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Solid-state surface luminescence of polycyclic aromatic hydrocarbons adsorbed on cellulose diacetate matrices

机译:在纤维素二饱和基质上吸附的多环芳烃的固态表面发光

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摘要

The spectral-kinetic characteristics of luminescence of 17 polycyclic aromatic hydrocarbons (PAH) sorbed from a "water-organic solvent" medium on cellulose diacetate (CDA) matrices were studied. A significant increase in the fluorescence signal on the CDA matrix was observed for 13 PAHs in comparison with aqueous solutions. The highest detection sensitivity was found for pyrene, benzo(a)pyrene, and benzo(k)fluoranthene. The fluorescence spectra of two PAH indicator pairs (anthracene-phenanthrene and pyrene-fluoranthene) used to control toxicant emission sources were studied with the simultaneous presence of isomers in the analyte, depending on the excitation wavelength. For both isomer pairs, it has been found that the spectra of their solid-state luminescence overlap insignificantly, the characteristic peaks do not coincide and do not overlap, the sensitivities of detection are close to each other, which makes it possible to consider this technique as promising to control PAH contamination sources.
机译:研究了来自“水 - 有机溶剂”培养基(CDA)基质的17个多环芳烃(PAH)吸附的17个多环芳烃(PAH)的光谱 - 动力学特征。与水溶液相比,观察到CDA基质上的荧光信号的显着增加。发现芘,苯并(A)芘和苯并(k)氟化物的最高检测灵敏度。使用用于控制毒物发射源的两种PAH指示器对(蒽 - 菲和芘 - 氟)的荧光光谱在分析物中同时存在于分析物中的异构体,取决于激发波长。对于两对异构体对,已经发现它们的固态发光的光谱重叠,特征峰不会重合并且不重叠,检测的敏感性彼此接近,这使得可以考虑这种技术作为对控制PAH污染来源的承诺。

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