The history and development of a rigorous metrological basis for pH measurements

• Published in: Journal of solid state electrochemistry 2011, Vol.15 (1), p.69-76
• Main Authors: Spitzer, Petra, Pratt, Kenneth W.
• Format: Article
• Language: English
• Subjects: Analytical Chemistry; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Condensed Matter Physics; Electrochemistry; Energy Storage; Physical Chemistry; Review
• ISSN: 1432-8488; 1433-0768
• DOI: 10.1007/s10008-010-1106-9

This paper discusses the basis and historical development of the traceability chain for pH. The quantity pH, first introduced in 1909, is among the most frequently measured analytical quantities. The practical measurement of the pH value of a sample is inexpensive, easy to perform, and yields a rapid result. However, the problems posed by the traceability of pH are not easy to solve. Most pH measurements are performed by potentiometry, using a glass electrode as the pH sensor. Such pH electrodes must be calibrated at regular intervals. Confidence in the reliability of pH measurements requires establishment of a metrological hierarchy including an uncertainty budget for calibration that links the pH measured in the sample to an internationally agreed and stated reference. For pH, this reference is the primary measurement of pH. A traceability chain can be established that links field measurements of pH to primary buffer solutions that are certified using this primary method. This allows the user in the field to estimate the measurement uncertainty of the measured pH data. As the realization of the primary measurement is sophisticated and time-consuming, primary standards are generally realized at national metrology institutes. A number of potentiometric methods are suitable for the determination of the pH of reference buffer solutions by comparison with the primary standard buffers. The choice between the methods should be made according to the uncertainty required for the application. For reference buffer solutions that have the same nominal composition as the primary standard, the differential potentiometric cell, often called the Baucke cell, is recommended.