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Nanoparticle with endgrafted chains in polymeric solution

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Title: Nanoparticle with endgrafted chains in polymeric solution


1
Nanoparticle with end-grafted chains in polymeric
solution
  • Analee Miranda, Undergraduate
  • Applied Math/Physics
  • Department of Mathematics
  • University of California, Riverside

2
Introduction
  • Polymer brushes attached to a colloidal surface
    can be engineered through grafting techniques
    available in todays chemical engineering
    industries

3
Why investigate these structures?We need to
look at some facts about colloidal science first
  • The introduction of nanoparticles into any system
    creates energy instability

4
The Facts
  • Colloid-Colloid Interactions aid in the
    destabilization of the colloid-polymer mixture
    causing effects such as aggregation

5
The Facts
  • Colloidal Dispersion is difficult to achieve

6
How the facts become problems to different
Industries
  • Drug Development
  • The biggest problem facing formulation
    development providers is solubility.
    www.researchediting.com
  • Industrial Chemicals/Cosmetics
  • Color infusion is dependent on dispersion of
    colloidal molecules into polymer solutions
  • Petrochemicals
  • The tendency of heavy organics from its oil phase
    into an aggregate causes arterial blockage
  • Bio-Engineering
  • Stable colloidal-polymer dispersion is necessary
    to produce biocompatible delivery methods

7
Potential Solutions
  • Introduction of Polymer Brushes to
  • lyophobic colloidal surfaces. This may induce
    thermodynamic stabilization
  • any colloidal surface interrupts aggregate
    formation by shielding colloids
  • any colloidal surface increases solubility by
    engineering a connection between tails of polymer
    brushes and wet-polymers

8
Monte Carlo Method
  • By using Density Functional Theory, the reduced
    Grand potential of a system based on different
    factors is calculated.
  • We first investigated a system in which the
    nanoparticle does not carry the polymer brush in
    order to observe the instability.
  • We then investigated the same system with the
    polymer brush in order to determine the
    improvements in system stability that the polymer
    brush provides.

9
Potential Model
  • Inter-segment interactions Cut and Shift
    Lennard Jones Potential
  • Segment-Nanoparticle interactions Yukawa
    Potential. The energy parameter is negative to
    induce a very strong repulsion

10
Effect of Size Ratio Between Colloid and Segment
Diameters
11
Effect of Size Ratio Between Colloid and Segment
Diameters
  • We can see that at very low surface coverage as
    the size ratio increases, the system becomes less
    stable.
  • For the highest surface coverage, as the size
    ratio increases, the system becomes more stable.
  • We can also see a sharp increase in stability as
    the size ratio increases, which suggests an
    optimum rate of stability with an increasing size
    ratio for the highest surface coverage

12
Effect of Chain Length of Free Polymers
13
Effect of Chain Length of Free Polymers
  • We calculated two different densities. We can see
    that for the lower density, it is easier for the
    system to become more stable. The desired effect
    is not as great for the higher density.
  • We can also see that the stability of the system
    reaches a maximum and does not undergo much
    transition as the chain length increases.

14
Effect of the chain length of Polymer Brushes
15
Effect of the chain length of Polymer Brushes
  • Again, we see that the maximum stability can be
    attained by adding more polymer brushes to the
    nanoparticle surface.
  • Increasing the chain length of the polymer
    brushes at this optimal condition can also yield
    a more stable system.
  • The chain length of polymer brushes has a slight
    effect at lower surface coverage.

16
Effect of Surface Coverage of Polymer Brush to
Colloid
17
Effect of Surface Coverage of Polymer Brush to
Colloid
  • We can now fully comprehend that as the surface
    coverage of polymer brushes on the colloid
    increases, the system becomes more stable.
  • We can also see that at low densities, we see
    more stability in the system

18
Conclusion
  • Using density functional theory, we were able to
    prove the function of polymer brushes in the
    colloid systems, i.e., improve the stability of
    colloid dispersion or increase the solubility of
    colloid particles.
  • The best results were achieved with low-density
    polymer solution with a high surface coverage of
    long polymer-brushes.

19
Acknowledgements
  • Dr. Jianzhong Wu, Department of Chemical
    Engineering, Bourns College of Engineering,
    University of California, Riverside
  • Zhidong Li, Department of Chemical Engineering,
    Bourns College of Engineering, University of
    California, Riverside
  • National Science Foundation

20
Abstract
  • Colloidal stability is critically important in a
    variety of biomedical and materials applications
    of nanoparticles. A conventional approach is to
    tether nanoparticles with a layer of highly
    soluble Polymer Chains, thereby introducing
    nanoparticle functionality and preventing
    nanoparticle aggregation by stearic repulsion.
    However, the microscopic structure and surface
    energy of Polymer Chains coated nanoparticles are
    not completely understood. This is particularly
    true if one considers the variation of
    interfacial properties with the particle size,
    the chemistry of Polymer Chains, their chain
    length and flexibility, and grafting density.

21
  • In this work, we have investigated the solvation
    energy and interfacial microscopic structure of
    isolated Polymer Chains -protected nanoparticles
    in polymer solutions through density functional
    theory. At low surface coverage of end-grafted
    Polymer Chains, the insertion of large
    nanoparticle is energetically unfavorable and the
    surface energy rises monotonically with the
    particle size. In this case, the increase of the
    Polymer Chains chain length alters the thickness
    of the protection layer but has only minor effect
    on the interfacial energy. At sufficiently high
    surface coverage, however, the surface energy of
    a large nanoparticle or longer Polymer Chains
    chains is much more negative than that of a small
    particle or short Polymer Chains chains,
    suggesting an increase in solubility with the
    particle size. In both cases, longer polymer
    chains and lower polymer concentration lead to
    improved stability of nanoparticles.

22
References
  • D.H. Everett. (1988) Basic principles of colloid
    science. London Royal Society of Chemistry.
  • Yuri S. Lipatov. Translated from Russian by A.
    Kozi. (1988) Colloid chemistry of polymers.
    Amsterdam New York Elsevier.
  • J. Mahanty B. W. Ninham. (1976) Dispersion
    forces. London New York Academic Press.
  • Ian D. Morrison Sydney Ross. (2002) Colloidal
    dispersions suspensions, emulsions, and foams.
    New York Wiley-Interscience.
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