keyence_sop
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keyence_sop [2020/11/10 19:02] – furst | keyence_sop [2021/04/27 17:41] (current) – furst | ||
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- | Name | + | Name (Last, First) |
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Group or Company | Group or Company | ||
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- | Signature | + | Signature |
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====Overview: | ====Overview: | ||
* This training provides an introduction to using and operating the Keyence microscope including: | * This training provides an introduction to using and operating the Keyence microscope including: | ||
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====Safety==== | ====Safety==== | ||
+ | * Do not leave lighting elements on | ||
+ | * Do not crash the objectives | ||
+ | * If replacing the bulb in the MI-150 wear gloves to avoid getting oil on the halogen lamp bulb | ||
- | + | =====Microscope Setup===== | |
- | ====Microscope Setup==== | + | ====At the microscope:==== |
- | **At the microscope:** | + | - **Changing objectives** |
- | - Changing objectives | + | - Press the button on the top of the objective (right above the Y axis of rotation screw) |
- | - Press the button on the top of the objective (right above the Y axis of rotation screw) | + | |
- Twist the camera body counterclockwise and carefully lift directly off. Set carefully on its side to avoid damaging the lenses in the camera assembly | - Twist the camera body counterclockwise and carefully lift directly off. Set carefully on its side to avoid damaging the lenses in the camera assembly | ||
- Loosen the large plastic wingnut screw located above the axis of rotation adjustment on the objective. (DO NOT ADJUST AXIS OF ROTATION SCREWS) | - Loosen the large plastic wingnut screw located above the axis of rotation adjustment on the objective. (DO NOT ADJUST AXIS OF ROTATION SCREWS) | ||
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- Make sure zoom knob is locked into a set zoom level detent | - Make sure zoom knob is locked into a set zoom level detent | ||
- Follow steps to initialize the XY stage | - Follow steps to initialize the XY stage | ||
- | - Tilting the head | + | - **Tilting the head** |
- | - The microscope head is able to tilt up to 90 degrees clockwise in order to better image samples. Caution should be taken to avoid crashing the objective into the sample or stage when head is tilted. | + | - The microscope head is able to tilt up to 90 degrees clockwise in order to better image samples. Caution should be taken to avoid crashing the objective into the sample or stage when head is tilted. |
- Loosen the tilt lock knob a turn or two max (until the knob loosens) | - Loosen the tilt lock knob a turn or two max (until the knob loosens) | ||
- With a HAND ON THE MICROSCOPE HEAD rotate the locking lever counter clockwise to its vertical position | - With a HAND ON THE MICROSCOPE HEAD rotate the locking lever counter clockwise to its vertical position | ||
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- Lock the head in its tilted position using the large tilt lock knob. Make sure knob is snug before letting go of the head but do not overtighten | - Lock the head in its tilted position using the large tilt lock knob. Make sure knob is snug before letting go of the head but do not overtighten | ||
- If desired angle is greater then 60 degrees, pull the locking pin out away from the microscope before retightening the tilt lock knob. This should allow the microscope head to tilt up to 90 degrees. Be incredibly careful as the stage and objective will become very close at angles above 60 degrees. | - If desired angle is greater then 60 degrees, pull the locking pin out away from the microscope before retightening the tilt lock knob. This should allow the microscope head to tilt up to 90 degrees. Be incredibly careful as the stage and objective will become very close at angles above 60 degrees. | ||
- | - Changing lighting elements | + | - **Changing lighting elements** \\ {{: |
- Switching to fiberoptic Epi-illumination for 100-1000x objective | - Switching to fiberoptic Epi-illumination for 100-1000x objective | ||
- With the 100-1000x objective installed turn on the MI-150 fiberoptic lamp | - With the 100-1000x objective installed turn on the MI-150 fiberoptic lamp | ||
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- Remove the black and white disk in the center of the stage being careful not to bump the objective | - Remove the black and white disk in the center of the stage being careful not to bump the objective | ||
- In the drawer containing the objectives there is also a class disk which can be placed in the stage center. | - In the drawer containing the objectives there is also a class disk which can be placed in the stage center. | ||
- | - Moving/ | + | - **Moving/ |
- X,Y movement | - X,Y movement | ||
- | - X and Y positioning of the sample can be done using the joystick on the console | + | - X and Y positioning of the sample can be done using the joystick on the console |
- Double clicking a location on the sample on the Keyence screen will center that part of the sample | - Double clicking a location on the sample on the Keyence screen will center that part of the sample | ||
- Z movement | - Z movement | ||
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- | **At the Computer: | + | ====At the Computer: |
- | - Initialize the XY stage | + | - **Initialize the XY stage** |
- The XY stage needs to be initialized every time a objective is switched or the microscope is power cycled | - The XY stage needs to be initialized every time a objective is switched or the microscope is power cycled | ||
- The microscope should prompt the user after objective is switched but can be done manually through " | - The microscope should prompt the user after objective is switched but can be done manually through " | ||
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- Be sure the black side of the XY stage disk is facing up and is fully in place | - Be sure the black side of the XY stage disk is facing up and is fully in place | ||
- click " | - click " | ||
- | - Software lighting and Image Quality | + | - **Software lighting and Image Quality** |
- Within Software lighting two tabs are available: | - Within Software lighting two tabs are available: | ||
- | - Brightness | + | - Brightness |
- Adjust shutter speed and camera settings (set to auto) | - Adjust shutter speed and camera settings (set to auto) | ||
- | - Lighting | + | - Lighting |
- Epi-illumination | - Epi-illumination | ||
- Adjust/turn on internal objective illumination (press " | - Adjust/turn on internal objective illumination (press " | ||
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- When 100-1000x objective is installed Epi-illumination is handled by the fiberoptic MI-150 located next to the microscope | - When 100-1000x objective is installed Epi-illumination is handled by the fiberoptic MI-150 located next to the microscope | ||
- Increased contrast can be achieved by turning on HDR under the Image Quality tab | - Increased contrast can be achieved by turning on HDR under the Image Quality tab | ||
- | - Depth up | + | - **Depth up** |
- The Keyence microscope is capable of taking hundreds of images as it raises the objective to capture an image larger depth of field. This is useful for observing objects that do not lie on a flat plane and would normally not be completely in focus. This image also contains depth mapping data which can be used to not only take XY and Z measurements, | - The Keyence microscope is capable of taking hundreds of images as it raises the objective to capture an image larger depth of field. This is useful for observing objects that do not lie on a flat plane and would normally not be completely in focus. This image also contains depth mapping data which can be used to not only take XY and Z measurements, | ||
- Select "depth up" from the right hand side bar then "quick composition and 3D" | - Select "depth up" from the right hand side bar then "quick composition and 3D" | ||
- | - Focus the microscope slightly below the lowest point on the object | + | - Focus the microscope slightly below the lowest point on the object |
- | - Click "3D Display" | + | - Click "3D Display" |
- | - Measure | + | - **Measure** |
- | - Measurements can be taken by selecting the " | + | - Measurements can be taken by selecting the " |
- | - Stitching | + | - Select the desired tool and desired points to measure from on the sample. The microscope will automatically display the length of lines or radius of arcs/ |
- | - saving images | + | |
+ | - **Stitching** | ||
+ | - Center surround stitching \\ {{: | ||
+ | - Center the sample in the frame and select " | ||
+ | - select " | ||
+ | - click "Start stitching" | ||
+ | - Stitch after specifying the area \\ {{: | ||
+ | - Click select range | ||
+ | - Position the microscope as the minimum x position and select left, then maximum x position and select right | ||
+ | - Position the microscope as the minimum y position and select top, then maximum y position and select bottom | ||
+ | - Select start stitching and the microscope will automatically stitch together an image from the bounds set | ||
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+ | ====Post Imaging==== | ||
+ | * If using another objective, please replace the 20-200x objective and initialize the microscope before leaving | ||
+ | * Be sure to turn off the microscope light as well as the fiberoptic MI-150 when imaging is finished | ||
+ | * If different light diffusers or polarizers are used during imaging please replace the original glass before leaving | ||
- | ====Maintenance==== | ||
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Tool Lead: \\ | Tool Lead: \\ | ||
Contact: andrewfurst@ucsb.edu | Contact: andrewfurst@ucsb.edu | ||
- | ====Safety | + | |
+ | ====Safety==== | ||
+ | * Do not leave lighting elements on | ||
+ | * Do not crash the objectives | ||
+ | * If replacing the bulb in the MI-150 wear gloves to avoid getting oil on the halogen lamp bulb | ||
====Safe Operation Procedures Review==== | ====Safe Operation Procedures Review==== | ||
- | ====Post Processing==== | + | |
- | ====Maintenance==== | + | |
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keyence_sop.1605034932.txt.gz · Last modified: 2020/11/10 19:02 by furst