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Troubles

Field of view is cut off, or 
illuminated irregularly.

Causes

The nosepiece is not changed properly.

Remedies

Slightly rotate the nosepiece until it 
clicks into position.

2. Troubles in optical system:

The centre of the bulb is not 
coincidence with the centre of the 
objective.

There are dust or dirt on the glass 
surface of the lenses.

Position the bulb correctly.

Remove the dust and dirt.

Dust and dirt is visible in 

the field of view.

The condenser is too low.

Raise the condenser up.

Image quality is poor: 
insufficient contrast and 
image details lack 

definition.

There is no cover glass on the slide.

Put the cover glass on the slide.

The top lens of the objective is dirty.

Clean it.

Immersion objective is used without 
immersion oil.

Apply immersion oil.

There are bubbles in the immersion oil. Drive the bubbles out.

Special immersion oil is not used.

Use the special immersion oil.

The diameter of the iris diaphragm is too 

large or small

.

The condenser is not correctly 

positioned in the light path or inclined.

Position the condenser.

One side of the viewing 

field is dark

.

Image moves while 

focusing

The specimen is not caught stably by 
the clamp.

The image is yellow.

Blue filter is not used.

The viewing field is too 
dark

.

P.8

Remove the dust and dirt.

There are dust or dirt on the specimen 
surface.

There are dust or dirt on the glass 
surface of the lenses.

Remove the dust and dirt.

The cover glass is too thick or thin.

Choose the cover glass 0.17mm thick.

The specimen is mounted on the stage 

upside down.

Reverse the specimen.

There are dust or dirt on the glass 
surface of the lenses.

Remove the dust and dirt.

There are dust or dirt on the surface of 
the prisms.

Remove the dust and dirt.

Adjust the diameter of the iris 

diaphragm

.

The condenser is too low.

Raise the condenser up.

Slightly rotate the nosepiece until it 
clicks into position.

The objective is not correctly positioned 

in the light path.

The clamp is not fixed stably.

Fix the clamp stably on the stage.

Slightly rotate the nosepiece until it 
clicks into position.

The objective is not correctly positioned 

in the light path.

Catch the specimen stably.

Apply the blue filter.

The diameter of the iris diaphragm is too 
small

.

Adjust the diameter of the iris 

diaphragm larger

.

The condenser is too low.

Raise the condenser up.

There are dust or dirt on the glass 
surface of the lenses.

Remove the dust and dirt.

Summary of Contents for A11.1303 Series

Page 1: ...www optoecu com 1 15 sale cnoec com A11 1303 Student Biological Microscope Instruction Manual...

Page 2: ...oubleshoot them by yourself according the manual please contact us or our representative in you area 3 Safety Before change a bulb or need to open the base ensure that the microscope has been disconne...

Page 3: ...Focusing System P 5 10 Illumination System P 5 D How to Use and Assemble P 6 E Trouble Shooting P 7 1 Troubles in Operating P 7 2 Troubles in Optical System P 8 3 Troubles in Electric System P 8 F Mai...

Page 4: ...F20X or Huygenian eyepieces as 5X 6X 10X 12 5X 15X 16X The specifications of WF10X are showed as following P 1 a b e c d f Fig 1 The Principle Draft In this microscope the standard outfit of the objec...

Page 5: ...Down 17 Swtich 18 Plate for Adjusting Brightness 16 Screw for Bulb Changing 8 Screw for Centring the Condenser Fig 2 The Structure Draft 3 Mechanical tube length 160mm 4 Conjugated distance between o...

Page 6: ...process software help you to preview measure compare count save and delete Connecting the CCD camera with the TV the micro image will be showed for teaching V type dual observing head 360 rotatable On...

Page 7: ...screen User friendly sophisticated micro image process software help you to preview measure compare count save and delete 3 Insert the CCD camera with the CCD Linker Connecting the CCD camera with th...

Page 8: ...the knob 25 built in rack and pinion mechanical system controls the condenser up or down Usually raise the condenser higher when 100X or 40X objective is used Down the condenser lower when 10X or 4X...

Page 9: ...b D How to use and assemble 1 Unpack the microscope and its parts carefully Check and sort out all parts according to the packing list 2 For the convenience of packaging and delivering the components...

Page 10: ...e 4X and 10X objectives can never come into contacting with your micro slide specimen because of our built in stop The 40X and 100X objectives may occasionally touch the micro slide specimen But becau...

Page 11: ...ld is dark Image moves while focusing The specimen is not caught stably by the clamp The image is yellow Blue filter is not used The viewing field is too dark P 8 Remove the dust and dirt There are du...

Page 12: ...to choose model XSP21 01V or XSP21 01T microscope 1 See Fig 4 and connect the CCD camera with the microscope as following steps 1 Take the plastic dust cover off from the viewing head and screw the v...

Page 13: ...nd its PL pilot lamp is lighting 3 Whether the TV is turned on the mode AV or VIDEO 4 Whether the rod on the right of trinocular head is pushed out 5 Whether the microscope is focused correctly At thi...

Page 14: ...can observe by using common eyepiece at the same time of showing the micro image in the PC screen The electron eyepiece is also used in model XSP21 01M or XSP21 01B microscope See Fig 6 and connect th...

Page 15: ...een as the following ways 1 Turn the plate 19 to make the illuminator darker 2 Turn the plate 10 to make the diameter of the iris diaphragm smaller 3 Rotate the knob 23 to lower the ABBE condenser Whe...

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