Professional Documents
Culture Documents
1
Content
Content ..............................................................................................................................................
Preface ................................................................................................................................................
2
z Preface
Please read the manual carefully in order to maintain the system correctly.
Appropriately keep the service manual somewhere is easily available in order to use it at your
disposal.
Components: Analysis unit (host), operation unit (computer system), result output unit
(printer), accessories and consumables.
Standard No:
Registration Address:
Production Address:
z Reader
Readers of the manual should be Dirui company or the maintenance staff authorized by Dirui.
z Content
●The instrument should used only for medical professionals or trained doctors, nurses or
experimentalist.
●Correct handling the waste liquid and instrument consumables is a must, and the blood contained
in waste liquid may have been contaminated by pathogens, therefore, please handle the waste
liquid and instrument consumables according to the regulations coping with medical waste,
●Samples, quality control, calibrator, waste liquid, etc. possessing potential biological infectious
danger may be pungent to the eyes, skin and mucous membranes. Operator should comply with
the safe operation of the laboratory and wear personal protective equipment (such as laboratory
protective clothing, gloves, etc.) when exposing to the related items in the laboratory.
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●Rinse it immediately with plenty of water once skin or eyes have contacted with the reagent.
●Avoid contacting with the sharp sampling probe which may be appendiculate with blood, quality
control and calibrator having potential biological infectious hazard; in the sampling process, a
certain distance should be maintained between the sampling probe and the bottom of container,
otherwise it will affect the accuracy of the assimilated volume solution. Forasmuch, avoid blood
●Do not use resin oil, benzene to clean the outside dirt, because it may cause changes in color and
shape. Scrub it with a soft or wet cloth, and clean it with diluted cleaning liquid or alcohol for the
serious.
●Do not use the expired reagent, and forbid dust, dirt, bacteria going in reagent after unseal.
●The outcome of the analysis can not be reliable if the analyzer worked at room temperature
●Do not unplug the printer, bar code scanner at the power-on state.
●Using the specified types of external equipment is must.
●Background check, namely, the analyzer works by using diluent instead of sample diluent.
●The outcome of the analysis can not be reliable if abnormality occurs to the analyzer when it is
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Part one Specification
Name:Auto-Hematology Analyzer
Model:BCC3000B
Frequency:50/60Hz
Dimension:
Weight:25Kg
MCV(fL) 0.0~300.0
1.4.2 Accuracy
The average and measurement error on standard machine should be in the following range with
quality control or calibrator used for testing 10 times.
Whole blood model WBC ±3% or ±0.5×109/L
RBC ±2% or±0.03×1012/L
PLT ±5% or±10×109/L
Dilution model WBC ±5% or±0.4×109/L
RBC ±3% or±0.05×1012/L
PLT ±8% or±15×109/L
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1.4.3 Repeatability
Variation parameter in the 95% confidence interval should be within the following range in 10
times continuous tests by normal fresh blood and QC blood.
1) Whole blood model
Parameter Range Repeatability
(CV%)
WBC 4.0×109/L or more ≤4.0%
1.4.4 linearity
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60 samples/h
1.5 Function
1.5.1 Memory
1.5.2 Printer
1) External printer:
2) Internal Printer:
1.5.5 QC
X Control or L-J Control
1.5.6 Calibration
Manual calibration
Fresh blood calibration
1.6 Reagent
1.7 Fuse
7
250v 2A;
Temperature: -20℃~+50℃
8
Part two. Electrical System
Analysis solution
Pulse Time
Adopting counting principle of Coulter electrical impedance (see figure 1). Resistance sensor
is constituted by electrodes of one glass gem microporous tube and that of a pair of contraposition
gem microporous tube inside and outside. Constant current is automatically added on electrodes
when testing.
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A certain amount of electrolyte should be contained in the inspected, namely test can be
carried out when the inspected and diluent resistance ratio of standard particle used by calibrator
must be equal under the specified resistance ratio, which is the condition of resistance test
Resistance method analyzers adopt negative pressure to siphon sample to force the inspected
pass the small cylindrical gem micropore whose inside is filled with the inspected to form the
constant liquid resistance (R0). The increment of resistance ΔR occurs the moment a spherical
standard particle whose diameter is d in the inspected passes the gem micropore because the
resistivity of particle is more than that of the inspected, which is calculated by Coulter formula:
well. The degree of increased voltage depends on the volume of small aperture sensing zone
taken by non-conductive cells, namely, the bigger the cell are, the bigger the pulse caused are.
z Amplifying: because the pulse signal generated when passing through the micropore is very
weak so that the counting circuit can not be touched off directly, the pulse signal should be
z Screening: All kinds of particles can generate corresponding pulse signals when passing
micropore whose level (pulse range) is direct proportion to particle volume. Besides blood
cells and cells in blood, the debris in blood, impurities in diluent all can generate fake signals
which can make counted result higher. Screening means that the fake signals which are lower
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than reference level should be taken out by using discriminator to improve the accuracy of
counting cells according to the reference level provided by threshold value adjustor.
z Threshold value: Adjust the reference level in the specified scope so that the result of the
z Shaping: The amplified and Screened signal wave shapes of cell pulse differ and need to
be shaped by shaper to be the wave that V is consistent with shape, and which is standard
z Counting: The pulse signals of blood cells are sent into the counting system after amplifying,
screening, shaping, and sent collecting peak value of pulse into the CPU simultaneously.
Incorporate the overlapping calibration formula into the instrument testing program by the
instrument logical circuit and math calculation and calculating formula. The instrument can
calibrate result easily after judging and calculating when the situation that two cells pass the
micropore simultaneously.
To rule out the noise and small red blood cell interference, the accurate counting result of
platelet without noise interference and impact of platelet can be obtained by electronic curve
fitting to count the large platelets which are not counted in accordance with normal volume of
2.2.1 In the counting of pulse, correctly differentiating erythrocyte, leukocyte, platelet one of key
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The number of human erythrocyte are about 1000 times as many as that of leukocyte, so
counting the number of human leukocyte can be carried out simultaneously when counting
erythrocyte.
z The number of human erythrocyte are about 1000 times as many as that of
leukocyte, so counting the number of human leukocyte can be carried out simultaneously when
counting erythrocyte.
Working principle:The pulse values of counting cells are different because of different types.
When the threshold value voltage of circuit is V1, start to count erythrocyte and leukocyte,
and the pulse of platelet is screened. The result is the number of erythrocyte. When the
threshold value voltage of circuit is between V2 and V1, the result is the number of platelet.
Add hemolytic agent in sample, and erythrocytes are dissolved. Leukocytes are dehydrated
to some extend in the controlled conditions, and the volume of leukocyte depends on the number
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of tangible substances. Small cells in leukocyte, for instance, lymphocyte is mononuclear cell
with small nuclear, small particles and size of 35 ~ 98fL; large cells in leukocyte, for instance,
mononuclear cell, eosinophil, basophil l, the original cells and late promyelocyte shrink to98~
160fL, which are called middle cell in leukocyte, or median cell. The following shows the
distribution or histogram of leukocyte volume. The different region classification fitting of the
histogram and integral calculating can obtain the count of the leukocyte trisection classification
(LYM#,MON#,GAN#).
Small cell (lymphocyte)
Middle cell (mononuclear cell)
Big cell (neutrophili)
The red blood cell starts to be dissolved after add the hemolytic agent to diluted blood and the
hemoglobin is released, and hemoglobin derivatives are generated after the latter combines
with the hemolytic agent. Enter into the hemoglobin test system and execute colorimetry in a
the content of Hb in the liquid, and HGB concentration can be calculated by the instrument.
HGB calculating formula:
Lambert-Beer law
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K: constant,I0: transmitted light intensity of blank sample
2.4 Volume testing principle
Start sensor
Start sensor
1. Start counting and empty the tube 2. Liquid level descends when
3. Count starts when liquid level 4. Count finishes when liquid level
passing start sensor passing finish sensor
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2.4 Electrical overall figure
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5 A5 Main control board (PCB NO.110703241)
20 P1 Air pump
22 S1 Button switch
16
37 V15 Two-pass solenoid valve
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Real time Internal
clock printer
Serial flash
Drive
board
interface LCD screen
Touch screen
Liquid level sensor
Control interface of amplification board
RS232 interface
External printer
1.1 Layout
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2、Drive board
Power drive board carries out controlling deflection motor, up-down motor and injector motor
according to the instruction of upper machine, and controls pumps and valves by receiving the
switch signal of upper machine. Power mainly consists of three models: switch control module,
motor control module and power module. Power supply
19
Power supply
Drive module of solenoid
valve
Drive module of motor
Serial port
Mainboard interface
Drive module
2.1 Layout
20
2、 Analog board
21
Analog board is reasonable for changing original signal into the signal which meets the A/D
conversion requirement, including WBC and RBC + PLT amplification unit, HGB amplification
unit, the temperature measurement unit, vacuum measurement unit, power supply monitoring unit,
processing unit of small hole voltage, electronic analog switch module etc..
Temperature sensor
温度传感器
Voltage check 电压检测
检波波形
Check wave start point
Amplifier Amplifier 起 点
放大器 放大器 Sensitivity
灵敏度increasement
增 益
Absorbance
WBC
吸光度 Main control board
主控板
Converting
HGB 放大器
Amplifier 放大器
Amplifier 模数转换
RBC
检波波形
RBC Check
起 wave
点 start point
放大器
Amplifier
放大器
Amplifier
灵敏度
Sensitivity increasement
增 益
100V voltage Amplifier
放大器
100V电压电路
circuit
模拟检测模块原理框图
Principle frame of simulation check module
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3.1 Layout
23
4、Volume computation
Volume computation board, by detecting the liquid volume with the light sensor of
computation tube, ensures the WBC and RBC + PLT test accuracy.
4.1 Layout
24
5、Display board
Control the interface through the main board.
5.1 Layout
25
6、Printing board
Singlechip LPC2114 on the board communicates with the main control board CPU through
the serial port, and printing of characters and waveforms and sending real-time status of counter to
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the host CPU to display is achieved in accordance with the instruction of main control board CPU
with total two sets power supply on the board. Printing head heating voltage is provided with the
voltage that has been converted from 24V DC voltage, and CPU power supply is provided with
5V by the main board.
串行数据输入
Serial data
input
Motor drive
Heater of paper‐in
Power 打印头加热器 进纸电机电机驱
打印机电源
电路 of
circuit motor 动
supply of
print head
printer
Figure Circuit frame of printer
图 1: 打印机电路框图
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6.1 Layout
28
7. Power supply board
Providing system power supply:+5v,±12v。
7.1 Layout
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Part three Liquid line
In the whole blood mode, diluted sample of ratio about 1:269 is formed by mixing 13ul of
whole blood sample and 3.5mL of diluent that are assimilated by counter, which is divided into
two parts. Counting sample of ratio about 1:44872, obtained by mixing the 15.6ul diluted sample
and 2.6mL diluent, is used for counting erythrocyte and platelet; counting sample of ratio about
1:308, obtained by mixing the rest of diluted sample and 0.5mL hemolytic agent, is used for
13μL whole blood sample
3.5 mL diluent
Sample of diluting ratio about 1:269
全血工作模式稀释流程
In the pre-diluting mode, diluted sample of ratio about 1:36 is formed by mixing 20ul of
peripheral blood sample and 0.7mL of diluent (diluted externally). Diluted sample of ratio about
1:384, obtained by mixing 0.3mL previous diluted sample with 2.9ml diluent that is assimilated by
counter, is divided into two parts. Counting sample of ratio about 1:43355, obtained by mixing the
24.8ul diluted sample and 2.8mL diluent, is used for counting erythrocyte and platelet; counting
sample of ratio about 1:428, obtained by mixing the rest of the previous diluted sample and
0.36mL hemolytic agent, is used for measuring the concentration of hemoglobin and counting
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leukocyte.
20μL peripheral blood sample
0.7mL diluent
Sample of diluting ratio about 1:36
2.9mL diluent
Sample of diluting ratio
about 1:384
0.36mLhemolytic agent About 2.8mL diluent
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2
20 3 4
6 5 7
8
9
10
14
11 12
13
15
16
21
17
18 19
1,10: Buffering bottle
2: Liquid absorbing pump
3,4,6,7: light sensor
5,8: Flowmeter
9: Cleaning liquid bottle
11: Hemolysin bottle
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12: Positive pressure pump
13: Pressure sensor
14: Hemolysin pump
15: Sampling pump
16: Diluting pump
17: Diluent pump
18: Sampling probe
19: Rinsing bath
20: Hydraulic pump
21: Pressure pump
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Part five. Maintenance
Figure 3-1
4.2 Valve check
Valve switch can be checked whether it is normal in the valve interface. System liquid lines
will not work normally if the valve fails.
Steps are as follows:
Press V1~V18 to start check before select the items “V1”、“V2”、“V3”……“V18” if the “OFF”
is shown in the corresponding result column of items. After check, the status key shows as “ON”.
It can be inferred preliminarily that valve works normally if the sound that valve and switch issue
sounds normally in the process of checking. Contrarily, failure may happen to valve.
~Valve Check~
Valve Valve Valve Valve Valve
V1 OFF V5 OFF V9 OFF V13 OFF V17 OFF
V2 OFF V6 OFF V10 OFF V14 OFF V18 OFF
V3 OFF V7 OFF V11 OFF V15 OFF
V4 OFF V8 OFF V12 OFF V16 OFF
Figure3-2
Confirm Exit
Figure 3-2
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4.3、Description and use of menu of instrument system check and diagnosis
Total 19 tests, such as counter hardware, machinery parts and liquid line components, are
tested by system, and it is shown that whether the component is in normal state or whether the
time of the test is in the range of time.
System testing is fluid path for a total of 19 tests showed or to the time required for this operation.
Check whether 2.5ml and 50ul, 10ml, deflection and up-down motors run normally in all
directions.
System Testing
2. If the result is normal, “Normal”(Y) will be displayed in the corresponding result column of the
"Test Item" .
3.If test results are abnormal, failure (N) will be displayed in the corresponding result column of
the "Test Item", and refer to malfunction at this time or measure the test points of relative valtage.
4.4 Maintenance
Daily 1, if instrument is not shut down for 24-hour, conducting "counting cell
2、QC
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Every 3 days if instrument is not shut down for 24-hour, conduct "Immerse probe top"
Weekly If instrument is shut down normally every day, conduct "Immerse probe
top" weekly
● If the counting cell is contaminated, implement “Counting cell cleansing " operation;
● When the counter is not used for more than two weeks, implement " Exhaust liquid line"
operation in "System maintenance" menu to complete the counter liquid line exhausting and
Press 【Eliminate block】 key manually or execute “Burn gem hole” and “Back-flush gem hole”
operation.
● Reliable analysis result can be obtained when the counter works in a normal circumstance. So,
4.5 Method
10 ways are available in the system maintenance interface
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Part five Maintenance Guide
Initially, it is needed to check whether the wiring of instrument is loose and the connecting of
liquid lines, pipelines of diluent, cleanser and waste liquid is good. Check system status
instrumentally and systematically check relevant function when start the instrument.
1. Boot
No. Function Malfunction Solution
1 Displaying Displaying 1. Adjust backlighting potentiometer
“loading…” failure 2. Check whether the LCD connection is loose
3. 3. Rewrite BOOT program
2 Entering self-check Displaying 1. Re-weld mainboard ARM chip and FPGA chip
interface failure 2. Rewrite ARM main program
3. Replace mainborad
3 Motor failure 1. Check whether the corresponding light sensor is
normal
2. Check whether the motor wire and light sensor
wire are loose.
4 System status Status 1. Check analog board
abnormal 2. Check whether the wire of temperature sensor is
loose.
5 System check Corresponding Replace mainborad EPCS4
AD status
normal, break
error
6 Sampling volume Sampling 1. Check whether the corresponding injection pump
check volume error is loose
2. Check whether there are bubbles or leakage to
corresponding pipeline
7 Blank check PLT test*** 1. Check whether poor soldering exists at RBC
sensor connecting wire
2. Exchange RBC sensor and WBC sensor
connecting wire
Replace the RBC cup body if WBC counting
abnormal
3.Replace analog board
8 PLT bland pass Replace diluent
failure
9 WBC bland
pass failure
10 Histogram-out Histogram setup option failure
failure
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11 Sampling probe 1. check 2 # pipeline
leaking 2. check 4 # pipeline
12
2. Maintenance in testing
38
6, open, clean the front and
back counting cells of counter and
the gem hole, and replace
microporous gasket.
7, Cut off the inflow of
hemolysin to exclude hemolysin
interference.
8,Check the lower
connected pipes of counting cell,
rinse the lower pipeline if it is Repair analog board
dirty.
9, valve dirty, not tightly
closed, poor opening.
10, replace counting cell.
11, analog board broken failure
5 PLT background 1、 whether the background Replace reagent
value high value is stable
2、 whether there is ground wire
3、 watch the histogram
4、 use probe cleaning liquid to
immerse counting cell
5、 open, clean the front and
back counting cells of
counter and the gem hole,
and replace microporous
gasket.
6、 Pipeline on the surface of Replace cell and check analog
cell is dirty and rinse it. board
7、 Counting cell can’t be
emptied; V11 valve dirty,
not tightly closed, poor
opening.
8、 Electrode of count failure
9、 Analog board
39
broken.
5, analog board
6, HGB adjustment alarm
7, Watch the background of
HGB voltage
8, immerse, clean WBC
cell
7 HGB background 1, clean WBC cell if it has
voltage not stable dirt.
2, whether there is water
membrane between the outside of
cell and HGB rack.
3, HGB illuminates and
receives connection oxidation
4, analog board
8 RBC、PLT blood 1, the cell is not emptied,
sample value low and poor valve opening.
2, whether sampling needle
is sampling and diluting normally.
3, analog board
4, whether sample
assimilating is normal and re-set
it height
9 WBC blood 1, the cell is not emptied,
sample value low and poor valve opening. (RBC
value low at the same time)
2, sampling probe blocked,
sampling volume inadequate RBC
value low(at the same time)
3, leakage occurs between
sampling probe and 10mL
syringe (RBC value low at the
same time)
10 WBC/RBC Bubbles simultaneously
bubble 1, check whether there is diluent
2, check whether there is diluent
in the two cells.
3, check whether the 10mL
syringe is filled with liquid; if not,
leakage occurs in 10mL syringe
or pipeline.
4,10ml syringe upper pipeline is
kinked, and pipeline is blocked
(10mL motor issues failure at the
40
same time).
Bubbles singly
1, back cell leaks
2, valve membrane broken
3, pipeline leaks
4,valve is not closed tightly or
valve membrane is broken.
11 when counting 1, Diluent and rinsing liquid
blood sample, are connected in reverse.
WBC value is 2, vacuum degree is low
normal; RBC 3, waste liquid pipe is
value is less than kinked and liquid exhausting is
1; PLT is 0 or a poor.
few dozen or 4, vacuum filter is blocked
normal 5, vacuum pump failure
6, valve is closed tightly.
7, vacuum tank and
relevant pipelines leak
8, vacuum sensor of analog
board are crystallized and
blocked.
12 Motor failure 1, the relevant line blocked
2, motor broken
3, light sensor broken
4, drive board failure
13 Hard to classify 1, what’s the WBC total number
WBC 2, check the background and
eliminate its interference factors
3, check whether the histogram is
compressed
4, what’s the voltage of small
hole
5, check whether it is diluent of
the original factory or it is
expired.
6, check whether it is whole
blood or peripheral blood, and
whether anticoagulant ratio is
followed EDTA K2
7, check whether specimen is
from children and specimen
storage time
41
high or low
3. Malfunction Code
Malfunction Malfunction
No. Malfunction Code Solution
description cause
1. Press “confirm” button
to reset motor
2. Check the diluting pump
32—41、48、49、 Diluting motor
Diluting motor motor
53—55、 61、 62、 abnormal with
1 failure 3. Check driver board
64、65、66、 abnormal sound
4. Check driver board power
187—189
supply
5. check LCP2131
6.Replace driver chip 3977
1. Press “confirm” button
to reset motor
Sample motor 2. Check the sample motor
Sample motor
16—22、24、 abnormal with 3. Check driver board
2 failure
25—28、179、185 abnormal sound 4. Check driver board power
supply
5. check LCP2131
6.Replace driver chip 3977
1. Press “confirm” button
to reset motor
2. Check the rotating motor
Rotating motor Rotating motor
3. check light sensor
abnormal with failure or light
3 112、115、116 4Check driver board
abnormal sound sensor is not
5. Check driver board power
checked
supply
6. check LCP2131
7.Replace driver chip 3977
1. Press “confirm” button
to reset motor
2. Check the s up-down
Up-down motor Up-down motor
motor
50、113、114、117、 abnormal with failure or light
4 3. Check light sensor
118 abnormal sound sensor is not
4. Check driver board power
checked
supply
5. check LCP2131
6.Replace driver chip 3977
5 176—178、184、186 Clean swab; motor failure 1. Press “confirm” button
42
automatically reset to reset motor
if not assimilating 2. Check the sample and
sample diluting pump motor
3. Check driver board
4. Check driver board power
supply
5. check LCP2131
6.Replace driver chip 3977
1 Check the analog board
Reset signal and mainboard cable.
6 180—183 Circuit failure
abnormal 2. Check the analog board
and mainboard
1. Check liquid line
2. Check analog board
3. Check +12 V voltage
4. Replace U19
5,Replace potentiometer
Liquid line and VR negative pressure and
7 2—5 Pressure abnormal analog board VR3 positive pressure
failure 6.Replace pressure sensor
negative pressure U21 and
U23 positive pressure
7.Replace U14 negative
pressure and U15 positive
pressure
1, Replace diluent,
cleaning liquid in the
maintenance interface
2, Check HGB background
voltage
3, check white blood cell
Liquid line counting cell, and check the
bubbles, relevant pipeline and
counting cell solenoid valves (3、1、4、
8 201 HGB Blank error cracks, bad light 5)if there is no liquid.
penetrating, bad 4, Check± 12V voltage
colorimetric (corresponding failure 202)
terminals 5, check the colorimetric
terminal
6, check the 100V voltage
and 56V Voltage
7, check Q14 (IRF210)
8, check U32 (UC3438)
9, check U12
43
1. Check analog board and
mainboard
2. Check the cable between
56v failure, the analog board and mainboard
lower probe, 3.Observe analog board
9 202 temperature alarm Circuit failure indicator
issues when probe 4. check ± 12V power
up and down supply voltage
5. Check 100 voltage,
6. check ZD1
7. Check 56V voltage
1. check whether the lead
of ration tube and its light
sensor is damaged
2. Check light sensors P1,
P2, P3, P4
Ration tube
3.Check potentiometers
10 203 Ration tube failure light sensor
VR1, VR2, VR3, VR4
failure
4. Check U2A, U2B, U2C,
U2D
5. Check whether solenoid
valves 7,17,8,18 are normal.
6. Check driver board
1,Implement washing,
1. Erythrocyte
immersing, eliminating
test unit hole
Counting cell liquid block, burning, back flush
blocked
Ration overtime overflows, and it is and other maintenance
11 2. leukocyte test
issued that ration is measures
unit hole
over time 2, clean gem hole
blocked
3, Clean No. 2,10,11,12
3.valve blocked
valves.
44
Part SIX Mechanical Unit Disassembly
3 2
5
Gem hole
Rubber pad
6
4
Figure 1
1、Setscrew 2、Transducer 3、Vacuum chamber
4、Ruby (microporous) 5、Mesoporous tube 6、Rubber gasket
Figure 2
Install the fluorine rubber gasket, gem microporous 100 (mind direction) and vacuum chamber
components into the transducer, and lock them tightly on the transducer by self-tapping screws;
2、Disassembly and component of HGB Rack
45
HGB rack on WBC count pool
Figure 3
HGB rack installation hole
Figure 4
Install LED component, optoelectronic receiving tubes into the O-ring into the transducer, and
lock them tightly by pan head screws.
2 4
3
7
Cable 21
Cable 20
Illustration
46
1、Guide closing tube 2、Cross pan head screw 3、Bracket of rotating motor 4、Step motor
5、Cross pan head screw 6、Cross pan head screw
7、Linear motor 8 Bracket of up-down motor
1)、Paint the screw thread on cross pan head screw with screw thread fastening agent, lock the step
motor(cable 21) tightly on the bracket component of the rotating motor with screws, and fix the
guide closing tube on the bracket of rotating motor with cross pan head screw as the following
figures shows, which assembles rotating motor components.
2)、Paint the screw thread on cross pan head screw with screw thread fastening agent, lock the
Linear motor(cable 20) tightly on the bracket component of the up-down motor with screws
(Note:lifting lead screw is forbidden when moving motor)as the following figures shows, which
assembles up-down motor components. Note: Sequently, put the components on table with
leadscrew up and motor down
3.2 Installation of components of connecting items, slider and rotating arm
4 10
1
9
3 5
8
2
6
7
Illustration
1、Connecting item 2、Cross countersunk head screw 3、Swab bracket 4、Cross pan
head screw 5、flange board of screw nut 6、N
7、Up-down light sensor 8、Cross countersunk head screw 9、Up-down slider 10、swaying
arm of sampling probe
1)、fix the swab bracket on the connecting item with the Cross countersunk head screw (2)to
assemble connecting items as the following figure shows;
2)、①Buckle the up-down slider and swaying arm of sample probe as the direction of figure 4
shows. (Note: the trough of sampling probe swaying arm should be buckled down to the bottom of
the slider circular button)
②fix the flange board of screw nut on the swaying arm of sampling probe with the cross
countersunk head screw(4).
③fix the nut on the up-down slider with the cross pan head screw(8), and fix up-down light
sensor on the up-down slider with cross pan head screw to assemble the slider and the components
of swaying arm .
47
3.3 Installation of screw nut components, up-down motor and connecting components.
3
2
4
5 6 Cable 20
Illustration
1、Rotating light sensor 2、Screw nut(spline shaft) 3、Deep groove ball Bearing
4、Up-down motor component 5、Interspace connection board 6、Internal hexagon head screw
1)、Install deep groove ball Bearing at the short end of optical axis of screw nut (bearing is
supposed to be install at the bottom of short end of optical axis), assemble rotating light sensor
on the screw nut to form the screw nut components as figure shows:
2)、Paint the screw thread on hexagon countersunk head screw with screw thread fastening agent,
fix the bracket of up-down motor on middle connection board to form the up-down motor and
middle connection components
48
3.4 Component installation and component connection of rotating motor and supporting
components:
1
3 4
2
7
5
Illustration
1、Slider and swaying components 2、Screw nut components
3、Linear axis 4、Rotating motor and middle connection components 5、Flange outer ball bearing
6、Rotation support 7、Rotating motor components
1)、Install the linear axis and screw nut components on up-down motor board, and install slider
and swaying components on the screw rod of up-down motor as figure shows:
2)、Install flange outer ball bearing on the screw rod of up-down motor, and install rotation support
on the axis end of step motor to form rotating motor and supporting components as figure shows:
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3.5 Overall assembly
0.2
Cable 21 Cable 20
1
2
3
Cable 21
Illustration
1 Connection components 2 、 Rotating motor and supporting components
3、Hexagon countersunk screw 4、Screw thread fastening agent
Assemble the connection components on the long end of screw nut, install the up-down motor
screw rod and one end of linear axis into the corresponding holes of rotating motor board,
adjust the parallelism of rotating motor board and up-down motor board to make sure the
difference of the two boards is less than 0.2mm, paint the screw thread on the hexagon
countersunk screw with fastening agent and fix the rotating motor bracket on the middle
connection board as figure 9 shows:
Note: after completion of installation, move the slider manually to make sure it moves smoothly.
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1.Disassembly and structure of liquid pressure unit
4.1 Installation of left and right block
1 7 6
2 3
4 5
illustration
1、Friction sleeve 2、Cross countersunk screw 3、Cross pan head screw 4、Light sensor
5、Shaft ring 6、Linear axis 7、Left block
1,Assemble linear bearing into left block, fix it with shaft ring
2,Lock the friction sleeve tightly with cross countersunk screw on the right block.
3,Lock the light sensor on the left block with pan head screw as figure shows:
4, Ibid to the right block
1 4
2
Cable 23 Cable 22
3
Illustration
1、Cross pan head screw 2、Motor seal sleeve 3、Linear motor 4、Lower board
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Assemble the motor seal sleeve into lower board, with whose top end pointing at the middle
area of upper and lower board, assemble the Linear motor into the lower board and lock it
tightly with pan head screw to form motor components with the cable coming out direction as
figure shows:
4.3 Installation of middle connection board and upper and lower boards
1
2
3 4
Illustration
Adjust the distance of upper and lower boards, and lock the upper and lower boards tightly at the
screw holes of both ends of middle connection board after paint hexagon column head screw with
screw thread fastening agent as figure shows:
1
2 3 4 5 6
Illustration
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1, Install the middle rod into the middle, lock it tightly after paint it with screw thread fastening
agent MSSU4-6, assemble the linear bearing rod into the left and right blocks respectively, rotate
into the corresponding positions of upper and lower boards and lock them tightly after paint them
with screw thread fastening agent 2-MSSU4-6, and keep the end levels of the three rods and
outside end of upper board at the same level.
2、Tighten the screw rod in the left block and right block after push it through the motor seal
sleeve, and lock the motor axis tightly on the left and right blocks with 2 MSSU4-10 hexagon set
screws with chamfered end , which is painted screw thread fastening agent.
3 、 Insert 3 cylindrical pin into corresponding positions of hydraulic connector, hydraulic
connector1 as figure shows;
Overall assembly 2:
2 3 4 5 6
7 8 9
Illustration
1、2.5ml injection pump 2、Screw 3、50ul injection pump 4、10ml injection pump
5 、 injection pump interface 1 6 、 Hydraulic interface 7 、 Baffle 1
8、Baffle 9、Cross pan head screw
1, Tighten injection pump interface 1 on the 50ul injection pump, spread the glue 704 evenly on
the injection pump and the connecting point of connector. The same way to install the hydraulic
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connector the other two injection pumps and they are available until glue is congealed.
2、Install the end of 3 injection pump components intoФ3 pin hole, and lock the other end on the
left and right blocks with 3 stainless steel screws as figure shows; Note: It is forbidden to shake
the 50ul injection when pulling down the left and right blocks to motor.
3、Lock the baffle 1 and baffle on the upper board with 4-M3x8 pan head screw as figure shows:
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