Discrete Free-Surface Millifluidics for Rapid Capture and Analysis of

Jan 6, 2014 - Interdepartmental Program in Biomolecular Science and Engineering, University of California, Santa Barbara, California 93106,. United St...
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Discrete Free-Surface Millifluidics for Rapid Capture and Analysis of Airborne Molecules Using Surface-Enhanced Raman Spectroscopy Brian D. Piorek,*,†,‡ Chrysafis Andreou,†,§ Martin Moskovits,†,∥ and Carl D. Meinhart†,‡ †

Institute for Collaborative Biotechnologies, University of California, Santa Barbara, California 93106, United States Department of Mechanical Engineering, University of California, Santa Barbara, California 93106, United States § Interdepartmental Program in Biomolecular Science and Engineering, University of California, Santa Barbara, California 93106, United States ∥ Department of Chemistry, University of California Santa Barbara, Santa Barbara, California 93106, United States ‡

ABSTRACT: A lithography-free, low-cost, free-surface millifluidic device is reported using discrete liquid interfaces for capturing and detecting gas-phase analyte molecules at low partial pressures out of a gas flow of time-varying composition. The architecture, based on segmented flow, consists of alternating regions of liquid and gas wherein the liquid regions contain surface-enhanced Raman spectroscopy (SERS)-active silver nanoparticles, while the gas regions contain trace quantities of vapor-phase analyte, thereby controlling and optimizing transport and mixing of the gas-phase analyte with the liquid phase. Once absorbed in the liquid phase, the entrained analyte molecules induce aggregation of the aqueous silver nanoparticles. The resulting aggregates consisting of nanoparticles and adsorbed analyte molecules produce intense SERS spectra that reliably identify the absorbed analyte in real time. The approach can be used to determine the time-variable trace chemical composition of a gas stream with applications in, for example, environmental monitoring and online industrial process monitoring, or as a SERS-based detector following gas chromatographic separation. The operation of the system is demonstrated using 4-aminobenzenethiol vapor at 750 ppb, and the detection response time is