Compliance with the CE Directiveswww.hannainst.com
Dear Customer,
Thank you for choosing a Hanna product. Please read this instruction
manual carefully before using the meter. 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. These instruments are in compliance
with
directives.
TABLE OF CONTENTS
PRELIMINARY EXAMINATION ....... 3
GENERAL DESCRIPTION ............... 3
SPECIFICATIONS ......................... 4
PRINCIPLE OF OPERATION .......... 4
FUNCTIONAL DESCRIPTION .......... 6
GUIDE TO DISPLAY CODES .......... 7
TIPS FOR AN ACCURATE
MEASUREMENT ........................ 10
PARAMETERS REFERENCE TABLE 11
OPERATIONAL GUIDE ................ 12
ABBREVIATIONS ....................... 13
INTRODUCTION ........................ 14
SAMPLE PREPARATION .............. 17
AMMONIA LR ........................... 21
AMMONIA MR .......................... 23
AMMONIA HR ........................... 25
NITRATE LR .............................. 27
NITRATE MR ............................. 29
NITRATE HR ............................. 31
PHOSPHORUS LR ..................... 33
PHOSPHORUS MR .................... 35
PHOSPHORUS HR ..................... 37
POTASSIUM LR ......................... 39
POTASSIUM MR ........................ 41
POTASSIUM HR ........................ 43
POTASSIUM UHR ...................... 45
INTERFACE WITH PC ................. 45
STANDARD METHODS ............... 47
BATTERY REPLACEMENT ............ 47
ACCESSORIES ........................... 48
WARRANTY ............................... 49
CE DECLARATION
OF CONFORMITY....................... 50
HANNA LITERATURE .................. 51
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
•Thermometry
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.
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.
2
51
CE DECLARATION OF CONFORMITY
Recommendations for Users
Before using these products, make sure that they are entirely suitable for the environment in which
they are used.
Operation of these instruments in residential area could cause unacceptable interferences to radio
and TV equipments, 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 perform any measurement in microwave ovens.
PRELIMINARY EXAMINATION
Remove the instrument from the packing material and examine it
carefully to make sure that no damage has occurred during shipment.
If there is any damage, notify your Dealer.
Each HI 83215 Meter is supplied complete with:
• Four Sample Cuvets and Caps
• One Transport Cap
• 2x 9 V Battery
• 12 VDC Transformer (HI 710005 or HI 710006)
Note: Save all packing material until you are sure that the instrument
functions correctly. Any defective item must be returned in its
original packing with the supplied accessories.
GENERAL DESCRIPTION
HI 83000 Series is a line of 17 different bench, microprocessor-based
photometers that measure more than 50 parameters in water and
wastewater. These multipurpose meters are manufactured to measure
the most important parameters of the application they have been
especially designed for:
HI 83099 Laboratories, with CODHI 83200 Laboratories
HI 83203 AquacultureHI 83205 Boilers & Cooling Towers
HI 83206 Environmental TestingHI 83207 Industrial Wastewater
HI 83208 Water ConditioningHI 83209 Education
HI 83210 Pulp & Paper MillsHI 83211 Chemical Manufacturers
HI 83212 Power Plant UtilitiesHI 83213 Municipal Wastewater
HI 83214 Wastewater Treatment Applic. HI 83215 Nutrient Analyses
HI 83216 Pool & Spa Applic.HI 83218 Environmental Applic.
HI 83226 Pool & Spa Applic.
All meters use an exclusive positive-locking system to ensure that the
cuvet is in the same position every time it is placed into the
measurement cell.
The reagents are in liquid or powder form and are supplied in bottles
or in packets. The amount of reagent is precisely dosed to ensure the
maximum repeatability.
Display codes aid the user in routine operations.
The meters have an auto-shut off feature, turning the unit off after 10
minutes of non-use.
The HI 83000 Series can be connected to a personal computer via the
HI 920010 three wire RS 232 cable. The HI 92000 Hanna Windows
Compatible Software aids the user to manage all test data.
®
50
3
SPECIFICATIONS
WARRANTY
Light LifeLife of the instrument
Light DetectorSilicon Photocell
Environment0 to 50°C (32 to 122°F);
max 95% RH non-condensing
Power Supply2x 9 V batteries / 12 to 20 VDC through voltage
adapter
Auto-Shut offAfter 10' of non-use
Dimensions230 x 165 x 70 mm (9.0 x 6.5 x 2.8")
Weight640 g (22.6 oz.)
For specifications related to each single parameter (e.g. range, accuracy, etc.), refer to the related measurement section.
PRINCIPLE OF OPERATION
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 physicochemical characteristics of substance according to the Lambert-Beer
Law:
-log
A
ελc d
I
/I
o
or
ελc d
All Hanna Instruments meters are warranted for two years against
defects in workmanship and materials when used for their intended
purpose and maintained according to instructions.
This warranty is limited to repair or replacement free of charge.
Damages due to accidents, misuse, tampering or lack of prescribed
maintenance are not covered.
If service is required, contact the dealer from whom you purchased the
instrument. 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.
Hanna Instruments reserves the right to modify the design, construction and appearance of its products without advance notice.
Where:
-log
= Absorbance (A)
I/I
o
= intensity of incident light beam
I
o
= intensity of light beam after absorption
I
ελ= molar extinction coefficient at wavelength λ
c = molar concentration of the substance
d = optical path through the substance
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.
4
49
ACCESSORIES
REAGENT SETS
HI 93706-01 100 Phosphorus tests
HI 93706-03 300 Phosphorus tests
HI 93715-01 100 Ammonia tests
HI 93715-03 300 Ammonia tests
HI 93728-01 100 Nitrate tests
HI 93728-03 300 Nitrate tests
HI 93750-01 100 Potassium tests
HI 93750-03 300 Potassium tests
OTHER ACCESSORIES
HI 721310 9V battery (10 pcs)
HI 731318 Tissue for wiping cuvets (4 pcs)
HI 731321 Glass cuvets (4 pcs)
HI 731325N New cap for cuvet (4 pcs)
HI 740034 Cap for 100 mL beaker (6 pcs)
HI 740036 100 mL plastic beaker (6 pcs)
HI 740157 Plastic refilling pipette (20 pcs)
HI 92000Windows
HI 920010 PC connection cable
HI 93703-50 Cuvets cleaning solution (230 mL)
HI 740223 170 mL plastic beaker
HI 740224 170 mL plastic beakers (12 pcs)
HI 740225 60 mL graduated syringe
HI 740226 5 mL graduated syringe
HI 740227 Filter assembly
HI 740228 Filter discs (25 pcs)
HI 740229 100 mL Polypropylene cylinder
HI 740230 230 mL Demineralized water
HI 93703-54 Dried resin (100 g)
HI 93703-55 Activated Carbon (50 pcs)
®
Compatible Software
Given that the absorption of a compound strictly depends on the
wavelength of the incident light beam, a narrow spectral bandwidth
should be selected as well as a proper central wavelength to optimize
measurements.
The optical system of Hanna's HI 83000 multiparameter photometers
is based on special subminiature tungsten lamps and narrow-band
interference filters to guarantee both high performance and reliable
results.
Four measuring channels (at four different wavelengths) allow a wide
range of tests.
HI 83000 Block diagram (optical layout)
A microprocessor controlled special tungsten lamp emits radiation
which is first optically conditioned and beamed to the sample contained in the cuvet. The optical path is fixed by the diameter of the
cuvet. Then the light is spectrally filtered to a narrow spectral bandwidth, to obtain a light beam of intensity
or
I
I
.
o
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.
The measurement process is carried out in two phases: first the meter
is zeroed and then the actual measurement is performed.
The cuvet 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) cuvets are optically identical to provide the same measurement conditions. Whenever possible
use the same cuvet for both.
It is also necessary that the surface of the cuvet is 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
cuvet walls with hands.
Furthermore, in order to maintain the same conditions during the
zeroing and the measuring phases, it is necessary to close the cuvet to
prevent any contamination.
48
5
FUNCTIONAL DESCRIPTION
STANDARD METHODS
FRONT PANEL
1) Cuvet Holder
2) Dual Level Liquid Crystal Display
3) Programs List
4) READ DIRECT, to perform measurement immediately
5) TIMER, to perform measurements after a preprogrammed
countdown
6) ZERO, to zero the meter prior to measurement
7) Program ▼ and ▲, to select the desired parameter
8) ON/OFF, to turn the meter on and off
REAR PANEL
1) Power Socket 12V to 20V DC 2.5 Watt
2) RS 232 Socket
3) Batteries Compartment
DescriptionProgram RangeMethod
Ammonia, LR10.0 to 10.0 mg/LNessler
Ammonia, MR20.0 to 50.0 mg/LNessler
Ammonia, HR30 to 100 mg/LNessler
Nitrate, LR40.0 to 30.0 mg/LCadmium Reduction
Nitrate, MR50 to 150 mg/LCadmium Reduction
Nitrate, HR60 to 300 mg/LCadmium Reduction
Phosphorus, LR70.0 to 10.0 mg/LAminoacid
Phosphorus, MR80.0 to 50.0 mg/LAminoacid
Phosphorus, HR90 to 100 mg/LAminoacid
Potassium, LR100.0 to 20.0 mg/LTurbidimetric
Potassium, MR1110 to 100 mg/LTurbidimetric
Potassium, HR1220 to 200 mg/LTurbidimetric
BATTERY REPLACEMENT
Besides to the 12 VDC supply, this meter can also be fed by two 9V
batteries.
To prolong battery life, switch your meter off after use. However, the
meter has an auto-shut off feature that will turn itself off after 10
minutes of non-use.
A blinking "LOBAT" on the display, while a
measurement is in progress, indicates low
voltage and the batteries should be replaced.
If the batteries are not replaced immediately, in order to prevent erroneous readings
due to low voltage, "-BA-" is displayed soon
afterwards. At this point the batteries must
be changed.
Battery replacement must only take place in a non-hazardous area
using two 9V alkaline batteries.
Remove the battery cover on the back of photometer, attach two fresh
9V batteries, while paying attention to the correct polarity, and
replace the cover.
The meter will turn on automatically when a new battery is connected.
You can turn it off by pressing ON/OFF.
6
47
Note: Windows Terminal® and all the other terminal programs that
support the ANSI escape sequence, represent the DLE character by the
string ‘^P’ and the CR character by the string ‘^M’.
Type of Commands
/OFF - Turn the meter OFF
/PDR - Press Read Direct
/PTR - Press Timer
/PZR - Press Zero
/PUP - Program Up
/PDN - Program Down
/PTM - Turn Test Mode On
/Brx - Set the baud rate
1 - 3002 - 600
3 - 12004 - 2400
/KBL - Lock Keyboard
/KBU - Unlock Keyboard
?PR# - Send Current Program Number (1 to 12)
?BRQ - Send current baud rate
1 - 1502 - 300
3 - 6004 - 1200
5 - 2400
?CNQ - Send Concentration (three bytes)
conc
decimal point
unit
m - ppmb - ppb
t - pptu - pcu
h - pH
?ERR - send error / status information
0 - No error
1 - CAP
2 - HI
3 - ZERO
4 - LO
5 - IDLE
6 - ZERO DONE
7 - TIMED READ
Windows® and Windows Terminal® are registered Trademark of "Microsoft Co."
TELIX® is registered Trademark of "Deltacomm"
GUIDE TO DISPLAY CODES
Note: The secondary LCD below shows a generic "P– –", whereas the
meter will indicate the exact program number (e.g. "P1" for
Ammonia LR).
This indicates that the meter is in a ready
state and zeroing can be performed.
Sampling in progress. This flashing prompt
appears each time the meter is performing a measurement.
The microprocessor is adjusting the light
level, indicated by a scrolling "SIP".
This indicates that the meter is in a zeroed
state and measurement can be performed.
The instrument is performing an internal
check-up.
The blinking "LOBAT" indicates that the
battery voltage is getting low and the batteries need to be replaced.
This indicates that the batteries are dead
and must be replaced.
46
7
ERROR MESSAGESERROR MESSAGES
ERROR MESSAGES
ERROR MESSAGESERROR MESSAGES
a) on zero reading:a) on zero reading:
a) on zero reading:
a) on zero reading:a) on zero reading:
Light over range. The cuvet is not inserted
correctly and an eccess ambient light is
reaching the detector. If the cuvet is properly
inserted, then contact your dealer or the
nearest Hanna Customer Service Center.
The lamp is not working properly. Contact
your dealer or the nearest Hanna Customer
Service Center.
The lamp is not working properly. Contact
your dealer or the nearest Hanna Customer
Service Center.
This indicates that the meter has lost its
configuration. Contact your dealer or the
nearest Hanna Customer Service Center.
This indicates that the zeroing procedure
failed due to a low signal-to-noise ratio. In
this case press ZERO again.
The instrument cannot adjust the light
level. Please check that the sample does
not contain any debris.
There is not enough light to perform a
measurement. Please check the preparation of the zero cuvet.
POTASSIUM ULTRA HIGH RANGE
For samples containing more than 200 ppm of Potassium: first follow
the sample preparation procedure described at page 19 for NUTRIENTS
SOLUTION (HR). 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 43.
Read the result in mg/L of Potassium on the display and multiply the
reading by 5 to obtain the real concentration of Potassium in your
sample.
INTERFACE WITH PC
To connect your meter to the PC use the optional HI 920010 (avail-
able from your Hanna Dealer). Make sure that your meter is switched
off and plug the connectors, one into the meter RS 232C socket, the
other into the serial port of your PC.
Note: Cables other than HI 920010 may use a different configura-
tion, in which case, communication between the meter and the PC
may not be possible.
SETTING THE BAUD RATE
The transmission speed (baud rate) of the meter and the external
device must be identical. The meter is factory set to 2400.
If you wish to change this value, please contact your nearest Hanna
Center.
SENDING COMMANDS FROM PC
With terminal programs such as, for example, Telix®, Windows Terminal®, it is possible to remotely control your Hanna Instruments bench
meter. Use HI 920010 cable to connect the meter to the PC, start the
terminal program and set the communication options as follows: 8, N,
1, no flow control.
Command Types
To send a command to the pH meter the scheme is:
There is too much light to perform a measurement. Please check the preparation of
the zero cuvet.
8
<DLE> <command> <CR>
This line makes the computer send a Data Link Escape character (/ or
?), the command expressed as a number or a 3-character sequence
and a CR character.
45
• Press ZERO and “SIP” will appear on the display.
b) on sample reading:b) on sample reading:
b) on sample reading:
b) on sample reading:b) on sample reading:
There is too much light for the sample
measurement. Please check if the right
sample cuvet is inserted.
• Wait for a few seconds and the display will
show “-0.0-”. Now the meter is zeroed
and ready for measurement.
• Remove the cuvet and add
the content of one packet
of HI 93750B reagent. Replace the cap and mix
gently for one minute by
turning slowly the cuvet upside down.
• Reinsert the cuvet 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
DIRECT. In both cases “SIP” will blink during measurement.
The sample and zero cuvet are inverted.
A zero reading was not taken. Follow the
instruction described in the measurement
procedures for zeroing the meter.
Under range. A blinking "0.00" indicates
that the sample absorbs less light than the
zero reference. Check the procedure and
make sure that you use the same cuvet for
reference (zero) and measurement.
1) A flashing value of the maximum concentration indicates an over range condition. The concentration of the sample is
beyond the programmed range: dilute the
sample and rerun the test.
2) A flashing value lower than the maximum concentration indicates a low signalto-noise ratio condition. In this case accuracy of the result is not guaranteed. Repeat
the reading procedure.
• The instrument directly displays concentration in mg/L (ppm) of
potassium (K).
• To convert the reading to mg/L of potassium oxide (K2O), multiply
by a factor of 1.20.
• For ULTRA HIGH RANGE samples: follow procedure described at
page 45.
INTERFERENCES
The following ions do not interfere below the concentrations reported:
Ammonium 10 ppmCalcium 10000 ppm as CaCO
Chloride 12000 ppmMagnesium 8000 ppm as CaCO
Sodium 8000 ppm
Potassium HR
44
3
3
9
TIPS FOR AN ACCURATE MEASUREMENT
The instructions listed below should be carefully followed during testing
to ensure best accuracy.
• Color or suspended matter in large amounts may cause interference,
therefore, these should be removed by treatment with active carbon
and by prior filtration.
• For a correct filling of the cuvet: the liquid
in the cuvet forms a convexity on the top;
the bottom of this convexity must be at
the same level of the 10 mL mark.
• Proper use of the dropper: to get good reproducible results, tap the dropper on the
table for several times and wipe the outside
of the dropper tip with a cloth. Always keep
the dropper bottle in a vertical position while
dosing the reagent.
• 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.
10m
L
POTASSIUM HIGH RANGE
SPECIFICATIONS
Range20 to 200 mg/L
Resolution5 mg/L
Accuracy±30 mg/L ±7% of reading
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
AA
HI 93750
A-0Potassium Reagent6 drops
AA
BB
HI 93750
B-0Powder Reagent1 packet
BB
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (HR)
procedure at page 19.
• Select the program number corresponding to Potassium HR on the
secondary LCD by pressing PROGRAM t and s.
(a
)
(b
)
(c
)
• It is important that the sample does not contain any debris. This
would corrupt the readings.
• Do not let the reacted sample stand too long after reagent is
added, or accuracy will be lost.
• In order to avoid reagent leaking and to obtain more
accurate measurements, it is recommended to close
the cuvet firstwith the supplied HDPE
plastic stopperand then with the black cap.
• Each time the cuvet is used, the cap must be tightened
to the same degree.
10
• Fill the cuvet with 10 mL of sample, up to the
mark.
• Add six drops of HI 93750A,
replace the cap and swirl the
x
6
solution.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
43
10m
Potassium HR
L
• Press ZERO and “SIP” will appear on the display.
• Wait for a few seconds and the display will
show “-0.0-”. Now the meter is zeroed
and ready for measurement.
• Remove the cuvet and add
the content of one packet
of HI 93750B reagent. Replace the cap and mix
gently for one minute by
turning slowly the cuvet upside down.
• Whenever the cuvet is placed into
the measurement cell, it must be
dry outside, and completely free of
fingerprints, oil or dirt. Wipe it
thoroughly with HI 731318 or a
lint-free cloth prior to insertion.
• 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 cuvet for zeroing and
measurement.
• It is important to discard the sample immediately after the reading
is taken because the glass might become permanently stained.
• All the reaction times reported in this manual are referred to 20°C
(68°F). As a general rule of thumb, they should be doubled at
10°C (50°F) and halved at 30°C (86°F).
• Reinsert the cuvet 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
DIRECT. In both cases “SIP” will blink during measurement.
• The instrument directly displays concentration in mg/L (ppm) of
potassium (K).
• To convert the reading to mg/L of potassium oxide (K2O), multiply
by a factor of 1.20.
INTERFERENCES
The following ions do not interfere below the concentrations reported:
Ammonium 10 ppm
Calcium 10000 ppm as CaCO
Chloride 12000 ppm
Magnesium 8000 ppm as CaCO
Sodium 8000 ppm
Plug the 12VDC adapter (HI 710005 - 110VDC, or HI 710006 -
220VDC) into the DC socket. Plug the adapter into the outlet.
Alternatively, remove the battery cover on the back of the meter;
attach 2 fresh 9V batteries and replace the cover.
Note:Insure the main line is surge protected.
Note: Always turn the meter off before unplugging it to insure no data
is lost.
MEASUREMENT PROCEDURE
• Turn the meter on by pressing ON/OFF.
• The meter will first perform an LCD self
diagnostic test by displaying a full set of
figures.
• Then it will show a scrolling
"215 Hanna Inst" message.
SPECIFICATIONS
Range10 to 100 mg/L
Resolution2.5 mg/L
Accuracy±15 mg/L ±7% of reading
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
AA
HI 93750
A-0Potassium Reagent6 drops
AA
BB
HI 93750
B-0Powder Reagent1 packet
BB
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (MR)
procedure at page 18.
• Select the program number corresponding to Potassium MR on the
secondary LCD by pressing PROGRAM t and s
• When the LCD displays “----”, the meter
is ready. On the secondary LCD "P1" will
appear to inform that the first parameter
measurement procedure (Ammonia LR)
can be performed.
• Press the PROGRAM t and PROGRAM s keys to select the
desired parameter.
12
• Fill the cuvet with 10 mL of sample, up to the
mark.
• Add six drops of HI 93750A,
replace the cap and swirl the
solution.
x
6
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
41
10m
Potassium MR
L
• Press ZERO and “SIP” will appear on the display.
Note: in the following measurement
sections, a generic "P– –" will be placed
on the secondary LCD instead of the exact
related message (e.g. "P1" for Ammonia
LR).
• Wait for a few seconds and the display will
show “-0.0-”. Now the meter is zeroed and
ready for measurement.
• Remove the cuvet and add
the content of one packet
of HI 93750B reagent. Replace the cap and mix
gently for one minute by
turning slowly the cuvet upside down.
• Reinsert the cuvet 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
DIRECT. In both cases “SIP” will blink during measurement.
• Before performing a test read carefully all the instructions related
to the selected parameter.
For the program number, see the table on page 12 or look at the list
printed on the mask of the meter.
ABBREVIATIONS
°C°C
°C:degree Celsius
°C°C
°F°F
°F:degree Fahrenheit
°F°F
HRHR
HR:High Range
HRHR
kg/hakg/ha
kg/ha: kilograms per hectare
kg/hakg/ha
LCDLCD
LCD:Liquid Crystal Display
LCDLCD
LRLR
LR:Low Range
LRLR
L/haL/ha
L/ha:liters per hectare
L/haL/ha
mm/hamm/ha
mm/ha: millimeters per hectare
mm/hamm/ha
mg/Lmg/L
mg/L: milligrams per liter (ppm)
mg/Lmg/L
mLmL
mL:milliliter
mLmL
MRMR
MR:Medium Range
MRMR
UHRUHR
UHR:Ultra High Range
UHRUHR
• The instrument directly displays concentration in mg/L (ppm) of
potassium (K).
• To convert the reading to mg/L of potassium oxide (K2O), multiply
by a factor of 1.20.
INTERFERENCES
The following ions do not interfere below the concentrations reported:
Ammonium 10 ppm
Calcium 10000 ppm as CaCO
Chloride 12000 ppm
Magnesium 8000 ppm as CaCO
Sodium 8000 ppm
Potassium LR
3
3
40
13
INTRODUCTION
POTASSIUM LOW RANGE
THE ROLE OF NUTRIENTS IN THE GROWTH AND
PRODUCTION OF PLANTS
The three elements that are mostly needed by the plants are nitrogen
(N), phosphorus (P) and potassium (K). They are called the macronutrients while other elements, needed by plants in smaller amounts, are
called microelements. In hydroponics, plants need a balanced nutritive
solution, composed of macro and microelements.
Shortage or excess of even only one nutritive element may cause an
imbalance in plant physiology and in the absorption of the other
nutrients. Nutrients shortages may result in irregular plant growth, low
resistance to diseases, scarce production both in quantity and quality,
while nutrients excess may cause waste of fertilizer, pollution of the
groundwater and the possible accumulation of dangerous substances
in the crops produced.
NITROGEN
Nitrogen (N) is mostly absorbed by plants as nitrates (NO
smaller amount, in the form of ammonium (NH
adequate ratio between the two forms is generally used in nutritive
ACTION• is fundamental for plants in phase of growth
• promotes the lengthening of trunks and sprouts
• increases the production of foliage
• helps to absorb other nutrients
(in particular phosphorus)
• assists a bigger production for both size and
number of fruits
SHORTAGE• slower growth
EFFECTS• smaller leaves
• yellowing of leaves
• smaller fruits
• premature ripening
EXCESS EFFECTS• reduction in resistance to diseases and atmo-
spheric agents
• increase of water demand (caused by an excessive
production of leaves)
• bad quality of fruits
• delayed ripening
• reduction in potassium absorption
-
) and, in
3
SPECIFICATIONS
Range0.0 to 20.0 mg/L
Resolution0.5 mg/L
Accuracy±3.0 mg/L ±7% of reading
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
AA
HI 93750
A-0Potassium Reagent6 drops
AA
BB
HI 93750
B-0Powder Reagent1 packet
BB
REAGENT SETS
HI 93750-01 Reagents for 100 tests
HI 93750-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the IRRIGATION WATER (LR)
procedure at page 17.
• Select the program number corresponding to Potassium LR on the
secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of sample, up to the
mark.
• Add six drops of HI 93750A,
replace the cap and swirl the
x
6
solution.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
10m
L
14
39
Potassium LR
• Wait for a few seconds and the
display will show "-0.0-". Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 10 drops of HI 93706A
x10
Molybdate reagent.
• Add the content of one packet of
HI 93706B-0 Phosphorus Reagent
B (Amino Acid) to the cuvet.
Replace the cap and shake gently
until dissolution is complete.
• Reinsert the cuvet 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
DIRECT. In both cases "SIP" will blink during measurement.
• The instrument directly displays concentration in mg/L of phosphorus
on the Liquid Crystal Display.
• To convert the reading to mg/L of phosphate (PO
3–
), multiply by
4
a factor of 3.07.
INTERFERENCES
Calcium above 10000 mg/L as CaCO
Chloride above 150000 mg/L as Cl
Ferrous iron above 100 mg/L
Magnesium above 40000 mg/L as CaCO
Sulfide
3
–
3
PHOSPHORUS
Phosphorus (P) has an important role in many fundamental biochemical and physiological processes. Plants take up phosphorus in the form
of phosphate ion (PO
PRESENT INDNA and RNA, ATP, ADP
ACTION• stimulates the roots growth
SHORTAGE• delayed ripening
EFFECTS• slower growth
EXCESS EFFECTS• premature ripening
3-
).
4
• stimulates blooming
• stimulates fecundation and ripeness
• strengthens the plant tissues
• is necessary in the formation of seeds
• small leaves
• decrease of production (smaller fruits and difficult
seeds formation)
• reduction of root system
• excess of fruit-setting
• negative effects on the absorption of some micro elements such as iron, zinc, boron and copper
POTASSIUM
Potassium (K) is essential in proteic synthesis. The problem of lack of
potassium is quite frequent in calcareous soils.
Potassium is absorbed as K+.
PRESENT INtissues responsible for the growth of plants (primary
and secondary meristems), embryos and cell vacuole
ACTION• improves the quality of fruits and flowers
• gives more resistance both to frost and to
diseases caused by fungi (increases the cuticular
thickness)
• regulates the cellular turgidity (helps to regulate the
osmotic processes and increases the resistance to
dryness)
• regulates the stomatic opening and closing (it means
a strong influence on transpiration and photo synthesis)
SHORTAGE• slower growth
EFFECTS• smaller fruits, less colored and less preserved
• increase of transpiration
• less resistance to the cold
Phosphorus HR
38
15
EXCESS EFFECTS• reduced absorption of calcium and magnesium
• increase of water consumption
• increase of the substrate salinity
IRRIGATION WATER (LOW RANGE)
In agricultural areas it is quite common to find altered values in the
chemical composition of irrigation waters. The problem concerns mostly
the high nitrate concentration, usually determined by excessive fertilization or irrational liquid manure spreading. The analysis of irrigation
waters allows us to find out which are the substances present in major
or minor quantity and to organize an advantageous fertilization plan.
For example, if the quantity of water utilized for crop cultivation is 250
mm/ha (= 2500000 L/ha) and the nitrate (NO
-
) concentration is
3
150 mg/L (34 mg/L as nitrate-nitrogen NO3-N), soil receives 85 kg/
ha of nitrogen. In choosing type and quantity of fertilizer to be used, it
is important to consider this information, in order not to waste fertilizer
nor to induce soil pollution.
NUTRIENTS SOLUTIONS (MEDIUM AND HIGH RANGE)
The nutrients requirements of the plants are determined by the type of
plant, its age and the environmental conditions. The control of chemical composition of nutrients solutions given to the plants is an operation
that allows a correct preparation of the fertilizer. In analyzing the
solution, it is possible to choose between medium range and high
range values, depending on the concentration of substances.
Medium range usually covers the analysis of residual solutions in
recycling systems. The nutritive elements are differently absorbed by
the plants, hence the nutrient solution loses substances, becomes
impoverished and must be enriched.
High range normally corresponds to the typical values of nutrients
solutions. It is therefore possible to verify that the solution given to the
plants contains the correct quantities of nutritive substances.
PHOSPHORUS HIGH RANGE
SPECIFICATIONS
Range0 to 100 mg/L
Resolution1 mg/L
Accuracy±5 mg/L ±4% of reading
Typical EMC Dev. ±1 mg/L
Light SourceTungsten lamp with narrow band interference
filter @ 525 nm
MethodAdaptation of the Standard Methods for the
Examination of Water and Wastewater, 18
edition, Amino Acid method. The reaction be-
tween phosphorus 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 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (HR)
procedure at page 19.
• Select the program number corresponding to Phosphorus HR on
the secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of unreacted
sample (up to the mark) and replace
the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP” will blink on
the display.
10m
L
th
16
37
Phosphorus HR
• Wait for a few seconds and the
display will show "-0.0-". Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 10 drops of HI 93706A
x10
Molybdate reagent.
• Add the content of one packet of
HI 93706B-0 Phosphorus Reagent
B (Amino Acid) to the cuvet.
Replace the cap and shake gently
until dissolution is complete.
• Reinsert the cuvet 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
DIRECT. In both cases "SIP" will blink during measurement.
SAMPLE PREPARATION
LIST OF MATERIAL
Each instrument HI 83215 is supplied with the following accessories
for sample preparation:
• 4 cuvettes (10 mL);
• 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).
SAMPLE PREPARATION PROCEDURE
Note: If the water sample to be analyzed is very turbid, let it stand in
a beaker for a while until most of the solid particles have
settled. Then, use the pipette to transfer the supernatant solution to the other beaker and prepare the samples as described
below. During this operation, take care not to induce air bubbles
into the solution, in order not to displace the settled solids at
the bottom of the beaker.
• The instrument directly displays concentration in mg/L of phosphorus
on the Liquid Crystal Display.
• To convert the reading to mg/L of phosphate (PO
3–
), multiply by
4
a factor of 3.07.
INTERFERENCES
Calcium above 10000 mg/L as CaCO
Chloride above 150000 mg/L as Cl
Ferrous iron above 100 mg/L
Magnesium above 40000 mg/L as CaCO
Sulfide
Phosphorus MR
3
–
3
36
IRRIGATION WATER (LR):
• Measure with the graduated cylinder about 100 mL of
sample.
• If the solution contains some turbidity
or color, pour it in the
large 170mL beaker
and add a powder
packet of active carbon.
17
• Mix well using the spoon
and then wait for 5
minutes.
filte
r
dis
c
• Unscrew the filter assembly,
put a filter disc inside and
close it again.
• Connect the filter assembly
to the 60 mL syringe by
the screw rim.
• Take off 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
100mL beaker by pushing
gently the syringe plunger.
The sample is now ready.
Note: Filter at least 40 mL of solution if all the four parameters
have to be tested. 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.
NUTRIENTS SOLUTION (MR):
PHOSPHORUS MEDIUM RANGE
SPECIFICATIONS
Range0.0 to 50.0 mg/L
Resolution0.5 mg/L
Accuracy±2.5 mg/L ±4% of reading
Typical EMC Dev. ±0.5 mg/L
Light SourceTungsten lamp with narrow band interference
filter @ 525 nm
MethodAdaptation of the Standard Methods for the
Examination of Water and Wastewater, 18
edition, Amino Acid method. The reaction be-
tween phosphorus 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 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (MR)
procedure at page 18.
• Select the program number corresponding to Phosphorus MR on
the secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of unreacted
sample (up to the mark) and replace
the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP” will blink on
the display.
10m
L
th
• Use the graduated cylinder to measure exactly 20 mL
of sample.
18
35
Phosphorus MR
• Wait for a few seconds and the
display will show "-0.0-". Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 10 drops of HI 93706A
x10
Molybdate reagent.
• Add the content of one packet of
HI 93706B-0 Phosphorus Reagent
B (Amino Acid) to the cuvet.
Replace the cap and shake gently
until dissolution is complete.
• Reinsert the cuvet 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
DIRECT. In both cases "SIP" will blink during measurement.
• Remove the cap and fill the
Demineralizer Bottle with tap
water.
• Replace the cap and shake
gently for
at least 2 minutes.
• Open the upper part of the
Demineralizer Bottle cap and squirt
gently 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 the resin
has to be replaced.
• Pour the solution in the large 170mL
beaker, replace the cap and invert
several times to mix.
• The instrument directly displays concentration in mg/L of phosphorus
on the Liquid Crystal Display.
• To convert the reading to mg/L of phosphate (PO
3–
), multiply by
4
a factor of 3.07.
INTERFERENCES
Calcium above 10000 mg/L as CaCO
Chloride above 150000 mg/L as Cl
Ferrous iron above 100 mg/L
Magnesium above 40000 mg/L as CaCO
Sulfide
Phosphorus LR
3
–
3
34
• If the solution contains some turbidity
or color, add a powder packet of
active carbon and follow the
procedure described for Irrigation
Water.
NUTRIENTS SOLUTION (HR):
• Use the 5 mL syringe twice to add to
the graduated cylinder exactly 10
mL of sample.
Note: To measure exactly 5 mL of
19
5mLx2
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.
obablelevelofli
pr
taken
upbysyringe
i
d
qu
• Remove the cap and fill the
Demineralizer Bottle with tap
water.
• Replace the cap and shake gently
at least 2 minutes.
for
• Open the upper part of the
Demineralizer Bottle cap and squirt
gently the demineralized water into
the cylinder, up to the 100 mL
mark.
• Pour the solution in the large
170mL beaker, replace the cap
and invert several times to mix.
PHOSPHORUS LOW RANGE
SPECIFICATIONS
Range0.0 to 10.0 mg/L
Resolution0.1 mg/L
Accuracy±0.5 mg/L ±4% of reading
Typical EMC Dev. ±0.1 mg/L
Light SourceTungsten lamp with narrow band interference
filter @ 525 nm
MethodAdaptation of the Standard Methods for the
Examination of Water and Wastewater, 18
edition, Amino Acid method. The reaction be-
tween phosphorus 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 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the IRRIGATION WATER (LR)
procedure at page 17.
• Select the program number corresponding to Phosphorus LR on
the secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of unreacted
10m
sample (up to the mark) and replace
the cap.
L
th
• If the solution contains some turbidity or color, add a powder
packet of active carbon and follow the procedure described for
Irrigation Water.
20
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP” will blink on
the display.
33
Phosphorus LR
• Remove the cuvet and add the content of one
packet of HI 93728 reagent.
AMMONIA LOW RANGE
• Replace the cap and immediately shake
vigorously for
exactly 10 seconds by moving the cuvet up and down.
Continue to mix by inverting the cuvet gently and
slowly for 50 seconds, while
taking care not to induce
air bubbles. A deposit remains, but this does not
affect the measurement. Time and way
of shaking could sensitively affect the
measurement.
• Reinsert the cuvet 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 DIRECT. In both cases "SIP" will blink during measurement.
• The instrument directly displays concentration in mg/L of nitratenitrogen on the Liquid Crystal Display.
• To convert the reading to mg/L of nitrate (NO
–
), multiply by a
3
factor of 4.43.
INTERFERENCES
Interference may be caused by:
Ammonia and amines, as urea and primary aliphatic amines
Chloride above 100 ppm (negative interference)
Chlorine above 2 ppm (positive interference)
Copper
Iron(III) (positive interference)
Strong oxidizing and reducing substances
Sulfide (it must be absent)
SPECIFICATIONS
Range0.0 to 10.0 mg/L
Resolution0.1 mg/L
Accuracy±0.1 mg/L ±4% of reading
Typical EMC±0.1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference filter
@ 420 nm
MethodAdaptation of the ASTM Manual of Water and
Environmental Technology, D1426-92, 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 in seawater)
HI 93715B-0Second Reagent4 drops (10 drops in seawater)
REAGENT SETS
HI 93715-01 Reagents for 100 tests
HI 93715-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the IRRIGATION WATER (LR)
procedure at page 17.
• Select the program number corresponding to Ammonia LR on the
secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of unreacted sample, up
to the mark, and replace the cap.
• Place the cuvet into the holder and ensure
that the notch on the cap is positioned
securely into the groove.
• Press ZERO and “SIP” will blink on the display.
10m
L
Nitrate HR
32
21
Ammonia LR
• Wait for a few seconds and the
display will show “-0.0-”. Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 4 drops of the First reagent
(6 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Add 4 drops of the Second reagent
(10 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Reinsert the cuvet into the
instrument.
NITRATE HIGH RANGE
SPECIFICATIONS
Range0 to 300 mg/L
Resolution5 mg/L
Accuracy±10 mg/L ±8% of reading
x
4
x
4
Typical EMC±5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference fil-
ter @ 525 nm
MethodAdaptation of the cadmium reduction method. The
reaction between nitrate-nitrogen 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 48.
• 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 DIRECT. In both cases “SIP” will blink during
measurement.
• The instrument directly displays concentration in mg/L of ammonia
nitrogen (NH3-N) on the display.
• To convert the reading to mg/L of ammonia (NH3), multiply by a
factor of 1.21.
• To convert the reading to mg/L of ammonium (NH
+
), multiply by
4
a factor of 1.29.
INTERFERENCES
acetone, alcohols, aldehydes, glycine, hardness above 1 g/L, iron,
organic chloramines, sulfide, various aliphatic and aromatic amines.
Ammonia LR
22
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION
(HR) procedure at page 19.
• Select the program number corresponding to Nitrate HR on
the secondary LCD by pressing PROGRAM t and s.
• Using the pipette, add to the cuvet 6 mL of sample, up to
half of its height, and replace the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP”
will blink on the display.
• Wait for a few seconds and the display
will show “-0.0-”. Now the meter is
zeroed and ready for measurement.
31
Nitrate HR
• Remove the cuvet and add the content of one
packet of HI 93728 reagent.
• Replace the cap and immediately shake
vigorously for
exactly 10 seconds by moving the cuvet up and down.
Continue to mix by inverting the cuvet gently and
slowly for 50 seconds, while
taking care not to induce
air bubbles. A deposit remains, but this does not
affect the measurement. Time and way
of shaking could sensitively affect the
measurement.
• Reinsert the cuvet 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 DIRECT. In both cases "SIP" will blink during measurement.
• The instrument directly displays concentration in mg/L of nitratenitrogen on the Liquid Crystal Display.
• To convert the reading to mg/L of nitrate (NO
–
), multiply by a
3
factor of 4.43.
INTERFERENCES
Interference may be caused by:
Ammonia and amines, as urea and primary aliphatic amines
Chloride above 100 ppm (negative interference)
Chlorine above 2 ppm (positive interference)
Copper
Iron(III) (positive interference)
Strong oxidizing and reducing substances
Sulfide (it must be absent)
AMMONIA MEDIUM RANGE
SPECIFICATIONS
Range0.0 to 50.0 mg/L
Resolution0.5 mg/L
Accuracy±0.5 mg/L ±4% of reading
Typical EMC±0.5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference fil-
ter @ 420 nm
MethodAdaptation of the ASTM Manual of Water and
Environmental Technology, D1426-92, 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 in seawater)
HI 93715B-0Second Reagent4 drops (10 drops in seawater)
REAGENT SETS
HI 93715-01 Reagents for 100 tests
HI 93715-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (MR)
procedure at page 18.
• Select the program number corresponding to Ammonia MR on the
secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of unreacted sample, up
to the mark, and replace the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP” will blink on the display.
10m
L
Nitrate MR
30
23
Ammonia MR
• Wait for a few seconds and the
display will show “-0.0-”. Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 4 drops of the First reagent
(6 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Add 4 drops of the Second reagent
(10 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Reinsert the cuvet into the
instrument.
NITRATE MEDIUM RANGE
SPECIFICATIONS
Range0 to 150 mg/L
Resolution2.5 mg/L
Accuracy±5 mg/L ±8% of reading
x
4
x
4
Typical EMC±2.5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference fil-
ter @ 525 nm
MethodAdaptation of the cadmium reduction method. The
reaction between nitrate-nitrogen 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 48.
• 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 DIRECT. In both cases “SIP” will blink during
measurement.
• The instrument directly displays concentration in mg/L of ammonia
nitrogen (NH3-N) on the display.
• To convert the reading to mg/L of ammonia (NH3), multiply by a
factor of 1.21.
• To convert the reading to mg/L of ammonium (NH
+
), multiply by
4
a factor of 1.29.
INTERFERENCES
acetone, alcohols, aldehydes, glycine, hardness above 1 g/L, iron,
organic chloramines, sulfide, various aliphatic and aromatic amines.
Ammonia MR
24
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION
(MR) procedure at page 18.
• Select the program number corresponding to Nitrate MR on
the secondary LCD by pressing PROGRAM t and s.
• Using the pipette, add to the cuvet 6 mL of sample, up to
half of its height, and replace the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP”
will blink on the
display.
• Wait for a few seconds and the display
will show “-0.0-”. Now the meter is
zeroed and ready for measurement.
29
Nitrate MR
• Remove the cuvet and add the content of one
packet of HI 93728 reagent.
AMMONIA HIGH RANGE
• Replace the cap and immediately shake
vigorously for
exactly 10 seconds by moving the cuvet up and down.
Continue to mix by inverting the cuvet gently and
slowly for 50 seconds, while
taking care not to induce
air bubbles. A deposit remains, but this does not
affect the measurement. Time and way
of shaking could sensitively affect the
measurement.
• Reinsert the cuvet 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 DIRECT. In both cases "SIP" will blink during measurement.
• The instrument directly displays concentration in mg/L of nitratenitrogen on the Liquid Crystal Display.
• To convert the reading to mg/L of nitrate (NO
–
), multiply by a
3
factor of 4.43.
INTERFERENCES
Interference may be caused by:
Ammonia and amines, as urea and primary aliphatic amines
Chloride above 100 ppm (negative interference)
Chlorine above 2 ppm (positive interference)
Copper
Iron(III) (positive interference)
Strong oxidizing and reducing substances
Sulfide (it must be absent)
SPECIFICATIONS
Range0 to 100 mg/L
Resolution1 mg/L
Accuracy±1 mg/L ±4% of reading
Typical EMC±1 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference fil-
ter @ 420 nm
MethodAdaptation of the ASTM Manual of Water and
Environmental Technology, D1426-92, 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 in seawater)
HI 93715B-0Second Reagent4 drops (10 drops in seawater)
REAGENT SETS
HI 93715-01 Reagents for 100 tests
HI 93715-03 Reagents for 300 tests
For other accessories see page 48.
MEASUREMENT PROCEDURE
Note: for sample preparation follow the NUTRIENTS SOLUTION (HR)
procedure at page 19.
• Select the program number corresponding to Ammonia HR on the
secondary LCD by pressing PROGRAM t and s.
• Fill the cuvet with 10 mL of sample, up to the
mark, and replace the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and “SIP” will blink on the display.
10m
L
Nitrate LR
28
25
Ammonia HR
• Wait for a few seconds and the
display will show “-0.0-”. Now
the meter is zeroed and ready for
measurement.
• Remove the cuvet.
• Add 4 drops of the First reagent
(6 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Add 4 drops of the Second reagent
(10 drops in case of seawater
analysis). Replace the cap and
mix the solution by inverting the
cuvet a couple of times.
• Reinsert the cuvet into the
instrument.
NITRATE LOW RANGE
SPECIFICATIONS
Range0.0 to 30.0 mg/L
Resolution0.5 mg/L
Accuracy±1.0 mg/L ±8% of reading
x
4
x
4
Typical EMC±0.5 mg/L
Deviation
Light SourceTungsten lamp with narrow band interference fil-
ter @ 525 nm
MethodAdaptation of the cadmium reduction method. The
reaction between nitrate-nitrogen 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 48.
• 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 DIRECT. In both cases “SIP” will blink during
measurement.
• The instrument directly displays concentration in mg/L of ammonia
nitrogen (NH3-N) on the display.
• To convert the reading to mg/L of ammonia (NH3), multiply by a
factor of 1.21.
• To convert the reading to mg/L of ammonium (NH
+
), multiply by
4
a factor of 1.29.
INTERFERENCES
acetone, alcohols, aldehydes, glycine, hardness above 1 g/L, iron,
organic chloramines, sulfide, various aliphatic and aromatic amines.
Ammonia HR
26
MEASUREMENT PROCEDURE
Note: for sample preparation follow the IRRIGATION WATER (LR)
procedure at page 17.
• Select the program number corresponding to Nitrate LR on
the secondary LCD by pressing PROGRAM t and s.
• Using the pipette, fill the cuvet with 6mL of sample, up to
half of its height, and replace the cap.
• Place the cuvet into the holder and
ensure that the notch on the cap is
positioned securely into the groove.
• Press ZERO and
“SIP” will blink on
the display.
• Wait for a few seconds and the display will
show “-0.0-”. Now the meter is zeroed
and ready for measurement.
27
Nitrate LR
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