JDR JDR Most Cited Articles
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Misra, D. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Misra, D. N.

Journal of Dental Research, Vol 75, 1418-1425, Copyright © 1996 by International & American Associations for Dental Research Online Journals


ARTICLES

Interaction of citric acid with hydroxyapatite: surface exchange of ions and precipitation of calcium citrate

D. N. Misra
American Dental Association Health Foundation, Paffenbarger Research Center, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA.

The use of citric acid is efficacious and distinctive in the demineralization of dentinal root surfaces for periodontal regeneration and in the etching and conditioning of enamel or dentin for bonding restorative resins. To decipher the role of citric acid in these applications, it is important that one have a basic understanding of its interaction with synthetic hydroxyapatite. The uptake or removal of citrate ions from aqueous solutions of citric acid (4 to 100 mmol/L, 10 mL) by hydroxyapatite (1 g) was studied at 22 degrees C after a given reaction period (from 3 hr to 11 days) by immediate spectrophotometric monitoring of the concentrations of the filtrates (214 nm). The concentrations of calcium, phosphate, and hydrogen ions were also determined in the same solutions. The interaction: (i) is a time-independent ionic-exchange process with the substrate when the initial acid concentrations are dilute (4 to 12.5 mmol/L), and (ii) is a reactive process that is time-dependent for higher acid concentrations. The exchange process shows an adsorption of about one citrate ion per (100) face of the unit cell of hydroxyapatite for a maximally exchanged surface. The curves representing the reactive process may be quantitatively or qualitatively explained on the basis of the supersaturation of the solutions with respect to calcium citrate and its slow precipitation. The physico-chemical analysis of the needle-shaped birefringent crystals of the precipitate from the supersaturated solutions confirms the precipitate to be Ca3(citrate)2.4H2O.


This article has been cited by other articles:


Home page
Soil Sci.Home page
B. Sutter, L. R. Hossner, and D. W. Ming
Dissolution Kinetics of Iron-, Manganese-, and Copper-Containing Synthetic Hydroxyapatites
Soil Sci. Soc. Am. J., March 1, 2005; 69(2): 362 - 370.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
IADR Journals Advances in Dental Research ®
Journal of Dental Research ® Critical Reviews (1990-2004)
Copyright © 1996 Institutional Access Guidelines