Neon and CO2 Adsorption on Open Carbon Nanohorns

被引:25
作者
Krungleviciute, Vaiva [2 ]
Ziegler, Carl A. [2 ]
Banjara, Shree R. [2 ]
Yudasaka, Masako [1 ]
Iijima, S. [1 ]
Migone, Aldo D. [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Nanotube Res Ctr, Tsukuba, Ibaraki 3058565, Japan
[2] So Illinois Univ, Dept Phys, Carbondale, IL 62901 USA
基金
美国国家科学基金会;
关键词
METAL-ORGANIC FRAMEWORKS; NANOTUBE BUNDLES; SURFACE-AREA; KINETICS; SEPARATION; GASES; TEMPERATURE; GRAPHITE;
D O I
10.1021/la401033u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present the results of a thermodynamics and kinetics study of the adsorption of neon and carbon dioxide on aggregates of chemically opened carbon nanohorns. Both the equilibrium adsorption characteristics, as well as the dependence of the kinetic behavior on sorbent loading, are different for these two adsorbates. For neon the adsorption isotherms display two steps before reaching the saturated vapor pressure, corresponding to adsorption on strong and on weak binding sites; the isosteric heat of adsorption is a decreasing function of sorbent loading (this quantity varies by about a factor of 2 on the range of loadings studied), and the speed of the adsorption kinetics increases with increasing loading. By contrast, for carbon dioxide there are no substeps in the adsorption isotherms; the isosteric heat is a nonmonotonic function of loading, the value of the isosteric heat never differs from the bulk heat of sublimation by more than 15%, and the kinetic behavior is opposite to that of neon, with equilibration times increasing for higher sorbent loadings. We explain the difference in the equilibrium properties observed for neon and carbon dioxide in terms of differences in the relative strengths of adsorbate-adsorbate to adsorbate-sorbent interaction for these species.
引用
收藏
页码:9388 / 9397
页数:10
相关论文
共 34 条
[1]  
[Anonymous], CHEM PHYS LETT
[2]   What chemicals will we need to capture CO2? [J].
Bara, Jason E. .
GREENHOUSE GASES-SCIENCE AND TECHNOLOGY, 2012, 2 (03) :162-171
[3]   Thermodynamics and structure of hydrogen, methane, argon, oxygen, and carbon dioxide adsorbed on single-wall carbon nanotube bundles [J].
Bienfait, M ;
Zeppenfeld, P ;
Dupont-Pavlovsky, N ;
Muris, M ;
Johnson, MR ;
Wilson, T ;
DePies, M ;
Vilches, OE .
PHYSICAL REVIEW B, 2004, 70 (03) :035410-1
[4]  
Bruch L. W., 1997, Physical Adsorption: Forces and Phenomena
[5]   Physisorption kinetics in carbon nanotube bundles [J].
Burde, Jared T. ;
Calbi, M. Mercedes .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (13) :5057-5063
[6]   Early Removal of Weak-Binding Adsorbates by Kinetic Separation [J].
Burde, Jared T. ;
Calbi, M. Mercedes .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (05) :808-812
[7]   Kinetics of External Adsorption on Nanotube Bundles: Surface Heterogeneity Effects [J].
Burde, Jared T. ;
Zuniga-Hansen, Nayeli ;
Park, Chong L. ;
Calbi, M. Mercedes .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (39) :16945-16950
[8]  
Calbi MM, 2008, ADSORPTION BY CARBONS, P187, DOI 10.1016/B978-008044464-2.50013-4
[9]   Industrial applications of metal-organic frameworks [J].
Czaja, Alexander U. ;
Trukhan, Natalia ;
Mueller, Ulrich .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (05) :1284-1293
[10]  
Drain L. E., 1958, T FARADAY SOC, V49, P650