Sugimoto Tadao, Zhou Xingping, Muramatsu Atsushi
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Katahira 2-1-1, Aobaku, Sendai 980-8577, Japan.
J Colloid Interface Sci. 2002 Aug 15;252(2):339-46. doi: 10.1006/jcis.2002.8454.
The mole fractions of hydroxo complexes of titanium(IV) ion in an aqueous solution with 0.10 mol dm(-3) NaClO4 at 25 degrees C have been determined as a function of pH by a newly developed analytical procedure based on UV spectrophotometry, using a metastable homogeneous solution of 1.25 x 10(-4) mol dm(-30 in total concentration of Ti(IV). Also, the total concentration of the hydroxo complexes in equilibrium with Ti(OH)4 solid, or the solubility of Ti(OH)4 solid in an inhomogeneous system, has been obtained by ICP measurement for the solution phase. A combination of these data yielded the absolute concentration of each complex species in equilibrium with Ti(OH)4 solid. Finally, Ti(OH)+3 complex has been assigned to the precursor for the formation of anatase TiO2 nanoparticles transformed from Ti(OH)4 gel from a comparison between the above equilibrium data and a kinetic study on the formation rate of the anatase TiO2 particles in the gel-sol system.
在25℃下,通过一种基于紫外分光光度法新开发的分析程序,测定了在含有0.10 mol dm⁻³ NaClO₄的水溶液中,钛(IV)离子羟基配合物的摩尔分数与pH的函数关系,该程序使用了总浓度为1.25×10⁻⁴ mol dm⁻³的Ti(IV)的亚稳态均相溶液。此外,通过对溶液相进行电感耦合等离子体测量,获得了与Ti(OH)₄固体处于平衡状态的羟基配合物的总浓度,即Ti(OH)₄固体在非均相体系中的溶解度。这些数据相结合,得出了与Ti(OH)₄固体处于平衡状态的每种配合物物种的绝对浓度。最后,通过比较上述平衡数据与凝胶-溶胶体系中锐钛矿TiO₂颗粒形成速率的动力学研究,确定Ti(OH)₃⁺配合物是由Ti(OH)₄凝胶转变而来的锐钛矿TiO₂纳米颗粒形成的前体。