三苯基膦
钼
热分解
残留物(化学)
磷化氢
材料科学
热重分析
金属
药物化学
化学
有机化学
催化作用
冶金
作者
Sanghee Kim,Byeong Yeob Choi,Sun-Hee Park,Ki Sung Kang,Min-Chul Chung,Hong-Ki Choi
标识
DOI:10.1166/jnn.2021.19217
摘要
(PPh 3 )Mo(CO) 5 and (PPh 3 ) 2 Mo(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. (PPh 3 ) 2 Mo(CO) 4 could also be synthesized by the reaction of (PPh 3 )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 (PPh 3 )Mo(CO) 5 , (PPh 3 ) 2 Mo(CO) 4 , and Mo-octoate was also examined by the thermogravimetric analysis. The TGA curve of (PPh 3 )Mo(CO) 5 and (PPh 3 ) 2 Mo(CO) 4 showed a similar weight-loss pattern. (PPh 3 )Mo(CO) 5 and (PPh 3 ) 2 Mo(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 (PPh 3 )Mo(CO) 5 and (PPh 3 ) 2 Mo(CO) 4 at the reaction temperature (430 °C) of hydrocracking. The amount of coke formed after hydrocracking over (PPh 3 )Mo(CO) 5 and (PPh 3 ) 2 Mo(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 (PPh 3 ) 2 Mo(CO) 4 was considerably effective in reducing coke formation.
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