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
RSC ADVANCES | 2016年 / 6卷 / 60期
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.
引用
收藏
页码:55382 / 55392
页数:11
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