Evaluation of a New Reagent-Ion Source and Focusing Ion-Molecule Reactor for Use in Proton-Transfer-Reaction Mass Spectrometry

Jordan Krechmer, Felipe Lopez-Hilfiker, Abigail Koss, Manuel Hutterli, Carsten Stoermer, Benjamin Deming, Joel Kimmel, Carsten Warneke, Rupert Holzinger, John Jayne, Douglas Worsnop, Katrin Fuhrer, Marc Gonin, Joost De Gouw*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We evaluate the performance of a new chemical ionization source called Vocus, consisting of a discharge reagent-ion source and focusing ion-molecule reactor (FIMR) for use in proton-transfer-reaction time-of-flight mass spectrometry (PTR-TOF) measurements of volatile organic compounds (VOCs) in air. The reagent ion source uses a low-pressure discharge. The FIMR consists of a glass tube with a resistive coating, mounted inside a radio frequency (RF) quadrupole. The axial electric field is used to enhance ion collision energies and limit cluster ion formation. The RF field focuses ions to the central axis of the reactor and improves the detection efficiency of product ions. Ion trajectory calculations demonstrate the mass-dependent focusing of ions and enhancement of the ion collision energy by the RF field, in particular for the lighter ions. Product ion signals are increased by a factor of 10 when the RF field is applied (5000-18000 cps ppbv-1), improving measurement precision and detection limits while operating at very similar reaction conditions as traditional PTR instruments. Because of the high water mixing ratio in the FIMR, we observe no dependence of the sensitivity on ambient sample humidity. In this work, the Vocus is interfaced to a TOF mass analyzer with a mass resolving power up to 12000, which allows clear separation of isobaric ions, observed at nearly every nominal mass when measuring ambient air. Measurement response times are determined for a range of ketones with saturation vapor concentrations down to 5 × 104 μg m-3 and compare favorably with previously published results for a PTR-MS instrument.

Original languageEnglish
Pages (from-to)12011-12018
Number of pages8
JournalAnalytical Chemistry
Volume90
Issue number20
DOIs
Publication statusPublished - 16 Oct 2018

Funding

The Authors are grateful to Paul Ziemann for the response time experiments performed in his laboratory and to Demetrios Pagonis and Jose-Luis Jimenez for useful discussions about the method. This manuscript is part of a project that has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement no. 654109.

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