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Ordered mesoporous carbons: citric acid-catalyzed synthesis, nitrogen doping and CO2 capture

机译:有序介孔碳:柠檬酸催化的合成,氮掺杂和CO2捕集

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摘要

Ordered mesoporous carbon materials (OMCs) were synthesized with the use of citric acid as an environmentally friendly catalyst to catalyze the polymerization of resorcinol/formaldehyde resin. The obtained carbon materials with high thermal stability have a 2D hexagonal mesopore system with uniform pore size of ~5.2 nm and high surface area of 612~851 m~2 g~(-1), which were available under a wide composition range of reaction systems at the reaction temperature of 50-80 °C and the molar ratio of formaldehyde to citric acid of ≥3. The presence of citric acid in the synthesis system can enhance the hydrogen bonding between the triblock copolymer and resol and further introduce more micropores to the final carbon material, which is favorable for CO2 adsorption. The nitridation of the OMCs in ammonia flow at the temperature of 650-1000 °C is demonstrated to be effective in introducing basic functionalities that enhances the specific interaction of CO2 and adsorbent. The N-doped OMCs exhibit enhanced CO2 uptake with a CO2 capture capacity of 3.46 mmol g~(-1) for the 1000 °C-nitrided sample. Both textural and surface chemistry influenced the CO2 capture performance of the resultant mesoporous carbon adsorbents.
机译:使用柠檬酸作为环境友好的催化剂,以催化间苯二酚/甲醛树脂的聚合反应,合成了有序的介孔碳材料(OMC)。所获得的具有高热稳定性的碳材料具有二维六角形介孔体系,孔径约5.2 nm,比表面积高612〜851 m〜2 g〜(-1),可在较宽的反应组成范围内使用。反应温度为50-80°C且甲醛与柠檬酸的摩尔比≥3。合成系统中柠檬酸的存在可以增强三嵌段共聚物和甲阶酚醛树脂之间的氢键,并向最终的碳材料中引入更多的微孔,这有利于CO2的吸附。在650-1000°C的温度下,氨流中OMC的氮化被证明可有效引入基本功能,从而增强CO2和吸附剂的特定相互作用。 N掺杂的OMC对1000°C渗氮样品的CO2吸收能力增强,CO2捕获能力为3.46 mmol g〜(-1)。质地和表面化学都影响所得中孔碳吸附剂的CO 2捕集性能。

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