A resin composition is produced by a method including a washing step of washing a resin composition with water. The resin composition contains fine polymer particles (A) and a resin (B). The fine polymer particles (A) have a graft part that is constituted by a polymer containing, as one or more structural units, one or more structural units derived from at least one type of monomer selected from the group consisting of aromatic vinyl monomers, vinyl cyanide monomers, and (meth)acrylate monomers. The resin (B) has a given viscosity, in a case where a total amount of the fine polymer particles (A) and the resin (B) is regarded as 100% by weight, an amount of the fine polymer particles (A) being 1% by weight to 70% by weight and an amount of the resin (B) being 30% by weight to 99% by weight.

A resin composition is produced by a method including a washing step of washing a resin composition with water. The resin composition contains fine polymer particles (A) and a resin (B). The fine polymer particles (A) have a graft part that is constituted by a polymer containing, as one or more structural units, one or more structural units derived from at least one type of monomer selected from the group consisting of aromatic vinyl monomers, vinyl cyanide monomers, and (meth)acrylate monomers. The resin (B) has a given viscosity, in a case where a total amount of the fine polymer particles (A) and the resin (B) is regarded as 100% by weight, an amount of the fine polymer particles (A) being 1% by weight to 70% by weight and an amount of the resin (B) being 30% by weight to 99% by weight.

A method for preparing a super absorbent polymer and a superabsorbent polymer prepared from the same are disclosed herein. In some embodiments, a method includes mixing super absorbent polymer particles, water and an additive form a hydrated super absorbent polymer, wherein the super absorbent polymer particles comprise a base polymer powder including a cross-linked polymer polymerized from a water-soluble ethylenically unsaturated monomer having an acidic group of which at least a part is neutralized, and a surface cross-linked layer formed on the base polymer powder, wherein the surface cross-linked layer is formed by further cross-linking the cross-linked polymer, and wherein the additive including a polyoxyalkylene aliphatic hydrocarbon ether carboxylic acid. The method can appropriately control the water content of the super absorbent polymer by water-addition or the like to suppress crushing or the like during transfer, and also can suppress deterioration of physical properties.

Disclosed is a production method for a poly(vinyl alcohol) having a degree of saponification of 97.0 mol % or more, comprising: a pulverization step of pulverizing a first poly(vinyl alcohol) having a particulate form to obtain a second poly(vinyl alcohol) having an adjusted particle size, and a heating step of heating the second poly(vinyl alcohol).

Disclosed is a production method for a poly(vinyl alcohol) having a degree of saponification of 97.0 mol % or more, comprising: a pulverization step of pulverizing a first poly(vinyl alcohol) having a particulate form to obtain a second poly(vinyl alcohol) having an adjusted particle size, and a heating step of heating the second poly(vinyl alcohol).

The method for preparing a super absorbent polymer according to the present disclosure reduces the generating amount of a fine powder while realizing the same particle size distribution in the process of pulverizing the dried polymer, thereby reducing the load of the fine powder reassembly, drying, pulverizing and classifying steps.

A process for the production of a graft copolymer composition is presented, which is based on acrylonitrile-styrene-acrylate (ASA) or acrylonitrile-butadiene-styrene (ABS) graft copolymers. The graft copolymers obtained by emulsion polymerization and precipitation show improved dewatering behavior after precipitation. Based on this method ASA and ABS graft copolymers with low residual humidity can be obtained. Furthermore, the invention relates to a process for the production of a thermoplastic molding composition comprising at least one thermoplastic styrene copolymer, in particular a styrene-acrylonitrile copolymer, the graft copolymer obtained by the process, and optional further components.

A process for the production of a graft copolymer composition is presented, which is based on acrylonitrile-styrene-acrylate (ASA) or acrylonitrile-butadiene-styrene (ABS) graft copolymers. The graft copolymers obtained by emulsion polymerization and precipitation show improved dewatering behavior after precipitation. Based on this method ASA and ABS graft copolymers with low residual humidity can be obtained. Furthermore, the invention relates to a process for the production of a thermoplastic molding composition comprising at least one thermoplastic styrene copolymer, in particular a styrene-acrylonitrile copolymer, the graft copolymer obtained by the process, and optional further components.

The present invention relates to a method for preparing superabsorbent polymer that introduces a plate type and rod-shaped clay additive in the superabsorbent polymer, and thus exhibits basic properties of a superabsorbent polymer equivalent to or much better than the existing superabsorbent polymer through multi-crosslinking, and particularly, can improve absorbency under pressure (AUP), and a superabsorbent polymer obtained thereby.

Acrylic rubber bale excellent in storage stability and processability, a method for producing the same, a rubber mixture obtained by mixing the acrylic rubber bale, and a cross-linked product of the rubber mixture are provided. The acrylic rubber bale includes an acrylic rubber having a reactive group and a weight average molecular weight (Mw) of 100,000 to 5,000,000, wherein an amount of gel insoluble in methyl ethyl ketone is 50% by weight or less, and a specific gravity is 0.8 or more.