A coating composition comprising a crosslinkable polyester polymer comprising an isocyanurate group and a crosslinkable group; a crosslinker; and an acid catalyst, wherein at least one of the crosslinkable polyester polymer and the crosslinker comprises an iodine-containing polymer.

A type of fully dull polyester drawn yarns and a preparing method thereof are disclosed. The preparing method is to melt spinning a modified polyester with the fully drawn yarn (FDY) technique, and the modified polyester is a product of an esterification and successive polycondensation reactions of evenly mixed terephthalic acid, ethylene glycol, 2,5,6,6-tetramethyl-2,5-heptanediol, a fluorinated dicarboxylic acid, a matting agent, a calcined multiphase solid acid base powder and a doped Bi.sub.2O.sub.3 powder. The obtained fiber has an intrinsic viscosity drop of 18-26% when stored at 25° C. and R.H. 65% for 60 months. The method of improving the degradation performance of polyester fiber through the incorporation of 2,5,6,6-tetramethyl-2,5-heptanediol, the fluorinated dicarboxylic acid, the doped Bi.sub.2O.sub.3 powder and the calcined multiphase solid acid base powder is easy to operate.

A type of feather-like polyester fiber and a preparing method thereof are disclosed. The preparing method is to manufacture filament from a modified polyester through a POY process with a four-fold flat spinneret and a successive DTY processes, wherein said modified polyester is the product of the esterification and the successive polycondensation reactions of evenly mixed terephthalic acid, ethylene glycol, main-chain silicated diol and fluorinated dicarboxylic acid, and the spinneret is the one set with four-fold flat shaped orifices. The obtained fiber has a dye uptake of 89.6-93.7% when dyed at 130 C., and has an intrinsic viscosity drop of 13-20% when stored at 25 C. and R.H. 65% for 60 months. This invention is simple to apply and features a product with good dyeing and degradation performance.

A type of fully dull polyester drawn yarns and a preparing method thereof are disclosed. The preparing method is to melt spinning a modified polyester with the fully drawn yarn (FDY) technique, and the modified polyester is a product of an esterification and successive polycondensation reactions of evenly mixed terephthalic acid, ethylene glycol, 2,5,6,6-tetramethyl-2,5-heptanediol, a fluorinated dicarboxylic acid, a matting agent, a calcined multiphase solid acid base powder and a doped Bi.sub.2O.sub.3 powder. The obtained fiber has an intrinsic viscosity drop of 18-26% when stored at 25 C. and R.H. 65% for 60 months. The method of improving the degradation performance of polyester fiber through the incorporation of 2,5,6,6-tetramethyl-2,5-heptanediol, the fluorinated dicarboxylic acid, the doped Bi.sub.2O.sub.3 powder and the calcined multiphase solid acid base powder is easy to operate.

A type of feather-like polyester fiber and a preparing method thereof are disclosed. The preparing method is to manufacture filament from a modified polyester through a POY process with a four-fold flat spinneret and a successive DTY processes, wherein said modified polyester is the product of the esterification and the successive polycondensation reactions of evenly mixed terephthalic acid, ethylene glycol, main-chain silicated diol and fluorinated dicarboxylic acid, and the spinneret is the one set with four-fold flat shaped orifices. The obtained fiber has a dye uptake of 89.6-93.7% when dyed at 130 C., and has an intrinsic viscosity drop of 13-20% when stored at 25 C. and R.H. 65% for 60 months. This invention is simple to apply and features a product with good dyeing and degradation performance.

A type of wool-like polyester filament and preparing method thereof are disclosed. The preparing method is manufacturing filament from a modified polyester through a POY process and a successive DTY processes, wherein the modified polyester is the product of the esterification and the successive polycondensation reactions of evenly mixed terephthalic acid, 1,4-butanediol, fluorinated dicarboxylic acid, tert-butyl branched hexanediol and 2,5,6,6-tetramethyl-2,5-heptanediol. The obtained fiber has a dye uptake of 90.32-93.27% and a K/S value of 22.15-23.42 when dyed at 100 C., and has an intrinsic viscosity drop of 17-20% when stored at 25 C. and R.H. 65% for 60 months. This invention features a method with ease of application and a product with good dyeing and degradation performance.

The present invention relates to a radiation curable composition comprising: (I) A radiation curable component comprising a compound having at least one ethylenically unsaturated group and (II) A chlorinated polyester component that is prepared from (A) A polyol component which is substantially free of any Bisphenol A derivative compound and which is substantially free of any cyclic ether polyol compound, said polyol component comprising a polyol compound (Ai) which is cyclic and which has at least two hydroxyl groups, and (B) A polycarboxylic acid component comprising a compound (Bi) having at least one chlorine group and at least two carboxyl groups, (C) optionally at least one monoalcohol compound, (D) optionally at least one monocarboxylic acid compound, (III) optionally at least one polycarboxylic acid compound substantially free of chlorine groups.

The present disclosure is directed to resins and to polymers, copolymers, and blends formed therefrom.

The present disclosure is directed to resins and to polymers, copolymers, and blends formed therefrom.

A polyarylate resin includes at least one type of repeating unit represented by a general formula (1), at least one type of repeating unit represented by a general formula (2), and a terminal group represented by a general formula (3). R.sup.1, R.sup.2, R.sup.3, and R.sup.4 each represent, independently of one another, a hydrogen atom or a methyl group. R.sup.5 and R.sup.6 each represent, independently of each other, a hydrogen atom or a C.sub.1-4 alkyl group. R.sup.5 and R.sup.6 may bond together to represent a C.sub.5-7 cycloalkylidene group. X.sup.1 represents a divalent group represented by a chemical formula (2A), (2B), (2C), or (2D) with the proviso that when only one type of repeating unit represented by the general formula (2) is included, X.sup.1 does not represent a divalent group represented by the chemical formula (2D). R.sup.f represents a chain aliphatic group having at least one fluoro group. ##STR00001##