Jiang Jianwen, Sandler Stanley I
Center for Molecular and Engineering Thermodynamics, Department of Chemical Engineering, University of Delaware, Newark, Delaware 19716, USA.
Langmuir. 2004 Dec 7;20(25):10910-8. doi: 10.1021/la0492254.
The adsorption of a nitrogen and oxygen mixture (air) on two types of single-walled carbon nanotube bundles at both sub- and supercritical temperatures is studied using grand canonical Monte Carlo molecular simulation. On an infinite periodic hexagonal bundle without an external surface, adsorption at a subcritical temperature is of type I. With increasing pressure, nitrogen adsorption first increases and then decreases until saturation; oxygen adsorption continues increasing, displacing nitrogen, until saturation. Both nitrogen and oxygen first form annuli inside the nanotubes, then with increased coverage they occupy the nanotube centers, and at the highest coverage some oxygen also adsorbs in the interstitial channels between the nanotubes. The selectivity of nitrogen over oxygen decreases with increasing pressure and reaches a constant near saturation. Adsorption at a supercritical temperature is also of type I, with both nitrogen and oxygen adsorption increasing with increasing pressure, though the selectivity of nitrogen to oxygen first increases slightly and then decreases with increasing pressure. On a small isolated hexagonal bundle with an external surface, adsorption at a subcritical temperature is of type II. With increasing pressure, nitrogen adsorption first increases, then decreases, and finally increases again due to wetting by liquid air, while oxygen adsorption increases continually. Both nitrogen and oxygen adsorb first at the internal annuli and at the grooves, and with increasing pressure, they then adsorb at the ridges and at the nanotube centers; at higher pressures, only oxygen adsorbs in the interstitial channels, and multilayer adsorption and wetting occur on the external surface as the bulk phase approaches saturation. The selectivity, like that of subcritical temperature adsorption on the infinite periodic bundle, decreases with increasing pressure and reaches a constant upon wetting. Adsorption at a supercritical temperature is of type I, with both nitrogen and oxygen adsorption increasing with increasing pressure. The selectivity of nitrogen to oxygen, like that of supercritical temperature adsorption on the infinite periodic bundle, first increases slightly and then decreases with increasing pressure. These results indicate that the adsorption selectivity strongly depends on temperature but only weakly depends on the type of the bundle and that a nitrogen--oxygen mixture (air) might be separated by competitive adsorption on the carbon nanotube bundles.
采用巨正则蒙特卡罗分子模拟方法,研究了氮气和氧气混合物(空气)在亚临界和超临界温度下在两种类型的单壁碳纳米管束上的吸附情况。在没有外表面的无限周期性六边形管束上,亚临界温度下的吸附为I型。随着压力增加,氮气吸附先增加后减少直至饱和;氧气吸附持续增加,取代氮气,直至饱和。氮气和氧气首先在纳米管内部形成环,然后随着覆盖度增加,它们占据纳米管中心,在最高覆盖度时,一些氧气也吸附在纳米管之间的间隙通道中。氮气对氧气的选择性随压力增加而降低,在接近饱和时达到恒定值。超临界温度下的吸附也是I型,氮气和氧气的吸附都随压力增加而增加,尽管氮气对氧气的选择性先略有增加,然后随压力增加而降低。在有外表面的小孤立六边形管束上,亚临界温度下的吸附为II型。随着压力增加,氮气吸附先增加,然后减少,最后由于液态空气的润湿作用再次增加,而氧气吸附持续增加。氮气和氧气首先在内环和凹槽处吸附,随着压力增加,它们随后在脊和纳米管中心吸附;在更高压力下,只有氧气吸附在间隙通道中,当本体相接近饱和时,在外表面发生多层吸附和润湿现象。选择性与无限周期性管束上亚临界温度吸附时一样,随压力增加而降低,在润湿时达到恒定值。超临界温度下的吸附为I型,氮气和氧气的吸附都随压力增加而增加。氮气对氧气的选择性与无限周期性管束上超临界温度吸附时一样,先略有增加,然后随压力增加而降低。这些结果表明,吸附选择性强烈依赖于温度,但仅微弱依赖于管束类型,并且氮气 - 氧气混合物(空气)可能通过在碳纳米管束上的竞争吸附而被分离。