User:Nadiezda Fernandez-Oropeza/Notebook/Notebook/2010/09/15: Difference between revisions

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====Related topics====
====Related topics====
====Primary Rays====
* Primary Ray
====Intensity of Illumination====
* Intensity of Illumination
====Optical Resolution====
* Optical Resolution





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Kohler Illumination

  • Discussion of Kholer Illumination and related topics

Kohler illumination is a method used in transmission-or –reflection microscopy that optimizes the specimen illumination. It was first introduced by August Kohler in 1893 and it is also known as double diaphragm illumination. Prior to Kohler illumination technique, all the other techniques could not prevent the filament of the light bulb (light source) from being visible in the sample plane. Kohler’s technique gets rid of this problem by creating parallel light rays to pass through the specimen, so that they are not in focus when creating the image of the specimen. The advantages of Kohler Illumination are: an evenly illuminated field and a bright image without glare and minimum heating of the specimen.

Process

The light is generated by the light source and it is first captured by the Collector Lens. The focal length from the collector to the light source to has to match the length of the filament. This way, it is ensured that the filament image is the right size when projected into the condenser aperture.

Then the light reaches the Field Lens, which brings the image of the filament into focus at the plane of the sub-stage condenser aperture diaphragm.

In some microscopes after the field lens there is a mirror that reflects the focused light that passed through the field lens and directs it to the Field Diaphragm.

The Field Diaphragm serves as filter and a virtual source of light since it regulates the amount of light that will reach the condenser. Therefore, it is one of the most important parts of the microscope. It also has the advantage of not affecting the optical resolution, numerical aperture, or the intensity of illumination. It can prevent glare as well.

After passing through the field diaphragm, the light reaches the Condenser. The function of a Condenser is to concentrate the light and generate what is known as a cone of light. On the condenser’s base there is another diaphragm called the Aperture Diaphragm. Its correct aperture is critical for proper Kohler illumination, since it determines the angle of the light cone reaching the specimen and consequently the Numerical Aperture.

Numerical Aperture is number that characterizes the range of angles over which the system can accept or emit light. It is given by the following equation:

                                             NA=nsinθ

Where, n is the index of refraction and θ is the half-angle of the maximum cone of light that can enter or exit the lens.

Something important to take into consideration is that the aperture or closure of the field diaphragm does not affect the angle and numerical aperture of the light cone. However, its closure slightly decreases the size of the lower portions of the light cones. Also, it is important to notice that the aperture or closure of the aperture diaphragm should not control the illumination intensity.

Set up for Kohler Illumination

  1. Switch on the light source
  2. Place the sample on the stage and then open the field diaphragm to its maximum aperture and notice whether or not the sample is illuminated.
  3. Focus the sample.
  4. Close the field diaphragm to its maximum and with the condenser focusing knobs bring the diaphragm edges to best focus possible.
  5. Center the image with the edges of the field diaphragm within the FOV.
  6. When it is centered, open the field diaphragm until its edge is outside the field.
  7. To reduce glare adjust the condenser diaphragm.
  8. Adjust the light intensity with a neutral density filter.

Related topics

  • Primary Ray
  • Intensity of Illumination
  • Optical Resolution