Abstract: A biodegradable injection mouldable polymer composition including on a dry weight basis from 45-85% w/w by weight of a starch and/or a modified high amylose starch, from 2-15% w/w by weight of a water soluble polymer preferably selected from polyvinyl alcohol, polyvinyl acetate and copolymers of ethylene and vinyl alcohol which have a melting point compatible with the molten state of the starch components, and from 5-45% w/w by weight of one or more polyol plasticizers having a molecular weight in the range of 50-6000, more preferably 50-2500, and still more preferably 100-400 and preferably selected from the group consisting of sorbitol, glycerol, maltitol, xylitol, mannitol, erythritol, polyglycerol, glycerol trioleate, tributyl citrate, acetyl tri-ethyl citrate, glyceryl triacetate, 2,2,4-trimethyl-1,3-pentanediol diisobutyrate, polyethylene oxide, ethylene glycol, diethylene glycol or polyethylene glycol; more preferably glycerol, maltitol, sorbitol, erythritol and xylitol.

Abstract: Disclosed are hydrophobic polyester-polycarbonate polyols which are the reaction product of (a) a polyester polyol and (b) one or more polycarbonate polyols. The polyester polyol (a) is the reaction product of: (i) one or more hydrophobic monomers, (ii) one or more organic acids, and (iii) one or more alcohols having an OH functionality of 2 or more. The polyester-polycarbonate polyols may be both amorphous and liquid at room temperature and have excellent hydrolytic stability. The hydrolytic and chemical performance of the polyester-polycarbonate polyols described herein is superior to that of commercially available hydrophobically modified polyester polyols and to that of commercially available polyester-polycarbonate polyols as described herein.

Abstract: A method for producing a liquid crystal polyester according to the present invention is a method for producing a liquid crystal polyester, comprising subjecting a composition in which a dicarboxylic acid compound, a hydroxycarboxylic acid compound, and a dihydroxy compound are contained to melt polycondensation, and subjecting an obtained reaction product to solid phase polycondensation, wherein the composition contains, based on a total of the dicarboxylic acid compound, the hydroxycarboxylic acid compound, and the dihydroxy compound, 2 to 30 mole % of a dicarboxylic acid compound represented by the following formula (1), and 40 to 80 mole % of p-hydroxybenzoic acid, a polycondensation temperature of the above melt polycondensation is 315° C. or less, and a polycondensation temperature of the above solid phase polycondensation is 315° C. or less.

Abstract: The present invention relates to aliphatic or aliphatic-aromatic polyesters and copolyesters comprised of biobased ?-hydroxyfatty acids or derivatives thereof, processes for the preparation thereof, and compositions thereof having improved properties. The copolyesters of the present invention may also contain additional components that can be selected from aliphatic or aromatic diacids, diols and hydroxyacids obtained from synthetic and natural sources. The biobased ?-hydroxyfatty acids that comprise the polyesters and copolyesters of the present invention are made using a fermentation process from pure fatty acids, fatty acid mixtures, pure fatty acid ester, mixtures of fatty acid esters, and triglycerides from various sources. The polyesters of the present invention may contain various amounts and types of ?-carboxyfatty acids depending on the engineered yeast strain used for the bioconversion as well as the feedstock(s) used.

Abstract: Process and methods for making glycolic acid chemical intermediates and derivatives from biomass are described herein.

Abstract: A blend of polylactic acid resin and copolyester resin and a molded article using the same having superior impact resistance and heat resistance are disclosed. The blend of polylactic acid resin and copolyester resin includes: 5 to 95 weight % of polylactic acid resin; and 5 to 95 weight % of copolyester resin which is a copolymerization product of an acid component including terephthalic acid and a diol component including 5 to 99 mol % of 1,4-cyclohexanedimethanol and 1 to 60 mol % of isosorbide(bio monomer), and has a repeated structure of an acid moiety derived from the acid component and a diol moiety derived from the diol component.

Abstract: A composite hydrogel comprises an amphiphilic triblock copolymer (ABA) and a loaded micelle bound by noncovalent interactions. The loaded micelle comprises a biologically active substance and an amphiphilic diblock copolymer (CD). The A blocks comprise a steroidal repeat unit (repeat unit 1) having both a backbone carbonate and a side chain bearing a steroid functional group. Each of the A blocks has a degree of polymerization of about 0.5 to about 4.0. The B block comprises a first poly(alkylene oxide) backbone. The C block comprises a second poly(alkylene oxide) backbone. The D block comprises a steroidal repeat unit (repeat unit 2) having both a backbone carbonate group and a side chain comprising a steroid functional group. The composite hydrogel is capable of controlled release of the biologically active substance.

Abstract: The present disclosure is directed to a polyester having renewable 1,3-propanediol. This invention is further directed to a coating composition comprising the polyester having components derived from renewable resources.

Abstract: A polyester resin with a superior heat-resistance and color as well as high content of a compound derived from biomass due to copolymerization of lactic acid or a compound derived therefrom and isosorbide, and a method for preparing the same are disclosed. The polyester resin is copolymerized with diacid components including terephthalic acid; diol components including 1 to 60 mol % of isosorbide and 1 to 90 mol % of ethylene glycol with respect to total diol components; and 1 to 50 weight % of lactic acid or a compound derived therefrom with respect to total reactants for resin polymerization, wherein, the polyester resin has the repeated structure of diacid moiety derived from the diacid components, diol moiety derived from the diol components and hydroxy monoacid moiety derived from the lactic acid or the compound derived therefrom.

Abstract: A process for producing an IPA/PET copolymer fiber that is homogenous having a substantially level, single IPA copolymer content, said fiber having improved pilling resistance and dye uptake.

Abstract: A process for the continuous production of a biodegradable polyester, where a mixture of aliphatic dihydroxy compounds, aliphatic and aromatic dicarboxylic acids or their liquid esters, and, optionally, further comonomers is mixed, without addition of a catalyst, to give a paste, and i) this mixture with at least a portion of the catalyst, is continuously esterified or, transesterified; ii) the transesterification or, esterification product obtained in i) is continuously precondensed with any remaining amount of catalyst to an intrinsic viscosity of from 20 to 70 cm3/g; iii) the product obtainable from ii) is continuously polycondensed to an intrinsic viscosity of from 60 to 170 cm3/g, and iv) the product obtainable from iii) is reacted continuously with a chain extender in a polyaddition reaction to an intrinsic viscosity of from 150 to 320 cm3/g. The invention further relates to biodegradable polyesters obtained by this process.

Abstract: A radiation curable coating comprising the reaction product of a polyol and a polycarboxylic acid/anhydride is disclosed. The reaction product may be made from at least some biomass derived compound. Coatings wherein this reaction product is further reacted with a hydroxyl-carboxylic acid and/or a compound having a radiation curable moiety are also disclosed, as are substrates coated with any of these coatings.

Abstract: This invention relates to poly(ester amide)s (PEAs) comprising inactivated terminal amino and carboxyl groups, methods of synthesizing the inactivated PEAs and uses for them in the treatment of vascular diseases.

Abstract: The thermoplastic resin in accordance with the present invention includes a unit (A) by 25 mol % to 60 mol %, the unit (A) having a biphenyl group, a linear unit (e.g., a linear aliphatic hydrocarbon chain) (B) by 25 mol % to 60 mol %, and a unit (C) by 1 mol % to 25 mol %, the unit (C) having a substituent selected from the group consisting of non-fused aromatic groups, fused aromatic groups, heterocyclic groups, alicyclic groups, and alicyclic heterocyclic groups, each of which has an effect of folding a main chain.

Abstract: A laser composition comprises a combination of: (a) from more than 45 to less than 94 weight percent of a crystalline or semi-crystalline thermoplastic polyester component selected from poly(butylene terephthalate), poly(ethylene terephthalate), poly(butylene terephthalate) copolymers poly(ethylene terephthalate) copolymers, and combinations thereof; (b) from greater than 6 to less than 25 weight percent of an amorphous thermoplastic poly(ester) copolymer, poly(ester-carbonate), or combination thereof; (c) optionally, from 1 to 30 weight percent of a filler; and (d) optionally, from 0.01 to 5 weight percent of an antioxidant, mold release agent, colorant, stabilizer, or a combination thereof; wherein an article having a 2 mm thickness and molded from the composition has (i) a near infrared transmission at 960 nanometers of greater than 30 percent and (ii) a Vicat softening temperature of at least 170° C.

Abstract: This invention relates to certain poly(1,4-cyclohexylenedimethylene terephthalate) copolyesters which are useful for the preparation of clear and tough thick wall molded parts, produced at good cycle times. The copolyesters can be molded into desired shapes such as cosmetic jars, fragrance caps, tool handles, and toothbrushes. These molded articles can have thick or thin walls and may be molded in a two shot molding process. The copolyesters also have good flow and reduced cycle times.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising 80 to 100 mole % terephthalic acid residues; optionally, 0 to 20 mole % aromatic dicarboxylic acid residues or aliphatic dicarboxylic acid residues; 20 to 30 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and 70 to 80 mole % 1,4-cyclohexanedimethanol residues. The polyesters may be manufactured into articles such as fibers, films, bottles or sheets.

Abstract: A polymer and a method for its preparation are provided. The polymer comprises poly(lactide), poly(lactide/glycolide) or poly(lactic acid/glycolic acid) segments bonded by ester linkages to both ends of an alkanediol core unit. The polymer is for use in a controlled release formulation for a medicament, preferably leuprolide acetate. The controlled release formulation is administered to a patient as a subcutaneous depot of a flowable composition comprising the polymer, a biocompatible solvent, and the medicament. Controlled release formulations comprising the polymer release leuprolide for treatment of prostate cancer patients over periods of 3-6 months.

Abstract: Disclosed are polyester resins and solvent borne thermosetting coating compositions that include these resins in combination with at least one crosslinker. The polyester resins contain 2,2,4,4-tetramethyl-1,3-cyclobutanediol and exhibit a combination of good solubility in organic solvents and high hardness with good flexibility in a coating composition.

Abstract: Disclosed is a thermo-shrinkable polyester film having superior thermal shrinkage properties. The thermo-shrinkable polyester film has a strength of 3.5˜6.5 kg/mm2 in a direction perpendicular to a main shrinking direction at an initial elongation less than 10%, an elongation at rupture of 50˜700% in a direction perpendicular to a main shrinking direction, a thickness uniformity (?R) of 4 or less and a shrinkage ratio of 5% or less in a direction perpendicular to a main shrinking direction, thus preventing the rupture thereof in a rolling process and so on and ensuring process stability and productivity.

Abstract: A hyper-branched polyester and a method of making the same having a tri-functional monomer A3, a di-functional monomer B2 and a mono-functional monomer C1 having a monomer ratio of A3:B2:C1 from about 1:0.2:2 to about 1:1.4:0.2 for use in a chemically processed electrophotographic toner providing a lower fusing temperature. In one form, the hyper-branched polyester includes a tri-hydroxy monomer, a di-acid and its derivatives, and a mono-acid and its derivatives. In other forms, a substituted anhydride and a long chain hydrocarbon carboxylic acid and its derivatives may also be included in the di-functional monomer.

Abstract: A polyester resin for a toner is a polycondensate of a carboxylic acid component and an alcohol component including rosin diol that is represented by the following formula (1) and has an alicyclic structure (alicyclic alcohol), wherein R1 and R2 each independently represents hydrogen or a methyl group, L1 represents a divalent linking group having an alicyclic structure, L2 and L3 each independently represents a divalent linking group selected from a group consisting of a carbonyl group, a carboxyl group, an ether group, a sulfonyl group, a chain-like alkylene group which may have a substituent, a cyclic alkylene group, a phenylene group, and combinations thereof, and A1 and A2 represent a rosin ester group, provided that a divalent linking group having the alicyclic structure represented by L1 may be a divalent linking group having an alicyclic structure formed through linking with any of R1, R2, L2 or L3.

Abstract: A process for the production of a polymeric film comprising a copolyester having an acid component and a diol component, said acid component comprising a dicarboxylic acid and a sulfomonomer containing a sulfonate group attached to the aromatic nucleus of an aromatic dicarboxylic acid, said process comprising the steps of: (i) melt-extruding a layer of said copolyester; (ii) stretching the extrudate in at least one direction; (iii) heat-setting the film by raising the temperature of the stretched film to a temperature T1 in a first heating zone such that (TM?T1 is in the range of from 5 to 30° C., and then raising the temperature of the film to a temperature T2 in a second heating zone such that (TM?T2 is in the range of from 0 to 10° C.

Abstract: The invention relates to heat-curing powder-lacquer compositions exhibiting a matte surface after curing of the coating, as well as to a simple method for production of the same.

Abstract: Disclosed are solvent borne thermosetting coating compositions that contain a curable polyester resin blended with an acrylic copolymer, a crosslinker, and a solvent. The polyester resin contains 2,2,4,4-tetramethyl-1,3-cyclobutanediol and exhibits good dry time, compatibility with acrylic resins, sag resistance and hardness development in a coating composition. The coating compositions can be used to prepare clear coat or pigmented coatings for automotive OEM, auto refinish, and other applications.

Abstract: This invention provides a coating composition for use on a food-contact surface of a container (e.g., a food or beverage can) that includes a polymer having one or more segments of Formula I: —O—Ar—Rn—C(O)—O—R1—O—C(O)—Rn—Ar—O— wherein each Ar is independently a divalent aryl group (i.e., an arylene group) or heteroarylene group; R1 is a divalent organic group; each R is independently a divalent organic group; and n is 0 or 1. Containers comprising the polymer and methods of making such containers are also provided.

Abstract: Disclosed are polyester resins and solvent borne thermosetting coating compositions that include these resins in combination with at least one crosslinker. The polyester resins contain 2,2,4,4-tetramethyl-1,3-cyclobutanediol and exhibit a combination of good solubility in organic solvents and high hardness with good flexibility in a coating composition.

Abstract: A polymer obtainable by polycondensation or polyaddition of monomeric compounds, wherefor accompanying use is made as monomeric compound of 2-(2-methylbutyl)-2-propyl-1,3-propanediol of the formula I or its alkoxylated derivatives (also referred to collectively below as C11 diol).

Abstract: The present invention relates to a clear, semicrystalline article comprising a polyester comprising terephthalic acid residues as the dicarboxylic acid component, and 1 to 15 mole % of 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues and 85 to 99 mole % of 1,4-cyclohexanedimethanol residues as the glycol component. The article may be in the form of a film or sheet, a bottle, or a fiber. The article, when produced by a process involving strain-induced crystallization, is characterized with high crystallinity.

Abstract: This invention relates to a biodegradable polyester which is particularly suitable for use for the manufacture of wrapping films for packaging, comprising units deriving from at least one diacid and at least one diol, characterised by a high static friction coefficient in comparison with conventional biodegradable polyesters. A further object of this invention is a wrapping film comprising the said biodegradable polyester.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising terephthalic acid residues; optionally, aromatic dicarboxylic acid residues or aliphatic dicarboxylic acid residues; 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues; and cyclohexanedimethanol residues. The polyesters have a desirable combination of inherent viscosity and glass transition temperature (“Tg”). The polyesters can have an inherent viscosity from 0.35 to 1.2 dL/g as determined in 60/40 (wt/wt) phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C. and a Tg of 85 to 115° C. The polyesters may be manufactured into articles such as fibers, films, bottles or sheets.

Abstract: A heat-shrinkable polyester film having a thermal shrinkage ratio of 15% or more in the longitudinal direction when treated at 100° C. for 10 seconds, a tensile strength at rupture in the longitudinal direction of 7 kgf/mm2 or more, and a difference between elongations at the hardening and yield points in the longitudinal direction of 15% or more exhibits superior properties, such as high tensile strength and crack-resistance in the longitudinal direction, suitable for labeling or shrink-wrapping containers.

Abstract: The invention is generally directed to baby bottles and other articles produced by blow molding from polymeric materials having glass transition temperatures ranging from 100° C. to 130° C., as well as to processes for producing them. These articles can be exposed to boiling water and can be produced by using a suitable combination of a stretch ratio of less than 3 and a preform temperature at least 20° C. greater than the glass transition temperature (Tg) of the polymeric material.

Abstract: Biodegradable polyesters are made by synthesizing copolymers derived from biodegradable hydroxyacid monomers as well as from hydroxyacid monomers containing a functional group such as an azide group, a halogen group, a thioacetate group, and the like. Preferably, the functionalized biodegradable polyester copolymers are derived from a functionalized hydroxyacid such as a homolog of lactic acid and/or glycolic acid with the copolyester thus containing functional groups on the backbone thereof. These biodegradable polyesters can be utilized wherever biodegradable polyesters are currently used, and also serve as a polymer to which various medical and drug delivery systems can be attached.

Abstract: Polyesters described herein are prepared in whole or in part from biomass. In one aspect, a copolyester is formed from monomers of 2,5-furan dicarboxylic acid, or a lower alkyl ester thereof, at least one aliphatic or cycloaliphatic C3-C10 diol, and terephthalic acid. In another aspect, a polyester is formed from monomers of 2,5-furan dicarboxylic acid, or a lower alkyl ester thereof, and isosorbide. In some aspects, the polyester is polyethylene isosorbide furandicarboxylate, poly(2,5-furandimethylene adipate), or polyvanillic ester. The polyesters may have desirable physical and thermal properties and can be used to partially or wholly replace polyesters derived from fossil resources, such as poly(ethylene terephthalate).

Abstract: Disclosed herein are process for preparing cyclic esters comprising unsaturated functional groups. Also disclosed are copolymers prepared from the cyclic esters. The copolymers can be used to form microparticles, polymer micelles, etc., which are useful in drug delivery applications.

Abstract: The present invention relates to an unsaturated polyester resin comprising itaconate ester units as reactive unsaturation, wherein the resin comprises itaconate, citraconate and mesaconate ester units. Preferably, the resin comprises itaconate, citraconate and mesaconate ester units in an amount of from 40 to 90 mol % itaconate, from 2 to 30 mol % citraconate and from 5 to 40 mol % mesaconate in which 100 mol % is the total amount of itaconate, citraconate and mesaconate esters units.

Abstract: The present invention relates to a biaxial oriented polyester film and process for preparing the same, the said film is having an average ellipticity of not more than 0.6, Poisson ratio of not more than 0.7 (at elongation greater than 25%) all along the width of web and residual enthalpy in the range of 12% to 20%, a continuous reduction in residual film area up to an elongation of 100%.

Abstract: Disclosed is a material for fiber manufacturing comprising a liquid crystal polyester satisfying the following requirements (a) and (b): (a) the weight-average molecular weight is equal to or less than 30000 and the polydispersity is equal to or less than 2.5; and (b) the melt viscosity measured at 360° C. with conditions of a nozzle pore diameter of 0.5 mm and a shear velocity of 1000 s?1 using a flow feature testing machine is equal to or less than 70 Pa·s.

Abstract: The processes disclosed herein provide methods for dehydrating diols such that dimers of the diols are formed and incorporated into polyesters during polycondensation. Control over this phenomenon provides unique polymer compositions with a range of thermo-mechanical properties, crystallinity, bio-content and biodegradability. Generation of a wide range of properties allows development of polymers that can be used for a wide range of applications.

Abstract: Disclosed is a material for fiber manufacturing obtained by melt kneading while degassing a liquid crystal polyester satisfying the following requirements (a) and (b): (a) the flow starting temperature is equal to or greater than 280° C. and equal to or less than 360° C.; and (b) the melting viscosity measured at 360° C. with conditions of a nozzle pore diameter of 0.5 mm and a shear velocity of 1000 s?1 using a flow feature testing machine is equal to or less than 70 Pa·s.

Abstract: The invention relates to an unsaturated polyester resin comprising a) a lactic acid-modified unsaturated polyester and b) a copolymerizable comonomer, with replacement, with lactic acid, in the composition of an initial polyester, of: i) up to 90 mol % of phthalic anhydride of the acid component of the initial polyester, the acid component comprising from 80 to 20 mol % of maleic anhydride (MA) or fumaric acid, and from 20 to 80 mol % of phthalic anhydride (PA), the polyol component of the initial polyester comprising from 50 to 100 mol % of propylene glycol (PG) and from 0 to 50 mol % of a polyol among ethylene glycol (EG), diethylene glycol (DEG), dipropylene glycol (DPG) and/or 1,3-butylene glycol and/or 1,4-butanediol and/or neopentyl glycol (NPG), ii) up to 100% of a polyol from DPG and DEG, present in an initial overall molar amount ranging up to 50% of the polyol component of the initial polyester and also comprising PG, with the acid component of the initial polyester being maleic anhydride (MA) or f

Abstract: Disclosed are hot-melt adhesives prepared from aromatic-aliphatic polyesters containing terephthalic acid in combination with adipic acid, glutaric acid, or a mixture thereof, as diacid components and a diol component containing 1,4-butanediol, 1,6-hexanediol, or a combination thereof. These adhesives set up rapidly within a well-defined temperature window. The hot-melt adhesives can be used in a variety of applications, but are especially suited as seaming adhesives for roll-applied labels. These adhesives have melting temperatures and crystallization properties that allow their application at temperatures cool enough to prevent curling and premature shrinkage of the shrink label during seaming, and yet produce strong label seams that can withstand the elevated temperatures of a shrink tunnel without sacrificing line speed. Also disclosed are labeled containers and a process for applying a roll-on, shrink label to a container using the hot-melt adhesives of the invention.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising 2,5-furandicarboxylic acid residues; optionally, aromatic dicarboxylic acid residues and/or modifying aliphatic dicarboxylic acid residues and 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues. The polyesters may be manufactured into articles such as fibers, films, bottles, coatings, or sheets.

Abstract: A toner, including a crystalline resin as a binder resin, wherein the toner comprises a THF-soluble component in a weight-average molecular weight not less than 20,000, and has a 50% wettability not less than 20% by volume when subjected to a methanol wettability test.

Abstract: Described are polyesters comprising (a) a dicarboxylic acid component comprising 2,5-furandicarboxylic acid residues; optionally, aromatic dicarboxylic acid residues and/or modifying aliphatic dicarboxylic acid residues, 2,2,4,4-tetramethyl-1,3-cyclobutanediol residues and 1,4-cyclohexanedimethanol. The polyesters may be manufactured into articles such as fibers, films, bottles, coatings, or sheets.

Abstract: The present invention relates to oligoesters and their use for the creation of additives. Oligoester containing additives and/or oligoesters themselves may be used for formulating pharmaceutical preparations, cosmetics or personal care products such as shampoos and conditioners. These oligoesters are particularly useful for the creation of multi-purpose additives that can impart conditioning, long substantivity and/or UV protection. Individual oligoesters and oligoester mixtures are described.

Abstract: Described are polyester compositions comprising at least one polyester which comprises terephthalic acid residues, 2,2,4,4-tetramethyl-l,3-cyclobutanediol, and 1,4-cyclohexanedimethanol, wherein the inherent viscosity of said polyester is from 0.55 to 0.68 dL/g as determined in 60/40(wt/wt) phenol/tetrachloroethane at a concentration of 0.5 g/100 ml at 25° C.; wherein said polyester has a Tg from 110 to 160° C.; wherein the polyester composition comprises no polycarbonate; wherein the melt viscosity of the polyester is less than 10,000 poise as measured at 1 radian/second on a rotary melt rheometer at 290° C.; and wherein the polyester has a notched Izod impact strength, of at least 7.5 ft-lb/in.ch at 23° C. according to ASTM D256 with a 10-mil notch in a ? inch thick bar. The polyesters may be manufactured into articles of manufacture as fibers, films, bottles or sheets.

Abstract: A breathable, heat-sealable composite film comprising first and second layers of polymeric material wherein (i) the polymeric material of the first layer comprises copolyester comprising monomeric units derived from one or more diol(s); one or more dicarboxylic acid(s); and one or more poly(alkylene oxide) glycol(s); and (ii) the second layer is a heat-sealable polymeric layer, and a process for the production thereof.

Abstract: Disclosed is a composition comprising an aliphatic-aromatic copolyester consisting essentially of a dicarboxylic acid component that includes a terephthalic acid component and a linear aliphatic dicarboxylic acid component; and a glycol component consisting essentially of a linear aliphatic glycol component and 0 to 4 mole percent based on 100 mole percent total glycol component of a dialkylene glycol component; starch; optionally water; and polyol plasticizer. Also disclosed are shaped articles such as films which exhibit greater than expected tear strength and methods for preparing the films.