2012
DOI: 10.1016/j.jnoncrysol.2012.07.028
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Thermal stability and optical property of ormocers (organically modified ceramics) nanoparticles produced from copolymerization between amino-silanes and tetraethoxysilane

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Cited by 19 publications
(8 citation statements)
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“…5(c)), it is easier to form a hydrophobic network for shielding the nanoparticle from water, resulting in a high water contact angle. The thermal gravimetric analysis results of the pristine and functionalised nanoparticles (silane:silica ratio = 200 µL$g -1 for both silanes) show a similar trend for mass loss over a wide range of temperature (100°C to 800°C), which agree with previous studies on the thermal properties of pristine and functionalised silica nanoparticles [34][35][36][37]. The similar mass loss for both pristine and functionalised nanoparticles indicate that the mass of the methyl-and octyl-functional groups is negligible with respect to the mass of the nanoparticle (Fig.…”
Section: Characterisation Of Silica Nanoparticlesupporting
confidence: 90%
“…5(c)), it is easier to form a hydrophobic network for shielding the nanoparticle from water, resulting in a high water contact angle. The thermal gravimetric analysis results of the pristine and functionalised nanoparticles (silane:silica ratio = 200 µL$g -1 for both silanes) show a similar trend for mass loss over a wide range of temperature (100°C to 800°C), which agree with previous studies on the thermal properties of pristine and functionalised silica nanoparticles [34][35][36][37]. The similar mass loss for both pristine and functionalised nanoparticles indicate that the mass of the methyl-and octyl-functional groups is negligible with respect to the mass of the nanoparticle (Fig.…”
Section: Characterisation Of Silica Nanoparticlesupporting
confidence: 90%
“…2.c. [22,23]. The crystallites size of (Si) can be estimated from diffraction pattern analysis by measuring FWHM and applying Scherrer's equation.…”
Section: Resultsmentioning
confidence: 99%
“…XRD is considered as a reference technique for the product powder characterization [10]. Figure 1(c) (t = 5 hours), the SiO 2 -peak high intensity appeared at 2θ = 20˚ that corresponds to the complete transformation to amorphous-SiO 2 [13]. Then, the preparation conditions during the crystalline-SiO 2 formation are [4.5 and 6 weight % KOH at t = 4 hours].…”
Section: Resultsmentioning
confidence: 99%