Kiba Shosuke, Haga Jun-ichi, Hashimoto Sachika, Nakato Teruyuki
Division of Bio-Applications and Systems Engineering, Institute of Symbiotic Science and Technology, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei-shi, Tokyo 184-8588, Japan.
J Nanosci Nanotechnol. 2010 Dec;10(12):8341-8. doi: 10.1166/jnn.2010.2665.
Layered hexaniobate K4Nb6O17 was modified with dodecylammonium ions and octadecyltrimethoxysilane molecules, which were held in the interlayer spaces by electrostatic interactions and covalent attachment to the layers, respectively. Interlayer spacing of the niobate was expanded by incorporation of the bulky organic species. Vapor adsorption isotherms of benzene and water indicated hydrophobic interlayer microenvironments of the organically modified niobates. Both of the modified niobates fairly adsorbed phenol dissolved in water. The photocatalytic activity of hexaniobate allowed the organically modified materials to photocatalytically decompose phenol upon UV irradiation. Decomposition time courses and quantitative analysis of phenol present in the system indicated that the phenol molecules adsorbed on the niobates were preferentially degraded. XRD and IR analyses of the modified niobates indicated that the silylated niobate was more durable than the ion-exchanged sample; the former kept the structure during the photocatalytic process while the latter was partly collapsed.
层状六铌酸钾K4Nb6O17用十二烷基铵离子和十八烷基三甲氧基硅烷分子进行了改性,它们分别通过静电相互作用和与层的共价连接而保持在层间空间中。通过引入庞大的有机物种,铌酸盐的层间距得以扩大。苯和水的蒸汽吸附等温线表明了有机改性铌酸盐的疏水层间微环境。两种改性铌酸盐都能很好地吸附溶解在水中的苯酚。六铌酸盐的光催化活性使有机改性材料在紫外光照射下能够光催化分解苯酚。系统中苯酚的分解时间进程和定量分析表明,吸附在铌酸盐上的苯酚分子优先被降解。改性铌酸盐的XRD和IR分析表明,硅烷化铌酸盐比离子交换样品更耐用;前者在光催化过程中保持结构,而后者部分坍塌。