scholarly journals The design of an atmospheric pressure ionization/time‐of‐flight mass spectrometer using a beam deflection method

1992 ◽  
Vol 63 (1) ◽  
pp. 139-148 ◽  
Author(s):  
Ce Ma ◽  
Steven M. Michael ◽  
Mingta Chien ◽  
Jianzhong Zhu ◽  
David M. Lubman
Keyword(s):  
Mass Spectrometer ◽  
Atmospheric Pressure ◽  
Time Of Flight ◽  
Beam Deflection ◽  
Atmospheric Pressure Ionization ◽  
Ionization Time ◽  
Flight Mass Spectrometer

Vacuum Ultraviolet Single-Photon Ionization Time-of-Flight Mass Spectrometer

2011 ◽  
Vol 39 (10) ◽  
pp. 1470-1475 ◽  
Author(s):  
Guo-Bin TAN ◽  
Wei GAO ◽  
Zheng-Xu HUANG ◽  
Yi HONG ◽  
Zhong FU ◽  
...  
Keyword(s):  
Mass Spectrometer ◽  
Vacuum Ultraviolet ◽  
Single Photon ◽  
Time Of Flight ◽  
Ionization Time ◽  
Single Photon Ionization ◽  
Flight Mass Spectrometer ◽  
Photon Ionization

scholarly journals A small high-irradiance laser ionization time-of-flight mass spectrometer

2009 ◽  
Vol 44 (5) ◽  
pp. 780-785 ◽  
Author(s):  
Jian He ◽  
Rongfu Huang ◽  
Quan Yu ◽  
Yiming Lin ◽  
Wei Hang ◽  
...  
Keyword(s):  
Mass Spectrometer ◽  
Time Of Flight ◽  
High Irradiance ◽  
Laser Ionization ◽  
Ionization Time ◽  
Flight Mass Spectrometer

scholarly journals Characterisation of the transfer of cluster ions through an atmospheric pressure interface time-of-flight mass spectrometer with hexapole ion guides

2019 ◽  
Vol 12 (10) ◽  
pp. 5231-5246 ◽  
Author(s):  
Markus Leiminger ◽  
Stefan Feil ◽  
Paul Mutschlechner ◽  
Arttu Ylisirniö ◽  
Daniel Gunsch ◽  
...  
Keyword(s):  
Mass Spectrometer ◽  
Atmospheric Pressure ◽  
Time Of Flight ◽  
Mass Range ◽  
Transmission Efficiency ◽  
Binding Energies ◽  
Cluster Ions ◽  
Ion Transfer ◽  
Flight Mass Spectrometer ◽  
Ion Guides

Abstract. Here we present an alternative approach of an atmospheric pressure interface (APi) time-of-flight mass spectrometer for the study of atmospheric ions and cluster ions, the so-called ioniAPi-TOF. The novelty is the use of two hexapoles as ion guides within the APi. In our case, hexapoles can accept and transmit a broad mass range enabling the study of small precursor ions and heavy cluster ions at the same time. Weakly bound cluster ions can easily de-cluster during ion transfer depending on the voltages applied to the ion transfer optics. With the example system of H3O+(H2O)n=0-3, we estimate that cluster ions with higher binding energies than 17 kcal mol−1 can be transferred through the APi without significant fragmentation, which is considerably lower than about 25 kcal mol−1 estimated from the literature for APi-TOFs with quadrupole ion guides. In contrast to the low-fragmenting ion transfer, the hexapoles can be set to a high-fragmenting declustering mode for collision-induced dissociation (CID) experiments as well. The ion transmission efficiency over a broad mass range was determined to be on the order of 1 %, which is comparable to existing instrumentation. From measurements under well-controlled conditions during the CLOUD experiment, we demonstrate the instrument's performance and present results from an inter-comparison with a quadrupole-based APi-TOF.

scholarly journals Organic aerosol source apportionment in Zurich using an extractive electrospray ionization time-of-flight mass spectrometer (EESI-TOF-MS) – Part 2: Biomass burning influences in winter

2019 ◽  
Vol 19 (12) ◽  
pp. 8037-8062 ◽  
Author(s):  
Lu Qi ◽  
Mindong Chen ◽  
Giulia Stefenelli ◽  
Veronika Pospisilova ◽  
Yandong Tong ◽  
...  
Keyword(s):  
Electrospray Ionization ◽  
Source Apportionment ◽  
Mass Spectrometer ◽  
Biomass Burning ◽  
Time Of Flight ◽  
Organic Aerosol ◽  
Climate Impacts ◽  
Ionization Time ◽  
Flight Mass Spectrometer ◽  
Tof Ms

Abstract. Real-time, in situ molecular composition measurements of the organic fraction of fine particulate matter (PM2.5) remain challenging, hindering a full understanding of the climate impacts and health effects of PM2.5. In particular, the thermal decomposition and ionization-induced fragmentation affecting current techniques has limited a detailed investigation of secondary organic aerosol (SOA), which typically dominates OA. Here we deploy a novel extractive electrospray ionization time-of-flight mass spectrometer (EESI-TOF-MS) during winter 2017 in downtown Zurich, Switzerland, which overcomes these limitations, together with an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS) and supporting instrumentation. Positive matrix factorization (PMF) implemented within the Multilinear Engine (ME-2) program was applied to the EESI-TOF-MS data to quantify the primary and secondary contributions to OA. An 11-factor solution was selected as the best representation of the data, including five primary and six secondary factors. Primary factors showed influence from cooking, cigarette smoke, biomass burning (two factors) and a special local unknown event occurred only during two nights. Secondary factors were affected by biomass burning (three factors, distinguished by temperature and/or wind direction), organonitrates, monoterpene oxidation, and undetermined regional processing, in particular the contributions of wood combustion. While the AMS attributed slightly over half the OA mass to SOA but did not identify its source, the EESI-TOF-MS showed that most (>70 %) of the SOA was derived from biomass burning. Together with significant contributions from less aged biomass burning factors identified by both AMS and EESI-TOF-MS, this firmly establishes biomass burning as the single most important contributor to OA mass at this site during winter. High correlation was obtained between EESI-TOF-MS and AMS PMF factors where specific analogues existed, as well as between total signal and POA–SOA apportionment. This suggests the EESI-TOF-MS apportionment in the current study can be approximately taken at face value, despite ion-by-ion differences in relative sensitivity. The apportionment of specific ions measured by the EESI-TOF-MS (e.g., levoglucosan, nitrocatechol, and selected organic acids) and utilization of a cluster analysis-based approach to identify key marker ions for the EESI-TOF-MS factors are investigated. The interpretability of the EESI-TOF-MS results and improved source separation relative to the AMS within this pilot campaign validate the EESI-TOF-MS as a promising approach to source apportionment and atmospheric composition research.

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