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汞探针衍生化结合液相色谱-原子荧光光谱法测定空气样品中的硫化氢和挥发性硫醇

Determination of hydrogen sulfide and volatile thiols in air samples by mercury probe derivatization coupled with liquid chromatography-atomic fluorescence spectrometry.

作者信息

Bramanti Emilia, D'Ulivo Lucia, Lomonte Cristina, Onor Massimo, Zamboni Roberto, Raspi Giorgio, D'Ulivo Alessandro

机构信息

Italian National Research Council, CNR-Istituto per i Processi Chimico-Fisici, Laboratory of Instrumental Analytical Chemistry, Via G. Moruzzi 1, 56124 Pisa, Italy.

出版信息

Anal Chim Acta. 2006 Oct 2;579(1):38-46. doi: 10.1016/j.aca.2006.07.004. Epub 2006 Jul 8.

Abstract

A new procedure is proposed for the sampling and storage of hydrogen sulphide (H2S) and volatile thiols (methanethiol or methyl mercaptan, ethanethiol and propanethiol) for their determination by liquid chromatography. The sampling procedure is based on the trapping/pre-concentration of the analytes in alkaline aqueous solution containing an organic mercurial probe p-hydroxymercurybenzoate, HO-Hg-C6H4-COO- (PHMB), where they are derivatized to stable PHMB complexes based on mercury-sulfur covalent bonds. PHMB complexes are separated on a C18 reverse phase column, allowing their determination by liquid chromatography coupled with sequential non-selective UV-vis (DAD) and mercury specific (chemical vapor generation atomic fluorescence spectrometry, CVGAFS) on-line detectors. PHMB complexes, S(PHMB)2CH3S-PHMB, C2H5S-PHMB and C3H7S-PHMB, are stable alt least for 12 h at room temperature and for 3 months if stored frozen (-20 degrees C). The best analytical figures of merits in the optimized conditions were obtained by CVGAFS detection, with detection limits (LODc) of 9.7 microg L(-1) for H2S, 13.7 microg L(-1) for CH(3)SH, 17.7 microg L(-1) for C2H5SH and 21.7 microg L(-1) for C3H7SH in the trapping solution in form of RS-PHMB complexes, the relative standard deviation (R.S.D.) ranging between 1.0 and 1.5%, and a linear dynamic range (LDR) between 10 and 9700 microg L(-1). Conventional UV absorbance detectors tuned at 254 nm can be employed as well with comparable R.S.D. and LDR, but with LODc one order of magnitude higher than AFS detector and lower specificity. The sampling procedure followed by LC-DAD-CVGAFS analysis has been validated, as example, for H2S determination by a certified gas permeation tube as a source of 3.071+/-0.154 microg min(-1) of H2S, giving a recovery of 99.8+/-7% and it has been applied to the determination of sulfur compounds in real gas samples (biogas and the air of a plant for fractional distillation of crude oil).

摘要

本文提出了一种新的用于采集和储存硫化氢(H₂S)及挥发性硫醇(甲硫醇、乙硫醇和丙硫醇)的方法,以便通过液相色谱法对其进行测定。采样过程基于将分析物捕集/预浓缩于含有有机汞探针对羟基汞苯甲酸盐(HO-Hg-C₆H₄-COO⁻,简称PHMB)的碱性水溶液中,在该溶液中,分析物基于汞-硫共价键被衍生化为稳定的PHMB络合物。PHMB络合物在C₁₈反相柱上进行分离,从而可通过液相色谱结合顺序非选择性紫外可见(DAD)和汞特异性(化学蒸气发生原子荧光光谱法,CVGAFS)在线检测器对其进行测定。PHMB络合物,即S(PHMB)₂、CH₃S-PHMB、C₂H₅S-PHMB和C₃H₇S-PHMB,在室温下至少可稳定12小时,若冷冻保存(-20℃)则可稳定3个月。在优化条件下,采用CVGAFS检测可获得最佳分析性能指标:以RS-PHMB络合物形式存在于捕集溶液中的H₂S的检测限(LODc)为9.7 μg L⁻¹、CH₃SH为13.7 μg L⁻¹、C₂H₅SH为17.7 μg L⁻¹、C₃H₇SH为21.7 μg L⁻¹,相对标准偏差(R.S.D.)在1.0%至1.5%之间,线性动态范围(LDR)为10至9700 μg L⁻¹。调谐至254 nm的常规紫外吸收检测器也可使用,其R.S.D.和LDR相当,但LODc比AFS检测器高一个数量级,且特异性较低。例如,通过以3.071±0.154 μg min⁻¹的H₂S作为气源的经认证的气体渗透管对H₂S进行测定,验证了采用LC-DAD-CVGAFS分析的采样过程,回收率为99.8±7%,该方法已应用于实际气体样品(沼气和原油分馏厂的空气)中硫化合物的测定。

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