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Enhancement of CO2 adsorption on phenolic resin-based mesoporous carbons by KOH activation

机译:通过KOH活化增强在酚醛树脂基介孔碳上的CO2吸附

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Carbons with high surface area and large volume of ultramicropores were synthesized for CO2 adsorption. First, mesoporous carbons were produced by soft-templating method using triblock copolymer Pluronic F127 as a structure directing agent and formaldehyde and either phloroglucinol or resorcinol as carbon precursors. The resulting carbons were mainly mesoporous with well-developed surface area, large total pore volume, and only moderate CO2 uptake. To improve CO2 adsorption, these carbons were subjected to KOH activation to enhance their microporosity. Activated carbons showed 2-3-fold increase in the specific surface area, resulting from substantial development of microporosity (3-5-fold increase in the micropore volume). KOH activation resulted in enhanced CO2 adsorption at 760mmHg pressure: 4.4mmolg~(-1) at 25 °C, and 7mmolg~(-1) at 0°C. This substantial increase in the CO2 uptake was achieved due to the development of ultramicroporosity, which was shown to be beneficial for C02 physisorption at low pressures. The resulting materials were investigated using low-temperature nitrogen physisorption, CO2 sorption, and small-angle powder X-ray diffraction. High CO2 uptake and good cyclability (without noticeable loss in CO2 uptake after five runs) render ultramicroporous carbons as efficient CO2 adsorbents at ambient conditions.
机译:合成了具有高表面积和大量超微孔的碳用于CO2吸附。首先,使用三嵌段共聚物Pluronic F127作为结构导向剂,使用甲醛和间苯三酚或间苯二酚作为碳前体,通过软模板法生产中孔碳。产生的碳主要是介孔的,具有发达的表面积,大的总孔体积和仅中等的二氧化碳吸收。为了改善CO2的吸附,这些碳经过KOH活化以增强其微孔性。活性炭显示出比表面积增加了2至3倍,这是由于微孔性的显着发展(微孔体积增加了3-5倍)所致。 KOH活化在760mmHg压力下增强了CO2吸附:在25°C下为4.4mmolg(-1),在0°C下为7mmolg(-1)。由于超微孔性的发展,实现了二氧化碳吸收的显着增加,这被证明有利于低压下的二氧化碳物理吸附。使用低温氮物理吸附,CO2吸附和小角度粉末X射线衍射研究所得材料。高CO2吸收和良好的可循环性(五次运行后没有明显的CO2吸收损失)使超微孔碳在环境条件下成为有效的CO2吸附剂。

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