A collisional focusing ion guide for coupling an atmospheric pressure ion source to a mass spectrometer

Author(s):  
A.V. Tolmachev ◽  
I.V. Chernushevich ◽  
A.F. Dodonov ◽  
K.G. Standing
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.


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

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.


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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