1985
DOI: 10.1351/pac198557030531
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Definition of pH scales, standard reference values, measurement of pH and related terminology (Recommendations 1984)

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Cited by 314 publications
(136 citation statements)
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“…A second factor to be noted whilst studying the effect of temperature on the AQ reduction wave is how the pH of the solution will vary with temperature, as the dissociation constants of the components of the buffer solutions vary as the temperature is changed. Therefore, four IUPAC standard buffers (pH 1.5, 4.6, 6.2 and 9.2) were utilised in these studies which have a known pH at a set of temperatures [25]. The corresponding square wave voltammograms obtained in both pH 4.6 (acetate buffer) and pH 9.2 (borax buffer) over a range of temperatures from 20 to 70 8C are detailed in Fig.…”
Section: Voltammetric Response Of Aqcarbon At Elevated Temperature Frmentioning
confidence: 99%
“…A second factor to be noted whilst studying the effect of temperature on the AQ reduction wave is how the pH of the solution will vary with temperature, as the dissociation constants of the components of the buffer solutions vary as the temperature is changed. Therefore, four IUPAC standard buffers (pH 1.5, 4.6, 6.2 and 9.2) were utilised in these studies which have a known pH at a set of temperatures [25]. The corresponding square wave voltammograms obtained in both pH 4.6 (acetate buffer) and pH 9.2 (borax buffer) over a range of temperatures from 20 to 70 8C are detailed in Fig.…”
Section: Voltammetric Response Of Aqcarbon At Elevated Temperature Frmentioning
confidence: 99%
“…This should avoid the confusion that would be caused by several inconsistent pH scales. This work will necessarily involve a reevaluation of the presently accepted definitions and conventions incorporated in the pH values of the SRMs issued by NBS and of the recommended standards of organizations such as the International Union of Pure and Applied Chemistry [31].…”
Section: Resultsmentioning
confidence: 99%
“…that the difference in electric potential between the electrode solution and buffer solution is the same as that between the electrode solution and sample solution (Covington, 1985). This error is referred to as liquid junction error and has been discussed in several articles describing the potentiometric measurement of pH (Dickson et al, 2007;Illingworth, 1981;Easley and Byrne, 2012).…”
Section: D Macleod Et Al: Technical Note 719mentioning
confidence: 99%