C08G63/826

Oxygen scavenging compositions requiring no induction period

The present invention provides a composition comprising: a polyester base polymer; an oxidizable polyether-based additive; and a transition metal catalyst, wherein the polyester base polymer is substantially free of antimony. Containers made include a wall made of the composition. The polyester base polymer may preferably include polyethylene terephthalate and include less than about 100 ppm of antimony, less than about 50 ppm, less than about 10 ppm, or between about 0 and about 2 ppm. Containers made from the composition are substantially clear and exhibit excellent oxygen scavenging properties with little to no induction period.

PROCESS FOR PREPARING POLY(TRIMETHYLENE FURANDICARBOXYLATE) USING ZINC CATALYST
20230257520 · 2023-08-17 ·

A process is disclosed herein comprising the steps: a) contacting a mixture comprising furandicarboxylic acid dialkyl ester, 1,3-propanediol, a zinc compound, and optionally a poly(alkylene ether) diol, at a temperature in the range of from about 120° C. to about 220° C. to form prepolymer, wherein the mole ratio of the furandicarboxylic acid dialkyl ester to the 1,3-propanediol is in the range of from 1:1.3 to 1:2.2; and b) heating the prepolymer under reduced pressure to a temperature in the range of from about 220° C. to about 260° C. to form polymer. The mixture of step a) can further comprise an anthraquinone compound.

POLYESTER COPOLYMER FOR EXTRUSION
20220127417 · 2022-04-28 ·

The polyester copolymer according to the present disclosure can be extrusion-molded, and thus, can be usefully applied for the preparation of various containers.

CASHEW NUT SHELL LIQUID DERIVATIVES AND METHODS FOR MAKING AND USING SAME

The present invention is directed to Cashew Nut Shell Liquid derivatives and methods for making and using same. The invention is also directed to Cashew Nut Shell Liquid based monomers and polymers for making antimicrobials, antioxidants, adhesives, coatings, corrosion retardants composites, cosmetics, detergents, soaps, de-icing products, elastomers, food, flavors, inks, lubricants, oil field chemicals, personal care products, polymers, structural polymers, engineered plastics, 3D printable polymers, techno-polymers, rubbers, sealants, solvents, surfactants and varnishes.

Controlled production of polyglycolic acid and glycolide
11814474 · 2023-11-14 · ·

Provided is a process for producing a product having polyglycolic acid and glycolide from methyl glycolate. The process comprises esterification, polycondensation and optimization. Also provided are a product produced by the process and a method of changing the amount of the polyglycolic acid in the product by modifying the amount of an esterification catalyst and/or adjusting the reaction temperature.

IMPROVED OXYGEN BARRIER OF 1,4-BUTANEDIOL CONTAINING POLYMERS
20230357494 · 2023-11-09 ·

In a first aspect, the invention relates to a polymer composition comprising (i) a polyester; and (ii) an oxidizable organic polymer consisting of a branched or unbranched alkyl chain, which comprises at least one oxidizable C═C double bond. A second aspect of the invention relates to the use of the polymer composition according to the first aspect for the preparation of a polymer article. In a third aspect, the invention relates to a polymer article comprising the polymer composition according to the first aspect. In a fourth aspect, the invention relates to a method for preparing a polymer composition having oxygen consumption activity.

Method for preparing biogenic guanidine complex, method for preparing polyethylene terephthalate (PET), and method for preparing poly (ethylene isophthalate-co-terephthalate) (PEIT)

A method for preparing a biogenic guanidine complex, the method including: mixing dimethyl sulfoxide (DMSO) with water in a volume ratio thereof of 1:1 to yield a solvent DMSO-H.sub.2O; adding organic guanidine (G) and a compound MX.sub.2 in a molar ratio G/MX.sub.2=1:1 or 2:1 to the solvent DMSO-H.sub.2O, where the organic guanidine (G) is selected from arginine (Arg), guanidinoacetic acid (Gaa), creatine (Cra), creatinine (Cran), guanine (Gua), and agmatine (Agm); M represents Fe.sup.2+, Mg.sup.2+, or Zn.sup.2+; and X represents Cl.sup.−, CH.sub.3COO.sup.−, or CH.sub.3CH(OH)COO.sup.−; stirring the solvent DMSO-H.sub.2O containing the organic guanidine and the compound MX.sub.2; recycling the solvent DMSO-H.sub.2O through vacuum distillation and obtaining a solid; transferring the solid to a Buchner funnel, and washing the solid with deionized water and ethanol consecutively; and removing the deionized water and ethanol through vacuum filtration, and drying the solid. Biogenic guanidine complex can be used for production of Polyethylene terephthalate or Poly(ethylene isophthalate-co-terephthalate).

OXYGEN SCAVENGING COMPOSITIONS REQUIRING NO INDUCTION PERIOD
20220282083 · 2022-09-08 ·

A multilayer plastic bottle comprising at least one layer comprising a composition, said composition comprising: polyethylene terephthalate that is substantially free of antimony; an oxidizable polyether-based additive; and a transition metal catalyst, wherein the bottle has an oxygen permeability of not more than about 3.0 cm.sup.3 mm/(m.sup.2 atm day) immediately after the bottle is formed.

Sustainable polymer compositions and methods
11180609 · 2021-11-23 · ·

In one aspect, the present invention encompasses compositions of sustainable polycarbonate polymers, methods of producing such polymers, and methods for evaluating whether certain constituents of a polymer chain are derived from biomass or a fossil carbon source.

PROCESS FOR PREPARING POLY(TRIMETHYLENE FURANDICARBOXYLATE) USING ZINC CATALYST
20210269589 · 2021-09-02 ·

A process is disclosed herein comprising the steps: a) contacting a mixture comprising furandicarboxylic acid dialkyl ester, 1,3-propanediol, a zinc compound, and optionally a poly(alkylene ether) diol, at a temperature in the range of from about 120° C. to about 220° C. to form prepolymer, wherein the mole ratio of the furandicarboxylic acid dialkyl ester to the 1,3-propanediol is in the range of from 1:1.3 to 1:2.2; and b) heating the prepolymer under reduced pressure to a temperature in the range of from about 220° C. to about 260° C. to form polymer. The mixture of step a) can further comprise an anthraquinone compound.