Physics Investigatory Project
Physics Investigatory Project
Physics Investigatory Project
INDEX OF DIFFERENT
SOLUTIONS BY USING
TRAVELLING MICROSCOPE
KANICA CHOPRA
2014-2015
STUDENT S INFORMATION
NAME
KANICA CHOPRA
CLASS
XII A
SCHOOL
ROLL NO
YEAR
2014-2015
CERTIFICATE OF
AUTHENTICITY
This is to certify that KANICA CHOPRA a student of class
XII A has
REFRECTIVE
TRAVELLINNG
INDEX
OF
DIFFERENT
MICROSCOPE
Under
SOLUTION
the
BY
guidance
USING
of
(Examiner)
(Subject teacher)
ACKNOWLEDEGEMENT
This project would not have been feasible without the proper and
rigorous guidance of my Physics Teacher
_____________________________who
guided
me
Mrs.
throughout
this
INTRODUCTION
This test is based on the work done by Wilson [1935] and Milk
Regulations 1963. This test is used to check the contamination of
bacteria in te sample of milk. It tells us about the viable count of
Bacteria that may be present in the milk. So by this particular test
we can have a clue about the quality of milk we have that whether
it is invaded by bacteria or not and in which quantity these are
present.
A compound microscope is a microscope fitted with two or more convex lenses. The high magnification
produced by these lenses together enables a detailed study of micro-organisms, cells and tissues. These types
of microscopes are therefore widely used in scientific and medical research.
Zacharias Janssen, a Dutch spectacle maker, invented the compound microscope in 1590.Galileo unveiled
his version in 1610. Several other scientists and inventors later helped refine its design and working
capabilities.
The basic design of a compound light microscope consists of convex lenses fitted at either end of a hollow
tube. This tube is fitted on an adjustable, rotary nosepiece. There is an adjustable stage under the nosepiece;
specimen slides are placed or fitted on this stage for observation through the lenses. The stage has a window
or hole in it through which a light source can illuminate the specimen under observation.
The light source can be a mirror reflecting natural light or a lamp in the base. The illuminating beam passes
through the stage window and through the specimen. The light brightens the area around the specimen,
making the specimen stand out in contrast. The level of contrast is controlled by controlling the amount of
illumination. A brighter or dimmer effect is achieved by opening or closing an iris diaphragm under the stage,
or by adjusting the height of the lamp.
Compound microscope
The upper lenses of the compound microscope, the ones closer to the viewer's eye, are the ocular lenses or
the eyepiece. Monocular microscopes have one eyepiece, and binocular ones a double eyepiece. Trinocular
versions have a double eyepiece and a camera-fitting arrangement.
The objective lenses are the lower lenses closer to the object being viewed. There can be three or four different
ones located on the rotary nose-piece of a compound microscope. The nosepiece is rotated to select the
objective lenses that offer the magnification most suited for a particular specimen.
The four objective lenses are the scanning power objective, the low power objective, the high dry objective and
the oil immersion objective. They have magnifications of 4X, 10X, 40X and 100X respectively. The ocular
lenses usually have a magnification of 10X.
To get the total magnification factor, the eyepiece magnification is multiplied with the objective magnification.
So, with 10X ocular lenses and 100X objective lenses, a magnification of 1000X is achieved. This means, a
viewed object is magnified 1000 times its actual size. Higher magnifications are also possible.
When an object is in focus, the objective lenses form a real, inverted image of the object at a point inside the
principle focus of the ocular lenses. The ocular lenses then treat this inverted image as the object and
produce an upright image of it. This image is the enlarged one seen by the observer.
However, it is also important to note that light changes direction when it travels from one medium to another.
Therefore, another method to calculate the refractive index of a medium is to apply Snells law, which will be
very important later in our discussion of refractometers.
The refractive index of any other medium is defined relative to the refractive index of a vacuum, which is
assigned a value of 1. Thus, a refractive index of 1.33 for water means that light travels 1.33 times faster in a
vacuum than in water.
1. Temperature
o
A higher temperature means the liquid becomes less dense and less viscous, causing light to
travel faster in the medium. This results in a smaller value for the refractive index due to a
smaller ratio.
A lower temperature means the liquid becomes denser and has a higher viscosity, causing light
to travel slower in the medium. This results in a larger value for the refractive index due to a
larger ratio.
2. Wavelength of light
o
The refractive index varies with wavelength linearly because different wavelengths interfere to
different extents with the atoms of the medium.
It is important to use monochromatic light to prevent dispersion of light into different colours.
The sodium D line at 598 nm is the most frequently used wavelength of light for a
refractometer.
refractometer works based on the principle that light bends when it enters a different medium. This
instrument measures the angle of refraction of light rays passing through the unknown sample. This
measurement combined with the knowledge of the refractive index of the medium directly in contact with the
unknown sample, are used to determine the refractive index of the unknown sample by applying Snells law
described above.
The following cross sectional diagram illustrates the inner-workings of a refractometer. A light source shines
on the illuminating prism and light rays enter the sample moving in different directions. The largest angle of
incidence produced by a light ray (i) produces the largest possible angle of refraction (B). The other light
rays entering the refracting prism all have a smaller refraction angle and lie to the left of point C. A detector
at the back of the refracting prism produces the light and dark regions. In an Abbe refractometer, a detector
is not present and there is more optics but the general scheme remains the same. Samples with different
refractive indexes produce different angles of refraction which will cause a shift in the borderline between the
light and dark regions. The borderlines position is then used to establish the refractive index of different
samples.