Glassy correlations and microstructures in randomly cross-linked homopolymer blends.
نویسندگان
چکیده
We consider a microscopic model of a polymer blend that is prone to phase separation. Permanent cross-links are introduced between randomly chosen pairs of monomers, drawn from the Deam-Edwards distribution. Thereby, not only density but also concentration fluctuations of the melt are quenched-in in the gel state, which emerge upon sufficient cross-linking. We derive a Landau expansion in terms of the order parameters for gelation and phase separation, and analyze it on the mean-field level, including Gaussian fluctuations. The mixed gel is characterized by thermal as well as time-persistent (glassy) concentration fluctuations. Whereas the former are independent of the preparation state, the latter reflect the concentration fluctuations at the instant of cross-linking, provided the mesh size is smaller than the correlation length of phase separation. The mixed gel becomes unstable to microphase separation upon lowering the temperature in the gel phase. Whereas the length scale of microphase separation is given by the mesh size, at least close to the transition, the emergent microstructure depends on the composition and compressibility of the melt. Hexagonal structures, as well as lamellas or random structures with a unique wavelength, can be energetically favorable.
منابع مشابه
Microphase separation in cross-linked polymer blends. Efficient replica RPA post-processing of simulation data for homopolymer networks.
We investigate the behaviour of randomly cross-linked (co)polymer blends using a combination of replica theory and large-scale molecular dynamics simulations. In particular, we derive the analogue of the random phase approximation for systems with quenched disorder and show how the required correlation functions can be calculated efficiently. By post-processing simulation data for homopolymer n...
متن کاملPhase Behavior of Complementary Multiply Hydrogen Bonded End-Functional Polymer Blends
Blends of diamidonaphthyridine (Napy) end-functional poly(n-butyl acrylate) (PnBA) and ureidopyrimidinone (UPy) end-functional poly(benzyl methacrylate) (PbnMA) were studied as a function of the component molecular weights to compare with prior theoretical predictions. Macroscopic phase separation was observed to be prevented by the reversible association of end-functional polymers to form supr...
متن کاملGlassy states and microphase separation in cross-linked homopolymer blends
– The physical properties of blends of distinct homopolymers, cross-linked beyond the gelation point, are addressed via a Landau approach involving a pair of coupled order-parameter fields: one describing vulcanisation, the other describing local phase separation. Thermal concentration fluctuations, present at the time of cross-linking, are frozen in by cross-linking, and the structure of the r...
متن کاملEffect of homopolymer molecular weight on order-order transition in block copolymer and homopolymer blends.
The order-order transition temperature (T(OOT)) in blends of poly(styrene-b-isoprene-b-styrene) (S-I-S) triblock copolymer and polyisoprene (PI) homopolymer was investigated by using synchrotron small-angle X-ray scattering (SAXS). Pure triblock copolymer undergoes an order-order transition (OOT) from hexagonally ordered cylinder (HEX) to body centered cubic (BCC) phases. In order to investigat...
متن کاملDiblock Copolymer / Homopolymer Blends: Derivation of a Density Functional Theory
Melts of diblock copolymer / homopolymer blends exhibit multiscale phase separation: (i) macrophase separation into homopolymerand copolymer-rich macrodomains followed by (ii) microphase separation into Aand B-rich microdomains within the copolymer-rich macrodomains (cf. [16, 17, 26]). Following our previous derivation in [6], we derive a density functional theory for blends. This theory has be...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The Journal of chemical physics
دوره 124 21 شماره
صفحات -
تاریخ انتشار 2006