Beer-Lambert Law

From The School of Biomedical Sciences Wiki
Revision as of 19:04, 27 July 2010 by Nnjm2 (Talk | contribs)
Jump to: navigation, search

The amount of light passing through a substance is called transmittance, T or percent transmittance (%T), and is defined by the following equation:

T = I/Io, %T = I/Io x 100

Where Io is the intensity of the incident light and I is the intensity of the absorbed light. The amount of light of a specified wavelength absorbed by the substance depends on the length of the light path through the substance. The negative logarithm of the transmittance, the absorbance (A), is directly proportional to the amount of light absorbed and to the length of the light path and is described by the Lambert law, which is expressed as follows:

-log T = -log I/Io = A = K1b

Here b is the length of the medium, usually a solution in a cell, and K1 is a constant.


A comparison of the scales for percent transmittance and absorbance may be used to convert percent transmittance into absorbance.

The negative logarithm of the transmittance (absorbance) is also directly proportional to the concentration of the absorbing substance c and is expressed by Beer law as follows:

-log I/Io = -log T = A = k2c

Combining the two laws as the Lambert-Beer law gives the equation:

-logI/Io = -log T = A = ε.c.l

Where ε is a constant called the extinction coefficient incorporating K1 and k2 (also called molar absorbance). The extinction coefficient is dependent on the wavelength of the light passing through the substance and on the chemical nature of the substance; l is the path length (cm) and c is the concentration of the substance.


To use the Lambert-Beer law to determine the concentration of a substance, light of a specified wavelength must be chosen. A spectrum of the pure substance, that is, the absorbance of the substance as a function of the wavelength of the incident light is necessary. This is most easily obtained using a recording spectrophotometer with a double beam, which is able to scan the wavelengths and thus identify the wavelength(s) of maximum absorbance.


Quantitation of an unknown concentration of a substance in a given biological fluid is nearly always carried out by construction of a standard curve. In spectrophotometry, like many other analytical techniques, the instrument response (absorbance) is plotted against known concentrations of standard solutions. A plot of the absorbance versus concentration should give a linear curve whose slope is the extinction coefficient when the cell length is 1.00 cm.

The measurement of the amount of light absorbed may be either as percent transmittance (%T) or as absorbance (A). Absorbance is used more often than percent transmittance because this variable is linear with the concentration of the absorbing substance, whereas percent transmittance is exponential. The measurement of concentration is best achieved between 0.05 and 0.3 absorbance or between 90% and 50% transmittance. The errors in measuring absorbance values of 1 or 2 could be very large. The concentration of an unknown amount of a substance can be determined from a plot of the absorbance (A) versus concentration (standard curve).  The readings are taken by placing the sample in a cuvette and taking the measurements, at the correct wavelength, using a spectrophotometer.

To plot a standard curve a linear curve (straight line) is drawn to best fit the scatter of data points as shown below:

A very simple standard curve

When drawing a curve it is important that you:

  1. Use a sharp pencil to draw all lines and plot points
  2. If the line is supposed to be a straight line then use a ruler!
  3. Give the graph a title and label the axis (do not forget the units!)
  4. Use appropriate scales on the axis and provide sufficient value markers.
Personal tools