Acute Upper Respiratory Tract Infections Fractures, Dislocations, Derangement, and Sprains Migraine Headache Otitis Media Skin and Subcutaneous Infections
Languages:
English
Description:
Dr. Driver graduated from the Oregon Health & Science University School of Medicine in 1980. He works in Clarkston, WA and specializes in Emergency Medicine. Dr. Driver is affiliated with Tri-State Memorial Hospital.
Isbn (Books And Publications)
The Dynamic Decision Maker: Five Decision Styles for Executive and Business Success
Methods for separating olefins from non-olefins, such as parafins, including cycloparaffins, oxygenates and aromatics, are provided. The methods use metal salts to complex olefins, allowing the non-olefins to be separated by a variety of methods, including decantation and distillation. The metal salts are dissolved in ionic liquids, which tend to have virtually no vapor pressure, and which poorly solubilize the non-olefins. Accordingly, the non-olefins phase separate well, and can be distilled without carrying over any of the ionic liquid into the distillate. Preferred salts are Group IB salts, more preferably silver salts. A preferred silver salt is silver tetrafluoroborate. Preferred ionic liquids are those which form stable solutions or dispersions of the metal salts, and which do not dissolve the non-olefins. Further, if the olefins are subject to isomerization, the ionic liquid is preferably relatively non-acidic. The methods involve forming a solution of a suitable olefin-complexing salt in an appropriate ionic liquid.
Process For Making Fatty Acid Nitriles And Fatty Amines By Cross-Metathesis Of Normal Alpha Olefins
A process for preparing fatty amines by the cross-metathesis of normal alpha olefins and acrylonitrile to form an intermediate fatty acid nitrile which is hydrogenated to the corresponding fatty amine.
Process For Increasing The Yield Of Lubricating Base Oil From A Fischer-Tropsch Plant
David R. Johnson - Petaluma CA Christopher A. Simmons - El Cerrito CA Donald H. Mohr - Orinda CA Stephen J. Miller - San Francisco CA Stephen K. Lee - Oakland CA William L. Schinski - San Rafael CA Michael S. Driver - San Francisco CA
Assignee:
Chevron U.S.A. Inc. - San Ramon CA
International Classification:
C10G 6717
US Classification:
208 80, 208 78, 208950, 585304, 585327
Abstract:
A process for increasing the yield of C plus hydrocarbon products from a Fischer-Tropsch plant which comprises the steps of (a) separating a Fischer-Tropsch product into a wax fraction and a condensate fraction; (b) dewaxing the wax fraction to produce a high boiling intermediate; (c) hydrofinishing the high boiling intermediate; (d) dehydrating the alcohols in the condensate fraction to convert them into olefins; (e) oligomerizing the olefins to form higher molecular weight hydrocarbons; (f) hydrofinishing the oligomerization mixture; and (g) and recovering a C plus hydrocarbon product from the hydrofinishing zone.
Separation Of Olefins From Paraffins Using Ionic Liquid Solutions
Curtis L. Munson - Oakland CA Laura C. Boudreau - Lafayette CA Michael S. Driver - San Francisco CA William L. Schinski - San Rafael CA
Assignee:
Chevron U.S.A. Inc. - San Ramon CA
International Classification:
C09K 300
US Classification:
252184, 585856, 585857
Abstract:
Methods for separating olefins from non-olefins, such as paraffins, including cycloparaffins, oxygenates and aromatics, are provided. The methods use metal salts to complex olefins, allowing the non-olefins to be separated by a variety of methods, including decantation and distillation. The metal salts are dissolved in ionic liquids, which tend to have virtually no vapor pressure, and which poorly solubilize the non-olefins. Accordingly, the non-olefins phase separate well, and can be distilled without carrying over any of the ionic liquid into the distillate. Preferred salts are Group IB salts, more preferably silver salts. A preferred silver salt is silver tetrafluoroborate. Preferred ionic liquids are those which form stable solutions or dispersions of the metal salts, and which do not dissolve the non-olefins. Further, if the olefins are subject to isomerization, the ionic liquid is preferably relatively non-acidic. The methods involve forming a solution of a suitable olefin-complexing salt in an appropriate ionic liquid.
Process For Upgrading Fischer-Tropsch Syncrude Using Thermal Cracking And Oligomerization
David R. Johnson - Petaluma CA Christopher A. Simmons - El Cerrito CA Donald H. Mohr - Orinda CA Stephen J. Miller - San Francisco CA Stephen K. Lee - Oakland CA William L. Schinski - San Rafael CA Michael S. Driver - San Francisco CA William J. Cannella - Hercules CA
Assignee:
Chevron U.S.A. Inc. - San Ramon CA
International Classification:
C07C 204
US Classification:
585303, 585302, 585304, 585329, 585330, 208950
Abstract:
A process for upgrading a Fischer-Tropsch feedstock which comprises (a) recovering from a Fischer-Tropsch reactor a Fischer-Tropsch wax fraction and a Fischer-Tropsch condensate fraction, wherein the Fischer-Tropsch condensate fraction contains alcohols boiling below about 370Â C. ; (b) contacting the Fischer-Tropsch condensate fraction with a dehydration catalyst in a dehydration zone under dehydration conditions pre-selected to convert at least some of the alcohols present in said fraction into olefins and recovering a first intermediate effluent from said dehydration zone; (c) pyrolyzing the paraffins in the Fischer-Tropsch wax fraction in a thermal cracking zone under thermal cracking conditions pre-selected to crack the Fischer-Tropsch wax molecules to form olefins and collecting a second intermediate effluent from the thermal cracking zone; (d) passing the first and second intermediate effluents recovered from steps (b) and (c) to an oligomerization zone containing an oligomerization catalyst under oligomerization conditions to form an oligomerization mixture having a higher molecular weight than either of said first and second intermediate effluent; (e) hydrofinishing the oligomerization mixture in a hydrofinishing zone; and (f) recovering from the hydrofinishing zone a C plus hydrocarbon product, most preferably a lubricating base oil.
Alkylation Process Using An Alkyl Halide Promoted Ionic Liquid Catalyst
Thomas V. Harris - Benicia CA, US Michael Driver - San Francisco CA, US Saleh Elomari - Fairfield CA, US Hye-Kyung C. Timken - Albany CA, US
Assignee:
Chevron U.S.A., Inc - San Ramon CA
International Classification:
C07C 2/60 C07C 2/62
US Classification:
585906, 585725, 585727, 585728, 585724
Abstract:
A process for the production of a high quality gasoline blending components from refinery process streams by the alkylation of light isoparaffins with olefins using an ionic liquid catalyst is disclosed. The alkylation process comprises contacting a hydrocarbon mixture comprising at least one olefin having from 2 to 6 carbon atoms and at least one isoparaffin having from 3 to 6 carbon atoms under alkylation conditions, said catalyst comprising a mixture of at least one acidic ionic liquid and at least one alkyl halide. The alkylhalide by reacting to at least a portion of the olefin with a hydrogen halide.
Michael S. Driver - San Francisco CA, US Gunther Dieckmann - Walnut Creek CA, US
Assignee:
Chevron U.S.A., Inc. - San Ramon CA
International Classification:
C07C 2/60 C07C 2/62
US Classification:
585712, 585725, 585727, 585728, 585724
Abstract:
An alkylation process comprising contacting a first hydrocarbon feed comprising at least one olefin having from 2 to 6 carbon atoms and a second hydrocarbon feed comprising at least one isoparaffin having from 3 to 6 carbon atoms with a halide-based acidic ionic liquid catalyst under alkylation conditions to produce an alkylate containing an organic halide and contacting at least a portion of the alkylate with a hydrotreating catalyst in the presence of hydrogen under hydrotreating conditions to reduce the concentration of the organic halide is disclosed.
Method Of Making An Alkylated Aromoatic Using Acidic Ionic Liquid Catalyst
Michael Driver - San Francisco CA, US Curt B. Campbell - Hercules CA, US Thomas V. Harris - Benicia CA, US
Assignee:
Chevron Oronite Company, LLC - San Ramon CA
International Classification:
C07C 2/70 C07C 2/26
US Classification:
585323, 585455, 585456, 585521, 585511
Abstract:
A process for alkylating an aromatic compound containing no hydroxyl groups comprising reacting at least one non-hydroxyl containing aromatic compound with at least one olefinic oligomer in the presence of an acidic ionic liquid catalyst, wherein the olefinic oligomer has a carbon range of from about Cto about Cand is synthesized by oligomerizing at least one monoolefin monomer in the presence of an acidic ionic liquid catalyst.