Layered Double Hydroxide (LDH)-based Monolith with Interconnected Hierarchical Channels: Enhanced Sorption Affinity for Anionic Species
Journal of Materials Chemistry A 1 巻
7702-7708 頁
2013-04-24 発行
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この文献の参照には次のURLをご利用ください : https://ir.lib.hiroshima-u.ac.jp/00053535
| ファイル情報(添付) | |
| タイトル ( eng ) |
Layered Double Hydroxide (LDH)-based Monolith with Interconnected Hierarchical Channels: Enhanced Sorption Affinity for Anionic Species
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| 作成者 |
Tokudome Yasuaki
Nakanishi Kazuki
Takahashi Masahide
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| 収録物名 |
Journal of Materials Chemistry A
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| 巻 | 1 |
| 開始ページ | 7702 |
| 終了ページ | 7708 |
| 抄録 |
Monolithic layered double hydroxides (LDHs) with interconnected channels have been expected to enhance sorption rate as well as increase accumulation of anions. Although powder molding can form easy-handled LDH compacts, interconnected channel formation therein has not been achieved. Herein, we demonstrate cm-scale monolithic LDH-based composites with interconnected hierarchical channels via a spontaneous sol−gel reaction. The synthesis was performed on Mg−Al hydrotalcite-type LDHs starting from metal chlorides aqueous/ethanolic solution with poly(ethylene oxide) incorporated. Addition of propylene oxide triggers sol−gel reaction to form monolithic xerogels with a formula of [Mg0.66Al0.33(OH)2Cl0.33·2.92H2O]·3.1Al(OH)3. LDH crystals together with aluminum hydroxide crystals homogeneously build up gel skeletons with well-defined hierarchical channels. The interconnected channels in μm range (macrochannel) are formed as a phase-separated structure, whereas the channels in nm range (nanochannel) are as interstices of primary particles. The channel architectures are preserved in the course of rehydration process, affording enhanced sorption affinity for anion species in the process. Both of macro and mesochannels as well as high charge density of the obtained LDHs (Mg/Al=2.0) contribute enhanced anion sorption in the monolithic xerogels. The materials obtained here opens up applications of high performance adsorbent and ion-storage free from diffusion limitation.
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| 内容記述 |
The present work is partially supported by Grant-in-Aid for Scientific Research (B) (No. 22360276), and Grant-in-Aid for Young Scientists (B) (No. 24750206) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), administrated by Japan Society for the Promotion of Science (JSPS). Y. T. is also partially supported financially by a research grant from The Murata Scientific Foundation.
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| 言語 |
英語
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| 資源タイプ | 学術雑誌論文 |
| 出版者 |
Royal Society of Chemistry
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| 発行日 | 2013-04-24 |
| 権利情報 |
This is not the published version. Please cite only the published version. この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。
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| 出版タイプ | Author’s Original（十分な品質であるとして、著者から正式な査読に提出される版） |
| アクセス権 | オープンアクセス |
| 収録物識別子 |
[ISSN] 2050-7496
[DOI] 10.1039/c3ta11110e
[DOI] https://doi.org/10.1039/C3TA11110E
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