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Systematic optimization of a pyromellitic acid background electrolyte for capillary electrophoresis with indirect UV-vis detection and online pre-concentration analysis of thiosalt anions in treated mine tailings

机译:间接电泳检测和处理过的矿山尾矿中硫代盐阴离子的在线预富集分析对均苯四酸本底电解液进行毛细管电泳的系统优化

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摘要

A CZE method using indirect UV-vis detection was developed for the simultaneous separation and determination of five thiosalt anions: sulfate (SO42-), thiosulfate (S2O32-), trithionate (S3O62-), tetrathionate (S4O62-) and pentathionate (S5O62-). As with many inorganic anions, absorbance by some thiosalt species in the UV-vis range is poor or non-existent. Fully ionized pyromellitate ion (PMA), with a high molar absorptivity, was evaluated as the chromophoric probe for analysis of these species. The factors considered in optimization of the method were: composition of the background electrolyte (BGE) (concentrations of PMA and electroosmotic flow (EOF) modifiers, pH of BGE, applied electric potential (V) and plug size of water for online sample pre-concentration. The optimal conditions were: [PMA] = 2.00 mM, [hexamethonium (HM2+)] = 0.80 mM, pH = 8.0, E = -30 kV and online sample pre-concentration (stacking) with 90 mbar s injection of water followed by 250 mbar s injection of thiosalt standard sample before application of separation voltage. The five thiosalt anions were separated in under 3 min with good resolution and sensitivity obtained for all the analyte peaks. Limits of detection (LOD) were between 0.09 and 0.34 mu g mL(-1) without stacking; a three-fold increase in LODs to between 0.02 and 0.12 mu g mL(-1) was achieved after online pre-concentration.
机译:开发了一种使用间接UV-vis检测的CZE方法来同时分离和测定5种硫代盐阴离子:硫酸根(SO42-),硫代硫酸根(S2O32-),三硫代酸根(S3O62-),四硫代酸根(S4O62-)和五硫代磷酸根(S5O62- )。与许多无机阴离子一样,某些硫盐物种在紫外可见范围内的吸收率很低或根本不存在。具有高摩尔吸收率的完全离子化均苯四酸根离子(PMA)被评估为发色探针,用于分析这些物质。优化该方法时应考虑的因素包括:本底电解质(BGE)的成分(PMA和电渗流(EOF)改性剂的浓度,BGE的pH,施加的电势(V)和在线样品前加水的塞子尺寸)最佳条件为:[PMA] = 2.00 mM,[六甲铵(HM2 +)] = 0.80 mM,pH = 8.0,E = -30 kV,在线预浓缩(堆叠),然后注入水90 mbar s在施加分离电压之前,通过注入250 mbar s的硫代盐标准样品,在3 min内分离出5种硫代盐阴离子,对所有分析物峰均具有良好的分离度和灵敏度,检测限(LOD)在0.09至0.34μg之间mL(-1)无需堆积;在线预浓缩后,LOD升高了三倍,达到0.02至0.12μgmL(-1)。

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