Dear Customer,
Thank you for choosing a Hanna product. Please read this instruction manual carefully before using the
instrument. This manual will provide you with the necessary information for the correct use of the
instrument. If you need additional technical information, do not hesitate to e-mail us at tech@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.
HANNA LITERATURE ...................................................... 131
PRELIMINARY EXAMINATION
Please examine this product carefully. Make sure that the instrument is not damaged. If any damage
occurred during shipment, please notify your local Hanna Office.
Each meter is supplied complete with:
• Four Sample Cuvettes and Caps
• Sample Preparation Kit (for turbid or concentrated samples see page 17)
• Cloth for wiping cuvettes (1 pcs)
• 60 mL glass bottle for dissolved oxygen analysis (1 pcs)
• Scissors
• AC/DC Power Adapter
• Instruction Manual
The sample preparation kit contains:
• 4 cuvettes (10 mL) with caps
• 2 plastic beakers (100 and 170 mL)
• 1 graduated cylinder (100 mL)
• 1 syringe with screw rim (60 mL)
• 1 syringe (5 mL)
• 1 filter assembly
• 25 filter discs
• 1 spoon
• 2 pipettes
• Carbon powder packets (50 pcs)
• 1 Demineralizer Bottle with filter cap for about 12 liters of deionized water (depending on the
hardness level of water to be treated)
Note: Save all packing material until you are sure that the instrument works correctly. Any defective item
must be returned in its original packing with the supplied accessories.
GENERAL DESCRIPTION
HI 83200 is a multiparameter bench photometer dedicated for Laboratory analysis. It measures 45 different
methods using specific liquid or powder reagents. The amount of reagent is precisely dosed to ensure
maximum reproducibility.
HI 83200 bench photometer can be connected to a PC via an USB cable. The optional HI 92000
Windows® Compatible Software helps users manage all their results.
HI 83200 has a powerful interactive user support that assists the user during the analysis process.
Each step in the measurement process is help supported. A tutorial mode is available in the Setup Menu.
23
ABBREVIATIONS
PRINCIPLE OF OPERATION
EPA:US Environmental Protection Agency
°C:degree Celsius
°F:degree Fahrenheit
µg/L:micrograms per liter (ppb)
mg/L:milligrams per liter (ppm)
g/L:grams per liter (ppt)
mL:milliliter
HR:high range
MR:medium range
LR:low range
PAN:1-(2-pyridylazo)-2-naphtol
TPTZ:2,4,6-tri-(2-pyridyl)-1,3,5-triazine
SPECIFICATIONS
Light LifeLife of the instrument
Light DetectorSilicon Photocell
Environment0 to 50°C (32 to 122°F);
max 90% RH non-condensing
Power Supplyexternal 12 Vdc power adapter
built-in rechargeable battery
Dimensions235 x 200 x 110 mm (9.2 x 7.87 x 4.33")
Weight0.9 Kg
For specifications related to each method (e.g. range, resolution, etc.) refer to the related measurement
section.
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 substance according to the Lambert-Beer Law:
-log I/Io = ελ c d
or
A = ελ c d
Where:
-log I/I
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 HI 83200 is based on special subminiature tungsten lamps and narrow-band
interference filters to guarantee both high performance and reliable results.
Five measuring channels allow a wide range of tests.
= Absorbance (A)
o
Io= intensity of incident light beam
I = intensity of light beam after absorption
ελ= molar extinction coefficient at wavelength λ
c= molar concentration of the substance
d = optical path through the substance
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.
For each method, the accuracy is expressed in the
related measurement section.
Instrument block diagram (optical layout)
A microprocessor controlled special tungsten lamp emits radiation which is first optically conditioned and beamed
through 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 Io or I.
The photoelectric cell collects the radiation I that 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.
45
ESC
RCL
HELP
SETUP
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) cuvette are optically identical to provide the
same measurement conditions. Most methods use the same cuvette for both, so it is important that measurements
are taken at the same optical point. The instrument and the cuvette cap have special marks that must be
aligned in order to obtain better reproducibility.
The surface of the cuvette must be clean and not scratched. This is 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 measurement phases,
it is necessary to cap the cuvette to prevent any contamination.
1) Open Cuvette Lid
2) Indexing mark
3) Cuvette point
4) Liquid Crystal Display (LCD)
5) Splash proof keypad
6) ON/OFF power switch
7) Power input connector
8) USB connector
FUNCTIONAL DESCRIPTION
INSTRUMENT DESCRIPTION
KEYPAD DESCRIPTION
The keypad contains 8 direct keys and 3 functional keys with the following functions:
Press to perform the function displayed above it on the LCD.
Press to exit the current screen.
Press to access the select method menu.
Press to move up in a menu or a help screen, to increment a set value, to access second level
functions.
Press to move down in a menu or a help screen, to decrement a set value, to access second
level functions.
Press to log the current reading.
Press to recall the log.
Press to display the help screen.
Press to access the setup screen.
67
TIPS FOR AN ACCURATE MEASUREMENT
The instructions listed below should be carefully followed during testing to ensure most accurate results.
• Color or suspended matter in large amounts may cause interference, and should be removed by
treatment with active carbon and filtration: refere to Sample Preparation Chapter (page 17).
• Ensure the cuvette is filled correctly: the liquid in the cuvette forms a convexity on the top; the bottom
of this convexity must be at the same level as the 10 mL mark.
COLLECTING AND MEASURING SAMPLES
• 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.
• Proper use of the powder reagent packet:
(a) use scissors to open the powder packet;
(b) push the edges of the packet to form a spout;
(c) pour out the content of the packet.
USING CUVETTES
• Proper mixing is very important for reproducibility of the measurements. The right way of mixing a
cuvette is specified for each method in the related chapter.
(a) invert the cuvette a couple of times or for a specified time: hold the cuvette in the vertical position. Turn
the cuvette upside-down and wait for all of the solution to flow to the cap end, then return the cuvette
to the upright vertical position and wait for all of the solution to flow to the cuvette bottom. This is one
inversion. The correct speed for this mixing technique is 10-15 complete inversions in 30 seconds.
This mixing technique is indicated with “invert to mix” and the following icon:
(c)(a)(b)
USING LIQUID AND POWDER REAGENTS
• Proper use of the dropper:
(a) for reproducible results, tap the dropper on the table for several times and wipe the outside of the
dropper tip with a cloth.
(b) always keep the dropper bottle in a vertical position while dosing the reagent.
(a)(b)
89
(b) shaking the cuvette, moving the cuvette up and down. The movement may be gentle or vigorous.
This mixing method is indicated with “shake gently” or “shake vigorously”, and one of the following
icons:
shake gentlyshake vigorously
• Pay attention to push the cuvette completely down in the holder and to align the white point on the
cap to the indexing mark on the meter.
• In order to avoid reagent leaking and to obtain more accurate
measurements, close the cuvette first with the supplied HDPE plastic
stopper and then 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 free of fingerprints, oil or dirt. Wipe it thoroughly with
HI 731318 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. For
best accuracy, respect the timings described in each specific method.
• 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 when possible (for most precise results
follow the measurement procedures carefully).
• Discard the sample immediately after the reading is taken, or the glass might become permanently
stained.
• All the reaction times reported in this manual are at 25 °C (77 °F). In general, the reaction time
should be increased for temperatures lower than 20 °C (68 °F), and decreased for temperatures higher
than 25 °C (77 °F).
INTERFERENCES
• In the method measurement section the most common interferences that may be present in an average
sample matrix have been reported. It may be that for a particular treatment process other compounds
do interfere with the method of analysis.
HEALTH & SAFETY
• The chemicals contained in the reagent kits may be hazardous if improperly handled.
• Read the Material Safety Data Sheet (MSDS) before performing tests.
• Safety equipment: Wear suitable eye protection and clothing when required, and follow instructions
carefully.
• Reagent spills: If a reagent spill occurs, wipe up immediately and rinse with plenty of water.
If reagent contacts skin, rinse the affected area thoroughly with water. Avoid breathing released vapors.
• Waste disposal: for proper disposal of reagent kits and reacted samples, refer to the Material Safety
Data Sheet (MSDS).
The meter can be powered from an AC/DC adapter (included) or from the built-in rechargeable battery.
Note: Always turn the meter off before unplugging it to ensure no data is lost.
When the meter switches ON, it verifies if the power supply adapter is connected. The battery icon on the
LCD will indicate the battery status:
- battery is charging from external adapter- battery fully charged (meter connected to AC/DC adapter)
• After the desired method is selected, follow the measurement described in the related section.
• Before performing a test you should read all the instructions carefully.
DATA MANAGEMENT
The instrument features a data log function to help you keep track of all your analysis. The data log can
hold 200 individual measurements. Storing, viewing and deleting the data is possible using the LOG
and
RCL keys
Storing data
stored with date and time stamps.
..
.
..
: You can store only a valid measurement. Press LOG
and the last valid measurement will be
- battery capacity (no external adapter)- battery Low (no external adapter)
- battery Dead (no external adapter)
METHOD SELECTION
• Turn the instrument ON via the ON/OFF power switch.
• The meter will perform an autodiagnostic test. During this test, the Hanna Instrument logo will appear
on the LCD. After 5 seconds, if the test was successful, the last method used will appear on the display.
• In order to select the desired method press the METHOD key and a screen with the available methods
will appear.
• Press the s t keys to highlight the desired method. Press Select.
Viewing and deleting
the last saved measurement. Additionally, you can delete the data records all at once.
: You can view and delete the data log by pressing the RCL key. You can only delete
CHEMICAL FORM
Chemical form conversion factors are pre-programmed into the instrument and are method specific. In order
to view the displayed result in the desired chemical form press s or t to access the second level function
and then press the Chem Frm key to toggle between the available chemical forms for the selected method.
SPECIAL CONVERSIONS
For Magnesium and Calcium Hardness, special conversion factors can be used to convert the readings from
mg/L to French degrees (°f), German degrees (°dH) and English degrees (°E) of hardness. This can be
achieved by pressing s or t to access the second level functions and then press the Unit key to toggle
between °f, °dH, °E and mg/L.
1213
SETUPSETUP
SETUP
SETUPSETUP
In the Setup mode the instrument’s parameters can be changed. Some parameters affect the measuring
sequence and others are general parameters that change the behavior or appearance of the instrument.
Press SETUP to enter the setup mode.
Press ESC or SETUP to return to the main screen.
A list of setup parameters will be displayed with currently
configured settings. Press HELP for additional information.
Press the s tkeys to select a parameter and change the
value as follows:
Backlight
Values: 0 to 8.
Press the Modify key to access the backlight value.
Use the ⊳u functional keys or the s t keys to increase
or decrease the value.
Press the Accept functional key to confirm or ESC to return to
the setup menu without saving the new value.
Contrast
Values: 0 to 20.
This option is used to set the display’s contrast.
Press the Modify key to change the display’s contrast.
Use the ⊳u functional keys or the s t keys to increase
or decrease the value.
Press the Accept key to confirm the value or ESC to return to
the setup menu without saving the new value.
Date / Time
This option is used to set the instrument’s date and time.
Press the Modify key to change the date/time.
Press the ⊳u functional keys to highlight the value to be modified
(year, month, day, hour, minute or second). Use the s tkeys to
change the value.
Press the Accept key to confirm or ESC to return to the setup without
saving the new date or time.
Time format
Option: AM/PM or 24 hour.
Press the functional key to select the desired time format.
Date format
Press the Modify key to change the Date Format.
Use the s t keys to select the desired format.
Press Accept functional key to confirm or ESC to return to the setup
menu without saving the new format.
Language
Press the corresponding key to change the language.
If the new language cannot be loaded, the previously selected
language will be reloaded.
Tutorial
Option: Enable or Disable.
If enabled this option will provide the user short guide related to
the current screen.
Press the functional key to enable/disable the tutorial mode.
Beeper
Option: Enable or Disable.
When enabled, a short beep is heard every time a key is pressed.
A long beep alert sounds when the pressed key is not active or an
error is detected.
Press the functional key to enable/disable the beeper.
1415
Instrument ID
Option: 0 to 9999.
This option is used to set the instrument’s ID (identification number).
The instrument ID is used while exchanging data with a PC.
Press the Modify key to access the instrument ID screen. Press the st keys in order to set the desired value.
Press the Accept key to confirm the value or ESC to return to the setup
menu without saving the new value.
Meter information
Press the Select key to view the instrument model, firmware version,
language version and instrument serial number.
Press ESC to return to the Setup mode.
HELP MODEHELP MODE
HELP MODE
HELP MODEHELP MODE
HELP MODE
HI 83200 offers an interactive contextual help mode that assists the user at any time.
SAMPLE PREPARATION
SAMPLE PREPARATION PROCEDURE
The following Sample Preparation Procedure applies in case of:
• Samples with color or suspended matter (turbidity).
• Concentrated samples, for which the analysis result is over the range of the parameter.
Use the accessories contained in the Sample Preparation Kit to prepare the sample according to the
following instructions.
COLORED OR TURBID SAMPLES:
Colored or suspended matter in large amounts may cause interference. They should be removed by
treatment with active carbon and filtration.
• If the water sample contains suspended matter, let it stand in a beaker until most of the solid particles
have settled. Then, use the pipette to transfer the supernatant solution to the other beaker. To prevent
the displacement of the settled solids at the bottom of the beaker, do not induce air bubbles into the
solution.
• Measure 100 mL of sample with the graduated cylinder.
• If the solution still contains some turbidity or color, pour
it in the large 170 mL beaker and add a powder packet
of active carbon.
To access the help screens press HELP.
The instrument will display additional information related to the
current screen. To read all the available information, scroll the
text using the s t keys.
Press the Support key to access a screen with Hanna service
centers and their contact details.
Press the Accessories key to access a list of instrument reagents
and accessories.
To exit support or accessories screens press ESC and the
instrument will return to the previous help screen.
To exit help mode press the HELP or ESC key again and the
meter will return to the previously selected screen.
1617
• Mix well using the spoon and then wait for 5 minutes.
• Unscrew the filter assembly, put a filter disc inside and
close it.
filter
disc
• Connect the filter assembly to the 60 mL syringe by the
screw rim.
• Remove the syringe plunger and fill the syringe with the
sample to be filtered. Pour the sample gently, trying to
avoid transferring of the actived carbon to the syringe.
• Reinsert the plunger and filter the solution into the 100 mL
beaker by pushing gently the syringe plunger.
The sample is now ready.
• Remove the cap and fill the Demineralizer Bottle with tap water.
• Replace the cap and shake gently for at least 2 minutes.
• If the solution is still turbid or colored, treat it again
with a packet of active carbon. After use, throw the filter
disc away and wash the syringe and the filter assembly
well. Always use a new disc for another sample.
CONCENTRATED SAMPLES:
If the analysis result is over the method range, the sample should be diluted. The following procedure
describe how to dilute the sample by a factor “N” (that is, to dilute by “N times”):
• Use the graduated cylinder to measure exactly V mL of
sample. For volumes V < 20 mL, accurately dose the
sample by mean of the syringe.
Note: To measure exactly 5 mL of sample with the syringe, push the plunger completely into the
syringe and insert the tip into the sample. Pull the plunger out until the lower edge of the seal is on
the 5 mL mark of the syringe.
• Open the upper part of the Demineralizer Bottle cap and gently squirt the demineralized water into the
cylinder, up to the 100 mL mark.
Note: The ion exchange resin contained in the Demineralizer Bottle is provided with an indicator
substance. The indicator will change from green to blue when the resin has been exhausted and needs
to be replaced.
• Pour the solution in the large 170 mL beaker, replace the cap and invert several times to mix.
probable level of liquid
taken up by syringe
1819
• If the solution contains some turbidity or color, add a powder packet of active carbon and follow the
procedure described in previous section Colored or Turbid Samples.
• Calculate the dilution factor N:
N = 100/V
Where:
V is the volume of original sample poured in the cylinder, expressed in mL, and 100 is the final volume
in the cylinder, expressed in mL.
• When performing the reading, pay attention to multiply the read value by the dilution factor in order
to obtain the real concentration of the analyte in the original sample:
Example:
Reading = value A
Dilution factor = N
Real value in the original sample = A x N
Note: The methods Potassium Medium Range and Potassium High Range require a dilution of 1:5
(N = 5, V = 20 mL) and 1:10 (N = 10, V = 10 mL) of the sample. As the dilution is always
done, it is already included in the final result and is not necessary to multiply by the dilution factor.
ALUMINUM
SPECIFICATIONS
Range0.00 to 1.00 mg/L
Resolution0.01 mg/L
Accuracy±0.02 mg/L ±4% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the aluminon method. The reaction between aluminum and reagents
causes a reddish tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93712A-0Ascorbic acid1 packet
HI 93712B-0Aluminon reagent1 packet
HI 93712C-0Bleaching powder1 packet
REAGENT SETS
HI 93712-01 Reagents for 100 tests
HI 93712-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
the
Method Selection
Aluminum
method using the procedure described in
section (see page 12).
• Fill a graduated beaker with 50 mL of sample.
• Add the content of one packet of HI 93712A-0 Ascorbic acid
and mix until completely dissolved.
• Add the content of one packet of HI 93712B-0 Aluminon
reagent and mix until completely dissolved. This is the sample.
• Fill two cuvettes with 10 mL of sample each (up to the mark).
2021
10 mL
# 1
10 mL
# 2
Aluminum
• Add the content of one packet of HI 93712C-0 Bleaching
powder to one of the two cuvettes. Replace the cap and shake
vigorously until completely dissolved. This is the blank.
# 1
• Place the blank into the holder and close the lid.
• Press Timer and the display will show the countdown prior to
# 1
zeroing the blank. Alternatively wait for 15 minutes and then press
Zero. The display will show "-0.0-" when the meter is zeroed and
ready for measurement.
# 2
• Remove the blank and insert the other cuvette into the instrument.
• Press the Read key and the meter will perform the reading. The instrument displays the results in
mg/L of aluminum.
ALKALINITY
SPECIFICATIONS
Range0 to 500 mg/L (as CaCO3)
Resolution5 mg/L
Accuracy±5 mg/L ±10 % of reading at 25 °C
Typical EMC±5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodColorimetric Method. The reaction causes a distinctive range of colors from yellow to
green to greenish blue to develop.
REQUIRED REAGENTS
CodeDescriptionQuantity/test
HI 93755-0Alkalinity Indicator Reagent 1 mL
REAGENT SETS
HI 93755-01 Reagents for 100 tests
HI 93755-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Alkalinity
Method Selection
method using the procedure described in the
section (see page 12).
10 mL
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of Al2O3.
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Iron above 20 mg/L, Alkalinity above 1000 mg/L, Phosphate above 50 mg/L; Fluoride must be absent.
Aluminum
2223
• Fill the cuvette with 10 mL of unreacted sample (up to the mark)
and replace the cap.
• Place the cuvette into the holder and close the lid
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
Alkalinity
• Remove the cuvette.
Note: Any chlorine present in the sample will interfere with the
reading. To remove the chlorine interference add one drop
of HI 93755-53 Chlorine Remover to the unreacted sample
• Carefully add exactly 1 mL of HI 93755-0 Liquid Alkalinity
Reagent using the supplied syringe.
• Replace the cap and invert 5 times.
• Reinsert the cuvette into the instrument and close the lid.
• Press Read to start the reading.
AMMONIA MEDIUM RANGE
SPECIFICATIONS
Range0.00 to 10.00 mg/L
Resolution0.01 mg/L
Accuracy±0.05 mg/L ±5% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the
Nessler method. The reaction between ammonia and reagents causes a yellow tint in
the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93715A-0First Reagent4 drops (6 drops for seawater)
HI 93715B-0Second Reagent 4 drops (10 drops for seawater)
REAGENT SETS
HI 93715-01 Reagents for 100 tests
HI 93715-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the mark)
Ammonia MR
the
Method Selection
and replace the cap.
section (see page 12).
ASTM Manual of Water and Environmental Technology, D1426-92
method using the procedure described in
,
10 mL
• The instrument displays the results in mg/L of alkalinity (CaCO3).
Note: If using a meter with software version 1.14 or earlier, readings can be improved for samples
with less than 75 ppm alkalinity by adding 0.7 mL of reagent instead of 1.0 mL.
Alkalinity
2425
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
Ammonia MR
• Remove the cuvette.
• Add 4 drops of HI 93715A-0 First Reagent (6 drops for
seawater analysis). Replace the cap and mix the solution.
• Add 4 drops of HI 93715B-0 Second Reagent (10 drops for
seawater analysis). Replace the cap and mix the solution.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the
measurement or, alternatively, wait for 3 minutes and 30 seconds
and press Read. When the timer ends the meter will perform the
reading. The instrument displays the results in mg/L of ammonianitrogen (NH3-N).
AMMONIA LOW RANGE
SPECIFICATIONS
Range0.00 to 3.00 mg/L
Resolution0.01 mg/L
Accuracy±0.04 mg/L ±4% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the
Nessler method. The reaction between ammonia and reagents causes a yellow tint in
the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93700A-0First Reagent4 drops (6 drops for seawater)
HI 93700B-0Second Reagent 4 drops (10 drops for seawater)
REAGENT SETS
HI 93700-01 Reagents for 100 tests
HI 93700-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the mark)
Ammonia LR
Method Selection
section (see page 12).
and replace the cap.
method using the procedure described in the
ASTM Manual of Water and Environmental Technology, D1426-92
,
10 mL
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of ammonia (NH3) and ammonium (NH
+
4
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
acetone, alcohols, aldehydes, glycine, hardness above 1 g/L, iron, organic chloramines, sulfide, various
aliphatic and aromatic amines.
Ammonia MR
2627
• Place the cuvette into the holder and close the lid.
).
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
Ammonia LR
• Remove the cuvette.
• Add 4 drops of HI 93700A-0 First Reagent (6 drops for
seawater analysis). Replace the cap and mix the solution.
• Add 4 drops of HI 93700B-0 Second Reagent (10 drops for
seawater analysis). Replace the cap and mix the solution.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the
measurement or, alternatively, wait for 3 minutes and 30 seconds and
press Read. When the timer ends the meter will perform the reading.
The instrument displays the results in mg/L of ammonia nitrogen(NH3-N).
BROMINE
SPECIFICATIONS
Range0.00 to 8.00 mg/L
Resolution0.01 mg/L
Accuracy±0.08 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
18
th
edition
pink tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93716-0DPD Reagent1 packet
REAGENT SETS
HI 93716-01 Reagents for 100 tests
HI 93716-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Bromine
Method Selection
method using the procedure described in the
section (see page 12).
Standard Methods for the Examination of Water and Wastewater,
, DPD method. The reaction between bromine and the reagent causes a
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of ammonia (NH3) and ammonium (NH
+
4
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by: acetone, alcohols, aldehydes, glycine, hardness above 1 g/L, iron, organic
chloramines, sulfide, various aliphatic and aromatic amines.
Ammonia LR
2829
• Fill the cuvette with 10 mL of unreacted sample (up to the
10 mL
mark) and replace the cap.
• Place the cuvette into the holder and close the lid.
).
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.
Bromine
• Remove the cuvette and add the content of one packet of
HI 93716-0 DPD reagent. Replace the cap and shake gently for
about 20 seconds to dissolve most of the reagent.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 2 minutes and 30 seconds and press Read. When the timer ends the meter will perform the
reading.
CALCIUM
SPECIFICATIONS
Range0 to 400 mg/L
Resolution10 mg/L
Accuracy±10 mg/L ±5% of reading at 25 °C
Light SourceTungsten lamp with narrow band interference filter @ 466 nm
MethodAdaptation of the Oxalate method.
REQUIRED REAGENTS
CodeDescriptionQuantity
-Buffer Reagent4 drops
HI 93752A-0 Ca Calcium Buffer Reagent7 mL
HI 93752B-0 Ca Calcium Oxalate Reagent1 mL
REAGENT SETS
HI 937521-01Reagents for 50 tests
HI 937521-03Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure at page 17.
• Select the
Calcium
method using the procedure described in the
Method Selection
section (see page 12).
• The instrument displays the results in mg/L of bromine.
INTERFERENCES
Interference may be caused by: Chlorine, Iodine, Ozone, Oxidized forms of Chromium and Manganese.
In case of water with hardness greater than 500 mg/L CaCO3, shake the sample for approximately
2 minutes after adding the reagent.
In case of water with alkalinity greater than 250 mg/L CaCO3 or acidity greater than 150 mg/L CaCO3,
the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the
sample with diluted HCl or NaOH.
Bromine
3031
• Using the 5 mL syringe add exactly 3.00 mL of sample to the cuvette.
3 mL of sample
• Use the pipette to fill the cuvette up to the
10 mL mark with the HI 93752A-0 Calcium
Buffer Reagent.
• Add 4 drops of Buffer Reagent.
Calcium
• Replace the cap and invert several times to mix.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when
the meter is zeroed and ready for measurement.
• Remove the cuvette.
• Using the 1 mL syringe, add exactly 1 mL of the
HI 93752B-0 Calcium Oxalate Reagent. Replace the
cap and invert the cuvette 10 times to mix (about
15 seconds).
• Press Timer or wait for 5 minutes. Then invert again
the cuvette 10 times to mix (about 15 seconds).
• Reinsert the cuvette into the instrument.
• Press Read to start the reading. The instrument displays the results in mg/L of Calcium.
FREE CHLORINE
FREE CHLORINEFREE CHLORINE
FREE CHLORINE
FREE CHLORINEFREE CHLORINE
SPECIFICATIONS
Range0.00 to 2.50 mg/L
Resolution0.01 mg/L
Accuracy±0.03 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
DPD reagent causes a pink tint in the sample.
EPA DPD method 330.5.
The reaction between free chlorine and the
REQUIRED REAGENTS
POWDER:
CodeDescriptionQuantity
HI 93701-0DPD1 packet
LIQUID:
CodeDescriptionQuantity
HI 93701A-FDPD1 Indicator3 drops
HI 93701B-FDPD1 Buffer3 drops
REAGENT SETS
HI 93701-F Reagents for 300 tests (liquid)
HI 93701-01 Reagents for 100 tests (powder)
HI 93701-03 Reagents for 300 tests (powder)
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
in the
Method Selection
Free Chlorine
method using the procedure described
section (see page 12).
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
• Place the cuvette into the holder and close the lid.
3233
10 mL
Free Chlorine
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette.
Powder reagents procedure
• Add the content of one packet of HI 93701 DPD reagent. Replace
the cap and shake gently for 20 seconds (or 2 minutes for
seawater analysis).
• Reinsert the cuvette into the instrument.
• Press Read to start the reading. The instrument displays the results in mg/L of free chlorine.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 1 minute and press Read. When the timer ends the meter will perform the reading. The instrument
displays the results in mg/L of free chlorine.
Liquid reagents procedure
• To an empty cuvette add 3 drops of HI 93701A-F DPD1
indicator and 3 drops of HI 93701B-F DPD1 buffer. Swirl
gently to mix, and immediately add 10 mL of unreacted
sample. Replace the cap and shake gently again.
x 3
x 3
INTERFERENCES
Interference may be caused by: Bromine, Iodine, Ozone, Oxidized forms of Chromium and Manganese.
In case of water with hardness greater than 500 mg/L CaCO3, shake the sample for approximately
2 minutes after adding the powder reagent.
In case of water with alkalinity greater than 250 mg/L CaCO3 or acidity greater than 150 mg/L CaCO3,
the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the
sample with diluted HCl or NaOH.
3435
Free ChlorineFree Chlorine
TOTAL CHLORINE
SPECIFICATIONS
Range0.00 to 3.50 mg/L
Resolution0.01 mg/L
Accuracy±0.03 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
DPD reagent causes a pink tint in the sample.
REQUIRED REAGENTS
POWDER:
CodeDescriptionQuantity
HI 93711-0DPD1 packet
LIQUID:
CodeDescriptionQuantity
HI 93701A-TDPD1 indicator3 drops
HI 93701B-TDPD1 buffer3 drops
HI 93701CDPD3 solution1 drop
REAGENT SETS
HI 93701-T Reagents for 300 total chlorine tests (liquid)
HI 93711-01 Reagents for 100 total chlorine tests (powder)
HI 93711-03 Reagents for 300 total chlorine tests (powder)
For other accessories see page 128.
EPA DPD method 330.5.
The reaction between the chlorine and the
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette.
Powder reagents procedure
• Add 1 packet of HI 93711 DPD reagent. Replace the cap and
shake gently for 20 seconds (or 2 minutes for seawater analysis).
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the
measurement or, alternatively, wait for 2 minutes and 30 seconds
and press Read. When the timer ends the meter will perform the
reading. The instrument displays the results in mg/L of total
chlorine.
MEASUREMENT PROCEDURE
• Select the
described in the
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
• Place the cuvette into the holder and close the lid.
Total Chlorine
Total Chlorine
Method Selection
method using the procedure
section (see page 12).
3637
10 mL
Liquid reagents procedure
• To an empty cuvette add 3 drops of HI 93701A-T
DPD1 indicator, 3 drops of HI 93701B-T DPD1 buffer
and 1 drop of HI 93701C DPD3 solution. Swirl gently
to mix and immediately add 10 mL of unreacted
sample. Replace the cap and shake gently again.
• Reinsert the cuvette into the instrument.
Total Chlorine
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 2 minutes and 30 seconds and press Read. When the timer ends the meter will perform the
reading.
• The instrument displays the results in mg/L of total chlorine.
Note: free and total chlorine have to be measured separately with fresh unreacted samples following
the related procedure if both values are requested.
INTERFERENCES
Interference may be caused by: Bromine, Iodine, Ozone, Oxidized forms of Chromium and Manganese.
In case of water with hardness greater than 500 mg/L CaCO3, shake the sample for approximately
2 minutes after adding the powder reagent.
In case of water with alkalinity greater than 250 mg/L CaCO3 or acidity greater than 150 mg/L CaCO3,
the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the
sample with diluted HCl or NaOH.
CHLORINE DIOXIDE
SPECIFICATIONS
Range0.00 to 2.00 mg/L
Resolution0.01 mg/L
Accuracy±0.10 mg/L ±5% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the Chlorophenol Red method. The reaction between chlorine dioxide and
reagents causes a colorless to purple tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93738A-0Reagent A1 mL
HI 93738B-0Dechlorinating Reagent B 1 packet
HI 93738C-0Reagent C1 mL
HI 93738D-0Reagent D1 mL
REAGENT SETS
HI 93738-01 Reagents for 100 tests
HI 93738-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
described in the
• Fill two graduated mixing cylinders (#1 & #2) up to the
25 mL mark with the sample.
Chlorine Dioxide
Method Selection
method using the procedure
section (see page 12).
# 1
25 mL
# 2
25 mL
Total Chlorine
• Add 0.5 mL of HI 93738A-0 Chlorine Dioxide Reagent to each cylinder (#1 & #2), close them and
invert several times to mix.
# 1# 2
3839
# 1 & # 2
Chlorine Dioxide
• Add the content of one packet of HI 93738B-0 Dechlorinating Reagent to one of the two cylinders
(#1), close and invert it several times until it is totally dissolved. This is the blank.
# 1
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Add precisely 0.5 mL of HI 93738C-0 Chlorine Dioxide Reagent to each cylinder (#1 & #2), close them
and invert several times to mix.
# 1 & # 2
# 1# 2
• Add 0.5 mL of HI 93738D-0 Chlorine Dioxide Reagent to each cylinder (#1 & #2), close them and
invert several times to mix. Cylinder #2 is the reacted sample.
# 1 & # 2
# 1
# 1# 2
10 mL
• Fill another cuvette with 10 mL of the reacted sample (#2) up
# 2
to the mark and replace the cap.
# 2
10 mL
• Insert the sample into the instrument.
• Press Read and the meter will perform the reading. The instrument displays the results in mg/L of
chlorine dioxide.
SAMPLING PROCEDURE
It is recommended to analyze chlorine dioxide samples immediately after collection. Chlorine dioxide samples
must be stored in sealed dark glass bottle, with minimal head space. Excessive heat (above 25°C/78°F),
agitation and exposure to light must be avoided.
INTERFERENCES
Interferences may be caused by strong oxidants.
• Fill a cuvette with 10 mL of the blank (#1) up to the mark
and replace the cap.
• Place the blank (#1) into the holder and close the lid.
Chlorine Dioxide
4041
# 1
Chlorine Dioxide
CHROMIUM VI HIGH RANGE
SPECIFICATIONS
Range0 to 1000 µg/L
Resolution1 µg/L
Accuracy±5 µg/L ±4% of reading at 25 °C
Typical EMC±1 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
Diphenylcarbohydrazide method. The reaction between chromium VI and the reagent
causes a purple tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93723-0Powder reagent1 packet
REAGENT SETS
HI 93723-01 Reagents for 100 tests
HI 93723-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the mark) and
Chromium VI HR
the
Method Selection
replace the cap.
section (see page 12).
ASTM Manual of Water and Environmental Technology, D1687-92
method using the procedure described in
10 mL
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 6 minutes and press Read. When the timer ends the meter will perform the reading. The
instrument displays concentration in
µµ
µg/L of chromium VI.
µµ
,
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in µg/L of Chromate (CrO
2
¯) and Dichromate (Cr2O
4
2
¯).
7
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette and add the content of one packet of
HI 93723-0 reagent. Replace the cap and shake vigorously
for about 10 seconds.
Chromium VI HR
4243
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Vanadium above 1 ppm. However, waiting 10 minutes before reading, the interference is removed
Iron above 1 ppm
Mercurous and mercuric ions cause slight inhibition of the reaction.
Chromium VI HR
CHROMIUM VI LOW RANGE
SPECIFICATIONS
Range0 to 300 µg/L
Resolution1 µg/L
Accuracy±1 µg/L ±4% of reading at 25 °C
Typical EMC±1 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
ASTM Manual of Water and Environmental Technology, D1687-92
Diphenylcarbohydrazide method. The reaction between chromium VI and the reagent
causes a purple tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93749-0Powder reagent1 packet
REAGENT SETS
HI 93749-01 Reagents for 100 tests
HI 93749-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the mark)
• Place the cuvette into the holder and close the lid.
Chromium VI LR
the
Method Selection
and replace the cap.
method using the procedure described in
section (see page 12).
10 mL
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 6 minutes and press Read. When the timer ends the meter will perform the reading. The instrument
displays concentration in µg/L of chromium VI.
,
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in µg/L of Chromate (CrO
2
¯) and Dichromate (Cr2O
4
2
¯).
7
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette and add the content of one packet of HI
93749-0 reagent. Replace the cap and shake vigorously for
about 10 seconds.
Chromium VI LR
4445
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Vanadium above 1 ppm. However, waiting 10 minutes before reading, the interference is removed.
Iron above 1 ppm
Mercurous and mercuric ions cause slight inhibition of the reaction.
Chromium VI LR
COLOR OF WATER
SPECIFICATIONS
Range0 to 500 PCU (Platinum Cobalt Units)
Resolution1 PCU
Accuracy±10 PCU ±5% of reading at 25 °C
Typical EMC± 1 PCU
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the
th
18
edition
REQUIRED ACCESSORIES
0.45 µm membrane for true color measurement.
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill one cuvette up to the mark with deionized water and replace
• Place the blank (# 1) into the holder and close the lid.
Color of Water
the
Method Selection
section (see page 12).
the cap. This is the blank.
Standard Methods for the Examination of Water and Wastewater,
, Colorimetric Platinum Cobalt method.
method using the procedure described in
# 1
10 mL
# 1
• Fill the second cuvette up to the mark with unfiltered sample
and replace the cap. This is the apparent color.
• Filter 10 mL of sample through a filter with a 0.45 µm
membrane into the third cuvette, up to the 10 mL mark and
replace the cap. This is the true color.
• Insert the apparent color cuvette (# 2) into the instrument
and close the lid.
• Press Read to start the reading.
• The meter displays the value of apparent color in PCU.
• Remove the cuvette, insert the true color cuvette (# 3) into the
instrument and ensure that the notch on the cap is positioned
securely into the groove.
10 mL
# 2
# 3
# 2
# 3
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the blank.
Color of Water
4647
• Press Read to start the reading. The meter displays the value of true color in PCU.
Color of Water
COPPER HIGH RANGE
• Remove the cuvette.
SPECIFICATIONS
Range0.00 to 5.00 mg/L
Resolution0.01 mg/L
Accuracy±0.02 mg/L ±4% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the
reagent causes a purple tint in the sample.
EPA method.
The reaction between copper and the bicinchoninate
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93702-0Bicinchoninate1 packet
REAGENT SETS
HI 93702-01 Reagents for 100 tests
HI 93702-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the mark)
Copper HR
Method Selection
and replace the cap.
section (see page 12).
method using the procedure described in the
• Add the content of one packet of HI 93702-0 Bicinchoninate.
Replace the cap and shake gently for about 15 seconds.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 45 seconds and press Read. When the timer ends the meter will perform the reading.
• The instrument displays the results in mg/L of copper.
10 mL
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
Copper HR
4849
INTERFERENCES
Interference may be caused by:
Silver
Cyanide
For samples overcoming buffering capacity of reagent (around pH 6.8), pH should be adjusted between 6
and 8.
Copper HR
COPPER LOW RANGE
• Remove the cuvette.
SPECIFICATIONS
Range0 to 1000 µg/L
Resolution1 µg/L
Accuracy±10 µg/L ±5% of reading at 25 °C
Typical EMC±1 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the
reagent causes a purple tint in the sample.
EPA method.
The reaction between copper and the bicinchoninate
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93747-0Bicinchoninate1 packet
REAGENT SETS
HI 93747-01 Reagents for 100 tests
HI 93747-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the
Copper LR
method using the procedure described in
the
Method Selection
mark) and replace the cap.
section (see page 12).
10 mL
• Add the content of one packet of HI 93747-0 Bicinchoninate.
Replace the cap and shake gently for about 15 seconds.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 45 seconds and press Read. When the timer ends the meter will perform the reading.
• The instrument displays the results in
µµ
µg/L of copper.
µµ
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
Copper LR
5051
INTERFERENCES
Interference may be caused by:
Silver
Cyanide
For samples overcoming buffering capacity of reagent (around pH 6.8), pH should be adjusted between 6
and 8.
Copper LR
CYANIDE
SPECIFICATIONS
Range0.000 to 0.200 mg/L
Resolution0.001 mg/L
Accuracy±0.005 mg/L ±3% of reading at 25 °C
Typical EMC Dev. ±0.001 mg/L
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the
th
edition
18
causes a blue tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93714A-0Reagent A1 spoon
HI 93714B-0Reagent B1 packet
HI 93714C-0Reagent C1 packet
REAGENT SETS
HI 93714-01 Reagents for 100 tests
HI 93714-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Cyanide
Method Selection
method using the procedure described in the
section (see page 12).
Standard Methods for the Examination of Water and Wastewater,
, Pyridine-Pyrazolone method. The reaction between cyanide and reagents
10 mL
Note: Pay attention to the way the spoon is filled:
- do not press the powder;
- do not overfill it.
• Place the HDPE plastic stopper and cap immediately, to
prevent the escape of chlorine gas which is developed during
the reaction, and shake gently for 30 seconds.
• Wait for 30 seconds leaving the cuvette tightly capped
and undisturbed, then add the content of one packet of
HI 93714B-0 reagent and shake gently for 10 seconds.
• Immediately add the content of one packet of HI 93714C-0
reagent, replace the cap and shake vigorously for 20 seconds.
• Reinsert the cuvette into the instrument.
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette and add 1 level spoon of HI 93714A-0
Cyanide Reagent. Remember to close the reagent bottle immediately
after use.
Cyanide
5253
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 25 minutes and press Read. When the timer ends the meter will perform the reading.
Note: Gently shake the cuvette 4 or 5 times during the first 20 minutes of the countdown prior to the
measurement. Accuracy is not affected by undissolved reagent powder.
• The instrument displays the results in mg/L of cyanide.
Cyanide
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of Potassium Cyanide (KCN).
• Press s or t to return to the measurement screen.
Note: for most accurate results perform the test at 20-25 °C.
INTERFERENCES
Interference may be caused by large amounts of turbidity that will cause high readings.
Oxidizing (such as chlorine) or reducing agents (such as sulfide or sulfur dioxide) are known to interfere with
the measurement. Distillation will remove these.
Samples with high pH values should be adjusted to approximately pH 7 before testing.
CAUTION: cyanides, their solutions, and hydrogen cyanide liberated by acids, are very poisonous.
CYANURIC ACID
SPECIFICATIONS
Range0 to 80 mg/L
Resolution1 mg/L
Accuracy±1 mg/L ±15% of reading at 25 °C
Typical EMC±1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the turbidimetric method. The reaction between cyanuric acid and the
reagent causes a white suspension in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93722-0Powder reagent1 packet
REAGENT SETS
HI 93722-01 Reagents for 100 tests
HI 93722-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
described in the
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
Cyanuric Acid
Method Selection
method using the procedure
section (see page 12).
10 mL
Cyanide
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the
meter is zeroed and ready for measurement.
5455
Cyanuric Acid
FLUORIDE
• Add the content of one packet of HI 93722-0 Cyanuric Acid
Reagent. Replace the cap and shake gently for about
10 seconds (dissolution is not complete).
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 45 seconds and press Read. When the timer ends the meter will perform the reading.
• The instrument displays concentration in mg/L of cyanuric acid.
SPECIFICATIONS
Range0.00 to 2.00 mg/L
Resolution0.01 mg/L
Accuracy±0.03 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the
th
18
edition
Standard Methods for the Examination of Water and Wastewater,
, SPADNS method. The reaction between fluoride and the liquid reagent
causes a red tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93729-0SPADNS Reagent4 mL
REAGENT SETS
HI 93729-01 Reagents for 100 tests
HI 93729-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Add 2 mL of HI 93729-0 SPADNS Reagent to two cuvettes.
Fluoride
Method Selection
method using the procedure described in the
section (see page 12).
Cyanuric Acid
• Fill one of the cuvettes with distilled water up to the mark,
replace the cap and invert several times to mix.
• Fill the other cuvette with sample up to the mark, replace the
cap and invert several times to mix.
• Place the cuvette with the reacted distilled water (# 1) into the
holder and close the lid.
5657
# 1
# 1
2 mL
10 mL10 mL
# 2
Fluoride
• Press Timer and the display will show the countdown prior to zeroing the blank or, alternatively, wait
for two minutes and press Zero. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
# 2
• Insert the other cuvette (# 2) with the reacted sample into the
instrument.
• Press Read to start reading. The instrument displays the results in mg/L of fluoride.
Note: For wastewater or seawater samples, before performing measurements, distillation is required.
For most accurate results, use two graduated pipettes to deliver exactly 8 mL of distilled water and
8 mL of sample.
INTERFERENCES
Interferences may be caused by:
Alkalinity (as CaCO3) above 5000 mg/L
Aluminum above 0.1 mg/L
Iron, ferric above 10 mg/L
Chloride above 700 mg/L
Phosphate, ortho above 16 mg/L
Sodium hexametaphosphate above 1.0 mg/L
Sulfate above 200 mg/L
Highly colored and turbid samples may require distillation
Highly alkaline samples can be neutralized with nitric acid.
CALCIUM HARDNESS
SPECIFICATIONS
Range0.00 to 2.70 mg/L
Resolution0.01 mg/L
Accuracy±0.11 mg/L ±5% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
th
18
edition,
reddish-violet tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93720A-0Ca & Mg indicator0.5 mL
HI 93720B-0Alkali solution0.5 mL
HI 93720C-0EGTA solution1 drop
REAGENT SETS
HI 93720-01 Reagents for 100 tests
HI 93720-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Rinse a graduated beaker several times with unreacted
• Add 0.5 mL of HI 93720A-0 Calcium indicator solution
• Add 0.5 mL of HI 93720B-0 Alkali solution and swirl to
Calcium Hardness
described in the
Method Selection
sample, before filling it to the 50 mL mark with the
sample.
and swirl to mix.
mix. Use this solution to rinse 2 cuvettes before filling
them up to the 10 mL mark.
Standard Methods for the Examination of Water and Wastewater,
Calmagite method. The reaction between calcium and reagents causes a
method using the procedure
section (see page 12).
# 1# 2
Fluoride
5859
Hardness Ca
• Add 1 drop of HI 93720C-0 EGTA solution to one cuvette (# 1), replace
the cap and invert the cuvette several times to mix. This is the blank.
# 1
# 1
• Place the blank (# 1) into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for
measurement.
# 2
• Remove the blank and insert the second cuvette (# 2)
into the instrument.
• Press Read to start the reading. The instrument displays concentration in mg/L of calcium
hardness, as CaCO3.
• Press the Unit key to change the current measurement unit. The results can be converted to French
degrees (°f), German degrees (°dH) and English degrees (°E).
• Press s or t to return to the measurement screen.
Note: This test will detect any calcium contamination in the beaker, measuring syringes or sample cells. To
test cleanliness, repeat the test multiple times until you obtain consistent results.
Note: For better accuracy wash glassware with HCl 6N.
SAMPLE DILUTION
This meter is designed to determine low levels of hardness, typically found in water purification systems.
When testing some other sources of water, it is not uncommon to come across levels of hardness that are
greater than the range of this meter.
This problem can be overcome through dilution. Dilutions must be performed with hardness-free water or the
readings will be erroneous.
A dilution to reduce the level of hardness by a factor of one hundred is performed as follows:
• Fill a 1 mL syringe with the sample.
• Place the syringe in a 50 mL beaker, making sure that the beaker is clean and empty, and inject 0.5
mL into the beaker.
• Fill the beaker up to the 50 mL mark with hardness-free water.
INTERFERENCES
Interference may be caused by excessive amounts of heavy metals.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of Calcium (Ca).
Hardness Ca
6061
Hardness Ca
MAGNESIUM HARDNESS
SPECIFICATIONS
Range0.00 to 2.00 mg/L
Resolution0.01 mg/L
Accuracy±0.11 mg/L ±5% of reading at 25 °C
Typical EMC±0.02 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
th
18
edition,
causes a reddish-violet tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93719A-0Mg indicator0.5 mL
HI 93719B-0Alkali solution0.5 mL
HI 93719C-0EDTA solution1 drop
HI 93719D-0EGTA solution1 drop
REAGENT SETS
HI 93719-01 Reagents for 100 tests
HI 93719-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Rinse a graduated beaker several times with unreacted sample,
Magnesium Hardness
described in the
Method Selection
before filling it to the 50 mL mark with the sample.
Standard Methods for the Examination of Water and Wastewater,
EDTA colorimetric method. The reaction between magnesium and reagents
method using the procedure
section (see page 12).
• Fill both cuvettes up to the 10 mL mark.
10 mL
# 1
10 mL
# 2
• Add 1 drop of HI 93719C-0 EDTA solution to one cuvette
(# 1), replace the cap and invert the cuvette several
times to mix. This is the blank.
# 1
• Add 1 drop of HI 93719D-0 EGTA solution to the second
cuvette (# 2), replace the cap and invert the cuvette
several times to mix. This is the sample.
# 2
# 1
• Place the blank (# 1) into the holder and close the lid.
• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.
# 2
• Add 0.5 mL of HI 93719A-0 Magnesium indicator solution,
then swirl to mix.
• Add 0.5 mL of HI 93719B-0 Alkali solution and swirl to mix.
Use this solution to rinse 2 cuvettes.
Hardness Mg
6263
• Remove the blank (# 1), insert the sample (# 2) into
the instrument, and close the lid.
• Press Read to start the reading. The instrument displays concentration in mg/L of magnesium
hardness, as CaCO3.
Hardness Mg
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of Magnesium (Mg).
• Press the Unit key to change the current measurement unit. The results can be converted to French
degrees (°f), German degrees (°dH) and English degrees (°E).
• Press s or t to return to the measurement screen.
Note: This test will detect any magnesium contamination in the beakers, measuring syringes or sample
cells. To test cleanliness, repeat the test multiple times until you obtain consistent results.
SAMPLE DILUTION
This meter is designed to determine hardness typically found in water purification systems. In order to
measure samples with high hardness, follow dilution procedure explained on page 61 (Ca Hardness).
HYDRAZINE
SPECIFICATIONS
Range0 to 400 µg/L
Resolution1 µg/L
Accuracy±4% of full scale reading at 25 °C
Typical EMC±2 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the
D1385-88,
and the liquid reagent causes a yellow tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93704-0Liquid Reagent24 drops
REAGENT SETS
HI 93704-01 Reagents for 100 tests
HI 93704-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill one cuvette up to the mark with 10 mL of distilled water.
Hydrazine
the
Method Selection
method using the procedure described in
section (see page 12).
ASTM Manual of Water and Environmental Technology, method
p-Dimethylaminobenzaldehyde method. The reaction between hydrazine
10 mL
# 1
INTERFERENCES
Interference may be caused by excessive amounts of heavy metals.
Hardness Mg
6465
• Place the cap, insert the cuvette # 1 into the holder and
# 1
close the lid.
• Press the Blank key to start adjusting the light level. The display will show “Blank done” when the
meter is ready to take a zero measurement.
• Fill a second cuvette with 10 mL of unreacted sample (up to
the mark) and replace the cap.
10 mL
# 2
Hydrazine
• Add 12 drops of the HI 93704-0 reagent to
each cuvette. Replace the caps and shake
gently to mix (about 30 seconds).
# 1# 2
# 1
• Place the blank (#1) into the holder and close the lid.
• Press Timer and the display will show the countdown prior to zeroing the blank. The display will
show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the blank.
# 2
• Insert the cuvette with the reacted sample (# 2) into the
instrument and close the lid.
IODINE
SPECIFICATIONS
Range0.0 to 12.5 mg/L
Resolution0.1 mg/L
Accuracy±0.1 mg/L ±5% of reading at 25 °C
Typical EMC±0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
18
th
edition
tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93718-0DPD Reagent1 packet
REAGENT SETS
HI 93718-01 Reagents for 100 tests
HI 93718-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to
• Place the cuvette into the holder and close the lid.
Iodine
method using the procedure described in
the
Method Selection
section (see page 12).
the mark) and replace the cap.
Standard Methods for the Examination of Water and Wastewater,
, DPD method. The reaction between iodine and the reagent causes a pink
10 mL
• Press Read to start the reading. The instrument displays concentration in
INTERFERENCES
Interference may be caused by:
Highly colored samples
Highly turbid samples
Aromatic amines
Hydrazine
6667
µµ
µg/L of hydrazine.
µµ
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cap and add the content of one packet of HI 93718-0
DPD reagent. Replace the cap and shake gently for about
30 seconds to dissolve most of the reagent.
Iodine
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 2 minutes and 30 seconds and press Read. When the timer ends the meter will perform the
reading.
• The instrument displays concentration in mg/L of iodine.
INTERFERENCES
Interference may be caused by: Bromine, Chlorine, Ozone, Oxidized forms of Chromium and Manganese.
In case of water with hardness greater than 500 mg/L CaCO3, shake the sample for approximately 2
minutes after adding the reagent.
In case of water with alkalinity greater than 250 mg/L CaCO3 or acidity greater than 150 mg/L CaCO3,
the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the
sample with diluted HCl or NaOH.
IRON HIGH RANGE
SPECIFICATIONS
Range0.00 to 5.00 mg/L
Resolution0.01 mg/L
Accuracy±0.04 mg/L ±2% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
The reaction between iron and reagents causes an orange tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93721-0Powder Reagent 1 packet
REAGENT SETS
HI 93721-01 Reagents for 100 tests
HI 93721-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” the meter is zeroed and ready for measurement.
Iron HR
method using the procedure described
in the
Method Selection
the mark) and replace the cap.
section (see page 12).
EPA Phenantroline method 315B,
for natural and treated waters.
10 mL
Iodine
• Remove the cuvette and add the content of one packet of
HI 93721-0 reagent. Replace the cap and shake until
dissolution is complete.
6869
Iron HR
IRON LOW RANGE
12
3
6
9
30"
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 3 minutes and press Read. When the timer ends the meter will perform the reading.
• The instrument displays concentration in mg/L of iron.
Range0 to 400 µg/L
Resolution1 µg/L
Accuracy±10 µg/L ±8% of reading at 25 °C
Typical EMC±1 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the TPTZ Method. The reaction between iron and the reagent causes a
violet tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93746-0TPTZ Reagent2 packets
REAGENT SETS
HI 93746-01 Reagents for 50 tests
HI 93746-03 Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill one graduated mixing cylinder up to the 25 mL mark
Iron LR
method using the procedure described in
the
Method Selection
with deionized water.
section (see page 12).
25 mL
• Add the content of one packet of HI 93746-0 TPTZ
reagent, close the cylinder and shake vigorously for 30
seconds. This is the blank.
• Fill a cuvette with 10 mL of the blank up to the mark and
10 mL
replace the cap.
• Place the cuvette into the holder and close the lid.
Iron HR
7071
Iron LR
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
12
3
6
9
30"
measurement.
• Remove the cuvette.
• Fill another graduated mixing cylinder up to the 25 mL
25 mL
mark with the sample.
• Add the content of one packet of HI 93746-0 TPTZ reagent,
close the cylinder and shake vigorously for 30 seconds. This
is the reacted sample.
• Fill a cuvette with 10 mL of the reacted sample up to the
mark and replace the cap.
10 mL
• Insert the sample into the instrument.
INTERFERENCES
Interference may be caused by:
Cadmium above 4.0 mg/L
3+
Chromium
Chromium
Cobalt above 0.05 mg/L
Copper above 0.6 mg/L
Cyanide above 2.8 mg/L
Manganese above 50.0 mg/L
Mercury above 0.4 mg/L
Molybdenum above 4.0 mg/L
Nickel above 1.0 mg/L
Nitrite ion above 0.8 mg/L
Sample pH should be between 3 and 4 to avoid developed color to
fade or turbidity formation.
above 0.25 mg/L
6+
above 1.2 mg/L
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 30 seconds and press Read. When the timer ends the meter will perform the reading. The
instrument displays concentration in
Iron LR
µµ
µg/L of iron.
µµ
7273
Iron LR
MAGNESIUM
SPECIFICATIONS
Range0 to 150 mg/L
Resolution5 mg/L
Accuracy±5 mg/L ±3% of reading at 25 °C
Light SourceTungsten lamp with narrow band interference filter @ 466 nm
MethodAdaptation of the Calmagite method
.
• Remove the cuvette.
• Using the other 1 mL syringe, add to the cuvette exactly 0.5 mL of sample.
Note: Do not mix up the two syringes!
• Replace the cap and invert several times to mix.
0.5 mL
of sample
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93752A-0 Mg Magnesium Buffer Reagent 1 mL
HI 93752B-0 Mg Magnesium Indicator Reagent 9 mL
REAGENT SETS
HI 937520-01Reagents for 50 tests
HI 937520-03Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the COLORED OR TURBID SAMPLES
procedure on page 17.
• Select the
• Using one 1 mL syringe add exactly 1.00 mL of HI 93752A-0
• Replace the cap and invert several times to mix.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
Magnesium
Method Selection
Mg Buffer reagent to the cuvette and use the pipette to fill the
cuvette up to the 10 mL mark with the HI 93752B-0 Mg
Indicator reagent.
measurement.
method using the procedure described in the
section (see page 12).
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 15 seconds and press Read. When the timer ends the meter will perform the reading.
• The instrument displays the results in mg/L of Magnesium (Mg).
INTERFERENCES
Interferences may be caused by:
Acidity (as CaCO3) above 1000 mg/L
Alkalinity (as CaCO3) above 1000 mg/L
Calcium (Ca2+) above 200 mg/L
Iron must be absent
Aluminum must be absent
Copper must be absent
Magnesium
7475
Magnesium
MANGANESE HIGH RANGE
SPECIFICATIONS
Range0.0 to 20.0 mg/L
Resolution0.1 mg/L
Accuracy±0.2 mg/L ±3% of reading at 25 °C
Typical EMC±0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
18
th
edition,
a pink tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93709A-0Citrate1 packet
HI 93709B-0Sodium periodate1 packet
REAGENT SETS
HI 93709-01 Reagents for 100 tests
HI 93709-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
described in the
• Fill the cuvette with 10 mL of unreacted sample (up to
the mark) and replace the cap.
Manganese HR
Method Selection
Standard Methods for the Examination of Water and Wastewater,
Periodate method. The reaction between manganese and reagents causes
method using the procedure
section (see page 12).
10 mL
• Add the content of one packet of HI 93709B-0 Sodium
Periodate reagent. Replace the cap and invert to mix with
gently movements for 2 minutes.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 1 minute and 30 seconds and press Read. When the timer ends the meter will perform the reading.
The instrument displays the results in mg/L of manganese.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of potassium permanganate (KMnO4) and
permanganate (MnO4).
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when
the meter is zeroed and ready for measurement.
• Remove the cuvette.
• Add the content of one packet of HI 93709A-0 Citrate
reagent. Replace the cap and invert to mix with gently
movements for 2 minutes.
Manganese HR
7677
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Calcium above 700 mg/L
Chloride above 70000 mg/L
Iron above 5 mg/L
Magnesium above 100000 mg/L.
Manganese HR
MANGANESE LOW RANGE
SPECIFICATIONS
Range0 to 300 µg/L
Resolution1 µg/L
Accuracy±10 µg/L ±3% of reading at 25 °C
Typical EMC±1 µg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the PAN Method. The reaction between manganese and the reagents
causes an orange tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93748A-0Ascorbic acid2 packets
HI 93748B-0Alkaline-cyanide sol.0.40 mL
HI 93748C-00.1% PAN indicator2 mL
HI 93703-51Dispersing Agent4-6 drops
REAGENT SETS
HI 93748-01 Reagents for 50 tests
HI 93748-03 Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill one cuvette with 10 mL of deionized water (up to the mark).
page 12).
Manganese LR
method using the procedure described in the
Method Selection
10 mL
section (see
• Add 0.2 mL of the HI 93748B-0 Alkaline-cyanide reagent
solution to each cuvette, replace the caps and invert gently
to mix for about 30 seconds.
• Add 1 mL of the HI 93748C-0 0.1% PAN indicator
solution to each cuvette, replace the caps and shake
gently.
• Add 3 drops of Dispersing Agent (HI 93703-51) to each
cuvette, replace the caps and invert gently to mix for
about 30 seconds.
• Place the cuvette with the reacted deionized water (blank)
into the holder and close the lid.
• Fill a second cuvette with 10 mL of sample (up to the mark).
• Add the content of one packet of HI 93748A-0 Ascorbic acid to
each cuvette, replace the caps and shake gently until completely
dissolved.
Manganese LR
7879
10 mL
• Press Timer and the display will show the countdown prior to zeroing the blank. Alternatively wait for
2 minutes and then press Zero. The display will show "-0.0-" when the meter is zeroed and ready for
measurement.
Manganese LR
• Insert the second cuvette with the reacted sample into the instrument.
• Press Read to start the reading. The instrument displays the results in
µµ
µg/L of manganese.
µµ
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in µg/L of potassium permanganate (KMnO
permanganate (MnO4).
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Aluminum above 20 mg/L
Cadmium above 10 mg/L
Calcium above 200 mg/L as CaCO
Cobalt above 20 mg/L
Copper above 50 mg/L
Iron above 10 mg/L
Lead above 0.5 mg/L
Magnesium above 100 mg/L as CaCO
Nickel above 40 mg/L
Zinc above 15 mg/L.
3
3
) and
4
MOLYBDENUM
SPECIFICATIONS
Range0.0 to 40.0 mg/L
Resolution0.1 mg/L
Accuracy±0.3 mg/L ±5% of reading at 25 °C
Typical EMC±0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the mercaptoacetic acid method. The reaction between molybdenum and
the reagents causes a yellow tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93730A-0Reagent A1 packet
HI 93730B-0Reagent B1 packet
HI 93730C-0Reagent C1 packet
REAGENT SETS
HI 93730-01 Reagents for 100 tests
HI 93730-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
in the
Method Selection
Molybdenum
method using the procedure described
section (see page 12).
mark) and replace the cap.
measurement.
10 mL
Manganese LR
8081Molybdenum
• Fill one graduated mixing cylinder up to the 25
mL mark with the sample.
• Add the content of one packet of HI 93730A-0
molybdenum reagent, close the cylinder and invert
it several times until completely dissolved.
• Add the content of one packet of HI 93730B-0
molybdenum reagent to the cylinder, close and
invert it several times until completely dissolved.
25 mL
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for five minutes and press Read. When the timer ends the meter will perform the reading. The
instrument displays concentration in mg/L of molybdenum.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of molybdate (MoO4) and sodium molybdate
(Na2MoO4).
• Add the content of one packet of HI 93730C-0
molybdenum reagent to the cylinder, close and
shake it vigorously.
• Fill an empty cuvette with 10 mL of sample up to
the mark and replace the cap.
• Insert the cuvette into the instrument.
Molybdenum
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Aluminum above 50 mg/L
Chromium above 1000 mg/L
Copper above 10 mg/L
Iron above 50 mg/L
Nickel above 50 mg/L
10 mL
8283
Nitrite, as NO2¯
Sulfate above 200 mg/L
Highly buffered samples or with extreme pH may exceed the buffering capacity of the reagents.
Molybdenum
NICKEL HIGH RANGE
SPECIFICATIONS
Range0.00 to 7.00 g/L
Resolution0.01 g/L
Accuracy±0.07 ±4% of reading at 25 °C
Typical EMC±0.02 g/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the photometric method. The reaction between nickel and the reagent
causes a blue tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93726-0Powder reagent1 packet
REAGENT SETS
HI 93726-01 Reagents for 100 tests
HI 93726-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Nickel HR
method using the procedure described in the
Method Selection
section (see page 12).
• Remove the cuvette and add the content of one packet of
HI 93726-0 reagent. Replace the cap and shake gently
until completely dissolved.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 1 minute and press Read. When the timer ends the meter will perform the reading.
• The instrument displays concentration in g/L of nickel.
• Fill the cuvette up to the mark with 10 mL of unreacted sample
and replace the cap.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
Nickel HR
8485
10 mL
INTERFERENCES
Interference may be caused by copper.
Nickel HR
NICKEL LOW RANGE
SPECIFICATIONS
Range0.000 to 1.000 mg/L
Resolution0.001 mg/L
Accuracy±0.010 mg/L ±7% of reading at 25 °C
Typical EMC±0.001 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the PAN method. The reaction between nickel and the reagents causes
an orange tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93740A-0Phthalate-phosphate2 packets
HI 93740B-00.3% PAN indicator2 mL
HI 93740C-0EDTA2 packets
HI 93703-51Dispersing Agent4-6 drops (only when necessary, see note)
REAGENT SETS
HI 93740-01 Reagents for 50 tests
HI 93740-03 Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Nickel LR
method using the procedure described in
the
Method Selection
section (see page 12).
Note: for best results perform your tests between 20-24°C.
• Press Timer and the display will show a countdown prior to adding reagent C or, alternatively, wait
for 15 minutes. Add one packet of HI 93740C-0 EDTA reagent to each beaker, cap and swirl to mix
until completely dissolved.
• Fill one cuvette up to the mark with 10 mL of the blank.
10 mL
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
10 mL
• Fill a second cuvette up to the mark with 10 mL of the reacted sample.
• Fill one graduated beaker with 25 mL of deionized water
(blank) and another one with 25 mL of sample.
• Add the content of one packet of HI 93740A-0 Phthalate-
phosphate reagent to each beaker. Cap and swirl gently until
the reagent is dissolved.
Note: If sample contains iron (Fe3+), it is important that all
powder be dissolved completely before continuing with following
step.
• Add 1 mL of HI 93740B-0 0.3% PAN solution to each
beaker, cap and swirl to mix.
Nickel LR
8687
• Insert the second cuvette into the instrument.
• Press Read to start the reading. The instrument displays the results in mg/L of nickel.
Note: a temperature above 30°C may cause turbidity. In this case, before zeroing and taking
readings, add 2-3 drops of Dispersing Agent (HI 93703-51) to each cuvette and swirl until turbidity
is removed.
Range0.0 to 30.0 mg/L
Resolution0.1 mg/L
Accuracy±0.5 mg/L ±10% of reading at 25 °C
Typical EMC±0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the cadmium reduction method. The reaction between nitrate and the
reagent causes an amber tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93728-0Powder reagent1 packet
REAGENT SETS
HI 93728-01 Reagents for 100 tests
HI 93728-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Using the pipette, fill the cuvette with 6 ml of sample, up to
Nitrate
method using the procedure described in the
Method Selection
half of its height, and replace the cap.
section (see page 12).
6 mL
Nickel LR
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette and add the content of one packet of HI 93728-0
reagent.
8889
Nitrate
• Replace the cap and immediately shake vigorously up
and down for exactly 10 seconds. Continue to mix by
inverting the cuvette gently for 50 seconds, while taking
care not to induce air bubbles. Powder will not completely dissolve. Time and way of shaking could sensitively
affect the measurement.
• Reinsert the cuvette into the instrument, taking care
not to shake it.
• Press Timer and the display will show the countdown
prior to the measurement or, alternatively, wait for
4 minutes and 30 seconds and press Read. When the timer
ends the meter will perform the reading. The instrument
displays the results in mg/L of nitrate-nitrogen.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of nitrate (NO3¯).
NITRITE HIGH RANGE
SPECIFICATIONS
Range0 to 150 mg/L
Resolution1 mg/L
Accuracy±4 mg/L ±4% of reading at 25 °C
Typical EMC±1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the Ferrous Sulfate method. The reaction between nitrite and the
reagent causes a greenish-brown tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93708-0Powder reagent1 packet
REAGENT SETS
HI 93708-01 Reagents for 100 tests
HI 93708-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette up to the mark with 10 mL of unreacted
Nitrite HR
method using the procedure described
in the
Method Selection
sample and replace the cap.
section (see page 12).
10 mL
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Ammonia and amines, as urea and primary aliphatic amines
Chloride above 100 ppm
Chlorine above 2 ppm
Copper
Iron(III)
Strong oxidizing and reducing substances
Sulfide must be absent
Nitrate
9091
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
Nitrite HR
NITRITE LOW RANGE
• Add the content of one packet of HI 93708-0 reagent.
Replace the cap and shake gently until completely dissolved.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 10 minutes and press Read. When the timer ends the meter will perform the reading. The
instrument displays concentration in mg/L of nitrite.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of nitrogen-nitrite (NO2¯-N) and sodium nitrite
(NaNO2).
SPECIFICATIONS
Range0.00 to 1.15 mg/L
Resolution0.01 mg/L
Accuracy±0.06 mg/L ±4% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
the reagent causes a pink tint in the sample.
EPA Diazotization method 354.1
. The reaction between nitrite and
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93707-0Powder reagent1 packet
REAGENT SETS
HI 93707-01 Reagents for 100 tests
HI 93707-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette up to the mark with 10 mL of unreacted
• Place the cuvette into the holder and close the lid.
Nitrite LR
method using the procedure described
in the
Method Selection
sample (up to the mark) and replace the cap.
section (see page 12).
10 mL
• Press s or t to return to the measurement screen.
Nitrite HR
9293
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
• Add the content of one packet of HI 93707-0 reagent.
Replace the cap and shake gently for about 15 seconds.
Nitrite LR
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 6 minutes and press Read. When the timer ends the meter will perform the reading. The instrument
displays concentration in mg/L of nitrite.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of nitrogen-nitrite (NO2¯-N) and sodium nitrite
(NaNO2).
DISSOLVED OXYGEN
SPECIFICATIONS
Range0.0 to 10.0 mg/L
Resolution0.1 mg/L
Accuracy±0.4 mg/L ±3% of reading at 25 °C
Typical EMC± 0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 420 nm
MethodAdaptation of the
18th edition,
and the reagents causes a yellow tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93732A-0Reagent A5 drops
HI 93732B-0Reagent B5 drops
HI 93732C-0Reagent C10 drops
REAGENT SET
HI 93732-01 Reagents for 100 tests
HI 93732-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Dissolved Oxygen
the
Method Selection
section (see page 12).
Standard Methods for the Examination of Water and Wastewater,
Azide modified Winkler method. The reaction between dissolved oxygen
method using the procedure described in
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by the following ions:
ferrous, ferric, cupric, mercurous, silver, antimonious, bismuth, auric, lead, metavanadate and chloroplatinate.
Strongly reducing and oxidizing reagents.
High levels of nitrate (above 100 mg/L) could yield falsely high readings due to a minute amount of
reduction to nitrite that could occur at these levels.
Nitrite LR
9495
• Fill one 60 mL glass bottle completely with the unreacted sample.
• Replace the cap and ensure that a small part of the sample spills
over.
• Remove the cap and add 5 drops of HI 93732A-0 and 5 drops of
HI 93732B-0.
• Add more sample, to fill the bottle completely. Replace the cap
again and ensure that a part of the sample spills over. This is to
make sure that no air bubbles have been trapped inside, which
could alter the reading.
• Invert several times the bottle. The sample becomes orange-yellow
and a flocculent agent will appear.
Dissolved Oxygen
• Let the sample stand and the flocculent agent will start to settle.
• After approximately 2 minutes, when the upper half of the bottle becomes limpid,
add 10 drops of HI 93732C-0.
• Replace the cap and invert the bottle until the settled flocculent dissolves completely.
The sample is ready for measurement when it is yellow and completely limpid.
10 mL
• Fill the cuvette up to the mark with 10 mL of the unreacted
(original) sample, and replace the cap. This is the blank.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the
meter is zeroed and ready for measurement.
• Remove the cuvette.
• Fill another cuvette up to the mark with 10 mL of the reacted
sample and replace the cap.
• Reinsert the cuvette into the instrument.
• Press Read to start the reading. The instrument will display the results in mg/L of dissolved oxygen.
OZONE
SPECIFICATIONS
Range0.00 to 2.00 mg/L
Resolution0.01 mg/L
Accuracy±0.02 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodColorimetric DPD Method. The reaction between ozone and the DPD reagent causes a
pink tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity/test
HI 93757-0DPD Powder Reagent1 packet
HI 93703-52-0 Glycine Powder (Optional Reagent) 1 packet
REAGENT SETS
HI 93757-01Reagents for 100 tests
HI 93757-03Reagents for 300 tests
HI 93703-52Glycine Powder, Optional Reagent for 100 tests
For other accessories see page 128.
IMPORTANT NOTE: Chlorine is a strong interferent for ozone determination. If the sample is suspected to
contain chlorine residues (free or total chlorine), please follow the alternative measurement procedure
described below:
• Perform the Standard Measurement Procedure and take note of the reading:
• On a fresh sample perform the Additional Measurement Procedure and take note of the reading:
• Subtract reading B from reading A to obtain the ozone concentration in mg/L:
mg/L (O3) =
value A
–
value B
.
STANDARD MEASUREMENT PROCEDURE
• Select the
in the
Method Selection
Ozone
method using the procedure described
section (see page 12).
value A
10 mL
.
value B
.
INTERFERENCES
Interferences may be caused by reducing and oxidizing materials.
Dissolved Oxygen
9697
• Fill the cuvette with 10 mL of unreacted sample, up to
the mark, and replace the cap.
• Place the cuvette into the holder and close the lid.
Ozone
• Press the Zero key. The display will show “-0.0-” the meter is zeroed and ready for measurement.
• Remove the cuvette.
• Add the content of one packet of HI 93757-0 Ozone
Reagent. Replace the cap and shake gently for 20
seconds.
• Replace the cuvette into the holder and close the lid.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 2 minutes and press Read. When the timer ends the meter will perform the reading.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
• Add the content of one packet of the optional reagent
HI 93703-52-0 Glycine Powder. Replace the cap and
shake gently until completely dissolved.
• Add the content of one packet of HI 93757-0 Ozone
Reagent. Replace the cap and shake gently for 20 seconds.
• Replace the cuvette into the holder and close the lid.
• The instrument displays concentration in mg/L of ozone (chlorine free samples only).
ADDITIONAL MEASUREMENT PROCEDURE
For samples containing chlorine
• Select the
• Fill the cuvette with 10 mL of unreacted sample, up to the
• Place the cuvette into the holder and close the lid.
Ozone
method using the procedure described in the
Method Selection
section (see page 12).
mark, and replace the cap.
10 mL
9899
• Press Timer and the display will show the countdown prior to the measurement or,
alternatively, wait for 2 minutes and press Read. When the timer ends the meter will perform the
reading.
• The instrument displays a concentration value refering to chlorine interference. Subtract this value from
the reading from the Standard Measurement Procedure: this will be the concentration in mg/L of
ozone in the sample.
INTERFERENCES
Interference may be caused by: Bromine, Chlorine Dioxide, Iodine.
Alkalinity above 250 mg/L CaCO3 will not reliably develop the full amount of color or it may rapidly fade.
To resolve this, neutralize the sample with diluted HCl.
In case of water with hardness greater than 500 mg/L CaCO3, shake the sample for approximately
2 minutes after adding the powder reagent.
OzoneOzone
pH
SPECIFICATIONS
Range6.5 to 8.5 pH
Resolution0.1 pH
Accuracy±0.1 pH at 25 °C
Typical EMC±0.1 pH
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the Phenol Red method. The reaction with the reagent causes a yellow
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93710-0Phenol Red Indicator5 drops
REAGENT SETS
HI 93710-01 Reagents for 100 pH tests
HI 93710-03 Reagents for 300 pH tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the pH method using the procedure described in the
Method Selection
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
to red tint in the sample.
section (see page 12).
10 mL
• Remove the cuvette and add 5 drops of HI 93710-0 Phenol
Red Indicator. Replace the cap and mix the solution.
• Reinsert the cuvette into the instrument.
• Press. the Read key to start the reading. The instrument displays the pH value.
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
pH
100101
pH
PHOSPHATE HIGH RANGE
SPECIFICATIONS
Range0.0 to 30.0 mg/L
Resolution0.1 mg/L
Accuracy±1 mg/L ±4% of reading at 25 °C
Typical EMC Dev. ±0.1 mg/L
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
th
edition,
18
causes a blue tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93717A-0Molybdate10 drops
HI 93717B-0Reagent B1 packet
REAGENT SETS
HI 93717-01 Reagents for 100 tests
HI 93717-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill the cuvette with 10 mL of unreacted sample (up to the
• Place the cuvette into the holder and close the lid.
in the
Method Selection
Phosphate HR
method using the procedure described
section (see page 12).
mark) and replace the cap.
Standard Methods for the Examination of Water and Wastewater,
Amino Acid method. The reaction between phosphate and reagents
10 mL
• Add the content of one packet of HI 93717B-0 Phosphate
HR Reagent B to the cuvette. Replace the cap and shake
gently until completely dissolved.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 5 minutes and press Read. When the timer ends the meter will perform the reading. The instrument
displays the results in mg/L of phosphate (PO
3
¯).
4
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of phosphorus (P) and phosphorus pentoxide
(P2O5).
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
• Add 10 drops of HI 93717A-0 Molybdate reagent.
Phosphate HR
102103
• Press s or t to return to the measurement screen.
INTERFERENCES
Sulfide
Chloride above 150000 mg/L )
Calcium above 10000 mg/L as CaCO
Magnesium above 40000 mg/L as CaCO
Ferrous iron above 100 mg/L
3
3
Phosphate HR
PHOSPHATE LOW RANGE
SPECIFICATIONS
Range0.00 to 2.50 mg/L
Resolution0.01 mg/L
Accuracy±0.04 mg/L ±4% of reading at 25 °C
Typical EMC Dev. ±0.01 mg/L
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the Ascorbic Acid method. The reaction between phosphate and the
reagent causes a blue tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93713-0Powder reagent1 packet
REAGENT SETS
HI 93713-01 Reagents for 100 tests
HI 93713-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
described in the
• Rinse, cap and shake the cuvette several times with unreacted
sample. Fill the cuvette with 10 mL of sample up to the
mark and replace the cap.
Phosphate LR
Method Selection
method using the procedure
section (see page 12).
10 mL
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 3 minutes and press Read. When the timer ends the meter will perform the reading. The instrument
displays concentration in mg/L of phosphate (PO
3
¯).
4
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of phosphorus (P) and phosphorus pentoxide
(P2O5).
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette and add the content of one packet of
HI 93713-0 reagent. Replace the cap and shake gently (for
about 2 minutes) until the powder is completely dissolved.
Phosphate LR
104105
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Iron above 50 mg/L
Silica above 50 mg/L
Silicate above 10 mg/L
Copper above 10 mg/L
Hydrogen sulfide, arsenate, turbid sample and highly buffered samples also interfere.
Phosphate LR
PHOSPHORUS
SPECIFICATIONS
Range0.0 to 15.0 mg/L
Resolution0.1 mg/L
Accuracy±0.3 mg/L ±4% of reading at 25 °C
Typical EMC Dev. ±0.2 mg/L
Light SourceTungsten lamp with narrow band interference filter @ 525 nm
MethodAdaptation of the
th
edition,
18
Standard Methods for the Examination of Water and Wastewater,
Amino Acid method. The reaction between phosphate and reagents
causes a blue tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93706A-0Molybdate10 drops
HI 93706B-0Amino Acid Powder1 packet
REAGENT SETS
HI 93706-01 Reagents for 100 tests
HI 93706-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
in the
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark) and replace the cap.
• Place the cuvette into the holder and close the lid.
Phosphorus
Method Selection
method using the procedure described
section (see page 12).
10 mL
• Add the content of one packet of HI 93706B-0 Phosphorus
Reagent B (Amino Acid) to the cuvette. Replace the cap
and shake gently until completely dissolved.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively,
wait for 5 minutes and press Read. When the timer ends the meter will perform the reading. The
instrument displays the results in mg/L of phosphorus (P).
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of phosphate (PO
3
¯) and phosphorus pentoxide
4
(P2O5).
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette.
• Add 10 drops of HI 937O6A-0 Molybdate reagent.
Phosphorus
106107
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Sulfide
Chloride above 150000 mg/L
Calcium above 10000 mg/L as CaCO
Magnesium above 40000 mg/L as CaCO
Ferrous iron above 100 mg/L
3
3
Phosphorus
12
3
6
9
1’
POTASSIUM HIGH RANGE
SPECIFICATIONS
Range20 to 200 mg/L
Resolution5 mg/L
Accuracy±30 mg/L ±7% of reading at 25 °C
Typical EMC±5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the Turbidimetric Tetraphenylborate method. The reaction between
Potassium and reagents causes turbidity in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93750A-0Potassium Reagent6 drops
HI 93750B-0Powder Reagent1 packet
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the CONCENTRATED SAMPLES procedure at page 18.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Remove the cuvette and add the content of one
packet of HI 93750B-0 reagent. Replace the cap and
gently mix for one minute by slowly turning the
cuvette upside down.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 2 minutes and press Read. When the timer ends the meter will perform the reading. The instrument
displays the results in mg/L (ppm) of potassium (K).
• Select the
described in the
Potassium HR
Method Selection
method using the procedure
section (see page 12).
10 mL
• Fill the cuvette with 10 mL of sample, up to the mark.
• Press s or t to access the second level functions.
• Add six drops of HI 93750A-0, replace the cap and swirl
• Press the Chem Frm key to convert the result in mg/L of potassium oxide (K2O).
the solution.
• Place the cuvette into the holder and close the lid.
• Press s or t to return to the measurement screen.
• For ULTRA HIGH RANGE samples: follow the procedure described at page 110.
Potassium HR
108109
Potassium HR
INTERFERENCES
Interferences may be caused by:
Ammonium above 10 ppm
Calcium above 10000 ppm as CaCO
3
Chloride above 12000 ppm
Magnesium above 8000 ppm as CaCO
3
Sodium above 8000 ppm
POTASSIUM ULTRA HIGH RANGE
For samples containing more than 200 ppm of Potassium: follow the sample preparation procedure
described at page 18 for CONCENTRATED SAMPLES. Then add to the graduated cylinder 20 mL of the
prepared sample (for HR) and fill the cylinder with demineralized water from the Demineralizer Bottle up
to the 100 mL mark.
Follow the MEASUREMENT PROCEDURE at page 108.
Read the result in mg/L of Potassium on the display and multiply the reading by 5 to obtain the actual
concentration of Potassium.
POTASSIUM MEDIUM RANGE
SPECIFICATIONS
Range10 to 100 mg/L
Resolution2.5 mg/L
Accuracy±15 mg/L ±7% of reading at 25 °C
Typical EMC±2.5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the Turbidimetric Tetraphenylborate method. The reaction between
Potassium and reagents causes turbidity in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93750A-0Potassium Reagent6 drops
HI 93750B-0Powder Reagent1 packet
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the CONCENTRATED SAMPLES procedure at page 18.
Potassium HR
• Select the
described in the
Potassium MR
Method Selection
method using the procedure
section (see page 12).
• Fill the cuvette with 10 mL of sample, up to the mark.
• Add six drops of HI 93750A-0, replace the cap and swirl
the solution.
• Place the cuvette into the holder and close the lid.
110111
10 mL
Potassium MR
12
3
6
9
1’
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette and add the content of one packet of
HI 93750B-0 reagent. Replace the cap and gently mix for
one minute by slowly turning the cuvette upside down.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the
measurement or, alternatively, wait for 2 minutes and press Read.
When the timer ends the meter will perform the reading. The
instrument displays the results in mg/L (ppm) of potassium (K).
POTASSIUM LOW RANGE
SPECIFICATIONS
Range0.0 to 20.0 mg/L
Resolution0.5 mg/L
Accuracy±3.0 mg/L ±7% of reading at 25 °C
Typical EMC±0.5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the Turbidimetric Tetraphenylborate method. The reaction between
Potassium and reagents causes turbidity in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93750A-0Potassium Reagent6 drops
HI 93750B-0Powder Reagent1 packet
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure at page 17.
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of potassium oxide (K2O).
• Select the
described in the
• Fill the cuvette with 10 mL of sample, up to the mark.
Potassium LR
Method Selection
method using the procedure
section (see page 12).
10 mL
• Add 6 drops of HI 93750A-0 Potassium Reagent,
replace the cap and swirl the solution.
• Press s or t to return to the measurement screen.
INTERFERENCES
Interferences may be caused by:
Ammonium above 10 ppm
Calcium above 10000 ppm as CaCO
Chloride above 12000 ppm
Magnesium above 8000 ppm as CaCO
Sodium above 8000 ppm
Potassium MR
3
3
112113
• Place the cuvette into the holder and close the lid.
Potassium LR
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.
12
3
6
9
1’
12
3
6
9
1’
• Remove the cuvette and add the content of one packet of
HI 93750B-0 reagent. Replace the cap and gently mix for
one minute by slowly turning the cuvette upside down.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the
measurement or, alternatively, wait for 2 minutes and press Read.
When the timer ends the meter will perform the reading. The
instrument displays the results in mg/L (ppm) of potassium (K).
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of potassium oxide (K2O).
SILICA
SPECIFICATIONS
Range0.00 to 2.00 mg/L
Resolution0.01 mg/L
Accuracy±0.03 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 610 nm
MethodAdaptation of the
Heteropoly Blue method. The reaction between silica and reagents causes a blue tint in
the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93705A-0Molybdate6 drops
HI 93705B-0Citric acid1 packet
HI 93705C-0Amino acid1 packet
REAGENT SETS
HI 93705-01 Reagents for 100 tests
HI 93705-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
Method Selection
• Fill the cuvette with 10 mL of unreacted sample (up to the
mark).
Silica
method using the procedure described in the
section (see page 12).
ASTM Manual of Water and Environmental Technology, D859,
10 mL
• Add 6 drops of HI 93705A-0 Molybdate reagent. Replace the
cap and swirl the solution.
• Press s or t to return to the measurement screen.
INTERFERENCES
Interferences may be caused by:
• Wait for 4 minutes, add the content of one packet of HI 93705B-0
Citric acid reagent and shake until it is completely dissolved.
• Place the cuvette into the holder and close the lid.
Silica
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.
• Remove the cuvette and add the content of one packet of
HI 93705C-0 Amino acid reagent and shake until it is
completely dissolved.
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown
prior to the measurement. Alternatively, wait for exactly 3
minutes and press Read. When the timer ends the meter
will perform the reading. The instrument displays
concentration in mg/L of silica (SiO2).
• Press s or t to access the second level functions.
• Press the Chem Frm key to convert the result in mg/L of Silicon (Si).
SILVER
SPECIFICATIONS
Range0.000 to 1.000 mg/L
Resolution0.005 mg/L
Accuracy±0.020 mg/L ±5% of reading at 25 °C
Typical EMC± 0.001 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm.
MethodAdaptation of the PAN method. The reaction between silver and reagents causes an
orange tint in the sample.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93737A-0Buffer Reagent A1 mL
HI 93737B-0Buffer Reagent B1 mL
HI 93737C-0Indicator Reagent C 2 mL
HI 93737D-0Fixing Reagent D2 mL
HI 93703-51Dispersing Agent4-6 drops
REAGENT SETS
HI 93737-01 Reagents for 50 tests
HI 93737-03 Reagents for 150 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
• Fill two graduated beakers with 25 mL of sample.
Silver
method using the procedure described in
the
Method Selection
Note: for best results perform your tests between 20-24°C.
section (see page 12).
# 1# 2
• Press s or t to return to the measurement screen.
INTERFERENCES
Interference may be caused by:
Phosphate above 60 mg/L
Phosphate above 75 mg/L
Sulfide and high concentration of iron
Eliminate color and turbidity interferences by zeroing the meter with the original water sample.
Silica
116117
• Add 1.0 mL of HI 93737A-0 Buffer reagent to one beaker
(the blank) and swirl gently to mix.
# 1
Silver
• Add exactly 1.0 mL of HI 93737B-0 Buffer reagent to the second
beaker (the sample) and swirl gently to mix. Press Timer and the
display will show the countdown prior to adding reagent C or,
alternatively, wait for 2 minutes.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
measurement.
• Then add exactly 1.0 mL of HI 93737C-0 Indicator reagent to
each beaker and swirl. Press Timer or, alternatively, wait for 2
minutes.
• Then, in both cases, add 1.0 mL of HI 93737D-0 Fixing reagent
to each beaker and swirl. Press Timer or, alternatively, wait for
2 minutes.
• Fill one cuvette up to the mark with 10 mL of the blank.
• Add 3 drops of Dispersing Agent (HI 93703-51), replace the cap
and invert gently to mix for about 10 seconds.
• Place the cuvette into the holder and close the lid.
# 1
# 1
# 2
# 2# 1
# 2
10 mL
# 1
• Fill a second cuvette up to the mark with 10 mL of the reacted sample.
• Add 3 drops of Dispersing Agent (HI 93703-51),
replace the cap and invert gently to mix for about 10
seconds.
• Insert the second cuvette into the instrument.
# 2
• Press Read to start the reading. The instrument displays the results in mg/L of silver.
Range0 to 100 mg/L
Resolution5 mg/L
Accuracy±5 mg/L ±3% of reading at 25 °C
Light SourceTungsten lamp with narrow band interference filter @ 466 nm
MethodSulfate is precipitated with barium chloride crystals. Light absorbance of the suspension
is measured.
REQUIRED REAGENTS
CodeDescriptionQuantity
HI 93751-0Indicator reagent1 packet
REAGENT SETS
HI 93751-01 Reagents for 100 tests
HI 93751-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure on page 17.
• Select the
• Fill a cuvette with 10 mL of unreacted sample (up to
• Place the cuvette into the holder and close the lid.
• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for
Sulfate
method using the procedure described
in the
Method Selection
section (see page 12).
the mark) and replace the cap.
measurement.
10 mL
• Add the content of one packet of HI 93751-0
Indicator reagent.
• Replace the cap and invert gently to mix for
1 minute (about 30 inversions).
• Reinsert the cuvette into the instrument.
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 5 minutes and press Read. When the timer ends the meter will perform the reading.
• The instrument displays concentration in mg/L of Sulfate (SO
2
¯).
4
INTERFERENCES
Interferences may be caused by:
Calcium (as CaCO3) above 20000 mg/L
Color or suspended matter in large amounts will interfere: suspended matter should be removed by previous
filtration.
Organic matter in large amounts may impede the precipitation of barium sulfate.
• Remove the cuvette.
Sulfate
120121
Sulfate
ZINC
SPECIFICATIONS
Range0.00 to 3.00 mg/L
Resolution0.01 mg/L
Accuracy±0.03 mg/L ±3% of reading at 25 °C
Typical EMC±0.01 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter @ 575 nm
MethodAdaptation of the
18
th
edition,
orange to a dark violet tint in the sample.
REQUIRED REAGENT
CodeDescriptionQuantity
HI 93731A-0Zinc Reagent1 packet
HI 93731B-0Cyclohexanone0.5 mL
REAGENT SETS
HI 93731-01 Reagents for 100 tests
HI 93731-03 Reagents for 300 tests
For other accessories see page 128.
MEASUREMENT PROCEDURE
• Select the
the
Method Selection
Zinc
method using the procedure described in
section (see page 12).
Standard Methods for the Examination of Water and Wastewater,
Zincon method. The reaction between zinc and the reagents causes an
• Place the cap and insert the cuvette into the instrument
and close the lid.
• Press the Zero key. The display will show “-0.0-” when
the meter is zeroed and ready for measurement.
• Remove the cuvette and add 0.5 mL of HI 93731B-0
Cyclohexanone to the cuvette.
Note: To prevent any contamination from the polycarbonate
cap, prior to replacing it, close the sample cuvette with
the supplied HDPE plastic stopper.
• Replace the cap and mix the sample for 15 seconds.
• Insert the sample into the instrument.
• Fill one graduated mixing cylinder up to the 20 mL mark
with the sample.
• Add the content of one packet of HI 93731A-0 Zinc
reagent, close the cylinder and invert several times to mix
until completely dissolved.
• Fill one cuvette with 10 mL of the reacted sample up to
the mark.
Zinc
122123
20 mL
• Press Timer and the display will show the countdown prior to the measurement or, alternatively, wait
for 3 minutes and 30 seconds and press Read. When the timer ends the meter will perform the
reading.
• The instrument displays the results in mg/L of zinc.
10 mL
Zinc
INTERFERENCES
Interference may be caused by:
Aluminum above 6 mg/L
Cadmium above 0.5 mg/L
Copper above 5 mg/L
Iron above 7 mg/L
Manganese above 5 mg/L
Nickel above 5 mg/L
ERRORS AND WARNINGS
The instrument shows clear warning messages when erroneous conditions appear and when measured values are
outside the expected range. These messages are described below.
No Light: The light source is not functioning properly.
Light Leak: There is an excess amount of ambient light reaching the
detector.
Inverted cuvettes: The sample and the zero cuvettes are inverted.
Battery Low: The battery capacity is lower than 10%.
Light Low: The instrument cannot adjust the light level. Please check
that the sample does not contain any debris.
Light High: There is too much light to perform a measurement. Please
check the preparation of the zero cuvette.
124125
DATA MANAGEMENT
STANDARD METHODS
The analyzed data can be managed using Hanna’s product HI92000, Windows® Compatible Software.
Windows® is registered Trademark of "Microsoft Co."
DescriptionRangeMethod
Aluminum0.00 to 1.00 mg/LAluminon
Alkalinity0 to 500 mg/LColorimetric
Ammonia MR0.00 to 10.00 mg/LNessler
Ammonia LR0.00 to 3.00 mg/LNessler
Bromine0.00 to 8.00 mg/LDPD
Calcium0 to 400 mg/LOxalate
Chlorine, Free0.00 to 2.50 mg/LDPD
Chlorine, Total0.00 to 3.50 mg/LDPD
Chlorine Dioxide0.00 to 2.00 mg/LChlorophenol Red
Chromium VI HR0 to 1000 µg/LDiphenylcarbohydrazide
Chromium VI LR0 to 300 µg/LDiphenylcarbohydrazide
Color of Water0 to 500 PCUColorimetric Platinum Cobalt
Copper HR0.00 to 5.00 mg/LBicinchoninate
Copper LR0 to 1000 µg/LBicinchoninate
Cyanide0.000 to 0.200 mg/LPyridine-Pyrazolone
Cyanuric Acid0 to 80 mg/LTurbidimetric
Fluoride0.00 to 2.00 mg/LSPADNS
Calcium Hardness0.00 to 2.70 mg/LColorimetric
Magnesium Hardness0.00 to 2.00 mg/LColorimetric
Hydrazine0 to 400 µg/Lp-Dimethylaminobenzaldehyde
Iodine0.0 to 12.5 mg/LDPD
Iron HR0.00 to 5.00 mg/LPhenantroline
Iron LR0 to 400 µg/LTPTZ
Magnesium0 to 150 mg/LCalmagite
Manganese HR0.0 to 20.0 mg/LPeriodate Oxidation
Manganese LR0 to 300 µg/LPAN
Molybdenum0.0 to 40.0 mg/LMercaptoacetic Acid
Nickel HR0.00 to 7.00 g/LPhotometric
Nickel LR0.000 to 1.000 mg/LPAN
Nitrate0.0 to 30.0 mg/LCadmium Reduction
Nitrite HR0 to 150 mg/LFerrous Sulfate
Nitrite LR0.00 to 0.35 mg/LDiazotization
Oxygen, Dissolved0.0 to 10.0 mg/LWinkler
Ozone0.00 to 2.00 mg/LDPD
pH6.5 to 8.5 pHPhenol Red
Phosphate HR0.0 to 30.0 mg/LAmino Acid
Phosphate LR0.00 to 2.50 mg/LAscorbic Acid
Phosphorus0.0 to 15.0 mg/LAmino Acid
Potassium HR20 to 200 mg/LTurbidimetric
Potassium MR10 to 100 mg/LTurbidimetric
Potassium LR0.0 to 20.0 mg/LTurbidimetric
Silica0.00 to 2.00 mg/LHeteropoly Blue
Silver0.000 to 1.000 mg/LPAN
Sulfate0 to 100 mg/LTurbidimetric
Zinc0.00 to 3.00 mg/LZincon
126127
ACCESSORIES
REAGENT SETS
HI 93700-01 100 ammonia LR tests
HI 93700-03 300 ammonia LR tests
HI 93701-01 100 free chlorine tests (powder)
HI 93701-03 300 free chlorine tests (powder)
HI 93701-F300 free chlorine tests (liquid)
HI 93701-T300 total chlorine tests (liquid)
HI 93702-01 100 copper HR tests
HI 93702-03 300 copper HR tests
HI 93704-01 100 hydrazine tests
HI 93704-03 300 hydrazine tests
HI 93705-01 100 silica tests
HI 93705-03 300 silica tests
HI 93706-01 100 phosphorus tests
HI 93706-03 300 phosphorus tests
HI 93707-01 100 nitrite LR tests
HI 93707-03 300 nitrite LR tests
HI 93708-01 100 nitrite HR tests
HI 93708-03 300 nitrite HR tests
HI 93709-01 100 manganese HR tests
HI 93709-03 300 manganese HR tests
HI 93710-01 100 pH tests
HI 93710-03 300 pH tests
HI 93711-01 100 total chlorine tests (powder)
HI 93711-03 300 total chlorine tests (powder)
HI 93712-01 100 aluminum tests
HI 93712-03 300 aluminum tests
HI 93713-01 100 phosphate LR tests
HI 93713-03 300 phosphate LR tests
HI 93714-01 100 cyanide tests
HI 93714-03 300 cyanide tests
HI 93715-01 100 ammonia MR tests
HI 93715-03 300 ammonia MR tests
HI 93716-01 100 bromine tests
HI 93716-03 300 bromine tests
HI 93717-01 100 phosphate HR tests
HI 93717-03 300 phosphate HR tests
HI 93718-01 100 iodine tests
HI 93718-03 300 iodine tests
HI 93719-01 100 Mg hardness tests
HI 93719-03 300 Mg hardness tests
HI 93720-01 100 Ca hardness tests
HI 93720-03 300 Ca hardness tests
HI 93721-01 100 iron HR tests
HI 93721-03 300 iron HR tests
HI 93722-01 100 cyanuric acid tests
HI 93722-03 300 cyanuric acid tests
HI 93723-01 100 chromium VI HR tests
HI 93723-03 300 chromium VI HR tests
HI 93726-01 100 nickel HR tests
HI 93726-03 300 nickel HR tests
HI 93728-01 100 nitrate tests
HI 93728-03 300 nitrate tests
HI 93729-01 100 fluoride tests
HI 93729-03 300 fluoride tests
HI 93730-01 100 molybdenum tests
HI 93730-03 300 molybdenum tests
HI 93731-01 100 zinc tests
HI 93731-03 300 zinc tests
HI 93732-01 100 dissolved oxygen tests
HI 93732-03 300 dissolved oxygen tests
HI 93737-01 50 silver tests
HI 93737-03 150 silver tests
HI 93738-01 100 chlorine dioxide tests
HI 93738-03 300 chlorine dioxide tests
HI 93740-01 50 nickel LR tests
HI 93740-03 150 nickel LR tests
HI 93746-01 50 iron LR tests
HI 93746-03 150 iron LR tests
HI 93747-01 100 copper LR tests
HI 93747-03 300 copper LR tests
HI 93748-01 50 manganese LR tests
HI 93748-03 150 manganese LR tests
HI 93749-01 100 chromium VI LR tests
HI 93749-03 300 chromium VI LR tests
HI 93755-01 100 alkalinity tests
HI 93755-03 300 alkalinity tests
HI 93755-53 Chlorine Remover
HI 937521-01 50 calcium tests
HI 937521-03 150 calcium tests
HI 937520-01 50 magnesium tests
HI 937520-03 150 magnesium tests
HI 93757-01 100 ozone tests
HI 93757-03 300 ozone tests
HI 93703-52-2 Glycine Powder, Optional Reagent for 100 tests
HI 93750-01 100 potassium HR tests
HI 93750-03 300 potassium HR tests
HI 93751-01 100 sulfate tests
HI 93751-03 300 sulfate tests
128129
OTHER ACCESSORIES
HI 731318cloth for wiping cuvettes (4 pcs)
HI 731321glass cuvettes (4 pcs)
HI 731325W new cap for cuvette (4 pcs)
HI 740034cap for 100 mL beaker (6 pcs)
HI 740036100 mL plastic beaker (6 pcs)
HI 74003860 mL glass bottle and stopper
HI 7401421 mL graduated syringe
HI 7401431 mL graduated syringe (6 pcs)
HI 740144pipette tip (6 pcs)
HI 740157plastic refilling pipette (20 pcs)
HI 74022025 mL glass cylinders with caps (2 pcs)
HI 740223170 mL plastic beaker
HI 740224170 mL plastic beakers (12 pcs)
HI 74022560 mL graduated syringe
HI 7402265 mL graduated syringe
HI 740227filter assembly
HI 740228filter discs (25 pcs)
HI 740229100 mL graduated cylinder
HI 740230230 mL demineralized water
HI 92000Windows compatible software
HI 920013PC connection cable
HI 93703-50 cuvette cleaning solution (230 mL)
HI 93703-54 dried resin (100 g)
HI 93703-55 activated carbon (50 pcs)
WARRANTY
All Hanna Instruments meters are warranted for two years against defects in workmanship and materials
when used for its intended purpose and maintained according to the instructions.
This warranty is limited to repair or replacement free of charge.
Damages due to accident, misuse, tampering or lack of prescribed maintenance are not covered.
If service is required, contact your dealer. If under warranty, report the model number, date of purchase,
serial number and the nature of the failure. If the repair is not covered by the warranty, you will be notified
of the charges incurred.
If the instrument is to be returned to Hanna Instruments, first obtain a Returned Goods Authorization Number
from the Customer Service Department and then send it with shipment costs prepaid. When shipping any
instrument, make sure it is properly packaged for complete protection.
To validate your warranty, fill out and return the enclosed warranty card within 14 days from the date of
purchase.
Recommendations for Users
Before using these products, make sure that they are entirely suitable for your specific application and for the environment in which they are used.
Operation of these instruments may cause unacceptable interferences to other electronic equipments, this requiring the operator to take all necessary steps to
correct interferences.
Any variation introduced by the user to the supplied equipment may degrade the instruments' EMC performance.
To avoid damages or burns, do not put the instrument in microwave ovens. For yours and the instrument safety do not use or store the instrument in hazardous
environments.
Hanna Instruments reserves the right to modify the design, construction and appearance of its products
without advance notice.
HANNA LITERATURE
Hanna publishes a wide range of catalogs and handbooks for an equally wide range of applications. The
reference literature currently covers areas such as:
• Water Treatment
• Process
• Swimming Pools
• Agriculture
• Food
• Laboratory
and many others. New reference material is constantly being added to the library.
For these and other catalogs, handbooks and leaflets contact your dealer or the Hanna Customer Service
Center nearest to you. To find the Hanna Office in your vicinity, check our home page at www.hannainst.com.
130131
Hanna Instruments Inc.
Highland Industrial Park
584 Park East Drive
Woonsocket, RI 02895 USA