As an alternative route for aromatics and hydrogen production, methane dehydroaromatization (MDA) is of significant academic and industrial interest due to the abundance of natural gas resources and the intensive demand for aromatics and CO-free hydrogen. In the present work, a simulation study on MDA in membrane reactors (MRs) was performed with the aim of co-producing aromatics and CO-free hydrogen with a highly improved efficiency. The effects of various parameters, including catalytic activity, membrane flux and selectivity, as well as the operating conditions on the MR performance were discussed with respect to methane conversion, hydrogen yield, and hydrogen purity. The results show that catalytic activity and membrane flux and selectivity have significant impacts on CH conversion and H yield, whereas H purity is mainly dominated by membrane selectivity. A highly improved MDA is confirmed to be feasible at a relatively low temperature and a high feed pressure because of the hydrogen extraction effect. To further improve MDA in MRs by intensifying H extraction, a simple configuration combining a fixed-bed reactor (FBR) and an MR together is proposed for MDA, which demonstrates good potential for the high-efficiency co-production of aromatics and CO-free hydrogen.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785898 | PMC |
http://dx.doi.org/10.3390/membranes12121175 | DOI Listing |
Phys Chem Chem Phys
July 2010
Department of Chemical and Biomolecular Engineering, The University of Melbourne, Parkville 3010, Victoria, Australia.
Glyoxal, HC(O)CHO, is an important trace component of the Earth's atmosphere, formed in biomass burning and in the photooxidation of volatile organic compounds (VOCs) like isoprene and aromatic hydrocarbons. The HC(O)CO free radical is the primary product of the glyoxal + OH reaction, and this study uses computational chemistry to show that the HC(O)CO radical can react with O(2) to regenerate the hydroxyl radical (OH) in the atmosphere. Master equation simulations indicate that the HC(O)C(O)O(2) peroxy radical adduct proceeds directly to CO(2) + CO + OH in a chemically activated mechanism, with minor collisional deactivation of the relatively unstable HC(O)C(O)O(2) peroxy radical.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!