首页|无金属组分的氮化碳材料催化CO2合成碳酸丙烯酯

无金属组分的氮化碳材料催化CO2合成碳酸丙烯酯

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以二氰二胺为前驱体,经热聚和热剥离制备了剥离石墨相氮化碳(eg-C3N4)材料,eg-C3N4 再经H2SO4 处理制得了eg-C3N4-S材料.采用N2-吸脱附、X射线衍射、傅里叶红外光谱、X射线光电子能谱和紫外-可见漫反射等方法对材料的孔结构、化学组成等理化性质进行了表征.结果显示,热剥离有效地提高了g-C3N4 的比表面积,而H2SO4 处理引入了羟基.在CO2 和环氧丙烷环加成合成碳酸丙烯酯的催化反应中,eg-C3N4-S材料相较于未经H2SO4 处理或未经热剥离的g-C3N4 材料具有更高的催化活性.在反应压力为 2.0 MPa,反应温度为 140℃条件下,环氧丙烷的转化率和碳酸丙烯酯选择性分别为85%和98%.
Synthesis of Propylene Carbonate from CO2 Catalyzed by Metal-free Carbon Nitride
The exfoliated graphitic carbon nitride(eg-C3N4)material was synthesized by thermal polymerization and thermal exfoliation using dicyanodiamide as a precursor,and the eg-C3N4-S materials were prepared by treatment of H2SO4.The physicochemical properties,including porous structure,chemical compositions etc.,of the materials were characterized by N2 adsorption-desorption,XRD,FT-IR,XPS and UV-Vis spectroscopy.The characterization results showed that exfoliation effectively increased the specific surface area of g-C3N4,while H2SO4 treatment introduced hydroxyl group.In the catalytic reaction of cycloaddition of CO2 with propylene oxide to propylene carbonate,eg-C3N4-S showed higher catalytic activity than g-C3N4 without H2SO4 treatment or thermal exfoliation.Under the reaction pressure of 2.0 MPa and temperature of 140℃,the propylene oxide conversion and propylene carbonate selectivity were 85%and 98%,respectively.

g-C3N4cyclic carbonateCO2 cycloaddition reaction

孙校华、张学文、王非、许杰、薛冰

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常州大学 石油化工学院,江苏 常州 213164

氮化碳 环碳酸酯 CO2环加成反应

国家自然科学基金项目中国石油—常州大学创新联合体科技创新人才项目

22278041CCIA2023-02

2024

分子催化
中国科学院兰州化学物理研究所

分子催化

CSTPCD北大核心
影响因子:2.622
ISSN:1001-3555
年,卷(期):2024.38(5)