C08C2/04

BINDER COMPOSITION FOR NON-AQUEOUS SECONDARY BATTERY POSITIVE ELECTRODE, COMPOSITION FOR NON-AQUEOUS SECONDARY BATTERY POSITIVE ELECTRODE, POSITIVE ELECTRODE FOR NON-AQUEOUS SECONDARY BATTERY, AND NON-AQUEOUS SECONDARY BATTERY, AND METHODS FOR PRODUCING COMPOSITION FOR NON-AQUEOUS SECONDARY BATTERY POSITIVE ELECTRODE, POSITIVE ELECTRODE FOR NON-AQUEOUS SECONDARY BATTERY, AND NON-AQUEOUS SECONDARY BATTERY

Provided is a binder composition for a non-aqueous secondary battery positive electrode that can form a positive electrode with which it is possible to obtain a non-aqueous secondary battery having excellent life characteristics even when aging treatment is carried out under low-temperature and low-depth of charge conditions. The binder composition contains a first binder, iron, and at least one of ruthenium and rhodium. The total iron, ruthenium, and rhodium content is no greater than 5×10.sup.−3 parts by mass per 100 parts by mass of the first binder.

HYDROGENATED NITRILE RUBBER WITH REDUCED CATALYST IMPURITY

The residual hydrogenation catalyst from the hydrogenated nitrile rubber solution is recovered by using two steps such as (1) the catalyst extraction step with an ammonium salt and water (optionally including an oxidation step) to extract catalyst from the HNBR polymer chain to the solvent and then (2) the separation/column recovery step with the column packed with functional ion exchange resins for the separation of ammonia-catalyst complex from hydrogenated nitrile rubber solution and the column recovery for the high catalyst recovery with functional groups of resins. The ammonium salt for the catalyst extraction step is selected from ammonium chloride, ammonium bromide, ammonium iodide, and ammonium acetate. The functional groups in the functional ion exchange resins for packing the column is selected from thiourea, thiouronium, thiol, amine, diamine, triamine, TMT, dithiocarbamate, and carbodithioate.

Method for producing hydrogenated conjugated diene polymer latex
10899851 · 2021-01-26 · ·

A method for producing a hydrogenated conjugated diene polymer latex includes: a hydrogenation step of dissolving or dispersing a hydrogenation catalyst containing a platinum group element in a latex of a conjugated diene polymer to hydrogenate a carbon-carbon unsaturated bond in the conjugated diene polymer; and an insoluble complex formation step of complexing the platinum group element in the latex with a complexing agent to form an insoluble complex, wherein pH of the latex at the insoluble complex formation step is controlled in a range of 5.0 to 8.0.

Process for recovery of residual hydrogenation catalyst from hydrogenated nitrile rubber solution

Residual hydrogenation catalyst produced from reduction of nitrile rubber is recovered by a chelation step using a chelating agent and a series of extraction using semi-coagulation with polar solvents and an optional washing steps for the separation of catalyst-chelating agent complex from hydrogenated nitrile rubber solution. The chelating agent is selected from xanthate, dithiocarbamate, and trithiocarbonate compounds.

Process for recovery of residual hydrogenation catalyst from hydrogenated nitrile rubber solution

Residual hydrogenation catalyst produced from reduction of nitrile rubber is recovered by a chelation step using a chelating agent and a series of extraction using semi-coagulation with polar solvents and an optional washing steps for the separation of catalyst-chelating agent complex from hydrogenated nitrile rubber solution. The chelating agent is selected from xanthate, dithiocarbamate, and trithiocarbonate compounds.

High molecular weight functionalized olefin copolymer quenching agent

This disclosure describes polymerization processes and processes for quenching polymerization reactions using reactive particulates, such as high molecular weight functionalized olefin copolymers, as quenching agents, typically in solution or bulk polymerization processes.

Binder composition for non-aqueous secondary battery positive electrode, composition for non-aqueous secondary battery positive electrode, positive electrode for non-aqueous secondary battery, and non-aqueous secondary battery, and methods for producing composition for non-aqueous secondary battery positive electrode, positive electrode for non-aqueous secondary battery, and non-aqueous secondary battery

Provided is a binder composition for a non-aqueous secondary battery positive electrode that can form a positive electrode with which it is possible to obtain a non-aqueous secondary battery having excellent life characteristics even when aging treatment is carried out under low-temperature and low-depth of charge conditions. The binder composition contains a first binder, iron, and at least one of ruthenium and rhodium. The total iron, ruthenium, and rhodium content is no greater than 510.sup.3 parts by mass per 100 parts by mass of the first binder.

Binder composition for non-aqueous secondary battery positive electrode, composition for non-aqueous secondary battery positive electrode, positive electrode for non-aqueous secondary battery, and non-aqueous secondary battery, and methods for producing composition for non-aqueous secondary battery positive electrode, positive electrode for non-aqueous secondary battery, and non-aqueous secondary battery

Provided is a binder composition for a non-aqueous secondary battery positive electrode that can form a positive electrode with which it is possible to obtain a non-aqueous secondary battery having excellent life characteristics even when aging treatment is carried out under low-temperature and low-depth of charge conditions. The binder composition contains a first binder, iron, and at least one of ruthenium and rhodium. The total iron, ruthenium, and rhodium content is no greater than 510.sup.3 parts by mass per 100 parts by mass of the first binder.

High Molecular Weight Functionalized Olefin Copolymer Quenching Agent
20190256619 · 2019-08-22 ·

This disclosure describes polymerization processes and processes for quenching polymerization reactions using reactive particulates, such as high molecular weight functionalized olefin copolymers, as quenching agents, typically in solution or bulk polymerization processes.

Hydrogenated nitrile rubber with reduced catalyst impurity

The residual hydrogenation catalyst from the hydrogenated nitrile rubber solution is recovered by using two steps such as (1) the catalyst extraction step with an ammonium salt and water (optionally including an oxidation step) to extract catalyst from the HNBR polymer chain to the solvent and then (2) the separation/column recovery step with the column packed with functional ion exchange resins for the separation of ammonia-catalyst complex from hydrogenated nitrile rubber solution and the column recovery for the high catalyst recovery with functional groups of resins. The ammonium salt for the catalyst extraction step is selected from ammonium chloride, ammonium bromide, ammonium iodide, and ammonium acetate. The functional groups in the functional ion exchange resins for packing the column is selected from thiourea, thiouronium, thiol, amine, diamine, triamine, TMT, dithiocarbamate, and carbodithioate.