Dramatic transport properties of carbon nanotube membranes for a robust protein channel mimetic platform

被引:44
作者
Hinds, Bruce [1 ]
机构
[1] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
基金
美国国家科学基金会;
关键词
Carbon nanotubes; Biomimetic; Water purification; Energy storage; Drug delivery; Membrane separations; Protein channel mimetics; Nanofluidics; Ion current; CHEMICAL-VAPOR-DEPOSITION; ELECTROOSMOTIC FLOW; MASS-TRANSPORT; FORCE MICROSCOPY; IONIC-DIFFUSION; WATER; MODEL; FUNCTIONALIZATION; PURIFICATION; DESALINATION;
D O I
10.1016/j.cossms.2011.05.003
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Carbon nanotube (CNT) membranes offer an exciting opportunity to mimic natural protein channels due to (1) a mechanism for dramatically enhanced fluid flow, (2) ability to place 'gatekeeper' chemistry at the entrance to pores, and (3) being electrically conductive to localize electric field or perform electrochemical transformations. The transport mechanisms through CNT membranes are primarily (1) ionic diffusion near bulk expectation, (2) gas flow enhanced 1-2 orders of magnitude primarily due to specular reflection, and (3) fluid flow 4-5 orders of magnitude faster than conventional materials due to a nearly ideal slip-boundary interface. Transport can be modulated by 'gatekeeper' chemistry at the pore entrance using steric hindrance, electrostatic attraction/repulsion, or biochemical state. Electroosmotic flow is seen to be highly power efficient and can act as a pump through regions of chemical selectivity. The fundamental requirements of mimicking protein channels are present in the CNT membrane system. This membrane structure is mechanically far more robust than lipid bilayer films, allowing for large-scale chemical separations, delivery or sensing based on the principles of protein channels. Applications ranging from water purification, energy generation and bio-separations are highlighted. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 66 条
[1]   Continuous production of aligned carbon nanotubes: a step closer to commercial realization [J].
Andrews, R ;
Jacques, D ;
Rao, AM ;
Derbyshire, F ;
Qian, D ;
Fan, X ;
Dickey, EC ;
Chen, J .
CHEMICAL PHYSICS LETTERS, 1999, 303 (5-6) :467-474
[2]  
[Anonymous], 2005, Handbook of Experimental Fluid Dynamics
[3]   Functionalization of carbon nanotubes by electrochemical reduction of aryl diazonium salts: A bucky paper electrode [J].
Bahr, JL ;
Yang, JP ;
Kosynkin, DV ;
Bronikowski, MJ ;
Smalley, RE ;
Tour, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (27) :6536-6542
[4]   Highly functionalized carbon nanotubes using in situ generated diazonium compounds [J].
Bahr, JL ;
Tour, JM .
CHEMISTRY OF MATERIALS, 2001, 13 (11) :3823-+
[5]   Chemical vapor deposition based synthesis of carbon nanotubes and nanofibers using a template method [J].
Che, G ;
Lakshmi, BB ;
Martin, CR ;
Fisher, ER ;
Ruoff, RS .
CHEMISTRY OF MATERIALS, 1998, 10 (01) :260-267
[6]   Designing carbon nanotube membranes for efficient water desalination [J].
Corry, Ben .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (05) :1427-1434
[7]   Ion exclusion by sub-2-nm carbon nanotube pores [J].
Fornasiero, Francesco ;
Park, Hyung Gyu ;
Holt, Jason K. ;
Stadermann, Michael ;
Grigoropoulos, Costas P. ;
Noy, Aleksandr ;
Bakajin, Olgica .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (45) :17250-17255
[8]  
Goldsmith J, J PHYS CHEM C UNPUB
[9]   Molecular Dynamics Simulation of Salt Rejection in Model Surface-Modified Nanopores [J].
Goldsmith, Jacob ;
Martens, Craig C. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (02) :528-535
[10]   A charge-driven molecular water pump [J].
Gong, Xiaojing ;
Li, Jingyuan ;
Lu, Hangjun ;
Wan, Rongzheng ;
Li, Jichen ;
Hu, Jun ;
Fang, Haiping .
NATURE NANOTECHNOLOGY, 2007, 2 (11) :709-712