A block copolymer consists mainly of structural units each derived from an ethylenically unsaturated monomer and has at least one mercapto group. The block copolymer has an Mn of 5,000-500,000 and has a block structure, which is an A-B-A triblock structure or a star-shaped block structure of [A-B]qX. The q is an integer of 2-6. The polymer block (A) has a glass transition temperature of 20° C. or higher. The polymer block (B) of the triblock structure has a glass transition temperature lower than 20° C., and the [polymer block (B)]qX of the star-shaped block structure has a glass transition temperature lower than 20° C. The X is an initiator residue or/and a coupling-agent residue or is a derivative thereof.

A block copolymer consists mainly of structural units each derived from an ethylenically unsaturated monomer and has at least one mercapto group. The block copolymer has an Mn of 5,000-500,000 and has a block structure, which is an A-B-A triblock structure or a star-shaped block structure of [A-B]qX. The q is an integer of 2-6. The polymer block (A) has a glass transition temperature of 20° C. or higher. The polymer block (B) of the triblock structure has a glass transition temperature lower than 20° C., and the [polymer block (B)]qX of the star-shaped block structure has a glass transition temperature lower than 20° C. The X is an initiator residue or/and a coupling-agent residue or is a derivative thereof.

A block copolymer consists mainly of structural units each derived from an ethylenically unsaturated monomer and has at least one mercapto group. The block copolymer has an Mn of 5,000-500,000 and has a block structure, which is an A-B-A triblock structure or a star-shaped block structure of [A-B]qX. The q is an integer of 2-6. The polymer block (A) has a glass transition temperature of 20° C. or higher. The polymer block (B) of the triblock structure has a glass transition temperature lower than 20° C., and the [polymer block (B)]qX of the star-shaped block structure has a glass transition temperature lower than 20° C. The X is an initiator residue or/and a coupling-agent residue or is a derivative thereof.

Functionalized polymer adsorbents for removing impurities from a feed stream comprising an active pharmaceutical ingredient (API) include particles of functionalized with at least one functional moiety capable of binding one or more contaminants, the polymer being a macroreticular polymer and the functionalized polymer adsorbents having a pore volume of at least 0.65 cm.sup.3/g. Alternatively, the adsorbent can comprise a polymer functionalized with either 2,4,6,-dimercaptotriazine-ethylenedithiol (DMT-EDT) adduct, 2,4,6,-trimercaptotriazine-ethylenedithiol (TMT-EDT) adduct, or a combination thereof, and the polymer can be either a macroreticular polymer or a swellable polymer. The adsorbents can be used in either continuous or batch processes for removing contaminants from an API-containing feed stream wherein the contaminants can include elemental impurities, particularly palladium.

Functionalized polymer adsorbents for removing impurities from a feed stream comprising an active pharmaceutical ingredient (API) include particles of functionalized with at least one functional moiety capable of binding one or more contaminants, the polymer being a macroreticular polymer and the functionalized polymer adsorbents having a pore volume of at least 0.65 cm.sup.3/g. Alternatively, the adsorbent can comprise a polymer functionalized with either 2,4,6,-dimercaptotriazine-ethylenedithiol (DMT-EDT) adduct, 2,4,6,-trimercaptotriazine-ethylenedithiol (TMT-EDT) adduct, or a combination thereof, and the polymer can be either a macroreticular polymer or a swellable polymer. The adsorbents can be used in either continuous or batch processes for removing contaminants from an API-containing feed stream wherein the contaminants can include elemental impurities, particularly palladium.

The present disclosure provides a multilayer film. In an embodiment, a multilayer film is provided and includes: a layer (A) comprising an olefin-based polymer; a layer (B) that is a tie layer comprising a sulfonamide derivative grafted olefin-based polymer (SD-g-PO); and a layer (C) comprising a polar component.

The present disclosure provides a multilayer film. In an embodiment, a multilayer film is provided and includes: a layer (A) comprising an olefin-based polymer; a layer (B) that is a tie layer comprising a sulfonamide derivative grafted olefin-based polymer (SD-g-PO); and a layer (C) comprising a polar component.

The present invention provides a sulfur-modified polyacrylonitrile having a total content of sulfur of from 30 mass % to 55 mass % and having a content of free sulfur of from 0.05 ppm by mass to 4 mass % determined by a solvent extraction method, an electrode active material containing the same, an electrode for a secondary battery including the electrode active material, a method of manufacturing the electrode, and a non-aqueous electrolyte secondary battery using the electrode.

The present invention provides a sulfur-modified polyacrylonitrile having a total content of sulfur of from 30 mass % to 55 mass % and having a content of free sulfur of from 0.05 ppm by mass to 4 mass % determined by a solvent extraction method, an electrode active material containing the same, an electrode for a secondary battery including the electrode active material, a method of manufacturing the electrode, and a non-aqueous electrolyte secondary battery using the electrode.

A preparation method of a hydrogel of a mercapto-modified macromolecular compound includes the steps of combining the mercapto-modified macromolecular compound with an acrylated macromolecular compound and/or an acrylated micromolecular crosslinker. The mercapto-modified macromolecular compound can be crosslinked with the acrylated macromolecular compound and/or the acrylated micromolecular crosslinker under physiological conditions to form the hydrogel. Due to the rapid mercapto-vinyl crosslinking reaction, the formed hydrogel system can be quickly gelled in situ after being injected into the body. The hydrogel is thus suitable for use in the fields of biomedicine, medical cosmetic plastic surgery and cosmetics.