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首页> 外文期刊>Applied Surface Science >Microporosity development in phenolic resin-based mesoporous carbons for enhancing CO_2 adsorption at ambient conditions
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Microporosity development in phenolic resin-based mesoporous carbons for enhancing CO_2 adsorption at ambient conditions

机译:酚醛树脂中孔碳的微孔发展,以增强环境条件下的CO_2吸附

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Soft-templating method was used to prepare mesoporous carbons. The synthesis in the presence of hydrochloric and citric acids involved resorcinol and formaldehyde as carbon precursors and triblock copolymer Pluronic F127 as a template. The as-synthesized samples underwent carbonization in flowing nitrogen at various temperatures; namely 600 ℃, 700 ℃ and 800 ℃. Two routes were used to develop microporosity in the mesoporous carbons studied. The first one involved introduction of tetraethyl orthosilicate to the reaction system. After silica dissolution with NaOH, an increase in microporosity was observed. The second method, chemical activation with KOH at 700℃, was explored as an alternative approach to create microporosity. It is noteworthy that the TEOS addition not only led to the development of microporosity but also to some improvement of mesoporosity. The post-synthesis KOH activation resulted in more significant increase in the microporosity as compared to the samples obtained by TEOS-assisted synthesis. The mesopore volume was somewhat lower for activated carbons as compared to that in mesoporous carbons. Both methods resulted in micro-mesoporous carbons with good adsorption properties; for instance, in the case of carbons prepared in the presence of TEOS, the best sample exhibited BET surface area of 1463 m~2/g and the total pore volume of 1.31 cm~3/g. For the KOH activated carbons the best adsorption parameters were as follows: the specific surface area = 1906 m~2/g, and the total pore volume = 0.98 cm~3/g. Both procedures used for microporosity development afforded carbons with good adsorption properties that can be useful for applications such as CO_2 adsorption, air and water purification.
机译:使用软模板法制备介孔碳。在盐酸和柠檬酸存在下的合成涉及间苯二酚和甲醛作为碳前体,三嵌段共聚物Pluronic F127作为模板。合成后的样品在各种温度下在流动的氮气中进行了碳化。即600℃,700℃和800℃。在研究的中孔碳中,有两种途径可用来发展微孔性。第一个涉及将原硅酸四乙酯引入反应体系。用NaOH溶解二氧化硅后,观察到微孔率增加。第二种方法是在700℃下用KOH进行化学活化,作为产生微孔的另一种方法。值得注意的是,添加TEOS不仅导致微孔性的发展,而且还导致中孔性的一些改善。与通过TEOS辅助合成获得的样品相比,合成后的KOH活化导致微孔率显着增加。与中孔碳相比,活性炭的中孔体积略低。两种方法均产生了具有良好吸附性能的中微孔碳。例如,在TEOS存在下制备碳的情况下,最佳样品的BET表面积为1463 m〜2 / g,总孔体积为1.31 cm〜3 / g。对于KOH活性炭,最佳吸附参数如下:比表面积= 1906 m〜2 / g,总孔体积= 0.98 cm〜3 / g。两种用于微孔发展的方法都提供了具有良好吸附性能的碳,这些碳可用于诸如CO_2吸附,空气和水净化等应用。

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