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Colorimeter - Beer’s Law, Lambert’s Law, Principle, Parts, Applications, FAQs

Colorimeter - Beer’s Law, Lambert’s Law, Principle, Parts, Applications, FAQs

Edited By Team Careers360 | Updated on Jun 24, 2022 05:02 PM IST

Colorimetry is a scientific technique that employs the Beer–Lambert rule to determine the concentration of coloured substances in solutions. A colorimeter is a colorimetry tool.It refers to a device that aids in the absorption of a given wavelength of light by specific solutions. It measures absorbance and wavelength between 400 and 700 nm (nanometer), i.e. from the visible spectrum of light. Using the Beer-Lambert rule, the colorimeter is often used to determine the concentration of a known solute in a given solution. In the year 1870, Louis J Duboscq devised the colorimeter

Working principle of colorimeter

Let as discuss the working principle of the colorimeter.The photometric technique is used in a colorimeter asserts that when a beam of incident light of intensity (I0) passes through a solution, a portion of it is reflected (Ir), absorbed (Ia), and the rest is transmitted (It)

I0 =Ir +Ia+It

Because of the measurement of (I0), (Ir) is deleted in colorimeters, and it is sufficient to determine the value of (Ia). This is accomplished by utilising cells with equal characteristics to keep the amount of light reflected (Ir) constant. After that, (I0), and (It), are calculated.

Colorimeter is based on two basic laws of photometry, which show the mathematical relationship between amount of light absorbed and the concentration of the substance.

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Beer’s Law

The amount of light absorbed is proportional to the amount of solute in solution, as per Beer's law.

Log10(I0/It)=as c

Where as=Absorbency index

c =Concentration of the solution

Lambert’s Law

According to Lambert's law, the amount of light absorbed and thickness or length of the solution are directly proportional

A = Log10(I0/It)= asb

Where,

A = Absorbance of the solution

as= Absorbancy index

b = thickness of the solution

Parts of Colorimeter

A colorimeter has five key components.

  1. Light Source

A tungsten filament is the most popular light source in colorimeters.

  1. Monochromator

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Filters or monochromators are used to separate the light from the light source to select a specific wavelength.

  1. Sample holder

Color solutions are held in test tubes or cuvettes, which are composed of glass at visible wavelengths.

  1. Photodetector system

An electric current is generated when light falls on the detection system, which reflects the Galvanometer reading.

  1. Measuring device

The current from the detector is routed into the Galvanometer, which displays a metre reading that is directly proportional to light intensity.

Colorimeter diagram

Working procedure of galvanometer

Working of Colorimeter

There are five steps involved in the working of colorimeter

  1. It is necessary to calibrate the colorimeter before beginning the experiment. It's done with the help of standard solutions containing the known solute concentration to be determined. Fill the cuvettes with standard solutions and set them in the colorimeter's cuvette holder.

  2. A light ray of a specific wavelength for the assay is sent in the direction of the solution. The light is filtered through a succession of lenses and filters. Colored light passes through lenses and the filter splits a beam of light into different wavelengths so that only the required wavelength can pass through the standard test solution in the cuvette.

  3. The laser beam is transmitted, reflected, and absorbed by the solution when it reaches the cuvette. The photodetector device monitors the intensity of transmitted light when the transmitted ray hits it. It turns the data into electrical impulses, which it then sends to the galvanometer.

  4. The galvanometer's electrical signals are shown in a digital format. The absorbance or optical density of the investigated solution is the digital representation of the electrical signals. If the solution absorbs more light, more light is absorbed by the solution, and if the solution absorbs less light, more light is transmitted through the solution, which determines the galvanometer reading

  5. Formula for determining the concentration of a chemical in a test solution.

A = ∈cl

For standard and test solutions

∈ and l are constant

AT= CT

AS= CS

From these equations,

AT× CS= AS× CT

CT= (AT/AS) × CS

Where,

CT= Concentration of the test solution

AT= Absorbance/optical density of test solution

CS= Standard concentration

AS= Absorbance / optical density of standard solution

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Applications of Colorimeter

  • The colorimeter is a device that measures the optical density or absorbance of a coloured chemical to determine its concentration

  • A substance can be identified using a colorimeter by analyzing its absorption spectra in the visible area of the light spectrum.

  • It can also be used to determine the reaction's course by observing the rate of creation and disappearance of the light-absorbing compound in the visible spectrum of light.

  • It is utilized to calculate biochemical samples including urine, cerebrospinal fluid, plasma, and serum in laboratories and hospitals.

  • It is utilized in the production of paint.

  • It can be found in the textile and food industries.

  • It is used to analyze proteins, glucose, and other biological components quantitatively.

  • It is used to determine the quality of water.

  • It is used to figure out how much haemoglobin is in your blood.

The main advantage of colorimeter is that it is a low-cost method that is commonly employed in the quantitative examination of coloured samples, as well as one that is simple to carry and transport. The disadvantage is that it is not feasible to analyze colourless chemicals, and it does not work in the IR or UV regions.

Colorimeter v/s Spectrophotometer

  • The spectrophotometer consists of moving parts, is heavier, and is only suitable for laboratory use. The colorimeter consists of fixed parts and is lighter and therefore suitable for use in the field.

  • The spectrophotometer measures the amount of light that passes through a sample. Colorimeter measures light absorption.

  • The wavelength selector of the spectrophotometer is monochromator, wavelength range. The wavelength selector on the colorimeter is a color filter with a fixed wavelength.

Also check-

NCERT Chemistry Notes:

Frequently Asked Question (FAQs)

1. What is the colorimeter's principle?

  The method of determining the concentration of a coloured chemical in a solution is known as colorimetry. A colorimeter, also known by the name philtre photometer. It is an analytical equipment that is needed to calculate the concentration of a solution by measuring the absorption of a specific wavelength of light.. The colorimeter's working principle is based on Beer-law, and  Lambert's which states that the amount of light absorbed by a colour solution is directly proportional to the  concentration of the solution and the thickness of the solution

2. What makes a colorimeter different from a spectrophotometer ?

Ans: Let's discuss the difference between colorimeter and spectrophotometer. A colorimeter is a device that characterises colour samples in order to acquire objective colour characteristics measurements. A spectrophotometer is a sort of photometer (a light-measurement equipment) that can determine the intensity or, more precisely, the wavelength of light as a function of colour.

3. A colorimeter uses what wavelength?

Ans: A solution's colour might be intrinsic or produced by adding another chemical to it. The colorimeter measures the amount of light that is reflected through a sample at a wavelength that the user specifies. The front panel arrow keys can be used to select one of four wavelengths: 430 nm, 470 nm, 565 nm, or 635 nm.

4. What is meant by a photoelectric colorimeter?

Ans: A photoelectric colorimeter is a device that is used to quantify various chemicals such as glucose, blood urea, and blood enzymes.

5. What are the uses of a colorimeter?

Ans: A colorimeter is a device that determines the concentration of a coloured substance by detecting its optical density or absorbance. A colorimeter can be used to identify a chemical by studying its absorption spectra in the visible light spectrum. It can also be used to determine the reaction's progress by looking at the pace at which the light-absorbing molecule appears and disappears in the visible spectrum of light.

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