The copolymerization of CO and styrene catalyzed by Pd/C toward the formation of polyketones （PK）was studied in the N-valeronitrile-N＆#39;-methylimidazolium hexafluorophosphate （[C4CNmim]＋PF6-） medium. The synth...The copolymerization of CO and styrene catalyzed by Pd/C toward the formation of polyketones （PK）was studied in the N-valeronitrile-N＆#39;-methylimidazolium hexafluorophosphate （[C4CNmim]＋PF6-） medium. The synthe-sized PK was characterized by Fourier transform infrared（FTIR）, elemental analysis, 13C-nuclear magnetic resonance （13C-NMR）, differential scanning calorimetry （DSC）, thermogravimetric analysis （TGA） and gel permeation chro-matography （GPC）. The supported ionic liquid film on the surface of Pd/C catalyst can prevent the products from covering the hole of active carbon due to its chemical stability and weak coordination ability with metal ions, and thus efficiently improve the catalytic activity. The effects of different amounts of ionic liquid on the catalytic activity and reusability of the catalyst and the molecular weight of PK were discussed. When the usage of ionic liquid is 10wt%（0.1 g ionic liquid/1 g active carbon carrier） and the theoretical content of Pd2＋is 5wt%（0.05 g Pd2＋/1 g active car-bon carrier）, the highest catalytic activity 2 963.64 gSTCO/（gPd＆#183;h） is achieved with the molecular weight and polydispersity index of PK as Mn=9 684, Mw=13 452 and Mw/Mn=1.389.展开更多
It has been found that cold plasma is a facile and environmentally benign method for synthesizing supported metal catalysts, and great efforts have been devoted to enlarging its applications. However, little work has ...It has been found that cold plasma is a facile and environmentally benign method for synthesizing supported metal catalysts, and great efforts have been devoted to enlarging its applications. However, little work has been done to disclose the influence mechanism, which is significant for controllable synthesis. In this work, hydrogen cold plasma was adopted to synthesize a palladium catalyst supported on activated carbon （Pd/C-P） using HzPdC14 as a Pd precursor followed by calcination in hydrogen gas to remove the chlorine ions. The Pd/C-P catalyst was found to be made of larger Pd nanoparticles showing a decreased migration to the support outer surface than that prepared by the conventional thermal hydrogen reduction method （Pd/C-C）. Meanwhile, the pore diameter of the activated carbon support is small （,-~4 nm）. Therefore, Pd/C-P exhibits lower CO oxidation activity than Pd/C-C. It was proposed that the strong interaction between the activated carbon and PdC142-, and the enhanced metal-support interaction caused by hydrogen cold plasma reduction made it difficult for Pd nanoparticles to migrate to the support outer surface. The larger-sized Pd nanoparticles for Pd/C-P may be due to the Coulomb interaction resulting in the disturbance of the metal-support interaction. This work has important guiding significance for the controllable synthesis of supported metal catalysts by hydrogen cold plasma.展开更多
基金Supported by the Tianjin Natural Science Foundation(No.07JCYBJC00600)
文摘The copolymerization of CO and styrene catalyzed by Pd/C toward the formation of polyketones （PK）was studied in the N-valeronitrile-N＆#39;-methylimidazolium hexafluorophosphate （[C4CNmim]＋PF6-） medium. The synthe-sized PK was characterized by Fourier transform infrared（FTIR）, elemental analysis, 13C-nuclear magnetic resonance （13C-NMR）, differential scanning calorimetry （DSC）, thermogravimetric analysis （TGA） and gel permeation chro-matography （GPC）. The supported ionic liquid film on the surface of Pd/C catalyst can prevent the products from covering the hole of active carbon due to its chemical stability and weak coordination ability with metal ions, and thus efficiently improve the catalytic activity. The effects of different amounts of ionic liquid on the catalytic activity and reusability of the catalyst and the molecular weight of PK were discussed. When the usage of ionic liquid is 10wt%（0.1 g ionic liquid/1 g active carbon carrier） and the theoretical content of Pd2＋is 5wt%（0.05 g Pd2＋/1 g active car-bon carrier）, the highest catalytic activity 2 963.64 gSTCO/（gPd＆#183;h） is achieved with the molecular weight and polydispersity index of PK as Mn=9 684, Mw=13 452 and Mw/Mn=1.389.
基金supported by National Natural Science Foundation of China (Grant Nos. 11505019, 21673026)Dalian Youth Science and Technology Project (Grant No. 2015R089)
文摘It has been found that cold plasma is a facile and environmentally benign method for synthesizing supported metal catalysts, and great efforts have been devoted to enlarging its applications. However, little work has been done to disclose the influence mechanism, which is significant for controllable synthesis. In this work, hydrogen cold plasma was adopted to synthesize a palladium catalyst supported on activated carbon （Pd/C-P） using HzPdC14 as a Pd precursor followed by calcination in hydrogen gas to remove the chlorine ions. The Pd/C-P catalyst was found to be made of larger Pd nanoparticles showing a decreased migration to the support outer surface than that prepared by the conventional thermal hydrogen reduction method （Pd/C-C）. Meanwhile, the pore diameter of the activated carbon support is small （,-~4 nm）. Therefore, Pd/C-P exhibits lower CO oxidation activity than Pd/C-C. It was proposed that the strong interaction between the activated carbon and PdC142-, and the enhanced metal-support interaction caused by hydrogen cold plasma reduction made it difficult for Pd nanoparticles to migrate to the support outer surface. The larger-sized Pd nanoparticles for Pd/C-P may be due to the Coulomb interaction resulting in the disturbance of the metal-support interaction. This work has important guiding significance for the controllable synthesis of supported metal catalysts by hydrogen cold plasma.
