Abstract

Solar carbothermal reduction of volatile metal oxides represents a promising pyro-metallurgical pathway for the sustainable conversion of both metal oxides and sunlight into metal commodities and fuels in a single process. Nevertheless, there are several scientific challenges in discovering suitable metal oxides candidates for the ease of oxygen extraction from metal oxides to enhance the reaction extent and in designing reactors for the efficient absorption of incident solar radiation to minimize losses. In this study, ZnO and MgO were considered as volatile metal oxides candidates, and their reaction behaviors were studied and compared through gas species production rate, metal oxides conversion, and yield. A solar reactor prototype was developed to facilitate solar carbothermal reduction of ZnO and MgO with different reducing agents comprising activated charcoal and carbon black. The process was operated in a batch operation mode under vacuum and atmospheric pressures to demonstrate the flexibility and reliability of this system for co-production of metals (Zn/Mg) and CO. As a result, decreasing total pressure enhanced conversion of ZnO and MgO, leading to increased Zn and Mg. However, in the case of ZnO, CO yield decreased with decreasing total pressure at the expense of favored CO2 as a result of the decrease of residence time. In contrast, CO2 formation was negligible in the case of MgO, and CO yield thus increased with decreasing pressure. Using activated charcoal as the reducing agent exhibited better conversion of both ZnO and MgO than carbon black thanks to the higher available specific surface area for chemical reactions. MgO and ZnO conversion above 97% and 78%, respectively, and high-purity Mg and Zn content were accomplished, as evidenced by the recovered products at the reactor outlet and filter containing pure metal. In addition, Mg product exhibited strong oxidation reactivity with air, thus requiring inert atmosphere for the handling of Mg-rich powders to avoid direct exposure to air.

Highlights

  • Harnessing the plentiful, clean, and renewable solar energy resource via solar thermochemical conversion processes is a promising avenue to convert intermittent solar radiation into chemical fuels and commodities [1]

  • ZnO and MgO have been considered as attractive volatile metal oxide candidates for solar carbothermal metallurgical processes towards Zn and Mg commodities production

  • This paper addresses the solar thermochemical reduction of ZnO and MgO using carbon-based feedstocks in a directly-irradiated cavity-type solar reactor for the clean production of energy-intensive fuels and materials

Read more

Summary

Introduction

Harnessing the plentiful, clean, and renewable solar energy resource via solar thermochemical conversion processes is a promising avenue to convert intermittent solar radiation into chemical fuels and commodities [1]. Volatile metal oxides such as ZnO/Zn [15], SnO2/SnO [16,17], and MgO/Mg [18] usually offer high oxygen exchange capacity and high entropy variation, as they can be completely reduced to their metallic elements (Zn and Mg), enhancing fuel production capacity. They come at the expense of an issue of recombination with oxygen (O2) during thermal reduction, since both products (metal and O2) are simultaneously released in the gaseous phase. The overall carbothermal reduction reactions of ZnO and MgO are represented in Equations (1) and (2), respectively

Objectives
Methods
Results
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.