کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4439566 | 1311025 | 2011 | 5 صفحه PDF | دانلود رایگان |
In this work, the dynamic range of gas chromatography (GC) combined with a thermal desorber (TD) was investigated through a series of calibration experiments. To this end, standard gases of reduced sulfur compounds (RSC: H2S, CH3SH, DMS, CS2 and DMDS) covering a relatively wide concentration range (2–100 nmol mol−1 (or ppb)) were analyzed by regulating sample loading range from 40 to 1200 mL (3.3–4900 pmol). It shows that the upper limits of GC–TD quantification are far higher than those of GC alone, although the cold trap unit in a TD suffers from breakthrough after a dose of RSC (e.g., 500 (DMDS) to 1600 pmol (H2S)). Its quantification uncertainties tend to grow systematically with decreases in standard concentrations and sample loading volume, especially with H2S. According to this study, the use of TD generally reduces the absolute detectability of GC by about one order of magnitude. Such reduction caused by TD application can be compensated efficiently with similar magnitude through the magnification of sample supply. Moreover, the TD system allows to increase sample volume (up to 3 orders of magnitude or above), it can ultimately help extend the practical range of RSC qualification in a fairly reliable manner.
► The dynamic range of GC–TD is investigated for gaseous reduced sulfur compounds.
► The method is tested by using their standard gases with a highly diverse range.
► The results allow to discriminate the TD-based detection property of each RSC.
► The use of TD can alter their quantification range relative to direct injection.
Journal: Atmospheric Environment - Volume 45, Issue 20, June 2011, Pages 3366–3370