DR. MICHAEL THOMAS SMITH, D.D.S.
Dentist at Wackerly St, Midland, MI
License number
Michigan 015385
Category
Dentist
Type
General Practice
Address
Address
2509 W Wackerly St, Midland, MI 48640
Phone
(989) 633-9811
Professional information
Dr. Michael T Smith, Midland MI - DDS (Doctor of Dental Surgery)
Specialties:
Dentistry
Address:
2509 W Wackerly St, Midland 48640
(989) 633-9811 (Phone)
(989) 633-9811 (Phone)
Languages:
English
Education:
Medical School
Graduates of Institutions Not Listed As Medical Schools
Graduates of Institutions Not Listed As Medical Schools
Michael Smith - Midland, MI
Work:
Dow Chemical Co
chemical operator Hancor - Findlay, OH
Outside Sales Representative Good Year Tire and rubbler manufacturer - Midland, MI
Manager
chemical operator Hancor - Findlay, OH
Outside Sales Representative Good Year Tire and rubbler manufacturer - Midland, MI
Manager
Education:
Delta College
Associates of Applied Science in chemical processing technology Northwood University
Bachelors of Business Administration in marketing/management, economics and international business University of Ohio
school and surveying University of Indiana
Associates of Applied Science in chemical processing technology Northwood University
Bachelors of Business Administration in marketing/management, economics and international business University of Ohio
school and surveying University of Indiana
Michael Smith - Midland, MI
Work:
Delta College
Chemcial processing AAS Rock Youth center
Independent sales Representative Hancor, Goodyear Tire and rubber co.
Chemcial processing AAS Rock Youth center
Independent sales Representative Hancor, Goodyear Tire and rubber co.
Education:
Delta College AAS
chemical Northwood University BBA
marketing/management, economic and international bu ine University of Ohio
school and surveying University of Indiana
community
chemical Northwood University BBA
marketing/management, economic and international bu ine University of Ohio
school and surveying University of Indiana
community
Michael Smith - Midland, MI
Work:
Envirotech Coatings
Shift Supervisor / Operator Pasquale & Sons, LLC - Midland, MI
Owner / Supervisor Envirotech Coatings - Midland, MI
Operator / Industrial Painter Smitty's Paint - Midland, MI
Owner / Supervisor
Shift Supervisor / Operator Pasquale & Sons, LLC - Midland, MI
Owner / Supervisor Envirotech Coatings - Midland, MI
Operator / Industrial Painter Smitty's Paint - Midland, MI
Owner / Supervisor
Education:
Delta College - Saginaw, MI
Business High Point High School - Beltsville, MD
Diploma in General Education
Business High Point High School - Beltsville, MD
Diploma in General Education
Silicone Composition And Cured Silicone Resin
US Patent:
2007026, Nov 8, 2007
Filed:
Nov 1, 2005
Appl. No.:
11/662857
Inventors:
Michael Smith - Midland MI, US
Bizhong Zhu - Midland MI, US
Bizhong Zhu - Midland MI, US
International Classification:
C08K 5/54, C08L 83/04
US Classification:
556431000
Abstract:
A silicone composition according to the present invention comprises (A) an organopolysiloxane resin having an average of at least two silicon-bonded alkenyl groups per molecule, (B) an organohydrogensilane in an amount sufficient to cure the composition, (C) an effective amount of a reactive diluent comprising (i) an organosiloxane having an average of at least two alkenyl groups per molecule and a viscosity of from 0.001 to 2 Pa·s at 25° C., wherein the viscosity of (C)(i) is not greater than 20% of the viscosity of component (A), and (ii) an organohydrogensiloxane having an average of at least two silicon-bonded hydrogen atoms per molecule and a viscosity of from 0.001 to 2 Pa·s at 25° C., in an amount sufficient to provide from 0.5 to 3 moles of silicon-bonded hydrogen atoms in (C)(ii) to moles of alkenyl groups in (C)(i), and (D) a catalytic amount of a hydrosilylation catalyst; and a cured silicone resin prepared by curing the silicone composition.
Method Of Making Branched Polysilane Copolymers
US Patent:
2009012, May 14, 2009
Filed:
Mar 29, 2006
Appl. No.:
11/884611
Inventors:
Travis Hein - Bay City MI, US
Russell King - Midland MI, US
Binh Thanh Nguyen - Midland MI, US
Herschel Henry Reese - Midland MI, US
Michael Andrew Smith - Midland MI, US
Hanh Xuan Vo - Midland MI, US
Russell King - Midland MI, US
Binh Thanh Nguyen - Midland MI, US
Herschel Henry Reese - Midland MI, US
Michael Andrew Smith - Midland MI, US
Hanh Xuan Vo - Midland MI, US
International Classification:
C08G 77/00
US Classification:
528 10
Abstract:
Branched polysilane copolymers are prepared via a Wurtz-type coupling reaction by reacting a mixture of two different dihalosilanes and a single trihalosilane with an alkali metal coupling agent in an organic liquid medium. The branched polysilane copolymers are recovered from the reaction mixture. Capped branched polysilane copolymers are prepared via the same Wurtz-type coupling reaction with addition of a capping agent to the reaction mixture. The capping agent is a monohalosilane, monoalkoxysilane, dialkoxysilane, or trialkoxysilane. The branched polysilane copolymers and the capped branched polysilane copolymers are soluble in organic liquid medium.
Method Of Making Branched Polysilanes
US Patent:
2007016, Jul 19, 2007
Filed:
May 10, 2005
Appl. No.:
11/578630
Inventors:
Travis Hein - Bay City MI, US
Russell King - Midland MI, US
Binh Nguyen - Midland MI, US
Herschel Reese - Midland MI, US
Michael Smith - Midland MI, US
Hanh Vo - Midland MI, US
Russell King - Midland MI, US
Binh Nguyen - Midland MI, US
Herschel Reese - Midland MI, US
Michael Smith - Midland MI, US
Hanh Vo - Midland MI, US
International Classification:
C08G 77/00
US Classification:
528010000, 528031000
Abstract:
In a first method, branched polysilanes are prepared via a Wurtz-type coupling reaction by reacting a mixture of a dihalosilanes and a trihalosilanes with an alkali metal coupling agent in an organic liquid medium. The reaction mixture is free of tetrahalosilanes. The branched polysilanes are recovered from the reaction mixture. In a second method, capped-branched polysilanes are prepared via the same Wurtz-type coupling reaction noted above, with the addition of a capping agent to the reaction mixture. The capping agent can be a monohalosilane, monoalkoxysilane, or trialkoxysilane. Capped-branched polysilanes are re-covered from the reaction mixture. The branched polysilanes are soluble in organic liquid mediums.