Catalytic cracking of n-hexane over HEU-1 zeolite for selective propylene production: Optimizing the SiO2/Al2O3 ratio by in-situ synthesis

被引:20
作者
Zhang, Ya-Fei [1 ,2 ]
Liu, Xiao-Ling [1 ,2 ]
Sun, Li-Yuan [1 ,2 ]
Xu, Qing-Hu [1 ,2 ]
Wang, Xu-Jin [1 ,2 ]
Gong, Yan-Jun [1 ,2 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] China Univ Petr, Key Lab Catalysis China Natl Petr Corp, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
High-silica HEU-1; n-Hexane; Catalytic cracking; Propylene; TEMPERATURE-PROGRAMMED OXIDATION; STRUCTURE-DIRECTING AGENT; SEED-ASSISTED SYNTHESIS; SILICA EU-1 ZEOLITE; SHAPE SELECTIVITY; ZSM-5; ZEOLITE; ACID SITES; HEXAMETHONIUM IONS; PARAFFIN CRACKING; HYDROGEN-TRANSFER;
D O I
10.1016/j.fuproc.2016.07.019
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
HEU-1 zeolites with different SiO2/Al2O3 ratios (60-530) were in-situ synthesized and systematically evaluated in n-hexane catalytic cracking reaction. The influencing factors including SiO2/Al2O3 ratio, weight hourly space velocity and reaction temperature were investigated to optimize the light olefin yield, especially propylene. Compared to HZSM-48 and HZSM-5 zeolites with similar SiO2/Al2O3 ratios, HEU-1-300 (SiO2/Al2O3 = ca. 300), for example, displays much higher yield of ethylene plus propylene than HZSM-48 and comparable with HZSM-5. Furthermore, the propylene yield (35.6%) on it is higher than HZSM-5 by 9.0 percentage points, thus leading to higher propylene/ethylene ratio of 2.1. This excellent cracking performance of HEU-1-300 is ascribed to the combination of its moderate Bronsted acidity, due to the optimal SiO2/Al2O3 ratio, and unique framework topology. Moreover, both HEU-1 and HZSM-48 zeolites present much lower aromatics selectivity in the gas effluent than HZSM-5. For HEU-1 zeolite, it displays significant product shape selectivity due to its confined channel system, even though the large void space favors the formation of large intermediate species or aromatics precursors, while there is transition state shape selectivity for HZSM-48 structure which possesses no enough void space available to accommodate the large and complex hydrocarbons. HEU-1 topological structure also has pronounced effect on the formation and oxidation of coke deposition. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:163 / 172
页数:10
相关论文
共 65 条
[1]  
Abrevaya H, 2007, STUD SURF SCI CATAL, V170, P1244
[2]   Development of hierarchical EU-1 zeolite by sequential alkaline and acid treatments for selective dimethyl ether to propylene (DTP) [J].
Ahmed, Mohamed H. M. ;
Muraza, Oki ;
Al-Amer, Adnan M. ;
Miyake, Koji ;
Nishiyama, Norikazu .
APPLIED CATALYSIS A-GENERAL, 2015, 497 :127-134
[3]   Development of desilicated EU-1 zeolite and its application in conversion of dimethyl ether to olefins [J].
Ahmed, Mohamed H. M. ;
Muraza, Oki ;
Al Amer, Adnan M. ;
Sugiura, Yusuke ;
Nishiyama, Norikazu .
MICROPOROUS AND MESOPOROUS MATERIALS, 2015, 207 :9-16
[4]   Catalytic cracking of heavy naphtha-range hydrocarbons over different zeolites structures [J].
Al-Shammari, Abdallah A. ;
Ali, Syed A. ;
Al-Yassir, Nabil ;
Aitani, Abdullah M. ;
Ogunronbi, Kehinde E. ;
Al-Majnouni, Khalid A. ;
Al-Khattaf, Sulaiman S. .
FUEL PROCESSING TECHNOLOGY, 2014, 122 :12-22
[5]  
[Anonymous], 2015, IEEE T CLOUD COMPUT
[6]   THE FRAMEWORK TOPOLOGY OF ZEOLITE EU-1 [J].
BRISCOE, NA ;
JOHNSON, DW ;
SHANNON, MD ;
KOKOTAILO, GT ;
MCCUSKER, LB .
ZEOLITES, 1988, 8 (01) :74-76
[7]   Reaction mechanism and kinetic modeling of hydroisomerization and hydroaromatization of fluid catalytic cracking naphtha [J].
Chen, Zhiping ;
Xu, Jian ;
Fan, Yu ;
Shi, Gang ;
Bao, Xiaojun .
FUEL PROCESSING TECHNOLOGY, 2015, 130 :117-126
[8]   Current views on the mechanism of catalytic cracking [J].
Corma, A ;
Orchillés, AV .
MICROPOROUS AND MESOPOROUS MATERIALS, 2000, 35-6 :21-30
[9]   Light cracked naphtha processing: Controlling chemistry for maximum propylene production [J].
Corma, A ;
Melo, FV ;
Sauvanaud, L ;
Ortega, F .
CATALYSIS TODAY, 2005, 107-08 :699-706
[10]   State of the art and future challenges of zeolites as catalysts [J].
Corma, A .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :298-312