Effect of graft density and molecular weight on mechanical properties of rubbery block copolymer grafted SiO2 nanoparticle toughened epoxy

Polymer ◽  
2013 ◽  
Vol 54 (15) ◽  
pp. 3961-3973 ◽  
Author(s):  
Jianing Gao ◽  
Junting Li ◽  
Su Zhao ◽  
Brian C. Benicewicz ◽  
Henrik Hillborg ◽  
...  
2015 ◽  
Vol 770 ◽  
pp. 87-92
Author(s):  
Sergey Panin ◽  
Lyudmila А. Kornienko ◽  
Nguyen Xuan Thuc ◽  
Larisa R. Ivanova ◽  
Mikhail A. Poltaranin ◽  
...  

In order to find out optimum filler to increase manufacturability (extrudability) of composites based on ultra-high molecular weight polyethylene (UHMWPE) matrix as well as to develop polymer-polymeric composites with improved tribological characteristics, the structure, mechanical properties and wear resistance of UHMWPE mixtures with elasticizing block-copolymer PA-b-LLDPE (UHMWPE + PA-b-LLDPE) was investigated under dry sliding friction. Applied aspect of the study is related to the selection of commercially available fillers being compatible with UHMWPE for manufacturing anti-frictional extrudable nanocomposites. It is shown that as compared with pure UHMWPE mechanical properties (ultimate strength, value of elongation at failure) do not vary substantially, but the wear rate under dry sliding friction of polymeric composites UHMWPE + n wt.% PA-b-LLDPE is reduced only when block copolymer weight fraction is less than ≤ 5 wt.%. By the polymeric filling an important technological characteristic - specific pressure of extrusion (that is proportional to melt flow index) might be decreased. Permolecular structure and wear track surfaces of polymer-polymer composites UHMWPE + n wt.% PA-b-LLDPE was examined and numerically characterized.


Author(s):  
Chang Dae Han

More often than not, the mechanical properties (e.g., impact and tensile properties) of immiscible polymer blends are very poor owing to the lack of adhesion between the constituent components, which originates from strong repulsive thermodynamic (segmental) interactions. Therefore, in the past, a great deal of effort (Barlow and Paul 1984; Fayt and Teyssie 1989; Fayt et al. 1981, 1987, 1989; Gupta and Purwar 1985; Ouhadi et al. 1986a; Park et al. 1992; Schwarz et al. 1988, 1989; Srinivasan and Gupta 1994; Traugott et al. 1983) has been made to improve the mechanical properties of two immiscible polymers by adding a third component (e.g., a block copolymer). In this chapter, we confine our attention primarily to the situations where a nonreactive third component is added to two immiscible homopolymers in order to improve their mechanical properties. A polymer blend consisting of two immiscible homopolymers (say, A and B) has a very narrow interface, as schematically shown in Figure 4.1, because they have strong repulsive segmental interactions giving rise to a positive value of the Flory–Huggins interaction parameter (χ), i.e., χAB > 0. Helfand and Tagami (1971, 1972) derived the following expression relating the interfacial thickness d of a pair of immiscible homopolymers of infinite molecular weight to χ: . . . d = 2b/(6χ)1/2 (4.1). . . where the Kuhn length b is assumed to be the same for both components. They also derived an expression for the interfacial tension γ between two immiscible homopolymers: . . . γ = (χ/6)1/2bρokBT . . . in terms of χ, where kB is the Boltzmann constant, T is the absolute temperature, and ρo is the reference density (the inverse of monomeric volume of a reference component). Equation (4.1) indicates that the interfacial thickness between two immiscible homopolymers will be larger when the extent of repulsive segmental interactions is less, and Eq. (4.2) indicates that the interfacial tension between two immiscible homopolymers will be lower when the extent of repulsive segmental interactions is less.


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2480
Author(s):  
Yi-Fang Chen ◽  
Jia-Wen Hong ◽  
Jung-Hong Chang ◽  
Belda Amelia Junisu ◽  
Ya-Sen Sun

We studied the influence of osmotic pressure on nanostructures in thin films of a symmetric weakly-segregated polystyrene-block-poly (methyl methacrylate), P(S-b-MMA), block copolymer and its mixtures with a polystyrene (PS) homopolymer of various compositions. Thin films were deposited on substrates through surface neutralization. The surface neutralization results from the PS mats, which were oxidized and cross-linked by UV-light exposure. Thus, thermal annealing produced perpendicularly oriented lamellae and perforated layers, depending on the content of added PS chains. Nevertheless, a mixed orientation was obtained from cylinders in thin films, where a high content of PS was blended with the P(S-b-MMA). A combination of UV-light exposure and acetic acid rinsing was used to remove the PMMA block. Interestingly, the treatment of PMMA removal inevitably produced osmotic pressure and consequently resulted in surface wrinkling of perpendicular lamellae. As a result, a hierarchical structure with two periodicities was obtained for wrinkled films with perpendicular lamellae. The formation of surface wrinkling is due to the interplay between UV-light exposure and acetic acid rinsing. UV-light exposure resulted in different mechanical properties between the skin and the inner region of a film. Acetic acid rinsing produced osmotic pressure. It was found that surface wrinkling could be suppressed by reducing film thickness, increasing PS content and using high-molecular-weight P(S-b-MMA) BCPs.


Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 404
Author(s):  
Nur Sharmila Sharip ◽  
Hidayah Ariffin ◽  
Tengku Arisyah Tengku Yasim-Anuar ◽  
Yoshito Andou ◽  
Yuki Shirosaki ◽  
...  

The major hurdle in melt-processing of ultra-high molecular weight polyethylene (UHMWPE) nanocomposite lies on the high melt viscosity of the UHMWPE, which may contribute to poor dispersion and distribution of the nanofiller. In this study, UHMWPE/cellulose nanofiber (UHMWPE/CNF) bionanocomposites were prepared by two different blending methods: (i) melt blending at 150 °C in a triple screw kneading extruder, and (ii) non-melt blending by ethanol mixing at room temperature. Results showed that melt-processing of UHMWPE without CNF (MB-UHMWPE/0) exhibited an increment in yield strength and Young’s modulus by 15% and 25%, respectively, compared to the Neat-UHMWPE. Tensile strength was however reduced by almost half. Ethanol mixed sample without CNF (EM-UHMWPE/0) on the other hand showed slight decrement in all mechanical properties tested. At 0.5% CNF inclusion, the mechanical properties of melt-blended bionanocomposites (MB-UHMWPE/0.5) were improved as compared to Neat-UHMWPE. It was also found that the yield strength, elongation at break, Young’s modulus, toughness and crystallinity of MB-UHMWPE/0.5 were higher by 28%, 61%, 47%, 45% and 11%, respectively, as compared to the ethanol mixing sample (EM-UHMWPE/0.5). Despite the reduction in tensile strength of MB-UHMWPE/0.5, the value i.e., 28.4 ± 1.0 MPa surpassed the minimum requirement of standard specification for fabricated UHMWPE in surgical implant application. Overall, melt-blending processing is more suitable for the preparation of UHMWPE/CNF bionanocomposites as exhibited by their characteristics presented herein. A better mechanical interlocking between UHMWPE and CNF at high temperature mixing with kneading was evident through FE-SEM observation, explains the higher mechanical properties of MB-UHMWPE/0.5 as compared to EM-UHMWPE/0.5.


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1137
Author(s):  
Sascha Stanic ◽  
Thomas Koch ◽  
Klaus Schmid ◽  
Simone Knaus ◽  
Vasiliki-Maria Archodoulaki

Blends of two long-chain branched polypropylenes (LCB-PP) and five linear polypropylenes (L-PP) were prepared in a single screw extruder at 240 °C. The two LCB-PPs were self-created via reactive extrusion at 180 °C by using dimyristyl peroxydicarbonate (PODIC C126) and dilauroyl peroxide (LP) as peroxides. For blending two virgin and three recycled PPs like coffee caps, yoghurt cups and buckets with different melt flow rate (MFR) values were used. The influence of using blends was assessed by investigating the rheological (dynamic and extensional rheology) and mechanical properties (tensile test and impact tensile test). The dynamic rheology indicated that the molecular weight as well as the molecular weight distribution could be increased or broadened. Also the melt strength behavior could be improved by using the two peroxide modified LCB-PP blends on the basis of PODIC C126 or PEROXAN LP (dilauroyl peroxide). In addition, the mechanical properties were consistently enhanced or at least kept constant compared to the original material. In particular, the impact tensile strength but also the elongation at break could be increased considerably. This study showed that the blending of LCB-PP can increase the investigated properties and represents a promising option, especially when using recycled PP, which demonstrates a real “up-cycling” process.


Polymers ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2018
Author(s):  
Muhammad Samsuri ◽  
Ihsan Iswaldi ◽  
Purba Purnama

Stereocomplexation is one of several approaches for improving polylactide (PLA) properties. The high molecular weight of poly L-lactide (PLLA) and poly D-lactide (PDLA) homopolymers are a constraint during the formation of stereocomplex PLAs (s-PLAs). The presence of s-PLA particles in PLA PLLA/PDLA blends can initiate the formation of s-PLA crystalline structures. We used the solution casting method to study the utilization of s-PLA materials from high molecular weight PLLA/PDLA blends for increasing s-PLA formation. The s-PLA particles initiated the formation of high molecular weight PLLA/PDLA blends, obtaining 49.13% s-PLA and 44.34% of the total crystalline fraction. In addition, the mechanical properties were enhanced through s-PLA crystalline formation and the increasing of total crystallinity of the PLLA/PDLA blends. The s-PLA particles supported initiation for s-PLA formation and acted as a nucleating agent for PLA homopolymers. These unique characteristics of s-PLA particles show potential to overcome the molecular weight limitation for stereocomplexation of PLLA/PDLA blends.


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