首页|ZrxCe1-xO2/NC催化CO2和苯乙烯-锅法制环碳酸酯

ZrxCe1-xO2/NC催化CO2和苯乙烯-锅法制环碳酸酯

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CO2与烯烃转化为环碳酸酯是当前一种有效的固碳策略,为此设计了一种掺氮多孔碳负载锆铈双金属(ZrxCe1-xO2/NC)催化剂.通过X射线衍射(XRD)、扫描电子显微镜(SEM)、N2-吸附、CO2和NH3程序升温脱附(CO2-TPD和NH3-TPD)等表征了催化剂的形貌、物相、孔结构以及酸碱两性特征.结果表明,该催化剂可在无卤条件下催化CO2和苯乙烯一锅法制备环碳酸酯,特别是Zr0.75Ce0.25O2/NC在2 MPa CO2下,采用80℃/8 h和150℃/8 h分段工艺,实现了74.87%的转化率和80.43%的环碳酸酯选择性,这归因于氧化铈(CeO2)和氧化锆(ZrO2)在碳载体上的均匀分散,以及丰富的酸-碱性位点协同作用.
One-Pot Synthesis of Cyclo-Carbonate from Styrene and CO2 over the ZrxCe1-xO2/NC Catalyst
The conversion of CO2 and olefin to cyclo-carbonate is one of effective carbon-immobilizing strategies.The zirconium-cerium bimetallic catalysts supported on the nitrogen-doped porous carbon(ZrxCe1-xO2/NC)were designed and prepared.Their morphology,crystal,pore structure and acid-base characters of the catalysts were monitored by X-Ray Diffraction(XRD),scanning electron microscope(SEM),N2 adsorption-desorption isotherm(N2-adsorption),CO2-temperature program desorption(CO2-TPD)and NH3-temperature program desorption(NH3-TPD).The results show that the catalyst can catalyse the one-pot synthesis of cyclo-carbonate by CO2 and styrene with halogen-free conditions.The Zr0.75Ce0.25O2/NC show the best conversion of 74.87%and selectivity of 80.43%under 2 MPa CO2 through a bi-period of 80℃/8 h and 150℃/8 h.This is attributed to the uniform dispersion of CeO2 and ZrO2 on the carbon support,as well as the synergistic effect of acid-base sites.

CO2styreneCeO2ZrO2porous carboncyclo-carbonate

周钰淼、梁栋、姚悦华、武越、赵婷、朱娜

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中北大学 化学与化工学院,山西 太原 030051

山西新华化学防护设备研究所,山西 太原 030008

山西大学 环境与资源学院,山西 太原 030006

CO2 苯乙烯 CeO2 ZrO2 多孔碳 环碳酸酯

国家自然科学基金山西省自然科学基金

22176117201901D111171

2024

中北大学学报(自然科学版)
中北大学

中北大学学报(自然科学版)

影响因子:0.258
ISSN:1673-3193
年,卷(期):2024.45(2)
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