完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Chang, Po-Hsueh | en_US |
dc.contributor.author | Chang, Yen-Po | en_US |
dc.contributor.author | Chen, San-Yuan | en_US |
dc.contributor.author | Yu, Ching-Tsung | en_US |
dc.contributor.author | Chyou, Yau-Pin | en_US |
dc.date.accessioned | 2014-12-08T15:21:39Z | - |
dc.date.available | 2014-12-08T15:21:39Z | - |
dc.date.issued | 2011 | en_US |
dc.identifier.issn | 1864-5631 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/15387 | - |
dc.identifier.uri | http://dx.doi.org/10.1002/cssc.201100357 | en_US |
dc.description.abstract | We present the design and synthesis of Ca-rich Ca-Al-O oxides, with Ca(2+)/Al(3+) ratios of 1:1, 3:1, 5:1, and 7:1, which were prepared by hydrothermal decomposition of coprecipitated hydrotalcite-like Ca-Al-CO(3) precursors, for high-temperature CO(2) adsorption at 500-700 degrees C. In situ X-ray diffraction measurements indicate that the coprecipitated, Ca-rich, hydrotalcite-like powders with Ca(2+)/Al(3+) ratios of 5:1 and 7:1 contained Ca(OH)(2) and layered double hydroxide (LDH) phases. Upon annealing, LDH was first destroyed at approximately 200 degrees C to form an amorphous matrix, and then at 450-550 degrees C, the Ca(OH)(2) phase was converted into a CaO matrix with incorporated Al(3+) to form a homogeneous solid solution without a disrupted lattice structure. CaO nanocrystals were grown by thermal treatment of the weakly crystalline Ca-Al-O oxide matrix. Thermogravimetric analysis indicates that a CO(2) adsorption capacity of approximately 51 wt.% can be obtained from Ca-rich Ca-Al-O oxides prepared by calcination of 7:1 Ca-Al-CO(3) LDH phases at 600-700 degrees C. Furthermore, a relatively high CO(2) capture capability can be achieved, even with gas flows containing very low CO(2) concentrations (CO(2)/N(2)=10%). Approximately 95.6% of the initial CO(2) adsorption capacity of the adsorbent is retained after 30 cycles of carbonationcalcination. TEM analysis indicates that carbonation-promoted CaCO(3) formation in the Ca-Al-O oxide matrix at 600 degrees C, but a subsequent desorption in N(2) at 700 degrees C, caused the formation CaO nanocrystals of approximately 10 nm. The CaO nanocrystals are widely distributed in the weakly crystalline Ca-Al-O oxide matrix and are present during the carbonationcalcination cycles. This demonstrates that Ca-Al-O sorbents that developed through the synthesis and calcination of Ca-rich Ca-Al LDH phases are suitable for long-term cyclic operation in severe temperature environments. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | adsorption | en_US |
dc.subject | carbon storage | en_US |
dc.subject | coprecipitation | en_US |
dc.subject | layered compounds | en_US |
dc.subject | hydrothermal synthesis | en_US |
dc.title | Ca-Rich Ca-Al-Oxide, High-Temperature-Stable Sorbents Prepared from Hydrotalcite Precursors: Synthesis, Characterization, and CO2 Capture Capacity | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/cssc.201100357 | en_US |
dc.identifier.journal | CHEMSUSCHEM | en_US |
dc.citation.volume | 4 | en_US |
dc.citation.issue | 12 | en_US |
dc.citation.spage | 1844 | en_US |
dc.citation.epage | 1851 | en_US |
dc.contributor.department | 材料科學與工程學系 | zh_TW |
dc.contributor.department | Department of Materials Science and Engineering | en_US |
dc.identifier.wosnumber | WOS:000297953400020 | - |
dc.citation.woscount | 18 | - |
顯示於類別: | 期刊論文 |