Academy Sport and Outdoors Mobile, AL Jun 2013 to Sep 2013 Freight Associate, Stock Associate, Merchandise Organizer and Customer Service RepresentativeRobert L. Fleming Physical Thaerphy Mobile, AL May 2012 to Jun 2012 InternLittle Ceaser's Pizza Mobile, AL Aug 2008 to Oct 2008 Customer Service Representative - Promoted sales
Education:
Spring Hill College Mobile, AL Public Relations and AdvertisingFaulkner State Community College May 2012 A.A. in Physical
A novel catalyst material of a boron containing substance for catalyzing the liquid phase oxidation of an olefin with an organic hydroperoxide to the corresponding oxirane is disclosed. The novel catalyst materials are characterized as binary or ternary boride compounds having the general formula M. sub. x B. sub. y or M. sub. x B. sub. y R. sub. z wherein x is an integer from 1-5; y is an integer from 1-2; z is an integer from 1-4; B is boron; M is an element selected from the groups II-A, III-B, IV-B, V-B, VI-B, VII-B, VIII, III-A, IV-A, and V-A of the Periodic Table, the rare earths, and the actinides; and R is an element different from M selected from the same group of elements in the Periodic Table as M. The preferred catalyst materials are those boron containing substances which are substantially insoluble in the reaction mixture containing the organic hydroperoxides, olefins and products. Also disclosed is a method for liquid phase epoxidation of an olefinic compound with an organic hydroperoxide at lower temperatures, e. g. 25. degree. C. to 200. degree. C.
Robert Malone Gipson - Austin TX John Gordon Milligan - Austin TX Floyd Edward Bentley - Austin TX
Assignee:
Jefferson Chemical Company, Inc. - Houston TX
International Classification:
C07C 3102 C07C 3302
US Classification:
260632R
Abstract:
Particular compositions of vinylidene alcohols are provided which are distinguishably characterized by their structure, their biodegradable nature, and by their very low pour point characteristics. These compositions can be used to provide useful surfactants and detergents and to form distinctive ethoxylate derivatives having unusual attributes, such as biodegradability, very high rates of water solubility, nongelling tendencies, and superior wetting ability; and certain of these ethoxylate compositions are synergistic in wetting ability and, unlike related ethoxylates of conventional alcohols, the ethoxylates of certain compositions possess cloud point temperatures within an especially desired range.
Substituted Alkylene Oxides From Substituted Alkylene Carbonates
Edward E. McEntire - Austin TX Robert M. Gipson - Austin TX
Assignee:
Texaco Dev. Corp. - White Plains NY
International Classification:
C07D30102
US Classification:
26034816
Abstract:
Alkyl substituted ethylene carbonates are converted to substituted ethylene oxides by heating the respective carbonates in the presence of a catalyst comprising alkali metal halides or lanthanum iodide. The alkyl substituted ethylene carbonates have the general formula ##STR1## where R is alkyl, aryl, substituted alkyl, substituted aryl, alkaryl or aralkyl.
Boride Catalyst For Epoxidizing Olefinic Compounds
A novel catalyst material of a boron containing substance for catalyzing the liquid phase oxidation of an olefin with an organic hydroperoxide to the corresponding oxirane is disclosed. The novel catalyst materials are characterized as binary or ternary boride compounds having the general formula M. sub. x B. sub. y or M. sub. x B. sub. y R. sub. z wherein x is an integer from 1-5; y is an integer from 1-2; z is an integer from 1-4; B is boron; M is an element selected from the groups II-A, III-B, IV-B, V-B, VI-B, VII-B, VIII, III-A, IV-A, and V-A of the Periodic Table, the rare earths, and the actinides; and R is an element different from M selected from the same group of elements in the Periodic Table as M. The preferred catalyst materials are those boron containing substances which are substantially insoluble in the reaction mixture containing the organic hydroperoxides, olefins and products. Also disclosed is a method for liquid phase epoxidation of an olefinic compound with an organic hydroperoxide at lower temperatures, e. g. , 25. degree. to 200. degree.
Boride Catalyst For Epoxidizing Olefinic Compounds
A novel catalyst material of a boron containing substance for catalyzing the liquid phase oxidation of an olefin with an organic hydroperoxide to the corresponding oxirane is disclosed. The novel catalyst materials are characterized as binary or ternary boride compounds having the general formula M. sub. x B. sub. y or M. sub. x B. sub. y R. sub. z wherein x is an integer from 1-5; y is an integer from 1-2; z is an integer from 1-4; B is boron; M is an element selected from the groups II-A, III-B, IV-B, V-B, VI-B, VII-B, VIII, III-A, IV-A, and V-A of the Periodic Table, the rare earths, and the actinides; and R is an element different from M selected from the same group of elements in the Periodic Table as M. The preferred catalyst materials are those boron containing substances which are substantially insoluble in the reaction mixture containing the organic hydroperoxides, olefins and products. Also disclosed is a method for liquid phase epoxidation of an olefinic compound with an organic hydroperoxide at lower temperatures, e. g. 25. degree. C to 200. degree.
Boride Catalyst For Epoxidizing Olefinic Compounds
A novel catalyst material of a boron containing substance for catalyzing the liquid phase oxidation of an olefin with an organic hydroperoxide to the corresponding oxirane is disclosed. The novel catalyst materials are characterized as binary or ternary boride compounds having the general formula M. sub. x B. sub. y or M. sub. x B. sub. y R. sub. z wherein x is an integer from 1-5; y is an integer from 1-2; z is an integer from 1-4; B is boron; M is an element selected from the groups II-A, III-B, IV-B, V-B, VI-B, VII-B, VIII, III-A, IV-A, and V-A of the Periodic Table, the rare earths, and the actinides; and R is an element different from M selected from the same group of elements in the Periodic Table as M. The preferred catalyst materials are those boron containing substances which are substantially insoluble in the reaction mixture containing the organic hydroperoxides, olefins and products. Also disclosed is a method for liquid phase epoxidation of an olefinic compound with an organic hydroperoxide at lower temperatures, e. g. 25. degree. C. to 200. degree. C.
David R. McCoy - Austin TX Robert M. Gipson - Austin TX
Assignee:
Texaco Inc. - White Plains NY
International Classification:
E21B 4322 C09K 300
US Classification:
252 855D
Abstract:
Hydrocarbons are recovered from a subterranean hydrocarbon-bearing formation penetrated by an injection well and a production well by displacing hydrocarbons toward the production well using an aqueous drive fluid such as water or brine containing dissolved therein: (a) a small amount of a nonionic surfactant formed by reacting an alcohol having not more than 6 carbon atoms or phenol first with butylene oxide and then with ethylene oxide and (b) a small amount of an anionic sulfate or sulfonate surfactant. Optionally the drive fluid may be saturated with natural gas, nitrogen and/or carbon dioxide at the injection pressure. A polymeric thickening agent also may be included in the drive fluid, if desired.
Low Foaming Nonionic Polyether Polycarbonate Surfactants And Functional Fluids
Michael Cuscurida - Austin TX Robert M. Gipson - Austin TX
Assignee:
Texaco Development Corp. - White Plains NJ
International Classification:
C11D 172 C11D 1875 C07C 6900
US Classification:
25217421
Abstract:
Improved surfactants and functional fluids are prepared by reacting a monofunctional initiator with an alkylene carbonate or with an alkylene oxide and carbon dioxide to form polyether polycarbonate materials. As surfactants, the resulting materials exhibit reduced foaming characteristics as compared to other nonionic surfactants. The viscosity-temperature relationships, flash points and pour points make them useful as functional fluids.
Isbn (Books And Publications)
The Unauthorized Collector's Guide to Garfield and the Gang
Robert Gipson (1977-1981), Billy Joe (1978-1982), Marca Tanner (1987-1991), Chris Barrett (1999-2003), Frank Vanburen (1972-1976), Barry Reseker (1975-1979)