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Determination of arsenic and arsenic compounds in natural gas samples
Author(s) -
Irgolic Kurt J,
Llger Drew,
Zingaro Ralph A,
Spall Dale,
Puri B K
Publication year - 1991
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.590050209
Subject(s) - arsenic , chemistry , arsenate , hydride , nitric acid , gas chromatography , environmental chemistry , natural gas , sulfuric acid , gas chromatography–mass spectrometry , mass spectrometry , chromatography , inorganic chemistry , organic chemistry , metal
Organic arsenic compounds (trialkylarsines) present in natural gas were extracted by 10 cm 3 of concentrated nitric acid from 1 dm 3 of gas kept at ambient pressure and temperature. The flask containing the gas and the acid was shaken for 1 h on a platform shaker set at the highest speed. The resulting solution was mixed with concentrated sulfuric acid and heated to convert all arsenic compounds to arsenate. Total arsenic was determined in the mineralized solutions by hydride generation. The arsenic concentrations in natural gas samples from a number of wells in several gas fields were in the range 0.01–63 μ As dm −3 . Replicate determinations of arsenic in a gas sample with an arsenic concentration of 5.9 μ dm −3 had a relative standard deviation of 1.7%. Because of the high blank values, the lowest arsenic concentration that could be reliably determined was 5 ng As dm −3 gas. Analysis of nonmineralized extracts by hydride generation identified trimethylarsine as the major arsenic compound in natural gas. Low‐temperature gas chromatography‐mass spectrometry showed more directly than the hydride generation technique, that trimethylarsine accounts for 55–80% of the total arsenic in several gas samples. Dimethylethylarsine, methyldiethylarsine, and triethylarsine were also identified, in concentrations decreasing with increasing molecular mass of the arsines.