C08G18/4288

Polyester polyols from thermoplastic polyesters and dimer fatty acids

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.

Hydroformylated triglycerides and uses thereof
11673850 · 2023-06-13 · ·

This disclosure provides methods for the chemical modification of triglycerides that are highly enriched in specific fatty acids and subsequent use thereof for producing functionally versatile polymers.

Aqueous dispersion of a copolymer

An aqueous dispersion containing at least one copolymer, the copolymer being preparable by initially charging an aqueous dispersion of at least one polyurethane, and then polymerizing a mixture of olefinically unsaturated monomers in the presence of the polyurethane, where a water-soluble initiator is used, the metered addition of the olefinically unsaturated monomers is effected in such a way that a concentration of 6.0% by weight, based on the total amount of olefinically unsaturated monomers, in the reaction solution is not exceeded over the entire duration of the reaction, and the mixture of the olefinically unsaturated monomers contains at least one polyolefinically unsaturated monomer.

Two-Component Solvent-Based Adhesive Composition
20220056324 · 2022-02-24 ·

The present disclosure provides a two-component solvent-less adhesive composition. The two-component solvent-less adhesive composition contains the reaction product of (A) an isocyanate component containing the reaction product of (i) an isocyanate monomer and (ii) a first dimer acid polyester polyol; and (B) a polyol component containing (i) a second dimer acid polyester polyol and (ii) optionally, a polyol selected from a polyether polyol, a polyester polyol, and combinations thereof. The two-component solvent-less adhesive composition contains from 15 wt % to 45 wt % units derived from dimer acid, based on the total weight of the two-component solvent-less adhesive composition.

Coating composition and use thereof
09796875 · 2017-10-24 · ·

The invention relates to a coating composition comprising: a) at least one alkyd binder with an oil content of at least 45 wt % and at most 85 wt %, a modified alkyd binder, or a combination thereof; b) at least one amine or imine component selected from the group comprising: polyaspartic acids and esters thereof, (meth)acrylate/aspartate amines, aldimines, ketimines, and combinations thereof; and c) at least one isocyanate compound.

Coating composition comprising a polyisocyanate and a polyol

The invention relates to a non-aqueous coating composition comprising a. a polyisocyanate, b. a polyol having an average functionality of more than 3 hydroxyl groups per molecule, c. a metal based curing catalyst for the addition reaction of isocyanate groups and hydroxyl groups, and d. a mercapto carboxylic acid, wherein the coating composition does not contain a carboxylic acid wherein the carbonyl group of the carboxylic acid is in conjugation with π-electron system.

Polyester-carbamate polymer and coating compositions thereof

A polyester-carbamate polymer and coating compositions containing the polymer are provided. The polyester-carbamate polymer preferably includes a polyester-carbamate backbone and one or more blocked isocyanate groups. A coating composition is provided that preferably includes the polyester-carbamate polymer and a thermoplastic dispersion. In a preferred embodiment, the coating composition is an organosol.

Storage-stable polyurethane casting compound for embedding hollow fibres in the production of filter elements

Disclosed are polyurethane encapsulating compounds for embedding hollow fibers of filter elements, obtainable by mixing a polyol component (A) and an isocyanate component (B), including at least one aromatic isocyanate, to give a reaction mixture and reacting the mixture to completion to give the polyurethane encapsulating compound. The polyol component (A) includes at least one fatty-acid-based polyol (a1) having a hydroxyl number of greater than 50 to less than 500 mg KOH/g and a functionality of from 2-6, and at least one bismuth catalyst (a2), obtainable by mixing a bismuth carboxylate (a2-1) with an amine compound (a2-11) having at least one tertiary nitrogen atom and at least one isocyanate-reactive hydrogen atom. The molar ratio of bismuth to amine compound (a2-11) is 1:0.5-1:50. Also disclosed are methods for producing filter elements using the polyurethane encapsulating compounds and to uses of the polyurethane encapsulating compounds for the embedding of hollow fibers.

Storage-stable polyurethane casting compound for embedding hollow fibres in the production of filter elements

Disclosed are polyurethane encapsulating compounds for embedding hollow fibers of filter elements, obtainable by mixing a polyol component (A) and an isocyanate component (B), including at least one aromatic isocyanate, to give a reaction mixture and reacting the mixture to completion to give the polyurethane encapsulating compound. The polyol component (A) includes at least one fatty-acid-based polyol (a1) having a hydroxyl number of greater than 50 to less than 500 mg KOH/g and a functionality of from 2-6, and at least one bismuth catalyst (a2), obtainable by mixing a bismuth carboxylate (a2-1) with an amine compound (a2-11) having at least one tertiary nitrogen atom and at least one isocyanate-reactive hydrogen atom. The molar ratio of bismuth to amine compound (a2-11) is 1:0.5-1:50. Also disclosed are methods for producing filter elements using the polyurethane encapsulating compounds and to uses of the polyurethane encapsulating compounds for the embedding of hollow fibers.

Reaction products containing hydroxyalkylterephthalates and methods of making and using same

The presently disclosed and/or claimed inventive concept(s) relates generally to oligomeric reaction products formed by the depolymerization of polyethylene terephthalate polymers and methods thereof. More specifically, the presently disclosed and/or claimed inventive concept(s) relates to oligomeric reaction products formed by the depolymerization of polyethylene terephthalate polymer obtained from, for example but not by way of limitation, waste products, such as beverage containers made from polyethylene terephthalate (PET). The oligomeric reaction products can, in one embodiment, be used as a starting material for polyurethanes. The presently disclosed and/or claimed inventive concept(s) also relates to processes for producing oligomeric reaction products from the depolymerization of polyethylene terephthalate. More particularly, the presently disclosed and/or claimed inventive concept(s) relates to a process of producing oligomeric reaction products of polyethylene terephthalate capable of controlling the removal of byproducts during the reaction. The presently disclosed and/or claimed inventive concept(s) also relates to ultraviolet curable urethane acrylate and polyethylene terephthalate compositions and methods of making and uses thereof.