Abstract

Sorption enhanced steam reforming of ethanol (SESRE), featured by yielding high purity of H(2) from one single reaction unit, is a new reaction process with a great potential for realizing sustainable H(2) production. The potential of such process with a CaO-based acceptor has been assessed by thermodynamic analysis and experimental demonstration. As predicted, ethanol can be reformed at relatively low temperatures (500-600 degrees C), still yielding high-quality H(2). Another major advantage of coupling CO(2) capture to the reforming process is predicted to be low risk in carbon formation. The SESRE reaction was carried out over a mixture of hydrotalcite-like material derived Co-Ni catalysts (Co-Ni/HTls) and calcined dolomite with a steam to carbon (S/C) ratio of 3 and temperatures ranging from 500 to 650 degrees C. The chosen reaction system was able to yield H(2) with purity fairly close to the theoretical prediction. Particularly, the best result was obtained over 40Ni and 20Co-20Ni/HTls at 550 degrees C, where the product gas had composition of more than 99 mol % H(2), ca. 0.4 mol % CH(4), 0.1 mol % CO, and 0.2 mol % CO(2). Special emphasis was put on the effect of steam on the stability of the CO(2) acceptor during the SESRE reaction. Hydration of CaO in the acceptor did not cause appreciable induction period, even at the low operating temperatures. However, different from a test under dry atmosphere (CO(2)/argon), the acceptor showed rapid deactivation in a multicycle operation of SESRE. A similar deactivation tend was given by a comparative test in a steam/CO(2)/Ar atmosphere.

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