光离子化
气相色谱离子检测器
气相色谱法
探测器
灵敏度(控制系统)
分析化学(期刊)
色谱法
微量气体
跟踪(心理语言学)
放电电离检测器
材料科学
化学
电离
光学
物理
离子
有机化学
工程类
哲学
语言学
电子工程
作者
Maxwell Wei-Hao Li,Abhishek Ghosh,Anandram Venkatasubramanian,Ruchi Sharma,Xiaolu Huang,Xudong Fan
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2021-05-24
卷期号:6 (6): 2348-2355
被引量:54
标识
DOI:10.1021/acssensors.1c00482
摘要
Rapid in situ detection and analysis of trace vapor concentrations at a sub-parts per billion to parts per trillion level remains a challenge for many applications such as indoor air-quality analysis and detection of explosives and narcotics. Micro-gas chromatography (μGC) together with a micro-photoionization detector (μPID) is a prominent method for portable analysis of complex vapor mixtures, but current μPID technology demonstrates poor detection performance compared to benchtop flame ionization detectors (FIDs). This work demonstrates the development of a significantly improved μPID with a sub-picogram detection limit (as low as ∼0.2 pg) comparable to or exceeding that of a benchtop FID, with a large linear dynamic range (>4 orders of magnitude) and robustness (high stability over 200 h of plasma activation). Based on this μPID, a complete μGC–PID system was built and tested on standard sample chromatograms in a laboratory setting to show the system's analytical capabilities and the detection limit down to sub-parts per trillion concentrations (as low as 0.14 ppt). Practical in-field chromatograms on breath and car exhaust were also generated to demonstrate applicability for in situ experimentation. This work shows that μGC–PID systems can be competitive with traditional GC–FID methods and thus opens a door to rapid trace vapor analysis in the field.
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