Beruflich Dokumente
Kultur Dokumente
Operating Manual
TABLE OF CONTENTS
4 INSTALLATION ............................................................................. 9
5 OPERATIONS .............................................................................. 11
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6.2 CHECK THE FUNCTION OF MAIN DEVICE ............................................. 18
6.2.1 Check the wavelength range .................................................. 18
6.2.2 Check the transmittance repeatability ..................................... 18
6.2.3 Check fixed-point noise ......................................................... 18
6.2.4 Check the wavelength repeatability ......................................... 19
6.3 IDENTIFYING AND HANDLING THE COMMON MALFUNCTIONS ................... 19
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1 Applications and Features
monitoring and quality control as qualitative and quantitative analyses. The main features
the indicators such as resolution, photometric accuracy, stray light and stability. And
Special precision pre-adjustment lamps and lamp holder fittings. Not necessary to
re-adjust optical path for installation which is convenient for users without any
strong acid/alkali, which enhances its anti-corrosion properties. Effusion dish and
liquid storage container, which can be removed and cleaned, are mounted on the
4-position colorimetric cell shelf, with optional rectangular optical path colorimetric
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2 Specifications and Standard Accessories
2. Wavelength range:360nm1000nm
(A):-0.32.999
(F):19999
(C):09999
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3. Rectangular colorimetric dish: 1cm, 2cm, 3cm, 5cm
4. 5cm optical path colorimetric dish shelf
5. Pr-Nd filters
6. Holmium trioxide filters
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3 Product Appearance and Function Keys
lamp lights.
presetting
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lamps lights up in the sequence of
5. Display window 4-digit LED number Displays data and error information
11. The pull rod of the groove shelf: changes the position of sample groove (4)
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6 5
7 4
8 3
9 2
2
1
12 13
10 11
14 15
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4 Installation
This instrument is suitable for analytical experiments under lab conditions, the following
requirements are demanded due to the fact that it works with PC:
4.1.2 It is mounted on a steady working platform, free from vibration, direct sunlight,
4.1.4 Clean the instrument surface with room temperature water, do not use cleaning
4.1.5 If the equipment is to be used on the spot, please use the original package while
being moved. On-site working environment usually complies with the above
4.2.1 Note: the instrument and computer are packed in paper cardboard boxes
4.2.2 Please check the package before unpacking. If the package is incomplete or
Collision traces are found, please contact the insurance and transportation
department.
4.2.3 Open along the sealing tapes; carefully remove the main device and computer
(please save the outer package for the later using). Check the main device's
Standard and optional components according to the packing list. Contact the
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4.3 Installation
4.3.1 Remove the fixing tapes which are for transportation, clean the surface, then
check the power switch at the bottom of the device. Make sure voltage
requirement is consist with the local power supply, then put the main device on
a stable working station, keeping clearance more than 10 cm away from the
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5 Operations
5.1.1. Warming up
After the instrument is started, lamps and electric components need heat balance;
Purpose: adjusts both sides of the basic scale (along with 100%T adjustment),
Operation: open the sample cover (automatically shut the light valve) or shade
the optical path with opaque materials in the sample cell, then press 0%, then
Purpose: adjusts both sides of the basic scale (along with zero adjustment), and
before zero adjustment as to make the automatic increase inside the device to the
full reach);
Operating: empty sample used as background is put into the light valve of the
sample cell, shut the sample cover (automatically open the light valve), press
Note: when adjusting 100 T, the automatic gain system re-adjustment may
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influence 0%T. Check 0%T after adjustment. If there's any change, re-adjust 0%
for once.
Use the only knob on the equipment to adjust the current measuring wavelength.
The wavelength displays on the window to the left of the knob. Read the readings
vertically.
Note: this machine uses precision-linkage cutoff filters system, so when the knob
rotates, there will be metal gratings. Low gratings at 360nm-1000nm are normal.
5.1.5. Change the groove position to get various samples into optical path.
In the standard specification, the testing sample groove shelf has four positions.
It can be controlled by the pull rod on the front of the device. Open the sample cell
cover to observe the positions: the closest one to the user is 0, then 1, 2, 3
end, then pull 1, 2, 3 outward respectively. When the rod is at the right
position, the user may feel it. Please push it a bit to make sure the position is right.
solids;
Concentration factors: sets concentration factors when direct reading with the
read directly; also directly reads the concentration when setting concentration
factors;
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Use MODE to adjust the scales, which displays with the lamps for transmittance,
Warm up 5.1.1
8 Read data
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5.2.3 Determine the transmittance of transparent solutions
Warm up 5.1.1
6 Read data
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responding concentration on the curve
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6 Read the displaying value, i.e. the concentration
value
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6 Maintenance and error recognition
6.1.1 Notice
6.1.1.3 Clean the colorimetric dish with petroleum ether after using, and dry it
with lens paper, is kept colorimetric dish box for the next use.
It is necessary to open the cover when it is required to check up the device, including the
inner structures, optical path, and electric circuit, or to replace the source lamp. The
6.1.2.2 Open the wavelength knob cover and remove the knob;
6.1.2.3 Remove five M4 screws from the bottom of the equipment, open the
cover to check the equipment (avoid touch the high-voltage part on the
The equipment uses the long-service combining source lamp pre-corrected by the factory.
6.1.3.2 Remove the old illuminant light's parts: remove the connecting cable, 2
6.1.3.3 6.1.3.3 Re-install the new illuminant parts according to the reverse order
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the parts, and make sure the rectangle spots in the middle of the incident
slit.
6.1.4.1 Lift the equipment up a little, and move the front end out of the desk;
6.1.4.2 Take out the container on the bottom (beware of liquids flowing out
6.1.4.3 Dump the liquid, clean the container with water and dry it;
After the equipment finishes testing and maintenance, use the following to check to make
6.2.1.1 Switch on the host and pre-heat for 30 min, the mode is on
transmittance;
6.2.1.2 Turn the wavelength knob to both sides of the wavelength range, press
100%, 100%T will be achieved. Open the sample cell door, 0% can adjust to 0%T.
6.2.2.1 Set the host's wavelength to 550nm, equipment to 0%T and 100%T.
6.2.2.2 Set the transmittance to 40%T and check the display value around the
samples which are evenly absorbed nearby successively for three times (i.e. neutral
6.2.3.1 Set the wavelength to 550nm, and adjust to 0%T and 100%T.
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6.2.3.2 Set the scale to absorbance.
6.2.3.3 Observe the data in the window, which should be within the range of
0.002A.
companies) as samples.
6.2.4.3 Regard air as blank, adjust the equipment to 0%T and 100%T, add the
sample into the optical path, read the responding wavelength values to standard peak
6.2.4.4 Repeat 6.2.4.3 three times, the wavelength reading errors should be
1.5nm.
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3) Energy not 1. Illuminant light not light 1. Broken illuminant light to be
measured 2. The light valve not open changed, or no voltage output
3. The colorimetric ware 2. Check if the light valve works
completely cover the light 3. Put in at the right position
4. No signal output 4. Receiver broken to be
changed, or not plugged in, or
back contact
4) Cannot adjust 1. Not enough light energy 1. Select the right gain key;
to 100%T 2. Colorimetric dish not in check the light from the
position illuminant light in the incident
slit; low light voltageadjust
higher
2. Adjust it to the right position
5) Abnormal 1. Wrong solutions to the 1. Dealt with properly
photometry samples 2. Reduce matching errors
2. Colorimetric dish not 3. Check with (Pr-Nd) glass and
match adjust wavelength
3. Big wavelength errors
6) Err3 displays 1. Wrong operation 1. Power off then on again
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