首页 | 本学科首页   官方微博 | 高级检索  
     检索      

硫辅助合成高孔隙率大孔氮化硼材料
引用本文:孙常慧,徐立强,马小健,钱逸泰.硫辅助合成高孔隙率大孔氮化硼材料[J].无机化学学报,2012,28(3):601-606.
作者姓名:孙常慧  徐立强  马小健  钱逸泰
作者单位:山东大学胶体与界面化学教育部重点实验室,济南,250100
基金项目:国家自然科学基金(No.20871075和20971079);973计划(No.2011CB935901)资助项目
摘    要:采用硫粉辅助的方法合成了具有一定有序孔洞结构的三维大孔氮化硼材料,具有高比表面积(230 m2.g-1)和高孔隙率(85.6%),并呈现开孔结构。在未加入硫粉的情况下则只形成完全无序的三维大孔氮化硼,并且比表面积和孔隙率分别降至122m2.g-1和73.7%。热重测试表明两种产品均具有良好的抗氧化性能。本文还对这种大孔材料的形成过程和硫粉的作用进行了初步的探讨。

关 键 词:氮化硼  大孔  孔隙率

Sulfur-Assisted Synthesis of Highly Porous Macroporous Boron Nitride Materials
SUN Chang-Hui,XU Li-Qiang,MA Xiao-Jian and QIAN Yi-Tai.Sulfur-Assisted Synthesis of Highly Porous Macroporous Boron Nitride Materials[J].Chinese Journal of Inorganic Chemistry,2012,28(3):601-606.
Authors:SUN Chang-Hui  XU Li-Qiang  MA Xiao-Jian and QIAN Yi-Tai
Institution:Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, China,Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, China,Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, China and Key Laboratory of Colloid and Interface Chemistry, Shandong University, Ministry of Education, Jinan 250100, China
Abstract:Three-dimensional(3D) macroporous boron nitride materials with a certain order of pore arrangements have been synthesized in the existence of sulfur powders.The as-obtained materials exhibit open macropores with high specific surface area of 230 m2·g-1 and high porosity of 85.6%.Without addition of sulfur disordered 3D macroporous boron nitride was formed only and its specific surface area and porosity were decreased to 122 m2·g-1 and 73.7%,respectively.Both of the products obtained with and without addition of sulfur show good oxidation resistance below 800 ℃.The formation process and the role of sulfur powders were studied.
Keywords:boron nitride  macroporous  porosity
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《无机化学学报》浏览原始摘要信息
点击此处可从《无机化学学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号