An evaluation on the extraction capability of anion exchange membranes for high-precision sulfur isotope measurement by multiple-collector inductively coupled plasma mass spectrometry
Abstract:Anion exchange membranes (AEMs) are adept at extracting sulfate for sulfur isotope analyses by multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) from natural samples typically with low sulfate concentrations.
“…Accurate determination of the sulfur isotope ratios of sulte, sulfate and thiosulfate in waters was achieved 84 in one analytical run by coupling IC to MC-ICP-MS. An S-containing IS (trimethylsulfoxide) was added to correct for mass bias, and oncolumn fractionation was corrected by external calibration. Use of a linear regression slope to calculate the isotope ratios of the transient signals resulted in a combined uncertainty of <0.25& for d 34 S in solution and a reproducibility of 0.5& for an injection of 1 mg of S. An anion-exchange membrane was evaluated 85 for the extraction of S from fresh and marine pore waters before determination of S isotope ratios by MC-ICP-MS. Recoveries were >90% when concentrations of competing ions (bicarbonate, carbonate, chloride, nitrate and phosphate) were limited to <0.5 mM per cm 2 of membrane. The lowest S concentration detectable without fractionation was 0.5 mM, but the recovery dropped at concentrations >0.01 mM probably as a result of reaching the breakthrough volume for the disc membrane.…”
This review covers advances in the analysis of air, water, plants, soils and geological materials by a range of atomic spectrometric techniques including atomic emission, absorption, fluorescence and mass spectrometry.
“…Accurate determination of the sulfur isotope ratios of sulte, sulfate and thiosulfate in waters was achieved 84 in one analytical run by coupling IC to MC-ICP-MS. An S-containing IS (trimethylsulfoxide) was added to correct for mass bias, and oncolumn fractionation was corrected by external calibration. Use of a linear regression slope to calculate the isotope ratios of the transient signals resulted in a combined uncertainty of <0.25& for d 34 S in solution and a reproducibility of 0.5& for an injection of 1 mg of S. An anion-exchange membrane was evaluated 85 for the extraction of S from fresh and marine pore waters before determination of S isotope ratios by MC-ICP-MS. Recoveries were >90% when concentrations of competing ions (bicarbonate, carbonate, chloride, nitrate and phosphate) were limited to <0.5 mM per cm 2 of membrane. The lowest S concentration detectable without fractionation was 0.5 mM, but the recovery dropped at concentrations >0.01 mM probably as a result of reaching the breakthrough volume for the disc membrane.…”
This review covers advances in the analysis of air, water, plants, soils and geological materials by a range of atomic spectrometric techniques including atomic emission, absorption, fluorescence and mass spectrometry.
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