Suppr超能文献

磷酸及磷酸钛官能化的MCM-41的合成、结构与酸性性质

Synthesis, structure, and acidic properties of MCM-41 functionalized with phosphate and titanium phosphate groups.

作者信息

Kovalchuk T V, Sfihi H, Korchev A S, Kovalenko A S, Il'in V G, Zaitsev V N, Fraissard J

机构信息

Kiev National T. Shevtchenko University, Chemistry Department, 60, Vladimirskaya str., Kiev 01033 Ukraine.

出版信息

J Phys Chem B. 2005 Jul 28;109(29):13948-56. doi: 10.1021/jp0580625.

Abstract

Mesoporous molecular sieves Si-MCM-41 (purely siliceous) and Ti-MCM-41 (partly covered with a surface layer of TiO2) were functionalized with phosphate groups by treatment with POCl3 (denoted -MCM-41(P)and Ti-MCM-41(P), respectively). With the use of TEM, X-ray diffraction, and N2 adsorption, it was shown that the initial hexagonal structure, the high specific surface area, and porosity are retained in the functionalized materials but are not as good as in the starting materials. 1H MAS NMR and 31P MAS NMR revealed that the surface of Si-MCM-41(P) consists of silicon phosphate and pyrophosphate species. That of Ti-MCM-41(P) additionally contains titanium dihydro-, hydro-, and pyrophosphate species, the latter being predominant. TPD of adsorbed ammonia for Si-MCM-41(P) and Ti-MCM-41(P) showed that functionalization leads to the creation of moderate and strong acid sites. A combination of mesoporous structure with acidic properties makes the MCM-41 functionalized with phosphate groups promising for use as solid acid catalysts.

摘要

介孔分子筛Si-MCM-41(纯硅质)和Ti-MCM-41(部分覆盖有TiO₂表面层)通过用POCl₃处理进行磷酰化官能团化(分别记为-MCM-41(P)和Ti-MCM-41(P))。通过透射电子显微镜(TEM)、X射线衍射和N₂吸附表明,官能团化材料保留了初始的六方结构、高比表面积和孔隙率,但不如起始材料。¹H 魔角旋转核磁共振(¹H MAS NMR)和³¹P 魔角旋转核磁共振(³¹P MAS NMR)表明,Si-MCM-41(P)的表面由磷酸硅和焦磷酸物种组成。Ti-MCM-41(P)的表面还额外含有二氢钛、氢钛和焦磷酸钛物种,其中焦磷酸钛物种占主导。Si-MCM-41(P)和Ti-MCM-41(P)吸附氨的程序升温脱附(TPD)表明,官能团化导致产生了中等强度和强酸性位点。介孔结构与酸性性质的结合使得磷酰化官能团化的MCM-41有望用作固体酸催化剂。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验