The present invention relates to a process for coating paper, wherein the coating material used is a biodegradable, aliphatic-aromatic polyester having a melt volume rate (MVR) according to EN ISO 1133 (190° C., 2.16 kg weight) of from 3 to 50 cm.sup.3/10 min.

The present invention relates to a process for coating paper, wherein the coating material used is a biodegradable, aliphatic-aromatic polyester having a melt volume rate (MVR) according to EN ISO 1133 (190° C., 2.16 kg weight) of from 3 to 50 cm.sup.3/10 min.

To provide a polycarbonate resin composition excellent in the surface hardness, the heat resistance, the moldability and the flame retardancy. A polycarbonate resin composition comprising at least a polycarbonate resin (a) and a polycarbonate resin (b) having structural units different from the polycarbonate resin (a), which satisfies the following requirements: (i) the pencil hardness of the polycarbonate resin (a) as specified by ISO 15184 is higher than the pencil hardness of the polycarbonate resin (b) as specified by ISO 15184; (ii) the glass transition point Tg(a) of the polycarbonate resin (a) and the glass transition point Tg(b) of the polycarbonate resin (b) satisfy the relation of the following (Formula 1):
Tg(b)−45° C. <Tg(a)<Tg(b)−10° C.  (Formula 1):
and (iii) the pencil hardness of the polycarbonate resin composition as specified by ISO 15184 is higher by at least two ranks than the pencil hardness of the polycarbonate resin (b) as specified by ISO 15184.

To provide a polycarbonate resin composition excellent in the surface hardness, the heat resistance, the moldability and the flame retardancy. A polycarbonate resin composition comprising at least a polycarbonate resin (a) and a polycarbonate resin (b) having structural units different from the polycarbonate resin (a), which satisfies the following requirements: (i) the pencil hardness of the polycarbonate resin (a) as specified by ISO 15184 is higher than the pencil hardness of the polycarbonate resin (b) as specified by ISO 15184; (ii) the glass transition point Tg(a) of the polycarbonate resin (a) and the glass transition point Tg(b) of the polycarbonate resin (b) satisfy the relation of the following (Formula 1):
Tg(b)−45° C. <Tg(a)<Tg(b)−10° C.  (Formula 1):
and (iii) the pencil hardness of the polycarbonate resin composition as specified by ISO 15184 is higher by at least two ranks than the pencil hardness of the polycarbonate resin (b) as specified by ISO 15184.

The present disclosure relates to a composite material comprising glass fiber and a polymer blend comprising polylactic acid (PLA) and polybutylene succinate (PBS), wherein the composite material comprises about 10 wt-% to about 80 wt-% of glass fibre, and wherein the polymer blend comprises about 20 wt-% to about 60 wt-% of PLA and about 40 wt-% to about 80 wt-% of PBS. The disclosure also relates to an article comprising the reinforced composite material.

The present disclosure relates to a composite material comprising glass fiber and a polymer blend comprising polylactic acid (PLA) and polybutylene succinate (PBS), wherein the composite material comprises about 10 wt-% to about 80 wt-% of glass fibre, and wherein the polymer blend comprises about 20 wt-% to about 60 wt-% of PLA and about 40 wt-% to about 80 wt-% of PBS. The disclosure also relates to an article comprising the reinforced composite material.

A polyethylene composition having increased environmental stress crack resistance comprises a polymer blend of a multimodal high density polyethylene (HDPE) and an additive of at least one of a polycarbonate-siloxane copolymer, a polyethylene glycol (PEG) having an average molecular weight (Mw) of at least 2000, and a random block copolymer comprising two different saturated alkane blocks between two aromatic hydrocarbon blocks. The additive is present in the polymer blend in an amount of from 1 wt. % or less by weight of the polymer blend.

Disclosed are aliphatic-aromatic biodegradable polyesters obtained from aliphatic dicarboxylic acids comprising azelaic acid, sebacic acid, suberic acid, brassylic acid and their esters; polyfunctional aromatic acids of renewable origin and particularly 2,5-furan dicarboxylic acid, and diols, such as 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-haxanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecanediol, 1,4-cyclohexanedimethanol, propylene glycol, neopentyl glycol, 2-methyl-1,3-propanediol, dianhydrosorbitol, dianhydromannitol, dianhydroiditol, cyclohexanediol, cyclohexane-methanediol, aromatic diols such as phenols, and furan diol. Also disclosed are blends of the polyesters with other biodegradable polymers of either natural or synthetic origin. The polyesters have properties and viscosity values that make them suitable, after adjusting their molecular weight, for use in numerous practical applications such as films, injection molded products, extrusion coatings, fibers, foams, thermoformed products, extruded profiles and sheets, extrusion blow molding, injection blow molding, rotomolding, stretch blow molding.

Disclosed are aliphatic-aromatic biodegradable polyesters obtained from aliphatic dicarboxylic acids comprising azelaic acid, sebacic acid, suberic acid, brassylic acid and their esters; polyfunctional aromatic acids of renewable origin and particularly 2,5-furan dicarboxylic acid, and diols, such as 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-haxanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, 1,13-tridecanediol, 1,4-cyclohexanedimethanol, propylene glycol, neopentyl glycol, 2-methyl-1,3-propanediol, dianhydrosorbitol, dianhydromannitol, dianhydroiditol, cyclohexanediol, cyclohexane-methanediol, aromatic diols such as phenols, and furan diol. Also disclosed are blends of the polyesters with other biodegradable polymers of either natural or synthetic origin. The polyesters have properties and viscosity values that make them suitable, after adjusting their molecular weight, for use in numerous practical applications such as films, injection molded products, extrusion coatings, fibers, foams, thermoformed products, extruded profiles and sheets, extrusion blow molding, injection blow molding, rotomolding, stretch blow molding.

The present invention relates to a process for the preparation of a spinnable composition (sC) by mixing at least one terephthalate polyester (A), at least one aliphatic-aromatic polyester (B), at least one oligomer (C) and optionally at least one additive (D). Moreover, the present invention relates to the spinnable composition (sC) obtained by this process, a process for the preparation of polyester fibers (PF) by extruding the spinnable composition (sC) through at least one spinneret, the polyester fibers (PF) obtained by this process, textile materials (T) comprising the polyester fibers (PF) a process for dying the textile materials (T), and the use of the oligomer (C) for the improvement of the rheology and/or the dyeability of a composition comprising at least one terephthalate polyester (A) and at least one aliphatic aromatic polyester (B).