Far Research, Inc. (Dba Far Chemical, Inc.
Commercial Director
Ascend Performance Materials Mar 2012 - Feb 2016
Technology Manager
Vertellus Aug 2010 - Mar 2012
Director of Applications Development
Evonik Goldschmidt Feb 2009 - Aug 2010
Plant Manager-Polyethers
Evonik Goldschmidt Aug 2007 - Feb 2009
Technology Manager-Silicones, North America
Education:
Carnegie Mellon University 1990 - 1994
Bachelors, Bachelor of Science, Chemistry
University of Florida
Doctorates, Doctor of Philosophy, Chemistry
Skills:
Coatings Polymers Chemistry Polymer Chemistry R&D Plastics Manufacturing Adhesives Resin Research and Development Process Engineering Product Development Polymer Science Commercialization Market Development Organic Chemistry Materials Business Development Cross Functional Team Leadership Management Additives Technology Transfer Strategic Planning Business Strategy Marketing Strategy Sales Stage Gate Change Management Communication Project Management Strategy Sales Management Portfolio Management Process Optimization Account Management New Product Implementations Innovation Management Sap Customer Relationship Management R
John D. Morris - Naperville IL Barbara E. Moriarty - Palatine IL Mingli Wei - Naperville IL Patrick G. Murray - Yorkville IL Jerry L. Reddinger - Round Rock TX
Fluorescent monomers are described and claimed which are synthesized by reacting a substituted or non-substituted naphthalic anhydride with an amine and with a moiety containing a polymerizable group. Such monomers are useful for the preparation of tagged treatment polymers. Such tagged treatment polymers are useful as scale inhibitors in industrial water systems.
Fluorescent Monomers And Tagged Treatment Polymers Containing Same For Use In Industrial Water Systems
John D. Morris - Naperville IL, US Barbara E. Moriarty - Palatine IL, US Mingli Wei - Naperville IL, US Patrick G. Murray - Yorkville IL, US Jerry L. Reddinger - Kingsport TN, US
Assignee:
Nalco Company - Naperville IL
International Classification:
C07D 487/02 C07D 471/02
US Classification:
546 52, 546 47
Abstract:
Fluorescent monomers are described and claimed which are synthesized by reacting a substituted or non-substituted naphthalic anhydride with an amine and with a moiety containing a polymerizable group. Such monomers are useful for the preparation of tagged treatment polymers. Such tagged treatment polymers are useful as scale inhibitors in industrial water systems.
Fluorescent Monomers And Tagged Treatment Polymers Containing Same For Use In Industrial Water Systems
John D. Morris - Naperville IL, US Barbara E. Moriarty - Palatine IL, US Mingli Wei - Naperville IL, US Patrick G. Murray - Yorkville IL, US Jerry L. Reddinger - Kingsport TN, US
Fluorescent monomers are described and claimed which are synthesized by reacting a substituted or non-substituted naphthalic anhydride with an amine and with a moiety containing a polymerizable group. Such monomers are useful for the preparation of tagged treatment polymers. Such tagged treatment polymers are useful as scale inhibitors in industrial water systems.
Fluorescent Monomers And Tagged Treatment Polymers Containing Same For Use In Industrial Water Systems
John D. Morris - Naperville IL, US Barbara E. Moriarty - Palatine IL, US Mingli Wei - Naperville IL, US Patrick G. Murray - Yorkville IL, US Jerry L. Reddinger - Kingsport TN, US
Assignee:
Nalco Company - Naperville IL
International Classification:
C07D 221/06
US Classification:
546 79
Abstract:
Fluorescent monomers are described and claimed which are synthesized by reacting a substituted or non-substituted naphthalic anhydride with an amine and with a moiety containing a polymerizable group. Such monomers are useful for the preparation of tagged treatment polymers. Such tagged treatment polymers are useful as scale inhibitors in industrial water systems.
Crosslinked Polysiloxanes, A Process For Their Preparation And Use Of The Crosslinked Polysiloxanes In Emulsifier Systems For Water-In-Oil Emulsions
Thomas Neumann - Bochum, DE Burghard Gruening - Essen, DE Anna Howe - Moseley VA, US Dana Adkins - Quinton VA, US Jerry Reddinger - Chesterfield VA, US
Assignee:
Evonik Goldschmidt GmbH - Essen
International Classification:
A61K 31/74 C08G 77/04
US Classification:
424 7802, 525474
Abstract:
The invention relates to crosslinked organopolysiloxanes which are linked by a polyether building block via the Si atoms, to emulsifier systems which have these crosslinked organopolysiloxanes, and also to cosmetic, dermatological or pharmaceutical formulations comprising a crosslinked organopolysiloxane or an emulsifier system comprising these.
Synergistic Amine Chain Extenders In Polyurea Spray Elestomers
Howard Klein - Singapore, SG Jerry Reddinger - Sewickley PA, US Kenneth Hillman - Spring TX, US Mark Posey - Spring TX, US
Assignee:
Huntsman Petrochemical Corporation - The Woodlands TX
International Classification:
C08G 18/00
US Classification:
528044000
Abstract:
Disclosed are derivatives of isophorone diamine exhibiting a synergistic relationship with other commonly employed chain extenders offerings enhanced efficacy with regard to slowing of the polyurea elastomer cure profile, and processes employing their use. According to the invention, extensions of the gel-free and tack-free times are more readily achieved at lower loading levels for these chain extender blends than are afforded through the sole use of the individual molecules.
Fluorescent Compounds For Use In Industrial Water Systems
Fluorescent compounds of the formula: wherein R and R are either both SO M, or one of R and R is SO M and the other is COOM, where M is selected from the group consisting of H, Na, K, Rb, Cs, Li or ammonium, are described and claimed. These inert flurorescent compounds have been found to be resistant to oxidizing biocides. One process for making these compounds is described and claimed as the condensation between a 1,8-naphthalic anhydride possessing the desired functionalities and the appropriately substituted o-phenylene diamine. Alternatively, o-amino-nitro-aromatics may be condensed with the various 1,8-naphthalic anhydrides when the in situ reduction of the nitro group is accomplished with a suitable reducing agent such as iron powder. The resulting fluorescent compounds can be used as inert fluorescent tracers in industrial water systems.
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