期刊
JOURNAL OF MEMBRANE SCIENCE
卷 598, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.memsci.2019.117780
关键词
-
资金
- National Science Foundation [CBET-1604700]
The existing process for hydrogen production from methane through steam-reforming requires multiple reactors and separators and is thus costly and energy-intensive. This paper reports a new concept of CO2-permselective membrane reactor for promoting hydrogen production via steam reforming of methane (SRM) with CO2 capture. The membrane reactor is made of a ceramic-carbonate dual-phase membrane with a two-layered asymmetric wall structure. Bismuth-yttrium-samarium oxide (Bi1.5Y0.3Sm0.2O3-delta, BYS) was added to the support layer to make it non-wettable by molten carbonate, leaving the samarium-doped ceria (Sm0.2Ce0.8O2-delta, SDC) layer to form a thin (similar to 150 mu m) CO2-permselective SDC/molten-carbonate dual-phase layer after molten carbonate infiltration. The output product composition from the membrane reactor confirms that in situ CO2 removal effectively promotes water-gas shift conversion in SRM and thus enhances hydrogen yield. At 900 degrees C with feed pressure at 1 atm, the membrane reactor achieves 90% hydrogen yield with 84% CO2 recovery, which poses significant improvement when compared with conventional fixed-bed reactor under similar conditions. Analysis of CO2 permeation activation energy suggests that surface reaction rate might have an effect on CO2 permeation flux for the thin SDC/molten-carbonate membranes. Under atmospheric conditions the CO2 permeation with reactive feed for SRM is lower than with non-reactive feed due to lower driving force under reactive conditions in the feed.
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