Patent classifications
C08G63/668
Polyester elastomer resin composition
A polyester elastomer resin composition having excellent anti-noise properties and wear resistance that achieves sustained wear resistance over a long period of time; enables lubricants to bleed out even in a low-temperature environment, so that the effects of the lubricants are maintained; and further prevents the lubricants from being dissolved in water, even when a molded article is washed with water. The polyester elastomer resin composition comprises a polyester elastomer (A), an aliphatic amide compound (B), and a copolyether (C), wherein the polyester elastomer (A) comprises a hard segment and a soft segment, the hard segment comprising a polyester that comprises, as constituents, an aromatic dicarboxylic acid and an aliphatic and/or alicyclic diol, the soft segment being at least one member selected from aliphatic polyethers, aliphatic polyesters, and aliphatic polycarbonates; the copolyether (C) comprises two or more different types of alkylene units and has a number average molecular weight of 1500 to 5000; and the aliphatic amide compound (B) is present in an amount of 0.01 to 1 part by mass, and the copolyether (C) is present in an amount of 0.1 to 10 parts by mass, per 100 parts by mass of the polyester elastomer (A).
Polyester elastomer resin composition
A polyester elastomer resin composition having excellent anti-noise properties and wear resistance that achieves sustained wear resistance over a long period of time; enables lubricants to bleed out even in a low-temperature environment, so that the effects of the lubricants are maintained; and further prevents the lubricants from being dissolved in water, even when a molded article is washed with water. The polyester elastomer resin composition comprises a polyester elastomer (A), an aliphatic amide compound (B), and a copolyether (C), wherein the polyester elastomer (A) comprises a hard segment and a soft segment, the hard segment comprising a polyester that comprises, as constituents, an aromatic dicarboxylic acid and an aliphatic and/or alicyclic diol, the soft segment being at least one member selected from aliphatic polyethers, aliphatic polyesters, and aliphatic polycarbonates; the copolyether (C) comprises two or more different types of alkylene units and has a number average molecular weight of 1500 to 5000; and the aliphatic amide compound (B) is present in an amount of 0.01 to 1 part by mass, and the copolyether (C) is present in an amount of 0.1 to 10 parts by mass, per 100 parts by mass of the polyester elastomer (A).
Topical preparations comprising biodegradable polyalkoxylated polyols polyester
Compounds contained herein relate to biodegradable thickening agents (e.g., polyalkoxylated polyol polyesters) having a viscosity that allows a product to be poured, yet retained on a desired surface to which it is applied. Embodiments of the compounds may be exemplified by the formula:
Q-[(OA).sub.n-OR].sub.m
Topical preparations comprising biodegradable polyalkoxylated polyols polyester
Compounds contained herein relate to biodegradable thickening agents (e.g., polyalkoxylated polyol polyesters) having a viscosity that allows a product to be poured, yet retained on a desired surface to which it is applied. Embodiments of the compounds may be exemplified by the formula:
Q-[(OA).sub.n-OR].sub.m
POLYESTER POLYMER NANOCOMPOSITES
Aspects of the present disclosure include compositions of and methods for producing a polymer-polysaccharide nanocomposite resin, including polymerizing an alkane diol monomer and an alkane diacid agent monomer in a mixture comprising dispersed polysaccharide nanocrystals, a catalyst and one or more optional additives under conditions sufficient to produce a polymer-polysaccharide nanocomposite resin. Aspects of the present disclosure further include compositions of and methods for producing a polybutylene succinate nanocomposite, including dispersing cellulose nanocrystals in 1,4 butanediol (BDO) to form a cellulose-BDO dispersion and esterifying the cellulose-BDO dispersion and succinate anhydride to form a plurality of polybutylene succinate oligomers. The polybutylene succinate oligomers are condensed to form a polybutylene succinate nanocomposite.
POLYESTER POLYMER NANOCOMPOSITES
Aspects of the present disclosure include compositions of and methods for producing a polymer-polysaccharide nanocomposite resin, including polymerizing an alkane diol monomer and an alkane diacid agent monomer in a mixture comprising dispersed polysaccharide nanocrystals, a catalyst and one or more optional additives under conditions sufficient to produce a polymer-polysaccharide nanocomposite resin. Aspects of the present disclosure further include compositions of and methods for producing a polybutylene succinate nanocomposite, including dispersing cellulose nanocrystals in 1,4 butanediol (BDO) to form a cellulose-BDO dispersion and esterifying the cellulose-BDO dispersion and succinate anhydride to form a plurality of polybutylene succinate oligomers. The polybutylene succinate oligomers are condensed to form a polybutylene succinate nanocomposite.
PHOTO-SENSITIVE COMPOSITION FOR INSULATING FILM FOR TOUCH PANEL OF ORGANIC LIGHT EMITTING DISPLAY DEVICE
Provided herein are a touch panel with excellent sensitivity by implementing an insulating film for a touch panel with a low dielectric constant from a photo-sensitive composition using hollow silica particles, and an organic light emitting display device to which the touch panel is applied.
PHOTO-SENSITIVE COMPOSITION FOR INSULATING FILM FOR TOUCH PANEL OF ORGANIC LIGHT EMITTING DISPLAY DEVICE
Provided herein are a touch panel with excellent sensitivity by implementing an insulating film for a touch panel with a low dielectric constant from a photo-sensitive composition using hollow silica particles, and an organic light emitting display device to which the touch panel is applied.
Polyester resin for toners, method for producing same, toner and method for producing toner
A polyester resin, including: (a) a constitutional unit derived from at least one tetravalent carboxylic acid selected from Compounds (A) and (B); a constitutional unit derived from a bisphenol A-alkylene oxide adduct; and a constitutional unit derived from an aliphatic alcohol having a boiling point of lower than or equal to 290° C., where the polyester resin is free of a constitutional unit derived from a monovalent carboxylic acid, an acid value of the polyester resin is 8 to 55 mg KOH/g, and an amount of the tetravalent carboxylic acid is 1 to 30 mol % when an total amount of the tetravalent carboxylic acid, and other polyvalent carboxylic acid excluding the Compounds (A) and (B) is set to 100 mol %, ##STR00001## where X.sup.1, X.sup.2, X.sup.3 and X.sup.4 each independently represent a trivalent organic group, and Z.sup.1 and Z.sup.2 each independently represent a single bond or a divalent organic group, wherein tetravalent carboxylic acid is, for example, 3,3′,4,4′-biphenyltetracarboxylic dianhydride, 2,2′,6,6′-biphenyltetracarboxylic dianhydride, 4,4′-oxydiphthalic dianhydride, 9,9-bis(3,4-dicarboxyphenyl) fluorene dianhydride, and/or 4,4′-(4,4′-isopropylidenediphenoxy) diphthalic anhydride.
Polyester resin for toners, method for producing same, toner and method for producing toner
A polyester resin, including: (a) a constitutional unit derived from at least one tetravalent carboxylic acid selected from Compounds (A) and (B); a constitutional unit derived from a bisphenol A-alkylene oxide adduct; and a constitutional unit derived from an aliphatic alcohol having a boiling point of lower than or equal to 290° C., where the polyester resin is free of a constitutional unit derived from a monovalent carboxylic acid, an acid value of the polyester resin is 8 to 55 mg KOH/g, and an amount of the tetravalent carboxylic acid is 1 to 30 mol % when an total amount of the tetravalent carboxylic acid, and other polyvalent carboxylic acid excluding the Compounds (A) and (B) is set to 100 mol %, ##STR00001## where X.sup.1, X.sup.2, X.sup.3 and X.sup.4 each independently represent a trivalent organic group, and Z.sup.1 and Z.sup.2 each independently represent a single bond or a divalent organic group, wherein tetravalent carboxylic acid is, for example, 3,3′,4,4′-biphenyltetracarboxylic dianhydride, 2,2′,6,6′-biphenyltetracarboxylic dianhydride, 4,4′-oxydiphthalic dianhydride, 9,9-bis(3,4-dicarboxyphenyl) fluorene dianhydride, and/or 4,4′-(4,4′-isopropylidenediphenoxy) diphthalic anhydride.