scholarly journals Tuned Surface and Mechanical Properties of Polymeric Film Prepared by Random Copolymers Consisting of Methacrylate-POSS and 2-(Methacryloyloxy)ethyl Phosphorylcholine

2018 ◽  
Vol 219 (8) ◽  
pp. 1700572 ◽  
Author(s):  
Suchismita Chatterjee ◽  
Takuya Matsumoto ◽  
Takashi Nishino ◽  
Tooru Ooya
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.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2263
Author(s):  
Maryam Safari ◽  
Itziar Otaegi ◽  
Nora Aramburu ◽  
Gonzalo Guerrica-Echevarria ◽  
Antxon Martínez de Ilarduya ◽  
...  

Isodimorphic behavior is determined by partial inclusion of comonomer segments within the crystalline structure and arises from the comparatively similar repeating chain units of the parental homopolymers. Isodimorphic random copolymers are able to crystallize irrespective of their composition and exhibit a pseudo-eutectic behavior when their melting point values are plotted as a function of comonomer content. At the pseudo-eutectic point or region, two crystalline phases can coexist. On the right-hand and the left-hand side of the pseudo-eutectic point or region, only one single crystalline phase can form which is very similar to the crystalline structures of the parent homopolymers. This article aims to study the synthesis method, structure, crystallization behavior and mechanical properties of isodimorphic random PBS-ran-PCL copolyesters. Moreover, this study provides a comprehensive analysis of our main recent results on PBS-ran-PCL random copolyesters with three different molecular weights. The results show that the comonomer composition and crystallization conditions are the major factors responsible for the crystalline morphology, crystallization kinetics and mechanical performance of isodimorphic random copolyesters. Our studies demonstrate that in the pseudo-eutectic region, where both crystalline phases can coexist, the crystallization conditions determine the crystalline phase or phases of the copolymer. The relationships between the comonomer composition and mechanical properties are also addressed in this work.


2011 ◽  
Vol 279 ◽  
pp. 120-125
Author(s):  
Jin Huan Li ◽  
Hai Yang Wang ◽  
Rui Hai Wang

Aromatic polybenzoxazoles (PBOs) are very promising materials for civil, aerospace and electronics industries due to their outstanding mechanical properties, good thermooxidative stability and chemical resistance. However, the feasibility of the wide applications is hindered due to the difficulty of their processing derived from the very rigid structure. Poly(aryl-ether benzoxazole) random copolymers (PAEXBOx) were prepared by nucleophilic polycondensation. Ary-ether ketone and aryl-ether sulfone segments along with flexible linkages and bulky groups were introduced to provide PAEXBOx with good solubility in organic solvents. PAEXBOx exhibit the improved Tgs, and intermediate properties between pristine PBOs and poly(acryl ether)s (PAEs). The structure and properties of the polymers were systematically characterized.


Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1055 ◽  
Author(s):  
Ke Wang ◽  
Qibo Deng

The thermal and mechanical properties of poly(ethylene-co-vinyl acetate) random copolymers (PEVA) and its covalently crosslinked analogues (cPEVA) were controlled by the overall crystallinity of the polymer networks. The cPEVAs with different VA-content were synthesized by thermally-induced crosslinking of linear PEVA with dicumyl peroxide (DCP). This work was mainly concerned with the effect of vinyl acetate (VA) content on the crosslinking density, thermal and mechanical properties of PEVAs and cPEVAs, respectively. The chemical composition was analyzed by thermogravimetric analysis and 1H-NMR. The thermal and mechanical properties of PEVAs and cPEVAs have been studied through a series of conventional analytical methods, including gel content determination, different scanning calorimetry, thermogravimetric analysis, dynamic mechanical thermal analysis and traditional mechanical measurements. The experimental results show that the thermal and mechanical properties of PEVAs and cPEVAs increase with decreasing the VA-content. A broad melting transition with a ΔTm in the range from 78 °C to 95 °C was observed for all polymer networks.


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