2019
DOI: 10.1016/j.ceramint.2019.01.067
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Synthesis and formation mechanism of amorphous silica particles via sol–gel process with tetraethylorthosilicate

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Cited by 50 publications
(29 citation statements)
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“…The physicochemical characterization of the synthesized MSNs was performed to ascertain the goodness of the material used as a carrier in this study. MSNs showed a broad band centered at 22 • in the XRD pattern ( Figure 1A), which is ascribable to a silica amorphous material (Dubey et al, 2015;Jiang et al, 2019). The ATR spectrum (Figure 1B) of the sample did exhibit the trademark signs of silica (Mourhly et al, 2015).…”
Section: Msns Characterizationmentioning
confidence: 97%
“…The physicochemical characterization of the synthesized MSNs was performed to ascertain the goodness of the material used as a carrier in this study. MSNs showed a broad band centered at 22 • in the XRD pattern ( Figure 1A), which is ascribable to a silica amorphous material (Dubey et al, 2015;Jiang et al, 2019). The ATR spectrum (Figure 1B) of the sample did exhibit the trademark signs of silica (Mourhly et al, 2015).…”
Section: Msns Characterizationmentioning
confidence: 97%
“…FT-IR characterization was performed on Sol-Si particles and samples of C/Sol-Si and C (Figure 3). To this end, the characteristic functional groups 21,22 of the tested samples were determined based on the IR absorption range. The Sol-Si particles showed characteristic IR bands in the region of 800 cm À1 (Si O Si symmetric stretching) and 450 cm À1…”
Section: Ft-ir Characterizationmentioning
confidence: 99%
“…In addition, the characteristic peak at 842 cm À 1 is attributed to the symmetric stretching vibration of SiÀ OÀ Si. [37] All FTIR spectra have strong SiÀ OÀ Si characteristic peaks, which indicates that lots of condensation reactions among SiÀ OH occurred and a large number of SiÀ OÀ Si bonds came into being during the synthesis of SiO 2 . The characteristic peaks at 795 cm À 1 and 950 cm À 1 are attributed to the stretching vibration and the bending vibration of SiÀ OH, respectively.…”
Section: Ftir Analysis Of Modified Siomentioning
confidence: 99%
“…The characteristic peaks at 795 cm À 1 and 950 cm À 1 are attributed to the stretching vibration and the bending vibration of SiÀ OH, respectively. [37][38][39] The characteristic peaks at 2961 cm À 1 and 2900 cm À 1 correspond to the stretching vibration absorption of À CH 3 , [40][41][42] the characteristic peak at 1255 cm À 1 corresponds to the symmetrical stretching vibration of SiÀ CH 3 , and the characteristic peak at 755 cm À 1 corresponds to the stretching vibration of -SiÀ (CH 3 ) 3 . [38,40,43] With the increase of TMES addition amount, the characteristic peak intensity of SiÀ OH decreased, while that for those characteristic peaks of SiÀ OÀ Si, À CH 3 , SiÀ CH 3 and À SiÀ (CH 3 ) 3 increased.…”
Section: Ftir Analysis Of Modified Siomentioning
confidence: 99%