Issue 12, 2009

Chemotrapping-atomic fluorescence spectrometric method as a field method for volatile arsenic in natural gas

Abstract

Volatile arsenic compounds in natural gas, existing in the form of trimethylarsine (TMAs), have been determined using gas cryo-trapping gas chromatography coupled to inductively coupled plasma-mass spectrometry (CT-GC-ICP-MS). The results from a number of different gas wells revealed a huge concentration spread ranging from below the detection limit of 0.2 up to 1800 µg/m3 TMAs (as As) in the gas. Due to the toxicity and corrosive nature of these arsines, they need near real time monitoring via a method that can easily be implemented on site, i.e. during gas exploitation. Here, we introduce a novel method which utilises silver nitrate impregnated silica gel tubes for quantitative chemotrapping of trimethylarsine (TMAs) from a natural gas matrix. Subsequent elution with hot nitric acid followed by online photo-oxidation hydride generation atomic fluorescence spectrometry (HG-AFS) is used for the determination of TMAs gas standards in nitrogen and natural gas samples, respectively. The chemotrapping method was validated using CT-GC-ICP-MS as a reference method. The recovery of arsenic from nitrogen or natural gas matrix ranged from 85 to 113% for a range of 20 to 2000 ng As. Trapping efficiency was >98%, from the methods LOD of 20 ng to 4.8 µg (absolute amount As) with sample sizes of 0.02 and 2 L gas. Method performance was established by comparing the results obtained for eight natural gas samples containing between 1 and 140 µg As/m3 with those achieved by the reference method (CT-GC-ICP-MS).

Graphical abstract: Chemotrapping-atomic fluorescence spectrometric method as a field method for volatile arsenic in natural gas

Article information

Article type
Paper
Submitted
06 Jul 2009
Accepted
28 Aug 2009
First published
25 Sep 2009

J. Environ. Monit., 2009,11, 2222-2230

Chemotrapping-atomic fluorescence spectrometric method as a field method for volatile arsenic in natural gas

M. K. Uroic, E. M. Krupp, C. Johnson and J. Feldmann, J. Environ. Monit., 2009, 11, 2222 DOI: 10.1039/B913322D

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