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Reverse water gas shift reaction over CuFe/Al2O3 catalyst in solid oxide electrolysis cell

Authors :
Kai Zhao
Jung-Il Yang
Qusay Bkour
Ji Chan Park
Su Ha
Xiaoxue Hou
M. Grant Norton
Shin Wook Kang
Source :
Chemical Engineering Journal. 336:20-27
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Catalytic reduction by the reverse water gas shift (RWGS) reaction is an efficient way to utilize carbon dioxide and reduce its environmental impact as a greenhouse gas. In this research, an active CuFe/Al 2 O 3 nano powder was developed as a high temperature reforming catalyst for the RWGS reaction. The powder was synthesized by a wet-impregnation method and the copper alloy was uniformly dispersed on the γ-Al 2 O 3 support. At a gas space velocity of 60,000 h −1 , the conversion of carbon dioxide was 42% at 700 °C, which is very close to the equilibrium conversion of 44%. The results indicated excellent reforming activity of the CuFe/Al 2 O 3 catalyst for the high temperature RWGS reaction. In addition, the catalyst was applied in the form of a reforming layer over a conventional Ni-based electrode of a solid oxide electrolysis cell (SOEC) for an integrated SOEC-RWGS system. Hydrogen produced from steam electrolysis over the Ni-based cathode can be efficiently utilized to reduce the carbon dioxide by the RWGS reaction over the CuFe/Al 2 O 3 -based reforming layer. In this bilayer design, the reforming layer maintained the high surface area necessary for achieving good reforming activity, while the electrode layer possessed a high degree of sintering to enhance its electrochemical function. A high conversion of carbon dioxide (37% at 700 °C) was obtained in our bilayer SOEC-RWGS system. This promising result suggests the feasibility of the integrated SOEC-RWGS system for an efficient co-electrolysis device.

Details

ISSN :
13858947
Volume :
336
Database :
OpenAIRE
Journal :
Chemical Engineering Journal
Accession number :
edsair.doi...........a5972169667af77bbb2bb29dbc160697
Full Text :
https://doi.org/10.1016/j.cej.2017.11.028