
US2561379A (en) | Aluminum carboxylic acid soap-heavy metal salt of hydroxy quinoline fungicidal composition and preparation thereof | |
US2628202A (en) | Soap useful for making lubricating greases | |
GB983243A (en) | Detergent briquettes | |
US2793132A (en) | Metallic soaps of fatty acids and alphahydroxy alkanoic acids | |
US2785989A (en) | Metallic soaps of fatty acids and polyhydroxy monocarboxylic acids | |
DE1696258A1 (en) | Process for the production of coated paper | |
US2945051A (en) | Metallic salts of commercial stearic acid | |
US2809121A (en) | Zinc stearate composition | |
US2424831A (en) | Composition for waterproofing and fireproofing textile material, and the treated material | |
US2995532A (en) | Corrosion preventive composition | |
US2763621A (en) | Method of converting a liquid hydrocarbon to a gel | |
US3081190A (en) | New composition of matter and methods involving the use of said composition of matter | |
US2289316A (en) | Metallic soap solution | |
US2995456A (en) | Complex zinc soaps | |
US1990811A (en) | Coating composition | |
US2695839A (en) | Method and compositions for killing weeds | |
US3100718A (en) | Copper borate antifouling pigment | |
GB721467A (en) | Improvements in or relating to coated solid particles | |
US2125594A (en) | Floor and wall covering material | |
US1031003A (en) | Waterproofing compound. | |
DE1158713B (en) | Process for the production of dispersible salts of homo- or copolymers of methacrylic acid | |
US2758123A (en) | Aluminum soaps | |
US2172955A (en) | Coating and impregnating process and product | |
US2507239A (en) | Protective coating compositions |