Surface chemistry and moisture sorption properties of wood coated with multifunctional alkoxysilanes by sol-gel process

被引:124
作者
Tshabalala, MA
Kingshott, P
VanLandingham, MR
Plackett, D
机构
[1] US Forest Serv, USDA, Forest Prod Lab, Madison, WI 53726 USA
[2] Riso Natl Lab, Danish Polymer Ctr, DK-4000 Roskilde, Denmark
[3] Natl Inst Stand & Technol, US Dept Commerce, Bldg Mat Div, Gaithersburg, MD 20899 USA
[4] Tech Univ Denmark, Danish Polymer Ctr, DK-2800 Lyngby, Denmark
关键词
polysaccharides; surface; coatings; polycondensation; morphology;
D O I
10.1002/app.12142
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Sol-gel surface deposition of a hydrophobic polysiloxane coating on wood was accomplished by using a mixture of a low molecular weight multifunctional alkoxysilane, methyltrimethoxysilane (MTMOS), and a high molecular weight multifunctional alkoxysilane, hexadecyltrimethoxysilane (HDTMOS). Investigation of the surface chemistry and morphology of the wood specimens by means of ATR-FTIR, energy-dispersive X-ray analysis, X-ray photoelectron spectroscopy, SEM, and atomic force microscopy indicated that the sol-gel process results in deposition of polysiloxane networks that are bonded to the wood by polycondensation with surface hydroxyl groups. The surface hydroxyl groups involved in the bonds appear to be located predominantly on the cellulose component of the wood. The sol-gel deposit on the wood substrates lowered the rates of water and water vapor sorption. The low molecular weight MTMOS apparently penetrated the outer surface layers of the wood and condensed with hydroxyls that may not be readily accessible to the high molecular weight HDTMOS. Once attached to such sites, it is reasonable to assume that some of these surface derivatives of MTMOS condensed with other molecules of MTMOS and HDTMOS with a long hydrocarbon chain to form a polysiloxane network that is hydrophobic. The ultimate effect of the sol-gel deposit can therefore be regarded as not only to decrease the surface concentration of hydrogen-bonding sites, but also to stereochemically hinder the formation of hydrogen bonds between such sites and water molecules. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:2828 / 2841
页数:14
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