Sound isolation properties of polycarbonate/clay and polycarbonate/silica nanocomposites

The soundproofing properties of polycarbonate (PC)/nanoclay and PC/nanosilica nanocomposites were studied through testing and theoretical analysis. Nanocomposite sheets with a 3 mm thickness were fabricated by direct hot-compression molding process. The nanoclay and nanosilica particles were incorporated into the PC matrix by a twin-screw extruder. The dispersion efficiency of 1, 3 and 5 wt% nanoclay and nanosilica in the PC matrix was investigated by transmission electron microscopy. Dynamic mechanical analysis was performed for evaluation of mechanical properties of nanocomposites. Sound transmission loss (STL) was measured by an impedance tube over the frequency range of 1600–6300 Hz, and further employed in sound proofing characterizations of nanocomposites. A new finite element model was developed to model the sound transmission loss in impedance tube test. The results showed that the PC/3 wt% nanoclay and 3 wt% nanosilica nanocomposites had an average maximum increase of 5.5 and 6 dB in STL values in the stiffness control region (1600–3600 Hz), respectively. On the other hand, the PC/3 wt% nanoclay and PC/3 wt% nanosilica nanocomposites showed the same sound isolation characteristics in the frequency range of 1600–3600 Hz. In addition, the finite element model developed for modeling the sound transmission loss in the impedance tube demonstrated a good correlation between the theoretical curves and the experimental results in the stiffness control region for both nanocomposites.     

Alendronic acid bearing ketone-formaldehyde resin and clay nanocomposites for fire-retardant polyurethanes

Cyclohexanone-formaldehyde resin and acetophenone-formaldehyde resin were in situ modified with sodium alendronate and the nanocomposites of cyclohexanone-formaldehyde resin with sepiolite and montmorillonite by adding the nanoclay into the resin formation media. The analysis of nanocomposites of nanoclay in the resin were carried out with X-ray diffraction. Exfoliated nanocomposites containing as much as 5 wt% sepiolite were obtained while the nanocomposites of montmorillonite were intercalated. The nanocomposites of alendronic acid-modified ketone-formaldehyde resin containing as much as 20 wt% sepiolite or 10 wt% montmorillonite were successfully produced in situ. Fourier transform infrared and nuclear magnetic resonance spectroscopies (NMR) were used for the structural characterization of the modified resins. The alendronic acid modified resins and their nanocomposites with the clays were used to produce reactive non-toxic fire retardant rigid polyurethane foam. The polyurethane foam containing alendronic acid-modified acetophenone-formaldehyde resin had a residue of 20% in the thermogravimetric analysis and was HB-grade in the horizontal fire test (HB) and self-extinguished in about 3–5 s during the test. Polyurethane foams containing alendronic acid and the nanoclay with the limiting oxygen index value of 20.8 were achieved.     

Mechanical response and rheological properties of polycarbonate layered‐silicate nanocomposites

The effect of clay loading on the mechanical behavior and melt state linear viscoelastic properties of intercalated polycarbonate (PC) nanocomposites was investigated. At low frequencies, the linear dynamic oscillatory moduli data revealed diminished frequency dependence with increasing nanoclay loading. The 3.5 and 5 wt% clay nanocomposites exhibited dramatically altered relaxation behavior, from liquid‐like to pseudo‐solid–like, compared to the pure PC and the 1.5 wt% clay nanocomposite. Thermal degradation of PC resulted from the melt compounding of organo‐modified nanoclays was evident from the reduction in the glass transition temperature and molecular weight of the PC nanocomposites. These nanocomposites also exhibited a significant decrease in the extent of tensile elongation and ductility with respect to the nanoclay incorporation. A concomitant decrease in the rheological properties at high frequencies was also observed, and was consistent with the lowering of the molecular weight of PC, particularly near or above the percolation threshold of nanoclay. These nanocomposites, nevertheless, exhibited elastic‐plastic deformation in compression, regardless of nanoclay content. Polym. Eng. Sci. 44:825–837, 2004. © 2004 Society of Plastics Engineers.     

Effect of sodium montmorillonite nanoclay on the water absorbency and cationic dye removal of carrageenan-based nanocomposite superabsorbents

Nanocomposite superabsorbents were synthesized by simultaneously solution copolymerization of acrylamide (AAm) and sodium acrylate (Na-AA) in the presence of carrageenan biopolymer and sodium montmorillonite (Na-MMt) nanoclay. Potassium persulfate (KPS) and methylenebisacrylamide (MBA) were used as initiator and crosslinker, respectively. The structure and morphology of the nanocomposites were investigated using XRD, FTIR, scanning electron microscopy (SEM), and TEM techniques. The influence of nanoclay and carrageenan contents as well as monomer weight ratios on the degree of swelling of nanocomposites was studied. The optimum water absorbency was obtained at 10 wt% of clay, 10 wt% of carrageenan, and 1:1 of monomers weight ratio. The obtained nanocomposites were examined to remove of crystal violet (CV) cationic dye from water. The effect of carrageenan and clay content on the speed of dye adsorption revealed that while the rate of dye adsorption is enhanced by increasing the clay content up to 14 wt% of clay, it was decreased as the carrageenan increased in nanocomposite composition. The results showed that the pseudo-second-order adsorption kinetic was predominated for the adsorption of CV onto nanocomposites. The experimental equilibrated adsorption capacity of nanocomposites was analyzed using Freundlich and Langmuir isotherm models. The results corroborated that the experimental data fit the Freundlich isotherm the best.     

Fabrication and characterization of functionally graded nanoclay/glass fiber/epoxy hybrid nanocomposite laminates

In this work, hardness, tensile, impact, bearing strength and water absorption tests were performed to study the mechanical properties of stepwise graded and non-graded hybrid nanocomposites. Three different stepwise graded nanocomposites and one non-graded (homogeneous) nanocomposite with the same geometry and total nanoclay content of 10 wt% were designed and prepared. Moreover, one neat glass fiber laminate was manufactured. The results of the tests indicated that addition of the graded and non-graded nanoclay improves hardness over neat glass fiber reinforcement. The maximum increase in hardness of about 53% over neat specimen is obtained for specimens that have the highest weight percentage (2 wt%) of the clay nanoparticles on its surface (S-specimen and the side of F-specimen that reinforced with 2 wt% nanoclay). The gradation process results in an increase in hardness of about 11% compared with non-graded (homogeneous) specimen. In addition, an improvement of 11.9% in strain-to-failure is achieved with specimen having greatest amount of nanoclay in the middle over neat glass fiber/epoxy composite. The other nanoclay-filled glass fiber composites have strain-to-failure close to neat glass fiber/epoxy. The addition of nanoclay reinforcement has insignificant effect on ultimate tensile strength, tensile modulus, water absorption, bearing strength and impact strength compared with neat glass fiber/epoxy.     

Improvement of Tensile and Flexural Properties in Epoxy/Clay Nanocomposites Reinforced with Weave Glass Fiber Reel

The tensile strength, tensile modulus, flexural strength and flexural modulus properties were investigated on epoxy/clay nanocomposites to assess the influence of nanoclay. Mechanical properties were significantly increased due to an increase in clay content up to 5 wt%, and decreased with a further increase in clay content. Optimal improvement of properties was observed with increased clay content up to 5 wt%. Duo properties of the glass fiber were improved by clay addition due to the improved interface between the glass fiber and epoxy. SEM analysis was conducted on different fractured surfaces to study the mechanical behavior.     

Biodegradable PBAT/Starch Nanocomposites

Starch-based biodegradable banocomposites of poly(butylene adipate-co-terephthalate) [PBAT] and organically modified nanoclays were prepared using melt intercalation technique in Haake Torque Rheocord 9000. Two different organically modified nanoclays Cloisite C20A and Cloisite C30B at various wt% (1, 3, 5) have been used for fabrication of nanocomposites. Starch was gelatinized to prepare thermoplastic starch (TPS) for increasing the compatibility with the PBAT matrix. Subsequently, films of PBAT/TPS blends at various TPS contents (10, 20, 30, 40) wt% and PBAT/TPS Organoclay biodegradable blend nanocomposites at different wt% of nanoclays were prepared using solvent casting method. The interfacial region between the biodegradable polymer matrix and the clays were also modified with grafting of Maleic anhydride (MA) with PBAT chains, during melt blending through two stage reactive extrusion process. Mechanical tests revealed an increase in tensile modulus and elongation at break with the incorporation of 30 wt% TPS and C30B nanoclay to the tune of 44.45% and 776.9% as compared with PBAT matrix. PBAT/TPS30 wt%/C30B3wt% shows maximum tensile modulus and elongation at break due to intercalation of silicate layers resulting from similarity in the surface polarity and interactions of C30B with TPS. Morphology of PBAT/TPS30%/C30B3% biodegradable blend nanocomposite studied using WAXD and SEM indicated intercalation and improved dispersion of TPS within PBAT with incorporation of C30B. Dynamical mechanical analysis of PBAT/TPS/C30B biodegradable blend nanocomposite revealed an increase of storage modulus and glass transition temperatures of PBAT with addition of nanoclays. Further Biodegradation test also confirmed higher biodegradability of PBAT in presence of TPS and C30B.     

Modified preparation of HDPE/clay nanocomposite by in situ polymerization using a metallocene catalyst

In this study, preparation of high-density polyethylene (HDPE)/clay nanocomposite by in situ polymerization of ethylene using a zirconocene catalyst (bis-(cyclopentadienyl) zirconium dichloride (Cp₂ZrCl₂)) was investigated. To obtain higher efficiency, nanoclay particles (Na-montmorillonite) were modified by ammonia (NH₃), NH₃/methylaluminoxane (MAO), NH₃/dodecylamine (DDA), and NH₃/MAO/DDA systems. The results showed that the activity of the catalyst supported on the nanoclay particles modified by NH₃/MAO (762 g_p/mmol (Zr) t [atm]) was higher than that of the one supported on the unmodified nanoclay as well as the other prepared modified nanoclay-supported catalyst systems. The catalyst activities versus MAO concentration in NH₃/MAO treatment system and versus DDA concentration in NH₃/DDA system showed a maximum. Unexpectedly, a very low catalyst activity (180 g_p/mmol(Zr) t [atm]) was obtained using NH₃/MAO/DDA system. X-ray diffraction patterns showed that the HDPE/clay nanocomposites prepared by NH₃/MAO/DDA treatment system had less intercalated structure. Fourier transform infrared (FTIR) spectroscopy confirmed that water molecules of the nanoclay particles were reduced by NH₃ modification. DSC results revealed that crystallinity of the HDPE/clay nanocomposites increased with the modification of the nanoclay particles. The maximum degree of crystallinity of 80.8% was obtained for HDPE/clay nanocomposites prepared by the nanoclay modified by NH₃. In addition, nanoclay modification with NH₃, NH₃/MAO, and NH₃/DDA systems resulted in higher thermal decomposition temperature (~30 °C higher than 480 °C of the unmodified one). Such increase was not observed for the NH₃/MAO/DDA treatment system. Dynamic mechanical analysis showed an increase in the elastic modulus of the nanocomposite samples prepared by modified nanoclay particles, as well. Meanwhile, modification of the nanoclay particles by NH₃ led to the highest elastic behavior compared to the other modification systems. It was about 4.6 GPa which was 28% higher than the elastic modulus of the nanocomposite prepared by unmodified nanoclay particles.     

Investigation of the high velocity impact behavior of nanocomposites

In this article, the ballistic behavior of the glass/epoxy/nanoclay hybrid nanocomposites is studied. The fiber glass used is a plain weave 200 g/m², while the nanoclay is an organically modified montmorillonite nanoclay (Closite 30B). The epoxy resin system is made of Epon 828 as the epoxy prepolymer and Jeffamine D‐400 as the curing agent. 0, 3, 5, 7, and 10 wt% of nanoclay particles are dispersed in the epoxy resin. Ballistic tests are performed using flat‐ended projectiles in impact velocities 134 m/s and 169 m/s. The results show that the energy absorption capability and mechanical properties of the composite can be significantly enhanced by adding nanoparticles. When the impact velocity is 134 m/s, near than the ballistic limit, the most increase in the energy absorption capability is observed in 3 wt% nanoclay while with the impact velocity 169 m/s, beyond the ballistic limit, the highest increase is observed in 10 wt% nanoclay. POLYM. COMPOS., 37:1173–1179, 2016. © 2014 Society of Plastics Engineers     

Electrospun PVDF/MWCNT/OMMT hybrid nanocomposites: preparation and characterization

Electrospinning technique was employed to prepare neat PVDF, nanoclay-PVDF and carbon nanotube (MWCNT)-PVDF nanocomposites, and nanoclay-carbon nanotube-PVDF hybrid nanocomposites. A mixture of dimethyl formamide/acetone (60/40) was used to fluidize the polymer and nanofillers. Electrospinning process was conducted under optimized conditions. Maximum modification was achieved at 0.15 wt% nanofiller. Rheological measurements on the prepared solutions revealed decreased material functions in the presence of nanoclay, whereas the rheological properties of MWCNT-PVDF solution did not show any significant reduction compared with those of neat PVDF solution. The behaviors of the hybrid nanocomposite solutions, though dependent on their composition and their material functions, increased with MWCNT concentration. These differences, together with variations in electrical properties of nanoclay and MWCNT, led to changes in morphology of the fiber during electrospinning process. Under electrospinning conditions designed for neat PVDF solution, mats with beads and with the highest fiber diameter were produced. Meanwhile, incorporation of both nanoclay and MWCNT into the solutions resulted in bead-free fibers with thinner diameter. Fourier transformed infrared spectrophotometry (FTIR) and X-ray diffractometry (XRD) were used to measure the β-phase crystalline content in electrospun mats. Complete agreement was found between the FTIR and XRD results. The lowest and highest β-phase contents were obtained for neat PVDF mat and hybrid nanocomposite mat containing 0.1 wt% clay, respectively. The mixing procedure of nanofillers and the PVDF solution was also found to be important. In case of hybrid nanocomposites, more β-crystals were formed when the nanoclay was first mixed in the absence of MWCNT.     

Improved mechanical and thermal properties of bamboo–epoxy nanocomposites

Natural fiber‐reinforced hybrid composites based on bamboo/epoxy/nanoclay were prepared. Ultrasound sonication was used for the dispersion of nanoclay in the bamboo–epoxy composites. The morphology of bamboo–epoxy nanocomposites was investigated by using scanning electron microscopy, transmission electron microscopy, and X‐ray diffraction. The results show that there exists an optimum limit in which the mechanical properties of composites improved by continuously increasing the nanoclay content. The tensile and flexural strength of bamboo–epoxy nanocomposites with 3 wt% nanoclay increased by 40% and 27%, respectively, as compared to pure composites. The highest value of impact strength was obtained for 1 wt% nanoclay content bamboo–epoxy nanocomposites. The enhanced impact strength of bamboo–epoxy nanocomposites was one of the key advantages brought by nanofiller. The results show that incorporation of nanoclay substantially increases the water resistance capability and thermal stability of bamboo–epoxy nanocomposites. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Improved thermal properties of jute fiber‐reinforced polyethylene nanocomposites

The thermal behavior of chemically modified jute fiber‐reinforced polyethylene (PE) nanocomposites was investigated. Nanocomposites were prepared by hot press molding technique using different fiber loadings (5, 10, 15, and 20 wt%) for both treated and untreated fibers. Jute fibers were chemically modified with benzene diazonium salt to increase their compatibility with the PE matrix. Surface and thermal properties were subsequently characterized. Fourier transform infrared spectroscopy and scanning electron microscopy analysis were used to study the surface morphology. Thermogravimetric analysis (TGA) and differential scanning calorimetry were carried out for thermal characterization. Fourier transform infrared spectroscopy and scanning electron microscopy study showed interfacial interaction among jute fiber, PE, and nanoclay. It was observed that, at optimum fiber content (15 wt%), treated jute fiber‐reinforced composites showed better thermal properties compared with that of untreated ones and also that nanoclay‐incorporated composites showed enhanced higher thermal properties compared with those without nanoclay. POLYM. COMPOS., 38:1266–1272, 2017. © 2015 Society of Plastics Engineers     

Analysis of synergistic effect of nanozinc/nanoclay additives on the corrosion performance of zinc‐rich polyurethane nanocomposite coatings

The aim of this study was to analyze the synergistic effect of clay and zinc nanopigments. Therefore different percentages of Montmorillonite clay nanolayers were added to zinc‐rich polyurethane nanocomposites. Ultrasonication process was used to prepare polyurethane/nanozinc/nanoclay nanocomposites. Then coatings were applied on steel panels with composition of 10 wt% nanozinc and 0.5, 1, 1.5, and 2 wt% nanoclay. TEM and XRD were used to analyze the structural characteristics of the nanocomposites. The results of the structure analysis revealed the size of nanomaterials and confirmed the appropriate dispersion in polymer matrix. The anticorrosive properties of the nanocomposites were investigated using salt fog test and electrochemical impedance spectroscopy (EIS). The results of EIS showed that addition of clay nanolayers improves the corrosion resistance of coatings and the best corrosion performance obtained for the nanocomposite sample with 2 wt% nanoclay. Also, according to the results of the salt spray test, the sample with 2 wt% nanoclay showed the least H₂O penetration and exfoliation adjacent to the scratches. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Mechanical,thermal and dynamic‐mechanical behavior of banana fiber reinforced polypropylene nanocomposites

Natural fiber‐reinforced nanocomposites based on polypropylene/nanoclay/banana fibers were fabricated by melt mixing in a twin‐screw extruder followed by compression molding in this current study. Maleic anhydride polypropylene copolymer (MA‐g‐PP) was used as a compatibilizer to increase the compatibility between the PP matrix, clay, and banana fiber to enhance exfoliation of organoclay and dispersion of fibers into the polymer matrix. Variation in mechanical, thermal, and physico‐mechanical properties with the addition of banana fiber into the PP nanocomposites was investigated. It was observed that 3 wt% of nanoclay and 5 wt% of MA‐g‐PP within PP matrix resulted in an increase in tensile and flexural strength by 41.3% and 45.6% as compared with virgin PP. Further, incorporation of 30 wt% banana fiber in PP nanocomposites system increases the tensile and flexural strength to the tune of 27.1% and 15.8%, respectively. The morphology of fiber reinforced PP nanocomposites has been examined by using scanning electron microscopy and transmission electron microscopy. Significant enhancement in the thermal stability of nanocomposites was also observed due to the presence of nanoclay under thermogravimetric analysis. Dynamic mechanical analysis tests revealed an increase in storage modulus (E′) and damping factor (tan δ), conforming the strong interaction between nanoclay/banana fiberand MA‐g‐PP in the fiber‐reinforced nanocomposites systems. POLYM. COMPOS., © 2011 Society of Plastics Engineers.     

Synthesis of β-myrcene-based macroporous nanocomposite foams: Altering the morphological and mechanical properties by using organo-modified nanoclay

Organo-modified nanoclay incorporated high internal phase emulsions (HIPEs) were successfully used for the preparation of macroporous nanocomposite foams. Due to the aim of obtaining mechanically improved foams, HIPEs were prepared by using a monomer mixture composed of β-myrcene and ethylene glycol dimethacrylate. Accordingly, two groups of macroporous nanocomposite foams were synthesized depending on the nanoclay type. The morphological analysis demonstrated that the pore openness of the resulting nanocomposites were significantly improved due to the decrease in the average cavity size and increase in the interconnected pore size. In terms of mechanical properties, it was found that filling 1 wt% of nanoclay which is surface modified by hydrogenated tallow lead to a 33% of increment in the compression modulus, as compared to the neat foam. However, loading 5 wt% of nanoclay having octadecylamine and aminopropyltriethoxysilane surface groups caused only 11% of increment in the compression modulus, as compared to the neat foam.     

Morphology and viscoelastic behavior of silicone rubber/EPDM/Cloisite 15A nanocomposites based on Maxwell model

Blends of silicone rubber (SR) and ethylene propylene diene monomer (EPDM) are immiscible due to different polarity and poor interfacial surface tension between their rubber chains. In this study, compatibilizing effect of a nanoclay addition in SR/EPDM blends was investigated. Viscoelasticity and morphology of nanocomposites based on SR and EPDM, containing 10, 20 and 30 wt% of EPDM and 3, 6 and 9 phr of nanoclay (Cloisite 15A), were studied. The curing behavior of the samples showed that the vulcanization rate and cross-link density of the blends increased with increases in SR content. Morphological study was conducted by XRD, SEM and EDX analyses and they indicated that the nanoparticles tended to disperse in the EPDM phase and consequently caused hardness and the elasticity of this phase in nanocomposites increased. Tensile properties of the samples showed a good fitting between that of experiments and the Maxwell model at initial time of testing (1.5 s) for all the blends. Sample parameters including modulus (E), viscosity (η) and relaxation time (τ) calculated by the Maxwell model revealed that those samples with higher content of nanoparticles exhibit higher modulus and lower relaxation time. The good match in tensile properties based on Maxwell model and those of the experimental data was attributed to good dispersion of nanoclay in the blends.     

Bulk and surface mechanical properties of clay modified HDPE used in liner applications

High‐density polyethylene (HDPE)/clay nanocomposites were prepared by melt blending process. The HDPE was mixed with different organoclays and polyethylene‐grafted‐maleic anhydride was used as a compatibiliser. A masterbatch procedure was used to obtain final organoclays concentrations of 1, 2.5 and 5 wt%. The effects of various types of nanoclays and their concentrations on morphological, thermal and mechanical properties of nanocomposites were investigated. Surface mechanical properties such as instrumented nanohardness, modulus of elasticity and creep were also measured using a nanoindentation technique. Young's, storage and loss moduli, were found to be higher than that of the neat polymer at low loading (2.5 wt%) for clay Cloisite 15A and at higher loading (5 wt%) for clay Nanomer 1.44P. The ultimate strength and the toughness decreased slightly compared to pure HDPE. The differential scanning calorimetry analysis revealed that the peak temperature of the nanocomposites increased with increased clay content while the crystallinity decreased. Also, dynamic mechanical analysis revealed the storage and loss moduli are enhanced by addition of nanoclay. Both mechanical and thermal properties of HDPE/Nanomer 1.44P nanocomposite showed interesting trends. All properties first dropped when 1 wt% of the clay was added. Thereafter, a gradual increase or decrease then followed as the loading of Nanomer was increased. These trends were observed for all mechanical properties. The results obtained from nanoindentation tests for surface mechanical properties also showed similar trend to that of bulk measurements. Based on these measurements a nanoclay additive for a liner grade HDPE was selected. © 2011 Canadian Society for Chemical Engineering     

Polyurethane adhesives containing functionalized nanoclays

The development and commercialization of nanoclays (NCs) offers new possibilities to tailor adhesives on the nanoscale range. Three types of functionalized nanoclays were included in the current study, two novel ones and one commercial nanoclay. The novel ones were based on aminosilane and amidoamine hyperbranched polymer, and the commercial nanoclay possessed hydroxyl functionality. All the three functionalities were expected to react with the polyurethane (PU) based thermoset adhesive. Fourier transform infrared (FT-IR) spectroscopy was used to follow the disappearance of the isocyanate group of the polyurethane thermoset adhesive. Thermo-mechanical properties were studied using dynamic mechanical analysis (DMA). Shear and peel properties of adhesively-bonded joints were evaluated using the appropriate test standards. Atomic force microscopy (AFM) was used to analyze the nanoscale morphology of cryogenically fractured surfaces. DMA measurements indicated that the glass transition temperature (T _g) of neat PU was 32°C. Incorporation of nanoclays in concentrations of 1, 3 and 5 wt% affected the glass transition temperature significantly. The functionalized nanoclays increased the T _g gradually to the range of 60 to 62°C for 5 wt% loading. The incorporation of functionalized nanoclays into PU improved the shear strength by 170, 160 and 195% for the hydroxyl-, aminosilane- and hyperbranched-treated NCs, respectively. The functionalized nanoclays exhibited higher peel strength compared to the neat PU by 30% for the hydroxyl modified clay and by 40% for aminosilane-modified clay (at 1 wt% concentration) and almost no change for the hyperbranched modified one. AFM analysis indicated that different fracture mechanisms occurred with respect to the type and concentration of nanoclay used.     

Synthesis and characterization of UV-curing epoxy acrylate coatings modified with organically modified rectorite

Epoxy acrylate (EA) coatings modified with organically modified rectorite (OREC) were synthesized employing the ultraviolet-curing technique. Two kinds of alkyl ammonium ions, octadecyltrimethylammonium chloride (OTAC) and [2-(methacryloyloxy)ethyl]trimethylammonium chloride (MAOTMA), were used to modify rectorite (REC). The methacrylate functionalities of MAOTMA were capable of reacting with the acrylate groups of EA. The structure of OREC was characterized by FTIR and XRD and the results indicated that the surfactants were successfully intercalated into the REC interlayers via cation exchange process. The morphology of nanocomposites was investigated by SEM and TEM. OREC showed better dispersion in EA matrix compared with unmodified REC. The T _g of neat EA obtained by DMA was 75.6°C, while for 5 wt% EA/MAOTMA-REC and EA/OTAC-REC nanocomposites it increased to 76.5 and 80.8°C, respectively. The nanocomposite with 3 wt% loading of OTAC-REC had the highest T _g (89.7°C). TGA revealed that the thermal stability of nanocomposites was enhanced by OTAC-REC and MAOTMA-REC and the thermal stability of EA/MAOTMA-REC nanocomposites was better than that of EA/OTAC-REC nanocomposites. The mechanical properties of nanocomposites containing OTAC-REC and MAOTMA-REC were better than those of nanocomposites containing unmodified REC. With increasing OREC content, the adhesive force of nanocomposites decreased slightly and the flexibility increased significantly.     

Synergetic association of grafted PLA and functionalized graphene on the properties of the designed nanocomposites

The synergetic association of poly(lactic acid) grafted with maleic anhydride (MA-g-PLA) containing 0.44 wt% of maleic anhydride and epoxy-functionalized graphene (GFe) on the properties of the designed nanocomposites was studied. Rheological, mechanical and barrier properties of PLA nanocomposites were studied using different content of epoxy-functionalized graphene and MA-g-PLA compatibilizer. The PLA/MA-g-PLA/GFe nanocomposites prepared by melt blending, containing 5 wt% of MA-g-PLA, yield a maximum in storage modulus G′ and a rheological plateau at low frequencies, with a content of epoxy-functionalized graphene comprised between 4 and 7 wt%. This phenomenon was ascribed to a pseudo-solid behavior resulting from the high degree of epoxy-functionalized graphene exfoliation due to strong interfacial interactions with PLA and epoxy-functionalized graphene. The better mechanical and barrier performances were obtained with PLA/GFe containing 10 wt% of epoxy-functionalized graphene and 5 wt% of MA-g-PLA compatibilizer. The variation of the percentage of compatibilizer showed that 5 wt% of maleated PLA was sufficient to improve the thermal, rheological, mechanical and barrier properties of the PLA nanocomposite containing 7 wt% of epoxy-functionalized graphene.