Tu Chi-Feng, Chen Yu-Chie
Department of Applied Chemistry, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan.
International College of Semiconductor Technology, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan.
Anal Chem. 2024 Jan 16;96(2):661-667. doi: 10.1021/acs.analchem.3c02589. Epub 2024 Jan 3.
In ambient ionization mass spectrometry (MS), a customized metal inlet is typically adapted to the orifice of the mass spectrometer for ease of introduction of the sample. We herein explore that the metal inlet coiled with a copper wire (∼50 μm) can be directly used as an ion source to induce corona discharge-like processes for ionization of analytes in the gas phase. When the metal inlet is subjected to a high voltage in the mass spectrometer, the electric field provided by the mass spectrometer enables the generation of corona discharge to ionize volatile/semivolatile analytes derived from the sample in the condensed phase. The limit of detection for azulene derived from the aqueous sample was as low as ∼1 pM. Moreover, we also demonstrated the feasibility of coupling ultraviolet-visible absorption spectroscopy with MS by using the metal inlet coiled with a thin copper wire as the interface. Integration of these two techniques enables the simultaneous acquisition of spectra from both instruments for quantitative and qualitative analysis of the sample. Furthermore, we showed that polar and nonpolar analytes in a mixture can be acquired in the same mass spectrum by simply depositing a sample droplet (∼20 μL) on a dielectric substrate near the copper wire-coiled metal inlet of the mass spectrometer. The ionization processes involved both electrospray ionization and corona discharge. To demonstrate the applicability of our method for detecting nonpolar and polar analytes in complex samples, we spiked a nonpolar analyte, benzo[]pyrene, to a spice sample and successfully detected analytes with different polarities using our approach.
在常压电离质谱(MS)中,通常会定制一个金属入口以适配质谱仪的孔口,便于引入样品。我们在此探究,用铜丝(约50μm)缠绕的金属入口可直接用作离子源,以引发类似电晕放电的过程,使气相中的分析物离子化。当金属入口在质谱仪中施加高电压时,质谱仪提供的电场能使电晕放电产生,从而使来自凝聚相样品的挥发性/半挥发性分析物离子化。从水性样品中得到的薁的检测限低至约1 pM。此外,我们还通过使用细铜丝缠绕的金属入口作为接口,证明了将紫外-可见吸收光谱与质谱联用的可行性。这两种技术的结合能够同时采集两台仪器的光谱,用于样品的定量和定性分析。此外,我们还表明,只需将一个样品液滴(约20μL)沉积在质谱仪铜丝缠绕金属入口附近的介电基板上,就能在同一质谱图中采集混合物中的极性和非极性分析物。电离过程涉及电喷雾电离和电晕放电。为了证明我们的方法对检测复杂样品中的非极性和极性分析物的适用性,我们将一种非极性分析物苯并[]芘添加到香料样品中,并使用我们的方法成功检测到了不同极性的分析物。