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Fluorescence Spectroscopy of Complex Aromatic Mixtures

机译:复杂芳香混合物的荧光光谱

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The contribution of two- to seven-ring polycyclic aromatic hydrocarbons (PAH) and of larger aromatic structures contained in complex PAH-laden mixtures collected in flames was evaluated by fluorescence spectroscopy. A composition procedure of the fluorescence spectra of individual PAHs, analyzed by gas chromatography/mass spectrometry (GC/MS) was applied for the evaluation of their contribution to the fluorescence spectra of PAH-laden mixtures. In this way, it was possible to put in evidence the contribution to the total fluorescence spectrum of high molecular weight aromatic species present in the PAH-laden mixtures and not detectable by GC/MS. Qualitative and quantitative interpretation of synchronous and conventional fluorescence spectra of PAH-laden mixtures formed in combustion processes was proposed. The composition procedure was showed to be reliable in the UV-visible region for samples dissolved in cyclohexane solutions, but failed in the UV region when the solvent contained heavy atoms, as in the case of dichloromethane. However, the heavy-atom solvent effect was not sufficient to explain the depression of the UV fluorescence signal. Energy transfer interaction between fluorene and other fluorescing PAHs was suggested to be also responsible for this effect on the basis of fluorescence studies performed on single PAHs and their mixtures in cyclohexane, methanol, and dichloromethane.
机译:通过荧光光谱法评估了火焰中收集的多环芳烃负载的复杂混合物中所含的二至七环多环芳烃(PAH)和较大的芳族结构的贡献。通过气相色谱/质谱法(GC / MS)分析了单个多环芳烃的荧光光谱的组成过程,以评估它们对含多环芳烃混合物的荧光光谱的贡献。以这种方式,有可能证明存在于PAH负载混合物中的高分子量芳族物质对总荧光光谱的贡献,而GC / MS无法检测到。提出了定性和定量解释燃烧过程中形成的多环芳烃混合物的同步和常规荧光光谱的方法。对于在环己烷溶液中溶解的样品,该组合物程序在UV可见区域是可靠的,但是当溶剂包含重原子时,在二氯甲烷中,该程序在UV区域中无效。但是,重原子溶剂效应不足以解释UV荧光信号的下降。根据对单个多环芳烃及其在环己烷,甲醇和二氯甲烷中的混合物进行的荧光研究,建议芴与其他荧光多环芳烃之间的能量转移相互作用也是造成这种效应的原因。

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