4.7 Article

Binding of methylmercury to humic acids (HA): Influence of solar radiation and sulfide addition reaction of HA

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 827, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.154356

关键词

Methylmercury; Humic acids; Binding interactions; 2DCOS; Spectroscopy

资金

  1. National Natural Science Foundation of China [21806140]
  2. China Postdoctoral Science Foundation [2019M662105, 2021T140610]
  3. Natural Science Foundation of Zhejiang Province [LY20B070010, 2017129004429]
  4. Zhejiang University of Technology, China

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This study investigated the influence of solar radiation and sulfide addition reaction on the complexation of methylmercury (MeHg) with dissolved organic matter (DOM). Fluorescence and FT-IR spectroscopic analysis showed that different treatments resulted in changes in the affinity of binding sites in DOM for MeHg.
Methylmercury (MeHg) is a neurotoxin that bioaccumulates in organisms and it forms strong complexes with reduced sulfur-containing ligands in dissolved organic matter (DOM). In the present study, the influences of solar radiation and sulfide addition reaction of humic acids (HA) on MeHg binding to HA were investigated using synchronous fluorescence and FT-IR two-dimensional correlation spectroscopic (2DCOS) analysis. Results showed that the complexation of fluorescent fractions of HA and sulfur-reacted HA (S-HA) with MeHg was not significantly affected by photoreaction treatments and the affinity of fluorescent fractions followed the order of protein-like fractions > humic-like fractions > fulvic-like fractions for both HA and S-HA. ET-IR 2DCOS analysis showed that the affinity of various binding sites in DOM for MeHg changed under different photoreaction treatments. Under dark treatment, small molecular compounds with low humification degree such as aromatic amino acids may be the site with the strongest binding ability to MeHg in HA, whereas aliphatic amino acids and sulfur-containing groups from sulfide addition reactions play a role in complexing of S-HA and MeHg. Under BS treatment (irradiation of DOM before MeHg binding), aliphatic compounds in HA preferentially bind to MeHg and aliphatic amino acids are the components with the strongest complexing ability; but for S-HA binding to MeHg, unsaturated functional groups and aromatic groups are more sensitive (alkenes > alkanes, phenols > alcohols). Under AS treatment (irradiation of DOM after MeHg binding), unsaturated bonds and aromatic compounds in HA preferentially bind to MeHg and aromatic amino acids show the strongest complexing ability; but for S-HA binding to MeHg, aliphatic groups show the strongest complexing ability (alkanes, alkencs > aromatics). These findings help us to better understand the complexation mechanisms between MeHg and DOM.

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