最近的气候变化正在引起世界各地的广泛关注。由于人为的CO 2排放被认为是造成这种令人担忧的现象的主要因素。因此,迫切需要减少碳足迹并消除大气中过量的二氧化碳。碳捕获、利用和储存是目前解决这一问题的最有希望的解决方案。本研究报告了一种从丰富的生物废物和氯化镁中生产新型分层多孔氮和碳负载 MgO 材料 (N@MgO/C) 的简单方法。通过几种表征技术彻底检查了制备样品的形貌。XRD、拉曼和 XPS 分析揭示了石墨碳的存在。FESEM 和 N 2 adsorption-desorption studies, reveal a hierarchical porous structure with a mesoporous texture and good surface area (258.98 m2/g). Furthermore, N@MgO/C demonstrated an excellent ability to adsorb CO2 at room temperature with maximum adsorption of 2.55 mmol/g remaining almost stable up to 4 cycles. Moreover, it exhibits good catalytic activity for the cycloaddition of CO2 with various epoxides at atmospheric pressure in the presence of CTAB under the solvent-free condition with a yield of 96% and high stability over five cycles without any modification in its morphology.
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Hierarchical porous nitrogen-doped carbon supported MgO as an excellent composite for CO2 capture at atmospheric pressure and conversion to value-added products
The recent climate change is causing widespread concern around the world. Since anthropogenic CO2 emissions are recognized as a major contributor to this alarming phenomenon. As a result, there is an urgent need to reduce the carbon footprint and eliminate excess carbon dioxide from the atmosphere. Carbon capture, utilization, and storage are currently the most promising solution to solve this problem. This study reports a simple method for producing a novel hierarchical porous nitrogen and carbon supported MgO material (N@MgO/C) from the abundant bio-waste and magnesium chloride. The topographies of the prepared samples were thoroughly examined by several characterization techniques. The XRD, Raman, and XPS analyses reveal the existence of graphitic carbon. FESEM, and N2 adsorption-desorption studies, reveal a hierarchical porous structure with a mesoporous texture and good surface area (258.98 m2/g). Furthermore, N@MgO/C demonstrated an excellent ability to adsorb CO2 at room temperature with maximum adsorption of 2.55 mmol/g remaining almost stable up to 4 cycles. Moreover, it exhibits good catalytic activity for the cycloaddition of CO2 with various epoxides at atmospheric pressure in the presence of CTAB under the solvent-free condition with a yield of 96% and high stability over five cycles without any modification in its morphology.