EP2816098A1 - Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification - Google Patents
Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification Download PDFInfo
- Publication number
- EP2816098A1 EP2816098A1 EP13172544.2A EP13172544A EP2816098A1 EP 2816098 A1 EP2816098 A1 EP 2816098A1 EP 13172544 A EP13172544 A EP 13172544A EP 2816098 A1 EP2816098 A1 EP 2816098A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricating oil
- compound
- oil composition
- oil
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000002816 fuel additive Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 239000005078 molybdenum compound Substances 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical class C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000010499 rapseed oil Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003582 thiophosphoric acids Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- IKXFIBBKEARMLL-UHFFFAOYSA-N triphenoxy(sulfanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=S)OC1=CC=CC=C1 IKXFIBBKEARMLL-UHFFFAOYSA-N 0.000 description 1
- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 239000004711 α-olefin 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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
- C10M135/18—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
-
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
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- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
-
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
-
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- 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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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/085—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
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- 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
- C10M2223/045—Metal containing thio derivatives
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- 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
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- 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
- C10M2223/049—Phosphite
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/78—Fuel contamination
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C10N2040/253—Small diesel engines
Definitions
- the base oil used in the present invention may conveniently comprise mixtures of one or more mineral oils and/or one or more synthetic oils; thus, the term "base oil” herein may refer to a blend containing more than one base oil.
- a preferred Fischer-Tropsch derived base oil for use herein has a pour point (as measured according to ASTM D 5950) of below -30°C, more preferably below -40°C, and most preferably below -45°C.
- Fischer-Tropsch derived base oil contains a blend of two or more Fischer-Tropsch derived base oils
- the above values apply to the blend of the two or more Fischer-Tropsch derived base oils.
- the total amount of base oil incorporated in the lubricating oil composition of the present invention is preferably in the range of from 60 to 99 wt.%, more preferably in the range of from 65 to 90 wt.% and most preferably in the range of from 70 to 85 wt.%, with respect to the total weight of the lubricating oil composition.
- R 5 and R 6 each represent a hydrocarbon group having 1 to 20 carbon atoms.
- the thiadiazole compound include 2,5-bis(n-hexyldithio)-1,3,4-thiadiazole, 2,5-bis(n-octyldithio)-1,3,4-thiadiazole, 2,5-bis(n-nonyldithio)-1,3,4-thiadiazole, 2,5-bis-(1,1,3,3-tetramethylbutyldithio)-1,3,4-thiadiazole, 3,5-bis(n-hexyldithio)-1,2,4-thiadiazole, 3,5-bis(n-octyldithio)-1,2,4-thiadiazole, 3,5-bis(n-nonyldithio)-1,2,4-thiadiazole, 3,5-bis(1,1,3,3-tetramethylbutyldithio)-1,2,4-thiadiaadia
- the thiocarbamate compound may include a metal-containing thiocarbamate or an ashless (non-metal-containing) thiocarbamate. Suitable examples include a zinc dialkyldithiocarbamate and 4,4'-methylene-bis-dibutyldithiocarbamate.
- Boron-containing compounds that may be conveniently used include borate esters, borated fatty amines, borated epoxides, alkali metal (or mixed alkali metal or alkaline earth metal) borates and borated overbased metal salts.
- seal fix or seal compatibility agents include, for example, commercially available aromatic esters.
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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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13172544.2A EP2816098A1 (fr) | 2013-06-18 | 2013-06-18 | Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13172544.2A EP2816098A1 (fr) | 2013-06-18 | 2013-06-18 | Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2816098A1 true EP2816098A1 (fr) | 2014-12-24 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP13172544.2A Withdrawn EP2816098A1 (fr) | 2013-06-18 | 2013-06-18 | Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification |
Country Status (1)
| Country | Link |
|---|---|
| EP (1) | EP2816098A1 (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019025561A1 (fr) | 2017-08-03 | 2019-02-07 | Universität Regensburg | Carburant issu de ressources renouvelables |
Citations (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0668342A1 (fr) | 1994-02-08 | 1995-08-23 | Shell Internationale Researchmaatschappij B.V. | Procédé de préparation d'une huile lubrifiante de base |
| EP0776959A2 (fr) | 1995-11-28 | 1997-06-04 | Shell Internationale Researchmaatschappij B.V. | Procédé pour la production d'huiles lubrifiantes |
| WO1997021788A1 (fr) | 1995-12-08 | 1997-06-19 | Exxon Research And Engineering Company | Huiles de base hydrocarbonees biodegradables et extremement efficaces |
| WO1998026030A1 (fr) | 1996-12-13 | 1998-06-18 | Exxon Research And Engineering Company | Compositions d'huile lubrifiante contenant des complexes de molybdene organiques |
| WO1999041332A1 (fr) | 1998-02-13 | 1999-08-19 | Exxon Research And Engineering Company | Huile de base a faible viscosite pour lubrifiants |
| WO2000008115A1 (fr) | 1998-08-04 | 2000-02-17 | Exxon Research And Engineering Company | Huile de base pour lubrifiant a stabilite amelioree vis-a-vis de l'oxydation |
| WO2000014179A1 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Base de lubrifiant synthetique de premiere qualite |
| WO2000014183A1 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Production de lubrifiant synthetique et de matiere de base pour lubrifiant sans deparaffinage |
| WO2000014187A2 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Lubrifiants synthetiques de premiere qualite |
| WO2000014188A2 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Lubrifiant de premiere qualite resistant a l'usure |
| WO2000015736A2 (fr) | 1998-09-11 | 2000-03-23 | Exxon Research And Engineering Company | Huiles lubrifiantes isoparaffiniques synthetiques a large fraction de distillation |
| EP1029029A1 (fr) | 1997-10-20 | 2000-08-23 | Mobil Oil Corporation | Compositions d'huiles de base de lubrifiant isoparaffiniques |
| WO2001018156A1 (fr) | 1999-09-08 | 2001-03-15 | Total Raffinage Distribution S.A. | Nouvelle huile de base hydrocarbonee pour lubrifiants a indice de viscosite tres eleve |
| WO2001057166A1 (fr) | 2000-02-04 | 2001-08-09 | Mobil Oil Corporation | Huiles lubrifiantes composees renfermant des huiles de base a haute performance derivees d'hydrocarbures paraffiniques |
| EP1058720B1 (fr) | 1998-02-27 | 2003-05-07 | Shell Internationale Researchmaatschappij B.V. | Composition lubrifiante |
| WO2007045629A1 (fr) | 2005-10-17 | 2007-04-26 | Shell Internationale Research Maatschappij B.V. | Composition d’huile lubrifiante |
| EP2248876A1 (fr) | 2008-02-14 | 2010-11-10 | Idemitsu Kosan Co., Ltd. | Composition lubrifiante |
| US20110245122A1 (en) * | 2010-04-01 | 2011-10-06 | Keith Strickland | Lubricating Oil Composition |
| EP2334770B1 (fr) * | 2008-07-15 | 2013-05-29 | ExxonMobil Research and Engineering Company | Procédé de stabilisation d huile de lubrification pour moteur diesel contre la dégradation par du biodiesel |
-
2013
- 2013-06-18 EP EP13172544.2A patent/EP2816098A1/fr not_active Withdrawn
Patent Citations (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0668342A1 (fr) | 1994-02-08 | 1995-08-23 | Shell Internationale Researchmaatschappij B.V. | Procédé de préparation d'une huile lubrifiante de base |
| EP0776959A2 (fr) | 1995-11-28 | 1997-06-04 | Shell Internationale Researchmaatschappij B.V. | Procédé pour la production d'huiles lubrifiantes |
| WO1997021788A1 (fr) | 1995-12-08 | 1997-06-19 | Exxon Research And Engineering Company | Huiles de base hydrocarbonees biodegradables et extremement efficaces |
| WO1998026030A1 (fr) | 1996-12-13 | 1998-06-18 | Exxon Research And Engineering Company | Compositions d'huile lubrifiante contenant des complexes de molybdene organiques |
| EP1029029A1 (fr) | 1997-10-20 | 2000-08-23 | Mobil Oil Corporation | Compositions d'huiles de base de lubrifiant isoparaffiniques |
| WO1999041332A1 (fr) | 1998-02-13 | 1999-08-19 | Exxon Research And Engineering Company | Huile de base a faible viscosite pour lubrifiants |
| EP1058720B1 (fr) | 1998-02-27 | 2003-05-07 | Shell Internationale Researchmaatschappij B.V. | Composition lubrifiante |
| WO2000008115A1 (fr) | 1998-08-04 | 2000-02-17 | Exxon Research And Engineering Company | Huile de base pour lubrifiant a stabilite amelioree vis-a-vis de l'oxydation |
| WO2000014187A2 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Lubrifiants synthetiques de premiere qualite |
| WO2000014188A2 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Lubrifiant de premiere qualite resistant a l'usure |
| WO2000014183A1 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Production de lubrifiant synthetique et de matiere de base pour lubrifiant sans deparaffinage |
| WO2000014179A1 (fr) | 1998-09-04 | 2000-03-16 | Exxon Research And Engineering Company | Base de lubrifiant synthetique de premiere qualite |
| WO2000015736A2 (fr) | 1998-09-11 | 2000-03-23 | Exxon Research And Engineering Company | Huiles lubrifiantes isoparaffiniques synthetiques a large fraction de distillation |
| WO2001018156A1 (fr) | 1999-09-08 | 2001-03-15 | Total Raffinage Distribution S.A. | Nouvelle huile de base hydrocarbonee pour lubrifiants a indice de viscosite tres eleve |
| WO2001057166A1 (fr) | 2000-02-04 | 2001-08-09 | Mobil Oil Corporation | Huiles lubrifiantes composees renfermant des huiles de base a haute performance derivees d'hydrocarbures paraffiniques |
| WO2007045629A1 (fr) | 2005-10-17 | 2007-04-26 | Shell Internationale Research Maatschappij B.V. | Composition d’huile lubrifiante |
| EP2248876A1 (fr) | 2008-02-14 | 2010-11-10 | Idemitsu Kosan Co., Ltd. | Composition lubrifiante |
| EP2334770B1 (fr) * | 2008-07-15 | 2013-05-29 | ExxonMobil Research and Engineering Company | Procédé de stabilisation d huile de lubrification pour moteur diesel contre la dégradation par du biodiesel |
| US20110245122A1 (en) * | 2010-04-01 | 2011-10-06 | Keith Strickland | Lubricating Oil Composition |
Non-Patent Citations (3)
| Title |
|---|
| "API Publication 1509", April 2002, AMERICAN PETROLEUM INSTITUTE (API |
| KIRK-OTHMER: "Encyclopedia of Chemical Technology", vol. 14, pages: 477 - 526 |
| VANDERBILT CHEMICALS: "Lubricant Additives", 31 January 2013 (2013-01-31), pages 1 - 36, XP055080763, Retrieved from the Internet <URL:http://www.rtvanderbilt.com/petro/p981.pdf> [retrieved on 20130924] * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019025561A1 (fr) | 2017-08-03 | 2019-02-07 | Universität Regensburg | Carburant issu de ressources renouvelables |
| WO2020025686A1 (fr) | 2017-08-03 | 2020-02-06 | Universität Regensburg | Carburant issu de ressources renouvelables |
| US20210324281A1 (en) * | 2017-08-03 | 2021-10-21 | Universität Regensburg | Fuel derived from renewable resources |
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