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