[go: up one dir, main page]

US2188943A - Lubricant and method of producing same - Google Patents

Lubricant and method of producing same Download PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
lubricant
extreme pressure
hydrocarbon
phenylene
lubricants
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US56451A
Inventor
William L Evers
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Oil Corp
Original Assignee
Socony Vacuum Oil Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Socony Vacuum Oil Co Inc filed Critical Socony Vacuum Oil Co Inc
Priority to US56451A priority Critical patent/US2188943A/en
Application granted granted Critical
Publication of US2188943A publication Critical patent/US2188943A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
    • C10M137/105Thio derivatives not containing metal
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/047Thioderivatives 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.

Landscapes

  • 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
US56451A 1935-12-28 1935-12-28 Lubricant and method of producing same Expired - Lifetime US2188943A (en)

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

Family

ID=22004485

Family Applications (1)

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)

* Cited by examiner, † Cited by third party
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

Cited By (7)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US2160273A (en) Lubricant
US2497521A (en) Oil compositions containing amine salts of boro-diol complexes
USRE22910E (en) E-oxcxs-m
US2236168A (en) Lubricant
US3533943A (en) Lubricant compositions
US2353558A (en) Addition agent for lubricating oil and method of making same
US2188943A (en) Lubricant and method of producing same
US2252675A (en) Stabilized hydrocarbon composition and stabilizing agent therefor
US2326140A (en) Lubricant
US2058343A (en) Petroleum product and method of making same
US2298640A (en) Lubricating composition
US2696473A (en) Halogen containing extreme pressure lubricant stabilized with a polyalkylene polyamine
US2293445A (en) Lubricant with high temperature stability
US2686760A (en) Hydraulic fluids and lubricating compositions
US2363880A (en) Lubricants
US2298636A (en) Lubricating composition
US2491772A (en) Extreme pressure lubricants
US2411153A (en) Mineral oil composition and improving agent
US2146543A (en) Lubricating oil
US2265819A (en) Hydrocarbon composition
US2181913A (en) Improved hydrocarbon composition
US2161584A (en) Petroleum lubricant composition
US2251686A (en) Lubricating compound
US2325076A (en) Lubricant
US2243485A (en) Lubricant