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  4. Carbonate-ceramic dual-phase membranes for high temperature carbon dioxide separation
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Carbonate-ceramic dual-phase membranes for high temperature carbon dioxide separation

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Description

Emission of CO2 into the atmosphere has become an increasingly concerning issue as we progress into the 21st century Flue gas from coal-burning power plants accounts for 40% of all carbon dioxide emissions. The key to successful separation and sequestration is to separate CO2 directly from flue gas (10-15% CO2, 70% N2), which can range from a few hundred to as high as 1000°C. Conventional microporous membranes (carbons/silicas/zeolites) are capable of separating CO2 from N2 at low temperatures, but cannot achieve separation above 200°C. To overcome the limitations of microporous membranes, a novel ceramic-carbonate dual-phase membrane for high temperature CO2 separation was proposed. The membrane was synthesized from porous La0.6Sr0.4Co0.8Fe0.2O3-d (LSCF) supports and infiltrated with molten carbonate (Li2CO3/Na2CO3/K2CO3). The CO2 permeation mechanism involves a reaction between CO2 (gas phase) and O= (solid phase) to form CO3=, which is then transported through the molten carbonate (liquid phase) to achieve separation. The effects of membrane thickness, temperature and CO2 partial pressure were studied. Decreasing thickness from 3.0 to 0.375 mm led to higher fluxes at 900°C, ranging from 0.186 to 0.322 mL.min-1.cm-2 respectively. CO2 flux increased with temperature from 700 to 900°C. Activation energy for permeation was similar to that for oxygen ion conduction in LSCF. For partial pressures above 0.05 atm, the membrane exhibited a nearly constant flux. From these observations, it was determined that oxygen ion conductivity limits CO2 permeation and that the equilibrium oxygen vacancy concentration in LSCF is dependent on the partial pressure of CO2 in the gas phase. Finally, the dual-phase membrane was used as a membrane reactor. Separation at high temperatures can produce warm, highly concentrated streams of CO2 that could be used as a chemical feedstock for the synthesis of syngas (H2 + CO). Towards this, three different membrane reactor configurations were examined: 1) blank system, 2) LSCF catalyst and 3) 10% Ni/y-alumina catalyst. Performance increased in the order of blank system < LSCF catalyst < Ni/y-alumina catalyst. Favorable conditions for syngas production were high temperature (850°C), low sweep gas flow rate (10 mL.min-1) and high methane concentration (50%) using the Ni/y-alumina catalyst.

Date Created
2011
Contributors
  • Anderson, Matthew Brandon (Author)
  • Lin, Jerry (Thesis advisor)
  • Alford, Terry (Committee member)
  • Rege, Kaushal (Committee member)
  • Anderson, James (Committee member)
  • Rivera, Daniel (Committee member)
  • Arizona State University (Publisher)
Topical Subject
  • chemical engineering
  • Carbon Dioxide
  • Dual-Phase Membrane
  • energy
  • Molten Carbonate
  • Syngas
  • Gas separation membranes
  • Flue gases
  • Carbon dioxide--Separation.
  • Carbon Dioxide
Resource Type
Text
Genre
Doctoral Dissertation
Academic theses
Extent
xx, 245 p. : ill. (some col.)
Language
eng
Copyright Statement
In Copyright
Reuse Permissions
All Rights Reserved
Primary Member of
ASU Electronic Theses and Dissertations
Peer-reviewed
No
Open Access
No
Handle
https://hdl.handle.net/2286/R.I.9003
Statement of Responsibility
Matthew Brandon Anderson
Description Source
Viewed on Dec. 7, 2011
Level of coding
full
Note
Partial requirement for: Ph. D., Arizona State University, 2011
Note type
thesis
Includes bibliographical references (p. 198-213)
Note type
bibliography
Field of study: Chemical engineering
System Created
  • 2011-08-12 03:49:47
System Modified
  • 2021-08-30 01:54:27
  •     
  • 1 year 6 months ago
Additional Formats
  • OAI Dublin Core
  • MODS XML

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