A flame-retardant polyamide composition can be prepared with a glow wire ignition temperature of not less than 775° C. Such a composition can include a polyamide having a melting point of not more than 290° C. as component A, fillers and/or reinforcers as component B, a phosphinic salt of the formula (I) as component C, a compound selected from the group of the Al, Fe, TiO.sub.p and Zn salts of ethylbutylphosphinic acid, of dibutylphosphinic acid, of ethylhexylphosphinic acid, of butylhexylphosphinic acid and/or of dihexylphosphinic acid as component D, a phosphonic salt of the formula (II) as component E, and a melamine polyphosphate having an average degree of condensation of 2 to 200 as component F. Additional components can be included in the composition.

A flame-retardant polyamide composition can be prepared with a glow wire ignition temperature of not less than 775° C. Such a composition can include a polyamide having a melting point of not more than 290° C. as component A, fillers and/or reinforcers as component B, a phosphinic salt of the formula (I) as component C, a compound selected from the group of the Al, Fe, TiO.sub.p and Zn salts of ethylbutylphosphinic acid, of dibutylphosphinic acid, of ethylhexylphosphinic acid, of butylhexylphosphinic acid and/or of dihexylphosphinic acid as component D, a phosphonic salt of the formula (II) as component E, and a melamine polyphosphate having an average degree of condensation of 2 to 200 as component F. Additional components can be included in the composition.

Provided is an aromatic polycarbonate resin composition, including, with respect to 100 parts by mass of an aromatic polycarbonate resin (A), 0.01 part by mass to 0.1 part by mass of an alicyclic epoxy compound (B), 0.2 part by mass to 0.6 part by mass of a polyether compound (C) having a polyoxyalkylene structure, and 0.005 part by mass to 1 part by mass of a phosphorus-based compound (D), wherein a difference between a YI value of a 5-millimeter thick molded body, which is obtained by molding the aromatic polycarbonate resin composition at 320° C., after a lapse of 3,000 hours under an environment at 85° C. and a humidity of 85%, and an initial YI value thereof is 3.0 or less.

Provided is an aromatic polycarbonate resin composition, including, with respect to 100 parts by mass of an aromatic polycarbonate resin (A), 0.01 part by mass to 0.1 part by mass of an alicyclic epoxy compound (B), 0.2 part by mass to 0.6 part by mass of a polyether compound (C) having a polyoxyalkylene structure, and 0.005 part by mass to 1 part by mass of a phosphorus-based compound (D), wherein a difference between a YI value of a 5-millimeter thick molded body, which is obtained by molding the aromatic polycarbonate resin composition at 320° C., after a lapse of 3,000 hours under an environment at 85° C. and a humidity of 85%, and an initial YI value thereof is 3.0 or less.

Provided is an aromatic polycarbonate resin composition, including, with respect to 100 parts by mass of an aromatic polycarbonate resin (A), 0.01 part by mass to 0.1 part by mass of an alicyclic epoxy compound (B), 0.2 part by mass to 0.6 part by mass of a polyether compound (C) having a polyoxyalkylene structure, and 0.005 part by mass to 1 part by mass of a phosphorus-based compound (D), wherein a difference between a YI value of a 5-millimeter thick molded body, which is obtained by molding the aromatic polycarbonate resin composition at 320° C., after a lapse of 3,000 hours under an environment at 85° C. and a humidity of 85%, and an initial YI value thereof is 3.0 or less.

Polymerizable compositions comprising a radically polymerizable resin can be polymerized in the absence of a peroxide initiator and other undesirable components. The polymerizable compositions and methods employ a manganese- or iron-containing salt or organic complex and a 1,3-dioxo compound with one or more other components. The polymerizable compositions have better storage stability and reduced gel time-drift.

Polymerizable compositions comprising a radically polymerizable resin can be polymerized in the absence of a peroxide initiator and other undesirable components. The polymerizable compositions and methods employ a manganese- or iron-containing salt or organic complex and a 1,3-dioxo compound with one or more other components. The polymerizable compositions have better storage stability and reduced gel time-drift.

Provided herein are methods of producing polymers from furan and optionally diol compounds, using an organocatalyst. A polymer composition comprising a polymer prepared by the method is contemplated. Provided herein are also polymer compositions, such as poly(alkylene-2,5-furandicarboxylate). In some embodiments, polymer compositions have any one of the characteristics discussed herein, or any combinations thereof.

Provided herein are methods of producing polymers from furan and optionally diol compounds, using an organocatalyst. A polymer composition comprising a polymer prepared by the method is contemplated. Provided herein are also polymer compositions, such as poly(alkylene-2,5-furandicarboxylate). In some embodiments, polymer compositions have any one of the characteristics discussed herein, or any combinations thereof.

Electrically conductive thermoplastic polymer composites of particulate thermoplastic polyester polymers, electrically conductive components (carbon nanofibers, graphene nanoplatelets, and/or conductive metal nanoparticulates), processing aids such as plasticizers, thermal stabilizers, etc., as well as nanoscopic particulate fillers such as nanoscopic titanium dioxide, etc., the electrically conductive components being distributed substantially uniformly in the composite to form an electrically conductive network. Also, methods for preparing thermoplastic polymer composites, a system for collecting extruded filaments prepared from thermoplastic polymer composites as a coil of filament, as well as method for tempering articles formed from thermoplastic polymer composites to increase the degree of crystallinity of the thermoplastic polymers and thus their mechanical strength properties.