Biomedical subjects

Scott W Sides

Publications and source records attributed to Scott W Sides.

5 recordsLinked to original sources

PubMed2006

Hybrid particle-field simulations of polymer nanocomposites.

We present a theoretical framework and computer simulation methodology for investigating the equilibrium structure and properties of mesostructured polymeric fluids with embedded colloids or nanoparticles. The method is based on a field-theoretic description of the fluid in which particle coordinates and chemical potential field variables are simultaneously updated. The fluid model can contain polymers of arbitrary chemical and architectural complexity, along with particles of all shapes, sizes, and surface treatments. Simulation results are compared with experiments conducted on polystyrene (PS)-functionalized Au nanoparticles in a PS-P2VP diblock copolymer melt.

Journal Article↗

PubMed2005

Introducing variable cell shape methods in field theory simulations of polymers.

We propose a new method for carrying out field-theoretic simulations of polymer systems under conditions of prescribed external stress, allowing for shape changes in the simulation box. A compact expression for the deviatoric stress tensor is derived in terms of the chain propagator, and it is used to monitor changes in the box shape according to a simple relaxation scheme. The method allows fully relaxed, stress free configurations to be obtained even in nontrivial morphologies, and it enables the study of morphology transitions induced by external stresses.

Journal Article↗

PubMed2005

Field-theoretic simulations of polymer solutions: finite-size and discretization effects.

In this work we analyze the finite-size and discretization effects that occur in field-theoretic polymer simulations. Following our previous work, we study these effects for a polymer solution in the canonical ensemble confined to a slit (with nonadsorbing walls) of width L, and focus on the behavior of two quantities: the chemical potential mu, and the correlation length xi. Our results show that the finite-size effects disappear for both quantities once the lateral size of the system L is larger than approximately 2xi. On the other hand, the chemical potential is dominated by the lattice discretization Deltax. The origins of this dependence are discussed in detail, and a scheme is proposed in which this effect is avoided. Our results also show that the density profiles do not depend on the lattice discretization if Deltax < approximately xi/4. This implies that the correlation length xi, extracted from the density profiles, is free of lattice size and lattice discretization artifacts once L is > approximately 2xi and Deltax < approximately xi/4.

Journal Article↗

PubMed2004

Composite mesostructures by nano-confinement.

In a physically confined environment, interfacial interactions, symmetry breaking, structural frustration and confinement-induced entropy loss can play dominant roles in determining molecular organization. Here we present a systematic study of the confined assembly of silica-surfactant composite mesostructures within cylindrical nanochannels of varying diameters. Using exactly the same precursors and reaction conditions that form the two-dimensional hexagonal SBA-15 mesostructured thin film, unprecedented silica mesostructures with chiral mesopores such as single- and double-helical geometries spontaneously form inside individual alumina nanochannels. On tightening the degree of confinement, a transition is observed in the mesopore morphology from a coiled cylindrical to a spherical cage-like geometry. Self-consistent field calculations carried out to account for the observed mesostructures accord well with experiment. The mesostructures produced by confined syntheses are useful as templates for fabricating highly ordered mesostructured nanowires and nanowire arrays.

Microscopy, Electron↗

PubMed2004

Continuous polydispersity in a self-consistent field theory for diblock copolymers.

An efficient algorithm is presented for numerically evaluating a self-consistent field theoretic (SCFT) model of an AB diblock copolymer that incorporates continuous polydispersity in one of the blocks. An interesting segregation effect is found in which chains of intermediate molecular weight are concentrated at domain interfaces. This model of continuous polydispersity is also implemented in the random phase approximation (RPA) to study the order-disorder transition and predicts that the stability of the disordered, homogeneous phase decreases as the polydispersity in one of the blocks increases. The RPA predictions are confirmed by SCFT calculations. Our approach and results are particularly relevant to block copolymers prepared by quasiliving synthesis techniques, where the polymerization of one block is much more controlled than the other block.

Journal Article↗