Membrane interface for selective introduction of volatile compounds directly into the ionization chamber of a mass spectrometer

1987 ◽  
Vol 59 (4) ◽  
pp. 597-601 ◽  
Author(s):  
M. E. Bier ◽  
R. G. Cooks
2016 ◽  
Vol 2016 ◽  
pp. 1-9
Author(s):  
Yury I. Lyakhovetsky ◽  
Elena A. Shilova ◽  
Alexandra P. Pleshkova ◽  
Alexander I. Belokon ◽  
Sergey O. Yakushin ◽  
...  

C60was shown to react with organosilanes Me4Si, Ph2SiH2, Ph2MeSiH, Ph4Si, andα-naphthylphenylmethylsilane in the electron ionization ion source of a mass spectrometer with the transfer of the corresponding organic radicals (Me, Ph, andα-naphthyl) from the silanes to the fullerene. The reactions were accompanied by hydrogen addition to some products and hydrogen loss from them. C70reacted with Me4Si analogously. A reaction mechanism involving homolytic dissociation of the silanes under electron impact to the corresponding organic radicals, which react further with C60at the surface of the ionization chamber of the mass spectrometer to give the respective adducts, was offered. A mechanistic study of the reaction of C60with Me4Si supported it. No silicon containing derivatives of the fullerenes were found. C60reacted with Ph4Si in solution under UV irradiation in a similar fashion furnishing phenyl derivatives of the fullerene. These results provide an additional support to the hypothesis formulated earlier thatthe homolytic reactive mass spectrometry of fullerenes (the reactions of fullerenes with other species in the ionization chambers of mass spectrometers and their mass spectral monitoring)can predict the reactivity of them toward the same reagents in solution to a significant extent.


2011 ◽  
Vol 54 (3) ◽  
pp. 390-396 ◽  
Author(s):  
V. T. Kogan ◽  
D. S. Lebedev ◽  
A. K. Pavlov ◽  
Yu. V. Chichagov ◽  
A. S. Antonov

1997 ◽  
Vol 69 (18) ◽  
pp. 3780-3790 ◽  
Author(s):  
David M. Chambers ◽  
Louis I. Grace ◽  
Brian D. Andresen

1951 ◽  
Vol 138 (890) ◽  
pp. 112-114

Studies with the mass spectrometer . By R. Bentley Under specified conditions, volatile compounds give a characteristic pattern of mass fragments when introduced into the ion source of a mass spectrometer (Smyth 1931; Hippie 1942; Roberts & Johnsen 1948). It was hoped that this method would disclose the molecular weight'of the volatile chemotactic material obtained from eggs of Fucus species, and provide information about its structure. Samples of the material (and several synthetic compounds) in evacuated breakseal tubes (figure 2, plate 8) were attached to tthe gas handling system of a mass spectrometer, evacuated to the seal, and the sample admitted to the ion source after breaking the seal in the usual way. A glass capillary leak was used, and the pressure of the sample behind the leak could be adjusted to a suitable value by operation of a Toepler pump. With a single exception, a cold trap was not used on the sample system.


2020 ◽  
Author(s):  
Markus Sebastian Leiminger ◽  
Tobias Reinecke ◽  
Markus Müller ◽  
Stefan Feil ◽  
Philipp Sulzer ◽  
...  

<p>The recently introduced PTR3-TOF mass spectrometer (Proton Transfer Reaction Time-Of-Flight) allows for a direct and quantitative detection of volatile organic compounds (VOC) and their oxidation products. With a design of the inlet system and the ionization chamber that allows analyte transfer with virtually no wall interactions, organics ranging from volatile to extremely low volatility (ELVOC) can be measured, even at ambient temperature. In addition, PTR3 has recently shown to detect and quantify RO<sub>2 </sub>radicals. Unlike the traditional PTR-MS ionization technique, the PTR3 is operated at an elevated reaction pressure of 50 to 80 mbar while reaction kinetics are precisely defined via radial electric fields emitted from a tripole ion guide. With this setup, outstanding sensitivities of more than 30,000 cps/ppbV are achieved.</p><p>Herein, we present an improved version of a PTR3-TOF instrument. The inlet comprises three cylindrically arranged ion sources allowing for fast electrical switching between a set of reagent ions including H<sub>3</sub>O<sup>+</sup>, NO<sup>+</sup>, O<sub>2</sub><sup>+</sup> and NH<sub>4</sub><sup>+</sup>. The tripole geometry is aerodynamically improved to further reduce surface interactions. Extraction of analyte ions from the PTR3 ionization chamber and subsequent transfer to the TOF mass analyzer is now enhanced by an ion booster in series to a hexapole ion guide. This setup enables a precise control of extraction energies to reduce unwanted collision induced fragmentation and at the same time efficiently transmits ions of a broad m/z range. Analyte ions are analyzed with a high-resolution Time-Of-Flight mass spectrometer achieving mass resolving powers of typically 13,000 to 15,000.</p><p>We have characterized the performance of this optimized PTR3-TOF instrument using pure chemical compounds of intermediate to low volatility, including carboxylic acids and peroxides. Hereby, the effects of PTR3 reaction conditions and ion extraction settings are studied. Monoterpene ozonolysis experiments demonstrate the performance in detecting aerosol precursors from intermediate to extremely low volatility. These new insights in gas phase chemistry are further combined with particle phase measurements conducted with a CHARON PTR-MS to emphasize the analytical capabilities of the PTR3.</p>


2015 ◽  
Vol 60 (10) ◽  
pp. 1549-1555 ◽  
Author(s):  
V. T. Kogan ◽  
A. V. Kozlenok ◽  
Yu. V. Chichagov ◽  
A. S. Antonov ◽  
D. S. Lebedev ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document