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Spectrophotometer
Spectrophotometer
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A spectrophotometer, also known as a spectrometer, is a scientific instrument that decomposes complex light components into spectral lines. The measurement range generally includes the visible light range of 380-780 nm and the ultraviolet light range of 200-380 nm. Different light sources have their own unique emission spectra, so different luminescent materials can be used as the light source for the instrument. The emission spectrum of tungsten lamp: The spectral light with a wavelength of 380-780nm emitted by the tungsten lamp light source can be refracted by a prism to obtain a continuous spectrum composed of red, orange, yellow, green, blue, indigo, and purple; This chromatography can be used as a light source for visible light spectrophotometers.

A spectrophotometer uses a light source that can generate multiple wavelengths. Through a series of spectroscopic devices, a specific wavelength light source is generated. After the light passes through the tested sample, some of the light is absorbed, and the absorbance value of the sample is calculated, which is then converted into the concentration of the sample. The absorbance value of the sample is directly proportional to its concentration. When monochromatic light radiation passes through a solution of the substance being measured, the amount absorbed by the substance is proportional to the concentration of the substance and the thickness of the liquid layer (optical path length), and the relationship is as follows:

A=-lg(I/I。)=-lgT=kLc

In the formula: A is the absorbance;
I. The intensity of the incident monochromatic light;
I is the transmitted monochromatic light intensity;
T is the transmittance of the substance;
K is the molar absorption coefficient;
L is the optical path length of the analyzed substance, which is the side length of the colorimetric dish;
C is the concentration of the substance;
The selective absorption wavelength and corresponding absorption coefficient of a substance for light are its physical constants. When the absorption coefficient of a certain pure substance is known under certain conditions, the test sample can be prepared into a solution under the same conditions, and its absorbance can be measured. The content of the substance in the test sample can be calculated from the above formula. In the visible light range, except for certain substances that absorb light, many substances themselves do not absorb light but can be measured after adding color reagents or processing to make them color under certain conditions, hence it is also known as colorimetric analysis. Due to the many factors that affect the depth of color during color development, and the frequent use of instruments with poor purity of monochromatic light, standard or control samples should be used simultaneously during measurement.
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