VISHALRAJ K
HCA20M10
*CONTENT*
Introduction
Principle
Beer’s law
Lambert’s law
Photoelectric colorimeter
Uses
Advantages & Disadvantages
*INTRODUCTION*
Colorimetry is the technology used in science
labs to measure the concentration of a
solution from its light absorbing properties.
It is similar to spectrophotometry.
Colorimetry was invited in the
year of 1870 by Louis J Doboscq.
*PRINCIPLE*
When a monochromatic light passes through
a coloured solution, some specific wavelength
of light are absorbed which is related to
colour intensity.
Log IO/IE = KCT
K > Constant
C > Concentration
T > Thickness
IO > Intensity
IE > Emitted
The amount of light absorbed or transmitted
by a colour solution is in accordance with two
law i.e. Beer’s & Lambert’s law.
*BEER’S LAW*
According to this law the amount of light
absorbed is proportional to the concentration
of the solute.
Intensity of the emitted light (IO) decreased
with increase in concentration.
*LAMBERT’S LAW*
The lambert’s law states that the amount of
light absorbed is directly proportional to the
length and thickness of the solution under
analysis.
Intensity of emitted light (IO) decreased with
increase in thickness and length.
*PHOTOELECTRIC COLORIMETER*
The Photoelectric colorimeter is commonly
employed for measurement of different
substance in the blood like glucose, blood
urea, blood enzymes, and others.
It is used for measuring the transmittance
and absorbance of light passing through a
liquid sample.
The different types of colorimeter are single
beam filter photometer, double beam
photometer, probe - type photometer, multi –
channel photometer, and portable photometer.
The colorimeter is widely used
in biochemical laboratories for
quantitative analysis of
specific substances in human
body fluids (blood and urine).
It measures absorbance and wavelength
between 400 to700 nm i.e. from the visible
spectrum of light of the electromagnetic
spectrum.
The light (tungsten lamp) passes through a
condensing lens .
And the filter helps to split a beam of light into
different wave lengths allowing only the
required wavelength to pass through it reach
the solution.
When the beam of light reaches solution, it is
transmitted, reflected, and absorbed by the
solution.
The transmitted rays falls on the photocell
system where it measures the intensity of
transmitted light.
Photocell converts it into the electrical signals
and send it to the galvanometer.
The electric signals measured by the
galvanometer are displayed in the digital
form.
*USES*
It is used in laboratories and hospitals to
estimate biochemical sample such as urine,
cerebrospinal fluid, plasma, serum, etc…
Used in quantitative analysis of proteins,
glucose, and other biochemical compounds.
Such as used to test water quality.
And to determine the concentration of
haemoglobin in the blood.
*ADVANTAGES & DISADVANTAGES*
Some benefits are as follows:
It is an expensive method, widely used in the
quantitative analysis of coloured samples,
easy to carry, and transport.
Some disadvantages are as follow:
Analysis of colourless compound is not
possible, does not working in IR and UV
regions.
 colorimetry

colorimetry

  • 1.
  • 2.
  • 3.
    *INTRODUCTION* Colorimetry is thetechnology used in science labs to measure the concentration of a solution from its light absorbing properties. It is similar to spectrophotometry. Colorimetry was invited in the year of 1870 by Louis J Doboscq.
  • 4.
    *PRINCIPLE* When a monochromaticlight passes through a coloured solution, some specific wavelength of light are absorbed which is related to colour intensity.
  • 5.
    Log IO/IE =KCT K > Constant C > Concentration T > Thickness IO > Intensity IE > Emitted The amount of light absorbed or transmitted by a colour solution is in accordance with two law i.e. Beer’s & Lambert’s law.
  • 6.
    *BEER’S LAW* According tothis law the amount of light absorbed is proportional to the concentration of the solute. Intensity of the emitted light (IO) decreased with increase in concentration.
  • 7.
    *LAMBERT’S LAW* The lambert’slaw states that the amount of light absorbed is directly proportional to the length and thickness of the solution under analysis. Intensity of emitted light (IO) decreased with increase in thickness and length.
  • 8.
    *PHOTOELECTRIC COLORIMETER* The Photoelectriccolorimeter is commonly employed for measurement of different substance in the blood like glucose, blood urea, blood enzymes, and others. It is used for measuring the transmittance and absorbance of light passing through a liquid sample.
  • 9.
    The different typesof colorimeter are single beam filter photometer, double beam photometer, probe - type photometer, multi – channel photometer, and portable photometer. The colorimeter is widely used in biochemical laboratories for quantitative analysis of specific substances in human body fluids (blood and urine).
  • 10.
    It measures absorbanceand wavelength between 400 to700 nm i.e. from the visible spectrum of light of the electromagnetic spectrum. The light (tungsten lamp) passes through a condensing lens . And the filter helps to split a beam of light into different wave lengths allowing only the required wavelength to pass through it reach the solution.
  • 11.
    When the beamof light reaches solution, it is transmitted, reflected, and absorbed by the solution. The transmitted rays falls on the photocell system where it measures the intensity of transmitted light. Photocell converts it into the electrical signals and send it to the galvanometer. The electric signals measured by the galvanometer are displayed in the digital form.
  • 12.
    *USES* It is usedin laboratories and hospitals to estimate biochemical sample such as urine, cerebrospinal fluid, plasma, serum, etc… Used in quantitative analysis of proteins, glucose, and other biochemical compounds. Such as used to test water quality. And to determine the concentration of haemoglobin in the blood.
  • 13.
    *ADVANTAGES & DISADVANTAGES* Somebenefits are as follows: It is an expensive method, widely used in the quantitative analysis of coloured samples, easy to carry, and transport. Some disadvantages are as follow: Analysis of colourless compound is not possible, does not working in IR and UV regions.