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Role of distributed oxygen addition and product removal in the oxidative coupling of methane
Author(s) -
Androulakis Ioannis P.,
Reyes Sebastián C.
Publication year - 1999
Publication title -
aiche journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.958
H-Index - 167
eISSN - 1547-5905
pISSN - 0001-1541
DOI - 10.1002/aic.690450417
Subject(s) - yield (engineering) , oxidative coupling of methane , oxygen , catalysis , chemistry , methane , product distribution , degradation (telecommunications) , hydrocarbon , plug flow reactor model , chemical engineering , organic chemistry , materials science , continuous stirred tank reactor , computer science , engineering , metallurgy , telecommunications
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 /CH 4 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.