Methane catalytic decomposition (MCD) over Ni/MCM-41 catalysts was tested in a microreactor to simultaneously produce hydrogen and carbon nanotubes (CNTs). The methane conversion reached 30% to 47% at a moderate tempe...Methane catalytic decomposition (MCD) over Ni/MCM-41 catalysts was tested in a microreactor to simultaneously produce hydrogen and carbon nanotubes (CNTs). The methane conversion reached 30% to 47% at a moderate temperature range from 400°C to 600°C and the catalytic activity of the catalysts remains stable during 500 min steam on time. CNTs were chiefly formed through tip-growth mode, due to the weak interaction between the metallic Ni and the support. Most of the Ni particles are located on the tip of the produced CNTs, which avoids rapid deactivation of the catalyst resulted from carbon encapsulation. Large Ni particles usually lead to the formation of CNTs with big diameter. During the reaction, the shape of Ni particles changed from pseudo-sphere to diamond-like. All the CNTs consist of multiple layer walls and are curved in certain degree.展开更多
A zirconium modified MCM-48 mesoporous material was synthesized by surfactant-templated method. Surface grafting Zr-MCM-48 with tungstophosphoric acid led to a great enhancement of both the number of the Br?nsted acid...A zirconium modified MCM-48 mesoporous material was synthesized by surfactant-templated method. Surface grafting Zr-MCM-48 with tungstophosphoric acid led to a great enhancement of both the number of the Br?nsted acid sites and acidity strength in comparison with the bare support. At 100°C, the 30 wt% H3PW12O40/Zr-MCM-48 contained 174 μmol/g Br?nsted acid sites which were 14.5 times greater than that of Zr-MCM-48. The Keggin structure of the grafted heteropolyacid was rather stable after calcination at 400°C for 2 h, approximately 93.3% of Keggin structure in the dispersed heteropolyacid were remained without destruction but slightly distorted in some degree, as evidenced by FTIR characterization and 31P NMR-MAS analysis. This H3PW12O40/Zr-MCM-48 solid with three dimensional mesoporous system, large surface area and very strong Br?nsted acidity will be a promising catalyst for acid catalytic reactions.展开更多
文摘Methane catalytic decomposition (MCD) over Ni/MCM-41 catalysts was tested in a microreactor to simultaneously produce hydrogen and carbon nanotubes (CNTs). The methane conversion reached 30% to 47% at a moderate temperature range from 400°C to 600°C and the catalytic activity of the catalysts remains stable during 500 min steam on time. CNTs were chiefly formed through tip-growth mode, due to the weak interaction between the metallic Ni and the support. Most of the Ni particles are located on the tip of the produced CNTs, which avoids rapid deactivation of the catalyst resulted from carbon encapsulation. Large Ni particles usually lead to the formation of CNTs with big diameter. During the reaction, the shape of Ni particles changed from pseudo-sphere to diamond-like. All the CNTs consist of multiple layer walls and are curved in certain degree.
文摘A zirconium modified MCM-48 mesoporous material was synthesized by surfactant-templated method. Surface grafting Zr-MCM-48 with tungstophosphoric acid led to a great enhancement of both the number of the Br?nsted acid sites and acidity strength in comparison with the bare support. At 100°C, the 30 wt% H3PW12O40/Zr-MCM-48 contained 174 μmol/g Br?nsted acid sites which were 14.5 times greater than that of Zr-MCM-48. The Keggin structure of the grafted heteropolyacid was rather stable after calcination at 400°C for 2 h, approximately 93.3% of Keggin structure in the dispersed heteropolyacid were remained without destruction but slightly distorted in some degree, as evidenced by FTIR characterization and 31P NMR-MAS analysis. This H3PW12O40/Zr-MCM-48 solid with three dimensional mesoporous system, large surface area and very strong Br?nsted acidity will be a promising catalyst for acid catalytic reactions.