Shi Lulu, Habib Ahsan, Bi Lei, Wen Luhong
Shanghai Institute of Technical Physics, Chinese Academy of Sciences, Shanghai 200083, Shanghai China.
The Research Institute of Advanced Technologies, Ningbo University, Ningbo 315211, Zhejiang China.
J Am Soc Mass Spectrom. 2024 Sep 4;35(9):2209-2221. doi: 10.1021/jasms.4c00248. Epub 2024 Aug 20.
Detection of illicit compounds like explosives and drugs of abuse at trace levels is crucial to provide public security and health safety. A dual ambient sampling system hollow cathode discharge (HCD) ion source was developed to investigate its performance. Here, trinitrotoluene (TNT), trinitrobenzene (TNB), hexamethylene triperoxide diamine (HMTD), and triacetone triperoxide (TATP) as explosives and methamphetamine (MA) as drugs of abuse were taken as model compounds. Two sample inlets, inlet-1 and inlet-2, are available for ambient sampling. In negative ion mode, N and air HCD plasmas are confined close to inlet-1, but in positive ion mode, they are confined close to inlet-2. Special design of the ion source makes it feasible to generate multiple ions from a single analyte, which assists in understanding the gas phase ionization mechanism. In negative ion mode, both TNT and TNB gave radical ions, [M], as major ions for N HCD plasma as they were introduced via inlet-1 or inlet-2. TNB gave radical ions for air and N HCD plasmas, while TNT exhibited adduct ions, [TNT-H], by using air HCD plasma. In positive ion mode, HMTD gave [HMTD + H] / 209 ions, while TATP only produced adduct ions with ammonia, [TATP + NH] / 240. Regardless of ion source inlet, MA showed protonated molecule ions, [MA + H] / 150. As analytes were introduced via inlet-1, the stability of the HCD background ion signal reduced, leading to a decrease in sensitivity. Unlike that in negative ion mode, introduction of ambient air in positive ion mode enhanced the sensitivity of the air HCD ion source through the formation of hydronium ions, which gave protonated molecule ions. Ionization mechanisms are also discussed.
痕量检测非法化合物如爆炸物和滥用药物对于保障公共安全和健康至关重要。开发了一种双环境采样系统空心阴极放电(HCD)离子源以研究其性能。在此,将三硝基甲苯(TNT)、三硝基苯(TNB)、六亚甲基三过氧化二胺(HMTD)和三丙酮三过氧化二胺(TATP)作为爆炸物以及甲基苯丙胺(MA)作为滥用药物作为模型化合物。有两个样品入口,入口1和入口2,可用于环境采样。在负离子模式下,N和空气HCD等离子体被限制在靠近入口1的位置,但在正离子模式下,它们被限制在靠近入口2的位置。离子源的特殊设计使得从单个分析物产生多个离子成为可能,这有助于理解气相电离机制。在负离子模式下,当TNT和TNB通过入口1或入口2引入时,它们都产生自由基离子[M]作为N HCD等离子体的主要离子。TNB在空气和N HCD等离子体中产生自由基离子,而TNT在使用空气HCD等离子体时表现出加合离子[TNT - H]。在正离子模式下,HMTD产生[HMTD + H] / 209离子,而TATP仅产生与氨的加合离子[TATP + NH] / 240。无论离子源入口如何,MA都显示出质子化分子离子[MA + H] / 150。当分析物通过入口1引入时,HCD背景离子信号的稳定性降低,导致灵敏度下降。与负离子模式不同,在正离子模式下引入环境空气通过形成水合氢离子增强了空气HCD离子源的灵敏度,水合氢离子产生质子化分子离子。还讨论了电离机制。