Friday, July 16, 2010

ISI Web of Knowledge Alert - Maibaum, L

ISI Web of Knowledge Citation Alert

Cited Article: Maibaum, L. A coarse-grained model of water confined in a hydrophobic tube
Alert Expires: 09 NOV 2010
Number of Citing Articles: 1 new records this week (1 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Methane Molecules Drive Water Molecules along Diameter-Gradient SWCNTs with Junctions

Authors:
Yu, HQ; Li, YF; Li, H; Zhang, K; An, CG; Liu, XF; Liew, KM

Author Full Names:
Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.; Liew, K. M.

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 114 (26): 8676-8679 JUL 8 2010

Language:
English

Document Type:
Article

KeyWords Plus:
WALLED CARBON NANOTUBES; TRANSPORT; MODEL; FLOW

Abstract:
We report the transport behavior of water molecules along a system of coaxial single-walled carbon nanotubes (SWCNTs) of different diameters with junctions under the driving force of methane molecules. The junctions are potential barriers to the transport of water molecules through SWCNTs. However, methane molecules can overcome these potential barriers and pull the water molecules across the junction region from one compartment to the next. Although a junction is an obstacle to water transport through SWCNTs, the presence of more junctions gives methane molecules a longer lasting driving force that helps them to pull the water molecules out of the SWCNTs.

Reprint Address:
Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.

Research Institution addresses:
[Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China; [Liew, K. M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China

E-mail Address:
lihuilmy@hotmail.com

Cited References:
DELLAGO C, 2003, PHYS REV LETT, V90, ARTN 105902.
HOLT JK, 2006, SCIENCE, V312, P1034, DOI 10.1126/science.1126298.
HUMMER G, 2001, NATURE, V414, P188.
KALRA A, 2004, J PHYS CHEM B, V108, P544, DOI 10.1021/jp035828x.
LI H, 2008, J CHEM PHYS, V128, UNSP 034707/1-5.
LIJIMA S, 1992, NATURE, V356, P776.
MAIBAUM L, 2003, J PHYS CHEM B, V107, P1189, DOI 10.1021/jp0267196.
MAJUMDER M, 2005, NATURE, V438, P44, DOI 10.1038/43844a.
MANIWA Y, 2005, CHEM PHYS LETT, V401, P534, DOI 10.1016/j.cplett.2004.11.112.
MANIWA Y, 2007, NAT MATER, V6, P135, DOI 10.1038/nmat1823.
MILLER SA, 2001, J AM CHEM SOC, V123, P12335.
POWER TD, 2002, J AM CHEM SOC, V124, P1858.
REN ZF, 1998, SCIENCE, V282, P1105.
SKOULIDAS AI, 2002, PHYS REV LETT, V89, ARTN 185901.
STRIOLO A, 2006, NANO LETT, V6, P633, DOI 10.1021/nl052254u.
SUNAND L, 2000, J AM CHEM SOC, V122, P12340.
TELEMAN O, 1987, MOL PHYS, V60, P193.
THOMAS JA, 2008, NANO LETT, V8, P2788, DOI 10.1021/nl8013617.
WANG Q, 2009, CARBON, V47, P1870, DOI 10.1016/j.carbon.2009.03.030.
WANG Q, 2009, NANO LETT, V9, P245, DOI 10.1021/nl802829z.
WANG QY, 1999, PHYS REV LETT, V82, P956.
YU HQ, 2010, CARBON, V48, P417, DOI 10.1016/j.carbon.2009.09.055.
ZAMBRANO HA, 2009, NANO LETT, V9, P66, DOI 10.1021/nl802429s.
ZHAO YC, 2008, ADV MATER, V20, P1772, DOI 10.1002/adma.200702956.
ZHEN Y, 1999, NATURE, V402, P273.

Cited Reference Count:
25

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/jp102810j

IDS Number:
617LP

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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: 09 NOV 2010
Number of Citing Articles: 4 new records this week (4 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
The Influence of the Rigidity of a Carbon Nanotube on the Structure and Dynamics of Confined Methanol

Authors:
Chaban, VV; Kalugin, ON; Habenicht, BF; Prezhdo, OV

Author Full Names:
Chaban, Vitaly V.; Kalugin, Oleg N.; Habenicht, Bradley F.; Prezhdo, Oleg V.

Source:
JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN 79 (6): Art. No. 064608 JUN 2010

Language:
English

Document Type:
Article

Author Keywords:
confined fluid; carbon nanotube; molecular dynamics simulation; methanol; intramolecular potentials; diffusion coefficient; hydrogen bond

KeyWords Plus:
LIQUID METHANOL; WATER; DIFFUSION; SUPERCAPACITOR; SIMULATION; TRANSPORT; MOLECULES

Abstract:
In this paper, we compare the behavior of liquid methanol confined by an open-ended single-walled nanotube (SWCNT) under four different simulation conditions by using the molecular dynamics (MD) simulations technique. The first model is a rigid and fixed SWCNT with all its carbon atoms fixed at their initial positions; the second is a flexible and fixed SWCNT with its centre-of-mass fixed at the center of the MD box and with the carbon-carbon bond potential applied; the third is a rigid and floating SWCNT, and the fourth is the most realistic flexible and floating SWCNT model-without fixed atoms and with bond potential. The microscopic structure and transport properties of bulk methanol confined by the four different SWCNTs were analyzed. No changes in the radial distribution functions of the hydrogen bond between MeOH molecules are found, and the self-diffusion constant and microscopic dipole relaxation time are essentially unaffected by the confinements. In spite of the fl!
exible/rigid or fixed/floating (15, 15) SWCNT model used, the structure and transport properties of confined MeOH are found to be very close in all the simulated cases. We conclude that using the approximation of rigid or/and fixed SWCNT does not lead to any systematic errors in properties of the confined liquid. The results show that simulations using rigid carbon nanotubes provide a reliable description of molecular diffusion and other solvent properties in a variety of applications, such electro-chemical devices, membranes and sensors that rely on these properties.

Reprint Address:
Chaban, VV, Kharkov Natl Univ, Dept Inorgan Chem, Kharkov, Ukraine.

Research Institution addresses:
[Chaban, Vitaly V.; Kalugin, Oleg N.] Kharkov Natl Univ, Dept Inorgan Chem, Kharkov, Ukraine; [Habenicht, Bradley F.; Prezhdo, Oleg V.] Univ Washington, Dept Chem, Seattle, WA 98195 USA

E-mail Address:
Oleg.N.Kalugin@univer.kharkov.ua; prezhdo@u.washington.edu

Cited References:
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Cited Reference Count:
29

Times Cited:
0

Publisher:
PHYSICAL SOC JAPAN; EISHIN-KAIHATSU BLDG, 5TH FLR, 5-34-3 SHINBASHI, MINATO-KU, TOKYO 105-0004, JAPAN

Subject Category:
Physics, Multidisciplinary

ISSN:
0031-9015

DOI:
10.1143/JPSJ.79.064608

IDS Number:
621XY

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Title:
Water on graphene surfaces

Authors:
Gordillo, MC; Marti, J

Author Full Names:
Gordillo, M. C.; Marti, J.

Source:
JOURNAL OF PHYSICS-CONDENSED MATTER 22 (28): Art. No. 284111 JUL 21 2010

Language:
English

Document Type:
Proceedings Paper

KeyWords Plus:
MOLECULAR-DYNAMICS SIMULATIONS; LIQUID WATER; CARBON NANOTUBES; SUPERCRITICAL WATER; HYDROPHOBIC SURFACE; COMPUTER-SIMULATION; CYLINDRICAL PORES; INFRARED-SPECTRA; INTERFACE; ADSORPTION

Abstract:
In this paper, we summarize the main results obtained in our group about the behavior of water confined inside or close to different graphene surfaces by means of molecular dynamics simulations. These include the inside and outside of carbon nanotubes, and the confinement inside a slit pore or a single graphene sheet. We paid special attention to some thermodynamical (binding energies), structural (hydrogen-bond distributions) and dynamic (infrared spectra) properties, and their comparison to their bulk counterparts.

Reprint Address:
Gordillo, MC, Univ Pablo Olavide, Dept Sistemas Fis Quim & Nat, Fac Ciencias Expt, Carretera Utrera,Km 1, E-41013 Seville, Spain.

Research Institution addresses:
[Gordillo, M. C.] Univ Pablo Olavide, Dept Sistemas Fis Quim & Nat, Fac Ciencias Expt, E-41013 Seville, Spain; [Marti, J.] Univ Politecn Cataluna, Dept Fis & Engn Nucl, E-08034 Barcelona, Catalonia, Spain

E-mail Address:
cgorbar@upo.es; jordi.marti@upc.edu

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Cited Reference Count:
69

Times Cited:
0

Publisher:
IOP PUBLISHING LTD; DIRAC HOUSE, TEMPLE BACK, BRISTOL BS1 6BE, ENGLAND

Subject Category:
Physics, Condensed Matter

ISSN:
0953-8984

DOI:
10.1088/0953-8984/22/28/284111

IDS Number:
617CB

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Title:
Methane Molecules Drive Water Molecules along Diameter-Gradient SWCNTs with Junctions

Authors:
Yu, HQ; Li, YF; Li, H; Zhang, K; An, CG; Liu, XF; Liew, KM

Author Full Names:
Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.; Liew, K. M.

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 114 (26): 8676-8679 JUL 8 2010

Language:
English

Document Type:
Article

KeyWords Plus:
WALLED CARBON NANOTUBES; TRANSPORT; MODEL; FLOW

Abstract:
We report the transport behavior of water molecules along a system of coaxial single-walled carbon nanotubes (SWCNTs) of different diameters with junctions under the driving force of methane molecules. The junctions are potential barriers to the transport of water molecules through SWCNTs. However, methane molecules can overcome these potential barriers and pull the water molecules across the junction region from one compartment to the next. Although a junction is an obstacle to water transport through SWCNTs, the presence of more junctions gives methane molecules a longer lasting driving force that helps them to pull the water molecules out of the SWCNTs.

Reprint Address:
Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.

Research Institution addresses:
[Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China; [Liew, K. M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China

E-mail Address:
lihuilmy@hotmail.com

Cited References:
DELLAGO C, 2003, PHYS REV LETT, V90, ARTN 105902.
HOLT JK, 2006, SCIENCE, V312, P1034, DOI 10.1126/science.1126298.
HUMMER G, 2001, NATURE, V414, P188.
KALRA A, 2004, J PHYS CHEM B, V108, P544, DOI 10.1021/jp035828x.
LI H, 2008, J CHEM PHYS, V128, UNSP 034707/1-5.
LIJIMA S, 1992, NATURE, V356, P776.
MAIBAUM L, 2003, J PHYS CHEM B, V107, P1189, DOI 10.1021/jp0267196.
MAJUMDER M, 2005, NATURE, V438, P44, DOI 10.1038/43844a.
MANIWA Y, 2005, CHEM PHYS LETT, V401, P534, DOI 10.1016/j.cplett.2004.11.112.
MANIWA Y, 2007, NAT MATER, V6, P135, DOI 10.1038/nmat1823.
MILLER SA, 2001, J AM CHEM SOC, V123, P12335.
POWER TD, 2002, J AM CHEM SOC, V124, P1858.
REN ZF, 1998, SCIENCE, V282, P1105.
SKOULIDAS AI, 2002, PHYS REV LETT, V89, ARTN 185901.
STRIOLO A, 2006, NANO LETT, V6, P633, DOI 10.1021/nl052254u.
SUNAND L, 2000, J AM CHEM SOC, V122, P12340.
TELEMAN O, 1987, MOL PHYS, V60, P193.
THOMAS JA, 2008, NANO LETT, V8, P2788, DOI 10.1021/nl8013617.
WANG Q, 2009, CARBON, V47, P1870, DOI 10.1016/j.carbon.2009.03.030.
WANG Q, 2009, NANO LETT, V9, P245, DOI 10.1021/nl802829z.
WANG QY, 1999, PHYS REV LETT, V82, P956.
YU HQ, 2010, CARBON, V48, P417, DOI 10.1016/j.carbon.2009.09.055.
ZAMBRANO HA, 2009, NANO LETT, V9, P66, DOI 10.1021/nl802429s.
ZHAO YC, 2008, ADV MATER, V20, P1772, DOI 10.1002/adma.200702956.
ZHEN Y, 1999, NATURE, V402, P273.

Cited Reference Count:
25

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/jp102810j

IDS Number:
617LP

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

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Title:
The Potential of Carbon Nanotube Membranes for Analytical Separations

Authors:
Lopez-Lorente, AI; Simonet, BM; Valcarcel, M

Author Full Names:
Lopez-Lorente, A. I.; Simonet, B. M.; Valcarcel, M.

Source:
ANALYTICAL CHEMISTRY 82 (13): 5399-5407 JUL 1 2010

Language:
English

Document Type:
Article

KeyWords Plus:
FAST MASS-TRANSPORT; ELECTROOSMOTIC FLOW; WATER; FABRICATION; BUCKYPAPERS; FILMS; TRANSPARENT; MODULATION; FILTERS; ARRAYS

Abstract:
Advances in nanotechnology have enabled the development of nanoporous membranes based on carbon nanotubes, which, by virtue of their exceptional properties, constitute excellent supports for analytical processes, including the selective separation of some molecules.

Reprint Address:
Valcarcel, M, Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain.

Research Institution addresses:
[Valcarcel, M.] Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain

E-mail Address:
qa1meobj@uco.es

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Cited Reference Count:
59

Times Cited:
0

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

Subject Category:
Chemistry, Analytical

ISSN:
0003-2700

DOI:
10.1021/ac902629n

IDS Number:
617AO

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ISI Web of Knowledge Alert - Thompson, P

ISI Web of Knowledge Citation Alert

Cited Article: Thompson, P. A general boundary condition for liquid flow at solid surfaces
Alert Expires: 09 NOV 2010
Number of Citing Articles: 1 new records this week (1 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Boundary Conditions at the Liquid-Liquid Interface in the Presence of Surfactants

Authors:
Hu, YX; Zhang, XR; Wang, WC

Author Full Names:
Hu, Yangxu; Zhang, Xianren; Wang, Wenchuan

Source:
LANGMUIR 26 (13): 10693-10702 JUL 6 2010

Language:
English

Document Type:
Article

KeyWords Plus:
MOLECULAR-DYNAMICS; SOLID-SURFACES; RHEOLOGICAL MEASUREMENTS; MONTE-CARLO; SHEAR-FLOW; SLIP; MICROSCOPY; ADSORPTION; GRAPHITE

Abstract:
In this work, we studied the flow boundary conditions for the interface between two immiscible liquids under the condition of low shear rates in the presence or absence of surfactants. Our simulation results indicate that the boundary conditions are substantially changed by the presence of surfactants. Similar to the liquid solid boundary, several boundary conditions at immiscible liquid liquid interfaces, including slip, no-slip, and locking boundary conditions, are observed depending on the interfacial surfactant concentration. The slip boundary condition is achieved only at zero or lower surfactant concentration. The locking boundary condition is observed when the surfactant concentration is large enough to form a fully developed monolayer whereas the no-slip condition occurs for systems with in values of surfactant concentration. The slip, no-slip, and locking boundary conditions yield the positive, zero, and negative slip lengths, respectively. We also investigated the !
dependence of boundary slip on shear rate at different interfacial surfactant concentrations. Compared to the systems without surfactants, the increase in slip with shear rate slows down because of the presence of surfactants, and consequently, the linear dependence of slip length changes to a nonlinear dependence. Simulation results also indicate that the shear rate also affects the surfactant distribution. In particular, when the surfactant concentration is high enough to form a fully developed monolayer, the higher shear rate would make the monolayer rupture.

Reprint Address:
Zhang, XR, Beijing Univ Chem Technol, Minist Educ, Key Lab Nanomat, Div Mol & Mat Simulat, Beijing 100029, Peoples R China.

Research Institution addresses:
[Hu, Yangxu; Zhang, Xianren; Wang, Wenchuan] Beijing Univ Chem Technol, Minist Educ, Key Lab Nanomat, Div Mol & Mat Simulat, Beijing 100029, Peoples R China

E-mail Address:
zhangxr@mail.buct.edu.cn

Cited References:
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Cited Reference Count:
30

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/la101025h

IDS Number:
616VX

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ISI Web of Knowledge Alert - Zhao, Y

ISI Web of Knowledge Citation Alert

Cited Article: Zhao, Y. Individual water-filled single-walled carbon nanotubes as hydroelectric power converters
Alert Expires: 09 NOV 2010
Number of Citing Articles: 1 new records this week (1 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Methane Molecules Drive Water Molecules along Diameter-Gradient SWCNTs with Junctions

Authors:
Yu, HQ; Li, YF; Li, H; Zhang, K; An, CG; Liu, XF; Liew, KM

Author Full Names:
Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.; Liew, K. M.

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 114 (26): 8676-8679 JUL 8 2010

Language:
English

Document Type:
Article

KeyWords Plus:
WALLED CARBON NANOTUBES; TRANSPORT; MODEL; FLOW

Abstract:
We report the transport behavior of water molecules along a system of coaxial single-walled carbon nanotubes (SWCNTs) of different diameters with junctions under the driving force of methane molecules. The junctions are potential barriers to the transport of water molecules through SWCNTs. However, methane molecules can overcome these potential barriers and pull the water molecules across the junction region from one compartment to the next. Although a junction is an obstacle to water transport through SWCNTs, the presence of more junctions gives methane molecules a longer lasting driving force that helps them to pull the water molecules out of the SWCNTs.

Reprint Address:
Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.

Research Institution addresses:
[Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China; [Liew, K. M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China

E-mail Address:
lihuilmy@hotmail.com

Cited References:
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LIJIMA S, 1992, NATURE, V356, P776.
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POWER TD, 2002, J AM CHEM SOC, V124, P1858.
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SKOULIDAS AI, 2002, PHYS REV LETT, V89, ARTN 185901.
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SUNAND L, 2000, J AM CHEM SOC, V122, P12340.
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WANG Q, 2009, NANO LETT, V9, P245, DOI 10.1021/nl802829z.
WANG QY, 1999, PHYS REV LETT, V82, P956.
YU HQ, 2010, CARBON, V48, P417, DOI 10.1016/j.carbon.2009.09.055.
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ZHEN Y, 1999, NATURE, V402, P273.

Cited Reference Count:
25

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/jp102810j

IDS Number:
617LP

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or 734-459-8565.

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ISI Web of Knowledge Alert - Majumder M

ISI Web of Knowledge Citation Alert

Cited Article: Majumder M. Nanoscale hydrodynamics - Enhanced flow in carbon nanotubes
Alert Expires: 09 NOV 2010
Number of Citing Articles: 4 new records this week (4 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Programmable transdermal drug delivery of nicotine using carbon nanotube membranes

Authors:
Wu, J; Paudel, KS; Strasinger, C; Hammell, D; Stinchcomb, AL; Hinds, BJ

Author Full Names:
Wu, Ji; Paudel, Kalpana S.; Strasinger, Caroline; Hammell, Dana; Stinchcomb, Audra L.; Hinds, Bruce J.

Source:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 107 (26): 11698-11702 JUN 29 2010

Language:
English

Document Type:
Article

Author Keywords:
electroosmosis; electrophoresis; smoking cessation; medical device

KeyWords Plus:
HAIRLESS GUINEA-PIGS; ELECTROOSMOTIC FLOW; MASS-TRANSPORT; SKIN; MODEL; PHARMACOKINETICS; IONTOPHORESIS; NALTREXONE; ELECTRODE; PRODRUGS

Abstract:
Carbon nanotube (CNT) membranes were employed as the active element of a switchable transdermal drug delivery device that can facilitate more effective treatments of drug abuse and addiction. Due to the dramatically fast flow through CNT cores, high charge density, and small pore dimensions, highly efficient electrophoretic pumping through functionalized CNT membrane was achieved. These membranes were integrated with a nicotine formulation to obtain switchable transdermal nicotine delivery rates on human skin (in vitro) and are consistent with a Fickian diffusion in series model. The transdermal nicotine delivery device was able to successfully switch between high (1.3 +/- 0.65 mu mol/hr-cm(2)) and low (0.33 +/- 0.22 mu mol/hr-cm(2)) fluxes that coincide with therapeutic demand levels for nicotine cessation treatment. These highly energy efficient programmable devices with minimal skin irritation and no skin barrier disruption would open an avenue for single application long!
-wear patches for therapies that require variable or programmable delivery rates.

Reprint Address:
Stinchcomb, AL, Univ Kentucky, Coll Pharm, Lexington, KY 40536 USA.

Research Institution addresses:
[Paudel, Kalpana S.; Strasinger, Caroline; Hammell, Dana; Stinchcomb, Audra L.] Univ Kentucky, Coll Pharm, Lexington, KY 40536 USA; [Wu, Ji; Hinds, Bruce J.] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA

E-mail Address:
audra.stinchcomb@uky.edu; bjhinds@engr.uky.edu

Cited References:
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BRAND RM, 1995, J CONTROL RELEASE, V33, P285.
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FEYERABEND C, 1985, BRIT J CLIN PHARMACO, V19, P239.
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KIM S, 2007, NANO LETT, V7, P2806, DOI 10.1021/nl071414u.
MAJUMDER M, 2005, NATURE, V438, P44, DOI 10.1038/43844a.
MAJUMDER M, 2007, LANGMUIR, V23, P8624, DOI 10.1021/la700686k.
MAJUMDER M, 2008, J MEMBRANE SCI, V316, P89, DOI 10.1016/j.memsci.2007.09.068.
MALIN DH, 2001, PHARMACOL BIOCHEM BE, V70, P551.
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WILLS S, 2005, DRUGS ABUSE.

Cited Reference Count:
30

Times Cited:
0

Publisher:
NATL ACAD SCIENCES; 2101 CONSTITUTION AVE NW, WASHINGTON, DC 20418 USA

Subject Category:
Multidisciplinary Sciences

ISSN:
0027-8424

DOI:
10.1073/pnas.1004714107

IDS Number:
618DT

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

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Title:
Methane Molecules Drive Water Molecules along Diameter-Gradient SWCNTs with Junctions

Authors:
Yu, HQ; Li, YF; Li, H; Zhang, K; An, CG; Liu, XF; Liew, KM

Author Full Names:
Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.; Liew, K. M.

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 114 (26): 8676-8679 JUL 8 2010

Language:
English

Document Type:
Article

KeyWords Plus:
WALLED CARBON NANOTUBES; TRANSPORT; MODEL; FLOW

Abstract:
We report the transport behavior of water molecules along a system of coaxial single-walled carbon nanotubes (SWCNTs) of different diameters with junctions under the driving force of methane molecules. The junctions are potential barriers to the transport of water molecules through SWCNTs. However, methane molecules can overcome these potential barriers and pull the water molecules across the junction region from one compartment to the next. Although a junction is an obstacle to water transport through SWCNTs, the presence of more junctions gives methane molecules a longer lasting driving force that helps them to pull the water molecules out of the SWCNTs.

Reprint Address:
Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.

Research Institution addresses:
[Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China; [Liew, K. M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China

E-mail Address:
lihuilmy@hotmail.com

Cited References:
DELLAGO C, 2003, PHYS REV LETT, V90, ARTN 105902.
HOLT JK, 2006, SCIENCE, V312, P1034, DOI 10.1126/science.1126298.
HUMMER G, 2001, NATURE, V414, P188.
KALRA A, 2004, J PHYS CHEM B, V108, P544, DOI 10.1021/jp035828x.
LI H, 2008, J CHEM PHYS, V128, UNSP 034707/1-5.
LIJIMA S, 1992, NATURE, V356, P776.
MAIBAUM L, 2003, J PHYS CHEM B, V107, P1189, DOI 10.1021/jp0267196.
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Cited Reference Count:
25

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/jp102810j

IDS Number:
617LP

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

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Title:
Analytic Solutions and Model Assessment for Electrokinetic Flow in Hydrophobic Microchannels with Various Boundary Conditions of Interfacial Electric and Slippage Phenomena

Authors:
Wang, JC; Soong, CY; Hwang, PW

Author Full Names:
Wang, J. C.; Soong, C. Y.; Hwang, P. W.

Source:
JOURNAL OF THE CHINESE SOCIETY OF MECHANICAL ENGINEERS 31 (3): 209-220 JUN 2010

Language:
English

Document Type:
Article

Author Keywords:
fluid slippage; microchannel flow; apparent zeta potential; hydrophobic wall; interfacial phenomena

KeyWords Plus:
SUPERHYDROPHOBIC SURFACE; LIQUID SLIP; MICROFLUIDICS

Abstract:
The present study is concerned with a theoretical analysis of pressure-driven electrokinetic flows in hydrophobic microchannels with emphasis on the slip effects under coupling of interfacial electric and fluid slippage phenomena. Nonlinear equations coupling hydrodynamics and electrical field are formulated and the corresponding linear version can be obtained by invoking Debye-Huckel approximation. To facilitate analytic solutions, the electrokinetic parameter K (defined as the ratio of channel semi-height to Debye length) is assumed high enough with electric double layer non-overlapping. Three zeta potential boundary conditions (BCs) including commonly used material true zeta potential and two kinds of slip-dependent relations are considered. Through comparisons of the six analytic solutions (linear and nonlinear models each with 3 BCs), the present analysis provides an assessment of various models with slip effects on electrokinetic flow in hydrophobic microchannels.

Reprint Address:
Soong, CY, Feng Chia Univ, Dept Aerosp & Syst Engn, Taichung 40724, Taiwan.

Research Institution addresses:
[Wang, J. C.; Soong, C. Y.; Hwang, P. W.] Feng Chia Univ, Dept Aerosp & Syst Engn, Taichung 40724, Taiwan

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Cited Reference Count:
20

Times Cited:
0

Publisher:
CHINESE SOC MECHANICAL ENGINEERS; 4F NO 60 SEC 2 PA TE RD, TAIPEI, 10401, TAIWAN

Subject Category:
Engineering, Mechanical

ISSN:
0257-9731

IDS Number:
620EA

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

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Title:
The Potential of Carbon Nanotube Membranes for Analytical Separations

Authors:
Lopez-Lorente, AI; Simonet, BM; Valcarcel, M

Author Full Names:
Lopez-Lorente, A. I.; Simonet, B. M.; Valcarcel, M.

Source:
ANALYTICAL CHEMISTRY 82 (13): 5399-5407 JUL 1 2010

Language:
English

Document Type:
Article

KeyWords Plus:
FAST MASS-TRANSPORT; ELECTROOSMOTIC FLOW; WATER; FABRICATION; BUCKYPAPERS; FILMS; TRANSPARENT; MODULATION; FILTERS; ARRAYS

Abstract:
Advances in nanotechnology have enabled the development of nanoporous membranes based on carbon nanotubes, which, by virtue of their exceptional properties, constitute excellent supports for analytical processes, including the selective separation of some molecules.

Reprint Address:
Valcarcel, M, Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain.

Research Institution addresses:
[Valcarcel, M.] Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain

E-mail Address:
qa1meobj@uco.es

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Cited Reference Count:
59

Times Cited:
0

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

Subject Category:
Chemistry, Analytical

ISSN:
0003-2700

DOI:
10.1021/ac902629n

IDS Number:
617AO

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Cited Article: Holt JK. Fast mass transport through sub-2-nanometer carbon nanotubes
Alert Expires: 09 NOV 2010
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PT J
*Record 1 of 3.
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*Order Full Text [ ]
AU Wu, J
Paudel, KS
Strasinger, C
Hammell, D
Stinchcomb, AL
Hinds, BJ
AF Wu, Ji
Paudel, Kalpana S.
Strasinger, Caroline
Hammell, Dana
Stinchcomb, Audra L.
Hinds, Bruce J.
TI Programmable transdermal drug delivery of nicotine using carbon
nanotube membranes
SO PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF
AMERICA
LA English
DT Article
DE electroosmosis; electrophoresis; smoking cessation; medical device
ID HAIRLESS GUINEA-PIGS; ELECTROOSMOTIC FLOW; MASS-TRANSPORT; SKIN; MODEL;
PHARMACOKINETICS; IONTOPHORESIS; NALTREXONE; ELECTRODE; PRODRUGS
AB Carbon nanotube (CNT) membranes were employed as the active element of
a switchable transdermal drug delivery device that can facilitate more
effective treatments of drug abuse and addiction. Due to the
dramatically fast flow through CNT cores, high charge density, and
small pore dimensions, highly efficient electrophoretic pumping through
functionalized CNT membrane was achieved. These membranes were
integrated with a nicotine formulation to obtain switchable transdermal
nicotine delivery rates on human skin (in vitro) and are consistent
with a Fickian diffusion in series model. The transdermal nicotine
delivery device was able to successfully switch between high (1.3 +/-
0.65 mu mol/hr-cm(2)) and low (0.33 +/- 0.22 mu mol/hr-cm(2)) fluxes
that coincide with therapeutic demand levels for nicotine cessation
treatment. These highly energy efficient programmable devices with
minimal skin irritation and no skin barrier disruption would open an
avenue for single application long-wear patches for therapies that
require variable or programmable delivery rates.
C1 [Paudel, Kalpana S.; Strasinger, Caroline; Hammell, Dana; Stinchcomb, Audra L.] Univ Kentucky, Coll Pharm, Lexington, KY 40536 USA.
[Wu, Ji; Hinds, Bruce J.] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA.
RP Stinchcomb, AL, Univ Kentucky, Coll Pharm, Lexington, KY 40536 USA.
EM audra.stinchcomb@uky.edu
bjhinds@engr.uky.edu
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NR 30
TC 0
PU NATL ACAD SCIENCES; 2101 CONSTITUTION AVE NW, WASHINGTON, DC 20418 USA
SN 0027-8424
DI 10.1073/pnas.1004714107
PD JUN 29
VL 107
IS 26
BP 11698
EP 11702
SC Multidisciplinary Sciences
GA 618DT
UT ISI:000279332300011
ER

PT J
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*Order Full Text [ ]
AU Yu, HQ
Li, YF
Li, H
Zhang, K
An, CG
Liu, XF
Liew, KM
AF Yu, H. Q.
Li, Y. F.
Li, H.
Zhang, K.
An, C. G.
Liu, X. F.
Liew, K. M.
TI Methane Molecules Drive Water Molecules along Diameter-Gradient SWCNTs
with Junctions
SO JOURNAL OF PHYSICAL CHEMISTRY B
LA English
DT Article
ID WALLED CARBON NANOTUBES; TRANSPORT; MODEL; FLOW
AB We report the transport behavior of water molecules along a system of
coaxial single-walled carbon nanotubes (SWCNTs) of different diameters
with junctions under the driving force of methane molecules. The
junctions are potential barriers to the transport of water molecules
through SWCNTs. However, methane molecules can overcome these potential
barriers and pull the water molecules across the junction region from
one compartment to the next. Although a junction is an obstacle to
water transport through SWCNTs, the presence of more junctions gives
methane molecules a longer lasting driving force that helps them to
pull the water molecules out of the SWCNTs.
C1 [Yu, H. Q.; Li, Y. F.; Li, H.; Zhang, K.; An, C. G.; Liu, X. F.] Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut & Proc Mat, Jinan 250061, Peoples R China.
[Liew, K. M.] City Univ Hong Kong, Dept Bldg & Construct, Kowloon, Hong Kong, Peoples R China.
RP Li, H, Shandong Univ, Minist Educ, Key Lab Liquid Solid Struct Evolut &
Proc Mat, Jinan 250061, Peoples R China.
EM lihuilmy@hotmail.com
CR DELLAGO C, 2003, PHYS REV LETT, V90, ARTN 105902
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10.1016/j.cplett.2004.11.112
MANIWA Y, 2007, NAT MATER, V6, P135, DOI 10.1038/nmat1823
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POWER TD, 2002, J AM CHEM SOC, V124, P1858
REN ZF, 1998, SCIENCE, V282, P1105
SKOULIDAS AI, 2002, PHYS REV LETT, V89, ARTN 185901
STRIOLO A, 2006, NANO LETT, V6, P633, DOI 10.1021/nl052254u
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TELEMAN O, 1987, MOL PHYS, V60, P193
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WANG Q, 2009, NANO LETT, V9, P245, DOI 10.1021/nl802829z
WANG QY, 1999, PHYS REV LETT, V82, P956
YU HQ, 2010, CARBON, V48, P417, DOI 10.1016/j.carbon.2009.09.055
ZAMBRANO HA, 2009, NANO LETT, V9, P66, DOI 10.1021/nl802429s
ZHAO YC, 2008, ADV MATER, V20, P1772, DOI 10.1002/adma.200702956
ZHEN Y, 1999, NATURE, V402, P273
NR 25
TC 0
PU AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1520-6106
DI 10.1021/jp102810j
PD JUL 8
VL 114
IS 26
BP 8676
EP 8679
SC Chemistry, Physical
GA 617LP
UT ISI:000279282600012
ER

PT J
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*Order Full Text [ ]
AU Lopez-Lorente, AI
Simonet, BM
Valcarcel, M
AF Lopez-Lorente, A. I.
Simonet, B. M.
Valcarcel, M.
TI The Potential of Carbon Nanotube Membranes for Analytical Separations
SO ANALYTICAL CHEMISTRY
LA English
DT Article
ID FAST MASS-TRANSPORT; ELECTROOSMOTIC FLOW; WATER; FABRICATION;
BUCKYPAPERS; FILMS; TRANSPARENT; MODULATION; FILTERS; ARRAYS
AB Advances in nanotechnology have enabled the development of nanoporous
membranes based on carbon nanotubes, which, by virtue of their
exceptional properties, constitute excellent supports for analytical
processes, including the selective separation of some molecules.
C1 [Valcarcel, M.] Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain.
RP Valcarcel, M, Univ Cordoba, Dept Analyt Chem, E-14071 Cordoba, Spain.
EM qa1meobj@uco.es
CR AGO H, 2000, APPL PHYS LETT, V77, P79
ANDREWS R, 1999, CHEM PHYS LETT, V303, P467
ANDREWS R, 2001, NASA C PUBLICATION
BASHEER C, 2006, ANAL CHEM, V78, P2853, DOI 10.1021/ac060240i
BRADYESTEVEZ AS, 2008, SMALL, V4, P481, DOI 10.1002/smll.200700863
CAO AY, 2005, SCIENCE, V310, P1307, DOI 10.1126/science.1118957
CHE GL, 1998, NATURE, V393, P346
CHEN HB, 2006, J MEMBRANE SCI, V269, P152, DOI
10.1016/j.memsci.2005.06.030
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ISI Web of Knowledge Alert - Lichter S

ISI Web of Knowledge Citation Alert

Cited Article: Lichter S. Mechanisms for liquid slip at solid surfaces
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Title:
Viscoelastie Modeling with Interfacial slip of a Protein Monolayer Electrode-Adsorbed on an Acoustic Wave Biosensor

Authors:
Ellis, JS; Thompson, M

Author Full Names:
Ellis, Jonathan S.; Thompson, Michael

Source:
LANGMUIR 26 (13): 11558-11567 JUL 6 2010

Language:
English

Document Type:
Article

KeyWords Plus:
QUARTZ-CRYSTAL MICROBALANCE; SURFACE-PLASMON RESONANCE; MOLECULAR-DYNAMICS SIMULATION; SOLID-LIQUID INTERFACE; BOUNDARY-CONDITION; NEWTONIAN LIQUIDS; KELVIN NANOPROBE; NETWORK ANALYSIS; THIN-FILMS; WALL SLIP

Abstract:
Transverse-shear mode acoustic wave devices have been used as real-time, label-free detectors of conformational shifts in biomolecules on surfaces. However, material changes in the biochemical monolayers and coupling between the substrate and the surrounding liquid make it difficult to isolate the desired signal, so an understanding of these phenomena is required. An important step in this understanding is knowledge of the material properties of the linker layer that attaches a biochemically selective molecule to the gold surface, in our case, neutravidin. With the goal of obtaining material properties for a neutravidin monolayer, for use in future studies, neutravidin adsorption to the gold surface of an acoustic wave biosensor is described as a viscoelastic monolayer using one-dimensional modeling. Neutravidin is described as forming hydrated, viscoelastie monolayers, and slip is allowed at all interfaces. An impedance model is numerically lit to experimental values using !
a two-parameter minimization algorithm and values for the shear modulus of the neutravidin monolayer, in agreement with literature values for similar proteins, are obtained. Slip is found on the electrode surface prior to neutravidin adsorption. These results will be used for future modeling studies involving this protein as a linker protein.

Reprint Address:
Thompson, M, Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada.

Research Institution addresses:
[Ellis, Jonathan S.; Thompson, Michael] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada; [Ellis, Jonathan S.; Thompson, Michael] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3C9, Canada

E-mail Address:
mikethom@chem.utoronto.ca

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Cited Reference Count:
118

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/la100798c

IDS Number:
616VX

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