Effect of lignin on mechanical,biodegradability, morphology,and thermal properties of polypropylene/polylactic acid/lignin biocomposite

ABSTRACT

The effects of lignin on mechanical, biodegradability, morphology, and thermal properties of PP/PLA/lignin were investigated. PP/PLA/lignin film were manufactured by adding PP, PLA, lignin and compatibilizer into rheomix at 200°C, at 70?rev?min^?1 for 30?minthen pressed using Hydraulic Hot Press at 200°C–210°C, at 6 bar for 20?min. The functional groups of PP/PLA/lignin were analyzed using FTIR. The surface morphology, mechanical properties and thermal stability was measured by SEM, tensile strenght and TGA respectively. TThe FTIR intensity of vibration peak of –CH₃?cm^-1 from PP/lignin and PP/PLA/lignin at 997–993, 1458–1451 and 2966–2904?cm^-1 was lower than neat PP. The addition of lignin into PP/lignin, PLA/lignin and PP/PLA/lignin can reduce tensile strength and elongation at break. The thermal stability PP/PLA/lignin was lower than the PP/lignin but higher compared to PP/PLA biocomposites. The biodegradability of PP/PLA/lignin biocomposites was two times higher than that of PP/lignin.     

Interface design in 3D-SiC/Al-Si-Mg interpenetrating composite fabricated by pressureless infiltration

3D-SiC/Al-Si-Mg interpenetrating composites (IPCs) were fabricated by pressureless infiltration method. Interfaces in the 3D-SiC/Al-Si-Mg IPCs were modificated by using two different kinds of aluminum alloy Al-15Si-10Mg and Al-9Si-6Mg to infiltrate into 3D-SiC performs and different treated 3D-SiC preforms unoxidized or preoxidized in air at 1000?°C, 1100?°C and 1200?°C for 2?h respectively. Results showed that desired interfaces can be achieved in both IPCs made with those two aluminum alloys, as demonstrated by their excellent comprehensive properties. When the Al-15Si-10Mg alloy with excessive Si content is used for infiltration, interfaces in 3D-SiC/Al-Si-Mg IPC fabricated with the unoxidized 3D-SiC preform are directly bonded through atomic matching without any interfacial reaction and the composite has the properties of a thermal conductivity (TC) of 224.5?W/(m?°C), a thermal expansion coefficient (CTE) (RT ~ 300?°C) of 7.04?×?10^?6/°C and a bending strength (BS) of 277?MPa. When the Al-9Si-6Mg alloy with a lower Si content is used for infiltration, interface zone with a thickness around 200?nm forms in the 3D-SiC/Al-Si-Mg IPC fabricated with the 3D-SiC preform preoxidized at 1000?°C. The reaction-bonded interface is composed of AlN and MgAl₂O₄ which have better interface affinity with SiC and can isolate SiC effectively from liquid Al against the formation of detrimental Al₄C₃ phase. The composite has the properties of a TC of 219.5?W/(m °C), a CTE (RT ~ 300?°C) of 7.66?×?10^?6/°C and a BS of 318?MPa.     

Strain rate-dependent deformation behaviors of multi-layer carbon fiber reinforced polymer laminates

This paper focuses on the contributions of diversities of strain rate and orientations for aggravating the diversities of micro failure behaviors on carbon fiber reinforced polymer (CFRP) laminates. A miniature horizontal type tensile tester is employed to conduct experiments with strain rate ranging from 2.6 × 10⁻⁶ s⁻¹ to 2.6 × 10⁻³ s⁻¹. The CFRP laminates are obtained based upon a thermoset toughened epoxy matrix (termed CF/Epoxy) with ply orientations of (0°/0°) and (0°/90°). Significant differences in deformation behaviors of CFRP laminates are determined through tests. The study clearly reveals the strain rate-dependent deformation modes of CFRP laminates, involving pure fiber fracture, epoxy crack with stepped surface and interface failure with residual voids, determines the “low-high-low” variation tendency of Young's modulus and strength as a function of strain rate. Ply orientation-dependent differences in deformation behaviors are also investigated via severe interfacial shearing effect. A unified model consisted of four deformation modes to is clarified to analyze the complexity of CFRP laminates failure mechanism.     

Synthesis and Properties of Random Copolymers of Functionalised Polybenzimidazoles for High Temperature Fuel Cells

A series of polybenzimidazoles (PBIs) incorporating main chain sulphonic acid groups were synthesised as random copolymers with p‐PBI in varying ratios using polyphosphoric acid (PPA) as both the polymerisation solvent and polycondensation reagent. The PPA process was used to produce high molecular weight phosphoric acid (PA) doped PBI gel membranes in a one‐step procedure. These membranes exhibit excellent mechanical properties (0.528–2.51 MPa tensile stress and 130–300% tensile strain) even at high acid doping levels [20–40 mol PA/PRU (polymer repeat unit)] and high conductivities (0.148–0.291 S cm^–1) at elevated temperatures (>100 °C) with no external humidification, depending on copolymer composition. Fuel cell testing was conducted with hydrogen fuel and air or oxygen oxidants for all membrane compositions at temperatures greater than 100 °C without external feed gas humidification. Initial studies showed a maximum fuel performance of 0.675 V for the 25 mol% s‐PBI/75 mol% p‐PBI random copolymer at 180 °C and 0.2 A cm^–2 with hydrogen and air, and 0.747 V for the same copolymer at 180 °C and 0.2 A cm^–2 with hydrogen and oxygen.     

Friction and wear mechanisms of PA66/PPS blend reinforced with carbon fiber

The mechanical and tribological properties of carbon fiber (CF) reinforced polyamide 66 (PA66)/polyphenylene sulfide (PPS) blend composite were studied in this article. It was found that CF reinforcement greatly increases the mechanical properties of PA66/PPS blend. The friction coefficient of the sample decreases with the increase of CF content. When CF content is lower (below 30%), the wear resistance is deteriorated by the addition of CF. However, the loading of higher than 30% CF significantly improves the tribological properties of the blend. The lowest friction coefficient (0.31) and the wear volume (1.05 mm³) were obtained with the PA66/PPS blend containing 30% CF. The transfer film and the worn surface formed by sample during sliding were examined by scanning electron microscopy. The observations revealed that the friction coefficient of PA66/PPS/CF composite depends on the formation and development of a transfer film on the counterface. The abrasive wear caused by ruptured CFs (for lower CF content) and the load bearing ability of CFs (for higher CF content) are the major factors affecting the wear volume. In addition, the improvements of mechanical properties, thermal conductivity, and self‐lubrication of bulk CFs are also contributed to the wear behavior of PA66/PPS/CF composite. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Corn Cob Lignin-based Porous Carbon Modified Reduced Graphene Oxide Film For Flexible Supercapacitor Electrode

Flexible supercapacitors (FSCs) have attracted widespread attention of many researchers as a type of portable energy storage devices. However, there are still challenges in preparing renewable and inexpensive electrode materials. Herein, we prepared the porous carbon (PC) by the two-step process involving hydrothermal method and low-temperature heat treatment using corn cob lignin as the carbon source, and different types for PC were obtained by changing the temperature of low temperature heat treatment (100?°C–300?°C). The flexible electrode film was prepared by combining the obtained corn cob lignin-based PC with reduced graphene oxide (RGO), in addition, we investigated the effect of PC obtained by different low-temperature heat treatment (100?°C, 150?°C, 200?°C, 250?°C, and 300?°C) on the electrochemical properties of the composite electrode. The optimal low-temperature heat treatment temperature (250?°C) was determined and the PC250/RGO film electrodes displayed a high area specific capacitance of 636 mF/cm² with a mass of 2.2?mg/cm² (specific capacitance of 289?F/g) at 0.2?mA/cm² and 82% of the capacitance was retained after 10,000 charge and discharge cycles at 5?mA/cm², at the same time on the electrode film flexibility test, the influence of different bending angle on the electrochemical properties can be ignored. The assembled supercapacitor had the advantages of flexible, lightweight, low price, and environment friendly, which can achieve area specific capacitance of 324.5 mF/cm² at 0.2?mA/cm² and 91.8% capacitance retention after 1000 charging/discharging cycles. These good electrochemical properties illustrate the application prospects of composite electrode materials in wearable and portable electronic devices.     

Effect of hybrid polysphosphazene coating treatment on carbon fibers on the interfacial properties of CF/PA6 composites

Carbon fiber (CF) reinforced polyamide 6 (PA6) composite has an extensive application. However, the performances of CF/PA6 composite are constrained by the poor interfacial adhesion between CF and PA6 matrix. In this article, in order to strengthen the interfacial adhesion of CF/PA6 composite, a layer of poly(cyclotriphosphazene-co-4,4′-sulfonyldiphonel) (PZS) hybrid coating with plenty of PZS microspheres (PZSMS) was successfully introduced onto CF surface through facile in situ polymerization. After surface modification, the surface morphologies and the surface chemical structures of fibers changed distinctly. On one hand, the PZSMS provided more contact points and increased mechanical interlocking between CF and PA6 matrix. On the other hand, numerous hydrogen bonds between CF and PA6 were formed due to a great amount of unique polar groups on modified CF surface. Consequently, in comparison with untreated CF, the interfacial shear strength of CF-PZSMS/PA6 composites was improved from 37.68 ± 3.16 to 53.79 ± 3.38 MPa, by 42.75 ± 3.02%. The results indicated that PZS hybrid coating on fiber surface effectively improved the interfacial adhesion of CF/PA6 composites, and the stronger hydrogen bonding and the enhanced mechanical interlocking synergistically played a major role in such significant improvements.     

Effect of syndiotactic polystyrene on the crystallization behavior of isotactic polypropylene/syndiotactic polystyrene blends with and without β‐nucleating agent

Blends of isotactic polypropylene (PP) and syndiotactic polystyrene (sPS) with and without β‐nucleating agent were prepared using a twin‐screw extruder at 290 °C. Blends of PP/sPS with β‐nucleating agent mainly show β crystalline form, irrespective of high (20 °C min^?1) or low (2 °C min^?1) previous cooling rates. This suggests that the cooling rates have little effect on the polymorphic composition of PP in PP/sPS blends. The effect of sPS on the crystallization of PP is compared with that of polyamide 6 (PA6). The increase in crystallization temperature of PP is smaller in the presence of sPS than in the presence of PA6; the fold surface free energy of PP/sPS is larger than that of PP/PA6 blends. These results reveal that compared with PA6, sPS has much weaker α‐nucleation effect on the crystallization of PP. The weak α‐nucleation effect of sPS is attributed to the high lattice mismatch between PP and sPS crystals.     

Morphological and nanomechanical characterization of anisotropic interfacial characteristic regions in CF/PA6 composites at different cooling rates

Macroscopic tensile tests on neat PA6 and CF/PA6 prepregs showed that the cooling rate significantly affects the mechanical properties of CF/PA6 composites because of their different crystallization behaviors both at the fiber surface and in the matrix. Polarizing optical microscopy, static nanoindentation (SNI), and dynamic mechanical imaging (DMI) tests were used to characterize the anisotropic morphologies and nanomechanical performances of the interfacial characteristic regions in CF/PA6 composites at five different cooling rates. As a result, the seven interfacial characteristic regions inside the CF/PA6 composites were clearly distinguished. The interphase thickness of the CF/PA6 composites decreased with a decrease in the cooling rate. On the contrary, the interphase modulus and transcrystallinity thickness and modulus showed significant increases with a decrease in the cooling rate. The DMI and SNI test results were in agreement with each other and with the macromechanical test results. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44106.     

Studies on PA6–PP–wollastonite composite compatibilised by PP–graft–maleic anhydride prepared via pan milling

Abstract

A composite of PA6–PP–wollastonite compatibilised by PP-g-maleic anhydride has been prepared using pan type milling equipment, and its structure and properties investigated by IR, DSC, melt index measurements, SEM, and mechanical testing. The experimental results show that during pan milling, PP, PA6, and wollastonite are effectively pulverised, reaching better mixing owing to the very strong shear forces and pressure exerted by the pan type milling equipment. In particular, some PA6 polymer chains are grafted onto the wollastonite surface and the pan milling affects the crystallinity of PA6 and PP to some degree. The compatibiliser prepared via solid phase grafting of maleic anhydride onto PP via pan milling shows a reasonably good compatibilising effect on the composite, improving the morphology and therefore the mechanical properties of the composite. If combined with suitable coupling agent, the PA6–PP–wollastonite compatibilised by PP-g-maleic anhydride prepared via pan milling (wollastonite content 30 wt-%) possesses much better mechanical properties, its tensile strength increases from 54·6 to 58·6 MPa, and its notched Izod impact strength increases from 29·4 to 48·7 J m^-1, compared with the uncompatibilised system. Pan milling is a novel way to achieve desired structure and hence improved properties of polymer based materials via the polymer processing procedure.     

Influence of a synthetic ureido nucleating agent on crystallization behavior and mechanical properties of polyamide 6

A synthetic ureido mixture prepared from the reaction of 4,4′‐diphenylmethane disocynanate (MDI) and cyclohexylamine without using any harmful organic solvents, has been used as a nucleating agent (PNA) for polyamide 6 (PA6). The effect of PNA on the crystallization and mechanical properties of PA6 has been studied by means of differential scanning calorimetry (DSC), polarized optical microscopy (POM), tensile test, melt flow index (MFI), and X‐ray diffraction (XRD). The results show that PNA is an effective nucleation agent for PA6. PNA affects the nucleation mechanism of PA6, and substantially accelerates the crystallization rate of PA6 and gives rise to smaller crystal size. In comparison with PA6, the crystallization temperature (T_c) of PA6/PNA (100/0.5) increases 21.3°C and the degree of sub‐cooling (ΔT_c) decreases 23.7°C. Furthermore, because of the heterogeneous nucleation induced by PNA, the spherulites of PA6 become even and tiny based on POM observation. Polymorph transform has been obtained from XRD analysis. The virgin PA6 is free of γ‐phase crystals, presented as α‐phase crystals in this study, but γ‐phase crystal appears after the introduction of PNA. The mechanical and thermal properties of PA6 are obviously improved by the addition of PNA. POLYM. ENG. SCI., 55:2011–2017, 2015. © 2015 Society of Plastics Engineers     

Biaxial flexural strength and Weilbull characteristics of adhesively luted hybrid and reinforced CAD/CAM materials to dentin: effect of self-etching ceramic primer versus hydrofluoric acid etching

Abstract

This study evaluated the influence of the surface treatment and aging on the biaxial flexural strength of ceramic materials cemented to a dentin analogue. One hundred twenty disc-shaped specimens were allocated into 12 groups considering three study factors: ceramic material (lithium disilicate, leucite-based ceramic and hybrid ceramic), surface treatment (10% hydrofluoric acid etching?+?silane or self-etching glass-ceramic primer) and Aging (with 10,000 thermocycles of 5–37–55?°C or without). A tri-layer assembly was designed to mimic a cemented restoration (Variolink N) into a dentin analogue. All samples were submitted to the biaxial flexural strength assay. The flexural strength in MPa was calculated using the finite element method for each sample considering thickness, material properties, and the load to fracture during the in vitro test. Fractographic analysis was also performed. The data was evaluated using three-way ANOVA and Tukey test (α?=?5%). ANOVA showed influence for the Material*Treatment*Aging interaction on the flexural strength (p?=?0.011). The highest strength was calculated for lithium disilicate ceramic?+?self-etching ceramic primer without aging (499?±?17?MPa)^A and the lowest value for hybrid ceramic material?+?acid etching with aging (424?±?48?MPa)^E. According to the Weibull modulus, the most predictable strength was calculated for lithium disilicate?+?acid etching after aging. Acid etching or self-etching ceramic primer promotes similar immediate biaxial flexural strength for each evaluated ceramic. In the long-term, superior strength was observed using acid etching for lithium disilicate and the self-etching ceramic primer for the hybrid ceramic while no difference was observed for leucite-based ceramic.

Clinical implications: Some protocols combining the CAD/CAM ceramic material and the surface treatment could present suitable and stable flexural strength.     

CMK-3 nanostructured carbon: Effect of temperature and time carbonization on textural properties and H2 storage

Abstract

CMK-3 carbons were synthesized varying the carbonization conditions and studying the effect of the templates calcined at different temperatures. The textural characterization of different SBA-15 templates calcined at 350, 450, and 550?°C shows a variation of the specific surface area below 10%. Based on the results, the SBA-15 obtained at 350?°C (the more affordable condition) was used as the final template for the CMK-3 synthesis. The results show that varying the time (from 2 to 6?h) and the temperature (from 600 to 900?°C) on the carbonization step, the textural, structural, and morphological properties of the carbons do not vary in a meaningful way. Thus, a CMK-3 carbon synthesized (using as template an SBA-15 calcined at 350?°C) obtained at 600?°C during 2?h was chosen to be used as adsorbent in hydrogen storage in order to stablish the relationship between the textural properties and its performance. Regarding the hydrogen storage, capacities of 15?mg H₂ g^?1 (1.5% w/w), and up to 28?mg H₂ g^?1 (2.8% w/w) were obtained at 1 and 10?bar, respectively. At high pressure, an important influence of the large micropores and narrow mesopores on the hydrogen adsorption was found.     

Tris-benzil crosslinked polyphenylquinoxalines

Polyphenylquinoxalines (PPQ) were crosslinked with a tris-benzil comonomer, to alleviate the inherenthigh temperature thermoplasticity, and evaluated as matrices in graphite reinforced composites. The room temperature flexural strength/modulus of Modmor IJ laminates were as high as 245,000 psi/16,6 × 10⁶ psi. Essentially 100 percent retention of ambient mechanical properties was obtained at 371°C using a PPQ matrix from the fully-crosslinked polymer prepared from 4,4′-bis(4″-oxybenzilyl) benzil (BOBB) and 3,3′-diaminQbenzrdine. The degree of high temperature thermoplasticity in the composite was found to be more closely related to the final postcure temperature than to the BOBB crosslink density. The thermoplasticity essentially disappeared when the BOBB comonomer-PPQ laminates were postcured at 482–510°C in nitrogen. Substitution of DMAC for the commonly used m-cresol solvent system allowed facile preparation of prepreg to fabricate low-void laminates and NOL rings.     

Effects of time and temperature on the tension-tension fatigue behavior of short fiber reinforced polyamides

To support the fatigue design of the cyclically stressed plastics parts, such as automotive under-the-hood and exterior components, we analyzed the short-term and long-term mechanical performance (tensile strength, fatigue strength, and fatigue life) of short glass fiber reinforced polyamides PA 6 and PA 66. Comprehensive tension-tension fatigue tests were conducted with reference to the latest ASTM, ISO, and Japanese industrial standards for plastics, at temperatures from −40°C to 121°C, on materials aged at 121°C for 0, 100, 500, and 1000 h. Tests were conducted at a loading frequency f = 5 Hz, stress ratio R = 0.1, and in a wide range of cycles to failure from 2 × 10³ to 2 × 10⁶. Without aging and for both PA 6 and PA 66, the highest fatigue strength or fatigue life was found at −40°C; it decreased significantly at 23°C, and decreased further at 121°C. The fatigue strength of PA 6 was found to be higher than that of PA 66 at −40°C, but the reverse was seen at 23°C. At 121°C, the fatigue strengths of PA 6 and PA 66 were virtually the same. Aging at 121°C improved the tensile strength of PA 6 and PA 66 as aging time increased from 100 to 1000 h, and this process seemed to be more influential for PA 6.     

Highly efficient preparation of multi-angle continuous carbon fibre reinforced hydroxyapatite composites by electrostatic splitting method

An electrostatic splitting device was self-designed and manufactured for highly efficient preparation of multi-angle continuous carbon fibre (CF)-reinforced ceramic-based composites and was used to prepare multi-angle continuous CF and nano-hydroxyapatite (nHA)-coated CF reinforced HA composites with improved CF dispersion and content. The compressive strength of sintered [0°/90°] CF reinforced hydroxyapatite (CF/HA) composites is more than two and a half times that of hydroxyapatite and is superior to that of cortical bone (26.42–110.7%). Compared with hydroxyapatite, fracture toughness of [0°/0°], [0°/90°] and [? 45°/+ 45°] CF/HA composites increase by 28.83%, 66.32% and 115.95%, respectively. The strength and fracture toughness (30.2 MPa·m^1/2) of [? 45°/+ 45°] CF/HA bioceramics display synchronously improving. Micromechanical property and crack propagation process of the composites were simulated in depth. Based on optimised dispersion and arrangement of CF, the introduction of nHA coating enhances the mechanical properties of nHA-coated CF reinforced HA composites because nHA coating can block the generation and propagation of cracks.     

Fibre reinforced composites of multifunctional epoxy resins

Glass and carbon fibre reinforced epoxy composites were fabricated for N,N,N′,N′-tetraglycidyl-4,4′-diaminodiphenyl methane (TGDDM) and its formulated systems with tri- and di-functional reactive epoxy diluents using 30% diaminodiphenyl sulphone (DDS) as a curing agent. The epoxy laminates were evaluated for their physical, chemical and mechanical properties [at room (26°C) and high (100°C) temperatures]. A marginal increase (<20%) in the mechanical properties of CFRP was found compared with GFRP laminates. Incorporation of epoxy diluents altered the mechanical properties of the composites significantly. The incorporation of triglycidyl-4-aminophenol diluent to TGDDM systems resulted in an improvement in mechanical properties of about 2–6%.     

Improving mechanical and thermal properties of short carbon fiber/polyamide 6 composites through a polydopamine/nano-silica interface layer

Carbon fiber (CF) reinforced matrix composites have been applied widely, however, the interfacial adhesion of composites is weak due to smooth and chemically inert of CF surface. To solve this problem, A polydopamine/nano-silica (PDA-SiO₂) interfacial layer on carbon fiber surface was constructed via polydopamine and nano- SiO₂ (CF-PDA-SiO₂) by a facile and effective method to reinforce polyamide 6 composites (CFs/PA6). The effects of PDA-SiO₂ interfacial layer on crystallization structure and behavior, thermal properties, and mechanical properties of CFs/PA6 composites were investigated. Furthermore, interfacial reinforcement mechanism of composites has been discussed. This interfacial layer greatly increased the number of active groups of CF surface and its wettability obviously. The tensile strength of CF-PDA-SiO₂/PA6 composites increased by 28.09%, 19.37%, and 26.22% compared to untreated-CF/PA6, CF-PDA/PA6, and CF-SiO₂/PA6 composites, respectively, which might be caused by the increased interfacial adhesion between CF and PA6 matrix. The thermal stability, crystallization temperature, crystallinity, and glass transition temperature (T_g) of CF-PDA-SiO₂/PA6 composites improved correspondingly, attributing to the heterogeneous nucleation of nano-SiO₂ in the crystalline area and hydrogen bonds with molecular chains of PA6 in the amorphous area. This work provides a novel strategy for the construction of interfaces suitable for advanced CF composites with different structures.     

Effect of the talc filler content on the mechanical properties of polypropylene composites

This research examines the effect of a microsize/nanosize talc filler on the physicochemical and mechanical properties of filled polypropylene (108MF10 and 33MBTU from Saudi Basic Industries Corp. and HE125MO grade from Borealis) composite matrices. A range of mechanical properties were measured [tensile properties, bending properties, fracture toughness, notched impact strength (at the ambient temperature and ?20°C), strain at break, and impact strength] along with microhardness testing and thermal stability testing from 40 to 600°C as measured by differential thermal analysis and thermogravimetric analysis. Increasing filler content lead to an increase in the mechanical strength of the composite material with a simultaneous decrease in the fracture toughness. The observed increase in tensile strength ranged from 15 to 25% (the maximum tensile strength at break was found to be 22 MPa). The increase in mechanical strength simultaneously led to a higher brittleness, which was reflected in a decrease in the mean impact strength from the initial 18 kJ/m² (for the virgin polypropylene sample) to 14 kJ/m², that is, a 23% decrease. A similar dependency was also obtained for the samples conditioned at ?20°C (a decrease of 12.5%). With increasing degree of filling of the talc–polypropylene composite matrix, the thermooxidative stability increased; the highest magnitude was obtained for the 20 wt % sample (decomposition temperature = 482°C, cf. 392°C for the virgin polymer). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

The effect of imidazolated PPO with different alkyl chains on its performance as a high temperature proton exchange membrane

ABSTRACT

Designed and synthesized a series of imidazolium-functionalized Poly (2, 6-dimethyl-1, 4-phenylene oxide) (Im-PPO) containing pendant imidazole groups, which were used to supply functional sites for acid–base interaction with the doping phosphoric acid. The imidazolium-functionalized Poly (2, 6-dimethyl-1, 4-phenylene oxide) membranes obtained by the solution-casting method were doped with phosphoric acid (PA). The PA content, swelling, and tensile strength of the different membranes doped with PA were measured. With the increase of the length of side chains on the imidazole groups, the membrane showed different properties. The proton conductivity at a level of 3.7 × 10^?2 S/cm was achieved at 160°C by the MeIm-PPO imidazolium composite membrane.