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Updated: May 7, 2026

Quantitative Detection of Trace Explosive Vapors by Programmed Temperature Desorption Gas Chromatography-Electron Capture Detector
Published on: July 25, 2014
A nanoparticle-coated chemiresistor array as a microscale gas chromatograph detector for explosive marker compounds:
1Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA. ezellers@umich.edu.
Abstract:
The effects of flow rate and temperature on the performance of a microscale gas chromatographic (μGC) detector consisting of a chemiresistor (CR) array coated with different thiolate-monolayer-protected gold nanoparticles (MPNs) are described with respect to the analysis of three gas-phase markers of the explosive trinitrotoluene (TNT): 2,4-dinitrotoluene (2,4-DNT), 2,6-dinitrotoluene (2,6-DNT), and 2,3-dimethyl-2,3-dinitrobutane (DMNB). In chamber tests, sensors were stable at 70 °C for several days in air, with <2% sensitivity drift per day and virtually no change in the array response patterns. In tests with a conventional upstream GC column, increasing the array temperature from 55-80 °C (1.2 mL min(-1)) led to similar (i.e., 4-6.6-fold) decreases in sensitivity, increases in the limits of detection (LODs), and increases in (estimated) chromatographic resolution. Increasing the flow rate from 1.1-3.7 mL min(-1) (70 °C) led to ∼1.3-2-fold decreases in sensitivity and LOD for 2,4-DNT and 2,6-DNT, a ∼2-fold net increase in LOD for DMNB (passes through a maximum), and a <2-fold increase in resolution. Results indicate that the rates of desorption of the marker vapors out of the MPN films are important determinants of observed trends. With Si-micromachined focuser/injector and separation column devices placed upstream of a CR array held at 70 °C, a mixture of the two primary markers, 2,4-DNT and DMNB, and four similarly volatile alkane interferents was separated in 1.5 min at 3 mL min(-1).
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