Title: Determination of Methylamines and Trimethylamine-N-oxide in particulate matter by non-suppressed ion chromatography Authors
|Erupe, Mark -|
|Liberman-Martin, Allegra -|
|Malloy, Quentin -|
|Yonis, Yonis -|
|Cocker, Iii, David -|
|Purvis-Roberts, Kathleen -|
Submitted to: Journal of Chromatography
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: January 19, 2010
Publication Date: March 26, 2010
Repository URL: http://hdl.handle.net/10113/41387
Citation: Erupe, M.E., Liberman-Martin, A., Silva, P.J., Malloy, Q.G., Yonis, Y., Cocker, III, D.R., Purvis-Roberts, K. 2010. Determination of Methylamines and Trimethylamine-N-oxide in particulate matter by non-suppressed ion chromatography. Journal of Chromatography. 1217(13):2070-2073. Interpretive Summary: A method to analyze particulate amines was developed. This method utilizes ion chromatography with non-suppressed conductivity detection. Methylamines (methylamine, dimethylamine, trimethylamine, and trimethylamine-n-oxide) can be rapidly separated with good sensitivity. The method was applied to product analysis of particulates collected from laboratory reactions of agricultural gas-phase amines with atmospheric oxidants. Results of these analyses indicate that little of the particulate mass can be accounted for by cationized and amine-n-oxide compounds. This indicates that the fate of amines emitted into the air may lie along a different chemical pathway than that suggested in the literature.
Technical Abstract: An ion chromatography method with non-suppressed conductivity detection was developed for the simultaneous determination of methylamines (methylamine, dimethylamine, trimethylamine) and trimethylamine-N-oxide in particulate matter air samples. The analytes were well separated by means of cation-exchange chromatography using a 3 mM nitric acid/3.5% acetonitrile (v/v) eluent solution and a Metrosep C 2 250 (250 mm × 4 mm i.d.) separation column. The effects of the different chromatographic parameters on the separation were also investigated. Detection limits of methylamine, dimethylamine, trimethylamine, and trimethylamine-N-oxide were 43, 46, 76 and 72 µg/L, respectively. The relative standard deviations of the retention times were between 0.42% and 1.14% while the recoveries were between 78.8% and 88.3%. The method is suitable for determining if methylamines and trimethylamine-N-oxide are a significant component of organic nitrogen aerosol in areas with high concentration of these species.