Instruction Manual: Ion-Selective Electrode Monitor
Instruction Manual: Ion-Selective Electrode Monitor
IM/8232–SO1_2
Model 8232 Ammonia Monitor
Special Range 0.05 to 2000 mg l–1
We are an established world force in the design and manufacture of instrumentation for industrial
process control, flow measurement, gas and liquid analysis and environmental applications.
As a part of ABB, a world leader in process automation technology, we offer customers Cert. No. Q05907
The quality, accuracy and performance of the Company’s products result from over 100 years
Lenno, Italy – Cert. No. 9/90A
experience, combined with a continuous program of innovative design and development to
incorporate the latest technology.
Stonehouse, U.K.
The UKAS Calibration Laboratory No. 0255 is just one of the ten flow calibration plants operated
by the Company, and is indicative of our dedication to quality and accuracy.
0255
Electrical Safety
This equipment complies with the requirements of CEI/IEC 61010-1:2001-2 'Safety Requirements for Electrical Equipment for
Measurement, Control and Laboratory Use'. If the equipment is used in a manner NOT specified by the Company, the protection
provided by the equipment may be impaired.
Symbols
One or more of the following symbols may appear on the equipment labelling:
Warning – Refer to the manual for instructions Direct current supply only
Protective earth (ground) terminal Both direct and alternating current supply
Information in this manual is intended only to assist our customers in the efficient operation of our equipment. Use of this manual for
any other purpose is specifically prohibited and its contents are not to be reproduced in full or part without prior approval of the
Technical Publications Department.
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1 INTRODUCTION
1.1 Description understood steps. The sample is presented from the user's
The Model 8232 Ammonia Monitor is a microprocessor based pipework to a constant head unit and any excess is allowed to
analyser using an ABB ammonia ion-selective probe. This overflow. This allows sample, under controlled pressure
equipment is used for environmental water monitoring. conditions, to be presented to a multi-channel peristaltic pump
which proportions sample and reagent solutions through the
monitor to the mixing point. The resulting combined solution is
1.2 Training then temperature controlled to remove the effects of sample
Due to the specialised nature of the above instrument, it is and ambient temperature variations. The conditioned solution
recommended that, where the end users personnel have had is then delivered to the probe, under constantly flowing
no previous experience of maintaining this equipment, training conditions, where the ion measurement takes place.
be provided by this Company.
The probe generates a millivolt output which is proportional to
Such training is available via the local Company in the UK, or the ion concentration. This output is processed by the
Overseas Agent elsewhere and may be carried out either on microprocessor-based electronics section to calculate the
the users premises or at the factory. actual sample concentration.
Ammonia 8232
User Junction Box
(behind case)
Solenoid Valves
(behind case)
Ammonia Probe
Case Lock
Push-to-Release
Latch
Hinged Door
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2 INSTALLATION
2.1 Accessories 2.4 Sampling Requirement
2 x reagent bottles 1 x ammonia probe kit In addition to being as close as possible to the monitor, the
4 x calibration bottles 1 x spares kit sampling point must provide a thoroughly mixed
representative sample. The sample must also conform to the
following conditions:
2.2 Location
The monitor should be installed in a clean, dry, well ventilated a) Sample flow rates must be between 5 ml min–1 and
and vibration-free location giving easy access, and where 1250 ml min–1.
short sample lines can be used. Rooms containing corrosive
gases or vapours (e.g., chlorination equipment or chlorine gas b) Sample temperature should be within 20 °C of the ambient
cylinders) should be avoided. It is also advisable to have temperature and within the range 0 to 40°C.
adjacent drains near ground level, so that the waste outlet
from the monitor can be as short as possible, together with c) Particles must be less than 10 mg l–1 and the size must not
maximum fall. Power supplies should also be adjacent. exceed 60 μm. Above these levels it is essential that the
Ambient temperature: within the range 5 to 40°C. filter supplied is fitted in both the sample and emergency
inlets.
188 Open
235
Position
Junction
Box
Cable
780 Entry 95° Max.
Fixing 890 Point
Centres angle of Closed
Position 542
opening
550
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…2 INSTALLATION
2.6 External Electrical Connections – Fig. 2.3 The connections are as follows:
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2 INSTALLATION…
2.7 Relay Contact Protection and Interference (part no. B9303) as shown in Fig. 2.5A. If the instrument
Suppression – Fig. 2.5 malfunctions the value of the RC network is too low for
If the relays are used to switch loads on or off the relay suppression and an alternative value must be used. If the
contacts can become eroded due to arcing. Arcing also correct RC suppressor unit cannot be obtained, contact the
produces radio frequency interference (r.f.i.) which can cause manufacturer of the switched device for details of the RC unit
instrument malfunctions and incorrect readings. To minimize required.
the effects of r.f.i., arc suppression components are required;
these are resistor/capacitor networks for a.c. applications, or For d.c. applications fit a diode as shown in Fig. 2.5B. For
diodes for d.c. applications. These components can be general applications use an alternative IN5406 type (600 V
connected either across the load or directly across the relay peak inverse voltage at 3 A – part no. B7363).
contacts.
Note. For reliable switching the minimum voltage must be
For a.c. applications the value of the resistor/capacitor greater than 12 V and the minimum current greater than
network depends on the load current and inductance that is 100 mA.
switched. Initially fit a 100 R/0.022 μF RC suppressor unit
ON Mains Fuse –
Mains 1A, 250V AC (T)
230V
F1 250V 1A
Transformer
OFF
PUMP Pump
ON / OFF
ON Switch
Cable Gland
Relay
Board F3 F2
N/C
C RELAY
1
N/O
N/C
C RELAY
N/O
2
User
N/C
CAL
Cable
C
N/C
and Heater C
OUT
OF
SERVICE
Indicators N/O
N/C
C
OUT
OF
Note. The mains and pump ON/
SAMPLE
HEATER N/O
OFF switches are situated on the
+
- O/P 1 right hand side of the junction box.
+ O/P 2
-
External
User
Internal Connection
Interconnection Terminals
Cable Terminals
Interconnection Cable from/to
Microprocessor Unit and Instrument
Components (wet section)
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…2 INSTALLATION 3 SETTING UP
NC C NO Relay Contacts
Diode
+ Load
–
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4 LIQUID HANDLING SECTION
4.1 Principle of Operation – Fig. 4.1
The monitor uses an ABB Ammonia Probe. This contains a
glass pH electrode, whose pH-sensitive glass membrane forms
a slightly convex tip, and a robust, long-life reference electrode.
The two electrodes are combined into a single assembly, and
are connected as a pH measuring pair through an internal
reservoir of filling solution containing ammonium ions.
The filling solution is 0.1 M ammonium chloride saturated with Filling Body
silver chloride and is separated from the sample by a gas- Solution Body
permeable hydrophobic membrane fitted in the tip of the Aperture Seal
probe. Sample is caused to flow past the probe membrane,
whereupon the partial pressures of ammonia gas in the two
Washer
solutions on either side of the membrane equilibrate,
transferring gas across the membrane. At equilibrium, the
Membrane
concentration of ammonia in the thin film of filling solution
between the probe membrane and the glass electrode pH
membrane equals that in the sample. The resultant change in Electrode
pH value of the thin film is measured by the pH electrode pair End Cap
which thus develops an output potential related to the
Reference
ammonia concentration in the sample. Like most ion-selective Element
electrodes, the Ammonia Probe produces an output which is
Filling
logarithmic with respect to concentration.
Solution
To Electronics Section
Three Channel
Peristaltic Pump Heat Exchanger Ammonia
Block Probe
Out of Sample Constant Head Unit Heater
Float Switch Mat
From Reaction
Flowcell Sample / Calibrate Coils
Solenoid Valves
SV1 SV2
Sample
Contaminated Overflow Sample Orange Heater Coil Temperature
Drain Drain Inlet Channel Drain via
Red Sensor
Constant
Channel Head Unit
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…4 LIQUID HANDLING SECTION 5 ELECTRONICS SECTION
4.2 General Operation – Fig. 4.2 5.1 Electronic Layout – Fig. 5.1
The sequence of events is: The electronic section comprises two separate sections:
a) The sample enters the constant head unit from below and
any excess is allowed to overflow to drain. • The User Junction Box at the top right hand side.
The constant head unit is fitted with a float switch to signal • The Microprocessor Unit at the top left hand side.
an 'Out of Sample' condition. This switch is used by the
monitor to initiate the 'Out of Sample' alarm.
5.2 User Junction Box
b) From the constant head unit the sample is drawn through The User Junction Box contains the relays for the heater,
the normally open ports of the solenoid valves SV1 and solenoid valves and alarms, and all the user external
SV2 by one channel of the peristaltic pump. connection terminals, with the exception of the serial interface
(if fitted).
c) The reagents are drawn through another channel of the
peristaltic pump, and then mixed with the sample. The tube Once installed there should be no need to remove the junction
diameters are arranged so as to obtain the correct ratio of box cover on a regular basis. However, to assist in any fault
sample and reagents. finding procedure, there are l.e.d's on the p.c.b. to indicate if
the relays and heater are being energised.
d) The probe is housed in a temperature controlled block
which includes a heat exchanger to remove the effects of Switches for the mains and pump/heater are situated on the
sample and ambient temperature variations. The probe right hand side of the junction box, together with a mains
produces an electrical potential when exposed to the indication lamp and mains fuse – see Fig. 2.3.
reacted sample which changes in proportion to changes in
concentration of the ion being measured. The probe is
connected to the electronic section where, after digital 5.3 Microprocessor Unit
conversion, the signal is processed by the microprocessor. The Microprocessor Unit contains the analogue input
processing, microprocessor, alarm and current output
e) After measurement the sample flows to waste via the generation, and (if fitted) the serial interface output.
contaminated drain connection.
The programme controls, digital and dot-matrix displays,
f) During calibration the monitor introduces two calibration alarm indication and status l.e.d's are all mounted on the front
solutions sequentially in place of the sample by means of panel of the microprocessor unit.
the solenoid valves SV1 and SV2.
User Junction
Microprocessor Unit
Box
Mains Supply 115 to 230 V
Current Outputs
External
Serial
Interface Interconnection
Connections Cables
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5 ELECTRONICS SECTION
Hold
Used to inhibit any change in the alarm relay/l.e.d.
status and the start of any auto calibration. The
feature is used during maintenance ('Hold' l.e.d. Connections
illuminated). Cover
Note. If the 'Hold' facility is inadvertently left Fig. 5.2 Location of Controls, Displays and L.E.D.s
switched-in, it is automatically cancelled after
a period of approximately 3 hours has elapsed. 5.5 Displays – Fig. 5.2
Two blue vacuum fluorescent displays are provided:
Enter
Used for storing the programmed function
parameters and values in the instrument's a) The upper is a 5-digit 7-segment type display which
nonvolatile memory. indicates the measured variable.
Note. The instrument responds instantly to b) The lower is a 20-character dot matrix type which provides
any programme change but the new value is user information during setting up and in normal operation.
lost in the event of a power interruption if it has
not been 'Entered'.
5.6 L.E.D. Indication – Fig. 5.2
Parameter Advance – used for selecting a particular There are five l.e.d's (indicators situated between the two
parameter from a programme page. displays) which provide information on the current status of the
monitor. From left to right the indicators are as follows:
Used for increasing or decreasing a parameter
value or stepping up or down through a selection of Used to indicate a concentration alarm state
parameters applicable to a particular function. (either high or low). This indicator is used in
A1 or A2
association with an external alarm relay output.
Note. Continued pressure on the 'Raise' or
'Lower' switches causes the rate of change of Used to indicate when the 'Hold' button has been
the displayed value to increase. To make small operated.
Hold
adjustments, operate the switches
momentarily. Indicates when a calibration sequence is taking
Cal place.
Page Advance – used, via the security code, for
selection of individual programme pages. Indicates when the monitor was unable to carry
Fail out a successful calibration.
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10
Operating Page 1
Ammonia <unit> SECURITY CODE 0 SET UP INPUT CURRENT OUTPUT SET UP ALARMS
Millivolts xx.xmV Control Temp. – – • –°C OP1 Cal Hold (Yes/No) A1 Enabled (Yes/No)
Control Temp xx.x°C Display as N Op1 Law. (Log/Lin) A1 Action (High/Low) No
Slope xxx.x% Ion Units (Units) OP1 FSD –– •–– A1 Failsafe (Yes/No)
or Date DD:MM:YY Display Zero – • – –°C OP1 Zero – • – – Lin A1 Hysteresis –%
Mode Time HH:MM:SS Display FSD – – • – –°C OP2 Cal Hold (Yes/No) A1 Delay ––m
Next AutCal DD:MM:YY Note 4 Incorrect OP2 Law (Log/Lin) A1 Setpoint –– •––
Code (Yes/No)
Last Cal DD:MM:YY Note 5 OP2 FSD –– •–– A2 Enabled
OP2 Zero – • – – Lin A2 Action (High/Low)
No
Test Output Zeros A2 Failsafe (Yes/No)
6 PROGRAMMING
Note 5.
‘Last Cal’ is the date of the last automatic or manual calibration.
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…6 PROGRAMMING
Control Temperature
Control Temp xx • x °C
The heater block control temperature is displayed in degrees Celsius.
or or
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6 PROGRAMMING…
Enter
Store.
Cal
Advance to next parameter.
Enter
Store.
Cal
Advance to next parameter.
Ion Standard 2
Ion Std 2 – –•– –
Set the value of the 'High' standard solution (Std 2). The concentrations of the two
or standard solutions must differ from each other by a factor of at least four.
Enter
Store.
Cal
Advance to next parameter.
Yes
Calibrating Std 1 Calibrating Standard 1
The upper display shows the ammonia concentration value. The display remains
until a stable output is obtained from the probe.
Electrode Millivolts
Electrode mV – –•–
Cal Note. Pressing Cal during a calibration aborts the sequence and returns to
normal operation.
When a stable probe output is detected the display automatically advances to the
next parameter.
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…6 PROGRAMMING
Note. Pressing Cal during a calibration aborts the sequence and returns to
Cal
normal operation.
When a stable probe output is detected the display automatically advances to the
next parameter.
or or
or or
Nitrate <units>
Incorrect code. Advance to the first of the programming pages – Set Up Input Page.
SET UP INPUT
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6 PROGRAMMING…
or Set the required block control temperature within the range 5 to 45 °C in 0.1 °C
increments.
Enter Store.
Display as
Display Type (Ammonium, Ammonia or Nitrogen)
NH4?
Select display as ammonium (NH4+), ammonia (NH3) or nitrogen (N).
N? or
NH3?
Enter Store.
Set the required value for display within the range 0.05 to 20.00.
Enter Store.
Example– If the setting is 1.0 the full scale is automatically set to 100.0.
Enter
Store.
or or
CURRENT OUTPUT
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…6 PROGRAMMING
Enter Store.
Enter Store.
or Set the required concentration value for Current Output 1 full scale.
Enter Store.
Log
OP1 Zero – •–– Output 1 Zero
Note. If the output 1 Law is linear (Lin), this parameter is omitted and the zero
current output is automatically set to '0'.
Enter Store.
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6 PROGRAMMING…
Enter Store.
Enter Store.
or Set the required concentration value for Current Output 2 full scale.
Enter Store.
Log
OP2 Zero – •–– Output 2 Zero
Note. If the Output 2 Law is linear (Lin), this parameter is omitted and the zero
current output is automatically set to '0'.
Enter Store.
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…6 PROGRAMMING
Set the Security Code required, between 0 and 19999. This value must then be
or
entered again to access the secure parameters from Operating Page 1.
Enter
Store.
or or
SET UP ALARMS
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6 PROGRAMMING…
Enter Store.
Yes
A1 Action High Alarm A1 Action
Select the alarm action required, 'High' or 'Low' – see Table 6.1.
Low or
Enter Store.
Enter Store.
or Example – A 5% differential setting operates 2.5% above and below the setpoint.
Enter Store.
Set the required delay time between 0 and 60 minutes in 1 minute increments.
Enter Store.
(a)
Continued on next page.
(b)
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…6 PROGRAMMING
Enter Store.
Enter Store.
or or
SET UP CLOCK
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6 PROGRAMMING…
Enter Store.
Enter Store.
Enter Store.
Enter Store.
Enter Store.
(a)
Continued on next page.
(b)
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…6 PROGRAMMING
(a)
(b)
Set Minutes –– Set Minutes
Enter Store.
Enter Store.
or Set the day of the month when the first automatic calibration is to be carried out.
or Set the month when the first automatic calibration is to be carried out.
or Set the year when the first automatic calibration is to be carried out.
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6 PROGRAMMING…
Flashing
or Set the hour of the day when the first automatic calibration is to be carried out.
or Set the minute of the hour when the first automatic calibration is to be carried out.
Enter Store.
or or
Incorrect Code
Advance to next programming page.
Correct Code
or or
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…6 PROGRAMMING
or or
CALIBRATION
†
Resistance boxes have an inherent residual resistance
which may range from a few milliohms to one ohm. This
value must be taken into account when simulating input
levels, as must the overall tolerances of the resistors within
the box.
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6 PROGRAMMING…
Enter
Store. New value is accepted only when input is stable.
Enter
Store. New value is accepted only when input is stable.
Enter
Store. New value is accepted only when input is stable.
Enter
Store. New value is accepted only when input is stable.
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…6 PROGRAMMING
Set the milliammeter reading to the current output 1 zero level, i.e. 0 mA (zero-
or based ranges) or 4 mA (4 to 20 mA range).
Enter Store.
Set the milliammeter reading to the current output 1 full scale level, i.e. 1 mA,
or 10 mA or 20 mA as applicable.
Enter Store.
Set the milliammeter reading to the current output 2 zero level, i.e. 0 mA (zero-
or based ranges) or 4 mA (4 to 20 mA range).
Enter Store.
Set the milliammeter reading to the current output 2 full scale level, i.e. 1 mA,
or 10 mA or 20 mA as applicable.
Enter
Store.
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6 PROGRAMMING
Enter Store.
or or
Ammonia <unit>
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7 CALIBRATION
7.1 Calibration Sequence On initiation of the calibration sequence, either manual or
Calibration of the monitor is carried out by replacing the automatic, the 'Cal' l.e.d. is illuminated and the Calibration
sample solution sequentially with two standard solutions of Mode relay is energised. Two solenoid valves, SV1 and SV2
known concentration. This calibration sequence (see Table operate sequentially to shut off the sample and admit standard
7.1) can be initiated automatically at preset times, or manually solutions of known concentration, one low and one high (STD1
on demand. and STD2), to the sample path.
The sensor outputs obtained during calibration are used to Once a valve is energised, sufficient time (preset to suit the
calculate the calibration graph for the monitor and the sensor response time) is allowed for the previous solution to
accuracy of the standard solutions will, therefore, have a direct be displaced, and for the sensor to respond to the new
effect upon the overall accuracy of the monitor. Given accurate solution, before the sensor output is evaluated for stability by
standards, it is clear that the best accuracy would be expected the microprocessor. When a stable output is achieved the next
at the two calibration points. Ideally, the concentrations of the stage in the sequence is initiated.
two standards should bracket the expected sample
concentration closely, but the latter often varies quite widely. In After calibration the probe outputs corresponding to the two
practice it is convenient, and often the best compromise, to standard solutions are used to calculate a new calibration
use standards whose concentrations are one decade apart, graph for the monitor, thus compensating for any drift in probe
i.e. differ by a factor of 10, and bracket the expected range of or liquid handling performance characteristics since the last
sample concentrations. For example, if the range of sample calibration, and the new slope value can be displayed in
concentrations is expected to be 5 to 10 ppm, then standards Operating Page 1 (100% slope is the theoretical value).
of 2 and 20 ppm could be used – see Section 8.1.2 concerning
low concentration ammonia standards. If the values are within limits, 'CALIBRATION PASSED' is
displayed.
Note. The concentrations of the two standard solutions
must differ from each other by a factor of at least four. 'CAL FAILED (SLOPE)' is displayed if the slope value is
outside acceptable limits and 'CAL FAILED (SLOW)' is
displayed if the sensor output failed to stabilise within 15
minutes after the end of Cal Time 1 or Cal Time 2.
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8 MAINTENANCE
8.1 Chemistry 8.1.2 Standard Solutions
Neither ammonium ion content nor total ammonia can be Two standard solutions of known concentration appropriate to
measured directly in an untreated sample, since the probe can the measuring range are required for calibration of the monitor.
respond only to free ammonia gas. The ammonium ions must To prepare a stock solution of 10,000 mg l–1 follow instructions
therefore be converted to free ammonia by adjusting the pH of below:
the sample solution to a value greater than 11. This is effected
by addition of a sodium hydroxide solution to the sample a) Ammonia as N – Dissolve 38.21 (±0.01) g analytical
before it is presented to the probe. This reagent also has a reagent grade ammonium chloride (NH4Cl) (dried) in
second function, i.e., to fix the total concentration of dissolved approximately 200 ml of high purity water.
species in the final solution at approximately 0.2M.
Ammonia as NH3 – Dissolve 31.47 (±0.01) g analytical
reagent grade ammonium chloride (NH4Cl) (dried) in
In water industry applications a water softener, EDTA, is
approximately 200 ml of high purity water.
added prior to the sodium hydroxide addition. Besides
preventing hardness precipitation, this also overcomes Ammonia as NH4+ – Dissolve 29.72 (±0.01) g analytical
inaccuracies caused by complexing of ammonia with some reagent grade ammonium chloride (NH4Cl) (dried) in
metal ions. In power applications where the hardness levels approximately 200 ml of high purity water.
are very low this second reagent is not required, so the bottle
tube, pump tube and first reaction coil can be removed. b) Transfer the solution to a one litre volumetric flask and
make up to the mark with more high purity water.
The reagent and standard solutions described below are
required to maintain the monitor in operation. Where possible, c) Dilute the appropriate stock solution with more high purity
they should be freshly made and stored in plastic (e.g. water to make the two standard solutions for the measuring
polythene) bottles. Typical reagent solution consumption for a range of the monitor. Store in plastic bottles.
continuously operating monitor is approximately 10 litres per
month. The monitor uses 50 to 80 ml of each standard solution Note. Low value ammonia standard solutions should be
each calibration cycle; consumption of the standard solution, avoided. For example, at ambient temperatures of about
also depends on the frequency with which this cycle is carried 25 °C, and under normal light conditions, a 0.5 mg -1 NH3
out. solution is expected to lose at least 10% of its
concentration over a seven day period. Because of the
8.1.1 Reagent Solutions instability of such solutions, it is not possible to
Two reagent solutions are used in the ammonia monitor. Care programme a standard solution of lower concentration
must be exercised to ensure that the correct reagent is fed into than 0.2 mg l–1 NH3 on this monitor. Solutions as low as
each channel. They are prepared as follows: 0.2 mg l–1 can be prepared with care, but must be used
immediately, making it an unsuitable concentration for
Reagent 1 – Orange Channel long term use with the monitor.
Dissolve 315 (±5) g laboratory reagent grade di-sodium EDTA
in approximately 8 litres of high purity water and make up to 10
litres with more high purity water. Note. The mass relationship of ammonium (NH4+) to
ammonia (NH3) is 18/17 and ammonia (NH3) to nitrogen
Note. If the monitor is to be used on power plant (N) is 17/14.
applications the reagent will not be required due to the
insignificant concentration of hardness in the sample.
8.2 Scheduled Servicing
Reagent 2 – Red Channel The following servicing schedule has been produced as a
Dissolve 1000 (±10) g analytical reagent grade sodium general guide only. Because the monitor has been designed
hydroxide (NaOH) in approximately 8 litres of high purity for a very wide range of applications, where the nature of the
water. Allow the solution to cool and then make up to ten litres sample can vary considerably, it may be necessary to amend
with more high purity water. the schedule to suit the particular installation and sample
conditions.
Warning. This solution is extremely caustic; avoid
8.2.1 Regular Visual Checks
contact with the skin and eyes. If contact occurs, wash
It is recommended that the monitor and the sampling system is
with plenty of clean water.
visually inspected on a regular basis to assure correct
functioning of the system and to check the integrity of the
readings.
a) Check for leaks, particularly around the sample and drain
pipework connections.
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…8 MAINTENANCE
d) Check liquid levels in the reagent and standard solution Note. Once growth is visible the problem is already
containers. serious.
e) Check for malfunction indications on the instrument The recommended agent for cleaning tubing and pipework is
display. sodium hypochlorite solution containing about 0.1%
(1000 mg l–1) available chlorine.
Note. The mains and pump/heater switches are situated
on the right hand side of the User Junction Box. Cleaning Solution
To prepare 500 ml of cleaning solution, dilute 5 ml of
8.2.2 Four Weekly concentrated sodium hypochlorite (NaOCl) solution
a) Inspect all tubing and flowcell for leaks or deterioration, (containing approximately 10% available chlorine) with de-
and for signs of accumulation of solid deposits. ionised water and make up to 500 ml with more de-ionised
water.
b) Clean monitor pipework if there are signs of algae visible.
Note. The solution is unstable. Make only enough for
c) Check the level of the filling solution in the probe and immediate requirements and discard any surplus after
top-up if necessary. use.
d) Discard old reagent and standard solutions. Clean
containers thoroughly before refilling with fresh solutions – Warning. Sodium hypochrorite is an irritant. Contact with
see Section 8.1. acids liberates toxic gas. Avoid contact with skin and eyes.
If contact occurs, wash with plenty of clean water.
Note. It is vital that the containers are not topped up.
Method
e) Examine the sample input pipe for leaks and deterioration. Where an Ultrafilter is used, clean according to the manual
with a 0.05% (500 mg l–1) chlorine solution (i.e. half the
f) Ensure the drain is in good order and free from obstruction. concentration of the above solution). Tubing between the
Ultrafilter and the analyser should also be flushed through,
8.2.3 Two Monthly along with the constant head tank.
Refurbish the probe – see Section 8.2.7.
a) Remove sensors for short-term storage before cleaning –
8.2.4 Twelve Monthly see Section 8.3.1
a) Service pump, tubing and capstans – see Section 8.2.8.
b) Remove the reagent and calibration solution take-up tubes
b) Replace all internal plumbing tubing – see Section 8.2.9. from their respective containers. Fill a calibration container
with the sodium hypochlorite cleaning solution, place it in
c) Carry out the normal 4 weekly schedule not already the calibration container recess and immerse the take-up
covered above. tubes in the solution.
8.2.5 Cleaning Sample Pipework c) Operate 'Cal' to initiate a calibration sequence to draw the
A common problem in measuring water samples from rivers, solution through the solenoid valves tubing and flowcell.
treatment works, etc., is the presence of bacteriological
growth in the sample. d) Remove any dislodged debris from the flowcell and clean
the constant-head unit with the cleaning solution using the
In the form of algae it creates a problem by growing inside bottle brush provided. The tube between the constant-
tubing supplying sample to analysers, as well as in the head unit and SV1 can be cleaned with the cleaning
monitors and associated ABB Kent-Taylor Ultrafilters, if used. solution using the syringe.
If severe, this growth may cause blockages in tubing or valves
and/or fouling of flowcells and sensors. e) Repeat the process using high purity water to flush out the
sodium hypochlorite solution.
In addition, the algae may affect the concentration of the
measured parameter in the sample. This is particularly severe If, after cleaning, there are still signs of discoloration or
in ammonia monitors, where algal growth in supply lines deposits in the monitor tubing, it should be discarded and
causes 'ammonia stripping' and a reduction in the measured replaced with new tubing throughout. In cases where the
concentration. Other parameters, however, may also be monitor tubing is blocked or very heavy deposits are found, it
affected. may be necessary to simply replace the tubing without
attempting to clean it.
It is therefore essential to maintain sterile conditions. This
requires periodic cleaning, at a frequency dependent on
sample conditions. It is suggested that a regular maintenance
programme is introduced, rather than wait for visible signs of
the presence of algal growth.
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8 MAINTENANCE…
It is advisable when changing standard or reagent solutions to c) Proceed from step c) in Assembling the Probe below.
replace the container and remove the empty/used one for
thorough cleaning. Assembling the Probe
a) Unscrew the end cap from the probe body. Rinse the probe
Note. It must be emphasised that containers which are to body with distilled or de-ionised water. Allow to drain.
be used for ammonia standard solutions must be very
thoroughly washed out after chlorine treatment because b) Remove the teat from the glass electrode. Rinse the
any residual chlorine will react with ammonia and hence electrode with distilled or de-ionised water. Dry with a
change the standard concentration. In addition to paper tissue.
thorough washing with water, it is suggested that the
containers are rinsed with a portion of the ammonia c) Screw the glass electrode into the body until the tip of the
standard before finally filling. electrode is flush with the end face of the probe. Note the
number on the electrode cap in line with the mark on the
8.2.6 Consumables Spares Kit body. Unscrew the electrode cap four full turns.
If one is not supplied, it should be ordered before the end of the
first year of operation. This kit includes all the components d) Drop a membrane (coloured white) into the end cap and
which are recommended for replacement annually (see place the sealing washer centrally upon it.
Section 10). This annual refurbishment ensures a high level of
reliability from the monitor over a period of many years. e) Screw the end cap firmly onto the body, taking care not to
Another kit should be ordered when the old one is used so that wrinkle the membrane. Ensure that the body seal and the
all the items are available throughout the following year's membrane sealing washer are both under compression.
operation. The consumable spares kit is in addition to the
electrode spares kit. f) Holding the probe upright, inject the filling solution
provided through the filling hole until there is a 50 to 60 mm
The kit contains the following: depth of solution inside so that the reference element is
immersed in the solution. Wipe any excess filling solution
• one set of pump tubing from the body.
• one set of pump capstans
• a complete set of plumbing tubing g) Tap the end of the probe with the finger to dislodge any air
• sundry items – 'O' rings, tube connectors, pump tube bubbles which have been trapped between the end of the
bungs and fuses glass electrode and the membrane. Screw the glass
• plastic syringe and bottle brush – for cleaning pipework, electrode down four turns to the flush position again and
valves, flowcell and constant-head unit. then a further 1.0 ±0.1 turns. The tip of the electrode should
now be pressing against the membrane. In some
circumstances, particularly if the electrode response is
sluggish, the screw may be given a further 0.2 to 0.3 turn.
Beware of overtightening, which can puncture the
membrane.
h) Push the probe cap onto the top of the probe body so that
it covers the filling hole.
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…8 MAINTENANCE
i) Hinge down the temperature controlled block cover to gain 8.2.9 Replacement of Plumbing Tubing
access to the block. Fit the assembled probe into the All necessary items are included in the Consumable Spares
recess in the temperature controlled block, ensuring that Kit.
the probe sits at the bottom of the recess. Rotate the
retaining clip to hold the probe in position. Do not touch the a) Remove probe for short term storage.
delicate membrane with any hard or sharp objects.
b) Remove each section of the sample and reagent plumbing
j) With sample and reagents flowing, ensure that liquid is tubing in turn and replace with new tubing of the same
delivered on to the membrane, flows over its surface and length.
drips off the lower edge of the probe end cap into the drain
recess, as shown. c) Remove drain tubing and replace with new tubing of the
same length.
k) Replace the cover on the temperature controlled block.
d) Clean the constant head unit, solenoid valves and sample
l) Connect probe lead to the coaxial socket above the heating coil in the flowcell with a syringe filled with sodium
temperature controlled block. hypochlorite solution.
Sample
Delivery
Tube
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8 MAINTENANCE…
5
If required, fit new pump tube 2 Disconnect each pump tube from its
bungs and shims, from the kit, to respective tube connector at the rear
the left hand side of the pump. of the case, pull through the
grommets and discard.
6
Pass new pump tubes, from the 7
kit, through the tube bungs and Locate the tubes centrally on the pump rollers.
case grommets. Connect to the
appropriate tube connector at the
rear of the case.
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…8 MAINTENANCE
8.3 Shutdown Procedure d) Clean sample pipework both inside and outside the
8.3.1 Short Term monitor, constant head unit, and filtration system (if used).
The monitor can be left with the power switched off for up to 24
hours without any detrimental effects. When returned to e) Remove pressure plate from peristaltic pump.
normal monitoring mode, the monitor should be run on sample
for 30 minutes, followed by a calibration – see Section 7.
8.4 Unscheduled Servicing
If the probe is left in the monitor with no liquids flowing, the The monitor indicates abnormal operation by means of signals
internal filling solution becomes more concentrated by on the 20 character dot matrix display and l.e.d's. The
evaporation of water through the membrane. The probe output indications are listed in Table 8.1.
drifts when normal operation is resumed and many hours may
be required to re–establish stability. In such cases normal 8.4.1 Malfunction of the Monitor
performance can sometimes be restored by unscrewing the It should always be remembered that any unpredictable
glass electrode 2 to 3 turns and then returning it to its original problems may be due to the standard or reagent solutions, or
position, thus allowing fresh filling solution to flow between it their flow through the flowcell. If any doubts exist regarding the
and the membrane. If this procedure is not successful replace integrity of the solutions, they should be replaced with freshly
the membrane and filling solution. prepared solutions in the early stages of the fault finding
investigations.
If the probe is likely to be out of use for more than one day,
remove from the monitor and store with the lower part of the Note. The accuracy of the monitor is governed by the
body immersed in a small quantity of liquid in a beaker or other condition of these solutions which may be incorrectly
suitable vessel. 0.1M ammonium chloride is the best storage made or contaminated.
solution (but it is essential that all traces of the storage solution
are rinsed away with clean water before use); otherwise, a In general, any problems are likely to be due to the electrodes,
small amount of the EDTA reagent (Reagent 1) is suitable. which may require refurbishment (see Section 8.4.3), but may
be due to other parts of the liquid handling section of the
8.3.2 Long Term monitor.
When the monitor is required to be shut down for more than 24
hours, proceed as follows: Mechanical components which are involved with the liquid
a) Switch of the monitor. handling, for example, pumps, valves, tubing and tubing
connections etc., should be systematically checked for correct
b) Close the sample valve upstream of the monitor. operation, and for leaks or blockages which change the
chemical conditions around the sensor. The majority of all
c) Dismantle the probe and return to its box. First the glass problems are found to be associated with the chemistry and
electrode is unscrewed, then the rest of the probe emptied, the liquid handling section.
rinsed and drained. Store the glass electrode with its end in
a teat containing a neutral buffer solution, taking care not to
cover the reference element.
'CALIBRATING Std 1 (or 2)' Normal when calibration is taking place. 'Std 1' or 'Std 2'
Cal L.E.D. flashing refers to the standard solution being admitted at the time.
'CALIBRATION PASSED' A recent two point calibration has been successfully carried out.
'CAL. FAILED (SLOPE)' The slope value calculated from the probe outputs in the two
Fail L.E.D. flashing standard solutions was outside the acceptable limits.
'CAL. FAILED (SLOW)' The monitor was unable to achieve a stable output from the
Fail L.E.D. flashing probe.
'TEMP. CONTROL ERROR' The sensor flowcell temperature is significantly different from the
Control Temperature.
'OUT OF SAMPLE' Indicates loss of sample.
Hold L.E.D. 'ON' This indicates the Hold button has been pressed to freeze the
concentration alarm states and to activate the Out of Service
alarm relay. Pressing the button again returns the monitor to
normal operation after a period of 3 hours.
Table 8.1 Unscheduled Servicing Messages
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8 MAINTENANCE
8.4.2 Monitor Diagnostic Information b) Clean membrane by washing with a jet of clean water from
Out of Service Alarm a wash–bottle or syringe.
This alarm relay output is a normally energised relay which de-
energises in the following circumstances: c) Check, and top up as necessary, the filling solution in the
a) Loss of mains supply. probe. There should be a 50 to 60 mm depth inside the
probe so that the reference element is immersed in the
b) Calibration Failed – the calculated electrode slope value is solution.
outside the acceptable limits or the response of the probe
is too slow. The 'CAL FAIL' l.e.d. on the front panel is d) Osmotic effects, i.e. total concentration of dissolved
illuminated with the appropriate text on the 20-character species in samples too high.
display.
e) Puncture of the membrane (usually visible), disassemble
c) Block temperature out of limits – the measured probe and reassemble – see Section 8.2.7.
temperature of the Block is not within 5 °C of the Control
Temperature. 'TEMP. CONTROL ERROR' is indicated on f) Interference (from for example high concentrations of
the 20-character display. anionic detergents).
d) 'OUT OF SAMPLE' alarm – a float switch in the g) Check glass electrode – see Section 8.5.
constant head unit detects the loss of sample. 'OUT OF
SAMPLE' is indicated on the 20-character display. h) Check reference element – see Section 8.5.
e) 'OUT OF SERVICE' alarm – displayed when the pump is In the 'CAL. FAILED (SLOW)' case the failure is usually due to
switched off. slow sensor response, but may be due to an unstable (noisy or
drifting) sensor output:
Note. The heater is switched off by the software when an a) Check sensor connections in the coaxial plugs and
'OUT OF SAMPLE' condition is detected. sockets, and inside the microprocessor unit.
b) Clean membrane by washing with a jet of clean water from 8.5 General Maintenance of the Probe
a wash–bottle or syringe.
8.5.1 Ageing of the Glass Electrode
c) Disassemble probe and reassemble – see Section 8.2.7. After the probe has been in use for some months, the
performance of the glass electrode may eventually deteriorate
d) Check glass electrode – see Section 8.5. due to its continued use in weakly buffered solutions at near
neutral pH. The response of the probe becomes sluggish and
Slope Value Grossly Abnormal the response slope drops. The electrode may frequently be
a) Check, and top up as necessary, the filling solution in the restored to its initial condition by soaking for 12 hours in 0.1M
probe. There should be a 50 to 60 mm depth of solution hydrochloric acid. The performance of the electrode may be
inside the probe. checked as described below.
b) Disassemble probe and reassemble – see Section 8.2.7. 8.5.2 Checking the Performance of the Glass
Electrode
c) Check glass electrode – see Section 8.5. The glass electrode may be checked independently of the
probe with a laboratory calomel reference electrode by testing
d) Check reference element – see Section 8.5. the pair in pH buffer solutions.
Noisy, unstable response or slow response Immerse the glass electrode to a depth of 5 to 10 mm. There
a) Check liquid delivery on to the probe membrane – see must be no liquid contact with the reference element.
Section 8.2.7 (j).
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…8 MAINTENANCE
Connect the electrodes to a pH meter and calibrate with pH c) If the element is not uniform in colour repeat the ammonia/
buffers in the usual way. The glass electrode may be found to nitric acid process.
be somewhat slower in response than a conventional bulb–
type electrode, but adequate scale length should be obtained, d) When clean, rinse with distilled water and immediately
typically better than 98% of the theoretical slope value. transfer to the plating solution such that the reference
element is completely immersed.
8.5.3 Reference Element
During the lifetime of the probe, the internal reference element Chloridisation –
may show signs of deterioration, indicated by the removal of a) Attach the screen of the combination electrode cable to the
the grey/brown silver chloride coating, exposing the buff/light negative terminal of the constant current supply and
grey silver element beneath. This is a normal process, the rate immerse the lower 50 mm of the electrode in the plating
of removal depending on probe operating conditions and solution so that the reference element is covered. Immerse
maintenance. a silver counter electrode in the plating solution and
connect to the positive terminal of the supply.
When new and in good condition this element is completely
and evenly coated. Loss of a large part of this coating causes b) Pass a current of 2 mA for approximately 30 seconds.
probe drift, but can be restored by re–chloridising the element, Carefully tap the electrode to remove all bubbles and then
using the following procedure: reverse the connections to the supply (i.e. the electrode to
be plated is connected to the positive terminal).
8.5.4 Procedure for Chloridising the Reference
Element c) Pass a current of 2 mA for 30 minutes after which
time the electrode will be a dark brown or grey colour. A
Requirements – more uniform coating may be obtained by employing
• Plating solution – hydrochloric acid (HCl) 0.1M, 500 ml. moderate stirring during the process.
Note. Do not use acid preserved with mercuric ions. d) Remove the electrode from the plating solution, rinse
with distilled water and dry with a tissue.
• Cleaning solutions – Ammonia solution (NH3) 50% vol./
vol., 200 ml.
To prepare, dilute 100 ml analytical reagent grade 8.6 Microprocessor Unit Error Messages
concentrated ammonia solution, s.g. 0.88, with 100 ml The instrument incorporates an automatic self-diagnostic
distilled water and stir. checking facility for detection of input and output errors. If such
a fault occurs, one of the error messages detailed below is
• Nitric acid (HNO3), 25% vol./vol. 200 ml. shown on the dot matrix display.
To prepare; cautiously pour 50 ml analytical reagent
grade, concentrated nitric acid, s.g. 1.42, into 150 ml 'CHAN 1 INPUT ERROR'
distilled water, stirring continuously. Allow to cool before This error message is usually caused by an open circuit
use. sensor input allowing the input to drift outside the range of
±400 mV. This may be due to any of the following:
Warning. Stored ammonia solutions and concentrated
a) Low level of filling solution in the probe.
nitric and hydrochloric acids are irritants and very
corrosive. Take great care not to inhale the fumes of either
b) Open circuit electrode internally, e.g. broken
or to get any on the skin or clothing. Any slight spillage on
connection.
skin, clothing or working surface must be washed away
with plenty of water.
c) Broken electrical connections between the probe and
the Microprocessor Unit sensor input.
• Constant current supply, 2 mA d.c. output.
d) Sensor coaxial plugs not correctly inserted.
• Silver wire (counter electrode).
'TEMP INPUT ERROR'
• 1 beaker.
'PRT OUT OF LIMITS'
'TEMP REF. ERROR'
Cleaning –
'THIRD LEAD ERROR'
a) Immerse the lower 50 mm of the combination electrode
(i.e. so that the silver reference element is covered) in the
The above four error messages refer to electrical problems
ammonia solution for about 1 minute. Remove and rinse
with the temperature sensor input – usually an open or short-
with distilled water.
circuited connection.
b) Immerse the electrode to the same depth in the 25% nitric
acid until the silver element is a uniform creamy white. This
process usually takes about 1 minute, but the element
must be inspected frequently as prolonged immersion is
detrimental.
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9 SPECIFICATION
Range: .................... Ammonia 0.05 to 2000 mg l–1. Concentration Alarm
Adjustment: ........... Programmable over range.
Repeatability: ........ ±2% of reading.
Concentration Alarm
Reproducibility: .... ±3% of reading. Differential: ............ 0 to 5%.
Response Time: .... Less than 10 minutes for 90% step Concentration Alarm
change. Delay: ..................... 0 to 60 minutes.
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10 SPARES LIST
Consumable Spares Strategic Spares
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APENDIX A – REPLACING SOFTWARE EPROM
Warning. Switch off the monitor and electrically isolate it A.2 Access the PCB – Fig. A.2
before carrying out the following steps.
Unlock and open cover plate and 1
hinge out to expose captive
A.1 Access the Transmitter Unit – Fig. A.1 screws.
Fluoride 8231
Fig. A.2 Procedure to Access the Processor PCB
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…APPENDIX A
A.4 Changing the EPROM – Fig. A.4 A.5 Completing the Procedure
1) Fit the PCB using the reverse procedure in
Fig. A.3.
Extract IC1 using an approved tool Fit the replacement IC
1 2
– see Caution in Section A.1. – press home firmly. Important Note. Ensure that the washers
are fitted between the PCB cover and the
See Section A.5 for
3 PCB.
reassembly instructions.
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