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I. INTRODUCTION
J. Goh (ed.), The 15th International Conference on Biomedical Engineering, IFMBE Proceedings 43,
DOI: 10.1007/978-3-319-02913-9_116, Springer International Publishing Switzerland 2014
456
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Fig. 1 Front View of the substrate for tapping potential drift in CNT
Tapping Expected Potential Drift:
The Synthesized CNTs will be fabricated on a specially
designed substrate with three layers in it. Consequently the
head and end layer are insulating in nature and the middle
layer is conductive, from which the Electrodes to the
Electrochemical Workstation are positioned is shown in the
Fig 1.The CNT are coated in the central locus since they
possess superconductive behavior through which the Bio
Fluids are flown and tested. Fig 2. explains the CNT placed
or coated on another material surface as the capillary bed
along the direction of Bio Fluid Flow. The consecutive
Ionic interaction on the surface of the CNT occurs. Kral
and Shapiro et al [7] theoretically proved the generation of
electric current in Carbon Nano Tubes immersing in a
flowing Liquid.
A.K.Sood et al [8] reports the experimental observation
of the voltage generated by the flow of a polar liquid over
Single Walled Carbon Nano Tube (SWNT) Bundles. It was
observed that the induced voltage tends to saturate at flow
velocities as low as 10-5 m/s with 0.65mv generation. This
led to voltage based on pulsating asymmetrical thermal
ratchet model. The Bio Fluid Ions that could interact with
the CNTare namely Na+,K+,Ca2+,Mg2+[9]. Majorly Lymph
of 6 to 10 Liters and Blood of 3.5 to 5.5 Liters full fills the
idea of flowing on the surface of SWNT reporting the
velocity gradient (shear) at the Liquid-Solid Interface.Both
the Intracellular and Extracellular Fluids serve with this
property. The Flow induced current is relatively weak
independent on the Liquid Viscosity.
458
Fig. 3.Bio Fludic Ions Movement over the surface of the CNT
Simulated Structure
Fig. 5.FT-IR Analysis Report
IV. IRON OXIDE SYNTHESIS
V. CNT GROWTH ON IMPLANTABLE MEDICAL DEVICE
Procedure: Iron Oxide is prepared using the CoPrecipitation method with Ammonium Ferrous sulphate of
0.01M and Iron (III) Chloride of 0.02M as precursor. Cetyl
Tri methyl Ammonium Bromide (CTAB) is used as a
surfactant to confine the size of the products at Nano Scale.
Liquor Ammonia is used as reducing agent, which is added
to the precursor solution under constant stirring. The
precipitate was washed using ultra centrifuge and dried at
1050 C overweight.
Fe(NH4)(SO4)2.H2O + 2FeCl3 + 8NHOH
FeO4 + 6NH4Cl + 4H2O + 2(NH4)2SO4
(I)
Characterization: The Dried out sample is collected and
tested for the size. Fig. 4 shows the Particle Size Analysis
result of Iron Oxide obtained with an average size of
148.5nm.Fig. 5 shows the FT IR Analysis report that the
peak 750cm-1 range was due to stretching of metal oxide
bonds, the range between 1500-1600cm-1 and 34003600cm-1 was due to hydroxide group.
Fig. 4.Particle Size Analysis report for Iron Oxide size -148.5nm
ACKNOWLEDGMENT
The authors would like extend sincere Thanks to SNR Sons
Charitable Trust, Department of Nano Technology, and
Department of Biomedical Engineering of Sri Ramakrishna
Engineering College for supporting both by knowledge and
wealth. We also wish to thank our collaborators and the
Almighty who stands always with us.
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Author: Prof.G.Gopu
Institute: Sri Ramakrishna Engineering College
Street: Vattamalaipalayam NGGO Colony (PO)
City:
Coimbatore
Country: India
Email: gopugovindasamy@gmail.com