Bibliographic Citation | |
Full Text | |
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DOI | 10.2172/795766 |
Title | CO2 SELECTIVE CERAMIC MEMBRANE FOR WATER-GAS SHIFT REACTION WITH CONCOMITANT FOR THE RECOVERY OF CO2 |
Creator/Author | Unknown |
Publication Date | 2002 May 08 |
OSTI Identifier | OSTI ID: 795766 |
Report Number(s) | FC26-00NT40922--09 |
DOE Contract Number | FC26-00NT40922 |
DOI | 10.2172/795766 |
Other Number(s) | TRN: US200213%%5 |
Resource Type | Technical Report |
Resource Relation | Other Information: PBD: 8 May 2002 |
Research Org | National Energy Technology Lab., Pittsburgh, PA (US); National Energy Technology Lab., Morgantown, WV (US) |
Sponsoring Org | US Department of Energy (US) |
Subject | 08 HYDROGEN; 01 COAL, LIGNITE, AND PEAT; ADSORPTION; CERAMICS; CRYSTAL GROWTH; LEACHING; MEMBRANES; SYNTHESIS; CARBON DIOXIDE; SEPARATION PROCESSES; WATER GAS PROCESSES; SHIFT PROCESSES |
Description/Abstract | The reversibility study using TGA/MS has been completed. Our result shows that the hydrotalcite material we proposed exhibits a high degree of CO{sub 2} reversibility. In addition, at higher temperatures (>200 C), insignificant adesorption of water was observed. Combining these results, we conclude that the hydrotalcite we choose is an ideal candidate material for high temperature gas separations requiring hydrothermal stability. We also have focused on the optimization of membrane synthesis. The gel formed after combining the reagents is an ideal precursor for deposition within the porous membrane based upon the Al/Mg ratio analysis and impurity leaching study. Finally, we experimentally verify the crystal growth temperature ranging from 100 to 150 C. The crystal growth is also highly dependent upon the time. Our study shows a general growth pattern from 0 to >4 hours. In the next quarter, we will utilize the information obtained here to initiate the optimization of membrane synthesis. |
Country of Publication | United States |
Language | English |
Format | Size: 10 pages |
Availability | OSTI as DE00795766 To purchase this media from NTIS, click here |
System Entry Date | 2007 Apr 16 |
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