Ionode IJ-Ag2S User Manual

Page 1
User maintenance and troubleshooting
GOOD CHEMISTRY
Symptom Possible cause Remedy
Drift Junction blocked Remove and clean sleeve
Membrane unclean or contaminated
Noisy Poor connection
Inaccurate readings or poor reproduc­ibility
to meter Junction not
immersed fully Insufcient
electrolyte or bubble
Contaminated standard(s)
Improperly made standards
Contamination from electrolyte
Remove sleeve. Gently polish membrane with P1200 “Wet & Dry”
Check connection
Lower electrode into solution below junction
Rell electrolyte
Make up fresh calibration standards and recalibrate
Recalibrate using freshly made standards
Use 1M potassium nitrate in sleeve
Warranty
IJ electrodes have a warranty of 12 months from date of purchase. Any electrode found to be faulty due to manufacture within this time will be replaced. Ionode reserves the right to limit or modify product warranty if it is deemed that the electrode has been used in unsuitable applications. Electrodes with broken stems, connectors or cables are not covered by warranty. Electrode life may be reduced in chemically aggressive or abrasive samples and at high temperatures.
Visit www.ionode.com for more information.
All specications and values are subject to change without notice. © 2012
Images are illustrative only.
Operators Manual
Short-Form
Intermediate Junction Series
IJ-Ag2S
SILVER/SULPHIDE
ION SELECTIVE
ELECTRODE
Temperature differences between calibration and sample measurement
No ISA used Add ISA
Incorrect pH Adjust pH
Sensitivity to light Perform calibration and
Ensure calibration and sample measurements are done at the same temperature
measurements in dark beakers or away from bright light
All specications and values are subject to change without notice. © 2009
Parameter Operating Range
Concentration range S2- 0.003 –32,100 mg/L
Temperature range 0 – 60ºC pH range S
Reference Type Double Junction Ag/AgCl/rellable Sensor materials Polycrystalline solid state
Body and sleeve Polypropylene/PEEK Overall length 150mm Barrel diameter 12mm Cable length 1m standard, longer to order.
Connector BNC standard, others on request
Ag+ 0.01 – 107,900 mg/L
2-
12-14
Ag+ 2-8
membrane
Maximum 20m
Page 2
Introduction
This guide contains the basic information for proper use of your new Silver/Sulphide Ion-selective electrode.
Preparation
IJ series electrodes are shipped without sleeve electrolyte, and must be lled prior to use. To ll, hold the electrode by the sleeve and gently ease off the rubber wetting cap. Prepare as follows:
1. 2.
1.
Invert the electrode. Hold the electrode just below the sleeve and with careful rotation and pulling along the axis of the electrode, remove the sleeve. DO NOT BEND.
3.
3.
Slide the sleeve back onto the electrode ensuring the black O-
ring is well seated within the electrode body. Do not exert side­ways force. Any excess electrolyte will be expelled from the end of the electrode through the ground junction. Ensure there are no air bubbles in the sleeve.Wash off any excess electrolyte before use.
2.
Fill the annular space with electrolyte to approximately half to three quarter full. 1M potassium nitrate is normally recommended.
Application
The Ionode IJ-Ag sulphide and silver ions (Ag The limit of detection is 0.003 ppm (Sulde), and 0.01 ppm (Silver). The electrode can also be used for low level cyanide and halide titrations.
S Ion selective electrode measures free
2
+
) in aqueous solutions.
Interfering Ions
Mercury ions should be absent. Ions that complex with measured species.
Cleaning
If the membrane is poisoned by interferences, the surface may be renewed by careful polishing with ne wet-and­dry (P1200 grade). The membrane surface should have a polished metallic appearance. Always inspect the membrane before use, and clean if necessary. Organic contaminants can be removed with ethanol. DO NOT use the electrode in chlorinated hydrocarbons.Routinely remove the sleeve and replace the potassium nitrate electrolyte.
Electrolyte Replacement
The electrode has an inbuilt double junction Ag/AgCl with a replaceable sleeve electrolyte. 1M potassium nitrate is suitable for most applications. Please consult Ionode Customer Service if you wish to use a different sleeve electrolyte.
Calibration Standards
Standard solutions should preferably bracket the expected measurement range. Sulphide standards are susceptible to oxidation and are not commercially available; these are to be made fresh and the titer determined by standardisation with Lead Perchlorate or equivalent.
The need for ISA (Ionic Strength Adjuster)
It is important to use ISA, so that the Ionic Strength of standards and samples is independent of the concentration of the measured ion. It is also important for pH adjustment. Use 10M NaOH or SAOB (Sulphide Anti-Oxidant Buffer) for Sulphide determination. Sodium nitrate or similar can normally be used for silver and halide determination.
Calibration Procedure
Before use, the electrode should be calibrated by measuring a series of known standard solutions by serial dilution of stock standard. For sulphide measurement, each decade of concentration will have a theoretical difference of 29mV (@25C). Similarly, for silver determination, the theoretical difference is 59mV. In practice, the measured differences will be less than these values. Acceptable values for slope are -56±4mV for Ag
+
and -28±4mV for S2-.
Other measurement Techniques
An unknown concentration can be determined by adding a small known amount of a concentrated standard to a known volume of sample. Other incremental techniques include sample addition, standard subtraction and analyte subtraction. More details can be obtained from the Theory Section at www.ionode.com
Typical silver calibration curve
Typical sulphide calibration curve
Titration of Chloride
The electrode may also be used as an indicator to follow the progress of a chloride (or other halide) titration using silver nitrate. During the titration, the added silver reacts with the halide ions forming a silver halide precipitate. At the stoichiometric end point, a large potential change occurs as silver ions end up in excess. These titrations may be performed manually or automatically using an automatic titrator.
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