User manual EUTECH INSTRUMENTS SODIUM GLASS

[. . . ] Instruction Manual Sodium Electrode EUTECH INSTRUMENTS PTE LTD. INSTRUCTION MANUAL SODIUM ION ELECTRODE Sodium Electrode Instruction Manual TABLE OF CONTENTS GENERAL INSTRUCTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 REQUIRED EQUIPMENT. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 REQUIRED SOLUTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 GENERAL PREPARATION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 ELECTRODE PREPARATION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 ELECTRODE SLOPE CHECK (WITH PH/MV METER) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 ELECTRODE SLOPE CHECK (WITH ION METER) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 MEASUREMENT. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 MEASURING HINTS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 SAMPLE REQUIREMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 UNITS OF MEASUREMENT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 MEASUREMENT PROCEDURE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . [. . . ] A new calibration curve should be prepared daily 7. Direct Measurement of Sodium (using an ion meter) 1. By serial dilution of the 0. 1M or 1, 000 ppm sodium standard, prepare two sodium standards whose concentration is near the expected sample concentration. Add 2 ml of ISA to each 100 ml of standard. Place the more dilute solution on the magnetic stirrer and begin stirring at a constant rate. Assure that the meter is in the concentration mode. Lower the electrode tips into the solution. Adjust the meter to the concentration of the sodium standard and fix the value in the memory according to the meter manufacturer's instructions after stabilization of the reading. Rinse the electrodes with electrode rinse solution and blot dry. Place the more concentrated solution on the magnetic stirrer and begin stirring at a constant rate. Lower the electrode tips into the solution. Adjust the meter to the concentration of the sodium standard and fix the value in the memory according to the meter manufacturer's instructions after stabilization of the reading. For low level measurements, place the rinsed, dried electrodes into a solution containing 100 ml of distilled water and 2 ml of ISA. After stabilization, fix the blank value in the meter according to the meter manufacturer's instructions. Place 100 ml of the sample and 2 ml of ISA in a 150 ml beaker. Place the beaker on the magnetic stirrer, and begin stirring. 2. 3. 4. 5. 6. 7. 8. 5 Sodium Electrode Instruction Manual 9. After rinsing the electrodes and blotting dry, place the electrode tips in the solution and wait for the reading to stabilize. Read the concentration directly from the meter display. The calibration should be checked every two hours. Assuming no change in ambient temperature, place the electrode tips in the first sodium standard. After the reading has stabilized, compare it to the original reading recorded in Step 4 above. A reading difference by more than 0. 5 mV or a change in the ambient temperature will necessitate the repetition of Steps 2-8 (9) above. The meter should be recalibrated daily. 10. Low Level Sodium Determination (using a pH/mV meter) This procedure is recommended for solutions with ionic strength less than 1. 0X10-2M and a sodium concentration less than 1X10-5M or 1 ppm. If the solution is high in ionic strength, but low in sodium, use the same procedure, but prepare a calibration solution with a composition similar to the sample. [. . . ] Electrode charge will be carried unequally across the solution boundary resulting in a potential difference between the two solutions, since ions diffuse at different rates. When making measurements, it is important to remember that this potential be the same when the reference is in the standardizing solution as well as in the sample solution or the change in liquid junction potential will appear as an error in the measured electrode potential. The composition of the liquid junction filling solution in the reference electrode is most important. The speed with which the positive and negative ions in the filling solutions diffuse into the sample should be as nearly equal as possible, that is, the filling solution should be equitransferent. [. . . ]