Intensification of Ethylene Production from Naphtha via a Redox Oxy-Cracking Scheme: Process Simulations and Analysis

被引:57
作者
Haribal, Vasudev Pralhad [1 ]
Chen, Yun [1 ,2 ]
Neal, Luke [1 ]
Li, Fanxing [1 ]
机构
[1] North Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
Ethylene; Naphtha cracking; Process intensification; Chemical looping; Process simulations; OXIDATIVE DEHYDROGENATION; STEAM CRACKING; PILOT-PLANT; ETHANE; CATALYSTS; OLEFINS; PROPANE;
D O I
10.1016/j.eng.2018.08.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Ethylene production by the thermal cracking of naphtha is an energy-intensive process (up to 40 GJ heat per tonne ethylene), leading to significant formation of coke and nitrogen oxide (NOx), along with 1.8-2 kg of carbon dioxide (CO2) emission per kilogram of ethylene produced. We propose an alternative process for the redox oxy-cracking (ROC) of naphtha. In this two-step process, hydrogen (H-2) from naphtha cracking is selectively combusted by a redox catalyst with its lattice oxygen first. The redox catalyst is subsequently re-oxidized by air and releases heat, which is used to satisfy the heat requirement for the cracking reactions. This intensified process reduces parasitic energy consumption and CO2 and NOx emissions. Moreover, the formation of ethylene and propylene can be enhanced due to the selective combustion of H-2. In this study, the ROC process is simulated with ASPEN Plus (R) based on experimental data from recently developed redox catalysts. Compared with traditional naphtha cracking, the ROC process can provide up to 52% reduction in energy consumption and CO2 emissions. The upstream section of the process consumes approximately 67% less energy while producing 28% more ethylene and propylene for every kilogram of naphtha feedstock. (C) 2018 THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company.
引用
收藏
页码:714 / 721
页数:8
相关论文
共 28 条
[1]  
Ball M, 2015, COMPENDIUM HYDROGEN
[2]   Supported vanadium oxide-based catalysts for the oxidehydrogenation of propane under cyclic conditions [J].
Ballarini, N ;
Cavani, F ;
Cericola, A ;
Cortelli, C ;
Ferrari, M ;
Trifirò, F ;
Capannelli, G ;
Comite, A ;
Catani, R ;
Cornaro, U .
CATALYSIS TODAY, 2004, 91-2 :99-104
[3]   PERFORMANCE AND AGING OF CATALYSTS FOR THE SELECTIVE HYDROGENATION OF ACETYLENE - A MICROPILOT-PLANT STUDY [J].
BATTISTON, GC ;
DALLORO, L ;
TAUSZIK, GR .
APPLIED CATALYSIS, 1982, 2 (1-2) :1-17
[4]   Dehydrogenation and oxydehydrogenation of paraffins to olefins [J].
Bhasin, MM ;
McCain, JH ;
Vora, BV ;
Imai, T ;
Pujadó, PR .
APPLIED CATALYSIS A-GENERAL, 2001, 221 (1-2) :397-419
[5]   Oxidative Conversion of Hexane to Olefins-Influence of Plasma and Catalyst on Reaction Pathways [J].
Boyadjian, C. ;
Agiral, A. ;
Gardeniers, J. G. E. ;
Lefferts, L. ;
Seshan, K. .
PLASMA CHEMISTRY AND PLASMA PROCESSING, 2011, 31 (02) :291-306
[6]  
Boyadjian CA, 2010, THESIS
[7]   Catalytic oxidative cracking of hexane as a route to olefins [J].
Boyadjian, Cassia ;
Lefferts, Leon ;
Seshan, K. .
APPLIED CATALYSIS A-GENERAL, 2010, 372 (02) :167-174
[8]   Oxidative dehydrogenation of ethane and propane: How far from commercial implementation? [J].
Cavani, F. ;
Ballarini, N. ;
Cericola, A. .
CATALYSIS TODAY, 2007, 127 (1-4) :113-131
[9]  
Contractor R.M., 1987, CATAL TODAY, V1, P49, DOI [10.1016/0920-5861(87)80026-3, DOI 10.1016/0920-5861(87)80026-3]
[10]   Pt0.02Sn0.003Mg0.06 on γ-alumina:: a stable catalyst for oxidative dehydrogenation of ethane [J].
de Graaf, EA ;
Rothenberg, G ;
Kooyman, PJ ;
Andreini, A ;
Bliek, A .
APPLIED CATALYSIS A-GENERAL, 2005, 278 (02) :187-194