吸附
膨润土
化学
磷酸盐
朗缪尔
化学工程
弗伦德利希方程
离子交换
解吸
朗缪尔吸附模型
腐植酸
无机化学
有机化学
离子
工程类
肥料
作者
Huan Xi,Qingqing Li,Yan Yang,Jianfeng Zhang,Feng Guo,Xiaogang Wang,Shimei Xu,Shiping Ruan
标识
DOI:10.1016/j.clay.2020.105919
摘要
The development of an effective phosphate removal strategy is still considered to be an important challenge in the field of wastewater remediation. In this study, novel alginate immobilized Zr-bentonite hydrogel beads were synthesized assisted by Zr-modification and Na2CO3 + HCl pore forming (abbreviated as NH-SA-ZrBT), that led to an enhancement in the specific surface area and porosity. The novel NH-SA-ZrBT adsorbent exhibited a high stability and adsorption selectivity for phosphate from complex water environments with various competitive anions, NaCl salinity and humic acid. The isotherm was fitted well by both Langmuir and Freundlich models, suggesting that the adsorption process was the chemisorption and the hydrogel beads could function through a variety of mechanisms. The maximum adsorption capacity of NH-SA-ZrBT for phosphate was calculated to be 63.61 mg/g at 25 °C by Langmuir model and had a high retention of 92.2% after five adsorption-desorption cycles. The kinetic data were better fitted by the pseudo-second model. Considering the zeta potential and XPS data before and after the phosphate adsorption, the adsorption mechanism was proposed to be a combination of electrostatic attraction, ligand exchange and inner sphere complexation. The present study demonstrates a new strategy for the fabrication of stable, separable and low-cost bentonite-containing hydrogel beads for phosphate removal from complex wastewater.
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