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Edward G Samsel, 73936 Louray Dr, Baton Rouge, LA 70808

Known as:
Edward Dr Samsel Edward Gerrard Samsel Ed Samsel
Related to:
Mary Tate 88

Edward Samsel Phones & Addresses

936 Louray Dr, Baton Rouge, LA 70808    225-7667640   

11580 Perkins Rd, Baton Rouge, LA 70810   

Naperville, IL   

Idaho Falls, ID   

Fort Collins, CO   

936 Louray Dr, Baton Rouge, LA 70808    225-9786216   

Work

Position: Machine Operators, Assemblers, and Inspectors Occupations

Emails

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Career records & work history

Lawyers & Attorneys

Edward Samsel Photo 1

Edward Samsel - Lawyer

Specialties:
Real Property Tax Administration
ISLN:
904066133
Admitted:
1983
University:
The Ohio State University, B.S., 1969
Law School:
The Ohio State University, J.D., 1983

Edward Samsel resumes & CV records

Resumes

Edward Samsel Photo 13

Edward Samsel

Location:
Baton Rouge, LA
Industry:
Chemicals
Work:
Albemarle Corporation Jun 1990 - Jun 2012
R and D Advisor
Education:
Princeton University 1977 - 1982
Doctorates, Doctor of Philosophy, Chemistry Idaho State University College of Business 1970 - 1974
Skills:
Chemical Engineering, Polymers, R&D, Process Simulation, Catalysis, Additives, Chemistry, Process Engineering, Process Optimization, Polymer Chemistry, Coatings, Plastics, Polymer Science, Petrochemical, Resin
Edward Samsel Photo 14

Edward Samsel

Location:
United States

Publications & IP owners

Wikipedia

Edward Samsel Photo 15

Edward Eugeniusz Samsel Wolna Encyklopedia

Edward Eugeniusz Samsel (ur. 2 stycznia 1940 w Myszycu k. omy, zm. 17 stycznia 2003 w Biaymstoku), polski duchowny katolicki, biskup pomocniczy ...

Us Patents

Process For Linear Alpha Olefins

US Patent:
6444867, Sep 3, 2002
Filed:
May 17, 2001
Appl. No.:
09/860173
Inventors:
Edward G. Samsel - Baton Rouge LA
Franke N. Brooks - Batavia IL
Assignee:
BP Corporation North America Inc. - Chicago IL
International Classification:
C07C 288
US Classification:
585637, 585318
Abstract:
Linear alpha olefins are typically produced by starting with a trialkylaluminum compound, such as triethylaluminum, and then subjecting the trialkylaluminum compound to alkyl chain growth conditions in the presence of ethylene and elevated temperature and pressure, frequently in the presence of a chain growth catalyst. Under such alkyl chain growth conditions, the alkyl groups attached to the aluminum may be extended by two carbon atoms per reaction with ethylene. The process is permitted to continue until the alkyl groups have reached the desired length at which point they are displaced from the trialkylaluminum compund as alpha olefins, usually in the presence of an excess of ethylene and a displacement catalyst. This invention discloses a new chain growth catalyst system comprising, in combination, non-bridged metallocenes and aluminum complexes having amidinate ligands and inert anions.

Process For The Preparation Of (Aminoalkylamino)Alkyl Halides And Conversion To Amifostine

US Patent:
2008027, Nov 6, 2008
Filed:
Nov 1, 2006
Appl. No.:
12/092516
Inventors:
Edward G. Samsel - Baton Rouge LA, US
Assignee:
ALBEMARLE CORPORATION - Baton Rouge LA
International Classification:
C07F 9/165
C07C 209/74
US Classification:
558146, 564496, 558 87
Abstract:
The present invention relates to processes for the preparation of (ω-aminoalkylamino)alkyl halides, their conversion to S-ω-(ω-aminoalkylamino)alkyl phosphothioates, and purification of the crystalline products of the reaction. The preparation process for the (ω-aminoalkylamino)alkyl halides comprises contacting an appropriate alcohol with a brominating agent in the presence of a sulfone solvent under temperature and pressure conditions suitable to effect salt formation without subsequent premature precipitation. The process is especially useful for converting (ω-aminoalkylamino)ethyl alcohol to amifostine.

Process For Manufacturing Bisphosphonic Acids

US Patent:
2009013, May 28, 2009
Filed:
Mar 16, 2007
Appl. No.:
12/282725
Inventors:
Edward G. Samsel - Baton Rouge LA, US
Tse-Chong Wu - Baton Rouge LA, US
Assignee:
ALBEMARLE CORPORATION - Baton Rouge LA
International Classification:
C07D 221/02
C07D 233/54
C07D 213/02
C07F 9/38
US Classification:
546 23, 548112, 546 22, 562 13
Abstract:
A manufacturing process for the preparation of bisphosphonic acids and in particular zoledronic acid is provided wherein diglyme, monoglyme, or a mixture thereof, is utilized to produce a homogenous, water soluble, solid reaction mass that upon cooling, dissolving in water and stripping results in a high purity product and comparatively good yield. wherein Ri is selected from the group consisting of

Catalyzed Chain Growth Process

US Patent:
5210338, May 11, 1993
Filed:
May 12, 1992
Appl. No.:
7/881928
Inventors:
Edward G. Samsel - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 2954
C07C 288
C07C 31125
C07F 506
US Classification:
568911
Abstract:
An improved process for the preparation of higher aluminum alkyls by a chain growth reaction of an. alpha. -olefin and especially ethylene with a lower molecular weight aluminum alkyl or aluminum hydride uses a catalyst system which comprises at least one of (a) a metallocene of a transition metal and an aluminoxane (b) a cationic transition metal metallocene complex with an inert, non-coordinating anion, and (c) a cationic transition metal metallocene complex with an inert, non-coordinating anion and a hydrocarbylaluminoxane. Higher purity alpha olefins can be recovered by olefin displacement. Alternatively, linear primary alcohols can be produced by oxidation and hydrolysis.

Actinide Catalyzed Chain Growth Process

US Patent:
5276220, Jan 4, 1994
Filed:
Jun 18, 1992
Appl. No.:
7/900387
Inventors:
Edward G. Samsel - Baton Rouge LA
David C. Eisenberg - Baton Rouge LA
Assignee:
Ethyl Corporation - Richmond VA
International Classification:
C07C 2954
C07C 31125
C07C 288
C07F 506
US Classification:
568911
Abstract:
An improved process for preparing an alkyl chain growth product by the chain growth reaction of. alpha. -olefin in an aluminum alkyl uses a catalyst system which comprises an actinide metallocene.

Enantioselective Synthesis Of L-(-)-4- Boronophenylalanine (L-Bpa)

US Patent:
5157149, Oct 20, 1992
Filed:
Jun 4, 1991
Appl. No.:
7/710208
Inventors:
Edward G. Samsel - Baton Rouge LA
Assignee:
The United States of America as represented by the United States
Department of Energy - Washington DC
International Classification:
C07F 502
US Classification:
562 7
Abstract:
A method of making substantially pure L-BPA is disclosed. The method includes the steps of reacting 4-bromobenzaldehyde with ethylene glycol to form 4-bromobenzaldehyde ethylene glycol acetal, sequentially reacting 4-bromobenzaldehyde ethyleneglycol acetal with Mg to produce the Grignard reagent and thereafter reacting with tributyl borate and then converting to an acid environment to form 4-boronobenzaldehyde, reacting 4-boronobenzaldehyde with diethanol amine to form 4-boronobenzaldehyde diethanolamine ester, condensing the 4-boronobenzaldehyde diethanolamine ester with 2-phenyl-2-oxazolin-5-one to form an azlactone, reacting the azlactone with an alkali metal hydroxide to form z-. alpha. -benzoylamino-4-boronocinnamic acid, asymmetrically hydrogenating the z-. alpha. -benzoylamino-4-boronocinnamic acid in the presence of a catalyst of a cheltate complex of rhodium (I) with chiral bisphosphines to form L-(+)-N-benzoyl-4-boronophenylalanine, and thereafter acidifying the L-(+)-N-benzoyl-4-boronophenylalanine in an organic medium to produce L-BPA.

Production Of Chiral Non-Racemic 2-Halopropionic Acid Or Salt Thereof

US Patent:
6184415, Feb 6, 2001
Filed:
Nov 1, 1999
Appl. No.:
9/431515
Inventors:
Edward G. Samsel - Baton Rouge LA
Christi R. Bedell - Baton Rouge LA
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
C07C 5315
US Classification:
562602
Abstract:
It has been discovered that it is possible to produce enantioselectively, a chiral 2-haloalkanoic acid or salt thereof, by subjecting a 2-halo-. alpha. ,. beta. -alkenoic acid or salt, e. g. , a 2-haloacrylic acid or salt, to asymmetric hydrogenation in the presence of an enantiometrically-enriched (BINAP)Ru(II) catalyst. In contrast to asymmetric hydrogenation of olefinic compounds having an electron rich, electropositive substituent in the 2-position, the substituent in the 2-position is an electronegative, electron-withdrawing halide substituent. The reaction is accelerated by inclusion of an alkali metal halide or quaternary ammonium halide in the reaction mixture.

Conversion Of Deep Internal Olefins Into Primary Alkylaluminum Compounds By Isomerization-Displacement

US Patent:
5597937, Jan 28, 1997
Filed:
May 11, 1995
Appl. No.:
8/438686
Inventors:
Edward G. Samsel - Baton Rouge LA
Assignee:
Albemarle Corporation - Richmond VA
International Classification:
C07F 506
US Classification:
556190
Abstract:
A deep olefin internal olefin is reacted with a C. sub. 3-4 primary alkyl aluminum chloride in the liquid phase in the presence of a catalyst system formed from (i) a dicyclopentadienyl dihalide or halohydride of zirconium or hafnium and (ii) a hydridic co-catalyst component. Unlike prior art procedures, negligible quantities of by-product paraffins are formed in the process.

Possible Relatives

David A Samsel  Dawn A Samsel  Daniel R Samsel  Dennis Samsel  Dianne E Samsel  Donald S Samsel  Fred J Samsel  Edward M Johnson  Edward M Stan  Edward W Stanchak 

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