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Martin D Dolfi, 77Kalamazoo, MI

Martin Dolfi Phones & Addresses

Portage, MI   

701 Ridgefields Rd, Kingsport, TN 37660   

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Martin D Dolfi

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Work

Company: Pfizer Position: Ehs sr specialist

Industries

Pharmaceuticals

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Martin Dolfi resumes & CV records

Resumes

Martin Dolfi Photo 9

Ehs Senior Specialist

Location:
Kalamazoo, MI
Industry:
Pharmaceuticals
Work:
Pfizer
EHS Sr Specialist
Eastman Chemical 1978 - 1999
Sr Process Engineer

Publications & IP owners

Us Patents

Process For Dehydrohalogenating Aromatic Halides

US Patent:
4925998, May 15, 1990
Filed:
Dec 27, 1988
Appl. No.:
7/290678
Inventors:
Thomas J. Abraham - Knoxville TN
Eric J. Fugate - Jonesborough TN
Guy R. Steinmetz - Kingsport TN
Martin D. Dolfi - Kingsport TN
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07C 120
US Classification:
585469
Abstract:
Disclosed is a process for dehydrohalogenating an aromatic bromide or iodide by contacting the aromatic halide with hydrogen at elevated pressure in the presence of an alkyl halide-forming compound and a Group VIII metal catalyst. The presence of the alkyl halide-forming compound, such as an alkanol, diol, triol or derivative thereof, facilitates the dehydrohalogenation reaction and permits the recovery of the halogen ad alkyl halides from which the bromide and iodide values can be economically recovered.

Process For The Production Of Sterol And Tocopherol Concentrates

US Patent:
5424457, Jun 13, 1995
Filed:
May 27, 1994
Appl. No.:
8/250221
Inventors:
Charles E. Sumner - Kingsport TN
Scott D. Barnicki - Kingsport TN
Martin D. Dolfi - Kingsport TN
Assignee:
Eastman Chemical Company - Kingsport TN
International Classification:
C07J 7500
C07J 900
US Classification:
549408
Abstract:
A process is provided which allows the isolation of sterols and a tocopherol concentrate in high yields from a deodorizer distillate (DOD) mixture obtained from the processing of, for example, soybean oils. Treatment of DOD with methanol at preferably 200. degree. -220. degree. C. in the presence of a monoalkyl- or dialkyl-tin compound results in the conversion of fatty acids and fatty acid esters into fatty acid methyl esters (FAME) and the liberation of free sterols and glycerin without appreciable degradation of tocopherols or sterols. The process can also be carried out in two steps where glycerin is used in the initial step and the fatty acids are converted into glycerides allowing the water of reaction to be removed as it is formed. The FAME produced by both methods are removed by a stripping operation to give a concentrate that allows the isolation of sterols in high yield and high purity and the isolation of a tocopherol concentrate by molecular distillation.

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