Co2+ - assisted continuous flow UV-induced Hg vapor generation coupled with a modified MSIS gas–liquid separator and microwave plasma atomic emission spectrometry

Dimitar Stoitsov
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Abstract

Co2+ and Ni2+ were investigated as potential sensitizers for the continuous flow UV-induced Hg vapor generation utilizing 10% (v/v) HCOOH as a low-molecular weight carboxylic acid and a modified multimode sample introduction system (MSIS) as a gas–liquid separator (GLS) coupled with microwave plasma atomic emission spectrometry (MP-AES). In contrast with Co2+, Ni2+ was found to suppress the sensitivity at different concentration levels. Thus, Co2+ was selected as a suitable sensitivity enhancement reagent and its concentration (1.50 mg dm−3) was optimized improving the empirical and the instrumental limit of detection (LOD) for Hg2+ to 0.10 µg dm−3 and 0.01 µg dm−3, respectively. The possible reasons for the observed effects of Co2+ and Ni2+ on the sensitivity were discussed. The Co2+—assisted UV-induced Hg vapor generation coupled with the modified MSIS GLS and MP-AES provided significantly lower instrumental LOD (ILOD) in comparison with other hyphenated Hg vapor generation procedures in the atomic spectrometry previously reported in the literature.

Graphical abstract

Abstract Image

Co2+辅助连续流紫外诱导汞蒸气生成与改良型MSIS气液分离器和微波等离子体原子发射光谱联用技术
利用 10% (v/v) HCOOH 作为低分子量羧酸和改进的多模样品导入系统 (MSIS) 作为气液分离器 (GLS),并结合微波等离子体原子发射光谱法 (MP-AES),研究了 Co2+ 和 Ni2+ 作为潜在敏化剂用于连续流紫外诱导汞蒸气生成的情况。与 Co2+ 相比,Ni2+ 在不同浓度水平下会抑制灵敏度。因此,Co2+ 被选为合适的灵敏度增强试剂,其浓度(1.50 毫克 dm-3)经过优化后,Hg2+ 的经验检测限和仪器检测限(LOD)分别提高到 0.10 微克 dm-3 和 0.01 微克 dm-3。讨论了 Co2+ 和 Ni2+ 对灵敏度产生影响的可能原因。与之前文献中报道的原子光谱法中的其他连体汞蒸气发生程序相比,Co2+辅助的紫外诱导汞蒸气发生与改进的MSIS GLS和MP-AES相结合,可显著降低仪器LOD(ILOD)。
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