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A condenser (right) and its respective diaphragm (left) A condenser is an optical lens that renders a divergent light beam from a point light source into a parallel or converging beam to illuminate an object to be imaged. Condensers are an essential part of any imaging device, such as microscopes, enlargers, slide projectors, and telescopes.
A bright-field microscope has many important parts including; the condenser, the objective lens, the ocular lens, the diaphragm, and the aperture. Some other pieces of the microscope that are commonly known are the arm, the head, the illuminator, the base, the stage, the adjusters, and the brightness adjuster.
The microscope's condenser is brought up close underneath the specimen to produce a wide divergence of polarised rays through a small point, and light intensity increased as much as possible (e.g., turning up the bulb and opening the diaphragm). A high power objective lens is typically used.
The Nomarski prism causes the two rays to come to a focal point outside the body of the prism, and so allows greater flexibility when setting up the microscope, as the prism can be actively focused. 3. The two rays are focused by the condenser for passage through the sample. These two rays are focused so they will pass through two adjacent ...
Light enters the microscope for illumination of the sample. A specially sized disc, the patch stop (see figure), blocks some light from the light source, leaving an outer ring of illumination. A wide phase annulus can also be reasonably substituted at low magnification. The condenser lens focuses the light towards the sample. The light enters ...
An inverted microscope is a microscope with its light source and condenser on the top, above the stage pointing down, while the objectives and turret are below the stage pointing up. It was invented in 1850 by J. Lawrence Smith , a faculty member of Tulane University (then named the Medical College of Louisiana).
The resolution of a microscope is defined as the minimum separation needed between two objects under examination in order for the microscope to discern them as separate objects. This minimum distance is labelled δ. If two objects are separated by a distance shorter than δ, then they will appear as a single object in the microscope.
A requirement for this method is that the incoming beam of light is as parallel as possible. This requires the closing down of the sub-stage condenser iris. Closing the sub-stage condenser iris decreases the resolution of the particle and increases the depth of field over which other objects may interfere with the effect seen.