Patent classifications
C08J5/02
Latex composition
A latex composition has a latex of a carboxyl group-containing conjugated diene rubber (A), and a plasticizer (B) having a SP value of 15 (cal/cm.sup.3).sup.1/2 or less, wherein the content of a plasticizer (B) is 0.1 to 15 parts by weight based on 100 parts by weight of the carboxyl group-containing conjugated diene rubber (A) included in the latex.
Laminate production method
A method for producing a laminate including a substrate and a rubber layer, the rubber layer having a thickness of 200 m or more from the surface of the substrate, the method including contacting the substrate in a heated state with a polymer latex having a viscosity of 2,000 to 100,000 mPa.Math.s at 25 C. to thereby coagulate the polymer in contact therewith to form the rubber layer.
Laminate production method
A method for producing a laminate including a substrate and a rubber layer, the rubber layer having a thickness of 200 m or more from the surface of the substrate, the method including contacting the substrate in a heated state with a polymer latex having a viscosity of 2,000 to 100,000 mPa.Math.s at 25 C. to thereby coagulate the polymer in contact therewith to form the rubber layer.
SYNTHETIC ELASTOMERIC ARTICLE AND METHOD FOR THE PRODUCTION THEREOF
The present application relates to an elastomeric article, such as a glove, comprising: (i) an elastomeric film comprising one or more film layers, and including an external surface and an internal surface, (ii) an antimicrobial agent that is effective against both beneficial and harmful microorganisms on the external surface of the elastomeric film, and (iii) a skin-protective agent selected from a probiotic, a prebiotic, or a combination thereof on the internal surface of the elastomeric film; wherein the inner surface of the film is free of an antimicrobially-effective amount of an antimicrobial agent that is effective against both beneficial and harmful microorganisms. The elastomeric articles may further comprise a barrier film layer that provides separation between the antimicrobial agent and the skin-protective agent. Also described are methods for the manufacture of such articles.
Latex Composition for Dip-Forming, Method for Preparing the Composition and Article Formed by the Composition
A latex composition for dip forming, and more particularly, to a latex composition for dip forming includes carboxylic acid-modified nitrile-based copolymer latex; and a phenolic emulsifier, wherein the phenolic emulsifier is included in an amount of 0.08 parts by weight to 6 parts by weight (based on a solid content) based on 100 parts by weight of the carboxylic acid-modified nitrile-based copolymer latex. A method for preparing the latex composition and a formed article produced using the latex composition are also provided.
Latex Composition for Dip-Forming, Method for Preparing the Composition and Article Formed by the Composition
A latex composition for dip forming, and more particularly, to a latex composition for dip forming includes carboxylic acid-modified nitrile-based copolymer latex; and a phenolic emulsifier, wherein the phenolic emulsifier is included in an amount of 0.08 parts by weight to 6 parts by weight (based on a solid content) based on 100 parts by weight of the carboxylic acid-modified nitrile-based copolymer latex. A method for preparing the latex composition and a formed article produced using the latex composition are also provided.
Glove
A glove according to the present invention includes a glove body configured to cover a hand of a wearer. The glove body has an outermost layer including a matrix resin and cellulose particles and constituting an outer surface of the glove. The outermost layer includes the cellulose particles in the range of more than 1 part to 9 parts or less by mass based on 100 parts by mass of the matrix resin. At least some of the cellulose particles are at least partially exposed from the outer surface.
PRODUCTION METHOD FOR DIP-MOLDED ARTICLE
A method for producing a dip-molded article, including a dip-molding step of dip-molding a latex composition containing a latex of a carboxyl group-containing conjugated diene-based rubber (A) and a water-soluble metal compound (B) using a dip mold to form a dip-molded layer on the surface of the dip mold; a moisture content adjustment step of adjusting the moisture content of the dip-molded layer formed on the surface of the dip mold to 1 to 30 wt %; and a beading step of performing beading after the adjusting of the moisture content, the beading including peeling a portion of the dip-molded layer formed on the surface of the dip mold from the dip mold.
ARTICLES OF POLY(BUTYLENE SUCCINATE) AND COPOLYMERS THEREOF
Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.
MEDICAL DEVICES CONTAINING COMPOSITIONS OF POLY(BUTYLENE SUCCINATE) AND COPOLYMERS THEREOF
Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.