Dixie E. Goins - Orangeburg SC Silas W. Holmes - Columbia SC Edward A. Burt - Orangeburg SC
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 3714
US Classification:
568789
Abstract:
A process using heterogeneous resin-bonded aluminum phenoxide catalyst to alkylate phenols, the catalyst per se, and a process for making the catalyst. The inventive alkylation process uses ortho-tert-butylphenoxide bonded to a phenolformaldehyde condensation resin heterogeneous catalyst to prepare 2,6-di-tert-butylphenol from isobutylene and ortho-tert-butylphenol.
Niomi L. Krzystowczyk - Orangeburg SC Steven P. Diefenbach - Baton Rouge LA Edward A. Burt - Lexington SC
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
B01J 3100 B01J 3700 B01J 3739 C08F 402 C08F 460
US Classification:
502107
Abstract:
A process is described which comprises heating a methylalumoxane solution in an aromatic hydrocarbon solvent at a temperature of at least 35. degree. C. for at least 0. 5 hour in an inert, dry atmosphere such that the resulting heat-treated composition provides, in a supported metallocene catalyst produced using the heat-treated composition, increased activity as compared to the same supported metallocene catalyst produced in the same way except for using a portion of the methylalumoxane solution that has not been heat-treated. Before the heating the methylalumoxane of the solution contains from about 5 to about 35 mole percent unreacted trimethylaluminum, and was formed by partial hydrolysis of trimethylaluminum with free water in an organic solvent.
Dixie E. Goins - Baton Rouge LA Silas W. Holmes - Columbia SC Edward A. Burt - Orangeburg SC
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
B01J 3106
US Classification:
502152
Abstract:
A process using heterogeneous resin-bonded aluminum phenoxide catalyst to alkylate phenols, the catalyst per se, and a process for making the catalyst. The inventive alkylation process uses ortho-tert-butylphenoxide bonded to a phenolformaldehyde condensation resin heterogeneous catalyst to prepare 2,6-di-tert-butylphenol from isobutylene and ortho-tert-butylphenol.
Dixie E. Goins - Orangeburg SC Harold V. Huggins - Orangeburg SC Edward A. Burt - Orangeburg SC Silas W. Holmes - Columbia SC
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 3711 C07C 3806
US Classification:
568789
Abstract:
A process for the production of a 2,6-dialkylphenol in high yield wherein the alkyl groups are secondary or tertiary with a reduced overall production of 4-alkylphenol by-products by the aluminum phenoxide catalyzed pressure reaction of isobutylene with phenol and a mixture of 2,4-dialkylphenol and 2,4,6-trialkylphenol which may be obtained, in a cyclic process, as a bottom stream from the distillation of the reaction mixture to obtain the 2,6-dialkylphenol product.
Alkylation Process Of Alkyl-Benzene With Olefin Using A Sodium-And-Potassium Catalyst
David J. Koehl - Orangeburg SC Edward A. Burt - Lexington SC Patrick T. Ward - Austin TX
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
C07C 264 C07C 15067 C07C 266
US Classification:
585452
Abstract:
An alkylbenzene is alkylated with an alkene, in the presence of a sodium/potassium alloy catalyst, on a saturated carbon atom which is alpha to the ring at temperatures which are lower than the temperatures used in a current commercial process. In a pre-alkylation reaction, the catalyst is reacted with a compound which has a saturated carbon atom alpha to a double bond in order to form a catalytic species. Higher amounts of catalyst are used in the pre-alkylation reaction than in the analogous reaction of the current commercial process. Following alkylation, the phase which contains the alkylation product is separated from the phase which contains the catalytic species. The process produces less isomeric and other soluble byproducts, and enables the efficacious production of longer chain alkylbenzenes without the formation of insoluble tars characteristic of the current commercial process.
Silas W. Holmes - Columbia SC Edward A. Burt - Orangeburg SC Dixie E. Goins - Orangeburg SC
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 3714 C07C 3906
US Classification:
568781
Abstract:
A process for producing 2,4-di-substituted phenols wherein an olefin is reacted with phenol in the presence of a heterogeneous catalyst comprising an aluminum phenoxide bonded to an acidic solid polymeric resin to preferably form 2,4-di-substituted phenol. A process for preparing a heterogeneous catalyst and a heterogeneous catalyst having the structure (Resin --A--). sub. m Al(--OC. sub. 6 R. sub. 5). sub. n (11) wherein Resin is a solid polymeric resin having acidic functional groups A, m is 1 or 2, n is 2 or 3 and the R are independently selected from H, alkyl, cycloalkyl, and aralkyl. Preferably, a styrene-divinylbenzene polymeric resin of a macroreticular structure is used for the alkylation process and A is --SO. sub. 3 --.
Weylchem Group of Companies Jul 2014 - Oct 2017
Contract Process Technology Advisor
Si Group Jul 2014 - Oct 2017
Engineering Consultant
Nephron Pharmaceuticals Jan 1, 2014 - Jul 2014
Quality Manager
Albemarle Corporation Jan 2008 - Feb 2014
Director Process Technology
Albemarle Corporation Jan 2000 - Jan 2008
Senior Process Technology Advisor
Education:
University of South Carolina 1979 - 1981
Bachelor of Engineering, Bachelors, Chemical Engineering
Florida Technological University 1974 - 1979
Bachelors, Bachelor of Science, Chemistry
Oak Ridge High School
University of Central Florida
Skills:
Chemical Engineering Process Optimization Process Engineering Process Simulation Chemistry Design of Experiments Root Cause Analysis Coatings Gmp Polymers Analytical Chemistry Technology Transfer Polymer Chemistry Polymer Science R
Edmund Burt also known as Edward Burt (died 4 January 1755) was a Scottish military figure, engineer and author. He was the author of the Letters from a ...