Back to Search Start Over

Solvent-free hydrothermal synthesis of gamma-aluminum oxide nanoparticles with selective adsorption of Congo red.

Authors :
Zhang, Huimin
Ruan, Yang
Feng, Yong
Su, Minhua
Diao, Zenghui
Chen, Diyun
Hou, Li'an
Lee, Po-Heng
Shih, Kaimin
Kong, Lingjun
Source :
Journal of Colloid & Interface Science. Feb2019, Vol. 536, p180-188. 9p.
Publication Year :
2019

Abstract

Graphical abstract Abstract Aluminum hydroxide and oxide have been widely used for decontamination due to their environmentally friendly nature and cost effectiveness. Aluminum (hydro) oxides are the main phases of aluminum-derived environment materials. Herein, the solvent-free hydrothermal synthesis of gamma-aluminum oxide (γ-Al 2 O 3) nanoparticles and phase transformation of AlOOH into γ-Al 2 O 3 are reported. Hydrothermal treatment of NH 3 ·H 2 O-induced aluminum precipitate resulted in the formation of AlOOH, which was an intermediate product of γ-Al 2 O 3. AlOOH was transformed into highly crystalline 20-nm γ-Al 2 O 3 particles through calcination at 500 °C due to dehydration. The transformation was confirmed through X-ray diffraction (XRD) and thermogravimetric (TG) analyses. The resulting γ-Al 2 O 3 had superior adsorption ability for the anionic Congo red (CR) dye than for the cationic methylene blue (MB) and malachite green (MG) dyes. The selective adsorption ability of CR instead of MB was attributed to the electrostatic attraction and hydrogen bonds between the amino group and azo double bond of CR, and between the amino group and hydroxyl group in γ-Al 2 O 3. Thus, this study investigated crystalline phase transformation into γ-Al 2 O 3 and selective adsorption capacity of CR, which provides important information regarding the synthesis of crystalline γ-Al 2 O 3 adsorbent, with selective adsorption ability for decontamination applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
536
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
133215565
Full Text :
https://doi.org/10.1016/j.jcis.2018.10.054