Effect of reaction temperature on grafting of γ-aminopropyl triethoxysilane (APTES) onto kaolinite

被引:113
作者
Yang, Shu-qin [1 ,2 ]
Yuan, Peng [1 ]
He, Hong-ping [1 ]
Qin, Zong-hua [1 ,2 ]
Zhou, Qing [1 ,2 ]
Zhu, Jian-xi [1 ]
Liu, Dong [1 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Mineral & Metallogeny, Guangzhou Inst Geochem, Guangzhou 510640, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Kaolinite; gamma-Aminopropyl triethoxysilane; Grafting; ORGANIC DERIVATIVES; AMINO-SILANE; SURFACE; MONTMORILLONITE; INTERCALATION; WATER; FUNCTIONALIZATION; ALKYLAMINES; LAPONITE; DIMETHYL;
D O I
10.1016/j.clay.2012.04.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The effect of the temperature (175, 185, 195 and 220 degrees C) on the grafting of gamma-aminopropyl triethoxysilane (APTES) on the interlayer hydroxyl groups of kaolinite pre-intercalated with DMSO were investigated using Fourier transform infrared spectroscopy, X-ray diffraction, thermal analysis and elemental analysis. The ARIES-modified kaolinite prepared at 220 degrees C showed a structure with high content of APTES and high thermal stability, in which the APTES molecules were grafted on to the inner-surface hydroxyl groups of kaolinite and arranged in the form of cross-linked monolayers. The ARIES-modified kaolinites prepared at 175, 185 and 195 degrees C exhibited inhomogeneous interlayer structure with pseudo-bilayer arrangements composed of grafted APTES molecules and hydrogen-bound DMSO or APTES molecules coexisting with monolayer arrangements. The monolayer arrangement of APTES corresponded to the basal spacing of about 1.00 nm and the pseudo-bilayer arrangement 1.73-1.89 nm. High reaction temperature was advantageous to the formation of the monolayer arrangement by promoting the exchange of the DMSO molecules by APTES molecules in the interlayer space of kaolinite, as well as the transformation of hydrogen-bound APTES molecules into grafted molecules. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 14
页数:7
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