HANNA HI 83200 Multiparameter Bench Photometer Instruction Manual

Below you will find brief information for Multiparameter Bench Photometer HI 83200. The HI 83200 is a multiparameter bench photometer dedicated for laboratory analysis. It measures 44 different methods using specific liquid or powder reagents. The 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.

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Instruction Manual

HI 83200

Multiparameter Bench

Photometer for Laboratories

w w w . h a n n a i n s t . c o m

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 [email protected].

PRELIMINARY EXAMINATION ............................................. 3

GENERAL DESCRIPTION ..................................................... 3

ABBREVIATIONS ............................................................... 4

SPECIFICATIONS .............................................................. 4

PRECISION AND ACCURACY ............................................... 4

PRINCIPLE OF OPERATION ................................................ 5

FUNCTIONAL DESCRIPTION ............................................... 6

TIPS FOR AN ACCURATE MEASUREMENT ........................... 8

HEALTH & SAFETY .......................................................... 11

METHOD REFERENCE TABLE ............................................. 11

OPERATIONAL GUIDE ....................................................... 12

SETUP ........................................................................... 14

HELP MODE ................................................................... 16

SAMPLE PREPARATION .................................................... 17

ALUMINUM .................................................................... 21

ALKALINITY .................................................................... 23

AMMONIA MR ................................................................ 25

AMMONIA LR ................................................................. 27

BROMINE ...................................................................... 29

CALCIUM ....................................................................... 31

FREE CHLORINE ............................................................. 33

TOTAL CHLORINE ............................................................ 36

CHLORINE DIOXIDE ......................................................... 39

CHROMIUM VI HR .......................................................... 42

CHROMIUM VI LR ........................................................... 44

COLOR OF WATER ........................................................... 46

COPPER HR .................................................................... 48

COPPER LR .................................................................... 50

CYANURIC ACID .............................................................. 52

FLUORIDE ...................................................................... 54

CALCIUM HARDNESS ....................................................... 56

MAGNESIUM HARDNESS ................................................. 59

HYDRAZINE .................................................................... 62

IODINE .......................................................................... 64

IRON HR ........................................................................ 66

IRON LR ......................................................................... 68

MAGNESIUM .................................................................. 71

MANGANESE HR ............................................................. 73

MANGANESE LR ............................................................. 75

MOLYBDENUM ............................................................... 78

NICKEL HR ..................................................................... 81

NICKEL LR ...................................................................... 83

NITRATE ......................................................................... 86

NITRITE HR .................................................................... 88

NITRITE LR ..................................................................... 90

DISSOLVED OXYGEN ........................................................ 92

OZONE .......................................................................... 94 pH ................................................................................ 97

PHOSPHATE HR .............................................................. 99

PHOSPHATE LR ............................................................. 101

PHOSPHORUS ............................................................. 103

POTASSIUM HR ............................................................ 105

POTASSIUM MR ............................................................ 108

POTASSIUM LR ............................................................. 110

SILICA ......................................................................... 112

SILVER ........................................................................ 114

SULFATE ...................................................................... 117

ZINC ............................................................................ 119

ERRORS AND WARNINGS ............................................... 121

DATA MANAGEMENT ...................................................... 122

STANDARD METHODS .................................................... 123

ACCESSORIES .............................................................. 124

WARRANTY .................................................................. 127

HANNA LITERATURE ...................................................... 127

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.

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 funnel

• 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 44 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.

ABBREVIATIONS

EPA: US Environmental Protection Agency

°C: degree Celsius

°F: degree Fahrenheit

µ g/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 Life Life of the instrument

Light Detector Silicon Photocell

Environment 0 to 50°C (32 to 122°F);

Power Supply max 90% RH non-condensing external 12 Vdc power adapter built-in rechargeable battery

Dimensions

Weight

235 x 200 x 110 mm (9.2 x 7.87 x 4.33")

0.9 Kg

For specifications related to each method (e.g. range, resolution, etc.) refer to the related measurement section.

PRECISION AND ACCURACY

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.

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 physical-chemical characteristics of substance according to the Lambert-Beer Law:

-log I / I o

λ c d or

A =

λ c d

Where:

-log I / I o

I o

= Absorbance (A)

= intensity of incident light beam

I = intensity of light beam after absorption

= molar extinction coefficient at wavelength c = molar concentration of the substance

λ 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.

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.

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 I o

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.

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.

FUNCTIONAL DESCRIPTION

INSTRUMENT DESCRIPTION

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

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.

ESC

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.

RCL

HELP

SETUP

Press to recall the log.

Press to display the help screen.

Press to access the setup screen.

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.

Probable level of liquid taken up by syringe

(a) (b) (c)

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)

• 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;

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:

(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 gently

9 shake 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).

Method

METHOD REFERENCE TABLE

Method Method description

Aluminum

Alkalinity

Ammonia MR

Ammonia LR

Bromine

Calcium

Free Chlorine

Total Chlorine

Chlorine Dioxide

Chromium VI HR

Chromium VI LR

Color of Water

Copper HR

Copper LR

Page

Cyanuric Acid

Fluoride

Calcium Hardness 56

Magnesium Hardness 59

Hydrazine

Iodine

Iron HR

Iron LR

Method description

Magnesium

Manganese HR

Manganese LR

Molybdenum

Nickel HR

Nickel LR

Nitrate

Nitrite HR

Nitrite LR

Dissolved Oxygen

Ozone pH

Phosphate HR

Phosphate LR

Phosphorus

Potassium HR

Potassium MR

Potassium LR

Silica

Silver

Sulfate

Zinc

Page

101

112

114

117

119

103

105

108

110

OPERATIONAL GUIDE

POWER CONNECTION AND BATTERY MANAGEMENT

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)

- 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 st keys to highlight the desired method. Press Select.

• 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: You can store only a valid measurement. Press LOG and the last valid measurement will be stored with date and time stamps.

Viewing and deleting: You can view and delete the data log by pressing the RCL key. You can only delete the last saved measurement. Additionally, you can delete the data records all at once.

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.

SETUP

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 t keys 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 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 t keys 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 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.

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 s t 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.

HI 83200 offers an interactive contextual help mode that assists the user at any time.

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.

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.

• Mix well using the spoon and then wait for 5 minutes.

• Fold a filter disc twice as shown in the figure. Separate one side from the other three to form a cone. Insert the folded filter disc in the funnel.

• Filter the treated sample into an empty beaker.

The sample is now ready.

• 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.

• 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 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 170 mL beaker, replace the cap and invert several times to mix.

• 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

Range

Resolution

Accuracy

Typical EMC

Deviation

Light Source

Method

0.00 to 1.00 mg/L

0.01 mg/L

±0.02 mg/L ±4% of reading at 25 °C

±0.01 mg/L

Tungsten lamp with narrow band interference filter @ 525 nm

Adaptation of the aluminon method. The reaction between aluminum and reagents causes a reddish tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93712 A-0 Ascorbic acid

HI 93712 B-0 Aluminon reagent

HI 93712 C-0 Bleaching powder

Quantity

1 packet

REAGENT SETS

HI 93712-01 Reagents for 100 tests

HI 93712-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Aluminum method using the procedure described in the Method Selection 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).

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 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.

# 1

# 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.

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in mg/L of Al

• 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

ALKALINITY

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0 to 500 mg/L (as CaCO

5 mg/L

±5 mg/L ±10 % of reading at 25 °C

±5 mg/L

)

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Colorimetric Method . The reaction causes a distinctive range of colors from yellow to green to greenish blue to develop.

REQUIRED REAGENTS

Code Description

HI 93755-0 Alkalinity Indicator Reagent

REAGENT SETS

HI 93755-01 Reagents for 100 tests

HI 93755-03 Reagents for 300 tests

For other accessories see page 124.

Quantity/test

1 mL

MEASUREMENT PROCEDURE

• Select the Alkalinity method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

23 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.

• The instrument displays the results in mg/L of alkalinity (CaCO

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

AMMONIA MEDIUM RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 10.00 mg/L

0.01 mg/L

±0.05 mg/L ±5% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the

Nessler method. The reaction between ammonia and reagents causes a yellow tint in the sample.

ASTM Manual of Water and Environmental Technology, D1426-92,

REQUIRED REAGENTS

Code Description

HI 93715 A-0 First Reagent

Quantity

4 drops (6 drops for seawater)

HI 93715 B-0 Second 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 124.

MEASUREMENT PROCEDURE

• Select the Ammonia MR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

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 ammonia nitrogen (NH

-N).

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in mg/L of ammonia (NH

) and ammonium (NH

+ ).

• 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

AMMONIA LOW RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 3.00 mg/L

0.01 mg/L

±0.04 mg/L ±4% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the

Nessler method. The reaction between ammonia and reagents causes a yellow tint in the sample.

ASTM Manual of Water and Environmental Technology, D1426-92,

REQUIRED REAGENTS

Code Description

HI 93700 A-0 First Reagent

Quantity

4 drops (6 drops for seawater)

HI 93700 B-0 Second 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 124.

MEASUREMENT PROCEDURE

• Select the Ammonia LR method using the procedure described in the

Method Selection section (see page 12).

10 mL

• 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.

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.

The instrument displays the results in mg/L of ammonia nitrogen

(NH

-N).

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in mg/L of ammonia (NH

) and ammonium (NH

+ ).

• 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

BROMINE

SPECIFICATIONS

Range 0.00 to 8.00 mg/L

Resolution

Accuracy

0.01 mg/L

±0.08 mg/L ±3% of reading at 25 °C

Typical EMC

Deviation

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the

Standard Methods for the Examination of Water and Wastewater, th edition, DPD method. The reaction between bromine and the reagent causes a pink tint in the sample.

REQUIRED REAGENTS

Code

HI 93716-0

Description

DPD Reagent

REAGENT SETS

HI 93716-01 Reagents for 100 tests

HI 93716-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Bromine method using the procedure described in the

Method Selection section (see page 12).

10 mL

• 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.

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.

• 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 CaCO

2 minutes after adding the reagent.

, shake the sample for approximately

In case of water with alkalinity greater than 250 mg/L CaCO

or acidity greater than 150 mg/L CaCO

, 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

CALCIUM

SPECIFICATIONS

Range

Resolution

0 to 400 mg/L

10 mg/L

Accuracy ±10 mg/L ±5% of reading at 25 °C

Light Source Tungsten lamp with narrow band interference filter @ 466 nm

Method Adaptation of the Oxalate method.

REQUIRED REAGENTS

Code

HI 93752

Description

Buffer Reagent

A-0 Ca Calcium Buffer Reagent

Quantity

4 drops

7 mL

HI 93752 B-0 Ca Calcium Oxalate Reagent 1 mL

REAGENT SETS

HI 937521-01

HI 937521-03

Reagents for 50 tests

Reagents for 150 tests

For other accessories see page 124.

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).

• 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.

INTERFERENCES:

Interferences may be caused by:

Acidity (as CaCO

) above 1000 mg/L

Alkalinity (as CaCO

) above 1000 mg/L

Magnesium (Mg 2+ ) above 400 mg/L

Calcium

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 2.50 mg/L

0.01 mg/L

±0.03 mg/L ±3% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the EPA DPD method 330.5. The reaction between free chlorine and the

DPD reagent causes a pink tint in the sample.

REQUIRED REAGENTS

POWDER :

Code

HI 93701-0

Description

DPD

Quantity

1 packet

LIQUID:

Code Description Quantity

HI 93701 A-F DPD1 Indicator 3 drops

HI 93701 B-F DPD1 Buffer 3 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 124.

MEASUREMENT PROCEDURE

• Select the Free Chlorine method using the procedure described in the Method Selection section (see page 12).

• Fill the cuvette with 10 mL of unreacted sample (up to the mark) and replace the cap.

10 mL

• Place the cuvette into the holder and close the lid.

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 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.

Free Chlorine

• Reinsert the cuvette into the instrument.

• Press Read to start the reading. The instrument displays the results in mg/L of free chlorine.

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 CaCO

, shake the sample for approximately

2 minutes after adding the powder reagent.

In case of water with alkalinity greater than 250 mg/L CaCO

or acidity greater than 150 mg/L CaCO

, the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the sample with diluted HCl or NaOH.

Free Chlorine

TOTAL CHLORINE

SPECIFICATIONS

Range 0.00 to 3.50 mg/L

Resolution

Accuracy

0.01 mg/L

±0.03 mg/L ±3% of reading at 25 °C

Typical EMC

Deviation

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the EPA DPD method 330.5. The reaction between the chlorine and the

DPD reagent causes a pink tint in the sample.

REQUIRED REAGENTS

POWDER:

Code

HI 93711-0

Description

DPD

LIQUID:

Code Description

HI 93701 A-T DPD1 indicator

HI 93701 B-T DPD1 buffer

HI 93701 C DPD3 solution

Quantity

1 packet

Quantity

3 drops

1 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 124.

MEASUREMENT PROCEDURE

• Select the Total Chlorine method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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 36

• 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.

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.

37 Total Chlorine

• 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 CaCO

2 minutes after adding the powder reagent.

, shake the sample for approximately

In case of water with alkalinity greater than 250 mg/L CaCO

or acidity greater than 150 mg/L CaCO

, the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the sample with diluted HCl or NaOH.

Total Chlorine 38

CHLORINE DIOXIDE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

0.00 to 2.00 mg/L

0.01 mg/L

±0.10 mg/L ±5% of reading at 25 °C

±0.01 mg/L

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the Chlorophenol Red method. The reaction between chlorine dioxide and reagents causes a colorless to purple tint in the sample.

REQUIRED REAGENT

Code Description

HI 93738 A-0 Reagent A

Quantity

1 mL

HI 93738 B-0 Dechlorinating Reagent B 1 packet

HI 93738 C-0 Reagent C 1 mL

HI 93738 D-0 Reagent D 1 mL

REAGENT SETS

HI 93738-01 Reagents for 100 tests

HI 93738-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Chlorine Dioxide method using the procedure described in the Method Selection section (see page 12).

# 1 # 2

• Fill two graduated mixing cylinders (#1 & #2) up to the

25 mL mark with the sample.

25 mL 25 mL

• 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

# 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

• 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 # 2

• 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.

# 1

10 mL

Chlorine Dioxide 40

• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.

• Fill another cuvette with 10 mL of the reacted sample (#2) up to the mark and replace the cap.

# 2

• Insert the sample into the instrument.

10 mL

# 2

• 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.

Chlorine Dioxide

CHROMIUM VI HIGH RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0 to 1000 µ g/L

µ g/L

±5

µ g/L ±4% of reading at 25 °C

±1

µ g/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation 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

Code

HI 93723-0

Description

Powder reagent

Quantity

1 packet

REAGENT SETS

HI 93723-01 Reagents for 100 tests

HI 93723-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Chromium VI HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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 the content of one packet of

HI 93723-0 reagent. Replace the cap and shake vigorously for about 10 seconds.

Chromium VI HR 42

• 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 µµµµµ g/L of chromium VI.

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in µ g/L of Chromate (CrO

2 ¯) and Dichromate (Cr

2 ¯).

• 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.

43 Chromium VI HR

CHROMIUM VI LOW RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

0 to 300 µ g/L

1 µ g/L

±1 µ g/L ±4% of reading at 25 °C

±1 µ g/L

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation 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

Code Description

HI 93749-0 Powder reagent

Quantity

1 packet

REAGENT SETS

HI 93749-01 Reagents for 100 tests

HI 93749-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Chromium VI LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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 the content of one packet of

HI 93749-0 reagent. Replace the cap and shake vigorously for about 10 seconds.

Chromium VI LR 44

• Reinsert the cuvette into the instrument.

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in µ g/L of Chromate (CrO

2 ¯) and Dichromate (Cr

2 ¯).

• 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.

45 Chromium VI LR

COLOR OF WATER

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0 to 500 PCU (Platinum Cobalt Units)

1 PCU

±10 PCU ±5% of reading at 25 °C

± 1 PCU

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Colorimetric Platinum Cobalt method.

REQUIRED ACCESSORIES

0.45 µ m membrane for true color measurement.

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Color of Water method using the procedure described in the Method Selection section (see page 12).

10 mL

• Fill one cuvette up to the mark with deionized water and replace the cap. This is the blank.

# 1

• Place the blank (# 1) into the holder and close the lid.

# 1

• 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 46

• 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 µ m 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.

# 2

• Press Read to start the reading.

• The meter displays the value of apparent color in PCU.

10 mL

# 2

# 3

• 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.

# 3

• Press Read to start the reading. The meter displays the value of true color in PCU.

47 Color of Water

COPPER HIGH RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 5.00 mg/L

0.01 mg/L

±0.02 mg/L ±4% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the EPA method. The reaction between copper and the bicinchoninate reagent causes a purple tint in the sample.

REQUIRED REAGENTS

Code

HI 93702-0

Description Quantity

Bicinchoninate 1 packet

REAGENT SETS

HI 93702-01 Reagents for 100 tests

HI 93702-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Copper HR method using the procedure described in the

Method Selection section (see page 12).

• Fill the cuvette with 10 mL of unreacted sample (up to the mark) and replace the cap.

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 48

• Remove the cuvette.

• 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.

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.

49 Copper HR

COPPER LOW RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

0 to 1000 µ g/L

1 µ g/L

±10 µ g/L ±5% of reading at 25 °C

±1 µ g/L

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the EPA method. The reaction between copper and the bicinchoninate reagent causes a purple tint in the sample.

REQUIRED REAGENTS

Code

HI 95747-0

Description Quantity

Bicinchoninate 1 packet

REAGENT SETS

HI 95747-01 Reagents for 100 tests

HI 95747-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Copper LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

Copper LR 50

• Remove the cuvette.

• Add the content of one packet of HI 95747-0 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 µµµµµ g/L of copper.

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.

51 Copper LR

CYANURIC ACID

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0 to 80 mg/L

1 mg/L

±1 mg/L ±15% of reading at 25 °C

±1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the turbidimetric method. The reaction between cyanuric acid and the reagent causes a white suspension in the sample.

REQUIRED REAGENTS

Code

HI 93722-0

Description

Powder reagent

REAGENT SETS

HI 93722-01 Reagents for 100 tests

HI 93722-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Cyanuric Acid method using the procedure described in the Method Selection section (see page 12).

• Fill the cuvette with 10 mL of unreacted sample (up to the mark) and replace the cap.

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.

Cyanuric Acid 52

• 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.

Cyanuric Acid

FLUORIDE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 2.00 mg/L

0.01 mg/L

±0.03 mg/L ±3% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, SPADNS method. The reaction between fluoride and the liquid reagent causes a red tint in the sample.

REQUIRED REAGENT

Code

HI 93729-0

Description

SPADNS Reagent

REAGENT SETS

HI 93729-01 Reagents for 100 tests

HI 93729-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

4 mL

MEASUREMENT PROCEDURE

• Select the Fluoride method using the procedure described in the Method Selection section (see page 12).

• Add 2 mL of HI 93729-0 SPADNS Reagent to two cuvettes.

• 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.

# 1

10 mL

# 1

2 mL

10 mL

# 2

Fluoride 54

• 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.

• Insert the other cuvette (# 2) with the reacted sample into the instrument.

# 2

• 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 CaCO

) 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.

55 Fluoride

CALCIUM HARDNESS

SPECIFICATIONS

Range 0.00 to 2.70 mg/L

Resolution

Accuracy

Typical EMC

Deviation

0.01 mg/L

±0.11 mg/L ±5% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Calmagite method. The reaction between calcium and reagents causes a reddish-violet tint in the sample.

REQUIRED REAGENTS

Code Description Quantity

HI 93720 A-0 Ca & Mg indicator 0.5 mL

HI 93720 B-0 Alkali solution 0.5 mL

HI 93720 C-0 EGTA solution 1 drop

REAGENT SETS

HI 93720-01 Reagents for 100 tests

HI 93720-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Calcium Hardness method using the procedure described in the Method Selection section (see page 12).

• Rinse a graduated beaker several times with unreacted sample, before filling it to the 50 mL mark with the sample.

• Add 0.5 mL of HI 93720A-0 Calcium indicator solution and swirl to mix.

• Add 0.5 mL of HI 93720B-0 Alkali solution and swirl to mix. Use this solution to rinse 2 cuvettes before filling them up to the 10 mL mark.

# 1 # 2

Hardness Ca 56

• 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

• Place the blank (# 1) into the holder and close the lid.

# 1

• 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 CaCO

• 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).

57 Hardness Ca

• 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.

Hardness Ca 58

MAGNESIUM HARDNESS

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 2.00 mg/L

0.01 mg/L

±0.11 mg/L ±5% of reading at 25 °C

±0.02 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, EDTA colorimetric method. The reaction between magnesium and reagents causes a reddish-violet tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93719 A-0 Mg indicator

HI 93719 B-0 Alkali solution

HI 93719 C-0 EDTA solution

HI 93719 D-0 EGTA solution

Quantity

0.5 mL

1 drop

REAGENT SETS

HI 93719-01 Reagents for 100 tests

HI 93719-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Magnesium Hardness method using the procedure described in the Method Selection section (see page 12).

• Rinse a graduated beaker several times with unreacted sample, before filling it to the 50 mL mark with the sample.

• 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.

59 Hardness Mg

• 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.

• Place the blank (# 1) into the holder and close the lid.

# 2

# 1

• Press the Zero key. The meter will show “-0.0-” when the meter is zeroed and ready for measurement.

# 2

• 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 CaCO

Hardness Mg 60

• 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 58 (Ca Hardness).

INTERFERENCES

Interference may be caused by excessive amounts of heavy metals.

61 Hardness Mg

HYDRAZINE

SPECIFICATIONS

Range

Resolution

0 to 400 µ g/L

µ g/L

Accuracy

Typical EMC

Deviation

±4% of full scale reading at 25 °C

±2 µ g/L

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the ASTM Manual of Water and Environmental Technology, method

D1385-88, p-Dimethylaminobenzaldehyde method. The reaction between hydrazine and the liquid reagent causes a yellow tint in the sample.

REQUIRED REAGENT

Code

HI 93704-0

Description Quantity

Liquid Reagent 24 drops

REAGENT SETS

HI 93704-01 Reagents for 100 tests

HI 93704-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Hydrazine method using the procedure described in the Method Selection section (see page 12).

10 mL

• Fill one cuvette up to the mark with 10 mL of distilled water.

# 1

• Place the cap, insert the cuvette # 1 into the holder and 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.

Hydrazine 62

10 mL

# 2

• 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

• 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.

• Insert the cuvette with the reacted sample (# 2) into the instrument and close the lid.

# 2

• Press Read to start the reading. The instrument displays concentration in µµµµµ g/L of hydrazine.

INTERFERENCES

Interference may be caused by:

Highly colored samples

Highly turbid samples

Aromatic amines

Hydrazine

IODINE

SPECIFICATIONS

Range

Resolution

Accuracy

0.0 to 12.5 mg/L

0.1 mg/L

±0.1 mg/L ±5% of reading at 25 °C

Typical EMC

Deviation

±0.1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, DPD method. The reaction between iodine and the reagent causes a pink tint in the sample.

REQUIRED REAGENTS

Code

HI 93718-0

Description

DPD Reagent

REAGENT SETS

HI 93718-01 Reagents for 100 tests

HI 93718-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Iodine method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• 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.

• 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 CaCO

, shake the sample for approximately

2 minutes after adding the reagent.

In case of water with alkalinity greater than 250 mg/L CaCO

or acidity greater than 150 mg/L CaCO

, the color of the sample may develop only partially, or may rapidly fade. To resolve this, neutralize the sample with diluted HCl or NaOH.

65 Iodine

IRON HIGH RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 5.00 mg/L

0.01 mg/L

±0.04 mg/L ±2% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the EPA Phenantroline method 315B, for natural and treated waters.

The reaction between iron and reagents causes an orange tint in the sample.

REQUIRED REAGENTS

Code

HI 93721-0

Description Quantity

Powder Reagent 1 packet

REAGENT SETS

HI 93721-01 Reagents for 100 tests

HI 93721-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Iron HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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-” the meter is zeroed and ready for measurement.

• Remove the cuvette and add the content of one packet of

HI 93721-0 reagent. Replace the cap and shake until dissolution is complete.

Iron HR 66

• 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.

INTERFERENCES

Interference may be caused by:

Molybdate Molybdenum above 50 ppm

Calcium above 10000 ppm (as CaCO

)

Magnesium above 100000 ppm (as CaCO

)

Chloride above 185000 ppm.

Iron HR

IRON LOW RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

0 to 400 µ g/L

1 µ g/L

±10 µ g/L ±8% of reading at 25 °C

±1 µ g/L

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the TPTZ Method. The reaction between iron and the reagent causes a violet tint in the sample.

REQUIRED REAGENTS

Code

HI 93746-0

Description Quantity

TPTZ Reagent 2 packets

REAGENT SETS

HI 93746-01 Reagents for 50 tests

HI 93746-03 Reagents for 150 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Iron LR method using the procedure described in the Method Selection section (see page 12).

25 mL

• Fill one graduated mixing cylinder up to the 25 mL mark with deionized water.

• 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 replace the cap.

• Place the cuvette into the holder and close the lid.

10 mL

Iron LR 68

• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.

• Remove the cuvette.

• Fill another graduated mixing cylinder up to the 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.

25 mL

• Fill a cuvette with 10 mL of the reacted sample up to the mark and replace the cap.

• Insert the sample into the instrument.

10 mL

• 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 µµµµµ g/L of iron.

69 Iron LR

INTERFERENCES

Interference may be caused by:

Cadmium above 4.0 mg/L

Chromium 3+ above 0.25 mg/L

Chromium 6+ above 1.2 mg/L

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.

Iron LR

MAGNESIUM

SPECIFICATIONS

Range

Resolution

0 to 150 mg/L

5 mg/L

Accuracy ±5 mg/L ±3% of reading at 25 °C

Light Source Tungsten lamp with narrow band interference filter @ 466 nm

Method Adaptation of the Calmagite method .

REQUIRED REAGENTS

Code Description Quantity

HI 93752 A-0 Mg Magnesium Buffer Reagent 1 mL

HI 93752 B-0 Mg Magnesium Indicator Reagent 9 mL

REAGENT SETS

HI 937520-01

HI 937520-03

Reagents for 50 tests

Reagents for 150 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure on page 17.

• Select the Magnesium method using the procedure described in the

Method Selection section (see page 12).

• Using one 1 mL syringe add exactly 1.00 mL of HI 93752A-0

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.

• 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.

71 Magnesium

• 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!

0.5 mL of sample

• Replace the cap and invert several times to mix.

• 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 2+ ).

INTERFERENCES

Interferences may be caused by:

Acidity (as CaCO

) above 1000 mg/L

Alkalinity (as CaCO

) above 1000 mg/L

Calcium (Ca 2+ ) above 200 mg/L

Iron must be absent

Aluminum must be absent

Copper must be absent

Magnesium

MANGANESE HIGH RANGE

SPECIFICATIONS

Range

Resolution

0.0 to 20.0 mg/L

0.1 mg/L

Accuracy

Typical EMC

Deviation

±0.2 mg/L ±3% of reading at 25 °C

±0.1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Periodate method. The reaction between manganese and reagents causes a pink tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93709 A-0 Citrate

Quantity

1 packet

HI 93709 B-0 Sodium periodate 1 packet

REAGENT SETS

HI 93709-01 Reagents for 100 tests

HI 93709-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Manganese HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• 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

• 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 (KMnO

4 permanganate (MnO

) and

• 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

Range

Resolution

Accuracy

Typical EMC

0 to 300 µ g/L

1 µ g/L

±10 µ g/L ±3% of reading at 25 °C

±1 µ g/L

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the PAN Method. The reaction between manganese and the reagents causes an orange tint in the sample.

REQUIRED REAGENT

Code Description

HI 93748 A-0 Ascorbic acid

HI 93748 B-0 Alkaline-cyanide sol.

HI 93748 C-0 0.1% PAN indicator

HI 93703-51 Dispersing Agent

Quantity

2 packets

0.40 mL

2 mL

4-6 drops

REAGENT SETS

HI 93748-01 Reagents for 50 tests

HI 93748-03 Reagents for 150 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Manganese LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• Fill one cuvette with 10 mL of deionized water (up to the mark).

• Fill a second cuvette with 10 mL of sample (up to the mark).

10 mL

• Add the content of one packet of HI 93748A-0 Ascorbic acid to each cuvette, replace the caps and shake gently until completely dissolved.

75 Manganese LR

• 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.

• 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 76

• Insert the second cuvette with the reacted sample into the instrument.

• Press Read to start the reading. The instrument displays the results in µµµµµ g/L of manganese.

• Press s or t to access the second level functions.

• Press the Chem Frm key to convert the result in µ g/L of potassium permanganate (KMnO

4 permanganate (MnO

) and

• 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.

77 Manganese LR

MOLYBDENUM

SPECIFICATIONS

Range

Resolution

Accuracy

0.0 to 40.0 mg/L

0.1 mg/L

±0.3 mg/L ±5% of reading at 25 °C

±0.1 mg/L Typical EMC

Deviation

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the mercaptoacetic acid method. The reaction between molybdenum and the reagents causes a yellow tint in the sample.

REQUIRED REAGENT

Code Description

HI 93730 A-0 Reagent A

HI 93730 B-0 Reagent B

HI 93730 C-0 Reagent C

REAGENT SETS

HI 93730-01 Reagents for 100 tests

HI 93730-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Molybdenum method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

Molybdenum 78

• 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.

• 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.

25 mL

10 mL

Molybdenum

• 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 (MoO

(Na

MoO

) and sodium molybdate

• 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

Nitrite, as NO

Sulfate above 200 mg/L

Highly buffered samples or with extreme pH may exceed the buffering capacity of the reagents.

Molybdenum 80

NICKEL HIGH RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 7.00 g/L

0.01 g/L

±0.07 ±4% of reading at 25 °C

±0.02 g/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the photometric method. The reaction between nickel and the reagent causes a blue tint in the sample.

REQUIRED REAGENTS

Code

HI 93726-0

Description Quantity

Powder reagent 1 packet

REAGENT SETS

HI 93726-01 Reagents for 100 tests

HI 93726-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Nickel HR method using the procedure described in the Method Selection section (see page 12).

• Fill the cuvette up to the mark with 10 mL of unreacted sample and replace the cap.

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.

81 Nickel HR

• 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.

INTERFERENCES

Interference may be caused by copper.

Nickel HR

NICKEL LOW RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

Light Source

Method

0.000 to 1.000 mg/L

0.001 mg/L

±0.010 mg/L ±7% of reading at 25 °C

±0.001 mg/L

Tungsten lamp with narrow band interference filter @ 575 nm

Adaptation of the PAN method. The reaction between nickel and the reagents causes an orange tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93740 A-0 Phthalate-phosphate

HI 93740 B-0 0.3% PAN indicator

HI 93740 C-0 EDTA

HI 93703-51 Dispersing Agent

REAGENT SETS

HI 93740-01 Reagents for 50 tests

HI 93740-03 Reagents for 150 tests

For other accessories see page 124.

Quantity

2 packets

2 mL

2 packets

4-6 drops (only when necessary, see note)

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.

• 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 (Fe 3+ ), 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.

83 Nickel LR

• 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.

• Fill a second cuvette up to the mark with 10 mL of the reacted sample.

10 mL

• 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.

Nickel LR 84

INTERFERENCES

Interference may be caused by:

Co 2+ must not be present

Fe 2+ must not be present

Al 3+ above 32 mg/L

Ca 2+ above 1000 mg/L (as CaCO

)

Cd 2+ above 20 mg/L

Cl¯ above 8000 mg/L

Cr 3+ above 20 mg/L

Cr 6+ above 40 mg/L

Cu 2+ above 15 mg/L

F¯ above 20 mg/L

Fe 3+ above 10 mg/L

K + above 500 mg/L

Mg 2+ above 400 mg/L

Mn 2+ above 25 mg/L

Mo 6+ above 60 mg/L

Na + above 5000 mg/L

Pb 2+ above 20 mg/L

Zn 2+ above 30 mg/L

Nickel LR

NITRATE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.0 to 30.0 mg/L

0.1 mg/L

±0.5 mg/L ±10% of reading at 25 °C

±0.1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the cadmium reduction method. The reaction between nitrate and the reagent causes an amber tint in the sample.

REQUIRED REAGENTS

Code

HI 93728-0

Description Quantity

Powder reagent 1 packet

REAGENT SETS

HI 93728-01 Reagents for 100 tests

HI 93728-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Nitrate method using the procedure described in the Method Selection section (see page 12).

• Using the pipette, fill the cuvette with 6 ml of sample, up to half of its height, and replace the cap.

6 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.

• Remove the cuvette and add the content of one packet of

HI 93728-0 reagent.

Nitrate 86

• 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 (NO

¯).

• 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

87 Nitrate

NITRITE HIGH RANGE

SPECIFICATIONS

Range 0 to 150 mg/L

Resolution

Accuracy

Typical EMC

Deviation

1 mg/L

±4 mg/L ±4% of reading at 25 °C

±1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the Ferrous Sulfate method. The reaction between nitrite and the reagent causes a greenish-brown tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93708-0 Powder reagent

REAGENT SETS

HI 93708-01 Reagents for 100 tests

HI 93708-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Nitrite HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• Remove the cuvette.

Nitrite HR 88

• 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 (NO

(NaNO

¯-N) and sodium nitrite

• Press s or t to return to the measurement screen.

89 Nitrite HR

NITRITE LOW RANGE

SPECIFICATIONS

Range 0.00 to 1.15 mg/L

Resolution

Accuracy

Typical EMC

Deviation

0.01 mg/L

±0.06 mg/L ±4% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the EPA Diazotization method 354.1. The reaction between nitrite and the reagent causes a pink tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93707-0 Powder reagent

REAGENT SETS

HI 93707-01 Reagents for 100 tests

HI 93707-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Nitrite LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• Fill the cuvette up to the mark 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.

• 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 90

• Reinsert the cuvette into the instrument.

• 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 (NO

(NaNO

¯-N) and sodium nitrite

• 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.

91 Nitrite LR

DISSOLVED OXYGEN

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.0 to 10.0 mg/L

0.1 mg/L

±0.4 mg/L ±3% of reading at 25 °C

± 0.1 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 420 nm

Method Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Azide modified Winkler method. The reaction between dissolved oxygen and the reagents causes a yellow tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93732 A-0 Reagent A

HI 93732 B-0 Reagent B

HI 93732 C-0 Reagent C

REAGENT SET

HI 93732-01 Reagents for 100 tests

HI 93732-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

5 drops

10 drops

MEASUREMENT PROCEDURE

• Select the Dissolved Oxygen method using the procedure described in the Method Selection section (see page 12).

• 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 92

• 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.

INTERFERENCES

Interferences may be caused by reducing and oxidizing materials.

93 Dissolved Oxygen

OZONE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 2.00 mg/L

0.01 mg/L

±0.02 mg/L ±3% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Colorimetric DPD Method. The reaction between ozone and the DPD reagent causes a pink tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93757-0 DPD Powder Reagent

Quantity/test

1 packet

HI 93703-52-0 Glycine Powder (Optional Reagent) 1 packet

REAGENT SETS

HI 93757-01 Reagents for 100 tests

HI 93757-03 Reagents for 300 tests

HI 93703-52 Glycine Powder, Optional Reagent for 100 tests

For other accessories see page 124.

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: value A.

• On a fresh sample perform the Additional Measurement Procedure and take note of the reading: value B.

• Subtract reading B from reading A to obtain the ozone concentration in mg/L: mg/L (O

) = value A – value B.

STANDARD MEASUREMENT PROCEDURE

• Select the Ozone method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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 94

• 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.

• The instrument displays concentration in mg/L of ozone (chlorine free samples only).

ADDITIONAL MEASUREMENT PROCEDURE

For samples containing chlorine

• Select the Ozone method using the procedure described in the Method Selection 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.

10 mL

Ozone

• 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.

• 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 CaCO

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 CaCO

2 minutes after adding the powder reagent.

, shake the sample for approximately

Ozone 96

pH

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

6.5 to 8.5 pH

0.1 pH

±0.1 pH at 25 °C

±0.1 pH

Light Source Tungsten lamp with narrow band interference filter @ 525 nm

Method Adaptation of the Phenol Red method. The reaction with the reagent causes a yellow to red tint in the sample.

REQUIRED REAGENTS

Code

HI 93710-0

Description

Phenol Red Indicator

Quantity

5 drops

REAGENT SETS

HI 93710-01 Reagents for 100 pH tests

HI 93710-03 Reagents for 300 pH tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the pH method using the procedure described in the

Method Selection section (see page 12).

• Fill the cuvette with 10 mL of unreacted sample (up to the mark) and replace the cap.

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.

97 pH

• 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.

pH 98

PHOSPHATE HIGH RANGE

SPECIFICATIONS

Range

Resolution

0.0 to 30.0 mg/L

0.1 mg/L

Accuracy ±1 mg/L ±4% of reading at 25 °C

Typical EMC Dev. ±0.1 mg/L

Light Source

Method

Tungsten lamp with narrow band interference filter @ 525 nm

Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Amino Acid method. The reaction between phosphate and reagents causes a blue tint in the sample.

REQUIRED REAGENTS

Code

HI 93717 A-0

HI 93717 B-0

Description

Molybdate

Reagent B

Quantity

10 drops

1 packet

REAGENT SETS

HI 93717-01 Reagents for 100 tests

HI 93717-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Phosphate HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• Remove the cuvette.

• Add 10 drops of HI 93717A-0 Molybdate reagent.

99 Phosphate HR

• 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 ¯).

• 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

• 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

Phosphate HR 100

PHOSPHATE LOW RANGE

SPECIFICATIONS

Range

Resolution

0.00 to 2.50 mg/L

0.01 mg/L

Accuracy ±0.04 mg/L ±4% of reading at 25 °C

Typical EMC Dev. ±0.01 mg/L

Light Source

Method

Tungsten lamp with narrow band interference filter @ 610 nm

Adaptation of the Ascorbic Acid method. The reaction between phosphate and the reagent causes a blue tint in the sample.

REQUIRED REAGENTS

Code Description

HI 93713-0 Powder reagent

REAGENT SETS

HI 93713-01 Reagents for 100 tests

HI 93713-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

• Select the Phosphate LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• 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.

101 Phosphate LR

• 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 ¯).

• 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

• 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 102

PHOSPHORUS

SPECIFICATIONS

Range 0.0 to 15.0 mg/L

Resolution

Accuracy

0.1 mg/L

±0.3 mg/L ±4% of reading at 25 °C

Typical EMC Dev. ±0.2 mg/L

Light Source

Method

Tungsten lamp with narrow band interference filter @ 525 nm

Adaptation of the Standard Methods for the Examination of Water and Wastewater,

18 th edition, Amino Acid method. The reaction between phosphate and reagents causes a blue tint in the sample.

REQUIRED REAGENTS

Code

HI 93706 A-0

HI 93706 B-0

Description Quantity

Molybdate 10 drops

Amino Acid Powder 1 packet

REAGENT SETS

HI 93706-01 Reagents for 100 tests

HI 93706-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Phosphorus method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

• Remove the cuvette.

• Add 10 drops of HI 937O6A-0 Molybdate reagent.

103 Phosphorus

• 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 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

• 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

Phosphorus 104

POTASSIUM HIGH RANGE

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

Light Source

Method

20 to 200 mg/L

5 mg/L

±30 mg/L ±7% of reading at 25 °C

±5 mg/L

Tungsten lamp with narrow band interference filter @ 610 nm

Adaptation of the Turbidimetric Tetraphenylborate method. The reaction between

Potassium and reagents causes turbidity in the sample.

REQUIRED REAGENTS

Code Description

HI 93750 A-0

HI 93750 B-0

Potassium Reagent

Powder Reagent

REAGENT SETS

HI 93750-01 Reagents for 100 tests

HI 93750-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

6 drops

1 packet

MEASUREMENT PROCEDURE

Note: for sample preparation follow the CONCENTRATED SAMPLES procedure at page 18.

• Select the Potassium HR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

105 Potassium HR

• 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).

• 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 (K

O).

• Press s or t to return to the measurement screen.

• For ULTRA HIGH RANGE samples: follow the procedure described at page 107.

Potassium HR 106

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 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 105.

Read the result in mg/L of Potassium on the display and multiply the reading by 5 to obtain the actual concentration of Potassium.

107 Potassium HR

POTASSIUM MEDIUM RANGE

SPECIFICATIONS

Range 10 to 100 mg/L

Resolution

Accuracy

Typical EMC

Deviation

Light Source

Method

2.5 mg/L

±15 mg/L ±7% of reading at 25 °C

±2.5 mg/L

Tungsten lamp with narrow band interference filter @ 610 nm

Adaptation of the Turbidimetric Tetraphenylborate method. The reaction between

Potassium and reagents causes turbidity in the sample.

REQUIRED REAGENTS

Code Description

HI 93750 A-0

HI 93750 B-0

Potassium Reagent

Powder Reagent

REAGENT SETS

HI 93750-01 Reagents for 100 tests

HI 93750-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

6 drops

1 packet

MEASUREMENT PROCEDURE

Note: for sample preparation follow the CONCENTRATED SAMPLES procedure at page 18.

• Select the Potassium MR method using the procedure described in the Method Selection section (see page 12).

10 mL

• 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.

Potassium MR 108

• 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).

• 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 (K

O).

• 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

109 Potassium MR

POTASSIUM LOW RANGE

SPECIFICATIONS

Range 0.0 to 20.0 mg/L

Resolution

Accuracy

Typical EMC

Deviation

Light Source

Method

0.5 mg/L

±3.0 mg/L ±7% of reading at 25 °C

±0.5 mg/L

Tungsten lamp with narrow band interference filter @ 610 nm

Adaptation of the Turbidimetric Tetraphenylborate method. The reaction between

Potassium and reagents causes turbidity in the sample.

REQUIRED REAGENTS

Code Description

HI 93750 A-0

HI 93750 B-0

Potassium Reagent

Powder Reagent

REAGENT SETS

HI 93750-01 Reagents for 100 tests

HI 93750-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

6 drops

1 packet

MEASUREMENT PROCEDURE

Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure at page 17.

• Select the Potassium LR method using the procedure described in the Method Selection section (see page 12).

10 mL

• Fill the cuvette with 10 mL of sample, up to the mark.

• Add 6 drops of HI 93750A-0 Potassium Reagent, replace the cap and swirl the solution.

• Place the cuvette into the holder and close the lid.

Potassium LR 110

• 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).

• 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 (K

O).

• 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

111 Potassium LR

SILICA

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 2.00 mg/L

0.01 mg/L

±0.03 mg/L ±3% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 610 nm

Method Adaptation of the

Heteropoly Blue method. The reaction between silica and reagents causes a blue tint in the sample.

ASTM Manual of Water and Environmental Technology, D859,

REQUIRED REAGENTS

Code Description

HI 93705 A-0 Molybdate

HI 93705 B-0 Citric acid

HI 93705 C-0 Amino acid

Quantity

6 drops

1 packet

REAGENT SETS

HI 93705-01 Reagents for 100 tests

HI 93705-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Silica method using the procedure described in the

Method Selection section (see page 12).

10 mL

• Fill the cuvette with 10 mL of unreacted sample (up to the mark).

• Add 6 drops of HI 93705A-0 Molybdate reagent. Replace the cap and swirl the solution.

• Wait for 4 minutes, add the content of one packet of HI 93705B-0

Citric acid reagent and shake until it is completely dissolved.

• Wait for 1 minute. This is the blank.

• Place the cuvette into the holder and close the lid.

Silica 112

• 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 (SiO

• 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).

• 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.

113 Silica

SILVER

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.000 to 1.000 mg/L

0.005 mg/L

±0.020 mg/L ±5% of reading at 25 °C

± 0.001 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm.

Method Adaptation of the PAN method. The reaction between silver and reagents causes an orange tint in the sample.

REQUIRED REAGENTS

Code

HI 93737 A-0

HI 93737 B-0

HI 93737 C-0

HI 93737 D-0

Description Quantity

Buffer Reagent A 1 mL

Buffer Reagent B 1 mL

Indicator Reagent C 2 mL

Fixing Reagent D 2 mL

HI 93703-51 Dispersing Agent 4-6 drops

REAGENT SETS

HI 93737-01 Reagents for 50 tests

HI 93737-03 Reagents for 150 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Silver method using the procedure described in the Method Selection section (see page 12).

Note: for best results perform your tests between 20-24°C.

• Fill two graduated beakers with 25 mL of sample.

# 1 # 2

• Add 1.0 mL of HI 93737A-0 Buffer reagent to one beaker

(the blank) and swirl gently to mix.

# 1

Silver 114

• 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.

# 2

• 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.

# 1 # 2

• 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.

115

# 1

# 1 # 2

10 mL

# 1

Silver

• Press the Zero key. The display will show “-0.0-” when the meter is zeroed and ready for measurement.

• 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.

# 2

• Insert the second cuvette into the instrument.

10 mL

# 2

• Press Read to start the reading. The instrument displays the results in mg/L of silver.

INTERFERENCES

Interference may be caused by:

above 30 mg/L

above 1000 mg/L as CaCO

above 20 mg/L

Cl¯ above 8000 mg/L

above 1.5 mg/L

above 20 mg/L

above 40 mg/L

above 15 mg/L

F¯ above 20 mg/L

above 1.5 mg/L

above 10 mg/L

above 500 mg/L

Mn 2+ above 25 mg/L

Mg 2+

above 1000 mg/L as CaCO

above 5000 mg/L

above 1.5 mg/L

above 20 mg/L

above 30 mg/L

Silver 116

SULFATE

SPECIFICATIONS

Range

Resolution

0 to 100 mg/L

5 mg/L

Accuracy ±5 mg/L ±3% of reading at 25 °C

Light Source Tungsten lamp with narrow band interference filter @ 466 nm

Method Sulfate is precipitated with barium chloride crystals. Light absorbance of the suspension is measured.

REQUIRED REAGENTS

Code

HI 93751-0

Description

Indicator reagent

REAGENT SETS

HI 93751-01 Reagents for 100 tests

HI 93751-03 Reagents for 300 tests

For other accessories see page 124.

Quantity

1 packet

MEASUREMENT PROCEDURE

Note: for sample preparation follow the COLORED OR TURBID SAMPLES procedure on page 17.

• Select the Sulfate method using the procedure described in the Method Selection section (see page 12).

• Fill a cuvette with 10 mL of unreacted sample (up to the mark) and replace the cap.

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.

• Remove the cuvette.

117 Sulfate

• 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 ¯).

INTERFERENCES

Interferences may be caused by:

Calcium (as CaCO

) above 20000 mg/L

Chloride (as Cl¯) above 40000 mg/L

Magnesium (as MgCO

) above 10000 mg/L

Silica (as SiO

) above 500 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.

Sulfate

118

ZINC

SPECIFICATIONS

Range

Resolution

Accuracy

Typical EMC

Deviation

0.00 to 3.00 mg/L

0.01 mg/L

±0.03 mg/L ±3% of reading at 25 °C

±0.01 mg/L

Light Source Tungsten lamp with narrow band interference filter @ 575 nm

Method Adaptation of the

Standard Methods for the Examination of Water and Wastewater, th edition, Zincon method. The reaction between zinc and the reagents causes an orange to a dark violet tint in the sample.

REQUIRED REAGENT

Code Description

HI 93731 A-0 Zinc Reagent

Quantity

1 packet

HI 93731 B-0 Cyclohexanone 0.5 mL

REAGENT SETS

HI 93731-01 Reagents for 100 tests

HI 93731-03 Reagents for 300 tests

For other accessories see page 124.

MEASUREMENT PROCEDURE

• Select the Zinc method using the procedure described in the Method Selection section (see page 12).

• Fill one graduated mixing cylinder up to the 20 mL mark with the sample.

20 mL

• 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.

119

10 mL

Zinc

• 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.

• 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.

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

Zinc

120

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.

121

DATA MANAGEMENT

The analyzed data can be managed using Hanna’s product HI92000, Windows ® Compatible Software .

Windows ® is registered Trademark of "Microsoft Co."

122

Description

Aluminum

Alkalinity

Ammonia MR

Ammonia LR

Bromine

Calcium

Chlorine, Free

Chlorine, Total

Chlorine Dioxide

Chromium VI HR

Chromium VI LR

Color of Water

Copper HR

Copper LR

Cyanuric Acid

Fluoride

Calcium Hardness

Magnesium Hardness

Hydrazine

Iodine

Iron HR

Iron LR

Magnesium

Manganese HR

Manganese LR

Molybdenum

Nickel HR

Nickel LR

Nitrate

Nitrite HR

Nitrite LR

Oxygen, Dissolved

Ozone pH

Phosphate HR

Phosphate LR

Phosphorus

Potassium HR

Potassium MR

Potassium LR

Silica

Silver

Sulfate

Zinc

STANDARD METHODS

Range

0.00 to 1.00 mg/L

0 to 500 mg/L

0.00 to 10.00 mg / L

0.00 to 3.00 mg / L

0.00 to 8.00 mg/L

0 to 400 mg/L

0.00 to 2.50 mg / L

0.00 to 3.50 mg / L

0.00 to 2.00 mg/L

0 to 1000 µ g/L

0 to 300 µ g/L

0 to 500 PCU

0.00 to 5.00 mg/L

0 to 1000

µ g/L

0 to 80 mg/L

0.00 to 2.00 mg/L

0.00 to 2.70 mg/L

0.00 to 2.00 mg/L

0 to 400

µ g/L

0.0 to 12.5 mg/L

0.00 to 5.00 mg/L

0 to 400

µ g/L

0 to 150 mg/L

0.0 to 20.0 mg/L

0 to 300 µ g/L

0.0 to 40.0 mg/L

0.00 to 7.00 g/L

0.000 to 1.000 mg/L

0.0 to 30.0 mg / L

0 to 150 mg/L

0.00 to 0.35 mg/L

0.0 to 10.0 mg/L

0.00 to 2.00 mg/L

6.5 to 8.5 pH

0.0 to 30.0 mg/L

0.00 to 2.50 mg/L

0.0 to 15.0 mg / L

20 to 200 mg/L

10 to 100 mg/L

0.0 to 20.0 mg/L

0.00 to 2.00 mg/L

0.000 to 1.000 mg/L

0 to 100 mg/L

0.00 to 3.00 mg/L

Method

Aluminon

Colorimetric

Nessler

DPD

Oxalate

DPD

Chlorophenol Red

Diphenylcarbohydrazide

Colorimetric Platinum Cobalt

Bicinchoninate

Turbidimetric

SPADNS

Colorimetric

Colorimetric p-Dimethylaminobenzaldehyde

DPD

Phenantroline

TPTZ

Calmagite

Periodate Oxidation

PAN

Mercaptoacetic Acid

Photometric

PAN

Cadmium Reduction

Ferrous Sulfate

Diazotization

Winkler

DPD

Phenol Red

Amino Acid

Ascorbic Acid

Amino Acid

Turbidimetric

Heteropoly Blue

PAN

Turbidimetric

Zincon

123

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-F 300 free chlorine tests (liquid)

HI 93701-T 300 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 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

124

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 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

HI 95747-01 100 copper LR tests

HI 95747-03 300 copper LR tests

125

OTHER ACCESSORIES

HI 731318 cloth for wiping cuvettes (4 pcs)

HI 731321 glass cuvettes (4 pcs)

HI 731325W new cap for cuvette (4 pcs)

HI 740034 cap for 100 mL beaker (6 pcs)

HI 740036 100 mL plastic beaker (6 pcs)

HI 740038 60 mL glass bottle and stopper

HI 740142 1 mL graduated syringe

HI 740143 1 mL graduated syringe (6 pcs)

HI 740144 pipette tip (6 pcs)

HI 740157 plastic refilling pipette (20 pcs)

HI 740220 25 mL glass cylinders with caps (2 pcs)

HI 740223 170 mL plastic beaker

HI 740224 170 mL plastic beaker (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 graduated cylinder

HI 740230 230 mL demineralized water

HI 92000 Windows compatible software

HI 920013 PC connection cable

HI 93703-50 cuvette cleaning solution (230 mL)

HI 93703-54 dried resin (100 g)

HI 93703-55 activated carbon (50 pcs)

126

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.

127

Hanna Instruments Inc.

Highland Industrial Park

584 Park East Drive

Woonsocket, RI 02895 USA

Technical Support for Customers

Tel. (800) 426 6287

Fax (401) 765 7575

E-mail [email protected]

www.hannainst.com

Local Sales and Customer Service Office

Printed in EUROPE

(ROMANIA)

128

MAN83200 04/12

Key features

Measures 44 different methods
Uses specific liquid or powder reagents
Connects to a PC via an USB cable
Optional HI 92000 Windows® Compatible Software
Powerful interactive user support

Frequently asked questions

The HI 83200 is a multiparameter bench photometer dedicated for Laboratory analysis. It measures 44 different methods using specific liquid or powder reagents.

The HI 83200 can measure 44 different methods.

Yes, the HI 83200 can be connected to a PC via an USB cable.

The optional HI 92000 Windows® Compatible Software helps users manage all their results.

Yes, the HI 83200 has a powerful interactive user support that assists the user during the analysis process.

Instruction Manual

Multiparameter Bench

Photometer for Laboratories

TABLE OF CONTENTS

PRELIMINARY EXAMINATION

GENERAL DESCRIPTION

ABBREVIATIONS

SPECIFICATIONS

PRECISION AND ACCURACY

PRINCIPLE OF OPERATION

FUNCTIONAL DESCRIPTION

TIPS FOR AN ACCURATE MEASUREMENT

HEALTH & SAFETY

METHOD REFERENCE TABLE

OPERATIONAL GUIDE

SETUP

SAMPLE PREPARATION

ALUMINUM

ALKALINITY

AMMONIA MEDIUM RANGE

AMMONIA LOW RANGE

BROMINE

CALCIUM

TOTAL CHLORINE

CHLORINE DIOXIDE

CHROMIUM VI HIGH RANGE

CHROMIUM VI LOW RANGE

COLOR OF WATER

COPPER HIGH RANGE

COPPER LOW RANGE

CYANURIC ACID

FLUORIDE

CALCIUM HARDNESS

MAGNESIUM HARDNESS

HYDRAZINE

IODINE

IRON HIGH RANGE

IRON LOW RANGE

MAGNESIUM

MANGANESE HIGH RANGE

MANGANESE LOW RANGE

MOLYBDENUM

NICKEL HIGH RANGE

NICKEL LOW RANGE

NITRATE

NITRITE HIGH RANGE

NITRITE LOW RANGE

DISSOLVED OXYGEN

OZONE

INTERFERENCES

pH

PHOSPHATE HIGH RANGE

PHOSPHATE LOW RANGE

PHOSPHORUS

POTASSIUM HIGH RANGE

POTASSIUM MEDIUM RANGE

POTASSIUM LOW RANGE

SILICA

SILVER

SULFATE

ZINC

ERRORS AND WARNINGS

DATA MANAGEMENT

STANDARD METHODS

ACCESSORIES

WARRANTY

HANNA LITERATURE

What is the HI 83200?

How many methods can the HI 83200 measure?

Can I connect the HI 83200 to a PC?

What is the optional HI 92000 Windows® Compatible Software used for?

Does the HI 83200 have user support?

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