Absorbance: Difference between revisions

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{{Redirect|Optical density|other uses|Refractive index|and|Nucleic acid quantitation|and|Neutral-density filter}}
{{Redirect|Optical density|other uses|Refractive index|and|Nucleic acid quantitation|and|Neutral-density filter}}


'''Absorbance''' is defined as "the logarithm of the ratio of incident to transmitted radiant power through a sample (excluding the effects on cell walls)".<ref name="GoldBook"/> Alternatively, for samples which scatter light, absorbance may be defined as "the negative logarithm of one minus absorptance, as measured on a uniform sample".<ref name=":0">{{GoldBookRef |title=decadic absorbance |file=D01536 }}</ref> The term is used in many technical areas to quantify the results of an experimental measurement. While the term has its origin in quantifying the absorption of light, it is often entangled with quantification of light which is "lost" to a detector system through other mechanisms. What these uses of the term tend to have in common is that they refer to a logarithm of the ratio of a quantity of light incident on a sample or material to that which is detected after the light has interacted with the sample.
{{Technical|date=July 2025}}
 
In [[Spectrophotometry|spectroscopy]], '''absorbance''' (abbreviated as '''A''')<ref>{{Cite encyclopedia |title=A |encyclopedia=Henderson's Dictionary of Biological Terms |last=Lawrence |first=Eleanor |page=1 |isbn=0-470-21446-5}}</ref> is a logarithmic value which describes the portion of a beam of [[Electromagnetic radiation|light]] which does not pass through a sample. Whilst the name refers to the [[Absorption (electromagnetic radiation)|absorption]] of light, other interactions of light with a sample (reflection, scattering) may also contribute to [[attenuation]] of the beam passing through the sample. The term "internal absorbance" is sometimes used to describe beam attenuation caused by absorption, while "attenuance" or "experimental absorbance" can be used to emphasize that beam attenuation can be caused by other phenomena.<ref name=":1" />  
The term [[Absorption (electromagnetic radiation)|absorption]] refers to the physical process of absorbing light, while absorbance does not always measure only absorption; it may measure [[attenuation]] (of transmitted radiant power) caused by absorption, as well as reflection, scattering, and other physical processes. Sometimes the term "attenuance" or "experimental absorbance" is used to emphasize that radiation is lost from the beam by processes other than absorption, with the term "internal absorbance" used to emphasize that the necessary corrections have been made to eliminate the effects of phenomena other than absorption.<ref name=":1" />


== History and uses of the term absorbance ==
== History and uses of the term absorbance ==


=== Beer-Lambert law ===
=== Beer-Lambert law ===
The roots of the term absorbance are in the [[Beer-Lambert law#Beer–Lambert law|Beer–Lambert law]]. As light moves through a medium, it will become dimmer as it is being "extinguished". Bouguer recognized that this extinction (now often called attenuation) was not linear with distance traveled through the medium, but related by what we now refer to as an exponential function.
The roots of the term absorbance are in the [[Beer-Lambert law#Beer–Lambert law|Beer–Lambert law]] (or Beer's law). As light moves through a medium, it will become dimmer as it is being "extinguished". [[Pierre Bouguer]] recognized that this extinction (now often called attenuation) was not linear with distance traveled through the medium, but related to what is now referred to as an exponential function.


If <math>I_0</math> is the intensity of the light at the beginning of the travel and <math>I_d</math> is the intensity of the light detected after travel of a distance {{nowrap|<math>d</math>,}} the fraction transmitted, {{nowrap|<math>T</math>,}} is given by
If <math>I_0</math> is the intensity of the light at the beginning of the travel and <math>I_d</math> is the intensity of the light detected after travel of a distance {{nowrap|<math>d</math>,}} the fraction transmitted, {{nowrap|<math>T</math>,}} is given by:


<math display="block">T=\frac {I_d}{I_0} = \exp(-\mu d)\,,</math>
<math display="block">T=\frac {I_d}{I_0} = \exp(-\mu d)\,,</math>


where <math>\mu</math> is called an [[Propagation constant#Attenuation constant|attenuation constant]] (a term used in various fields where a signal is transmitted though a medium) or coefficient. The amount of light transmitted is falling off exponentially with distance. Taking the natural logarithm in the above equation, we get
where <math>\mu</math> is called an [[Propagation constant#Attenuation constant|attenuation constant]] (a term used in various fields where a signal is transmitted though a medium) or coefficient. The amount of light transmitted decreases exponentially with distance. Taking the natural logarithm in the above equation, we get:


<math display="block">-\ln(T) = \ln \frac {I_0}{I_d} = \mu d\,.</math>
<math display="block">-\ln(T) = \ln \frac {I_0}{I_d} = \mu d\,.</math>


For scattering media, the constant is often divided into two parts,<ref>{{Cite book |last=Van de Hulst |first=H. C. |title=Light Scattering by Small Particles |publisher=John Wiley and Sons |year=1957 |isbn=9780486642284 |location=New York}}</ref> {{nowrap|<math>\mu = \mu_s + \mu_a </math>,}} separating it into a scattering coefficient <math>\mu _s</math> and an absorption coefficient {{nowrap|<math>\mu_a</math>,}} obtaining
For scattering media, the constant is often divided into two parts,<ref>{{Cite book |last=Van de Hulst |first=H. C. |title=Light Scattering by Small Particles |publisher=John Wiley and Sons |year=1957 |isbn=9780486642284 |location=New York}}</ref> {{nowrap|<math>\mu = \mu_s + \mu_a </math>,}} separating it into a scattering coefficient <math>\mu _s</math> and an absorption coefficient {{nowrap|<math>\mu_a</math>,}} obtaining:


<math display="block">-\ln(T) = \ln \frac {I_0}{I_s} = (\mu_s + \mu_a) d\,.</math>
<math display="block">-\ln(T) = \ln \frac {I_0}{I_s} = (\mu_s + \mu_a) d\,.</math>


If a size of a detector is very small compared to the distance traveled by the light, any light that is scattered by a particle, either in the forward or backward direction, will not strike the detector. (Bouguer was studying astronomical phenomena, so this condition was met.) In such case, a plot of <math>-\ln(T)</math> as a function of wavelength will yield a superposition of the effects of absorption and scatter. Because the absorption portion is more distinct and tends to ride on a background of the scatter portion, it is often used to identify and quantify the absorbing species. Consequently, this is often referred to as [[absorption spectroscopy]], and the plotted quantity is called "absorbance", symbolized as {{nowrap|<math>\Alpha</math>.}} Some disciplines by convention use decadic (base 10) absorbance rather than Napierian (natural) absorbance, resulting in: <math>\Alpha_{10} = \mu_{10}d </math> (with the subscript 10 usually not shown).
If the size of a detector is very small compared to the distance traveled by the light, any light that is scattered by a particle, either in the forward or backward direction, will not strike the detector. (Bouguer was studying astronomical phenomena, so this condition was met.) In such cases, a plot of <math>-\ln(T)</math> as a function of wavelength will yield a superposition of the effects of absorption and scattering. Because the absorption portion is more distinct and tends to ride on a background of the scatter portion, it is often used to identify and quantify the absorbing species. Consequently, this is often referred to as [[absorption spectroscopy]], and the plotted quantity is called "absorbance", symbolized as {{nowrap|<math>\Alpha</math>.}} Some disciplines by convention use decadic (base 10) absorbance rather than Napierian (natural) absorbance, resulting in: <math>\Alpha_{10} = \mu_{10}d </math> (with the subscript 10 usually not shown).


=== Absorbance for non-scattering samples ===
=== Absorbance for non-scattering samples ===
Within a homogeneous medium such as a solution, there is no scattering. For this case, researched extensively by [[August Beer]], the concentration of the absorbing species follows the same linear contribution to absorbance as the path-length. Additionally, the contributions of individual absorbing species are additive. This is a very favorable situation, and made absorbance an absorption metric far preferable to absorption fraction (absorptance). This is the case for which the term "absorbance" was first used.
Within a homogeneous medium such as a solution, there is no scattering. In this case, researched extensively by [[August Beer]], the concentration of the absorbing species follows the same linear contribution to absorbance as the path-length. Additionally, the contributions of individual absorbing species are additive. This is a very favorable situation, and made absorbance an absorption metric far preferable to absorption fraction (absorptance). This is the case for which the term "absorbance" was first used.


A common expression of the [[Beer's law]] relates the attenuation of light in a material as: {{nowrap|<math>\Alpha = \varepsilon\ell c </math>,}} where <math>\Alpha </math> is the '''absorbance;''' <math>\varepsilon </math> is the [[molar attenuation coefficient]] or [[Molar absorptivity|absorptivity]] of the attenuating species; <math>\ell </math> is the optical path length; and <math>c </math> is the concentration of the attenuating species.
A common expression of the Beer's law relates the attenuation of light in a material as: {{nowrap|<math>\Alpha = \varepsilon\ell c </math>,}} where <math>\Alpha </math> is the '''absorbance;''' <math>\varepsilon </math> is the [[molar attenuation coefficient]] or [[Molar absorptivity|absorptivity]] of the attenuating species; <math>\ell </math> is the optical path length; and <math>c </math> is the concentration of the attenuating species.


=== Absorbance for scattering samples ===
=== Absorbance for scattering samples ===
For samples which scatter light, absorbance is defined as "the negative logarithm of one minus absorptance (absorption fraction: <math>\alpha</math>) as measured on a uniform sample".<ref name=":0" /> For decadic absorbance,<ref name=":1">{{cite book |doi=10.1002/0470027320.s8401 |chapter=Glossary of Terms used in Vibrational Spectroscopy |title=Handbook of Vibrational Spectroscopy |year=2006 |last1=Bertie |first1=John E. |isbn=0471988472 |editor1-first=Peter R |editor1-last=Griffiths }}</ref> this may be symbolized as {{nowrap|<math>\Alpha_{10}=-\log_{10}(1-\alpha)</math>.}} If a sample both transmits and [[Diffuse reflectance spectroscopy#Remission|remits light]], and is not luminescent, the fraction of light absorbed {{nowrap|(<math>\alpha</math>),}} remitted {{nowrap|(<math>R</math>),}} and transmitted {{nowrap|(<math>T</math>)}} add to 1: {{nowrap|<math>\alpha + R + T =1</math>.}} Note that {{nowrap|<math>1-\alpha = R+T </math>,}} and the formula may be written as {{nowrap|<math>\Alpha _{10}=-\log_{10}(R+T)</math>.}} For a sample which does not scatter, {{nowrap|<math>R=0 </math>,}} and {{nowrap|<math>1-\alpha = T</math>,}} yielding the formula for absorbance of a material discussed below.
For samples which scatter light, absorbance is defined as "the negative logarithm of one minus absorptance (absorption fraction: <math>\alpha</math>) as measured on a uniform sample".<ref name=":0">{{GoldBookRef|title=decadic absorbance|file=D01536}}</ref> For decadic absorbance,<ref name=":1">{{cite book |doi=10.1002/0470027320.s8401 |chapter=Glossary of Terms used in Vibrational Spectroscopy |title=Handbook of Vibrational Spectroscopy |year=2006 |last1=Bertie |first1=John E. |isbn=0471988472 |editor1-first=Peter R |editor1-last=Griffiths }}</ref> this may be symbolized as {{nowrap|<math>\Alpha_{10}=-\log_{10}(1-\alpha)</math>.}} If a sample both transmits and [[Diffuse reflectance spectroscopy#Remission|remits light]], and is not luminescent, the fraction of light absorbed {{nowrap|(<math>\alpha</math>),}} remitted {{nowrap|(<math>R</math>),}} and transmitted {{nowrap|(<math>T</math>)}} add to 1: {{nowrap|<math>\alpha + R + T =1</math>.}} Note that {{nowrap|<math>1-\alpha = R+T </math>,}} and the formula may be written as {{nowrap|<math>\Alpha _{10}=-\log_{10}(R+T)</math>.}} For a sample which does not scatter, {{nowrap|<math>R=0 </math>,}} and {{nowrap|<math>1-\alpha = T</math>,}} yielding the formula for absorbance of a material discussed below.


Even though this absorbance function is very useful with scattering samples, the function does not have the same desirable characteristics as it does for non-scattering samples. There is, however, a property called [[Representative layer theory#Absorbing Power: The Scatter Corrected Absorbance of a sample|absorbing power]] which may be estimated for these samples. The [[Representative layer theory#Absorbing Power: The Scatter Corrected Absorbance of a sample|absorbing power]] of a single unit thickness of material making up a scattering sample is the same as the absorbance of the same thickness of the material in the absence of scatter.<ref>{{cite book |doi=10.1255/978-1-901019-05-6 |title=Interpreting Diffuse Reflectance and Transmittance: A Theoretical Introduction to Absorption Spectroscopy of Scattering Materials |year=2007 |last1=Dahm |first1=Donald |last2=Dahm |first2=Kevin |isbn=9781901019056 }}</ref>
Even though this absorbance function is very useful with scattering samples, the function does not have the same desirable characteristics as it does for non-scattering samples. There is, however, a property called [[Representative layer theory#Absorbing Power: The Scatter Corrected Absorbance of a sample|absorbing power]] which may be estimated for these samples. The [[Representative layer theory#Absorbing Power: The Scatter Corrected Absorbance of a sample|absorbing power]] of a single unit thickness of material making up a scattering sample is the same as the absorbance of the same thickness of the material in the absence of scatter.<ref>{{cite book |doi=10.1255/978-1-901019-05-6 |title=Interpreting Diffuse Reflectance and Transmittance: A Theoretical Introduction to Absorption Spectroscopy of Scattering Materials |year=2007 |last1=Dahm |first1=Donald |last2=Dahm |first2=Kevin |isbn=9781901019056 }}</ref>
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* {{mvar|τ{{sub|λ}}}} is the spectral optical depth in wavelength.
* {{mvar|τ{{sub|λ}}}} is the spectral optical depth in wavelength.


Although absorbance is properly unitless, it is sometimes reported in "absorbance units", or AU. Many people, including scientific researchers, wrongly state the results from absorbance measurement experiments in terms of these made-up units.<ref>{{cite journal |doi=10.1021/jz4006916 |title=How to Make Your Next Paper Scientifically Effective |journal=J. Phys. Chem. Lett. |date=2013 |volume=4 |pages=1578–1581 |issue=9|last1=Kamat |first1=Prashant |last2=Schatz |first2=George C. |pmid=26282316 |doi-access=free }}</ref>
Although absorbance is properly unitless, it is sometimes reported in "absorbance units", or AU. Many people, including scientific researchers, wrongly state the results from absorbance measurement experiments in terms of these made-up units.<ref>{{cite journal |doi=10.1021/jz4006916 |title=How to Make Your Next Paper Scientifically Effective |journal=J. Phys. Chem. Lett. |date=2013 |volume=4 |pages=1578–1581 |issue=9|last1=Kamat |first1=Prashant |last2=Schatz |first2=George C. |pmid=26282316 |bibcode=2013JPCL....4.1578K |doi-access=free }}</ref>


== Relationship with attenuation ==
== Relationship with attenuation ==
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* <math display="inline">E = \Phi_\mathrm{e}^\mathrm{e} / \Phi_\mathrm{e}^\mathrm{i}</math> is the emittance of that material.
* <math display="inline">E = \Phi_\mathrm{e}^\mathrm{e} / \Phi_\mathrm{e}^\mathrm{i}</math> is the emittance of that material.


According to the [[Beer–Lambert law]], {{math|1=''T'' = 10<sup>−''A''</sup>}}, so
According to the Beer's law, {{math|1=''T'' = 10<sup>−''A''</sup>}}, so
* <math>\mathrm{ATT} = 1 - 10^{-A} + E \approx A \ln 10 + E, \quad \text{if}\ A \ll 1,</math>
* <math>\mathrm{ATT} = 1 - 10^{-A} + E \approx A \ln 10 + E, \quad \text{if}\ A \ll 1,</math>
and finally
and finally
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The use of the term "molar absorptivity" for molar attenuation coefficient is discouraged.<ref name=GoldBook />
The use of the term "molar absorptivity" for molar attenuation coefficient is discouraged.<ref name=GoldBook />


==Measurements==
==Use in Analytical Chemistry==
 
Absorbance is a widely used measurement in quantitative [[absorption spectroscopy]]. While the attenuation of a light beam can be also be described by ''transmittance'' (the ratio of transmitted incident light), the logarithmic formulation of absorbance is convenient for sample quantification: under conditions where the Beer's law is valid, absorbance will be linearly proportional to sample thickness and the concentration of the absorptive species.<ref name=":2">{{Cite book |last1=Ham |first1=Bryan M. |title=Analytical chemistry: a toolkit for scientists and laboratory technicians |last2=MaHam |first2=Aihui |date=2024 |publisher=John Wiley & Sons, Inc |isbn=978-1-119-89445-2 |edition=2nd |location=Hoboken, New Jersey |pages=235–237}}</ref>
===Logarithmic vs. directly proportional measurements===
The amount of light transmitted through a material diminishes [[Exponential function|exponentially]] as it travels through the material, according to the Beer–Lambert law ({{math|1=''A'' = (''ε'')(''l'')}}). Since the absorbance of a sample is measured as a logarithm, it is directly proportional to the thickness of the sample and to the concentration of the absorbing material in the sample. Some other measures related to absorption, such as transmittance, are measured as a simple ratio so they vary exponentially with the thickness and concentration of the material.
 
{| class="wikitable sortable" style="text-align: center;"
|+ Absorbances and equivalent transmittances
|-
! scope="col" | Absorbance: <math display="inline">-\log_{10}\left(\Phi_\mathrm{e}^\mathrm{t}/\Phi_\mathrm{e}^\mathrm{i}\right)</math>
! scope="col" | Transmittance: <math display="inline">\Phi_\mathrm{e}^\mathrm{t}/\Phi_\mathrm{e}^\mathrm{i}</math>
|-
| 0
| 1
|-
| 0.1
| 0.79
|-
| 0.25
| 0.56
|-
| 0.5
| 0.32
|-
| 0.75
| 0.18
|-
| 0.9
| 0.13
|-
| 1
| 0.1
|-
| 2
| 0.01
|-
| 3
| 0.001
|}
 
===Instrument measurement range===
Any real measuring instrument has a limited range over which it can accurately measure absorbance. An instrument must be calibrated and checked against known standards if the readings are to be trusted. Many instruments will become non-linear (fail to follow the Beer–Lambert law) starting at approximately 2 AU (~1% transmission). It is also difficult to accurately measure very small absorbance values (below {{val|e=-4}}) with commercially available instruments for chemical analysis. In such cases, [[Laser absorption spectrometry|laser-based absorption techniques]] can be used, since they have demonstrated detection limits that supersede those obtained by conventional non-laser-based instruments by many orders of magnitude (detection has been demonstrated all the way down to {{val|5e-13}}). The theoretical best accuracy for most commercially available non-laser-based instruments is attained in the range near 1 AU. The path length or concentration should then, when possible, be adjusted to achieve readings near this range.
 
===Method of measurement===
Typically, absorbance of a dissolved substance is measured using [[absorption spectroscopy]]. This involves shining a light through a solution and recording how much light and what wavelengths were transmitted onto a detector. Using this information, the wavelengths that were absorbed can be determined.<ref>{{cite web|last1=Reusch|first1=William|title=Visible and Ultraviolet Spectroscopy|url=https://www2.chemistry.msu.edu/faculty/reusch/virttxtjml/Spectrpy/UV-Vis/spectrum.htm|access-date=2014-10-29}}</ref> First, measurements on a "blank" are taken using just the solvent for reference purposes. This is so that the absorbance of the solvent is known, and then any change in absorbance when measuring the whole solution is made by just the solute of interest. Then measurements of the solution are taken. The transmitted spectral radiant flux that makes it through the solution sample is measured and compared to the incident spectral radiant flux. As stated above, the spectral absorbance at a given wavelength is
 
<math display="block">A_\lambda = \log_{10}\!\left(\frac{\Phi_{\mathrm{e},\lambda}^\mathrm{i}}{\Phi_{\mathrm{e},\lambda}^\mathrm{t}}\right)\!.</math>
 
The absorbance spectrum is plotted on a graph of absorbance vs. wavelength.<ref>{{cite web|last1=Reusch|first1=William|title=Empirical Rules for Absorption Wavelengths of Conjugated Systems|url=https://www2.chemistry.msu.edu/faculty/reusch/virttxtjml/Spectrpy/UV-Vis/uvspec.htm#uv1|access-date=2014-10-29}}</ref>


An [[Ultraviolet-visible spectroscopy#Ultraviolet–visible spectrophotometer]] will do all this automatically. To use this machine, solutions are placed in a small [[cuvette]] and inserted into the holder. The machine is controlled through a computer and, once it has been "blanked", automatically displays the absorbance plotted against wavelength. Getting the absorbance spectrum of a solution is useful for determining the concentration of that solution using the Beer–Lambert law and is used in [[HPLC]].
For quantitative purposes, absorbance is often measured on a sample solution held in a [[cuvette]], where the solution is sufficiently dilute that the linear relationship of the Beer's law holds. The cuvette provides a known and consistent path length for the light beam passing through the sample.<ref name=":2" /> Measuring first the absorbance of the cuvette and a "blank" solution containing no analyte, differences in absorbance between samples can be used to quantity the analyte. Spectrometers generally measure absorbance separately for a range of wavelengths: this data is then plotted as absorbance vs. wavelength.<ref>{{cite web|last1=Reusch|first1=William|title=Empirical Rules for Absorption Wavelengths of Conjugated Systems|url=https://www2.chemistry.msu.edu/faculty/reusch/virttxtjml/Spectrpy/UV-Vis/uvspec.htm#uv1|access-date=2014-10-29}}</ref>


==Shade number==
==Shade number==

Latest revision as of 00:55, 13 December 2025

Template:Short description Script error: No such module "about". Script error: No such module "redirect hatnote".

Script error: No such module "Unsubst". In spectroscopy, absorbance (abbreviated as A)[1] is a logarithmic value which describes the portion of a beam of light which does not pass through a sample. Whilst the name refers to the absorption of light, other interactions of light with a sample (reflection, scattering) may also contribute to attenuation of the beam passing through the sample. The term "internal absorbance" is sometimes used to describe beam attenuation caused by absorption, while "attenuance" or "experimental absorbance" can be used to emphasize that beam attenuation can be caused by other phenomena.[2]

History and uses of the term absorbance

Beer-Lambert law

The roots of the term absorbance are in the Beer–Lambert law (or Beer's law). As light moves through a medium, it will become dimmer as it is being "extinguished". Pierre Bouguer recognized that this extinction (now often called attenuation) was not linear with distance traveled through the medium, but related to what is now referred to as an exponential function.

If I0 is the intensity of the light at the beginning of the travel and Id is the intensity of the light detected after travel of a distance d, the fraction transmitted, T, is given by:

T=IdI0=exp(μd),

where μ is called an attenuation constant (a term used in various fields where a signal is transmitted though a medium) or coefficient. The amount of light transmitted decreases exponentially with distance. Taking the natural logarithm in the above equation, we get:

ln(T)=lnI0Id=μd.

For scattering media, the constant is often divided into two parts,[3] μ=μs+μa, separating it into a scattering coefficient μs and an absorption coefficient μa, obtaining:

ln(T)=lnI0Is=(μs+μa)d.

If the size of a detector is very small compared to the distance traveled by the light, any light that is scattered by a particle, either in the forward or backward direction, will not strike the detector. (Bouguer was studying astronomical phenomena, so this condition was met.) In such cases, a plot of ln(T) as a function of wavelength will yield a superposition of the effects of absorption and scattering. Because the absorption portion is more distinct and tends to ride on a background of the scatter portion, it is often used to identify and quantify the absorbing species. Consequently, this is often referred to as absorption spectroscopy, and the plotted quantity is called "absorbance", symbolized as A. Some disciplines by convention use decadic (base 10) absorbance rather than Napierian (natural) absorbance, resulting in: A10=μ10d (with the subscript 10 usually not shown).

Absorbance for non-scattering samples

Within a homogeneous medium such as a solution, there is no scattering. In this case, researched extensively by August Beer, the concentration of the absorbing species follows the same linear contribution to absorbance as the path-length. Additionally, the contributions of individual absorbing species are additive. This is a very favorable situation, and made absorbance an absorption metric far preferable to absorption fraction (absorptance). This is the case for which the term "absorbance" was first used.

A common expression of the Beer's law relates the attenuation of light in a material as: A=εc, where A is the absorbance; ε is the molar attenuation coefficient or absorptivity of the attenuating species; is the optical path length; and c is the concentration of the attenuating species.

Absorbance for scattering samples

For samples which scatter light, absorbance is defined as "the negative logarithm of one minus absorptance (absorption fraction: α) as measured on a uniform sample".[4] For decadic absorbance,[2] this may be symbolized as A10=log10(1α). If a sample both transmits and remits light, and is not luminescent, the fraction of light absorbed (α), remitted (R), and transmitted (T) add to 1: α+R+T=1. Note that 1α=R+T, and the formula may be written as A10=log10(R+T). For a sample which does not scatter, R=0, and 1α=T, yielding the formula for absorbance of a material discussed below.

Even though this absorbance function is very useful with scattering samples, the function does not have the same desirable characteristics as it does for non-scattering samples. There is, however, a property called absorbing power which may be estimated for these samples. The absorbing power of a single unit thickness of material making up a scattering sample is the same as the absorbance of the same thickness of the material in the absence of scatter.[5]

Optics

In optics, absorbance or decadic absorbance is the common logarithm of the ratio of incident to Template:Em radiant power through a material, and spectral absorbance or spectral decadic absorbance is the common logarithm of the ratio of incident to Template:Em spectral radiant power through a material. Absorbance is dimensionless, and in particular is not a length, though it is a monotonically increasing function of path length, and approaches zero as the path length approaches zero.

Mathematical definitions

Absorbance of a material

The absorbance of a material, denoted Template:Mvar, is given by[6]

A=log10ΦeiΦet=log10T,

where

Absorbance is a dimensionless quantity. Nevertheless, the absorbance unit or AU is commonly used in ultraviolet–visible spectroscopy and its high-performance liquid chromatography applications, often in derived units such as the milli-absorbance unit (mAU) or milli-absorbance unit-minutes (mAU×min), a unit of absorbance integrated over time.[7]

Absorbance is related to optical depth by

A=τln10=τlog10e,

where Template:Mvar is the optical depth.

Spectral absorbance

Spectral absorbance in frequency and spectral absorbance in wavelength of a material, denoted AνScript error: No such module "Check for unknown parameters". and AλScript error: No such module "Check for unknown parameters". respectively, are given by[6]

Aν=log10Φe,νiΦe,νt=log10Tν,Aλ=log10Φe,λiΦe,λt=log10Tλ,

where

Spectral absorbance is related to spectral optical depth by

Aν=τνln10=τνlog10e,Aλ=τλln10=τλlog10e,

where

Although absorbance is properly unitless, it is sometimes reported in "absorbance units", or AU. Many people, including scientific researchers, wrongly state the results from absorbance measurement experiments in terms of these made-up units.[8]

Relationship with attenuation

Attenuance

Absorbance is a number that measures the attenuation of the transmitted radiant power in a material. Attenuation can be caused by the physical process of "absorption", but also reflection, scattering, and other physical processes. Absorbance of a material is approximately equal to its attenuanceScript error: No such module "Unsubst". when both the absorbance is much less than 1 and the emittance of that material (not to be confused with radiant exitance or emissivity) is much less than the absorbance. Indeed,

Φet+Φeatt=Φei+Φee,

where

  • Φet is the radiant power transmitted by that material,
  • Φeatt is the radiant power attenuated by that material,
  • Φei is the radiant power received by that material, and
  • Φee is the radiant power emitted by that material.

This is equivalent to

T+ATT=1+E,

where

  • T=Φet/Φei is the transmittance of that material,
  • ATT=Φeatt/Φei is the Template:Em of that material,
  • E=Φee/Φei is the emittance of that material.

According to the Beer's law, T = 10AScript error: No such module "Check for unknown parameters"., so

  • ATT=110A+EAln10+E,if A1,

and finally

  • ATTAln10,if EA.

Attenuation coefficient

Absorbance of a material is also related to its decadic attenuation coefficient by

A=0la(z)dz,

where

  • Template:Mvar is the thickness of that material through which the light travels, and
  • a(z)Script error: No such module "Check for unknown parameters". is the decadic attenuation coefficient of that material at Template:Mvar.

If a(z) is uniform along the path, the attenuation is said to be a linear attenuation, and the relation becomes A=al.

Sometimes the relation is given using the molar attenuation coefficient of the material, that is its attenuation coefficient divided by its molar concentration:

A=0lεc(z)dz,

where

  • Template:Mvar is the molar attenuation coefficient of that material, and
  • c(z)Script error: No such module "Check for unknown parameters". is the molar concentration of that material at Template:Mvar.

If c(z)Script error: No such module "Check for unknown parameters". is uniform along the path, the relation becomes

A=εcl.

The use of the term "molar absorptivity" for molar attenuation coefficient is discouraged.[6]

Use in Analytical Chemistry

Absorbance is a widely used measurement in quantitative absorption spectroscopy. While the attenuation of a light beam can be also be described by transmittance (the ratio of transmitted incident light), the logarithmic formulation of absorbance is convenient for sample quantification: under conditions where the Beer's law is valid, absorbance will be linearly proportional to sample thickness and the concentration of the absorptive species.[9]

For quantitative purposes, absorbance is often measured on a sample solution held in a cuvette, where the solution is sufficiently dilute that the linear relationship of the Beer's law holds. The cuvette provides a known and consistent path length for the light beam passing through the sample.[9] Measuring first the absorbance of the cuvette and a "blank" solution containing no analyte, differences in absorbance between samples can be used to quantity the analyte. Spectrometers generally measure absorbance separately for a range of wavelengths: this data is then plotted as absorbance vs. wavelength.[10]

Shade number

Some filters, notably welding glass, are rated by shade number (SN), which is 7/3 times the absorbance plus one:[11]

SN=73A+1=73(log10T)+1.

For example, if the filter has 0.1% transmittance (0.001 transmittance, which is 3 absorbance units), its shade number would be 8.

See also

References

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