This work aims to develop fundamental insights about the underlying surface and bulk chemical processes instrumental to the efficiency of chemical looping combustion (CLC). CLC, which uses a solid-state oxygen carrier (e.g., metal oxides) to drive hydrocarbon combustion, is a promising combustion alternative that minimizes byproduct formation and facilities capture of CO2. In this work, we compare the performance of different transition metal oxides, namely iron, copper, cobalt, manganese, and nickel oxides, as oxygen carriers in CLC using CH4 as the reducing agent. Experiments used a continuous flow reactor across temperatures ranging from 500 to 800 oC and feed flowrates from 12.5 to 250 h-1. In addition to monitoring size-, temperature- and flow rate-dependent performance trends for CH4 conversion to CO2, microscopic and spectroscopic techniques were used to investigate the solid-state mechanism of oxygen carrier reduction and the coupled surface chemical and bulk material processes influencing performance. Bulk (XRD) and surface (XPS) analysis reveal that oxygen carrier reduction can be generally represented by two models, the unreacted shrinking core model (USCM) and the nuclei growth model (NNGM). The reduction of some metal oxides can also proceed via a two-stage solid-state mechanism; for example, hematite reduction to magnetite follows USCM, while the subsequent reductions of magnetite to wustite and wustite to iron metal follow NNGM. Furthermore, our results reveal that minimizing the particle size promotes oxygen carrier performance, but only for metal oxides reduced according to the USCM, where metal oxide reduction initiates on the particle surface. In contrast, no benefit of decreasing particle size was observed for materials reduced according to the NNGM because the reaction initiates in the particle bulk, such that a more critical determinant of reactivity may be the available oxygen carrier volume rather than surface area. Beyond these fundamental insights, cycling experiments were also performed to provide more practical information about the effect of oxygen carrier particle size on their long-term performance in CLC applications.
Fundamental insights into chemical looping combustion (CLC): a materials characterization approach to understanding mechanisms and size effects in oxygen carrier performance
Abstract
Details
- Title: Subtitle
- Fundamental insights into chemical looping combustion (CLC): a materials characterization approach to understanding mechanisms and size effects in oxygen carrier performance
- Creators
- Hayder Abdulkhaleq Khudhair Alalwan - University of Iowa
- Contributors
- David M. Cwiertny (Advisor)Vicki H. Grassian (Advisor)C. Allan Guymon (Committee Member)Eric E. Nuxoll (Committee Member)Sara E. Mason (Committee Member)
- Resource Type
- Dissertation
- Degree Awarded
- Doctor of Philosophy (PhD), University of Iowa
- Degree in
- Chemical and Biochemical Engineering
- Date degree season
- Summer 2018
- DOI
- 10.17077/etd.4arcwa2g
- Publisher
- University of Iowa
- Number of pages
- xx, 186 pages
- Copyright
- Copyright © 2018 Hayder A. Alalwan
- Language
- English
- Description illustrations
- illustrations (some color)
- Description bibliographic
- Includes bibliographical references (pages 165-178).
- Public Abstract (ETD)
The world-wide consumption of fossil fuels such as crude oil, natural gas and coal is ever increasing due to rising energy demands. The regular method to generate energy from fossil fuels is by burning it with air, which releases pollutants such as carbon monoxide (CO) and carbon dioxide (CO2) that have negative impacts to the environment. Thus, approaches that limit the formation or promote the capture of these byproduct gases will improve environmental quality, and in the case of CO2, help combat global warming.
One of the most promising techniques to facilitate CO2 capture is chemical looping combustion (CLC). In CLC, a hydrocarbon fuel is burned using the oxygen present in metal oxides (not air), after which the metal oxides are re-generated inside an adjacent reactor that contains only air (not fuel). The products of CLC is simply CO2 and steam, allowing CO2 to be easily captured by condensing the steam.
In this thesis, we provide new insights into the reaction of methane (CH4), the main component of natural gas, with five metal oxides commonly proposed for CLC (α-Fe2O3, NiO, CuO, Co2O3, and Mn2O3). We found that reduction of α-Fe2O3 and Mn2O3 by CH4 follows the unreacted shrinking core (USCM) model. According to the USCM, metal oxides first release their surface oxygen, forming a reduced layer or shell that retreats toward the more oxidized particle core as the reaction proceeds. For Co3O4, CuO, and NiO, our results show that their reduction follows the Nucleation and Nuclei Growth Model (NNGM), where core oxygen migrates to the particle surface to react with CH4. We propose for the first time links between these reduction models and whether particle size is an influential factor in controlling metal oxide performance during CLC. Furthermore, we provide practical performance considerations related to CLC such as the impact of the reaction temperature and gas flow rate on the efficiency of combustion and the potential for unwanted byproducts being generated via side reactions. Collectively, this work will help to develop better materials for CLC and promote technology scale up to commercial level.
- Academic Unit
- Chemical and Biochemical Engineering
- Record Identifier
- 9983777060402771