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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 2016-2021 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 7817-7821 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 5687-5693 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present results of numerical simulations of a new model for the clustering process in self-associating polymer systems. We focus on two experimentally interesting systems; telechelic ionomers and reverse micelles. The clustering dynamics introduced by us is an extension of the Eden method, previously used in the context of single particle aggregation. The structure of the aggregates seen in the simulations is qualitatively similar to that observed in experimental systems. The quantitative predictions of the model are found to be similar to those found in simulations of a model based on a diffusion-limited-aggregation-type process.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6899-6909 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report results of a detailed numerical study of the phase separation process in a three dimensional model of polymer blends. The model system considered by us is described by Flory–Huggins–de Gennes free-energy functional. For a critical quench, we numerically integrate the corresponding time evolution equation for the conserved order parameter based on the above free-energy functional. We study the time dependence of the characteristic domain size as well as the pair correlation function and the structure factor for several quench temperatures. The results indicate that the growth law for the characteristic domain size is given by a modified Lifshitz–Slyozov law and the growth law exponent is independent of the quench temperature. We also find that both the pair correlation function and the structure factors show dynamical scaling at late times.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 6423-6428 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We numerically study morphology of symmetric diblock copolymer films with a thickness smaller than the bulk equilibrium period. These films are cast on either flat or corrugated substrates. Our results show that the formation of uniformly sized lateral domains that appear randomly on a flat surface can be controlled by using topographically patterned substrates. This is in excellent agreement with recent experimental studies. Control of lateral pattern fails if (i) the distance between the steps of the substrate is smaller than the bulk lamellar wavelength, or (ii) the lateral size of the corrugation is larger than the bulk lamellar wavelength. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 10582-10587 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We study phase separation of quenched polymer solutions under an external shear flow by using a stochastic molecular dynamics method. We observe the formation of a stringlike pattern of polymer domains normal to the direction of the shear flow. The characteristic size of the layered domains has a power law relation with the shear rate. Shear-induced rheological behavior of the mixture is also examined in terms of the excess viscosity. We find that the maximum excess viscosity scales as the shear rate, and that the numerical value of the power-law exponent agrees well with theoretical scaling predictions. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 801 (1996), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 748-749 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We carry out Monte Carlo simulations in both lattice and off-lattice geometry, to study the configurational properties of a system of two polymer-coated plates. We compare our results with numerical and analytical self-consistent-field theories. For the short chain-lengths considered here, we find both compression and interpenetration of the polymer brushes as the plate separation is decreased, instead of the "classical-limit'' picture of compression with no interpenetration.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 3310-3317 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Surface-induced ordering in block copolymer melts is studied numerically. For symmetric copolymers, the thickness of the surface-enrichment layer is found to scale as Req∼Nθ with θ≈0.6, suggesting the system is undergoing a surface-induced strong segregation. The density profile perpendicular to the interacting surface is described quite well by the form predicted by Fredrickson in a mean-field analysis. In asymmetric copolymers, the surface is found to have a profound effect on domain formation. For some off-critical compositions, domains were found to form near the surface with a geometry different from that in the bulk; while for stronger asymmetry in composition, minority domains were nucleated near the wall only, long before any formed in the bulk. These interesting pattern formation processes should be observable in experiments using a depth profiling technique.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 9418-9423 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have carried out a systematic investigation of the kinetics of domain growth of a model binary mixture in contact with a fractal network similar to the fumed silica network used in recent experiments with polymer blends. This network has selective affinity for one component of the blend. We study the morphology of the growing domains and the wetting layer, the growth exponent, and dynamical scaling behavior for a critical composition of the mixture. We find that the characteristic size of domains grows as t1/3 for deep quenches, as long as the average domain size is small compared to the average "pore" radius of the unoccupied region. This suggests that the kinetics of domain growth at intermediate times is not appreciably perturbed by the presence of the network. For off-critical compositions, we study domain growth in two different situations where either the majority or the minority component of the blend wets the network. When the majority component wets the network, a network-induced nucleation is possible for sufficiently off-critical mixtures due to the reduction or elimination of the local nucleation barrier for the minority phase near the network. For this reason, minority droplets nucleate predominantly near the network before they appear in the bulk. When the minority phase wets the network, a slowdown in wetting layer growth is found to occur at late times due to a depletion of the system of its minority component. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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