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UV cavity enhanced absorption spectroscopy of the hydroxyl radical
Authors:G?Hancock  Email author" target="_blank">VL?KasyutichEmail author
Institution:(1) Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, UK
Abstract:We present the application of a continuous-wave ultra-violet tuneable light source for detection of the hydroxyl radical (OH) using cavity-enhanced absorption spectroscopy of the Q11(2) and Q21(2) absorption lines in the A2Sgr+(vprime=0)larrKHgr2Pgr3/2(vprimeprime=0) band at ca. 308 nm. A tuneable infra-red diode laser operating at 835 nm and either an Ar+ laser or a single frequency continuous-wave intracavity frequency-doubled diode laser, both operating at ca. 488 nm, were used to produce 0.1–0.5 mgrW of tuneable radiation at ca. 308 nm by sum frequency generation in a betaBaB2O4 crystal. Cavity enhanced absorption spectroscopy was used to detect OH generated by UV photolysis of water vapour in argon, nitrogen, neon and helium at atmospheric pressure. A noise-equivalent (1sgr) absorption sensitivity of 2.1×10-7 cm-1Hz-1/2 measured over 128 scans in a time of 1.16 s was demonstrated with mirrors of reflectivity 0.9963 in a cavity of length 58.5 cm for a sim2 cm-1 scanning range at a UV power of sim0.5 mgrW. An OH detection limit (1sgr) of 3.84×109 moleculethinspcm-3 was estimated in argon at atmospheric pressure. OH collisional broadening in humidified N2, Ar, Ne and He was determined at atmospheric pressure . PACS 39.30.+w; 42.55.Px; 42.62.Fi; 42.68.Ca
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