US2578851A - Lubricating greases - Google Patents
Lubricating greases Download PDFInfo
- Publication number
- US2578851A US2578851A US115314A US11531449A US2578851A US 2578851 A US2578851 A US 2578851A US 115314 A US115314 A US 115314A US 11531449 A US11531449 A US 11531449A US 2578851 A US2578851 A US 2578851A
- Authority
- US
- United States
- Prior art keywords
- grease
- oil
- metal
- soap
- alkyl
- 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
- 230000001050 lubricating effect Effects 0.000 title claims description 12
- 239000004519 grease Substances 0.000 claims description 58
- 230000000740 bleeding effect Effects 0.000 claims description 14
- 150000001408 amides Chemical class 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 21
- 229910052751 metal Inorganic materials 0.000 description 20
- 239000002184 metal Substances 0.000 description 20
- -1 phthalyl alkyl amide Chemical class 0.000 description 17
- 239000000203 mixture Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- 239000002480 mineral oil Substances 0.000 description 8
- 229910052791 calcium Inorganic materials 0.000 description 7
- 239000011575 calcium Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 235000010446 mineral oil Nutrition 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 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 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 150000004692 metal hydroxides Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- OTVDESMGXUUCQW-UHFFFAOYSA-N 2-(dodecylcarbamoyl)benzoic acid Chemical compound CCCCCCCCCCCCNC(=O)C1=CC=CC=C1C(O)=O OTVDESMGXUUCQW-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- KJJKANHJKSOLRK-UHFFFAOYSA-N 2-(hexadecylcarbamoyl)benzoic acid Chemical compound CCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1C(O)=O KJJKANHJKSOLRK-UHFFFAOYSA-N 0.000 description 1
- CYMRPDYINXWJFU-UHFFFAOYSA-N 2-carbamoylbenzoic acid Chemical class NC(=O)C1=CC=CC=C1C(O)=O CYMRPDYINXWJFU-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- GDNCXORZAMVMIW-UHFFFAOYSA-N dodecane Chemical group [CH2]CCCCCCCCCCC GDNCXORZAMVMIW-UHFFFAOYSA-N 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- MDLWEBWGXACWGE-UHFFFAOYSA-N octadecane Chemical group [CH2]CCCCCCCCCCCCCCCCC MDLWEBWGXACWGE-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/12—Partial amides of polycarboxylic acids
- C10M2215/122—Phtalamic acid
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/10—Groups 5 or 15
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/16—Groups 8, 9, or 10
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- This invention relates tonovel lubricating greases and, more particularly, to soap-thickened mineral oils having a modified gel structure.
- Another object of this invention is to manufacture a grease in which oil separation or bleeding does not take place.
- a further object of this invention is to provide a grease which can be used on high pressure bearings.
- the soaps generally employed as thickeners include the sodium, calcium, aluminum and zinc or other metal salts of fatty materials derived from animal or vegetable fats or fatty acids.
- the metal of the soap can be an alkali metal, an alkaline earth metal, and various other metals such as lead, chromium, tin, iron, cobalt, nickel, cadmium, mercury, etc., and
- the fats or fatty acids can betallow, lard, cotton- 8 Claims. (01. 252- 333) a 2 facture. the addition of a metal phthalyl alkyl amide to any grease comprising a mineral oil thickened to the consistency of a grease with a soap.
- a roller bearing grease was prepared having the following composition: I
- N-alkyl phthalamidates We obtain particularly good results from the sodium, calcium andaluminum N-alkyl phthalamidates; however, satisfactory metal salts of N-alkyl phthalamides can be prepared from potassium, or other alkali metal, barium, strontium, magnesium, chromium, nickel, cobalt, Zinc, lead, tin, copper, cadmium, bismuth, etc.
- the primary alkyl amines which we employ in the preparation of the metal phthalyl alkyl amides are amines having the following generic formula:
- n is a number between 6 and 18.
- Some of the amines of this generic class are no-Fawn amine.
- Mono-lauryl amine Mono-myristyl amine
- Mono-palmityl amine Mono-stearyl amine and other primary alkyl amines having the above formula. Any of the aboveamines may be used with advantage in making our metal phthalyl alkyl amides.
- mixtures of such amines may be employed. For instance, one commercially available mixture of such amines is the so-called cocoamine prepared by converting the mixed acids of coconut oil into corresponding amines by well known methods.
- cocoamine prepared by converting the mixed acids of coconut oil into corresponding amines by well known methods.
- EXAMPLE A the improvement agent was prepared in situ in mineral oil from phthalic anhydride, dodecylamine and aluminum hydroxide, the agent so prepared having the following formula:
- the aluminum phthalyl dodecyl amide produced in situ in oil had .the following properties:
- R is an octadecyl radical
- metalphthalyl alkyl amides which are deac'zsgeer scribed in the aboverexammes .havebeen; used as additives in mineral lubricating oils because of the-antirust and anticorrosion properties which they, confer "upon thelubricants in which they are incorporated.
- the gel is notably stabilized against bleeding and oil evaporation.
- the grease does not become rancid over a long storage period because the metal phthalyl alkyl amide acts as a buffer to the soap solution.
- the grease compositions of our invention have all been rigidly tested according to the methods prescribed in Army-Navy Aeronautical Specifications for Grease, AN-G-ba for lubricating performance, life, bleeding, evaporation, apparent viscosity, plasticity and low temperature torque. These tests clearly establish the fact that the gel structure of the original grease has been modified. The following comparative tests show the amount of bleeding and evaporation according to the Army-Navy standard specification tests.
- the greases prepared according to our invention wgive eminently, satisfactory lubrication, es; pecially when used on highgpressurebearings;at high surface temperatures. These greases are not consumed at an excessive rate while they are lubricating such hot bearings. In all cases the compositions give satisfactory lubrication in such applications as gun mechanisms, roller bearings and similar mechanisms.
- a lubricating grease which comprises a major amount of a soap-oil grease, and a minor amount, sufficient to prevent bleeding, of ame'tal phthalyl alkyl am'ide having the formula wherein R is an alkyl group containing from 8 to 20 carbon atoms, X is a whole number equal to the valence of M, and M is a metal.
- a lubricating grease having a modified gel structure comprising a major amount of a soapoil grease and a minor amount, from 0.1 to 5.0 per cent by weight of said soap-oil grease of a metal phthalyl alkyl amide having the formula t i I wherein R is an alkyl group containing from 8 to 20 carbon atoms, X is a whole number equal to the valence of M, and M is a metal.
- a lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufiicient to prevent bleeding, of a sodium phthalyl alkyl amide having the formula wherein R is an alkyl group containing from 8 to 20 carbon atoms.
- a lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufiicient to prevent bleeding, of a calcium phthalyl alkyl amide having the formula ll 1% I l 15 wherein R is an alkyl group containing from 8 to 20 carbon atoms.
- a lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufficient to prevent bleeding, 011m aluminum phthalyLaIkyl 8.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Dec. 18, 1951 LUBRICATING GREASES Herschel G. Smith, Wallingford, Troy L. Cantrell, Lansdowne, and Mark L. Hill, Boothwyn, Pa., assignors to Gulf Oil Corporation, Pittsburgh, Pa., a corporation of Pennsylvania.
N Drawing. Application September 12, 1949,
1 Serial No. 115,314
This invention relates tonovel lubricating greases and, more particularly, to soap-thickened mineral oils having a modified gel structure.
Dimculties have been encountered in the use of conventional mineral oil greases because of the fact that these conventional greases sometimes have indefinite and unstable gel structure. Slight variations in soaps or other basic ingredients produce changes in the gel structure which result in oil separation and limit the efficiency of the grease; its service life and the uses to which it can be applied.
It is therefore an object of this inventionto produce a soap-thickened grease which has a modified gel structure. 7
Another object of this invention is to manufacture a grease in which oil separation or bleeding does not take place.
A further object of this invention is to provide a grease which can be used on high pressure bearings.
These objects are accomplished in accordance with the present invention by the preparation of a grease which comprises a major amount of a mineral oil thickened to a grease with a soap and a minor amount, sufficient to prevent bleeding, of a metal phthalyl alkyl amide (a metalsalt of an N-alkyl phthalamidic acid) having the Q alert? "4 i' generic formula wherein M is a metal, a: is a whole number equal to the valence of M, and R is an alkyl group containing from 8 to carbon atoms.
In a soap-thickened mineral oil type'of grease, the soaps generally employed as thickeners include the sodium, calcium, aluminum and zinc or other metal salts of fatty materials derived from animal or vegetable fats or fatty acids. For example, the metal of the soap can be an alkali metal, an alkaline earth metal, and various other metals such as lead, chromium, tin, iron, cobalt, nickel, cadmium, mercury, etc., and
the fats or fatty acids can betallow, lard, cotton- 8 Claims. (01. 252- 333) a 2 facture. the addition of a metal phthalyl alkyl amide to any grease comprising a mineral oil thickened to the consistency of a grease with a soap. By
, the termfsoap-oil grease or soap-thickened grease we refer. to these commonly known greases.
vIn the preparation of the greases of .our invention the soap-oil greases are usually prepared first, and subsequently, from 0.1 to 5.0v
per cent by weight on the grease of the metal phthalyl alkyl amide is incorporated in the,
grease. However, the metal phthalyl alkyl amide may be added during the manufacture ofv ,the grease, for example, by being dissolved in the mineral oil used in compounding the grease.
The nature of our lubricating grease compo--, sition will be more clearly: understood .by ref.--
. erence to the following examples.
EXAMPLE I A grease having the following composition was prepared by the conventional pressure saponification method:
No.- 1 lard oil ..gal1ons '150 Water do 150 pale coastal oil (156 S. U. S. at
100 F.) allons 900- Powdered hydrated lime pounds 198 No. 1 inedible tallow do 100 The lubricant was then dehydrated and, during the stirring and cooling operation, 1 per .cent by weight of the calcium salt of amidic acid was added.
EXAMPLE? A cup grease having the following composition in parts by weight was prepared by the pressure saponification method:
During the stirring and cooling operation, 1 per cent by weight of the calcium salt of N-dodecylphthalamidic acid was incorporated there- EXAMPLE III A recoil mechanism grease having the following composition in parts by weight was prepare by'the pressure saponification method:
Two per cent by weight of the aluminum salt-- of N-dodecylphthalamidic acid was subsequently incorporated therein.
Our invention therefore contemplates c nthal EXAMPLE w A roller bearing grease was prepared having the following composition: I
Per cent by weight Sodium tallow soap 14 400 S. U. S. lubricating oil 7 at 100 F. 86
The above grease was treated with 1 per cent-"by weight of the sodium salt of N-hexadecylphthalamidic acid.
The viscosities expressed for the oils in the above examples are in Saybolt Universal seconds at 100 F. It is obvious that any of the soap-oil greases can be usedin accordance with our invention and that the above examples are merely illustrative. Variations will naturally occur to those skilled in the art.
The metalphthalyl alkyl amides which are incorporated in the soap-oil greasesin accordance with this invention are readily prepared, as will be shown, from metal hydroxides,- phthalic anhydride and primary alkyl amines; or, in the event the metal hydroxide of a particular metal is difficult to react, as, for example, the heavy metal hydroxides, the desired heavy metal N- alkyl phthalamidate' can be readily prepared by first preparing an alkali metal N-alkyl phthalamidate and reacting the latter with a water soluble salt of the desired heavy metal by a conventional double decomposition or metathesis reaction. We obtain particularly good results from the sodium, calcium andaluminum N-alkyl phthalamidates; however, satisfactory metal salts of N-alkyl phthalamides can be prepared from potassium, or other alkali metal, barium, strontium, magnesium, chromium, nickel, cobalt, Zinc, lead, tin, copper, cadmium, bismuth, etc.
The primary alkyl amines, which we employ in the preparation of the metal phthalyl alkyl amides are amines having the following generic formula:
wherein n is a number between 6 and 18. Some of the amines of this generic class are no-Fawn amine. Mono-lauryl amine Mono-myristyl amine Mono-palmityl amine Mono-stearyl amine and other primary alkyl amines having the above formula. Any of the aboveamines may be used with advantage in making our metal phthalyl alkyl amides. Furthermore, mixtures of such amines may be employed. For instance, one commercially available mixture of such amines is the so-called cocoamine prepared by converting the mixed acids of coconut oil into corresponding amines by well known methods. The
commercial cocoamine has an'average molecular weight of about 200-210 and contains a pounds so obtained, the new improvement agents being formed in situ in the oil.
The following examples illustrate various methods of preparing our metal phthalyl alkyl amides.
EXAMPLE A In this example, the improvement agent was prepared in situ in mineral oil from phthalic anhydride, dodecylamine and aluminum hydroxide, the agent so prepared having the following formula:
H OEJLFCHH camera The procedure employed in preparing this com-v pound was as follows:
Into an iron vessel equipped with means for heating, stirring and cooling, were charged 444 pounds of phthalic :anhydride to whichv 555 pounds of dodecyl amine wereslowly added. To this mixture were added 2000 pounds of a Texas oil having a viscosity of 70S. U. S. at F. and,
the components. were thoroughly agitated and slowly heatedto F.- After one'hour, 435 pounds of alumina (gelatinous 18 per cent Al(OH)3) were added and the mixture was kept at F. until the formation of water was com-,
pleted and no more water could be drawn off. From the kettle 2966 pounds of aluminum phthalyl dodecyl amide oil mixture were obtained.
The aluminum phthalyl dodecyl amide produced in situ in oil had .the following properties:
Gravity, API 20.8 Viscosity, SUV:
Neutralization No. a 1.11
ExAMPLEB A calcium phthalyl alkyl amide having the following formula:
wherein R is an octadecyl radical, was prepared substantially anhydrous oil solution of the cal'- 1 cium N-mono-octadecyl amido phthalate compounds so obtained was then cooled to room temperature.
The metalphthalyl alkyl amides which are deac'zsgeer scribed in the aboverexammes .havebeen; used as additives in mineral lubricating oils because of the-antirust and anticorrosion properties which they, confer "upon thelubricants in which they are incorporated. The-calcium and aluminum salts of phthalamidic acid are described in U. S. Letters Patent Nos.=2,3vs,442.and 2,378,443. It is truethat, as in the caseof mineral oil s, metal phthalyl alkyl amides also render grease compositions non-corrosive, to metal parts. Our invention, however, resides in'the discovery that entirely new and unexpectedresults are obtained byethe addition of metal phthalyl alkyl amides to soapeoil greases. j l a J'r-Q l xWe have discovered that themetal phthalyl alkyl. amides modify the ;gel structure" .of-the grease. Due to the fact that the grease has a different gel structure, the following properties of the grease are improved:
(1) The new gel structure does not break down as readily as the gel structure in the unmodified grease.
(2) A more plastic grease is produced.
(3) The texture of the grease is smoother and more uniform.
(4) The gel is notably stabilized against bleeding and oil evaporation.
Moreover, the grease does not become rancid over a long storage period because the metal phthalyl alkyl amide acts as a buffer to the soap solution.
The grease compositions of our invention have all been rigidly tested according to the methods prescribed in Army-Navy Aeronautical Specifications for Grease, AN-G-ba for lubricating performance, life, bleeding, evaporation, apparent viscosity, plasticity and low temperature torque. These tests clearly establish the fact that the gel structure of the original grease has been modified. The following comparative tests show the amount of bleeding and evaporation according to the Army-Navy standard specification tests.
Bleeding and evaporation test TEST AN-G-3a Per cent of separated oil due to bleed- Grease ing and evaporation after 50 hours (212 F.)
Grease prepared according to Example I and n lodified with 1% of calcium N-dodecyl phthalami ate Grease prepared according to Example I but not modified i. 24 Cup grease prepared according to Example II and modified with 1% of calcium N-dodecyl phthalamidate 0 Cup grease prepared according to Example II but not modified 28 Recoil mechanism grease prepared according to Example III and modified with 2% of aluminum Ndodecy1 phthalamidate 0, 1 Recoil mechanism grease prepared cc Example III but not modified l2 Roller bearing grease prepared according to Example IV and modified with 1.0% 01 sodium N-hexadecyl phthalamidate 0 Roller bearing grease prepared according to Example IV but not modified 5 The above tests clearly indicate the stability of our greases against bleeding or separation, particularly since our greases showed no signs of bleeding during the fifty-four hour test period. In fact, the unmodified greases showed some bleeding within 48 hours while the modified grease was still without separation after a two-week period.
The greases prepared according to our inventionwgive eminently, satisfactory lubrication, es; pecially when used on highgpressurebearings;at high surface temperatures. These greases are not consumed at an excessive rate while they are lubricating such hot bearings. In all cases the compositions give satisfactory lubrication in such applications as gun mechanisms, roller bearings and similar mechanisms.
Resort may be had to such modifications and variations as fall within the spirit of the invention and the scope of the appended claims.
We claim:
1. A lubricating grease which comprises a major amount of a soap-oil grease, and a minor amount, sufficient to prevent bleeding, of ame'tal phthalyl alkyl am'ide having the formula wherein R is an alkyl group containing from 8 to 20 carbon atoms, X is a whole number equal to the valence of M, and M is a metal.
2. A lubricating grease having a modified gel structure, comprising a major amount of a soapoil grease and a minor amount, from 0.1 to 5.0 per cent by weight of said soap-oil grease of a metal phthalyl alkyl amide having the formula t i I wherein R is an alkyl group containing from 8 to 20 carbon atoms, X is a whole number equal to the valence of M, and M is a metal.
3. A lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufiicient to prevent bleeding, of a sodium phthalyl alkyl amide having the formula wherein R is an alkyl group containing from 8 to 20 carbon atoms.
4. The grease of claim 3 wherein R is a hexadecyl radical.
5. A lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufiicient to prevent bleeding, of a calcium phthalyl alkyl amide having the formula ll 1% I l 15 wherein R is an alkyl group containing from 8 to 20 carbon atoms.
6. The grease of claim 5 wherein R is a dodecyl radical.
'7. A lubricating grease having a modified gel structure which comprises a major amount of a soap-oil grease and a minor amount, sufficient to prevent bleeding, 011m aluminum phthalyLaIkyl 8. The grease of claim 7 wherein R is a dodecyl amide having the formula radical.
HERSCHEL G. SMITH. TROY L. CANTRELL. 5 MARK L. HILL.
L 5 REFERENCES CITED 0 O The following references are of record in the file of this patent:
1 I I UNITED STATES PATENTS C-NH HNC Number Name Date L, g 2,370,442 Smith et a1 June 19, 1945 2,378,443 Smith et a1 June 19, 1945 g zgi gzsi fi gmup wntammg mm 8 15 2,408,102 Smith et a1 Sept. 24, 1946 2,403,103 Smith et a1 Sept. 24, 1946
Claims (1)
1. A LUBRICATING GREASE WHICH COMPRISES A MAJOR AMOUNT OF A SOAP-OIL GREASE, AND A MINOR AMOUNT, SUFFICIENT TO PREVENT BLEEDING, OF A METAL PHTHALYL ALKYL AMIDE HAVING THE FORMULA
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US115314A US2578851A (en) | 1949-09-12 | 1949-09-12 | Lubricating greases |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US115314A US2578851A (en) | 1949-09-12 | 1949-09-12 | Lubricating greases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2578851A true US2578851A (en) | 1951-12-18 |
Family
ID=22360567
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US115314A Expired - Lifetime US2578851A (en) | 1949-09-12 | 1949-09-12 | Lubricating greases |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2578851A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2820012A (en) * | 1954-12-14 | 1958-01-14 | California Research Corp | High temperature phthalamate grease compositions |
| US2983682A (en) * | 1959-07-10 | 1961-05-09 | Gulf Research Development Co | Lubricating oil thickened to a grease consistency with a mixture of a tetraphenylphthalyl compound and an organophilic siliceous compound |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2378442A (en) * | 1944-01-04 | 1945-06-19 | Gulf Oil Corp | Mineral oil composition |
| US2378443A (en) * | 1944-12-02 | 1945-06-19 | Gulf Oil Corp | Mineral oil composition |
| US2408103A (en) * | 1945-03-19 | 1946-09-24 | Gulf Oil Corp | Mineral oil composition |
| US2408102A (en) * | 1945-03-19 | 1946-09-24 | Gulf Oil Corp | Oil compositions |
-
1949
- 1949-09-12 US US115314A patent/US2578851A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2378442A (en) * | 1944-01-04 | 1945-06-19 | Gulf Oil Corp | Mineral oil composition |
| US2378443A (en) * | 1944-12-02 | 1945-06-19 | Gulf Oil Corp | Mineral oil composition |
| US2408103A (en) * | 1945-03-19 | 1946-09-24 | Gulf Oil Corp | Mineral oil composition |
| US2408102A (en) * | 1945-03-19 | 1946-09-24 | Gulf Oil Corp | Oil compositions |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2820012A (en) * | 1954-12-14 | 1958-01-14 | California Research Corp | High temperature phthalamate grease compositions |
| US2983682A (en) * | 1959-07-10 | 1961-05-09 | Gulf Research Development Co | Lubricating oil thickened to a grease consistency with a mixture of a tetraphenylphthalyl compound and an organophilic siliceous compound |
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