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Enhancement of Carbon dioxide adsorption capacity on synthesized oxygen-doped nanocarbons via solution plasma process and nitridation

机译:通过溶液等离子体工艺和氮化增强合成氧掺杂纳米碳的二氧化碳吸附能力

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Recently, the adsorption of carbon dioxide (CO_2) on solid sorbent is now focused since it overcomes the drawbacks of previous conventional CO_2 capture process by CO_2 scrubbing via liquid amine, in terms of lower energy requirements for regeneration and ease of separation. Carbon-based sorbent has high potential to make this done due to its high surface area to its volume ratio, as well as high thermal and chemical stability. In this report, oxygen-doped nanocarbon (o-CN) was synthesized from a homogeneous mixture of benzene and metal working fluid (MWF) via in-liquid plasma process, so called solution plasma process (SPP). Then it was nitrided under ammonia atmosphere at high temperature (800 °C) to enhance its capacity. CO_2 adsorption was done by volumetric analysis at 25 °C. The experimental results revealed that CO_2 adsorption capacity was increased by nitridation by creating microporosity and nitrogen-containing functional groups on the sorbent. The maximum capacity was achieved at 1.63 mmol g~(-1) on nanocarbon synthesized from benzene mixed with 15 vol% MWF, nitrided at 800 °C (no-CN) which was greater than nanocarbon synthesized by pure benzene about 5-fold. The study of thermodynamics revealed that the CO_2 adsorption on no-CN was exothermic, less random and exergonic. Nitrided sorbent showed more negative isosteric enthalpy of adsorption than pristine carbon referring to stronger binding forces to sorbate molecule. Moreover, no-CN exhibited a better selectivity of CO_2 adsorption than of N2, and it can withstand on multi-cycle use.
机译:最近,在固体吸附剂上的二氧化碳(CO_2)的吸附现在,因为它克服了通过液态胺通过液态胺克服的先前传统CO_2捕获过程的缺点,就较低的能量要求进行再生和易于分离。碳基吸附剂具有高潜力,使其在其高度的高度与其体积比以及高热和化学稳定性的高度造型中进行。在本报告中,通过内肠和金属加工液(MWF)的均匀混合物通过内液相体加工合成氧掺杂的纳米碳(O-CN),所以称为溶液等离子体工艺(SPP)。然后在高温(800℃)下氨气气氛遍历,以增强其容量。 CO_2吸附在25℃下通过体积分析完成。实验结果表明,通过在吸附剂上产生微孔和含氮官能团来增加CO_2吸附能力。在用15Vol%MWF中合成的纳米氧化物的1.63mmol G〜(-1)下实现最大容量,氮化为800℃(NO-CN),其大于纯苯约为5倍的纳米碳。热力学的研究表明,NO-CN上的CO_2吸附是放热的,较少随机和出汗。氮化的吸附剂显示出比原始碳对吸附的吸附更多的负旁边焓,所述碳对山梨酯分子较强的结合力。此外,NO-CN表现出比N2的CO_2吸附的更好选择性,并且可以承受多循环使用。

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