Hexadecyl-functionalized lamellar mesostructured silicates and alumino silicates designed for polymer-clay nanocomposites. Part I. Clay synthesis and structure

被引:12
作者
Chastek, TT
Que, EL
Shore, JS
Lowy, RJ
Macosko, C
Stein, A
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[3] S Dakota State Univ, Dept Chem & Biochem, Brookings, SD 57007 USA
基金
美国国家科学基金会;
关键词
lamellar mesostructures; synthetic clays; alummosilicates;
D O I
10.1016/j.polymer.2005.03.006
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Motivated by a need for synthetic clays that can be dispersed and exfoliated in polymer melts without added compatibilizers, lamellar mesostructured silicates and aluminosilicates with covalently attached hexadecyl functional groups (C-16-LMS and C-16-LMAS, respectively) were prepared by sol-gel syntheses and their structures were characterized. Based on XRD and TEM data, lamellar products with layer spacings of 4.8-4.9 nm were obtained between room temperature and 60 degrees C (C-16-LMS) or 70 degrees C (C-16-LMAS). The degree of condensation of the aluminosilicate layers increased at the higher synthesis temperatures. Attachment of organic groups to the inorganic sheets was confirmed by Si-29 solid state MAS NMR and IR spectroscopy. The sheets of C-16-LMS consisted of single or double layers of tetrahedral silicate groups, each attached to a hexadecyl chain. C-16-LMAS was composed of pyrophyllite-like layers (Si:Al = 2) with an octahedral aluminum layer sandwiched between two tetrahedral silicate layers and hexadecyl surface groups. Tetrahedral aluminum sites were also present. The clay layer spacing could be increased to 5.2 nm by addition of tetraethoxysilanes during the synthesis (C-16-SiO2-LMAS). C-16-SiO2-LMAS was structurally similar to C-16-LMAS; however, the presence of additional silicate groups in this structure increased the inorganic layer thickness and introduced further structural disorder. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4421 / 4430
页数:10
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