US2541789A - Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid - Google Patents
Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid Download PDFInfo
- Publication number
- US2541789A US2541789A US740723A US74072347A US2541789A US 2541789 A US2541789 A US 2541789A US 740723 A US740723 A US 740723A US 74072347 A US74072347 A US 74072347A US 2541789 A US2541789 A US 2541789A
- Authority
- US
- United States
- Prior art keywords
- phosphorized
- sulfurized
- additive
- per cent
- oil
- 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
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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/08—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-nitrogen bonds
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
-
- 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
Definitions
- This invention relates to lubricants and additives and, more particularly, to additives which have the ability to render a blend of lubricating oil with the additive capable of carrying a high load and also showing a low pour point.
- esters of decenoic, myristoleic, palmitoleic, oleic, erucic, and tetracosenoic acids combined with any one of the polyhydroxy alcohols, such as glycol, glycerol, propylene glycol and butylene glycol as typical examples.
- the polyhydroxy alcohols such as glycol, glycerol, propylene glycol and butylene glycol as typical examples.
- compounds which are completely esterified alcohols those in which only partial esterification has taken place are also suitable, for example, the mono-, diand triesters of glycerol and monoand (ii-esters of glycols can be used.
- the sulfurization can be carried out using flowers of sulfur or a sulfur compound.
- the phosphorization can be accomplished with elemental phosphorus or a phosphorus compound.
- the sulfurization or phosphorization reaction is conducted by blowing air through the reaction mixture at a rate sufiicient to make the reaction selfsustaining thermally. This process is described in detail in United States Patent Application, Serial Number 636,286, filed December 20, 1945, by Elmer W. Brennan and Norman D. Williams (now Patent No. 2,483,571).
- compositions may be used which contain small amounts of polyethenoid acids or esters thereof as well as small amounts of ethanoid compounds.
- Compositions deviating from pure compounds are exemplified by such products as partially hydrogenated sunflower, corn and rapeseed oils in which the hydrogenation is carried to a point where the acid radicals having more unsaturation than a single double bond are hydrogenated to a single double bond radical.
- Olive oil is fairly satisfactory as a starting material.
- the fatty acid content of compositions useful as starting materials in accordance with my invention should be not less than per cent of monoethenoid acids and not more than 10 per cent of acids of greater unsaturation.
- a composition was prepared by mixing 5 parts by weight of Gulf Coast mineral oil (having a Saybolt-Viscosity at F. of 200 to 210 seconds, and at 210 F. of 43 to 45 seconds) and 87.6 parts by weight of glycerol oleates composed of approximately 70 per cent by weight of glycerol trioleate, 20 per cent by weight of glycerol dioleate and 10 per cent by weight of glycerol monooleate. The mixture was slowly heated to a temperature of approximately 270 F., whereupon 7.4 parts by weight of finely ground flowers of sulfur was added over a period of about 10 minutes. After the addition of the sulfur was completed the room temperature.
- Gulf Coast mineral oil having a Saybolt-Viscosity at F. of 200 to 210 seconds, and at 210 F. of 43 to 45 seconds
- glycerol oleates composed of approximately 70 per cent by weight of glycerol trioleate, 20 per cent by weight of glycerol di
- blend No. 3 shown in Table II, displays unusual properties which make it perform like an S. A. E. 80-S. A. E. grade lubricant, because the channel and extrapolated viscosity at zero Fahrenheit meet the requirements of the S. A. E. 80 grade, while the viscosity at 210 Frplaces it in the S. A. E. 90 grade. Not only do the bench tests and graphs of its physical properties point to its unusual nature, but actual field tests indicate it to be a superior lubricant, as the test described below will establish.
- a new clean differential unit was installedi'n a 1946 De Soto sedan in which the axle housing had previously been thoroughly cleaned.
- the housing was filled with the test lubricant corresponding in composition to N0. 3 above, and the car was driven for ten miles at a rate of 30 miles per hour in order to warm the engine and provide a moderate amount of rear axle break in, v
- the car was then driven for 1,000 miles athigh-speed ⁇ l S-P Base: sulfurized-phosphorized propyleneglycol dioleate.
- sulfurization may be effected by means of elemental sulfur in an amount of from 1 to per cent by weight, and preferably 5 to 8.5 per cent by weight of sulfur based on the sulfurized product.
- the base can be prepared by sulfurizing the ester in accordance with the method disclosed in United States Patent 2,352,818, of July 4, 1944, to Whittier et al., using approximately 5 to per cent by weight of the sulfur chloride based on the ester.
- the phosphorization step is preferably effected by means of phosphorus sesquisulfide at temperatures of about 220 to 230 F., but other phosphorus compounds, including halides, oxyhalides, sulfides, and oxides such as phosphorus trichloride, phosphorus oxychloride, phosphorus pentasulfide and phosphorus pentoxide, as well as elemental phosphorus and compounds such as tin phosphide, may be used.
- the amount of phosphorus in the base should not exceed 2 per cent, and preferably should be only a fraction of 1 per cent, for example 0.2 to 0.6 per cent based on the weight of the sulfurized base.
- Additives made in accordance with my invention may be used in lubricating oils in amounts ranging from approximately 0.5 to per cent or more by weight of the finished lubricant depending upon the service for which the lubricant is intended.
- additives prepared in accordance with my invention may be blended with all types of mineral lubricating oil, I prefer to keep the amount of high viscosityindex oil, as exemplified by Mid-Continent solvent refined oil, to a minimum except when employing propylene glycol dioleate as the additive, because generally the sulfurized-phosphorized fatty materials have limited compatibility with high viscosity-index oil.
- the sulfurized-phosphorized propylene glycol dioleate appears to be unique in possessing the additional property of being quite completely compatible with the solvent refined oils.
- a lubricant comprising a major portion of a Mid-Continent Solvent Refined petroleum lubricating oil and a minor portion of a composition as the principal additive; effective to improve its load carrying characteristics, which additive consists substantially of a sulfurized and phosphorized ester from the group consisting of propylene and butylene glycol dioleates, the sulfur content of said additive being about 1 to 10 per cent, and the phosphorus content being about 0.2 to 0.6 per cent, said additive being soluble in said oil.
- a lubricant in accordance with claim 1 in which the ester is sulfurized with sulfur in an amount equal to about 5 to 8.5 per cent by weight of the sulfurized product, and the sulfurized product is phosphorized with phosphorus sesquisulfide in an amount equivalent to 0.2 to 0.6 per cent of phosphorus based on the sulfurized product.
- a lubricant in accordance with claim 4 in which the sulfurized and phosphorized propylene glycol dioleate is present in an amount of about 15 per cent by weight of the total lubricant, and the lubricant contains about 1 per cent of dibenzyl disulfide.
- a lubricant additive consisting of sulfurized and phosphorized ester from the group consisting of propylene and butylene glycol dioleates, said additive containing about 0.2 to about 0.6 per cent of phosphorus, and aboutl to 10 per cent of sulfur, and being soluble in Mid-Continent Solvent Refined blended oils.
- a lubricant additive in accordance with claim 7 in which the propylene glycol dioleate is sulfurized with elemental sulfur, and the sulfurized product is phosphorized with phosphorus sesquisulfide.
- a lubricant additive consisting substantially of the phosphorized reaction product of sulfur and propylene glycol dioleate mixed with a small amount of mineral oil, said additive being soluble in Mid-Continent Solvent Refined petroleum lubricating oil and prepared by reacting about 5 to 8.5 per cent by weight of sulfur with propylene glycol dioleate, and then reacting the sulfurized product with 0.2 to 0.6 per cent by weight of phosphorus sesquisulfide based on the sulfurized product.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Feb. 13, 1951 MINERAL OIL LUBRICANT CONTAINING SULFURIZED AND PHOSPHORIZED PRO- PYLENE AND BUTYLENE GLYCOL ESTERS OF OLEIC ACID Joseph B. Stucker, Des Plaines, Ill., assignor to The Pure Oil Company, Chicago, 111., a corporation of Ohio No Drawing. Application April 10, 1947, Serial No. 740,723
9 Claims. (01. 252-46.6)
This invention relates to lubricants and additives and, more particularly, to additives which have the ability to render a blend of lubricating oil with the additive capable of carrying a high load and also showing a low pour point.
In United States Patent 2,211,306, of August 13,
1940, to Whittier, assigned to The Pure Oil Company, there is disclosed and claimed a process for preparing an extreme pressure lubricant additive which involves sulfurizing a fatty body or oil and subsequently phosphorizing the sulfurized product. Such extreme pressure additives have been in successful use for many years, and have proved to be quite satisfactory. However, when made from ordinary fatty oils, such as lard oil, these additives have one disadvantage, namely, the lubricant which is a blend of the additive with a mineral oil does not have as low a pour point as might be desired. In addition to this disadvantage, the lubricants also display a somewhat limited compatibility with Mid-Continent solvent refined oils.
Accordingly, it is an object of the invention to provide an extreme pressure additive which when blended with minerals oils will endow the blend with low pour point characteristics and improved compatibility with Mid-Continent solvent refined oils.
Other objects and advantages of the invention will in part be obvious and in part appear hereinafter.
I have discovered that sulfurized and phosphorized extreme pressure additives displaying high load carrying characteristics and low pour points can be prepared in accordance with the method disclosed and claimed in United States Patent 2,211,306, if the fatty body is an ester of a polyhydroxy alcohol and a monoethenoid acid having the general formula CnH21L202, and containing from about to 24 carbon atoms in the molecule. In particular, I have found that the esters of glycerol and glycols having more than 2 carbon atoms are valuable starting materials. Compounds suitable for the preparation of additives in accordance with my invention include esters of decenoic, myristoleic, palmitoleic, oleic, erucic, and tetracosenoic acids combined with any one of the polyhydroxy alcohols, such as glycol, glycerol, propylene glycol and butylene glycol as typical examples. Although it is preferable, generally, to use compounds which are completely esterified alcohols, those in which only partial esterification has taken place are also suitable, for example, the mono-, diand triesters of glycerol and monoand (ii-esters of glycols can be used.
In preparation of the sulfurized-phosphorized base, the sulfurization can be carried out using flowers of sulfur or a sulfur compound. Similarly, the phosphorization can be accomplished with elemental phosphorus or a phosphorus compound. When the fatty material or ester is cooked with the sulfur or phosphorus compound, it is customary practice to do so in an open kettle while stirring the reactants. However, better results in the form of precise control over the reaction and the product are obtainable when the sulfurization or phosphorization reaction is conducted by blowing air through the reaction mixture at a rate sufiicient to make the reaction selfsustaining thermally. This process is described in detail in United States Patent Application, Serial Number 636,286, filed December 20, 1945, by Elmer W. Brennan and Norman D. Williams (now Patent No. 2,483,571).
Instead of using pure polyhydroxy alcoholmono-ethenoid acid esters, compositions may be used which contain small amounts of polyethenoid acids or esters thereof as well as small amounts of ethanoid compounds. Compositions deviating from pure compounds are exemplified by such products as partially hydrogenated sunflower, corn and rapeseed oils in which the hydrogenation is carried to a point where the acid radicals having more unsaturation than a single double bond are hydrogenated to a single double bond radical. Olive oil is fairly satisfactory as a starting material. In general, the fatty acid content of compositions useful as starting materials in accordance with my invention should be not less than per cent of monoethenoid acids and not more than 10 per cent of acids of greater unsaturation. a
In order to demonstrate the invention a composition was prepared by mixing 5 parts by weight of Gulf Coast mineral oil (having a Saybolt-Viscosity at F. of 200 to 210 seconds, and at 210 F. of 43 to 45 seconds) and 87.6 parts by weight of glycerol oleates composed of approximately 70 per cent by weight of glycerol trioleate, 20 per cent by weight of glycerol dioleate and 10 per cent by weight of glycerol monooleate. The mixture was slowly heated to a temperature of approximately 270 F., whereupon 7.4 parts by weight of finely ground flowers of sulfur was added over a period of about 10 minutes. After the addition of the sulfur was completed the room temperature. To 99.6 parts of the sulfurized base thus prepared was added 0.4 part by weight 7 of finely divided phosphorus sesquisulfide and the mixture heated with constant agitation to a tem-' perature of approximately 220 to 230 F. The heating was continued for a period of approximately hours and the mixture then allowed to cool. The resulting product was non-corrosive to the copper strip test and did not fume when heated to 300 to 350 F. Blends of '18 per cent by weight of the sulfurized phosphorized product with mineral oil were prepared to obtain compositions corresponding to an 80 S. A. E. and a 90 S.'A. E. gravity oil. These blendswere tested for viscosity, viscosity index, pour point, and Timken test and compared with similar blends of phosphorized-sulfurized lard oil made in accordance with the specific example set forth in the manner just described in which glycerol oleates were used. The results Of these tests are set forth in the following table:
Table I Examples Composition, percent By Weight:
Saybolt V. I. 57 Poor, F -00 +5 0 0 Timken Testfl" Load" 77 86 33 Beam .c 30. 0 20.0 S.-.A.'E., 750 155 275 100 Viscosity Gulf Coast Pale Oil.
2 200 Viscosity Gulf Coast Pale Oil.
3 160 Viscosity Gull Coast'Bright Stock at 210 l Blend of Gulf Coast Pale Oil and Bright Stock to desired viscosity.
5 Blend of Gulf Coast Pale Oil and Bright Stock to, desired viscosity.
B 8-1 Ester-Propylene glycol dioleate. 7 Timken test:.load in pounds; beam in, thousands of pounds per square inch.
From an inspection of the table, it is apparent that the blends made by sulfurizing and phosphorizing the glycerol oleate had higher viscosity indexes than the sulfurized-phosphorized lard oil blends, and the pour points of the sulfurizedphosphorized glycerol oleate blends Were considerably lower. For example, the 90 S. A. E. grade, #4 in the table, had a pour point degrees lower than the 80 S. A. E. grademade from the lard oil, #1 in the table. The Timken tests for the sulfurized-phosphorized glycerol .oleate compositions were at least as good as the sulfur ized-phosphorized lard oil compositions, and, in general, were superior from a load carrying standpoint.
Brends' prepared in accordance with the second and fourth examples in the table weresubjected to actual service tests in the transmissions and differentials of a number of different automobiles. After 4,000 to 5,000 miles of operation, the gears showed no evidence of wear, and the lubricant exhibited high stability. Low temperature characteristics of the lubricant were excellent as evidenced by the fact that after the automobile had been allowed to stand outdoors at temperatures approaching minus 10 F. the gears could be shifted with ease.
Additional blends of extreme pressure additives made from sulfurized-phosphorized propylene glycol dioleate and Mid-Continent solvent refined oils were made and tested. It was found that the propylene glycol dioleate, in addition to making a good extreme pressure additive, also displayed unusual compatibility with the Mid- Continent solvent refined oil. In regulating the compatibility of this additive with the Mid-Continent solvent refined oil, it is well to employ a relatively pure oleic acid in the preparation of the ester, because the 5 to 1 8 per cent ofv poly-- ethenoid acids occurring in commercial oleic acid detract from the compatibilityof the sulfurized. phosporized material, and will cause the separation of a small amount of tarry matter from the blends. In the following table, there are summarized the properties of a iew typical blends, made from propylene glycol dioleate and Mid- Continent solvent refined oils in combination witha few additives:
Examples Composition, percent By Weight:
S-P Base Timken 4 Test:
Load
Beam S. A/E. at 750 R. P. M
It should be noted that blend No. 3, shown in Table II, displays unusual properties which make it perform like an S. A. E. 80-S. A. E. grade lubricant, because the channel and extrapolated viscosity at zero Fahrenheit meet the requirements of the S. A. E. 80 grade, while the viscosity at 210 Frplaces it in the S. A. E. 90 grade. Not only do the bench tests and graphs of its physical properties point to its unusual nature, but actual field tests indicate it to be a superior lubricant, as the test described below will establish.
A new clean differential unit was installedi'n a 1946 De Soto sedan in which the axle housing had previously been thoroughly cleaned. The housing was filled with the test lubricant corresponding in composition to N0. 3 above, and the car was driven for ten miles at a rate of 30 miles per hour in order to warm the engine and provide a moderate amount of rear axle break in, v The car was then driven for 1,000 miles athigh-speed} l S-P Base: sulfurized-phosphorized propyleneglycol dioleate.
60 to 90 miles per hour. At the end of this period, the rear axle unit operated perfectly quietly and on disassembly, the ring, pinion and differential gear were found to be in essentially their pristine condition, for they showed no trace of scoring.
In preparing the additive in accordance with my invention, sulfurization may be effected by means of elemental sulfur in an amount of from 1 to per cent by weight, and preferably 5 to 8.5 per cent by weight of sulfur based on the sulfurized product. Also the base can be prepared by sulfurizing the ester in accordance with the method disclosed in United States Patent 2,352,818, of July 4, 1944, to Whittier et al., using approximately 5 to per cent by weight of the sulfur chloride based on the ester. The phosphorization step is preferably effected by means of phosphorus sesquisulfide at temperatures of about 220 to 230 F., but other phosphorus compounds, including halides, oxyhalides, sulfides, and oxides such as phosphorus trichloride, phosphorus oxychloride, phosphorus pentasulfide and phosphorus pentoxide, as well as elemental phosphorus and compounds such as tin phosphide, may be used. The amount of phosphorus in the base should not exceed 2 per cent, and preferably should be only a fraction of 1 per cent, for example 0.2 to 0.6 per cent based on the weight of the sulfurized base.
It will be seen, therefore, that by sulfurizing and phosphorizing a fatty body composed chiefly of esters of polyhydroxy alcohols and monoethenoid acids a lubricant additive having high load carrying characteristics and unexpected low temperature characteristics can be obtained. Additives made in accordance with my invention may be used in lubricating oils in amounts ranging from approximately 0.5 to per cent or more by weight of the finished lubricant depending upon the service for which the lubricant is intended. Although additives prepared in accordance with my invention may be blended with all types of mineral lubricating oil, I prefer to keep the amount of high viscosityindex oil, as exemplified by Mid-Continent solvent refined oil, to a minimum except when employing propylene glycol dioleate as the additive, because generally the sulfurized-phosphorized fatty materials have limited compatibility with high viscosity-index oil. The sulfurized-phosphorized propylene glycol dioleate appears to be unique in possessing the additional property of being quite completely compatible with the solvent refined oils.
This application is a continuation-in-part of my application Serial Number 653,438, filed March 9, 1946.
What is claimed is:
1. A lubricant comprising a major portion of a Mid-Continent Solvent Refined petroleum lubricating oil and a minor portion of a composition as the principal additive; effective to improve its load carrying characteristics, which additive consists substantially of a sulfurized and phosphorized ester from the group consisting of propylene and butylene glycol dioleates, the sulfur content of said additive being about 1 to 10 per cent, and the phosphorus content being about 0.2 to 0.6 per cent, said additive being soluble in said oil.
2. A lubricant in accordance with claim 1 in which the ester is sulfurized with sulfur in an amount equal to about 5 to 8.5 per cent by weight of the sulfurized product, and the sulfurized product is phosphorized with phosphorus sesquisulfide in an amount equivalent to 0.2 to 0.6 per cent of phosphorus based on the sulfurized product.
3. A lubricant in accordance with claim 1 in which the petroleum lubricating oil is a blend of Mid-Continent Solvent Refined bright stock and neutral oil, and the additive is a sulfurizedphosphorized propylene glycol dioleate.
4. A compounded mineral oil-lubricant in accordance with claim 1 in which the additive is sulfurized and phosphorized propylene glycol dioleate.
5. A lubricant in accordance with claim 4 in which the sulfurized and phosphorized propylene glycol dioleate is present in an amount of about 15 per cent by weight of the total lubricant, and the lubricant contains about 1 per cent of dibenzyl disulfide.
6. A lubricant additive consisting of sulfurized and phosphorized ester from the group consisting of propylene and butylene glycol dioleates, said additive containing about 0.2 to about 0.6 per cent of phosphorus, and aboutl to 10 per cent of sulfur, and being soluble in Mid-Continent Solvent Refined blended oils.
7. A lubricant additive in accordance with claim 6 in which the ester is propylene glycol dioleate.
8. A lubricant additive in accordance with claim 7 in which the propylene glycol dioleate is sulfurized with elemental sulfur, and the sulfurized product is phosphorized with phosphorus sesquisulfide.
9. A lubricant additive consisting substantially of the phosphorized reaction product of sulfur and propylene glycol dioleate mixed with a small amount of mineral oil, said additive being soluble in Mid-Continent Solvent Refined petroleum lubricating oil and prepared by reacting about 5 to 8.5 per cent by weight of sulfur with propylene glycol dioleate, and then reacting the sulfurized product with 0.2 to 0.6 per cent by weight of phosphorus sesquisulfide based on the sulfurized product.
JOSEPH B. STUCKER.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,211,231 Henderson Aug. 13, 1940 2,211,306 Whittier et al Aug. 13, 1940 2,242,260 Prutton May 20, 1941 2,418,422 Palmer Apr. 1, 1947 2,441,587 Musselman May 18, 1948 2,480,873 Musselman Sept. 6, 1949 2,483,600 Stucker Oct. 4, 1949
Claims (1)
1. A LUBRICANT COMPRISING A MAJOR PORTION OF A MID-CONTINENT SOLVENT REFINED PETROLEUM LUBRICATING OIL AND A MINOR PORTION OF A COMPOSITION AS THE PRINCIPAL ADDITIVE, EFFECTIVE TO IMPROVE ITS LOAD CARRYING CHARACTERISTICS, WHICH ADDITIVE CONSISTS SUBSTANTIALLY OF A SULFURIZED AND PHOSPHORIZED ESTER FROM THE GROUP CONSISTINJG OF PROPYLENE AND BUTYLENE GLYCOL DIOLEATES, THE SULFUR CONTENT OF SAID ADDITIVE BEING ABOUT 1 TO 10 PER CENT, AND THE PHOSPHORUS CONTENT BEING ABOUT 0.2 TO 0.6 PER CENT, SAID ADDITIVE BEING SOLUBLE IN SAID OIL.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US740723A US2541789A (en) | 1947-04-10 | 1947-04-10 | Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US740723A US2541789A (en) | 1947-04-10 | 1947-04-10 | Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
US2541789A true US2541789A (en) | 1951-02-13 |
Family
ID=24977786
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US740723A Expired - Lifetime US2541789A (en) | 1947-04-10 | 1947-04-10 | Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid |
Country Status (1)
Country | Link |
---|---|
US (1) | US2541789A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2628939A (en) * | 1947-11-21 | 1953-02-17 | Monsanto Chemicals | Mineral oil composition |
DE948811C (en) * | 1952-08-01 | 1956-09-06 | Pure Oil Co | Additive to mineral lubricating oils |
US4908400A (en) * | 1987-02-16 | 1990-03-13 | Du Pont-Showa Denko Co., Ltd. | Plasticizer for chloroprene rubber and plasticized chloroprene rubber |
US4959168A (en) * | 1988-01-15 | 1990-09-25 | The Lubrizol Corporation | Sulfurized compositions, and additive concentrates and lubricating oils containing same |
US20060016118A1 (en) * | 2004-07-26 | 2006-01-26 | Andrew Zuk | Fishing lure and kit |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2211306A (en) * | 1935-12-19 | 1940-08-13 | Pure Oil Co | Lubricant and method of preparing same |
US2211231A (en) * | 1935-12-19 | 1940-08-13 | Pure Oil Co | Lubricant and method of preparing same |
US2242260A (en) * | 1937-01-22 | 1941-05-20 | Lubri Zol Dev Corp | Lubricating composition |
US2418422A (en) * | 1944-12-11 | 1947-04-01 | Sinclair Refining Co | Lubricant |
US2441587A (en) * | 1944-07-25 | 1948-05-18 | Standard Oil Co | Method of preparing composition of matter suitable for use as a lubricant and as an addition agent to lubricants |
US2480873A (en) * | 1944-12-18 | 1949-09-06 | Standard Oil Co | Lubricants |
US2483600A (en) * | 1946-05-16 | 1949-10-04 | Pure Oil Co | Preparation of high-viscosity extreme pressure base by airblowing |
-
1947
- 1947-04-10 US US740723A patent/US2541789A/en not_active Expired - Lifetime
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2211306A (en) * | 1935-12-19 | 1940-08-13 | Pure Oil Co | Lubricant and method of preparing same |
US2211231A (en) * | 1935-12-19 | 1940-08-13 | Pure Oil Co | Lubricant and method of preparing same |
US2242260A (en) * | 1937-01-22 | 1941-05-20 | Lubri Zol Dev Corp | Lubricating composition |
US2441587A (en) * | 1944-07-25 | 1948-05-18 | Standard Oil Co | Method of preparing composition of matter suitable for use as a lubricant and as an addition agent to lubricants |
US2418422A (en) * | 1944-12-11 | 1947-04-01 | Sinclair Refining Co | Lubricant |
US2480873A (en) * | 1944-12-18 | 1949-09-06 | Standard Oil Co | Lubricants |
US2483600A (en) * | 1946-05-16 | 1949-10-04 | Pure Oil Co | Preparation of high-viscosity extreme pressure base by airblowing |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2628939A (en) * | 1947-11-21 | 1953-02-17 | Monsanto Chemicals | Mineral oil composition |
DE948811C (en) * | 1952-08-01 | 1956-09-06 | Pure Oil Co | Additive to mineral lubricating oils |
US4908400A (en) * | 1987-02-16 | 1990-03-13 | Du Pont-Showa Denko Co., Ltd. | Plasticizer for chloroprene rubber and plasticized chloroprene rubber |
US4959168A (en) * | 1988-01-15 | 1990-09-25 | The Lubrizol Corporation | Sulfurized compositions, and additive concentrates and lubricating oils containing same |
US20060016118A1 (en) * | 2004-07-26 | 2006-01-26 | Andrew Zuk | Fishing lure and kit |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3740333A (en) | Compositions useful as sperm oil substitutes | |
US2540570A (en) | Extreme pressure lubricant | |
US2541789A (en) | Mineral oil lubricant containing sulfurized and phosphorized propylene and butylene glycol esters of oleic acid | |
US2483571A (en) | Reaction of organic substances with phosphorous sesquisulfide | |
US2179061A (en) | Manufacture of lubricating compositions | |
US2211231A (en) | Lubricant and method of preparing same | |
US2528732A (en) | Reaction products of diesters of dithiophosphoric acid and mineral oil compositions containing the same | |
US2483600A (en) | Preparation of high-viscosity extreme pressure base by airblowing | |
US2250545A (en) | Lubricating composition | |
US2542161A (en) | Mineral oil lubricant containing phosphorized and sulfurized glyceryl trioleate | |
US2167439A (en) | Sulphur cutting o | |
US2411153A (en) | Mineral oil composition and improving agent | |
US2303558A (en) | Premium cup grease of improved heat and texture stability | |
US2871191A (en) | Greases stabilized with organic carbonates | |
US2367355A (en) | Lubricant | |
US2382121A (en) | Lubricant and method of preparing same | |
US2873254A (en) | Extreme pressure lubricants | |
US2268232A (en) | High film strength lubricant and method of preparing same | |
US2550406A (en) | Extreme pressure lubricants | |
US2720491A (en) | Extreme pressure lubricant | |
US2969326A (en) | Lubricant composition | |
US2830024A (en) | Extreme pressure gear lubricant | |
US2910438A (en) | Preparation of an extreme pressure additive and gear oil containing same | |
US2830023A (en) | Complex ester-phosphorus sulfide reaction products and lubricants containing them | |
US2628940A (en) | Extreme pressure lubricant |