Dongfei Xu’s research while affiliated with Shanghai University and other places

A series of Al-P-O catalysts (Al-xP-O) were prepared using a P123-assisted one-pot method at different P/Al molar ratios and used for O-methylation of catechol and methanol. The influences of the P/Al molar ratio and P123 addition on catalyst structure and surface acid-base characteristics were investigated in detail. Increasing the P/Al molar ratio more favored crystalline aluminophosphate. The P123-assisted Al3+ and PO43− are known to be stabilized through weak steric force so that the formation of crystalline aluminophosphate could be inhibited at higher P/Al molar ratios. The results showed that the prepared Al-P-O catalysts possessed appropriate weak acid and weak base sites, which was beneficial to the reaction of catechol and methanol. The Al-1.1P-O catalyst synthesized with the assistance of P123 exhibited superior catalytic performances, with 52.5% catechol conversion and higher guaiacol selectivity of 97.6%.

Guaiacol produced by O-methylation of catechol with methanol over solid catalysts is a green environmental synthesis route. In order to achieve high catalytic efficiency, it is quite necessary to employ low-cost catalysts with high activity and stability. Herein, series of aluminophosphate catalysts were synthesized by a simple precipitation route modified by Zr. The characterization results indicated that the prepared Al-P-Zr catalysts possessed appropriate weak acid and weak base sites, which were beneficial for the O-methylation of catechol with methanol. Different Zr amount and calcined temperature exerted a significant influence on physicochemical properties of the catalysts and catalytic performance. The Al-P-Zr catalysts containing Zr/Al molar ratio of 0.012 calcined under 400 °C showed the optimal catalytic activity and long-term stability for vapor-phase selective O-methylation of catechol with methanol.

A new mesoporous alumina-supported molybdenum carbide (Mo2C/γ-MA) has been successfully prepared by one-step hydrolysis method without template, followed by carbonization with a mixed gas of CH4 and H2. The Mo2C particles (2.5 ± 0.3 nm) are homogeneously dispersed in the γ-alumina (γ-MA) framework and exhibit high catalytic activity and stability for thiophene hydrodesulfurization (HDS). Taking 1 wt% thiophene (3810 ppm S) as an example, the Mo2C/γ-MA exhibits 92% thiophene conversion, higher than the MoS2/γ-MA (85%), and other molybdenum carbides supported over commercial alumina and γ-MA prepared by the impregnation method. The stability test demonstrated that the Mo2C/γ-MA almost showed no deactivation during 150 h reaction, and no obvious carbon deposition and sulfurization of Mo2C species were observed over the spent Mo2C/γ-MA. The high HDS activity and stability of the Mo2C/γ-MA for HDS could be attributed to the formation of small Mo2C nanoparticles, appropriate surface acidity and the strong interaction between Mo2C species and alumina inhibiting the sulfurization of Mo2C species.