Friday, June 17, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

Cited Article: Hummer, G. Water conduction through the hydrophobic channel of a carbon nanotube
Alert Expires: 22 AUG 2011
Number of Citing Articles: 2 new records this week (2 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
The role of activation energy and reduced viscosity on the enhancement of water flow through carbon nanotubes

Authors:
Babu, JS; Sathian, SP

Author Full Names:
Babu, Jeetu S.; Sathian, Sarith P.

Source:
JOURNAL OF CHEMICAL PHYSICS 134 (19): Art. No. 194509 MAY 21 2011

Language:
English

Document Type:
Article

KeyWords Plus:
ABSOLUTE REACTION-RATES; MOLECULAR-DYNAMICS; ROOM-TEMPERATURE; TRANSPORT; DIFFUSION; NANOFLUIDICS; SIMULATION; MEMBRANES; LIQUIDS; STORAGE

Abstract:
Molecular dynamics simulations are carried out to study the pressure driven fluid flow of water through single walled carbon nanotubes. A method for the calculation of viscosity of the confined fluid based on the Eyring theory of reaction rates is proposed. The method involves the calculation of the activation energy directly from the molecular dynamics trajectory information. Computations are performed using this method to study the effect of surface curvature on the confined fluid viscosity. The results indicate that the viscosity varies nonlinearly with the carbon nanotube diameter. It is concluded that the reason behind the observed enhancement in the rate of fluid flow through carbon nanotubes could be the nonlinear variation of viscosity. (C) 2011 American Institute of Physics. [doi:10.1063/1.3592532]

Reprint Address:
Sathian, SP, Natl Inst Technol Calicut, Computat Nanotechnol Lab, Sch Nano Sci & Technol, Kozhikode 673601, India.

Research Institution addresses:
[Babu, Jeetu S.; Sathian, Sarith P.] Natl Inst Technol Calicut, Computat Nanotechnol Lab, Sch Nano Sci & Technol, Kozhikode 673601, India

E-mail Address:
sarith@nitc.ac.in

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Cited Reference Count:
33

Times Cited:
0

Publisher:
AMER INST PHYSICS; CIRCULATION & FULFILLMENT DIV, 2 HUNTINGTON QUADRANGLE, STE 1 N O 1, MELVILLE, NY 11747-4501 USA

Subject Category:
Physics, Atomic, Molecular & Chemical

ISSN:
0021-9606

DOI:
10.1063/1.3592532

IDS Number:
770SX

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Title:
A review of water treatment membrane nanotechnologies

Authors:
Pendergast, MM; Hoek, EMV

Author Full Names:
Pendergast, MaryTheresa M.; Hoek, Eric M. V.

Source:
ENERGY & ENVIRONMENTAL SCIENCE 4 (6): 1946-1971 JUN 2011

Language:
English

Document Type:
Review

KeyWords Plus:
REVERSE-OSMOSIS MEMBRANES; ALIGNED CARBON NANOTUBES; FILM NANOCOMPOSITE MEMBRANES; ATOMIC-FORCE MICROSCOPY; COPOLYMER THIN-FILMS; MANGANESE-CATALYZED OZONATION; POLYAMIDE MOLECULAR-STRUCTURE; CELLULOSE-ACETATE MEMBRANES; SUPPORTED ZEROVALENT IRON; METAL-OXIDE NANOPARTICLES

Abstract:
Nanotechnology is being used to enhance conventional ceramic and polymeric water treatment membrane materials through various avenues. Among the numerous concepts proposed, the most promising to date include zeolitic and catalytic nanoparticle coated ceramic membranes, hybrid inorganic-organic nanocomposite membranes, and bio-inspired membranes such as hybrid protein-polymer biomimetic membranes, aligned nanotube membranes, and isoporous block copolymer membranes. A semi-quantitative ranking system was proposed considering projected performance enhancement (over state-of-the-art analogs) and state of commercial readiness. Performance enhancement was based on water permeability, solute selectivity, and operational robustness, while commercial readiness was based on known or anticipated material costs, scalability (for large scale water treatment applications), and compatibility with existing manufacturing infrastructure. Overall, bio-inspired membranes are farthest from commercial reality, but offer the most promise for performance enhancements; however, nanocomposite membranes offering significant performance enhancements are already commercially available. Zeolitic and catalytic membranes appear reasonably far from commercial reality and offer small to moderate performance enhancements. The ranking of each membrane nanotechnology is discussed along with the key commercialization hurdles for each membrane nanotechnology.

Reprint Address:
Pendergast, MM, Univ Calif Los Angeles, Dept Civil & Environm Engn, Nanomat & Membrane Technol Res Lab, 5732-G Boelter Hall,POB 951593, Los Angeles, CA 90095 USA.

Research Institution addresses:
[Pendergast, MaryTheresa M.; Hoek, Eric M. V.] Univ Calif Los Angeles, Dept Civil & Environm Engn, Nanomat & Membrane Technol Res Lab, Los Angeles, CA 90095 USA; [Hoek, Eric M. V.] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA

E-mail Address:
emvhoek@ucla.edu

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Cited Reference Count:
230

Times Cited:
0

Publisher:
ROYAL SOC CHEMISTRY; THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND

Subject Category:
Chemistry, Multidisciplinary; Energy & Fuels; Engineering, Chemical; Environmental Sciences

ISSN:
1754-5692

DOI:
10.1039/c0ee00541j

IDS Number:
772FG

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Friday, June 3, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

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)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Size and temperature effects on the viscosity of water inside carbon nanotubes

Authors:
Ye, HF; Zhang, HW; Zhang, ZQ; Zheng, YG

Author Full Names:
Ye, Hongfei; Zhang, Hongwu; Zhang, Zhongqiang; Zheng, Yonggang

Source:
NANOSCALE RESEARCH LETTERS 6 (1): Art. No. 87 DEC 2010

Language:
English

Document Type:
Article

KeyWords Plus:
MOLECULAR-DYNAMICS; TRANSPORT; CONDUCTION; CHANNEL

Abstract:
The influences of the diameter (size) of single-walled carbon nanotubes (SWCNTs) and the temperature on the viscosity of water confined in SWCNTs are investigated by an "Eyring-MD" (molecular dynamics) method. The results suggest that the relative viscosity of the confined water increases with increasing diameter and temperature, whereas the size-dependent trend of the relative viscosity is almost independent of the temperature. Based on the computational results, a fitting formula is proposed to calculate the size-and temperature-dependent water viscosity, which is useful for the computation on the nanoflow. To demonstrate the rationality of the calculated relative viscosity, the relative amount of the hydrogen bonds of water confined in SWCNTs is also computed. The results of the relative amount of the hydrogen bonds exhibit similar profiles with the curves of the relative viscosity. The present results should be instructive for understanding the coupling effect of the size
and the temperature at the nanoscale.

Reprint Address:
Zhang, HW, Dalian Univ Technol, State Key Lab Struct Anal Ind Equipment, Dept Engn Mech, Fac Vehicle Engn & Mech, Dalian 116023, Peoples R China.

Research Institution addresses:
[Ye, Hongfei; Zhang, Hongwu; Zhang, Zhongqiang; Zheng, Yonggang] Dalian Univ Technol, State Key Lab Struct Anal Ind Equipment, Dept Engn Mech, Fac Vehicle Engn & Mech, Dalian 116023, Peoples R China; [Zhang, Zhongqiang] Jiangsu Univ, Ctr Micro Nano Sci & Technol, Zhenjiang 212013, Peoples R China

E-mail Address:
zhanghw@dlut.edu.cn

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Cited Reference Count:
25

Times Cited:
0

Publisher:
SPRINGER; 233 SPRING ST, NEW YORK, NY 10013 USA

Subject Category:
Nanoscience & Nanotechnology; Materials Science, Multidisciplinary; Physics, Applied

ISSN:
1931-7573

DOI:
10.1186/1556-276X-6-87

IDS Number:
763AQ

========================================================================

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Title:
Nanoconfinement induced anomalous water diffusion inside carbon nanotubes

Authors:
Ye, HF; Zhang, HW; Zheng, YG; Zhang, ZQ

Author Full Names:
Ye, Hongfei; Zhang, Hongwu; Zheng, Yonggang; Zhang, Zhongqiang

Source:
MICROFLUIDICS AND NANOFLUIDICS 10 (6): 1359-1364 JUN 2011

Language:
English

Document Type:
Article

Author Keywords:
Diffusion mechanism; Diffusion coefficient; Carbon nanotube; Confined water; Molecular dynamics

KeyWords Plus:
SINGLE-FILE DIFFUSION; MOLECULAR-DYNAMICS; TRANSPORT; FLUID

Abstract:
The diffusion mechanism and coefficient of water confined in carbon nanotubes (CNTs) of diameter ranging from 8 to 54 are studied by molecular dynamics simulations. It is found that the motions of water molecules inside the CNTs of diameter smaller than 12.2 follow a two-stage diffusion mechanism. Initially, the water diffusion exhibits a long-time super- or sub-diffusion mechanism, and thereafter it transits to the single-file type inside the (6, 6) CNT and shifts to the Fickian type inside the larger CNTs. As for the CNTs of diameter larger than 12.2 , the diffusion of the confined water occurs through the Fickian mechanism, which is identical to that of the bulk water. The simulation results further reveal that the diffusion coefficient of the confined water is non-monotonically dependent on the diameter, which can be ascribed to the double-edged effect of CNTs, i.e., the surface effect and the size effect.

Reprint Address:
Zhang, HW, Dalian Univ Technol, Fac Vehicle Engn & Mech, Dept Engn Mech, State Key Lab Struct Anal Ind Equipment, Dalian 116023, Peoples R China.

Research Institution addresses:
[Ye, Hongfei; Zhang, Hongwu; Zheng, Yonggang; Zhang, Zhongqiang] Dalian Univ Technol, Fac Vehicle Engn & Mech, Dept Engn Mech, State Key Lab Struct Anal Ind Equipment, Dalian 116023, Peoples R China; [Zhang, Zhongqiang] Jiangsu Univ, Ctr Micro Nano Sci & Technol, Zhenjiang 212013, Peoples R China

E-mail Address:
zhanghw@dlut.edu.cn

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Times Cited:
0

Publisher:
SPRINGER HEIDELBERG; TIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY

Subject Category:
Nanoscience & Nanotechnology; Instruments & Instrumentation; Physics, Fluids & Plasmas

ISSN:
1613-4982

DOI:
10.1007/s10404-011-0772-y

IDS Number:
763TF

========================================================================

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Title:
Non local effects in the forced vibration of an elastically connected double-carbon nanotube system under a moving nanoparticle

Authors:
Simsek, M

Author Full Names:
Simsek, Mesut

Source:
COMPUTATIONAL MATERIALS SCIENCE 50 (7): 2112-2123 MAY 2011

Language:
English

Document Type:
Article

Author Keywords:
Vibration; Nonlocal elasticity theory; Carbon nanotube; Nanoparticle; Moving load

KeyWords Plus:
NONLOCAL CONTINUUM-MECHANICS; TIMOSHENKO BEAM THEORY; SMALL LENGTH SCALE; WAVE-PROPAGATION; TRANSVERSE VIBRATIONS; MODEL; LOAD; ADSORPTION; SENSORS

Abstract:
This study presents an analytical method for the forced vibration of an elastically connected double-carbon nanotube system (DCNTS) carrying a moving nanoparticle based on the nonlocal elasticity theory. The two nanotubes are identical and are connected with each other continuously by elastic springs. The problem is also solved numerically by using the Galerkin method and the time integration method of Newmark to establish the reliability of the analytical method. Two sets of critical velocity exist for DCNTS. The closed-form solutions for the dynamic deflections of the two nanotubes are derived for these two sets of critical velocity for the first time in this study. The influences of the nonlocal parameter, aspect ratio, velocity of the moving nanoparticle and the elastic layer between the nanotubes on the dynamic responses are discussed. The study shows that the dynamic behavior of the double-carbon nanotube system is greatly influenced by the nonlocal effects. The dynamic
deflections predicted by the classical theory are always smaller than those predicted by the nonlocal theory due to the nonlocal effects. Thus, the classical beam models are not suitable in modeling carbon nanotubes with small aspect ratio, and nonlocal effects should be taken into account. Furthermore, the velocity of the nanoparticle and the stiffness of the elastic layer have significant effects on the dynamic behavior of DCNTS. (C) 2011 Elsevier B.V. All rights reserved.

Reprint Address:
Simsek, M, Yildiz Tech Univ, Dept Civil Engn, Davutpasa Campus, TR-34210 Esenler, Turkey.

Research Institution addresses:
Yildiz Tech Univ, Dept Civil Engn, TR-34210 Esenler, Turkey

E-mail Address:
msimsek@yildiz.edu.tr

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84

Times Cited:
0

Publisher:
ELSEVIER SCIENCE BV; PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS

Subject Category:
Materials Science, Multidisciplinary

ISSN:
0927-0256

DOI:
10.1016/j.commatsci.2011.02.017

IDS Number:
764RN

========================================================================

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Title:
Molecular Dynamics Simulation of the Antiamoebin Ion Channel: Linking Structure and Conductance

Authors:
Wilson, MA; Wei, CY; Bjelkmar, P; Wallace, BA; Pohorille, A

Author Full Names:
Wilson, Michael A.; Wei, Chenyu; Bjelkmar, Paer; Wallace, B. A.; Pohorille, Andrew

Source:
BIOPHYSICAL JOURNAL 100 (10): 2394-2402 MAY 18 2011

Language:
English

Document Type:
Article

KeyWords Plus:
NERNST-PLANCK THEORY; FORMING POLYPEPTIDE; POTASSIUM CHANNELS; ALPHA-HEMOLYSIN; BACTERIAL PORIN; ALAMETHICIN; MEMBRANE; MODELS; TRANSPORT; FORCE

Abstract:
Molecular-dynamics simulations were carried out to ascertain which of the potential multimeric forms of the transmembrane peptaibol channel, antiamoebin, is consistent with its measured conductance. Estimates of the conductance obtained through counting ions that cross the channel and by solving the Nernst-Planck equation yield consistent results, indicating that the motion of ions inside the channel can be satisfactorily described as diffusive. The calculated conductance of octameric channels is markedly higher than the conductance measured in single channel recordings, whereas the tetramer appears to be nonconducting. The conductance of the hexamer was estimated to be 115 +/- 34 pS and 74 +/- 20 pS, at 150 mV and 75 mV, respectively, in satisfactory agreement with the value of 90 pS measured at 75 mV. On this basis, we propose that the antiamoebin channel consists of six monomers. Its pore is large enough to accommodate K+ and Cl- with their first solvation shells intact. T
he free energy barrier encountered by K+ is only 2.2 kcal/mol whereas Cl- encounters a substantially higher barrier of nearly 5 kcal/mol. This difference makes the channel selective for cations. Ion crossing events are shown to be uncorrelated and follow Poisson statistics.

Reprint Address:
Pohorille, A, Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA.

Research Institution addresses:
[Wilson, Michael A.; Wei, Chenyu; Pohorille, Andrew] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA; [Wilson, Michael A.; Wei, Chenyu; Bjelkmar, Paer; Pohorille, Andrew] NASA, Ames Res Ctr, Exobiol Branch, Moffett Field, CA 94035 USA; [Wallace, B. A.] Univ London, Inst Struct & Mol Biol, Birkbeck Coll, Dept Crystallog, London, England

E-mail Address:
Andrew.Pohorille@nasa.gov

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62

Times Cited:
0

Publisher:
CELL PRESS; 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, MA 02139 USA

Subject Category:
Biophysics

ISSN:
0006-3495

DOI:
10.1016/j.bpj.2011.03.054

IDS Number:
767BS

========================================================================

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Title:
Mass Transport through Carbon Nanotube Membranes in Three Different Regimes: Ionic Diffusion and Gas and Liquid Flow

Authors:
Majumder, M; Chopra, N; Hinds, BJ

Author Full Names:
Majumder, Mainak; Chopra, Nitin; Hinds, Bruce J.

Source:
ACS NANO 5 (5): 3867-3877 MAY 2011

Language:
English

Document Type:
Article

Author Keywords:
membrane; separations; biomimetic; nanofluidics

KeyWords Plus:
MOLECULAR-DYNAMICS SIMULATIONS; WATER; SEPARATION; NANOPORES; MIXTURES; SURFACES; CHANNEL; PORES; FILMS; SLIP

Abstract:
Transport phenomena through the hollow conduits of carbon nanotubes (CNTs) are subjects of intense theoretical and experimental research. We have studied molecular transport over the large spectrum of ionic diffusion to pressure-driven gaseous and liquid flow. Plasma oxidation during the fabrication of the membrane introduces carboxylic acid groups at the CNT entrance, which provides electrostatic "gatekeeper" effects on ionic transport. Diffusive transport of ions of different charge and size through the core of the CNT is close to bulk diffusion expectations and allows estimation of the number of open pores or porosity of the membrane. Flux of gases such as N-2, CO2, Ar, H-2, and CH4 scaled Inversely with their molecular weight by an exponent of 0.4, close to expected kinetic theory velocity expectations. However, the magnitude of the fluxes was similar to 15- to 30-fold higher than predicted from Knudsen diffusion kinetics and consistent with specular momentum reflection i
nside smooth pores. Polar liquids such as water, ethanol, and isopropyl alcohol and nonpolar liquids such as hexane and decane were dramatically enhanced, with water flow over 4 orders of magnitude larger than "no-slip" hydrodynamic flow predictions. As direct experimental proof for the mechanism of near perfect slip conditions within CNT cores, a stepwise hydrophilic functionalization of CNT membranes from as-produced, tip-functionalized, and core-functionalized was performed. Pressure-driven water flow through the membrane was reduced from 5 x 10(4) to 2 x 10(2) to less than a factor of 5 enhancement over conventional Newtonian flow, while retaining nearly the same pore area.

Reprint Address:
Hinds, BJ, Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA.

Research Institution addresses:
[Majumder, Mainak; Hinds, Bruce J.] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA; [Chopra, Nitin; Hinds, Bruce J.] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA

E-mail Address:
bjhinds@engr.uky.edu

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Cited Reference Count:
57

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Multidisciplinary; Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary

ISSN:
1936-0851

DOI:
10.1021/nn200222g

IDS Number:
767AD

========================================================================

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Title:
Self-Cleaning Flexible Infrared Nanosensor Based on Carbon Nanoparticles

Authors:
Yuan, LY; Dai, JJ; Fan, XH; Song, T; Tao, YT; Wang, K; Xu, Z; Zhang, J; Bai, XD; Lu, PX; Chen, J; Zhou, J; Wang, ZL

Author Full Names:
Yuan, Longyan; Dai, Junjie; Fan, Xiaohong; Song, Ting; Tao, Yu Ting; Wang, Kai; Xu, Zhi; Zhang, Jun; Bai, Xuedong; Lu, Peixiang; Chen, Jian; Zhou, Jun; Wang, Zhong Lin

Source:
ACS NANO 5 (5): 4007-4013 MAY 2011

Language:
English

Document Type:
Article

Author Keywords:
carbon nanoparticles; flexible electronics; infrared sensor; self-cleaning; polydimethylsiloxane

KeyWords Plus:
NANOWIRE TRANSISTOR ARRAYS; SEMICONDUCTING POLYMER; PHOTOVOLTAIC DEVICES; RAMAN-SPECTROSCOPY; NANOTUBE FILMS; PHOTOCONDUCTIVITY; SURFACES; SOOT; PHOTODETECTORS; SPECTRA

Abstract:
Highly flexible, robust, and sensitive Infrared nanosensors were fabricated based on carbon nanoparticles that were synthesized through a simple and low-cost flame method. The infrared nanosensor devices showed sharp infrared photoresponse with a response time of similar to 68 ms and a maximum photocurrent change of similar to 52.9%. The devices showed a superhydrophobic property with a contact angle larger than 150 degrees and a sliding angle of similar to 4 degrees. The mechanism for the enhanced Infrared photoresponse from carbon nanoparticles is discussed.

Reprint Address:
Zhou, J, Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan 430074, Peoples R China.

Research Institution addresses:
[Yuan, Longyan; Dai, Junjie; Fan, Xiaohong; Song, Ting; Wang, Kai; Zhang, Jun; Lu, Peixiang; Zhou, Jun; Wang, Zhong Lin] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan 430074, Peoples R China; [Tao, Yu Ting; Chen, Jian] Sun Yat Sen Univ, Instrumental Anal & Res Ctr, Guangzhou 510275, Guangdong, Peoples R China; [Yuan, Longyan; Dai, Junjie; Fan, Xiaohong; Song, Ting; Wang, Kai; Zhang, Jun; Lu, Peixiang; Zhou, Jun; Wang, Zhong Lin] Huazhong Univ Sci & Technol, Coll Optoelect Sci & Engn, Wuhan 430074, Peoples R China; [Xu, Zhi; Bai, Xuedong] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China; [Wang, Zhong Lin] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA

E-mail Address:
jun.zhou@mail.hust.edu.cn; zlwang@gatech.edu

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Cited Reference Count:
57

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Multidisciplinary; Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary

ISSN:
1936-0851

DOI:
10.1021/nn200571q

IDS Number:
767AD

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Friday, May 20, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

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:
Measurement of the Rate of Water Translocation through Carbon Nanotubes

Authors:
Qin, XC; Yuan, QZ; Zhao, YP; Xie, SB; Liu, ZF

Author Full Names:
Qin, Xingcai; Yuan, Quanzi; Zhao, Yapu; Xie, Shubao; Liu, Zhongfan

Source:
NANO LETTERS 11 (5): 2173-2177 MAY 2011

Language:
English

Document Type:
Article

Author Keywords:
Nanofluidics; water flow velocity; enhancement factor; slip length; CNT-FET

KeyWords Plus:
ELECTRICAL BREAKDOWN; RAMAN-SPECTROSCOPY; FLOW; TRANSPORT; GROWTH

Abstract:
We present an approach for measuring the water flow rate through individual ultralong carbon nanotubes (CNTs) using field effect transistors array defined on individual tubes. Our work exhibits a rate enhancement of 882-51 and a slip length of 53-8 nm for CNTs with diameters of 0.81-1.59 nm. We also found that the enhancement factor does not increase monotonically with shrinking tube diameter and there exists a discontinuous region around 0.98-1.10 nm. We believe that these single-tube level results would help understand the intrinsic nanofluidics of water in CNTs.

Reprint Address:
Liu, ZF, Peking Univ, Coll Chem & Mol Engn, State Key Lab Struct Chem Unstable & Stable Speci, Ctr Nanochem,Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China.

Research Institution addresses:
[Qin, Xingcai; Xie, Shubao; Liu, Zhongfan] Peking Univ, Coll Chem & Mol Engn, State Key Lab Struct Chem Unstable & Stable Speci, Ctr Nanochem,Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China; [Yuan, Quanzi; Zhao, Yapu] Chinese Acad Sci, Inst Mech, State Key Lab Nonlinear Mech, Beijing 100190, Peoples R China

E-mail Address:
zfliu@pku.edu.cn

Cited References:
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Cited Reference Count:
21

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Multidisciplinary; Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary; Physics, Applied; Physics, Condensed Matter

ISSN:
1530-6984

DOI:
10.1021/n1200843g

IDS Number:
761CN

========================================================================

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Title:
Effect of Electric Field on Liquid Infiltration into Hydrophobic Nanopores

Authors:
Xu, BX; Qiao, Y; Zhou, QL; Chen, X

Author Full Names:
Xu, Baoxing; Qiao, Yu; Zhou, Qulan; Chen, Xi

Source:
LANGMUIR 27 (10): 6349-6357 MAY 17 2011

Language:
English

Document Type:
Article

KeyWords Plus:
CARBON NANOTUBES; MOLECULAR-DYNAMICS; SILICA-GEL; WATER; SURFACES; CAPILLARITY; SIMULATIONS; NANOSCALE; TRANSPORT; CHANNELS

Abstract:
Understanding the variation of nanofluidic behavior in the presence of an external electric field is critical for controlling and designing nanofluidic devices. By studying the critical infiltration pressure of liquids into hydrophobic nanopores using molecular dynamics (MD) simulations and experiments, important insights can be gained on the variation of the effective liquid solid interfacial tension with the magnitude and sign of electric field, as well as its coupling with the pore size and the solid and liquid species. It is found that the effective hydrophobicity reduces with the increase of electric intensity and/or pore size, and the behavior is asymmetric with respect to the direction of the electric field. The underlying molecular mechanisms are revealed via the study of the density profile, contact angle, and surface tension of confined liquid molecules.

Reprint Address:
Chen, X, Columbia Univ, Columbia Nanomech Res Ctr, Dept Earth & Environm Engn, New York, NY 10027 USA.

Research Institution addresses:
[Xu, Baoxing; Chen, Xi] Columbia Univ, Columbia Nanomech Res Ctr, Dept Earth & Environm Engn, New York, NY 10027 USA; [Qiao, Yu] Univ Calif San Diego, Dept Struct Engn, La Jolla, CA 92093 USA; [Zhou, Qulan] Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Xian 710049, Peoples R China; [Chen, Xi] Xi An Jiao Tong Univ, Sch Aerosp, Xian 710049, Peoples R China; [Chen, Xi] Hanyang Univ, Dept Civil & Environm Engn, Seoul 133791, South Korea

E-mail Address:
qlzhou@mail.xjtu.edu.cn; xichen@columbia.edu

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43

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Multidisciplinary; Chemistry, Physical; Materials Science, Multidisciplinary

ISSN:
0743-7463

DOI:
10.1021/la200477y

IDS Number:
760AL

========================================================================

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Title:
Vibrational Energy Transfer between Carbon Nanotubes and Nonaqueous Solvents: A Molecular Dynamics Study

Authors:
Nelson, TR; Chaban, VV; Prezhdo, VV; Prezhdo, OV

Author Full Names:
Nelson, Tammie R.; Chaban, Vitaly V.; Prezhdo, Victor V.; Prezhdo, Oleg V.

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 115 (18): 5260-5267 MAY 12 2011

Language:
English

Document Type:
Article

KeyWords Plus:
SOLVATION DYNAMICS; HYDRATED ELECTRON; AB-INITIO; SIMULATION; WATER; ACETONITRILE; RELAXATION; FUNCTIONALIZATION

Abstract:
We report molecular dynamics (MD) simulation of energy exchange between single-walled carbon nanotubes (CNTs) and two aprotic solvents, acetonitrile and cyclohexane. Following our earlier study of hydrated CNTs, we find that the time scales and molecular mechanisms of the energy transfer are largely independent of the nature of the surrounding medium, and therefore, should hold for other media including polymer matrices and DNA. The vibrational energy exchange between CNT and solvents exhibits two time-scales. Over half of the energy is transferred in less than one picosecond, indicating that the dominant exchange mechanism is inertial relaxation. It occurs by collisions of solvent molecules with CNT walls, facilitated by the short-range Lennard-Jones interaction. Additional several picoseconds are required for the remainder of the vibrational energy exchange, corresponding to the diffusive relaxation mechanism and involving collective molecular motions. The faster stage of t
he CNT-solvent energy exchange occurs on the same time-scale, and therefore, competes with the vibrational energy relaxation inside CNTs. The energy exchange time-scales are significantly influenced by the arrangement of solvent molecules inside CNTs. Generally, the effects of confinement on the dynamics can be rationalized by analysis of the solvent structure. For the same CNT diameter, the extent of the confinement effect strongly depends on the size of the solvent molecules. Icelike properties in water seen in small CNTs disappear in CNTs with intermediate diameters. In acetonitrile and cyclohexane, medium size CNTs still show strong confinement effects. Rotational motions of acetonitrile molecules are inhibited, and the cyclohexane density is dramatically decreased. The disbalance between the local temperatures of the inside and outside regions of the solvent equilibrates through a tube-mediated interaction, rather than by a direct coupling between the two solvent subsys
tems. In all cases, the CNT-solvent energy transfer is media!
ted by s
low motions in the frequency range of CNT radial breathing modes.

Reprint Address:
Prezhdo, OV, Univ Rochester, Dept Chem, Rochester, NY 14627 USA.

Research Institution addresses:
[Chaban, Vitaly V.; Prezhdo, Oleg V.] Univ Rochester, Dept Chem, Rochester, NY 14627 USA; [Nelson, Tammie R.] Univ Washington, Dept Chem, Seattle, WA 98195 USA; [Prezhdo, Victor V.] Jan Kochanowski Univ, Inst Chem, PL-25406 Kielce, Poland

E-mail Address:
oleg.prezhdo@rochester.edu

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53

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Physical

ISSN:
1520-6106

DOI:
10.1021/jp108776q

IDS Number:
757ZA

========================================================================

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Title:
Vibrational Spectroscopy of Water in Narrow Nanopores

Authors:
Weinwurm, M; Dellago, C

Author Full Names:
Weinwurm, Marcus; Dellago, Christoph

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 115 (18): 5268-5277 MAY 12 2011

Language:
English

Document Type:
Article

KeyWords Plus:
ULTRAFAST INFRARED-SPECTROSCOPY; HYDROGEN-BOND DYNAMICS; CARBON NANOTUBES; LIQUID WATER; MOLECULAR SIMULATION; DILUTE HOD; D2O; CONDUCTION; TRANSPORT; MODELS

Abstract:
Inside narrow pores, for instance, realized as carbon nanotubes, water forms structures that strongly differ from the structure of bulk liquid water or ice. Here we compute vibrational spectra of such systems using molecular dynamics simulation combined with quantum mechanical perturbation theory. We focus on the spectroscopic response of single-file water chains in pores with subnanometer diameter, finding characteristic signatures of dangling and hydrogen-bonded hydrogen configurations occurring in this particular form of water. These features in the absorption spectra permit us to distinguish single-file water from the stacked-ring structures that form in wider pores. As previously observed in bulk liquid water, the vibrational frequency of the OH stretch of an HDO molecule in a system of D2O molecules is essentially determined by the electric field acting at the position of the hydrogen atom, providing a way to link the spectroscopic response to the local charge distribut
ion of specific molecular arrangements.

Reprint Address:
Dellago, C, Univ Vienna, Fac Phys, Boltzmanngasse 5, A-1090 Vienna, Austria.

Research Institution addresses:
[Weinwurm, Marcus; Dellago, Christoph] Univ Vienna, Fac Phys, A-1090 Vienna, Austria

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Cited Reference Count:
49

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Physical

ISSN:
1520-6106

DOI:
10.1021/jp109037q

IDS Number:
757ZA

========================================================================

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Title:
Effect of Curvature on the alpha-Helix Breaking Tendency of Carbon Based Nanomaterials

Authors:
Balamurugan, K; Singam, ERA; Subramanian, V

Author Full Names:
Balamurugan, K.; Singam, E. R. Azhagiya; Subramanian, V.

Source:
JOURNAL OF PHYSICAL CHEMISTRY C 115 (18): 8886-8892 MAY 12 2011

Language:
English

Document Type:
Article

KeyWords Plus:
MOLECULAR-DYNAMICS; NANOTUBE MEMBRANES; FORCE-FIELD; SIMULATION; PROTEINS; PEPTIDE

Abstract:
Our previous study on the interaction of alpha-helical peptide with single walled carbon nanotubes (CNTs) has revealed the structural basis for the helix breaking tendency of the CNT and associated energetics (J. Phys. Chem. B 2010, 114, 14048). In this study, a systematic attempt has been made to explore the relationship between the curvature of carbon nanomaterials (NMs) and their alpha-helix breaking tendency. The interaction of a model alpha-helical peptide, polyalanine consisting of 40 residues (PA(40)) with CNTs of different chiralities ((6,6), (10,10), (14,14), and (18,18)) and planar graphene sheet has been investigated using molecular dynamics (MD) simulation approach. The structural changes in the helical peptide which is adsorbed onto the surface of the NMs of different curvatures have been derived from the MD simulation. The role of electrostatic and van der Waals energies in the interaction process has also been obtained from the MD trajectory. Results show that
the extent of helix breakage induced by the NMs is inversely proportional to their curvature; that is, the helix breaking tendency is minimum for the CNT having the highest curvature and maximum for the planar graphene sheet.

Reprint Address:
Subramanian, V, Cent Leather Res Inst, Chem Lab, Council Sci & Ind Res, Madras 600020, Tamil Nadu, India.

Research Institution addresses:
[Balamurugan, K.; Singam, E. R. Azhagiya; Subramanian, V.] Cent Leather Res Inst, Chem Lab, Council Sci & Ind Res, Madras 600020, Tamil Nadu, India

E-mail Address:
subuchem@hotmail.com

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Cited Reference Count:
40

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/jp110898r

IDS Number:
757ZB

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Title:
Salty water desalination using carbon nanotubes membrane

Authors:
Tofighy, MA; Shirazi, Y; Mohammadi, T; Pak, A

Author Full Names:
Tofighy, Maryam Ahmadzadeh; Shirazi, Yaser; Mohammadi, Toraj; Pak, Afshin

Source:
CHEMICAL ENGINEERING JOURNAL 168 (3): 1064-1072 APR 15 2011

Language:
English

Document Type:
Article

Author Keywords:
Carbon nanotubes membrane; Salty water desalination; Taguchi method

KeyWords Plus:
METAL-IONS; CVD

Abstract:
Carbon nanotube (CNT) film was synthesized directly on macroporous surface of a-alumina support by chemical vapor deposition (CVD) of cyclohexanol and ferrocene in nitrogen atmosphere at 650 degrees C, and oxidized using HNO3 and H2SO4 and then employed as membrane in desalination process (sodium chloride removal from water). In order to enhance the performance of the oxidized CNTs membrane, effects of operating parameters on the yield of desalinated water (separation percent and permeate flux) were studied. Four parameters at three levels were selected: feed concentration (10,000, 20,000 and 30,000 ppm), temperature (25. 35 and 45 degrees C), pressure (4, 7 and 10 bar) and flow rate (200, 350 and 5001/h). Taguchi method was used to plan a minimum number of experiments and to find the optimal conditions. The results showed that increasing feed concentration, temperature and flow rate as well as decreasing pressure optimize the performance of the oxidized CNTs membrane (separa
tion percent and permeate flux). Analysis of variance (ANOVA) was applied and it was found that temperature is the most influential factor on the oxidized CNTs membrane performance (its contribution percentage was calculated to be about 60%). (C) 2011 Elsevier B.V. All rights reserved.

Reprint Address:
Mohammadi, T, Iran Univ Sci & Technol IUST, Res Ctr Membrane Separat Proc, Fac Chem Engn, Tehran, Iran.

Research Institution addresses:
[Tofighy, Maryam Ahmadzadeh; Shirazi, Yaser; Mohammadi, Toraj; Pak, Afshin] Iran Univ Sci & Technol IUST, Res Ctr Membrane Separat Proc, Fac Chem Engn, Tehran, Iran

E-mail Address:
torajmohammadi@iust.ac.ir

Cited References:
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Cited Reference Count:
33

Times Cited:
0

Publisher:
ELSEVIER SCIENCE SA; PO BOX 564, 1001 LAUSANNE, SWITZERLAND

Subject Category:
Engineering, Environmental; Engineering, Chemical

ISSN:
1385-8947

DOI:
10.1016/j.cej.2011.01.086

IDS Number:
761BI

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Friday, May 13, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

Cited Article: Hummer, G. Water conduction through the hydrophobic channel of a carbon nanotube
Alert Expires: 22 AUG 2011
Number of Citing Articles: 2 new records this week (2 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
A mechanical model for single-file transport of water through carbon nanotube membranes

Authors:
Chan, Y; Hill, JM

Author Full Names:
Chan, Yue; Hill, James M.

Source:
JOURNAL OF MEMBRANE SCIENCE 372 (1-2): 57-65 APR 15 2011

Language:
English

Document Type:
Article

Author Keywords:
Single-file transport; Continuous approximation; Classical phonon theory; Carbon nanotube; Water molecules

KeyWords Plus:
DIFFUSION; CHANNEL; FULLERENES; ATOMS; IONS; BEHAVIOR; FLOW

Abstract:
Carbon nanotubes can be embedded into a polymer matrix to manufacture nanotube membranes generating rapid water transport. In particular, for nanotubes of small radii, the single-file transport of water diffusing rapidly and concertedly through densely filled carbon nanotubes has been reported. In this paper, we provide an additional methodology to investigate such problems by employing both applied mathematical modelling and classical phonon theory. Our approach has the merit of giving rise to rapid computational times in comparison to the molecular dynamics simulations approach. The total energy of a water molecule inside a carbon nanotube can be determined analytically using point-point interactions and the continuous approximation. In addition, we may use classical phonon theory for the collective motion of water molecules inside the nanotube to formulate the basic equations of motion for water diffusing through a carbon nanotube. Upon making a 'sufficiently long' hypoth!
esis, the average water flow time can be deduced analytically. Furthermore, we incorporate external forces at the tube ends and show that water is virtually incompressible for external forces up to 3 pN. We also determine the variation of the water flow time under random fluctuations in the presence of the external forces and find that the random effect diminishes as the external force increases. This outcome could open up a precise engineering approach for using such nanotube membranes in numerous applications. (C) 2011 Elsevier B.V. All rights reserved.

Reprint Address:
Chan, Y, Univ Adelaide, Nanomech Grp, Sch Math Sci, Adelaide, SA 5005, Australia.

Research Institution addresses:
[Chan, Yue; Hill, James M.] Univ Adelaide, Nanomech Grp, Sch Math Sci, Adelaide, SA 5005, Australia

E-mail Address:
yue.chan@adelaide.edu.au

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Cited Reference Count:
43

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.2011.01.040

IDS Number:
754CI

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Title:
Phase transition of nanotube-confined water driven by electric field

Authors:
Fu, ZM; Luo, Y; Ma, JP; Wei, GH

Author Full Names:
Fu, Zhaoming; Luo, Yin; Ma, Jianpeng; Wei, Guanghong

Source:
JOURNAL OF CHEMICAL PHYSICS 134 (15): Art. No. 154507 APR 21 2011

Language:
English

Document Type:
Article

KeyWords Plus:
WALLED CARBON NANOTUBES; ICE-NANOTUBES; TRANSPORT-PROPERTIES; CHANNEL; DYNAMICS; NMR

Abstract:
The effects of electric field on the phase behaviors of water encapsulated in a thick single-walled carbon nanotube (SWCNT) (diameter = 1.2 nm) have been studied by performing extensive molecular dynamics simulations at atmospheric pressure. We found that liquid water can freeze continuously into either pentagonal or helical solidlike ice nanotube in SWCNT, depending on the strengths of the external electric field applied along the tube axis. Remarkably, the helical one is new ice phase which was not observed previously in the same size of SWCNT in the absence of electric field. Furthermore, a discontinuous solid-solid phase transition is observed between pentagonal and helical ice nanotubes as the strengths of the external electric field changes. The mechanism of electric-field-induced phase transition is discussed. The dependence of ice structures on the chiralities of SWCNTs is also investigated. Finally, we present a phase diagram of confined water in the electric field-!
temperature plane. (C) 2011 American Institute of Physics. [doi:10.1063/1.3579482]

Reprint Address:
Wei, GH, Fudan Univ, State Key Lab Surface Phys, Key Lab Computat Phys Sci, Minist Educ, Shanghai 200433, Peoples R China.

Research Institution addresses:
[Fu, Zhaoming; Luo, Yin; Wei, Guanghong] Fudan Univ, State Key Lab Surface Phys, Key Lab Computat Phys Sci, Minist Educ, Shanghai 200433, Peoples R China; [Fu, Zhaoming; Luo, Yin; Wei, Guanghong] Fudan Univ, Dept Phys, Shanghai 200433, Peoples R China; [Ma, Jianpeng] Rice Univ, Verna & Marrs McLean Dept Biochem & Mol Biol, Baylor Coll Med, Houston, TX USA; [Ma, Jianpeng] Rice Univ, Dept Bioengn, Houston, TX USA

E-mail Address:
ghwei@fudan.edu.cn

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Cited Reference Count:
32

Times Cited:
0

Publisher:
AMER INST PHYSICS; CIRCULATION & FULFILLMENT DIV, 2 HUNTINGTON QUADRANGLE, STE 1 N O 1, MELVILLE, NY 11747-4501 USA

Subject Category:
Physics, Atomic, Molecular & Chemical

ISSN:
0021-9606

DOI:
10.1063/1.3579482

IDS Number:
754FM

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