| Patent Number |
Title Of Patent |
Date Issued |
| D602852 |
Tire |
October 27, 2009 |
|
| D602422 |
Tire |
October 20, 2009 |
|
| 7622431 |
Lubricating oil compositions |
November 24, 2009 |
| Reaction products of an acidic organic compound, a boron compound, and an alkoxylated amine and/or alkoxylated amide. Also disclosed are lubricating oil compositions and fuel compositions containing the reaction products. |
| 7621971 |
Detergent/anti-oxidant additives for fuels |
November 24, 2009 |
| A composition is disclosed that comprises the reaction product of an acidic organic compound, a boron compound, and a basic organic compound. The composition is useful as a detergent additive for lubricants and hydrocarbon fuels. |
| 7618467 |
Detergent / anti-oxidant additives for fuels and lubricants |
November 17, 2009 |
| A composition is disclosed that comprises the reaction product of an acidic organic compound, a boron compound, and a basic organic compound. The composition is useful as a detergent additive for lubricants and hydrocarbon fuels. |
| 7618466 |
Fuel compositions |
November 17, 2009 |
| Reaction products of an acidic organic compound, a boron compound, and an alkoxylated amine and/or alkoxylated amide. Also disclosed are lubricating oil compositions and fuel compositions containing the reaction products. |
| 7615168 |
Flame retardants and flame retarded polymers |
November 10, 2009 |
| There is presented a new flame retardant composition comprising a brominated aromatic composition and a butyl substituted phenyl phosphate. |
| 7612156 |
Polymers of bromostyrenes having controlled molecular weight |
November 3, 2009 |
| A controlled molecular weight polymer of styrene is provided having bromine substituted thereon. Control of molecular weight is achieved by the use of alpha-methyl styrene dimer as a chain transfer agent. The brominated polymer of styrene is useful as a flame retardant, particularly |
| 7608568 |
Tetraaromatic diamine compounds as antioxidants |
October 27, 2009 |
| Tetraaromatic diamine compounds having the general formula: ##STR00001## are provided wherein a is 0-3; b, c and d independently are integers from 0-5, R.sup.1 and R.sup.2 together with the carbon atoms to which they are bonded are joined together to form a substituted or unsubstituted C |
| 7601255 |
Process for removal of residual catalyst components |
October 13, 2009 |
| A process for reducing the level of residual catalyst comprising one or more alkylhalide, alkoxyhalide, metal halide, metal oxyhalide, alkyl metal, alkoxy metal, boron compound and coordinated metal compound wherein the metal is a Group III, Group IV, Group V, Group VI and/or Group V |
| 7585909 |
.beta.-crystalline polypropylenes |
September 8, 2009 |
| Disclosed herein are p-urea phenyl derivatives of the formula: ##STR00001## wherein R.sub.1 and R.sub.2 are independently selected hydrocarbyl groups. These derivatives are useful as haze reducing agents in propylene polymers and copolymers. |
| 7579306 |
Method for improving the oxidative stability of industrial fluids |
August 25, 2009 |
| An oxidatively stable biodegradable industrial fluid is disclosed, wherein the industrial fluid is comprised of an epoxidized vegetable oil or synthetic ester in combination with at least one antioxidant. A method for improving the oxidation stability of industrial fluids is also dis |
| 7572849 |
Urea phenyl derivatives and their use as polypropylene nucleating agents |
August 11, 2009 |
| Disclosed herein are urea phenyl derivatives of the formula: ##STR00001## wherein each R is an independently selected hydrocarbyl group and n is 2 or 3, and their use as nucleating agents for propylene polymers. |
| 7572753 |
Tetrazole fungicides |
August 11, 2009 |
| The use of certain tetrazole compounds as fungicides is disclosed wherein said compounds are of the structural formula: ##STR00001## wherein: R is selected from the group consisting of phenyl groups of the structural formula: ##STR00002## and thienyl groups of the structural formula: |
| 7569630 |
.beta.-Crystalline polypropylenes |
August 4, 2009 |
| Disclosed herein are aromatic amide derivatives of the formulae: ##STR00001## wherein X.sub.1 and X.sub.2 are independently selected from the group consisting of --OH, --OR, --OM, --NH.sub.2, and --NHR; M is a metal; and R, R.sub.1, and R.sub.2 are independently selected hydrocarb |
| 7563929 |
Alkylation of N'-phenyl-N-alkylphenylenediamines in ionic liquid and N'-phenyl-N-alkyl(alkylphen |
July 21, 2009 |
| A process for alkylation of a N'-phenyl-N-alkyl-p-phenylenediamine of specified formula in an ionic liquid unexpectedly produces a N'-phenyl-N-alkyl(alkylphenylene)diamine of a second specified formula. The use of an inorganic liquid permits convenient separation of the alkylated rea |
| 7553896 |
Ortho-nitrosophenols as polymerization inhibitors |
June 30, 2009 |
| Disclosed herein is a method for inhibiting the premature polymerization of ethylenically unsaturated monomers comprising adding to said monomers an effective amount of at least one nitroso inhibitor of the structure: ##STR00001## wherein R.sub.1, R.sub.2, R.sub.3, and R.sub.4 are i |
| 7550551 |
Brominated flame retardant |
June 23, 2009 |
| A process for preparing a polybromoaryl ether comprising adding to a solvent for the polybromoaryl ether a mixture of (1) at least one compound of the structure HO--Ar--X.sub.1, X.sub.2, X.sub.3, X.sub.4, X.sub.5, wherein Ar is an aryl group and X.sub.1, X.sub.2, X.sub.3, X.sub.4, an |
| 7541319 |
1,3-dithiolane-2-thione additives for lubricants and fuels |
June 2, 2009 |
| Fuels, especially hydrocarbon fuels, and lubricants, especially lubricating oils, contain a class of anti-corrosion, anti-wear, anti-fatigue, and extreme pressure additives that are derived from 1,3-dithiolane-2-thiones. |
| 7521401 |
Dithiocarbamyl .beta.-hydroxy fatty acid esters as additives for lubricants and fuels |
April 21, 2009 |
| Fuels, especially hydrocarbon fuels, and lubricants, especially lubricating oils, contain dithiocarbamyl .beta.-hydroxy fatty acid esters, a class of anti-corrosion, anti-wear, anti-fatigue, and extreme pressure additives that are derived from epoxidized fatty acid esters. The additi |
| 7514485 |
Compatibilizers for composites of PVC and cellulosic materials |
April 7, 2009 |
| Disclosed herein is a method for improving the physical properties of cellulose fiber-containing material/PVC composites comprising adding to said composites an effective amount of at least one compatibilizer comprising an organometallic zirconium compound. The preferred organometall |
| 7511029 |
Pesticidal diazene oxide carboxylates |
March 31, 2009 |
| Pesticidal compounds having the structural formula ##STR00001## wherein: R.sup.2 is C.sub.1-C.sub.6 branched or straight chain alkyl; C.sub.1-C.sub.4 branched or straight-chain haloalkyl; or C.sub.3-C.sub.6 cycloalkyl; m is 0, 1, or 2; X is selected from the group consisting of: C. |
| 7449119 |
Methods for controlling Mycobacterium chelonae and removing bacterial cell membrane fragments fr |
November 11, 2008 |
| Compositions containing chlorine and/or bromine in combination with chlorine dioxide are found to be synergistic against non-tuberculosis mycobacterium such as Mycobacteria chelonae. |
| 7399757 |
Pesticidal diazene oxide carboxylates |
July 15, 2008 |
| Pesticidal compounds having the structural formula ##STR00001## wherein R.sup.1 and R.sup.2 are each, independently, C.sub.1-6 alkyl, compositions comprising the compounds and methods for their use as pesticides. |
| 7390928 |
Alkylation of N'-phenyl-N-alkylphenylenediamines in ionic liquid, N'-phenyl-N-alkyl (alkylphenyl |
June 24, 2008 |
| A process for alkylation of a N'-phenyl-N-alkyl-p-phenylenediamine of specified formula in an ionic liquid unexpectedly produces a N'-phenyl-N-alkyl(alkylphenylene)diamine of a second specified formula. The use of an inorganic liquid permits convenient separation of the alkylated rea |
| 7378554 |
Ring alkylation of aniline or an aniline derivative using ionic liquid catalysts |
May 27, 2008 |
| A process for ring-alkylating aniline or an aniline derivative in which aniline or an aniline derivative is reacted with an alkylating agent in the presence of an ionic liquid which includes a Lewis acid and a quaternary cation, to produce a ring-alkylated alkylaniline or a ring-alky |
| 7361788 |
Direct alkylation of N-alkyl-N'-phenyl-p-phenylenediamine |
April 22, 2008 |
| A single-step process is disclosed for the ring alkylation of at least one N-alkyl-N'-phenyl-phenylenediamine with at least one olefin wherein the process comprises heating a mixture of the N-alkyl-N'-phenyl-phenylenediamine(s) and olefin(s) in the presence of a catalytic amount of a |
| 7145038 |
Alkylation of a diphenylamine compound in ionic liquid |
December 5, 2006 |
| A process for alkylation of a diphenylamine compound in an ionic liquid. The use of an ionic liquid permits convenient separation of the alkylated reaction product from the reaction mixture. |
