Scanning electrochemical microscopy as a quantitative probe of acid-induced dissolution: theory and application to dental enamel
McGeouch, Carrie-Anne, Edwards, Martin A., Mbogoro, Michael M., Parkinson, Charles and Unwin, Patrick R.. (2010) Scanning electrochemical microscopy as a quantitative probe of acid-induced dissolution: theory and application to dental enamel. Analytical Chemistry, Vol.82 (No.22). pp. 9322-9328. ISSN 0003-2700Full text not available from this repository.
Official URL: http://dx.doi.org/10.1021/ac101662h
This Article reports the use of scanning electrochemical microscopy (SECM) for the quantitative study of acid-induced dissolution. An ultramicroelectrode (UME) is used to generate a flux of protons galvanostatically just above a sample surface, creating controlled acid challenges relevant to acid erosion. The electrochemical technique produces etch features in the sample, which are characterized by white light interferometry (WLI). The technique has been applied to bovine enamel where understanding the kinetics of dissolution is important in the context of acid erosion. Dissolution has been observed as a fast process, but the high rates of mass transport in SECM allow the surface kinetics of dissolution to be evaluated. Key attributes of SECM for these studies are the ability to deliver high, controllable, and local acid challenges in a defined way and that multiple dissolution measurements can be performed on one sample, eliminating intersample variability effects. A novel moving boundary finite element model has been designed to describe the etching process, which allows the etch kinetics to be evaluated quantitatively, simply by measuring the size and shape of etch features over time.
|Item Type:||Journal Article|
|Subjects:||Q Science > QD Chemistry|
|Divisions:||Faculty of Science > Molecular Organisation and Assembly in Cells (MOAC)|
|Journal or Publication Title:||Analytical Chemistry|
|Publisher:||American Chemical Society|
|Date:||15 November 2010|
|Number of Pages:||7|
|Page Range:||pp. 9322-9328|
|Access rights to Published version:||Restricted or Subscription Access|
|Funder:||Engineering and Physical Sciences Research Council (EPSRC), GlaxoSmithKline, European Regional Development Fund (ERDF)|
Actions (login required)