US2188943A - Lubricant and method of producing same - Google Patents
Lubricant and method of producing same Download PDFInfo
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- US2188943A US2188943A US56451A US5645135A US2188943A US 2188943 A US2188943 A US 2188943A US 56451 A US56451 A US 56451A US 5645135 A US5645135 A US 5645135A US 2188943 A US2188943 A US 2188943A
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- Prior art keywords
- lubricant
- extreme pressure
- hydrocarbon
- phenylene
- lubricants
- Prior art date
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- 239000000314 lubricant Substances 0.000 title description 34
- 238000000034 method Methods 0.000 title description 3
- 229930195733 hydrocarbon Natural products 0.000 description 19
- 150000002430 hydrocarbons Chemical class 0.000 description 19
- 239000004215 Carbon black (E152) Substances 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 16
- -1 phenylene, para hydroxy phenylene, tolyl Chemical group 0.000 description 14
- 239000003921 oil Substances 0.000 description 13
- 230000001050 lubricating effect Effects 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 12
- 239000004615 ingredient Substances 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 8
- MRQLRZQLPODMPG-UHFFFAOYSA-N tris(phenylsulfanyl)phosphane Chemical compound C=1C=CC=CC=1SP(SC=1C=CC=CC=1)SC1=CC=CC=C1 MRQLRZQLPODMPG-UHFFFAOYSA-N 0.000 description 8
- 150000003254 radicals Chemical class 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000005840 aryl radicals Chemical group 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 125000005023 xylyl group Chemical group 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000010835 comparative analysis Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000004351 phenylcyclohexyl group Chemical group C1(=CC=CC=C1)C1(CCCCC1)* 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000001993 wax 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
- C10M137/105—Thio derivatives not containing metal
-
- 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
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/047—Thioderivatives not containing metallic elements
Definitions
- Characterizing extreme pressure into gredients commonly used have included free sulfur, chemically bound sulfur, chlorinated or ganic hydrocarbons, and the like. Such materails have the common'disadvantage of corroding the metallic surface intended to be lubricated. 86 Metallic soaps such as metal oleates, naphthenates, sulphonates, and the like, have also been used, but have been found to give only moderate aid in extreme pressure lubrication.
- This invention is based upon the discovery that 5 novel lubricants having exceptional ability to lubricate effectively under conditions of extreme pressure loading may be produced by incorporating with a hydrocarbon lubricant oil a small proportion of a compound having the general 10 formula /SR PSR where R is an aryl radical, selected from the group consisting of radicals of the general types selected from the group consisting of hydrogen,
- aryl compounds generally preferred for the purposes of this invention are 30 those corresponding to the above general formula where R is selected from the groups (a) and (b) as defined above and where the R's are preferably hydrogen or alkyl. Where R is alkyl, one or more of such alkyl substituents may be an alkyl .35 of high molecular weight, such as, for example,
- the thiophosphites preferred for the purposesof this invention are the triaryltrithiophosphites.
- compounds of the preferred class suitable for the purposes of this invention there may be given triphenyl trithiophosphite, the tritolyl trithiophosphites, and the trinaphthyl trithiophosphites.
- the preferred compounds with which this invention is concerned may be generally described as the reaction products resulting from the reaction of a compound of the nature a thiophenol, or substituted or condensed thiophenol, with phosphorus trlchloride.
- the preferred proportions are three molecular amounts of the thicphenol substance to one molecular amountof the phosphorus trichloride.
- the preferred embodiment of this invention contemplates an extreme pressure lubricant comprising a small proportion of a triaryl trithiophosphite, that is a compound of the general formula (ARS)3P, with a hydrocarbon mineral oil.
- This new composition possesses distinct advantages as an extreme pressure lubricant capable of maintaining an oily lubricant film under high unit loading and preventing seizure of the metallic parts in contact under extreme pressures.
- triphenyl trithiophosphite (CeH5S)3P. This and other aryl trithiophosphites are easily prepared. For example, one molecular proportion of phosphorus trichlorlde is gradually added to three molecular proportions of thiophenol. Hydrochloric acid gas is evolved and is measured as it forms, since the formation of each molecular amount of product.
- the reaction proceeds without difficulty at ordinary temperatures, but I have found it best to finally heat the mixture to about 160 C. in order to insure complete reaction.
- the reaction mixture so produced is chiefly triphenyl trithiophosphite.
- the main impurities are dissolved HCl and a small amount of thiophenol. These may be removed by distilling until a temperature (in the liquid) of 150 C. is reached.
- a hydrocarbon solvent such as Stoddard" (which has a boiling range of 300 F. to 400 F.) prior to the distillation. aids in the complete removal of impurities.
- the residual product solidifies at about 74 C.
- triphenyl trithiophosphite is a white crystalline product which is quite soluble in mineral oil. It does not darken the original color of the mineral oil and it has no tendency to separate from the oil or to form sludge under normal storage conditions. It is a stable substance of high boiling point. Similar compounds may be similarly prepared from any of the thiophenols or substituted or condensed thiophenols as outlined above, having similarly effective properties. The same is true for the preparation of the triaryltrithiophosphites in general.
- novel extreme pressure lubricants herein disclosed are quite effective for the purposes intended and are stable under conditions of heating far in excess of those to which they are ordinarily subjected in actual use.
- Lubricating oils so prepared are not corrosive to the metals encountered in use,- since they do not darken or corrode copper or steel when maintained in contact with them for 24 hours at 300 F.
- extreme pressure inbricating composition means either (and includes all) the finished lubricant as actually used, the characterizing extreme pressure lubricant itself, or any intermediate extreme pressure lubricant base, admixture or dilution containing the active ingredient.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small proportion of a triaryltrithiophosphite.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small proportion, sunicient to act as a characterizing extreme pressure ingredient, of a compound of the general formula s-n 19 5-1! ⁇ SR where at least one It is a radical selected from the group consisting of 7 a B! R! I -OB/and and where the R's are selected from the group which consists of hydrogen and alkyl.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, suflicient to act as a characterizing extreme pressure ingredient.
- atriaryltrithiophosphite of the general formula where the R's are radicals selected from the group which consists of hydrogen and alkyl.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, sumcient to act as a characterizing extreme pressure ingredient of a triaryltrithiophosphite oi the general formula s-a PBR where each of the said R's is a radical of the general type and where the R's are radicals selected from the group consisting of hydrogen and alkyl.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount of a compound selected from the group consisting of triphenyltrithiophosphites, tritolyltrithiophosphites. and trinaphthyltrithiophosphites, suflicient to increase the loadbearing capacity thereof.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and small amount of a triaryltrithiophosphite wherein the aryl radicals are selected from the group consisting of phenyl, tolyl, naphthyl, meta-hydroiw-phenylene, para-hydroxy-phenylene, tolyl, xylyl, xenyl (or biphenyl), methyl-xenyl, ethylxenyl, anisyl, ortho-phenetyl, chlor-phenylene (o,m,p), brom-phenylene (o,m,p), nitro-phenylene (o,m,p),, amino-phenylene (o,m,p), methylnaphtbylene, phenyl-naphthylene, chlor-naphthylenes, brom-naphthylenes, nitro-naphthylenes, amino-naph
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, but not in excess oi 5%. of a triaryltrithiophosphite.
- An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, but not in excess of 5%. of a compound selected from the group consisting of triphenyl trithiophosphites, tritolyl trithiophosphites, and trinaphthyl trithiophosphites. sumcient to increase the load bearing capacity thereof.
- the method of lubricating relatively moving bearing surfaces engaged under extreme pressure which comprises maintaining between said surfaces a hydrocarbon lubricant illm and at the same time chemically acting upon said engaged surfaces with a minor proportion of a triaryltrithiophosphite contained within the lubricant film.
- a lubricating composition comprising a hydrocarbon lubricant and in admixture therewith a minor proportion of a triaryl trithio phosphite in which at least one aryl radical has at least one relatively long alkyl substituent oi the general character corresponding to paramn wax.
- Patent Office I I Signed-and sealed this 18th day of June, A. D. 19h0.
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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
Patented Feb. 6, 1940 UNITED STATES PATENT OFFICE LUBRICANT AND won F PRODUCING William L. Evers, Woodbury, N. 1., assignor to Sooony-Vacuum Oil Company, Incorporated, New York, N. Y., a corporation of New York No Drawing. Application December as, 1935,
' Serial Ito. 56,451
11 Claims.
The present trend in automobile design toward rapid acceleration and the use of hypoid gears has increased .the unit loading on rear axles. In many cases the unit pressures encountered are sumciently great to rupture the lubricating filmv hydrocarbons of high viscosity of the general na- 80 ture of cylinder stocks. Upon the increase. of pressures as referred to above, it was found that mineral hydrocarbon lubricants alone were not capable of maintaining film and/or lubrication under the conditions encountered, and resort was had to extreme pressure lubricants consisting of the usual mineral hydrocarbon oils together with a characterizing ingredient which imparted extreme pressure lubricating properties to the lubricant. Characterizing extreme pressure into gredients commonly used have included free sulfur, chemically bound sulfur, chlorinated or ganic hydrocarbons, and the like. Such materails have the common'disadvantage of corroding the metallic surface intended to be lubricated. 86 Metallic soaps such as metal oleates, naphthenates, sulphonates, and the like, have also been used, but have been found to give only moderate aid in extreme pressure lubrication.
It is an object of this invention to rovide an extreme pressure lubricant, together with a base for use in compounding. same, which lubricant has superior properties, such as load carrying capacity, stability, maintenance of extreme pres- It is an object of this invention to premethods of preparing lubricants containing these novel characterizing ingredients, lubrication of mechanisms involving extreme unit pressures, and other advantages as hereinafter appear.
This invention is based upon the discovery that 5 novel lubricants having exceptional ability to lubricate effectively under conditions of extreme pressure loading may be produced by incorporating with a hydrocarbon lubricant oil a small proportion of a compound having the general 10 formula /SR PSR where R is an aryl radical, selected from the group consisting of radicals of the general types selected from the group consisting of hydrogen,
hydroxy, aryl, alkyl, alkaryl, arakyl, halogen; nitro, or amino. The aryl compounds generally preferred for the purposes of this invention are 30 those corresponding to the above general formula where R is selected from the groups (a) and (b) as defined above and where the R's are preferably hydrogen or alkyl. Where R is alkyl, one or more of such alkyl substituents may be an alkyl .35 of high molecular weight, such as, for example,
an alkyl corresponding to a crystalline petroleum wax. The thiophosphites preferred for the purposesof this invention are the triaryltrithiophosphites. As examples of compounds of the preferred class suitable for the purposes of this invention, there may be given triphenyl trithiophosphite, the tritolyl trithiophosphites, and the trinaphthyl trithiophosphites.
Other compounds of this general type, generally suitable for the same purposes, particu larly where in any given compound all three Rs are the same, may be produced with radicals selected from the following group: Metahydroxy phenylene, para hydroxy phenylene, tolyl, xylyl, xenyl (or biphenyl). methyl-xenyl, ethyl-xenyl, anisyl, ortho-phenetyl, chlor-phenylene -(o,m,p) brom-phenylene (o,m,p), nitrophenylene (o,m,p), amino-phenylene (o,m,p), methyl-naphthylene, phenyl-naphthylene, chlor- Bl naphthylenes, brom-naphthylenes, nitro-naphthylenes, amino-naphthylenes, corresponding anthryls, and the hydrogenated or cycle forms of the above, usually designated as saturated closed ring compounds as, for example, cyclohexyl, methyl cyclohexyl, phenyl cyclohexyl, benzyl cyclohexyl, halogen, nitro and amino cyclohexyls and the like.
The preferred compounds with which this invention is concerned may be generally described as the reaction products resulting from the reaction of a compound of the nature a thiophenol, or substituted or condensed thiophenol, with phosphorus trlchloride. The preferred proportions are three molecular amounts of the thicphenol substance to one molecular amountof the phosphorus trichloride.
The preferred embodiment of this inventioncontemplates an extreme pressure lubricant comprising a small proportion of a triaryl trithiophosphite, that is a compound of the general formula (ARS)3P, with a hydrocarbon mineral oil. This new composition possesses distinct advantages as an extreme pressure lubricant capable of maintaining an oily lubricant film under high unit loading and preventing seizure of the metallic parts in contact under extreme pressures.
-As an example of my new extreme pressure compounds, and their method of manufacture, I 2
may describe the manufacture of triphenyl trithiophosphite, (CeH5S)3P. This and other aryl trithiophosphites are easily prepared. For example, one molecular proportion of phosphorus trichlorlde is gradually added to three molecular proportions of thiophenol. Hydrochloric acid gas is evolved and is measured as it forms, since the formation of each molecular amount of product.
is accompanied by the evolution of three molecular amounts of 1101 gas, and its measurement forms an easy means of control. ,The reaction proceeds without difficulty at ordinary temperatures, but I have found it best to finally heat the mixture to about 160 C. in order to insure complete reaction. The reaction mixture so produced is chiefly triphenyl trithiophosphite. The main impurities are dissolved HCl and a small amount of thiophenol. These may be removed by distilling until a temperature (in the liquid) of 150 C. is reached. The addition of a hydrocarbon solvent such as Stoddard", (which has a boiling range of 300 F. to 400 F.) prior to the distillation. aids in the complete removal of impurities. The residual product solidifies at about 74 C. and if desired may be obtained in a very pure form by recrystallizing from a solvent such as ethyl alcohol. The crude product, however, may be used for the purposes of this invention without this further purification. The specific compound thus formed, triphenyl trithiophosphite, is a white crystalline product which is quite soluble in mineral oil. It does not darken the original color of the mineral oil and it has no tendency to separate from the oil or to form sludge under normal storage conditions. It is a stable substance of high boiling point. Similar compounds may be similarly prepared from any of the thiophenols or substituted or condensed thiophenols as outlined above, having similarly effective properties. The same is true for the preparation of the triaryltrithiophosphites in general.
As an example of the ability of extreme pressure lubricants containing these novel characterizing ingredients, the following tabular data is presented. In evaluating oils or lubricants of this type use may be made of the Almen Pin Test Machine described by Mouaey and Almen (Free. A. P. I. 1931, page '17) where a pin is rotated in bearings so designed that increasing pressure may be applied to the lubricated surface. This machine is used widely in such comparative evaluations. In the following tabulation of results from the Almen Pin Test Machine, column 1 shows the pressure in pounds per square inch applied to the. lubricated contact surface. The other columns show the torque in foot pounds transmitted through the pin at the given pressures with the respectively described lubricants, and also show the pressure at which lubrication failed, resulting in seizure of the surface of the bearing and pin.
Almen tests of samples Origi- Containing Containing Containing. 2% samnai vis- 113% 2% ple alter Weights cons (CaHlShP (CsEhShP zgl shbt oil 1, 000 2, 000 0. 7 o. 7 0. 7 3, 000 1. 0 1. 0 1. 0 8, 000 2. 4 2. 7 2. 4 9, 000 2. I 2. 9 2. 6 10, 000 3. 9 3. 2 2. 9 19, 000 4. 2 3. 8 3. 9 20, 000 4. 5 8. 8 4. 0 21, 000 4. 8 3. 9 4. 1 22, 000 0. 0 Seized 4. l 23, 000 Seized 4. 2 24, 000 4. 2 25, 000 6. 0 20,000 Seized In the above described tests, the oil used in column 2 is a mineral hydrocarbon oil of cylinder stock type having the following characteristics:
This is oil of the type commonly used in compounding extreme pressure lubricants, and in the absence of characterizing ingredients is frequently used alone, although the data show it to be quite ineflective for the purpose. This same oil was used in compounding the oils whose tests appear in columns 3 to 6, inclusive. In column 3, it was compounded with 1% of triphenyl trithiophosphite. In column 4, it was compounded with 2% of that ingredient, and in column 5 with 5%. In column 6, the oil of column 1 was compounded with 2% of triphenyl trithiophosphite, and in order to test the persistence of the characterizing ingredient upon exposure to heat, the sample was subjected to heat at 300 F. for 24 hours, afterward being cooled and tested with the results shown in column 6. Generally similar results may be obtained with the other compounds mentioned above and thegeneral classes of compounds defined above. The novel extreme pressure lubricants herein disclosed are quite effective for the purposes intended and are stable under conditions of heating far in excess of those to which they are ordinarily subjected in actual use. Lubricating oils so prepared are not corrosive to the metals encountered in use,- since they do not darken or corrode copper or steel when maintained in contact with them for 24 hours at 300 F.
' The amount of these novel ingredients which may be added to mineral hydrocarbon oils to produce extreme pressure lubricants will vary from about 1 to about 5%, although it is preferred to use about 2% to produce lubricants of desired properties.
In the clatns, the term "extreme pressure inbricating composition" means either (and includes all) the finished lubricant as actually used, the characterizing extreme pressure lubricant itself, or any intermediate extreme pressure lubricant base, admixture or dilution containing the active ingredient.
I claim:
1. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small proportion of a triaryltrithiophosphite.
2. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small proportion, sunicient to act as a characterizing extreme pressure ingredient, of a compound of the general formula s-n 19 5-1! \SR where at least one It is a radical selected from the group consisting of 7 a B! R! I -OB/and and where the R's are selected from the group which consists of hydrogen and alkyl.
4. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, suflicient to act as a characterizing extreme pressure ingredient. of atriaryltrithiophosphite of the general formula where the R's are radicals selected from the group which consists of hydrogen and alkyl.
5. An extreme pressure lubricating composition, consisting of a hydrocarbon lubricant and a small amount, sumcient to act as a characterizing extreme pressure ingredient of a triaryltrithiophosphite oi the general formula s-a PBR where each of the said R's is a radical of the general type and where the R's are radicals selected from the group consisting of hydrogen and alkyl.
6. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount of a compound selected from the group consisting of triphenyltrithiophosphites, tritolyltrithiophosphites. and trinaphthyltrithiophosphites, suflicient to increase the loadbearing capacity thereof.
'7. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and small amount of a triaryltrithiophosphite wherein the aryl radicals are selected from the group consisting of phenyl, tolyl, naphthyl, meta-hydroiw-phenylene, para-hydroxy-phenylene, tolyl, xylyl, xenyl (or biphenyl), methyl-xenyl, ethylxenyl, anisyl, ortho-phenetyl, chlor-phenylene (o,m,p), brom-phenylene (o,m,p), nitro-phenylene (o,m,p),, amino-phenylene (o,m,p), methylnaphtbylene, phenyl-naphthylene, chlor-naphthylenes, brom-naphthylenes, nitro-naphthylenes, amino-naphthylenes.
8. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, but not in excess oi 5%. of a triaryltrithiophosphite.
9. An extreme pressure lubricating composition consisting of a hydrocarbon lubricant and a small amount, but not in excess of 5%. of a compound selected from the group consisting of triphenyl trithiophosphites, tritolyl trithiophosphites, and trinaphthyl trithiophosphites. sumcient to increase the load bearing capacity thereof.
10. The method of lubricating relatively moving bearing surfaces engaged under extreme pressure which comprises maintaining between said surfaces a hydrocarbon lubricant illm and at the same time chemically acting upon said engaged surfaces with a minor proportion of a triaryltrithiophosphite contained within the lubricant film.
11. A lubricating composition comprising a hydrocarbon lubricant and in admixture therewith a minor proportion of a triaryl trithio phosphite in which at least one aryl radical has at least one relatively long alkyl substituent oi the general character corresponding to paramn wax.
WILLIAMLIVIRB.
CERTIFICATE OF- CORRECTIQN.
' 'February', 1"9L O Patent No. 2,18 3%.
WILLIAM L. EVERS.
Itixxhereby certified that error appearsin the printed speeification of the above numbered patent.- requiring correction as foilows: Page 1, first column, linel forthevmrd "automdbile" read --autohotive--; line-52+55, for "materails" read materials--;samepage, second co}umh, li#e55,fbr "Rs" r'ead "R'spage 5, first column, l1nes5 and 514., and seeorid column, lines 1 and 21, claims 2, 5, h, end 5'respective1y, for "R;s" read and that the said Letters Pater 1t should-he read with this correction therein that the same may conform to the record of the 09.3
Patent Office I I Signed-and sealed this 18th day of June, A. D. 19h0.
He r my Van Arsdale,
(Seal) Aeting Commissioner of Patents
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56451A US2188943A (en) | 1935-12-28 | 1935-12-28 | Lubricant and method of producing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56451A US2188943A (en) | 1935-12-28 | 1935-12-28 | Lubricant and method of producing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2188943A true US2188943A (en) | 1940-02-06 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US56451A Expired - Lifetime US2188943A (en) | 1935-12-28 | 1935-12-28 | Lubricant and method of producing same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2188943A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2476037A (en) * | 1945-04-05 | 1949-07-12 | Socony Vacuum Oil Co Inc | Wax-substituted diaryl dithiophosphoric acids and salts thereof |
| US2571332A (en) * | 1947-12-30 | 1951-10-16 | Socony Vacuum Oil Co Inc | Thiophenethiol-phosphorus halide reaction products in lubricating compositions |
| US2571333A (en) * | 1947-12-30 | 1951-10-16 | Socony Vacuum Oil Co Inc | Thiophenethiols-phosphorus halide reaction products |
| US2836535A (en) * | 1954-02-11 | 1958-05-27 | Monsanto Chemicals | Phosphorus-sulfur compounds |
| US3071548A (en) * | 1959-12-14 | 1963-01-01 | Universal Oil Prod Co | Stabilization of organic substances |
| US3296134A (en) * | 1964-04-30 | 1967-01-03 | Shell Oil Co | Mineral lubricating oil containing bisphenol, detergent and phosphite additive |
| US3446738A (en) * | 1964-02-10 | 1969-05-27 | Sinclair Research Inc | Ester base lubricant compositions containing an aromatic amine and an organic thiophosphite or thiophosphonate |
-
1935
- 1935-12-28 US US56451A patent/US2188943A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2476037A (en) * | 1945-04-05 | 1949-07-12 | Socony Vacuum Oil Co Inc | Wax-substituted diaryl dithiophosphoric acids and salts thereof |
| US2571332A (en) * | 1947-12-30 | 1951-10-16 | Socony Vacuum Oil Co Inc | Thiophenethiol-phosphorus halide reaction products in lubricating compositions |
| US2571333A (en) * | 1947-12-30 | 1951-10-16 | Socony Vacuum Oil Co Inc | Thiophenethiols-phosphorus halide reaction products |
| US2836535A (en) * | 1954-02-11 | 1958-05-27 | Monsanto Chemicals | Phosphorus-sulfur compounds |
| US3071548A (en) * | 1959-12-14 | 1963-01-01 | Universal Oil Prod Co | Stabilization of organic substances |
| US3446738A (en) * | 1964-02-10 | 1969-05-27 | Sinclair Research Inc | Ester base lubricant compositions containing an aromatic amine and an organic thiophosphite or thiophosphonate |
| US3296134A (en) * | 1964-04-30 | 1967-01-03 | Shell Oil Co | Mineral lubricating oil containing bisphenol, detergent and phosphite additive |
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