ABSTRACT
Cadmium (Cd) contamination in cropland poses a significant threat to the quality of agricultural products, but even though in-situ remediation has been extensively applied, non-selective immobilization remains an issue. In order to develop a material that specifically immobilizes Cd in soil, a layered double hydroxide, intercalated with mercaptosuccinic acid (MSA-CFA), was synthesized through co-precipitation. In this case, the MSA-CFA's maximum adsorption capacity was increased from the 513.8 mg·g-1 for unintercalated hydrotalcite CFA to 692.6 mg·g-1. Besides, MSA-CFA efficiently removed 99.25 % of Cd from soil water-extract solution and immobilized up to 70.03 % of bio-available Cd. However, interestingly, its immobilization effects on beneficial metal elements Fe, Mn and Zn were milder, being equivalent to 2/7, 5/7 and 1/2 that of lime, respectively. Moreover, XRD and XPS techniques revealed isomorphous substitution with calcium and sulfhydryl complexation during the Cd adsorption by MSA-CFA. Compared with CFA, the increased adsorption capacity of MSA-CFA for Cd was due to intercalated MSA acting as a new adsorption site, while the enhanced selectivity was contributed by sulfhydryl's affinity for Cd. Altogether, MSA-CFA showed great promise as a competitive and highly efficient candidate amendment in Cd-contaminated soil remediation.
ABSTRACT
There is an urgent need to investigate on the distribution and fate of short-chain analogues and emerging per- and polyfluoroalkyl substances (PFASs) in groundwater, and little research on their source apportionment and health risks through the drinking water exposure pathway has been carried out. In present study, the concentration and source of 22 PFASs, including five alternatives: 6:2 fluorotelomer sulfonate (6:2 FTS), potassium 9-chlorohexadecafluoro-3-oxanonane-1-sulfonate (F-53B), hexafluoropropylene oxide trimer acid (HFPO-TA), hexafluoropropylene oxide dimer acid (HFPO-DA) and ammonium 4, 8-dioxa-3H-perfluorononanoate (ADONA), were analyzed in 88 groundwater samples from wells in Jiangxi Province, southeastern China. The total PFASs concentration (Σ18PFASs) in groundwater varied from 1.27 to 381.00 ng/L (mean 47.60 ng/L). Short-chain perfluorobutanoic acid (PFBA) and perfluoropentanoic acid (PFPeA) were the most abundant perfluorinated carboxylic acids (PFCAs), and short-chain perfluorobutanesulfonate (PFBS) was the most abundant perfluorinated sulfonic acids (PFSAs) in groundwater samples. The quantitative source apportionment by nonnegative matrix/tensor factorization coupled with k-means clustering (NMFk) model suggested that short-chain homologues and emerging alternatives have been used as substitutes for legacy PFOS and PFOA. Furthermore, the human risk assessment results showed that the estimated daily intakes (EDIs) for short-chain PFCAs were higher than that of PFOA, whereas the EDIs of PFBS, 6:2 FTS and F-53B were comparable to that of PFOS.
