Simulation of random copolymers at selective interfaces and of cross-linked polymer blends

Author(s):  
Jens-Uwe Sommer ◽  
Stefan Lay ◽  
Alexander Blumen
2015 ◽  
Vol 25 (5) ◽  
pp. 1267-1276 ◽  
Author(s):  
Xiang Xu ◽  
Zhixin Xu ◽  
Pei Chen ◽  
Xiaodong Zhou ◽  
Anna Zheng ◽  
...  

Author(s):  
Chang Dae Han

The polymer industry has been challenged to produce new polymeric materials by blending two or more homopolymers or random copolymers or by synthesizing graft copolymers. To meet the challenge, various methods have been explored, namely, (1) by synthesizing a new monomer, polymerizing it, and then blending it with an existing homopolymer or random copolymer, (2) by copolymerizing existing monomers and then blending it with an existing homopolymer or random copolymer, (3) by chemically modifying an existing homopolymer or random copolymer and then blending it with other homopolymers or copolymers already available, or (4) by synthesizing new compatibilizer(s) to improve the mechanical properties of two immiscible homopolymers or random copolymers that otherwise have unacceptable mechanical properties. There are numerous monographs (Cooper and Estes 1979; Han 1984; Paul and Newman 1978; Platzer 1971, 1975; Sperling 1974; Utracki 1990) describing various aspects of polymer blends. In the 1970s, Han and coworkers (Han 1971, 1974; Han and Kim 1975; Han and Yu 1971a, 1971b, 1972; Han et al. 1973, 1975; Kim and Han 1976) conducted seminal experimental studies on the rheology of immiscible polymer blends and related the observed rheological behavior to blend morphology. Independently, in the same period, Vinogradov and coworkers (Ablazova et al. 1975; Brizitsky et al. 1978; Tsebrenko et al. 1974, 1976; Vinogradov et al. 1975) conducted a series of experimental studies relating the blend rheology to blend morphology. Van Oene (1972, 1978) also pursued, independently, experimental studies for a better understanding of rheology–morphology relationships in immiscible polymer blends. Since then, using different polymer pairs, numerous researchers have conducted experimental studies, which were essentially the same as, or very similar to, the previous experimental studies of Han and coworkers, Vinogradov and coworkers, and van Oene in the 1970s. It is fair to state that those studies in the 1980s and 1990s have not revealed any significant new findings.


Author(s):  
Afzana Anwer ◽  
S. Eilidh Bedford ◽  
Richard J. Spontak ◽  
Alan H. Windle

Random copolyesters composed of wholly aromatic monomers such as p-oxybenzoate (B) and 2,6-oxynaphthoate (N) are known to exhibit liquid crystalline characteristics at elevated temperatures and over a broad composition range. Previous studies employing techniques such as X-ray diffractometry (XRD) and differential scanning calorimetry (DSC) have conclusively proven that these thermotropic copolymers can possess a significant crystalline fraction, depending on molecular characteristics and processing history, despite the fact that the copolymer chains possess random intramolecular sequencing. Consequently, the nature of the crystalline structure that develops when these materials are processed in their mesophases and subsequently annealed has recently received considerable attention. A model that has been consistent with all experimental observations involves the Non-Periodic Layer (NPL) crystallite, which occurs when identical monomer sequences enter into register between adjacent chains. The objective of this work is to employ electron microscopy to identify and characterize these crystallites.


Author(s):  
E. G. Rightor

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.


Author(s):  
William A. Heeschen

Two new morphological measurements based on digital image analysis, CoContinuity and CoContinuity Balance, have been developed and implemented for quantitative measurement of morphology in polymer blends. The morphology of polymer blends varies with phase ratio, composition and processing. A typical morphological evolution for increasing phase ratio of polymer A to polymer B starts with discrete domains of A in a matrix of B (A/B < 1), moves through a cocontinuous distribution of A and B (A/B ≈ 1) and finishes with discrete domains of B in a matrix of A (A/B > 1). For low phase ratios, A is often seen as solid convex particles embedded in the continuous B phase. As the ratio increases, A domains begin to evolve into irregular shapes, though still recognizable as separate domains. Further increase in the phase ratio leads to A domains which extend into and surround the B phase while the B phase simultaneously extends into and surrounds the A phase.


Polymer News ◽  
2005 ◽  
Vol 30 (9) ◽  
pp. 296-300
Author(s):  
F. Esposito ◽  
V. Casuscelli ◽  
M. V. Volpe ◽  
G. Carotenuto ◽  
L. Nicolais

Sign in / Sign up

Export Citation Format

Share Document