|Publication number||US3442808 A|
|Publication date||May 6, 1969|
|Filing date||Nov 1, 1966|
|Priority date||Nov 1, 1966|
|Publication number||US 3442808 A, US 3442808A, US-A-3442808, US3442808 A, US3442808A|
|Inventors||Randel Q Little, Thornton P Traise, Roger W Watson|
|Original Assignee||Standard Oil Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (213), Classifications (43)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent LUBRICATING OIL ADDITIVES Thornton P. Traise, Chicago Heights, Ill., and Randel Q. Little, Munster, and Roger W. Watson, Highland, Ind., assignors to Standard Oil Company, Chicago, 11]., a corporation of Indiana No Drawing. Filed Nov. 1, 1966, Ser. No. 591,084 Int. Cl. Cm 3/26, 3/22; C07d 27/08 US. Cl. 25249.6 12 Claims ABSTRACT OF THE DISCLOSURE Lubricating oil additives prepared by reacting alkenyl succinic anhydride with the Mannich condensation product prepared by condensing alkyl substituted phenol, formaldehyde and polyalkylene polyamine. The additives can optionally be further reacted with a boron compound such as boric acid, boric anhydride or a boric acid ester.
This invention concerns new chemical compositions and lubricating oil compositions containing the same. The subject matter of the instant invention also concerns a novel class of chemical compositions which act as dispersants when incorporated as additives into engine lubricating oils. The invention particularly concerns new Mannich condensation products.
The prior art portrays a need for improved engine lubricating oil additives which function as dispersants to retain in suspension insoluble particles such as the products of fuel combustion, those of incipient oxidation, and those of lubricant deterioration. The control of the deterioration of lubricating oils has long been a problem particularly in the formulation of the compositions of lubricating oil additives.
It has been known for many years that deterioration of hydrocarbon lubricating oils causes the formation of substances which deleteriously aifect the surfaces which the lubricants are developed to protect through the maintenance of reduced frictional forces between said surfaces. Lubricating oil deterioration not only causes the formation of surface-deleterious substances, but it also results in the agglomeration of sludge-like materials in the lubricants and the deposition of varnish on the surfaces.
For many years it has been a practice to include as additives in lubricating oils, chemical compositions which tend to reduce oil deterioration and the consequent formation of the sludge and varnish-like materials. Broadly included in the classification of additives are corrosion and oxidation inhibitors, and dispersing agents. These additives generally function to reduce the corrosion of the surfaces to be protected, to stabilize the lubricating oil, to inhibit deterioration by oxidation, and to function as dispersants which tend to prevent the agglomeration of sludge and the deposition of varnish and sludge caused by the formation of the products of deterioration.
Frequently, the inclusion into lubricating oils of corrosion, oxidation, and dispersant agents is highly desirable; however, the problems of compatibility of these three or more functional agents creates serious problems in the formulation of useful additive-containing lubricating oils. Much research and development effort has been expended in the search for improved lubricating oil additives which function in the above-enumerated manner. The research efforts have been directed toward the development of three or more separate agents, as well as a single agent, or a plurality of compatible agents that will perform all of the desired functions when incorporated into hydrocarbon lubricating oils.
Various Mannich condensation products are known in the prior art as lubricating oil additives; however, the
Patented May 6, 1969 teachings of the disclosures indicate that these Mannich products have previously been considered for use as oxidation inhibitors and as anti-wear additives. The former tend to reduce the rate of formation of oxidation products and the latter tend to coat surfaces with films and reduce friction resulting in less wear; consequently, there is some reduction of particulate and product contamination of the lubricating oil medium. It is also well known that various Mannich products produced for use as oxidation inhibitors and anti-wear additives demonstrate limited solubility in lubricating oil, which factor is also an undesirable characteristic of an additive. In view of the above, it has long been attempted to develop Mannich products and derivatives thereof which have novel functional properties as well as improved solubility in lubricating oils when incorporated therein.
Accordingly, it is an object of this invention to provide new compositions of matter.
It is an additional object of this invention to provide new compositions of matter which are useful as dispersants in lubricating oil compositions.
Another object of this invention is to provide lubricating oil dispersants which have improved solubility in said oil and which exhibit superior compatibility with other oil included additives.
An additional object of this invention is to provide a novel process for the preparation of compositions useful as dispersants.
Another object of this invention is to provide improved lubricating compositions.
Other objects and advantages of the invention disclosed and claimed herein will become apparent from the specification, including various embodiments, examples, and the claims.
It has been discovered that the solubility of Mannich condensation products is appreciably improved by reacting the Mannich products with a polyalkenyl succinic anhydride at a temperature sufficient to remove water of condensation. The modified Mannich reaction products impart excellent dispersant properties to the lubricating oil compositions while maintaining an unusually high degree of solubility within said lubricating oil compositions. The invention includes the reaction of an alkylphenol, formaldehyde, and a polyalkylene amine to form a Mannich product. The ratio of phenol, formaldehyde, and amine is from about l:1:0.5 to about 1:2.522. The conventional Mannich product so formed is known to have anti-wear and oxidation-inhibiting properties but limited oil solubility. This conventional Mannich product is then reacted with a polyalkenyl succinic anhydride to yield the highly effective low-temperature dispersants for lubricating oils. The Mannich polyalkenyl succinic an hydride reaction product can be treated with a small amount of a boron-containing compound to provide an other modified Mannich reaction product. Boration further improves compatibility with other additives. Each of these products exhibits surprising and superior dispersant properties when incorporated into lubricating oils. Each of these products also maintains a high degree of solubility with the lubricating oil additive-containing matrix.
By polyalkenyl succinic anhydride is meant the reaction product of maleic anhydride with a polymer of a monoolefin having three or four carbon atoms, such as propylene or butylene. The polymers should be a viscous liquid polyolefin having a viscosity measured in Saybolt Universal Seconds (SUS) at 210 F. of from about 50 sec. to about 10,000 sec. Such viscous liquid polypropylenes and polybutylenes (including polyisobutylenes) are well known to those skilled in the art and they can be conveniently prepared, for example, by polymerizing propylene-and-butylene containing hydrocarbon fractions in the presence of aluminum chloride or other Friedel- Crafts catalysts. These viscous liquid polypropylenes and polybutylenes contain a limited amount of residual unsaturation so that they can be reacted with maleic anhydride to form an alkenyl succinic anhydride. These polypropylenes and polybutylenes can be reacted with substituted maleic anhydrides with other anhydrides of similar unsaturated aliphatic dicarboxylic acids to form corresponding alkenyl derivatives.
Typically a polybutenyl succinic anhydride can be prepared by reacting about 0.85 mole of maleic anhydride per mole of polybutene, the polybutene having a molecular weight of about 860. Although not all of the maleic anhydride enters into the reaction at about 450 F., only about 5 weight percent is thermally decomposed and a small amount is stripped out. The yield of polybutenyl succinic anhydride is about 50-80% based on the polybutene used.
Suitable Mannich products for modification according to the process of this invention are prepared by condensing an alkylphenol, formaldehyde, and a polyalkylene amine. The alkylphenol may be a C -C alkyl substituted phenol, preferably a C alkyl substituted phenol (nonylphenol). the polyalkylene polyamine is derived from ethylenediamine or condensation products of ethylenediamine, such as diethylene triamine, triethylene tetramine, tetraethylenepentamine, or pentaethylene hexamine. Tetraethylenepentamine (TEPA) is the preferred polyalkylene polyamine.
Example I.Preparation of conventional Mannich product The preparation of a conventional Mannich product is a condensation of TEPA with nonylphenol and formaldehyde. Three thousands three hundred twenty nine lbs. of TEPA, 17.6 lb. moles, is added to a 2,000 gallon kettle blanketed with an inert gas such as nitrogen. One thousand nine hundred thirty six lbs. of nonylphenol is added over a 30-minute period with thorough mixing and the temperature is adjusted to within the range of about 100-110 F. One thousand four hundred twenty five lbs. of 37% aqueous formaldehyde containing 17.6 lb. moles of CH O, is charged to the above mixture over a period of about three hours. The temperature will rise to about 130-150 F. and the reacting material is held for about two hours with stirring. Subsequently, the reactants are heated to about 300 F. in the presence of an inert gas such as nitrogen and about 145 gallons of water is distilled therefrom. The reacting material is held at 300 F. for about one hour prior to cooling to ambient temperature.
The properties of the above reaction product are as follows:
Activity, percent 100 Nitrogen, percent 20-21 Gravity, lb./gal. 8.53 Vis. 210 F., SSU 333 Flash, F. 420 Molecular weight 622 Example II.-Modification of conventional Mannich product thousand three hundred sixty eight lbs. of the Mannich condensation product prepared in accordance with the foregoing description is added over a period of about two hours during which the temperature increases about 20 F. The material is heated to about 300 F. within about one hour, and the reactants are held at about 300 F. for three hours in the presence of an inert gas such as nitrogen. Subsequently, the material is filtered through a sparkler filter.
The properties of the above reaction product as as follows:
Activity, percent 40 Nitrogen, percent 2.1 Gravity, lbs/gal. 7.56 Vis. 210 F., SSU 600 Flash, F. 380
Example III.Alkylenyl succinimide modified Mannich About 648 grams (6 moles) of para cresol and 2270 grams (12 moles) tetrae-thylenepentamine were combined in a 5-liter flask equipped with a stirrer. About 972 grams of 37% formaldehyde (12 moles) were added over a period of four hours. The exothermic heat increased the reaction temperature to about 133 F. The product was then heated between about 311 F. and 327 F. with nitrogen blowing over a period of about ten hours. A total of about 570 ml. of water were distilled out. The product yield was 3000 grams.
About 382 grams (.75 moles) of the above Mannich product were dissolved in 300 grams of chloroform and combined with 2580 grams of polybutenyl succinic anhydride containing a polybutenyl substitient having a viscosity of about 1000 SUS at 210 F. (1.5 mols) and 750 grams of S-grade oil in a 5-liter flask and heated between about 210-302 F. for about ten hours. The volatile material was allowed to escape as vapor. The yield of this product was 3625 grams and it contained 3.41% nitrogen and 0.15% chlorine.
Example IV.-Alkylenyl succinimide modified Mannich 648 grams (6 moles) of mixed cresol were placed in a 5-liter flask equipped with a stirrer. Through a dropping funnel, 2270 grams (12 moles) of tetraethylenepentamine was added. A small exothermic heat was observed. 972 grams (12 moles) of 37% formaldehyde was added dropwise. The mixture was heated between about l22-302 F. for 16 hours with nitrogen blowing. 345 ml. of water were condensed in a trap. The yield of product was 3121 grams. The nitrogen content was 25%.
The polyalkyleneyl succinic anhydride modification of the above Mannich was prepared as follows. 382.5 grams of the above Mannich (.75 mole) was added to a mixture of 2580 grams of 54% active polybutenyl succinic anhydride containing a polybutenyle substituent having a viscosity of about 1000 SUS at 210 F. (1.5 moles) and 564 grams of S-gnade oil in a 5 -liter flask. The mixture was heated with nitrogen blowing for about ten hours between about 77 and 302 F. The yield of product was 3452 grams and contained 2.70% nitrogen.
Example V-Alkyleneyl succinimide modified Mannich Phenol was alkylated with polypropylene as follows. About 1600 grams (2 moles) of polypropylene, l-liter of hexane and 210 grams of a phenol-B1 complex (about 2 moles) were reacted in a 5-liter flask at ambient temperatures for approximately two hours. The product was washed with water and steam stripped to about 302 F., then dried by blowing with an inert gas. The yield was 1657 grams, the molecular weight 885, and the hydroxyl number was 51.
The Mannich product of the above phenol was prepared as follows. 1600 grams of the alkyl phenol (1.8 moles) and 681 grams of tetraethylenepentamine (3.6 moles) were combined in a 5-liter flask equipped with a stirrer. About 294 grams of 37% formaldehyde (3.6 moles) were added dropwise. The mixture was heated with stirring for about ten hours between about 122 and 144 F. About 170 mls. of water were collected in a trap. The yield was 2222 grams.
The succinimide of the above Mannich was prepared as follows. About 1000 grams of the Mannich (.772 mole) was dissolved in 100 mls. of toluene and added dropwise to 2660 grams of a polybutenyl succinic anhydride containing a polybutenyl substituent having a viscosity of about 1000 SUS at 210 F. (1.54 moles) heated to about 257 F. in a 5-liter stirred flask. The mixture was heated with nitrogen gas blowing for about ten hours at about 25 7-302 F. The yield was 3623 grams. The product contained 2.78% nitrogen.
By way of mere illustration and not limitation, the compostiion of the modified Mannich reaction products disclosed herein may be shown structurally in accordance varnish and sludge ratings are made from the individual ratings of the following engine parts. Varnish:
Piston Rocker arm cover Push rod cover Cylinder walls Oil pan Sludge:
Push rod chamber Rocker arm assembly Rocker arm cover Oil screen Oil pan Push rod cover Timing gear cover Valve deck The varnish and sludge rating for each and every one of the foregoing parts is made. Then an average rating is with the following: made for each type of part, for example, the varnish OH R 0 o R N- oznmmnozmrmom CHzNHCzHKNHCaHOr-N t- B. R
wherein R is a polyolefin constituent derived from a mono-olefin having three to four carbon atoms, preferably a polybutylene having a viscosity at 210 F. of from about 50 to 10,000 SUS: n equals 0-10, preferably about 3; and R and R are hydrogen or a 0 -0 alkyl-substituent, preferably, R being hydrogen and R being C The aforementioned boron modification of the modified Mannich product may be carried out with boric acid, a boric acid ester, a boric anhydride, etc., at a temperature of from about 120-400" F., using from 0.2 to 2.0 or more moles of boron per mole of modified Mannich reaction product. Although up to as high as 1.5 atoms of boron per gram atom of nitrogen can be reacted, it is desirable to have a boron to nitrogen (B/ N) ratio within the range of about 0.05 to 1.0, preferably the (B/N) weight ratio is in the range of 0.10 to 0.5, inclusive.
Lubricating oils containing Mannich condensation products in accordance with this invention were tested in the Lincoln M.S. V Test Sequence designed by Ford Motor Company. The Lincoln Sequence test procedure evaluates low temperature dispersancy characteristics of a lubricating oil. Briefly, the test consists of using the oil to be tested as a lubricating oil in a V-8 Lincoln engine under prescribed test conditions. Accordingly, 5 quartes of oil are placed in the crankcase and the engine is started and run in accordance with the 4-hour cycle:
The 4-hour cycle is repeated a total of 48 times (192 hours running time). After each 16 hours of operation the engine is shut down for 8 hours. The oil level is adjusted with fresh oil to a level of 5 quarts. At the termination of the test, the hot oil is drained. The engine is then disassembled and examined for deposits of varnish and sludge among other observable results.
In the Lincoln M.S. Test Sequence V, after the formulated lubricant oil has been tested and the engine disassembled for inspection of the parts thereof for sludge and varnish deposits among other inspections, the total ratings for each of the eight pistons are added and divided by 8 for the average piston varnish. The sum of the average ratings for each class of parts is found for both sludge and varnish. The rating of total varnish is the sum of the average ratings of the five classes of parts. A varnish rating of 7.0 or higher for each class of parts is considered to be passing.
The rating of total sludge is the sum of the average ratings for the eight classes of parts multiplied by /s since the perfect total sludge rating is 50. The perfect total varnish rating is also 50.
Lincoln Engine Tests 1, 2, and 3 In the first and second formulations subjected to the Lincoln Sequence Test the blend of additives included 3.75% of the Mannich condensation product made in accordance with the teachings of EXAMPLE II and was combined with 1.0% of an overbased magnesium sulfonate that is readily available commercially and 1% of a zinc dialkyldithio-phosphate oxidation inhibitor also commercially available. The third formulation included 2.5% by weight of the novel dispersants of this invention and the other additives of formulations 1 and 2 were present in the same amounts. All three tests were effective in demonstrating the high performance of the novel dispersant additive as shown below in Table I.
TABLE I.L1NCOLN MS V RESULTS Oil ring 011 screen Sludge Varnish filling, plugging,
Oil formation rating rating percent percen Engine tests 4, 5, 6, and 7 phenate and 1% by weight zinc dialkyldithio-phosphate. Formulation No. 5 included 1% overbased magnesium sulfonate and 1% zinc dialkyldithio-phosphate.
In formulations Nos. 6 and 7 ingredients were added to a SAE 30 lubricating oil. In formulation 6 the additives included 5% of the novel dispersant, 1% of an oberbased calcium sulfonate and 1% of a zinc dialkyldithiophosphate. The combination of additives in formulation 7 included 6.0% of the novel dispersant of this invention, 4% basic calcium phenate, 2% of an overbased calcium sulfonate and 1% of a zinc dialkyldithio-phosphate. All the constituents except the novel dispersant of this invention are readily available on the open market. The test results of these formulations were effective in demonstrating the superiority of the novel dispersants as shown in Table II below.
TABLE II.FORD 289 ENGINE TEST RESULTS Oil ring Oil screen Sludge Varnish filling, plugging Oil formation rating rating percent percent Percent Ashless dispersant 5 Polymethacrylate viscosity index improver 5 300 TBN calcium sulfonate l Alkenyl succinic acid 0.2 Zinc dithiophosphate 0.7
The instant novel dispersant disclosed and claimed herein is compared below with another ashless dispersant commercially available. The ratings for varnish and sludge are given on a scale where 10 is perfectly clean.
Dispersant Instant Other Test miles (thousands)- 11 12 6 Rocker arm cover rating:
Varnish 9. 7 9. 7 9. 4 Sludge- 9. 8 9. 7 9. 2
The dispersants prepared as disclosed herein can be used as addition agents in lubricating oils and especially in lubricating oils for use in internal combusion engines. The addition agents impart excellent low temperature dispersancy characteristics to the lubricating oil. Although amounts of the dispersancy addition agent may be varied as desired, it is believed advantageous to use at least about 0.2 weight percent and up to 20 weight percent of the addition agent of this invention and preferably 0.5 to 10 weight percent in a suitable lubricating oil. Although the preferred lubricating oils are the mineral lubricating oils, the use of the additive compositions is not restricted thereto. Other lubricating oil bases can be used, such as hydrocarbon oils, both natural and synthetic, for example, those obtained by the polymerization of olefins, as well as synthetic lubricating oils of the alkylene oxide type and the monoand polycarboxylic acid ester type, such as the esters of adipic acid, sebacic acid, azelaic acid; it is also contemplated that various other well-known additives, such as anti-oxidants, anti-foam agents, pour point depressors, extreme pressure agents, corrosion inhibitors, anti-wear agents, etc., may be incorporated in lubricating oils containing the additives of our invention.
Concentrates of a suitable oil base containing more than 10 percent, for example, up to 75 percent or more, of the additive of this invention alone or in combination with other additives may be prepared and can be used for blending with hydrocarbon oils or other oils in the proportions desired for the particular conditions of use to give a finished lubricating product containing the additives of this invention. In order to exemplify the use of the reaction products prepared in accordance herewith as low dispersancy lubricating oil addition agents, examples of formulated lubricating oils containing such reaction products were prepared.
While in the foregoing specification this invention had been described in relation to preferred embodiment thereof, and many details have been set forth for the purpose of illustration, it will be apparent to those skilled in the art that the invention is susceptible to other embodiments and that many of the details set forth herein can be varied considerably without departing from the basic principles of the invention.
What is claimed is:
1. A composition comprising the reaction product of heating to a temperature sufficient to remove water of condensation, a Mannich compound obtained by condensing an alkyl substituted phenol, formaldehyde and a polyalkylene polyamine with 1-2 moles of alkenyl succinic anhydride, said alkenyl substituent being derived from a polyolefin having a viscosity at 210 F. of from about $0 to about 10,000 Saybolt Universal Seconds.
2. The composition of claim 1 reacted at a temperature of from about -400 F. with a small amount of boron containing compound selected from the group consisting of boric acid, boric acid esters and boric anhydride, in a mole ratio of from 0.2 to at least 2.0 moles of boron per mole of said composition of claim 1.
3. The composition of claim 1 wherein the phenol is a mono-substituted phenol.
4- The composition of claim 1 wherein the phenol is a di-alkyl substituted phenol.
5. A lubricant composition comprising a major proportion of a lubricating oil and from about 0.2-20% by wt. of the composition of claim 1.
6. The composition of claim 1 wherein the alkenyl substituent is a polybutene having a molecular weight within the range of about BOO-10,000.
7. A composition comprising the reaction product of heating to a temperature of from about 77 F. to about 302 F. a Mannich compound obtained by condensing a nonylphenol, formaldehyde and tetraethylenepentamine with l-2 moles of alkenyl succinic anhydride, said alkenyl substituent being derived from a polyolefin having a viscosity at 210 F. of from about 50 to about 10,000 Saybolt Universal Seconds.
8. The composition of claim 7 reacted at a temperature of from about 120-400 F. with a small amount of boron containing compound selected from the group consisting of boric acid, boric acid esters and boric anhydride, in a mole ratio of from 0.2 to at least 2.0 moles of boron per mole of said composition of claim 7.
9. A lubricant composition comprising a major proportion of a lubricating oil and from about 0.2-20% by wt. of the composition of claim 8.
10. A composition comprising the reaction product of heating to a temperature of from about 77 F. to about 302 F., a Mannich compound obtained by condensing a cresol, formaldehyde, and tetraethylenepentamine with l-2 moles of alkenyl succinic anhydride, said alkenyl substituent being derived from a polyolefin having a vis cosity at 210 F. of from about 50 to about 10,000 Saybolt Universal Seconds.
11. A lubricant composition comprising a major proportion of a lubriacting oil and from about 0.2-20% by wt. of the composition of claim 10.
12. A process for producing a lubricant additive composition comprising the steps of reacting about 2 moles of alkenyl succinic anhydride, said alkenyl substituent being derived from a polyolefin having a viscosity of 210 References Cited UNITED STATES PATENTS Le Suer 25249.6 Norman et a1. 2525 1.5 Le Suer 25249.6 Le Suer et a1 25251.5 Le Suer 25251.5
10 OTHER REFERENCES Noller: Chemistry of Organic Compounds, (1951), published by W. B. Sanders Co., Philadelphia, Pa., pp. 494 and 495 most pertinent copy available in Sci. Lib. QD
PATRICK P. GARVIN, Primary Examiner.
US. Cl. X.R.
mg UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent: No. 3, m2,808 Dated May 6, 1969 Invent0r(S) gngggtgg P. l'gise, Bggdel Q. Little and R oger W. Watson It is certified that error aupears in the above-identified paten't and that said Letters Patent are hereby corrected as shown below:
column 3, line 2 the word "the" should be capitalized; line 35, the word "thousands" should be --thouse.nd--. Column h, line 10, the word "as" (first occurrence) should be --are--. Column 5, line 5 the word "quartes" should be --quarts--; in the table, under "Phase 2", the first number should be --2-- instead of 2"; under "Phase 3" the first number should be --75-- instead of "7"; under "Phase 3", opposite "Water Jacket" the numbers "ITO-1T0" should be --lT0-lTS--; opposite "O11 sump" the numbers "205-215" should be --205-2l0--. Column 6, Table I, first column should be headed --011 Formulation" instead of "011 formation"; in the heading of the last column, "percen" should be --percent--. Column 7, Table II, first column, the heading 'Oil formation" should be --Oil Formulation"; line 25, the word "mottor" should be --motor--. Column 8, line 12, the word "embodiment" should be --embodiments--; line 70, the word "lubriacting" should be "lubricating"; line 75, the word "of" should be --a.t--.
SIGNED AND SEALED MAR 1 71970 Atteat:
Edw mums s sohunns .m
o o Attesting Off Commissioner of Pat-eats
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3087936 *||Aug 18, 1961||Apr 30, 1963||Lubrizol Corp||Reaction product of an aliphatic olefinpolymer-succinic acid producing compound with an amine and reacting the resulting product with a boron compound|
|US3219666 *||Jul 21, 1961||Nov 23, 1965||Derivatives of succinic acids and nitrogen compounds|
|US3254025 *||Apr 6, 1962||May 31, 1966||Lubrizol Corp||Boron-containing acylated amine and lubricating compositions containing the same|
|US3272746 *||Nov 22, 1965||Sep 13, 1966||Lubrizol Corp||Lubricating composition containing an acylated nitrogen compound|
|US3338832 *||Mar 28, 1966||Aug 29, 1967||Lubrizol Corp||Lubricating oil containing reaction product of certain acylated nitrogen containing intermediates and a boron compound|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4011167 *||Jul 9, 1975||Mar 8, 1977||Mobil Oil Corporation||Lubricant compositions containing metal complexes as detergents|
|US4105571 *||Aug 22, 1977||Aug 8, 1978||Exxon Research & Engineering Co.||Lubricant composition|
|US4219431 *||Jul 28, 1976||Aug 26, 1980||Mobil Oil Corporation||Aroyl derivatives of alkenylsuccinic anhydride as lubricant and fuel additives|
|US4248725 *||Mar 19, 1979||Feb 3, 1981||Chevron Research Company||Dispersants having antioxidant activity and lubricating compositions containing them|
|US4317739 *||Oct 10, 1980||Mar 2, 1982||Standard Oil Company (Indiana)||Aminated sulfurized olefin funtionalized with a boron compound and formaldehyde|
|US4354950 *||Dec 29, 1980||Oct 19, 1982||Texaco Inc.||Mannich base derivative of hydroxyaryl succinimide and hydrocarbon oil composition containing same|
|US4379064 *||Mar 20, 1981||Apr 5, 1983||Standard Oil Company (Indiana)||Oxidative passivation of polyamine-dispersants|
|US4749505 *||Jul 8, 1985||Jun 7, 1988||Exxon Chemical Patents Inc.||Olefin polymer viscosity index improver additive useful in oil compositions|
|US4820432 *||Jul 24, 1987||Apr 11, 1989||Exxon Chemical Patents Inc.||Lactone-modified, Mannich base dispersant additives useful in oleaginous compositions|
|US4826615 *||Aug 10, 1988||May 2, 1989||Exxon Chemical Patents Inc.||Lubricating oil composition containing dual additive combination for low temperature viscosity improvement (PTF-004)|
|US4828742 *||Jul 24, 1987||May 9, 1989||Exxon Chemical Patents, Inc.||Lactone-modified, mannich base dispersant additives useful in oleaginous compositions|
|US4891145 *||Jan 29, 1986||Jan 2, 1990||Exxon Chemical Patents Inc.||Lubricating oil composition|
|US4913830 *||Jan 9, 1989||Apr 3, 1990||Exxon Chemical Patents Inc.||Lactone-modified, mannich base dispersant additives useful in oleaginous compositions|
|US4940552 *||Apr 30, 1982||Jul 10, 1990||Amoco Corporation||Passivation of polyamine dispersants toward fluorohydrocarbon compositions|
|US4954572 *||Nov 7, 1988||Sep 4, 1990||Exxon Chemical Patents Inc.||Dispersant additives prepared from monoepoxy alcohols|
|US4957645 *||Feb 29, 1988||Sep 18, 1990||Exxon Chemical Patents Inc.||Oil soluble dispersant additives useful in oleaginous compositions|
|US4957650 *||Feb 3, 1989||Sep 18, 1990||Exxon Chemical Patents Inc.||Lubricating oil composition containing dual additive combination for low temperature viscosity improvement|
|US4971711 *||Jan 9, 1989||Nov 20, 1990||Exxon Chemical Patents, Inc.||Lactone-modified, mannich base dispersant additives useful in oleaginous compositions|
|US5017299 *||Aug 1, 1988||May 21, 1991||Exxon Chemical Patents, Inc.||Novel ethylene alpha-olefin copolymer substituted Mannich base lubricant dispersant additives|
|US5026495 *||Dec 29, 1988||Jun 25, 1991||Exxon Chemical Patents Inc.||Oil soluble dispersant additives useful in oleaginous compositions|
|US5030369 *||Dec 29, 1988||Jul 9, 1991||Exxon Chemical Patents Inc.||Oil soluble dispersant additives useful in oleaginous compositions|
|US5043084 *||May 30, 1989||Aug 27, 1991||Exxon Chemical Patents, Inc.||Novel polymer substituted amino phenol mannich base amido-amine dispersant additives (PT-742)|
|US5047160 *||Dec 29, 1988||Sep 10, 1991||Exxon Chemical Patents Inc.||Polyanhydride modified adducts or reactants and oleaginous compositions containing same|
|US5053150 *||Dec 4, 1990||Oct 1, 1991||Exxon Chemical Patents Inc.||Polyepoxide modified adducts or reactants and oleaginous compositions containing same|
|US5057617 *||Nov 7, 1988||Oct 15, 1991||Exxon Chemical Patents Inc.||Dispersant additives prepared from monoepoxy thiols|
|US5085788 *||Jul 27, 1990||Feb 4, 1992||Exxon Chemical Patents Inc.||Oil soluble dispersant additives useful in oleaginous compositions|
|US5102570 *||Dec 31, 1990||Apr 7, 1992||Texaco Inc.||Acylated mannich base mono and/or bis-succinimide lubricating oil additives|
|US5124055 *||Mar 16, 1990||Jun 23, 1992||Ethyl Petroleum Additives, Inc.||Lubricating oil composition|
|US5124056 *||May 30, 1989||Jun 23, 1992||Exxon Chemical Patents Inc.||Polymer substituted amido-amine Mannich Base lubricant dispersant additives|
|US5128056 *||Mar 20, 1991||Jul 7, 1992||Exxon Chemical Patents Inc.||Ethylene alpha-olefin copolymer substituted amino phenol mannich base lubricant dispersant additives|
|US5156757 *||Dec 31, 1990||Oct 20, 1992||Texaco Inc.||Acylated mannich thioalkylphenol mono and/or bis-succinimide lubricating oil additives|
|US5186851 *||Apr 7, 1992||Feb 16, 1993||Exxon Chemical Patents Inc.||Ethylene alpha-olefin copolymer substituted mannich base lubricant dispersant additives|
|US5200103 *||Feb 1, 1990||Apr 6, 1993||Exxon Chemical Patents Inc.||Ethylene alpha-olefin copolymer substituted Mannich base lubricant dispsersant additives|
|US5205947 *||Jun 27, 1991||Apr 27, 1993||Exxon Chemical Patents Inc.||Dispersant additives comprising amine adducts of dicarboxylic acid monoepoxy thiol reaction products|
|US5217634 *||Sep 9, 1991||Jun 8, 1993||Exxon Chemical Patents Inc.||Polyepoxide modified adducts or reactants and oleaginous compositions containing same|
|US5219480 *||Aug 1, 1988||Jun 15, 1993||Exxon Chemical Patents Inc.||Ethylene alpha-olefin mannich base viscosity index improver/dispersant additives derived from amino phenols and monosecondary amines|
|US5230817 *||Mar 28, 1991||Jul 27, 1993||Exxon Chemical Patents Inc.||Polyanhydride modified adducts or reactants and oleaginous compositions containing same|
|US5256325 *||Feb 2, 1993||Oct 26, 1993||Exxon Chemical Patents Inc.||Polyanhydride modified adducts or reactants and oleaginous compositions containing same|
|US5259968 *||Oct 14, 1992||Nov 9, 1993||Exxon Chemical Patents Inc.||Dispersant additive comprising the reaction product of a polyanhydride and a mannich condensation product|
|US5268115 *||Oct 26, 1992||Dec 7, 1993||Exxon Chemical Patents Inc.||Alkyl-substituted hydroxyaromatic compounds useful as a multifunctional viscosity index improver|
|US5275748 *||Feb 2, 1993||Jan 4, 1994||Exxon Chemical Patents Inc.||Polyanhydride modified adducts or reactants and oleaginous compositions containing same|
|US5292444 *||Oct 2, 1992||Mar 8, 1994||Exxon Research And Engineering Company||Lube oil compositions containing fullerene-grafted polymers|
|US5292813 *||Oct 2, 1992||Mar 8, 1994||Exxon Research & Engineering Co.||Fullerene-grafted polymers and processes of making|
|US5306313 *||Jul 29, 1993||Apr 26, 1994||Exxon Chemical Patents Inc.||Dispersant additive comprising the reaction product of a polyanhydride and a mannich condensation product|
|US5328620 *||Dec 21, 1992||Jul 12, 1994||The Lubrizol Corporation||Oil additive package useful in diesel engine and transmission lubricants|
|US5334329 *||Oct 7, 1988||Aug 2, 1994||The Lubrizol Corporation||Lubricant and functional fluid compositions exhibiting improved demulsibility|
|US5340487 *||Aug 19, 1993||Aug 23, 1994||Exxon Chemical Patents Inc.||Dispersant adducts comprising alcohol adducts of dicarboxylic acid monoepoxy thiol reaction products|
|US5345002 *||Oct 9, 1992||Sep 6, 1994||Exxon Chemical Patents Inc.||Ethylene alpha-olefin copolymer substituted hydroxy aromatic compounds|
|US5382698 *||May 2, 1994||Jan 17, 1995||Exxon Chemical Patents Inc.||Borated ethylene alpha-olefin copolymer substituted Mannich base lubricant dispersant additives|
|US5385687 *||Aug 4, 1993||Jan 31, 1995||Exxon Chemical Patents Inc.||Polyanhydride modified adducts or reactants and oleaginous compositions containing same|
|US5407591 *||Aug 19, 1991||Apr 18, 1995||Exxon Chemical Patents Inc.||Oil soluble dispersant additives comprising the reaction product of a mannich base and a polyepoxide|
|US5430105 *||Nov 22, 1993||Jul 4, 1995||Exxon Chemical Patents Inc.||Low sediment process for forming borated dispersant|
|US5433874 *||Sep 28, 1994||Jul 18, 1995||Exxon Chemical Patents Inc.||Ethylene α-olefin copolymer substituted mannich base lubricant dispersant additives|
|US5482519 *||Nov 4, 1994||Jan 9, 1996||Exxon Chemical Patents Inc.||Polyepoxide modified adducts or reactants and oleaginous compositions containing same|
|US5558802 *||Sep 14, 1995||Sep 24, 1996||Exxon Chemical Patents Inc||Multigrade crankcase lubricants with low temperature pumpability and low volatility|
|US5565128 *||Oct 12, 1994||Oct 15, 1996||Exxon Chemical Patents Inc||Lubricating oil mannich base dispersants derived from heavy polyamine|
|US5580484 *||Dec 30, 1994||Dec 3, 1996||Exxon Chemical Patents Inc.||Lubricating oil dispersants derived from hydroxy aromatic succinimide Mannich base condensates of heavy polyamine|
|US5629434 *||Sep 25, 1995||May 13, 1997||Exxon Chemical Patents Inc||Functionalization of polymers based on Koch chemistry and derivatives thereof|
|US5643859 *||Jun 17, 1994||Jul 1, 1997||Exxon Chemical Patents Inc.||Derivatives of polyamines with one primary amine and secondary of tertiary amines|
|US5646332 *||Jun 17, 1994||Jul 8, 1997||Exxon Chemical Patents Inc.||Batch Koch carbonylation process|
|US5650536 *||Jun 17, 1994||Jul 22, 1997||Exxon Chemical Patents Inc.||Continuous process for production of functionalized olefins|
|US5652201 *||Jul 11, 1995||Jul 29, 1997||Ethyl Petroleum Additives Inc.||Lubricating oil compositions and concentrates and the use thereof|
|US5652202 *||Aug 15, 1995||Jul 29, 1997||Exxon Chemical Patents Inc.||Lubricating oil compositions|
|US5696064 *||Aug 23, 1995||Dec 9, 1997||Exxon Chemical Patents Inc.||Functionalization of polymers based on Koch chemistry and derivatives thereof|
|US5698722 *||Jun 6, 1995||Dec 16, 1997||Exxon Chemical Patents Inc.||Functionalization of polymers based on Koch chemistry and derivatives thereof|
|US5703256 *||Dec 16, 1996||Dec 30, 1997||Exxon Chemical Patents Inc.||Functionalization of polymers based on Koch chemistry and derivatives thereof|
|US5717039 *||Jun 6, 1995||Feb 10, 1998||Exxon Chemical Patents Inc.||Functionalization of polymers based on Koch chemistry and derivatives thereof|
|US5767046 *||May 15, 1997||Jun 16, 1998||Exxon Chemical Company||Functionalized additives useful in two-cycle engines|
|US5814111 *||Aug 6, 1996||Sep 29, 1998||Shell Oil Company||Gasoline compositions|
|US6034184 *||Jun 23, 1998||Mar 7, 2000||Mobil Oil Corporation||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers: Mannich reaction products|
|US6054539 *||Jul 31, 1998||Apr 25, 2000||Mobil Oil Corporation||Selectively hydrogenated polymer compositions: polybutadiene-isoprene-polybutadiene|
|US6103676 *||Jun 23, 1998||Aug 15, 2000||Mobil Oil Corporation||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers: hydroformylation/reductive amination reaction products|
|US6162768 *||Jun 23, 1998||Dec 19, 2000||Mobil Oil Corporation||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers: free radically initiated direct grafting reaction products|
|US6215033||Dec 11, 1998||Apr 10, 2001||Mobil Oil Corporation||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers: blends with lower molecular weight components|
|US6228817||Jun 23, 1998||May 8, 2001||Mobil Oil Corporation||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers|
|US6248702||Nov 30, 1998||Jun 19, 2001||Mobil Oil Corporation||Dispersant and dispersant viscosity index improvers from selectively hydrogenated aryl-substituted olefin containing diene copolymers|
|US6319881||Jul 12, 1999||Nov 20, 2001||Exxonmobil Oil Corporation||Haze free oil additive compositions containing dispersants from selectively hydrogenated diene copolymers|
|US6423670||Mar 14, 2001||Jul 23, 2002||Infineum International Ltd.||Lubricating oil compositions|
|US6525004||May 1, 2001||Feb 25, 2003||Infineum International Inc.||Combustion improving additive for small engine lubricating oils|
|US6627584||Jan 28, 2002||Sep 30, 2003||Ethyl Corporation||Automatic transmission fluid additive comprising reaction product of hydrocarbyl acrylates and dihydrocarbyldithiophosphoric acids|
|US6743266||Aug 13, 2002||Jun 1, 2004||Texaco, Inc.||Fuel additive composition for improving delivery of friction modifier|
|US6835217||Sep 20, 2000||Dec 28, 2004||Texaco, Inc.||Fuel composition containing friction modifier|
|US6855674||Dec 2, 2002||Feb 15, 2005||Infineum International Ltd.||Hydroxy aromatic Mannich base condensation products and the use thereof as soot dispersants in lubricating oil compositions|
|US7049273 *||Jul 17, 2002||May 23, 2006||Afton Chemical Intangibles Llc||Hybridized olefin copolymer additives|
|US7214649||Dec 31, 2003||May 8, 2007||Afton Chemical Corporation||Hydrocarbyl dispersants including pendant polar functional groups|
|US7563314||Nov 30, 2005||Jul 21, 2009||Xerox Corporation||Ink carriers containing nanoparticles, phase change inks including same and methods for making same|
|US7645728||Jan 12, 2010||Afton Chemical Corporation||Lubricant and fuel additives derived from treated amines|
|US7655084||Dec 12, 2005||Feb 2, 2010||Xerox Corporation||Carbon black inks and method for making same|
|US7743738||Mar 1, 2007||Jun 29, 2010||Afton Chemical Corporation||Scavenging phosphorus, sulfur, and lead from combustion exhaust using tungsten compounds and lubricant|
|US7786209||Sep 21, 2007||Aug 31, 2010||Xerox Corporation||Nanostructured particles, phase change inks including same and methods for making same|
|US7794512||Mar 16, 2007||Sep 14, 2010||Afton Chemical Corporation||Supplying tungsten to a combustion system or combustion system exhaust stream containing iron|
|US7833953||Aug 28, 2006||Nov 16, 2010||Afton Chemical Corporation||Lubricant composition|
|US7879775||Jul 14, 2006||Feb 1, 2011||Afton Chemical Corporation||Lubricant compositions|
|US7888299||Jan 13, 2004||Feb 15, 2011||Afton Chemical Japan Corp.||Extended drain, thermally stable, gear oil formulations|
|US7902133||Jul 14, 2006||Mar 8, 2011||Afton Chemical Corporation||Lubricant composition|
|US7947636||Feb 27, 2004||May 24, 2011||Afton Chemical Corporation||Power transmission fluids|
|US8029861||Sep 23, 2008||Oct 4, 2011||Xerox Corporation||Ink carriers containing low viscosity functionalized waxes, phase change inks including same, and methods for making same|
|US8080699||Aug 28, 2009||Dec 20, 2011||Chemtura Corporation||Two-stage process and system for forming high viscosity polyalphaolefins|
|US8123344||Aug 4, 2008||Feb 28, 2012||Xerox Corporation||Ink carriers containing surface modified nanoparticles, phase change inks including same, and methods for making same|
|US8177897||Nov 17, 2008||May 15, 2012||Xerox Corporation||Phase change inks containing graphene-based carbon allotrope colorants|
|US8415284||Nov 5, 2009||Apr 9, 2013||Afton Chemical Corporation||Olefin copolymer VI improvers and lubricant compositions and uses thereof|
|US8420583||Jan 24, 2008||Apr 16, 2013||Afton Chemical Corporation||Olefin copolymer dispersant VI improver and lubricant compositions and uses thereof|
|US8546311||Mar 10, 2009||Oct 1, 2013||Volkswagen Aktiengesellsschaft||Method for lubricating a clutch-only automatic transmission component requiring lubrication|
|US8557752||Mar 22, 2006||Oct 15, 2013||Afton Chemical Corporation||Lubricating compositions|
|US8563489||Sep 17, 2008||Oct 22, 2013||Chemtura Corporation||Alkylated 1,3-benzenediamine compounds and methods for producing same|
|US8703669||Feb 17, 2009||Apr 22, 2014||Afton Chemical Corporation||Ultra-low sulfur clutch-only transmission fluids|
|US8933001||Mar 31, 2010||Jan 13, 2015||Chevron Oronite Company Llc||Method for improving fluorocarbon elastomer seal compatibility|
|US9133581||Mar 14, 2013||Sep 15, 2015||Calera Corporation||Non-cementitious compositions comprising vaterite and methods thereof|
|US20030173251 *||Dec 2, 2002||Sep 18, 2003||Antonio Gutierrez||Hydroxy aromatic mannich base condensation products and the use thereof as soot dispersants in lubricating oil compositions|
|US20040014612 *||Jul 17, 2002||Jan 22, 2004||Esche Carl K.||Hybridized olefin copolymer additives|
|US20040147410 *||Jan 13, 2004||Jul 29, 2004||Milner Jeffrey L||Extended drain, thermally stable, gear oil formulations|
|US20050065043 *||Sep 23, 2003||Mar 24, 2005||Henly Timothy J.||Power transmission fluids having extended durability|
|US20050070446 *||Sep 25, 2003||Mar 31, 2005||Ethyl Petroleum Additives, Inc.||Boron free automotive gear oil|
|US20050101494 *||Nov 10, 2003||May 12, 2005||Iyer Ramnath N.||Lubricant compositions for power transmitting fluids|
|US20050101496 *||Nov 6, 2003||May 12, 2005||Loper John T.||Hydrocarbyl dispersants and compositions containing the dispersants|
|US20050143265 *||Dec 31, 2003||Jun 30, 2005||Loper John T.||Hydrocarbyl dispersants including pendant polar functional groups|
|US20050181959 *||Feb 17, 2004||Aug 18, 2005||Esche Carl K.Jr.||Lubricant and fuel additives derived from treated amines|
|US20050192185 *||Feb 27, 2004||Sep 1, 2005||Saathoff Lee D.||Power transmission fluids|
|US20050202979 *||Mar 9, 2005||Sep 15, 2005||Ethyl Petroleum Additives, Inc.||Power transmission fluids with enhanced extreme pressure characteristics|
|US20060003905 *||Jul 2, 2004||Jan 5, 2006||Devlin Cathy C||Additives and lubricant formulations for improved corrosion protection|
|US20060025314 *||Oct 11, 2004||Feb 2, 2006||Afton Chemical Corporation||Power transmission fluids with enhanced extreme pressure and antiwear characteristics|
|US20060217273 *||Mar 22, 2006||Sep 28, 2006||Nubar Ozbalik||Lubricating compositions|
|US20060223716 *||Apr 4, 2005||Oct 5, 2006||Milner Jeffrey L||Tractor fluids|
|US20060264339 *||May 19, 2005||Nov 23, 2006||Devlin Mark T||Power transmission fluids with enhanced lifetime characteristics|
|US20060287202 *||Jun 15, 2005||Dec 21, 2006||Malcolm Waddoups||Low ash or ashless two-cycle lubricating oil with reduced smoke generation|
|US20070054813 *||Oct 25, 2006||Mar 8, 2007||Chip Hewette||Boron free automotive gear oil|
|US20070111906 *||Nov 12, 2005||May 17, 2007||Milner Jeffrey L||Relatively low viscosity transmission fluids|
|US20070131138 *||Dec 12, 2005||Jun 14, 2007||Xerox Corporation||Carbon black inks and method for making same|
|US20080009426 *||Aug 15, 2007||Jan 10, 2008||Iyer Ramnath N||Lubricant Compositions and Methods Comprising Dispersant and Detergent|
|US20080015124 *||Jul 14, 2006||Jan 17, 2008||Devlin Mark T||Lubricant composition|
|US20080015125 *||Jul 14, 2006||Jan 17, 2008||Devlin Mark T||Lubricant compositions|
|US20080015127 *||Jul 14, 2006||Jan 17, 2008||Loper John T||Boundary friction reducing lubricating composition|
|US20080051305 *||Aug 28, 2006||Feb 28, 2008||Devlin Mark T||Lubricant composition|
|US20080098930 *||Nov 1, 2006||May 1, 2008||Xerox Corporation||Colorant dispersant|
|US20080103250 *||Sep 21, 2007||May 1, 2008||Xerox Corporation||Nanostructed particles, phase change inks including same and methods for making same|
|US20080119377 *||Nov 22, 2006||May 22, 2008||Devlin Mark T||Lubricant compositions|
|US20080182768 *||Dec 20, 2007||Jul 31, 2008||Devlin Cathy C||Lubricant composition for bio-diesel fuel engine applications|
|US20080274921 *||Jun 14, 2007||Nov 6, 2008||Ian Macpherson||Environmentally-Friendly Lubricant Compositions|
|US20090011963 *||Jul 6, 2007||Jan 8, 2009||Afton Chemical Corporation||Truck fleet fuel economy by the use of optimized engine oil, transmission fluid, and gear oil|
|US20090031614 *||Aug 1, 2007||Feb 5, 2009||Ian Macpherson||Environmentally-Friendly Fuel Compositions|
|US20090071067 *||Sep 17, 2007||Mar 19, 2009||Ian Macpherson||Environmentally-Friendly Additives And Additive Compositions For Solid Fuels|
|US20090156441 *||Dec 12, 2007||Jun 18, 2009||Rowland Robert G||Cycloalkyl phenylenediamines as deposit control agents for lubricants|
|US20090156445 *||Dec 13, 2007||Jun 18, 2009||Lam William Y||Lubricant composition suitable for engines fueled by alternate fuels|
|US20090156449 *||Sep 17, 2008||Jun 18, 2009||Rowland Robert G||Alkylated 1,3-benzenediamine compounds and methods for producing same|
|US20100028537 *||Feb 4, 2010||Xerox Corporation||Ink Carriers Containing Surface Modified Nanoparticles, Phase Change Inks Including Same, and Methods for Making Same|
|US20100075038 *||Mar 25, 2010||Xerox Corporation||Ink Carriers Containing Low Viscosity Functionalized Waxes, Phase Change Inks Including Same, And Methods For Making Same|
|US20100124611 *||Nov 17, 2008||May 20, 2010||Xerox Corporation||Phase Change Inks Containing Graphene-Based Carbon Allotrope Colorants|
|US20100152078 *||Feb 12, 2010||Jun 17, 2010||Ian Macpherson||Environmentally-friendly lubricant compositions|
|US20100279901 *||Nov 4, 2010||Iyer Ramnath N||Methods for providing steel-on-steel friction and/or steel-on-paper friction with lubricant compositions for power transmitting fluids|
|DE102008005330A1||Jan 21, 2008||Aug 7, 2008||Afton Chemical Corp.||Schmiermittelzusammensetzung für Biodieselkraftstoffmotorverwendungen|
|DE102009001301A1||Mar 3, 2009||Sep 24, 2009||Audi Ag||Verfahren zum Schmieren einer Komponente nur für die Kupplung eines automatischen Getriebes, welche Schmierung erfordert|
|DE102009012567A1||Mar 11, 2009||Oct 1, 2009||Afton Chemical Corp.||Clutch-only transmission fluid useful for lubrication comprises oil formulated with additive components having metal detergent, phosphorus-based wear preventative, phosphorylated and boronated dispersant, sulfurized extreme pressure agent|
|DE102012223638A1||Dec 18, 2012||Jun 27, 2013||Infineum International Ltd.||Verfahren zur Herabsetzung der Abnahmerate der Basizität einer Schmierölzusammensetzung, die in einem Motor verwendet wird|
|EP0304175A1 *||Jul 25, 1988||Feb 22, 1989||Exxon Chemical Patents Inc.||Lactone-modified, Mannich base dispersant additives useful in oleaginous compositions|
|EP0317353A2||Nov 18, 1988||May 24, 1989||Exxon Chemical Patents Inc.||Use of oil soluble dispersant additives in oleaginous compositions|
|EP0357215A1 *||Jul 25, 1989||Mar 7, 1990||Exxon Chemical Patents Inc.||Ethylene alpha-olefin mannich base viscosity index improver/dispersant additives|
|EP0399764A1||May 21, 1990||Nov 28, 1990||Ethyl Petroleum Additives Limited||Lubricant compositions|
|EP0558835A1||Jan 30, 1992||Sep 8, 1993||Albemarle Corporation||Biodegradable lubricants and functional fluids|
|EP0713908A1||Nov 21, 1995||May 29, 1996||Ethyl Corporation||Power transmission fluids|
|EP1568759A2||Feb 24, 2005||Aug 31, 2005||Afton Chemical Corporation||Power transmission fluids|
|EP1669435A1||Dec 9, 2005||Jun 14, 2006||Afton Chemical Corporation||Dispersant reaction product with antioxidant capability|
|EP1959003A2||Jan 28, 2008||Aug 20, 2008||Infineum International Limited||Soot dispersants and lubricating oil compositions containing same|
|EP2017329A1||Apr 17, 2008||Jan 21, 2009||Afton Chemical Corporation||Environmentally-Friendly Lubricant Compositions|
|EP2025737A1||Jul 30, 2008||Feb 18, 2009||Afton Chemical Corporation||Environmentally-friendly fuel compositions|
|EP2072611A1||Nov 11, 2008||Jun 24, 2009||Afton Chemical Corporation||Lubricant composition suitable for engines fueled by alternate fuels|
|EP2075264A1||Dec 4, 2008||Jul 1, 2009||Infineum International Limited||Method of forming polyalkene substituted carboxylic acid compositions|
|EP2075315A1||Jul 18, 2008||Jul 1, 2009||Infineum International Limited||Additive Compositions with Michael adducts of N-substituted phenylenediamines|
|EP2083024A1||Sep 12, 2008||Jul 29, 2009||Afton Chemical Corporation||Olefin copolymer dispersant VI improver and lubricant compositions and uses thereof|
|EP2083063A1||Jan 14, 2009||Jul 29, 2009||Infineum International Limited||Lubricating oil composition|
|EP2090642A1||Jan 27, 2009||Aug 19, 2009||Infineum International Limited||Engine lubrication|
|EP2116590A1||Feb 2, 2006||Nov 11, 2009||Infineum International Limited||Soot dispersants and lubricating oil compositions containing same|
|EP2206764A1||Feb 4, 2009||Jul 14, 2010||Infineum International Limited||Aniline compounds as ashless TBN sources and lubricating oil compositions containing same|
|EP2230292A1||Nov 8, 2004||Sep 22, 2010||Afton Chemical Corporation||Methods of lubricating transmissions|
|EP2236590A1||Apr 6, 2009||Oct 6, 2010||Infineum International Limited||Lubricating oil composition|
|EP2239314A1||Mar 31, 2010||Oct 13, 2010||Infineum International Limited||Lubricating oil composition|
|EP2290041A2||Jul 29, 2010||Mar 2, 2011||Infineum International Limited||A lubricating oil composition|
|EP2302023A2||Oct 2, 2003||Mar 30, 2011||R.T. Vanderbilt Company, Inc.||Synergistic organoborate compositions and lubricating compositions containing same|
|EP2319904A1||Sep 6, 2010||May 11, 2011||Infineum International Limited||Lubrication and lubricating oil compositions comprising phenylene diamines|
|EP2325291A1||Oct 20, 2010||May 25, 2011||Afton Chemical Corporation||Olefin Copolymer VI improvers and lubricant compositions and uses thereof|
|EP2366761A1||Feb 10, 2011||Sep 21, 2011||Infineum International Limited||Morpholine derivatives as ashless TBN sources and lubricating oil compositions containing same|
|EP2366762A1||Oct 2, 2003||Sep 21, 2011||R.T. Vanderbilt Company Inc.||Synergistic organoborate compositions and lubricating compositions containing same|
|EP2371933A1||Feb 1, 2007||Oct 5, 2011||The Lubrizol Corporation||Tartaric acid derivatives as fuel economy improvers and antiwear agents in crankcase oils and preparation thereof|
|EP2371934A1||Mar 24, 2011||Oct 5, 2011||Infineum International Limited||Lubricating oil composition|
|EP2420552A1||Aug 19, 2010||Feb 22, 2012||Infineum International Limited||EGR Equipped Diesel Engines and Lubricating Oil Compositions|
|EP2420553A1||Apr 17, 2008||Feb 22, 2012||Afton Chemical Corporation||Environmentally-Friendly Lubricant Compositions|
|EP2436753A1||Oct 2, 2003||Apr 4, 2012||R.T. Vanderbilt Company Inc.||Synergistic organoborate compositions and lubricating compositions containing same|
|EP2460870A1||Oct 2, 2003||Jun 6, 2012||R.T. Vanderbilt Company, Inc.||Synergistic organoborate compositions and lubricating compositions containing same|
|EP2574656A1||Sep 28, 2011||Apr 3, 2013||Infineum International Limited||Lubricating oil compositions|
|EP2620207A2||Oct 30, 2009||Jul 31, 2013||Calera Corporation||Non-cementitious compositions comprising CO2 sequestering additives|
|EP2687583A1||Jul 12, 2013||Jan 22, 2014||Infineum International Limited||Lubricating oil compositions containing sterically hindered amines as ashless TBN sources|
|EP2727984A1||Sep 13, 2013||May 7, 2014||Infineum International Limited||Marine engine lubrication|
|EP2735603A1||Oct 16, 2013||May 28, 2014||Infineum International Limited||Marine engine lubrication|
|EP2740782A1||Dec 9, 2013||Jun 11, 2014||Infineum International Limited||Lubricating oil compositions containing sterically hindered amines as ashless tbn sources|
|EP2765179A1||Jan 7, 2014||Aug 13, 2014||Infineum International Limited||Marine engine lubrication|
|EP2851412A1||Sep 4, 2014||Mar 25, 2015||Infineum International Limited||Marine engine lubrication|
|EP2940110A1||Apr 29, 2015||Nov 4, 2015||Infineum International Limited||Lubricating oil compositions|
|WO1986004601A1||Jan 29, 1986||Aug 14, 1986||Lubrizol Corp||Sulfur-containing compositions, and additive concentrates and lubricating oils containing same|
|WO1999067301A1 *||May 26, 1999||Dec 29, 1999||Mobil Oil Corp||Dispersants and dispersant viscosity index improvers from selectively hydrogenated polymers: mannich reaction products|
|WO2008154334A1||Jun 6, 2008||Dec 18, 2008||Infineum Int Ltd||Additives and lubricating oil compositions containing same|
|WO2010096325A1||Feb 11, 2010||Aug 26, 2010||The Lubrizol Corporation||Amine derivatives as friction modifiers in lubricants|
|WO2010115594A1||Mar 31, 2010||Oct 14, 2010||Infineum International Limited||Marine engine lubrication|
|WO2011025636A1||Aug 4, 2010||Mar 3, 2011||Chemtura Corporation||Two-stage process and system for forming high viscosity polyalphaolefins|
|WO2011059583A1||Sep 29, 2010||May 19, 2011||Chemtura Corporation||Lubrication and lubricating oil compositions|
|WO2011126640A2 *||Mar 7, 2011||Oct 13, 2011||Chevron Oronite Company Llc||Method for improving fluorocarbon elastomer seal compatibility|
|WO2011143051A1||May 6, 2011||Nov 17, 2011||The Lubrizol Corporation||Tartaric acid derivatives in hths fluids|
|WO2012033668A1||Aug 30, 2011||Mar 15, 2012||The Lubrizol Corporation||Hydroxychroman derivatives as engine oil antioxidants|
|WO2012141855A1||Mar 21, 2012||Oct 18, 2012||R.T. Vanderbilt Company, Inc.||Molybdenum dialkyldithiocarbamate compositions and lubricating compositions containing the same|
|WO2012154708A1||May 8, 2012||Nov 15, 2012||The Lubrizol Corporation||Aromatic imides and esters as lubricant additives|
|WO2013012987A1||Jul 19, 2012||Jan 24, 2013||The Lubrizol Corporation||Overbased friction modifiers and methods of use thereof|
|WO2013013026A1||Jul 19, 2012||Jan 24, 2013||The Lubrizol Corporation||Carboxylic pyrrolidinones and methods of use thereof|
|WO2013070376A2||Oct 11, 2012||May 16, 2013||Vanderbilt Chemicals, Llc||Lubricant composition|
|WO2013090051A1||Dec 4, 2012||Jun 20, 2013||Chemtura Corporation||Cross products and co-oligomers of phenylenediamines and aromatic amines as antioxidants for lubricants|
|WO2014088814A1||Nov 21, 2013||Jun 12, 2014||The Lubrizol Corporation||Pyran dispersants|
|U.S. Classification||508/192, 508/240, 508/194, 508/189, 548/520, 564/160, 548/405|
|International Classification||C10M159/16, C07D207/412, C07D207/40|
|Cooperative Classification||C07D207/412, C10M2223/045, C10M2207/34, C10M2207/281, C10M2215/04, C10M159/16, C10M2215/28, C10M2207/283, C10N2270/02, C10M2209/103, C10M2219/044, C10M2215/086, C10M2207/129, C10M2215/082, C10M2217/06, C10M2207/123, C10N2210/02, C10M2219/046, C10M2205/00, C10M2215/08, C10M2215/26, C10N2210/03, C10M2207/027, C10M2207/028, C10M2227/061, C10M2209/084, C10M2207/286, C10M2217/046, C10M2227/06, C10M2207/282, C10M2207/22|
|European Classification||C10M159/16, C07D207/412|