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A helium microwave plasma torch (MPT) was coupled to time-of-flight mass spectrometry (TOFMS) for the detection of halogenated hydrocarbons separated by capillary gas chromatography (GC). The GC-MPT-TOFMS system offered excellent stability over the course of the experiments and avoided mass spectral peak distortions caused by spectral skew. In the initial studies, empirical formulas based on the halogen-to-carbon ratio were predicted utilizing a flow cell apparatus. The MPT proved to be very robust and could handle large amounts of organic vapor. Results from this study indicate that, for both aromatic and aliphatic halogenated hydrocarbons, the ratios of carbon to chlorine signals correlate well (r = 0.994) with the ones expected from their chemical composition. This study was later extended to include chromatographic separation. For a series of homologous aliphatic halogenated hydrocarbons, a correlation coefficient of 0.999 was obtained for both peak heights and peak areas obtained from a single chromatogram. A novel Nichrome wire-heated transfer line was developed to ensure that the capillary column was heated efficiently from the GC oven to the MPT and then through the length of the MPT up to the microwave plasma itself. No appreciable peak broadening and no detectable memory effects were associated with the heated transfer line. The GC-MPT-TOFMS system offered equal sensitivity for I, Br, and Cl. Absolute detection limits for the halogenated hydrocarbons ranged from 160 to 330 fg, constituting an improvement by a factor of 5-35 over earlier results obtained with MIPs supported in a TM010 cavity and combined with quadrupole-based mass spectrometry. In addition, the effect of molecular gases on the MPT performance was investigated. Up to about 1% (v/v) of either oxygen or hydrogen in the central channel helium flow attenuated the signal levels for both carbon and chlorine, with the larger loss seen in the chlorine signal.

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