Hanna Instruments HI 4008 User manual

1
HI 4008HI 4008
HI 4008HI 4008
HI 4008
HI 4108HI 4108
HI 4108HI 4108
HI 4108
Cupric Ion
Selective Electrode
Instruction Manual
Half-cell
Combination
COMBINATION
CUPRIC
HI 4108
CUPRIC
HI 4008

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HI 4008 Cupric Half-cellHI 4008 Cupric Half-cell
HI 4008 Cupric Half-cellHI 4008 Cupric Half-cell
HI 4008 Cupric Half-cell
HI 4108 Cupric Combination ElectrodeHI 4108 Cupric Combination Electrode
HI 4108 Cupric Combination ElectrodeHI 4108 Cupric Combination Electrode
HI 4108 Cupric Combination Electrode
I.I.
I.I.
I. Introduction:Introduction:
Introduction:Introduction:
Introduction:
The Hanna HI 4008 and HI 4108 are ion selective elec-
trodes designed for the measurement of cupric ions in
aqueous solutions. The HI 4008 is a solid state half-cell
sensor that requires a separate reference. The HI 4108 is a
combination ion selective electrode.
IIII
IIII
II. SpecificationsSpecifications
SpecificationsSpecifications
Specifications
Type: Solid State electrode with
a cupric sulfide /silver sul-
fide membrane.
Interfering ions: Silver and mercury must
be absent. Any ion that forms a more insoluble sulfide than
cupric sulfide will interfere with the electrode response. These
include bismith (Bi3+), iron (Fe2+) ,bromide(Br-) and
chloride (Cl-) if they are in high concentrations. Long term
exposure in this ion will poison the cupric surface. Oxidation
of the cupric surface will also poison the electrode.
Operating Temperature: 0-80°C
Operating pH: 3 to 7 pH
(4-6 recommended)
Dimensions: 12 mm (OD) X 120 mm
nominal insertion
(0.47” X 4.72”)
Connection: BNC
Ion(s) measured: Cupric (Cu 2++
++
+)
Measurement range: 0.1M to 1X 10-6 M
6355 to 0.065 ppm

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III.III.
III.III.
III. Theory of OperationTheory of Operation
Theory of OperationTheory of Operation
Theory of Operation:::::
The HI 4108 or HI 4108 cupric electrodes are potentiometric
devices used for the rapid determination of free cupric ions
in samples and as a detector for the titration of cupric with
EDTA. Cupric sensors are “electrodes of the third kind”
because they detect cations which also form low-solubility
salts with sulfide anions that also form low-solubility salts
with silver.
The electrode functions as a sensor or ionic conductor. The
HI 4008 requires a separate reference electrode to complete
its electrolytic circuit. The HI 4108 incorporates a reference
electrode. The mixed cupric sulfide/ silver sulfide mem-
brane produces a potential change due to changes in the
sample’s cupric ion activity. When the ionic strength of the
sample is fixed by the addition of ISA, the voltage is pro-
portional to the concentration of cupric ions in solution and
the electrode follows the Nernst equation.
E= Ea+2.3 RT/nF log A ion
E= observed potential
Ea= Reference and fixed internal voltages
R= gas constant (8.314 volt coulomb/K Mole)
n= Charge on ion (2+)
A i=ion activity in sample
T= absolute temperature in K
F= Faraday constant (9.648 x 104 coulombs/mole)

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IV.IV.
IV.IV.
IV. Design elements of the HI 4008 and HI 4108Design elements of the HI 4008 and HI 4108
Design elements of the HI 4008 and HI 4108Design elements of the HI 4008 and HI 4108
Design elements of the HI 4008 and HI 4108
electrodeselectrodes
electrodeselectrodes
electrodes
Upper Cap
Spring
O-Ring
Ceramic Junction
on Inner Stem
Fill Hole
O-Ring and
Plug
Sensing
Membrane
Outer Sleeve
Upper
Threads
Liquid junction
Cap
Sensing
Membrane
Sensor
Handle
CUPRIC
HI 4008

5
V.V.
V.V.
V. Equipment required:Equipment required:
Equipment required:Equipment required:
Equipment required:
•Hanna HI 5315 Double Junction Reference Electrode
with HI 7072 Fill Solution for use with HI 4008 half-
cell.
•Hanna HI 4222 pH/ISE/mV meter or other suitable
ion or pH/mV meter. (Note: log/linear graph paper is
useful if an ISE (ion) meter is not available).
•Hanna HI 180 Magnetic Stirrer or equivalent with TFE
coated stirring bars (HI 731320). Note: isolate bea-
kers from stirrer motor heat by placing insulating
material such as foam or cork between them.
•Hanna HI 76404 Electrode Holder or equivalent.
•Plastic beakers (HI 740036P) or other suitable mea-
surement vessel.
VI.VI.
VI.VI.
VI. Solutions RequiredSolutions Required
Solutions RequiredSolutions Required
Solutions Required
For Cupric Measurements
0.1 M cupric standard, (500 mL) HI 4008-01
ISA, (500 mL) HI 4000-00
For direct cupric measurements- Using volumetric pipettes
and glassware, make dilutions of HI 4008-01 to bracket
the concentration of the samples. Note: 0.1M cupric stan-
dard is equivalent to 6355 ppm. Standards with concen-
trations <10-3 M (63.6 ppm) should be prepared daily.
Store in tightly closed plastic bottle. To 100 parts standard
or sample add 2 mL of ISA.

6
VIIVII
VIIVII
VII. General GuidelinesGeneral Guidelines
General GuidelinesGeneral Guidelines
General Guidelines
•Concentrated samples (>0.10 M) should be diluted
before measurement. Multiply the final result by the
corresponding dilution factor.
•Calibration standards and sample solutions should
have the same ionic strength.
•For high ionic strength samples use standard addi-
tion or titration methods.
•Calibration standards and sample solutions should
be at same temperature.
•The magnetic stirrer may generate heat. Thermally
insulate beaker containing standard or sample from
magnetic stirrer by placing cork or other insulative
sheet between beaker and stirrer plate.
•Calibration standards and sample solutions should
be stirred at the same rate using identical sized TFE
coated stir bars.
•Rinse electrode pair with distilled or deionized water
between samples and gently dab dry with soft dis-
posable absorbent toweling. Do not rub electrodes.
•Avoid Cu(OH)2
precipitation by maintaining pH be-
tween 4 and 6 pH.
•Presoaking the cupric sensor tip in a dilute standard
will optimize response. Use concentrations approxi-
mately10-3M.
•A scratched, pitted, or oxidized pellet surface can cause
drift, a loss of low level response, or poor repeatability.
Optimum response can be restored by removing the
damaged surface with the microabrasive strip HI 4000-
70. Use gloves to protect skin.
•Avoid large changes in temperature (thermal shock)
as it may damage the sensor.

7
•Gas bubbles may form from solution out-gassing due
to temperature change. Gently tap body of sensor to
dislodge them from sensing membrane.
HI 4008
•Remove protective cover from sensor tip.
HI 4108
•Remove the protective plastic wrap that covers the
ceramic junction before assembling sensor for the first
time.
•HI 7072 reference fill solution should be added daily
to electrolyte reservoir before electrode use.
•During measurement always operate electrode with
the fill hole open.
•During normal use, fill solution will slowly drain out
of the tapered cone junction at the lower portion of the
electrode. Excessive loss (>4 cm drop within 24 hours)
is not normal. If this occurs verify cap is tightened and
the interface between the internal cone and outer
body is free of debris.
•Add fill solution daily to maintain a good head pres-
sure. For optimum response, this level should be main-
tained and not be allowed to drop more than 2-3 cm
(1-inch) below fill hole. Fill solution must cover the
ceramic found on the inner stem.
•If an erratic measurement occurs, check to see if for-
eign matter is seen trapped near the internal cone.
Drain, wipe off outer cone while depressing cap, re-
lease cap and refill with fresh fill solution.

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VIII.VIII.
VIII.VIII.
VIII. Electrode PreparationElectrode Preparation
Electrode PreparationElectrode Preparation
Electrode Preparation
HI 4008
1. Remove protective cover from sensor tip.
2. Prepare reference electrode by filling outer electrolyte
reservoir with HI 7072.
3. Place sensor and reference electrodes into electrode
holder and connect cable connectors to meter.
HI 4108
1. Unwrap plastic film seal found over ceramic junction
on inner stem and discard. This is only used for ship-
ping and long term storage.
2. Rinse inner stem with deionized water making certain
to wet the o-ring found on the inner stem.
3. Reassemble electrode by gently pushing the inner
assembly into the outer body, sliding spring down
cable, and screwing cap into place.
4. Remove fill hole cover and o-ring on fill hole spout.
5. Using the dropper pipette provided, add a few drops
HI 7072 fill solution to the electrode, wetting the o-
ring and rinsing out the fill solution chamber.
Deionized
Water
Remove
Parafilm

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6. Holding the body of the electrode gently press upper
cap with your thumb. This permits the fill solution to
drain out of the body. Release cap and verify elec-
trode returns to its original position. (You may need to
gently assist for this to occur).
7. Tighten the electrode cap onto the body and fill elec-
trode body until fill solution volume is just below fill
hole.
8. Position electrode in a Hanna HI 76404 electrode
holder (or equivalent) and connect plug to meter.
HI 4108
CUPRIC
COMBINATION

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IX.IX.
IX.IX.
IX. Quick Check of Electrode SlopeQuick Check of Electrode Slope
Quick Check of Electrode SlopeQuick Check of Electrode Slope
Quick Check of Electrode Slope
•Connect sensors to pH/mV/ISE meter
•Place meter in mV mode.
•Place 100 mL of deionized water into a beaker with
stir bar and 2 mL of HI 4000-00 ISA. Add stir bar and
place on magnetic stirrer.
•Place electrodes into prepared sample.
•Add 1 mL of the stock standard HI 4008-01 (or .01 M
or .001 M standard by dilution) to the beaker.
Record the mV value when reading has stabilized.
•Add an additional 10 mL of standard HI 4008-01 (or
same dilute standard) to the solution. Record the mV
when reading has stabilized. This value should be
more positive than the previous noted.
•Determine the difference between the two mV values.
An acceptable value for this slope is +27 ± 4 mV.
X.X.
X.X.
X. Corrective actionCorrective action
Corrective actionCorrective action
Corrective action
•Verify protective cap has been removed (HI 4008).
•Verify plastic film has been removed from inner stem
(HI 4108).
•Verify electrodes are connected properly to meter and
meter is powered.
•Verify standard has been properly stored. Remake
standards if appropriate.
•If the sensor slope just misses the suggested slope
window, soaking the sensor in a dilute standard may
solve the problem. (<10-3 M standard).
•A scratched, pitted or oxidized sensing surface can be
polished with HI 4000-70 polishing strip. Cut off
approximately 1 inch of the micro-abrasive strip. Wear
protectice gloves. Wet the frosted side with deionized
water and place against damaged membrane of the
electrode. Place your gloved thumb against the shiny
backing and slowly rotate back and forth while
applying gentle pressure. Continue polishing until
you are satisfied with the surface. If dark deposits
appear on polishing strip move the paper slightly

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and continue polishing.
•If the membrane is damaged, the response becomes
extremely sluggish, or the slope of the electrode has
decreased significantly, and procedures above have
not helped, the sensor should be replaced.
XI.XI.
XI.XI.
XI. Direct Calibration and MeasurementDirect Calibration and Measurement
Direct Calibration and MeasurementDirect Calibration and Measurement
Direct Calibration and Measurement
This method is a simple procedure for measuring many
samples. A direct reading ISE meter (HI 4222 or equiva-
lent) determines concentration of the unknown by a direct
reading after calibrating the meter with the standards. The
meter is calibrated with two or more freshly made stan-
dards that are in the linear measurement range of the
unknowns. Two mL of ISA (HI 4000-00) is added to each
100 mL volume of standard or sample. More calibration
standards are required in non-linear regions. Unknowns
are read directly.
Samples with concentration greater than 0.1 M should be
diluted to be within the working range of the electrodes.
The final result must be multiplied by the corresponding
dilution factor to determine the actual concentration.
A pH/mV meter in mV mode with semi-log graph paper
may also be used. Two or more freshly prepared standards
that are in the measurement range of the unknowns are
measured in mV mode on the meter.
These values are plotted on the semi-log paper and the
points are connected to form a straight-line curve. When
samples are measured, their mV values are converted to
concentration by following the mV to the concentration axis
on the semi-log plot.

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Procedure
1) Follow sections VIII and IX to prepare sensors for
measurement.
2) Follow section VI to prepare standards / solution.
Standards should bracket and fall within the range of
interest.
Two mL HI 4000-00 ISA is added to 100 mL of both
samples and standards. Add stir bar and mix before
taking measurements.
3) Follow section VII; General Guidelines to optimize test
set-up.
4) During calibration it is best to start with lower concen-
tration samples first. Wait for a stable measurement
before recording values. Slightly longer equilibra-
tions are required at lower concentrations .
5) To prevent carry over and contamination of samples,
rinse sensors with deionized and dab dry with
absorbant laboratory tissue between samples.
XII.XII.
XII.XII.
XII. Other Measurement TOther Measurement T
Other Measurement TOther Measurement T
Other Measurement Techniquesechniques
echniquesechniques
echniques
Known Addition (for Cu2+)
An unknown concentration can be determined by adding a
known amount (volume and concentration) of measured
ion to a known volume of the sample. A mV value is taken
before and after the addition of standard, and using the
equation provided, the unknown concentration is found.
T
y
pical Linearit
y
for HI 4008 and HI 4108 Cupric
Electrodes
0
20
40
60
80
100
120
140
160
180
0.511.522.533.544.555.566.57
-Lo
g
[M]
mV

13
This technique is called Known Addition. The method can
use an ideal sensor slope, but actual determined slopes at
the temperature of measurement should be used if known.
The volume and concentration of the added standard must
cause a mV change of at least 8 mV. This method is
preprogrammed in the Hanna HI 4222 pH/ISE/mV meter,
which simplifies the method greatly. The method works
well for samples with high ionic strengths.
Example: Cupric ion determination in samples with con-
centrations less than 1 X 10 -3 M using known addition.
1. A 50 mL sample of unknown concentration (Vsample)
is placed in a clean plastic beaker with a cupric sensor
with 1 mL of HI 4000-00 ISA (VISA=1 mL) a. The stable
mV value (mV 1) is recorded after the sample is mixed.
2. 5mL (Vstd) of 10-1M standard (Cstd) is added to the
beaker and the mV value increases as does the con-
centration. ∆E is calculated as mV2-mV1. The un-
known cupric concentration in the original sample
(Csample) can then be determined by the following
equation.
Csample =
(VT)10∆E/S - (VS’)
CstandardVstandard
Vsample
VS’
3. The procedure can be repeated with a second stan-
dard addition to verify slope and operation of the
method.
Titration of cupric
A cupric electrode may be used as an indicator to follow the
progress and detect the endpoint of a complexation titra-
tion of cupricions with EDTA standard. During the titration
the sensor follows the decreasing cupric concentration while
small additions of EDTA titrant are added. The Cupric ion
reacts with the EDTA and removes
(V
sample
+V
standard
+V
ISA
)= V
T
(V
sample
+V
ISA
)= V
S’

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the free ions from the measurement pool.
Cu2+ + EDTA <—>Cu-EDTA
The EDTA reacts with the cupric ion forming a complex. The
EDTA also can react with a host of other metals. Working at
a pH between 4 and 6 optimizes the pH of the Cu-EDTA
complex, and also discourages complexing with other ions
that form stable complexes at high pH. Consult a
comprehensive Analytical Chemistry Treatise for techniques
concerning your particular interferent. The end point is
assumed to be at the inflection of the mV versus titrant
volume curve. Measurements may be automated by use of
the Hanna Titrator HI 901 or titrated manually.
Notes:
• Use of the an acetic acid buffer may increase the end
point break. Prepare buffer by diluting glacial acetic
acid (17.4 M) to 1M and adjust to pH 4 with KOH.
Add 1part buffer to 10 parts sample.
• Addition of ISA is suggested (2 mL/100 mL sample).
• The EDTA titrant should be 10X more concentrated
than the expected Cupric concentration.
• Competing metals will need to be identified and
removed or masked.
Plot generated on Hanna HI 901 Titrator duringPlot generated on Hanna HI 901 Titrator during
Plot generated on Hanna HI 901 Titrator duringPlot generated on Hanna HI 901 Titrator during
Plot generated on Hanna HI 901 Titrator during
automated Cupric ion titration using HI 4108 asautomated Cupric ion titration using HI 4108 as
automated Cupric ion titration using HI 4108 asautomated Cupric ion titration using HI 4108 as
automated Cupric ion titration using HI 4108 as
indicator electrode.indicator electrode.
indicator electrode.indicator electrode.
indicator electrode.

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XIV. SXIV. S
XIV. SXIV. S
XIV. Storage and Care of the HI 4008 andtorage and Care of the HI 4008 and
torage and Care of the HI 4008 andtorage and Care of the HI 4008 and
torage and Care of the HI 4008 and
HI 4108 sensorsHI 4108 sensors
HI 4108 sensorsHI 4108 sensors
HI 4108 sensors
The HI 4008 and HI 4108 sensor can be stored in very
dilute standards (<10-3M) for short periods of time.
The HI4008 should be stored dry with it’s protective cap
on for longer periods. For longer term storage of the
model HI 4108 combination electrode ;Drain and wash
of salts with distilled or deionized water. Unscrew the
upper cap and move outer sleeve up cable. Wrap the
ceramic junction on the inner stem with Parafilm®or
other sealing wrap. Place the protective cap provided
over the dried membrane and store in original storage
box provided with electrode.
XVXV
XVXV
XV..
..
. Conversion TConversion T
Conversion TConversion T
Conversion Tables For Cuables For Cu
ables For Cuables For Cu
ables For Cu2+2+
2+2+
2+ MultiplyMultiply
MultiplyMultiply
Multiply
Moles/L (M) to ppm (mg/L) 6.354 x 104
ppm (mg/L) to M (moles/L) 1.574 x 10-4
XIII.XIII.
XIII.XIII.
XIII.pHpH
pHpH
pH
HI 4108 and HI 4008 electrodes may be used in solutions
with pH values between 4 and 6. Samples above pH 6
may form Cu(OH)2. Adjust these samples with nitric acid.

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MAN4108 02/07
WARRANTYWARRANTY
WARRANTYWARRANTY
WARRANTY
Hanna Instruments Ion Selective Electrodes are warranted
to be free of defects in material and workmanship for 6
months from date of purchase when used for their intended
purpose and maintained according to instructions. If they
fail to work when first used contact your dealer immediately.
Damage due to accidents, misuse, misapplication, tampering
or lack of prescribed maintenance is not covered.
Hanna Instruments reserves the right to modify the design,
construction or appearance of its products without advance
notice.