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A thermodynamic equilibrium analysis on steam reforming process to utilize acetone-butanol-ethanol-water mixture obtained from biomass fermentation as biorenewable fuel has been performed to produce clean energy carrier H 2 via non-stoichiometric approach namely Gibbs free energy minimization method. The effect of process variables such as temperature (573–1473 K), pressure (1–10 atm), and steam/fuel molar feed ratio ( F ABE  = 5.5–12) have been investigated on equilibrium compositions of products, H 2 , CO, CO 2 , CH 4 and solid carbon. The best suitable conditions for maximization of desired product H 2 , suppression of CH 4 , and inhibition of solid carbon are 973 K, 1 atm, steam/fuel molar feed ratio = 12. Under these conditions, the maximum molar production of hydrogen is 8.35 with negligible formation of carbon and methane. Furthermore, the energy requirement per mol of H 2 (48.96 kJ), thermal efficiency (69.13%), exergy efficiency (55.09%), exergy destruction (85.36 kJ/mol), and generated entropy (0.29 kJ/mol.K) have been achieved at same operating conditions. [ABSTRACT FROM AUTHOR]

Abstract: The thermodynamic analysis of steam reforming of methanol without and with fractional removal of H2 and CO2 in adsorption, membrane and adsorption-membrane hybrid reactor systems to produce fuel cell grade H2 with minimal carbon formation is investigated. The results indicate that the removal of undesired CO2 by CO2 adsorbent is most effective process for the production of high purity H2 than H2 removal by membrane. However, the membrane is effective only above 30% H2 removal. It is possible to obtain H2 yield of 2.6 with negligibly small amount of CO and carbon formation at T = 405 K, P = 1 atm, 80% removal of CO2 and 100% methanol conversion. Identical results are achieved even at lower temperature of 345 K in adsorption-membrane hybrid reactor system at 80% removal of H2 and CO2. Thus high grade H2 can be produced by single step process and further processing to reduce CO by PROX reactor is not necessary. [Copyright &y& Elsevier]