Chen Dong, Wang Linlin, Chen Xiaopeng, Wei Xiaojie, Liang Jiezhen, Jiang Jiao, Liang Baofang
School of Chemistry and Chemical Engineering, Guangxi University, Nanning 53004, People's Republic of China.
Guangxi Key Laboratory of Petrochemical Resources Processing and Process Intensification Technology, Guangxi University, Nanning 53004, People's Republic of China.
R Soc Open Sci. 2018 May 23;5(5):172052. doi: 10.1098/rsos.172052. eCollection 2018 May.
A Ni-based catalyst (Ni-PVP/PFC3R) with polyvinyl pyrrolidone (PVP) as a dispersant supported in a pretreated fluid catalytic cracking catalyst residue (PFC3R) was synthesized and applied to C9 petroleum resin (C9 PR) hydrogenation. For comparison, a Ni catalyst without PVP (Ni/PFC3R) was prepared in the same way. Ni-PVP/PFC3R exhibited higher activity and better stability. The catalysts were characterized by X-ray diffraction, scanning electron microscope, H-temperature programmed reduction/temperature programmed desorption, Fourier transform infrared spectroscopy and the Brunauer-Emmett-Teller method. The catalysts had a smaller crystallite size and stronger interactions between the Ni species and the PFC3R support in the presence of PVP. The effects of nickel loading, H pressure, temperature and reaction time for C9 PR hydrogenation over Ni-PVP/PFC3R were investigated. The bromine number was reduced to 1.25 under the following conditions: nickel content of 12 wt%, PVP amount of 1.5 wt%, temperature of 270°C, H pressure of 8 MPa and reaction time of 240 min.
合成了一种以聚乙烯吡咯烷酮(PVP)为分散剂负载于预处理流化催化裂化催化剂残渣(PFC3R)中的镍基催化剂(Ni-PVP/PFC3R),并将其应用于C9石油树脂(C9 PR)加氢反应。作为对比,以同样方式制备了不含PVP的镍催化剂(Ni/PFC3R)。Ni-PVP/PFC3R表现出更高的活性和更好的稳定性。通过X射线衍射、扫描电子显微镜、H2程序升温还原/程序升温脱附、傅里叶变换红外光谱和布鲁诺尔-埃米特-泰勒法对催化剂进行了表征。在PVP存在下,催化剂的微晶尺寸更小,镍物种与PFC3R载体之间的相互作用更强。研究了镍负载量、氢气压力、温度和反应时间对Ni-PVP/PFC3R上C9 PR加氢反应的影响。在以下条件下,溴值降至1.25:镍含量为12 wt%、PVP用量为1.5 wt%、温度为270°C、氢气压力为8 MPa和反应时间为240 min。