Tsunami - Beckman Institute Laser Resource Center
Tsunami - Beckman Institute Laser Resource Center
Tsunami - Beckman Institute Laser Resource Center
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I ,111 111 I<br />
Maintenance<br />
CAUTION<br />
Do not use lens tissue designated for cleaning eye glasses. Such tissue<br />
contains silicones. These molecules bind themselves to the optic<br />
coatings and can cause permanent damage. Also, do not use cotton<br />
swabs, e.g., Q-Tips" . Solvents dissolve the glue used to fasten the<br />
cotton to the stick, resulting in contaminated coatings. Only use<br />
photographic lens tissue to clean optical components.<br />
General Procedures for Cleaning Optics<br />
With the exception of the rod, the AOM, the GTI (ps configuration), and<br />
prisms (fs configuration), all optics must be removed from their mounts<br />
for cleaning. However, only mirrors MS, the output coupler Mlo, the<br />
Brewster windows, and the beam splitter must be removed from their<br />
holder to clean the second surface.<br />
CAUTION<br />
DO NOT remove or adjust fs prisms Prl to Pr4, or adjust the mirror<br />
mounts of M6, M7, M8, or Ms. These optics are prealigned at the factory<br />
and are not to be disturbed unless specifically told to do so elsewhere<br />
in this manual. A service call might be required if disturbed.<br />
WARNING<br />
When replacing optics holders, DO NOT tighten them too much or<br />
you will press the optic against the three steel alignment balls too hard<br />
and chip the optic. Simply screw on the holder until you feel contact.<br />
Also, be careful not to cross-thread the holder when you screw it on.<br />
1. Use a squeeze bulb or dry nitrogen to clean away any dust or grit before<br />
cleaning optics with solvent. If canned air is used, hold the can in<br />
an upright position to avoid liquid freon from contaminating the optic.<br />
2. Whenever possible, clean the optic using the "drop and drag" method<br />
(Figure 9-1).<br />
a. Hold the optic horizontal with its coated surface up. Place a sheet<br />
of lens tissue over it, and squeeze a drop or two of acetone or<br />
methanol onto it.<br />
b. Slowly draw the tissue across the surface to remove dissolved<br />
contaminants and to dry the surface.<br />
Pull the tissue slow enough so the solvent evaporation front<br />
immediately follows the tissue.