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通过一种新颖的死时间校正方法来扩展质子转移反应飞行时间质谱仪的动态范围。

Extending the dynamic range of proton transfer reaction time-of-flight mass spectrometers by a novel dead time correction.

机构信息

IASMA Research and Innovation Centre, Fondazione Edmund Mach, Food Quality and Nutrition Area, Via E. Mach 1, 38010 S. Michele a/A, Italy.

出版信息

Rapid Commun Mass Spectrom. 2011 Jan 15;25(1):179-83. doi: 10.1002/rcm.4819.

Abstract

Proton transfer reaction time-of-flight mass spectrometry (PTR-TOF-MS) allows for very fast simultaneous monitoring of volatile organic compounds (VOCs) in complex environments. In several applications, food science and food technology in particular, peaks with very different intensities are present in a single spectrum. For VOCs, the concentrations range from the sub-ppt all the way up to the ppm level. Thus, a large dynamic range is necessary. In particular, high intensity peaks are a problem because for them the linear dependency of the detector signal on VOC concentration is distorted. In this paper we present, test with real data, and discuss a novel method which extends the linearity of PTR-TOF-MS for high intensity peaks far beyond the limit allowed by the usual analytical correction methods such as the so-called Poisson correction. Usually, raw data can be used directly without corrections with an intensity of up to about 0.1 ions/pulse, and the Poisson correction allows the use of peaks with intensities of a few ions/pulse. Our method further extends the linear range by at least one order of magnitude. Although this work originated from the necessity to extend the dynamic range of PTR-TOF-MS instruments in agro-industrial applications, it is by no means limited to this area, and can be implemented wherever dead time corrections are an issue.

摘要

质子转移反应飞行时间质谱(PTR-TOF-MS)可用于非常快速地同时监测复杂环境中的挥发性有机化合物(VOCs)。在许多应用中,特别是食品科学和食品技术,单个光谱中存在强度非常不同的峰。对于 VOCs,浓度范围从亚 ppt 一直到 ppm 水平。因此,需要很大的动态范围。特别是高强度的峰是一个问题,因为对于它们,探测器信号对 VOC 浓度的线性依赖性会被扭曲。在本文中,我们提出了一种新方法,并通过实际数据进行了测试和讨论,该方法将 PTR-TOF-MS 的线性度扩展到高强度峰,远远超出了通常的分析校正方法(例如所谓的泊松校正)允许的范围。通常,在不进行校正的情况下,强度高达约 0.1 个离子/脉冲的原始数据可直接使用,而泊松校正允许使用强度为几个离子/脉冲的峰。我们的方法通过至少一个数量级进一步扩展了线性范围。尽管这项工作源于在农业工业应用中扩展 PTR-TOF-MS 仪器动态范围的必要性,但它绝不仅限于此领域,只要存在死时间校正问题,就可以实施该方法。

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