C08F8/06

REMOVAL OF THIOCARBONYLTHIO END GROUPS FROM POLYMERS

Embodiments of the present disclosure describe a method of removing an end group from a polymer comprising contacting a polymer having a thiocarbonylthio end group, or a solution containing such a polymer, with an excess of a borane compound in the presence of oxygen. Embodiments of the present disclosure further describe a method of polymerization comprising contacting one or more monomers with an initiator and a chain transfer agent to form a polymer having a thiocarbonylthio end group in a reaction solution and contacting the polymer with a borane compound in the presence of oxygen to remove the thiocarbonylthio end group from the polymer.

REMOVAL OF THIOCARBONYLTHIO END GROUPS FROM POLYMERS

Embodiments of the present disclosure describe a method of removing an end group from a polymer comprising contacting a polymer having a thiocarbonylthio end group, or a solution containing such a polymer, with an excess of a borane compound in the presence of oxygen. Embodiments of the present disclosure further describe a method of polymerization comprising contacting one or more monomers with an initiator and a chain transfer agent to form a polymer having a thiocarbonylthio end group in a reaction solution and contacting the polymer with a borane compound in the presence of oxygen to remove the thiocarbonylthio end group from the polymer.

Method of producing protected particles of cathode active materials for lithium batteries
11223049 · 2022-01-11 · ·

A method of producing a powder mass for a lithium battery, the method comprising: (a) providing a solution containing a sulfonated elastomer dissolved in a solvent or a precursor in a liquid form or dissolved in a solvent; (b) dispersing a plurality of particles of a cathode active material in the solution to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing/curing the precursor to form the powder mass, wherein the powder mass comprises multiple particulates and at least a particulate comprises one or a plurality of particles of a cathode active material being encapsulated by a thin layer of sulfonated elastomer having a thickness from 1 nm to 10 μm, a fully recoverable tensile strain from 2% to 800%, and a lithium ion conductivity from 10.sup.−7 S/cm to 5×10.sup.−2 S/cm at room temperature.

Method of producing protected particles of cathode active materials for lithium batteries
11223049 · 2022-01-11 · ·

A method of producing a powder mass for a lithium battery, the method comprising: (a) providing a solution containing a sulfonated elastomer dissolved in a solvent or a precursor in a liquid form or dissolved in a solvent; (b) dispersing a plurality of particles of a cathode active material in the solution to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing/curing the precursor to form the powder mass, wherein the powder mass comprises multiple particulates and at least a particulate comprises one or a plurality of particles of a cathode active material being encapsulated by a thin layer of sulfonated elastomer having a thickness from 1 nm to 10 μm, a fully recoverable tensile strain from 2% to 800%, and a lithium ion conductivity from 10.sup.−7 S/cm to 5×10.sup.−2 S/cm at room temperature.

Method for preparing graft copolymer and thermoplastic resin molded article

The present invention relates to a method for preparing a graft copolymer including polymerizing a conjugated diene-based monomer to prepare a small-size conjugated diene-based polymer; enlarging the small-size conjugated diene-based polymer to prepare a large-size conjugated diene-based polymer; and polymerizing the small-size conjugated diene-based polymer, the large-size conjugated diene-based polymer, an aromatic vinyl-based monomer and a vinyl cyan-based monomer to prepare a graft copolymer, wherein a weight ratio of the small-size conjugated diene-based polymer and the large-size conjugated diene-based polymer is 10:90 to 40:60 in preparing the graft copolymer.

CURE AND FUNCTIONALIZATION OF OLEFIN/SILANE INTERPOLYMERS

A process to form a crosslinked composition comprising thermally treating a composition at a temperature ≥ 25° C., in the presence of moisture, and wherein the composition comprises the following components: a) an olefin/silane interpolymer, b) a cure catalyst selected from the following: i) a metal alkoxide, ii) a metal carboxylate, iii) a metal sulfonate, iv) an aryl sulfonic acid, v) a tris-aryl borane, vi) any combination of two or more from i)-v). Also, a composition comprising the following components a and b, as described above. A process to form an olefin/alkoxysilane interpolymer, and the corresponding composition, said process comprising thermally treating a composition comprising the following components: a) an olefin/silane interpolymer, b) an alcohol, and c) a Lewis acid.

CURE AND FUNCTIONALIZATION OF OLEFIN/SILANE INTERPOLYMERS

A process to form a crosslinked composition comprising thermally treating a composition at a temperature ≥ 25° C., in the presence of moisture, and wherein the composition comprises the following components: a) an olefin/silane interpolymer, b) a cure catalyst selected from the following: i) a metal alkoxide, ii) a metal carboxylate, iii) a metal sulfonate, iv) an aryl sulfonic acid, v) a tris-aryl borane, vi) any combination of two or more from i)-v). Also, a composition comprising the following components a and b, as described above. A process to form an olefin/alkoxysilane interpolymer, and the corresponding composition, said process comprising thermally treating a composition comprising the following components: a) an olefin/silane interpolymer, b) an alcohol, and c) a Lewis acid.

Method for producing low molecular weight polytetrafluoroethylene, low molecular weight polytetrafluoroethylene, and powder

Powder including low molecular weight polytetrafluoroethylene having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having an average particle size of 1.0 to 50 μm, and containing 30 or more carboxyl groups at ends of the molecule chain per 10.sup.6 carbon atoms in the main chain, wherein the powder is substantially free from C8-C14 perfluorocarboxylic acids and salts thereof.

Method for producing low molecular weight polytetrafluoroethylene, low molecular weight polytetrafluoroethylene, and powder

Powder including low molecular weight polytetrafluoroethylene having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having an average particle size of 1.0 to 50 μm, and containing 30 or more carboxyl groups at ends of the molecule chain per 10.sup.6 carbon atoms in the main chain, wherein the powder is substantially free from C8-C14 perfluorocarboxylic acids and salts thereof.

Method for producing low molecular weight polytetrafluoroethylene, low molecular weight polytetrafluoroethylene, and powder

Powder including low molecular weight polytetrafluoroethylene having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having a melt viscosity of 1×10.sup.2 to 7×10.sup.5 Pa.Math.s at 380° C., having an average particle size of 1.0 to 50 μm, and containing 30 or more carboxyl groups at ends of the molecule chain per 10.sup.6 carbon atoms in the main chain, wherein the powder is substantially free from C8-C14 perfluorocarboxylic acids and salts thereof.