C08G63/19

A METHOD FOR MANUFACTURING AN OLIGOMERIC POLYETHYLENE TEREPHTHALATE (PET) SUBSTRATE

A method for producing an oligomeric polyethylene terephthalate (PET) substrate for use in a recycled PET (rPET) manufacturing process, comprising (i) adding recycled bis-hydroxylethylenete rephthalate (rBHET) and an under-esterified purified terephthalic acid (PTA) oligomer to a reaction zone; and ii) reacting the rBHET and the under-esterified PTA oligomer in the reaction zone to produce an oligomeric PET substrate represented by the formula (I), wherein R1 is a carboxyl end group or a hydroxyl end group, R2 is a carboxyl end group or a hydroxyl end group, and n is a degree of polymerisation (Dp).

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A METHOD FOR IMPROVING L* COLOR IN A PET POLYMER

A method for improving L* color of polyethylene terephthalate polymer, the method including bis-hydroxylethyl-eneterephthalate being polycondensed to produce said polyethylene terephthalate polymer in a polyethylene terephthalate manufacturing process, and wherein said process requires an antimony-containing catalyst, the method comprising the steps of: i) adding said antimony-containing catalyst at a temperature in a range of a melting point of said BHET to an upper temperature of 220° C.; and ii) exposing said BHET in a molten state to glycol removal before addition of said antimony-containing catalyst.

Sustainable Polyester from Recycled Polyethylene Terephthalate

A method includes depolymerizing post-consumer or post-industrial recycled polyethylene terephthalate (rPET) to form bis(2-hydroxyethyl) terephthalate (BHET), and reacting at least a portion of the BHET with a catalyst to form an alcohol. The alcohol includes cyclohexanedimethanol (CHDM) or 1,4-phenylenedimethanol (PDM). Further steps of the method include polymerizing the alcohol in the presence of additional BHET to form a polyester. The polyester may include poly(cyclohexylenedimethylene terephthalate (PCT), polyethylene terephthalate glycol (PETG) copolyester, polycyclohexylene dimethylene terephthalate glycol (PCTG) copolyester, polycyclohexylene dimethylene terephthalate acid (PCTA), or a monomer having repeating units with the structure (I), wherein n is an integer having a value of at least 20.

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Sustainable Polyester from Recycled Polyethylene Terephthalate

A method includes depolymerizing post-consumer or post-industrial recycled polyethylene terephthalate (rPET) to form bis(2-hydroxyethyl) terephthalate (BHET), and reacting at least a portion of the BHET with a catalyst to form an alcohol. The alcohol includes cyclohexanedimethanol (CHDM) or 1,4-phenylenedimethanol (PDM). Further steps of the method include polymerizing the alcohol in the presence of additional BHET to form a polyester. The polyester may include poly(cyclohexylenedimethylene terephthalate (PCT), polyethylene terephthalate glycol (PETG) copolyester, polycyclohexylene dimethylene terephthalate glycol (PCTG) copolyester, polycyclohexylene dimethylene terephthalate acid (PCTA), or a monomer having repeating units with the structure (I), wherein n is an integer having a value of at least 20.

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Plateable Polymer Composition
20230167234 · 2023-06-01 ·

A plateable polymer composition is provided. The polymer composition comprises 100 parts by weight of a polymer matrix that includes a thermotropic liquid crystalline polymer, from about 10 parts to about 80 parts by weight of silicate fibers, and a noble metal catalyst.

Plateable Polymer Composition
20230167234 · 2023-06-01 ·

A plateable polymer composition is provided. The polymer composition comprises 100 parts by weight of a polymer matrix that includes a thermotropic liquid crystalline polymer, from about 10 parts to about 80 parts by weight of silicate fibers, and a noble metal catalyst.

POLYMETRIC BIOMATERIALS DERIVED FROM PHENOLIC MONOMERS AND THEIR MEDICAL USES

The present invention provides new classes of phenol compounds, including those derived from tyrosol and analogues, useful as monomers for preparation of biocompatible polymers, and biocompatible polymers prepared from these monomeric phenol compounds, including novel biodegradable and/or bioresorbable polymers. These biocompatible polymers or polymer compositions with enhanced bioresorbability and processibility are useful in a variety of medical applications, such as in medical devices and con-trolled-release therapeutic formulations. The invention also provides methods for preparing these monomeric phenol compounds and biocompatible polymers.

DEOXYBENZOIN CONTAINING FLAME RETARDANT POLYMER COMPOSITIONS

The present invention relates to specific deoxybenzoin containing flame retardant polyesters and flame retardant thermoplastic polymer molding compositions comprising deoxybenzoin containing flame retardant polyesters as well as their preparation and use for producing moldings, fibers or foils.

DEOXYBENZOIN CONTAINING FLAME RETARDANT POLYMER COMPOSITIONS

The present invention relates to specific deoxybenzoin containing flame retardant polyesters and flame retardant thermoplastic polymer molding compositions comprising deoxybenzoin containing flame retardant polyesters as well as their preparation and use for producing moldings, fibers or foils.

Sheet formed from carbon fiber reinforced thermoplastic resin, and production method of said sheet

A sheet formed from carbon fiber reinforced thermoplastic resin with high moldability, and a production method of said resin is provided. This sheet is formed from a carbon fiber reinforced thermoplastic resin that contains carbon fibers, dichloromethane, and a thermoplastic resin containing at least one of a polycarbonate resin and a polyarylate resin. The aforementioned at least one of a polycarbonate resin and a polyarylate resin has a terminal structure derived from a monohydric phenol represented by formula (1) and a constituent unit derived from a dihydric phenol, and the content of the dichloromethane contained in the sheet is 10-10,000 ppm by mass. (In formula (1), R.sub.1 represents an alkyl group with 8-36 carbons, or an alkenyl group with 8-36 carbons, and R.sub.2-R.sub.5 independently represent a hydrogen, a halogen, an alkyl group with 1-20 carbons optionally having a substituent, or an aryl group with 6-12 carbons optionally having a substituent.) ##STR00001##