专利摘要:
A storage stable lubricating composition having improved anti-friction and anti-wear properties is provided by a base oil composition containing an additive combination of (1) a zinc dihydrocarbyl dithiophosphate, (2) an ester of a polycarboxylic acid and a glycol and (3) an ashless dispersant containing a high molecular weight aliphatic hydrocarbon oil solubilizing group attached thereto and wherein either the zinc or ester component or both are predispersed prior to adding them to the lubricating composition.
公开号:SU936818A3
申请号:SU782652605
申请日:1978-08-21
公开日:1982-06-15
发明作者:Шоб Хэрольд;Эдвин Вэдди Вальтер
申请人:Эксон Рисерч Энд Инджиниринг Компани (Фирма);
IPC主号:
专利说明:

one
This invention relates to a storage stable lubricant. Memory containing complex add. Ku, I improve anti-friction and anti-wear properties.
As is known, under the conditions referred to as boundary lubrication, it becomes necessary to lubricate two rubbing surfaces or otherwise protect them in order to prevent wear and ensure continuous movement. There, the 1. friction between the two surfaces increases the energy consumption required for the movement, and where the movement is an integral part of the energy conversion system, lubrication is highly desirable, reducing this friction to a minimum. It is also known that friction and H-Jnos can be reduced with varying success by adding appropriate additives or their combinations to a natural or synthetic lubricant.
material. In the same way possible. provide continuous motion by adding one or more appropriate additives. five
Metallic dialcdithiophosphates are a number of well-known additives that have anti-acid anti-wear properties.
Known additives of this class are dialkyldithiophosphates of zinc, using e a .e in lubricant compositions ij.
While zinc compounds
5 have excellent oxidation stability and excellent anti-wear properties, but they increase or significantly limit the ability to lower
20 between moving parts, therefore the use of compositions containing them leads to significant loss of energy when countering friction, even when anti-friction agents are included in the composition. 3 Lubricating compositions containing as additives mixtures based on MacnopacTBOpHNbix dimeric acids and polyols 2j and esters obtained by the interaction of components of this kind 3 have good anti-wear properties. However, the f3} blend may not be used in crankcase oils, since the acid component is corrosive and interacts with the usual zinc component, commonly used to reduce wear on the valve remover; while using cheaper, shorter chain glycols for the purpose of obtaining more economically viable mixtures, these glycols boil away under normal operating conditions. In addition, the ester components also tend to interact with zinc dialkyldithiophosphate and thus cause possible precipitation or precipitation from the lubricant composition in the form of droplets, i.e. it is an unstable connection. A lubricant composition containing base oil, metal dihydrocarbon dithiophosphate, in particular zinc di () alkyl dithiophosphate and dispersant, is a product of the interaction of polyalkenyl succinic acid and polyamine t. The known composition has detergent properties, however, it has unsatisfactory anti-wear properties. The aim of the invention is to reduce friction while maintaining other performance properties. The goal is achieved by the fact that the lubricant composition containing base oil, di (Cd-Cg) alkyldithio zinc phosphate and dispersant, additionally contains linoleic acid dimer ester and diethylene glycol and a dispersant selected from the group comprising the reaction product of succinic acid polyisobutenyl anhydride, pentaerythritol and polyamine, the product of the reaction of the anhydride of polyiso5 Tenh1 succinic acid and polyamine, the boron-containing product of the interaction of the anhydride polyisobutylene n-tartaric acid and polyamine, the product of the Effects of polyisobutenyl succinic anhydride and tris (hydroxymethyl) -aminomethane with the following components, wt.%: 8 Di () alkyl dithiophosphate of zinc Linoleic acid dimer ester and diethylene glycol Dispergator 0.25-6.3 Base oil Up to 100 The described additives can used in standard base oils along with other conventional additives and additives. However, an important condition of the invention is that in order to obtain formulations that are resistant to storage and retain their exceptional anti-friction and anti-wear properties, zinc dialkyldithiophosphate and linoleic acid dimer and diethylene glycol ester must be pre-dispersed. By predisposing, it is necessary to understand the separate mixing of the false ester or zinc component with an ashless dispersant, which can be dissolved in oil, to produce a substantially clear and fully miscible solution. This mixing process can be accelerated by heating the solution to a temperature in the order of. If this proprietary process is not carried out, the zinc component, after a certain period of time, begins to interact with complex ether or form a complex compound with it, falling out of solution at the same time, which entails a loss of stability and valuable compositional properties. In order to eliminate this disadvantage, the cncy dialkyldithiophosphate or the ester is dispersed separately from each other before being mixed with the other components in the lubricant composition. It should be noted that the residual additives can be added in a standard or conventional manner with the sole condition that the zinc and complex ester components are not combined with each other (or partially) before at least one of them is not pre-dispersed. The base oils used in the composition according to the invention include mineral lubricating oils, synthetic lubricating oils and their mixtures. Synthetic oils include complex-dyspiric oils, such as di (2-ethylhexyl) sebacate, azel.shpip adipate, complex layers of dicarboxylic acids, glycol or monobasic acids or monohydric alcohols, silicone oils , sulfide esters, organic carbonates and other known synthetic oils. In order to obtain the desired oil, to the oils-compositions according to the invention, other additives may be added. Such additives include commonly used additives: oxidation inhibitors — phenothiazine or phenyl-O-naphthylamine; anticorrosive agents — lecithin or sorbitan monooleate; detergents — barium phenol; lower hardening temperature; copolymers of vinyl acetate and formic acid esters and alcohols, and alcohols, and alcohols, and alcohols, and alcohols, alcohols, and alcohols, alcohols and alcohols. oils, viscosity index enhancers, olefin copolymers, polymethacrylates, and the like. In particular, the basic alkaline earth metal salts of organic sulfonic acid, petroleum sulfonic acid, or synthetic alkarylsulphonic acid are useful additives. Among petroleum sulfonates, the most useful products are those obtained by sulfonation of the corresponding petroleum fractions with subsequent removal of acid precipitates and purification of the product. Synthetic alkaryl sulphonic acids are usually obtained from alkyl benzenes, such as the Friedel-Crafts benzene reaction products with a polymer, for example tetrapropylene. Relevant acids so
HOCH CK2 OCH CH OC {CH2) (CHg) 5 CH
HOCH CH OCH CHiOC (CHj)
In preparing various formulations, various dispersants are used.
A. Ashless disperser is obtained by the interaction of polyisobutynyl succinic acid anhydride (APIBAC) with a polyisobutenyl residue (PIB) with an average molecular weight (CMBJ of about 900 with an equimolar amount of pentaerythritol and a smaller amount of polyamine mixture containing polyoxyprolineamineamine amine, i.e. 0.35 wt.%. Pro-
(Cli.ljC
Hi
These types of products are supplied by the company Lubrisol Corporation under the trade name Lubrisol 6401.
B. A borated ashless dispersant is obtained by condensation of 2.1 mol of APIBAC PIB with about 1300 MW dissolved in mineral oil Solvent Neutral 150 in order to obtain 50% solution, with i mol of tetraethylenepentamine. The ASHABAC solution is heated to about 150 ° C with stirring, the polyamine is loaded into the reactor for 4 hours, after which it can be obtained in the at86 by sulfonation of alkyl derivatives of such compounds as diphenylenoxidianthrene, phenolthioxin, diphenylenesulfine, phenothiazine, diphenyloxide, diphenylsulfide, diphenylamine, acetylamine, phenylthiazine, diphenyloxymethyl, diphenyloxymethyl, diphenyloxymethyl, and phenylthioxine. hydra of naphthalene, etc. Basic alkaline earth metal sulfonates are obtained by reacting an alkaline earth metal base, for example, lime, magnesium oxide or magnesium with sulfur in the presence of sulfonic acid or neutral metal sulfate sulfate, usually calcium, magnesium or barium salts. These neutral salts, in turn, can be obtained from free acids by reacting with an appropriate alkaline earth metapla or Hsa base by double decomposition of an alkali metal sulfonate by known methods. Example 1. To obtain formulations, engine oil of type 10 W, -40 SE, containing 1.5 wt./about E, is calculated on the total weight of the lubricating oil of zinc dialkyldithiophosphate (containing 80% of the active substance in mineral oil), in which the alkyl groups are are a mixture of such groups containing about 4-5 C atoms (obtained by reacting with a mixture of about 65% isobutyl alcohol and 35% amyl 0.1%, calculated on the total weight of ester lubricant obtained by sterilization of dimer acid and diztilen glycol structural According to formula 7 of the nitrogen atmosphere, light fractions are distilled off for 3 hours. The temperature is kept within the range of about 140-165 ° C. during the reaction and distillation. While the resulting product is released at about 135-165 ° C, 1.4 mol is added over 34 hours. boric acid in mineral oil, after which the light fractions are distilled off again in a nitrogen atmosphere.After frosting and evaporation in a rotary evaporator, the concentrate (50% by weight of the reaction product) contains about 1.46% by weight, nitrogen and 0.32% .% boron. B. The ashless dispersant is obtained by charging 1.0 mol ASHABAC with a PIB group with a CMB of about 1300 dissolved in 500 ml of Solvent Neutral 150, 0.36 mol of zinc acetate dihydrate as a promoter and 1.9 motif (oxymethyl) aminomethane ( TOAM in a glass reactor. After heating for 4 hours at approximately 168-174 ° C., the expected amount of water is obtained. After filtration and evaporation on a rotary evaporator, the concentration (50% by weight of the active ingredient) contains, according to analysis, 1.0% by weight of nitrogen. G. Bezsolnyh dispersant is prepared according to Example B, using 1.3 mol APIBN (beer has SMV about 900) without boronation. Contains 2.1 wt.% of nitrogen. Upon receipt of the target lubricant composition, the ester component of each composition is first dispersed in the following amounts of ashless dispersers: A 5.25 wt.% dispersant (mixture of 46.5 wt.% active ingredient in mineral lubricating oil) B and C 5.25 wt.% dispersant (mixture of 50 wt.% active ingredient in mineral lubricating oil) D 6.3 wt.% dispersant (mixture 50 wt.% by weight of active ingredient in mineral lubricating oil) Ester part of each composition (0, J wt.%) is dispersed in the description of dispersants for about 2 hours, stirring for 2 hours, followed by the addition of a crankcase oil containing anticorrosive agents, i.e. overbased magnesium sulphonate, a detergent additive, an improvement in the s88 index of an ethylene-propylene copolymer bone and a specified zinc dialkyldithiophosphate (1.5 wt.% - 80% active ingredient in mineral oil). Unlike formulations in which zinc dialkyldithiophosphate is added to the ester prior to prior dispersing one of these two components, all of the products described show resistance to storage for several months at room temperature. The composition containing the dispersant G is characterized by a somewhat reduced storage resistance, which appears to drop out in the form of droplets after two weeks at room temperature. Example2. In this experiment, two compositions, prepared analogously to Example 1 and containing dialkyl dithiophosphate dialster and ester, are tested for relative friction and wear, using the method with a ball or cylinder. For comparison purposes, standard oil of type 10 W - 30 SE, containing only a zinc component, is also tested for relative friction and wear. The device used in this experiment consists of a fixed metal ball working against a rotating ts1-tindra. The load on the ball and the rotation of the cylinder can be varied throughout the experiment or from experience to experience, as well as the duration of the test. However, as a rule, the steel against the steel, constant revolutions per minute and constant experience (load 4 kg, 0.26 rpm and 70 min in each case) work at a constant load. Actual wear is determined by measuring the volume metal removed from the cylinder compared with the standard. The actual friction is determined by the force required to make the rotation compared to the standard. 1. In the first composition, standard oil 10 W - 40 SE is mixed for lubrication (same as in example 1), containing dispersant G and 1.5% by weight of zinc dialkydithiophosphate (80% active ingredient in mineral oil and other standard additives , including anticorrosive additive, detergent, additive that improves the viscosity index, but without linoleic acid dimer ester and diethylene glycol.
权利要求:
Claims (1)
[1]
Claim
----------------------- eComposition ..... - ·· ·. . . -. - - - - ·.Relative ball / cylinder data Friction Wear 1 1.00 1.00 P 0.59 0.62 W 0.62 0.48
In addition to the friction and wear test, where in the lubricant composition containing dialkyldithiophosphate and ester of dimer of linoleic acid and diethylene glycol, grades P and III show an improvement in these properties, composition 1 (without ester) and composition III are subjected to a standard test (Seguence III with Test in the engine in order to determine the deterioration of the valve puller (see table. 2) ..
•Table
A lubricating composition containing a base masld, zinc di (C ^ -Cj) -alkidithiophosphate and a dispersant, characterized in that, in order to reduce friction, the composition further comprises an ester of linoleic acid dimer and diethylene glycol and a dispersant selected from the group comprising the product 'the action of the polyisobutenyl succinic acid anhydride, pentaerythritol and polyamine, the reaction product of the polyisobutenyl succinic acid anhydride and polyamine, the boron-containing product of the interaction of the polyisobutenyl succinic acid anhydride and polyamine, the product of the interaction of the anhydride of polyisobutenyl succinic acid and Tris (oxymethyl) -aminomethane, in the following ratio of components, wt.%:
Di (C ^ -C ^) zinc alkyldithiophosphate
Linoleic Acid Dimer Diethylene Glycol Dispersant Base Oil
1,5
0.1
0.25-6.3 to 100
类似技术:
公开号 | 公开日 | 专利标题
SU936818A3|1982-06-15|Lubrication composition
US6841521B2|2005-01-11|Methods and compositions for reducing wear in heavy-duty diesel engines
US4479883A|1984-10-30|Lubricant composition with improved friction reducing properties containing a mixture of dithiocarbamates
US6479440B1|2002-11-12|Alkaline earth alkylaryl sulfonates, their application as an additive for lubricating oil, and methods of preparation
EP0217591B1|1989-11-23|Normally liquid c18 to c24 monoalkyl catechols
US5164102A|1992-11-17|Lubricating oil composition
US5807813A|1998-09-15|Lubricating oil composition
CA1180320A|1985-01-02|Co-dispersant stabilized friction modifierlubricating oil composition
EP0562062A1|1993-09-29|Fluorocarbon seal protective additives for lubrication oils
EP0285455B1|1992-01-29|Sulphur-containing borate esters
US3377281A|1968-04-09|Lubricating composition
US4115287A|1978-09-19|Lubricating compositions
US6204226B1|2001-03-20|Mixture of alkyl-phenyl-sulfonates of alkaline earth metals, its application as an additive for lubricating oil, and methods of preparation
JP2749623B2|1998-05-13|Lubricating oil composition
EP0039998B1|1984-04-18|Lubricating oil composition containing sediment-reducing additive
US4960528A|1990-10-02|Lubricating oil composition
CA1273344A|1990-08-28|Succinimide complexes of borated alkyl catechols andlubricating oil compositions containing same
EP0051998B1|1985-04-10|Lubricating oil composition
US5028345A|1991-07-02|Lubricating oil composition
US3822284A|1974-07-02|1-and 3-substituted |carbazole
EP0041851B1|1984-03-21|Lubricant composition with stabilized metal detergent additive and friction reducing ester component
CA1224470A|1987-07-21|Succinimide complexes of borated fatty acid esters of glycerol and lubricating compositions containingsame
WO2001072933A2|2001-10-04|Oil compositions having improved fuel economy efficiency
EP0976810A1|2000-02-02|Mixture of alkyl-phenyl-sulfonates of alkaline earth metals, its application as an additive for lubricating oil, and methods of preparation
US3764535A|1973-10-09|Tetra-t-dodecylamarcapto-p-benzoquinone
同族专利:
公开号 | 公开日
AU520291B2|1982-01-21|
DK313778A|1979-02-23|
FR2401218A1|1979-03-23|
SE443368B|1986-02-24|
NO146643B|1982-08-02|
AT365631B|1982-02-10|
NL7807606A|1979-02-26|
CH638560A5|1983-09-30|
FI63594C|1983-07-11|
DE2833171A1|1979-03-01|
JPS5443207A|1979-04-05|
PH13339A|1980-03-13|
DK150640C|1987-11-02|
GB2002810B|1982-05-12|
US4105571A|1978-08-08|
BE869226A|1979-01-25|
AU3755678A|1980-01-03|
NO782506L|1979-02-23|
FI63594B|1983-03-31|
CA1097320A|1981-03-10|
BR7804924A|1979-04-10|
DK150640B|1987-05-04|
JPH0129838B2|1989-06-14|
FI782094A|1979-02-23|
ATA554178A|1981-06-15|
NO146643C|1982-11-10|
SE7807537L|1979-02-23|
IT7825224D0|1978-06-30|
GB2002810A|1979-02-28|
NZ187690A|1980-03-05|
FR2401218B1|1983-01-21|
ZA783637B|1979-06-27|
IT1098356B|1985-09-07|
IN148664B|1981-05-02|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

NL262417A|1960-03-15|
US3180832A|1963-03-07|1965-04-27|Exxon Research Engineering Co|Oil compositions containing anti-wear additives|
US3381022A|1963-04-23|1968-04-30|Lubrizol Corp|Polymerized olefin substituted succinic acid esters|
FR1396645A|1963-04-23|1965-04-23|Lubrizol Corp|Lubricating oil additives|
DE1271877B|1963-04-23|1968-07-04|Lubrizol Corp|Lubricating oil|
US3281356A|1963-05-17|1966-10-25|Lubrizol Corp|Thermally stable water-in-oil emulsions|
NL296139A|1963-08-02|
US3216936A|1964-03-02|1965-11-09|Lubrizol Corp|Process of preparing lubricant additives|
US3446737A|1966-08-18|1969-05-27|Exxon Research Engineering Co|Friction reducing additive comprising metal soap solubilized in oil by an ncontaining dispersant|
US3442808A|1966-11-01|1969-05-06|Standard Oil Co|Lubricating oil additives|
US3429817A|1968-02-29|1969-02-25|Exxon Research Engineering Co|Diester lubricity additives and oleophilic liquids containing the same|
US3562159A|1968-06-26|1971-02-09|Lubrizol Corp|Synthetic lubricants|
US3576743A|1969-04-11|1971-04-27|Lubrizol Corp|Lubricant and fuel additives and process for making the additives|
US3632511A|1969-11-10|1972-01-04|Lubrizol Corp|Acylated nitrogen-containing compositions processes for their preparationand lubricants and fuels containing the same|
US3804763A|1971-07-01|1974-04-16|Lubrizol Corp|Dispersant compositions|
US3933659A|1974-07-11|1976-01-20|Chevron Research Company|Extended life functional fluid|US4244829A|1978-03-07|1981-01-13|Exxon Research & Engineering Co.|Hydrocarbon-soluble epoxidized fatty acid esters as lubricity modifiers for lubricating oils|
GB2056482A|1979-08-13|1981-03-18|Exxon Research Engineering Co|Lubricating oil compositions|
DE3163160D1|1980-05-08|1984-05-24|Exxon Research Engineering Co|Lubricating oil composition containing sediment-reducing additive|
US4505829A|1980-05-08|1985-03-19|Exxon Research & Engineering Co.|Lubricating oil composition containing sediment-reducing additive|
CA1159045A|1980-06-09|1983-12-20|David H. Rehrer|Lubricant composition with stabilized metal detergent additive and friction reducing ester component|
US4702850A|1980-10-06|1987-10-27|Exxon Research & Engineering Co.|Power transmitting fluids containing esters of hydrocarbyl succinic acid or anhydride with thio-bis-alkanols|
US4344853A|1980-10-06|1982-08-17|Exxon Research & Engineering Co.|Functional fluid containing metal salts of esters of hydrocarbyl succinic acid or anhydride with thio-bis-alkanols as antioxidants|
CA1159436A|1980-11-10|1983-12-27|Harold Shaub|Lubricant composition with improved friction reducing properties|
US4617134A|1980-11-10|1986-10-14|Exxon Research And Engineering Company|Method and lubricant composition for providing improved friction reduction|
US4325827A|1981-01-26|1982-04-20|Edwin Cooper, Inc.|Fuel and lubricating compositions containing N-hydroxymethyl succinimides|
US4388201A|1981-07-20|1983-06-14|Exxon Research & Engineering Co.|Co-dispersant stabilized friction modifier lubricating oil composition|
US4479883A|1982-01-06|1984-10-30|Exxon Research & Engineering Co.|Lubricant composition with improved friction reducing properties containing a mixture of dithiocarbamates|
US4459223A|1982-05-05|1984-07-10|Exxon Research And Engineering Co.|Lubricant oil composition with improved friction reducing properties|
US4637886A|1982-12-27|1987-01-20|Exxon Research & Engineering Co.|Macrocyclic polyamine and polycyclic polyamine multifunctional lubricating oil additives|
US4617026A|1983-03-28|1986-10-14|Exxon Research And Engineering Company|Method for improving the fuel economy of an internal combustion engine using fuel having hydroxyl-containing ester additive|
US5178782A|1985-03-12|1993-01-12|The Lubrizol Corporation|Metal salts of mixed aromatic/aliphatic phosphorodithioic acids|
US4760170A|1985-07-01|1988-07-26|Exxon Research & Engineering Co.|Solution process for preparing metal salt esters of hydrocarbyl substituted succinic acid or anhydride and alkanols|
US4707284A|1985-12-23|1987-11-17|Exxon Research And Engineering Company|Lube oil anti-wear agent|
GB8602627D0|1986-02-04|1986-03-12|Exxon Chemical Patents Inc|Marine lubricating composition|
US4776969A|1986-03-31|1988-10-11|Exxon Chemical Patents Inc.|Cyclic phosphate additives and their use in oleaginous compositions|
US4684473A|1986-03-31|1987-08-04|Exxon Research And Engineering Company|Lubricant oil composition with improved friction reducing properties|
JPH0535757B2|1986-06-09|1993-05-27|Idemitsu Kosan Co|
US4938880A|1987-05-26|1990-07-03|Exxon Chemical Patents Inc.|Process for preparing stable oleaginous compositions|
US4822505A|1987-07-31|1989-04-18|Exxon Research And Engineering Company|Load-carrying grease|
US5021173A|1988-02-26|1991-06-04|Exxon Chemical Patents, Inc.|Friction modified oleaginous concentrates of improved stability|
CA1329730C|1988-02-26|1994-05-24|Robert A. Oklejas|Power recovery pump turbine|
CA1336902C|1988-02-26|1995-09-05|Jacob Emert|Friction modified oleaginous concentrates of improvedstability|
US4952328A|1988-05-27|1990-08-28|The Lubrizol Corporation|Lubricating oil compositions|
US4981602A|1988-06-13|1991-01-01|The Lubrizol Corporation|Lubricating oil compositions and concentrates|
US5185090A|1988-06-24|1993-02-09|Exxon Chemical Patents Inc.|Low pressure derived mixed phosphorous- and sulfur-containing reaction products useful in power transmitting compositions and process for preparing same|
US4957649A|1988-08-01|1990-09-18|The Lubrizol Corporation|Lubricating oil compositions and concentrates|
US4938881A|1988-08-01|1990-07-03|The Lubrizol Corporation|Lubricating oil compositions and concentrates|
US5391307A|1989-07-07|1995-02-21|Tonen Corp.|Lubricating oil composition|
US5478463A|1989-09-07|1995-12-26|Exxon Chemical Patents Inc.|Method of reducing sludge and varnish precursors in lubricating oils|
US5118875A|1990-10-10|1992-06-02|Exxon Chemical Patents Inc.|Method of preparing alkyl phenol-formaldehyde condensates|
US5262508A|1990-10-10|1993-11-16|Exxon Chemical Patents Inc.|Process for preparing alkyl phenol-sulfur condensate lubricating oil additives|
AU634121B1|1991-08-23|1993-02-11|National Starch And Chemical Investment Holding Corporation|Toughened cyanoacrylate adhesive composition containing polyester polymers|
EP0558835B1|1992-01-30|2001-05-09|BP Amoco Corporation|Biodegradable lubricants and functional fluids|
US5427702A|1992-12-11|1995-06-27|Exxon Chemical Patents Inc.|Mixed ethylene alpha olefin copolymer multifunctional viscosity modifiers useful in lube oil compositions|
JPH07197068A|1993-12-30|1995-08-01|Tonen Corp|Lubricating oil composition|
US5763371A|1994-07-29|1998-06-09|Witco Corporation|Ethylene compressor lubricant containing phospate ester of a monoglyceride or diglyceride|
US5498355A|1994-09-20|1996-03-12|Ethyl Corporation|Lubricant compositions of enhanced performance capabilities|
US5732548A|1994-10-07|1998-03-31|Platinum Plus, Inc.|Method for reducing harmful emissions from two-stroke engines|
AU693624B2|1994-12-09|1998-07-02|Exxon Chemical Patents Inc.|Oil soluble complexes of phosphorus-containing acids useful as lubricating oil additives|
US6077455A|1995-07-17|2000-06-20|Exxon Chemical Patents Inc|Automatic transmission fluid of improved viscometric properties|
AU719520B2|1995-09-19|2000-05-11|Lubrizol Corporation, The|Additive compositions for lubricants and functional fluids|
US5674820A|1995-09-19|1997-10-07|The Lubrizol Corporation|Additive compositions for lubricants and functional fluids|
US6001141A|1996-11-12|1999-12-14|Ethyl Petroleum Additives, Ltd.|Fuel additive|
US5863873A|1997-04-08|1999-01-26|Exxon Chemical Patents Inc|Fuel economy additive and lubricant composition containing same|
US5885942A|1997-09-23|1999-03-23|Nch Corporation|Multifunctional lubricant additive|
US6750182B1|1998-10-09|2004-06-15|Exxonmobil Research And Engineering Company|Polar oil based industrial oils with enhanced sludge performance|
AU2168701A|1999-12-20|2001-07-03|Unichema Chemie Bv|Esters and their use in lubrificant compositions for extreme pressure applications|
US20020132343A1|2001-03-19|2002-09-19|Clark Lum|System and method for delivering umbilical cord-derived tissue-matched stem cells for transplantation|
US8337804B2|2003-04-28|2012-12-25|Centrum Fur Angewandte NanotechnologieGmbh|Synthesis of nanoparticles comprising metalvanadate|
US20040220059A1|2003-05-01|2004-11-04|Esche Carl K.|Low sulfur, low ash, low and phosphorus lubricant additive package using overbased calcium oleate|
US20040224858A1|2003-05-06|2004-11-11|Ethyl Corporation|Low sulfur, low ash, and low phosphorus lubricant additive package using overbased calcium phenate|
JP4614049B2|2004-03-31|2011-01-19|東燃ゼネラル石油株式会社|Engine oil composition|
US20050250656A1|2004-05-04|2005-11-10|Masahiro Ishikawa|Continuously variable transmission fluid|
EP1761617A1|2004-06-30|2007-03-14|The Lubrizol Corporation|Lubricant additive composition suitable for lubricating, preventing deposit formation, or clean-up of two-stroke engines|
US7875576B2|2004-07-29|2011-01-25|Chevron Oronite Company Llc|Lubricating oil composition for internal combustion engines|
US7250126B2|2004-08-11|2007-07-31|Fleetguard, Inc.|Acid-neutralizing filter media|
EP1757673B1|2005-08-23|2020-04-15|Chevron Oronite Company LLC|Lubricating oil composition for internal combustion engines|
US10100266B2|2006-01-12|2018-10-16|The Board Of Trustees Of The University Of Arkansas|Dielectric nanolubricant compositions|
WO2007082299A2|2006-01-12|2007-07-19|The Board Of Trustees Of The University Of Arkansas|Nanoparticle compositions and methods for making and using the same|
JP2008007700A|2006-06-30|2008-01-17|Kyodo Yushi Co Ltd|Metalworking oil composition, metalworking method and metal workpiece|
US10752997B2|2006-10-19|2020-08-25|P&S Global Holdings Llc|Methods and apparatus for making coatings using ultrasonic spray deposition|
MX2009004149A|2006-10-19|2009-08-07|Univ Arkansas|Methods and apparatus for making coatings using electrostatic spray.|
US7858566B2|2006-10-27|2010-12-28|Chevron Oronite Company Llc|Lubricating oil additive composition and method of making the same|
US7816309B2|2006-10-27|2010-10-19|Chevron Oronite Company Llc|Lubricating oil additive composition and method of making the same|
US8466096B2|2007-04-26|2013-06-18|Afton Chemical Corporation|1,3,2-dioxaphosphorinane, 2-sulfide derivatives for use as anti-wear additives in lubricant compositions|
WO2008157467A2|2007-06-19|2008-12-24|Afton Chemical Corporation|Pyrrolidine-2,5-dione derivatives for use in friction modification|
US20090005277A1|2007-06-29|2009-01-01|Watts Raymond F|Lubricating Oils Having Improved Friction Stability|
US8623797B2|2007-06-29|2014-01-07|Infineum International Limited|Boron-containing lubricating oils having improved friction stability|
US20090143263A1|2007-12-03|2009-06-04|Bloch Ricardo A|Lubricant composition comprising a bi-modal side-chain distribution lofi|
US9518244B2|2007-12-03|2016-12-13|Infineum International Limited|Lubricant composition comprising a bi-modal side-chain distribution LOFI|
DE102009012567B4|2008-03-11|2016-11-10|Afton Chemical Corp.|Transmission oils with very little sulfur only for coupling and their use|
US8703669B2|2008-03-11|2014-04-22|Afton Chemical Corporation|Ultra-low sulfur clutch-only transmission fluids|
DE102009001301A1|2008-03-11|2009-09-24|Volkswagen Ag|Method for lubricating a component only for the clutch of an automatic transmission, which requires lubrication|
JP2010179085A|2008-07-11|2010-08-19|Canon Inc|Biological information acquisition apparatus|
US20120015854A1|2008-08-08|2012-01-19|Ravishankar Periagaram S|Olefinic Copolymer Compositions for Viscosity Modification of Motor Oil|
US8378042B2|2009-04-28|2013-02-19|Exxonmobil Chemical Patents Inc.|Finishing process for amorphous polymers|
WO2013115912A1|2012-02-03|2013-08-08|Exxonmobil Chemical Patents Inc.|Process for the production of polymeric compositions useful as oil modifiers|
US9127151B2|2009-04-28|2015-09-08|Exxonmobil Chemical Patents Inc.|Polymer compositions having improved properties as viscosity index improvers and use thereof in lubricating oils|
US20110046029A1|2009-08-20|2011-02-24|Milner Jeffrey L|Combinations of Phosphorus-Containing Compounds For Use As Anti-Wear Additives In Lubricant Compositions|
US8618033B2|2010-01-22|2013-12-31|Exxonmobil Chemical Patents Inc.|Ethylene copolymers, methods for their production, and use|
CN102725319B|2010-01-27|2014-10-15|埃克森美孚化学专利公司|Copolymers, compositions thereof, and methods for making them|
KR101486833B1|2010-07-28|2015-01-29|엑손모빌 케미칼 패턴츠 인코포레이티드|Ethylene based copolymer compositions as viscosity modifiers and methods for making them|
EP2598570B1|2010-07-28|2017-11-15|ExxonMobil Chemical Patents Inc.|Viscosity modifiers comprising blends of ethylene-based copolymers|
SG186165A1|2010-07-28|2013-01-30|Exxonmobil Chem Patents Inc|Viscosity modifiers comprising blends of ethylene-based copolymers|
US20120028865A1|2010-07-28|2012-02-02|Sudhin Datta|Viscosity Modifiers Comprising Blends of Ethylene-Based Copolymers|
US8822393B2|2010-11-19|2014-09-02|Chevron U.S.A. Inc.|Lubricant for percussion equipment|
US9133413B2|2011-12-21|2015-09-15|Infineum International Limited|Viscosity index improvers for lubricating oil compositions|
US9139794B2|2012-02-03|2015-09-22|Exxonmobil Chemical Patents Inc.|Process for the production of polymeric compositions useful as oil modifiers|
US10316176B2|2012-02-03|2019-06-11|Exxonmobil Chemical Patents Inc.|Polymer compositions and methods of making them|
US9012578B2|2012-04-19|2015-04-21|Exxonmobil Chemical Patents Inc.|Blocky ethylene propylene copolymers and methods for making them|
US8486870B1|2012-07-02|2013-07-16|Ajay P. Malshe|Textured surfaces to enhance nano-lubrication|
US8476206B1|2012-07-02|2013-07-02|Ajay P. Malshe|Nanoparticle macro-compositions|
US10227544B2|2013-08-15|2019-03-12|Infineum International Limited|Automotive transmission fluid compositions for improved energy efficiency|
US20150051129A1|2013-08-15|2015-02-19|Infineum International Limited|Transmission Fluid Compositions for Improved Energy Efficiency|
SG10201405796PA|2013-09-23|2015-04-29|Chevron Japan Ltd|A Fuel Economy Engine Oil Composition|
US9340746B1|2015-04-13|2016-05-17|Afton Chemical Corporation|Low viscosity transmission fluids with enhanced gear fatigue and frictional performance|
GB201718527D0|2017-11-09|2017-12-27|Croda Int Plc|Lubricant formulation & friction modifier additive|
EP3762475A1|2018-03-08|2021-01-13|ExxonMobil Chemical Patents Inc.|Ethylene-propylene branched copolymers as viscosity modifiers with enhanced fuel economy|
US20210040250A1|2018-03-08|2021-02-11|Exxonmobil Chemical Patents Inc.|Ethylene-propylene linear copolymers as viscosity modifiers|
WO2019236418A1|2018-06-05|2019-12-12|Exxonmobil Chemical Patents Inc.|Alcohol-polyalphaolefins and methods thereof|
WO2021041406A1|2019-08-27|2021-03-04|Chevron Oronite Company Llc|Ethylene copolymers and use as viscosity modifiers|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
US05/826,544|US4105571A|1977-08-22|1977-08-22|Lubricant composition|
[返回顶部]