Differential mobility spectrometry of chlorocarbons with a micro-fabricated drift tube

• Published in: Analyst (London) Vol. 129; no. 4; pp. 297 - 304
• Main Authors: EICEMAN, G. A, KRYLOV, E. V, TADJIKOV, B, EWING, R. G, NAZAROV, E. G, MILLER, R. A
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 01.01.2004
• Subjects: Analytical chemistry; Applied sciences; Chemistry; Chromatographic methods and physical methods associated with chromatography; Environmental Monitoring - instrumentation; Environmental Monitoring - methods; Exact sciences and technology; Gas chromatographic methods; Global environmental pollution; Hydrocarbons, Chlorinated - analysis; Mass Spectrometry - instrumentation; Mass Spectrometry - methods; Pollution; Water Pollutants, Chemical - analysis; Trace analysis; Ion source; In situ; Air; Analyzer; Silica; Chemical ionization; Positive ion; Gas chromatography; Chlorocarbon; Detection limit; Bentonite; Environment; Membrane; Differential spectrometry; Negative ion; Gas phase; Differential method; Adduct; Effluent; Monitoring
• ISSN: 0003-2654; 1364-5528
• DOI: 10.1039/b316326a

Chlorocarbons were ionized through gas phase chemistry at ambient pressure in air and resultant ions were characterized using a micro-fabricated drift tube with differential mobility spectrometry (DMS). Positive and negative product ions were characterized simultaneously in a single drift tube equipped with a 3 mCi (63)Ni ion source at 50 degrees C and drift gas of air with 1 ppm moisture. Scans of compensation voltage for most chlorocarbons produced differential mobility spectra with Cl(-) as the sole product ion and a few chlorocarbons produced adduct ions, M (.-) Cl(-). Detection limits were approximately 20-80 pg for gas chromatography-DMS measurements. Chlorocarbons also yielded positive ions through chemical ionization in air and differential mobility spectra showed peaks with characteristic compensation voltages for each substance. Field dependence of mobility was determined for positive and negative ions of each substance and confirmed characteristic behavior for each ion. A DMS analyzer with a membrane inlet was used to continuously monitor effluent from columns of bentonite or synthetic silica beads to determine breakthrough volumes of individual chlorocarbons. These findings suggest a potential of DMS for monitoring subsurface environments either on site or perhaps in situ.