Abstract: The present invention relates to a block copolymer, being the reaction product of: at least one functionalized polyfarnesene comprising a polymeric chain derived from farnesene and having at least one functional terminal end selected from the group comprising hydroxyl, amino, epoxy, isocyanato, and carboxylic acid; and at least one lactide; forming at least one polyfarnesene block and at least one polylactide block. The present invention also relates to a process for preparing said block copolymer, a polymer composition comprising said block copolymer, an article comprising said block copolymer, the use of said block copolymers as impact modifier and the use of said block copolymer as compatibilizer.

Abstract: A process for manufacturing defined functional lactic acid oligomers, can include contacting lactide with at least one compound that is a transfer agent. Oligomers can be prepared according to the process.

Abstract: A process for the manufacture of a block copolymer includes a reaction of a lactide monomers in the presence of a catalyst with a polymer to form the block copolymer having a lactic acid chain, wherein a polymer selected from polypropylene, polyethylene, polysiloxane, polybutylene succinate, polytrimethylene carbonate, polyester, polyether, polystyrene, polyisoprene, polycarbonate, polyalkylenecarbonate, polyvinyl alcohol, polyurethane, or polyacrylate; and wherein the polymer contains n number of OH and/or NH2 group(s), n is an integer greater than or equal to 1 and Moles ? ? of ? ? Lactide ( Moles ? ? of ? ? Compound * n ) ? 70 , and the reaction is performed at a temperature of at least 70° C. The process includes step of quenching of the reaction in order to form the lactic acid chains consisting of 70 or less of the lactide monomers, and the quenching agent is an acid chloride having a formula of Cl—CO—R9, wherein R9 is 1-pentenyl or aminoethyl.

Abstract: A method can include immortal ring-opening homopolymerisation of cyclic carbonates or cyclic esters in the presence of a catalytic system, or sequential two-step ring-opening block copolymerisation of one or more cyclic monomers selected from cyclic carbonates or cyclic esters in the presence of the catalytic system. The catalytic system can include a phenolate supported metallic complex. The catalytic system can also include an alcohol or a primary amine containing aliphatic and/or aromatic moieties. The alcohol or primary amine can be present in a molar ratio with respect to the metallic complex that is larger than 1.

Abstract: The present invention relates to the field of tailored di-, tri- and multi-block as well as gradient polyesters/polycarbonates copolymers prepared by introducing monomers simultaneously in the reaction medium in the presence of an organometallic, metal salt or organic catalyst.

Abstract: Poly(carbonate-urethane) or poly(ester-urethane) may be characterized in that of carbonate soft segments have molecular weights Mn ranging between 10,000 and 250,000 g/mol. The segments' length may be monitored by the ring-opening polymerization condition. The process of preparing the poly(carbonate-urethane) or poly(ester-urethane) may include immortal ring-opening polymerization of a cyclic carbonate or of a cyclic ester or diester monomers in the presence of a first catalyst system and diols or polyols. The process may include chemical modification of the hydroxyl chain-end groups into carboxylic groups in the presence of a second catalyst system. The process may include a coupling reaction with at least 2 equivalents of a second cyclic carbonate, enabling coupling with the carboxylic moiety in the presence of a third catalyst system.

Abstract: This invention relates to the synthesis of polycarbonates prepared from carbonate monomers derived from the biomass in the presence of a system comprising an organometallic transfer agent and alcohol. It also relates to the polymers resulting from these cyclic compounds.

Abstract: Polycarbonates prepared from carbonate monomers derived from the biomass are synthesized in the presence of an organometallic transfer agent and an alcohol. The number average molecular weight Mn of the final polymer increases with increasing the monomer/alcohol ratio.

Abstract: Poly(carbonate-urethane) or poly(ester-urethane) may be characterised in that of carbonate soft segments have molecular weights Mn ranging between 10,000 and 250,000 g/mol. The segments' length may be monitored by the ring-opening polymerisation condition. The process of preparing the poly(carbonate-urethane) or poly(ester-urethane) may include immortal ring-opening polymerisation of a cyclic carbonate or of a cyclic ester or diester monomers in the presence of a first catalyst system and diols or polyols. The process may include chemical modification of the hydroxyl chain-end groups into carboxylic groups in the presence of a second catalyst system. The process may include a coupling reaction with at least 2 equivalents of a second cyclic carbonate, enabling coupling with the carboxylic moiety in the presence of a third catalyst system.

Abstract: The present invention discloses new catalyst systems based on complexes of divalent metals supported by chelating phenoxy ligands for immortal ring-opening polymerization of cyclic esters and cyclic carbonates.

Abstract: The present invention discloses new catalyst systems based on complexes of divalent metals supported by chelating phenoxy ligands for immortal ring-opening polymerisation of cyclic esters and cyclic carbonates.

Abstract: The present invention discloses a method for preparing poly(carbonate-urethane) or poly(ester-urethane) without isocyanate.

Abstract: The present invention discloses new catalyst systems based on complexes of divalent metals supported by chelating phenoxy ligands for immortal ring-opening polymerisation of cyclic esters and cyclic carbonates.

Abstract: A process for manufacturing defined functional lactic acid oligomers can include contacting lactide with at least one compound that is a transfer agent. Oligomers can be prepared according to the process.

Abstract: A method can include immortal ring-opening homopolymerisation of cyclic carbonates or cyclic esters in the presence of a catalytic system, or sequential two-step ring-opening block copolymerisation of one or more cyclic monomers selected from cyclic carbonates or cyclic esters in the presence of the catalytic system. The catalytic system can include a phenolate supported metallic complex. The catalytic system can also include an alcohol or a primary amine containing aliphatic and/or aromatic moieties. The alcohol or primary amine can be present in a molar ratio with respect to the metallic complex that is larger than 1.

Abstract: The present invention relates to the field of tailored di-, tri- and multi-block as well as gradient polyesters/polycarbonates copolymers prepared by introducing monomers simultaneously in the reaction medium in the presence of an organometallic, metal salt or organic catalyst.

Abstract: The present invention discloses the use of polycarbonate to increase the crystallisation rate of polylactides while maintaining its the mechanical properties.

Abstract: This invention relates to the synthesis of polycarbonates prepared from carbonate monomers derived from the biomass in the presence of a system comprising an organometallic transfer agent and alcohol. It also relates to the polymers resulting from these cyclic compounds.

Abstract: This invention relates to the synthesis of polycarbonates prepared from carbonate monomers derived from the biomass in the presence of a system comprising an organometallic transfer agent and alcohol. It also relates to the polymers resulting from these cyclic compounds.

Abstract: The present invention discloses a method for preparing polycarbonate-urethane) or poly(ester-urethane) without isocyanate