US2364830A - Lubricating oil - Google Patents
Lubricating oil Download PDFInfo
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- US2364830A US2364830A US345989A US34598940A US2364830A US 2364830 A US2364830 A US 2364830A US 345989 A US345989 A US 345989A US 34598940 A US34598940 A US 34598940A US 2364830 A US2364830 A US 2364830A
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- Prior art keywords
- oil
- polymer
- rubber
- sulfurized
- lubricating oil
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- 239000010687 lubricating oil Substances 0.000 title description 30
- 229920000642 polymer Polymers 0.000 description 72
- 229920001971 elastomer Polymers 0.000 description 70
- 239000005060 rubber Substances 0.000 description 70
- 239000003921 oil Substances 0.000 description 60
- 239000000203 mixture Substances 0.000 description 23
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 14
- 229910052801 chlorine Inorganic materials 0.000 description 14
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 12
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 11
- 229910052717 sulfur Inorganic materials 0.000 description 11
- 239000011593 sulfur Substances 0.000 description 11
- 239000010688 mineral lubricating oil Substances 0.000 description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 9
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 9
- 229910052796 boron Inorganic materials 0.000 description 9
- 239000007795 chemical reaction product Substances 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 9
- 229960000583 acetic acid Drugs 0.000 description 8
- 238000005260 corrosion Methods 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 239000012362 glacial acetic acid Substances 0.000 description 7
- -1 halogen acids Chemical class 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 6
- 239000002199 base oil Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 101150039167 Bex3 gene Proteins 0.000 description 1
- 229920001368 Crepe rubber Polymers 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- 229910021623 Tin(IV) bromide Inorganic materials 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical class BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 1
- NSAODVHAXBZWGW-UHFFFAOYSA-N cadmium silver Chemical compound [Ag].[Cd] NSAODVHAXBZWGW-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical compound Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- LTSUHJWLSNQKIP-UHFFFAOYSA-J tin(iv) bromide Chemical compound Br[Sn](Br)(Br)Br LTSUHJWLSNQKIP-UHFFFAOYSA-J 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000008096 xylene Substances 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
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
-
- 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
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/041—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds involving sulfurisation of macromolecular compounds, e.g. polyolefins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
Definitions
- An extreme pressure lubricant is generally composed of a hydrocarbon lubricating oil and a minor proportion of an ingredient which imparts extreme pressure characteristics to the oil; i. e., characteristics which enable the oil to form between the engaged surfaces a lubricating film capable of withstanding high pressures.
- the lubricating oil compositions of the present invention contain a lubricating oil and an oil soluble sulfurized rubber polymer, preferably a sulfurized rubber polymer which also contains combined chlorine.
- an oil soluble sulfurized rubber polymer preferably a sulfurized rubber polymer which also contains combined chlorine.
- the polymer acts to inhibit bearing corrosion, to impart extreme pressure characteristics to the oil, or to improve other properties of the oil such as the viscosity index.
- This product is preferably prepared by depolymerizing a dispersion of rubber in a suitable aromatic solvent such as benzene, reacting the depolymerized rubber in the presence of a-halide or halogen acid of tin or boron to form a resinous polymer, and precipitating and separating the resinous polymer.
- a suitable aromatic solvent such as benzene
- the depolymerization of the rubber is preferably effected with the use of an agent such as glacial acetic acid, hydrochloric acid, chlor-acetic acid,
- stannic chloride stannic bromide
- boron trichloride boron fluoride
- fiuoroboric acid chloro-stannic acid
- chloro-stannous acid chloro-stannous acid and the corresponding brom acids
- anhydrous stannic chloride being preferred.
- a valuable product is prepared from an oil soluble rubber polymer of the class disclosed in my prior patents, preferably the oil soluble polymer described in my Patent No. 2,199,352.
- an oil soluble rubber polymer of the class disclosed in my prior patents preferably the oil soluble polymer described in my Patent No. 2,199,352.
- the sulfurization of this polymer is preferably accomplished with the use of sulfur chloride.
- an oil soluble rubber polymer is ,flrst prepared as described in my Patent No. 2,199,352.
- benzol 95% containing 15 cc. of glacial acetic acid.
- the dispersion is allowed to stand twenty-four hours, and the air is then swept out with a nitrogen stream.
- 10 cc. of anhydrous fuming stannic chloride is added to this depolymerized rubber dispersion.
- the mixture is allowed to stand twentyfour hours at room temperature.
- the product is then run into 3500 cc.
- the rubber polymer prepared as above described which polymer is conveniently referred to as a depolymerized rubber polymer, is then reacted with sulfur chloride so as to introduce sulfur and chlorine into the product.
- This is conveniently accomplished by dissolving the depolymerized rubber polymer in an aromatic solvent such as toluene, xylene, or benzol, preferably benzol, and then introducing the sulfur chloride' The reaction takes place easily, and heating is unnecessary.
- the resulting solution may then be treated as by filtering to remove impurities.
- the sulfurized polymer is then separated from the remainder of the solution. This'rnay be done by running the solution into a suitable liquid in which the sulfurized polymer is insoluble, preferably an alcohol.
- the precipitate is then filtered, washed free of acid, preferably with additional precipitating solvent, and dried.
- This sulfurized rubber polymer has varied properties which make it valuable for addition to different types of lubricating oils. For example, by adding the product to a furfural refined Mid- Continent SAE N0. 30 lubricating oil in the pro- Viscosity SIT/100 F 513 630 Viscosity SIT/210 F 62 70 L Viscosity index (Dean 6: Davis) 87 96+ Lead index 8 30 Q'Ihe lead index 'givenabove isan arbitrary empirical figure which is the measure of resis-- tivity of the oil to bearing corrosion. It is obtained'by multiplying the leadnumber of the oil by 1,000.
- the lead number of the oil represents the maximum percentage of lead as lead naphthenate which can be added to the oil without substantial corrosion when the bearing is immersed in the oil and the oil passed therethrough at-a temperature of about 325350 F. for five hours in the presence of air.
- the amount of corrosion is determined by weighing the bearing before and after the test. For example, if the oil has a lead index of 10, this means that 0.01% of lead as lead naphthenate is the maximum amount which can be added to the oil without substantial corrosion of the bearing.
- the compounded oil described above displays improved viscosity characteristics over the base 011, where it is desired to increase the viscosity index of an oil to a greater extent this may be done by using, a larger proportion of the sulfurized rubber polymer. For example, by mixing a furfural refined Mid-Continent SAE No. 20 lubricating oil with 2.6% by weight of the sulfurized rubber polymer a compounded oil possessing the following properties as compared with the properties of the base oil is obtained.
- the compounded oil is supressure characteristics, as shown by the relative Almen values.
- Other.Almen tests using 1.0% and 0.5% of the sulfurized polymer show that the use of these proportions improves the extreme pressure characteristics to noticeable degrees, although not as'much as the proportion used in compounding the oil identified in the table.
- the proportions of sulfurized rubber polymer used it is possible to vary the extrem pressure characteristics of the oil.
- a sulf-urized rubber polymer that differs from that specifically disclosed above in a higher content of sulfur and chlorine may be prepared as follows. '20 grams of depolymerized rubber polymer is'dissolved in 500 cc. of benzol 'and 10 cc. of sulfur chloride is added to the solution- The resulting mixture is permitted to stand'for 24 hours, after which the mixture is run into 2000 cc. of ethyl alcohol. A brownish yellow precipitate, consisting essentiallyof the sulfurized rubber polymer, is formed. This precipitate is filtered off, washed, and dried.
- This product which is a dry powder, contains 5.58% sulfur and 1.8 chlorine; It is 'i'nade up into a compounded 011 containing 2.6% sulfurized rubber polymer, 58.4% SAE #10 oil, and 39.0% SAE #20 oil (furfural refined Mid-Continent lubricating oils).
- the sulfur- I ized polymers which contain combined chlorine apparently possess exceptionally good extreme compounded oil as compared with the mixed base oil has the following properties:
- this sulfurized rubber polypolymer in the specification and claims it will be understood that it is not meant that the polymer is necessarily wholly soluble in a hydrocarbon oil, since in some cases the polymer may be only partly soluble. In using a partly soluble sulfurized rubber polymer it is usually advisable to mix the base oil with an amount of polymer in excess of that which it is desired to dissolve in the oil and then to filter the resulting mixture to remove the undissolved portion of the polymer.
- the properties of the sulfurized rubberpolymers can be varied by varying the amount of sulfur chloride used in their preparation.
- the sulfurized rubber polymer preferably should not contain more than 10% sulfur by weight, and where a wholly soluble product is desired the product should contain on the order of 2 to 4% sulfur.
- Alubricating oil composition comprising a lubricating oil and an oil soluble sulfurized rub ber polymer.
- a lubricating. oil composition comprising a mineral lubricating oil and an oil soluble sulfurized rubber polymer, said rubber polymer being the reaction product of rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron.
- a lubricating oil composition comprising a mineral lubricating oil and an oil soluble sulfur-' ized rubber polymer, said rubber polymer being the reaction product of depolymerized rubberwith a compound selected fromthe group consisting of the halides and halogen acids of tin and boron.
- a lubricating oil composition comprising a. mineral lubricating oil and an oil soluble sulfurized rubber polymer containing combined chlorine.
- a lubricating oil composition comprising a mineral lubricating oil and a minor proportion of
- the lubricating oil compositions of the invention may contain base oils of various types depending upon the type of product desired. For example, if a cutting oil is intended to be prepared, then the lubricating oil cosity from about 170 to 300 up to 1000 at 100 F.
- oils ofthe cylinder stock type having viscosities of about 100 to 200 at 210 F., may be used.
- the invention therefore provides lubricating oil compositions which possess valuable properties imparted to them by the oil soluble sulfurized an oil soluble sulfurized rubber polymer containing not more than 10 per cent of sulfur, said rubber polymer being the reaction product of rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron, said sulfurized rubber polymeralso containing combined chlorine.
- a lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing not morethan 10 per cent of sulfur, said rubber polymer being the reaction product of depolymerized rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron, said sulfurized rubber polymer also containing combined chlorine.
- a lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber polymer containing not more than 10 per cent of sulfur and being the reaction product of sulfur chloride with an oil soluble rubber polymer which is the reaction product of rubber with a compound selected from thegroup consisting of the halides and halogen acids of tin and boron.
- a lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber polymer containing not more than 10 per cent of sulfur and being the reaction product of sulfur chloride with an oil soluble rubber polymer which is the reaction product of depolymerized rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron.
- a lubricating oil composition comprising a mineral lubricating oil and 0.1 to 10 percent of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber-poly-- mer being prepared by reacting rubber with glacial acetic acid and with stannic chloride to produce a depolymerized rubber polymer, the reaction with the glacial acetic acid and with the stannic chloride being carried out in the presence of benzol, and reacting the depolymerized rubber polymer in solution in benzol with sulfur chloride to produce the sulfurizedrubberpolymer.
- a lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer prepared by reacting rubber with a depoly'merizing amount of glacial acetic acid and with stannic chloride to produce a depolymerized rufober polymer, the reaction with the glacial acetic acid and with stannic chloride being carried out in the presence of benzol, and reacting the depolymerized rubber pohrmer in solution in benzol with sulfur chloride to produce a sulfurized' rubber olymer.
- a lubricating oil composition comprising a mineral lubricating oil and a minorproportion of an oil soluble sulfuri'zed ru'bber polymer con- I taining combined chlorine, said suliurized I'll-b7 her polymer being prepared by dispersing rubb'er I in benzol, adding glacial acetic acid to the resulting dispersion to produce a dispersion of depolymerized rubber, treating the depolymerized rubber in the presence of benzol with stannic chloride, and reacting the resulting product with sulfur chloride to introduce not more than 10 per cent sulfur therein.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
. or more particulars.
Patented Dec. 12,1944
LUBRICATING on.
Charles C. Towne, Beacon, N. Y., asslgnor, by
mesne assignments, to The Texas Company, New York, N. Y., a corporation of Delaware No Drawing. Application July 17, 1940, Serial No. 345,989
11 Claims.
metallic materials such as cadmium-silver, cadmium-nickel, and copper-lead alloys. While these bearing materials have definite advantages, they have the disadvantage of being susceptible to corrosion under certain extreme conditions, especially by the modern highly refined motor oils. According to the present invention, the tendency of such oils to corrode bearings under extreme conditions of operation is overcome without impairing other desired properties of the oil, such, for example, as high viscosity index.
Another problem that is presented by the design of modern machinery is the necessity for providing lubricating oils capable of withstanding the high pressures encountered between engaged surfaces, such as the hypoid gears used in motor vehicles. Since the ordinary type of hydrocarbon lubricating oil is incapable of withstanding such pressures, there have been developed socalled extreme pressure lubricants. An extreme pressure lubricant is generally composed of a hydrocarbon lubricating oil and a minor proportion of an ingredient which imparts extreme pressure characteristics to the oil; i. e., characteristics which enable the oil to form between the engaged surfaces a lubricating film capable of withstanding high pressures.
It is an object of the invention to provide lubricating oil compositions containing an additive which imparts to the compositions one or more desirable properties. Another object of the inventionis to provide lubricating oil compositions which possess the valuable properties of high refined oils while at the same time having a decreased tendency to cause corrosion of hard metal bearings. A further object of the invention is to provide lubricating oil compositions possessing improved extreme pressure characteristics. Another object of the invention is to provide'novel sulfurized products which when added to lubrieating oils are adapted to improve the oils in one all Other objects of the invention will in part be obvious and will in part appear hereinafter.
The lubricating oil compositions of the present invention contain a lubricating oil and an oil soluble sulfurized rubber polymer, preferably a sulfurized rubber polymer which also contains combined chlorine. Depending primarily upon the characteristics of the base oil and the proportions in which the sulfurized rubber polymer is employed, the polymer acts to inhibit bearing corrosion, to impart extreme pressure characteristics to the oil, or to improve other properties of the oil such as the viscosity index.
In my United States Patent No. 2,078,472, I have described a lubricating oil containing a resinous rubber polymer which consists essentially of a reaction product of rubber with a halide or halogen acid of tin or boron. In my United States Patent No. 2,086,399, I have described a method for treating the resinous rubber polymer so as to remove impurities therefrom. When preparing a polymer as described in these patents a substantial proportion of oil insoluble polymer is produced which is not suitable, in some instances, for compounding with oils. In my United States Patent No. 2,199,352, I have described a resinous rubber polymer which is substantially completely oil soluble. This product is preferably prepared by depolymerizing a dispersion of rubber in a suitable aromatic solvent such as benzene, reacting the depolymerized rubber in the presence of a-halide or halogen acid of tin or boron to form a resinous polymer, and precipitating and separating the resinous polymer. In this process the depolymerization of the rubber is preferably effected with the use of an agent such as glacial acetic acid, hydrochloric acid, chlor-acetic acid,
acidified benzol, sulfur dioxide, hydrogen sulfide,
benzoic acid, mercurous chloride, and ammonia. Examples of suitable halides and halogen acids of tin or boron which may be used in the preparation of the rubber polymers described in my prior patents are stannic chloride, stannic bromide, boron trichloride, boron fluoride, fiuoroboric acid, chloro-stannic acid, chloro-stannous acid and the corresponding brom acids, anhydrous stannic chloride being preferred.
In accordance with one feature of the present invention a valuable product is prepared from an oil soluble rubber polymer of the class disclosed in my prior patents, preferably the oil soluble polymer described in my Patent No. 2,199,352. By sulfurizing a polymer of this class a product is obtained which is adapted for addition to l vdrocarbon oils, such as petroleum lubricating oils,
to improve the properties thereof. The sulfurization of this polymer is preferably accomplished with the use of sulfur chloride.
In preparing an oil soluble sulfurized'rubber polymer in accordance with a preferred manner of proceeding, an oil soluble rubber polymer is ,flrst prepared as described in my Patent No. 2,199,352. Thus 50 grams of crepe rubber are dispersed in 1500 cc. of benzol (90%) containing 15 cc. of glacial acetic acid. The dispersion is allowed to stand twenty-four hours, and the air is then swept out with a nitrogen stream. To this depolymerized rubber dispersion, there is added 10 cc. of anhydrous fuming stannic chloride. The mixture is allowed to stand twentyfour hours at room temperature. The product is then run into 3500 cc. of 95% ethyl alcohol which effects precipitation of the resinous polymer. The precipitation is completed by stirring for two to three hours. The precipitated polymer is then filtered off, washed free of acid with alcohol, and dried. It will be understood in this connection that it is not necessary to prepare the depolymerized rubber dispersion as a separate step, but that the rubber may be added to the benvol containing the acetic acid and the stannic chloride.
The rubber polymer prepared as above described, which polymer is conveniently referred to as a depolymerized rubber polymer, is then reacted with sulfur chloride so as to introduce sulfur and chlorine into the product. This is conveniently accomplished by dissolving the depolymerized rubber polymer in an aromatic solvent such as toluene, xylene, or benzol, preferably benzol, and then introducing the sulfur chloride' The reaction takes place easily, and heating is unnecessary. The resulting solution may then be treated as by filtering to remove impurities. In any case the sulfurized polymer is then separated from the remainder of the solution. This'rnay be done by running the solution into a suitable liquid in which the sulfurized polymer is insoluble, preferably an alcohol. The precipitate is then filtered, washed free of acid, preferably with additional precipitating solvent, and dried.
As a specific example of the above procedure, 20 grams of the depolymerized rubber polymer in solution in 500 cc. of benzol is treated with 5 cc. of sulfur chloride. The resulting reaction mixture is permitted to stand for four hours and is then filtered through Filter-'Cel. The filtered solution containing a sulfurized rubber polymer is then run slowly into 2500 cc. of 95% ethyl alcohol. As a result of this procedure, the sulfurized r-ubber polymer is precipitated. The precipitate is filtered, washed 'with alcohol and dried. The
product is a brownish yellow powder, highly soluble in hydrocarbon oils. It contains about 3% sulfur and about 0.42% chlorine.
This sulfurized rubber polymer has varied properties which make it valuable for addition to different types of lubricating oils. For example, by adding the product to a furfural refined Mid- Continent SAE N0. 30 lubricating oil in the pro- Viscosity SIT/100 F 513 630 Viscosity SIT/210 F 62 70 L Viscosity index (Dean 6: Davis) 87 96+ Lead index 8 30 Q'Ihe lead index 'givenabove isan arbitrary empirical figure which is the measure of resis-- tivity of the oil to bearing corrosion. It is obtained'by multiplying the leadnumber of the oil by 1,000. The lead number of the oil represents the maximum percentage of lead as lead naphthenate which can be added to the oil without substantial corrosion when the bearing is immersed in the oil and the oil passed therethrough at-a temperature of about 325350 F. for five hours in the presence of air. The amount of corrosion is determined by weighing the bearing before and after the test. For example, if the oil has a lead index of 10, this means that 0.01% of lead as lead naphthenate is the maximum amount which can be added to the oil without substantial corrosion of the bearing. Thus the results given in the above table show that the sulfurized rubber it has the property of inhibiting corrosion by lubricating oils of the type tested. The results given also show that the sulfurized rubber polymer improves the viscosity index characteristics of the oil.
Although the compounded oil described above displays improved viscosity characteristics over the base 011, where it is desired to increase the viscosity index of an oil to a greater extent this may be done by using, a larger proportion of the sulfurized rubber polymer. For example, by mixing a furfural refined Mid-Continent SAE No. 20 lubricating oil with 2.6% by weight of the sulfurized rubber polymer a compounded oil possessing the following properties as compared with the properties of the base oil is obtained.
. It will be noted that the compounded oil is supressure characteristics, as shown by the relative Almen values. Other.Almen tests using 1.0% and 0.5% of the sulfurized polymer show that the use of these proportions improves the extreme pressure characteristics to noticeable degrees, although not as'much as the proportion used in compounding the oil identified in the table. Thus, by varying the proportions of sulfurized rubber polymer used, it is possible to vary the extrem pressure characteristics of the oil.
A sulf-urized rubber polymer that differs from that specifically disclosed above in a higher content of sulfur and chlorine may be prepared as follows. '20 grams of depolymerized rubber polymer is'dissolved in 500 cc. of benzol 'and 10 cc. of sulfur chloride is added to the solution- The resulting mixture is permitted to stand'for 24 hours, after which the mixture is run into 2000 cc. of ethyl alcohol. A brownish yellow precipitate, consisting essentiallyof the sulfurized rubber polymer, is formed. This precipitate is filtered off, washed, and dried. This product, which is a dry powder, contains 5.58% sulfur and 1.8 chlorine; It is 'i'nade up into a compounded 011 containing 2.6% sulfurized rubber polymer, 58.4% SAE #10 oil, and 39.0% SAE #20 oil (furfural refined Mid-Continent lubricating oils).
.Only a part of the sulfurized rubber polymer dissolves in the oil, and to remove the undissolved portion the compound oil is filtered through Filter-Cel at a temperature of 212 F. The filtered 1 rubber polymersof the invention. The sulfur- I ized polymers which contain combined chlorine apparently possess exceptionally good extreme compounded oil as compared with the mixed base oil has the following properties:
Mixed base Compounded oil 1 oil L Viscosity SUIIOO F 221 240 Viscosity SU/210 F 47. 1 49 Viscosity index (Dean 6: Davi 88 99 Almen value (breakdown, lbs.).. 9. 38. 9
It will be noted that this sulfurized rubber polypolymer in the specification and claims it will be understood that it is not meant that the polymer is necessarily wholly soluble in a hydrocarbon oil, since in some cases the polymer may be only partly soluble. In using a partly soluble sulfurized rubber polymer it is usually advisable to mix the base oil with an amount of polymer in excess of that which it is desired to dissolve in the oil and then to filter the resulting mixture to remove the undissolved portion of the polymer.
From what has been said heretofore, it will be evident that the properties of the sulfurized rubberpolymers can be varied by varying the amount of sulfur chloride used in their preparation. In general the sulfurized rubber polymer preferably should not contain more than 10% sulfur by weight, and where a wholly soluble product is desired the product should contain on the order of 2 to 4% sulfur.
The proportions in which the sulfurized rub-.
it is ordinarily advisable to use from /3 to 5% of a polymer.
pressure characteristics because of this chlorine content.
I Since changes may be made in the compositions and processes above described without departing from the scope of the invention, it is intended that all'matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
I claim:
' 1. Alubricating oil composition comprising a lubricating oil and an oil soluble sulfurized rub ber polymer.
2. A lubricating. oil composition comprising a mineral lubricating oil and an oil soluble sulfurized rubber polymer, said rubber polymer being the reaction product of rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron. I
3. A lubricating oil composition comprising a mineral lubricating oil and an oil soluble sulfur-' ized rubber polymer, said rubber polymer being the reaction product of depolymerized rubberwith a compound selected fromthe group consisting of the halides and halogen acids of tin and boron.
4. A lubricating oil composition comprising a. mineral lubricating oil and an oil soluble sulfurized rubber polymer containing combined chlorine.
5. A lubricating oil composition comprisinga mineral lubricating oil and a minor proportion of As previously indicated, the lubricating oil compositions of the invention may contain base oils of various types depending upon the type of product desired. For example, if a cutting oil is intended to be prepared, then the lubricating oil cosity from about 170 to 300 up to 1000 at 100 F.
may be advantageous. Further, in the preparation of an extreme pressure lubricant, higher viscosity lubricating oils such as oils ofthe cylinder stock type, having viscosities of about 100 to 200 at 210 F., may be used.
The invention therefore provides lubricating oil compositions which possess valuable properties imparted to them by the oil soluble sulfurized an oil soluble sulfurized rubber polymer containing not more than 10 per cent of sulfur, said rubber polymer being the reaction product of rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron, said sulfurized rubber polymeralso containing combined chlorine.
6. A lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing not morethan 10 per cent of sulfur, said rubber polymer being the reaction product of depolymerized rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron, said sulfurized rubber polymer also containing combined chlorine.
7. A lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber polymer containing not more than 10 per cent of sulfur and being the reaction product of sulfur chloride with an oil soluble rubber polymer which is the reaction product of rubber with a compound selected from thegroup consisting of the halides and halogen acids of tin and boron.
8. A lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber polymer containing not more than 10 per cent of sulfur and being the reaction product of sulfur chloride with an oil soluble rubber polymer which is the reaction product of depolymerized rubber with a compound selected from the group consisting of the halides and halogen acids of tin and boron.
9. A lubricating oil composition comprising a mineral lubricating oil and 0.1 to 10 percent of an oil soluble sulfurized rubber polymer containing combined chlorine, said sulfurized rubber-poly-- mer being prepared by reacting rubber with glacial acetic acid and with stannic chloride to produce a depolymerized rubber polymer, the reaction with the glacial acetic acid and with the stannic chloride being carried out in the presence of benzol, and reacting the depolymerized rubber polymer in solution in benzol with sulfur chloride to produce the sulfurizedrubberpolymer.
10. A lubricating oil composition comprising a mineral lubricating oil and a minor proportion of an oil soluble sulfurized rubber polymer prepared by reacting rubber with a depoly'merizing amount of glacial acetic acid and with stannic chloride to produce a depolymerized rufober polymer, the reaction with the glacial acetic acid and with stannic chloride being carried out in the presence of benzol, and reacting the depolymerized rubber pohrmer in solution in benzol with sulfur chloride to produce a sulfurized' rubber olymer.
11.. A lubricating oil composition comprising a mineral lubricating oil and a minorproportion of an oil soluble sulfuri'zed ru'bber polymer con- I taining combined chlorine, said suliurized I'll-b7 her polymer being prepared by dispersing rubb'er I in benzol, adding glacial acetic acid to the resulting dispersion to produce a dispersion of depolymerized rubber, treating the depolymerized rubber in the presence of benzol with stannic chloride, and reacting the resulting product with sulfur chloride to introduce not more than 10 per cent sulfur therein.
CHARLES C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US345989A US2364830A (en) | 1940-07-17 | 1940-07-17 | Lubricating oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US345989A US2364830A (en) | 1940-07-17 | 1940-07-17 | Lubricating oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2364830A true US2364830A (en) | 1944-12-12 |
Family
ID=23357448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US345989A Expired - Lifetime US2364830A (en) | 1940-07-17 | 1940-07-17 | Lubricating oil |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2364830A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2481257A (en) * | 1946-03-08 | 1949-09-06 | Standard Oil Dev Co | Lubricating composition |
| US3269950A (en) * | 1964-05-20 | 1966-08-30 | Texaco Inc | Lubricating composition containing amide, imide and thiocyanate complexes of zinc and tin |
| US4320017A (en) * | 1980-10-10 | 1982-03-16 | Standard Oil Company (Indiana) | Sulfurized/aminated mixture of ethylene-based polyolefin and polyisobutylene for lubricating oil |
| US4352911A (en) * | 1980-10-10 | 1982-10-05 | Standard Oil Company (Indiana) | Sulfurized/aminated mixture of ethylene-based polyolefin and polyisobutylene |
-
1940
- 1940-07-17 US US345989A patent/US2364830A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2481257A (en) * | 1946-03-08 | 1949-09-06 | Standard Oil Dev Co | Lubricating composition |
| US3269950A (en) * | 1964-05-20 | 1966-08-30 | Texaco Inc | Lubricating composition containing amide, imide and thiocyanate complexes of zinc and tin |
| US4320017A (en) * | 1980-10-10 | 1982-03-16 | Standard Oil Company (Indiana) | Sulfurized/aminated mixture of ethylene-based polyolefin and polyisobutylene for lubricating oil |
| US4352911A (en) * | 1980-10-10 | 1982-10-05 | Standard Oil Company (Indiana) | Sulfurized/aminated mixture of ethylene-based polyolefin and polyisobutylene |
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