Comparison and Synthesis of Molybdenum Carbonyl Complexes Substituted with Mono- and Bis-Triphenylphosphine Ligands for Hydrocracking of Vacuum Residue

(PPh3)Mo(CO)5 and (PPh3)2Mo(CO)4 were synthesized by the reaction of molybdenum hexacar-bonyl with triphenylphosphine and applied as precursors to hydrocracking of vacuum residue under high-pressure and high-temperature conditions. (PPh3)2Mo(CO)4 could also be synthesized by the reaction of (PPh3)Mo(CO)5 with triphenyl phosphine. A commercial precursor (Mo-octoate) for hydrocracking of vacuum residue was used for comparison. The thermal decomposition behavior of (PPh3)Mo(CO)5, (PPh3)2Mo(CO)4, and Mo-octoate was also examined by the thermogravimetric analysis. The TGA curve of (PPh3)Mo(CO)5 and (PPh3)2Mo(CO)4 showed a similar weight-loss pattern. (PPh3)Mo(CO)5 and (PPh3)2Mo(CO)4 were decomposed into Mo metal and ligands rapidly in the range of 140 °C~270 °C. There were no ligands bound to a metal center of (PPh3)Mo(CO)5 and (PPh3)2Mo(CO)4 at the reaction temperature (430 °C) of hydrocracking. The amount of coke formed after hydrocracking over (PPh3)Mo(CO)5 and (PPh3)2Mo(CO)4 was 2.3% and 0.5%, respectively. Upgrading the qualities of heavy oils is an important issue in the energy industry. It is not easy to achieve the complete conversion of vacuum residue due to coke forming during hydrocracking of vacuum residue. This study showed that (PPh3)2Mo(CO)4 was considerably effective in reducing coke formation.

Synthesis of butadiene/isoprene–styrene di-block copolymer with high cis-1,4 unit content based on a neodymium phosphate ester

A novel synthesis strategy of butadiene/isoprene–styrene di-block copolymer with high cis-1,4 content was explored based on a neodymium phosphate catalyst, by adjusting the electron cloud density of the catalytic active center via triphenyl phosphine.