A crosslinking method of UHMWPE irradiated by electron beam using TMPTMA as radiosensitizer

Trimethylolpropane trimethylacrylate/Ultra high molecular weight polyethylene (TMPTMA/UHMWPE) composite and pure UHMWPE plates were made by compression molding and electron beam (EB) irradiation crosslinking methods. Fourier transform infrared spectroscopy (FTIR), Soxhlet extractor, electromechanical tester, and wear tester were used for the characterization of the structure, mechanical properties, and tribological performance of the crosslinked UHMWPE. FTIR analyses show that trans‐vinylene (965 cm^?1) absorption increases with the increasing dose and the trans‐vinylene intensity of TMPTMA/UHMWPE is higher than that of UHMWPE at the same dose, and Soxhlet experiments reveal that gel fraction increases with the increasing dose, both proving that crosslinking took place in all the irradiated samples. The results of the tensile tests indicate a significant decrease in elongation at break, but the stress of UHMWPE increases to 47 MPa at 10 kGy and then decreases with the increasing dose. The stress of TMPTMA/UHMWPE composites keeps at about 39 MPa before 50 kGy and then decreases with the increasing dose because of plasticization effect. The stress changes indicate that crosslinking and degradation occurred at the same time. Wear rate of 100 kGy 1% TMPTMA/UHMWPE is 1.76 × 10^?7mg/Nm, only 23.5% of wear rate of 0 kGy UHMWPE and 44.2% of wear rate of 100 kGy UHMWPE. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

High temperature melted,radiation cross-linked,vitamin E stabilized oxidation resistant UHMWPE with low wear and high impact strength

In a previous communication we showed improvement in the wear resistance and toughness of cross-linked ultrahigh molecular weight polyethylene (UHMWPE) for total joint implants by radiation cross-linking after high temperature melting (HTM). In this study, we hypothesized that introduction of vitamin E into UHMWPE before high temperature melting could improve the oxidative stability of these UHMWPEs with low wear and high toughness. Vitamin E was blended with UHMWPE powder at concentrations of 0.1 and 0.2 wt% and consolidated, followed by melting at 300 and 320 °C for 5 h, and subsequent irradiation with electron beam to 150 kGy. These vitamin E/UHMWPE blends showed improved tensile and impact toughness and good wear resistance in comparison with the radiation cross-linked vitamin E/UHMWPE blends. Aggressive accelerated aging with or without pro-oxidant lipids showed that vitamin E-blended, high temperature melted and subsequently irradiated UHMWPE had good oxidation resistance.     

Binary and ternary particulated composites: UHMWPE/CACO3/HDPE

A study of the influence of employing ultrahigh molecular weight polyethylene (UHMWPE) on the toughness of CaCO₃/high‐density polyethylene (HDPE) composites was carried out. Binary and ternary HDPE‐based composites with calcium carbonate in the range of 0–40% and UHMWPE in the range of 0–50% were produced by twin‐screw extrusion followed by compression molding. From tensile and impact tests, it was found that increasing calcium carbonate content increased tensile modulus, but decreased tensile strength, strain at break, and impact resistance. The addition of UHMWPE helped to increase the strain at break and impact resistance of composites moderately without decreasing modulus or strength. The degree of toughening was found to increase with increasing UHMWPE content, but to decrease as the filler volume fraction was increased. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 1503–1513, 2000     

The influence of EB-crosslinking on barrier properties of HDPE–mica composites

High-density polyethylene (HDPE) was compounded with untreated and surface-treated mica (10, 20, 40 wt %) and composites were injection-molded. The composites were radiation crosslinked (100, 300, 700 kGy) and hydrocarbon permeability, tensile impact strength, and tensile strength at 25 and 80°C of the composites were examined. The permeability of HDPE decreased from 7 to 3.6 g/(d × m²) by compounding the polymer with 20 wt % mica, and the permeability was additionally reduced to 1.3 g/(d × m²) by irradiation of the compounds (700 kGy). When surface-treated mica was used, the permeability of the composite furthermore decreased to about 1.0 g/(d × m²). Upon irradiation, the E modulus measured at 25°C increased 5% when the dose was 300 kGy. At 80°C, the corresponding increase was 40%. The tensile impact strength of an unfilled polymer increased more than three times by an irradiation dose of 700 kGy, and for a polymer with 10 wt % mica, the tensile impact strength was twice the level of an unirradiated composite. © 1996 John Wiley & Sons, Inc.     

Mechanical properties study of micro‐ and nano‐hydroxyapatite reinforced ultrahigh molecular weight polyethylene composites

This is a comparative study between ultrahigh molecular weight polyethylene (UHMWPE) reinforced with micro‐ and nano‐hydroxyapatite (HA) under different filler content. The micro‐ and nano‐HA/UHMWPE composites were prepared by hot‐pressing method, and then compression strength, ball indentation hardness, creep resistance, friction, and wear properties were investigated. To explore mechanisms of these properties, differential scanning calorimetry, infrared spectrum, wettability, and scanning electron microscopy with energy dispersive spectrometry analysis were carried out on the samples. The results demonstrated that UHMWPE reinforced with micro‐ and nano‐HA would improve the ball indentation hardness, compression strength, creep resistance, wettability, and wear behavior. The mechanical properties for both micro‐ and nano‐HA/UHMWPE composites were comparable with pure UHMWPE. The mechanical properties of nano‐HA/UHMWPE composites are better compared with micro‐HA/UHMWPE composites and pure UHMWPE. The optimum filler quantity of micro‐ and nano‐HA/UHMWPE composites is found to be at 15 wt % and 10 wt %, separately. The micro‐ and nano‐HA/UHMWPE composites exhibit a low friction coefficient and good wear resistance at this content. The worn surface of HA/UHMWPE composites shows the wear mechanisms changed from furrow and scratch to surface rupture and delamination when the weight percent of micro‐ and nano‐HA exceed 15 wt % and 10 wt %. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42869.     

不同材料填充超高摩尔质量聚乙烯复合材料的力学性能分析

对纳米Al2O3、玻纤粉、石墨、微珠粉等材料填充的UHMWPE复合材料进行了拉伸、强度和磨损性能试验。结果表明：不同填料对UHMWPE性能的影响不一样，几种填料填充UHMWPE后，其硬度及耐磨性有不同的改善，而拉伸强度和断裂伸长率有不同程度的下降；其中以质量分数为10％的纳米Al2O3填充UHMWPE综合性能最佳；石墨填充材料的加入会使UHMWPE拉伸强度和断裂伸长率下降较大，脆性增大，但可较好地改善UHMWPE的耐磨性。     

Effect of entangled state of nascent UHMWPE on structural and mechanical properties of HDPE/UHMWPE blends

In this study, a synthesized ultra‐high molecular weight polyethylene (UHMWPE) with a less entangled state and a commercial UHMWPE with a highly entangled state were blended with high‐density polyethylene (HDPE) by melt blending, respectively. Rheology, 2D small‐angle X‐ray scattering (2D‐SAXS), differential scanning calorimetry (DSC), and tensile test were used to study the relationship between the microstructure and the mechanical properties of blends. It was demonstrated that the UHMWPE with the less entangled state was easy to be oriented at a given flow. More mechanical networks were achieved among the HDPE matrix and the UHMWPE chains due to the fewer entanglements of synthesized UHMWPE, improving the melting recovery of blends. Furthermore, notably oriented structures (shish‐kebabs) with increased long‐periods were made in the blends of weakly entangled UHMWPE and HDPE. The tensile strength of this blend was thus enhanced, i.e., the tensile strength raised for neat HDPE from 45.7 to 83.1 MPa for HDPE/UHMWPE blends containing 10 wt % of less entangled UHMWPE. However, the phase separation of blends was characterized when more weakly entangled UHMWPE was incorporated. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44728.     

Mechanical and tribological properties of short discontinuous UHMWPE fiber reinforced UHMWPE

The tribological properties of Ultra-High Molecular Weight Polyethylene have generated new concern regarding the long-term clinical performance of total joint replacements. To extend the lifetime of artificial joints, it is necessary to decrease the wear rate of UHMWPE. One possible solution is the incorporation of UHMWPE fibers. Mixing of the two components was accomplished by swirling the UHMWPE powder and chopped UHMWPE fibers with compressed nitrogen. During this mixture procedure opposite surface charges will be generated on the UHMWPE powder and UHMWPE fiber. The electrostatic attraction could be responsible for the coherence of the two components, leading a composite with fairly uniformly distributed and randomly oriented fibers was obtained. With this method a fiber volume fraction up to 60 volume percent could be achieved. In this composite the matrix and fibers are of the same chemical nature. The inherent chemical compatibility of the composite components is likely to promote good bonding at the interface, through which a composite with excellent mechanical properties is made. The ultimate stress and modulus of the 60 volume percent composite show an improvement of 160 and 600 percent, respectively, in comparison with the neat UHMWPE. The wear rates were determined with a pin-on-roll apparatus with a nominal contact stress of 3 MPa at a sliding velocity of 0.24 m/s. The volumetric wear rate decreases with the incorporation of the UHMWPE fibers. Received: 28 November 1996/Revised: 20 January 1997/Accepted: 23 January 1997     

Preparation and characterization of exfoliated layered double hydroxide/silicone rubber nanocomposites

Silicone rubber (SR)/Mg–Al layered double hydroxide (LDH) nanocomposites were prepared by the solution intercalation of SR crosslinked by a platinum‐catalyzed hydrosilylation reaction into the galleries of dodecyl sulfate intercalated layered double hydroxide (DS–LDH). X‐ray diffraction and transmission electron microscopy analysis showed the formation of exfoliated structures of organomodified LDH layers in the SR matrix. The tensile strength and elongation at break of SR/DS–LDH (5 wt %) were maximally improved by 53 and 38%, respectively, in comparison with those of the neat polymer. Thermogravimetric analysis indicated that the thermal degradation temperature of the exfoliated SR/DS–LDH (1 wt %) nanocomposites at 50% weight loss was 20°C higher than that of pure SR. Differential scanning calorimetry analysis data confirmed that the melting temperature of the nanocomposites increased at lower filler loadings (1, 3, and 5 wt %), whereas it decreased at a higher filler loading (8 wt %). The relative improvements in the solvent‐uptake resistance behavior of the SR/DS–LDH nanocomposites were also observed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of polyethylene‐graft‐maleic anhydride as a compatibilizer on the mechanical and tribological behaviors of ultrahigh‐molecular‐weight polyethylene/copper composites

Ultrahigh‐molecular‐weight polyethylene/copper (UHMWPE/Cu) composites compatibilized with polyethylene‐graft‐maleic anhydride (PE‐g‐MAH) were prepared by compression molding. The effects of the compatibilizer on the mechanical, thermal, and tribological properties of the UHMWPE/Cu composites were investigated. These properties of the composites were evaluated at various compositions, and worn steel surfaces and composite surfaces were examined with scanning electron microscopy and X‐ray photoelectron spectroscopy. The incorporation of PE‐g‐MAH reduced the melting points of the composites and increased their crystallinity to some extent. Moreover, the inclusion of the PE‐g‐MAH compatibilizer greatly increased the tensile rupture strength and tensile modulus of the composites, and this improved the wear resistance of the composites. These improvements in the mechanical and tribological behavior of the ultrahigh‐molecular‐weight‐polyethylene‐matrix composites with the PE‐g‐MAH compatibilizer could be closely related to the enhanced crosslinking function of the composites in the presence of the compatibilizer. Moreover, the compatibilizer had an effect on the transfer and oxidation behavior of the filler Cu particulates, which could be critical to the application of metallic‐particulate‐filled polymer composites in engineering. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 948–955, 2004     

Structure and properties of UHMWPE fiber/carbon fiber hybrid composites

Ultrahigh molecular weight polyethylene (UHMWPE) fiber/carbon fiber hybrid composites were prepared by inner‐laminar and interlaminar hybrid way. The mechanical properties, dynamic mechanical analysis (DMA), and morphologies of the composites were investigated and compared with each other. The results show that the hybrid way was the major factor to affect mechanical and thermal properties of hybrid composites. The resultant properties of inner‐laminar hybrid composite were better than that of interlaminar hybrid composite. The bending strength, compressive strength, and interlaminar shear strength of hybrid composites increased with an increase in carbon fiber content. The impact strength of inner‐laminar hybrid composite was the largest (423.3 kJ/m²) for the UHMWPE fiber content at 43 wt % to carbon fiber. The results show that the storage modulus (E′), dissipation factor (tan δ), and loss modulus (E″) of the inner‐laminar hybrid composite shift toward high temperature remarkably. The results also indicate that the high‐performance composite with high strength and heat resistance may be prepared by fibers' hybrid. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1880–1884, 2006     

Surface modification of UHMWPE fibers by means of polyethylene wax grafted maleic anhydride treatment

A novel surface modification method for ultrahigh molecular weight polyethylene (UHMWPE) fibers to improve the adhesion with epoxy matrix was demonstrated. Polyethylene wax grafted maleic anhydride (PEW‐g‐MAH) was deposited on the UHMWPE fibers surface by coating method. The changes of surface chemical composition, crystalline structure, mechanical properties of fiber and composite, wettability, surface topography of fibers and adhesion between fiber and epoxy resin before and after finishing were studied, respectively. The Fourier transform infrared spectroscopy spectra proved that some polar groups (MAH) were introduced onto the fiber surface after finishing. The X‐ray diffraction spectra indicated that crystallinity of the fiber was the same before and after finishing. Tensile testing results showed that mechanical properties of the fiber did not change significantly and the tensile strength of 9 wt % PEW‐g‐MAH treated fiber reinforced composite showed about 10.75% enhancement. The water contact angle of the fibers decreased after finishing. A single‐fiber pull out test was applied to evaluate the adhesion of UHMWPE fibers with the epoxy matrix. After treatment with 9 wt % PEW‐g‐MAH, a pull‐out force of 1.304 MPa which is 53.59% higher than that of pristine UNMWPE fibers was achieved. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46555.     

Abrasive wear performance and antibacterial assessment of untreated and treated ZnO‐reinforced polymer composite

In this work, the response of different filler loading of zinc oxide (ZnO) reinforced ultra‐high‐molecular‐weight polyethylene (UHMWPE) on mechanical, abrasive wear, and antibacterial properties were studied. Two variants of untreated ZnO‐reinforced UHMWPE (U‐ZPE) and treated ZnO‐reinforced UHMWPE (T‐ZPE) with aminoproplytriethoxysilane (APTES) were used to compare the improvement of the mechanical, abrasive wear, and antibacterial properties. The abrasive wear and friction behaviors were monitored using a pin‐on‐disc (POD) test rig with different applied loads and sliding speeds against 400‐grit size of silicon carbide (SiC) abrasive paper under dry sliding conditions. The antibacterial assessments of the composites were tested against two common human body bacteria, that is, Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). Results have shown that T‐ZPE possess higher ultimate tensile strength and elongation at break values as compared to U‐ZPE. Furthermore, the T‐ZPE have higher wear resistance compared to U‐ZPE and pure UHMWPE. The average coefficient of friction (COF) of UHMWPE was not significantly affected by the addition of both untreated and treated ZnO filler. The wear mechanisms were studied under scanning electron microscopy (SEM). Both U‐ZPE and T‐ZPE composites showed active inhibition against E. coli and S. aureus bacteria. POLYM. COMPOS., 34:1020–1032, 2013. © 2013 Society of Plastics Engineers     

Radiation-induced crosslinking of UHMWPE in the presence of co-agents: chemical and mechanical characterisation

Radiation-induced crosslinking has been shown to have a beneficial effect on the wear resistance of ultra high molecular weight polyethylene (UHMWPE). Since we postulate that crosslinking takes place through reactions involving terminal double bonds, unsaturated additives were added to UHMWPE in this study to enhance crosslinking. UHMWPE specimens soaked in 1,7-octadiene, methylacetylene and ethylene, respectively, were irradiated with electron beam to different doses in single or multiple passages. FTIR spectroscopy was used for the chemical characterisation of the crosslinked polymer. Tensile tests were performed with all samples in order to monitor changes in the mechanical properties.Gel fraction measurements proved that crosslinking took place in all the irradiated samples, but 1,7-octadiene turned out to be the most effective additive for the present purpose, exhibiting a good efficiency in enhancing crosslinking. The FTIR analyses showed that consumption of vinyl double bonds is proportional to the irradiation dose, with an efficiency which increases with increasing their initial concentration, confirming the hypothesis of the involvement of these groups in the crosslinking process. In the case of UHMWPE with 1,7-octadiene irradiated to high doses in multiple passages, the results of the tensile tests indicated a significant decrease in both elongation at break (up to 65%) and ultimate stress (up to 25%). A possible explanation of the diminished strength of the crosslinked material has also been proposed.     

Effects of gamma irradiation with and without compatibilizer on the mechanical properties of polypropylene/wood flour composites

In this study, polypropylene/wood flour (Hevea brasiliensis) composites at 40 wt% filler content were prepared using a twin-screw extruder and an injection moulding machine. The effects of gamma irradiation with and without maleic anhydride graft polypropylene (PP-g-MA) compatibilizer (3% relative to the wood flour content) on the flexural properties, tensile properties, and creep behavior were investigated. The irradiation in nitrogen and air atmospheres was performed at various radiation doses (i.e. 5, 10, 20 and 30 kGy). The results revealed the improvement of mechanical properties and creep behavior was found in the presence of gamma irradiation at low radiation doses (5 and 10 kGy), while the composites irradiated at radiation doses over 10 kGy rendered the decrease of mechanical properties. Furthermore, at the same radiation dose, the composites irradiated in nitrogen atmosphere tended to provide significantly higher mechanical properties than the ones irradiated in air atmosphere. Interestingly, the great enhancement of creep resistance was observed, i.e. the tensile strains (6 h of static loading) of the irradiated composites (at 10 kGy) with and without compatibilizer were approximately 36% and 19% lower than that of the untreated composite, respectively. In addition, the Burger’s creep model is applied in order to determine the creep parameters of the composites.     

Interfacial evaluation of epoxy/carbon nanofiber nanocomposite reinforced with glycidyl methacrylate treated UHMWPE fiber

Interface interactions of fiber–matrix play a crucial role in final performance of polymer composites. Herein, in situ polymerization of glycidyl methacrylate (GMA) on the ultrahigh molecular weight polyethylene (UHMWPE) fibers surface was proposed for improving the surface activity and adhesion property of UHMWPE fibers towards carbon nanofibers (CNF)‐epoxy nanocomposites. Chemical treatment of UHMWPE fibers was characterized by FTIR, XPS analysis, SEM, and microdroplet tests, confirming that the grafting of poly (GMA) chains on the surface alongside a significant synergy in the interfacial properties. SEM evaluations also exhibited cohesive type of failure for the samples when both GMA‐treated UHMWPE fiber and CNF were used to reinforce epoxy matrix. Compared with unmodified composite, a ～319% increase in interfacial shear strength was observed for the samples reinforced with both 5 wt % GMA‐grafted UHMWPE and 0.5 wt % of CNF. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43751.     

Effects of reinforcements and gamma-irradiation on wear performance of ultra-high molecular weight polyethylene as acetabular cup liner in hip-joint arthroplasty: A review

Improving the wear resistance of ultra-high molecular weight polyethylene (UHMWPE), the gold standard polymer for acetabular component in hip joint arthroplasty, is the most important challenge in joint arthroplasty. The possible ways that have been approached to this challenge are by: (i) engineering multi-phase that is, both carbonaceous and noncarbonaceous fillers-based polyethylene composites, which unite the inherent attributes of each element available in the system. The wear rate of carbonaceous composite is nearly 50% lower (5.11–6.69 × 10⁻⁵ mm³/Nm) than that of noncarbonaceous composite (10–12.5 × 10⁻⁵ mm³/Nm), thus, recognized as a potential reinforcement, and (ii) coupling gamma-irradiation, which is a mandated sterilization process, with multi-phase nanocomposite to understand the free radical-scavenging effect of fillers and improved interfacial adhesion strength between fillers and matrix. After the exposure of gamma-rays (50–100 kGy), the free radicals formed by bond breakage in both the reinforcements and the matrix recombine to form covalent/Van der Waals bond in the interface. Thus, dramatical improvement in wear resistance of both types of composites with 2–4 times decreased wear rate is observed compared to that of composites under un-irradiated condition. However, enhancing the interfacial adhesion between two different phases is a major constraint in the design of UHMWPE composites. Many methods such as functionalization of reinforcements, and irradiation on functionalized UHMWPE composites that can be approached to address this constraint are documented in this review.     

Simultaneously enhanced mechanical properties and thermal properties of ultrahigh‐molecular‐weight polyethylene with polydopamine‐coated α‐alumina platelets

Polydopamine (PDA) was employed to modify micrometric Al₂O₃ platelets to improve the interfacial compatibility between α‐Al₂O₃ powder and ultrahigh‐molecular‐weight polyethylene (UHMWPE). The structure of PDA‐coated Al₂O₃ and UHMWPE composites was investigated via Fourier transform infrared spectroscopy, scanning electron microscopy and X‐ray photoelectron spectroscopy. The thermal stability and mechanical performance of the samples were also evaluated. It is clear that UHMWPE/PDA‐Al₂O₃ composites exhibit better mechanical properties, higher thermal stability and higher thermal conductivity than UHMWPE/Al₂O₃ composites, owing to the good dispersion of Al₂O₃ powder in the UHMWPE matrix and the strong interfacial force between the macromolecules and the inorganic filler caused by the presence of PDA. The tensile strength and the tensile elongation at break of UHMWPE/PDA‐Al₂O₃ composite with 1 wt% PDA‐Al₂O₃ are 62.508 MPa and 462%, which are 1.96 and 1.98 times higher than those of pure UHMWPE, respectively. The thermal conductivity of UHMWPE/PDA‐Al₂O₃ composite increases from 0.38 to 0.52 W m^?1 K^?1 with an increase in the dosage of PDA‐Al₂O₃ to 20 wt%. The results show that the prepared PDA‐coated Al₂O₃ powder can simultaneously enhance the mechanical properties and thermal conductivity of UHMWPE. © 2018 Society of Chemical Industry     

Effect of surface modification of Kevlar fibre on friction and wear properties of UHMWPE composites

Abstract

The effects of Kevlar fibre additions and, particularly, the surface modification of the Kevlar fibres, on the sliding wear behaviour of the ultra high molecular weight polyethylene (UHMWPE) composites were investigated. The results showed that the sliding friction coefficient of the UHMWPE composites increased with the fibre content increase. The wear resistance of the UHMWPE composite was highest when the Kevlar fibre content was ～10 vol.-% and decreased as the applied normal load was increased. It was found that the silane modification of the Kevlar fibres improved the wear resistance and tensile strength of the UHMWPE composites as well.     

The effects of hybrid fillers on thermal,mechanical, physical,and antimicrobial properties of ultrahigh‐molecular‐weight polyethylene‐reinforced composites

The effects of hybrid filler of zinc oxide and chitosan (chitosan–ZnO) on thermal, flexural, antimicrobial, chemical resistance, and hardness properties of ultrahigh‐molecular‐weight polyethylene (UHMWPE) composites with varying concentration of zinc oxide (ZnO) and further hybridized by chitosan (CS) were successfully studied. The composites were prepared using mechanical ball milling and followed by hot compression molding. The addition of ZnO to the UHMWPE matrix had lowered the melting temperature (T _m) of the composite but delayed its degradation temperature. Further investigation of dual filler incorporation was done by the addition of chitosan to the UHMWPE/ZnO composite and resulted in the reduction of UHMWPE crystallization. The flexural strength and modulus had a notably high improvement through ZnO addition up to 25 wt% as compared to neat UHMWPE. However, the addition of chitosan had resulted in lower flexural strength than that of 12 wt% ZnO UHMWPE composite but still higher than that of neat UHMWPE. It was experimentally proven that the incorporation of ZnO and chitosan particles within UHMWPE matrix had further enhanced the antimicrobial properties of neat UHMWPE. Chemical resistance was improved with higher ZnO content with a slight reduction of mass change after the incorporation of chitosan. The hardness value increased with ZnO addition but higher incorporation of chitosan had lowered the hardness value. These findings have significant implications for the commercial application of UHMWPE based products. It appears that these hybrid fillers (chitosan–ZnO)‐reinforced UHMWPE composites exhibit superior overall properties than that of conventional neat UHMWPE. POLYM. COMPOS., 38:1689–1697, 2017. © 2015 Society of Plastics Engineers