The effect of loading rates and particle geometry on compressive properties of polypropylene/zinc oxide nanocomposites: Experimental and numerical prediction

Compressive properties, of particulate filled polymer matrix composites, are affected (to a certain extent) by the geometry of the particles, as well as the loadingrates. Therefore, this article presents the results on the compressive properties of polypropylene/zinc oxide nanocomposites across strain rates from 10⁻² to 10⁻³ s⁻¹. The specimens were tested using a Universal Testing Machine for static loading and a conventional Split Hopkinson Pressure Bar apparatus for dynamic loading. Results show that the yield stress and 2.5% flow stress, of both PP/ZnO nanocomposites, showed a positive increment with increasing strain rates. However, the yield strain shows a contradictory pattern, where it decreased with increasing strain rates. PP/ZnO‐white seal recorded higher strain rate sensitivity, dissipation energy, stiffness, and strength properties, than that of PP/ZnO‐pharmaceutical, over a wide range of strain rates investigated. Interestingly, the Eyring theory almost agreed with the experimental results. Overall, based on the experimental and numerical results, we do believe that particle geometry, as well as strain rates, has a significant influence on the compressive properties of polypropylene/zinc oxide nanocomposites specimens. POLYM. COMPOS., 2012. © 2011 Society of Plastics Engineers     

Surface‐activated nanosilica treated with silane coupling agents/polypropylene composites: Mechanical,morphological, and thermal studies

This work reports the mechanical, morphological, and thermal properties of the polypropylene (PP) nanocomposites containing nanosilica (nano‐SiO₂) which were treated by different functional group silane coupling agents. Four types of silane coupling agents namely aminopropyltriethoxy silane (APTES), glycidyloxypropyltrimethoxy silane (GPTMS), trimethoxysilylpropyl methacrylate (TMPM), and dichlorodimethyl silane (DCMS) were used to modify the surface‐activated nanosilica. To enhance the effectiveness of the coupling, nanosilica was chemically activated and analyzed through FTIR and X‐ray photo electron spectroscopy (XPS). The highest tensile strength was recorded by the activated nanocomposites treated with APTES followed by nanocomposite treated with GPTMS, TMPM, and DCMS, respectively. The addition of silane coupling agents into nano‐SiO₂/PP system further improved the tensile modulus of the PP nanocomposites. From the transmission electron microscopy (TEM) analysis, activated nanosilica treated with APTES showed better nanosilica dispersion in the PP matrix and lesser agglomeration occurred when compared with the other silane coupling agents which were used in this study. Surface activation process does not effectively increase the degree of crystallinity and thermal stability on the PP nanocomposites. However, with the assistance of the surface treatment, it was found that the thermal behavior of the PP nanocomposites had been enhanced. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Polypropylene–nanosilica‐filled composites: Effects of epoxy‐resin‐grafted nanosilica on the structural,thermal, and dynamic mechanical properties

This article reports a comparative study of polypropylene (PP) nanocomposites synthesized with nanosilica (NS) and diglycidyl ether of bisphenol A, an epoxy‐resin‐grafted nanosilica (ENS), as nanofillers. These nanocomposites were prepared with the melt‐mixing method at a constant loading level of 2.5 wt %; this loading level was much lower than that used for fillers in conventional composites. The effects of pure NS and ENS on the thermal, structural, mechanical, and dynamic mechanical properties of PP were analyzed with wide‐angle X‐ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical analysis, and scanning electron microscopy. The transmission electron microscopy studies showed a better dispersion of ENS in the PP matrix, that is, in the polypropylene‐epoxy‐resin‐grafted nanosilica (PP–ENS) nanocomposite, in comparison with NS in the PP matrix, that is, in the polypropylene–nanosilica (PP–NS) nanocomposite. Also, the thermogravimetric analysis results showed a higher thermal stability for PP–ENS than PP–NS. Furthermore, the dynamic mechanical analysis studies showed an increase in the elastic modulus and glass‐transition temperature for PP–ENS with respect to PP–NS. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2117–2124, 2006     

Nanosilica‐reinforced Epoxidized natural rubber nanocomposites: Effect of Epoxidation level on morphological and mechanical properties

Epoxidized natural rubbers (ENRs) with three different epoxide contents (i.e., 20, 35, and 50 mol% indicated as ENR20, ENR35, and ENR50, respectively) were prepared. They were then reinforced with 3‐methyacryloxypropyl trimethoxysilane‐modified nanosilica (MPTS‐SiO₂). Influence of epoxide level in ENR molecules on morphological, mechanical, and dynamic mechanical properties of the ENR nanocomposites was investigated. The scanning electron microscopy results revealed larger agglomerates of SiO₂ were found in the ENR composites with higher epoxide content. Furthermore, the strength and moduli of the ENR nanocomposites increased with increasing epoxide content. However, the optimal tensile strength and elongation at break were observed in the nanocomposites with the intermediate level of epoxide contents. The correlation between the strength properties and the interfacial silica‐matrix adhesion indicated that the maximum interfacial adhesion of the nanocomposites was observed in the nanocomposite with ENR35. Also, DMA results indicated stronger interaction between ENR35 and MPTS‐SiO₂ due to higher storage modulus. POLYM. COMPOS., 38:1151–1157, 2017. © 2015 Society of Plastics Engineers     

Influence of incorporation sequence of silica nanoparticles on morphology,crystallization behavior,mechanical properties,and thermal resistance of melt blended thermoplastic natural rubber

Thermoplastic natural rubber nanocomposites based on epoxidized natural rubber (ENR) and polypropylene blends at a fixed blend ratio of 50/50 wt% reinforced with small amount (2.5 wt%) of nanosilica (SiO₂) were prepared by melt‐mixing through three different incorporation sequences in an internal mixer. The effects of incorporation techniques on morphology, crystallization behavior, mechanical properties, dynamic, rheological characteristics, and thermal resistance of thermoplastic natural rubber (TPNR) nanocomposites were investigated. It was found that the dispersion of nanosilica in TPNRs was significantly dependent on the incorporation sequence. In the case where SiO₂ was premixed in ENR before blending with polypropylene (PP), the final morphology showed the good dispersion of SiO₂ in ENR phase, while the SiO₂ particles were localized near the PP interface when SiO₂ was premixed the in PP first. Whereas, when the three components were simultaneously mixed, the SiO₂ particles were mainly dispersed in the PP phase. It was also found that the improvements of Young's modulus, tensile strength, damping behavior, and thermal stability of TPNR nanocomposites were more pronounced when the SiO₂ particles localized in ENR phase. By contrast, the presence of SiO₂ particles in PP domain either near the interface or inside the PP phase affected the reduction in crystallinity of PP phase and showed a negative effect on mechanical properties due to the poor interface interaction between PP and SiO₂ particles. POLYM. COMPOS., 33:1911–1920, 2012. © 2012 Society of Plastics Engineers     

Mechanical properties and morphologies of polypropylene composites synergistically filled by styrene‐butadiene rubber and silica nanoparticles

The mechanical properties and morphologies of PP/SBR/SiO₂ nanocomposites have been studied using mechanical testing, wide‐angle X‐ray diffraction (WAXD), polarizing optical microscopy (POM), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The mechanical properties of neat polypropylene can be considerably improved by synergistically filling with SiO₂ and SBR nanoparticles, especially for the notched Izod impact strength. The results from the WAXD, POM, SEM, DSC, and TGA measurements reveal that: (i) the β‐phase crystal structure of PP is formed when SiO₂ and SBR nanoparticles are synergistically filled with polypropylene and its formation plays a role for the enhancement of the impact strength for PP/SBR/SiO₂ nanocomposites; (ii) the dispersion of SiO₂ and SBR nanoparticles in PP/SBR/SiO₂ composites is homogeneous, indicating that synergistic incorporating method decreases the aggregation of nanoparticles and thus increases the sites for dissipation of shock for impact energy in PP/SBR/SiO₂ nanocomposites; (iii) the thermal analysis shows high thermal stability for the PP/SBR/SiO₂ nanocomposites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Characterization of nanosilica‐filled epoxy composites for electrical and insulation applications

We report in this article the results of nanosilica (SiO₂)‐filled epoxy composites with different loadings and their electrical, thermal, mechanical, and free‐volume properties characterized with different techniques. The morphological features were studied by transmission electron microscopy, and differential scanning calorimetry was used to investigate the glass‐transition temperature (T_g) of the nanocomposites. The properties of the nanocomposites showed that the electrical resistivity (ρ), ultimate tensile strength, and hardness of the composites increased with SiO₂ weight fraction up to 10 wt % and decreased thereafter; this suggested that the beneficial properties occurred up to this weight fraction. The temperature and seawater aging had a negative influence on ρ; that is, ρ decreased with increases in the temperature and aging. The free‐volume changes (microstructural) in the composite systems correlated with seawater aging but did not correlate so well with the mechanical properties. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

PMMA‐grafted‐silica/PVC nanocomposites: Mechanical performance and barrier properties

Poly(vinyl chloride) (PVC)/SiO₂ nanocomposites were prepared via melt mixture using a twin‐screw mixing method. To improve the dispersion degree of the nanoparticles and endow the compatibility between polymeric matrix and nanosilica, SiO₂ surface was grafted with polymethyl methacrylate (PMMA). The interfacial adhesion was enhanced with filling the resulting PMMA‐grafted‐SiO₂ hybrid nanoparticles characterized by scanning electron microscopy. Both storage modulus and glass transition temperature of prepared nanocomposites measured by dynamic mechanical thermal analysis were increased compared with untreated nanosilica‐treated PVC composite. A much more efficient transfer of stresses was permitted from the polymer matrix to the hybrid silica nanoparticles. The filling of the hybrid nanoparticles caused the improved mechanical properties (tensile strength, notched impact strength, and rigidity) when the filler content was not more than 3 wt %. Permeability rates of O₂ and H₂O through films of PMMA‐grafted‐SiO₂/PVC were also measured. Lower rates were observed when compared with that of neat PVC. This was attributed to the more tortuous path which must be covered by the gas molecules, since SiO₂ nanoparticles are considered impenetrable by gas molecules. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Coincorporation of nano‐silica and nano‐calcium carbonate in polypropylene

In this study, various polypropylene (PP) nanocomposites were prepared by melt blending method. The effects of different spherical nanofillers, such as 50 nm CaCO₃ and 20 nm SiO₂, on the linear viscoelastic property, crystallization behavior, morphology and mechanical property of the resulting PP nanocomposites were examined. Rheological study indicated that coincorporation of nano‐SiO₂ and nano‐CaCO₃ favored the uniform dispersion of nanoparticles in the PP matrix. Differential scanning calorimeter (DSC) and polarizing optical microscopy (POM) studies revealed that the coincorporation of SiO₂ and CaCO₃ nanoparticles could effectively improve PP crystallizability, which gave rise to a lower supercooling temperature (ΔT), a shorter crystallization half‐life (t_1/2) and a smaller spherulite size in comparison with those nanocomposites incorporating only one type of CaCO₃ or SiO₂ nanoparticles. The mechanical analysis results also showed that addition of two types of nanoparticles into PP matrix gave rise to enhanced performance than the nanocomposites containing CaCO₃ or SiO₂ individually. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Study on structure and properties of SSBR/SiO2 co‐coagulated rubber and SSBR filled with nanosilica composites

The morphological structure, glass transition, mechanical properties, and dynamic mechanical properties of star‐shaped solution‐polymerized styrene‐butadiene rubber (SSBR) synthesized by a multifunctional organic lithium initiator and SiO₂‐SSBR composite (N‐SSBR) prepared through adding a small amount of nanosilica modified by silane coupling agent to star‐shaped SSBR synthetic solution and co‐coagulating, and their nanocomposites filled with 20 phr nanosilica were investigated, respectively. The results showed that the silica particles were well dispersed with nanosize in N‐SSBR, which glass‐transition temperature (T_g) was 2°C higher than SSBR. N‐SSBR/SiO₂ nanocomposite exhibited lower Payne effect and internal friction loss, higher mechanical properties, and its T_g was 2°C higher than SSBR/SiO₂ nanocomposite. N‐SSBR might promote the dispersion of nanosilica powder in matrix and could be applied to green tire tread materials. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and properties of polylactide–silica nanocomposites

Poly(lactic acid) (PLA)/SiO₂ nanocomposites were prepared via melt mixing with a Haake mixing method. To improve the dispersion of nanoparticles and endow compatibility between the polymer matrix and nanosilica, SiO₂ was surface‐modified with oleic acid (OA). The interfacial adhesion of the PLA nanocomposites was characterized by field‐emission scanning electron microscopy. The storage modulus and glass‐transition temperature values of the prepared nanocomposites were measured by dynamic mechanical thermal analysis. The linear and nonlinear dynamic rheological properties of the PLA nanocomposites were measured with a parallel‐plate rheometer. The effects of the filling content on the dispersability of the OA–SiO₂ nanoparticles in the PLA matrix, the interface adhesion, the thermomechanical properties, the rheological properties, and the mechanical properties were investigated. Moreover, the proper representation of the oscillatory viscometry results provided an alternative sensitive method to detect whether aggregation formed in the polymeric nanocomposites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Static and dynamic compressive properties of polypropylene/zinc oxide nanocomposites

The effect of strain rate is widely recognized as an essential factor that influences the mechanical properties of polymer matrix composites. Despite its importance, no previous work has been reported on the high‐strain rate behavior of polypropylene/zinc oxide nanocomposites. Based on this, static and dynamic compression properties of polypropylene/zinc oxide nanocomposites, with particle contents of 1%, 3%, and 5% by weight, were successfully studied at different strain rates (i.e., 0.01 s^?1, 0.1 s^?1, 650 s^?1, 900 s^?1, and 1100 s^?1) using a universal testing machine and a split Hopkinson pressure bar apparatus. For standardization, approximately 24 nm of zinc oxide nanoparticles were embedded into polypropylene matrix for each of the tested polypropylene/zinc oxide nanocomposites. Results show that the yield strength, the ultimate strength, and the stiffness properties, of polypropylene/zinc oxide nanocomposites, were greatly affected by both particle loading and applied strain rate. Furthermore, the rate sensitivity and the absorbed energy of all tested specimens showed a positive increment with increasing strain rate, whereas the thermal activation volume showed a contrary trend. In addition, the fractographic analysis and particle dispersion of all composite specimens were successfully obtained using a field emisission scanning electron microscopy. POLYM. ENG. SCI., 54:949–960, 2014. © 2013 Society of Plastics Engineers     

Mechanical properties and morphology of polypropylene‐calcium carbonate nanocomposites prepared by dynamic packing injection molding

In this article, dynamic packing injection molding (DPIM) technology was used to prepare injection samples of Polypropylene‐Calcium Carbonate (PP/CaCO₃) nanocomposites. Through DPIM, the mechanical properties of PP/nano‐CaCO₃ samples were improved significantly. Compared with conventional injection molding (CIM), the enhancement of the tensile strength and impact strength of the samples molded by DPIM was 39 and 144%, respectively. In addition, the tensile strength and impact strength of the PP/nano‐CaCO₃ composites molded by DPIM increase by 21 and 514%, respectively compared with those of pure PP through CIM. According to the SEM, WAXD, DSC measurement, it could be found that a much better dispersion of nano‐CaCO₃ in samples was achieved by DPIM. Moreover, γcrystal is found in the shear layer of the DPIM samples. The crystallinity of PP matrix in DPIM sample increases by 22.76% compared with that of conventional sample. The improvement of mechanical properties of PP/nano‐CaCO₃ composites prepared by DPIM attributes to the even distribution of nano‐CaCO₃ particles and the morphology change of PP matrix under the influence of dynamic shear stress. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Dynamic properties of star‐shaped,solution‐polymerized styrene–butadiene rubber and its cocoagulated rubber‐filled with silica/carbon black

The dynamic properties, including the dynamic mechanical properties, flex fatigue properties, dynamic compression properties, and rolling loss properties, of star‐shaped solution‐polymerized styrene–butadiene rubber (SSBR) and organically modified nanosilica powder/star‐shaped styrene–butadiene rubber cocoagulated rubber (N‐SSBR), both filled with silica/carbon black (CB), were studied. N‐SSBR was characterized by ¹H‐NMR, gel permeation chromatography, energy dispersive spectrometry, and transmission electron microscopy. The results show that the silica particles were homogeneously dispersed in the N‐SSBR matrix. In addition, the N‐SSBR/SiO₂/CB–rubber compounds' high bound rubber contents implied good filler–polymer interactions. Compared with SSBR filled with silica/CB, the N‐SSBR filled with these fillers exhibited better flex fatigue resistance and a lower Payne effect, internal friction loss, compression permanent set, compression heat buildup, and power loss. The nanocomposites with excellent flex fatigue resistance showed several characteristics of branched, thick, rough, homogeneously distributed cross‐sectional cracks, tortuous flex crack paths, few stress concentration points, and obscure interfaces with the matrix. Accordingly, N‐SSBR would be an ideal matrix for applications in the tread of green tires. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40348.     

Propylene‐ethylene copolymer nanocomposites: Epoxy resin grafted nanosilica as a reinforcing filler

In the present work it is shown that low nanoparticle‐loaded polymer composites with improved mechanical performance can be prepared by a conventional melt blending technique in which the nanoparticles are chemically pregrafted by diglycidyl ether of bisphenol‐A (DGEBA). Two composites, each with 2.5 wt% filler, were developed. The first one was obtained by melt blending propylene‐ethylene copolymer (EP) with nanosilica in a co‐rotating sigma internal mixer. The second one was obtained by melt blending the same EP, but with DGEBA grafted nanosilica. The addition of epoxy resin grafted nanosilica to the polymer matrix produced a homogeneous dispersion of particles in the form of micro domains. The results of tensile tests indicate that epoxy resin grafted nanosilica particles (SiO₂‐g‐DGEBA) provide EP with stiffening, strengthening, and toughening effects at a 2.5 wt% loading level. This is a much lower level compared to most particulate fillers used for composites. There was no noticeable improvement in the mechanical properties when nanosilica was added to the neat polymer. However, the addition of SiO₂‐g‐DGEBA particles to the polymer matrix led to an increase of both elastic modulus and toughness (from 0.36 to 0.54 GPa, and 19.06 to 21.05 MJ/m³, respectively). POLYM. ENG. SCI., 26:806–812, 2005. © 2005 Society of Plastics Engineers     

Interfacial influence on mechanical properties of polypropylene/polypropylene‐grafted silica nanocomposites

Three types of polypropylene‐grafted silica (PGS‐2 K, PGS‐8 K and PGS‐30 K) with different grafting chain lengths were prepared. After melt‐blending PGS with polypropylene (PP), we studied the PP/PGS interface properties and the influence of PP/PGS interfaces on mechanical properties of nanocomposites. The strong matrix/particle interface was observed in PP/PGS‐30 K nanocomposites with 5 wt % particle loading as evidenced by 2.5 °C increased glass transition temperature (T_g) compared with neat PP, whereas the weak matrix/particle interface was observed in PP/PGS‐2 K nanocomposites with decreased T_g. The variations in the matrix/particle interfacial strength lead to a transition in the yield stress of nanocomposites. Compared with the unfilled PP, the yield stress of the PP/PGS‐2 K nanocomposites is decreased by 0.7 MPa, and the yield stress of the PP/PGS‐30 K nanocomposites is enhanced by 1.4 MPa. In addition, benefiting from good dispersion, the PP/PGS‐masterbatch nanocomposites with a strong matrix/particle interface not only exhibit increased Young's modulus and yield stress, but also the strain at break remains in line with the unfilled PP, which is in contrast to the conventional wisdom that the gain in modulus and strength must be at the expense of the decreased break strain. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45887.     

Effects of epoxy resin‐modified zinc‐ion‐coated nanosilica on structural,thermal and dynamic mechanical properties of propylene‐ethylene copolymer

This paper reports a comparative study of propylene–ethylene copolymer (EP) nanocomposites synthesized using zinc‐ion (Zn²⁺)‐coated nanosilica (ZNS) and the diglycidyl ether of bisphenol‐A (DGEBA, an epoxy resin)‐modified zinc‐ion‐coated nanosilica (EZNS) as nanofillers. These nanocomposites were prepared using the ‘melt mixing’ method at a constant loading level of 2.5 wt%. This loading level is much lower than that used for fillers in conventional composites. The EP nanocomposites were characterized using wide‐angle X‐ray diffractometer (WAXD), a thermo gravimetric analyzer (TGA), a differential scanning calorimeter (DSC), a dynamic mechanical analyzer (DMA) and scanning electron microscopy (SEM). DMA results showed a higher storage modulus for EP‐epoxy‐modified Zn²⁺‐coated nanosilica nanocomposite (EP‐EZNS) with respect to EP and EP‐Zn²⁺‐coated nanosilica nanocomposite (EP‐ZNS). In addition, TGA thermograms showed an increase in degradation temperature of EP in the presence of EZNS. Copyright © 2006 Society of Chemical Industry     

A study on the role of polypropylene fibers and silica nanoparticles on the compression properties of silicone rubber composites as a material of finger joint implant

In this study, different contents of SiO₂ nanoparticles and polypropylene fibers were added to silicone rubber matrix as a material of finger joint implants and mechanical properties of these composites were investigated before and after being soaked in simulated body fluid. Results of compression test revealed that compression stress of silicone rubber by addition of the 2 wt% silica and 2 wt% PP fibers increased from 0.98 to 1.9 and 2.37 MPa, respectively. These stresses decreased after being soaked in SBF and water absorption results proved this. Increasing silica contents caused an increase in water absorption while increasing PP fibers showed contrary behavior.     

Effect of phenol functionalization of carbon nanotubes on properties of natural rubber nanocomposites

This paper reports the results of studies on the effect of phenol functionalization of carbon nanotubes (CNTs) on the mechanical and dynamic mechanical properties of natural rubber (NR) composites. Fourier transform infrared spectrometry (FTIR) indicates characteristic peaks for ether and aromatic rings in the case of phenol functionalized CNT. Although differential scanning calorimetric (DSC) studies show no changes in the glass‐rubber transition temperature (T_g) of NR in the nanocomposites due to surface modification of CNT, dynamic mechanical studies show marginal shifting of T_g to higher temperature, the effect being pronounced in the case of functionalized CNT. Stress‐strain plots suggest an optimum loading of 5 phr CNT in NR formulations and the phenolic functionalization of CNT does not affect significantly the stress‐strain properties of the NR nanocomposites. The storage moduli register an increase in the presence of CNT and this increase is greater in the case of functionalized CNT. Loss tangent showed a decrease in the presence of CNT, and the effect is more pronounced in the case of phenol functionalized CNT. Transmission electron microscopy (TEM) reveals that phenol functionalization causes improvement in dispersion of CNT in NR matrix. This is corroborated by the increase in electrical resistivity in the case of phenol functionalized CNT/NR composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of nanoparticles on the morphology and properties of PET/PP in situ microfibrillar reinforced composites

In this work, the effect of SiO₂ nanoparticles on the morphology and properties of PET/PP in situ microfibrillar reinforced composites (MFC) obtained from slit die extrusion and hot stretching‐quenching was investigated. The scanning electron micrographs revealed that the nanoparticles could have different effects on microfibril formation of PET/PP MFC depending on their concentration. Addition of appropriate content of nanoparticles (e.g., 1.6 and 8 wt%) facilitated the PET droplet‐fibril transition during stretching due to the presence of nanosilica in the PP matrix, which increased the viscosity of PP matrix and then improved the droplet deformability. However, at higher loading (e.g., 12 wt%), the aggregation of silica nanoparticles around the PET droplets prevented disperse phase coalescence during drawing and then reduced the fibrillation ability of PET minor phase. The dynamic rheological test performed at 190°C showed that the increased spatial restriction of the nanoparticles improved the viscoelastic moduli and complex viscosity of PET/PP MFC. DSC results indicated that nanosilica had little heterogeneous nucleation effect on the PP matrix of PET/PP MFC. Additionally, nanoparticles could present drastic improvement in the degradation behavior of PET/PP MFC under thermo‐oxidative conditions and increased the modulus of PET/PP MFC. POLYM. COMPOS., 38:2718–2726, 2017. © 2015 Society of Plastics Engineers