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A series of thioether cross-linked membranes based on sulfonated poly(arylene ether ketone)s containing propenyl groups were prepared to solve the problem of high methanol permeability for proton electrolyte membrane in direct methanol fuel cells (DMFCs). For this purpose, 4,4′-thiobisbenzenethiol was selected as cross-linker, and the cross-linked structure was formed via thiol-ene click chemical reaction between propenyl and thiol groups. Compared with pristine membrane, the thioether cross-linked membranes exhibited improved mechanical properties and dimensional stabilities. As the cross-linker increased, the swelling ratio decreased from 11.01% to 8.64% at 20°C and from 15.18% to 10.69% at 80°C. Furthermore, the modified membranes exhibited reduced methanol permeability coefficients (down to 4.03 × 10−7 cm2 s−1), which was nearly half of the pristine membrane (7.66 × 10−7 cm2 s−1). Due to the thioether units, the cross-linked membranes showed enhanced oxidative stabilities, and the longest elapsed time in Fenton’s reagent was 225 min, which was 2.5 times longer than that of pristine polymeric membrane. Although the proton conductivity decreased upon the addition of cross-linker agent, the selectivity value increased due to the lower methanol permeability. Thus, all the results implied that the thioether cross-linked membranes were promising alternative materials for DMFCs application. [ABSTRACT FROM AUTHOR]

Two kinds of glass fibers with round (RdGF) and rectangle cross-sections (RcGF) were used to reinforce polyphenylene sulfide (PPS), respectively. In this way, the effect of fiber cross-section shape on rheological and mechanical properties of the composites was studied for the first time. Results showed that the viscosity of the composites reinforced with RcGF was much lower than that of RdGF composites, owing to their higher sensitivity to flow. As a result, PPS/RcGF composites could be injection-molded at high fiber contents. Moreover, RcGF showed a better reinforcing effect on mechanical properties of PPS. So the use of RcGF could better balance the contradiction between processability and reinforcing effect for glass fiber-reinforced composites. Various characterizations were carried out to reveal the reinforcing mechanism. This work demonstrated the importance of fiber cross-section shape on design and production of fiber-reinforced composites. [ABSTRACT FROM AUTHOR]

Bioresource natural sisal fiber ( SF) was used to prepare single fiber-reinforced isotactic polypropylene ( iPP) composites. Three kinds of interfacial crystalline morphologies, spherulites, medium nuclei density transcrystallinity ( MD-TC) and high nuclei density transcrystallinity ( HD-TC), were obtained in the single fiber-reinforced composites by implementing quiescent or dynamic shear-enhanced crystallization and by modulating the compatibility interaction between SF and iPP. The development of interfacial shear strength ( IFSS) during the interfacial crystallization process was demonstrated for the first time using a combination of single-fiber fragmentation testing and optical microscope observation. A close correlation between IFSS and morphological characteristics of interfacial crystallization was well elucidated. The increases in IFSS were very different for spherulitic, MD-TC and HD-TC morphologies. The highest IFSS obtained was 28 MPa, after the formation of HD-TC, which was about 62% of the tensile strength of neat iPP (45 MPa). These results offer powerful and direct evidence that interfacial crystallization could play an important role in the enhancement of interfacial adhesion of real SF/ iPP composites. © 2013 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

As part of a continuous effort to develop high performance isotactic polypropylene (iPP) based on β-form crystalline and morphological change induced by rare earth nucleator (WBG), various WBG contents (from 0.025 to 1.0 wt%) were adopted to prepare β-nucleated iPP at a fixed final molten temperature (240°C) in this study. The crystallinity, polymorphic composition, and crystalline morphology were inspected in detail by a series of crystallographic characterizations, including calorimeter, X-ray diffraction, polarized light microscopy (PLM), and electron microscopy. Furthermore, the self-organization and re-crystallization behavior of β-nucleating agent occurred during cooling was characterized by rheometry. Finally, the dependence of mechanical properties, including tensile strength, elongation at break, and impact strength, on WBG content was discussed based on the variations in β-form content and crystalline morphology. Interestingly, it is found that while the WBG content is below 0.1 wt%, the toughness of β-nucleated iPP increases with increase in WBG content due to additional β-form content; as the WBG content is in range of 0.1-0.5 wt%, the toughness increases at a lower rate with increase in WBG content due to β-crystalline morphological change. However, a decrease in toughness is observed while nucleator content is above 0.5 wt% as WBG remains undissolved in iPP upon the adopted processing conditions. The result of this study provides valuable information for potential industrial applications. Copyright © 2010 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]