Aqueous phase reforming of biodiesel byproduct glycerol over mesoporous Ni-Cu/CeO2 for renewable hydrogen production

Aqueous phase reforming (APR), regarded as one method for inexpensive H-2 production, was widely studied due to lower temperature and unnecessary to vaporize water and fuels. In this study, the mesoporous CeO2, regarded as a metal oxide carrier, was first prepared by colloidal solution combustion, and then the Ni-Cu bimetallic supported on mesoporous CeO2 was successfully synthesized to investigate the catalytic performance in APR of biodiesel byproduct glycerol. The results show that the Cu element in the catalysts can effectively improve water-gas shift (WGS) reaction and inhibit the formation of methane, which increases the H-2 production rate from 125.08 to 195.57 mu mol.min(-1).g cat(-1). The higher reaction temperature is beneficial to the H-2 production rate, but not to H-2 selectivity. Kinetics analysis indicates that catalyst of 1Ni2Cu/CeO2 + 0.2gCaO has the lowest apparent activation energy (29.86 kJ.mol(-1)). CaO is introduced as an absorbent to improve WGS reaction and reduce methanation reactions through in-situ CO2 removal and capture. The reaction path and mechanism of APR of glycerol are also discussed in this paper.

Automated summary

This study successfully synthesized a Ni-Cu bimetallic catalyst supported on CeO2, which can effectively increase the H-2 production rate and inhibit methane formation in aqueous phase reforming. Furthermore, the addition of CaO can reduce the activation energy, improve the water-gas shift reaction, and decrease methane production.