This is an old revision of the document!
An Ion Selective electrode can be thought of as a battery when immersed in a solution. It will develop a voltage relating to the dissolved ion concentration of a particular salt in solution. The Ion meter receives the voltage from the ISE electrode and converts it into a ppm value for display. To be more specific, the circuit compares the voltage from the specific ion electrode to the voltage produced from the reference electrode and displays the difference on the ion concentration meter as a ppm value.
ISE electrodes are available in many shapes and lengths to fit a wide variety of applications. Normally, the sensing electrode has a flat membrane imbedded with a specific ion sensitive material. The membrane is in contact with an internal electrode conductor element (Ag-AgCl) connected to the electrode lead, which is connected to the pH or concentration meter. The voltage, which will develop for the ISE electrode, is a function of the ion sensitive membrane. Response of the electrode may be described as the voltage developed between the inside and the outside of the ion sensitive membrane. The ion sensitive membrane composition will determine the electrode’s response time and its sensitivity to other ions.
As noted, the ISE membrane is a half cell and needs a companion reference electrode half cell to function. A reference electrode consists of a non-conductive body and a liquid junction maintaining contact between the internal electrolyte and external fluid sample being measured. An internal electrode conductor element (Ag-AgCl) immersed in the internal electrolyte is connected to the electrode lead, which is connected to the pH meter. A good reference electrode will produce an output voltage that is very stable. For example, one of the most common reference electrode systems is based on silver/silver chloride/potassium chloride. This reference system consists of a silver wire electrolytically coated with silver chloride or dipped in a paste of silver chloride. This metal/metal salt combination is dipped in a concentrated potassium chloride solution saturated with silver chloride. Contact between the saturated KCl and the measured sample solution, the liquid junction is made through a porous ceramic pin. The voltage which is produced by this system is constant and unaffected by the pH of the sample. The internal filling solution should not contain KCl if it will interfere with the sample, if there is a chance that the liquid junction will clog due to precipitation, or if it is immiscible with the sample. Consort ISE's have a double junction electrode with a second internal junction containing no KCl or a modified internal filling solution can be used. The double junction configuration also isolates the silver ion from direct contact with the sample fluid, decreasing the probability of sample contamination. An electrode using potassium nitrate as an outer reference filling solution is one example. Many other outer fill solutions are known.
Combination ISE’s are advantageous in that they are often less expensive than a pair of individual half-cell electrodes and the more compact geometry allows use in smaller volumes of samples.
The first grouping of ISE’s are the solid state type which have a solid pellet as a sensing membrane connected to a contact wire. There is no inner filling solution and the membrane pellet is virtually insoluble. Pellet composition determines the mV response to ions. This group includes bromide, cadmium, chloride, copper, cyanide, iodide, lead, silver, and sulfide ion selective electrodes.
The second grouping of ISE’s are the PVC membrane type which have an inner filling solution in contact with a PVC membrane. Electrode response is due to the presence of ion-exchange material imbedded in the PVC sponge. Certain ion exchangers are selective for certain ions. This group includes ammonium, calcium, fluoroborate, nitrate, perchlorate, potassium, surfactant, and water hardness ion selective electrodes.
The third grouping of ISE’s are the glass/crystal membrane type which have an inner filling solution in contact with a glass/crystal membrane. The chemical composition of the glass/crystal make it respond to specific ions by creating a certain mV potential. The most recognizable and most frequently used ISE electrode of this type is the Fluoride electrode. Sodium ISE's also fall into this category.
The final grouping of replaceable membrane ISE’s are the gas sensing membrane type which include ammonia, carbon dioxide, and nitrogen oxide electrodes. Gas Sensors have a gas-permeable membrane separating the sample from a special internal fill solution. Gas diffuses across the membrane, reacts with the solution, and causes a change in solution pH. The pH change is measured with the internal pH element and corresponds to the gas concentration.
Considering all the analytical tools available, why choose ISE’s? They can be used from 0.1 to 10,000 ppm, have advantages over colorimetric or gravimetric methods, and the electrode bodies are shock-proof and chemically-resistant. Electrodes, once calibrated, can monitor concentration continuously, analyze the sample within 1 to 2 minutes, and be placed in samples without sample pretreatment or destruction of the sample. Best of all, electrodes are inexpensive and great screening tools for identifying dissolved salts in samples.
Consort has for all ISE's the option to choose between a sealed version or a refillable version with replaceable membrane. Both versions are similarly constructed as a combination electrode of a double junction reference electrode with a specific Ion sensitive membrane. The main differences are:
The sealed electrodes will have a durability for the life of either the reference electrode or either the life of the ion sensitive membrane. The life of the replaceable types can be extended when the membranes are worn, not when the reference electrode is polluted or worn.