Abstract: A polybutylene succinate (PBS) nanocomposite material includes a matrix comprising polybutylene succinate chains, and nanocelluloses dispersed between the polybutylene succinate chains. The PBS composite material may be produced by polymerizing 1,4-butanediol and succinic acid or a derivative thereof in a mixture of 1,4-butanediol and succinic acid or a derivative thereof with nanocelluloses. The PBS nanocomposite material and the method have improved properties, which does not require a surface hydrophobization pretreatment process of cellulose, melt kneading, and solution mixing processes.

Abstract: A self-restoring polyurethane-based polymer obtained by polymerization of a composition containing an aromatic disulfide diol represented by Chemical Formula, HO—Ar1—S—S—Ar2—OH, an alicyclic polyisocyanate, and a polyol. Ar1 and Ar2 each are independently a substituted or unsubstituted C6-C30 arylene group. The composition satisfies Equation, 0.1?M[disulfide]/M[OH]. M[disulfide] is a total mole number of the aromatic disulfide diol in the composition, and M[OH] is a total mole number of the aromatic disulfide diol and the polyol in the composition.

Abstract: The present invention relates to a polymer composite material comprising an aramid nanofiber (ANF), and a method for preparing same. More specifically, the present invention relates to an arylene ether-based polymer or arylene ether imide-based polymer composite material which is obtained by mixing an arylene ether-based polymer or an arylene ether imide-based polymer with aramid nanofibers dispersed in a polar aprotic solution or by adding and polymerizing monomers in the dispersion of aramid nanofibers.

Abstract: Disclosed is a composite film including a nanocellulose film including cellulose nanofibers stacked in a structure including a plurality of pores; and a polycarbonate resin filling the pores in the nanocellulose film and including a repeating unit that comprises a moiety derived from isosorbide.

Abstract: A polybutylene succinate (PBS) nanocomposite material includes a matrix comprising polybutylene succinate chains, and nanocelluloses dispersed between the polybutylene succinate chains. The PBS composite material may be produced by polymerizing 1,4-butanediol and succinic acid or a derivative thereof in a mixture of 1,4-butanediol and succinic acid or a derivative thereof with nanocelluloses. The PBS nanocomposite material and the method have improved properties, which does not require a surface hydrophobization pretreatment process of cellulose, melt kneading, and solution mixing processes.

Abstract: A self-restoring polyurethane-based polymer obtained by polymerization of a composition containing an aromatic disulfide diol represented by Chemical Formula, HO—Ar1—S—S—Ar2—OH, an alicyclic polyisocyanate, and a polyol. Ar1 and Ar2 each are independently a substituted or unsubstituted C6-C30 arylene group. The composition satisfies Equation, 0.1?M[disulfide]/M[OH]. M[disulfide] is a total mole number of the aromatic disulfide diol in the composition, and M[OH] is a total mole number of the aromatic disulfide diol and the polyol in the composition.

Abstract: The present invention provides a method for producing polythiophene star copolymer capable of being self-doped by an external stimulus, which includes the steps of: forming a polythiophene macroinitiator made by introducing a living radical polymerizable functional group into an end of polythiophene or a derivative thereof; forming through living radical polymerization a polymer macroinitiator for providing by an external stimulus at least a dopant selected from the group consisting of sulfonic acid radical, carboxylic acid radical and phosphoric acid radical; and polymerizing the polythiophene macroinitiator added with the polymer macroinitiator and at least one kind of divinyl monomer to produce the polythiophene star copolymer. The polythiophene star copolymer capable of being self-doped by an external stimulus according to the present invention is a self-doped material to stably increase conductivity, and can be used as a material for a conductive film.

Abstract: Provided are a CNT-polymer complex and a process for preparing the same. The CNT-polymer complex includes carbon nanotubes (CNT) coated with a block copolymer of a conjugated polymer and a non-conjugated polymer, wherein the non-conjugated polymer comprises at least one monomer selected from the group consisting of styrene, butadiene, isoprene, methacryl, acryl, acryl amide, methacryl amide, acrylonitrile, vinyl acetate, vinyl pyridine and vinyl pyrrolidone in which at least one selected from the group consisting of a sulfone group, carboxyl group, acryl group and phosphate group is protected with a protective group, and provides at least one dopant selected from the group consisting of a sulfone group, carboxyl group, acryl group and phosphate group by external stimuli so that self-doping is allowed; and the complex is soluble to an organic solvent in a neutral state but is insoluble to any solvent after subjecting it to external stimuli.

Abstract: Provided are a CNT-polymer complex and a process for preparing the same. The CNT-polymer complex includes carbon nanotubes (CNT) coated with a block copolymer of a conjugated polymer and a non-conjugated polymer, wherein the non-conjugated polymer comprises at least one monomer selected from the group consisting of styrene, butadiene, isoprene, methacryl, acryl, acryl amide, methacryl amide, acrylonitrile, vinyl acetate, vinyl pyridine and vinyl pyrrolidone in which at least one selected from the group consisting of a sulfone group, carboxyl group, acryl group and phosphate group is protected with a protective group, and provides at least one dopant selected from the group consisting of a sulfone group, carboxyl group, acryl group and phosphate group by external stimuli so that self-doping is allowed; and the complex is soluble to an organic solvent in a neutral state but is insoluble to any solvent after subjecting it to external stimuli.

Abstract: The present invention provides a method for producing polythiophene star copolymer capable of being self-doped by an external stimulus, which includes the steps of: forming a polythiophene macroinitiator made by introducing a living radical polymerizable functional group into an end of polythiophene or a derivative thereof; forming through living radical polymerization a polymer macroinitiator for providing by an external stimulus at least a dopant selected from the group consisting of sulfonic acid radical, carboxylic acid radical and phosphoric acid radical; and polymerizing the polythiophene macroinitiator added with the polymer macroinitiator and at least one kind of divinyl monomer to produce the polythiophene star copolymer. The polythiophene star copolymer capable of being self-doped by an external stimulus according to the present invention is a self-doped material to stably increase conductivity, and can be used as a material for a conductive film.