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UV-Visible Spectrophotometry | Inorganic Chemistry PDF Download

Introduction

The Principle of UV-Visible Spectroscopy is based on the absorption of ultraviolet light or visible light by chemical compounds, which results in the production of distinct spectra. Spectroscopy is based on the interaction between light and matter. When the matter absorbs the light, it undergoes excitation and de-excitation, resulting in the production of a spectrum.
When matter absorbs ultraviolet radiation, the electrons present in it undergo excitation. This causes them to jump from a ground state (an energy state with a relatively small amount of energy associated with it) to an excited state (an energy state with a relatively large amount of energy associated with it). It is important to note that the difference in the energies of the ground state and the excited state of the electron is always equal to the amount of ultraviolet radiation or visible radiation absorbed by it.

UV-Visible Spectroscopy and the Beer-Lambert Law

The statement of the Beer-Lambert law can be written as follows: When a beam of monochromatic light is made incident on a solution that contains a substance that absorbs the monochromatic light, the rate at which the intensity of the beam decreases along the thickness of the solution is directly proportional to the concentration of the absorbing substance in the solution and is also directly proportional to the intensity of the incident monochromatic radiation.

As per the Beer-Lambert law, the greater the number of absorbing molecules (that have the ability to absorb light of a specific wavelength), the greater the extent of absorption of the radiation.
To learn more about the principle of UV-Visible spectroscopy and other related concepts such as infrared spectroscopy, register with BYJU’S and download the mobile application on your smartphone.

The document UV-Visible Spectrophotometry | Inorganic Chemistry is a part of the Chemistry Course Inorganic Chemistry.
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FAQs on UV-Visible Spectrophotometry - Inorganic Chemistry

1. What is UV-Visible spectrophotometry?
Ans. UV-Visible spectrophotometry is a technique used to measure the absorption of ultraviolet (UV) and visible light by a substance. It is commonly used in various fields such as chemistry, biochemistry, and environmental science to determine the concentration of a substance in a solution.
2. How does UV-Visible spectrophotometry work?
Ans. UV-Visible spectrophotometry works by passing a beam of UV or visible light through a sample and measuring the amount of light absorbed by the sample. The instrument used, called a spectrophotometer, consists of a light source, monochromator, sample holder, and detector. The monochromator selects a specific wavelength of light, which is then passed through the sample. The detector measures the intensity of the transmitted light, and the absorption of the sample is calculated based on the difference between the incident and transmitted light.
3. What are the applications of UV-Visible spectrophotometry?
Ans. UV-Visible spectrophotometry has a wide range of applications. It is commonly used in pharmaceutical industries to determine the concentration of drugs in formulations. It is also used in environmental analysis to measure the concentration of pollutants in water and air. In biochemistry, UV-Visible spectrophotometry is used to study the interaction of biomolecules, such as proteins and nucleic acids, with light. Additionally, it is utilized in quality control processes of food and beverage industries to assess the color and purity of products.
4. How is a calibration curve created in UV-Visible spectrophotometry?
Ans. A calibration curve is created in UV-Visible spectrophotometry by measuring the absorbance of a series of standard solutions with known concentrations. The standard solutions should cover a range of concentrations that are expected in the samples being analyzed. The absorbance values obtained from the standards are plotted against their respective concentrations, and a linear regression analysis is performed to establish a calibration curve. This curve is then used to determine the concentration of unknown samples based on their absorbance values.
5. What are the advantages of UV-Visible spectrophotometry?
Ans. UV-Visible spectrophotometry offers several advantages. It is a rapid and non-destructive technique that requires minimal sample preparation. It is also a widely available and cost-effective method. UV-Visible spectrophotometry can be used for both qualitative and quantitative analysis, making it versatile. Additionally, it has a high sensitivity, allowing for the detection of low concentrations of substances.
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