Silyl celluloses (SiC) were prepared by reacting cellulose with chloropropyltrichlorosilane (CPTCSi) andchloropropyltriethoxysilane (CPTESi) in LiCl/N
N-dimethylacetamide (DMAc). The Si content in the silyl cellulose could becontrolled by adjustment of the molar ratio of silane and cellulose. FT-IR spectra showed that cellulose was readily reactedwith the above two silane reagents
and the reactivity of CPTCSi is higher than that of CPTESi. It was presumed that the reaction process belongs to graft-polymerization.The results of differential thermal analysis (DTA) indicated that the thermostability of the materials produced increased with the increase of Si content in the sample.The acid resistance of the samples SiC in 1 mol/L HCl aqueous solution was improved significantly.When Si content was ca.20%
the silyl cellulose has excellent thermostability
hydrophobicity
low density and stability in 1 mol/L HCl aqueous solution
owing to crosslinking of cellulose chain with silane.
Abstract
Silyl celluloses (SiC) were prepared by reacting cellulose with chloropropyltrichlorosilane (CPTCSi) andchloropropyltriethoxysilane (CPTESi) in LiCl/N
N-dimethylacetamide (DMAc). The Si content in the silyl cellulose could becontrolled by adjustment of the molar ratio of silane and cellulose. FT-IR spectra showed that cellulose was readily reactedwith the above two silane reagents
and the reactivity of CPTCSi is higher than that of CPTESi. It was presumed that the reaction process belongs to graft-polymerization.The results of differential thermal analysis (DTA) indicated that the thermostability of the materials produced increased with the increase of Si content in the sample.The acid resistance of the samples SiC in 1 mol/L HCl aqueous solution was improved significantly.When Si content was ca.20%
the silyl cellulose has excellent thermostability
hydrophobicity
low density and stability in 1 mol/L HCl aqueous solution
owing to crosslinking of cellulose chain with silane.
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