In situ synthesis of hierarchical cobalt-aluminum layered double hydroxide on boehmite surface for efficient removal of arsenate from aqueous solutions: Effects of solution chemistry factors and sorption mechanism
- Authors
- Lee, Seon Yong; Jung, Kyung-Won; Choi, Jae-Woo; Lee, Young Jae
- Issue Date
- 15-7월-2019
- Publisher
- ELSEVIER SCIENCE SA
- Keywords
- Arsenic removal; Layered double hydroxide; Boehmite; Hierarchical structure; Anion exchange; Ligand exchange
- Citation
- CHEMICAL ENGINEERING JOURNAL, v.368, pp.914 - 923
- Indexed
- SCIE
SCOPUS
- Journal Title
- CHEMICAL ENGINEERING JOURNAL
- Volume
- 368
- Start Page
- 914
- End Page
- 923
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/64098
- DOI
- 10.1016/j.cej.2019.03.043
- ISSN
- 1385-8947
- Abstract
- A facile route is reported for the in situ formation of three-dimensionally structured hierarchical Co-Al layered double hydroxide (CoAl-LDH) crystals on a boehmite surface (CoAl-LDH@boehmite) via the dissolution of boehmite followed by the coprecipitation of Co and Al ions on the boehmite surface. The physicochemical properties of the as-prepared materials were characterized and tested for evaluating their sorption affinity toward arsenate (As(V)) in an aqueous solution. The characterization results confirmed that the plate-like CoAlL-DH nanocrystals were densely and uniformly formed on the boehmite surface with a three-dimensional hierarchical structure. Batch experiments were conducted systematically to evaluate the effects of the sorbent dosage, initial pH, competitive anions, and temperature on the sorption behavior of CoAl-LDH@boehmite. The sorption kinetics and isotherms studies indicated that the As(V) sorption processes could be well described by the pseudo-second-order and Sips isotherm models, respectively. The sorption mechanisms were confirmed by various solid phase analyses, including X-ray diffraction, Fourier transform infrared, transmission electron microscopy, X-ray photoelectron spectroscopy, and extended X-ray absorption fine structure. These findings suggest that the intercalation of As(V) into the interlayer region via anion exchange and bidentate-binuclear innersphere surface complexation due to ligand exchange were responsible for the removal of As(V) by CoAl-LDH@boehmite.
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