C08G61/08

ALKENE ISOMERIZATION AS AN ENTRY TO EFFICIENT ALTERNATING RING-OPEINING METATHESIS POLYMERIZATION (i-AROMP)
20180002481 · 2018-01-04 ·

This invention relates to the field of polymers and olefin polymerization, and more specifically olefin metathesis polymerization. Specifically, the present invention provides a polymer comprising rigorously alternating AB subunits and methods of formation of the AB alternating polymers. In the polymers and process of the invention, the A monomer is derived from a cyclobutene derivative, and the B monomer is derived from a cyclohexene derivative. The polymerization takes place in the presence of an olefin metathesis catalyst.

ALKENE ISOMERIZATION AS AN ENTRY TO EFFICIENT ALTERNATING RING-OPEINING METATHESIS POLYMERIZATION (i-AROMP)
20180002481 · 2018-01-04 ·

This invention relates to the field of polymers and olefin polymerization, and more specifically olefin metathesis polymerization. Specifically, the present invention provides a polymer comprising rigorously alternating AB subunits and methods of formation of the AB alternating polymers. In the polymers and process of the invention, the A monomer is derived from a cyclobutene derivative, and the B monomer is derived from a cyclohexene derivative. The polymerization takes place in the presence of an olefin metathesis catalyst.

Superconducting coil device and method for producing same

A superconducting coil device (10) includes: a coil case (20) housing a superconducting coil (30); a superconducting coil (30) housed in the coil case (20); and a resin part (50) formed of a polymer (51) filled in a gap between an inner wall of the coil case (20) and the superconducting coil (30). The resin part (50) is formed of a polymer (51) obtained by polymerizing a polymerizable composition containing a first monomer having a norbornene ring structure.

Superconducting coil device and method for producing same

A superconducting coil device (10) includes: a coil case (20) housing a superconducting coil (30); a superconducting coil (30) housed in the coil case (20); and a resin part (50) formed of a polymer (51) filled in a gap between an inner wall of the coil case (20) and the superconducting coil (30). The resin part (50) is formed of a polymer (51) obtained by polymerizing a polymerizable composition containing a first monomer having a norbornene ring structure.

Phase difference film and production method for the same
11709302 · 2023-07-25 · ·

Provided is a phase difference film formed of a resin containing a polymer having crystallizability. The phase difference film has an NZ factor of less than 1 and an in-plane retardation Re that satisfies 125 nm≤Re≤345 nm. The polymer has a crystallization degree of 15% or more. Alternatively, the polymer is an alicyclic structure-containing polymer being a hydrogenated product of a ring-opening polymer of dicyclopentadiene.

Phase difference film and production method for the same
11709302 · 2023-07-25 · ·

Provided is a phase difference film formed of a resin containing a polymer having crystallizability. The phase difference film has an NZ factor of less than 1 and an in-plane retardation Re that satisfies 125 nm≤Re≤345 nm. The polymer has a crystallization degree of 15% or more. Alternatively, the polymer is an alicyclic structure-containing polymer being a hydrogenated product of a ring-opening polymer of dicyclopentadiene.

ASSOCIATIVE POLYMERS AND RELATED COMPOSITIONS, METHODS AND SYSTEMS
20230235127 · 2023-07-27 ·

Described herein are associative polymers capable of controlling a physical and/or chemical property of non-polar compositions and related compositions, methods and systems. Associative polymers herein described have a non-polar backbone and functional groups presented at ends of the non-polar backbone, with a number of the functional groups presented at the ends of the non-polar backbone formed by associative functional groups capable of undergoing an associative interaction with another associative functional group with an association constant (k) such that the strength of each associative interaction is less than the strength of a covalent bond between atoms and in particular less than the strength of a covalent bond between backbone atoms.

ASSOCIATIVE POLYMERS AND RELATED COMPOSITIONS, METHODS AND SYSTEMS
20230235127 · 2023-07-27 ·

Described herein are associative polymers capable of controlling a physical and/or chemical property of non-polar compositions and related compositions, methods and systems. Associative polymers herein described have a non-polar backbone and functional groups presented at ends of the non-polar backbone, with a number of the functional groups presented at the ends of the non-polar backbone formed by associative functional groups capable of undergoing an associative interaction with another associative functional group with an association constant (k) such that the strength of each associative interaction is less than the strength of a covalent bond between atoms and in particular less than the strength of a covalent bond between backbone atoms.

Post-Synthesis Backbone Modification of Polypentenamer Rubber and Related Tire Compositions

Rubber compounds may comprise: an epoxidized polypentenamer rubber (CPR) and/or a hydrolyzed epoxidized CPR; and a filler comprising silica particles. One nonlimiting example is rubber compound comprising: phr to 90 phr of a styrene-butadiene rubber (SBR), a natural rubber (NR), and/or a butadiene rubber (BR); 10 phr to 50 phr of a epoxidized CPR and/or a hydrolyzed epoxidized CPR; and 10 phr to 200 phr of a filler comprising silica particles, wherein the SBR, the NR, the BR, the epoxidized CPR, and the hydrolyzed epoxidized CPR combined equal 100 parts. Rubber compounds comprising epoxidized CPR and/or a hydrolyzed epoxidized CPR; and a filler comprising silica particles may be useful in tire compositions.

Post-Synthesis Backbone Modification of Polypentenamer Rubber and Related Tire Compositions

Rubber compounds may comprise: an epoxidized polypentenamer rubber (CPR) and/or a hydrolyzed epoxidized CPR; and a filler comprising silica particles. One nonlimiting example is rubber compound comprising: phr to 90 phr of a styrene-butadiene rubber (SBR), a natural rubber (NR), and/or a butadiene rubber (BR); 10 phr to 50 phr of a epoxidized CPR and/or a hydrolyzed epoxidized CPR; and 10 phr to 200 phr of a filler comprising silica particles, wherein the SBR, the NR, the BR, the epoxidized CPR, and the hydrolyzed epoxidized CPR combined equal 100 parts. Rubber compounds comprising epoxidized CPR and/or a hydrolyzed epoxidized CPR; and a filler comprising silica particles may be useful in tire compositions.