Uv Vis

SQ-2800 Single Beam
Scanning UV/Visible
Spectrophotometer
User’s Guide
United Products & Instruments Inc.

182 Ridge Road, Suite E, Dayton, NJ 08810
U.S.A.
Tel: 732-274-1155 / 1-800-588-9776

Fax: 732-274-1151
www.unico1.com
H H [email protected]
Contents
Safety ……………………………………………………………………………………… 2
General …………………………………………………………………………………… 2
Electrical ………………………………………………………………………………….. 2
Warning ………………………………………………………………….……………….. 2
Performance ………………………………………………………..……………..…… 3
Radio Interference …………………..………………………………………………….. 3
Introduction ………………………………………………………….………………… 3
Working Principle ………………………………………………………..…..……….. 4
Unpacking Instructions …………..……………………………………………………. 5
Specifications ……………………………………………..………………..……….… 5
Installation ……………………………………………………………………………..…. 5
Operation ………………………………………………………..……………………..… 6
Prepare the Spectrophotometer ………………………………………..………..… 6
Description of keys ………… ………………………………………..……….. 6
Turn on spectrophotometer … ……………………………………………….….. 7
Basic operation………………………………………………………………………. 8
Analyze Sample ………………………………………………..………………………… 13
Basic Mode ……………………………………………………………………….…..13
Quantitative …………………………………………………………………….….. 15
Wavelength Scan …………………..…………………………………………….... 21
Kinetics …….……………………………………………………………………..… 26
DNA/Protein ………………………………………………………….…………… 28
Multi Wavelength …………………………………………………………………....31
Setting and Calibration ……………………………………………….……………. 33
Utility …………………………………………….………………………………….… 33
Defined Tests ……………………………..…………………………………………… 43
Appendix A ………………………………………………………………..………… 46
Appendix B ………………………………………………………………………..… 47
Appendix C ………………………………………………………………………..… 54
2
Safety:
The safety statements in this manual comply with the requirements of the
HEALTH AND SAFETY AT WORK ACT, 1974.
Read the following before installing and using the instrument and its
accessories. The UNICO SQ-2800 should be operated by appropriate
laboratory technicians.
General:
The apparatus described in this manual is designed to be used by properly
trained personnel in a suitably equipped laboratory. For the correct and safe
use of this apparatus it is essential that laboratory personnel follow generally
accepted safe procedures in addition to the safety precautions called for in
this manual.
The covers on this instrument may be removed for servicing. However, the
inside of the power supply unit is a hazardous area and its cover should not
be removed under any circumstances. There are no serviceable components
inside this power supply unit. For UNICO SQ-2800, avoid touching the high
voltage power supply at all times.
Some of the chemicals used in spectrophotometry are corrosive and/or

inflammable and samples may be radioactive, toxic, or potentially infective.
Care should be taken to follow the normal laboratory procedures for handling
chemicals and samples.
Electrical:
Before switching on the apparatus, make sure it is set to the voltage of the
local power supply (see Installation).
The power cord shall be inserted in a socket provided with a protective earth
contact. The protective action must not be negated by the use of an extension
cord without a protective conductor.
Warning:
Any interruption of the protective conductor inside or outside the apparatus or
disconnection of the protective earth terminal is likely to make the apparatus
dangerous. Intentional interruption is prohibited.
Whenever it is likely that the protection has been impaired, the apparatus
shall be made inoperative and be secured against any unintended operation.
NEVER touch or handle the power supply on UNICO SQ-2800 due to the high
voltage.
The protection is likely to be impaired if, for example, the apparatus
 Shows visible damage
 Fails to perform the intended measurements
 Has been subjected to prolonged storage under unfavorable conditions
3
 Has been subjected to severe transport stresses
Performance:
To ensure that the instrument is working within its specification, especially
when making measurements of an important nature, carry out performance
checks with particular reference to wavelength and absorbance accuracy.
Performance checks are detailed in this manual.
Radio Interference:
For compliance with the EMC standards referred to in the EC Declaration of
Conformity, it is necessary that only shielded cables supplied by us are used
when connecting the instrument to computers and accessories.
Introduction:
The UNICO SQ-2800 model spectrophotometer (Fig 1) is a single beam,
general purpose instrument designed to meet the needs of the Conventional
Laboratory, The UNICO SQ-2800 model spectrophotometer is ideal for
various applications, such as: Chemistry, Biochemistry, Biotechnology,
Petrochemistry, Environmental Protection, Food and Beverage Labs, Water
and Waste Water Labs and other fields of quality control and research.
The UNICO SQ-2800 model spectrophotometer incorporates a 320×240 dot

matrix LCD display for photometric results, easy operation and wavelength
range of 190nm to 1100nm. This instrument is ideal for measurements in the
visible and ultraviolet wavelength region of the electromagnetic spectrum.
Sample Compartment Lid LCD Display
Rod Keypad
4
Power Power Contrast Adjuster Printer
Supply Fan Socket of LCD Interface
Power 110V/220V Serial

Switch Select Switch Comm.
Fig 1
Working Principle:
The spectrophotometer consists of five parts:
1) Halogen or deuterium lamps to supply the light;
2) A Monochromator to isolate the wavelength of interest and eliminate the
unwanted second order radiation;
3) A sample compartment to accommodate the sample solution;
4) A detector to receive the transmitted light and convert it to an electrical
signal;
5) A digital display to indicate absorbance or transmittance. The block
diagram (Fig 2) below illustrates the relationship between these parts.
Block diagram for the Spectrophotometer
100%T
0A
Light Mono- Sample Detector Display
Source chromator Compartment
Fig 2
In your spectrophotometer, light from the lamp is focused on the entrance slit
of the monochromator where the collimating mirror directs the beam onto the
grating. The grating disperses the light beam to produce the spectrum, a
portion of which is focused on the exit slit of the monochromator by a
collimating mirror. From here the beam is passed to a sample compartment
through one of the filters, which helps to eliminate unwanted second order
radiation from the diffraction grating. Upon leaving the sample compartment,
the beam is passed to the silicon photodiode detector and causes the detector
to produce an electrical signal that is displayed on the digital display.
5
Unpacking Instructions:
Carefully unpack the contents and check the materials against the following
packing list to ensure that you have received everything in good condition.
Packing List
Description Quantity
Spectrophotometer............................................... 1
Mains Lead........................................................... 1
Cuvettes............................................................... Set of 4, glass
Cuvettes............................................................... Set of 2, quartz
Dust Cover........................................................... 1
Manual.................................................................. 1
Specifications:
 Wavelength Range: 190~1100nm
 Spectral Bandpass: 4 nm
 Wavelength Accuracy: ±0.8nm
 Wavelength Repeatability: ±0.5nm
 Stray Radiant Energy: ＜0.15%@220nm&340nm
 Photometric Range: 0-200%T, -0.3~3.0A
 Noise: <0.001A @ 500nm 0A
 Drift: <0.002A/h @ 500nm
 Power Requirements: AC 110V/60Hz or 220V/50Hz
 Dimensions: 550W × 420L × 270H mm
 Light Source: Tungsten Halogen/Deuterium
 Weight: 18 kg / 44 lbs
Installation:
1. After carefully unpacking the contents, check the materials with the
packing list to ensure that you have received everything in good
condition.
2. Place the instrument in a suitable location away from direct sunlight.

In order to have the best performance from your instrument, keep it as
far as possible from any strong magnetic or electrical fields or any
electrical device that may generate high-frequency fields. Set the unit
up in an area that is free of dust, corrosive gases and strong
vibrations.
3. Remove any obstructions or materials that could hinder the flow of air
under and around the instrument.
4. Use the appropriate power cord and plug into a grounded outlet.
5. Turn on your UNICO SQ-2800 model spectrophotometer. Allow it to

warm up for 15 minutes before taking any readings. We suggest you
then do the Calibrate System with the Search 656.1nm to set the
wavelength to the deuterium lamp emission line.
6
NOTE: This symbol means Caution, Risk of Danger. Refer to this Manual (see Appendix B –
Lamp Replacement)
Operation:
Prepare the spectrophotometer
Fig 3 is the control panel. User can perform all operations by pressing the
keys and all the results and operation information are displayed on the LCD.
LCD
Function
F1 F2 F3 F4
keys
1 2 3 4 5
CLEAR
ABC DEF GHI JKL
Numeric
6 7 8 9 keys
0 +/-/.
MNO PQRS TUV WXYZ
0Abs ESC
PRINT SETλ
100%T STOP
ESC Control
CELL
STOP keys
LOAD SAVE START ENTER
Fig 3
Description of keys
[LOAD] Load data or curve saved before;
[SAVE] Save data or curve;
[SET λ] Set wavelength;
[0Abs/100%T] Blank or scan the base line;
[PRINT] Print test results or screen
[START] Start testing or scanning sample;
[ESC/STOP] Exit to previous screen or cancel the operation;
[ENTER] Confirm the inputted data or selected item; Go into next setup or
screen;
[F1] - [F4] Function based on the information on the screen;
[0] - [9] Input number or letter; consecutively press a numeric key to select
a character;
[+/-/.] Input +, - or dot;
[CLEAR] Clear all characters when you are inputting or clear curve displays
on the screen;
[＜] , [＞] Change “X” scale; Search point after scan; [＜] clear a character;
[∧] , [∨] Change “Y” scale; Search peak after scan; Scroll items for selecting;
7
Change capital/small letter last typed in; Browse the items for selection;
[CELL] Set cell position.
Turn on spectrophotometer
Turn on spectrophotometer by pressing the Power Switch (IO) (see Fig 1).
The instrument starts to initiate and the steps are as below:
1. The instrument will check memory first (Fig 4), please wait or press
any key to skip this step, after positioning filter, auto-cell changer(if installed)
and D2/W lamps, the screen display as Fig 4A. 15 minutes pass or press
[ESC], the screen display as Fig 5, Select “No” to skip to main menu (Fig 7)
and select “Yes” (recommended) to calibrate system (Fig 6). The calibrating
process includes “get dark current”, “searching 656.1nm” and “check energy”.
After finish the calibration system, go to main menu too (Fig 7).
2. If the data in memory has been lost, the instrument will directly
calibrate system without any choice for you.
3. If no auto-cell changer installed “cell #1” will disappear in Fig 7
WL : 6 5 6 . 1 n m RAM C h ecked: 16 k b
Wa it u n t il E a s yRTOS b oote d : D2
W
Ch ec k m em or y . . . . . . . .
Un ited Pr od u cts & In s tr u m en ts In c.
Fig 4
WL : 656.1nm 1 6 :2 0 :0 5
Wa it u n til E a s yRTO S b ooted : D2

W
Ch e ck m e m or y . . . . . . . .√
In it Pr in ter . . . . . . . . . . .√
In it Com m Por t . . . . . . . .√
Sta r t Ke r n e l . . . . . . . . . .√
Pos ition in g . . . . . . . . . . √
Wa r m u p 1 5 m in u te s . . .
Pr e s s E SC to s k ip . . .
Fig 4A
8
WL : 656.1nm 1 6 :2 0 :1 8
Wa it u n til E a s yRTO S b ooted : D2

W
Ch e ck m e m or y . . . . . . . .√
In it Pr in ter . . . . . . . . . . .√
In it Com m Por t . . . . . . . .√
Sta r t Ke r n e l . . . . . . . . . .√
Pos ition in g . . . . . . . . . . √
Wa r m u p 1 5 m in u te s . . . √ .
Sys te m c a lib r a tin g? No
Fig 5
WL : 656.1nm 1 6 :2 8 :0 3
Wa it u n til E a s yRTOS b ooted : D2

Ch e ck m em or y . . . . . . . .√ W
In it Pr in te r . . . . . . . . . . .√
In it Com m Por t . . . . . . . √ .
Sta r t Ke r n el . . . . . . . . . .√
Pos ition in g . . . . . . . . . . √
In it AD Con ver ter . . . . . √ .
Se a r ch 6 5 6 . 1 n m . . . . . .√
Ch e ck E n er gy . . . . . . √
Un ite d Pr od u c ts & In s tr u m en ts In c .
Fig 6
WL : 656.1nm 1 6 :3 1 : 3 5
D2
UNICO SPECTROPHOTOMETER W
C ell #1
SPE CTRO-QUE ST
1 Ba s ic m od e 5 DNA/ Pr ote in
2 Qu a n tita tive 6 Mu lti WL
3 WL s ca n 7 Utility
4 Kin e tics 8 De fin e d te s t
Un ite d Pr od u c ts & In s tr u m e n ts In c .
Fig 7
Basic operation
Blank
 Push the blank cuvette into the lightpath.
 Press the key [0Abs/100%T] for blanking
Note: 1. If the reference solution is too thick, “Energy Low…”will appear

following the “Blanking…”on the screen (Fig 8). If “Energy too Low…” appears
following the “Blanking…”, the test will be paused and “Warning…”will appear
on the screen.(Fig 9).
2. If no automatic changer installed “cell #1” and “Max E” will

disappear in Fig 8.
9
WL : 656.1nm En ergy Low. . .
D2
Bla n k in g W
C ell #1
Ma x E
F1 :Un it F2 :Mod e F3 : F Fa c tor F4 : Sta n d a r d
Fig 8
NOTE:
1. Blanking is automatic after a wavelength change
DO NOT OPEN SAMPLE COMPARTMENT LID DURING BLANKING.
2. The dark current don’t be taken after power on, if you bypass the calibrating
system. It is recommended to take the dark current after warm up. See page 38.
WL : 656.1nm En ergy t oo Lo w. . .
D2
Wa r n in g…... W
C ell #1
Ma x E
F1 :Un it F2 :Mod e F3 : F Fa c tor F4 : Sta n d a r d
Fig 9
Set wavelength (Example: set wavelength in “Basic mode”)
 Press [SET λ] (Fig 10).
WL : 656.1nm 12 : 3 5: 27
D2
0 .0 0 1 Ab s W
C ell #1
Ma x E
F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d
Fig 10
 Use numeric keypad to input wavelength (Fig 11).

10
WL : 656.1nm 12 : 3 5: 27
D2
0 .0 0 1 Ab s W
C ell #1
Ma x E
Ple a s e in p u t wl: 4 5 0
Fig 11
 Press [ENTER] to change the wavelength from 656.1nm to

450.0nm, and then blank; after blanking, the screen displays as
Fig 12.
WL : 450.0nm 12 : 3 5: 27
D2
0 .0 0 0 Ab s W
C ell #1
Ma x E
Fig 12
Load or delete data or curve (Take the “WL scan” test for example)
 Press [3] in Fig 7 go into “WL scan”. After [LOAD] being pressed,
the first file (ABC.wav) in memory will appear on the bottom line
of screen .Showed as Fig 13. Press [∧] or [∨] to browse the files
stored in memory. Then if :
1. The key [ENTER] be pressed, the file selected will be loaded and
displays on the screen. Fig 14.
Note
1) The file selected must match “WL scan” test’s type. if not，the
“file type error…” will appear on the right of top line.
2) Different test has different file type. Refer to table 1 on page
12.
2. The key [CLEAR] be pressed the file selected will be deleted by

selecting “Yes”.
11
WL : 680.0nm %T: 1 2: 35 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSca le
200.0 Wa velen gth (n m ) 680.0
F1 :Setu p F2 :Mod e F3 :Se a r c h
Fig 13
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSca le
200.0 Wa velen gth (n m ) 680.0
Fig 14
Table 1
Test File Type
Quantitative Curve ***.fit
Quantitative Test Result ***.qua
WL Scan ***.wav
Kinetics ***.kin
DNA/Protein ***.dna
Multi WL ***.mul
WL Validity ***. wlv
Accu. Validity ***.phv
Save data or curve (Example: Save curve in “WL scan”)

 Press the key [SAVE] in Fig 14 to save curve.
 Name the curve by pressing the numeric keypad (Fig 15), press
the key [ENTER] to confirm.
Note
1) Pressing numeric key continually to scroll characters and pressing [∧],
[∨] to alter capital letter to miniscule. Table 2 shows all characters built
in.
2) If the name already exists in memory, the warning “duplicated name,
are you sure？” will appear . “Yes” for overwrite and “No” for Exit.
3) The length of filename is less than 4.
12
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSca le
200.0 Wa velen gth (n m ) 680.0
Ple a s e in p u t File Na m e :2
Fig 15
Table 2
key representing key representing key representing
0 0,+,-,* ,/ 1 1,#,?,:,I 2 2,A,B,C,=
3 3,D,E,F,% 4 4,G,H,I,{ 5 5,J,K,L,}
6 6,M,N,O,~ 7 7,P,Q,R,S, 8 8,T,U,V,“
9 9,W,X,Y,Z +/-/. -, .,
Print test report (For example: Print the report in “Basic mode”, Fig 16)
Press the key [PRINT] to print the report (curve or data you have loaded or
tested, Fig 17).
WL : 546.0nm 12 : 3 5: 27
D2 Fig 16
0 .2 2 1 Ab s W
C ell #1
Ma x E
Fig 17
Before measurement
 Make a blank reference solution by filling a clean cuvette (or test tube)
half full with distilled or de-ionized water or other specified solvent. Wipe
the cuvette with tissue to remove the fingerprints and droplets of liquid.
 Fit the blank cuvette into the 4-cell linear changer and place the cuvette in
the slot nearest you. For the SQ-2800, push the changer so that the
cuvette is in the light path (Push the rod in). Close the lid.
13
Analyze Sample
For different user requirements, we have provided different test methods.
1 Basic Mode
Push the blank cuvette into the light path. In main menu (Fig 7), press [1] to
enter “Basic mode” test. After automatically blanking, it will display as Fig 18
(automatic changer installed) or Fig 19 (automatic changer uninstalled) and
wait for the operator. [ESC/STOP] to exit.
Note: If no automatic changer installed “cell #1” and “Max E” will disappear in
Fig 18
WL : 656.1nm 12 : 3 5: 27
D2
0 .0 0 0 Ab s W
C ell #1
Ma x E
Fig 18
WL : 6 5 6 . 1 n m 12 : 3 5: 27
D2
0 .0 0 0 Ab s W
Ma x E
Fig 19
 Test
There are three modes (T%, Abs, Conc/factor) for you to select by
pressing [F2] to make choice.
1. Abs mode
Push the blank cuvette into the light path. Press [F2] to select Abs
mode, Press [0Abs/100%T] for Blanking, and then push the sample into
lightpath to take reading (Fig 20)
14
WL : 6 5 6 . 1 n m 1 2 : 3 5: 27
D2
0 .1 0 4 Ab s W
C ell #1
Ma x E
Fig 20
2. T% mode
The operation is the same as Abs test mode but pressing [F2] to select
T% mode.
3. Conc/Factor mode
Press [F1] to select a concentration unit (Fig 21). If no unit is suitable
for your test, please select the item “Other”, press enter and input a new
unit by pressing the numeric keypad (Fig 22).
WL : 656.1nm 12 : 3 5: 27
D2
0 .0 0 0 m g/ m l W
C ell #1
F fa c tor 2.000
Ma x E
Ple a s e s e le c t u n it: %
Fig 21
WL : 656.1nm 1 2: 35 : 2 7
D2
0 .0 0 0 m g/ m l W
C ell #1
F fa c tor 2.000
Ma x E
Ple a s e in p u t s e lf d e fin e d u n it: c
Fig 22
Push the blank cuvette into the light path and press [0Abs/100%T] for
Blanking. There are now two choices:
1) Press [F3] to input known F value, Fig 23. Then push the sample into
lightpath to take reading of concentration. Push sample of known
concentration into the lightpath
15
WL : 656.1nm 1 2: 35 : 2 7
D2
0 .0 0 0 m g/ m l W
C ell #1
Ma x E
Ple a s e in p u t F fa c tor : 4
Fig 23
2) Press [F4] to input known Conc value, Fig 24. Then push the sample
into lightpath to take reading of concentration.
WL : 656.1nm 1 2 : 3 5: 2 7
D2
W
0 .0 0 0 m g/ m l C ell #1
F=4 . 0 0 0
Ma x E
Fig 24
Note:
1) You can select wavelength at any time by pressing [SET λ]. After your
selection, instrument always blanks automatically.
2) If F value is more than 9999, the “out of range” will display on screen.
 Print Test Report

Press [PRINT] to print test results (Fig 25).
Fig 25
2 Quantitative
Press [2] in Main Menu for “Quantitative” Test (Fig 26). Press [ESC/STOP] to
exit.
Note: .If no automatic changer installed “cell #1” will disappear in Fig 26.
16
WL : 7 0 0 . 0 n m Ab s : 12 : 3 5: 27
Qu a n tita tive Tes t D2

W
ID Ab s Con c . (m g/ L) C ell #1
WL(n m )
700.0
Se a r ch
Scr oll
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
F1 :Un it F2 :Sta n d a r d Cu r ve
Fig 26
 How to operation
 Press [F1] to select unit of concentration (Fig 27).
WL : 700.0nm Ab s : 12 : 3 5 : 2 7

W
WL(n m )
700.0
Se a r ch
Scr oll
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
Ple a s e s e le c t u n it: g/ L
Fig 27
 Press [SET λ] to select correction methods and enter the wavelength.

There are three correction methods (single, Isoabsorbance and 3
point, Fig 28).
Note: Please refer to the Appendix C for the correction method.
WL : 700.0nm Ab s : 12 : 3 5 : 2 7

W
WL(n m )
700.0
Se a r ch
Scr oll
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
Cor r e c tion m e th od : Sin gle WL
Fig 28
 Press [F2] in Fig 26 for more items to select .See Fig 29.
17
WL : 7 0 0 . 0 n m Ab s : 12 : 3 5: 27
Cal i br at i on t abl e D2
W
No Con c . (m g/ L) Ab s C ell #1
WL(n m )
700.0
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
F 1 :Meth od F2 : Pa r a m s F3 : Sta n d a r d F4 : Cu r ve
Fig 29
 Press [F1] in Fig 29 to select fitting method. There are 4 methods for
you to choose: Linear fit, linear fit through zero, square fit and cubic fit.
 Press [F2] in Fig 29 to enter directly a known standard curve. Fig 29A.
WL : 7 0 0 . 0 n m Ab s : 1 2 : 3 5: 27
Cal i br at i on t abl e D2
W
No Con c. (m g/ L) Ab s C ell #1
WL(n m )
700.0
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
In p u t K1 =1 . 0 3 3
Fig 29A
The constants to be entered are depending on which fitting method

selected. The table below lists the relation:
Fitting Method Fitting Equation constants

Linear fit through zero C=K1×A K1, r*
Linear fit C=K0+K1×A K0,K1,r*
Square fit C=K0+K1×A+K2×A2 K0,K1,K2
Cubic fit C=K0+K1×A+K2×A2+K3×A3 K0,K1,K2,K3
*r: regression co-efficient, default=1
 Press [F3] in Fig 29 to establish a standard curve by measuring a

group of standard samples. See Fig 30.
WL : 7 0 0 . 0 n m Ab s : 12 : 3 5: 2 7
Setu p Sta n da r d Con c. D2

W
1 0.000 WL(n m )
2 - m or e - 700.0
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
E d it th e n u m b er . . .
Fig 30
18
 Enter standard concentrations of samples by pressing the Numeric
keypad followed by [ENTER]. Press [∧] or [∨] to modify the inputted
data Fig31.
WL : 700.0nm Ab s : 1 2: 35 : 2 7
Setu p Sta n da r d Con c. D2

W
1 2.000 WL(n m )
2 3.000 700.0
3 - m or e-
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
In p u t Sta n d a r d Con c : 3
Fig 31
 Press [ESC/STOP] to finish inputting and to exit Fig 32.
 Push the blank cuvette into the light path, press [0Abs/%100T], the
instrument will step to the wavelength and blank. See Fig 32.
WL : 700.0nm Ab s : Bla n k …. …….

Ca libra tion ta ble D2
No Con c . (m g/ L) Ab s W
C ell #1
1 2.000
WL(n m )
2 3.000
700.0
3 4.000
4 5.000
5 6.000
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
F1 :Me th od F2 :Pa r a m s F3 :Sta n d a r d F4 :Cu r ve
Fig 32
 Pull the first sample cuvette of known concentration into the light path,
Press the key [START] to get values of standard curve one by one
(Fig 33).
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
Ca libra tion ta ble D2

No Con c . (m g/ L) Ab s W
C ell #1
1 2.000 0.247
WL(n m )
2 3.000 0.375
700.0
3 4.000 0.532
4 5.000 0.603
5 6.000 0.764
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
F1 :Me th od F2 :Pa r a m s F3 :Sta n d a r d F4 :Cu r ve
Fig 33
Note: If auto-cell changer is installed, the vary samples are measured by

pressing [CELL] following numbers (1-8) and pressing [ENTER] to
confirm.
19
 Press [F4] to draw the curve. You can get a different curve by
pressing [F1] to select a different fitting method. See Fig 34 -Fig 37.
For linear fits, “r” represent fitting coefficient of linear regression.

r=1 is best fitting. usually “r” is very close to 1.
Note: If there are few standard samples, it is not suitable for selecting
square fitting, especially cubic fitting, otherwise invalid fitting result will be
obtained.
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
D2
76
W
C ell #1
Con c.
0
-1.0 Abs 4.0

Pr e s s (E SC) to r e tu r n . . .
Fig 34 linear through zero fit
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
D2
76
W
C ell #1
Con c.
0
-1.0 Abs 4.0

Pr e s s (E SC) to r e tu r n . . .
Fig 35 square fit
WL : 656.1nm Ab s : 12: 35: 27 WL : 656.1nm Ab s : 12 : 3 5 : 2 7

D2 D2
914 38
76
W W
C ell #1 C ell #1
Con c.
Con c.
0
-1.0 Abs 4.0 -1.0 Abs 4.0

Pr e s s (E SC) to r e tu r n . . . Pr e s s (E SC) to r e tu r n . . .
Fig 36 cubic fit Fig 37 linear fit
 Press [SAVE] to save calibration if required

 Press [ESC/STOP] to exit
 Quantitative Test
20
Before test, the standard curve must be obtained. There are three ways
for you to obtained it (a, b or c).
a) Standard curve built up and saved in the instrument. In Fig 33 press

[Load] and then press [∧] or [∨] to select the file with type ***.fit. At last
press [ENTER] to confirm.
b) Known standard curve, which is not saved in the instrument. See
page 17 for Fig 29 enter a known standard curve directly.
c) Use the standard samples for the test. First the standard curve must
be established using the method shown in page 17.
Note: All sample results must be taken in screen Fig 26.
 Push the blank cuvette into the light path and press [0Abs/100%T] for
blanking.
 Pull the sample cuvette into the light path, press the key [START], the
results will be displayed on the screen (Fig 38). If there is more than one
sample, repeat for the next sample.
WL : 700.0nm Ab s : 12 : 3 5: 27

ID Ab s Con c . (m g/ L) W
C ell #1
1 0.062 0.062
WL(n m )
2 0.061 0.061
700.0
3 0.062 0.061
4 0.061 0.061
Se a r ch
Scr oll
C=1 . 0 0 0 *A^ 1 r =1 . 0 0 0
F1 :Un it F2 :Sta n d a r d Cu r ve
Fig 38
 Press (SAVE) to save the results and fitting parameters
Press the key [PRINT] to print the test report (Fig 39).
Fig 39
21
3 Wavelength Scan
Press [3] in main menu for “WL Scan” test (Fig 41). [ESC/STOP] to exit.
To load a previous curve, press [LOAD] and select a previously stored curve
(.wav)
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSca le
0
YSca le
200.0 Wa velen gth (n m ) 680.0
Fig 41
 Scan sample
1. Press [F1] to setup, input the start wavelength, and end wavelength
by pressing the numeric keypad (Fig 42).
Note: The SQ-2800 scans from high to low wavelength. Browse and
select the items of scan step and scan speed by pressing [∧] or [∨].
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
680.0
%T
Step :
1.0nm
XSc a le
YSc a le
0
200.0 Wa velen gth (n m ) 680.0

Sc a n fr om : 6 8 0
Fig 42
Note: “Scan step” allows the selection of 0.1nm, 0.2nm, 0.5nm, 1nm, 2nm
and 5nm. “Scan speed” allows the selection of “HI”, “MEDIUM” and
“LOW”. For survey scan we suggest 5nm, HI. For detailed scan we
suggest 0.5nm, HI
22
2. Press [F2] to select the test mode, “Abs”, “%T” or ”E”’ (Fig 43).
WL : 656.1nm Ab s : 12 : 3 5 : 2 7
D2
1 20. 0
W
C ell #1
Fr om :
200.0
To:
680.0
%T
Step :
1.0nm
XSc a le
0
YSc a le
200.0 Wa velen gth (n m ) 680.0
Ple a s e s e le c t m od e: Ab s
Fig 43
3. Push the blank cuvette into the light path, press [0Abs/100%T] to
scan the base line (Fig 44). Press the key [ESC/STOP] to stop
scanning;
WL : 520.0nm Sca n to 2 0 0 . 0 n m
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSc a le
200.0 Wa velen gth (n m ) 680.0
Pr e s s (E SC) to s top . . .
Fig 44
4. Pull the sample cuvette into the light path, press [START] to scan the
sample (Fig 45) [ESC/STOP] to stop scanning. When scan has
finished the beeper beeps 3 times (Fig 46).
WL : 417.0nm %T: 3 6 . 7 3 Sca n to 2 0 0 . 0 n m WL : 680.0nm %T: 12 : 3 5 : 2 7

D2 D2
12 0.0
12 0.0
W W
C ell #1 C ell #1
Fr om : Fr om :
200.0 200.0
To: To:
%T
%T
680.0 680.0
Step : Step :
1.0nm 1.0nm
XSc a le XSc a le
0
YSca le YSca le
200.0 Wa velen gth (n m ) 680.0 200.0 Wa velen gth (n m ) 680.0
Pr e s s (E SC) to s top . . . F1 :Setu p F2 :Mod e F3 :Se a r c h
Fig 45 Fig 46
23
5. If you want to change the scale, press [＜] or [＞] to change “x” scale
(Fig 47), input upper limit and lower limit by pressing the numeric
keypad. To change “y”scale press [∧] or [∨]. After these inputs the
instrument will redraw the curve (Fig 48).
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSca le
200.0 Wa velen gth (n m ) 680.0
Min X:3 0 0
Fig47
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
10 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
XSc a le
0
YSca le
300.0 Wa velen gth (n m ) 500.0
Fig 48
6. Press [F3] to search the Abs/%T value of the scan. There are two
ways for you to search (Fig 49).
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
Poin t
0
Pea k
200.0 Wa velen gth (n m ) 680.0
F1 :Set Pea k He igh t
Fig 49
a) Peak to peak, press [F1] to set “peak height” and input value by
pressing the numeric keypad (Fig 50). Press [∨] to search the
peak from left to right and press [∧] to search from right to left.
The value of every peak found will be displayed on the screen
24
one at a time (Fig 51).
WL : 680.0nm %T: 12 : 3 5 : 2 7
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
Poin t
0
Pe a k
200.0 Wa velen gth (n m ) 680.0
Ple a s e in p u t p ea k h e igh t: 0 . 1 0 0
Fig 50
WL : 452.0nm %T:2 2 . 3 8 12 : 3 5: 27
D2
12 0.0
W
C ell #1
Fr om :
200.0
To:
%T
680.0
Step :
1.0nm
Poin t
0
Pe a k
200.0 Wa velen gth (n m ) 680.0
F1 :Set p ea k He igh t
Fig 51
b) Point to point, Press [ ＞ ] to search the point from left to right and
press [ ＜ ] to search from right to left. The search step interval is
the same as the scan step. The value of every point searched will
be displayed on the screen.
 Save Curve
Press [SAVE] to save the curve. Note: Load/Save requires the first scan
display page Fig 48. Press ESC if in Search to return to the required page

Press [PRINT] to print the curve you have loaded or scanned (Fig 52).
Note: The report always is printed in Fig 46
25
Fig 52
26
4 Kinetics
Press [4] in main menu for “Kinetics” (Fig 53). [ESC/STOP] to exit.
To load a previous kinetics result, press [LOAD] and select a previously
stored result (.kin)
Tim : 6 0 s Ab s : 1 2: 3 5: 27
D2
3. 000
W
C ell #1
Tota l T
180s
In te va l
Abs
1.0s
XSca le
0
YSca le
0 Tim e(s ) 180
F1 :Setu p F2 :Mod e F3 :Pr oce s s F4 :Se a r ch
Fig 53
 Test
1. Press [F1] to set “Total Time”, ”Delay Time”, ”Time interval”, and input
the value by pressing the numeric keypad (Fig 54).
Tim : 6 0 s Ab s : 1 2: 3 5: 27
D2
3. 000
W
C ell #1
Tota l T
180s
In te va l
Abs
1.0s
XSca le
0
YSca le
0 Tim e(s ) 180
Tota l Tim e:1 8 0
Fig 54
2. Select the test mode (“Abs” or “%T”) by pressing [F2] (Fig 55).
Tim : 6 0 s Ab s : 1 2: 3 5: 27
D2
3. 000
W
C ell #1
Tota l T
180s
In te va l
Abs
1.0s
XSca le
0
YSca le
0 Tim e(s ) 180
Ple a s e s e le c t m od e:Ab s
Fig 55
3. Set wavelength by pressing [SET λ]. Pull the blank cuvette into the
light path, press [0Abs/100%T] for blanking
4. Pull the sample cuvette into the light path, press [START] to scan the
27
sample. After the delay time, the beeper beeps 3 times and time-scan
starts. At the end of the time-scan, the beeper also beeps 3 times (Fig
56);
Tim : 1 8 0 s Ab s : 1 2: 3 5: 27
D2
1. 000
W
C ell #1
Tota l T
180s
In te va l
Abs
1.0s
0 XSca le
YSca le
0 Tim e(s ) 180
F1 :Setu p F2 :Mod e F3 :Pr oce s s F4 :Se a r c h
Fig 56
5. Press [F3] to process the data, and enter “Begin Time”, ”End Time”
and ”Factor” (Fig 57) and the value in I.U. will be calculated and
displayed (Fig 58). The average straight line between the Begin Time
and End Time will be calculated. The gradient of this line gives the
rate of change of ΔA/min.
Note: I.U. = Factor X ΔA/min
Tim : 6 0 s Ab s : 1 2: 3 5: 27
D2
3. 000
W
C ell #1
Tota l T
180s
In te va l
Abs
1.0s
XSca le
0
YSca le
0 Tim e(s ) 180
Be gin Tim e :0
Fig 57
Tim : 1 8 0 s Ab s : 1 2: 3 5: 27
D2
1. 000
W
C ell #1
Tota l T
180s
In te va l
1.0s
Abs
I. U. =
+0 . 3 6 4
XSca le
0
YSca le
0 Tim e(s ) 180
F1 :Setu p F2 :Mod e F3 :Pr oce s s F4 :Se a r c h
Fig 58
6. If you want to change the scale, please refer to step 5 of “WL scan”.
7. Press [F4] to search the Abs/%T value in relation to the time axis.
28
Search point to point by pressing the key [＜] or [＞]. Please refer to
step 6 of “WL scan”.
 Save Curve
Press the key [SAVE] to save curve. Note: Load/Save requires the first
kinetics display page Fig 56. Press ESC if in Search to return to the required
page.

Press the key [PRINT] to print the curve you have loaded or scanned (Fig 59).
Fig 59
5 DNA/Protein
Press [5] in main menu for “DNA/Protein” (Fig 60). [ESC/STOP] to exit.
29
Note: The algorithm of the test refer to Appendix A please.
WL : 900.0nm 12 : 3 5 : 2 7
DNA/ Protein m ea s u r em en t D2
W
No Item s Res u lt U n it C ell #1
WL(n m )
260.0
280.0
320.0
Se a r ch
Sc r oll
F1 :Coe ff F2 :Mod e F3 :U n it F4 :De fa u lt
Fig 60
To load previous DNA results, press [LOAD] and select a previously stored result (.dna)
 Test
1. To use a simpler or different algorithm, you can enter your own values
for f1-f4. Press [F1] to set f1-f4. Input the value by pressing the
numeric keypad (Fig 61).
WL : 900.0nm 1 2: 35 : 2 7
W
WL(n m )
260.0
280.0
320.0
Se a r ch
Sc r oll
In p u t f1 =6 2 . 9 0
Fig 61
2. Press [F2] to select test mode. “Absorbance difference 1” is for testing

at the wavelength 260nm, 280nm and 320nm (optional), and the
“Absorbance difference 2” is for testing at the wavelength 260nm,
280nm and 320nm (optional), Fig 62. Then select with/without
reference. If selected with reference (no), the A ref. will be “0” (Fig 63).
WL : 900.0nm 1 2: 35 : 2 7
W
WL(n m )
260.0
280.0
Se a r ch
Sc r oll
Me a s u m en t: Ab s or b a n ce d iffe r e n c e 1
Fig 62
30
WL : 900.0nm 1 2: 35 : 2 7
W
WL(n m )
260.0
280.0
Se a r ch
Sc r oll
With r e fer e n ce : Yes
Fig 63
3. Press [F3] to select the unit of concentration (Fig 64).
WL : 900.0nm 1 2: 35 : 2 7
W
WL(n m )
260.0
280.0
Se a r ch
Sc r oll
Ple a s e s e le c t u n it: m g/ m L
Fig 64
4. Push the blank cuvette into the light path, then press [0Abs/100%T]
for blanking.
5. Pull the sample cuvette into the light path, press [START] to test the
sample. The test result will be displayed on the screen (Fig 65).
WL : 900.0nm Ab s : 12 : 3 5: 27
No Item s Res u lt U n it W
1 A1 2.947 Ab s C ell #1
A2 2.842 Ab s WL(n m )
Ar e f 0.638 Ab s 260.0
280.0
C- DNA 65.91 m g/ m L 320.0
C- Pr o 1672 m g/ m L
Ra tio 1.048
Se a r ch
Sc r oll
F1 :Coe ff F2 :Mod e F3 :U n it F4 :De fa u lt
Fig 65
6. If there is more than one sample, repeat step 5 for the next sample.
7. Press the key [＜] or [＞] for searching. Input the sample number (Fig
66), the result will be displayed on the screen. Press the key [∧] or [∨]
to browse the test results one by one.
31
WL : 900.0nm Ab s : 12 : 3 5: 27
No Item s Res u lt U n it W
1 A1 2.947 Ab s C ell #1
A2 2.842 Ab s WL(n m )
Ar e f 0.638 Ab s 260.0
280.0
C- DNA 65.91 m g/ m L 320.0
C- Pr o 1672 m g/ m L
Ra tio 1.048
Se a r ch
Sc r oll
Se a r ch s a m p le:3
Fig 66
 Recall the default

Press the key [F4] to recall the default of the f1-f4.
 Save Data
Press the key [SAVE] to save data.

Press the key [PRINT] to print the test result (Fig 67).
Fig 67
6 Multi Wavelength
Press [6] in main menu for “Multi WL” (Fig 68). [ESC/STOP] to exit.
WL : 900.0nm Ab s : 12 : 3 5: 27
Mu lti Wa velen gth Tes t D2

W
No WL(n m ) Ab s C ell #1
500.0 1 WL
Se a r ch
Sc r oll
F1 :WL s etu p F2 :Mod e
Fig 68
To load previous Multi Wavelength results, press [LOAD] and select

previously stored results (.mul)
32
 Test
1. Press [F1] to setup a group of wavelengths for testing by pressing the
numeric keypad followed by [ENTER]. [∧] or [∨] to modify the inputted
data Fig 69. Press [ESC/STOP] to finish setup and exit.
Note: It is recommended to enter the highest wavelength first.
WL : 900.0nm Ab s : 12 : 3 5: 27

No WL(n m ) Ab s W
500.0 C ell #1
2 WL
400.0
546.0
Se a r ch
Sc r oll
Ple a s e in p u t wl:5 0 0
Fig 69
2. Press [F2] to select mode: T%, Abs (Fig 70).
WL : 900.0nm Ab s : 12 : 3 5: 27

No WL(n m ) Ab s W
C ell #1
500.0
3 WL
400.0
300.0
Se a r ch
Sc r oll
Ple a s e s e lec t m od e : Ab s
Fig 70
3. Push the blank cuvette into the light path, then press [0Abs/100%T]
for Blanking.
4. Pull the sample cuvette into the light path, press [START] to test. The
test results will be displayed on the screen (Fig 71).
WL : 500.0nm Ab s : 1 2: 35: 27

No WL(n m ) Ab s W
C ell #1
1 500.0 0.87 3 WL
400.0 0.42
300.0 0.81
Se a r c h
Sc r oll
F1 :WL s e tu p F2 :Mod e
33
Fig 71
5. If there is more than one sample, repeat step 4 for the next sample.
Note: When the test has finished, the wavelength will go to the first WL.
6. Press [＜] or [＞] for searching. Input the sample number, the result
will be displayed on the screen. Press [∧] or [∨] to browse the test
results one by one.
 Save Data
Press [SAVE] to save data.

Press [PRINT] to print the test results (Fig 72).
Fig 72
Setting and Calibration
7 Utility
Press [7] in Main menu for “Utility” (Fig 73). [ESC/STOP] to exit.
WL : 656.1nm 08: 04: 35

D2
C ell #1
SPE CTRO-QUE ST
1 WL Re s et 6 Acc u Va lid ity
2 Pr in te r 7 WL Va lid ity
3 La m p 8 Con n ec t to PC
4 Cloc k 9 Bee p e r on / off
5 Da r k cu r r en t
F1 De le te en tir e s a ve d file s
F2 Res tor e d e fa u lt
Un ited Pr od u c ts & In s tr u m en ts INC.
Fig 73
34
 WL Reset
Press [1] to reset wavelength (Fig 74).
WL : 482.0nm Ste p to 9 0 0 . 0 n m . . .
D2
C ell #1
SPE CTRO-QUE ST
1 WL Re s e t 6 Ac cu Va id ity
2 Pr in te r 7 WL Va id ity
3 La m p 8 Con n e c t to PC
4 Cloc k 9 Be ep e r on / off
F1 De le te en tir e s a ve d file s
F2 Res tor e d e fa u lt
U n ite d Pr od u cts & In s tr u m en ts INC.
Fig 74
 Printer
Press [2] to set printer (Fig 75). [ESC/STOP] to exit.
WL : 656.1nm 08: 04: 35

D2
C ell #1
S PE CTRO-QUE ST
1 Res et p r in ter
2 Selec t p r in t p or t
3 Selec t p r in te r
4 Pr in t r e p or t
Un ite d Pr od u c ts & In s tr u m e n ts INC.
Fig 75
1. Press [1] in Fig 75 to Reset Printer.
2. Press [2] in Fig 75 to select print port (LPT or Comm., Fig 76).
WL : 656.1nm 08: 04: 35

D2
C ell #1
SPE CTRO-QUE ST
1 Res et p r in ter
Se lec t th e p r in t p or t : LPT
Fig 76
3. Press [3] in Fig 75 to select printer (HP PCL (1 color cartridge), PCL
35
(black mode), Epson ESC/P or Epson/P2 or above, Fig 77).
WL : 656.1nm 08: 04: 35

D2
C ell #1
SPE CTRO-QUE ST
1 Res et p r in ter
Pr in te r : HP PCL (1 c olor c a r tr id ge)
Fig 77
4. Press [4] in Fig 75 to select print mode. If you select “Print screen”
mode, a little icon will be displayed on the top line of the screen (Fig 78),
if you select “Print report” mode, the little icon will disappear.
WL : 656.1nm 08: 04: 35

D2
S PE CTRO-QUE ST C ell #1
1 Res et p r in ter
4 Pr in t s cr ee n
Fig 78
 Lamp
Press [3] to set lamp (Fig 79). [ESC/STOP] to exit.
WL : 656.1nm 08: 04: 35

D2
SPE CTRO-QUE ST C ell #1
1 Switc h D2 : ON
2 Res et D 2 la m p u s a ge tim e
3 Switc h W: ON
4 Res et W la m p u s a ge tim e
5 Switc h p oin t
Fig 79
1. Press [1] in Fig 79 to switch on/off D2. Fig 80.
36
WL : 656.1nm 08: 04: 35
D2
C ell #1
S PE CTRO-QUE ST
1 Switc h D2 : OF F
3 Switc h W: OF F
5 Switc h p oin t
Fig 80
2. Press [2] in Fig 79 to reset usage time of D2 (Fig 81). Press [∧] or [∨] to
select “Yes” or “No”, and then press [ENTER].
WL : 656.1nm 08: 04: 35

D2
C ell #1
S PE CTRO-QUE ST
1 Switc h D2 : ON
3 Switc h W: ON
5 Switc h p oin t
5 h r s u s ed . Ar e you s u r e ? NO
Fig 81
3. Press [3] in Fig 79 to switch on/off W. The indication is also on the top
right corner of the screen (Fig 82).
WL : 656.1nm 08: 04: 35

D2
C ell #1
SPE CTRO-QUE ST
1 Switc h D2 : ON
3 Switc h W: OF F
5 Switc h p oin t
Fig 82
4. Press [4] in Fig 79 to reset usage of W (Fig 83). Press [∧] or [∨] to select
“Yes” or “No”, and then press [ENTER].
37
WL : 656.1nm 08: 04: 35
D2
C ell #1
S PE CTRO-QUE ST
1 Switc h D2 : ON
3 Switc h W: ON
5 Switc h p oin t
5 h r s u s ed . Ar e you s u r e ? NO
Fig 83
5. Press [5] in Fig 79 to set the switch usage point of D2 and W lamp (Fig
84).
WL : 656.1nm 08: 04: 35

D2
C ell #1
S PE CTRO-QUE ST
1 Switc h on / off D 2
3 Switc h on / off W
5 Switc h p oin t
In p u t th e D 2 / W s w itc h p oin t:3 4 0 . 0
Fig 84
 Clock
Press [4] In Fig 73 to set the display mode and modify the clock (Fig 85).
[ESC/STOP] to exit.
WL : 656.1nm 08: 04: 35

D2
C ell #1
SP E CTRO-QUE S T
1 Set Tim e
2 Set Da te
3 Sh ow Tim e m od e
4 Sh ow Da te m od e
Fig 85
1. Press [1] in Fig 85 to modify time by pressing the numeric keypad (Fig
86).
38
WL : 656.1nm 08: 04: 35
D2
C ell #1
S PE CTRO-QUE ST
1 Set Tim e
2 Set Da te
Ple a s e in p u t th e tim e:0 8 . 0 4 . 3 5
Fig 86
2. Press [2] in Fig 85 to modify date by pressing the numeric keypad.
3. Press [3] in Fig 85 to set the date display on the top right corner of the
screen.
4. Press [4] in Fig 85 to set the time display on the top right corner of the
screen (Fig 87).
WL : 656.1nm 08: 04: 35

D2
C ell #1
S PE CTRO-QUE ST
1 Set Tim e
2 Set Da te
Fig 87
Note: Make sure press DOT ([+/-/.] button) between numbers. For example,
January 20, 2005, should input like: 20.01.05
 Dark Current
Press [5] In Fig 73 to get dark current (Fig 88).
WL : 656.1nm G et d a r k cu r r en t
D2
C ell #1
SPE CTRO-QUE ST
1 WL Res et 6 Acc u Va lid ity
2 Pr in ter 7 WL Va lid ity
3 La m p 8 Con n ec t to PC
4 Cloc k 9 Bee p er on / off
F1 De lete en tir e s a ved file s

F2 Re s tor e d e fa u lt
Un ited Pr od u c ts & In s tr u m e n ts INC.
Fig 88
39
 Accu Validity
Press [6] In Fig 73 to do Accu validity (Fig 89). [ESC/STOP] to exit.
WL : 900.0nm Ab s : 12 : 3 5: 27
Ph otom etric Va lidity Tes t D2

W
No WL(n m ) Ab s (Std ) Ab s Re s u lt C ell #1
F1 : Sta n d a r d F2 : Mod e F3 : Tole r a n c e
Fig 89
1. Press [SET λ] to set the wavelength. Press [ENTER] to edit and input
wavelength by pressing the numeric keypad (Fig 90). [ESC/STOP] to
finish inputting and exit.
WL : 900.0nm Ab s : 12 : 3 5: 27

No WL(n m ) Ab s (Std ) Ab s Re s u lt W
C ell #1
1 440.0
2 546.0
3 - m or e-
Ple a s e in p u t wl:5 4 6
Fig 90
2. Press [F1] to set the standard value, Press [ENTER] to edit and input by
pressing the numeric keypad (Fig 91). [ESC/STOP] to finish inputting and
exit.
WL : 900.0nm %T: 12 : 3 5 : 2 7

No WL(n m ) %T(Std ) %T Re s u lt W
C ell #1
1 440.0 9.28
2 546.0 0.000
3 635.0 0.000
Se lec t
In p u t th e s ta n d a r d :0
Fig 91
3. Press [F2] to select test mode (Abs or %T, Fig 92).
40
WL : 900.0nm %T: 12 : 3 5 : 2 7

C ell #1
1 440.0 9.28
2 546.0 8.45
3 635.0 5.66
Ple a s e s e le c t m od e: %T
Fig 92
4. Press [F3] to set tolerance (Fig 93).Input the value by pressing the
numeric keypad.
WL : 900.0nm %T: 12 : 3 5 : 2 7

C ell #1
1 500.0 9.28
2 600.0 8.45
3 700.0 5.66
In p u t tole r a n ce :0 . 0 0 5
Fig 93
5. Press [0Abs/100%T] for Blanking.
6. Put the sample (calibrated neutral density filter) into the light path. Press
[START] to check. The results will be displayed on the screen (Fig 94). If
the discrepancy between the results and the calibrated standards is not
more than the tolerance, “pass” will be displayed after the test result.
Otherwise, “fail” will be displayed.
7. The result can be saved, loaded and printed by pressing [SAVE], [LOAD]
and [PRINT].
WL : 900.0nm %T: 12 : 3 5 : 2 7

C ell #1
1 500.0 9.28 9.28 pa ss
2 600.0 8.45 8.45 pa s s
3 700.0 5.66
Fig 94
41
 WL Validity
Press [7] in Fig 73 to WL validity (Fig 95). [ESC/STOP] to exit.
WL : 900.0nm Ab s : 12 : 3 5: 27
Wa velen gth Va lidity Tes t D2

No WL(n m ) Pe a k (n m ) T% Res u lt W
C ell #1
F1 : Se t p ea k s F2 : Mod e F3 : Toler a n ce
Fig 95
1. Press [F1] to set the standard peak. Press [ENTER] to edit and input
wavelength by pressing the numeric keypad (Fig 96). [ESC/STOP] to
finish inputting and exit.
WL : 900.0nm %T: 12 : 3 5 : 2 7

No WL(n m ) Pe a k (n m ) %T Res u lt W
C ell #1
1 241.4
2 361.0
3 417.0
4 537.6
5 641.4
6 807.4
Se lec t
In p u t th e s ta n d a r d :0
Fig 96
WL : 900.0nm %T: 12 : 3 5 : 2 7
D2
Wa velen gth Va lidity Tes t W
No WL(n m ) Pea k (n m ) %T Re s u lt C ell #1
1 241.4
2 361.0
3 417.0
4 537.6
5 641.4
6 807.4
Ple a s e s e le c t m od e: %T
Fig 97
42
3. Press [F3] to set tolerance (Fig 98). Input the value by pressing the
numeric keypad.
WL : 900.0nm %T: 12 : 3 5 : 2 7

No WL(n m ) Pe a k (n m ) %T Res u lt W
C ell #1
1 241.4
2 361.0
3 417.0
4 537.6
5 641.4
6 807.4
Se lec t
In p u t tole r a n ce :0 . 8
Fig 98
4. Press [0Abs/100%T] for blanking.
5. Put the sample (calibrated holmium liquid) into the light path. Press
[START] to check. The results will be displayed on the screen (Fig
99). If the discrepancy between the results and the calibrated values
is not more than the tolerance, “pass” will be displayed after the test
results. Otherwise, “fail” will be displayed.
WL : 900.0nm %T: 12 : 3 5 : 2 7
D2
Wa velen gth Va lidity Tes t W
No WL(n m ) Pe a k (n m ) %T Re s u ltC ell #1
1 241.4 239.7 40.06 pass
2 361.0 360.4 42.82 pass
3 417.0 416.9 37.63 pass
4 537.6 537.2 16.50 pass
5 641.4 641.3 24.33 pass
6 807.4 807.7 92.38 pass
Fig 99
6. The result can be saved, loaded and printed by pressing [SAVE],

[LOAD] and [PRINT]
 Connect to PC
Press [8] in Fig 73 to connect to PC (Fig 100), if the instrument is on-line with
the PC. The screen displays as Fig 100A. Press [ESC/STOP] to exit.
43
WL : 656.1nm 08: 04: 35
D2
SPE CTRO-QUE ST
Con n ec tin g to c om p u ter . . .
Fig 100
WL : 656.1nm 08: 04: 35

D2
UNICO SPECTROPHOTOMETER
W
SPE CTRO-QUE ST
Con tr olle d b y PC . . .
Fig 100A
 Beeper on/off
Press [9] in Fig 73 to turn on/off the beeper
 Delete entire saved files

Press [F1] in Fig 73 to delete entire saved files. After the delete the files,
double confirm need to do.
 Restore default
Press [F2] in Fig 73 to restore the default parameters.
8 Defined Test (auto-cell changer required)
Press [8] in main menu for “defined test” (Fig 101). [ESC/STOP] to exit.
WL : 900.0nm 12 : 3 5 : 2 7
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 1 Sa m p le
No. Ab s
1
F1 : Me th or d F2 :Mod e
Fig 101
44
1. Press [F1] to setup method (Fig 102). There are 8 items (1 ref. 1 sample,
1 ref. 2 samples, 1 ref. 3 samples, 1 ref. 4 samples, 1 ref. 5 samples, 1
ref. 6 samples, 1 ref. 7 samples, N refs. N samples) for selecting. We take
“ 1 ref. 4 samples” for example, Fig 102
WL : 900.0nm 12 : 3 5 : 2 7
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 4 Sa m p le s
No. Ab s
1
2
3
4
Se lec t d e fin e te s t: 1 Ref. , 4 s a m p les
Fig 102
WL : 900.0nm 12 : 3 5 : 2 7
D2
0 .0 0 0 Ab s W
4 Re f, 4 Sa m p le
No. Ab s
1
2
3
4
Ple a s e s e le c t m od e: Ab s
Fig 103
3. Put the reference into cell NO.1 and 4 samples into cell NO.2-NO.5.Set
wavelength.
4. Press [START] .Automatically the reference is taken in cell NO.1,the 4

samples are taken in cell NO.2-NO.5. The results are displayed as Fig
104.
WL : 900.0nm 1 2: 35 : 2 7
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 1 Sa m p le
No. Ab s
1 0.227
2 0.289
3 0.338
4 1.106
F1 : Meth or d F2 :Mod e
Fig 104
5. Select “N refs. N samples”, Take “8 refs. 8 samples” for example.

45
6. After setup wavelength and mode (%T or Abs),put 8 references into CELL
NO.1-NO.8.
7. Press [START], the screen display as Fig 105, the “Place 1st group…”
appear on the right of top line, Press [0Abs/100%T], the 8 references are
taken automatically and the screen change to Fig 106.
WL : 900.0nm Pla ce 1 s t gr ou p . .
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 1 Sa m p le
No. Ab s
1
2
3
4
5
6
7
8
Fig 105
WL : 900.0nm Pla ce 2 n d gr ou p . .
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 1 Sa m p le
No. Ab s
1
2
3
4
5
6
7
8
Fig 106
8. Remove 8 references and put 8 samples into CELL NO.1-NO.8, Press the
[START], the results are taken automatically . Fig 107.
WL : 900.0nm 1 2: 45 : 5 7
D2
0 .0 0 0 Ab s W
C ell #1
1 Re f, 1 Sa m p le
No. Ab s
1 0.127
2 0.189
3 0.238
4 0.806
5 1.442
6 1.567
7 1.669
8 1.741
Fig 107
46
Appendix A
DNA/Protein Test Algorithm
Test Name Method Wavelength Calculations Parameters Displayed

Units
DNA MEASUREMENT
DNA/Protein Absorbance A1=A260nm DNA f1=62.9 DNA: μg/ml
difference A2=A280nm concentration: f2=36.0
Concentration (260,280) Aref=A320nm (A1-Aref)f1-(A2- f3=1552 Protein:
(optional) Aref)f2 f4=757.3 μg/ml
and Protein
concentration
DNA purity (A2-Aref)f3-(A1-
Aref)f4
Absorbance A1=A260nm DNA f1=49.1
difference A2=A230nm concentration: f2=3.48
(260,230) Aref=A320nm (A1-Aref)f1-(A2- f3=183
(optional) Aref)f2 f4=75.8
Protein
concentration
(A2-Aref)f3-(A1-
Aref)f4
Absorbance A1=A260nm None No units
ratio A2=A280nm or A -A (ratio)
Ratio= 1 ref
A230nm A -A
Aref=A320nm 2 ref
(optional)
47
Appendix B
Lamp Replacement
A. TO REPLACE DEUTERIUM LAMP
1. Turn off and unplug the instrument (VERY

IMPORTANT: HIGH VOLTAGE).
2. Remove the cuvette holder rod by unscrewing the rod

counterclockwise.
3. Remove the all screws around the sides of the spectrophotometer. See
Fig A1
Fig A1
4. Very carefully remove the cover of the instrument and place in right
side of the instrument. Fig A2
48
Fig A2
HINT: If it is necessary to remove the cover from the right side of the
instrument, carefully remove 3 connectors (CZ6, CZ4 and J3) on PCB marked
SST8.417.100. Be sure to reconnect after replacing the lamp!
Fig A3
J3
CZ6 CZ4
Fig A3
49
5. Remove the grey metal protection cover. Using screwdrivers remove
the two top screws and the two bottom screws, and then place the
protective cover to the side. See Fig A4
Fig A4
6. Disconnecting the connector J7 on the PCB marked SST8.411.128.

Unscrew the screw that holds the lamp bracket to the instrument base.
Pull the entire lamp and lamp holder assembly out. See Fig A5
50
J7
Fig A5
7. Replace the pre-aligned lamp with a lamp (Fig A6) provided by UNICO
or an authorized UNICO Service Provider. This comes pre-assembled
with lamp socket.
Fig A6
CAUTION: THE LAMP MAY BE HOT! TAKE PRECAUTIONS TO

PREVENT POSSIBLE BURNS.
51
8. Reconnect the connector J7 to the PCB marked SST8.411.128.
9. Re-fit the grey metal protection cover, Fig A4. Temporarily re-fit the
main cover and fix with two screws, one each side.
Switch on and remove the grommet from the middle of the rear panel. You
can now look through the hole and view the image of the lamp on the slit.
Check the lamp alignment Fig A7. If the image is not covering the slit, the
lamp alignment needs adjustment. This requires running the SQ-2802
without the covers, with high voltages accessible, and so should only be
performed by a suitably qualified engineer.
If adjustment is required, remove the cover and grey protection cover, put
on UV protection glasses and turn on the instrument. Adjust to make the
image central on the slit, Fig A7.
Install the grey metal protection cover and cover of instrument.
Focus on
the slit
Fig A7
CAUTION: Wear UV protection glasses when replacing deuterium lamp.
52
10. Re-fit all the screws around the sides of the spectrophotometer, Fig A1.
11. Re-set the lamp usage time. Select “Utility”, lamp, and re-set D2 usage
time.
B. TO REPLACE TUNGSTEN-HALOGEN LAMP
1. The step 1-step 5 are the same as the REPLACING DEUTERIUM.
2. Remove the lamp from the ceramic base.
3. Insert the new lamp (Fig A8), pushing it in as far as it will go.
4. Re-fit the grey metal protection cover, Fig A4. Temporarily re-fit the main
cover and fix with two screws, one each side.
Switch on and remove the grommet from the middle of the rear panel. You
can now look through the hole and view the image of the lamp on the slit.
Check the lamp alignment Fig A9. If the image is not covering the slit, the
lamp alignment needs adjustment. This requires running the SQ-2802
without the covers, with high voltages accessible, and so should only be
performed by a suitably qualified engineer.
If adjustment is required, remove the cover and grey protection cover and
turn on the instrument. Adjust to make the image central on the slit, Fig A9.
Install the grey metal protection cover and instrument cover.
Fig A8
53
Focus on
the slit
Fig A9
CAUTION: DO NOT HANDLE THE LAMP WITH BARE FINGERS. USE

TISSUE OR CLOTH WHEN HANDLING LAMP.
The oil from your fingers can cause the lamp to burn out prematurely.
5. Re-fit all the screws around the sides of the spectrophotometer, Fig A1
6. Install the gray metal protection cover and cover of instrument.
7. Re-set the tungsten lamp usage time. Select Utility, lamp and re-set W
lamp usage time.
54
Appendix C
A number of correction techniques can be used to eliminate or reduce

interference errors. In general, if the source of the error is known and is
consistent from sample to sample, the error can be eliminated. On the other
hand, if the source is unknown and varies from sample to sample, the error
can be reduced but not eliminated. Correction techniques can always require
data from at least two wavelengths. The more sophisticated correction
techniques require multiwavelength or spectral data.
A.1 Isoabsorbance
When a known interfering component with a known spectrum is present, the

error introduced by this component at the analytical wavelength for the target
analyze can be eliminated by selecting a reference wavelength at which the
interfering compound exhibits the same absorbance as it does at the
analytical wavelength. The absorbance at this reference wavelength is
subtracted from the absorbance at the analytical wavelength, as shown in
Figure A1.The residual absorbance is the true absorbance of the analyze.
This technique is less reliable when the spectra of the analyze and of the
interferent are highly similar. Moreover, it can correct for only one
interference.
Fig A1 Isoabsorbance correction
55
A.2 Three-point correction
The three-point or Morton-Stubbs correction uses two reference wavelengths,

usually those on either side of the analytical wavelength.
The background interfering absorbance at the analytical wavelength is then

estimated using linear interpolation (see Figure A2).This method represents
an improvement over the single-wavelength reference technique because it
corrects for any background absorbance that exhibits a linear relationship to
the wavelength. In many cases, if the wavelength range is narrow, it will be a
reasonable correction for non-linear background absorbance such as that
resulting from scattering of from a complex matrix.
Fig A2
56

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SQ-2800 Single Beam

United Products & Instruments Inc.

Tel: 732-274-1155 / 1-800-588-9776

Some of the chemicals used in spectrophotometry are corrosive and/or

The UNICO SQ-2800 model spectrophotometer incorporates a 320×240 dot

Sample Compartment Lid LCD Display

Power 110V/220V Serial

Block diagram for the Spectrophotometer

2. Place the instrument in a suitable location away from direct sunlight.

5. Turn on your UNICO SQ-2800 model spectrophotometer. Allow it to

Prepare the spectrophotometer

3. If no auto-cell changer installed “cell #1” will disappear in Fig 7

Un ited Pr od u cts & In s tr u m en ts In c.

Wa it u n til E a s yRTO S b ooted : D2

Wa it u n til E a s yRTO S b ooted : D2

Sys te m c a lib r a tin g? No

Wa it u n til E a s yRTOS b ooted : D2

 Press the key [0Abs/100%T] for blanking

Note: 1. If the reference solution is too thick, “Energy Low…”will appear

2. If no automatic changer installed “cell #1” and “Max E” will

F1 :Un it F2 :Mod e F3 : F Fa c tor F4 : Sta n d a r d

F1 :Un it F2 :Mod e F3 : F Fa c tor F4 : Sta n d a r d

Set wavelength (Example: set wavelength in “Basic mode”)

 Press [SET λ] (Fig 10).

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

 Use numeric keypad to input wavelength (Fig 11).

 Press [ENTER] to change the wavelength from 656.1nm to

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

2. The key [CLEAR] be pressed the file selected will be deleted by

Save data or curve (Example: Save curve in “WL scan”)

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

For different user requirements, we have provided different test methods.

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

Ple a s e in p u t s e lf d e fin e d u n it: c

F1 :Un it F2 :Mod e F3 :F Fa c tor F4 :Sta n d a r d

 Print Test Report

Qu a n tita tive Tes t D2

 Press [F1] to select unit of concentration (Fig 27).

Qu a n tita tive Tes t D2

 Press [SET λ] to select correction methods and enter the wavelength.

Note: Please refer to the Appendix C for the correction method.

Qu a n tita tive Tes t D2

The constants to be entered are depending on which fitting method

Fitting Method Fitting Equation constants

 Press [F3] in Fig 29 to establish a standard curve by measuring a

Setu p Sta n da r d Con c. D2

Setu p Sta n da r d Con c. D2

WL : 700.0nm Ab s : Bla n k …. …….

Ca libra tion ta ble D2

Note: If auto-cell changer is installed, the vary samples are measured by

For linear fits, “r” represent fitting coefficient of linear regression.

-1.0 Abs 4.0

Fig 34 linear through zero fit

-1.0 Abs 4.0

Fig 35 square fit

WL : 656.1nm Ab s : 12: 35: 27 WL : 656.1nm Ab s : 12 : 3 5 : 2 7