Role of distributed oxygen addition and product removal in the oxidative coupling of methane

被引:22
作者
Androulakis, IP [1 ]
Reyes, SC [1 ]
机构
[1] Exxon Res & Engn Co, Corp Res Labs, Annandale, NJ 08801 USA
关键词
D O I
10.1002/aic.690450417
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Modeling and optimization of C-2 hydrocarbon production via the oxidative coupling of methane (OCM) were studied. The model includes both homogeneous and heterogeneous reactions. Focusing on the use of detailed reaction networks, previously validated experimentally, and the critical role of oxygen in both methane activation and product degradation, this work systematically explores the use of controlled oxygen addition and product removal schemes that improve OCM performance. Based on a plug flow reactor that is divided into N-p stages, within which oxygen is added and/or products are removed, a rigorous optimization algorithm is developed that simultaneously maximizes C-2 yields and minimizes O-2 consumption. In the absence of catalyst and product removal, the C-2 yield is maximized at a fixed O-2/CH4 ratio, but this maximum yield is independent of the form in which the oxygen is added (cofeed or staged). When a catalyst is added, the optimal C-2 yields show only gradual improvements with oxygen distribution because the benefits of the lower oxygen reaction order on the catalyst are adversely affected by concomitant surface degradation reactions. The largest yield improvements are obtained when the C-2 hydrocarbons are removed at each stage before they undergo oxidation reactions. Thus, when staged oxygen addition is combined with product removal in the presence of a catalyst, C-2 yields as high as 87% are achieved in about 20 stages. Such yield values are consistent with experiments in which continuous product separation schemes have been used.
引用
收藏
页码:860 / 868
页数:9
相关论文
共 40 条
[1]   CONVERSION OF METHANE BY OXIDATIVE COUPLING [J].
AMENOMIYA, Y ;
BIRSS, VI ;
GOLEDZINOWSKI, M ;
GALUSZKA, J ;
SANGER, AR .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1990, 32 (03) :163-227
[2]   KINETICS AND MECHANISM OF THE HETEROGENEOUS OXIDATION OF METHYL RADICALS ON SAMARIUM(III) OXIDE - IMPLICATIONS FOR THE OXIDATIVE COUPLING OF METHANE [J].
AMOREBIETA, VT ;
COLUSSI, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (13) :3856-3861
[3]  
AMOREBIETA VT, 1996, J AM CHEM SOC, V118, P10326
[4]  
Andrianova ZS, 1996, KINET CATAL+, V37, P246
[5]  
Baerns M., 1986, US Patent, Patent No. [4608449 A, 4608449]
[6]  
Brenan K.E., 1995, Numerical Solution of Initial-Value Problems in Differential-Algebraic Equations
[7]   SIMULATION OF A CATALYTIC MEMBRANE REACTOR FOR OXIDATIVE COUPLING OF METHANE [J].
CHENG, S ;
SHUAI, X .
AICHE JOURNAL, 1995, 41 (06) :1598-1601
[8]   BENEFICIAL EFFECT OF OXYGEN DISTRIBUTION ON METHANE CONVERSION AND C-2-SELECTIVITY IN OXIDATIVE COUPLING OF METHANE TO C-2-HYDROCARBONS OVER LANTHANUM-PROMOTED MAGNESIUM-OXIDE [J].
CHOUDHARY, VR ;
CHAUDHARI, ST ;
RAJPUT, AM ;
RANE, VH .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (20) :1526-1527
[9]   Optimum yield of the purely heterogeneous oxidative dimerization of methane [J].
Colussi, AJ ;
Amorebieta, VT .
JOURNAL OF CATALYSIS, 1997, 169 (01) :301-306
[10]   Steady-state production of olefins in high yields during the oxidative coupling of methane: Utilization of a membrane contactor [J].
Cordi, EM ;
Pak, S ;
Rosynek, MP ;
Lunsford, JH .
APPLIED CATALYSIS A-GENERAL, 1997, 155 (01) :L1-L7