(80c) Metal Oxide Based Solar Driven Two-Step Methane Reforming and Water Splitting Cycle | AIChE

(80c) Metal Oxide Based Solar Driven Two-Step Methane Reforming and Water Splitting Cycle

Authors 

Bhosale, R. - Presenter, Qatar University
H2 production via metal oxide based solar thermochemical splitting of H2O is considered as one of the alternatives for the gasification and reforming of fossil fuels, pyrolysis and reforming of biomass, ethanol decomposition, and others. Various metal oxide based thermochemical cycles such as zinc oxide cycle, tin oxide cycle, iron oxide cycle, ferrite cycle, ceria cycle, perovskite cycle, and others have been investigated towards the solar production of H2 via water splitting reaction. The major limitation associated with this process is the requirement of a very high temperature for the reduction of the metal oxide. This issue can be addressed if the metal oxide based H2O splitting process is coupled with the CH4 reforming process.

Recently, metal oxide (MO) based two-step CH4 reforming and H2O/CO2 splitting cycle receiving much attention for co-production of syngas and H2. As explained above, in first step, the MO is reduced using CH4 as the reducing agent producing synags (combined H2 and CO). The reduced MO can be re-oxidized using H2O, CO2, or combined stream of H2O/CO2 for the production of H2, CO, or syngas. In this study, the equilibrium thermodynamic analysis is performed to study the effect of CH4/metal oxide ratio on equilibrium compositions and the temperatures required to achieve higher levels of fuel production. Likewise, the solar reactor efficiency analysis is conducted to determine the solar-to-fuel energy conversion efficiency of this cycle. The investigated metal oxide is further synthesized and characterized using various analytical techniques. The synthesized metal oxide is tested towards CH4 reforming and H2O/CO2 splitting reaction using a thermogravimetric analyzer (coupled with GC-MS). Effects of CH4 concentration, reforming and splitting temperatures on the fuel production is also explored. The obtained results are compared with previous thermochemical cycles and will be presented in detail.