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超越比尔定律:准理想二元液体混合物

Beyond Beer's Law: Quasi-Ideal Binary Liquid Mixtures.

作者信息

Mayerhöfer Thomas G, Ilchenko Oleksii, Kutsyk Andrii, Popp Jürgen

机构信息

40096Leibniz Institute of Photonic Technology (IPHT), Jena, Germany.

Institute of Physical Chemistry and Abbe Center of Photonics, 9378Friedrich Schiller University, Jena, Germany.

出版信息

Appl Spectrosc. 2022 Jan;76(1):92-104. doi: 10.1177/00037028211056293. Epub 2021 Dec 29.

Abstract

We have recorded attenuated total reflection infrared spectra of binary mixtures in the (quasi-)ideal systems benzene-toluene, benzene-carbon tetrachloride, and benzene-cyclohexane. We used two-dimensional correlation spectroscopy, principal component analysis, and multivariate curve resolution to analyze the data. The 2D correlation proves nonlinearities, also in spectral ranges with no obvious deviations from Beer's approximation. The number of principal components is much higher than two and multivariate curve resolution carried out under the assumption of the presence of a third component, results in spectra which only show bands of the original components. The results negate the presence of third components, since any complex should have lower symmetry than the individual molecules and thus more and/or different infrared-active bands in the spectra. Based on Lorentz-Lorenz theory and literature values of the optical constants, we show that the nonlinearities and additional principal components are consequences of local field effects and the polarization of matter by light. Lorentz-Lorenz theory is, however, not able to explain, for example, the different blueshifts of the strong A band of benzene in the three mixtures. Obviously, infrared spectroscopy is sensitive to the short-range order around the molecules, which changes with content, their shapes, and their anisotropy.

摘要

我们记录了(准)理想体系中二元混合物苯 - 甲苯、苯 - 四氯化碳和苯 - 环己烷的衰减全反射红外光谱。我们使用二维相关光谱、主成分分析和多元曲线分辨来分析数据。二维相关证明了非线性,即使在与比尔近似无明显偏差的光谱范围内也是如此。主成分数量远多于两个,并且在假设存在第三种成分的情况下进行的多元曲线分辨,得到的光谱仅显示原始成分的谱带。结果否定了第三种成分的存在,因为任何复合物的对称性都应低于单个分子,因此光谱中应有更多和/或不同的红外活性谱带。基于洛伦兹 - 洛伦茨理论和光学常数的文献值,我们表明非线性和额外的主成分是局部场效应和光对物质极化的结果。然而,洛伦兹 - 洛伦茨理论无法解释例如三种混合物中苯的强A带不同的蓝移现象。显然,红外光谱对分子周围的短程有序敏感,短程有序会随含量、分子形状及其各向异性而变化。

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