Following the Ions through a Mass Spectrometer with Atmospheric Pressure Interface: Simulation of Complete Ion Trajectories from Ion Source to Mass Analyzer

2016 ◽  
Vol 88 (14) ◽  
pp. 7033-7040 ◽  
Author(s):  
Xiaoyu Zhou ◽  
Zheng Ouyang
2009 ◽  
Vol 6 (1) ◽  
pp. 39-46
Author(s):  
Francis Beaudry ◽  
Robert B. Moore

An intermediate electrode was developed to improve the transfer of ions in atmospheric pressure from a first location, the ion source, to a second location, the mass spectrometer. The new apparatus increase the efficiency of mass analysis of molecular constituents of liquids, including trace analysis of chemical entities, in which an electrospray (ES) or IonSpray™ (IS) technique is used to produce electrically charged droplets which divide and evaporate to form gaseous ions of the molecular constituents. The gas phase ions are transported to the mass spectrometer by an electric field generated by a new electrode design that separates the two fundamental functions of an electrospray or an IonSpray™, which are the nebulization of charged droplets and the transport of ions into the mass analyzer. The results suggest that the new apparatus provide a gain in signal intensity up to 10 compared with the commercial product. A significant improvement in ion transport results in higher precision and accuracy and/or reduction of the amount of material needed for analysis.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6760
Author(s):  
De-Yi Huang ◽  
Meng-Jiy Wang ◽  
Jih-Jen Wu ◽  
Yu-Chie Chen

Atmospheric pressure chemical ionization (APCI)-mass spectrometry (MS) and electrospray ionization (ESI)-MS can cover the analysis of analytes from low to high polarities. Thus, an ion source that possesses these two ionization functions is useful. Atmospheric surface-assisted ionization (ASAI), which can be used to ionize polar and nonpolar analytes in vapor, liquid, and solid forms, was demonstrated in this study. The ionization of analytes through APCI or ESI was induced from the surface of a metal substrate such as a titanium slab. ASAI is a contactless approach operated at atmospheric pressure. No electric contacts nor any voltages were required to be applied on the metal substrate during ionization. When placing samples with high vapor pressure in condensed phase underneath a titanium slab close to the inlet of the mass spectrometer, analytes can be readily ionized and detected by the mass spectrometer. Furthermore, a sample droplet (~2 μL) containing high-polarity analytes, including polar organics and biomolecules, was ionized using the titanium slab. One titanium slab is sufficient to induce the ionization of analytes occurring in front of a mass spectrometer applied with a high voltage. Moreover, this ionization method can be used to detect high volatile or polar analytes through APCI-like or ESI-like processes, respectively.


2020 ◽  
Author(s):  
Rustam Lukmanov ◽  
Marek Tulej ◽  
Valentine Riedo ◽  
Niels Ligterink ◽  
Coenraad De Koning ◽  
...  

<p>In-situ Mars exploration requires new promising instrumentation that will be capable of delivering highly accurate chemical information about soils and rocks present at the Martian surface. Specific attention is drawn to the instruments that are capable of identifying extinct or extant microbes within the bulk of various solid samples (Tulej et al., 2015; Westall et al., 2015; Wiesendanger et al., 2018). A miniature Laser Ablation/Ionization Mass Spectrometer (LIMS) developed at the University of Bern is among the valid candidates (Wurz et al., 2012). The size of the mass analyzer is only Ø 60 mm × 160 mm and thus capable of being deployed on a rover or lander platform. In this contribution, we will present data collected from a 1.88 Ga Gunflint sample using a deep UV fs laser system as ablation ion source. The gunflint chert sample contains a population of microfossils entombed in the silica matrix and was chosen as a Martian analogue. Using the high stability of the UV laser and consequent uniform ablation, we performed large-scale spectra collection (90’000) in two modes - chemical imaging and depth profiling. With the current setup, we achieved a diameter of the analytical spot of ~10 µm for the depth profiling and ~5 µm for the imaging. Our results reveal that our LIMS instrument can identify the location of the microfossil lamination area as well as single microfossils by chemical means. We show how single mass unit spectral decomposition and subsequent kernel clustering reveal masses and intensity regions unique to the microfossils and inorganic host, thus providing the opportunity for automated identification of the spectra that are collected from the microfossils. We also show how transforming spectral intensities into spectral proximities can help to navigate the rich multidimensional datasets. We also address common interpretation problems in LIMS, when multiple mineralogical inclusions contribute to the output spectra acquired within the single analytical spot using ρ-networks and Principal Component Analysis (PCA). In combination with analysis of spectral proximities, this approach is particularly useful in attempts to assess the biogenicity of the putative terrestrial microfossils as well as potential Martian microfossils. Additionally, we discuss the data analysis pipeline and chemical composition of the microfossils and surrounding inorganic host in detail. </p> <p>Tulej M., Neubeck A., Ivarsson M., Riedo A., Neuland M. B., Meyer S., and Wurz P. (2015) Chemical Composition of Micrometer-Sized Filaments in an Aragonite Host by a Miniature Laser Ablation/Ionization Mass Spectrometer. Astrobiology, 15: 669-682.</p> <p>Westall F., Foucher F., Bost N., Bertrand M., Loizeau D., Vago J. L., Kminek G., Gaboyer F., Campbell K. A., Bréhéret J.-G. and others. (2015) Biosignatures on Mars: What, Where, and How? Implications for the Search for Martian Life. Astrobiology, 15: 998-1029.</p> <p>Wiesendanger R., Wacey D., Tulej M., Neubeck A., Ivarsson M., Grimaudo V., Moreno-García P., Cedeño-López A., Riedo A., Wurz P. and others. (2018) Chemical and Optical Identification of Micrometer-Sized 1.9 Billion-Year-Old Fossils by Combining a Miniature Laser Ablation Ionization Mass Spectrometry System with an Optical Microscope. Astrobiology, 18: 1071-1080.</p> <p>Wurz P., Abplanalp D., Tulej M., Iakovleva M., Fernandes V. A., Chumikov A., and Managadze G. G. (2012) Mass spectrometric analysis in planetary science: Investigation of the surface and the atmosphere. Solar System Research, 46: 408-422.</p> <p> </p>


2013 ◽  
Vol 85 (19) ◽  
pp. 9003-9012 ◽  
Author(s):  
Alexey A. Sysoev ◽  
Denis M. Chernyshev ◽  
Sergey S. Poteshin ◽  
Alexander V. Karpov ◽  
Oleg I. Fomin ◽  
...  

Author(s):  
Clara Markert ◽  
Marco Thinius ◽  
Laura Lehmann ◽  
Chris Heintz ◽  
Florian Stappert ◽  
...  

AbstractElectrospray ionization (ESI) generates bare analyte ions from charged droplets, which result from spraying a liquid in a strong electric field. Experimental observations available in the literature suggest that at least a significant fraction of the initially generated droplets remain large, have long lifetimes, and can thus aspirate into the inlet system of an atmospheric pressure ionization mass spectrometer (API-MS). We report on the observation of fragment signatures from charged droplets penetrating deeply the vacuum stages of three commercial mass spectrometer systems with largely different ion source and spray configurations. Charged droplets can pass through the ion source and pressure reduction stages and even into the mass analyzer region. Since droplet signatures were found in all investigated instruments, the incorporation of charged droplets is considered a general phenomenon occurring with common spray conditions in ESI sources.


2016 ◽  
Vol 18 (33) ◽  
pp. 22962-22972 ◽  
Author(s):  
Jikku M. Thomas ◽  
Siqin He ◽  
Carlos Larriba-Andaluz ◽  
Joseph W. DePalma ◽  
Murray V. Johnston ◽  
...  

Uptake of water molecules by dimethylamine–sulfuric acid cluster ions mitigates dissociation in atmospheric pressure ion source mass spectrometer inlets.


2001 ◽  
Vol 40 (Part 1, No. 4B) ◽  
pp. 2688-2693 ◽  
Author(s):  
Masafumi Kitano ◽  
Yasuyuki Shirai ◽  
Atsushi Ohki ◽  
Shinichi Babasaki ◽  
Tadahiro Ohmi

2007 ◽  
Vol 13 (4) ◽  
pp. 249-257 ◽  
Author(s):  
Changjuan Guo ◽  
Zhengxu Huang ◽  
Wei Gao ◽  
Huiqing Nian ◽  
Huayong Chen ◽  
...  

A heated capillary tube combined with a radio-frequency-only quadrupole has been coupled with a home-made, high-resolution orthogonal-injection, time-of-flight mass spectrometer to improve ion transmission from the atmospheric pressure to the low-pressure regions. With an electrospray ion source, the performance of the interface on the intensity of spectra was investigated. For electrospray ionization, the ion intensity detected on the time-of-flight mass spectrometer was seen to increase three-fold compared with an orifice interface. It has been shown that the enhanced ion inlet designs can not only increase the ion translation efficiency, but also improve the detection limits of the mass spectrometer. Coupling atmospheric pressure matrix-assisted laser desorption/ionization with the improved interface resulted in an instrument detection limit as low as 2.5 fmol.


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