Cited Article: Hummer, G. Water conduction through the hydrophobic channel of a carbon nanotube
Alert Expires: 22 AUG 2011
Number of Citing Articles: 6 new records this week (6 in this e-mail)
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Title:
A review of reverse osmosis membrane materials for desalination-Development to date and future potential
Authors:
Lee, KP; Arnot, TC; Mattia, D
Author Full Names:
Lee, Kali Peng; Arnot, Tom C.; Mattia, Davide
Source:
JOURNAL OF MEMBRANE SCIENCE 370 (1-2): 1-22 MAR 15 2011
Language:
English
Document Type:
Review
Author Keywords:
Desalination; Reverse osmosis (RO); Membrane material; Membrane performance; Nano-materials
KeyWords Plus:
CARBON NANOTUBE MEMBRANES; FILM COMPOSITE MEMBRANE; POLYAMIDE MOLECULAR-STRUCTURE; ATOMIC-FORCE MICROSCOPY; CARBIDE-DERIVED CARBON; RIGID STAR AMPHIPHILES; NANOFILTRATION MEMBRANES; SEAWATER DESALINATION; INTERFACIAL POLYMERIZATION; ZEOLITE MEMBRANES
Abstract:
Reverse osmosis (RO) is currently the most important desalination technology and it is experiencing significant growth. The objective of this paper is to review the historical and current development of RO membrane materials which are the key determinants of separation performance and water productivity, and hence to define performance targets for those who are developing new RO membrane materials. The chemistry, synthesis mechanism(s) and desalination performance of various RO membranes are discussed from the point of view of membrane materials science. The review starts with the first generation of asymmetric polymeric membranes and finishes with current proposals for nano-structured membrane materials. The paper provides an overview of RO performance in relation to membrane materials and methods of synthesis.
To date polymeric membranes have dominated the RO desalination industry. From the late 1950s to the 1980s the research effort focussed on the search for optimum polymeric membrane materials. In subsequent decades the performance of RO membranes has been optimised via control of membrane formation reactions, and the use of poly-condensation catalysts and additives. The performance of state-of-the-art RO membranes has been highlighted. Nevertheless, the advances in membrane permselectivity in the past decade has been relatively slow, and membrane fouling remains a severe problem.
The emergence of nano-technology in membrane materials science could offer an attractive alternative to polymeric materials. Hence nano-structured membranes are discussed in this review including zeolite membranes, thin film nano-composite membranes, carbon nano-tube membranes, and biomimetic membranes. It is proposed that these novel materials represent the most likely opportunities for enhanced RO desalination performance in the future, but that a number of challenges remain with regard to their practical implementation. (C) 2010 Elsevier B.V. All rights reserved.
Reprint Address:
Mattia, D, Univ Bath, Dept Chem Engn, Bath BA2 7AY, Avon, England.
Research Institution addresses:
[Lee, Kali Peng; Arnot, Tom C.; Mattia, Davide] Univ Bath, Dept Chem Engn, Bath BA2 7AY, Avon, England
E-mail Address:
D.Mattia@bath.ac.uk
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Cited Reference Count:
209
Times Cited:
0
Publisher:
ELSEVIER SCIENCE BV; PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
Subject Category:
Engineering, Chemical; Polymer Science
ISSN:
0376-7388
DOI:
10.1016/j.memsci.2010.12.036
IDS Number:
734RV
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Title:
Fluctuation Effects of the Electric Field Induced by Water on a Graphene Dot Band Gap
Authors:
Dalosto, SD; Tinte, S
Author Full Names:
Dalosto, Sergio D.; Tinte, Silvia
Source:
JOURNAL OF PHYSICAL CHEMISTRY C 115 (11): 4381-4386 MAR 24 2011
Language:
English
Document Type:
Article
KeyWords Plus:
NANORIBBONS; NANOTUBES; OXIDE
Abstract:
We investigate how a box of water molecules affects the HOMO LUMO gap of a rectangular graphene nanodot (GND) with two zigzag and two armchair edges, using a combination of first principles and molecular mechanics, and also classical molecular dynamics. A GND is solvated in a periodic box of water molecules, and the HOMO LUMO gap is computed for some snapshots taken from a molecular dynamics simulation. Although an isolated GND has a semiconductor state with degenerate alpha and beta gaps, we find that, in a solvated GND, that degeneracy broken and the gaps of both spins flavors oscillate following the time fluctuations in strength and direction of the electric field generated by the solvent at the edges. The average electric field generated by the water molecules causes an effect equivalent to applying a uniform electric field of 0.16 V/angstrom computed at the PBE level of theory. In particular, this field is not strong enough to change the GND semiconductor ground state to
a half-metallic one in nanodots with dimensions smaller than 2.5 nm, as those studied here. These results can be useful in the design of sensors based on graphene, indicating that important fluctuations in the energy gap can occur if water molecules are present.
Reprint Address:
Dalosto, SD, INTEC CONICET, Guemes 3450, RA-3000 Santa Fe, Argentina.
Research Institution addresses:
[Dalosto, Sergio D.] INTEC CONICET, RA-3000 Santa Fe, Argentina; Univ Nacl Litoral, RA-3000 Santa Fe, Argentina
E-mail Address:
dalosto@intec.unl.edu.ar
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Cited Reference Count:
44
Times Cited:
0
Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
Subject Category:
Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary
ISSN:
1932-7447
DOI:
10.1021/jp109297p
IDS Number:
735GK
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Title:
Syntheses, structures, and photoluminescence of lanthanide coordination polymers with pyridine-2,3,5,6-tetracarboxylic acid
Authors:
Yang, AH; Gao, HL; Cui, JZ; Zhao, B
Author Full Names:
Yang, Ai-Hong; Gao, Hong-Ling; Cui, Jian-Zhong; Zhao, Bin
Source:
CRYSTENGCOMM 13 (6): 1870-1876 2011
Language:
English
Document Type:
Article
KeyWords Plus:
ORGANIC SUPRAMOLECULAR COMPLEX; CYCLIC WATER HEPTAMER; SOLID-STATE; PYRAZINE-2,3,5,6-TETRACARBOXYLIC ACID; CRYSTAL-STRUCTURE; (H2O)(10) CLUSTER; 1,2,4,5-BENZENETETRACARBOXYLIC ACID; MOLECULAR RECOGNITION; FRAMEWORK STRUCTURES; ICE
Abstract:
Six lanthanide(III) coordination polymers with the formulae {[Ln(Hpdtc)(H2O)(3)]center dot H2O}(n) [Ln = La (1), Ce (2), Pr (3)], {[Ln(Hpdtc)(H2O)(2)]center dot 2H(2)O}(n) [Ln = Eu (4), Tb (5)] and {SmK(pdtc)(H2O)(4)} n (6) (H(4)pdtc = pyridine-2,3,5,6-tetracarboxylic acid) have been synthesized by reacting the corresponding rare earth salts or oxides with H(4)pdtc under hydrothermal conditions. In the three kinds of structure, H(4)pdtc displays three different coordination modes. H(4)pdtc is an elegant ligand with rich coordination sites and low symmetry, but has seldom been used to synthesize complexes. 1-6 are the first examples from lanthanide ions and H(4)pdtc. Furthermore, the novel wave-like T3(2)4(2)6(2) water tape with (H2O)(4) as the substructure is present in complex 6. The two complexes of Eu(III) and Tb(III) exhibit the corresponding characteristic luminescence.
Reprint Address:
Cui, JZ, Tianjin Univ, Dept Chem, Tianjin 300072, Peoples R China.
Research Institution addresses:
[Yang, Ai-Hong; Gao, Hong-Ling; Cui, Jian-Zhong] Tianjin Univ, Dept Chem, Tianjin 300072, Peoples R China; [Zhao, Bin] Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China
E-mail Address:
cuijianzhong@tju.edu.cn
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73
Times Cited:
0
Publisher:
ROYAL SOC CHEMISTRY; THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND
Subject Category:
Chemistry, Multidisciplinary; Crystallography
ISSN:
1466-8033
DOI:
10.1039/c0ce00397b
IDS Number:
729BV
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Title:
Raman spectroscopy of iodine molecules trapped in zeolite crystals
Authors:
Guo, WH; Wang, DD; Hu, JM; Tang, ZK; Du, SW
Author Full Names:
Guo, Wenhao; Wang, Dingdi; Hu, Juanmei; Tang, Z. K.; Du, Shengwang
Source:
APPLIED PHYSICS LETTERS 98 (4): Art. No. 043105 JAN 24 2011
Language:
English
Document Type:
Article
KeyWords Plus:
CARBON NANOTUBE; HYPERFINE INTERACTIONS; CHANNELS; STATE; NM
Abstract:
We study the Raman spectroscopy of neutral iodine molecules confined in the channels of zeolite AlPO4-5 (AFI) and AlPO4-11 (AEL) crystals, which shows that the molecular vibration states are significantly modified by the confinements from the nanosize channels. An iodine molecule trapped in the AEL crystal has an effective internuclear potential close to an ideal harmonic oscillator, while that in the AFI crystal behaves similarly to that in free space. The results are further confirmed by measuring the temperature dependence of Raman spectral width. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3549194]
Reprint Address:
Du, SW, Hong Kong Univ Sci & Technol, Dept Phys, Kowloon, Hong Kong, Peoples R China.
Research Institution addresses:
[Guo, Wenhao; Wang, Dingdi; Hu, Juanmei; Tang, Z. K.; Du, Shengwang] Hong Kong Univ Sci & Technol, Dept Phys, Kowloon, Hong Kong, Peoples R China
E-mail Address:
phzktang@ust.hk; dusw@ust.hk
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0
Publisher:
AMER INST PHYSICS; CIRCULATION & FULFILLMENT DIV, 2 HUNTINGTON QUADRANGLE, STE 1 N O 1, MELVILLE, NY 11747-4501 USA
Subject Category:
Physics, Applied
ISSN:
0003-6951
DOI:
10.1063/1.3549194
IDS Number:
712OR
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Title:
Control of Unidirectional Transport of Single-File Water Molecules through Carbon Nanotubes in an Electric Field
Authors:
Su, JY; Guo, HX
Author Full Names:
Su, Jiaye; Guo, Hongxia
Source:
ACS NANO 5 (1): 351-359 JAN 2010
Language:
English
Document Type:
Article
Author Keywords:
water molecule; transport; carbon nanotube; electric field; molecular dynamics simulation
KeyWords Plus:
NONPOLAR CAVITIES; DRUG-DELIVERY; ICE NANOTUBES; CHANNEL; MEMBRANES; COMPOSITES; MECHANISM; CLUSTERS; PROTEIN; DESALINATION
Abstract:
The transport of water molecules through nanopores is not only crucial to biological activities but also useful for designing novel nanofluidic devices. Despite considerable effort and progress that has been made, a controllable and unidirectional water flow is still difficult to achieve and the underlying mechanism is far from being understood. In this paper, using molecular dynamics simulations, we systematically investigate the effects of an external electric field on the transport of single-file water molecules through a carbon nanotube (CNT). We find that the orientation of water molecules inside the CNT can be well-tuned by the electric field and is strongly coupled to the water flux. This orientation induced water flux is energetically due to the asymmetrical water water interaction along the CNT ills. The wavelike water density profiles are disturbed under strong field strengths. The frequency of flipping for the water dipoles will decrease as the field strength is in
creased, and the flipping events vanish completely for the relatively large field strengths. Most importantly, a critical field strength E, related to the water flux is found. The water flux is increased as E is increased for E <= E-o while it is almost unchanged for E > E-c. Thus, the electric field offers a level of governing for unidirectional water flow, which may have some biological applications and provides a route for designing efficient nanopumps.
Reprint Address:
Guo, HX, Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Joint Lab Polymer Sci & Mat,State Key Lab Polymer, Beijing 100190, Peoples R China.
Research Institution addresses:
[Su, Jiaye; Guo, Hongxia] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Joint Lab Polymer Sci & Mat,State Key Lab Polymer, Beijing 100190, Peoples R China
E-mail Address:
hxguo@iccas.ac.cn
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75
Times Cited:
0
Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
Subject Category:
Chemistry, Multidisciplinary; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary
ISSN:
1936-0851
DOI:
10.1021/nn1014616
IDS Number:
710CA
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Title:
Helical Encapsulation of Graphene Nanoribbon into Carbon Nanotube
Authors:
Jiang, YY; Li, H; Li, YF; Yu, HQ; Liew, KM; He, YZ; Liu, XF
Author Full Names:
Jiang, Yanyan; Li, Hui; Li, Yunfang; Yu, Haiqing; Liew, Kim M.; He, Yezeng; Liu, Xiangfa
Source:
ACS NANO 5 (3): 2126-2133 MAR 2011
Language:
English
Document Type:
Article
Author Keywords:
molecular dynamics simulation; graphene nanoribbon; carbon nanotube; helical configuration; the pi-pi stacking interaction; nanoscale carriers
KeyWords Plus:
FORCE-FIELD; WATER; DYNAMICS; OXIDE; TRANSPORTATION; ENERGETICS; BEHAVIOR; CHANNEL; COMPASS; ESTERS
Abstract:
Molecular dynamics (MD) simulations were performed to study interaction between the graphene nanoribbon (GNR) and single-wall carbon nanotube (SWCNT). The GNR enters the SWCNT spontaneously to display a helical configuration which is quite similar to the chloroplast in the spirogyra cell. This unique phenomenon results from the combined action of the van der Waals potential well and the pi-pi stacking interaction. The size of SWCNT and GNR should satisfy some certain conditions in the helical encapsulation process. A DNA-like double helix would be formed inside the SWCNT with the encapsulation of two GNRs. A water cluster enclosed in the SWCNT has great effect on the formation of the GNR helix in the tube. Furthermore, we also studied the possibility that the spontaneous encapsulation of GNR is used for substance delivery. The expected outcome of these properties is to provide novel strategies to design nanoscale carriers and reaction devices.
Reprint Address:
Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.
Research Institution addresses:
[Jiang, Yanyan; Li, Hui; Li, Yunfang; Yu, Haiqing; He, Yezeng; Liu, Xiangfa] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China; [Liew, Kim M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China
E-mail Address:
lihuilmy@hotmail.com
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Cited Reference Count:
47
Times Cited:
0
Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
Subject Category:
Chemistry, Multidisciplinary; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary
ISSN:
1936-0851
DOI:
10.1021/nn103317u
IDS Number:
737LP
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