An object of the present invention is to provide a production method of a diene-based polymer that can control the crosslinking morphology. The present invention provides a method for producing a modified diene-based polymer having a structure represented by the formula (1), comprising a first step of mixing a diene-based polymer and a dithioester compound to prepare a mixture; and a second step of irradiating a ray to the mixture under an inert atmosphere.

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[In the formula (1), R.sup.1 and R.sup.2 represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, a hydrogen atom, or a halogen atom; and Z is an organic group, an organic group where a part of hydrogen atom of the above organic group is substituted, a hydrogen atom, or a halogen atom.]

The present invention relates to a modified conjugated diene-based polymer having excellent affinity with a filler and a method for preparing the same, and provides a modified conjugated diene-based polymer including: a first chain comprising a repeating unit derived from a conjugated diene-based monomer; and one or more graft chains comprising a derived unit from an oligomer and graft-bonded to the first chain, wherein the derived unit from an oligomer comprises a residual group derived from a radical reactive functional group, and a molecular weight distribution increase ratio defined by Mathematical Equation 1 is 20% or less, and a method for preparing the same.

The present invention relates to a modified conjugated diene-based polymer having excellent affinity with a filler and a method for preparing the same, and provides a modified conjugated diene-based polymer including: a first chain comprising a repeating unit derived from a conjugated diene-based monomer; and one or more graft chains comprising a derived unit from an oligomer and graft-bonded to the first chain, wherein the derived unit from an oligomer comprises a residual group derived from a radical reactive functional group, and a molecular weight distribution increase ratio defined by Mathematical Equation 1 is 20% or less, and a method for preparing the same.

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.

The invention relates to methods for achieving a step increase in the Mooney viscosity in production of high-molecular-weight polybutadiene having >95% by weight content of cis-1,4 units and <1% by weight 1,2-vinyl content, characterized in that 1) at least one monomer selected from butadiene and/or isoprene is polymerized at temperatures of from −20° C. to 150° C. in the presence of at least one inert, organic solvent and in the presence of at least one catalyst based on neodymium carboxylate, 2) the polymerization is then terminated by addition of protic compounds and 3) then sulphur chlorides are added to the polymer, and prior to addition these sulphur chlorides are treated with a carboxylic acid, fatty acid and/or fatty acid ester.

The invention relates to methods for achieving a step increase in the Mooney viscosity in production of high-molecular-weight polybutadiene having >95% by weight content of cis-1,4 units and <1% by weight 1,2-vinyl content, characterized in that 1) at least one monomer selected from butadiene and/or isoprene is polymerized at temperatures of from −20° C. to 150° C. in the presence of at least one inert, organic solvent and in the presence of at least one catalyst based on neodymium carboxylate, 2) the polymerization is then terminated by addition of protic compounds and 3) then sulphur chlorides are added to the polymer, and prior to addition these sulphur chlorides are treated with a carboxylic acid, fatty acid and/or fatty acid ester.

Method for the manufacture of the innerliner compound comprising: —a first mixing step wherein at least one cross-linkable unsaturated chain polymeric base and one filler system are mixed together; —a final mixing step wherein a vulcanization system is added and mixed with the mixture deriving from an earlier mixing step; and —an intermediate mixing step, interposed between said first mixing step and the final mixing step, and wherein lignin is added and mixed into the mixture deriving from a previous mixing step.

Method for the manufacture of the innerliner compound comprising: —a first mixing step wherein at least one cross-linkable unsaturated chain polymeric base and one filler system are mixed together; —a final mixing step wherein a vulcanization system is added and mixed with the mixture deriving from an earlier mixing step; and —an intermediate mixing step, interposed between said first mixing step and the final mixing step, and wherein lignin is added and mixed into the mixture deriving from a previous mixing step.

The present invention relates to articles comprising crosslinked polymer network comprising thioether crosslinks and process of making and using same. Such thiol-ene crosslinking reactions not only make the isocyanate crosslinking reaction unnecessary, but they also improve the article's strength due to chemical crosslinking between the article's resin layers, and reduce or eliminate post curing. Thus resulting in a sufficiently cured article in a much shorter time.

The present invention relates to articles comprising crosslinked polymer network comprising thioether crosslinks and process of making and using same. Such thiol-ene crosslinking reactions not only make the isocyanate crosslinking reaction unnecessary, but they also improve the article's strength due to chemical crosslinking between the article's resin layers, and reduce or eliminate post curing. Thus resulting in a sufficiently cured article in a much shorter time.