Properties of bamboo flour/high-density polyethylene composites reinforced with ultrahigh molecular weight polyethylene

In order to improve the properties of bamboo-plastic composites (BPCs), bamboo flour/high-density polyethylene (HDPE) composites were reinforced with ultrahigh molecular weight polyethylene (UHMWPE). The effects of UHMWPE on properties of composites were studied. The crystallinity of composites decreased slightly. Compared with non-UHMWPE added bamboo powder/HDPE composite, the composite with 6 wt % UHMWPE, showed decrease in water absorption to 0.41%, whereas its tensile strength and flexural strength increased to 34.51 and 25.88 MPa, respectively, a corresponding increase of 34.59 and 12.87%. The temperatures corresponding to initial degradation temperature (T_initial) and maximum degradation temperature (T_max) of the composite increased from 282.7 and 467.4 °C to 288.5 and 474.7 °C respectively. Scanning electron microscopic images showed that UHMWPE was well dispersed and fully extended as long fibers in the composite, forming a “three-dimensional physically cross-linked network structure,” which contributed to the improved properties of the composites. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48971.     

Thermal and mechanical properties of plasticized poly(L‐lactic acid)

Acetyl tri‐n‐butyl citrate (ATBC) and poly(ethyleneglycol)s (PEGs) with different molecular weights (from 400 to 10000) were used in this study to plasticize poly(L‐lactic acid) (PLA). The thermal and mechanical properties of the plasticized polymer are reported. Both ATBC and PEG are effective in lowering the glass transition (T_g) of PLA up to a given concentration, where the plasticizer reaches its solubility limit in the polymer (50 wt % in the case of ATBC; 15–30 wt %, depending on molecular weight, in the case of PEG). The range of applicability of PEGs as PLA plasticizers is given in terms of PEG molecular weight and concentration. The mechanical properties of plasticized PLA change with increasing plasticizer concentration. In all PLA/plasticizer systems investigated, when the blend T_g approaches room temperature, a stepwise change in the mechanical properties of the system is observed. The elongation at break drastically increases, whereas tensile strength and modulus decrease. This behavior occurs at a plasticizer concentration that depends on the T_g‐depressing efficiency of the plasticizer. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1731–1738, 2003     

Melt blending of polylactide and poly(methyl methacrylate): Thermal and mechanical properties and phase morphology characterization

Blends of polylactide with poly(methyl methacrylate), PLA/PMMA, were prepared by a semi‐industrial twin screw extruder and afterwards were injection molded. Blends were studied using different techniques as Fourier Transform Infrared Spectroscopy (FTIR), Dynamic Mechanical Analysis (DMA), Differential Scanning Calorimetry (DSC), Scanning Electron Microscopy (SEM), and mechanical properties by means of tensile and impact tests, were also studied. This work helped better understanding of apparently contradictory results reported in the literature for PLA/PMMA blends prepared by melt compounding. DSC first heating scan and DMA results showed partially miscible blends, whereas the second DSC heating scan showed miscible blends. For miscible blends, T_g values were predicted using Gordon‐Taylor equation. On the other hand, Small and Van Krevelen approaches were used to estimate the solubility parameters of neat PLA and neat PMMA, and Flory‐Huggins interaction parameter was calculated from solubility parameters. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42677.     

Hybrid biocomposites with enhanced thermal and mechanical properties for structural applications

The current work focuses on enhancing the mechanical and thermal properties of sisal fiber reinforced composites that were previously used in developing interior automotive trims. In order to extend their use in other structural applications, two hybrid biocomposites with the combination of sisal (SF) and glass fiber (GF)‐SF20/GF10 and SF10/GF20 were blended with polypropylene via extrusion and injection molding process. Critical material properties such as density, fogging, acoustic, mechanical, thermal, and rheological properties were evaluated and results were analyzed using ANOVA. Hybridization of SF and GF enhanced flexural strength and thermal properties of the biocomposites by 33 and 19%, respectively, while no significant change in acoustic, impact and rheological properties were observed. The properties of the hybrid biocomposites were compared with the material specification of a battery tray and it was found that these hybrid biocomposites could be better alternative materials in structural applications. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42452.     

Approach in Macadamia integrifolia residue based low-density polyethylene composites on mechanical and thermal performance

Macadamia nutshell residues are generated in large quantities, around 70%–77% for each ton produced, and it is a waste material with high techno-economic potential. This work purpose a sustainable alternative to valorize macadamia nutshell residues (MN) as reinforcing in low-density polyethylene (LDPE) composites through melt mixing, using different fiber contents (0, 5, 10, and 20 wt%), and investigate the influence of fibers (residues) in composites by mechanical tests and thermal analysis. The fibers addition has significantly increased the composites' stiffness compared with neat LDPE, causing a reduction of toughness and resilience, leading to lower impact energy absorption. The LPDE/MN20% composite obtained the best tensile and flexural mechanical performance, resulting in a maximum modulus, which implies an increase of 36.9% and 77.6% compared with the neat LDPE. The addition of macadamia fibers on the composites acted as nucleation points of spherulites, which promoted an increase in the crystallization degree. Consequently, better performance of mechanical properties was observed in the green composites. Thus, the macadamia nutshell residues present a promising future as filler in LDPE for enhancing composites' thermal and mechanical properties.     

聚乙二醇改性双马来酰亚胺-三嗪树脂/玻璃纤维布复合材料的热性能

聚乙二醇对树脂基玻璃纤维布复合材料增韧具有优良的效果,但其柔性链段的分子结构本质极大影响了复合材料的耐热性能。本文以聚乙二醇为改性剂制备了聚乙二醇/BT树脂/玻璃纤维布复合材料,系统研究了不同分子链长度以及不同含量的聚乙二醇对复合材料热性能的影响。研究结果表明：聚乙二醇的加入降低了复合材料的玻璃化转变温度、5%热失重温度以及800 ℃残炭率。在聚乙二醇相对分子质量为4000时,复合材料的热性能出现最大值。随聚乙二醇含量的增加,复合材料的热稳定性能逐步下降。由于聚乙二醇、BT树脂、玻璃纤维布之间较大的界面结合力,使基体树脂的链运动受到一定程度的限制,一定程度上缓解了由于聚乙二醇的加入而使复合材料的热稳定性能下降的趋势。研究结果为合理添加聚乙二醇而提高复合材料的韧性提供了热性能方面的参考依据。     

Thermal and mechanical properties of PES/PTFE composites and nanocomposites

Polyethersulphone/polytetrafluoroethylene (PES/PTFE) nanocomposites and composites were prepared by precipitation of PES into a PTFE latex‐containing nanoparticles. Different samples were obtained by varying the relative ratio between PES and PTFE. The complex crystallization process, discussed within the fractionated crystallization frame, allowed to identify and quantify different dispersion degree of the PTFE nanoparticles within the PES matrix. The different samples were thus divided into nanocomposite and composites. The effect of crystalline PTFE domains on the mobility of PES was investigated and discussed. The dynamic‐mechanical behavior was explained in terms of the particle aggregation state. The mechanical properties of the PES/PTFE composites were found to depend on both the dispersion and the concentration of the PTFE nanoparticles. In the glassy state the stiffness of the materials was found to increase with the dispersion degree, resulting higher for the nanocomposite with respect to composites. On the contrary, in the rubbery state the modulus was found proportional to the PTFE nanoparticles concentration, resulting higher in the composites with respect to the nanocomposite. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3624–3633, 2013     

Thermal and mechanical properties of woodflour/tannin adhesive composites

Composite materials formulated with a natural polyphenolic matrix (commercial tannin adhesive made from quebracho tannin extract), pine woodflour as reinforcing material, and hexamethylenetetramine as hardener were prepared and tested. Scanning electron microscopy of fractured samples was used to analyze the efficiency of the wetting and adhesion of the filler to the surrounding matrix. Thermogravimetric analysis was used in the thermal characterization of the woodflour and the tannin extract. Flexural, compression, and dynamic‐mechanical tests were performed on composites to study the relationship of the filler content and particle size with the composite final properties. Moreover, the influence of the moisture content on the physical and mechanical properties of the different composites was analyzed. Results indicated that the mechanical properties were severely affected by the absorbed moisture. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3074–3082, 2004     

Physical and mechanical properties of thermostatic fabrics treated with nanoencapsulated phase change materials

Textiles treated with nanoencapsulated phase change materials (nanoPCMs) were used to examine their suitability as clothing materials to prepare thermostatic clothes for absorbing or releasing heat according to heat fluctuation between the body and the environment. To this end, the physical and mechanical properties of fabrics treated with nanoPCMs, such as nano‐nonadecane and nano‐octadecane, were evaluated after we confirmed the morphology and thermal efficiency of the nanoPCMs. The nanoPCMs were almost spherical, with an irregular size distribution between 200 and 400 nm. The heat of fusion and peak temperature of melting for nano‐nonadecane, nano‐octadecane, and a balanced mix were measured at 102.6 J/g and 33.6°C, 144.7 J/g and 29.8°C, and 137.4 J/g and 31.8°C, respectively. However, the heat of fusion of the vapor‐permeable and water‐repellant (VPWR) fabrics treated with the nanoPCMs were only 6.8, 4.0, and 3.6 J/g, respectively, because the weight of fabric was added per unit area. The air permeability of the specimens without nanoPCMs was the lowest; that of the VPWR fabrics with nanoPCMs was relatively higher. The water vapor transmission of the VPWR fabrics with nanoPCMs was higher than the fabric without nanoPCMs, and the water resistance decreased in the same order. Compared to the mechanical properties of the fabric without nanoPCMs, the stiffness and roughness of the fabrics with nanoPCMs were improved, but the resilience and smoothness of the fabrics were slightly decreased. Consequently, the physical and mechanical properties of VPWR fabrics with nanoPCMs were superior to those of the fabric without nanoPCMs. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Thermal and mechanical properties of chitosan reinforced polyhydroxybutyrate composites

The article reports the results of studies on the effect of chitosan (0, 5, 10, 20, 30, and 40 wt %) on thermal and mechanical properties of poly(hydroxybutyrate) composites. The addition of chitosan causes an increase in the glass transition temperature (T_g) while a decrease in the enthalpy of fusion (ΔH_fus), crystallization (ΔH_cry) and percentage of crystallinity as determined by differential scanning calorimeter (DSC). The thermogravimetric analysis reveals that high amount of chitosan decreases the thermal stability of the composites. The Young's modulus of the composite increases and is high for the composite having 40 wt % of chitosan. Increase in the amount of chitosan decreases the elongation at break and impact strength of composites. Finally, the Young's modulus of the composites has been compared with the theoretical predictions. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Development of high Tg epoxy resin and mechanical properties of its fiber‐reinforced composites

A new epoxy resin with high glass transition temperature (T_g) (～ 180°C) and a viscosity low enough for infiltration into dry reinforcements at 40°C was developed for the vacuum‐assisted resin transfer molding process. To study the curing behavior and viscosity, several blends were formulated using multifunctional resin, aromatic hardener, and reactive diluents. Effects of these components on the viscosity and T_g were investigated by thermomechanical analysis, dynamic scanning calorimetry, and rheometer. Experimental results showed that a liquid aromatic hardener and multifunctional epoxy resin should be used to decrease the viscosity to <1 Pa·s at 40°C. Moreover, the addition of a proper reactive diluent decreased the viscosity and simultaneously minimized the deterioration of T_g. Mechanical properties of the composite produced with the optimized blend were evaluated at both room‐temperature and high‐temperature conditions. According to the results, the composite showed comparable mechanical properties with that of the current commercial resin. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Thermal and mechanical characterization of linear low‐density polyethylene/wood flour composites

A linear low‐density polyethylene (LLDPE) matrix was modified with an organic peroxide and by a reaction with maleic anhydride (MAn) and was simultaneously compounded with untreated wood flour in a twin‐screw extruder. The thermal and mechanical properties of the modified LLDPE and the resulting composites were evaluated. The degree of crystallinity was reduced in the modified LLDPE, but it increased with the addition of wood flour for the formation of the composites. Significant improvements in the tensile strength, ductility, and creep resistance were obtained for the MAn‐modified composites. This enhancement in the mechanical behavior could be attributed to an improvement in the compatibility between the filler and the matrix. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2775–2784, 2003     

聚乙二醇/石墨烯纳米片复合相变材料的制备及其性能研究

以聚乙二醇(PEG)作为相变工作物质,以具有优异导热性能的石墨烯纳米片(GNPs)作为导热填料,通过熔融共混法制备出一系列不同GNPs含量的PEG/GNPs复合相变材料。采用激光导热仪、差示扫描量热仪、扫描电子显微镜、X射线衍射仪、红外光谱仪等测试PEG/GNPs复合相变材料的导热性能、热物性、微观形貌、结晶性能及化学组成。结果表明,GNPs均匀分散于PEG基体中,形成能够加快热量传递的导热通路,复合材料体系的导热系数得以显著提高,而相变焓仅仅略微下降,当GNPs含量为2%时,复合材料体系的导热系数是PEG的249.7%,而相变焓损失率却仅为3.9%;PEG与GNPs二者间仅是物理吸附,并未发生化学反应,复合材料体系的结晶性能良好;PEG与GNPs复合相变材料的热响应速度更快,能源利用率因而更高。     

Thermal,mechanical, and structural properties of zno/polyethylene membranes made by thermally induced phase separation method

In this study, ZnO/polyethylene membranes were fabricated via thermally induced phase separation method. A set of tests including FE‐SEM, EDX, XRD, DSC, TGA, DMA, mechanical test, and pure water flux (PWF) for characterization of membranes were carried out. The results of EDX, XRD, and TGA analyses confirmed the presence of ZnO nanoparticles in the polymer matrix. The results of DSC analysis revealed that the melting point as well as the crystallinity of the membranes increased slightly with increasing ZnO content. However, glass transition temperature of the membranes was not affected by presence of the particles. Addition of nanoparticles also increased storage modulus, loss modulus. and tensile at break of the membranes due to the stiffness improvement effect of inorganic ZnO. Finally, it was observed that incorporation of the nanoparticles improved PWF of the membranes, whereas humic acid rejection decreased due to the increase in mean pore radius of membranes. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42338.     

Thermal and mechanical properties of polypropylene/wood‐flour composites

In this research, polypropylene/wood‐flour composites (WPCs) were blended with different contents of wood and/or maleated polypropylene (MAPP) and clay. We found that the addition of MAPP or clay in the formulation greatly improved the dispersion of the wood fibers in the composite; this suggested that MAPP or clay may have played the role of an adhesion promoter in the WPCs. The results obtained with clay indicate that it also acted as a flame retardant. The thermal tests carried out with the produced samples showed an increased crystallization temperature (T_c), crystallinity, and melting temperature (T_m) with wood loading. The increase of the two former parameters was explained by the incorporation of wood flour, which played the role of nucleating agent and induced the crystallization of the matrix polymer. On the other hand, the T_m increase was ascribed to the insulating properties of wood, which hindered the movement of heat conduction. The effects of UV irradiation on T_m and T_c were also examined. T_c increased with UV exposure time; this implied that UV degradation generated short chains with low molecular weight that could move easily in the bulk of the sample and, thus, catalyze early crystallization. The flexural strength and modulus increased with increasing wood‐flour content. In contrast, the impact strength and tensile strength and strain decreased with increasing wood‐flour content. All of these changes were related to the level of dispersion of the wood flour in the polymeric matrix. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

聚乙二醇/二氧化硅定形相变材料的制备

采用多孔二氧化硅（SiO₂）、聚乙二醇(PEG)等研究一种定形无机 有机复合相变材料的制备方法,并加入适当的促进剂和改性剂对复合材料进行了改性。利用多孔二氧化硅具有良好的吸附性能特点,将聚乙二醇相变材料吸附在二氧化硅微孔结构内,在毛细管力和表面张力的作用下,聚乙二醇在发生固液相变的时候很难从二氧化硅的微孔结构内渗透出来,从而解决了聚乙二醇在蓄热技术中应用时的液体流动问题。同时对相变材料进行了热性能分析,实验证明该复合相变材料具有形状稳定,导热率高,储热能力大等特点。     

Thermal expansion and mechanical properties of phenolic resin/ZrW2O8 composites

Phenolic resin/ZrW₂O₈ composites were successfully fabricated and their coefficient of thermal expansion (CTE) as well as mechanical properties was investigated. The CTE of the composites decreases from 46 × 10^–6 to 14 × 10^–6 K^?1 when the ZrW₂O₈ volume fraction increases from 0 to 52 vol %. The CTE of the composites is analyzed by some theoretical models; Schapery's upper bound provides the best estimate of the reduction in CTE. The Barcol hardness of the composites increases with an increase in the ZrW₂O₈ volume fraction. The bending strength of the composites with 19–25 vol % of ZrW₂O₈ fillers shows a maximum value of 130 MPa, which is 45% larger than that of phenolic resin without fillers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Miscibility,UV resistance,thermal degradation,and mechanical properties of PMMA/SAN blends and their composites with MWCNTs

Poly(methyl methacrylate)/poly(styrene‐co‐acrylonitrile) (PMMA/SAN) blends, with varying concentrations, were prepared by melt‐mixing technique. The miscibility is ensured by fixing the acrylonitrile (AN) content of styrene acrylonitrile (SAN) as 25% by weight. The blends were transparent as well. The Fourier transform infrared spectroscopic (FTIR) studies did not reveal any specific interactions, supporting the well accepted ‘copolymer repulsion effect’ as the driving mechanism for miscibility. Addition of SAN increased the stability of PMMA towards ultraviolet (UV) radiations and thermal degradation. Incorporation of even 0.05% by weight of multi‐walled carbon nanotubes (MWCNTs) significantly improved the UV absorbance and thermal stability. Moreover, the composites exhibited good strength and modulus. However, at higher concentrations of MWCNTs (0.5 and 1% by weight) the thermo‐mechanical properties experienced deterioration, mainly due to the agglomeration of MWCNTs. It was observed that composites with 0.05% by weight of finely dispersed and well distributed MWCNTs provided excellent protection in most extreme climatic conditions. Thus, PMMA/SAN/MWCNTs composites can act as excellent light screens and may be useful, as cost‐effective UV absorbers, in the outdoor applications. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43628.     

Preparation and properties of polyethylene terephthalate/polyethylene/near infrared reflective pigment composites

Polyethylene terephthalate/high density polyethylene (PET/HDPE) composites containing a near infrared reflective (NIR, nickel antimony titanium yellow rutile) pigment was prepared using ethylene‐glycidyl methacrylate‐vinyl acetate (EGMA‐VA) as a compatibilizer to increase the infrared reflection of PET/HDPE and limit the thermal heat accumulation in light of environmental and energy conservation concerns. HDPE was premixed with NIR to form N‐HDPE masterbatch. A good interfacial bonding between PET matrix and HDPE dispersed phase with the help of compatibilizer was confirmed through Fourier transform‐infrared spectra, scanning electron microscopy, and torque rheometer. For PET/N‐HDPE composites, the major X‐ray diffraction peaks and melting behaviors remained unchanged, indicating the limited alternation of crystalline structure for the composite systems with or without compatibilizer. The observed increment in the crystallization temperature of PET for the investigated PET/N‐HDPE composites was mainly due to the nucleation role of both inorganic NIR and HDPE. Tensile strength and elongation at break for compatibilized cases at various N‐HDPE contents conferred higher values than those of the corresponding counterparts without compatibilizer. Yet, Young's modulus for compatibilized systems was about 40% lower than that for systems without compatibilizer, attributed to the rubbery nature of EGMA‐VA. With the inclusion of NIR into HDPE to form PET/N‐HDPE composites with or without EGMA‐VA compatibilizer, the values of reflectance increased to a great degree. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40830.     

Thermal,dielectric, and mechanical properties of SiC particles filled linear low‐density polyethylene composites

A thermally conductive linear low‐density polyethylene (LLDPE) composite with silicon carbide (SiC) as filler was prepared in a heat press molding. The SiC particles distributions were found to be rather uniform in matrix at both low and high filler content due to a powder mixing process employed. Differential scanning calorimeter results indicated that the SiC filler decreases the degree of crystallinity of LLDPE, and has no obvious influence on the melting temperature of LLDPE. Experimental results demonstrated that the LLDPE composites displays a high thermal conductivity of 1.48 Wm^?1 K^?1 and improved thermal stability at 55 wt % SiC content as compared to pure LLDPE. The surface treatment of SiC particles has a beneficial effect on improving the thermal conductivity. The dielectric constant and loss increased with SiC content, however, they still remained at relatively low levels (<10² Hz); whereas, the composites showed poorer mechanical properties as compared to pure LLDPE. In addition, combined use of small amount of alumina short fiber and SiC gave rise to improved overall properties of LLDPE composites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009