A very large number of laboratories use absorbance when analyzing in experimental manipulations. By measuring how much light passes through, you can measure how much of a substance is present in the solution. Or, you can check how much of a reaction is going on.
When experimenting with biological systems, we frequently use absorbance to analyze them. In essence, we can measure how much light passes through, which allows us to see how compounds and enzymes work, and to measure the concentration of substances.
By checking how much light penetrates the solution, we can determine if the concentration is dark or light. Naturally, the darker the color, the more material can be inferred to be present there.
Terms such as the UV-visible absorption spectrum and Lambert–Beer law make the concept and principle of absorbance very difficult to understand. So, we can understand it as a method to measure the amount of a substance in a solution by making use of the property that light is less likely to pass through when the concentration is high.
Table of Contents
- 1 Conjugation in the Structural Formula Absorbs Light
- 2 Absorbance Is Related to Concentration and Distance
- 3 Determine the Wavelength of Measurement Using the UV-Visible Absorption Spectrum
- 4 Understanding the Principles of Absorption Spectra and Absorbance by UV-Visible Spectroscopy
Conjugation in the Structural Formula Absorbs Light
There are so many colored liquids around us. Why do they have these colors? It’s because it contains some compounds.
If it doesn’t contain any compounds, it’s pure water, so it’s clear. On the other hand, the liquid is colored as a result of the presence of some organic compound in it. It is important to understand that a colored liquid is always a liquid that contains some kind of compound.
Colored liquids always contain compounds that contain heavy metals or organic compounds that have a conjugated structure. In addition, colored liquids often contain compounds with a conjugated structure. For example, a compound that absorbs ultraviolet or visible light has the following structural formula.
For example, if it is a sunscreen, the product contains substances that absorb UV rays. In the case of tea, there are many organic compounds called polyphenols in the tea. As a result of the presence of these compounds, they absorb UV light and the solution has a color.
The benzene ring is the most famous conjugated structure. Compounds with a benzene ring all exhibit UV-visible absorption spectra. Because the benzene ring absorbs ultraviolet light, the UV-visible absorption spectrum peaks.
Measuring Differences in Light Transmission (Absorbance)
The presence of coloration means that the organic compound absorbs the color. We perceive a liquid to be colored because the compound absorbs light.
If an organic compound absorbs ultraviolet or visible light, the intensity of the light will be weakened by that amount. Also, if you shine light on a dark-colored solution, the light that comes out will be weaker by that amount.
It’s easy to imagine that the higher the concentration of compounds in the solution, the more light it absorbs and the less intense the light that comes out.
For example, if you use a black shading sheet, it will absorb all the light. However, if the black color is lighter, the light will pass through and reach you. On the other hand, the darker the black color, the more light it can block. In the same way, think of it as focusing on the transmission of light in the UV-visible absorption spectrum.
The principle behind the UV-visible absorption spectrum is the emission of energy
So why do organic compounds absorb ultraviolet (UV) and visible light (VIS)? Different substances absorb light at different wavelengths. The UV-VIS absorption spectrum describes the wavelengths that a solution absorbs.
Which light is absorbed and appears as the UV-VIS absorption spectrum depends on the compound dissolved in the solution. But why does it appear in the UV-visible absorption spectrum?
It is related to the excited state of the electrons.
Atoms have electrons and electrons are in a stable state (ground state). When energy is applied from the outside, the electron is temporarily in a high energy state. This is the excited state.
The migration of electrons from their original orbit to a higher-energy orbit is called electronic transition. When light energy hits a compound, it causes an electronic transition. However, molecules do not like high-energy states, so they try to return to the original stable state after the electronic transition. When the molecule returns to the stable state (ground state), it releases light and heat as energy.
There is a reason why when light hits a solution, the light is weakened after transmission. It’s because the compound absorbs the light energy and then releases the energy as heat or light. Naturally, the darker the solution, the more light it absorbs and the weaker the light is after transmission.
Even for black shading sheets, the shading sheets are hot after blocking a lot of light. This is because it absorbs light energy and stores a lot of energy as heat.
Absorbance Is Related to Concentration and Distance
This property is applied in scientific experiments. By measuring how much light is absorbed as the light passes through a liquid, we can measure the amount of material contained or the progress of the reaction.
There are two factors involved in absorbance: concentration and distance. The more concentrated the concentration, the more light will be absorbed accordingly. In addition, even if the concentration of the solution is the same, the longer the distance, the more light is absorbed.
For example, let’s say there is a solution in which the light intensity drops to 50% after the light passes through. If the length of this solution is doubled, the light will be 25% after transmission.
First 50% of the light is absorbed, then 50% of the light is absorbed. The result is 0.5 x 0.5 = 0.25 (25%). Understand that as the distance increases, the intensity of the light weakens as an exponential function.
Understanding Lambert–Beer Law
Once you learn these details, it is easy to understand Lambert–Beer law. Many people try to explain Lambert–Beer law by using difficult symbols and formulas. However, these do not make sense.
In Lambert–Beer law, the two names are combined.
It was discovered that when the concentration is the same, the absorbance is proportional to the distance (the length of light transmitted). This is called Lambert law (Bouguer law).
On the other hand, when the distance (length of light transmission) is the same, the absorbance depends on the concentration of the solution (molar concentration of the solute). This is called Beer law.
Lambert–Beer law is a combination of Lambert law (Bouguer law) and Beer law. However, it only states the obvious: the denser the solution is and the longer the distance, the weaker the light after transmission.
Use Absorbance, Not Transmittance
So what is the reason for using absorbance (A) instead of transmittance? This is because transmittance does not produce a straight line in the graph.
By measuring the intensity of the output light (I0) and the intensity of the transmitted light (I), the transmittance can be easily measured. The transmittance is shown below.
As mentioned before, the graph will bend when you use transmittance to give a number. I explained earlier that as the distance increases, the light gets weaker, like an exponential function: if you have 50% transmission, then when you double the distance, you don’t get zero transmission, you get 25% transmission.
So instead of transmittance, we use logarithm. If you add a minus sign to the logarithm, you will get a straight line graph.
Absorbance is the logarithm of the transmittance, plus a negative number. Because of the use of absorbance, the lines in the graph are straightened and the experimental data can be read.
Lambert–Beer law also uses other equations. The formula is as follows
- A (Absorbance) = εcl
- ε (Epsilon): Molar absorption coefficient
- c: Concentration of the solution
- l: Distance of light
In Lambert–Beer law, we explained that absorbance is proportional to concentration and distance. Therefore, the absorbance can be calculated by multiplying the concentration of the solution (c) by the distance of the light (l). Although the formula may seem difficult, it is a very simple one.
ε (epsilon) is called the molar absorbance coefficient. When c is 1 mol/L and l is 1 cm, the molar absorbance is ε.
If you are shown this formula at first, you will not understand what it means. However, once you understand Lambert–Beer and the meaning of absorbance, you will be able to understand it easily.
Determine the Wavelength of Measurement Using the UV-Visible Absorption Spectrum
These are the principles of Lambert-Bert’s law of absorbance measurement. So, how can we analyze it?
First of all, we have to know what kind of light the compound of interest absorbs. So let’s look at the UV-visible absorption spectrum. By exposing the compound to ultraviolet and visible light by a machine, the UV-visible absorption spectrum will appear. It looks something like the following.
From the data in the UV-visible absorption spectrum, decide which wavelengths of light you want to use in your experiment.
However, we usually use the wavelength that has the highest absorbance. This is the point at which light is easily absorbed and thus data can be obtained from the experiment.
Measuring the Absorbance Will Give You the Concentration of the Solution
After determining the wavelengths to be used by the UV-visible absorption spectrum, what is the next experimental operation to be performed?
The experiment varies from person to person. Some people want to know the concentration of a substance, while others want to know the progress of a reaction. But in any case, we can calculate the concentration of the solution by measuring the absorbance. We then produce the data.
In laboratories involved in biochemistry, including cell experiments, absorbance measurements are frequently used. For example, the following small plates are used to examine the degree of coloration.
Depending on how much color is generated, the concentration of a substance in the solution can be determined. It’s just a list of numbers (absorbance) that come up because it only measures absorbance. So by organizing the absorbance numbers, you will be able to get your data.
A great number of scientific experiments are being conducted in laboratories that make use of color differences, such as the quantification of substances, enzyme reactions, and the use of cells. By using the absorption of ultraviolet light and the use of chromophores, we can measure how much of a compound is present there by the degree of light absorption. As a result, we are able to collect experimental data.
For example, there are reagents that react with glucose (sugar) to produce color. If blood is collected and colored by reacting with the reagent, it is possible to measure the blood glucose level according to the intensity of the color. The measurement of absorbance has medical applications.
It is also used in scientific experiments and measurements in many other situations using Lambert–Beer law. Although it only measures absorbance as the transmission of light, it is one of the measurement technologies used in all aspects of our lives.
Proteins, For Example, May Themselves Absorb Light
In addition, substances themselves often absorb light when they are measured. There are only a few compounds that have a dye, but there are many compounds that absorb UV light. As mentioned above, if they have a conjugated structure, they will absorb UV light.
For example, in proteins, the UV-visible absorption spectrum can be seen. Proteins have peptide bonds and there is UV absorption related to this.
There are also aromatic amino acids (tyrosine and tryptophan) in proteins. Because they have a benzene ring in their structural formula, they have a conjugated structure and absorb UV light. For this reason, the concentration of proteins can be estimated by measuring absorbance.
-In General, Oher Than Ultraviolet Light Are Used to Measure Absorbances
Many organic substances, including proteins, have a conjugated structure and absorb UV light. Therefore, it is common to use visible light as the light source for absorbance analysis.
Although UV light can be used as a light source, any organic compound with a conjugated structure absorbs UV light. Therefore, when multiple substances are mixed in a solution, not only your target compound but also other substances will absorb UV light, making it difficult to obtain accurate data.
So we use other light (visible colors). For example, let’s say it reacts with a reagent to produce a red color. Shine the light on the solution. Then we can measure only the compounds that are dyed red by the reagent. Depending on the intensity of the red color, the concentration of the compound can be measured.
Utilizing visibly tinted reagents, UV-visible spectroscopy can be useful in many biochemical experiments.
Understanding the Principles of Absorption Spectra and Absorbance by UV-Visible Spectroscopy
By using UV-visible spectroscopy and using the UV-visible absorption spectrum, we can tell what wavelength of light the compound absorbs. We can then use Lambert–Beer law and measure the absorbance to get the desired number.
It is not possible to understand the principle and meaning of Lambert–Beer law by looking at the formula alone. There is no point in using a difficult mathematical formula. The concept of absorbance can be understood simply by knowing multiplication and logarithm.
These absorbance measurements are not only used in the laboratory, but are used in all kinds of research facilities. This includes a great many institutions, such as government agencies and hospitals. It is a very simple and even common method to determine the degree of absorption of light and give the concentration of a target compound.
The measurement of absorbance is used in a great many situations. By measuring absorbance, you should be able to derive the desired data.