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Method for determining the concentration of CADMIUM (Cd++)
in Aqueous Solutions


Electrode Specifications       Links to publications on the WWW     Go to Ion Selective Electrodes page

Apparatus Required:

Ion-Selective Electrode for cadmium ion (ELIT 8241 crystal membrane)

Reference electrode: double junction lithium acetate (ELIT 003n)

Dual electrode head (ELIT 201)

ELIT Computer Interface/Ion Analyser, or Ion/pH/mV meter.

Standard solution: 1000 ppm Cd as Cd(NO3)2

Buffer solution (ISAB): 5 Molar NaNO3.

150 ml polypropylene beakers, 100ml volumetric flask, 1, 2, 5, 10ml pipettes.

Calibration:

Before use, the electrodes must be calibrated by measuring a series of known standard solutions, made by serial dilution of the 1000ppm standard solution. For a full calibration, prepare 100ml of solutions containing 1000, 100, 10, 1, and 0.1ppm Cd. If the approximate range of concentrations of the samples is known, and this is within the linear range of the ISE, then it is only necessary to make two solutions (preferably a decade apart) which span this range.

NB: If the samples to be measured are expected to have a total ionic strength of greater than 0.001 Molar, or a pH of >7 then 2 ml of buffer solution should be added to each 100ml standard and mixed thoroughly to compensate for different activity coefficients between samples and standards.

Follow the instructions in the General Operating Instructions to measure these standard solutions and prepare a calibration graph.

Sample Preparation:

For samples with low ionic strength and pH < 7, no sample preparation is necessary. Simply take approximately 50 to 100 mls of sample in a plastic beaker, or even immerse the electrodes directly in a lake or river (but take care to avoid losing the electrodes!). For high ionic strength samples (or pH>7), take 100mls of sample and add 2 mls of buffer solution and stir well before measurement.

Sample Measurement:

Follow the instructions in the electrode operating instructions to measure a series of samples and record the results. Briefly, it is important to note that, if measuring in beakers, the electrodes must be washed and dried between each sample, to avoid cross contamination, and sufficient time must be allowed (2 or 3 minutes), before taking a reading after immersion, to permit the electrode signal to reach a stable value. For the highest precision, frequent recalibration is recommended (see operating instructions).

Results:

The results will be displayed as ppm and mol/l. If buffer solution has been added equally to standards and samples then these figures will not need adjusting because they will all be affected by the same dilution factor.

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Technical Specifications
for the Cadmium Ion-Selective Electrode
(ELIT 8241)

Click here to download a printer-friendly (pdf) Specification Sheet.

Introduction
The Cadmium Ion-Selective Electrode has a solid-state crystal membrane. The electrode is designed for the detection of cadmium ions (Cd+2 ) in aqueous solutions and is suitable for use in both field and laboratory applications.
The Cadmium Ion is a divalent cation.
One mole of ( Cd+2) has a mass of 112.411 grams; 1000ppm is 0.009M
Dissolve 2.744g Cadmium Nitrate tetra hydrate (Cd(NO3)2.4H2O) in 1 Litre water.

Physical Specifications
Length of body excluding gold contact = 130 mm
Length of body including gold contact = 140 mm
Diameter of body = 8 mm
DC resistance at 25°C < 2.5 MOhm
Minimum feasible sample volume = 5 mls

Chemical / Operational Specifications
Preconditioning / Standard solution : Normally 1000ppm Cd+2 as Cd(NO3)2
(But see General Operating Instructions )
Preconditioning time : 5 minutes
Optimum pH range : pH 3 to pH 7
Temperature range : 0 to 80°C
Recommended ISAB : 5M NaNO3 (Add 2% v/v)
Recommended reference electrode : double junction (ELIT 003)
Reference electrode outer filling solution : 0.1M CH3COOLi
Electrode slope at 25°C : 26±3 mV/decade
Concentration range : 0.1 to 11,000 ppm (9x10-7 to 0.1 Molar)
Response time : < 10 seconds
Defined as time to complete 90% of the change in potential after immersion in the new solution.
Time for stable reading after immersion : < 1 to > 5 minutes
Depending on concentration, use of ISAB, nature of sample and stabilisation time of liquid junction potential of reference electrode.
Potential drift (in 1000 ppm) < 3 mV/ day (8 hours)
Measured at constant temperature and with ISE and Reference Electrode continually immersed

Interference:
NB: All poly-crystalline membranes contain Silver Sulphide and thus will not give reliable readings if Ag or S ions are present in the solution. This electrode cannot be used in the presence of significant concentrations of Copper, or Mercury. Furthermore, any Iron or Lead ions in a concentration greater than one hundredth of that of the Cadmium will lead to spuriously high values – Selectivity coefficients for Iron (Fe+2) and Lead are approximately 10.

Note low pH range (3 to 7) for this electrode.


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