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Factors affecting quantitative analysis using Raman and resonance Raman spectroscopy.

机译:影响使用拉曼光谱和共振拉曼光谱进行定量分析的因素。

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摘要

This work deals with the quantitative use of Raman and resonance Raman spectroscopies. The types of difficulties that occur when using these spectroscopies are due to the many factors that affect Raman signals. In Chapter I, the general principles of Raman spectroscopy are discussed which include a description of the instrumentation, a comparison to IR spectroscopy, and a brief overview of the factors that affect the Raman signal.; The determination of azo dyes by resonance-enhanced Raman spectroscopy discussed in Chapter II describes the use of an internal standard to correct the Raman signal for fluctuations in excitation radiation power, optical alignment, and absorbance. Also, the use of frequency exclusion in the Fourier domain and data domain truncation to exclude fluorescence from the Raman signal will be discussed. Limits of detection in the parts-per-billion range are reported due to the resonance enhancement effect.; The use of Raman spectroscopy to detect and determine the concentration of minor components in a nominally pure solid is given in Chapter III. Background removal is accomplished through the use of an abscissa correction. Cross-correlation and least-squares fitting are used for quantitation to obtain limits of detection near 0.1%. Simulations are used to demonstrate how an iterative least-squares fitting program can be used to detect previously unknown impurities.; The effect of absorbance of the incident and scattered radiation on the Raman signal is discussed in Chapter IV. A correction set is derived that is based on an earlier work, but now includes a correction for the collection efficiency of the collecting optics and allows the user to apply the actual physical dimension of the path length.; In Chapter V, the use of a KrF excimer laser as the exciting source in a UV resonance Raman system is discussed. The generation of new lines in the UV by stimulated Raman scattering is described. Also, the problem of saturation and techniques to avoid its effects are discussed.
机译:这项工作涉及拉曼光谱和共振拉曼光谱学的定量使用。使用这些光谱仪时遇到的困难类型是由于许多影响拉曼信号的因素所致。在第一章中,讨论了拉曼光谱的一般原理,包括对仪器的描述,与红外光谱的比较以及对影响拉曼信号的因素的简要概述。第二章讨论了通过共振增强拉曼光谱测定偶氮染料的方法,该方法描述了使用内标校正拉曼信号的激发辐射功率,光学取向和吸光度的波动。同样,将讨论在傅立叶域中使用频率排除和数据域截断以从拉曼信号中排除荧光。由于共振增强作用,报告的检测极限在十亿分之一范围内。第三章介绍了使用拉曼光谱法检测和确定名义上纯净固体中次要成分的浓度。通过使用横坐标校正来完成背景去除。互相关和最小二乘拟合用于定量以获得接近0.1%的检测限。仿真被用来证明如何使用迭代最小二乘拟合程序来检测先前未知的杂质。第四章讨论了入射辐射和散射辐射的吸收度对拉曼信号的影响。得出的校正集是基于较早的工作,但现在包括对收集光学器件的收集效率的校正,并允许用户应用路径长度的实际物理尺寸。在第五章中,讨论了在紫外共振拉曼系统中使用KrF准分子激光器作为激发源。描述了通过受激拉曼散射在紫外线中生成新谱线。此外,讨论了饱和问题和避免其影响的技术。

著录项

  • 作者

    Womack, James David.;

  • 作者单位

    The Florida State University.;

  • 授予单位 The Florida State University.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 1988
  • 页码 119 p.
  • 总页数 119
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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