Hanna Instruments HI96733C User manual

INSTRUCTION MANUAL
HI96733C
Ammonia High Range ISM

Thank you for choosing a Hanna Instruments product.
Please read this instruction manual carefully before using the instrument.
This manual will provide you with the necessary information for correct use of
the instrument, as well as a precise idea of its versatility.
If you need additional technical information, do not hesitate to e‑mail us at
[email protected] or view our worldwide contact list at www.hannainst.com.
All rights are reserved. Reproduction in whole or in part is prohibited without the written consent
of the copyright owner, Hanna Instruments Inc., Woonsocket, Rhode Island, 02895, USA.
Dear
Customer,

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PRELIMINARY EXAMINATION .............................................................................................
GENERAL DESCRIPTION .....................................................................................................
ABBREVIATIONS ...............................................................................................................
SPECIFICATIONS ...............................................................................................................
PRECISION AND ACCURACY ...............................................................................................
PRINCIPLE OF OPERATION ................................................................................................
FUNCTIONAL DESCRIPTION ...............................................................................................
ERRORS AND WARNINGS ..................................................................................................
GENERAL TIPS FOR AN ACCURATE MEASUREMENT ..............................................................
STARTUP ..........................................................................................................................
MEASUREMENT PROCEDURE .............................................................................................
VALIDATION PROCEDURE ...................................................................................................
CALIBRATION PROCEDURE .................................................................................................
GLP .................................................................................................................................
BATTERY MANAGEMENT ....................................................................................................
BATTERY REPLACEMENT ....................................................................................................
ACCESSORIES ...................................................................................................................
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TABLE OF CONTENTS

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Please examine this product carefully. Make sure that the instrument is not damaged. If any damage
occurred during shipment, please contact your local Hanna Instruments Office.
Each HI96733 Ion Selective Meter is supplied complete with:
• Sample Cuvettes and Caps (2 pcs.)
• CAL CheckTM standard cuvettes
• 9V Battery
• Tissue for wiping cuvettes
• Instrument quality certificate
• Instruction Manual and Quick Reference Guide
• Rigid carrying case
Note: Save all packing material until you are sure that the instrument works correctly. Any
defective item must be returned in its original packing.
PRELIMINARY EXAMINATION

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The HI96733 is an auto diagnostic portable microprocessor meter that benefits from
Hanna Instruments’ years of experience as a manufacturer of analytical instruments. It has an
advanced optical system based on a special tungsten lamp and a narrow band interference filter
that allows most accurate and repeatable readings. All instruments are factory calibrated and the
electronic and optical design minimizes the need of frequent calibration.
With the powerful CAL CheckTM validation function, you are able to validate good performance
of your instrument at any time. The validation procedure is extremely user friendly. Just use the
exclusive Hanna Instruments ready‑made, NIST traceable standards to verify the performance of
the instrument and recalibrate if necessary.
The instrument is splash proof and the tungsten lamp and filter units are protected from dust or dirt
by a transparent cup. This makes the instruments fulfill field applications. Display messages aid the
user in routine operation. The meter has an auto‑shut off feature that will turn off the instrument
after 10 minutes of non use in measurement mode or after 1 hour if left in calibration mode.
The meter uses an exclusive positive‑locking system to ensure that the cuvette is in the same
position every time it is placed into the measurement cell. It is designed to fit a cuvette with a
larger neck making it easier to add both sample and reagents. The cuvette is made from special
optical glass to obtain best results.
The HI96733 meter measures the ammonium ion content in water samples in the 0.0 to
50.0 mg/L (ppm) range. The method is an adaptation from ASTM Manual of Water and
Environmental Technology, D1426‑92, Nessler Method.
The reagents are liquid form and are supplied in bottles. The amount of reagent is precisely dosed
to ensure the maximum repeatability.
Celsius degree
Fahrenheit degree
American Society for Testing and Materials
Liquid Crystal Display
milligrams per liter. mg/L is equivalent to ppm (parts per million)
milliliter
millivolt
°C:
°F:
ASTM:
LCD:
mg/L:
mL:
mV:
GENERAL DESCRIPTION ABBREVIATIONS

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SPECIFICATIONS
Range 0.0 to 50.0 mg/L (as NH4
+)
Resolution 0.1 mg/L for measurement
0.1 mg/L for calibration and validation
Accuracy
@25 °C (77 °F)
±0.5 mg/L ±5% of reading
Light Source Tungsten lamp
Light Detector Silicon Photocell with narrow band interference filter @420 nm
Method
Adaptation of the ASTM Manual of Water and Environmental Technology,
D1426‑92, Nessler Method. The reaction between ammonia and the reagents
causes a yellow tint in the sample.
Environment 0 to 50 °C (32 to 122 °F)
max 95 % RH non‑condensing
Battery Type 9V (1 pc.)
Auto‑Shut off After 10’ of non‑use in measurement mode; after 1 hour of non‑use in
calibration mode; with last reading reminder
Dimensions 192 x 104 x 69 mm (7.6 x 4.1 x 2.7”)
Weight 320 g (11.3 oz.)
REQUIRED REAGENTS
Code Description Quantity/test
HI93733A‑0 Nessler Reagent 4 drops
HI93733B‑0 Ammonia Reagent B 9 mL

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Precision is how closely repeated measurements
agree with each other. Precision is usually
expressed as standard deviation (SD).
Accuracy is defined as the nearness of a test result
to the true value.
Although good precision suggests good accuracy,
precise results can be inaccurate. The figure
explains these definitions.
In a laboratory using a standard solution of
6.00 mg/L ammonia nitrogen (NH3‑N) and
a representative lot of reagents, an operator
obtained with a single instrument a standard
deviation of 0.12 mg/L.
PRECISION AND ACCURACY
Absorption of Light is a typical phenomenon of interaction between electromagnetic radiation and
matter. When a light beam crosses a substance, some of the radiation may be absorbed by atoms,
molecules or crystal lattices.
If pure absorption occurs, the fraction of light absorbed depends both on the optical path length
through the matter and on the physical‑chemical characteristics of the substance according to the
Lambert‑Beer Law:
‑log I/Io= ελc d
or
A = ελc d
Where:
‑log I/Io= Absorbance (A)
Io = intensity of incident light beam
I = intensity of light beam after absorption
ε
λ= molar extinction coefficient at wavelength λ
c = molar concentration of the substance
d = optical path through the substance
PRINCIPLE OF OPERATION

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A microprocessor controlled special tungsten lamp emits radiation which is first optically conditioned
and beamed to the sample contained in the cuvette. The optical path is fixed by the diameter of
the cuvette. Then the light is spectrally filtered to a narrow spectral bandwidth, to obtain a light
beam of intensity Ioor I.
The photoelectric cell collects the radiation Ithat is not absorbed by the sample and converts it
into an electric current, producing a potential in the mV range.
The microprocessor uses this potential to convert the incoming value into the desired measuring
unit and to display it on the LCD.
The measurement process is carried out in two phases: first the meter is zeroed and then the actual
measurement is performed.
The cuvette has a very important role because it is an optical element and thus requires particular
attention. It is important that both, the measurement and the calibration (zeroing) cuvettes, are
optically identical to provide the same measurement conditions. Whenever possible use the same
cuvette for both. It is necessary that the surface of the cuvette is clean and not scratched. This to avoid
measurement interference due to unwanted reflection and absorption of light. It is recommended
not to touch the cuvette walls with hands.
Furthermore, in order to maintain the same conditions during the zeroing and the measuring phases,
it is necessary to close the cuvette to prevent any contamination.
Therefore, the concentration “c” can be calculated from the absorbance of the substance as the
other factors are known.
Photometric chemical analysis is based on the possibility to develop an absorbing compound from a
specific chemical reaction between sample and reagents. Given that the absorption of a compound
strictly depends on the wavelength of the incident light beam, a narrow spectral bandwidth should
be selected as well as a proper central wavelength to optimize measurements.
The optical system of Hanna Instruments’ HI96733 colorimeter is based on a tungsten lamp combined
with a narrow‑band interference filter to guarantee both high performance and reliable results.
HI96733 block diagram (optical layout)
PRINCIPLE OF OPERATION

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1) GLP/ key
2) CAL CHECK key
3) ZERO/CFM key
4) READ /TIMER key
5) ON/OFF key
6) Liquid Crystal Display (LCD)
7) Cuvette alignment indicator
8) Cuvette holder
INSTRUMENT DESCRIPTION
FUNCTIONAL DESCRIPTION
KEYPAD DESCRIPTION
• ON/OFF: to turn the meter on and off.
• ZERO/CFM: this is a bi‑functional key. Just press to zero the meter prior to measurement, or
to confirm edited values or to confirm factory calibration restore.
• READ /TIMER: this is a multi‑functional key. In measurement mode, press to make a
measurement, or press and hold for three seconds to start a pre‑programmed countdown prior
to measurement. In GLP mode press to view the next screen.
• CAL CHECK: this is a bi‑functional key. Just press to perform the validation of the meter, or
press and hold for three seconds to enter calibration mode.
• GLP/: this is a bi‑functional key. Just press to enter GLP mode. In calibration mode press
to edit the date and time.
OPERATING MODES
• Measurement mode: default operation mode, enables both validation and measurement.
• Calibration mode: may be entered by keeping CAL CHECK pressed for three seconds (the
“CAL” tag appears), it enables calibration of the instrument.
• GLP mode: may be entered by pressing GLP/(“GLP” appears), it enables consulting of
user calibration date or restore factory calibration.

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DISPLAY ELEMENTS DESCRIPTION
1) The measuring scheme (lamp, cuvette, detector), appears during different phases of zero
or reading measurement
2) Error messages and warnings
3) The battery icon shows the charging level of the battery
4) The hourglass appears when an internal checking is in progress
5) Status messages
6) The chronometer appears when the reaction timer is running
7) The month, day and date icons appear when a date is displayed
8) Four digit main display
9) Measuring units
10) Four digit secondary display
FUNCTIONAL DESCRIPTION

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The instrument shows clear messages when erroneous condition appears. Messages are also displayed
when the obtained values are outside expected range. The beeper is playing a beep on errors.
a) on zero reading
Light High: There is too much light to perform a measurement.
Please check the preparation of the zero cuvette.
Light Low: There is not enough light to perform a measurement.
Please check the preparation of the zero cuvette.
No Light:The instrument cannot adjust the light level. Please check
that the sample does not contain any debris.
Inverted cuvettes: The sample and the zero cuvette are inverted.
Zero: A zero reading was not taken. Follow the instructions of the
measurement procedure for zeroing the meter.
b) on sample reading
ERRORS AND WARNINGS

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Under range: A blinking “0.0” indicates that the sample absorbs
less light than the zero reference. Check the procedure and make sure
you use the same cuvette for reference (zero) and measurement.
Over Range: A flashing value of the maximum concentration
indicates an over range condition. The concentration of the sample
is beyond the programmed range: dilute the sample and re‑run
the test.
c) during calibration procedure
Standard Low: The standard reading is less than expected.
Standard High: The standard reading is higher than expected.
Cap error: Appears when external light enters in the analysis cell.
Assure that the cuvette cap is present.
Cooling lamp: The instrument waits for the lamp to cool down.
d) other errors and warnings
ERRORS AND WARNINGS

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Battery low: The battery must be replaced soon.
Dead battery: This indicates that the battery is dead and must be
replaced. Once this indication is displayed, the meter will lock up.
Change the battery and restart the meter.
ERRORS AND WARNINGS

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• Proper use of dropper:
(a) to get good reproducible results, tap the dropper on the table for several times and wipe
the outside of the dropper with a cloth.
(b) always keep the dropper bottle in a vertical position while dosing the reagent.
(a) (b)
The instructions listed below should be carefully followed during testing to ensure best accuracy.
• Color or suspended matter in large amounts may cause
interference, therefore these should be removed by treatment
with active carbon and by prior filtration.
• For a correct filling of the cuvette: the liquid in the cuvette
forms a concavity on the top; the bottom of this concavity
must be at the same level of the 10 mL mark.
• In order to measure exactly 0.5 mL of reagent with the 1 mL syringe:
(a) push the plunger completely into the syringe and insert the tip into the solution.
(b) pull the plunger up until the lower edge of the seal is exactly on the 0.0 mL mark.
(c) take out the syringe and clean the outside of the syringe tip. Be sure that no drops are
hanging on the tip of the syringe, if so eliminate them. Then, keeping the syringe in vertical
position above the cuvette, push the plunger down into the syringe until the lower edge of
the seal is exactly on the 0.5 mL mark. Now the exact amount of 0.5 mL has been added
to the cuvette, even if the tip still contains some solution.
GENERAL TIPS FOR AN ACCURATE MEASUREMENT

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• It is important that the sample does not contain any debris. This
would corrupt the reading.
• In order to avoid reagent leaking and to obtain more accurate
measurements, it is recommended to close the cuvette first with
the supplied HPDE plastic stopper and then with the black cap.
• Each time the cuvette is used, the cap must be tightened to
the same degree.
• Whenever the cuvette is placed into the measurement cell, it
must be dry outside, and completely free of fingerprints, oil
or dirt. Wipe it thoroughly with HI731318 or a lint‑free cloth
prior to insertion.
• Shaking the cuvette can generate bubbles in the sample, causing higher readings. To obtain
accurate measurements, remove such bubbles by swirling or by gently tapping the cuvette.
• Do not let the reacted sample stand too long after reagent is added, or accuracy will be lost.
• It is possible to take multiple readings in a row, but it is recommended to take a new zero
reading for each sample and to use the same cuvette for zeroing and measurement.
• After the reading it is important to discard immediately the sample, otherwise the glass might
become permanently stained.
• All the reaction times reported in this manual are referred to 25 °C (77 °F). In general, the
reaction time should be increased for temperatures lower than 20 °C (86 °F), and decreased
for temperatures higher than 25 °C (77 °F).
• In order to maximize accuracy, prior to a measurement follow the validation procedure to be
sure that the instrument is properly calibrated. If necessary, calibrate the instrument.
GENERAL TIPS FOR AN ACCURATE MEASUREMENT

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Prepare the instrument for measurement as follows:
• Unpack the instrument by removing the dust protection sleeve from the instrument cuvette
holder.
• Place the battery in the instrument as described in the “BATTERY REPLACEMENT” chapter.
• Place the instrument on a flat table.
• Do not place the instrument under direct sun light.
To compensate the meter for the sample turbidity or color, the measurement takes place in two
phases. First, the meter is zeroed using the unreacted sample. After the reagents are added the
reacted sample is measured.
• When the beeper sounds briefly and the LCD displays dashes, the meter is ready. The blinking
“ZERO” indicates that the instrument needs to be zeroed first.
• Fill one cuvette with 1 mL of unreacted sample, by means of the syringe.
• Turn the meter on by pressing ON/OFF. The display briefly shows all tags on.
STARTUPMEASUREMENT PROCEDURE

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• Press ZERO/CFM and the lamp, cuvette and detector icons will appear on the display, depending
on the measurement phase.
• After a few seconds, the display will show “-0.0-”. The meter is now zeroed and ready for
measurement.
• Using the plastik pipette, add 9 mL of HI93733B‑0 Ammonia Reagent B, up to the 10 mL
mark. Place the cap and swirl the solution to mix.
• Place the cuvette into the cuvette holder and ensure that the notch on the cap is positioned
securely into the groove.
MEASUREMENT PROCEDURE
10 mL
sample

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• Remove the cuvette, open it and add 4 drops of HI93733A‑0 Nessler Reagent. Replace the cap
and swirl the cuvette gently to mix.
• Replace the cuvette into the cuvette holder and ensure that the notch on the cap is positioned
securely into the groove.
• Press and hold READ /TIMER for three seconds. The display will show the countdown prior
to measurement. The beeper is playing a beep at the end of countdown period.
MEASUREMENT PROCEDURE
HI93733A-0
• Alternatively, wait for 3 minutes and 30 seconds and just press READ /TIMER.
In both cases, the lamp, cuvette and detector icons will appear on the display, depending on
the measurement phase.

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INTERFERENCES
• Organic compounds like: chloramines, various aliphatic and aromatic amines, glycine, (positive
error).
To eliminate these interferences distillation is required.
• Organic compounds like: aldehydes, alcohols (e.g. ethanol) or acetone (negative error).
To eliminate these interferences distillation is required.
• Sulfide (S2‑): may cause turbidity.
• Hardness above 1 g/L as Calcium Carbonate (CaCO3).
• At the end of measurement, the instrument directly displays concentration in mg/L of ammonium ion (NH4
+)
on the LCD. To convert the reading to mg/L of ammonia (NH3), multiply by the factor 0.944. To convert
the reading to mg/L of ammonia nitrogen (NH3‑N), multiply by the factor 0.776.
MEASUREMENT PROCEDURE

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Use the validation procedure to ensure that the instrument is properly calibrated.
Warning: Do not validate the instrument with any standard solutions other than the Hanna Instruments
CAL CheckTM Standards, otherwise erroneous results will be obtained. For accurate validation, please
perform test at room temperature: 18 to 25 °C (64.5 to 77.0 °F)
•Turn the meter on by pressing ON/OFF.
• When the beeper sounds briefly and the LCD displays dashes, the meter is ready.
VALIDATION PROCEDURE
• Press ZERO/CFM and the lamp, cuvette and detector icons will appear on the display, depending
on the measurement phase.
• Place the CAL CheckTM Standard HI96733‑11 Cuvette A into the cuvette holder and ensure that
the notch on the cap is positioned securely into the groove.