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Facile alkali-assisted synthesis of g-C3N4 materials and their high-performance catalytic application in solvent-free cycloaddition of CO2 to epoxides
被引:55
|作者:
Xu, Jie
[1
]
Shang, Jie-Kun
[1
]
Jiang, Quan
[1
]
Wang, Yue
[1
]
Li, Yong-Xin
[1
]
机构:
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Gehu Rd 1, Changzhou 213164, Jiangsu, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
GRAPHITIC CARBON NITRIDE;
PHOTOCATALYTIC HYDROGEN EVOLUTION;
EFFICIENT HETEROGENEOUS CATALYSTS;
SOLID BASE CATALYST;
CYCLIC CARBONATES;
IONIC LIQUIDS;
VISIBLE-LIGHT;
PROPYLENE CARBONATE;
DIOXIDE;
TRANSESTERIFICATION;
D O I:
10.1039/c6ra10509b
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A series of graphitic carbon nitride materials were synthesized using guanidine hydrochloride (GndCl) as a precursor with the aid of alkali treatment. The introduction of alkali successfully enabled GndCl to be transformed into g-C3N4 at much lower calcination temperatures (450-475 degrees C). The g-C3N4 samples synthesized under various conditions have been characterized by several techniques including XRD, FTIR, UV-vis, C-13 NMR, and XPS spectroscopy. The results confirmed that the alkali could effectively accelerate further condensation of melem-like fragments to g-C3N4. Meanwhile, a possible mechanism of alkali-assisted synthesis of g-C3N4 from GndCl has been proposed. In solvent-free catalytic cycloaddition of CO2 to propylene oxide to propylene carbonate (PC), g-C3N4-NaOH and g-C3N4-KOH materials demonstrated high and stable catalytic performances, affording PC yields of ca. 90% under optimized reaction conditions. Moreover, the activities were superior to those obtained over g-C3N4 prepared without alkali treatment. In addition, the catalytic activity along with preparation method for the present g-C3N4 has also been compared with other reported g-C3N4-based catalysts.
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页码:55382 / 55392
页数:11
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