Abstract

Novel ultra-high molecular weight polyethylene (UHMWPE)/nanoalumina (F100Ay), UHMWPE/acid-treated nanoalumina (F100Aox%-8-y) and UHMWPE/functionalized nanoalumina (F100Aox%-81PEg-MAHxy) as-prepared nanocomposite fibers were prepared by gel-spinning processes. The rod-like features of the original nanoalumina fillers were significantly etched into broken/shorter nanorods and/or shreds by oxalic acid solutions as their concentrations and/or treating time increased. As evidenced by Fourier transform infrared and transmission electron microscopy analysis, PEg-MAH molecules were successfully grafted onto acid-treated nanoalumina fillers through the reaction of the hydroxyl groups of nanoalumina fillers with the maleic anhydride groups of PEg-MAH molecules during their modification processes. The specific surface areas of each Aox%-81PEg-MAHxy functionalized nanoalumina filler reached a maximum value (≧470 m2/g), as the weight ratios of PEg-MAH to acid-treated nanoalumina approached the optimal value at 8. The achievable draw ratio ( Dra) values of F100Ay, F100Aox%-8-y and/or F100Aox%-81PEg-MAHxy as-prepared fibers approach a maximal value as the original, acid-treated and/or functionalized nanoalumina contents reach the optimal values at 0.1, 0.1 and 0.075 phr, respectively, in which, the maximal Dra values obtained for F100Aox%-81PEg-MAHx0.075 as-prepared fiber specimens are significantly higher than those of the F100A0.1 and F100Aox%-8-0.1 drawn fiber specimens prepared at the same draw ratios. Moreover, the maximal Dra values obtained for F100Aox%-81PEg-MAHx0.075 as-prepared fibers reached another maximal value as the functionalized nanoalumina fillers were modified using the optimal weight ratio of PEg-MAH to acid-treated nanoalumina at 8. Further investigation revealed that excellent orientation and tensile properties of the UHMWPE nanocomposite fibers can be obtained by ultradrawing the F100Aox%-81PEg-MAHxy as-prepared fibers with proper amounts of well-dispersed functionalized nanoalumina fillers.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.