Cited Article:    Holt JK. Fast mass transport through sub-2-nanometer carbon nanotubes
 Alert Expires:    18 OCT 2009
 Number of Citing Articles:    3 new records this week (3 in this e-mail)
 Organization ID:  3b97d1bbc1878baed0ab183d8b03130b
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AU Shiomi, J
   Maruyama, S
AF Shiomi, J.
   Maruyama, S.
TI Water transport inside a single-walled carbon nanotube driven by a
   temperature gradient
SO NANOTECHNOLOGY
LA English
DT Article
ID MOLECULAR-DYNAMICS SIMULATION; HEAT-CONDUCTION; MASS-TRANSPORT;
   ICE-NANOTUBES
AB In this work, by means of molecular dynamics simulations, we consider
   the mass transport of a water cluster inside a single-walled carbon
   nanotube (SWNT) with a diameter of about 1.4 nm. The influence of the
   non-equilibrium thermal environment on the confined water cluster has
   been investigated by imposing a longitudinal temperature gradient on
   the SWNT. It is demonstrated that the water cluster is transported with
   an average acceleration proportional to the temperature gradient.
   Additional equilibrium simulations suggest that the temperature
   dependence of the potential energy of the confined water is sufficient
   to realize the transport. In particular, for a system with a
   hydrophobic interface, the water-water intrinsic potential energy
   appears to play a dominant role. The transport simulations were also
   performed for a system with a junction between two different SWNTs. The
   results suggest that an angstrom difference in diameter may result in a
   large barrier for water being transported through a small diameter SWNT.
C1 [Shiomi, J.; Maruyama, S.] Univ Tokyo, Dept Mech Engn, Bunkyo Ku, Tokyo 1138656, Japan.
RP Shiomi, J, Univ Tokyo, Dept Mech Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo
   1138656, Japan.
EM shiomi@photon.t.u-tokyo.ac.jp
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NR 22
TC 0
PU IOP PUBLISHING LTD; DIRAC HOUSE, TEMPLE BACK, BRISTOL BS1 6BE, ENGLAND
SN 0957-4484
DI 10.1088/0957-4484/20/5/055708
PD FEB 4
PY 2009
VL 20
IS 5
AR 055708
SC Engineering, Multidisciplinary; Nanoscience & Nanotechnology; Materials
   Science, Multidisciplinary; Physics, Applied
GA 393LV
UT ISI:000262375700036
ER
PT J
*Record 2 of 3. 
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AU Kong, J
   Xu, Y
   Yung, KL
   Xie, YC
   He, L
AF Kong, Jie
   Xu, Yan
   Yung, Kai-Leung
   Xie, Yunchuan
   He, Lan
TI Enhanced Polymer Melts Flow though Nanoscale Channels under Vibration
SO JOURNAL OF PHYSICAL CHEMISTRY C
LA English
DT Article
ID MOLECULAR-DYNAMICS SIMULATION; WALLED CARBON NANOTUBES; WATER;
   NANOCHANNELS; BEHAVIOR; NANOCRYSTALS; CAPILLARIES; CONDUCTION;
   NANOFIBERS; INTERFACE
AB The enhanced poly(epsilon-caprolactone) melts flow behaviors though
   nanoscale channels under vibration were observed. The effect of
   vibration on the nanoflow is dependent on the vibration frequency of
   piezoelectric transducer that generates the vibration fields. The flow
   rate of poly(epsilon-caprolactone) melts in nanochannels increases with
   the increase of vibration frequency within the range from 2.0 to 14.0
   kHz. The observed enhanced flow through nanochannels under vibration is
   a new nanoscale phenomenon, which is potential in vibration-assisted
   nanofluidic, nanoimprint lithography, and micro-/nanoinjection molding
   etc.
C1 [Kong, Jie; Xu, Yan; Yung, Kai-Leung; Xie, Yunchuan; He, Lan] Hong Kong Polytech Univ, Dept Ind & Syst Engn, Kowloon, Hong Kong, Peoples R China.
   [Kong, Jie] NW Polytech Univ, Sch Sci, Dept Appl Chem, Xian 710072, Peoples R China.
RP Kong, J, Hong Kong Polytech Univ, Dept Ind & Syst Engn, Kowloon, Hong
   Kong, Peoples R China.
EM mfkongjie@hotmail.com
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NR 44
TC 0
PU AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1932-7447
DI 10.1021/jp809164k
PD JAN 15
PY 2009
VL 113
IS 2
BP 624
EP 629
SC Chemistry, Physical; Nanoscience & Nanotechnology; Materials Science,
   Multidisciplinary
GA 392TH
UT ISI:000262324600022
ER
PT J
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AU Li, YX
   Ito, T
AF Li, Yongxin
   Ito, Takashi
TI Size-Exclusion Properties of Nanoporous Films Derived from
   Polystyrene-Poly(methylmethacrylate) Diblock Copolymers Assessed Using
   Direct Electrochemistry of Ferritin
SO ANALYTICAL CHEMISTRY
LA English
DT Article
ID SELF-ASSEMBLED MONOLAYERS; DIRECT ELECTRON-TRANSFER; INDIUM OXIDE
   ELECTRODES; BLOCK-COPOLYMERS; NANOTUBE MEMBRANES; PROTEIN-TRANSPORT;
   GOLD ELECTRODES; TEMPLATES; SURFACE; POLYSTYRENE
AB This paper reports the size-exclusion properties of nanoporous films
   derived from polystyrene-poly(methylmethacrylate) diblock copolymers
   (PS-b-PMMA) for biomacro-molecules. These properties were assessed by
   measuring cyclic voltammetry of ferritin (12 nm in diameter) adsorbed
   onto recessed nanodisk-array gold electrodes (RNEs) fabricated from the
   nanoporous films having different effective pore diameters and surface
   functionalities. RNEs having 20-nm-diameter nanopores modified with a
   poly(ethylene glycol) (PEG) layer showed the redox currents of ferritin
   after their immersion in a ferritin solution (5 mg/mL) for longer than
   2 h. The currents originated from the direct electron transfer reaction
   of ferritin molecules immobilized on the underlying gold surface as a
   result of their penetration through the 20-nm-diameter nanopores. The
   PEG modification of the nanopore surface was required for the
   penetration of ferritin, probably because it reduced the nonspecific
   adsorption of ferritin to the nanopore surface. In contrast, no redox
   current of ferritin was observed for RNEs having PEG-modified
   15-nm-diameter nanopores after their immersion in the ferritin solution
   for 12 h, indicating the size-exclusion of ferritin from the 15-nm
   nanopores. The distinct size-exclusion properties of the
   PS-b-PMMA-derived nanoporous films reflect their uniform diameters and
   shapes and will provide a means for fabricating separation membranes
   for biomolecules with high size-based selectivity.
C1 [Li, Yongxin; Ito, Takashi] Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA.
RP Ito, T, Kansas State Univ, Dept Chem, 111 Willard Hall, Manhattan, KS
   66506 USA.
EM ito@ksu.edu
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NR 37
TC 0
PU AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 0003-2700
DI 10.1021/ac802201w
PD JAN 15
PY 2009
VL 81
IS 2
BP 851
EP 855
SC Chemistry, Analytical
GA 394WB
UT ISI:000262482700044
ER
EF
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