Selective hydroisomerization of isobutane to n-butane over WO3-ZrO2 supported Ni-Cu alloy

被引:16
作者
Wang, Shufang [1 ]
Cao, Minglun [1 ]
Sun, Shujuan [1 ]
Jiang, Hui [1 ]
Duan, Yaoyao [1 ]
Kong, Xiangjin [2 ]
Wang, Hefang [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300130, Peoples R China
[2] Liaocheng Univ, Shandong Prov Key Lab, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Storage & Nove, Liaocheng 252000, Shandong, Peoples R China
关键词
Isobutane; N-butane; Hydroisomerization; Ni-Cu alloy; Tungstated zirconia; Acidity; ISOMERIZATION ACTIVITY; CATALYTIC PERFORMANCE; TUNGSTATED ZIRCONIA; SULFATED-ZIRCONIA; ACID; HEPTANE; PT/WO3-ZRO2; CONVERSION; CRACKING; NI-CU/AL2O3;
D O I
10.1016/j.fuel.2020.118274
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
To develop a robust and efficient non-noble metal-based catalyst for selective hydroisomerization of short-chain iso-alkanes is of great importance, yet challenging. In the present studies, a series of WO3-ZrO2 supported Ni, Cu catalysts were prepared by incipient wetness impregnation. The characterization results of Mapping, XRD, H-2-TPR, TEM, and XPS confirmed the formation of Ni-Cu alloy in the bimetallic catalysts. The results of NH3-TPD indicated that the formation of Ni-Cu alloy increased the amount of medium acidic sites and total acidic sites. Isobutane hydroisomerization to n-butane was used as probe reaction to evaluate the catalytic activity. With the Cu addition up to 1 wt% over 1 wt% WO3-ZrO2, the hydrocracking reactions were inhibited, leading to both a significant increase in the selectivity to n-butane and an improved stability of the catalysts. Under the optimized condition, the yield of n-butane was 38.86% at 450 degrees C, 2.5 MPa with an H-2/alkane of 4:1, and a LHSV of 1 h(-1) over 1Ni1Cu/WZr. The activity of 1Ni1Cu/WZr remained almost unchanged after 123 h on stream. A possible reaction scheme was also proposed for the isobutane hydroisomerization to n-butane over 1Ni1Cu/WZr.
引用
收藏
页数:10
相关论文
共 40 条
[1]   On the nanogate-opening pressures of copper-doped zeolitic imidazolate framework ZIF-8 for the adsorption of propane, propylene, isobutane, and n-butane [J].
Awadallah-F, Ahmed ;
Hillman, Febrian ;
Al-Muhtaseb, Shaheen A. ;
Jeong, Hae-Kwon .
JOURNAL OF MATERIALS SCIENCE, 2019, 54 (07) :5513-5527
[2]   Composite catalysts of Pt/SO42--ZrO2 and Pt/WO3-ZrO2 for producing high octane isomerizate by isomerization-cracking of long paraffins [J].
Busto, M. ;
Dosso, L. A. ;
Vera, C. R. ;
Grau, J. M. .
FUEL PROCESSING TECHNOLOGY, 2012, 104 :128-135
[3]   Conversion of levulinic acid to N-substituted pyrrolidinones over a nonnoble bimetallic catalyst Cu15Pr3/Al2O3 [J].
Cao, Pengwei ;
Ma, Tengfei ;
Zhang, Hong-Yu ;
Yin, Guohui ;
Zhao, Jiquan ;
Zhan, Yuecheng .
CATALYSIS COMMUNICATIONS, 2018, 116 :85-90
[4]   Catalytic Performance of Re/Ga2O3/WO3/ZrO2 Catalyst for n-Hexane Isomerization [J].
Chen Chao ;
Qin Lizhen ;
Chen Xiaorong ;
Chen Changlin .
CHINESE JOURNAL OF CATALYSIS, 2009, 30 (09) :859-863
[5]  
Chen S. S., 1975, Journal of Physical and Chemical Reference Data, V4, P859, DOI 10.1063/1.555526
[6]   Al- and Ga-promoted WO3/ZrO2 strong solid acid catalysts and their catalytic activities in n-butane isomerization [J].
Chen, XR ;
Chen, CL ;
Xu, NP ;
Mou, CY .
CATALYSIS TODAY, 2004, 93-5 :129-134
[7]   Activation and isomerization of hydrocarbons over WO3/ZrO2 catalysts -: I.: Preparation, characterization, and X-ray photoelectron spectroscopy studies [J].
Di Gregorio, F ;
Keller, V .
JOURNAL OF CATALYSIS, 2004, 225 (01) :45-55
[8]   Activity, selectivity and stability of Ni-Pt loaded zeolite-β and mordenite catalysts for hydroisomerisation of n-heptane [J].
Eswaramoorthi, I ;
Bhavani, AG ;
Lingappan, N .
APPLIED CATALYSIS A-GENERAL, 2003, 253 (02) :469-486
[9]   Catalytic cycles for isobutane isomerization over sulfated-zirconia catalysts [J].
Fogash, KB ;
Hong, Z ;
Dumesic, JA .
CATALYSIS LETTERS, 1998, 56 (2-3) :85-93
[10]   Liquid-phase glycerol hydrogenolysis by formic acid over Ni-Cu/Al2O3 catalysts [J].
Gandarias, I. ;
Requies, J. ;
Arias, P. L. ;
Armbruster, U. ;
Martin, A. .
JOURNAL OF CATALYSIS, 2012, 290 :79-89