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SELECTIVE DETECTION OF PHENOL IMPURITIES IN WATER

机译:水中苯酚杂质的选择性检测

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CO2 laser ablation of the frozen water matrix, followed by resonance-enhanced multiphoton ionization technique coupled with reflection time-of-flight mass spectrometry, has been used for analysis of water polluted with phenol molecules. The linear dependence of the ion signal on the phenol concentration ranged from 0.1 mu g L(-1) to 10 mg L(-1) under identical experimental conditions. A detection limit of 0.1 pg L(-1) was achieved for phenol. It was shown that the overall sensitivity of 1 ng L(-1) (1 ppt) can be attained with the present experimental setup, The velocity distribution of the ablated phenol species was approximated by a Maxwell-like function at a temperature of 150 K, Contours of the S-0-S-1 (36352 cm(-1)) electronic transition of both thermally evaporated and CO2 laser-ablated phenol molecules have been obtained, Their comparison demonstrated that the rotational temperature, in the case of laser ablation of frozen water matrix, appeared to be lower than 140 K. It is believed that the cooling effect is due to jetlike expansion of water molecules into vacuum. A potential benefit of this phenomenon for spectroscopic and mass spectrometric studies of complex nonvolatile and thermally labile molecules is discussed.
机译:已使用CO2激光烧蚀冷冻水基质,然后采用共振增强多光子电离技术和反射飞行时间质谱技术,来分析被苯酚分子污染的水。在相同的实验条件下,离子信号对苯酚浓度的线性依赖性为0.1μg L(-1)至10 mg L(-1)。苯酚的检出限为0.1 pg L(-1)。结果表明,使用本实验装置可以达到1 ng L(-1)(1 ppt)的总体灵敏度。在150 K的温度下,通过麦克斯韦式函数估算烧蚀酚的速度分布。 ,获得了热蒸发的和CO2激光烧蚀的酚分子的S-0-S-1(36352 cm(-1))电子跃迁的轮廓,它们的比较表明,在激光烧蚀的情况下旋转温度冻结的水基质的α2似乎低于140K。据认为,冷却效果是由于水分子喷射状膨胀成真空所致。讨论了这种现象对复杂的非易失性和热不稳定分子的光谱学和质谱研究的潜在好处。

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