US3890363A - Oil additive - Google Patents

Oil additive Download PDF

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Publication number
US3890363A
US3890363A US473129A US47312974A US3890363A US 3890363 A US3890363 A US 3890363A US 473129 A US473129 A US 473129A US 47312974 A US47312974 A US 47312974A US 3890363 A US3890363 A US 3890363A
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Prior art keywords
additive
acid
dithiocarbamate
carbon atoms
formula
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US473129A
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Robert E Malec
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Ethyl Corp
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Ethyl Corp
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Priority to US00348625A priority Critical patent/US3833496A/en
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    • C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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    • C10M2205/026—Butene
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    • C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
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    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
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    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
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    • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
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    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
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Definitions

  • R' is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
  • R is an aliphatic hydrocarbon radical containing about 8-100 carbon atoms
  • R" is selected antirust additives in lubricating oils and greases.
  • Antiwear additives used in the past include compounds such as zinc dialkyldithiophosphates, sulfurized sperm oil, and the like. Antirust protection can be provided by compounds such as overbased calcium sulfonates. Long chain amines such as polybutenyl ethylenediamine have been used to improve dispersancy of lubricating oils.
  • lubricating oils and greases having improved antiwear and antirust properties are provided by including in the lubricating oil composition certain 3-mercaptoalkanoic acid, [(alkylamino)alkyl] dithiocarbamates such as 3- mercaptobutyric acid, [3(oleylamino)-propyl] dithiocarbamate.
  • R is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
  • R is an aliphatic hydrocarbon radical containing about 8-100 carbon atoms
  • R"" is selected from the group consisting of hydrogen and C alkyls and R is a divalent aliphatic hydrocarbon radical containing about 2-10 carbon atoms
  • R and R are selected from the group consisting of hydrogen and alkyl radicals containing about 14 carbon atoms
  • R" is selected from the group consisting of hydrogen and C alkyls
  • R' is selected from the group consisting of hydrogen and salt cations.
  • Useful salt cations include the cations of the alkaline earth metals such as calcium, magnesium, strontium, and barium; ammonium ions formed from ammonia; alkyl and alkenyl amines such as methylamine, dimethylamine, trimethylamine, triethylamine, tributylamine, ethanolamine, diethanolamine, triethanolamine, morpholine, stearylamine, oleylamine, palmylamine, laurylamine, eicosylamine, eicosenylamine, and the like; and other metal cations such as zinc, aluminum, nickel, manganese, iron, and the like.
  • alkaline earth metals such as calcium, magnesium, strontium, and barium
  • ammonium ions formed from ammonia
  • alkyl and alkenyl amines such as methylamine, dimethylamine, trimethylamine, triethylamine, tributylamine, ethanolamine, diethanolamine, triethanolamine, morph
  • a most preferred embodiment of this invention is an antiwear-antirust additive for lubricating oils and greases, said additive having the formula:
  • R is an aliphatic hydrocarbon radical containing from about 8-100 carbon atoms
  • R is a divalent aliphatic hydrocarbon radical containing from 2 to about 10 carbon atoms
  • R and R are selected from tl" group consisting of hydrogen and alkyl radicals containing l to about 4 carbon atoms. Since the compounds contain both a basic amine functional group and a carboxylic acid they can exist in the form of a zwitterion and are shown in that form in Formula [1.
  • additives include: 3-mercaptopropionic acid, [2(9- eicosenylamino)ethyl]dithiocarbamate 3-mercapto-2-methylbutyric acid, [6(octylamino)hexyl]dithioca'rbamate 3-mercaptoheptanoic cyl]dithiocarbamate 3-mercapto-2-methylhexanoic acid,
  • additives are readily prepared by reacting an aliphatic hydrocarbylaminohydrocarbylamine with carbon disulfide to form the corresponding hydrocarbylaminohydrocarbyl dithiocarbamic acid and reacting this with an appropriate alpha-unsaturated aliphatic carboxylic acid such as acrylic acid, crotonic acid, a-methyl crotonic acid, a,B-diethyl acrylic acid, B-butyl acrylic acid, a-butyl acrylic acid, and the like (N.
  • the aliphatic hydrocarbylaminohydrocarbylamines can be prepared by reacting an aliphatic hydrocarbyl chloride with an aliphatic diamine.
  • reaction of oleyl chloride with 1,3-propanediamine yields oleylaminopropylamine.
  • reaction of lauryl chloride with 1,6-hexanediamine forms laurylaminohyexylamine.
  • reaction of C -polybutenyl chloride with ethylenediamine forms C polybutenylaminoethylamine.
  • the polyolefin chlorides are readily formed by reacting a polyolefin (e.g., polypropylene, polybutene, and the like) with chlorine.
  • EXAMPLE 1 To a solution of 175 grams of N-oleyl-l,3- propanediamine and 175 grams of isopropyl'alcohol was added a solution of 40 grams of carbon disulfide and 40 grams of isopropyl alcohol over a one hour period at 0lOC. The unreacted carbon disulfide was distilled off and 50 grams each of crotonic acid, isopropyl alcohol and methanol was added. The mixture was stirred at 010C for 2 hours and then allowed to warm to room temperature. The product was diluted with hexane and washed with water, following which volatile material was distilled out under vacuum to yield 184 grams of a low melting solid.
  • EXAMPLE 2 A portion of the product from Example 1 was diluted with hexane, filtered, water washed, and then the hexane distilled out. The resultant product was diluted with neutral mineral oil to obtain a 67 weight percent active concentrate. This was diluted with hexane and washed with aqueous ammonia. Powdered solid carbon dioxide was added and stirred into the mixture. The mixture was then water washed, following which hexane was distilled out, leaving a viscous yellow liquid concentrate.
  • the additives are useful in lubricating oils and greases including both mineral and synthetic.
  • Synthetic oils include polyolefin oils (e.g., polybutene oil, decene oligomer, and the like), synthetic esters (e.g., dinonyl sebacate, trioctanoic acid ester of trimethylolpropane,
  • polyglycol oils and the like
  • Greases are madefrom these'oils by adding a thickening agent such as sodium, calcium, lithium, or aluminum salts of fatty acids such as stearic acid.
  • the oils and greases are prepared by blending an antiwear and antirust amount of the additive into the oil or grease.
  • a useful concentration is from about O.l to 5 weight percent.
  • the additives may be added in the form of a concentrate such as the mineral oil diluted concentrate described in Example 2.
  • additives may be included in the oil or grease compositions. These include such additives as zinc dialkyldithiophosphates, barium phenates, calcium phenates, calcium aryl sulfonates, magnesium aryl sulfonates, overbased calcium aryl sulfonates, barium polybutenyl phosphonates; antioxidants such as 4,4- methylenebis(2,6-di-tert-butylphenol), a-dimethylamino-2,6-di-tert-butyl-p-cresol; dispersants such as polybutenyl succinimides of ethylenepolyamines, polybutenyl ethylenediamines, viscosity index improvers such as polybutenes, ethylene-propylene copolymers, polylauryl methacrylates, and the like.
  • additives as zinc dialkyldithiophosphates, barium phenates, calcium phenates, calcium aryl sulfon
  • Tests have been carried out to demonstrate the antiwear and antirust properties of the additives.
  • the first is known as the four-ball cam and tappet test.
  • three steel balls are placed in a triangular manner in a circular retainer containing the test oil.
  • a fourth ball is placed on top of these three to form a triangular pyramid.
  • a 50 Kg load is placed on the top ball and it is rotated at 1800 rpm. for one hour with the oil heated to l 10C.
  • Criteria is the average scar diameter formed on the three bottom balls. A scar diameter of 1 mm or less is considered satisfactory.
  • R' is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
  • R is an aliphatic hydrocarbon radical containing from about 8-100 carbon atoms
  • R is a divalent aliphatic hydrocarbon radical containing from 2 to about 10 carbon atoms
  • R and R are selected from the group consisting of hydrogen and alkyl radicals containing 1 to about 4 carbon atoms.
  • R contains about 8-22 carbon atoms, R is the trimethylene radical, R is the methyl radical, and R is hydrogen.

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  • Oil, Petroleum & Natural Gas (AREA)
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Abstract

Compounds having the formula:

WHEREIN R''is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:

Description

United States Patent [1 1 Malec y 1 OIL ADDlTlVE Inventor: Robert E. Malec, Birmingham,
Mich.
Assignee: Ethyl Corporation, Richmond, Va.
Filed: May 24, 1974 Appl. No.: 473,129
Related US. Application Data u.s. Cl 260/455 A; 252/34; 252/475 Int. Cl. C07C 5 0 C07C 155 0 c07c 155/08 Field of Search 260/455 A References Cited UNITED STATES PATENTS 7/1958 Andersen et al "260/455 A 4/1965 Ross et'al. 260/455 A Primary Examiner-Lewis Gotts Assistant Examiner-D. R. Phillips Attorney, Agent, or FirmDonald L. Johnson; Robert A. Linn; Joseph D. Odenweller Division of Ser. No. 348,625, April 6, 1973, Pat. No.
[1-11 3,890,363 June 17, 1975 7 ABSTRACT Compounds having the formula;
5 ll R' -:m' I c -:-c!ivR3 R4 wherein R'is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
wherein R is an aliphatic hydrocarbon radical containing about 8-100 carbon atoms, R" is selected antirust additives in lubricating oils and greases.
6 Claims, No Drawings OIL ADDITIVE This application is a division of application Ser. No. 348,625, filed April 6, 1973, now US. Pat. No. 3,833,496.
BACKGROUND Additives are conventionally added to lubricating oil and grease to improve their properties. Antiwear additives used in the past include compounds such as zinc dialkyldithiophosphates, sulfurized sperm oil, and the like. Antirust protection can be provided by compounds such as overbased calcium sulfonates. Long chain amines such as polybutenyl ethylenediamine have been used to improve dispersancy of lubricating oils.
SUMMARY OF THE INVENTION According to the present invention, lubricating oils and greases having improved antiwear and antirust properties are provided by including in the lubricating oil composition certain 3-mercaptoalkanoic acid, [(alkylamino)alkyl] dithiocarbamates such as 3- mercaptobutyric acid, [3(oleylamino)-propyl] dithiocarbamate.
DESCRIPTION OF THE PREFERRED EMBODIMENTS A preferred embodiment of the invention is an antiwear-antirust additive for lubricating oils and greases having the formula:
wherein R is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
wherein R is an aliphatic hydrocarbon radical containing about 8-100 carbon atoms, R"" is selected from the group consisting of hydrogen and C alkyls and R is a divalent aliphatic hydrocarbon radical containing about 2-10 carbon atoms, R and R are selected from the group consisting of hydrogen and alkyl radicals containing about 14 carbon atoms, R" is selected from the group consisting of hydrogen and C alkyls and R' is selected from the group consisting of hydrogen and salt cations. Useful salt cations include the cations of the alkaline earth metals such as calcium, magnesium, strontium, and barium; ammonium ions formed from ammonia; alkyl and alkenyl amines such as methylamine, dimethylamine, trimethylamine, triethylamine, tributylamine, ethanolamine, diethanolamine, triethanolamine, morpholine, stearylamine, oleylamine, palmylamine, laurylamine, eicosylamine, eicosenylamine, and the like; and other metal cations such as zinc, aluminum, nickel, manganese, iron, and the like.
Representative examples of the above additives in clude:
2 3-mercaptopropionic acid, n-octyldithiocarbamate 3-mercaptobutyric acid, stearyldithiocarbamate calcium S-mercaptobutyrate, oleyldithiocarbamate zinc 3-mercaptopropionate, palmyldithiocarbamate trimethylammonium 3-mercaptohexanoate, C
polybutenyl dithiocarbamate manganese 3-mercaptobutyrate, stearyldithiocarbamate barium 3-mercaptoheptanoate, eicosyldithiocarbamate magnesium 3-mercaptobutyrate, eicosenyldithiocarbamate triethanolammonium 3-mercaptobutyrate, oleyldithiocarbamate A most preferred embodiment of this invention is an antiwear-antirust additive for lubricating oils and greases, said additive having the formula:
wherein R is an aliphatic hydrocarbon radical containing from about 8-100 carbon atoms, R is a divalent aliphatic hydrocarbon radical containing from 2 to about 10 carbon atoms, and R and R are selected from tl" group consisting of hydrogen and alkyl radicals containing l to about 4 carbon atoms. Since the compounds contain both a basic amine functional group and a carboxylic acid they can exist in the form of a zwitterion and are shown in that form in Formula [1. Representative examples of such additives include: 3-mercaptopropionic acid, [2(9- eicosenylamino)ethyl]dithiocarbamate 3-mercapto-2-methylbutyric acid, [6(octylamino)hexyl]dithioca'rbamate 3-mercaptoheptanoic cyl]dithiocarbamate 3-mercapto-2-methylhexanoic acid,
hexylbutylamino) butyl] dithiocarbamate 3-mercapto-2-butylheptanoic acid, [3(pentacontenylamino) propyl] dithiocarbamate B-mercaptobutyric acid,
tylamino)ethyl]dithiocarbamate S-mercaptopropionic acid, [3(octacontylamino)propyl]dithiocarbamate 3-mercaptohexanoic acid,
polybutenylamino) propyl] dithiocarbamate 3-mercaptobutyric acid, [3(C -p0lypropenylamino) propyl] dithiocarbamate 3-mercaptooctanoic acid, [3(dodecenylamino)bu- [2(hexacontyl]dithiocarbamate 3-mercaptopropionic acid, [3(tetracosylamino)propyl]dithiocarbamate 3-mercaptobutyric acid, [6(stearylamino)- hexyl]dithiocarbamate 3-mercaptopentanoic acid, [4(palmylamino)butyl]dithiocarbamate 3-mercaptobutyric acid, [3( 2- nonacontenylamino )propyl]dithiocarbamate A preferred class of additives are those of Formula I] wherein R contains about 8-22 carbon atoms, R is the trimethylene radical (CH R is the methyl radiacid, [l0(laurylamino)decal, and R is hydrogen. Examples of these compounds are:
3-mercaptobutyric acid, [3(oleylamino )propyl]dithiocarbamate 3-mercaptobutyric acid, [3(steary1amino)propyl]dithiocarbamate B-mercaptobutyric acid, [3(palmylamino)propyl ]dithiocarbamate The additives are readily prepared by reacting an aliphatic hydrocarbylaminohydrocarbylamine with carbon disulfide to form the corresponding hydrocarbylaminohydrocarbyl dithiocarbamic acid and reacting this with an appropriate alpha-unsaturated aliphatic carboxylic acid such as acrylic acid, crotonic acid, a-methyl crotonic acid, a,B-diethyl acrylic acid, B-butyl acrylic acid, a-butyl acrylic acid, and the like (N. Kreutzkamp et al, Arch. Pharm. 304, p. 477-481, July 1971 l The aliphatic hydrocarbylaminohydrocarbylamines can be prepared by reacting an aliphatic hydrocarbyl chloride with an aliphatic diamine. For example, reaction of oleyl chloride with 1,3-propanediamine yields oleylaminopropylamine. Likewise, reaction of lauryl chloride with 1,6-hexanediamine forms laurylaminohyexylamine. Similarly, reaction of C -polybutenyl chloride with ethylenediamine forms C polybutenylaminoethylamine. The polyolefin chlorides are readily formed by reacting a polyolefin (e.g., polypropylene, polybutene, and the like) with chlorine.
The following example illustrates the manner in which the additives can be prepared.
EXAMPLE 1 To a solution of 175 grams of N-oleyl-l,3- propanediamine and 175 grams of isopropyl'alcohol was added a solution of 40 grams of carbon disulfide and 40 grams of isopropyl alcohol over a one hour period at 0lOC. The unreacted carbon disulfide was distilled off and 50 grams each of crotonic acid, isopropyl alcohol and methanol was added. The mixture was stirred at 010C for 2 hours and then allowed to warm to room temperature. The product was diluted with hexane and washed with water, following which volatile material was distilled out under vacuum to yield 184 grams of a low melting solid.
EXAMPLE 2 A portion of the product from Example 1 was diluted with hexane, filtered, water washed, and then the hexane distilled out. The resultant product was diluted with neutral mineral oil to obtain a 67 weight percent active concentrate. This was diluted with hexane and washed with aqueous ammonia. Powdered solid carbon dioxide was added and stirred into the mixture. The mixture was then water washed, following which hexane was distilled out, leaving a viscous yellow liquid concentrate.
Modification of the above procedure by substitution of different starting hydrocarbylaminohydrocarbylamines and different alpha-unsaturated aliphatic carboxylic acids will lead to the other additives within the scope of this invention.
The additives are useful in lubricating oils and greases including both mineral and synthetic. Synthetic oils include polyolefin oils (e.g., polybutene oil, decene oligomer, and the like), synthetic esters (e.g., dinonyl sebacate, trioctanoic acid ester of trimethylolpropane,
and the like), polyglycol oils, and the like. Greases are madefrom these'oils by adding a thickening agent such as sodium, calcium, lithium, or aluminum salts of fatty acids such as stearic acid. The oils and greases are prepared by blending an antiwear and antirust amount of the additive into the oil or grease. A useful concentration is from about O.l to 5 weight percent. The additives may be added in the form of a concentrate such as the mineral oil diluted concentrate described in Example 2.
Other additives may be included in the oil or grease compositions. These include such additives as zinc dialkyldithiophosphates, barium phenates, calcium phenates, calcium aryl sulfonates, magnesium aryl sulfonates, overbased calcium aryl sulfonates, barium polybutenyl phosphonates; antioxidants such as 4,4- methylenebis(2,6-di-tert-butylphenol), a-dimethylamino-2,6-di-tert-butyl-p-cresol; dispersants such as polybutenyl succinimides of ethylenepolyamines, polybutenyl ethylenediamines, viscosity index improvers such as polybutenes, ethylene-propylene copolymers, polylauryl methacrylates, and the like.
Tests have been carried out to demonstrate the antiwear and antirust properties of the additives. The first is known as the four-ball cam and tappet test. In this test, three steel balls are placed in a triangular manner in a circular retainer containing the test oil. A fourth ball is placed on top of these three to form a triangular pyramid. A 50 Kg load is placed on the top ball and it is rotated at 1800 rpm. for one hour with the oil heated to l 10C. This test has previously been shown to correlate well with the cam and tappet wear of an internal combustion engine. Criteria is the average scar diameter formed on the three bottom balls. A scar diameter of 1 mm or less is considered satisfactory.
The test was carried out on a non-additive neutral oil and on triplicate samples containing 1 weight percent of the additive of Example 1 3-mercaptobutyric acid, [3(oleylamino)propyl] dithiocarbamate. The results obtained were as follows.
TABLE 1 Additive Average scar diameter (mm) None 2.3 Example I (1%) '0.92, 0.99, 0.89
TABLE 2 Additive Results None both fail Example 2 (1%) all pass These results demonstrate the excellent antiwear and antirust properties of the present additives.
I claim: 1. An antiwear-antirust additive for lubricating oils and greases, said additive having the formula:
c v u wherein R' is selected from the group consisting of aliphatic hydrocarbon radicals containing about 8-100 carbon atoms, and hydrocarbylaminohydrocarbyl radicals having the formula:
2. An antiwear-antirust additive of claim 1, said additive having the formula:
wherein R is an aliphatic hydrocarbon radical containing from about 8-100 carbon atoms, R is a divalent aliphatic hydrocarbon radical containing from 2 to about 10 carbon atoms, and R and R are selected from the group consisting of hydrogen and alkyl radicals containing 1 to about 4 carbon atoms.
3. An additive of claim 2 wherein R contains about 8-22 carbon atoms, R is the trimethylene radical, R is the methyl radical, and R is hydrogen.
4. An additive of claim 3 wherein R is the oleyl radical.
5. An additive of claim 3 wherein R is the stearyl radical.
6. An additive of claim 3 wherein R is the palmyl radical.

Claims (6)

1. AN ANTIWEAR-ANTIRUST ADDITIVE FOR LUBRICATING OILS AND GREASES, SAID ADDITIVE HAVING THE FORMULA:
2. An antiwear-antirust additive of claim 1, said additive having the formula:
3. An additive of claim 2 wherein R1 contains about 8-22 carbon atoms, R2 is the trimethylene radical, R3 is the methyl radical, and R4 is hydrogen.
4. An additive of claim 3 wherein R1 is the oleyl radical.
5. An additive of claim 3 wherein R1 is the stearyl radical.
6. An additive of claim 3 wherein R1 is the palmyl radical.
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Cited By (15)

* Cited by examiner, † Cited by third party
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US4360438A (en) * 1980-06-06 1982-11-23 R. T. Vanderbilt Company, Inc. Organomolybdenum based additives and lubricating compositions containing same
US4609480A (en) * 1983-09-19 1986-09-02 Idemitsu Kosan Company Limited Lubricant composition for improving fatigue life
US4758362A (en) * 1986-03-18 1988-07-19 The Lubrizol Corporation Carbamate additives for low phosphorus or phosphorus free lubricating compositions
US4859352A (en) * 1988-02-29 1989-08-22 Amoco Corporation Low temperature high performance grease
US4997969A (en) * 1988-12-12 1991-03-05 The Lubrizol Corporation Carbamate additives for lubricating compositions
US5674820A (en) * 1995-09-19 1997-10-07 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5693598A (en) * 1995-09-19 1997-12-02 The Lubrizol Corporation Low-viscosity lubricating oil and functional fluid compositions
US5705458A (en) * 1995-09-19 1998-01-06 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5726132A (en) * 1997-02-28 1998-03-10 The Lubrizol Corporation Oil composition for improving fuel economy in internal combustion engines
US5759965A (en) * 1995-10-18 1998-06-02 The Lubrizol Corporation Antiwear enhancing composition for lubricants and functional fluids
US5843873A (en) * 1994-11-15 1998-12-01 The Lubrizol Corporation Lubricants and fluids containing thiocarbamates and phosphorus
US5902776A (en) * 1995-09-19 1999-05-11 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5913112A (en) * 1991-03-06 1999-06-15 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing an insulated gate field effect semiconductor device having an offset region and/or lightly doped region
US20100283010A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity
US20100283011A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity

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US4076639A (en) * 1976-08-30 1978-02-28 Mobil Oil Corporation Lubricant compositions
US4863622A (en) * 1988-03-31 1989-09-05 Pennzoil Products Company Phosphorus-free antiwear/antifriction additives
US5180510A (en) * 1988-03-31 1993-01-19 Ethyl Petroleum Additives, Inc. Antioxidant additive and lubricating oil containing same
US4957643A (en) * 1988-05-20 1990-09-18 Ethyl Petroleum Additives, Inc. Lubricant compositions
US4885365A (en) * 1988-05-20 1989-12-05 Ethyl Petroleum Additives, Inc. Dithiocarbanate lubricant compositions
US5370806A (en) * 1989-12-21 1994-12-06 Mobil Oil Corporation Borated dihydrocarbyl dithiocarbamate lubricant additives and composition thereof
US5789357A (en) * 1997-01-10 1998-08-04 Uniroyal Chemical Company, Inc. Dithiocarbamyl carboxylic acids and their use as multifunctional additives for lubricating oils
US6001782A (en) * 1998-12-17 1999-12-14 The Lubrizol Corporation Metal overbased fatty amines further derivatized to contain covalently bound sulfer and/or phorphorus useful as antiwear/extreme pressure additives

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US3180791A (en) * 1960-12-28 1965-04-27 Montedison Spa Method of controlling fungi with organic sulfur ester compounds

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4360438A (en) * 1980-06-06 1982-11-23 R. T. Vanderbilt Company, Inc. Organomolybdenum based additives and lubricating compositions containing same
US4609480A (en) * 1983-09-19 1986-09-02 Idemitsu Kosan Company Limited Lubricant composition for improving fatigue life
US4758362A (en) * 1986-03-18 1988-07-19 The Lubrizol Corporation Carbamate additives for low phosphorus or phosphorus free lubricating compositions
US4859352A (en) * 1988-02-29 1989-08-22 Amoco Corporation Low temperature high performance grease
US4997969A (en) * 1988-12-12 1991-03-05 The Lubrizol Corporation Carbamate additives for lubricating compositions
US5913112A (en) * 1991-03-06 1999-06-15 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing an insulated gate field effect semiconductor device having an offset region and/or lightly doped region
US5843873A (en) * 1994-11-15 1998-12-01 The Lubrizol Corporation Lubricants and fluids containing thiocarbamates and phosphorus
US5693598A (en) * 1995-09-19 1997-12-02 The Lubrizol Corporation Low-viscosity lubricating oil and functional fluid compositions
US5705458A (en) * 1995-09-19 1998-01-06 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5902776A (en) * 1995-09-19 1999-05-11 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5674820A (en) * 1995-09-19 1997-10-07 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5759965A (en) * 1995-10-18 1998-06-02 The Lubrizol Corporation Antiwear enhancing composition for lubricants and functional fluids
US5726132A (en) * 1997-02-28 1998-03-10 The Lubrizol Corporation Oil composition for improving fuel economy in internal combustion engines
US20100283010A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity
US20100283011A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity
US8349215B2 (en) * 2008-01-10 2013-01-08 Clariant Finance (Bvi) Limited Corrosion inhibitors having increased biological degradability and minimized toxicity

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