4.4 Article

Determination of Ethyl Xanthate in Aqueous Solution by High Performance Liquid Chromatography-Inductively Coupled Plasma-Tandem Mass Spectrometry and Spectrophotometry

Journal

ANALYTICAL LETTERS
Volume 55, Issue 12, Pages 1857-1871

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00032719.2022.2031205

Keywords

High-performance liquid chromatography-inductively coupled plasma-tandem mass spectrometry; spectrophotometry; sulfur; xanthate

Funding

  1. Technology and Natural Sciences Doctoral Programme

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Xanthates, commonly used collectors in flotation processes, have high toxicity to the aquatic environment. However, there are limited methods for accurately determining low concentrations of xanthates in water samples. This study presents a sensitive, selective, and fast method for determining potassium ethyl xanthate (KEX) using high-performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS/MS). The method was optimized for diethyl dixanthogen [(EX)(2)] and showed potential for analyzing other xanthates and collectors with similar structures.
Xanthates are commonly used collectors in flotation processes but are highly toxic to the aquatic environment. However, there are few methods for reliable determination of low xanthate concentrations in water samples. In this work, a sensitive, selective, and fast method is presented for the determination of potassium ethyl xanthate (KEX). KEX was determined by high-performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS/MS) directly and as diethyl dixanthogen [(EX)(2)] after oxidation with triiodide. The HPLC method was optimized for (EX)(2) and the separated compounds were detected by ICP-MS/MS. The ICP-MS/MS was used in mass-shift mode using O-2 as the cell gas and S+ was measured as SO+ to reduce spectral interferences. Detection limits of 88 mu g L-1 for KEX and 20 mu g L-1 for (EX)(2) calculated from the peak area were obtained using mass-shift S-32(+) -> (SO+)-S-32-O-16. No significant matrix effects were present when spiking experiments of (EX)(2) were done to a sample collected from the tailings of a flotation process. The developed method demonstrates the potential of the HPLC-ICP-MS/MS for the determination of ethyl xanthate. This method may be extended to analyzing other xanthates and similarly structured sulfur containing collectors.

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