Tianhang Luo,Xuebing Xu,Maoqiang Jiang,Ying-zhou Lu,Hong Meng,Chun-xi Li
Polyacetylene (PA) was synthesized for the first time under mild conditions via polymerization of acetylene in n-octane with AlCl3 as a catalyst, whereby a series of PA-derived carbon materials were obtained. Their composition and structure were characterized and their electrochemical performance was evaluated systematically. It is found that acetylene gas at 1 MPa can polymerize explosively at room temperature under catalysis of AlCl3, forming acetylene black-like PA and a great amount of H2, while in the presence of n-octane solvent, acetylene polymerizes smoothly at higher temperature (30 to 300 °C), forming PA with a H(CHCH)nH structure. A series of PA-derived carbon materials are obtained by treating PA with KOH at 800 °C. The as-synthesizzed PA-100–KOH exhibits a high specific surface area (∼2500 m2 g−1), high specific capacitance (241 F g−1 at a current density of 0.1 A g−1 and 143 F g−1 at 5 A g−1), low AC resistance, and good cycling stability with 91.7% maintenance of capacity after 2000 cycles at a current density of 2 A g−1. This paper provides a new method for the facile synthesis of PA and a novel carbon source for supercapacitor electrode materials with excellent electrochemical performance and practical application.
Yang Han,Yuanyuan Liu,Shiwei Wang,Xuehui Ge,Xiaoda Wang,Ting Qiu
Tonalid, an important fragrance ingredient with widespread application, was synthesized via two Friedel-Crafts reactions, which were catalyzed by AlCl 3 . The traditional tonalid production was conducted in batch stirring tank reactors, suffering from low production capacity and the safety hazard of temperature runaway. To solve these problems, the continuous-flow technologies were developed for the high-efficiency and intrinsically safe synthesis of tonalid in microreactors. Catalyst AlCl 3 was neatly homogenized in proper solvents by forming complex with reactant, which was a necessary step for the continuous synthesis in microreactors. Several reaction conditions, including reactant molar ratio, catalyst concentration, temperature, and microchannel hydrodynamic diameter, were investigated for the two Friedel-Crafts reactions in microreactors. At optimized conditions, the yields of the two Friedel-Crafts reactions were 44.15% and 97.55%, respectively. In comparison with the batch reactors, the reaction times of these two reactions could both be reduced by nearly two thirds in microreactors at the similar yield.