US2161584A - Petroleum lubricant composition - Google Patents
Petroleum lubricant composition Download PDFInfo
- Publication number
- US2161584A US2161584A US93760A US9376036A US2161584A US 2161584 A US2161584 A US 2161584A US 93760 A US93760 A US 93760A US 9376036 A US9376036 A US 9376036A US 2161584 A US2161584 A US 2161584A
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- US
- United States
- Prior art keywords
- oil
- xanthate
- xanthyl
- ethyl
- ethyl ether
- 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.)
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- 239000000314 lubricant Substances 0.000 title description 25
- 239000000203 mixture Substances 0.000 title description 10
- 239000003208 petroleum Substances 0.000 title description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 28
- 239000003921 oil Substances 0.000 description 18
- 238000012360 testing method Methods 0.000 description 14
- 238000011068 loading method Methods 0.000 description 11
- 239000012991 xanthate Substances 0.000 description 11
- 239000003513 alkali Substances 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 9
- 230000001050 lubricating effect Effects 0.000 description 9
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical class CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 8
- -1 beta, beta dichlor ethyl Chemical group 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000012937 correction Methods 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- 239000011707 mineral Substances 0.000 description 6
- 235000010755 mineral Nutrition 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- JCBJVAJGLKENNC-UHFFFAOYSA-M potassium ethyl xanthate Chemical compound [K+].CCOC([S-])=S JCBJVAJGLKENNC-UHFFFAOYSA-M 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010835 comparative analysis Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- CONMNFZLRNYHIQ-UHFFFAOYSA-N 3-methylbutoxymethanedithioic acid Chemical class CC(C)CCOC(S)=S CONMNFZLRNYHIQ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 101100180399 Mus musculus Izumo1r gene Proteins 0.000 description 1
- UOJYYXATTMQQNA-UHFFFAOYSA-N Proxan Chemical class CC(C)OC(S)=S UOJYYXATTMQQNA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WIKDURKPSJEWGB-UHFFFAOYSA-N phenylmethoxymethanedithioic acid Chemical class SC(=S)OCC1=CC=CC=C1 WIKDURKPSJEWGB-UHFFFAOYSA-N 0.000 description 1
- PEEXCRJDFUVJRT-UHFFFAOYSA-M potassium;methoxymethanedithioate Chemical compound [K+].COC([S-])=S PEEXCRJDFUVJRT-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- AAJRIJBGDLLRAE-UHFFFAOYSA-M sodium;butoxymethanedithioate Chemical compound [Na+].CCCCOC([S-])=S AAJRIJBGDLLRAE-UHFFFAOYSA-M 0.000 description 1
- PGGWALFSVWIQLA-UHFFFAOYSA-M sodium;propoxymethanedithioate Chemical compound [Na+].CCCOC([S-])=S PGGWALFSVWIQLA-UHFFFAOYSA-M 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
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
-
- 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
Definitions
- This invention has for its object the provision of novel lubricants capable of maintaining a lubricant film under conditions of high unit pressure.
- a further object is the provision of novel ingredients or bases for use as characterizing ingredients, in admixture with petroleum fractions, to produce therefrom lubricants capable of maintaining a lubricant film under unit loadings much higher than those at which the petroleum fraction alone will fall.
- a most important object is the provision of a method of lubrication, making use of the novel extreme pressure lubricants and novel characterizing agents therefor which are herein disclosed.
- This invention is based upon the discovery that a class of compounds comprising the dixanthyl ethyl ethers are novel and valuable extreme pressure characterizing agents, capable of conferring 40 upon petroleum oil fractions, when in admixture therewith, the power to maintain a lubricating film under conditions of extreme pressure.
- Dixanthyl ethyl ethers may be prepared by the reaction of alkali xanthates with beta, beta dichlor ethyl ether.
- Alkali xanthates or thiccarbonates are readily prepared by reacting an alcohol with carbon disulphide in the presence of an alkali such as potassium hydroxide.
- the reaction involved is of the type ROI-1+ CS2+ KO H- TtOSCSK-l H2O where K may be potassium or sodium and where R is an alkyl, aralkyl, or other substituted alkyl radical. Many of these alkali xanthates are known and described in the literature.
- alkali xanthates useful for the purposes of this invention are the alkali salts of ethyl xanthate, isoamyl xanthate, isopropyl xanthate and benzyl xanthate.
- the xanthic acid salts of any of the alkyl, aralkyl, or simply substituted alkyl radicals will be found useful, as for example, sodium n-butyl xanthate, potassium phenyl ethyl xanthate, potassium methyl xanthate, potassium oleyl xanthate, potassium n-amylxanthate, and sodium n-propyl xanthate.
- alkali xanthates of the above group may be reacted with beta, beta dichlor ethyl ether to form high boiling oils which are oil-miscible and substantially insoluble in water, and which possess the property of conferring upon petroleum fractions with which they are mixed an improved ability to maintain a lubricating film under conditions of extreme pressure loading.
- potassium ethyl xanthate was prepared in accordance with the reaction previously discussed. Then 32 parts of this potassium ethyl xanthate was dissolved in 320 parts (by weight) of ethyl alcohol. Then 14.3 parts of beta, beta dichlor ethyl was added at room temperature about 2025 C. and the mixture refluxed for 5 hours, at approximately 78 C. The mixture was allowed to stand overnight to settle the precipitate of potassium chloride, which was then removed by filtration.
- the filtrate was distilled or the removal of alcohol, after which the distillation residue was taken up in benzol and washed with water to insure complete removal of any potassium chloride or of any remaining unreacted potassium ethyl xanthate.
- the benzol layer was then heated to 120 C. under 2.5 mm. pressure to remove benzol and unreacted beta, beta dichlor ethyl ether.
- the product so obtained was a yellow oil, misci ble in petroleum fractions and substantially insoluble in water.
- the proportions of ingredients used were in the ratio of 2 mols of the alkali xanthate for 1 mol of beta, beta dichlor ethyl ether. Sumcient ethyl alcohol was used to completely dissolve the alkali xanthate and to give a reaction mixture of suitable fluidity.
- Other solvents which might well be used are methyl alcohol, propyl alcohol, or any solvent which is a mutual solvent for the reacting compounds, and which does not itself react with the reagents.
- mineral oil pound in disclosed possess to a marked degree the ability to increase the power of a petroleum fraction to maintain a lubricating film under conditions of extreme pressure loading.
- novel E. P. characterizing compounds herein disclosed are described as oil-miscible, which term is used in the sense that they are sufliciently soluble in oil to accomplish the purposes of this invention. They are likewise described as substantially water-insoluble, which means that they are at least sufliciently water-insoluble to prevent their removal from admixture with oil by contact with water such as might occur during storage and/or handling and/or use.
- the limits of concentration of the dixanthyl ethyl ether compounds in oil which will be found useful for the purposes of this invention will normally range from a minimum of about 0.5% by weight to a maximum of about 5.0% by weight in the oil.
- a lubricant oil composition capable of maintaining a lubricating film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether.
- a lubricating composition comprising a major portion of a mineral hydrocarbon oil and in admixture therewith a small amount of diethyl xanthyl ethyl ether.
- a lubricant oil composition capable of maintaining a lubricant film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether, wherein the alkyl xanthyl radicals are selected from the group consisting of ethyl xanthyl, iso-amyl xanthyl, iso-propyl xanthyi, and benzyl xanthyl.
- reaction product resulting from interaction of an alkali xanthate and beta, beta dichlor ethyl ether is probably a. dialkyl xanthyl ethyl ether, formed according to the following reaction, in the case of an ethyl xanthate:
- mineral oil pound in disclosed possess to a marked degree the ability to increase the power of a petroleum fraction to maintain a lubricating film under conditions of extreme pressure loading.
- novel E. P. characterizing compounds herein disclosed are described as oil-miscible, which term is used in the sense that they are sufliciently soluble in oil to accomplish the purposes of this invention. They are likewise described as substantially water-insoluble, which means that they are at least sufliciently water-insoluble to prevent their removal from admixture with oil by contact with water such as might occur during storage and/or handling and/or use.
- the limits of concentration of the dixanthyl ethyl ether compounds in oil which will be found useful for the purposes of this invention will normally range from a minimum of about 0.5% by weight to a maximum of about 5.0% by weight in the oil.
- a lubricant oil composition capable of maintaining a lubricating film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether.
- a lubricating composition comprising a major portion of a mineral hydrocarbon oil and in admixture therewith a small amount of diethyl xanthyl ethyl ether.
- a lubricant oil composition capable of maintaining a lubricant film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether, wherein the alkyl xanthyl radicals are selected from the group consisting of ethyl xanthyl, iso-amyl xanthyl, iso-propyl xanthyi, and benzyl xanthyl.
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- 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 Juno 6, 1939 UNITED STATES PATENT OFFICE mom 0. Moran, Wenonah. and Everett w. Fuller, Woodbury, N. 1., assignors to Socony-Vacuum Oil Company. Inoorpora ted, New York,
N. Y., a corporation of New York No Drawing.
Application August 1, 1938,
Serial No. 93,760
3 Claims.
Advances in mechanical design of gears, adoption of new forms of gear teeth, higher speeds, and greater load demands in many mechanisms have recently resulted in the subjection of lubri- 5 cated contact areas, as in gear teeth to loads of extremely high unit value. Petroleum fractions alone have been proven incompetent to carry these extremely high unit loads without serious rupture of the lubricating film between contacting areas, often resulting in seizure. To provide lubricants capable of maintaining lubricant films under such conditions, resort has been had to blends of major proportions of petroleum fractions with minor proportions of characterizing ingredients of various kinds. Such compounded lubricants for service under conditions of high unit loading are known as extreme pressure lubricants, and the characterizing ingredients are known as E. P. (extreme pressure) ingredients, or E. P. bases. This invention has to do with such lubricants and such bases.
This invention has for its object the provision of novel lubricants capable of maintaining a lubricant film under conditions of high unit pressure. A further object is the provision of novel ingredients or bases for use as characterizing ingredients, in admixture with petroleum fractions, to produce therefrom lubricants capable of maintaining a lubricant film under unit loadings much higher than those at which the petroleum fraction alone will fall. A most important object is the provision of a method of lubrication, making use of the novel extreme pressure lubricants and novel characterizing agents therefor which are herein disclosed.
This invention is based upon the discovery that a class of compounds comprising the dixanthyl ethyl ethers are novel and valuable extreme pressure characterizing agents, capable of conferring 40 upon petroleum oil fractions, when in admixture therewith, the power to maintain a lubricating film under conditions of extreme pressure.
Dixanthyl ethyl ethers may be prepared by the reaction of alkali xanthates with beta, beta dichlor ethyl ether. Alkali xanthates or thiccarbonates are readily prepared by reacting an alcohol with carbon disulphide in the presence of an alkali such as potassium hydroxide. The reaction involved is of the type ROI-1+ CS2+ KO H- TtOSCSK-l H2O where K may be potassium or sodium and where R is an alkyl, aralkyl, or other substituted alkyl radical. Many of these alkali xanthates are known and described in the literature. Examples of alkali xanthates useful for the purposes of this invention are the alkali salts of ethyl xanthate, isoamyl xanthate, isopropyl xanthate and benzyl xanthate. In general, the xanthic acid salts of any of the alkyl, aralkyl, or simply substituted alkyl radicals will be found useful, as for example, sodium n-butyl xanthate, potassium phenyl ethyl xanthate, potassium methyl xanthate, potassium oleyl xanthate, potassium n-amylxanthate, and sodium n-propyl xanthate.
We have found that alkali xanthates of the above group may be reacted with beta, beta dichlor ethyl ether to form high boiling oils which are oil-miscible and substantially insoluble in water, and which possess the property of conferring upon petroleum fractions with which they are mixed an improved ability to maintain a lubricating film under conditions of extreme pressure loading.
As an example of the preparation of one of the novel E, P. ingredients of this invention, the preparation of diethyl xanthyl ethyl ether will be described. First, potassium ethyl xanthate was prepared in accordance with the reaction previously discussed. Then 32 parts of this potassium ethyl xanthate was dissolved in 320 parts (by weight) of ethyl alcohol. Then 14.3 parts of beta, beta dichlor ethyl was added at room temperature about 2025 C. and the mixture refluxed for 5 hours, at approximately 78 C. The mixture was allowed to stand overnight to settle the precipitate of potassium chloride, which was then removed by filtration. The filtrate was distilled or the removal of alcohol, after which the distillation residue was taken up in benzol and washed with water to insure complete removal of any potassium chloride or of any remaining unreacted potassium ethyl xanthate. The benzol layer was then heated to 120 C. under 2.5 mm. pressure to remove benzol and unreacted beta, beta dichlor ethyl ether. The product so obtained was a yellow oil, misci ble in petroleum fractions and substantially insoluble in water.
The proportions of ingredients used were in the ratio of 2 mols of the alkali xanthate for 1 mol of beta, beta dichlor ethyl ether. Sumcient ethyl alcohol was used to completely dissolve the alkali xanthate and to give a reaction mixture of suitable fluidity. Other solvents which might well be used are methyl alcohol, propyl alcohol, or any solvent which is a mutual solvent for the reacting compounds, and which does not itself react with the reagents.
It will be apparent to those skilled in the art that the reaction product resulting from interaction of an alkali xanthate and beta, beta dichlor ethyl ether is probably a. dialkyl xanthyl ethyl ether, formed according to the following reaction, in the case of an ethyl xanthate:
To illustrate the eiiectiveness of novel ingredicuts of the class herein disclosed as characterizing E. P. ingredients for the production of extreme pressure lubricants, the following tests are noted. These tests were made in the Almen Pin Test Machine, (Mougey 8i Almen, Free. A. P. I. 1931, page 77), wherein a steel pin is rotated in a bearing so designed that increasing loads of known amount may be added, the assembly being lubricated by the oil undergoing test. This test is in wide use for the comparative evaluation of lubricants of this type. In the following tabulation of such tests, Table I, the first vertical column shows the loading in pounds per square inch of bearing area, and columns 2 and 3 show the torque in foot pounds applied to the Almen pin:
TABLE I Almen pin test results Torque, foot pounds 1 Load, pounds 2 3 r square m inch Straight 3:
mineral oil pound in disclosed possess to a marked degree the ability to increase the power of a petroleum fraction to maintain a lubricating film under conditions of extreme pressure loading.
The novel E. P. characterizing compounds herein disclosed are described as oil-miscible, which term is used in the sense that they are sufliciently soluble in oil to accomplish the purposes of this invention. They are likewise described as substantially water-insoluble, which means that they are at least sufliciently water-insoluble to prevent their removal from admixture with oil by contact with water such as might occur during storage and/or handling and/or use.
The limits of concentration of the dixanthyl ethyl ether compounds in oil which will be found useful for the purposes of this invention will normally range from a minimum of about 0.5% by weight to a maximum of about 5.0% by weight in the oil.
It will be understood that the exemplary preparation of one of the novel E. P. characterizing compounds of this invention discussed herein is given only by way of example and is not in any way intended as a limitation. It is our intention to claim broadly all of the novelty inherent in this invention, subject only to those limitations expressed in the following claims.
We claim:
1. A lubricant oil composition capable of maintaining a lubricating film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether.
2. A lubricating composition comprising a major portion of a mineral hydrocarbon oil and in admixture therewith a small amount of diethyl xanthyl ethyl ether.
3. A lubricant oil composition capable of maintaining a lubricant film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether, wherein the alkyl xanthyl radicals are selected from the group consisting of ethyl xanthyl, iso-amyl xanthyl, iso-propyl xanthyi, and benzyl xanthyl.
ROBERT C. MORAN. EVERETT W. FULLER.
CERTIFICATE OF CORRECTION;
Patent No. 2,161,581;-
ROBERT C June 6, 1939. mm, ET AL.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 1, first column, line 51, for the word "fall" read fail; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 8th day of August, A. D. 19 9.
(Seal) Leslie Frazer, Acting Commissioner of Patents.
that the reaction product resulting from interaction of an alkali xanthate and beta, beta dichlor ethyl ether is probably a. dialkyl xanthyl ethyl ether, formed according to the following reaction, in the case of an ethyl xanthate:
To illustrate the eiiectiveness of novel ingredicuts of the class herein disclosed as characterizing E. P. ingredients for the production of extreme pressure lubricants, the following tests are noted. These tests were made in the Almen Pin Test Machine, (Mougey 8i Almen, Free. A. P. I. 1931, page 77), wherein a steel pin is rotated in a bearing so designed that increasing loads of known amount may be added, the assembly being lubricated by the oil undergoing test. This test is in wide use for the comparative evaluation of lubricants of this type. In the following tabulation of such tests, Table I, the first vertical column shows the loading in pounds per square inch of bearing area, and columns 2 and 3 show the torque in foot pounds applied to the Almen pin:
TABLE I Almen pin test results Torque, foot pounds 1 Load, pounds 2 3 r square m inch Straight 3:
mineral oil pound in disclosed possess to a marked degree the ability to increase the power of a petroleum fraction to maintain a lubricating film under conditions of extreme pressure loading.
The novel E. P. characterizing compounds herein disclosed are described as oil-miscible, which term is used in the sense that they are sufliciently soluble in oil to accomplish the purposes of this invention. They are likewise described as substantially water-insoluble, which means that they are at least sufliciently water-insoluble to prevent their removal from admixture with oil by contact with water such as might occur during storage and/or handling and/or use.
The limits of concentration of the dixanthyl ethyl ether compounds in oil which will be found useful for the purposes of this invention will normally range from a minimum of about 0.5% by weight to a maximum of about 5.0% by weight in the oil.
It will be understood that the exemplary preparation of one of the novel E. P. characterizing compounds of this invention discussed herein is given only by way of example and is not in any way intended as a limitation. It is our intention to claim broadly all of the novelty inherent in this invention, subject only to those limitations expressed in the following claims.
We claim:
1. A lubricant oil composition capable of maintaining a lubricating film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether.
2. A lubricating composition comprising a major portion of a mineral hydrocarbon oil and in admixture therewith a small amount of diethyl xanthyl ethyl ether.
3. A lubricant oil composition capable of maintaining a lubricant film under conditions of high unit loading comprising a major portion of a mineral hydrocarbon lubricant not so capable, and in admixture therewith a small amount of an oil-miscible, substantially water-insoluble dialkyl xanthyl ethyl ether, wherein the alkyl xanthyl radicals are selected from the group consisting of ethyl xanthyl, iso-amyl xanthyl, iso-propyl xanthyi, and benzyl xanthyl.
ROBERT C. MORAN. EVERETT W. FULLER.
CERTIFICATE OF CORRECTION;
Patent No. 2,161,581;-
ROBERT C June 6, 1939. mm, ET AL.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 1, first column, line 51, for the word "fall" read fail; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 8th day of August, A. D. 19 9.
(Seal) Leslie Frazer, Acting Commissioner of Patents.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93760A US2161584A (en) | 1936-08-01 | 1936-08-01 | Petroleum lubricant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93760A US2161584A (en) | 1936-08-01 | 1936-08-01 | Petroleum lubricant composition |
Publications (1)
Publication Number | Publication Date |
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US2161584A true US2161584A (en) | 1939-06-06 |
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US93760A Expired - Lifetime US2161584A (en) | 1936-08-01 | 1936-08-01 | Petroleum lubricant composition |
Country Status (1)
Country | Link |
---|---|
US (1) | US2161584A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2537518A (en) * | 1946-05-02 | 1951-01-09 | Pittsburgh Plate Glass Co | Diethylene glycol bis |
US2843546A (en) * | 1952-08-13 | 1958-07-15 | Huels Chemische Werke Ag | Lubricant |
US4019991A (en) * | 1975-02-27 | 1977-04-26 | Edwin Cooper & Company Limited | Sulphur containing lubricating oil additives |
US4981869A (en) * | 1980-11-26 | 1991-01-01 | Merz & Co., Gmbh & Co. | Xanthates as antitumor agents |
-
1936
- 1936-08-01 US US93760A patent/US2161584A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2537518A (en) * | 1946-05-02 | 1951-01-09 | Pittsburgh Plate Glass Co | Diethylene glycol bis |
US2843546A (en) * | 1952-08-13 | 1958-07-15 | Huels Chemische Werke Ag | Lubricant |
US4019991A (en) * | 1975-02-27 | 1977-04-26 | Edwin Cooper & Company Limited | Sulphur containing lubricating oil additives |
US4981869A (en) * | 1980-11-26 | 1991-01-01 | Merz & Co., Gmbh & Co. | Xanthates as antitumor agents |
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