Cd(II)-Sb(V)对典型土壤矿物和有机组分共吸附的普遍协同规律

IF 2.8 4区 工程技术 Q2 CHEMISTRY, APPLIED Adsorption Science & Technology Pub Date : 2022-01-18 DOI:10.1155/2022/9131597
Min Zhou, Rui-Jia Yang, X. Tan, Boqing Tie, M. Lei, H. Du
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引用次数: 1

摘要

重金属和类金属在污染土壤中共同存在,使它们的行为比单独存在更为复杂。对土壤矿物和有机成分的吸附决定了重金属的溶解度和迁移率。然而,关于金属(如Cd)和准金属(如Sb)与土壤组分的共吸附,以及是否存在普遍的共吸附规则,几乎没有可用的信息,需要阐明。本研究研究了Cd(II)和Sb(V)在两种酸性(pH)条件下对针铁矿、高岭石和细菌(蜡样芽孢杆菌)的共吸附行为 4.5)和碱性pH(pH 8.5).平衡吸附实验,结合扫描电子显微镜(SEM)能量色散X射线光谱(EDS)和X射线光电子能谱(XPS),确定了间歇吸附现象和可能的机理。批处理结果表明,在pH值下,Cd(II)的吸附更大 8.5,而Sb(V)在pH下的吸附更大 4.5.Cd或Sb的存在促进了彼此对针铁矿、高岭石和细菌的吸附,但略有不同的是,Sb(V)在酸性pH下更倾向于增强对Cd(II)的吸附,而Cd(Ⅱ)在碱性pH下更能增强对Sb(V)的吸附。SEM-EDS分析进一步表明,Cd和Sb的分布是共定位的。表面的FeOH、AlOH和COOH基团参与了Cd(II)和Sb(V)的结合,可能是通过形成内球络合物。可能形成了两种可能的三元络合物,即吸附剂-Cd2+-Sb(OH)6-和吸附剂Sb(OH-6-Cd2+。电荷效应和三元配合物的形成是Cd-Sb协同共吸附的原因。所获得的普遍协同规则表明,目前基于单个系统预测Cd(II)或Sb(V)螯合的模型可能低估了它们在共存情况下的固液分配比。研究结果对了解Sb和Cd在污染土壤中的化学行为具有重要意义。
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A Universal Synergistic Rule of Cd(II)-Sb(V) Coadsorption to Typical Soil Mineral and Organic Components
Heavy metals and metalloids are common cooccurrence in contaminated soils, making their behaviors more complex than their individual presences. Adsorption to soil minerals and organic components determines the solubility and mobility of heavy metals. However, little information is available regarding coadsorbing metals (e.g., Cd) and metalloids (e.g., Sb) to soil components, and whether there is a universal coadsorption rule needs to be illuminated. This study investigated the coadsorption behaviors of Cd(II) and Sb(V) to goethite, kaolinite, and bacteria (Bacillus cereus) at both acidic (pH 4.5) and alkaline pH (pH 8.5). Equilibrium adsorption experiments, coupled with scanning electron microscopy- (SEM-) energy-dispersive X-ray spectrum (EDS) and X-ray photoelectron spectroscopy (XPS), were applied to determine the batch adsorption phenomena and possible mechanisms. Batch results showed that Cd(II) adsorption was greater at pH 8.5 whereas Sb(V) adsorption was greater at pH 4.5. The presence of Cd or Sb promoted each other’s adsorption to goethite, kaolinite, and bacteria, but slight differences were that Sb(V) preferred to enhance Cd(II) adsorption at acidic pH, whereas Cd(II) was more able to increase Sb(V) adsorption at alkaline pH. SEM-EDS analyses further showed that the distribution of Cd and Sb was colocalized. The surface FeOH, AlOH, and COOH groups participated in the binding of Cd(II) and Sb(V), probably through the formation of inner-sphere complexes. Two possible ternary complexes, i.e., sorbent-Cd2+-Sb(OH)6– and sorbent-Sb(OH)6–-Cd2+, were possibly formed. Both the charge effect and the formation of ternary complexes were responsible for the collaborative coadsorbing of Cd-Sb. The universal synergistic rule obtained suggests that current models for predicting Cd(II) or Sb(V) sequestration based on single systems may underestimate their solid-to-liquid distribution ratio in a coexistence situation. The results obtained have important implications for understanding the chemical behavior of Sb and Cd in contaminated soils.
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来源期刊
Adsorption Science & Technology
Adsorption Science & Technology 工程技术-工程:化工
CiteScore
5.00
自引率
10.30%
发文量
181
审稿时长
4.5 months
期刊介绍: Adsorption Science & Technology is a peer-reviewed, open access journal devoted to studies of adsorption and desorption phenomena, which publishes original research papers and critical review articles, with occasional special issues relating to particular topics and symposia.
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