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Rapid Determination of Quinoline and 2-Hydroxyquinoline in Quinoline Biodegradation Process by Tri-Wavelength UV/Vis Spectroscopy

机译:三波长紫外/可见光谱法快速测定喹啉生物降解过程中的喹啉和2-羟基喹啉

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For the present study, a tri-wavelength UV/Vis spectrophotometric method for rapid determination of quinoline (Q) and 2-hydroxyquinoline (HQ) during Q biodegradation was developed. Based on the spectral measurements at 289 nm (the isosbestic point of Q and HQ), 326 and 380 nm, the spectral interference of extracellular polymeric substances (EPS) in the process samples could be minimized, and the amounts of Q and HQ could be simultaneously quantified. Our results indicated that the relative standard deviations in the repeatability tests were 2.7 and 1.7% for Q and HQ, respectively. The method validation was conducted by comparing the data obtained using the present method with those generated from high performance liquid chromatography (HPLC). The same set of samples from Q biodegradation process was used. The relative differences between the two methods were within 10%. In conclusion, the present method is simple, rapid, and suitable for the investigation in Q biodegradation processes.
机译:对于本研究,开发了一种三波长紫外/可见光分光光度法,用于在Q生物降解过程中快速测定喹啉(Q)和2-羟基喹啉(HQ)。根据289 nm(Q和HQ的等渗点),326和380 nm处的光谱测量结果,可以最大程度地减少过程样品中细胞外聚合物质(EPS)的光谱干扰,并且可以将Q和HQ的量同时量化。我们的结果表明,Q和HQ重复性测试中的相对标准偏差分别为2.7和1.7%。通过将使用本方法获得的数据与由高效液相色谱(HPLC)生成的数据进行比较,进行方法验证。使用来自Q生物降解过程的同一组样品。两种方法之间的相对差异在10%以内。综上所述,本方法简便,快速,适用于Q生物降解过程的研究。

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