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Anchoring a halogenated amine on the surface of a microporous activated carbon for carbon dioxide capture

机译:将卤化胺锚定在微孔活性炭表面以捕获二氧化碳

摘要

Activated carbon (AC) surface may be modified by grafting amine-containing compounds to improve theudCO2 adsorption capacity. Two solid sorbents were prepared by anchoring a halogenated amine, i.e., 2-udchloroethylamine hydrochloric acid (CEA) on the surface of a microporous AC using a two-stageudmodification. At the first stage, the samples of AC were oxidized by nitric acid to increase the amount ofudoxygen surface groups and at the second stage, the oxidized samples were modified by anchoring CEA onudthe surface to produce a superior CO2 adsorbent. The oxidized samples were compared with the aid ofudproximate and ultimate analysis, nitrogen adsorption–desorption at �196 8C (77 K) and temperatureudprogrammed desorption (TPD) to decide on the best oxidation conditions. The amine-modified samplesudwere analyzed in terms of texture, surface chemistry and CO2 adsorption. The latter was studied usingudisothermal CO2 capture, temperature-programmed (TP) CO2 adsorption and cyclic operation. Theudmodified samples had a lower surface area than the parent sample. The best modified sample presentedudan increase of 45% in CO2 capture capacity at 100 8C. Based on unit surface area, the modified samplesudshowed great CO2 capture capacities, compared to the virgin sample. Moreover, the modified samplesudpresented a less dependency of CO2 capacity on temperature. This indicates that the adsorptionudmechanism shifts from physisorption to chemisorption by increasing temperature.
机译:可以通过接枝含胺化合物来修饰活性炭(AC)表面,以提高udCO2吸附能力。通过使用两阶段的双改性,将卤化的胺,即2-二氯乙基胺盐酸(CEA)固定在微孔AC的表面上,制备了两种固体吸附剂。在第一阶段,用硝酸将AC样品氧化,以增加 udoxygen表面基团的数量;在第二阶段,通过将CEA锚固在 udud表面上,对氧化后的样品进行改性,以产生优异的CO2吸附剂。氧化后的样品通过 u近似和最终分析,氮在196 8C(77 K)下的吸附和解吸以及温度 udprogrammed解吸(TPD)的比较来确定最佳氧化条件。对胺改性的样品进行了织构,表面化学和CO2吸附分析。使用等温CO2捕集,程序升温(TP)CO2吸附和循环操作研究了后者。改性后的样品比母体样品的表面积低。最佳的改性样品在100 8 C下呈现出 udan的CO2捕集能力提高了45%的趋势。与原始样品相比,基于单位表面积,改性样品显示出强大的CO2捕集能力。此外,修改后的样品表明二氧化碳容量对温度的依赖性较小。这表明,随着温度的升高,吸附动力作用从物理吸附转变为化学吸附。

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