US2844536A - High temperature complex grease manufacturing processes - Google Patents
High temperature complex grease manufacturing processes Download PDFInfo
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- US2844536A US2844536A US426928A US42692854A US2844536A US 2844536 A US2844536 A US 2844536A US 426928 A US426928 A US 426928A US 42692854 A US42692854 A US 42692854A US 2844536 A US2844536 A US 2844536A
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- 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
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- 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
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
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- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/124—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
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- 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
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- 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
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- 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
- C10M2207/22—Acids obtained from polymerised unsaturated acids
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- 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
- C10M2207/28—Esters
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- 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2207/28—Esters
- C10M2207/30—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
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- 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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- 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
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
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- 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
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- 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—Semi-solids; greasy
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
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Description
United States Patent HIGH TEMPERATURE COMPLEX GREASE MANUFACTURING PROCESSES Arnold J. Morway, Clark, N. J assignor to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Application April 30, 1954 Serial No. 426,928
3 Claims. (Cl. 252-39) This invention relates to high temperature lubricating grease compositions and to a process for their preparation. Particularly, the invention relates to a process for the preparation of complex lubricating greases wherein the soap system consists of a combination of the salt of a low molecular weight acid and the soap of a high molecular weight acid wherein the mol ratio of the salt to the soap is above about 21:1. The improved process of this invention comprises the steps of preforming a salt-soap complex lubricating grease containing a saltsoap ratio of between about :1 to 50:1, adding a calculated amount of this salt-soap complex grease to a simple grease composition, heating the mixture to a temperature substantially below that necessary to complex the salt and soap and homogenizing the mixture to obtain a finished grease composition containing from 1 to mols of salt per mol of soap.
In the preparation of high temperature lubricating grease compositions of the type contemplated herein, it has been found necessary to use temperatures in the order of 450 to 500 F. in order to form a true complex of the low molecular weight acid salt and the high molecular weight acid soap. The instant invention relates to the preparation of these general type lubricating grease compositions wherein a salt-soap complex grease is preformed that contains a ratio of salt to soap of about 10:1 to 50:1, and admixing this preformed complex with a major proportion of a simple soap grease in a second step. The incorporation of the two greases may be accomplished at temperatures below about 350 F., representing a tremendous saving in heat and time of manufacture and also eliminating the necessity of subjecting the lubricating oil to high temperatures.
The invention will be more clearly described by reference to the following illustrative examples:
EXAMPLE I a. Preparation of high acetate soap concentrate Formulation: Percent weight Glacial acetic acid 25.20 Hydrogenated fish oil acids 2.00 Hydrogenated castor oil 2.00 Hydrated lime 17.40 Phenyl alpha-naphthylamine 1.00 Di-octyl azelate 52.40
Preparation Charged all ingredients to a fire heated kettle with the exception of the acetic acid and the phenyl alpha naphthylamine. Warmed to 135 F., then added the acetic acid and continued heating to 500 F. Cooled grease to 300 F., added phenyl alpha naphthylamine, cooled to 250 F. and homogenized by passage through a Gaulin homogenizer.
2,844,536 Patented July 22, 1958 ICC Water slurry of lime, fatty acid, and sutlicient ester to make a 20 soap concentrate are charged to kettle and cooked until dehydrated with a maximum kettle temperature of 265 F. The complex concentrate (a) and remainder of oil added with the inhibitor and the temperature raised briefly to 330 F., followed by slow cooling. At 200 F. 1.0% H 0 added and the grease is homogenized after brief stirring. The mol ratio of low molecular weight acid to high molecular weight acid in the complex soap was 3.8.
Inspections: After storage for 37 days Penetration, mm./ l0- Unworked 242 236 Worked 60 strokes 278 280 Unworked (after 48 hours) 235 Dropping point, F 500+ Appearance Smooth, homogeneous.
EXAMPLE II a. Preparation of high acetate soap concentrate MOL RATIO ACETIC ACID TO FATTY ACIDS 4O 1 Formulation: I Percent weight Glacial acetic acid 14.20 Fish oil acids, hydrogenated 0.85 Hydrogenated castor oil 0.85 Hydrated lime 9.70 Phenyl alpha naphthylamine 0.50 Mineral oil 79.90
The materials other than acetic acid and phenyl alpha naphthylamine were charged to a tire heated grease kettle and warmed to F. The acetic acid was charged and the mass heated to 500 F. The grease was cooled to 250 F., the phenyl alpha nap'hthylamine added and further cooled to 200 F. where it is homogenized if desired.
Properties:
Appearance Softsemi-tluid. Dropping point, F 500+. Stability Separates oil on standing unless homogenized.
b. Preparation of simple calcium soap grease- Formulation: Weight per-cent Animal fat 9.50 Hydrated lime 1.35 Water 0.95
' Mineral oil 88.52
Properties:
Appearance Excellengsmooth,
unifonm product. Penetrations 77 F. mm./lO- T a Unworked 300. Worked 60 strokes 310. Dropping point, F' 200 (water is evaporatedand soap 1 and 4 oil separates).
0. Preparation of finished grease: g
20% produce of a 80% product of b The grease of b as finished or at 300 F. before the addition .of water may be employed. In either case, 20% ofthe .grease of a is added before heating to 300 F. or at 300 F., held atthis temperature while agitating for approximately .3 hours, cooled rapidly to 200 F. and homogenized and packaged. 7
Properties: 7
Appearance Excellent smooth grease. Dropping point, F 450. Penetration 77 F. mm./l
Unworked 315. Worker 60 strokes 340. Worked 75,000 strokes 384. Wheel bearing test Pass. Leakage Small amount of grease in retainer cup.
EXAMPLE III a. The simple calcium soap grease preparation of Example IIb was repeated.
. b. Preparation of highacetate complex grease- Formulation: Percent weight Glacial acetic acid 25.20 Hydrogenated fish oil acids 2.00 Hydrogenated castor oil 2.00 Hydrated lime 17.40 Phenyl alpha-naphthyl 'ne 2.00 Mineral oil 51.40
Preparation All ingredients were charged to a fire heated kettle and heated to 500 F., and then cooled to 200 F. Phenyl alpha naphthylamine was added 'at 250 F. during the cooling cycle.
Penetration 77 F. mm./l0:
' Preparation The animal fat, mineral oil and hydrated lime were charged to a steam kettle and heated to 300 F. That temperature was maintained until the fat was completely saponified. Then there was added the grease described in Example IIIb. Mixing was continued at 300 F. for 2 hours. The mix was then cooled to 200 F. and the product was homogenized.
Properties; g
Appearance Excellent smooth uniform grease. Total saponifiable 12.46%. Mol ratio acetic acid to high molecular weight acids 1.8: 1. Penetrations 77 F. mm./10-
Unworked 300. Worked 60 strokes 310. Worked 10,000 strokes 360. Dropping point F 485.
EXAMPLE 'IV Percent Grease of Example IIb (simple calcium soap grease) 45.00 Grease of Example I'l'lb (complex calcium soap grease) 12.50 Mineral oil -4 42.50
I or Animal fat 4.28 Hydrogenated fish oil acids .50 Acetic acid 3.15 Hydrated lime 2.91 Phenyl alpha-naphthylarnine 0.25 Mineral ni 88.41
PreparatiomfiSimilar to Example lHc.
The mol ratio of acetic acid to high molecular weight acid was 2.8:1.
Properties:
Appearance Excellent. Total saponifiable 8.43. Penetrations 77 F. mm./10-- Unworked 323. Worked 60 strokes 340. Worked 10,000 strokes 362. Dropping point, F '500. Wheel bearing test Pass, excellent, no leakage and no fiuidization.
(Added 0.25% phenyl alpha naphthylamine inhibitor to grease before running following tests.)
. Norma Hofiman oxidation:
Hours to 5 p. s. i. drop in oxygen pressure Lubrication lifel0,000 R. P. M.-
250 F., hours 1128 As is shown by the examples above, the lubricating oil used may be either a naturally occurring mineral lubricating oil or a synthetic lubricating oil. It will be understood that the lubricating oil viscosity willpreferably be within a range of from about 35 SUS to about SUS at 210 F. In addition to diester synthetic lubricants illustrated by Example I, other forms of synthetic lubricating oils such as complex esters prepared by the coreaction of alcohols, dibasic acids and glycols, formals, polymerized olefins, ether alcohols, ether esters, ester ethers and the like may be used.
The complex grease compositions resulting from the instant inventive process preferably contain at least 1 mol of the low molecular weight acid per mol of the high molecular weight acid. The upper limit of the saltsoap ratio will be in the vicinity of 15 although it may be desirable for some purposes to have a ratio even higher than this.
It is generally desired that the finished grease composition contain between about 5% and 30% by weight of total salt soap complex. From 8 to '20 weight percent is preferred.
' Although in the examples cited above, calcium is the alkaline earth metal used, and although calcium is contemplated in the preferred embodiment of this invention, it will be understood that other alkaline earth metals such as barium, magnesium and strontium may be used as mixed bases. It has been found, however, that the alkali metal complexes yield grease compositions of undesirable properties when the mol ratio of low molecular weight acid to high molecular weight acid is in excess of about 2:1. Although it is preferred that both the salt and the soap be of the same metal, it is not necessary that this be so. For example, the calcium soap of the fatty acid may be used in conjunction with a barium salt of a low molecular weight acid.
The high molecular weight acids that are used in forming the grease compositions of this invention may be any of the commonly known grease making acids having from 12 to 30 carbon atoms, preferably from 18 to 22 carbon atoms, per molecule. These acids include stearic acid, hydroxy stearic acid, dihydroxy stearic acid, arachidic acid, hydrogenated fish oil acids, tallow acids, oleic acids, ricinoleic acids, etc.
The low molecular weight acid operable for forming the greases of this invention is preferably acetic acid. However, other saturated or unsaturated aliphatic monoor poly-carboxylic acids having about 1 to 6 carbon atoms per molecule are operable. A partial list of operable low molecular weight acids includes formic acid, acetic acid, propionic acid, butyric acid, furoic acid, acrylic acid, adipic acid, including their hydroxy derivatives such as lactic acid, etc.
To summarize briefly, this invention relates to an improved process for the preparation of complex salt-soap thickened lubricating grease compositions. The process involves two major steps wherein there is first formed a salt-soap complex lubricating grease which contains a high ratio of low molecular weight acid to high molecular weight acid, preferably a mol ratio of about 10:1 to 50:1. This complex is then admixed with a simple alkaline earth metal soap grease in a second step in proportions such that the finished composition contains a mol ratio of low molecular weight acid to high molecular weight acid of between about 1:1 and :1. The second step may be carried out at temperatures substantially below those necessary to form the salt soap complex, that is, substantially below about 350 F. The resulting grease compositions have all the desirable properties of similar prior art greases but have the advantage of subjecting the major portion of the lubricating oil to substantially lower temperatures than was hitherto thought possible.
What is claimed is:
1. A process for the preparation of a high temperature lubricating grease composition wherein a major proportion of the lubricating oil in the final composition has not been subjected to high temperatures above about 350 F. which comprises the steps of forming at a temperature in the range of 450 to 500 F., a complex-thickened grease from a lubricating oil, an alkaline earth metal soap of a grease-making acid having in the rangeof- 12 to 30 carbon atoms per molecule, and an alkaline earth metal salt of a monocarboxylic acid having in the range of 1 to 6 carbon atoms per molecule, with the mole ratio of salt to soap being in the range of 10:1 to 50:1, admixing at a temperature in the range of 300 to 350 F. a minor amount :of said complex-thickened grease with a major amount of simple soap grease formed from a lubricating oil .and an alkaline earth metal soap of a grease-making acid having in the range of 12 to 30 carbon atoms per molecule, in proportion such that the mole ratio of salt to soap in the finished formulation is in the range of 1:1 to 15:1 and the total salt-soap content thereof is in the range of 5 to 30% by weight, and homogenizing the admixture to obtain the finished composition.
2. The process of claim 1 wherein said alkaline earth metal salt is calcium acetate.
3. A process for the preparation of a high temperature lubricating grease composition wherein a major proportion of the lubricating oil in the final composition has not been subjected to high temperatures above about 350 F. which comprises the steps of forming at a temperature in the range of 450 to 500 F. a complex-thickened grease from a lubricating oil, a calcium soap of a grease-making acid having in the range of 12 to 30 carbon atoms per molecule and calcium acetate, the mole ratio of acetate to acid being in the range of 10:1 to 50:1, admixing at a temperature in the range of 300 to 350 F. a minor amount of said complex-thickened grease with a major amount of simple soap grease formed from a lubricating oil and a calcium soap of a grease-making acid having in the range of 12 to 30 carbon atoms per molecule, in proportion such that the mole ratio of acetate to soap in the finished formulation is in the range of 1:1 to 15 :1 and the total acetate-soap content thereof is in the range of 5 to 30% by weight, and homogenizing the admixture to obtain the finished composition.
References Cited in the file of this patent UNITED STATES PATENTS 2,417,428 McLennan Mar. 18, 1947 2,417,429 McLennan Mar. 18, 1947 2,417,430 McLennan Mar. 18, 1947 2,417,432 McLennan Mar. 18, 1947 2,417,439 McLennan Mar. 18, 1947 2,455,892 Fraser Dec. 7, 1948 2,468,098 Morway et a1 Apr. 26, 1949 2,487,080 Swenson Nov. 8, 1949 2,564,561 Carmichael et a1 Aug. 14, 1951 2,575,286 Morway et a1 Nov. 13, 1951 2,583,607 Sirianni et al. Feb. 2, 1952 2,588,279 OHalloran Mar. 4, 1952 2,618,599 King et al. Nov. 18, 1952
Claims (1)
1. A PROCESS FOR THE PREPARATION OF A HIGH TEMPERATURE LUBRICATING GREASE COMPOSITION WHEREIN A MAJOR PROPORTION OF THE LUBRICATING OIL IN THE FINAL COMPOSITION HAS NOT BEEN SUBJECTED TO HIGH TEMPERATURES ABOVE ABOUT 350*F. WHICH COMPRISES THE STEPS OF FORMING AT A TEMPERATURE IN THE RANGE OF 450* TO 500*F., A COMPLEX-THICKENED GREASE FROM A LUBRICATING OIL, AN ALKALINE EARTH METAL SOAP OF A GREASE-MAKING ACID HAVING IN THE RANGE OF 12 TO 30 CARBON ATOMS PER MOLECULE, AND AN ALKALINE EARTH METAL SALT OF A MONOCARBOXYLIC ACID HAVING IN THE RANGE OF 1 TO 6 CARBON ATOMS PER MOLECULE, WITH THE MOLE RATIO OF SALT TO SOAP BEING IN THE RANGE OF 10:1 TO 50:1, ADMIXING AT A TEMPERATURE IN THE RANGE OF 300* TO 350*F. A MINOR AMOUNT OF SAID COMPLEX-THICKENED GREASE WITH A MAJOR AMOUNT OF SIMPLE SOAP GREASE FORMED FROM A LUBRICATING OIL AND AN ALKALINE EARTH METAL SOAP OF A GREASE-MAKING ACID HAVING IN THE RANGE OF 12 TO 30 CARBON ATOMS PER MOLECULE, IN PROPORTION SUCH THAT THE MOLE RATIO OF 1:1 TO 15:1 AND THE TOTAL SALT-SOAP CONTENT THEREOF IS IN THE RANGE OF 5 TO 30% BY WEIGHT, AND HOMOGENIZING THE ADMIXTURE TO OBTAIN THE FINISHED COMPOSITION.
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US426928A US2844536A (en) | 1954-04-30 | 1954-04-30 | High temperature complex grease manufacturing processes |
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US426928A US2844536A (en) | 1954-04-30 | 1954-04-30 | High temperature complex grease manufacturing processes |
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US (1) | US2844536A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2908645A (en) * | 1955-04-28 | 1959-10-13 | Exxon Research Engineering Co | Blended lithium calcium base grease |
US2985590A (en) * | 1955-09-28 | 1961-05-23 | Exxon Research Engineering Co | Lubricating oil compositions comprising mercaptobenzothiazole ester derivatives |
US3077450A (en) * | 1960-07-01 | 1963-02-12 | Exxon Research Engineering Co | Oil compositions containing soapsalt mixtures |
US3155618A (en) * | 1960-04-05 | 1964-11-03 | Socony Mobil Oil Co Inc | Lubricant |
DE1233079B (en) * | 1953-10-21 | 1967-01-26 | Exxon Research Engineering Co | lubricant |
US5940247A (en) * | 1997-03-26 | 1999-08-17 | International Business Machines Corporation | Magnetic recording device with spindle motor lubricant of specified amine and carbamate concentrations/ratios |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2417432A (en) * | 1945-03-31 | 1947-03-18 | Union Oil Co | Lubricants |
US2417429A (en) * | 1945-04-16 | 1947-03-18 | Union Oil Co | Complex basic soap greases |
US2417439A (en) * | 1944-08-09 | 1947-03-18 | Overdick William | Chair |
US2417430A (en) * | 1945-03-31 | 1947-03-18 | Union Oil Co | Lubricants |
US2417428A (en) * | 1946-09-19 | 1947-03-18 | Union Oil Co | Lubricating composition |
US2455892A (en) * | 1946-08-27 | 1948-12-07 | Internat Lubricant Corp | Lubricating greases and method of making the same |
US2468098A (en) * | 1948-02-18 | 1949-04-26 | Standard Oil Dev Co | Grease composition |
US2487080A (en) * | 1947-11-28 | 1949-11-08 | Standard Oil Co | Grease |
US2564561A (en) * | 1944-05-20 | 1951-08-14 | Socony Vacuum Oil Co Inc | Grease composition |
US2575286A (en) * | 1949-07-29 | 1951-11-13 | Standard Oil Dev Co | Lubricating grease composition |
US2583607A (en) * | 1949-07-01 | 1952-01-29 | Honorary Advisory Council Sci | Complex soap greases |
US2588279A (en) * | 1950-02-02 | 1952-03-04 | Standard Oil Dev Co | Lubricating composition |
US2618599A (en) * | 1951-06-01 | 1952-11-18 | Standard Oil Dev Co | High melting point calcium grease of low soap content |
-
1954
- 1954-04-30 US US426928A patent/US2844536A/en not_active Expired - Lifetime
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2564561A (en) * | 1944-05-20 | 1951-08-14 | Socony Vacuum Oil Co Inc | Grease composition |
US2417439A (en) * | 1944-08-09 | 1947-03-18 | Overdick William | Chair |
US2417430A (en) * | 1945-03-31 | 1947-03-18 | Union Oil Co | Lubricants |
US2417432A (en) * | 1945-03-31 | 1947-03-18 | Union Oil Co | Lubricants |
US2417429A (en) * | 1945-04-16 | 1947-03-18 | Union Oil Co | Complex basic soap greases |
US2455892A (en) * | 1946-08-27 | 1948-12-07 | Internat Lubricant Corp | Lubricating greases and method of making the same |
US2417428A (en) * | 1946-09-19 | 1947-03-18 | Union Oil Co | Lubricating composition |
US2487080A (en) * | 1947-11-28 | 1949-11-08 | Standard Oil Co | Grease |
US2468098A (en) * | 1948-02-18 | 1949-04-26 | Standard Oil Dev Co | Grease composition |
US2583607A (en) * | 1949-07-01 | 1952-01-29 | Honorary Advisory Council Sci | Complex soap greases |
US2575286A (en) * | 1949-07-29 | 1951-11-13 | Standard Oil Dev Co | Lubricating grease composition |
US2588279A (en) * | 1950-02-02 | 1952-03-04 | Standard Oil Dev Co | Lubricating composition |
US2618599A (en) * | 1951-06-01 | 1952-11-18 | Standard Oil Dev Co | High melting point calcium grease of low soap content |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1233079B (en) * | 1953-10-21 | 1967-01-26 | Exxon Research Engineering Co | lubricant |
US2908645A (en) * | 1955-04-28 | 1959-10-13 | Exxon Research Engineering Co | Blended lithium calcium base grease |
US2985590A (en) * | 1955-09-28 | 1961-05-23 | Exxon Research Engineering Co | Lubricating oil compositions comprising mercaptobenzothiazole ester derivatives |
US3155618A (en) * | 1960-04-05 | 1964-11-03 | Socony Mobil Oil Co Inc | Lubricant |
US3077450A (en) * | 1960-07-01 | 1963-02-12 | Exxon Research Engineering Co | Oil compositions containing soapsalt mixtures |
DE1233080B (en) * | 1960-07-01 | 1967-01-26 | Exxon Research Engineering Co | lubricant |
US5940247A (en) * | 1997-03-26 | 1999-08-17 | International Business Machines Corporation | Magnetic recording device with spindle motor lubricant of specified amine and carbamate concentrations/ratios |
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