Effect of metal ions of chlorapatites on the topotaxial replacement by hydroxyapatite under hydrothermal conditions

被引:32
作者
Rendón-Angeles, JC
Yanagisawa, K
Ishizawa, N
Oishi, S
机构
[1] Kochi Univ, Fac Sci, Res Lab Hydrothermal Chem, Kochi 7808520, Japan
[2] Tokyo Inst Technol, Mat & Struct Lab, Yokohama, Kanagawa 2268503, Japan
[3] Shinshu Univ, Dept Environm Sci & Technol, Wakasato, Nagano 3808553, Japan
关键词
chlorapatite; hydrothermal treatment; ion-exchange; metal ion; dissolution-precipitation;
D O I
10.1006/jssc.2000.8888
中图分类号
O61 [无机化学];
学科分类号
070301 [无机化学]; 081704 [应用化学];
摘要
The effect of the metal ions in the chlorapatite structure on the topotaxial conversion to the hydroxyapatite structure was investigated, using three different types of chlorapatite single crystals, calcium, strontium, and barium chlorapatite, The topotaxial conversion to the hydroxyapatite structure was conducted under hydrothermal conditions at a range of temperature from 300 to 800 degreesC for intervals between 3 and 96 h in concentrated KOH solutions. The Cl- ion exchange in the calcium and strontium chlorapatite crystals was completed at 500 and 700 degreesC in a 6.25 M KOH solution, respectively, which resulted in the formation of hydroxyapatite structure. The transformed crystals retained their original shape and dimensions due to the topotaxial transformation. In contrast, the rate of the topotaxial conversion was further reduced on the barium chlorapatite crystals that contain metal ions with large size such as Ba, These crystals were only partially converted to hydroxyapatite even at 800 degreesC in 10 M KOH solution. Under these conditions, a dissolution of ion species of the topotaxially converted barium hydroxyapatite layer was observed, which resulted in the precipitation of new crystals on the surface of the remaining barium chlorapatite crystals. The structure of the new crystals was matched with the hexagonal apatite structure, but a great amount of K was incorporated in the structure. (C) 2000 Academic Press.
引用
收藏
页码:569 / 578
页数:10
相关论文
共 17 条
[1]
Brennan J., 1994, CHEM GEOL, V110, P195
[2]
MECHANISM OF SUBSTITUTION IN CARBONATED APATITES [J].
DRIESSENS, FCM ;
VERBEECK, RMH ;
KIEKENS, P .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 1983, 504 (09) :195-200
[3]
CONVERSION OF SINGLE CRYSTALS OF CHLORAPATITE INTO SINGLE CRYSTALS OF HYDROXYAPATITE [J].
ELLIOTT, JC ;
YOUNG, RA .
NATURE, 1967, 214 (5091) :904-&
[4]
FAVER JR, 1989, GEOCHIM COSMOCHIM AC, V53, P1621
[5]
KINETICS AND MECHANISMS OF REACTIONS OF HUMAN TOOTH ENAMEL IN BUFFERED SOLUTIONS OF HIGH FLUORIDE CONCENTRATIONS [J].
HIGUCHI, WI ;
VALVANI, SC ;
HEFFERREN, JJ .
ARCHIVES OF ORAL BIOLOGY, 1974, 19 (09) :737-746
[6]
HYDROTHERMAL EXCHANGE OF OH-, F- AND CL- IN HYDROTHERMAL APATITES AND THEIR BOUNDING [J].
LATIL, C ;
MAURY, R .
BULLETIN DE LA SOCIETE FRANCAISE MINERALOGIE ET DE CRISTALLOGRAPHIE, 1977, 100 (05) :246-250
[7]
LEGEROS RZ, 1968, B SOC CHIM FR, P1712
[8]
INCORPORATION OF CHLORINE INTO HYDROXYAPATITE [J].
MAITI, GC ;
FREUND, F .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1981, 43 (11) :2633-2637
[9]
MITUYA M, 1999, P JOINT M SOC IN MAT, P42
[10]
Some physico-chemical aspects of hydroxylapatite [J].
Narasaraju, TSB ;
Phebe, DE .
JOURNAL OF MATERIALS SCIENCE, 1996, 31 (01) :1-21