Beer–Lambert law

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An example of Beer–Lambert law: green laser light in a solution of Rhodamine 6B. The beam radiant power becomes weaker as it passes through solution

The Beer–Lambert law, also known as Beer's law, the Lambert–Beer law, or the Beer–Lambert–Bouguer law relates the attenuation of light to the properties of the material through which the light is traveling. The law is commonly applied to chemical analysis measurements and used in understanding attenuation in physical optics, for photons, neutrons or rarefied gases. In mathematical physics, this law arises as a solution of the BGK equation.


The law was discovered by Pierre Bouguer before 1729.[1] It is often attributed to Johann Heinrich Lambert, who cited Bouguer's Essai d'optique sur la gradation de la lumière (Claude Jombert, Paris, 1729)—and even quoted from it—in his Photometria in 1760.[2] Lambert's law stated that absorbance of a material sample is directly proportional to its thickness (path length). Much later, August Beer discovered another attenuation relation in 1852. Beer's law stated that absorbance is proportional to the concentrations of the attenuating species in the material sample in 1852.[3] The modern derivation of the Beer–Lambert law combines the two laws and correlates the absorbance to both the concentrations of the attenuating species as well as the thickness of the material sample.[4]

Beer–Lambert law

By definition, the transmittance of material sample is related to its optical depth τ and to its absorbance A as

T = \frac{\Phi_\mathrm{e}^\mathrm{t}}{\Phi_\mathrm{e}^\mathrm{i}} = e^{-\tau} = 10^{-A},


  • Φet is the radiant flux transmitted by that material sample;
  • Φei is the radiant flux received by that material sample.

The Beer–Lambert law states that, for N attenuating species in the material sample,

T = e^{-\sum_{i = 1}^N \sigma_i \int_0^\ell n_i(z)\mathrm{d}z} = 10^{-\sum_{i = 1}^N \varepsilon_i \int_0^\ell c_i(z)\mathrm{d}z},

or equivalently that

\tau = \sum_{i = 1}^N \tau_i = \sum_{i = 1}^N \sigma_i \int_0^\ell n_i(z)\,\mathrm{d}z,
A = \sum_{i = 1}^N A_i = \sum_{i = 1}^N \varepsilon_i \int_0^\ell c_i(z)\,\mathrm{d}z,


Attenuation cross section and molar attenuation coefficient are related by

\varepsilon_i = \frac{\mathrm{N_A}}{\ln{10}}\,\sigma_i,

and number density and amount concentration by

c_i = \frac{n_i}{\mathrm{N_A}},

where NA is the Avogadro constant.

In case of uniform attenuation, these relations become[5]

T = e^{-\sum_{i = 1}^N \sigma_i n_i\ell} = 10^{-\sum_{i = 1}^N \varepsilon_i c_i\ell},

or equivalently

\tau = \sum_{i = 1}^N \sigma_i n_i\ell,
A = \sum_{i = 1}^N \varepsilon_i c_i\ell.

Cases of non-uniform attenuation occur in atmospheric science applications and radiation shielding theory for instance.

The law tends to break down at very high concentrations, especially if the material is highly scattering. If the radiation is especially intense, nonlinear optical processes can also cause variances. The main reason, however, is the following. At high concentrations, the molecules are closer to each other and begin to interact with each other. This interaction will change several properties of the molecule, and thus will change the attenuation.

Expression with attenuation coefficient

The Beer–Lambert law can be expressed in terms of attenuation coefficient, but in this case is better called Lambert's law since amount concentration, from Beer's law, is hidden inside the attenuation coefficient. The (Napierian) attenuation coefficient μ and the decadic attenuation coefficient μ10 = μ/ln 10 of a material sample are related to its number densities and amount concentrations as

\mu(z) = \sum_{i = 1}^N \mu_i(z) = \sum_{i = 1}^N \sigma_i n_i(z),
\mu_{10}(z) = \sum_{i = 1}^N \mu_{10,i}(z) = \sum_{i = 1}^N \varepsilon_i c_i(z)

respectively, by definition of attenuation cross section and molar attenuation coefficient. Then the Beer–Lambert law becomes

T = e^{-\int_0^\ell \mu(z)\mathrm{d}z} = 10^{-\int_0^\ell \mu_{10}(z)\mathrm{d}z},


\tau = \int_0^\ell \mu(z)\,\mathrm{d}z,
A = \int_0^\ell \mu_{10}(z)\,\mathrm{d}z.

In case of uniform attenuation, these relations become

T = e^{-\mu\ell} = 10^{-\mu_{10}\ell},

or equivalently

\tau = \mu\ell,
A = \mu_{10}\ell.


Assume that a beam of light enters a material sample. Define z as an axis parallel to the direction of the beam. Divide the material sample into thin slices, perpendicular to the beam of light, with thickness dz sufficiently small that one particle in a slice cannot obscure another particle in the same slice when viewed along the z direction. The radiant flux of the light that emerges from a slice is reduced, compared to that of the light that entered, by e(z) = −μ(ze(z) dz, where μ is the (Napierian) attenuation coefficient, which yields the following first-order linear ODE:

\frac{\mathrm{d}\Phi_\mathrm{e}}{\mathrm{d}z}(z) = -\mu(z)\Phi_\mathrm{e}(z).

The attenuation is caused by the photons that did not make it to the other side of the slice because of scattering or absorption. The solution to this differential equation is obtained by multiplying the integrating factor

e^{\int_0^z \mu(z')\mathrm{d}z'}

throughout to obtain

\frac{\mathrm{d}\Phi_\mathrm{e}}{\mathrm{d}z}(z)\,e^{\int_0^z \mu(z')\mathrm{d}z'} + \mu(z)\Phi_\mathrm{e}(z)\,e^{\int_0^z \mu(z')\mathrm{d}z'} = 0,

which simplifies due to the product rule (applied backwards) to

\frac{\mathrm{d}}{\mathrm{d}z}\bigl(\Phi_\mathrm{e}(z)\,e^{\int_0^z \mu(z')\mathrm{d}z'}\bigr) = 0.

Integrating both sides and solving for Φe for a material of real thickness , with the incident radiant flux upon the slice Φei = Φe(0) and the transmitted radiant flux Φet = Φe( ) gives

\Phi_\mathrm{e}^\mathrm{t} = \Phi_\mathrm{e}^\mathrm{i}\,e^{-\int_0^\ell \mu(z)\mathrm{d}z},

and finally

T = \frac{\Phi_\mathrm{e}^\mathrm{t}}{\Phi_\mathrm{e}^\mathrm{i}} = e^{-\int_0^\ell \mu(z)\mathrm{d}z}.

Since the decadic attenuation coefficient μ10 is related to the (Napierian) attenuation coefficient by μ10 = μ/ln 10, one also have

T = e^{-\int_0^\ell \ln{10}\,\mu_{10}(z)\mathrm{d}z} = \bigl(e^{-\int_0^\ell \mu_{10}(z)\mathrm{d}z}\bigr)^{\ln{10}} = 10^{-\int_0^\ell \mu_{10}(z)\mathrm{d}z}.

To describe the attenuation coefficient in a way independent of the number densities ni of the N attenuating species of the material sample, one introduces the attenuation cross section σi = μi(z)/ni(z). σi has the dimension of an area; it expresses the likelihood of interaction between the particles of the beam and the particles of the specie i in the material sample:

T = e^{-\sum_{i = 1}^N \sigma_i \int_0^\ell n_i(z)\mathrm{d}z}.

One can also use the molar attenuation coefficients εi = (NA/ln 10)σi, where NA is the Avogadro constant, to describe the attenuation coefficient in a way independent of the amount concentrations ci(z) = ni(z)/NA of the attenuating species of the material sample:

T = e^{-\sum_{i = 1}^N \frac{\ln{10}}{\mathrm{N_A}}\varepsilon_i \int_0^\ell n_i(z)\mathrm{d}z} = \Bigl(e^{-\sum_{i = 1}^N \varepsilon_i \int_0^\ell \frac{n_i(z)}{\mathrm{N_A}}\mathrm{d}z}\Bigr)^{\ln{10}} = 10^{-\sum_{i = 1}^N \varepsilon_i \int_0^\ell c_i(z)\mathrm{d}z}.


Under certain conditions Beer–Lambert law fails to maintain a linear relationship between attenuation and concentration of analyte.[6] These deviations are classified into three categories:

  1. Real—fundamental deviations due to the limitations of the law itself.
  2. Chemical—deviations observed due to specific chemical species of the sample which is being analyzed.
  3. Instrument—deviations which occur due to how the attenuation measurements are made.

There are at least six conditions that need to be fulfilled in order for Beer–Lambert law to be valid. These are:

  1. The attenuators must act independently of each other.
  2. The attenuating medium must be homogeneous in the interaction volume.
  3. The attenuating medium must not scatter the radiation—no turbidity—unless this is accounted for as in DOAS.
  4. The incident radiation must consist of parallel rays, each traversing the same length in the absorbing medium.
  5. The incident radiation should preferably be monochromatic, or have at least a width that is narrower than that of the attenuating transition. Otherwise a spectrometer as detector for the power is needed instead of a photodiode which has not a selective wavelength dependence.
  6. The incident flux must not influence the atoms or molecules; it should only act as a non-invasive probe of the species under study. In particular, this implies that the light should not cause optical saturation or optical pumping, since such effects will deplete the lower level and possibly give rise to stimulated emission.

If any of these conditions are not fulfilled, there will be deviations from Beer–Lambert law.

Chemical analysis by spectrophotometry

Beer–Lambert law can be applied to the analysis of a mixture by spectrophotometry, without the need for extensive pre-processing of the sample. An example is the determination of bilirubin in blood plasma samples. The spectrum of pure bilirubin is known, so the molar attenuation coefficient ε is known. Measurements of decadic attenuation coefficient μ10 are made at one wavelength λ that is nearly unique for bilirubin and at a second wavelength in order to correct for possible interferences. The amount concentration c is then given by

c = \frac{\mu_{10}(\lambda)}{\varepsilon(\lambda)}.

For a more complicated example, consider a mixture in solution containing two species at amount concentrations c1 and c2. The decadic attenuation coefficient at any wavelength λ is, given by

\mu_{10}(\lambda) = \varepsilon_1(\lambda) c_1 + \varepsilon_2(\lambda) c_2.

Therefore, measurements at two wavelengths yields two equations in two unknowns and will suffice to determine the amount concentrations c1 and c2 as long as the molar attenuation coefficient of the two components, ε1 and ε2 are known at both wavelengths. This two system equation can be solved using Cramer's rule. In practice it is better to use linear least squares to determine the two amount concentrations from measurements made at more than two wavelengths. Mixtures containing more than two components can be analyzed in the same way, using a minimum of N wavelengths for a mixture containing N components.

The law is used widely in infra-red spectroscopy and near-infrared spectroscopy for analysis of polymer degradation and oxidation (also in biological tissue). The carbonyl group attenuation at about 6 micrometres can be detected quite easily, and degree of oxidation of the polymer calculated.

Beer–Lambert law in the atmosphere

This law is also applied to describe the attenuation of solar or stellar radiation as it travels through the atmosphere. In this case, there is scattering of radiation as well as absorption. The optical depth for a slant path is τ′ = , where τ refers to a vertical path, m is called the relative airmass, and for a plane-parallel atmosphere it is determined as m = sec θ where θ is the zenith angle corresponding to the given path. The Beer–Lambert law for the atmosphere is usually written

T = e^{-m(\tau_\mathrm{a} + \tau_\mathrm{g} + \tau_\mathrm{RS} + \tau_\mathrm{NO_2} + \tau_\mathrm{w} + \tau_\mathrm{O_3} + \tau_\mathrm{r} + \ldots)},

where each τx is the optical depth whose subscript identifies the source of the absorption or scattering it describes:

m is the optical mass or airmass factor, a term approximately equal (for small and moderate values of θ) to 1/cos θ, where θ is the observed object's zenith angle (the angle measured from the direction perpendicular to the Earth's surface at the observation site). This equation can be used to retrieve τa, the aerosol optical thickness, which is necessary for the correction of satellite images and also important in accounting for the role of aerosols in climate.

See also


  1. Pierre Bouguer, Essai d'optique sur la gradation de la lumière (Paris, France: Claude Jombert, 1729) pp. 16–22.
  2. J.H. Lambert, Photometria sive de mensura et gradibus luminis, colorum et umbrae [Photometry, or, On the measure and gradations of light, colors, and shade] (Augsburg ("Augusta Vindelicorum"), Germany: Eberhardt Klett, 1760). See especially p. 391.
  3. Beer (1852) "Bestimmung der Absorption des rothen Lichts in farbigen Flüssigkeiten" (Determination of the absorption of red light in colored liquids), Annalen der Physik und Chemie, vol. 86, pp. 78–88.
  4. Ingle, J. D. J.; Crouch, S. R. (1988). Spectrochemical Analysis. New Jersey: Prentice Hall.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  5. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "Beer–Lambert law".
  6. Mehta A.Limitations and Deviations of Beer–Lambert Law

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