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土壤胶体对工程纳米颗粒(TiCT MXene)聚集和降解的影响。

Effects of soil colloids on the aggregation and degradation of engineered nanoparticles (TiCT MXene).

机构信息

State Environmental Protection Key Laboratory of Synergetic Control and Joint Remediation for Soil & Water Pollution, College of Ecology and Environment, Chengdu University of Technology, Chengdu 610059, China; State Key Laboratory of Geohazard Prevention and Geoenvironment Protection, Chengdu University of Technology, Chengdu 610059, China.

State Environmental Protection Key Laboratory of Synergetic Control and Joint Remediation for Soil & Water Pollution, College of Ecology and Environment, Chengdu University of Technology, Chengdu 610059, China.

出版信息

Environ Res. 2022 Nov;214(Pt 1):113886. doi: 10.1016/j.envres.2022.113886. Epub 2022 Jul 12.

Abstract

Soil colloid is a nonnegligible factor when evaluating the environmental risk of engineered nanoparticles (ENPs) in the groundwater. In this study, the environmental fate of an emerging ENP (TiCT MXene) in the groundwater was investigated for the first time, which currently poses a severe environmental risk due to its cytotoxicity but has received little attention. The colloidal dispersion stability and degradation kinetics of TiCT MXene in the groundwater were evaluated by considering the effects of soil colloids prepared from sodium humate (SH), montmorillonite (MT), and a natural soil (NS) under variable solution chemistry. The results showed that the affinity of soil colloids with TiCT followed an SH > MT > NS sequence. Increasing SH concentration led to TiCT disaggregation by enhancing the electrical and steric repulsive forces, while MT and NS resulted in hetero-aggregation because of the elevated collision frequency. SH and MT enhanced the critical coagulation concentrations of TiCT by 100 and 10 folders, respectively, via surface coating process, while NS slightly reduced due to the bridging effects induced by the soluble cations. The soil colloids promoted TiCT degradation compared with their absence and in an SH > MT ≫ NS sequence. SH and MT were through forming Ti-O-C and Si-O-Ti bonds with TiCT via their carboxyl and hydroxyl groups, respectively, rendering the TiCT surface more reactive and faster degradation. NS showed a weak promotion effect because of its less affinity with TiCT and limited organic matter and clay contents with hydroxyl and carboxyl groups. This study demonstrated the unstable environmental behaviors of TiCT in the groundwater and mitigated its environmental risk concerns.

摘要

土壤胶体是评估地下水工程纳米颗粒(ENPs)环境风险时不可忽视的因素。在这项研究中,首次研究了一种新兴的 ENP(TiCT MXene)在地下水中的环境归宿,由于其细胞毒性,目前它构成了严重的环境风险,但却很少受到关注。通过考虑从腐植酸钠(SH)、蒙脱石(MT)和天然土壤(NS)制备的土壤胶体在不同溶液化学条件下的影响,评估了 TiCT MXene 在地下水中的胶体分散稳定性和降解动力学。结果表明,土壤胶体与 TiCT 的亲和力顺序为 SH > MT > NS。增加 SH 浓度会通过增强电和空间排斥力导致 TiCT 解聚,而 MT 和 NS 则会由于碰撞频率升高而导致异质聚集。SH 和 MT 通过表面涂层过程分别将 TiCT 的临界聚沉浓度提高了 100 倍和 10 倍,而 NS 则略有降低,这是由于可溶性阳离子引起的桥接效应。与不存在土壤胶体相比,土壤胶体促进了 TiCT 的降解,并且顺序为 SH > MT > NS。SH 和 MT 分别通过其羧基和羟基与 TiCT 形成 Ti-O-C 和 Si-O-Ti 键,使 TiCT 表面更具反应性并加速降解。NS 由于与 TiCT 的亲和力较低以及羟基和羧基含量有限,因此表现出较弱的促进作用。这项研究表明了 TiCT 在地下水中的不稳定环境行为,并减轻了其环境风险的担忧。

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