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Porous carbon materials based on biomass for acetone adsorption: Effect of surface chemistry and porous structure

机译:基于生物质的丙酮吸附多孔碳材料:表面化学和多孔结构的影响

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The relative influence of porous structure and functional groups of porous carbon materials for acetone adsorption is presented in this article. Here, we have successfully prepared oxygen and nitrogen doping porous carbons (ONPCs) by a hydrothermal method using waste tobacco stem as the carbon precursor and ethylenediamine as a nitrogen source. The resulting ONPCs have high specific surface (906-2940 m(2) g(-1)) and chemical compositions (1.80-5.22% N and 5.81-11.77% O). This carbon shows high acetone adsorption capacity (Le., 16.91 mmol g(-1) at 25 degrees C and 18 kPa). The pore volume and specific surface area of ONPCs were found to be determinative factors for acetone adsorption at high pressure, and the introduction of oxygen and nitrogen into carbon surface can improve acetone adsorption at low pressure. Molecular simulations results suggest that adsorption capacity of acetone is improved at low pressure after doping of oxygen and nitrogen functional groups, but equilibrium adsorption capacity is unchanged. This is in good agreement with the experimental results that these functional groups are primarily responsible for the materials' low-pressure acetone adsorption capacity. This work provides insights into material design and further development for acetone adsorption.
机译:本文提出了多孔碳材料的多孔结构和官能团对丙酮吸附的相对影响。在这里,我们已经成功地通过水热法以废烟茎为碳前驱体,以乙二胺为氮源,制备了氧和氮掺杂的多孔碳(ONPC)。所得的ONPC具有较高的比表面积(906-2940 m(2)g(-1))和化学成分(1.80-5.22%N和5.81-11.77%O)。该碳显示出高的丙酮吸附能力(Le。,在25摄氏度和18 kPa下为16.91 mmol g(-1))。发现ONPC的孔体积和比表面积是高压下丙酮吸附的决定性因素,在碳表面引入氧气和氮气可以改善低压下丙酮的吸附。分子模拟结果表明,在氧和氮官能团掺杂后,低压下丙酮的吸附能力有所提高,但平衡吸附能力没有变化。这些实验结果与这些官能团主要负责材料的低压丙酮吸附能力非常吻合。这项工作提供了对丙酮吸附材料设计和进一步开发的见识。

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