2015
DOI: 10.5539/jmsr.v5n1p1
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Spectroscopic and Thermal Studies of Polyalkoxysilanes and Silica-Chitosan Hybrid Materials

Abstract: Polymers of organoalkoxysilanes (or polyalkoxysilanes) were synthesized through sol-gel process using different organosilanes: Tetraethylorthosilicate (TEOS), (3-Glycidyloxypropyl) trimethoxysilane (GPTMS), Trimethoxy(propyl)silane (TMPS), and/or Triethoxy(octyl)silane (EOS). Different carboxylic acids (acetic, formic, and citric) were used to prepare polyalkoxysilanes, with citric acid acting as a reactant rather than a catalyst for the sol-gel reaction. Silica-chitosan hybrid materials were synthesized react… Show more

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Cited by 4 publications
(2 citation statements)
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“…The above-mentioned issues inspired authors to undertake research works aimed at comparison of changes in: (a) adsorption process [mean free adsorption Energy ( E fe )], kinetic diffusion properties [the intraparticle diffusion coefficient ( D p ) and film diffusion coefficient ( D f )], and thermodynamic parameters; (b) tensile strength, (c) tensile strain at break, (d) flexural strength, (g) thermal properties [thermogravimetric analysis (TGA)], (h) structural properties of samples [Fourier transform infrared spectroscopy (FT-IR)], and (i) surface free energy (solid-state carbon-13 nuclear magnetic resonance (solid state 13 C-NMR) spectroscopy [ 52 ]), and (j) mechanism of interaction, deformation of compounds, and adsorption energies [ONIOM and molecular dynamics (MD)]. The results are offered in the present paper.…”
Section: Introductionmentioning
confidence: 99%
“…The above-mentioned issues inspired authors to undertake research works aimed at comparison of changes in: (a) adsorption process [mean free adsorption Energy ( E fe )], kinetic diffusion properties [the intraparticle diffusion coefficient ( D p ) and film diffusion coefficient ( D f )], and thermodynamic parameters; (b) tensile strength, (c) tensile strain at break, (d) flexural strength, (g) thermal properties [thermogravimetric analysis (TGA)], (h) structural properties of samples [Fourier transform infrared spectroscopy (FT-IR)], and (i) surface free energy (solid-state carbon-13 nuclear magnetic resonance (solid state 13 C-NMR) spectroscopy [ 52 ]), and (j) mechanism of interaction, deformation of compounds, and adsorption energies [ONIOM and molecular dynamics (MD)]. The results are offered in the present paper.…”
Section: Introductionmentioning
confidence: 99%
“…Chitosan matrix signals appeared at 105.1 (C1), 82.6 (C4), 75.8 (C3 and C5), 61.6 (C6), 58.1 (C2), 174.4 (N-acetyl C = O signal) and 24.1 (N-acetyl-methyl CH 3 signal) ppm in the 13 C CP-MAS NMR spectra ( Figure 8 and Figure 9 ) [ 26 , 27 , 28 ]. The intensity of C2/C1 in the Ch, ChG05 and ChG10 spectra was 1.52, 1.29 and 1.28.…”
Section: Resultsmentioning
confidence: 99%