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A. Lynn AndersonSenior LecturerOffice: 368 GreenquistTelephone: (262) 595-2633Fax : (262) 595-2056andersoa@uwp.edu
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Courses Typically Taught
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Organic Laboratory 323, Chemistry 115, 215, Lecture and Lab |
Education
Organic Chemistry
Organic Chemistry
Chemistry
Experience
Teaching:
Chemistry 321 organic chemistry lecture
Chemistry 322 organic chemistry lecture
Chemistry 323 organic chemistry lab course
Chemistry 090 prep. for college chem. lecture
Chemistry 115 allied health science lab
Chemistry 215 allied health science lab
Chemistry 101 & 102 general chemistry lab
click here for a complete cv
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list of publications and patents
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Divisions: Fluorine, Organic, Polymer, Small Chemical Business
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PAST
During my employment at Sinclair Research, Inc. I studied the hydrochlorination of alkenes, acid and base catalyzed condensations, and alkene absorption in sulfuric acid.
While a senior research chemist at Michigan Chemical, I worked primarily on the synthesis of novel organic halogen compounds for use as flame retardants. The work led to the issuance of over 60 United States Patents and eventually to the commercialization of two products. A major success was the discovery of a flame retardant additive now manufactured under the trade name FF-680. This compound is accepted by the plastics industry as a non-toxic, environmentally acceptable replacement for the polybrominated biphenyls formerly used.
During the course of my employment in Michigan, I coordinated efforts with applications chemists/engineers on structure-property relationship studies for polymer additives. I developed industrial processes for flame retardants using the Williamson ether synthesis. Additional studies were performed for phase transfer catalysis assisted synthetic routes to flame retardants and herbicide intermediates. Halogenated telomers were suggested and studied as polymer modifiers. Exploratory research was conducted on unique halogenated intumescent compounds for potential civilian/military uses.
As a group leader at Stepan Chemical, I and members of my group conducted syntheses of flavor and fragrance compounds, feasibility studies of novel synthetic routes to surfactants, and the preparation of aldehydes via oxidation.
PRESENT
Since beginning my own consultancy, I have been involved in a wide array of projects. Significant projects include the following:
Chemical modification of corn starch
New thermoplastic elastomers
Thermal/photochemical stable organic bromine compounds
Alkylene oxide derivatives
4-Aminophenol derivatives
Institutional cleaning product formulations
Fluorocarbon fire extinguishers
Phase-transfer catalysis techniques applied to industrial processes
Flame retardant applications
Anionic and non-ionic surfactant syntheses
My plans for future work lie in three main areas.
1. Nucleophilic Substitution Reactions: For over twenty years I have maintained an on-going interest in this generalized reaction. The Williamson ether synthesis and metal hydride reactions, typically very efficient, have historically proven to be effective tools in organic synthesis. I intend to investigate further applications of these and other nucleophilic substitution reactions in the synthesis of highly symmetrical compounds.
2. Organic Halogen Compounds: Organic bromine and chlorine compounds, because of their accessibility, outnumber the corresponding fluorine and iodine analogs. Organobromine and chlorine compounds have very similar chemistry; in many cases the extremes of fluorine and iodine substitution give rise to unique chemistries. My intentions are to investigate this aspect of halogen chemistry in more detail.
3. N For One Synthesis: An ideal chemical process is one in which each molecule entering a chemical process exits as a useful new molecule. I wish to investigate synthetic routes with the potential of giving N =2,3,... useful molecules per reaction.
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2001, University of Wisconsin-Parkside. All rights reserved. Questions, comments and suggestions should be directed to kolb@uwp.edu |