Back to Search Start Over

Isobutane Made Practical as a Reagent Gas for Chemical Ionization Mass Spectrometry.

Authors :
Newsome GA
Steinkamp FL
Giordano BC
Source :
Journal of the American Society for Mass Spectrometry [J Am Soc Mass Spectrom] 2016 Nov; Vol. 27 (11), pp. 1789-1795. Date of Electronic Publication: 2016 Aug 15.
Publication Year :
2016

Abstract

As a reagent gas for positive- and negative-mode chemical ionization mass spectrometry (CI-MS), isobutane (i-C <subscript>4</subscript> H <subscript>10</subscript> ) produces superior analyte signal abundance to methane. Isobutane has never been widely adopted for CI-MS because it fouls the ion source more rapidly and produces positive CI spectra that are more strongly dependent on reagent gas pressure compared with methane. Isobutane was diluted to various concentrations in argon for use as a reagent gas with an unmodified commercial gas chromatograph-mass spectrometer. Analyte spectra were directly compared using methane, isobutane, and isobutane/argon mixtures. A mixture of 10% i-C <subscript>4</subscript> H <subscript>10</subscript> in argon produced twice the positive-mode analyte signal of methane, equal to pure isobutane, and reduced spectral dependence on reagent gas pressure. Electron capture negative chemical ionization using 1% i-C <subscript>4</subscript> H <subscript>10</subscript> in argon tripled analyte signal compared with methane and was reproducible, unlike pure isobutane. The operative lifetime of the ion source using isobutane/argon mixtures was extended exponentially compared with pure isobutane, producing stable and reproducible CI signal throughout. By diluting the reagent gas in an inert buffer gas, isobutane CI-MS experiments were made as practical to use as methane CI-MS experiments but with superior analytical performance. Graphical Abstract ᅟ.

Details

Language :
English
ISSN :
1879-1123
Volume :
27
Issue :
11
Database :
MEDLINE
Journal :
Journal of the American Society for Mass Spectrometry
Publication Type :
Academic Journal
Accession number :
27527096
Full Text :
https://doi.org/10.1007/s13361-016-1463-4