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Zeiss Axio Scope.A1 - Diagram of the Color Tables According to Michel-Lévy; Fig

Zeiss Axio Scope.A1
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OPERATION
Axio Scope.A1 Illumination and Contrasting Method Carl Zeiss
M60-2-0007 e 05/08 81
(3) Adjusting the microscope
Adjust the microscope as described in chapter
650H650H4.1.1 (3) for transmitted light/bright-field. Make sure
the eye distance is adjusted correctly on the binocular tube (see chapter
651H651H3.5.1).
Center the rotary stage Pol (
652H652HFig. 4-7/1).
Swing the polarizer (
653H653HFig. 4-7/3) in the beam path and position it to 0° if you are using a rotatable
polarizer.
Swing the analyzer module on the reflector turret in (
654H654HFig. 4-7/2) (or slide the analyzer slider into the
intermediate plate). Because of the crossed polarizers the field of view now appears dark.
Place the adjustment sample Pol on the microscope stage and turn until the sample appears dark.
Switch off the analyzer and align the graticule along the split cracks of the object.
Now switch the analyzer back on and remove the sample. The forward direction of polarizer and
analyzer are now parallel to the graticule (Polarizer EW, Analyzer NS).
Turn the rotary stage Pol with the sample, e.g. a synthetic fiber, so that the sample reaches maximal
darkness. The fiber is now parallel to one of the two graticule directions. If the deflection is significant
(5° and more) you will need to use a polarization microscope.
Do not change the eyepiece distance on the binocular tube any further in order to avoid
shifting the angular position of the graticule to the fiber.
Now turn the stage by approx. 45° until the
longitudinal axis of the fiber is pointing in NE-
SW direction (
655H655HFig. 4-9). The sample now shows
the strongest brightness (diagonal position). The
sample can have any color in this position.
Slide in the compensator λ.
Like the sample, the compensator λ is a
birefringent object, but it has a defined path
difference of 550 nm and a maximum oscillation
direction n
γ
pointing strongly to NE-SW.
When the compensator λ is put in, the sample
changes its color depending on its orientation (NE-
SW or NW-SE).
The changes in color are based on optical
interference. It is necessary to compare the
interference colors (phase differences) in both
diagonal positions (NE-SW and NW-SE).
Fig. 4-9 Diagram of the color tables
according to Michel-Lévy

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