研究论文

以硫酸钛为前驱体的简单溶胶-凝胶法合成纳米多孔二氧化钛粉末

  • 张新;吴俊升;肖葵;周建龙;杨仁春;李晓刚
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  • 1. 环境保护部核与辐射安全中心,北京 100082;2. 北京科技大学新材料技术研究院,北京 100083;3. 安徽工程大学生物与化学工程学院,安徽芜湖 241000

收稿日期: 2012-07-25

  修回日期: 2012-08-18

  网络出版日期: 2012-09-28

Simple Sol-Gel Route for Preparation of Nanosized Porous TiO2 Powders Using Inorganic Precursor

  • ZHANG Xin;WU Junsheng;XIAO Kui;ZHOU Jianlong;YANG Renchun;LI Xiaogang
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  • 1. Nuclear and Radiation Safety Center, Ministry of Environmental Protection, Beijing 100082, China;2. Advanced Materials and Technology Institute, University of Science and Technology Beijing, Beijing 100083, China;3. College of Biological and Chemical Engineering, Anhui Polytechnic University, Wuhu 241000, China

Received date: 2012-07-25

  Revised date: 2012-08-18

  Online published: 2012-09-28

摘要

以无机硫酸钛溶液为前驱体,甲酰胺为pH值调节剂,本文采用简单溶胶-凝胶法合成纳米多孔的TiO2粉末。运用X射线衍射(XRD)、扫描电镜(SEM)、透射电镜(TEM)和氮吸附脱附(N2 Adsorption/Desorption)等方法对合成的TiO2粉末进行了表征。结果表明,合成的TiO2粉末具有高的热稳定性,450—750℃的温度范围内焙烧后为单一的锐钛矿相结构,且850℃焙烧后主要相为锐钛矿相。随着焙烧温度的升高,TiO2粉末的晶粒长大,比表面积减少。550℃焙烧后的TiO2粉末是由平均晶粒尺寸约为10nm的颗粒聚集而成,其比表面积约为219.70m2·g-1,并且具有独特的双孔结构。

本文引用格式

张新;吴俊升;肖葵;周建龙;杨仁春;李晓刚 . 以硫酸钛为前驱体的简单溶胶-凝胶法合成纳米多孔二氧化钛粉末[J]. 科技导报, 2012 , 30(27) : 58 -60 . DOI: 10.3981/j.issn.1000-7857.2012.27.009

Abstract

NThe nanosized porous TiO2 powders were synthesized by using the titanium sulfate solution through a simple sol-gel route, where the formamide was used as the pH adjusting agent. The X-ray diffraction, the scanning electron microscopy, the transmission electron microscopy and the N2 Adsorption/Desorption were used to analyze the prepared samples. The results show that the prepared TiO2 powders have a high thermal stability and maintain as a monophasic anatase in cases of calcination from 450℃ to 750℃, furthermore, the main crystalline phase remains as that of anatase even at 850℃. The crystalline grains of TiO2 powders grow larger and the specific surface area is reduced with enhancing the calcination temperature. The microstructure of TiO2 powders is that of aggregation of nanocrystalline with diameter of approximately 10 nm in case of calcination at 550℃. The specific surface area of the prepared samples is approximately 219.70m2·g-1 after calcinating at 550℃ and there is a specific bimodal pore structure in the prepared samples.
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