2005
DOI: 10.1016/j.micromeso.2005.06.010
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Adsorption characteristics of carbon dioxide on organically functionalized SBA-15

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Cited by 534 publications
(481 citation statements)
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“…The FT-IR spectra patterns of KIT-6 and p-KIT-6 are shown in Fig. 3 are identied as the C-H stretching vibrations of methyl and methylene groups, 36 and the peak at 1431 is assigned to the C-H deformation vibration of the remaining Si-O-CH-, 37 which has not reacted with the hydroxyl groups through condensation. It should be noticed that the intensities of the peaks at about 3748 cm À1 , which is ascribed to free Si-OH groups, 38 decrease signicantly aer functionalization.…”
Section: Ft-irmentioning
confidence: 99%
“…The FT-IR spectra patterns of KIT-6 and p-KIT-6 are shown in Fig. 3 are identied as the C-H stretching vibrations of methyl and methylene groups, 36 and the peak at 1431 is assigned to the C-H deformation vibration of the remaining Si-O-CH-, 37 which has not reacted with the hydroxyl groups through condensation. It should be noticed that the intensities of the peaks at about 3748 cm À1 , which is ascribed to free Si-OH groups, 38 decrease signicantly aer functionalization.…”
Section: Ft-irmentioning
confidence: 99%
“…However, the IR band for hydrogen-bonded carbamic acids is not observed. Hiyoshi et al [33] assigned similar frequencies with different intensities of the ammonium carbamate ion pairs bands. NH stretching of ammonium carbamate at 3440 cm -1 was detected in FIGURE 4 (ii).…”
Section: Resultsmentioning
confidence: 98%
“…Referring to FIGURE 4 (iii), a band at 1552 cm -1 represent COO -asymmetric stretching of carbamate (ionic form) and NH deformation in NH 3 + was appeared at 1484 cm -1 [34]. A weak shoulder at 1432 cm -1 appeared on the band at 1468 cm -1 is due to COO -symmetric stretch [33][34][35][36][37]. Formation of these new absorption bands respectively due to the formation of alkylammonium carbamate by chemisorption of CO 2 towards ODA compounds.…”
Section: Resultsmentioning
confidence: 99%
“…25,26 The broad bands at 1980 and 1850 cm -1 are overtone vibrations of Si-O-Si groups. 27 The absorption at 932 cm -1 can be attributed to the stretching vibration of Si-OH. 25 The bands at 3300, 1595 and 770 cm -1 correspond to the symmetric stretching, deformation and wagging vibration of N-H, respectively.…”
mentioning
confidence: 99%
“…25,28 The absorption at 1660 cm -1 is due to deformation of the protonated amino groups R-NH 3 +  -O-Si. 27 Peaks at 2930, 2880, 2810, 1460, 1410, 1346, and 1276 cm -1 are due to the vibrations of methylene groups in the bridging spacer. 28,29 The absorption band at 690 cm -1 can be assigned to the Si-CH 2 stretching.…”
mentioning
confidence: 99%