Coal ash conversion into effective adsorbents for removal of heavy metals and dyes from wastewater

被引:178
|
作者
Wang, SB
Soudi, M
Li, L
Zhu, ZH
机构
[1] Curtin Univ Technol, Dept Chem Engn, Perth, WA 6845, Australia
[2] Univ Queensland, ARC Ctr Funct Nanomat, Brisbane, Qld 4072, Australia
关键词
fly ash; zeolite; basic dyes; heavy metals; adsorption; adsorption isotherm; kinetics;
D O I
10.1016/j.jhazmat.2005.10.034
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fly ash was modified by hydrothermal treatment using NaOH solutions under various conditions for zeolite synthesis. The XRD patterns are presented. The results indicated that the samples obtained after treatment are much different. The XRD profiles revealed a number of new reflexes, suggesting a phase transformation probably occurred. Both heat treatment and chemical treatment increased the surface area and pore volume. It was found that zeolite P would be formed at the conditions of higher NaOH concentration and temperature. The treated fly ash was tested for adsorption of heavy metal ions and dyes in aqueous solution. It was shown that fly ash and the modified forms could effectively absorb heavy metals and methylene blue but not effectively adsorb rhodamine B. Modifying fly ash with NaOH solution would significantly enhance the adsorption capacity depending on the treatment temperature, time, and base concentration. The adsorption capacity of methylene blue would increases with pH of the dye solution and the sorption capacity of FA-NaOH could reach 5 x 10(-5) mol/g. The adsorption isotherm could be described by the Langmuir and Freundlich isotherm equations. Removal of copper and nickel ions could also be achieved on those treated fly ash. The removal efficiency for copper and nickel ions could be from 30% to 90% depending on the initial concentrations. The increase in adsorption temperature will enhance the adsorption efficiency for both heavy metals. The pseudo second-order kinetics would be better for fitting the dynamic adsorption of Cu and Ni ions. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:243 / 251
页数:9
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