2007
DOI: 10.1016/j.micromeso.2007.06.043
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Active solid acid catalysts prepared by sulfonation of carbonization-controlled mesoporous carbon materials

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Cited by 157 publications
(132 citation statements)
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“…Owing to the complexity of many carbonaceous structures, the chemical shift ranges for various functional groups are not always clearly defined, and overlap is common. [105] However, complex carbonaceous structures can be analyzed in detail by combining data from multiple solid state NMR techniques.…”
Section: Solid-state Nmrmentioning
confidence: 99%
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“…Owing to the complexity of many carbonaceous structures, the chemical shift ranges for various functional groups are not always clearly defined, and overlap is common. [105] However, complex carbonaceous structures can be analyzed in detail by combining data from multiple solid state NMR techniques.…”
Section: Solid-state Nmrmentioning
confidence: 99%
“…An ordered mesoporous carbon was also functionalized with sulfonate groups by contacting the carbon with the vapor of fuming sulfuric acid inside an autoclave. [105] Under optimal conditions, a surface concentration of 1.3 mmol g À1 was achieved on this material, which served as an active and selective catalyst for several catalytic reactions, including rearrangement and condensation reactions.…”
mentioning
confidence: 99%
“…Sulfonated carbon materials, such as sulfonated hexagonal tube-like mesoporous carbon [23,26], sulfonated carbon nanotubes [34,35] and sulfonated amorphous carbon material [11] etc., have attracted considerable attention due to their applications in catalysis as Brønsted acid catalysts, and fuel cells [35]. We attempted to explore the functionalization of carbon nanocage CKT-3(A) with sulfophenyl group and its catalysis effect as solid Brønsted acid.…”
Section: Materials Characteristicsmentioning
confidence: 99%
“…Significant efforts have been devoted to the sulfonation of OMCs [20][21][22][23], and their potential applications in catalysis have been reported [24,25]. But those sulfonation processes were reported with two-dimensional hexagonal carbon as precursor.…”
Section: Introductionmentioning
confidence: 99%
“…The sulfonation of MNPsSi-PPh 3 was completed by the method of vapour-phase sulfonation as described [16]. The sulfonation was performed in a Teflon-lined autoclave where MNPsSi-PPh 3 powders of 3 g were contacted with the vapor from 50 mL 50 wt% SO 3 /H 2 SO 4 at 353 K for 72 h. The sulfonated samples were washed with hot deionized water ([353 K) to remove any physically adsorbed species until the sulfate ions were not detected in the upper layer solution.…”
Section: Sulfonation Of Mnpssi-pphmentioning
confidence: 99%