Cadmium and arsenic interactions under different molar ratios during coadsorption processes by excluding pH interference
文献类型: 外文期刊
作者: Tao, Liang 2 ; Huang, Minxue 1 ; Li, Hui 4 ; Chen, Wenjie 2 ; Su, Zixian 1 ; Guan, Yufeng 1 ;
作者机构: 1.South China Normal Univ, Sch Environm Sci, Guangzhou 510006, Peoples R China
2.Guangdong Acad Sci, Natl Reg Joint Engn Res Ctr Soil Pollut Control &, Inst Ecoenvironm & Soil Sci, Guangdong Key Lab Integrated Agroenvironm Pollut, Guangzhou 510650, Peoples R China
3.Guangdong Acad Agr Sci, Inst Agr Econ & Informat, Key Lab Urban Agr South China, Minist Agr & Rural Affairs, Guangzhou 510640, Peoples R China
4.South China Normal Univ, Sch Comp Sci, Guangzhou 510631, Peoples R China
5.Guangdong Univ Technol, Sch Environm Sci & Engn, Guangzhou 510006, Peoples R China
关键词: Coadsorption; pH interference; Electrostatic adsorption; Ternary complex; Surface precipitation
期刊名称:CHEMOSPHERE ( 影响因子:8.943; 五年影响因子:8.52 )
ISSN: 0045-6535
年卷期: 2022 年 291 卷
页码:
收录情况: SCI
摘要: Cadmium (Cd) and arsenic (As), two common heavy metals that are toxic to living bodies, are often commonly coadsorbed onto minerals in the soil environment and influenced by many surrounding factors. Among them, pH is the critical factor in determining the As(V)-Cd(II) interaction during coadsorption processes; hence, this study aimed to elucidate the regulatory mechanisms in determining the As(V)-Cd(II) interactions on gamma-Al2O3 interface after excluding pH interference. At pH 6.0, Cd(II) adsorption sharply increased at first and then decreased with increasing As(V) concentrations, and the turning point of As(V)/Cd(II) molar ratios was approximately 5. For comparison, As(V) adsorption remained stable at the beginning and then sharply increased with increasing Cd(II) concentrations, with the turning point at Cd(II)/As(V) molar ratios = 1. Through analysis by zeta potential, X-ray diffraction and high resolution transmission electron microscope, electrostatic adsorption and formation of ternary complexes were proven to be the critical mechanisms in deciding the reactivity of Cd(II), whereas formation of ternary complexes and surface precipitation were the dominant mechanisms controlling the stability of As(V). The results in this study allowed us to infer that the mechanism for the coadsorption of Cd(II) and As(V) at stable pH conditions included both competitive and synergistic effects.
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