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To accelerate the crystallization of poly(L-lactic acid) (PLLA) and enhance its crystallization ability, a multiamide nucleator (TMC) was introduced into the PLLA matrix. The thermal characteristics, isothermal and nonisothermal crystallization behavior of pure PLLA and TMC-nucleated PLLA were investigated by differential scanning calorimetry. The determination of thermal characteristics shows that the addition of TMC can significantly decrease the onset temperature of cold crystallization and meanwhile elevate the total crystallinity of PLLA. For the isothermal crystallization process, it is found that the overall crystallization rate is much faster in TMC-nucleated PLLA than in pure PLLA and increases as the TMC content is increased, however, the crystal growth form and crystalline structure are not influenced much despite the presence of TMC. In the case of nonisothermal crystallization, the nucleation efficiency and nucleation activity were estimated and the results indicate that excellent nucleation-promoting effect could be achieved when the weight percentage of TMC is chosen between 0.25% and 0.5%. Polarized optical microscopy observation reveals that the nuclei number of PLLA increases and the spherulite size reduces greatly with the addition of

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The silane-treated carbon fiber induced the formation of transcrystalline structure and enhanced the interfacial adhesion between the fiber and polyamide 6 matrix.

RH-derived carbon exhibits stable electrochemical performance. Moreover, the preparation process is very simple and low cost.

Biodegradable poly(butylene succinate) (PBS)/carbon fiber (CF) composites were prepared by melt blending method using twin-screw extruder followed by injection molding. Mechanical properties, crystallization behavior, morphology, crystal structure, and thermal stability of PBS/CF composites were investigated with different CF contents (0, 5, 10, 15, and 20 wt%). It was found that the tensile and impact properties of the composites were improved markedly with the addition of CF; while too much CF would lead to agglomeration and thus weaken the improvement. Scanning electron microscopic photographs on the fracture surfaces showed superior interfacial adhesion between fibers and PBS matrix. Crystallization peak temperature of PBS in its composites was increased due to the heterogeneous effect of CF. The spherulite size of PBS/CF composites decreased and the nucleation density increased drastically. The crystal structure was not affected by the incorporation of CF, as confirmed from the wide-angle X-ray diffraction analysis. thermogravimetric analysis showed that the thermal stability of PBS/CF composites was also enhanced. POLYM. COM-POS., 36:1335-1345, 2015