Investigation of the Tensile Strength and Chemical Interaction & Structure of Ultra-High Molecular Weight Polyethylene/ Silicon Carbide Nanocomposite  

preprint OA: closed CC-BY-4.0
📄 Open PDF View at publisher

Abstract

Purpose: In this research, nanocomposite of Ultra-High Molecular Weight Polyethylene (UHMWPE) reinforced with Silicon Carbide (SiC) nanoparticles was prepared and characterized in terms of chemical interaction, molecular structure, tensile strength, and dispersion state of nanoparticles in the UHMWPE matrix. Method: Nanocomposite of UHMWPE/SiC was prepared in gradient loadings (1.5, 3, 4.5 and 6 wt % of the SiC nanoparticles) by means of ultra-sonication mixing technique followed by compression molding. Results: : Physicochemical interaction of the UHMWPE matrix and the SiC nanoparticles at filler/polymer interface was suggested by Fourier-transfer Infrared spectroscopy (FTIR) results. X-ray diffraction (XRD) approved that the incorporation of SiC in the UHMWPE matrix did not change the orthorhombic crystalline structure of neat UHMWPE. However, an increase in crystallinity of 14 % was achieved with the 3 wt % of SiC. No significant change was observed in the average grain size comparing the pure UHMWPE to its nanocomposites. Conclusion: Enhancement in mechanical properties were achieved by 3 wt % SiC reinforced UHMWPE where young’s modulus, tensile strength and strain at break increased by an average of 13 %, 20 % and 46 % respectively. Scanning electron microscopy (SEM) approved good dispersion of SiC nanoparticles in UHMWPE matrix up to 3 wt%.

My notes (saved in your browser only)

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-05-19T01:45:01.086888+00:00
unpaywall
last seen: 2026-05-28T02:00:01.590549+00:00
License: CC-BY-4.0