Unified pH measurement

Agnes Heering, Ivo Leito, Markus Lahe, Martin Vilbaste

Published: 2021-09-25 DOI: 10.17504/protocols.io.bybxpspn

Abstract

The purpose of this document is to present technical guidance of measuring pHabsH2O difference (ΔpHabsH2O value) between two solutions by differential potentiometry in a cell with two compartments connected by a salt bridge filled with an ionic liquid.

Before start

Turn on the thermostat and electrometer at least half an hour before starting the work.

Steps

Software

1.

Start Quick IV Measurement Software.

Note
Computer cannot go to sleep during measurements or the communication between computer and instruments is lost and data collection stops.

2.

On the left hand pick Function “Source & Sampling”.

Position of the Function choice “Source & Sampling”.
Position of the Function choice “Source & Sampling”.

Note
Alternatively, open previously saved QIVM file with measurement settings.

3.

Right hand side click on tab “Channel Communication”. Click on “Search Channels”, which opens a new window. Select USB interface and search for the channel. After the search click on the channel name to choose the channel and close the window.

Position of the tabs “Channel Communication” and “Search Channels”.
Position of the tabs “Channel Communication” and “Search Channels”.

Note
This must be done every time the program is started.

4.

Settings can be saved as QIVM file, which can be used for measurements. The saved file can be opened under tab “File”. The settings will remain the same between the measurements if the program is not closed.

Program settings.
Program settings.

Filling the cell

5.
Cell from Gebr. Rettberg GmbH.
Cell from Gebr. Rettberg GmbH.

25.0°C

Equipment

ValueLabel
VistaShieldNAME
Faraday cageTYPE
GamryBRAND
VistaShieldSKU
https://www.gamry.com/LINK

Equipment

ValueLabel
UT cellNAME
Special water-jacketed glass cellTYPE
RettbergBRAND
Glass cellSKU
https://www.rettberg.biz/en/LINK

Equipment

ValueLabel
U2cNAME
ThermostatTYPE
MLWBRAND
U2cSKU

Note
The side ports must be open.

6.

Fill capillary with a syringe or pipette with the ionic liquid, so that the level of ionic liquid is 1 mm to 2 mm below the bottoms of the measurement compartments.0.1mL

Note
Ionic liquid has high viscosity, therefore flows very slowly, and can leave a film on the wall of the pipette tip or syringe during dispense.

7.

The test solutions are added simultaneously to both compartments, raising solution levels in the compartments synchronously.20mL

Note
Equal amount by weight (not volume!) of solutions must be used. The volume of the lighter solution is calculated from the weight of the heavier solution using the densities of the two solutions in hand. This is especially important for solutions containing acetonitrile.

Note
Minimum volume that can be used is 13 ml.
One option how to fill the cell. This configuration gives positive ΔpH values. Figure shows connections to a pH meter, a potentiostat and an electrometer.
One option how to fill the cell. This configuration gives positive ΔpH values. Figure shows connections to a pH meter, a potentiostat and an electrometer.

8.

After adding the test solutions, the air bubbles are removed from the capillary ends with a syringe or a pipette.

9.

Insert electrodes one-by-one.

Equipment

ValueLabel
EST-0601NAME
Glass electrode half-cellTYPE
Izmeritelnaya tekhnikaBRAND
EST-0601SKU
9.1.

Electrode is rinsed with water, gently dried, and then rinsed with solution to be measured.

10.

Connect electrodes to the instrument.

Equipment

ValueLabel
B2987A Electrometer / High Resistance MeterNAME
ElectrometerTYPE
KeysightBRAND
B2987ASKU
10.1.

Crocodile clips are as following:

red is signal and connects to ISE1,

black is shield and is connected to ISE2 and

green is guard. Green stays unused.

Connections to electrodes.
Connections to electrodes.

Note
Cable goes through the port in Faraday cage. Electrometer is not in the Faraday cage.

Equipment

ValueLabel
N1415A Triax to Alligator CableNAME
CableTYPE
Keysight TechnologiesBRAND
N1415ASKU

Measurement

11.

Start the measurement by clicking on the "Measure" button on the upper panel.

12.

Data collection. Point is taken at 10 s interval.

13.

Save data. Files are named as Date_ISE1_Solution1_vs_ISE2_solution2.

Note
SAVE THE FILE BEFORE NEW MEASUREMENT! Otherwise, data is lost. Data is given in volts and seconds.

13.1.

Go to table view, right click on the table, choose “Export as CSV…” and save the results. The data can be automatically imported into excel file while measuring or after (both under “Excel Navigation”), but this causes constant shift in the comma position.

Washing

14.

Remove the electrodes, rinse them and put them in storage solution.

15.

Remove the solutions.

16.

Rinse the cell with small amount of ethanol5mL

17.

Rinse three times with plenty of water20mL

18.

Rinse once with acetone to ease the drying. 5mL

19.

Dry cell with compressed air.

Data analysis

20.

Points from 30 min to 60 min are used for analysis.Points from 30 min to 60 min are used for analysis.Points from 30 min to 60 min are used for analysis.

Example of a good graph with non-aqueous system.
Example of a good graph with non-aqueous system.
21.

Take the average of the chosen data points.

22.

ΔpH = Δ E / average slope of the glass electrodes

Calibration of glass electrode half-cells

23.

Insert the ΔpH into the ladder.

Note
Symmetry 2020 , 12 (7), 1150; Symmetry 2020, 12 (7), 1150; https://doi.org/10.3390/sym12071150

Mesurement

24.

Repeat with a new pair of solutions.

25.

Repeat the data analysis with all the measured potentials.

26.

Insert the data into the ladder.

27.

Do the minimization process.

Note
Symmetry 2020 , 12 (7), 1150; Symmetry 2020, 12 (7), 1150; https://doi.org/10.3390/sym12071150

28.

Obtain the pH values for all the measured solutions from the minimization process.

29.

Calculate uncertainty.

Note
Analytica Chimica Acta , 2021 , 1182, 338923, Analytica Chimica Acta, 2021, 1182, 338923, doi.org/10.1016/j.aca.2021.338923

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