A bimodal polymer composition comprising a lower molecular weight homopolymer and a higher molecular weight copolymer wherein the bimodal polymer composition has a density of from about 0.930 gram per cubic centimeter (g/cc) to about 0.970 g/cc, a ratio of high load melt index:melt index of from about 10 to about 150 and an Environmental Stress Crack Resistance (ESCR) of from about 25 hours to about 300 hours when measured in accordance with ASTM D1693 or ASTM D2561. A chromium-catalyzed polymer composition comprising (i) a lower molecular weight homopolymer and (ii) a higher molecular weight copolymer, wherein the bimodal polymer composition has an Environmental Stress Crack Resistance (ESCR) of from about 25 hours to about 300 hours when measured in accordance with ASTM D1693 or ASTM D2561.

The present invention provides a process for making a silica masterbatch that contains hydrophobated silica, solution-made rubber and emulsion-made rubber. Hydrophobated silica is mixed into a latex emulsion. Solution-rubber crumb in an aqueous suspension is mixed into the latex emulsion, which is coagulated, and a crumb is recovered, further homogenized, dried and baled to yield the silica masterbatch. A well-dispersed mixture of hydrophobated silica and emulsion-made rubber is added into a steam distillation step of a solution-rubber process from which a silica masterbatch is recovered. The emulsion-made rubber can be omitted to make a silica masterbatch of solution rubber and silica without emulsion rubber. The silica masterbatch has physical properties similar to those found in a comparable dry-mixed composition, but the silica masterbatch can be incorporated more easily and less expensively into tires and other rubber products than the dry-mixed composition.

A polyester blend is made in a reaction of a linear polylactide resin and a thermoplastic epoxy group-containing polymer. The polyester blend is blended with a polyester having a glass transition temperature below 0C to form a polyester blend that is particular useful for making paperboard coatings in a melt extrusion process.

A rubber composition for a torsional damper, comprising 10 to 200 parts by weight of carbon black having an iodine adsorption of 100 to 600 mg/g, a DBP oil absorption of 138 to 330 cm.sup.3/.sub.100 g and a nitrogen adsorption specific surface area of 100 to 530 m.sup.2/g, and 5 to 100 parts by weight of a liquid polyolefin oligomer having a number average molecular weight Mn of 3,000 to 4,000, based on 100 parts by weight of at least one of ethylene-propylene-non-conjugated diene terpolymer rubber, ethylene-butene-non-conjugated diene terpolymer rubber and ethylene-propylene copolymer rubber, wherein in the total amount of ethylene and propylene or butene, the content of propylene or butene is 35 to 55 wt. %.

Crosslinkable polymeric compositions comprising (a) 10 to 99 weight percent of an ethylene-based interpolymer having the following properties: (i) a density of 0.93 g/cm.sup.3 or less, (ii) a high-shear viscosity (V100) at 190° C. and 10% strain of 1,200 Pa-s or less, and (iii) a shear thinning ratio (V0.1/V100) at 190° C. and 10% strain of at least 8; and (b) 0 to less than 10 weight percent of a filler, where the ethylene-based interpolymer is not prepared in a high-pressure reactor. Such crosslinkable polymeric compositions may be employed as insulation layers in flexible power cables.

A polyester blend is made in a reaction of a linear polylactide resin and a thermoplastic epoxy group-containing polymer. The polyester blend is blended with a polyester having a glass transition temperature below 0 C to form a polyester blend that is particular useful for making paperboard coatings in a melt extrusion process.

Through the present invention, by undergoing a step in which a straight-chain diorganopolysiloxane having silanol groups at both terminal ends of the molecular chain thereof, a hydrolyzable silane and/or a partial hydrolysis condensate thereof having a hydrolyzable group capable of detaching a lactic acid ester, and an amino-group-containing hydrolyzable organosilane and/or a partial hydrolysis condensate thereof are pre-mixed/reacted in advance and silanol groups at both terminal ends of the molecular chain of a main agent (base polymer) are blocked by specific hydrolyzable silyl groups, it is possible to manufacture a lactic-acid-ester-type room-temperature-curable organopolysiloxane composition excellent in all characteristics including curability, adhesive properties, workability, and the like that were not attainable by the conventional lactic-acid-ester-type room-temperature curable (RTV) silicone rubber composition.

The present invention relates to a coating composition for polyester film capable of printing on all types of printers with liquid and dry toners. The coating composition comprising of a combination of polyethylene carboxylic acid dispersion and homopolymer or copolymer of polyacrylate dispersion and/or homopolymer or copolymer of polyvinyl acetate dispersion, wherein acrylate and/or acetate content be is in the range of 1 to 50% of carboxylic acid content in the dispersion.

A gas barrier film according to the present invention includes: a resin film substrate; a first layer made of an aqueous coating agent (C) that contains a water soluble polymer (A) and an inorganic layered mineral (B); and a second layer made of a coating agent (D) that contains titanium oxide, the first layer and the second layer being disposed in this order on at least one surface of the resin film substrate.

A fiber-reinforced resin composition includes a polyamide resin and a polyolefin resin, and when one resin between the polyamide resin and the polyolefin resin is set as a first resin, and the other resin is set as a second resin, the composition has a sea-island structure including a continuous phase C consisting of the first resin and a dispersed phase c consisting of the second resin dispersed in the continuous phase C, and in a resin phase separation cross-sectional structure, a total of cross-sectional areas of dispersed phases having a cross-sectional area equal to or smaller than an average cross-sectional area of the reinforcing fiber is 20% or less with respect to a total of cross-sectional areas of all dispersed phases.