文献类型: 外文期刊
作者: Tao, Liang 2 ; Chen, Wenjie 2 ; Liu, Yuxin 2 ; Yang, Feng 2 ; Liu, Dong 4 ; Liang, Junfen 3 ; Liu, Saihong 5 ; Li, Hui 1 ;
作者机构: 1.South China Normal Univ, Sch Comp Sci, Guangzhou 510631, Peoples R China
2.Guangdong Acad Sci, Inst Ecoenvironm & Soil Sci, Natl Reg Joint Engn Res Ctr Soil Pollut Control &, Guangdong Key Lab Integrated Agroenvironm Pollut C, 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.Chinese Acad Sci, Guangzhou Inst Geochem, CAS Ctr Excellence Deep Earth Sci, Guangdong Prov Key Lab Mineral Phys & Mat, Guangzhou 510640, Peoples R China
5.Guangzhou Municipal Ecol Environm Bur, Huangpu Technol Ctr, Guangzhou 510530, Peoples R China
关键词: Soil acidification; Anthropic activities; Electrostatic adsorption; Ternary complex; Surface precipitation
期刊名称:CHEMOSPHERE ( 影响因子:8.8; 五年影响因子:8.3 )
ISSN: 0045-6535
年卷期: 2023 年 324 卷
页码:
收录情况: SCI
摘要: Soil acidification in southern China increases the environmental risk posed by heavy metals, especially cadmium (Cd), and has been accelerated by anthropic activities. Long-term fertilizer use increases the quantity of phos-phate (P) in soils, which affects the biogeochemistry of heavy metals in soil environments. In this study, various analytical methods were used to investigate the critical mechanisms controlling P(V)-Cd(II) interactions with goethite (alpha-FeOOH, a typical iron oxide widely distributed in red soil areas) with added P(V)/Cd(II) in different molar ratios (to simulate the annual P fertilizer surplus). After excluding pH interference by using organic buffers, Cd(II) adsorption processes on alpha-FeOOH were found to be enhanced by the presence of P(V), whereas the Cd(II) adsorption type changed from single inner-sphere complexation to both inner-and outer-sphere complexation. The results of a zeta potential analysis, X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS) showed different dominant mecha-nisms underlying the promotion of Cd(II) adsorption by P(V) at different P(V)/Cd(II) molar ratios. Electrostatic adsorption and the formation of ternary complexes were proven to be the critical mechanisms controlling the reactivity of Cd(II), where coprecipitation occurs at high P(V)/Cd(II) molar ratios and considerably enhances the fixation of Cd(II) and P(V). The mechanism for Cd(II) and P(V) coadsorption onto alpha-FeOOH under stable pH conditions was found to include both competitive and synergistic effects, and the results in this study show that more attention should be given to the impact of anthropic activities on the reactivity of heavy metals in the soil environment, especially farmland.
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