Issue 9, 2012

Assessment of pumped mercury vapour adsorption tubes as passive samplers using a micro-exposure chamber

Abstract

Mercury vapour adsorption tubes manufactured for pumped sampling and analysis have been evaluated for their performance as passive samplers. This has been done by exposing these tubes in a novel micro-exposure chamber. The uptake rates of these tubes have been found to be low (approximately 0.215 ml min−1) as compared to bespoke passive samplers for mercury vapour (typically in excess of 50 ml min−1). The measured uptake rates were shown to vary significantly between tubes and this was attributed to the variability in the air–sorbent interface and the proportion of the cross sectional area removed by the crimp in the quartz tubes used to secure the sorbent material. As a result of this variability the uptake rate of each tube must be determined using the micro-exposure chamber prior to deployment. Results have shown that the uptake rate determined in the micro-exposure chamber is invariant of concentration, and therefore these uptakes rates may be determined at a high mercury vapour concentration for many tubes at once in less than one hour. The uptake rate of the adsorption tubes under these conditions may be determined with a precision of 5%. Measurements made on a limited field trial in indoor and outdoor ambient air have shown that these tubes give results in acceptable agreement with more traditional pumped sampling methods, although longer sampling periods are required in order to reduce the uncertainty of the measurement, which is currently approximately 30%.

Graphical abstract: Assessment of pumped mercury vapour adsorption tubes as passive samplers using a micro-exposure chamber

Article information

Article type
Paper
Submitted
03 Feb 2012
Accepted
18 Jul 2012
First published
18 Jul 2012

J. Environ. Monit., 2012,14, 2456-2463

Assessment of pumped mercury vapour adsorption tubes as passive samplers using a micro-exposure chamber

R. J. C. Brown, M. K. Burdon, A. S. Brown and K. Kim, J. Environ. Monit., 2012, 14, 2456 DOI: 10.1039/C2EM30101F

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