The Beer-Lambert law relates the attenuation of light to the material’s properties through which the light travels. Beer-Lambert law is applied to chemical analysis measurements. Let us familiarise ourselves with the law by reading the article.
What is the Beer-Lambert Law?
Beer’s law states the following:
For a given material, the sample path length and concentration of the sample are directly proportional to the absorbance of the light.
Various Names for Beer-Lambert Law
The Beer-Lambert law, known by various names such as the Lambert-Beer law, Beer-Lambert–Bouguer law or the Beer’s law. The Beer-Lambert law is known by so many names because more than one law is involved.
- In 1729, Pierre Bouguer discovered the law.
- Later, in 1760, Johann Heinrich Lambert quoted Bouger’s discovery saying that the absorbance of a sample is directly proportional to the path length of light. Although Lambert dint claim the discovery, he was often credited with it.
- In 1852, August Beer discovered a related law which stated that the absorbance is proportional to the concentration of the sample.
Beer-Lambert Law Equation
Where,
I is the intensity
I0 is the initial intensity
μ is the coefficient of absorption
x is the depth in metrer
Beer-Lambert Law Applications
This law finds applications in various fields such as:
Analytical chemistry
This analysis mainly concentrates on the separation, quantification, and identification of matter by spectrophotometry. There is no involvement of extensive pre-processing of the sample to get the results. For example, bilirubin count in a blood sample can be determined by using a spectrophotometer.
In atmosphere
Solar or stellar radiation in the atmosphere can be described using this law. The law in atmospheric applications has a modified
Where,
a is the aerosols
g is the mixed gases
RS is the Raman scattering effect.
NO2 is Nitrogen dioxide
w is the water vapour absorption
O3 is Ozone
r is Rayleigh scattering
Beer-Lambert Law Limitations
Using this law it becomes easy to study the absorptivity coefficient of the sample when the concentration is low i.e. <10mM but as the concentration becomes high i.e. >10mM there is a deviation as the electrostatic interactions become more.
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