Enhanced mechanical and thermal properties of nanodiamond reinforced low density polyethylene nanocomposites

In this study, the reinforcement effects of low-content hydrophilic nanodiamond (ND) on linear low-density polyethylene (PE) nanocomposites were investigated. ND was incorporated in PE via simple solution blending. The obtained PE/ND nanocomposites were characterized using scanning electron microscopy, ultraviolet–visible spectra, X-ray diffraction, tensile test, thermogravimetry, and differential scanning calorimetry. Generally, PE/ND nanocomposites with poor interfacial interaction cause large agglomerates, resulting in brittle and poor mechanical properties. Owing to the different natures of non-polar PE and polar ND, the higher the ND content, the larger the agglomerates formed in the nanocomposites. However, PE/ND nanocomposites show unique mechanical properties, that is, the Young's modulus, tensile strength, elongation at break, and toughness increased upon the incorporation of ND. The Young's modulus of the PE/ND nanocomposites exceeded the theoretical value calculated using the Halpin–Tsai model. In addition, the toughness increased by 18% at only 0.5 wt% ND loading. Furthermore, there was an increase in the thermal degradation temperature, melting temperature, and crystallization temperature.     

Combined effect of isophthalic acid and polyethylene glycol in polyethylene terephthalate polymer on thermal,mechanical, and gas transport properties

The objective of this article is to study the combined effect of isophthalic acid (IPA) and polyethylene glycol (PEG‐400) in PET polymer and film on thermal, mechanical, and gas transport properties. The purpose of developing this material is to reduce the melting point, improve mechanical, thermal, and gas barrier properties. The chosen raw materials, namely, IPA and PEG for copolyester synthesis will replace partially the acid and diol monomers of PET. The molar concentration of comonomers (IPA and PEG‐400) were varied from 2 to 50% and the result shows that the gas barrier properties (namely O₂, CO₂, N₂, and water vapor transmission rate), mechanical, and thermal properties were lesser than that of PET polymer. On improving the crystallinity of PET‐isophthalate‐PEG (PET‐IP) copolymer, barrier properties are improved than that of PET polymer. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of chlorine dioxide gas on physical,thermal, mechanical,and barrier properties of polymeric packaging materials

The effects of gaseous chlorine dioxide (ClO₂) on properties and performance of 10 selected polymeric packaging materials, including polyethylene (PE), biaxially oriented poly(propylene), polystyrene, poly(vinyl chloride), poly(ethylene terephthalate) (PET), poly(lactic acid), nylon, and a multilayer structure of ethylene vinyl acetate (EVA)/ethylene vinyl alcohol (EVOH), were evaluated. Physical, mechanical, barrier, and color properties as well as infrared (IR) spectra were assessed before and after polymer samples were exposed to 3600 ppmV ClO₂ gas at 23°C for 24, 168, and 336 h. The IR spectra of the ClO₂‐treated samples revealed many changes in their chemical characteristics, such as the formation of polar groups in the polyolefin, changes in functional groups, main chain scission degradation, and possible chlorination of several materials. The ClO₂‐treated PE samples showed a decrease in tensile properties compared with the untreated (control) films. Decreases in moisture, oxygen, and/or carbon dioxide barrier properties were observed in the treated PE, PET, and multilayer EVA/EVOH/EVA samples. A significant increase (P < 0.05) in the barrier to O₂ was observed in the ClO₂‐treated nylon, possibly the result of molecular reordering, which was found through an increase in the crystallinity of the material. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Improved mechanical and barrier properties of starch film with reduced graphene oxide modified by SDBS

Starch is regarded as one of the most promising biopolymers to replace the fossil resources. However, due to the poor mechanical properties, high sensitivity to humidity, and low barrier property, the development of starch‐based materials has been limited. In this study, they improved the mechanical and barrier properties of starch film with reduced graphene oxide (RGO) modified by sodium dodecyl benzene sulfonate (SDBS). The hydrophilia of modified RGO (r‐RGO) was improved and result in a good dispersion in oxidized starch (OS) matrix. The tensile strength of the r‐RGO‐4/OS film increased to 58.5 MPa which was more than three times of the OS film (17.2 MPa). Besides, both the water vapor and oxygen barrier properties of r‐RGO/OS film were improved greatly compared with OS and GO/OS films. Moreover, the r‐RGO/OS film could protect against UV light effectively due to its lightproof performance. In conclusion, the r‐RGO/OS composite film has great potential applications in packaging industry. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44910.     

Effect of shear rate on structural,mechanical, and barrier properties of chitosan/montmorillonite nanocomposite film

The dispersion of MMT‐Na⁺ (montmorillonite) layers in a chitosan polymer matrix, using the homogenization, was performed. The effect of shear rate was characterized on the mechanical, barrier, and structural properties of nanocomposites. Elongation at break (EAB) was unaffected by shear rate, which decreased after homogenization, increased above 13,000 rpm, however, tensile strength (TS) dramatically increased up to 59 MPa at 16,000 rpm. Water vapor permeability (WVP) and oxygen permeability (OP) of the homogenized nanocomposite decreased more than that of untreated nanocomposite and OP was not significantly changed above 16,000 rpm of shear rate. XRD result and TEM images indicated that three types of tactoids, exfoliation, and intercalation were generated and the largest distance of 18.87 Å between MMT‐Na⁺ layers was produced at 16,000 rpm. The results indicate that homogenization was a beneficial method for effectively dispersing MMT‐Na⁺ layers in a chitosan polymer matrix and that a shear rate of 16,000 rpm was the effective condition. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Impact of compression molding conditions on the thermal and mechanical properties of polyethylene

Compression molding is a current technique in polymer processing. Despite numerous studies, effect of molding pressure on physical properties has surprisingly not been fully investigated. In this study, the thermal and mechanical behavior of the compression‐molded polyethylene were thus explored to better grasp the relationship between processing parameters and ensuing properties. The effect of the molding temperature, pressure, cooling rate, and temperature profile on the tensile and flexural moduli as well as melting point of polyethylene was studied. We conclude that higher tensile and flexural moduli are obtained by increasing pressure and molding temperature, as well as decreasing the cooling rate. Our results were corroborated by X‐ray diffraction and differential scanning calorimetry measurements. Moreover, the use of a temperature gradient with different temperatures for the upper and bottom plates of the mold leads to asymmetric samples whose tensile and flexural moduli are improved. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46176.     

Mechanical properties,oxygen barrier property,and chemical stability of RE3NbO7 for thermal barrier coating

Rare earth niobate (RE₃NbO₇, RE = Dy, Y, Er, Yb) ceramics have shown extremely low thermal conductivity but remain questionable in high temperature thermal barrier coating (TBC) applications with high thermal, mechanical, and chemical loads. Herein, we comprehensively characterize the properties of rare earth niobates, including mechanical properties, oxygen barrier properties, chemical stability, etc. It is found that the oxygen conductivities of the rare earth niobates are three orders of magnitude lower than 7wt.% yttria-stabilized zirconia (YSZ), indicating a remarkable oxygen barrier property to avoid oxidation of underlying metallic components. The corrosion resistance of rare earth niobate against calcium-magnesium-aluminum silicate (CMAS) is also significantly better than that of YSZ. Together with the extremely low thermal conductivity, the rare earth niobates exhibit a combination of excellent high temperature properties, which may become a promising candidate material of high temperature TBC of next generation gas turbines.     

Effect of different compatibilizers on the mechanical and thermal properties of starch/polypropylene blends

Starch was treated with three kinds of compatibilizers (coupling agents or modifying agents), KH‐550, KH‐570, and glycerin monostearate. Blends of polypropylene (PP) and treated starch were prepared by a twin‐screw extruder. The effects of the starch before and after treatments and the kinds and contents of the compatibilizers on the mechanical and thermal properties of the PP/starch blends were investigated in this study. We found that the mechanical properties (tensile strength, impact strength, and elongation at break) of the blends were obviously improved with increasing content of different kinds of compatibilizers. Meanwhile, the most significant improvement in the mechanical properties was obtained in the samples containing just a 1 wt % loading of compatibilizers, and KH‐570 had the best improved effects among the different kinds of compatibilizers. The results of thermogravimetric analysis demonstrate that to some extent, the thermal stability of the PP/starch blends was improved after the addition of compatibilizers. Scanning electron microscopy showed that the dispersion of starch in the PP matrix and adhesion between the starch and PP matrix were obviously improved after the addition of compatibilizers. KH‐570 not only had the best improved effects among the coupling agents but also still acted as a similar plasticizer. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43332.     

Low‐density polyethylene/plasticized tapioca starch blends with the low‐density polyethylene functionalized with maleate ester: Mechanical and thermal properties

In this study, the mechanical and thermal properties of low‐density polyethylene (LDPE)/thermoplastic tapioca starch blends were determined with LDPE‐g‐dibutyl maleate as the compatibilizer. Mechanical testing for the evaluation of the impact strength and tensile properties was carried our as per standard ASTM methods. Thermogravimetric analysis and differential scanning calorimetry were also used to assess the thermal degradation of the blends. Scanning electron micrographs were used to analyze fracture and blend morphologies. The results show significant improvement in the mechanical properties due to the addition of the compatibilizer, which effectively linked the two immiscible blend components. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1109–1120, 2006     

Effect of mechanical recycling on crystallization,mechanical, and rheological properties of recycled high-density polyethylene and reinforcement based on virgin high-density polyethylene

This study investigated the effects of mechanical recycling on the crystallization, mechanical, thermal, and rheological properties of recycled high-density polyethylene (rHDPE), as well as vHDPE/rHDPE pellets and films made by different compositions. The results confirmed the presence of contaminants in rHDPEs, and the crystalline diameter of rHDPE is smaller than that of virgin high-density polyethylene (vHDPE), with diameters ranging from 0.60 to 0.72 μm. The content of 75 wt% vHDPE in rHDPE film could repair the defects of crystalline morphology to approximate that of vHDPE films and significantly improve the elongation at break. The temperature required for the transition from crystalline to amorphous state of rHDPE film was 2°C lower than that of vHDPE, and the crystallization time and crystallinity declined compared to that of vHDPE. For rheological performance, the apparent shear viscosity and melt fluidity of rHDPE were worse than those of vHDPE. The blending of low rHDPE with vHDPE is a feasible option not only to reduce plastic waste but also to maintain acceptable properties of the blend composition.     

Mechanical and thermal properties of low density polyethylene composites filled with dye‐loaded shell powder

To achieve reinforcement and coloring in one combined process of polymer production, a dye‐loaded shell powder (DPSP) based on Congo red and pearl shell powder was prepared and used as a versatile bio‐filler in low‐density polyethylene (LDPE). The DPSP was characterized by means of X‐ray diffraction, Fourier transform infrared spectroscopy and thermogravimetric analysis. The mechanical, thermal, and colorimetric properties of prepared LDPE/DPSP composites were investigated as well. Adding DPSP could significantly increase the strength and stiffness of LDPE composites while giving an outstanding coloring performance. Moreover, the impact strength of LDPE composites was improved at lower filler loading rate, and the maximum incorporation content could reach 10 wt % with a good balance between toughness and stiffness of LDPE composites. The thermal performance studies confirmed an increase in thermal stability and heat resistance of LDPE composites with the incorporation of DPSP. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44118.     

Effect of different nanoparticles on thermal,mechanical and dynamic mechanical properties of hydrogenated nitrile butadiene rubber nanocomposites

Organically modified and unmodified montmorillonite clays (Cloisite NA, Cloisite 30B and Cloisite 15A), sepiolite (Pangel B20) and nanosilica (Aerosil 300) were incorporated into hydrogenated nitrile rubber (HNBR) matrix by solution process in order to study the effect of these nanofillers on thermal, mechanical and dynamic mechanical properties of HNBR. It was found that on addition of only 4 phr of nanofiller to neat HNBR, the temperature at which maximum degradation took place (T_max) increased by 4 to 16°C, while the modulus at 100% elongation and the tensile strength were enhanced by almost 40–60% and 100–300% respectively, depending upon nature of the nanofiller. It was further observed that T_max was the highest in the case of nanosilica‐based nanocomposite with 4 phr of filler loading. The increment of storage modulus was highest for sepiolite‐HNBR and Cloisite 30B‐HNBR nanocomposites at 25°C, while the modulus at 100% elongation was found maximum for sepiolite‐HNBR nanocomposite at the same loading. A similar trend was observed in the case of another grade of HNBR having similar ACN content, but different diene level. The results were explained by x‐ray diffraction, transmission electron microscopy, and atomic force microscopy studies. The above results were further explained with the help of thermodynamics. Effect of different filler loadings (2, 4, 6, 8, and 16 phr) on the properties of HNBR nanocomposites was further investigated. Both thermal as well as mechanical properties were found to be highest at 8 phr of filler loading. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effects of titanate treatment on morphology and mechanical properties of graphene nanoplatelets/high density polyethylene nanocomposites

The effect of graphene nanoplatelets (GNPs) and titanate coupling agent on morphology and mechanical properties of high density polyethylene (HDPE) nanocomposites was investigated. The titanate has a tendency to link chemically with the two dissimilar species GNPs and HDPE via proton coordination to generate a complete continuous phase for stress/strain transfer via the elimination of air voids and hydrophobicity. The interaction of titanate with GNPs and HDPE was effective to improve the dispersion of GNPs in HDPE composites. At constant weight (1 wt %) of titanate treatment for 2 and 5 wt % HDPE composites, we clearly observed a significantly high value of tensile strength and elongation at break than untreated composites. Particularly, composite containing 2 wt % GNPs in HDPE with titanate showed 66.5% improvement of the ultimate tensile strength and an enormously high value of elongation at break. The effect of GNPs dispersion and orientation in HDPE for the mechanical reinforcement was also evaluated based on the experimental modulus data to theoretical predictions made using the Halpin‐Tsai model. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42073.     

Influence of octyl substituted octakis(dimethylsiloxy)octasilsesquioxane on the morphology and thermal and mechanical properties of low density polyethylene

Low density polyethylene (LDPE) was melt blended with octyl substituted octakis(dimethylsiloxy)octasilsesquioxane (AS8) prepared in high yield by hydrosilylation of octene with octakis(hydrodimethylsiloxy)octasilsesquioxane. Two procedures were used to incorporate AS8 into LDPE at nanolevel and their efficiency was investigated by X‐ray diffraction (XRD), scanning electron microscopy, atomic force microscopy (AFM), differential scanning calorimetry, thermogravimetry and mechanical characterization. A slight increase of crystallite mean dimensions was observed by XRD in both types of LDPE‐AS8 composites compared with neat LDPE. Better AS8 dispersion was observed by AFM in the composite prepared by the first procedure and the increase of both tensile strength and elongation at break in this composite confirmed the nanolevel dispersion and interface improvement in this case. AS8 influence in the final stages of polyethylene fracture was illustrated by AFM of elongated tensile specimens and a new mechanism of AS8 action was suggested. An interesting behavior consisting of simultaneous improvement of elastic modulus, strength and ductility was detected in the low range of polyhedral oligomeric silsesquioxane concentration in LDPE (0.5 wt%). © 2013 Society of Chemical Industry     

Mechanical and thermal properties of high‐density polyethylene toughened with glass beads

Glass beads were used to improve the mechanical and thermal properties of high‐density polyethylene (HDPE). HDPE/glass‐bead blends were prepared in a Brabender‐like apparatus, and this was followed by press molding. Static tensile measurements showed that the modulus of the HDPE/glass‐bead blends increased considerably with increasing glass‐bead content, whereas the yield stress remained roughly unchanged at first and then decreased slowly with increasing glass‐bead content. Izod impact tests at room temperature revealed that the impact strength changed very slowly with increasing glass‐bead content up to a critical value; thereafter, it increased sharply with increasing glass‐bead content. That is, the Izod impact strength of the blends underwent a sharp transition with increasing glass‐bead content. It was calculated that the critical interparticle distance for the HDPE/glass‐bead blends at room temperature (25°C) was 2.5 μm. Scanning electron microscopy observations indicated that the high impact strength of the HDPE/glass‐bead blends resulted from the deformation of the HDPE matrix. Dynamic mechanical analyses and thermogravimetric measurements implied that the heat resistance and heat stability of the blends tended to increase considerably with increasing glass‐bead content. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2102–2107, 2003     

Thermal and mechanical properties of linear low‐density polyethylene/low‐density polyethylene/wax ternary blends

The thermal and mechanical properties of uncrosslinked three‐component blends of linear low‐density polyethylene (LLDPE), low‐density polyethylene (LDPE), and a hard, paraffinic Fischer–Tropsch wax were investigated. A decrease in the total crystallinity with an increase in both LDPE and wax contents was observed. It was also observed that experimental enthalpy values of LLDPE in the blends were generally higher than the theoretically expected values, whereas in the case of LDPE the theoretically expected values were higher than the experimental values. In the presence of higher wax content there was a good correlation between experimental and theoretically expected enthalpy values. The DSC results showed changes in peak temperature of melting, as well as peak width, with changing blend composition. Most of these changes are explained in terms of the preferred cocrystallization of wax with LLDPE. Young's modulus, yield stress, and stress at break decreased with increasing LDPE content, whereas elongation at yield increased. This is in line with the decreasing crystallinity and increasing amorphous content expected with increasing LDPE content. Deviations from this behavior for samples containing 10% wax and relatively low LDPE contents are explained in terms of lower tie chain fractions. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1748–1755, 2005     

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     

Implications of melt compatibility/incompatibility on thermal and mechanical properties of metallocene and Ziegler–Natta linear low density polyethylene (LLDPE) blends with high density polyethylene (HDPE): influence of composition distribution and branch content of LLDPE

In this paper, the implications of melt compatibility on thermal and solid‐state properties of linear low density polyethylene/high density polyethylene (LLDPE/HDPE) blends were assessed with respect to the effect of composition distribution (CD) and branch content (BC). The effect of CD was studied by melt blending a metallocene (m‐LLDPE) and a Ziegler‐Natta (ZN) LLDPE with the same HDPE at 190 °C. Similarly, the effect of BC was examined. In both cases, resins were paired to study one molecular variable at a time. Thermal and solid‐state properties were measured in a differential scanning calorimeter and in an Instron mechanical testing instrument, respectively. The low‐BC m‐LLDPE (BC = 14.5 CH₃/1000 C) blends with HDPE were compatible at all compositions: rheological, thermal and some mechanical properties followed additivity rules. For incompatible high‐BC (42.0 CH₃/1000 C) m‐LLDPE‐rich blends, elongation at break and work of rupture showed synergistic effects, while modulus was lower than predictions of linear additivity. The CD of LLDPE showed no significant effect on thermal properties, elongation at break or work of rupture; however, it resulted in low moduli for ZN‐LLDPE blends with HDPE. For miscible blends, no effect for BC or CD of LLDPE was observed. The BC of LLDPE has, in general, a stronger influence on melt and solid‐state properties of blends than the CD. Copyright © 2004 Society of Chemical Industry     

Effects of a coupling agent on the mechanical and thermal properties of ultrahigh molecular weight polyethylene/nano silicon carbide composites

Ultra‐high‐molecular‐weight polyethylene (UHMWPE)/nano silicon carbide (nano‐SiC) composites were prepared by compression molding. The effects of a coupling agent and the content of the filler on the filler dispersion and the mechanical and thermal properties of the composites were investigated. The results show that the mechanical properties of the composites first increased and then decreased with increasing SiC content. The macromolecular coupling agent exhibited a much better reinforcing effect than the small‐molecule coupling agent. The tensile strength of the composites with 3‐aminopropyltriethoxysilane (KH550), γ‐methacryloxypropyltrimethoxysilane (KH570), and silicone powders reached its maximum value when the silicon carbide (SiC) content was 3%. We found that a web of the UHMWPE/SiC/coupling agent was formed and played a significant role in improving the heat resistance of the composites. In addition, appropriate amounts of SiC could increase the crystallinity of UHMWPE via a process of heterogeneous nucleation. The comprehensive performance of the KH550/silicone/SiC/UHMWPE composites was the best. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Studies on mechanical and thermal properties of ternary blends of polyethylenes. I

Six film samples of varying compositions of linear low‐density polyethylene (LLDPE), 10–35 wt %, and high‐density polyethylene (HDPE), 40–65 wt %, having a fixed percentage of low‐density polyethylene (LDPE) at 25 wt % were extruded by melt blending in a single‐screw extruder (L/D ratio = 20 : 1) of uniform thickness of 2 mil. The tensile strength, elongation at break, and impact strength were found to increase up to 60 wt % HDPE addition, starting from 40 wt % HDPE, in the blends and then decreased. The blend sample B‐500 was found to be more thermally stable than its counterparts. The appearance of a single peak beyond 45 wt % HDPE content in the blend in dynamic DSC scans showed the formation of miscible blend systems and this was further confirmed by scanning electron microscopic analysis. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1691–1698, 2005