International Journal of Hydrogen Energy, Vol.42, No.10, 6713-6726, 2017
Membrane reformer module with Ni-foam catalyst for pure hydrogen production from methane: Experimental demonstration and modeling
Results of experiments and modeling of a compact (800 cm(3)) membrane reformer module for the production of 0.25-0.30 Nm(3)/h hydrogen by methane steam reforming are reported. The module consists of a two-sided composite membrane disc with a 50 pm Pd Ag layer and two adjacent 4 mm thick Ni foam discs (60 ppi). A nickel catalyst and a porous support were deposited on the foam discs to give the final composition of 10%Ni/10%MgO/Ni-foam. Membrane permeability by pure hydrogen was investigated, and coefficients of transverse hydrogen transport across the Ni foam to the membrane in the case of inlet binary N-2-H-2 mixture were refined in order to account for concentration polarization effect into the model. Activity of the catalytic discs was measured in a differential laboratory scale reactor at a pressure of 1 bar and temperature of 400-600 degrees C. Modules were tested at a 8-13 bar pressure of the mixture in the reforming zone and at 1 bar of pure hydrogen under the membrane, H2O/C = 2.5-3 and a module temperature of 550-680 degrees C (with and without hydrogen removal). Two modifications of the module were tested: consecutive (I-type) and parallel (II-type) flow of the reaction mixture around two sides of the membrane disc. In order to optimize construction of the module, calculations were made for revealing the effect of thickness of the Pd Ag membrane layer (5-50 mu m), thickness of the Ni foam discs (0.5-8 mm) and temperature (600-700 degrees C) on the hydrogen output of the module. A comparison of the values obtained in our experiments (>1 MW/m(3) and >0.7 kg(H-2)/h/m(2)) with the literature data reported by other authors showed that the developed modules are promising for practical application as components of a fuel processor section for mobile applications. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.