Patent classifications
C08F8/02
Polymer Nanodiscs for Biotechnology and Medical Applications
The present invention includes compositions, methods, and methods of making and using a nanoscale discoidal membrane comprising: an amphiphilic membrane patch comprising self-assembled molecular amphiphiles capable of supporting one or more membrane proteins in the amphiphilic membrane patch; and one or more amphipathic scaffold macromolecules that encase the nanoscale discoidal membrane.
Functionalized Resin Having A Polar Linker
- Fabian Peters ,
- Emily Baird Anderson ,
- John Dayton Baker, Jr. ,
- Terri Roxanne Carvagno ,
- Judicael Jacques Chapelet ,
- Wei Min Cheng ,
- Liu Deng ,
- Jacobus Gillis De Hullu ,
- Sebastian Finger ,
- Hubert Hirschlag ,
- Christopher Lee Lester ,
- Wentao Li ,
- Mutombo Joseph Muvundamina ,
- Mark Stanley Pavlin ,
- Carla Recker ,
- Christopher Thomas Scilla
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
Functionalized Resin Having A Polar Linker
- Fabian Peters ,
- Emily Baird Anderson ,
- John Dayton Baker, Jr. ,
- Terri Roxanne Carvagno ,
- Judicael Jacques Chapelet ,
- Wei Min Cheng ,
- Liu Deng ,
- Jacobus Gillis De Hullu ,
- Sebastian Finger ,
- Hubert Hirschlag ,
- Christopher Lee Lester ,
- Wentao Li ,
- Mutombo Joseph Muvundamina ,
- Mark Stanley Pavlin ,
- Carla Recker ,
- Christopher Thomas Scilla
Polar silane linkers are provided that attach to resins to form silane-functionalized resins. The functionalized resins can be bound to hydroxyl groups on the surface of silica particles to improve the dispersibility of the silica particles in rubber mixtures. Further disclosed are synthetic routes to provide the silane-functionalized resins, as well as various uses and end products that benefit from the unexpected properties of the silane-functionalized resins. Silane-functionalized resins impart remarkable properties on various rubber compositions, such as tires, belts, hoses, brakes, and the like. Automobile tires incorporating the silane-functionalized resins are shown to possess excellent results in balancing the properties of rolling resistance, tire wear, and wet braking performance.
VINYL THERMOSETTING RESIN COMPOSITION, PREPREG, LAMINATE, AND PRINTED CIRCUIT BOARD
A vinyl thermosetting resin composition, a prepreg, a laminate, and a printed circuit board are provided. The vinyl thermosetting resin composition has a vinyl thermosetting resin, a curing agent, and hollow borosilicate microspheres with surfaces chemically modified by a vinyl polyphenylene ether resin. The laminate not only has excellent overall properties such as low dielectric constant, low dielectric loss, low water absorption rate, good heat resistance, and the like, but also has only small fluctuations in dielectric constants between batches, which can satisfy the requirements for dielectric constant stability and/or thickness consistency of a substrate.
SYNTHESIS OF STAR ISOBUTYLENE-BASED THERMOPLASTIC ELASTOMERS
A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having either a styrene oligomer or -methyl styrene oligomer, wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.
SYNTHESIS OF STAR ISOBUTYLENE-BASED THERMOPLASTIC ELASTOMERS
A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having either a styrene oligomer or -methyl styrene oligomer, wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.
STAR ISOBUTYLENE-BASED THERMOPLASTIC ELASTOMERS
A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having a styrene oligomer wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.
STAR ISOBUTYLENE-BASED THERMOPLASTIC ELASTOMERS
A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having a styrene oligomer wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.
HIGH-STRENGTH LOW-CREEP THERMOPLASTIC ELASTOMER
A polystyrene-g-(polyisobutylene-b-polystyrene) is taught. The polystyrene-g-(polyisobutylene-b-polystyrene) is synthesized by first providing a polystyrene backbone. Once the polystyrene backbone is provided, the polystyrene backbone is acetylated to provide acetyl groups on the polystyrene backbone. Next, the acetyl groups are converted to C(CH.sub.3).sub.2OH groups. Finally, the living polymerization of isobutylene is initiated, which is then followed by the living block polymerization of styrene. A polymer network of polystyrene-g-(polyisobutylene-b-polystyrene)s is also provided.
HIGH-STRENGTH LOW-CREEP THERMOPLASTIC ELASTOMER
A polystyrene-g-(polyisobutylene-b-polystyrene) is taught. The polystyrene-g-(polyisobutylene-b-polystyrene) is synthesized by first providing a polystyrene backbone. Once the polystyrene backbone is provided, the polystyrene backbone is acetylated to provide acetyl groups on the polystyrene backbone. Next, the acetyl groups are converted to C(CH.sub.3).sub.2OH groups. Finally, the living polymerization of isobutylene is initiated, which is then followed by the living block polymerization of styrene. A polymer network of polystyrene-g-(polyisobutylene-b-polystyrene)s is also provided.