Ana Maria Oliveira-Brett

Prof. Ana Maria Oliveira-Brett

orcid

Research Focus & Metrics

Academic Career Length

43Years (1984-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2018 in Applied Materials Today
Verified
Journal Article
Closed access
LTLuciana I.N. Tomé
Luciana I.N. Tomé
VBVanessa Baião
Vanessa Baião
WSWanderson da Silva
Wanderson da Silva
CBChristopher Brett
Christopher Brett

1 January 2002 in Pure and Applied Chemistry
Verified
Journal Article
Closed access
PDF file
RBR. P. Buck
R. P. Buck
Sandra RondininiSandra Rondinini
Sandra Rondinini
ACA. K. Covington
A. K. Covington
FBF. G. K. Baucke
F. G. K. Baucke
CBChristopher Brett
Christopher Brett
GWG. S. Wilson
G. S. Wilson
The definition of a “primary method of measurement ” has permitted a full consideration of the definition of primary standards for pH, determined by a primary method (cell without transference, Harned cell), of the definition of secondary standards by secondary methods, and of the question whether pH, as a conventional quantity, can be incorporated within the internationally accepted system of measurement, the International System of Units (SI, Système International d’ Unités). This approach has enabled resolution of the previous compromise IUPAC 1985 Recommendations [Pure Appl. Chem. 57, 531 (1985)]. Furthermore, incorporation of the uncertainties for the primary method, and for all subsequent measurements, permits the uncertainties for all procedures to be linked to the primary standards by an unbroken chain of comparisons. Thus, a rational choice can be made by the analyst of the appropriate procedure to achieve the target uncertainty of sample pH. Accordingly, this document explains IUPAC recommended definitions, procedures, and terminology relating to pH measurements in dilute aqueous solutions in the temperature range 5-50 °C. Details are given of the primary and secondary methods for measuring pH and the rationale for the assignment of pH values with appropriate uncertainties to selected primary and secondary substances.

1 May 2011 in Journal of Electroanalytical Chemistry
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Journal Article
Closed access
Teodor Adrian EnacheTeodor Adrian Enache
Teodor Adrian Enache
AOAna Maria Oliveira-Brett
Ana Maria Oliveira-Brett

1 June 2015 in Analytica Chimica Acta
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Journal Article
Closed access
Madalina BarsanMadalina Barsan
Madalina Barsan
Mariana Emilia GhicaMariana Emilia Ghica
Mariana Emilia Ghica
CBChristopher Brett
Christopher Brett

1 August 2004 in Analytica Chimica Acta
Verified
Journal Article
Closed access
PJPatricia Janeiro
Patricia Janeiro
AOAna Maria Oliveira-Brett
Ana Maria Oliveira-Brett

23 February 2022 in Molecules
Verified
Journal Article
Open access
PDF file
CBChristopher Brett
Christopher Brett
Electrochemical impedance spectroscopy is finding increasing use in electrochemical sensors and biosensors, both in their characterisation, including during successive phases of sensor construction, and in application as a quantitative determination technique. Much of the published work continues to make little use of all the information that can be furnished by full physical modelling and analysis of the impedance spectra, and thus does not throw more than a superficial light on the processes occurring. Analysis is often restricted to estimating values of charge transfer resistances without interpretation and ignoring other electrical equivalent circuit components. In this article, the important basics of electrochemical impedance for electrochemical sensors and biosensors are presented, focussing on the necessary electrical circuit elements. This is followed by examples of its use in characterisation and in electroanalytical applications, at the same time demonstrating how fuller use can be made of the information obtained from complete modelling and analysis of the data in the spectra, the values of the circuit components and their physical meaning. The future outlook for electrochemical impedance in the sensing field is discussed.