A process for producing a polyester composition from recycled polyesters.

The present application discloses a bending-resistant polyester film and its production method thereof. The chemical structure of the bending-resistant polyester composition comprises monomers having elastic conformation. The film made from the composition of polyester of the present invention through production processes such as melt extrusion and biaxial drawing still has excellent flexibility and optical properties.

The present disclosure envisages a coating composition. The coating composition comprises a polymeric emulsion, silane functionalized fibres and a fluid medium. The silane functionalized fibres are present in an amount in the range of 0.05 wt. % to 10 wt. % of the coating composition. The polymeric emulsion is present in an amount in the range of 20 wt. % to 60 wt. % of the coating composition. The fluid medium is present in an amount in the range of 5 wt. % to 40 wt. % of the coating composition. The silane functionalized fibre comprises at least one polymer bonded to at least one silane group. The coating composition of the present disclosure exhibit improved properties such as better coverage when applied on a surface, mechanical properties, stain resistance properties and the like, when compared to coating composition without fibres.

The present invention relates to a functional coating obtained from an aqueous coating composition, which composition comprises a pigment and a polymeric binder, wherein the binder has a weight average molecular weight of from 2000 to 50000 g/mole, and an acid value of 40 to 250, and wherein the binder is a polyester comprising a side group introduced by a Diels-Alder and/or pericyclic Ene-reaction, wherein the side group contains an ionic group and/or an ion-forming group.

Disclosed are curable adhesive compositions comprising hydroxyl functional polymers and silane functionalized resins. Such adhesive compositions are capable of providing unexpected properties for various uses and end products. The adhesive may be used for woodworking, automotive, textile, appliances, electronics, bookbinding, and packaging. Suitable substrates can be metal, polymer film, plastics, wood, glass, ceramic, paper, and concrete.

An end capped condensation polymer may be formed by heating a condensation polymer in the presence of an end capping compound to form cleaved condensation polymer reacting at least a portion of the cleaved condensation polymer with the end capping compound to form the end capped condensation polymer. The end capped condensation polymers may be used to form additive manufactured articles having high solids loading and improved processing due to improved rheological behavior.

Copolymers of condensation polymers are formed by a method of cleaving and reacting with a chain extender to form an end capped cleaved condensation polymer that is further reacted with a second compound that may be comprised of a further chain extender and condensation polymer that react with a reactive group still remaining in the chain extender capping the cleaved condensation polymer. The method allows the formation of block copolymers, branched copolymers and star polymers of differing condensation polymers bonded through the residue of a chain extender.

Polyethylene glycol (PEG)-b-poly(β-amino ester) (PBAE) co-polymers (PEG-PBAE) and blends of PEG-PBAEs and PBAEs and their use for delivering drugs, genes, and other pharmaceutical or therapeutic agents safely and effectively to different sites in the body and to different cells, such as cancer cells, are disclosed.

An ion exchange resin and a method for preparing the same are provided. An ion exchange resin is formed by a composition, and the composition includes a crosslinking agent and an ionic compound with sulfonate ions. The ionic compound with sulfonate ions is formed by reacting an epoxy resin with an ionic monomer with sulfonate ions or an ionic polymer having sulfonate ions. The ionic monomer and the ionic polymer each has a hydroxyl group or an acid group at the ends. The ionic monomer or the ionic polymer is 40 to 80 parts by weight, and the epoxy resin is 15 to 25 parts by weight, based on 100 parts by weight of the ion exchange resin. An ion exchange resin with a network structure is formed after the ionic compound with sulfonate ions reacts with the crosslinking agent.

An ion exchange resin and a method for preparing the same are provided. An ion exchange resin is formed by a composition, and the composition includes a crosslinking agent and an ionic compound with sulfonate ions. The ionic compound with sulfonate ions is formed by reacting an epoxy resin with an ionic monomer with sulfonate ions or an ionic polymer having sulfonate ions. The ionic monomer and the ionic polymer each has a hydroxyl group or an acid group at the ends. The ionic monomer or the ionic polymer is 40 to 80 parts by weight, and the epoxy resin is 15 to 25 parts by weight, based on 100 parts by weight of the ion exchange resin. An ion exchange resin with a network structure is formed after the ionic compound with sulfonate ions reacts with the crosslinking agent.