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正交加速飞行时间质谱仪平台上的真空单光子和多光子电离的在线同时进行。

Simultaneous on-line vacuum single- and multi-photon ionization on an orthogonal acceleration time-of-flight mass spectrometer platform.

机构信息

Joint Mass Spectrometry Centre, Chair of Analytical Chemistry, Institute of Chemistry, University of Rostock, 18059 Rostock, Germany.

Photonion GmbH, 19061 Schwerin, Germany.

出版信息

Analyst. 2022 Aug 8;147(16):3662-3674. doi: 10.1039/d2an00774f.

Abstract

The development of orthogonal acceleration time-of-flight (oa-tof) technology is driven forward due to higher mass accuracy and resolving power than conventional linear/reflectron tof instruments. This is achieved with a more accurate definition of starting energies and coordinates of ions by spatial separation of ion generation and orthogonal ion extraction. Consequently, the ability to cover the whole mass spectral range without scanning is not given anymore. Therefore, continuous ion sources are favored for ensuring high duty cycles and thus high temporal resolution. For pulsed ion sources, high repetition rates are mandatory for covering large / ranges without losing their high temporal resolution. We have combined an oa-tof with deuterium lamp single-photon ionization (SPI) as a continuous ion source together with a pulsed 2000 Hz excimer (KrF) laser for resonance enhanced multi-photon ionization (REMPI). These two ionization techniques can be used simultaneously. To the best of our knowledge, this system is the first of its kind in combining a vacuum pulsed ionization source with an oa-tof instrument without any other ion storage hardware. The combination of a soft broadband ionization for organics (SPI) in combination with a very sensitive and selective soft ionization (REMPI) can be used for covering the whole mass range or in targeted on-line monitoring cases one or several smaller mass ranges. To demonstrate the simultaneous SPI/REMPI-oa-tof technique, two applicative areas are explored: on-line monitoring of coffee roast gas emissions and e-cigarette vapor. The complementary information from SPI and REMPI signals are combined in a way to exploit the advantages of both ionization types. In a further development step, a second data acquisition card is built into the system. This modification allows the independent storage of data from both ionization methods without mixing. For demonstration, a third example with a GC measurement is provided. The last example shows the possibility of modified sensitivities for different mass regions in REMPI data acquisition without affecting the SPI channel. The newly developed system shows high robustness in terms of measurements in real industrial environments. The simultaneous measurement technique provides a higher density of information in a single measurement, saving time and resources.

摘要

正交加速飞行时间(oa-tof)技术的发展得益于比传统线性/反射飞行时间仪器更高的质量精度和分辨率。这是通过空间分离离子产生和正交离子提取来更准确地定义离子的起始能量和坐标来实现的。因此,不再能够在不进行扫描的情况下覆盖整个质谱范围。因此,连续离子源有利于确保高占空比,从而实现高时间分辨率。对于脉冲离子源,必须提高重复频率才能在不损失其高时间分辨率的情况下覆盖大的质量范围。我们将 oa-tof 与氘灯单光子电离(SPI)相结合,作为连续离子源,同时使用脉冲 2000 Hz 准分子(KrF)激光器进行共振增强多光子电离(REMPI)。这两种电离技术可以同时使用。据我们所知,该系统是将真空脉冲电离源与 oa-tof 仪器结合使用的首例系统,没有任何其他离子存储硬件。将用于有机化合物的软宽带电离(SPI)与非常敏感和选择性的软电离(REMPI)相结合,可以用于覆盖整个质量范围,或者在有针对性的在线监测情况下,用于一个或几个较小的质量范围。为了演示同时的 SPI/REMPI-oa-tof 技术,我们探索了两个应用领域:在线监测咖啡烘焙气体排放和电子烟蒸汽。SPI 和 REMPI 信号的互补信息以一种方式组合,以利用两种电离类型的优势。在进一步的开发步骤中,系统中内置了第二张数据采集卡。此修改允许独立存储两种电离方法的数据而不混合。为了演示,提供了第三个带有 GC 测量的示例。最后一个示例显示了在不影响 SPI 通道的情况下,在 REMPI 数据采集时为不同质量区域修改灵敏度的可能性。新开发的系统在实际工业环境中的测量中具有很高的稳健性。同时测量技术在单次测量中提供了更高密度的信息,节省了时间和资源。

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