砷
化学
吸附
羟基自由基
无机化学
质子化
废水
等电点
亚砷酸盐
氧化物
核化学
激进的
离子
有机化学
环境工程
工程类
酶
作者
Wenbin Hu,Liming Yang,Penghui Shao,Hui Shi,Ziwen Chang,Difan Fang,Yun Wei,Yufa Feng,Yong Huang,Kai Yu,Xubiao Luo
标识
DOI:10.1021/acs.est.2c02675
摘要
Acid recycling and arsenic recovery from strongly acidic wastewater are goals of the metallurgical industry to reduce carbon emissions. In this study, arsenic was recovered using a hydroxyl-enriched CeO2 adsorbent, and the adsorption mechanism in a strongly acidic solution was investigated. The adsorption capacities of 88.59 mg/g for As(III) and 126.211 mg/g for As(V) at pH 1.0 are the highest reported values to date. It is revealed that the hydroxyl groups on the CeO2 surface can buffer hydrogen ions, and the isoelectric point of the material can be reduced to pH 1.52. The binding energy of arsenic is -1.25 eV for the hydroxyl-enriched CeO2 and -2.24 eV for CeO2 without hydroxyl groups. Additionally, the protonated hydroxyl groups reduce the oxidation energy of As(III) and promote the adsorption of arsenic by forming new active sites in the strongly acidic solution. Nearly 98.11% of arsenic (initial concentration is 886.8 mg/L) is removed within 24 h without pH adjustment, indicating the feasibility of hydroxyl-enriched CeO2 for recovering arsenic and acid. This work investigated the adsorption and proton-enhanced oxidation mechanism of arsenic by hydroxyl-enriched CeO2 in strongly acidic wastewater.
科研通智能强力驱动
Strongly Powered by AbleSci AI