Abstract

Since obtaining a highly oriented structure based on a large-scale commercial ultra-high molecular weight polyethylene (UHMWPE) is considered very difficult due to its high molecular weight and melting index, modifying the structure of these cheap commercial UHMWPE brands into a supra-molecular structure with fiber-forming properties by adding a small amount of polyethylene wax (PE-wax) will provide the possibility to obtain highly oriented UHMWPE products with enhanced mechanical and tribological properties. In this work, highly oriented UHMWPE/PE-wax films were prepared. The PE-wax affected the UHMWPE as an intermolecular lubricant. The obtained lamellar structure of the UHMWPE/PE-wax composites had a better processability. The UHMWPE and UHMWPE/PE-wax structures for the xerogels and the films were studied by using differential scanning calorimetry and scanning electron microscopy. The PE-wax presence enhanced the mechanical properties of the UHMWPE/PE-wax films to a high degree. The highest average value of the tensile strength was 1320 MPa (an increase of 78%) obtained by adding a PE-wax content of 1.0 wt.%, and the highest average value of the Young’s modulus was 56.8 GPa (an increase of 71%) obtained by adding a PE-wax content of 2.0 wt.%. The addition of the PE-wax increased the work of fracture values of the UHMWPE/PE-wax films up to 233%. The formation of the cavities was observed in the virgin UHMWPE films more than in the UHMWPE/PE-wax films, and the whitening of the oriented films was related to the crystallization process more than to the cavitation phenomenon. The coefficient of friction of the oriented UHMWPE/PE-wax films improved by 33% in comparison with the isotropic UHMWPE, and by 7% in comparison with the oriented virgin UHMWPE films.

Highlights

  • Among polymeric materials, ultrahigh molecular weight polyethylene (UHMWPE) is considered the best choice for medical and light-weight engineering applications in the construction and automotive industries, since it exhibits a unique toughness, abrasion, fatigue, and good chemical resistances, in addition to a very low coefficient of friction, strength, and biocompatibility [1,2,3,4,5]

  • In comparison with the polytetrafluoroethylene-based lubricant to improve the processability of the lamellar structure and the mechanical properties of the composites (PTFE, Teflon), which is considered a popular material used in a large number of tribological highly oriented UHMWPE/polyethylene wax (PE-wax) films

  • On the other hand, when the PE-wax content was in the range of 2.0–20.0 wt.%, the crystallinity of the UHMWPE/PE-wax xerogels decreased due to the presence of a large amount of the PE-wax that preserved its original state as a PE with a low crystallinity

Read more

Summary

Introduction

Ultrahigh molecular weight polyethylene (UHMWPE) is considered the best choice for medical and light-weight engineering applications in the construction and automotive industries, since it exhibits a unique toughness, abrasion, fatigue, and good chemical resistances, in addition to a very low coefficient of friction, strength, and biocompatibility [1,2,3,4,5]. Obtaining materials based on UHMWPE with an oriented supra-molecular structure and an enhanced mechanical performance is considered an important direction in the polymer science. The tensile strength and the modulus of elasticity for the ultra-oriented fibers based on UHMWPE can reach up to 4 GPa and 140 GPa, respectively [6]. Carrying out the orientation process, tensile stresses are applied on the films during the drawing process, that is to say, the stress and the deformation rates will control. The crystallization of the UHMWPE will speed up to a high degree and the mechanical properties will increase as a result of the drawing and the thermal orientation process of the amorphous phase, leading to an improvement in the UHMWPE films by increasing the molecular orientation [7,9]. The maximum attainable draw ratio (λ) of the polyethylene is related to the polymer molecular weight (Mw ) [10] and to the polymer concentration in the solvent solution [11]

Methods
Results
Conclusion
Full Text
Published version (Free)

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