Kinetics of dissolution of beta-tricalcium phosphate

被引:33
作者
Bohner, M
Lemaitre, J
Ring, TA
机构
[1] SWISS FED INST TECHNOL,POWDER TECHNOL LAB,EPFL,LTP,MX ECUBLENS,CH-1015 LAUSANNE,SWITZERLAND
[2] UNIV UTAH,DEPT CHEM & FUELS ENGN,SALT LAKE CITY,UT 84112
关键词
beta-tricalcium phosphate; kinetics; dissolution; pH; saturation;
D O I
10.1006/jcis.1997.4846
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
The rate of dissolution of beta-tricalcium phosphate (beta-Ca-3(PO4)(2); beta-TCP) has been measured in the solution system Ca(OH)(2)H3PO4-NaOH-HNO3-H2O. The effects of different parameters such as pH, temperature, time, and saturation have been investigated, At zero saturation, the logarithm of the dissolution rate is a linear function of the pH (log(j(0)) = 2.02 - 0.82 pH; r(2) = 0.993; in mmol/m(2)s), indicating diffusion-limited dissolution, A simple calculation of the theoretical rate of a diffusion-controlled process showed that our data are consistent with theory, Moreover, the activation energy for this process is low (E-act = 3.9 kcal/mol) also suggesting that the beta-TCP dissolution is controlled by diffusion processes, At increased saturation, the initial beta-TCP dissolution rate decreases much faster than that predicted assuming a diffusion-controlled model, However, this latter model gives a good prediction of the results if it is assumed that beta-TCP dissolution is controlled by the dissolution of an interfacial layer of hydroxyapatite (Ca-5(PO4)(3)OH;HAp): log(j)= -1.47 + 1.34 log(1 - S-HAp); r(2) = 0.959. The beta-TCP dissolution rate decreases very sharply with time, This effect increases at higher pH or saturation, Several explanations are proposed and discussed, even though none is conclusive. (C) 1997 Academic Press.
引用
收藏
页码:37 / 48
页数:12
相关论文
共 54 条
[1]
CRYSTAL-GROWTH AS A FUNCTION OF SEED SURFACE-AREA [J].
BARONE, JP ;
NANCOLLAS, GH ;
YOSHIKAWA, Y .
JOURNAL OF CRYSTAL GROWTH, 1983, 63 (01) :91-96
[2]
Bohner M., 1993, 3 EUROCERAMICS, P95
[3]
BOHNER M, 1993, THESIS SWISS FEDERAL
[4]
KINETICS OF HYDROXYAPATITE FORMATION AT LOW-TEMPERATURE [J].
BROWN, PW ;
FULMER, M .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1991, 74 (05) :934-940
[5]
Budz J A, 1987, Adv Dent Res, V1, P314
[6]
THE MECHANISM OF DISSOLUTION OF HYDROXYAPATITE AND CARBONATED APATITE IN ACIDIC SOLUTIONS [J].
BUDZ, JA ;
NANCOLLAS, GH .
JOURNAL OF CRYSTAL GROWTH, 1988, 91 (04) :490-496
[7]
Chander S., 1984, ADSORPTION SURFACE C, P29
[8]
THE KINETICS OF DISSOLUTION OF TOOTH ENAMEL - A CONSTANT COMPOSITION STUDY [J].
CHEN, WC ;
NANCOLLAS, GH .
JOURNAL OF DENTAL RESEARCH, 1986, 65 (05) :663-668
[9]
DISSOLUTION OF FLUORAPATITE - A CONSTANT-COMPOSITION KINETICS STUDY [J].
CHIN, KOA ;
NANCOLLAS, GH .
LANGMUIR, 1991, 7 (10) :2175-2179
[10]
KINETICS OF DISSOLUTION OF CALCIUM HYDROXYAPATITE .4. THE EFFECT OF SOME BIOLOGICALLY IMPORTANT INHIBITORS [J].
CHRISTOFFERSEN, J ;
CHRISTOFFERSEN, MR .
JOURNAL OF CRYSTAL GROWTH, 1981, 53 (01) :42-54