Chris Chappelow - Midland MI, US Edward Daugs - Midland MI, US Sterling Gatling - Midland MI, US Kevin Sikkema - Midland MI, US Maciej Turowski - Midland MI, US Ross Wallingford - Scott Depot WV, US
International Classification:
A61K 31/765 C08G 65/32
US Classification:
424078380, 525409000
Abstract:
The invention is directed toward novel high molecular weight and high purity mPEG alcohol compositions as well as a process for obtaining said compositions by removing PEG diols from the mPEG alcohol after polymerization is complete.
Injection Stretch Blow Molding Process Using Polylactide Resins
Kevin Cink - Brooklyn Park MN, US Richard Bopp - Golden Valley MN, US Kevin Sikkema - Midland MI, US
Assignee:
NATUREWORKS LLC - Minnetonka MN
International Classification:
B29C 49/06 B29C 49/10 B29C 49/64 B29C 49/22
US Classification:
264510000, 264532000, 264535000, 264537000
Abstract:
Containers are manufactured in an injection stretch molding process using a PLA resin having a specified ratio of lactic acid stereoisomers and stretch ratios. The process permits good quality containers to be made at good operating rates.
Analysis Of High Molecular Weight Mpeg Alcohol Compositions
Chris Chappelow - Midland MI, US Edward D. Daugs - Midland MI, US Sterling C. Gatling - Midland MI, US Kevin D. Sikkema - Midland MI, US Maciej Turowski - Midland MI, US Ross A. Wallingford - Scott Depot WV, US
International Classification:
G01N 33/44
US Classification:
436 85
Abstract:
The invention is directed toward novel high molecular weight and high purity mPEG alcohol compositions as well as a process for obtaining said compositions by removing PEG diols from the mPEG alcohol after polymerization is complete.
Mehmet Demirors - Midland MI Duane B. Priddy - Midland MI Nicolaas M. A. Hermans - Terneuzen, NL Rudi H. E. Veraart - Terneuzen, NL Albert J. Heuvelsland - Heikant, NL Kevin D. Sikkema - Midland MI
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08L 5104
US Classification:
525 86
Abstract:
The present invention is directed to rubber modified polymers which contain a non-block grafted rubber having a degree of grafting of at least 30 percent at the point of phase inversion and a specified amount of grafted vinyl aromatic polymer.
Preparation Of Ketone Containing Photodegradable Polymers
James J. O'Brien - Midland MI Kevin D. Sikkema - Midland MI Duane B. Priddy - Midland MI
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08F 200 C08F21636
US Classification:
526 75
Abstract:
A process for preparing polymers comprising pendant ketone functional moieties, the steps of the process comprising exposing a mixture comprising an ethylenically unsaturated addition polymerizable monomer and a. beta. -substituted ketone compound corresponding to the formula: XCH. sub. 2 --CHR'--C(O)R where X is a suitable leaving group, R' is hydrogen or R; and R is alkyl or aryl of up to 12 carbons to vinyl ketone monomer formation conditions to prepare the corresponding vinyl ketone monomer from the. beta. -substituted ketone compound and subsequently exposing the mixture to addition polymerization conditions to prepare the resulting polymer.
Kevin D. Sikkema - Midland MI Duane B. Priddy - Midland MI
Assignee:
The Dow Chemical Company - Midland MI
International Classification:
C08F22606 C08F22400
US Classification:
526258
Abstract:
Photodegradable and biodegradable polymers comprising both ketone functionality and hydrolyzable polymer ester or amide functionality and thermoplastic articles formed therefrom are disclosed.
- KANSAS CITY KS, US - AUSTIN TX, US KEVIN SIKKEMA - OVERLAND PARK KS, US JOHN BOOREM - KANSAS CITY KS, US AARON BOOREM - LEAVENWORTH KS, US KURT CHESHIRE - SHAWNEE KS, US KISHORE K. MOHANTY - AUSTIN TX, US KRISHNA PANTHI - CEDAR PARK TX, US HIMANSHU SHARMA - AUSTIN TX, US PINAKI GHOSH - AUSTIN TX, US
The present invention is directed to surfactants with small hydrophobes, which are of non-conventional hydrophobe size. The surfactants of the present invention utilize a small hydrophobic moiety with a polvalkoxylate chain comprising PO, BO and/or EO groups, with optional ionic groups, such as anionic, cationic and zwitterionic, to achieve the desired hydrophilic-lipophilic balance (HLB). The present invention is further directed to formulations comprising the surfactants of the invention, and methods of using the surfactants of the invention, including in enhanced oil recovery applications.
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