Polyester polyols made from thermoplastic polyesters are disclosed. The polyols can be made by heating a thermoplastic polyester such as virgin PET, recycled PET, or mixtures thereof, with a glycol to give a digested intermediate, which is then condensed with a dimer fatty acid to give the polyol. The invention includes a polyester polyol comprising recurring units of a glycol-digested thermoplastic polyester and a dimer fatty acid. The polyester polyol can also be made in a single step by reacting the thermoplastic polyester, glycol, and dimer acid under conditions effective to produce the polyol. High-recycle-content polyols having desirable properties and attributes for formulating polyurethane products, including aqueous polyurethane dispersions, can be made. The polyols provide a sustainable alternative to bio- or petrochemical-based polyols.

The invention relates to a method for producing an EBM bottle with 0.90 to 1.5 dL/g from a bottle-grade PET post-consumer recycling flake, i.e., a recycled, post-consumer PET with a viscosity of 0.65 to 0.84 dL/g, using extrusion processes, solid state polycondensation processes, and a blowing process.

Functionalized compounds including residues of one or more 1,1-disubstituted alkene compounds. Preferably the functionalized compound includes the residue of two or more 1,1-disubstituted alkene compounds, which are spaced apart. The functionalized compound may be produced by a transesterification reaction. The functionalized compounds may be employed in a polymerizable composition and may be used to prepare new polymers, (for example by reacting the alkene group).

Poly(glycerol sebacate) (PGS) polymers, which may be referred to as a functionalized poly(glycerol sebacate) polymers. The PGS polymers include pendant aliphatic carboxyl ate groups and/or pendant aryl carboxyl ate groups covalently bound to the glycerol group of the glycerol sebacate backbone of the polymer. Polymeric materials including a plurality of glycerol sebacate groups, where at least a portion of the individual glycerol sebacate groups have a pendant aliphatic carboxylate group and/or pendant aryl carboxyl ate group covalently bound to the glycerol group of the glycerol sebacate group. The PGS polymers or polymeric materials may be crosslinked PGS polymers or polymeric materials. The PGS polymers and polymeric materials may be made by post-polymerization functionalization. The PGS polymers and polymeric materials may be in fiber form. A material, which may be a fabric, may include a fiber or plurality of fibers. A material may be used to form a tissue graft.

Biodegradable compositions containing an aliphatic-aromatic copolyester derived from aromatic polyesters. Methods of making the compositions and articles made from the compositions.

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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A hydroxyl-terminated polyester resin, a preparation method therefor and use thereof. The hydroxyl-terminated polyester resin is composed of the following raw materials in parts by mass: 25-50 parts of a diol, 40-70 parts of a dibasic acid, 0.1-2 parts of glycidyl tertcarbonate, 0.5-4 parts of a hydroxylation reagent, 0.08-0.3 parts of a catalyst and 0.2-0.5 parts of an antioxidant. The acid value of the polyester resin is 1-8 mgKOH/g, the hydroxyl value is 20-30 mgKOH/g, the melt viscosity at 200° C. is 9000-13000 mPa.Math.s, the reactivity at 180° C. is 410-520 s, the glass transition temperature is 53-59° C., and the softening point is 101-106° C.

Provided is a composition comprising one or more epoxy phosphate esters wherein the structure comprises two or more polyester linkages. Also provided is a method of making the epoxy phosphate esters that comprises reacting one or more epoxy-terminated polyesters with one or more phosphoric acids. Further provided is an adhesive composition that comprises one or more epoxy phosphate esters, one or more multifunctional isocyanate prepolymers, and one or more multifunctional isocyanate-reactive compounds.

A method of forming a multimodal Polyalkylene Terephthalate (PAT) can include: providing a feed of a low molecular weight (LMW) PAT, the LMW PAT having a low average molecular weight; providing a feed of high molecular weight (HMW) PAT, the HMW PAT having a high average molecular weight, wherein the low average molecular weight is lower than the high average molecular weight; mixing the feed of LMW PAT with the feed of HMW PAT in a mixer to form a multimodal PAT; and providing the multimodal PAT as output. The multimodal PAT can include: a low average molecular weight of a low molecular weight (LMW) PAT; and a high average molecular weight of a high molecular weight (HMW) PAT mixed with the LMW PAT to form the multimodal PAT, wherein the multimodal PAT is devoid of talc.

A flame retardant with which fire retardancy is improved and the fire retardancy is able to be secured stably for a long time is provided. An internal layer 11 containing a polymer and a flame retardant factor layer 12 that is formed outside of the internal layer 11 and that contains a polymer to which at least one of a sulfonate group and a sulfonate base is bonded are included. Thereby, compared to a case that the flame retardant factor layer 12 is not included, moisture is hardly absorbed, and respective particles of the flame retardant are inhibited from being adhered to each other. Accordingly, blocking is inhibited.