The dissolution of Mg in C1-, F-, and OH-containing aqueous solutions has been investigated over a large potential range, from far into H, evolution at -3000 mV (see) to the passive state at -1400 mV (see). The steady state current-potential and the impedance have been measured using a new automa& e
Directional/acidic dissolution kinetics of (OH,F,Cl)-bearing apatite
✍ Scribed by Wan-Ju Tseng; Chung-Cherng Lin; Po-Wen Shen; Pouyan Shen
- Book ID
- 102872086
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 722 KB
- Volume
- 76A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
Directional dissolution of a natural (OH,F,Cl)‐bearing apatite has been studied at various solution pH values (0–3) and 30°C. This apatite showed abnormally high OH stretching frequencies due to the substitution of Cl for OH. The advance of dissolution front indicated that steady‐state directional dissolution for pH = 0–2 followed an apparent rate law of Rate = ka (in mole/m^2^h), where the rate constants (k) are 2.15 and 1.61; and the rate orders (n) are 1.44 and 1.30 for [0001] and <1120> directions, respectively. Previous study, however, indicated a smaller n value (n = 0.55–0.70) for fluorapatite powders at higher pHs. A nonlinear pH dependence of logarithmic dissolution rate at a wide pH range implied that the surface active sites and/or rate‐determining steps have changed when the acidity of solution and/or the composition of the apatite were changed. The opening of etch pits on basal planes further indicated that the dissolution rates along the three principal directions have the following relationship: [0001] > <1120> > <1010> for pH=0–1, but the order was reversed for pH > 3. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
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