Author:
Matsuyama Hiroyoshi,Young J. Francis
Abstract
Some high molecular weight cationic polymers, poly(diallyldimethylammonium chloride) (PDC) and poly(4-vinylbenzyltrimethylammonium chloride) (PVC), have been incorporated into the calcium silicate hydrate (C–S–H) structure during precipitation of quasicrystalline C–S–H from aqueous solution. Expansion of the interlayer spacing [0.9 nm (PDC), 1.5 nm (PVC)] and a high-carbon content provided evidence that these polymers were intercalated between layers of C–S–H when Ca/Si <1.0. Intercalation characteristic properties strongly depended on both of the type of polymer and Ca/Si ratio in C–S–H. Poly(4-vinyl-1-methylpyridinium bromide) and methyl glycol chitosan (iodide) also interacted with C–S–H, probably by surface adsorption. The C–S–H/polymer complexes were examined by Fourier transform infrared spectroscopy, 29Si nuclear magnetic resonance magic angle spinning, and 13C cross-polarization, magic angle spinning nuclear magnetic resonance spectroscopy. Mechanisms of intercalation of different kinds of polymers between the C–S–H layers are discussed.
Publisher
Springer Science and Business Media LLC
Subject
Mechanical Engineering,Mechanics of Materials,Condensed Matter Physics,General Materials Science
Cited by
59 articles.
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