Evaluation of functionalized isoreticular metal organic frameworks (IRMOFs) as smart nanoporous preconcentrators of RDX

被引:38
作者
Xiong, Ruichang [1 ]
Odbadrakh, Khorgolkhuu [2 ]
Michalkova, Andrea [3 ]
Luna, Johnathan P. [1 ]
Petrova, Tetyana [3 ]
Keffer, David J. [1 ]
Nicholson, Donald M. [4 ]
Fuentes-Cabrera, Miguel A. [5 ,6 ]
Lewis, James P. [2 ]
Leszczynski, Jerzy [3 ]
机构
[1] Univ Tennessee, Dept Chem & Biomol Engn, Knoxville, TN 37996 USA
[2] W Virginia Univ, Dept Phys, Morgantown, WV 26506 USA
[3] Jackson State Univ, Interdisciplinary Nanotox Ctr, Jackson, MS USA
[4] Oak Ridge Natl Lab, Comp Sci & Math Div, Oak Ridge, TN USA
[5] Univ Tennessee, Joint Inst Computat Sci, Oak Ridge, TN USA
[6] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN USA
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2010年 / 148卷 / 02期
基金
美国国家科学基金会;
关键词
Metal-organic framework; Explosive sensor; Preconcentrator; Molecular simulation; RDX; MOLECULAR-DYNAMICS SIMULATIONS; ADSORPTION; DIFFUSION; HYDROGEN; DESIGN; GASES; BINDING; MOF-5;
D O I
10.1016/j.snb.2010.05.064
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Classical molecular dynamics (MD) and Grand Canonical Monte Carlo (GCMC) simulations were used to generate self-diffusivities, adsorption isotherms and density distributions for hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) in five isoreticular metal-organic frameworks (IRMOFs), which varied in the cage size and in the presence and location of amine groups. These simulations were performed at room temperature (300 K) and low pressures (up to 1 ppm RDX). The atomic charges required for MD and GCMC simulations were calculated from quantum mechanical (QM) calculations using two different charge generation methods-Lowdin Population Analysis and Natural Bond Orbital Analysis. Both charge sets show that the presence of amine groups increases the amount of RDX adsorbed. The cage size and the location of amine groups also affect the loading of RDX. The amount of RDX adsorbed is correlated with the energy of adsorption. The activation energy for diffusion of RDX is not positively correlated with the energy of adsorption. The density distributions identify the location of the adsorption sites of RDX-exclusively in the big cage around the metal complex vertices and between benzene rings. In the absence of amine groups on the framework, one of nitro groups on RDX interacts closely with the metal complex. In the IRMOFs functionalized with amine groups, a second nitro group of the RDX interacts with an amine group, enhancing adsorption. With regard to the application as a smart nanoporous preconcentrator, these IRMOFs are found to concentrate RDX up to 3000 times compared to the gas phase, on a volumetric basis. From a simple Langmuir estimation, the selectivity of RDX over butane is up to 5000. The diffusion of RDX is sufficiently high for real time sensor applications. These results indicate IRMOFs can be tailored with functional groups to be highly selective nanoporous preconcentrators. (C) 2010 Elsevier B.V All rights reserved.
引用
收藏
页码:459 / 468
页数:10
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