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8/2/2019 IIM.tech Seminar I
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Presented by,Anusree Unnikrishnan
II M.Tech
CB.EN.P2CHE10001
Novel Microreactors for FunctionalNovel Microreactors for Functional
Polymer BeadsPolymer Beads.T . Nisisako et al. , Dept of Precision Engineering ,Graduate School of
Engineering, University of Tokyo, Chemical Engineering Journal ,2004.
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IntroductionPolymeric microspheres of uniform size in the diameter
range 10100 m have a great many applications in diverse
fields.
In liquid chromatography, mono-sized particles packed
optimally in columns provide significant improvement in
separation efficiency .
Regular-sized beads in liquid crystal displays give a clear
and uniform image.
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Introduction Cont.
Many other applications arise in science and technology
which includes:
y Particle-based bioassays
y Flow measurement : Particle image velocimetry (PIV)
y Microparticle - based displays
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Introduction Cont.Therefore studies have been carried out in engineering of
polymeric microspheres of the requisite diameter having a
tight distribution of sizes.
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Classical Methods
1m dia
a.)Dispersion Polymerization
b.)Seed Polymerization
10-100m dia
a.) Suspension
Polymerization
Microspheres
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Recent Techniques
Membrane Emulsification
Omi et al. successfully manufactured polystyrene
microspheres of 29m with a CV of close to 10% by
suspension polymerization of relatively uniform oil/water
emulsion produced by sirasu porous glass (SPG) membrane
emulsification.
Microfabricated channel arrays on silicon have been used
for preparing suspensions for polymerization and polymericdivinylbenzene beads of over 50 m with a CV below 5%
.
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Current Approach
Preparation of monodispersed droplets :
In this technique we make use of a microfluidic
systems in which two immiscible liquids areintroduced into separate microchannels , and then one
liquid is forced into the second liquid at a junction to
form microdroplets one by one.
Droplet formation a the junction is both rapid and
reproducible.
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Objective
To produce monodisperse polymeric microspheres of
diameter 30120 m by polymerization of a monomer
suspension, using a simple T-shaped channel
configuration.
We also engineer bicolored beads using another
microfluidic device
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Experimental Setup
1.) Generation of single-phase microdroplets :
T-shaped channel employed
Grooves and holes for supply ports and drain ports,
were machined into quartz chipsCovered by Fusion bonding with another quartz chip.
The channels were machined deeper and wider near
the drain port in order to measure the size of the
droplets as spheres are formed there.
The channel widens gradually so that the flow speed
changes only slowly.
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T-junction device
.
The organic phase
(monomer) flow channel
is at right angles to theaqueous phase flow
channel
This T-junction is
positioned at 3mm fromthe organic phase supply
port and 8mm from the
aqueous phase supply
port
Schematic of the T-shaped channel
(Channel sizes are written as width depth).
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Equipments Required
Glass microsyringes (1000 series, Hamilton Company,NV,
Syringe pumps (KDS200, KD Scientific Inc., PA, USA)
[ The pumps were tested in advance to confirm constant supply of liquids
by using pressure sensors ]
The glass microchip was assembled in a stainless jig(40mm
30mm8mm) and linked to syringes through polytetrafluoroethylene(PTFE) tubes and connectors.
An optical microscope (BX-51, OLYMPUS OPTICAL CO. Ltd., Japan)
A high-speed video camera (Fastcam-max, PHOTRON LIMITED,
Japan) :These were used to observe and record the microfluidic behavior
of the two immiscible liquids [so as to capture such phenomena as the
formation of microdroplets at junctions].
Images were downloaded digitally to an IBM-compatible PC, and the
droplet size was calculated from the images.
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The resulting droplets were collected in a beaker andcured either by UV light radiation (for 12 min) or ahot water bath (7080 C for 45 min).
To prevent clogging in the microchannels , allequipment was placed in a clean room.
The room was air-conditioned to a constant
temperature (293 K) to prevent thermally drivenfluctuations in the viscosity, surface tension and other
physical properties of the fluids.
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Results & Discussion
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Conclusion
We have reported here the production of polymeric
microspheres using confluent microflow systems.
Monomer droplets of uniform size were rapidly and
reproducibly formed in the crossflow junction, and polymerparticles with a CV below 2% were successfully prepared
by subsequent polymerization.
The particle size was reliably chosen in the range of 30
120m by controlling flow conditions.A flow diagram focusing on droplet breakup phenomena
was obtained.
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Conclusion Cont . . .
This simple technique will be applicable to a variety of
functional spheres: porous particles, magnetized beads,
microcapsules, and many others.
We showed a further functionality by preparinghemispherically colored droplets and microspheres that
were cured subsequently. These functional particles could
find application as materials in electric displays, as Gyricon
balls have done .The possibility of active control of the internal design of
particles now arises. This method shows great promise and
we believe that it will open up a new field of research in the
microfluidic synthesis of pioneering materials
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THANK YOUTHANK YOU