Phase separation in multicomponent polymer melts is a ubiquitous process in polymer engineering and consequently has also attracted abiding interest from simulation and theory. Whereas the equilibrium thermodynamics of macrophase separation and microphase separation in homopolymer blends and copolymers can be rather quantitatively described by Self-Consistent Field Theory (SCFT) or extensions that capture fluctuations, the kinetics of structure evolution poses challenges for a theoretical description. Examining simple, prototypical examples, we highlight the role of internal modes and indicate how Dynamic Self-Consistent Field Theory (D-SCFT) can be generalised to include the consequences of the subdiffusive single-chain dynamics for the co...
textThis research focuses on the computational modeling of fluctuations, interactions, phase behavio...
To provide a faster calculation of the block copolymer phase diagrams a simplified version of the se...
Polymer dynamics in the melt state cover a wide range in time and frequency, for both molecular weig...
Structure evolution in multicomponent polymer melts and in their network equivalents is investigated...
In this paper, we describe a numerical method for the calculation of collective diffusion relaxation...
In this paper we discuss a new generalized time-dependent Ginzburg-Landau theory for the numerical c...
We present detailed results from a molecular dynamics (MD) simulation of phase-separation kinetics i...
We review a formalism that can be used to calculate the microphase-separated crystallographic struct...
Several extensions to the phase behavior of binary polymer blends were investigated. Complicated and...
The segmental dynamics of miscible polymer blends have been the focus of much recent research since ...
In this paper we apply nonlocal kinetic coupling to the dynamic mean-field density functional method...
We report results of molecular-dynamics simulations of a model polymer melt consisting of short non-...
ABSTRACT: A balanced A-C diblock copolymer surfactant was used to organize mixtures of immiscible A ...
Summary The main theme of this thesis is the influence of polydispersity on the phase behavior of co...
Summary The main theme of this thesis is the influence of polydispersity on the phase behavior of co...
textThis research focuses on the computational modeling of fluctuations, interactions, phase behavio...
To provide a faster calculation of the block copolymer phase diagrams a simplified version of the se...
Polymer dynamics in the melt state cover a wide range in time and frequency, for both molecular weig...
Structure evolution in multicomponent polymer melts and in their network equivalents is investigated...
In this paper, we describe a numerical method for the calculation of collective diffusion relaxation...
In this paper we discuss a new generalized time-dependent Ginzburg-Landau theory for the numerical c...
We present detailed results from a molecular dynamics (MD) simulation of phase-separation kinetics i...
We review a formalism that can be used to calculate the microphase-separated crystallographic struct...
Several extensions to the phase behavior of binary polymer blends were investigated. Complicated and...
The segmental dynamics of miscible polymer blends have been the focus of much recent research since ...
In this paper we apply nonlocal kinetic coupling to the dynamic mean-field density functional method...
We report results of molecular-dynamics simulations of a model polymer melt consisting of short non-...
ABSTRACT: A balanced A-C diblock copolymer surfactant was used to organize mixtures of immiscible A ...
Summary The main theme of this thesis is the influence of polydispersity on the phase behavior of co...
Summary The main theme of this thesis is the influence of polydispersity on the phase behavior of co...
textThis research focuses on the computational modeling of fluctuations, interactions, phase behavio...
To provide a faster calculation of the block copolymer phase diagrams a simplified version of the se...
Polymer dynamics in the melt state cover a wide range in time and frequency, for both molecular weig...