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Xanthates, common mining flotation reagents, strongly bind thiophilic metals such as copper (Cu), lead (Pb), cadmium (Cd), and zinc (Zn) and consequentially change their bioavailability and mobility upon their discharge into the environment. However, accurate quantification of the metal-xanthate complexes has remained elusive. This study develops a novel and robust method that realizes the accurate quantification of the metal-xanthate complexes resulted from single and multiple reactions of three typical xanthates (ethyl, isopropyl, and butyl xanthates) and four thiophilic metals (Cu, Pb, Cd, and Zn) in water samples. This method uses sulfur (S) dissociation, followed by tandem solid phase extraction of C + PWAX and subsequent LC-MS/MS analysis. It has a wide linearity range (1-1000 μg/L, R ≥ 0.995), low method detection limits (0.002-0.036 μg/L), and good recoveries (70.6-107.0 %) at 0.01-10 mg/L of xanthates. Applications of this method showed ubiquitous occurrence of the metal-xanthate complexes as the primary species in flotation wastewaters, which the concentrations were 4.6-28.9-fold higher than those previously determined. It is the first quantitative method established for the analysis of metal-xanthate complexes in water samples, which is of great importance to comprehensively understand the fate and risks of xanthates in the environment.
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http://dx.doi.org/10.1016/j.jhazmat.2024.134873 | DOI Listing |
Water Res
July 2025
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA; Hawaii Pacific Neuroscience, 2230 Liliha Street, Honolulu, HI 96817, United States.
Mining activities release a substantial quantity of toxic metals and organic flotation reagents into the aquatic environment, causing severe pollution and potential health risks. However, the synergisms and mechanisms associated with these mixed pollutants are largely overlooked. The combined application of atomic force microscopy, high-resolution mass spectrometry, nuclear magnetic resonance spectroscopy, isothermal titration calorimetry, and quantum chemical calculations revealed that cadmium (Cd) was capable of forming tridentate coordination complexes with typical organic beneficiation reagents, namely xanthates (ethyl, isopropyl, and butyl xanthates).
View Article and Find Full Text PDFJ Hazard Mater
September 2024
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Xanthates, common mining flotation reagents, strongly bind thiophilic metals such as copper (Cu), lead (Pb), cadmium (Cd), and zinc (Zn) and consequentially change their bioavailability and mobility upon their discharge into the environment. However, accurate quantification of the metal-xanthate complexes has remained elusive. This study develops a novel and robust method that realizes the accurate quantification of the metal-xanthate complexes resulted from single and multiple reactions of three typical xanthates (ethyl, isopropyl, and butyl xanthates) and four thiophilic metals (Cu, Pb, Cd, and Zn) in water samples.
View Article and Find Full Text PDFACS Appl Eng Mater
May 2024
Department of Materials, The University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
A methodology to use laser printing, a form of electrophotography, to print metal chalcogenide complexes on paper, is described. After fusing the toner to paper, a heating step is used to cause the printed metal xanthate complexes to thermolyze within the toner and form three target metal chalcogenides: CuS, SnS, and ZnS. To achieve this, we synthesize a poly(styrene---butyl acrylate) thermopolymer that emulates the thermal properties of a commercial toner and is also solution processable with the metal xanthate complexes used: [Zn(SCOEt)], [Cu(SCOEt)·(PPh)], and [Sn(SCOEt)].
View Article and Find Full Text PDFDalton Trans
November 2019
School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Alkyl-xanthato gallium(iii) complexes of the form [Ga(SCOR)], where R = Me (1), Et (2), Pr (3), Pr (4), Bu (5), Bu (6) and Bu (7), have been synthesized and fully characterised. The crystal structures for 1 and 3-7 have been solved and examined to elucidate if these structures are related to their decomposition. Thermogravimetric analysis was used to gain insight into the decomposition temperatures for each complex.
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July 2018
Department of Chemistry, University of Zululand, Private Bag X1001, Kwa-Dlangezwa, 3880, South Africa.
Xanthate complexes are used in the low temperature atom efficient synthesis of some geological and technologically important ternary compounds. The process involves direct heating of a stoichiometric mixture of the metal xanthate complexes. The reactive melts of the xanthates, generated in the transition state, cleanly decompose to ternary metal sulfides.
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