Mechanical properties of surface‐modified ultra‐high molecular weight polyethylene fiber reinforced natural rubber composites

The mechanical properties of ultra‐high molecular weight polyethylene (UHMWPE) fibers reinforced natural rubber (NR) composites were determined, and the effects of fiber surface treatment and fiber mass fraction on the mechanical properties of the composites were investigated. Chromic acid was used to modify the UHMWPE fibers, and the results showed that the surface roughness and the oxygen‐containing groups on the surface of the fibers could be effectively increased. The NR matrix composites were prepared with as‐received and chromic acid treated UHMWPE fibers added 0–6 wt%. The treated UHMWPE fibers increased the elongation at break, tear strength, and hardness of the NR composites, especially the tensile stress at a given elongation, but reduced the tensile strength. The elongation at break increased markedly with increasing fiber mass fraction, attained maximum values at 3.0 wt%, and then decreased. The tear strength and hardness exhibited continuous increase with increasing the fiber content. Several microfibrillations between the fiber and NR matrix were observed from SEM images of the fractured surfaces of the treated UHMWPE fibers/NR composites, which meant that the interfacial adhesion strength was improved. POLYM. COMPOS., 38:1215–1220, 2017. © 2015 Society of Plastics Engineers     

Surface modification of ultra‐high‐molecular‐weight polyethylene. II. Effect on the physicomechanical and tribological properties of ultra‐high‐molecular‐weight polyethylene/poly(ethylene terephthalate) composites

We performed surface modification of ultra‐high‐molecular‐weight polyethylene (UHMWPE) through chromic acid etching, with the aim of improving the performance of its composites with poly(ethylene terephthalate) (PET) fibers. In this article, we report on the morphology and physicomechanical and tribological properties of modified UHMWPE/PET composites. Composites containing chemically modified UHMWPE had higher impact properties than those based on unmodified UHMWPE because of improved interfacial bonding between the polymer matrix and the fibers and better dispersion of the fibers within the modified UHMWPE matrix. Chemical modification of UHMWPE before the introduction of PET fibers resulted in composites exhibiting improved wear resistance compared to the base material and compared to unmodified UHMWPE/PET composites. On the basis of the morphological studies of worn samples, microploughing and fatigue failure associated with microcracking were identified as the principle wear mechanisms. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

Surface modification and physical properties of various UHMWPE‐fiber‐reinforced modified epoxy composites

Two surface modification methods—plasma surface treatment and chemical agent treatment—were used to investigate their effects on the surface properties of ultrahigh‐molecular‐weight polyethylene (UHMWPE) fibers. In the analyses, performed using electron spectroscopy for chemical analysis, changes in weight, and scanning electron microscope observations, demonstrated that the two fiber‐surface‐modified composites formed between UHMWPE fiber and epoxy matrix exhibited improved interfacial adhesion and slight improvements in tensile strengths, but notable decreases in elongation, relative to those properties of the composites reinforced with the untreated UHMWPE fibers. In addition, three kinds of epoxy resins—neat DGEBA, polyurethane‐crosslinked DGEBA, and BHHBP‐DGEBA—were used as resin matrices to examine the tensile and elongation properties of their UHMWPE fiber‐reinforced composites. From stress/strain measurements and scanning electron microscope observations, the resin matrix improved the tensile strength apparently, but did not affect the elongation. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 655–665, 2007     

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 alkaline and silane treatments on the water‐resistance properties of wood‐fiber‐reinforced recycled plastic composites

The water‐resistance properties of wood‐fiber‐reinforced recycled plastic composites (WRPCs) prepared from postconsumer high‐density polyethylene (HDPE) and wood fibers from saw mills were studied. Three methods consisting of an alkaline method (AM), a silane method (SM), and a combination of the alkaline and silane methods (ASM) were used to modify the wood fibers. The effects of fiber/matrix mix ratio and surface treatment on the moisture content, thickness swelling, and flexural strength change of the WRPCs, before and after immersion in 60°C water for 8 weeks, were studied and analyzed. The flexural fractured surfaces of the WRPCs before and after immersion in hot water were examined, and the fracture mechanism of the WRPCs was discussed. The results showed that the different surface treatments of the wood fibers had significant effects on the moisture content, thickness swelling, and flexural strength of the WRPCs after a long immersion time in hot water. For WRPCs treated by ASM, the moisture content was the lowest, the thickness swelling was at a minimum, and the flexural strength was the highest. Higher water absorption of composites with fiber treated by the AM or SM methods, as compared to those treated by ASM, could be attributed to the incomplete adhesion and wettability between the wood fibers and the polymer matrix, which may have caused more gaps and flaws at the interface. J. VINYL ADDIT. TECHNOL., 2008. © 2008 Society of Plastics Engineers.     

Vinculin focal adhesion of osteoblast‐like cells on PEEK coated with ultra‐thin polymer nano films

PEEK is the polymer of choice to replace metal encapsulants and other parts in active medical implants fixated into bone. The current challenge is to improve its biocompatibility with bone tissue to ultimately achieve osseointegration. PEEK sheets surfaces coated with plasma deposited nano thin polymer films using CH₄, (CH₄ + O₂) and (CH₄ + N₂) gases. PEEK samples plasma treated with nonpolymerizing gases (O₂) were also used for comparison. The adhesion performance of osteoblast like cells on the plasma‐treated PEEK surfaces and the presence of Vinculin in these cells were evaluated after long culturing period (12 days). X‐ray photoelectron spectroscopy and Auger spectroscopy were used to provide surface molecular information, surface hardness and molecular density. All plasma‐treated surfaces retained functionality after the sterilization process. PEEK surfaces with high number of oxygen functional groups and particularly oxygen rich thin polymer coating (plasma deposition using CH₄+O₂ gas mixture) resulted in strong cellular adhesion strength and large Vinculin amount. Further, osteoblast‐like cells responded better to surfaces with lower molecular density acting like another signal for cell adhesion. The osteoblast‐like cells response was weaker for surfaces with both thin films with nitrogen functional groups and nonfunctional (nonpolar) films. Furthermore, thin films rich in nitrogen functional groups repelled the cells, showed abnormal cells shape, smaller Vinculin amount and induced thicker cellular clusters with poor spread. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42181.     

Effect of Glycerol Coating on the Atmospheric Pressure Plasma Treatment of UHMWPE Fibers

In order to investigate how coatings of glycerol affects atmospheric pressure plasma treatment, ultra high molecular weight polyethylene (UHMWPE) fibers were first pretreated with 0.2 and 0.6 mol/l glycerol solutions, respectively, and then were modified by an atmospheric pressure plasma jet (APPJ) using helium as the carrier gas with a flow rate of 20 l/min, discharge power of 30 W and a radio frequency of 13.56 MHz. After the plasma treatment, scanning electron microscopy (SEM) and atomic force microscopy (AFM) analysis revealed that the glycerol coated-APPJ treated samples possessed smoother surface than the APPJ directly treated samples. The X-ray photoelectron spectroscopy (XPS) analysis indicated that the changed content of oxygen containing groups on the surface of the glycerol coated groups compared with the non-glycerol coated group was mainly due to the remaining glycerol on the fiber surfaces. The water contact angle test revealed that the wettability of the glycerol coated-APPJ treated fibers decreased slightly in comparison with the APPJ directly treated fibers. Furthermore, the microbond pull-out test indicated that the interfacial bonding of the fiber to epoxy resin decreased when the fiber was pretreated with glycerol before plasma treatment. Therefore, it was concluded that the presence of glycerol on fiber surface weakened the effectiveness of APPJ treatment of UHMWPE fibers in improving the interfacial bonding to epoxy. This was mainly attributed to the consumption of plasma energy in etching the glycerol layer on the fiber surface and a weak interfacial layer due to the presence of residual glycerol.     

Wear properties of 3‐aminopropyltriethoxysilane‐functionalized carbon nanotubes reinforced ultra high molecular weight polyethylene nanocomposites

Ultra high molecular weight polyethylene (UHMWPE) is extensively used as a material in various high‐end applications with superior mechanical properties. Carbon nanotubes (CNTs) reinforced UHMWPE (CNT/UHMWPE) nanocomposite is a promising material that can compensate for the weak durability of UHMWPE. In this study, multiwalled carbon nanotubes were oxidized and silanized using acid mixture and 3‐aminopropyltriethoxysilane, respectively, to improve the interfacial strength between CNTs and UHMWPE. The CNT/UHMWPE nanocomposite was fabricated using these oxidized and silanized CNTs. The treatment effect of CNTs on the wear behavior of the CNT/UHMWPE nanocomposites was investigated through wear tests. The oxidization and silanization of CNTs were confirmed by infrared spectroscopy. Scanning electron microscope analysis showed that the silane‐treated CNT/UHMWPE nanocomposites showed better dispersion and interfacial adhesion between UHMWPE and CNTs becaue of the newly formed functional groups on the CNTs. The friction coefficient and wear rate of silanized CNT/UHMWPE nanocomposite were also found to be lower than those of raw UHMWPE and oxidized CNT/UHMWPE nanocomposite. CNTs were functionalized using oxidation and silanization methods to improve the interfacial adhesion between CNTs and UHMWPE. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

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.     

Evaluation of Adhesion Property of UHMWPE Fibers/Nano-epoxy by a Pullout Test

Ultrahigh-molecular-weight polyethylene (UHMWPE) fibers have poor wetting and adhesion properties to polymer resins because of the inert surface of the fibers. In our previous study, a reactive nano-epoxy matrix, developed by making a modification on the matrix with reactive graphitic nanofibers (r-GNFs), showed improved wettability to UHMWPE fibers. In this work, fiber bundle pullout tests were conducted to evaluate the adhesion property between the UHMWPE fibers and the nano-epoxy matrices. Analysis of load-displacement curves from pullout tests shows that debonding initiation load and ultimate debonding load increased considerably, because of effective improvement of adhesion between the UHMWPE fibers and nano-epoxy matrix. Stress-controlled and energy-controlled models of interfacial debonding were applied for theoretical analyses. Results from ultimate IFSS, frictional shear stress, and critical energy-release rate are in good agreement with experimental results. Nano-epoxy matrix with 0.3 wt% r-GNFs shows effective improvement in terms of adhesion property between UHMWPE fiber and epoxy.     

Surface modification of ultra‐high molecular weight polyethylene fiber by different kinds of SiO2 nanoparticles

We successfully improved the interfacial adhesion strength between ultra‐high molecular weight polyethylene (UHMWPE) fiber and resin by the surface modification of UHMWPE fiber with two kinds of SiO₂ nanoparticles through gel spinning process. Modified effect of treated SiO₂ nanoparticles by coupling agent was superior to original SiO₂ nanoparticles. Compared with unmodified fibers, pull‐out tests of modified UHMWPE/treated SiO₂ fibers revealed that interfacial adhesion strength increased by the maximum of 10.95%, but corresponding breaking strength decreased by 8.51%. In addition, the interfacial adhesion strength and breaking strength could continue to enhance with increasing the additive amount of treated SiO₂ nanoparticles. The results of Differential Scanning Calorimetry (DSC), X‐ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy (SEM) indicated that the crystallinity of all modified fibers decreased while crystallite dimension increased, and the surface of modified fibers by treated SiO₂ nanoparticles exhibited polar functional group (C=O). The superiority of this modified technology was that it realized the bulk industrial production and maneuverability, low cost, and no pollution. POLYM. COMPOS., 38:1928–1936, 2017. © 2015 Society of Plastics Engineers     

Effects of surface modification by oxygen plasma on peel adhesion of pressure‐sensitive adhesive tapes

Surfaces of poly(isobutylene) (PIB) and poly(butylacrylate) (PBA) pressure‐sensitive adhesive tapes were treated by oxygen plasma, and effects of surface modification on their adhesive behavior were investigated from the viewpoint of peel adhesion. The peel adhesion between PIB and PBA pressure‐sensitive adhesive tapes and stainless steel has been improved by the oxygen plasma treatment. The surface‐modification layer was formed on PIB and PBA pressure‐sensitive adhesive surfaces by the oxygen plasma treatment. The oxygen plasma treatment led to the formation of functional groups such as various carbonyl groups. The treated layer was restricted to the topmost layer (50–300 nm) from the surface. The GPC curves of the oxygen plasma‐treated PBA adhesive were less changed. Although a degradation product of 1–3% was formed in the process of the oxygen plasma treatment of the PIB adhesive. There are differences in the oxygen plasma treatment between the PIB and PBA adhesives. A close relationship was recognized between the amount of carbonyl groups and peel adhesion. Therefore, the carbonyl groups formed on the PIB and PBA adhesive surfaces may be a main factor to improve the peel adhesion between the PIB and PBA adhesive and stainless steel. The peel adhesion could be controlled by changing the carbonyl concentration on the PIB and PBA adhesive surfaces. We speculate that the carbonyl groups on the PIB and PBA adhesive surface might provide an interaction with a stainless steel surface. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1392–1401, 2000     

Charaterization of UHMWPE fiber/matrix adhesion by dynamic mechanical spectrometry

The tensile and dynamic mechanical properties of polystyrene and a poly(styrene-co-buty1 acrylate-co-cyclohexy1 methacrylate) statistical terpolymer (terpolymer) reinforced by randomly oriented, discontinuous ultra-high molecular weight polyethylene (UHMWPE) fibers are presented in terms of the fiber/matrix interfacial properties. Using a thermomechanical block model based on the parallel rule of mixtures, the adhesion characteristics of poly(butyl acrylate) (PBA) and poly(cyclohexyl methacrylate) (PCHM) grafted, plasma treated, and untreated fibers were determined. The model successfully predicts the tan δ response of the composites including peak height variations and the development of additional loss dispersions associated with the interphase. Moreover, the model yields a fiber reinforcement efficiency factor, K, which gives a quantitative measure of adhesion. The contact angle of PBA and PCHM grafted high density polyethylene (HDPE) films are also included and are compared to the contact angle of plasma treated fibers. The results indicate that PBA and PCHM grafts enhance adhesion through polymer graft/matrix interactions, not simply by improved wetting.     

Atmospheric pressure helium + oxygen plasma treatment of ultrahigh modulus polyethylene fibers

Ultrahigh modulus polyethylene fibers were treated with atmospheric pressure helium + oxygen plasma in a capacitively coupled device at a frequency of 7.5 kHz. The fibers were treated for 0, 0.5, 1, 1.5, and 2 min. The surfaces of the fibers treated with He + O₂ plasma were etched and micro-cracks were formed. XPS analysis showed a 65ndash213% increase in oxygen content on the surfaces of all plasma-treated fibers, except for the 1.5 min group. An increase in the concentration of C—O and the appearance of C=O bonds on the surfaces of plasma-treated fibers were observed. In the micro-bond test, He + O2 plasma-treated groups had a 65–104% increase in interfacial shear strength over that of the control. The tensile strength of the fibers was either unchanged or decreased by 10–13% by the plasma treatments.     

低温等离子体处理UHMWPE纤维表面性能的多指标优化

利用正交表安排试验,对超高相对分子质量聚乙烯(UHMWPE)纤维进行空气低温等离子体处理,测试各处理条件下UHMWPE纤维的力学和表面摩擦性能;采用矩阵分析法对多指标正交试验结果进行优化分析,找出最优方案并进行黏着性试验验证。结果表明:经空气低温等离子体处理后,UHMWPE纤维的断裂强度有所减小,表面静、动摩擦因数有较大幅度的提高;处理纤维的最优方案为功率50 W、压强15 Pa、时间150 s,此时纤维的断裂强度损失率仅为2.53%,剥离功为未处理时的4.25倍,说明由矩阵分析法得出的最优方案在保证纤维断裂强度损失很小的情况下,黏着性得到了很大程度的改善。     

Synchronous toughening and reinforcing of polypropylene with ultrahigh‐molecular‐weight polyethylene via melt blending: Mechanical properties,morphology, and rheology

Blending systems based on polypropylene (PP) and ultrahigh‐molecular‐weight polyethylene (UHMWPE) were prepared via a melt extrusion by the four‐screw and the twin‐screw extruders, respectively. The mechanical evaluation demonstrated that the synchronous toughening and reinforcing effects could be achieved from the combination of the PP and the UHMWPE, in which the toughness and the tensile properties could be improved with increasing the UHMWPE content, and achieved optimal values at a weight ratio of PP/UHMWPE (85/15). EPDM can be used as a compatibilizer to improve the compatibility and the interfacial adhesion between the PP and the UHMWPE. This resulted in more effective toughening and reinforcing effects. In contrast, for the PP/UHMWPE blends prepared by the normal twin‐screw extruder, the poor dispersion capacity for the UHMWPE resulted in a deterioration of all mechanical parameters. Morphological observation revealed that the UHMWPE domain was well distributed as tiny particles in the PP matrix, which was confirmed by the differential scanning calorimetry analysis. The toughening effect was attributed to the energy dissipation caused by these rigid tiny particles that detached from the matrix to initiate the local matrix shear yield and formed the void. Rheological investigation demonstrated that there was an interesting composition dependence of viscosity, for which the melt viscosities of the PP/UHMWPE blends decreased when 5 wt % UHMWPE was added, and then began to increase as the UHMWPE content continued to increase. However, this dependence on composition became weaker because of the compatibilization of the EPDM. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3498–3509, 2006     

Ultradrawing properties of ultrahigh‐ molecular‐weight polyethylene/carbon nanotube fibers prepared at various formation temperatures

The influence of formation temperature on the ultradrawing properties of ultrahigh‐molecular‐weight polyethylene/carbon nanotube (UHMWPE/CNT) fiber specimens is investigated. Gel solutions of UHMWPE/CNT with various CNT contents were gel‐spun at the optimum concentration and temperature but were cooled at varying formation temperatures in order to improve the ultradrawing and tensile properties of the UHMWPE/CNT composite fibers. The achievable draw ratio (D_ra) values of UHMWPE/CNT as‐prepared fibers reach a maximum when they are prepared with the optimum CNT content and formation temperature. The D_ra value of UHMWPE/CNT as‐prepared fibers produced using the optimum CNT content and formation temperature is about 33% higher than that of UHMWPE as‐prepared fibers produced using the optimum concentration and formation temperature. The percentage crystallinity (W_c) and melting temperature (T_m) of UHMWPE/CNT as‐prepared fiber specimens increase significantly as the formation temperature increases. In contrast, W_c increases but T_m decreases significantly as the CNT content increases. Dynamic mechanical analysis of UHMWPE and UHMWPE/CNT fiber specimens exhibits particularly high α‐transition and low β‐transition, wherein the peak temperatures of α‐transition and β‐transition increase dramatically as the formation temperature increases and/or CNT content decreases. In order to understand these interesting drawing, thermal and dynamic mechanical properties of the UHMWPE and UHMWPE/CNT as‐prepared fiber specimens, birefringence, morphological and tensile studies of as‐prepared and drawn fibers were carried out. Possible mechanisms accounting for these interesting properties are proposed. Copyright © 2010 Society of Chemical Industry     

Surface modification of drawn gel-cast ultra-high molecular weight polyethylene films

Gel-spun ultra-high molecular weight polyethylene (UHMWPE) fibers have superior properties but their use in composite material applications is limited by their poor adhesion to polymer matrices. Previous studies have shown that etching improves the adhesion of epoxy to the fibers, but leads to a reduction in mechanical properties. The purpose of this research was to use uniaxially drawn gel-cast UHMWPE films as a model system since both films and fibers have a highly oriented fibrillar structural hierarchy. Etching has detrimental effects on the mechanical properties and crystallinity of these very thin films. The small amount of carbonyl and carboxyl groups added to the surface through etching raises the film's surface tension and enhances wetting by epoxy. Even though the unmodified film cannot be bonded with epoxy, the interlaminar shear strength between epoxy and the etched films approaches the cohesive strength of the epoxy. A combination of interfacial and UHMWPE cohesive failures is observed. The increase in adhesion is attributed to the slight increase in surface oxygen.     

Enzyme‐mediated grafting of acrylamide to ultrahigh molecular weight polyethylene fiber: A novel radical initiation system

The enzyme‐mediated grafting of acrylamide (AM) to ultrahigh molecular weight polyethylene (UHMWPE) fibers using horseradish peroxidase (HRP) was demonstrated. To optimize the reaction condition, the concentrations of monomer, H₂O₂, the initiator, and time were varied. The grafting results were discussed and a reaction mechanism was proposed. Function groups and structural change of the graft copolymer were determined by FTIR spectroscopic and scanning electron microscopy micrographs for proof of grafting and the results were discussed. Results show that the surface of treated fiber becomes rougher than the untreated surface. Compared to unmodified fiber, modified fiber surface had significantly increased the interfacial shear strength, and carbonyl‐stretching regions in the IR spectra. The interfacial shear strength of the UHMWPE fiber increased, clearly indicating that enzymatic‐grafted acrylamide could significantly increase the hydrophilicity of the surfaces of UHMWPE fibers. Moreover, the hydrophilicity of treated fiber depends on the monomer concentration, the initiator concentration, and oxidizing agent concentration as well as the time of the reaction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1011–1016, 2005     

Catalytic grafting: A new technique for polymer/fiber composites. II. Plasma treated UHMPE fibers/polyethylene composites

In this paper, the catalytic grafting technique for preparation of polymer/fiber composites is extended to plasma treated ultra-high modulus polyethylene (UHMPE) fiber/high density polyethylene (HDPE) system. The OH groups introduced on the UHMPE fiber surface by oxygen plasma treatment were used to chemically anchor Ziegler-Natta catalyst which then was followed by ethylene polymerization on the fiber surface. The morphology and interfacial behavior, as well as the mechanical properties, of the HDPE composites reinforced by catalytic grafted or ungrafted UHMPE fibers were investigated by SEM, DSC, polarized light optical microscopy, and tensile testing. The experimental results show that the polyethylene grafted on the fibers acted as a transition layer between the reinforcing UHMPE fibers and a commercial HDPE matrix. The interfacial adhesion was also significantly improved. Compared with the composite reinforced by ungrafted UHMPE fibers, the composite reinforced by catalytic grafted UHMPE fibers exhibits much better mechanical properties.