1996
DOI: 10.1016/0927-6513(96)00016-8
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Influence of the sorbate type on the XRD peak intensities of loaded MCM-41

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Cited by 368 publications
(228 citation statements)
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“…3b). This may be due to the difference of scattering contrast between the amorphous silicate framework and organic moieties which are located inside the channels of MCM-41 [32,43]. N-methylglucamine functionalization (NMG-MCM-41(3)) caused the disappearance of low intensity peaks, while there appears only a slight change in the intensity of (1 0 0) reflection as compared with that of propyl bromide-grafted MCM-41 (Fig.…”
Section: Characterization Of the Synthesized Sorbentmentioning
confidence: 95%
“…3b). This may be due to the difference of scattering contrast between the amorphous silicate framework and organic moieties which are located inside the channels of MCM-41 [32,43]. N-methylglucamine functionalization (NMG-MCM-41(3)) caused the disappearance of low intensity peaks, while there appears only a slight change in the intensity of (1 0 0) reflection as compared with that of propyl bromide-grafted MCM-41 (Fig.…”
Section: Characterization Of the Synthesized Sorbentmentioning
confidence: 95%
“…The presence of a single broad diffraction peak of the parent material alone (dashed-line peak) is typical of ordered mesoporous silica due to the amorphous nature of the walls, while the decrease in intensity (solid-line peak) was claimed to be indicative of the presence of a guest molecule inside the pores. 694 Clearer evidences of this is provided by the fluorescence confocal scanning laser microscopy images (see Figure 87b), which also indicated DNA penetration of the bulk of the micrometric particles.…”
Section: Interaction With Nucleic Acid-related Biomoleculesmentioning
confidence: 99%
“…It can also be seen here that the peak intensity of the hybrid material is lower than the pure MCM-48, which is since the uptake of molecules inside the pores reduces the scattering contrast between pore wall and pore, thus leading to a decrease in peak intensity. 39,43,44 Results for dye removal…”
Section: Structural Characterization Resultsmentioning
confidence: 99%
“…Step 1: MCM-48 was synthesized hydrothermally in a water bath at [40][41][42][43][44][45][46][47][48][49][50] C; 50 mL of deionized (DI) water was added to a 250-mL beaker immersed inside the water bath; 11.077 g CTAB was added and stirred vigorously for 30 min. After that, 9.6 mL TEOS and 3 mL NH 4 OH were added and sealed.…”
Section: Synthesis Of the Hybrid Mcm-48 Infused With Tio 2 Npsmentioning
confidence: 99%