4.7 Article

Single versus multi-metal sulfide systems: The role of cysteine and complex environmental conditions

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 750, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.scitotenv.2020.142274

关键词

Particle size fractionation; Thiol; Oxidative dissolution; Cysteine

资金

  1. Temple University Presidential Fellowship
  2. Temple University

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The presence of dissolved organic matter (DOM) can impact metal sulfide (MeS) precipitation and mobility. Thiol containing ligands like cysteine can effectively stabilize MeS nanoparticles in both single and multi-metal systems. Metal sequestration into MeS solids follows solubility products, with the behavior varying in multi-metal systems due to different NP sizes and dissolved concentrations. MeS stabilization by cysteine is influenced by the CYS:S ratio and the presence of Ca2+, impacting particle aggregation and metal dissolution.
The presence of dissolved organic matter (DOM) can impactmetal sulfide (MeS) precipitation and mobility. Thiol containing ligands such as cysteine have been shown to be effective capping agents in single metal MeS studies, allowing NPs to persist in oxic environments. In this study, both single (Cd or Zn) and multi-MeS (Cu, Pb, Cd, Zn, and As) nanoparticle (NP) formation was characterized to understand the impact of the thiol cysteine (CYS) on early stage (3 h) MeS NP behavior. Short duration singlemetal batch experiments, in the absence and presence of CYS, confirmed thatMeS species readily formed solidswith limited dissolved fraction; however, multi-metal systems exhibited divergent behavior reflecting awider range of NP sizes and an increased dissolved concentration. Multi-metal batch experiments revealed that metals were generally sequestered into MeS solids in accordance with MeS solubility products (i.e., from least to most soluble: Cu > Pb similar to Cd > Zn). CYS concentrations in excess of sulfide (10:1 CYS:S ratio) stabilized MeS within the Small NP size fraction (3.2 nm < d < 43 nm) and limited Pb, Cd, and Zn dissolution compared to molar ratios of 1:1. In the combined presence of CYS and Ca2+, multi-MeS particle aggregation increased substantially compared to monovalent systems. Dissolution increased for Pb and Zn as a function of matrix ionic strength whereas dissolved Cu trends changed as a function of cation valence state (e.g., Na+ vs. Ca2+). Most noteworthy, single-metal Zn and Cd batch experiments demonstrated that single-metal studies can overestimateMeS NP resistance to oxidative dissolution compared tomulti-metal counterparts. Thus, caution should be taken when broadly applying mechanisms and rates elucidated from single-metal systems. (C) 2020 Elsevier B.V. All rights reserved.

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