Department of Chemistry and Biochemistry, 0300 Old Main Hill, Utah State University, Logan, UT 84322-0300, USA.
J Chromatogr A. 2010 Mar 26;1217(13):2070-3. doi: 10.1016/j.chroma.2010.01.066. Epub 2010 Jan 29.
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 x 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 microg/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.
建立了一种非抑制型电导检测离子色谱法,用于同时测定大气颗粒物中甲基胺(甲胺、二甲胺、三甲胺)和三甲胺 N-氧化物。采用 3 mM 硝酸/3.5%乙腈(v/v)洗脱液和 Metrosep C2 250(250 mm×4 mm i.d.)分离柱,通过阳离子交换色谱法对分析物进行了很好的分离。还研究了不同色谱参数对分离的影响。甲胺、二甲胺、三甲胺和三甲胺 N-氧化物的检测限分别为 43、46、76 和 72 μg/L。保留时间的相对标准偏差在 0.42%至 1.14%之间,回收率在 78.8%至 88.3%之间。该方法适用于测定高浓度甲基胺和三甲胺 N-氧化物地区的有机氮气溶胶中这些物质是否为重要组成部分。