化学
烟气
多溴联苯醚
多氯代二苯并呋喃
气相色谱法
色谱法
甲苯
检出限
分馏
环境化学
多氯二苯并对二恶英
同族
火焰离子化检测器
分析化学(期刊)
污染物
有机化学
作者
Xu PengJun,Tao Bu,Nan Li,Sheng Zheng,Huijing Zhao,Saijun Fan,Zhou Zhi-Guang,Ren Yue,Qi Li,Jiping Chen
摘要
A method for simultaneous determination of pcdds, dl-pcbs, bfrs and pbdd/fs in flue gas from stationary source was developed. the sample was extracted by soxhlet apparatus with toluene, and followed by purification through sulfuric acid partition and multi. layer silica gel column separation. the target compounds were then all separated by passing through the active carbon. dispersed silica gel column and reversal eluting. gas chromatography coupled with a thermostable capillary column (short length, thin stationary phase film) was operated at pulse injection mode. high resolution mass spectrometry set at low-electron-energy ionization was used for quantification. the high- and low-brominated compounds were determined simultaneously. the detection limits of this method were 0. 081 - 1. 2 pg for pcdd/fs, 0. 100 - 32 pg for dl-pcbs, 0. 14 - 12 pg for pbdes, 0. 26 - 16 pg for new bfrs, 0. 44 - 3. 6 pg for tetra- to hepta-bdd/fs and 8. 2 - 12 pg for obdd/f. recoveries (rsds) in spiked flue gas samples were 88% - 115% (2. 9% - 6. 1%) for pcdd/fs, 84% - 118% (3. 2% - 10%) for dl-pcbs, 71% - 135% (2. 1% - 18%) for pbdes, 71% - 114% (2. 9% - 7. 4%) for new bfrs, 83% - 127% (5. 2% - 10%) for tetra- to hepta. bdd/fs and 52% - 149% (23% - 24%) for obdd/f. all quality control data fell within the acceptable range specified in analysis standards for flue gas.
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