12.7
紫外和可见光的吸光度使用紫外-可见分光光度计测量。包括发射紫外线辐射的氘灯和产生可见光辐射的钨灯用作紫外-可见分光光度计的光源。单色仪或棱镜被用作衍射光栅,即将入射光分解成不同的波长。狭缝系统用于将所需波长聚焦在样品池上。紫外可见分光光度计的样品必须处于液相。因此,固体有机化合物应在分析前溶解在合适…
紫外-可见分光光度计由光源(如用于紫外区的氘灯和用于可见区的钨灯)、单色器、样品池、 以及检测器组成。
可见光光谱法使用玻璃或塑料样品池,而紫外光谱法使用石英样品池。
棱镜将光束分解为其组成波长,通过狭缝和滤光片系统将所需波长聚焦到样品池上。
光电二极管检测器测量透过样品池的光强度。
在单光束仪器中,位于光源和样品之间的单色器允许一次分析一个波长。
或者,在双光束仪器中,单色器配备有分光器和反射镜,可将光束分成两束。样品光束穿过样品池,而参比光束则穿过参比样品。
通过减去两个光谱,可从获取的原始光谱中去除参比样品的贡献。
View the full transcript and gain access to JoVE Core videos
Q1: What are the main components of a UV-Vis spectrometer?
A UV-Vis spectrometer contains a light source (deuterium lamp for UV, tungsten lamp for visible light), a monochromator to split light into component wavelengths, a sample holder or cuvette, and a detector such as a photodiode. These components work together to measure how much light a sample absorbs at specific wavelengths during molecular electronic transitions.
Q2: Why are different cuvette materials used for UV versus visible spectroscopy?
Glass and plastic cuvettes are used for visible spectroscopy because they effectively transmit visible light with spectral cutoffs around 350 nm. UV spectroscopy requires quartz cuvettes with lower cutoffs around 200 nm to allow transmission of UV radiation. This material selection ensures accurate absorbance measurements across different wavelength regions.
Q3: How does a monochromator function in UV-Vis spectrometers?
A monochromator uses a prism or diffraction grating to split incoming light into its component wavelengths. A system of slits and filters then focuses the desired wavelength onto the sample cell. This allows the spectrometer to analyze one specific wavelength at a time, enabling precise measurement of light absorption.
Q4: What is the difference between single-beam and double-beam instruments?
In single-beam instruments, all light passes through the sample cell sequentially. Double-beam instruments split light into two beams using mirrors and splitters: one passes through the sample, the other through a reference. The spectra are subtracted to remove reference contributions, providing more accurate measurements by compensating for instrumental variations.
Q5: Why is solvent selection critical in UV-Vis spectroscopy?
Solvents absorb light and affect spectral fine structure. Nonpolar solvents like hexane do not form hydrogen bonds with solutes, preserving fine structure similar to gaseous phase spectra. Polar solvents like water form hydrogen bonds, eliminating fine structure. Choosing an appropriate solvent ensures accurate absorbance measurements and reveals desired spectral details.
Q6: What role does the detector play in measuring light intensity?
Detectors such as photodiodes, photomultiplier tubes, and photodiode arrays measure the intensity of light passing through the sample cell, referred to as I. Modern diode-array spectrophotometers use photodiode detectors to record the entire spectrum simultaneously, enabling rapid and comprehensive analysis of sample absorbance across multiple wavelengths.
Q7: Why must samples be in liquid form for UV-Vis spectrophotometry?
UV-Vis spectrophotometers require samples in liquid phase for accurate analysis. Solid organic compounds must be dissolved in a suitable solvent prior to measurement. This ensures uniform light interaction with the sample and allows the spectrometer to measure absorbance reliably. Understanding interaction of EM radiation with matter spectroscopy principles guides this requirement.