Manual N6000
Manual N6000
Manual N6000
SPECTROPHOTOMETER
OPERATION MANUAL
Double beam UV-VIS spectrophotometer
N6000/N6000PLUS/N6000SPLUS
UV-VIS spectrophotometer USER’S MANUAL
CONTENT
I. Spectrophotometer Overview ...................................................................................................................................
1. Basic operating principle ..................................................................................................................................
2. Performance Indicators Definitions ..................................................................................................................
3. Application .......................................................................................................................................................
4. Using conditions ...............................................................................................................................................
AI. Product features and installation
1. Features ............................................................................................................................................................
2. Performance indicators ....................................................................................................................................
3. Main Functions .................................................................................................................................................
4. Structure introduction ......................................................................................................................................
5. Instrument installation .....................................................................................................................................
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UV-VIS spectrophotometer USER’S MANUAL
I. Spectrophotometer Overview
1) The nature of absorption: spectrophotometric analysis method is the use of substances to choose a different
wavelength of light absorption characteristics established. Typically using a prism or grating to obtain
monochromatic light that passes through the continuous monochromatic solution, the solution was measured
and the absorption of each wavelength, the absorption spectrum curve obtained.
Absorption spectrum selective absorption of light from the material, which is the material of macroscopic
phenomena, and the nature of the molecular absorption is the result of internal movement and light interaction.
When molecules absorb certain wavelengths of spectral energy or by some wavelengths of the spectrum is absorbed
to form the absorption spectra. The smaller the energy absorption, the wavelength of light corresponding to the
absorption peak at a longer wavelength. When the infrared absorbent is formed in the infrared absorption
spectrum, if the energy absorption is larger, the shorter the wavelength corresponding to the absorption peak at a
shorter wavelength, when generating the ultraviolet absorption spectra of absorption in the ultraviolet region.
2) Absorption Law - Lambert Beer law: when a parallel beam through the homogeneous solution, the
absorbance of monochromatic light is proportional to the product of the solution concentration and thickness.
Premise absorption laws established numeric expression: ① the incident light is monochromatic ② the
absorption process without interaction of each substance, the absorbance of each substance has additivity ③
the role of light and matter is limited to the absorption process, no fluorescent and photochemical scattering
negligible fluorescence efficiency is very small in most cases the color system, and the fluorescence emission is
isotropic, only a small portion along the transmitted light direction into the detector, the measurement of
absorbance is low, resulting in a negative deviation. Depends on the instrument to measure the impact on the
absorption of fluorescence great extent on the optical absorption cell and detector design.
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C. Reflection and scattering, absorption law applies only to homogeneous medium absorption system, turbid
solution so that the measured increase in absorbance due to scattering, resulting in deviation from Beer's law
E. Beer's law deviation polychromatic contrast, the majority of the photometer can only get close to monochromatic
light with a narrow lumen, in fact, there is still a polychromatic nature, can lead to deviations from Beer's law.
Deviation depends on the two monochromatic molar absorptivity difference △ ε, | △ ε | is very small, can be
approximated that monochromatic, at low concentrations, curve remains linear, but larger concentrations, with
concentration increases, AC curve bend more serious, there is Beer's law applies only to dilute solutions
F. Stray light, stray light entering the detector means is unnecessary components to be tested at other
wavelengths outside the range of the wavelength spectral bandwidth. The main dispersive element from a
prism or grating spectrometer, a mirror, a lens surface scattering, dust and other inner walls of
monochromator components and diffuse reflection and other scars, the stray light can cause serious
measurement error. The instrument is the smallest wavelength of energy, usually at a maximum stray light
G. Slit width, the slit width of the spectrum affects not only the purity, but also affect the absorbance. When
quantitative analysis in order to obtain sufficient measuring signal, the slit should be larger, in the qualitative
analysis of the use of a smaller slit when the entrance slit and the exit slit width equal to the width of the slit
H. Wavelength scale ruler of error, the wavelength of the gauge that wavelength accuracy of the instrument,
such as a large error or correction, the spectral measurements produce errors that affect the accuracy of
absorbance measurements (in the absorption spectrum of the peak of the more significant )
I. Impact of non-parallel incident, one of the prerequisites ear than the law is the use of a parallel incident
beam to ensure that all beams through the same thickness of the absorbing medium, when a large deviation
from parallelism when the incident beam, obviously lead to deviations from Beer's law. If the instrument is in
moderate-intensity beam deviation from parallelism, absorbance measurement error is generally caused by
J. Photometric scale error, photometric accuracy of the scale that is transmittance, which directly affects the
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UV-VIS spectrophotometer USER’S MANUAL
international institutions often used as a photometer industry type and CT autocollimation two structures;
2) Wavelength range: means for wavelength photometer can difference between maximum and minimum
3) Wavelength accuracy means the actual wavelength difference between the real wavelength and the setting
structural analysis of the impact is enormous. Way to check wavelength accuracy of many spectral lines as a
standard filter praseodymium, neodymium, holmium oxide filter, holmium oxide wavelength standard
solution, deuterium lamp or low pressure mercury lamp emission and interference filters and so on.
4) Wavelength repeatability: Wavelength Repeatability is the ability of the instrument to return the original
wavelength. It reflects the wavelength drive mechanism and the stability of the whole instrument;
5) Spectral bandwidth (sensitivity, resolution): refers to a peak spectral bands when the slit on the detector
detected through a monochromator energy half-width, expressed in nm wavelength, from another perspective
to understand this concept will more user-friendly: first, the monochromator exit slit represents not just the
physical size or geometry, it also represents the optical sense, this is the spectral bandwidth, we know that the
light from the failure of a single monochromator wavelength, but at a narrow wavelength spectral band are
arranged in the order, the number of spectral wavelength band comprises, represented by the spectral
bandwidth. Spectral bandwidth is a direct response to the quality level of monochromatic light from the
monochromator out. The index with the instrument resolution and sensitivity are similar, but different, they
react photometer performance quality from different sides. Resolution refers to the size of the instrument to
distinguish two adjacent wavelengths ability Sensitivity is measured at low concentrations do, when the
concentration changes by one unit to the detector signal caused by the change amount, it is subject to a
calibration curve (standard curve as the horizontal axis, the absorbance on the vertical axis) and a precision
instrument itself restrictions. Two measurement precision of the method is the same, the greater the sensitivity
calibration curve slope, while the slope equal, the higher the sensitivity, the better precision. It is noted that, in
order to obtain accurate test results, the natural bandwidth of the spectral bandwidth of the instrument
(Spectral Bandwidth referred SBW) and the analysis of samples (Natural Bandwidth referred NBW) ratio
should be less than 0.1, more than 99.5% can be obtained so that the measurement accuracy.
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6) Stray light: wavelength of stray light is irradiated onto the non-selection signal generated by the detector. It
is an important source of photometric analysis of errors, stray light limit the accuracy of the General
7) Photometric range: Refers to meet the photometric test range in various technical indicators, represented by A or
T;
8) Photometric accuracy: the true average value refers to the degree of compliance with a plurality of
measured; photometric accuracy check is usually through the use of repeated measurements of the neutral
density filter carefully film to a standard photometric detection. A neutral density filter for light in a
wavelength range having almost the same transmittance (or absorbance) of the filter, and the use of its
wavelength insensitive characteristic bandwidth changes, to check the accuracy of the optical instrument and
repeatability.
9) Photometric Repeatability: refers several times under the same conditions as measured in parallel, each
10) Noise: the sum of the instrument detects the unwanted signals, which is the purpose of the relative signal.
Generally, the spectrophotometer has two sources of noise, one from the light source, the second is derived
from the internal electronic noise inherent in the instrument, such as: power supply, amplifier, AD conversion
and the like. To reduce noise, improve signal to noise ratio, there must be a good electrical design. Noise
measurement repeatability test under low concentrations, but also affect test accuracy. Noise by averaging
11) Drift: refers to the degree of deviation from the instrument over time the starting value. It depends on the
stability, light stability of the electrical device and the like. Single-beam instrument, the warm-up time has a
12) Baseline flatness: refers to the distribution of the full wavelength range of the instrument noise.
3. Application
Subjects available for physics, chemistry, medicine, biology, pharmacology, geology and other scientific
research, is widely used in chemical, pharmaceutical, biological and chemical, metallurgy, light industry,
materials, environmental protection, medicine and other industries and laboratory analysis of the industry's
most one important quality control instruments, is essential for routine laboratory instruments.
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UV-VIS spectrophotometer USER’S MANUAL
4. Using conditions
Equipment should be installed away from the hot and humid environment, the instrument should be used in
16-35 ℃ ,45-80% humidity conditions. Please try to stay away from issuing magnetic, electric, high-frequency
waves of electrical devices, do not install the instrument in the air chlorine, hydrochloric acid gas, hydrogen
sulfide gas, such as sulfurous acid gas, corrosive gas Excessive places. Place the instrument table should be
smooth, without vibrations; nearby fan of the instrument should be left enough space to exhaust smoothly.
Instrument is best to use a single power outlet, power should ensure good grounding. Doing so may result in
equipment not working properly. If the local voltage instability, give the instrument is equipped with power
supply. The instrument should avoid direct sunlight. Avoid dusty environments.
1. Features
With low stray light, a high resolution structure of the double-beam optical monochromator, the instrument
Not only the instrument has automatically set 0% T and 100% T and other control functions as well as the
concentration of computing and data processing functions of a variety of methods, but also to prevent user
errors with special features, no worries when using . Scientific design, the use of new technologies, the optical,
mechanical, electrical and computer technology combined with organic, both to improve product performance
Large screen graphic LCD display can display the data and maps. The extensive machine software can complete
quantitative analysis, qualitative analysis, kinetics, DNA/Protein and other tests. coupled with powerful storage and
printing capabilities, the computer can complete all testing, analysis and data output with no conncetion with PC.
Optional equipment is also available on the Windows platform running UV Professional user application
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2. Performance indicators
3. Main Function
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4.Structure introduction
Overall structure is consisted of three parts: optical system, power system and micro-computer
2) Bottom view:
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Filter: Due to the grating spectrum spectral overlap exists between the problem class times, so the use of filters
to eliminate spectral overlap problem.
Action slits, the slits in the monochromator is large, and the resolution of the instrument is not only related to
the dispersion of the grating and the size of the image (i.e., the slit width). The slit is too large, color band is
deteriorated, is not conducive to the qualitative analysis, quantitative analysis also affect the linear range of
the calibration curve, the slit is too small, flux decreased, reducing the signal to noise ratio, affect the
measurement accuracy, the slits there are two general representation of the width, the actual width of the slit
of a knife-edge between the two expressed (in mm), the other to represent the bandwidth of spectral bands (in
nm).
D. Spectroscopic Room: contains a half-mirror, focusing lens and reflector to achieve a beam monochromator
out into two beams of light in different directions
E. Sample Chamber: fixed 2-cell holder, one is for reference solution, and the other is for sample solution. 8-
cell changer is optional.
F.Signal Board: Transfer to the motherboard processed signal detection light amplification
G. Main board: instrument micro control unit, control instruments light source switch, the motor rotates, the
signal processor display, etc.
5. Instrument installation
1) After unpacking, carefully check the packing list inside the object is complete and intact;
2) Determine whether the work environment to meet the foregoing requirements, the ambient temperature 10
~ 35 ℃, relative humidity less than 85%, operating voltage (220 3 22) V / (50 3 1) H3
3) The instrument is placed on a horizontal platform, the instrument should avoid direct sunlight and away
from electromagnetic launchers and high-power electrical devices, the use of the environment can not have
dust, corrosive gases and vibration;
4) Around the instrument can not be any obstacle to the flow of air around the instrument;
5) The company supplied with a power cord and make sure there are well-grounded power outlet line;
6) Check the sample chamber, ensure that there is not any solution, and foreign matter and the process of self-
test to ensure that the sample compartment lid is closed, you can not half-open (this is very important
otherwise affect the instrument self-test results and normal use!!!).
7) Turn on the instrument. Then the instrument make self-test. after self-test, the instrument can be operated
normally. in case there is an error alarm halfway, please refer to the chapter of instrument troubleshooting.
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UV-VIS spectrophotometer USER’S MANUAL
3. Basic operation
1) How to adjust the blank
In any test interface, put the cuvette containing the reference solution into cuvette slot, and pull it into light
path., press【Zero】key to adjust the blank.
2) How to set the wavelength
In any measurement interface press【Goλ】key to set the current working wavelength
3) Store files in txt or cvs format ( to use Excel format for simple spreadsheet file)
Check the communication port of the instrument is working properly. The result is displayed correct as √ and
an error as ×, the buzzer alarm.
3.Filter positioning
Check the instrument's filter motor and its locator is working correctly. The result is displayed correct as √,
an error as ×, the buzzer alarm.
4.Light positioning
Check the instrument light switch motor and its locator is working correctly. The result is displayed correctly
√, an error is displayed result is ×, the buzzer alarm.
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5.Printer check
Check the printer interface device is working properly. The result is displayed correctly √, an error is
displayed result is ×, the buzzer alarm.
Open the instrument tungsten light source, check the operating parameters of tungsten lights are working
properly. If the parameter is not working properly, then re-set the operating parameters of a tungsten lamp.
Change detections are always displayed correctly, the result is always √.
Open deuterium light source instrument operating parameters to check the deuterium lamp is working
correctly. If the parameter is not working properly, then re-set the operating parameters of the deuterium
lamp. Change detections are always displayed correctly, the result is always √.
Check signal detector instrument is working correctly. The result is displayed correctly √, an error is
displayed result is ×, the buzzer alarm.
9.Wavelength Calibration
Wavelength parameter checking instrument is working properly. Correct, then the pop-up boxes, please
confirm whether the user input wavelength calibration if no user input within five seconds, then skip this. If
the argument is wrong wavelength, then start looking for a deuterium lamp to automatically correct the
characteristic peak wavelength. Wavelength calibration result is displayed by √, the correction is not passed,
then the result is ×, the buzzer alarm.
Read instrument dark current of energy, checking eligibility. If the dark current in the proper range, which
means that the dark current is correct, then displays the results of √. If the dark current exceeds the maximum
setting, the user is prompted dark current error. The results are displayed as ×, the buzzer alarm.
Instrument system baseline reading is correct. If correct, then the pop-up box that asks the user whether to re-enter
the correction system baseline, baseline correction system default does not automatically skip the 3 seconds. If an
error does not exist or the baseline, the baseline correction system directly. Showing results √, the correction is not
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UV-VIS spectrophotometer USER’S MANUAL
Note: After power on the instrument, the instrument will automatically self-test and initialization until after
initialization is complete, the instrument will warm up for 20 minutes, 20 minutes warm-up time or press
[ESC] to skip preheating case, the instrument being prompted preparatory work environment, which is the
instrument re-calibration dark current, set the working parameters, etc., and then enter the main menu.
V. Photometric measurement
1. Function description
Photometric measurements are measuring the absorbance of the sample at a single wavelength, transmittance
or energy value.
3. Press the set button, enter the measurement mode settings menu, select the desired test mode, press [ENTER] to
confirm. If you choose the energy model, energy window appears and prompts to select the amplifier gain.
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UV-VIS spectrophotometer USER’S MANUAL
3.Set wavelength
Set the current working wavelength range 190nm-1100nm, press the up and down button to open wavelength
setting window, press [0] - [9] to enter the desired wavelength, press [CLEAR] to clear the input, press
[ENTER] to confirm. Input errors or exceeds the set range buzzer alarm.
4. Correction 100%T/0Abs
In two samples simultaneously into the two slots reference solution, and then press the [3ERO] key, the instrument
will be blank correction in the current wavelength. Display calibration is completed 100.0% T or 0.000Abs.
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UV-VIS spectrophotometer USER’S MANUAL
5. Measurement data
Calibrated with reference solution 100% T/0Abs, remove the rear slot reference sample solution into the sample
solution, and then press the [START] button, then perform a test, the sample data are immediately added to the list.
6. Delete data
Delete files Press [CLEAR] button, delete files prompt box will pop up, this operation will delete all the test
data currently under test. Select [Yes], the file will be deleted all the data, select [No] will return the test
window.
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1) Curve fitting mode: there are first order fitting, first order fitting through zero, and second order fitting.
Curve building method: there are standard sample method and coefficient method. Stand sample method is
2) to
prepare sample first , build curve, and then test sample. Coefficient method is to enter the known coefficient
and build standard curve, then to test sample.
3) the number of samples: at least 2 samples. More sample numbers, more accurate testing data.
4) concentration units: Enter the concentration value of each standard sample, because the parameters of the
curve has established limits, please select the appropriate concentration units.
5) wavelength value is required.
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UV-VIS spectrophotometer USER’S MANUAL
2. Standard sample measuring
Put various standard samples into cuvette holder orderly, and enter the concentration value of each sample,
then press [enter] key, read the absorbance of the sample. The input is completed, the data of the standard
sample is calculated automatically according to the parameters of the curve, displayed on the screen. If the
parameter is wrong, then the buzzer alarm, exit to establish the curve function.
3. Sample test
Put sample into cuvette holder and press [start] key, to get the concentration value of the current sample.
By opening the previously established curves for measurements. Select the appropriate quantitative test file,
press the [Enter] key to open a standard curve file.
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3. Data test
Press [START] to start measuring. the current real-time map will be on the screen.
4. Data list
press [Menu] key to check the scanning data after scanning finish.
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5. Slope calculation
after scanning, press [Menu] key to set starting time and end time for slope calculate.
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3. System baseline
Before the beginning of the measurement wavelength scan, you must create a system baseline. If you have
previously established a system baseline, you can skip. A long time without updating the system, re-create the
system baseline.
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UV-VIS spectrophotometer USER’S MANUAL
Press [Menu] key to view the baseline data after building system baseline.
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Before starting the measurement, the user must establish a baseline, that is, correction of the reference sample
100% T and 0Abs.
5. Begin testing
The tested samples were placed in the light path, press [START] to start the test.
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After the test is complete, you can choose to find peaks and valleys peaks and valleys value of test results.
7. Data list
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2. Set parameter
3. Correction 100%T/0Abs
After these parameters are set, place two reference solution for both colorimetric anti-tank, and then press the
[3ERO] key, the instrument will go to pre-school set a good few wavelengths were blank, went after the end of
the prior setting the minimum wavelength, and displays 100.0% T or 0.000Abs.
4. Data test
Remove the rear slot of the reference sample solution (the front does not move), and placed in the sample
solution is measured, and then press the [START] button will measure a set of data, if a second sample to be
measured, replace the solution after press [START], once on.
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UV-VIS spectrophotometer USER’S MANUAL
1. Function description
Protein / nucleic acid comprising two tests: Measurement of protein and single-stranded nucleic acid testing.
The curve and parameter is installed inside instrument for the two tests and users can make tests without
building standard curve again.
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UV-VIS spectrophotometer USER’S MANUAL
2. Parameter selection
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3. Set zero
Put reference solution into light path after selecting mode, press [3ero] key to set zero.
4. Test
put sample solution into light path, press [Start] key to measure.
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UV-VIS spectrophotometer USER’S MANUAL
Long time operation of instrument probably lead to drift of dark current. this function can make correction
for full range of dark current. Please make sure to cover the sample chamber lid when test dark current.
This function is to locate 656.1nm wavelength characteristic curve by looking deuterium lamp, wavelength
calibration.
If the seek fails deuterium lamp characteristic curve, the wavelength is invalid instrument, the instrument will
not work.
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UV-VIS spectrophotometer USER’S MANUAL
Set the time and date of the instrument, set the year, month, day, hour, minute, second. By the arrow keys to
select the year, month, day, hour, minute, second, through the numeric keys currently selected content. Press
Enter to confirm your entry, press Esc to abandon input.
Note: The time and date after the instrument is switched off, will not power down lost.
Of deuterium lamps and tungsten light source light switches to control the display of each light source life.
Up and down keys to select the source, press Enter to confirm the selection, the arrow keys to select the state
of the light source, and press Enter to confirm the selection,
Note: Open deuterium lamp need preheating after 15 seconds, before they can open
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5. General
7. File system
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1. Routine precautions
Any instrument is concerned, the correct use is the best safeguard for equipment maintenance, with emphasis
on the use of the environment and mobile devices, in addition to the requirements previously proposed for use,
we must also pay attention to the following issues:
1) Use the environment clean, the host instrument when not in use can be used to cover up the cloth cover to
prevent dust accumulation, the thermostat should be placed in long-term storage of dry indoor better,
2) The sample is placed over the pool should pay attention to the color being careful not to let the solution
spilled into the sample chamber, to prevent corrosion, for some volatile sample, we recommend using the
cuvette lid to prevent the impact of volatile gases to light , thus affecting the accuracy of the test equipment,
3) Any optical instrument road section screws and nuts, are not going to loose, to prevent the optical path
deviations affect the instrument is working properly,
4) The instrument must not mirror all the hard and soft hands or objects to touch, once leaving traces, will
produce stray light and reduce the effective energy punish and even cause damage to man-made instruments,
5) Instrument handling should be handled with care, can not be placed on the instrument shell weight, so as to
avoid affecting the optical path shift stability and accuracy,
6) The instrument can not work in bright light to ensure the accuracy of measurements,
7) Instrument power do not always do wavelength calibration, but can not always do, wavelength calibration
is recommended once a week in order to improve the accuracy of the measured data,
8) The instrument can not be left unused for a long time, so instead of reducing life, if not for some time, it is
recommended boot 1-2 times a week, each about half an hour.
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UV-VIS spectrophotometer USER’S MANUAL
2. Instrument Care and Maintenance
1) Check the sample chamber lens: regular checks on both sides of the sample chamber is about bias in quartz
lens position, look at whether fingerprints and other stains, if stains serious impact on the accuracy of the
measured value will be found after the stain, after a clean cloth moistened with alcohol to wipe in one direction
can decontamination is recommended to check once a month,
2) Wavelength accuracy check: Buy a calibrated holmium oxide solution in the instrument wavelength
scanning interface scanning range corresponding absorption spectra, measured by the detection of
reconciliation between the peak value of the calibration standard, the error is between wavelength accuracy of
the instrument error, it is recommended to check once a year,
3) Wavelength Accuracy cursory examination: After the completion of the self-test instrument interface into
any of the tests, set the wavelength to 546nm, and then open the sample chamber, take a small piece of white
paper on the left side of the lens at any of the sample chamber, watching the display in the white color of the
light sheet of paper, if the wavelength of light green indicates substantially correct, and when the result of the
test is larger away from their past experiences can be checked at any time.
1. Power failure
Failures Causes Solutions
No electrical outlet Check the external power supply
Power cord not plugged in Re-seated host power
Replace the spare fuse embedded or purchase
Socket switch inline fuse burned
the same size fuse 3A
Boot no reaction
Please contact the manufacturer or your local
Instrument socket switch is broken
dealer
Internal power supply board or Please contact the manufacturer or your local
transformer burned dealer
Opening the housing service personnel under
Internal wiring is loose display
the guidance of re-seated
Internal +5 V power supply is not Opening the housing service personnel under
Instrumentation normal or loose cable the guidance of re-seated
display is not Internal procedures by the
Service personnel under the guidance of
normal unexpected collapse of the
re-programming process
high-frequency voltage shock
The motherboard is not working Please contact the manufacturer or your local
properly dealer
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2. Self-test failure
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3. Other failure
Normal self tungsten Tungsten lights over 2000 hours or Refer to Chapter XV to replace
lamp wavelength bad tungsten lamp
region of low energy or Use too long causes the internal Please contact the manufacturer or
unstable optics moldy your local dealer
Experimental cuvette with a glass Use quartz cuvette
Both sides of the sample chamber Lens cleaning paper moistened with
Wavelength calibration
is too dirty lens alcohol to wipe dry
test normal low energy
Deuterium lamp is lit more than Refer to Chapter XV deuterium lamp
deuterium lamp or
2000 hours or bad replacement
unstable areas
Use too long causes the internal Please contact the manufacturer or
optics moldy your local dealer
2) Remove the lamp compartment cover three fixing screws and gently remove the lamp compartment cover.
(Note: If the instrument has been open for some time the lamp compartment cover will be very hot, please be
careful burns!!!)
3) Find the objects shown in the following figure, loose fastening sheet metal screws, pull out a tungsten lamp,
and the new tungsten lamp according to the original position seated, and put on a solid metal piece tighten the
screws (to ensure tungsten light positive)
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UV-VIS spectrophotometer USER’S MANUAL
Tungsten lamp
Metal sheet
4) Turn on the instrument, make tungsten lamp light, and convert the light source switching mirror to
5) Loosen the screws seat switch motors, seat motors to move the focus to switch into the slit in the smallest
6) Replace the lamp compartment cover (be careful not to press the right side of the line) and the instrument
housing (do not press the display line), and tighten the corresponding screws,
7) Re-POST, after the completion of the self-test mode in the wavelength photometric measurements were walked
340nm, 370nm, 1000nm, 1100nm let automatic zero. If it does not display the low energy lamp replacement is
completed, if there is low energy, repeat the above steps, if not enough, please contact the company sales staff.
2) Remove the lamp compartment cover three fixing screws and gently remove the lamp compartment cover.
(Note: If the instrument has been open for some time the lamp compartment cover will be very hot, please be
careful burns!!!)
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UV-VIS spectrophotometer USER’S MANUAL
3) Find the objects shown in the figure, as shown in Figure unscrew the screws and disconnect the plug on the
power supply board to remove the deuterium lamp socket, then put the new deuterium lamp installed in
accordance with the original position (note deuterium lamp light mouth will toward objective), and plug it in
the power supply board,
4) Turn on the instrument, make deuterium lamp light, and convert the light source switching mirror to
5) Loosen the screws fixed lens holder, fine-tune the focus lens holder into the slot on the smallest and
7) Loosen the screws seat switch motors, seat motors to move the focus to switch into the slit in the smallest
8) Replace the lamp compartment cover (be careful not to press the right side of the line) and the instrument
housing (do not press the display line), and tighten the corresponding screws,
9) Re-POST, after the completion of the self-test mode in the wavelength photometric measurements were
walked 200nm, 330nm, 340nm, 370nm, 1000nm, 1100nm let automatic zero. If you no longer displays low
energy lamp replacement is completed, if there is low energy, repeat the above steps, if not enough, please
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