Systematic utilization of layered double hydroxide nanosheets for effective removal of methyl orange from an aqueous system by pi-pi stacking-induced nanoconfinement
- Authors
- Ko, Su-Joung; Yamaguchi, Tetsuo; Salles, Fabrice; Oh, Jae-Min
- Issue Date
- 1-Jan-2021
- Publisher
- ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
- Keywords
- Anionic dye removal; LDH; Monte Carlo simulation; Size effect; Intercalation
- Citation
- JOURNAL OF ENVIRONMENTAL MANAGEMENT, v.277
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF ENVIRONMENTAL MANAGEMENT
- Volume
- 277
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/5473
- DOI
- 10.1016/j.jenvman.2020.111455
- ISSN
- 0301-4797
1095-8630
- Abstract
- Systematic utilization of carbonated Mg-Al layered double hydroxide (LDH) nanosheets for methyl orange removal was investigated with respect to particle dimensions. LDHs with the smallest dimensions were carefully synthesized to have a small lateral size as well as high dispersibility. The other particles, with medium and large sizes, were prepared by hydrothermal treatment and urea hydrolysis to have larger sizes and higher crystallinity. According to kinetics and isotherm analyses, the smallest LDH showed efficient adsorption of methyl orange (1250 mg/g-LDH), which was remarkably higher than the adsorption by the other LDHs with larger lateral sizes. Unlike the larger lateral-sized LDHs, the small ones were shown to utilize all accessible adsorption sites on the nanosheets, generating nanoconfinement of methyl orange molecules. Transmission electron microscopy (TEM) and powder X-ray diffraction (PXRD) patterns indicated that the LDHs with lateral dimensions of-40 nm fully utilized interlayer nanospace. Monte Carlo simulation suggested that the intercalated methyl orange was stabilized not only through electrostatic interactions with the LDH layer but also by pi-pi stacking between the methyl orange molecules, which is thought to be the driving force for replacement of carbonate anions.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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