Yasukawa Akemi, Ueda Eiichi, Kandori Kazuhiko, Ishikawa Tatsuo
School of Chemistry, Osaka University of Education, 4-698-1 Asahigaoka, Kashiwara-shi, Osaka 582-8582, Japan.
J Colloid Interface Sci. 2005 Aug 15;288(2):468-74. doi: 10.1016/j.jcis.2005.03.007.
Particles of carbonated barium-calcium hydroxyapatite solid solutions (BaCaHap) with different Ba/(Ba+Ca) (X(Ba)) atomic ratios were prepared by a wet method at 100 degrees C and characterized by various means. The crystal phases and structures of the products strongly depended on the composition of the starting solution, that is, the Ba/(Ba+Ca) atomic ratio ([X(Ba)]) and H3PO4 concentration ([H3PO4]) in the solution. BaCaHap with X(Ba)0.43 could be prepared at [X(Ba)]0.7 by changing [H3PO4], but could never be obtained at [X(Ba)]=0.8-0.95 regardless of [H3PO4]. The carbonated calcium hydroxyapatite particles prepared at [X(Ba)]=0 were fine and short rod-shaped particles (ca. 14x84 nm). With increasing [X(Ba)] from 0 to 0.8, the particles obtained became large spherical agglomerates. The carbonated barium hydroxyapatite particles formed at [X(Ba)]=1 were long rod-shaped agglomerates (ca. 0.2x2 microm) of fine primary particles. The amount of CO2 adsorbed irreversibly on a series of BaCaHaps showed a minimum at (Ba+Ca)/(P+C) atomic ratio of around 1.56, which agreed well with the minimum cation/P ratio obtained for the other hydroxyapatites, as already reported.
通过湿法在100℃下制备了具有不同Ba/(Ba + Ca)(X(Ba))原子比的碳酸钡 - 钙羟基磷灰石固溶体(BaCaHap)颗粒,并采用多种方法对其进行了表征。产物的晶相和结构强烈依赖于起始溶液的组成,即溶液中的Ba/(Ba + Ca)原子比([X(Ba)])和H3PO4浓度([H3PO4])。通过改变[H3PO4],在[X(Ba)]0.7时可以制备出X(Ba)0.43的BaCaHap,但无论[H3PO4]如何,在[X(Ba)] = 0.8 - 0.95时都无法得到。在[X(Ba)] = 0时制备的碳酸羟基磷灰石颗粒细小且呈短棒状(约14×84nm)。随着[X(Ba)]从0增加到0.8,所得颗粒变为大的球形团聚体。在[X(Ba)] = 1时形成的碳酸钡羟基磷灰石颗粒是由细小初级颗粒组成的长棒状团聚体(约0.2×2μm)。一系列BaCaHaps上不可逆吸附的CO2量在(Ba + Ca)/(P + C)原子比约为1.56时显示出最小值,这与已报道的其他羟基磷灰石获得的最小阳离子/P比非常吻合。