Compatibilizing effect of maleated polypropylene on the mechanical properties of injection molded polypropylene/polyamide 6/functionalized-TiO2 nanocomposites

TiO₂ nanoparticles were pretreated with excessive toluene-2,4-diisocyanate to synthesize TDI-functionalized TiO₂ (TiO₂-NCO), and then the polypropylene/polyamide 6/(PP/PA6, 70/30 wt%) blends containing 3 phr of the TDI-functionalized TiO₂ were prepared using twin-screw extruder followed by injection molding. Maleated polypropylene (PP-g-MAH) was used to compatibilize the blends. The mechanical properties of PP/PA6 blends based nanocomposites were studied through tensile and flexural tests. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to assess the fracture surface morphology and the dispersion of the TDI-functionalized TiO₂, respectively. The dynamic mechanical properties of PP/PA6 based nanocomposites were analyzed by using dynamic mechanical thermal analyzer (DMTA). The strength and stiffness of the PP/PA6 compounds were improved significantly in the presence of PP-g-MAH. This has been attributed to the synergistic effect of TDI-functionalized TiO₂ and PP-g-MAH. The PP-g-MAH compatibilized PP/PA6 compounds showed a homogeneous morphology supporting the compatibility improvement between PP, PA6 and TDI-functionalized TiO₂. TEM results revealed that the TDI-functionalized TiO₂ nanoparticles were exfoliated and uniformly dispersed in blends matrix. Possible chemical interactions between PP, PA6, TDI-functionalized TiO₂ and PP-g-MAH were proposed based on the experimental work.     

Fabrication of the new structure high toughness PP/HA-PP sandwich nano-composites by rolling process

In this study a designed rolling setup was used to fabricate new structure polypropylene/hydroxyapatite-polypropylene (PP/HA-PP) sandwich nano-composites. To check the effect of rolling process and PP layers content on the structure and mechanical properties of these sandwich composites, different mechanical tests and analysis were performed on these composites. Results of tensile, bending and buckling tests show the rolling process improves the strength, modulus and flexural rigidity of composites significantly while with increasing the PP layers content from 10 vol.% to 20 vol.% decreases the stiffness, flexural rigidity and modulus of composites slightly. Results of impact test demonstrate the rolling process and increasing the volume percentage of the PP layers in sandwich composites cause a dramatic improve in impact absorbed energy of the PP/HA-PP sandwich composites. The results of Differential Scanning Calorimetry (DSC) analysis confirm the rolling process increases the crystallinity and molecular alignment of polypropylene in composites. The results of mechanical tests and DSC analysis show the increasing of polypropylene molecular alignment by rolling process is the most dominant reason of improvement the mechanical properties of sandwich composites.     

Mechanical properties and morphological characterization of exfoliated graphite–polypropylene nanocomposites

This research explores the potential of using exfoliated graphite nanoplatelets, xGnP, (graphene sheets ∼10 nm thickness, ∼1 μm diameter), as reinforcement in polypropylene, PP. xGnP–PP nanocomposites were fabricated by melt mixing and injection molding. The feasibility of using xGnP–PP nanocomposites was investigated by evaluating the flexural strength, modulus and impact strength and studying the morphology of this system as a function of xGnP loading and aspect ratio and by comparing the xGnP–PP with composites made with commercial available reinforcements such as carbon fibers, carbon black and clays. It is concluded that the smaller aspect ratio xGnP has the strongest impact on the mechanical properties of PP, at loadings up to 5 vol.%, compared to the other reinforcements used, which reflects the compatibility between the exfoliated graphite nanoplatelets and the PP matrix and the exceptional mechanical properties of xGnP, similar to crystalline graphite.     

Mechanical performance of epoxy matrix hybrid nanocomposites containing carbon nanotubes and nanodiamonds

A novel class of epoxy matrix hybrid nanocomposites has been developed containing multiwalled carbon nanotubes (MWCNTs) and nanodiamonds (NDs) to explore the combined effect of nanoreinforcements on the mechanical performance of nanocomposites. Both the nanofillers were functionalized before incorporating into epoxy matrix to promote interfacial interactions. The concentrations of both MWCNTs and NDs in the nanocomposites were increased systematically, i.e. 0.05 wt.%, 0.1 wt.% and 0.2 wt.% while composites containing individual nanoreinforcements were also manufactured for comparison. The developed nanocomposites were characterized microstructurally by scanning electron microscopy (SEM) and mechanically by tensile, flexural, impact and hardness tests. Homogeneous dispersion of MWCNTs and NDs was observed under SEM, which resulted in the enhancement of mechanical properties of nanocomposites. The composites containing 0.2 wt.% MWCNTs and 0.2 wt.% NDs showed 50% increase in hardness while tensile strength and modulus enhanced to 70% and 84%, respectively. Flexural strength and modulus also showed a rise of 104% and 56%, respectively. Interestingly, fracture strain also increased in both the tensile and flexural testing. The impact resistance increased to 161% showing a significant improvement in the toughness of hybrid nanocomposites.     

Effect of a novel coupling agent,alkyl ketene dimer,on the mechanical properties of wood–plastic composites

The objective of this study was to investigate the incorporation of poplar wood fibers both with and without a novel coupling agent, alkyl ketene dimer (AKD), on the mechanical properties of wood fiber/polypropylene (PP) composites. The resulting properties were compared to those obtained with the most commonly used coupling agent, maleic anhydride grafted PP (MAPP). Tensile and impact strengths of the composites decreased with increasing poplar wood fibers content. Tensile modulus of the composites increased by the incorporation of the wood fibers content up to 70 wt% but further increment in the wood fibers decreased the tensile modulus. At the constant content of poplar wood fibers (70 wt%), the tensile strength determined for the coupled composites with 5% AKD increased by 41% in comparison with the non-coupled composites while the tensile modulus increased by 45%, the impact strength of the coupled composites increased by 38%. The performance of 5% AKD on the mechanical properties of the composites is a little better than 3% MAPP. The good performance of 5% AKD is attributed to the enhanced compatibility between the poplar wood fibers and the polymer matrix. The increase in mechanical properties of the composites demonstrated that AKD is an effective coupling agent for wood fiber/PP composites.     

The role of epoxy matrix occlusions within BaTiO3 nanoparticles on the dielectric properties of functionalized BaTiO3/epoxy nanocomposites

In this work, the effects of controlled nanoparticles aggregations of barium titanate (BaTiO₃) on the dielectric properties of epoxy nanocomposites are investigated in detail with respect to different experimental parameters like frequency, ceramic content and temperature. Dispersing silanized BaTiO₃ nanopowder under ultrasonic and stir, nanocomposites of epoxy-amine matrix with different morphologies are obtained. The nanoparticles silane functionalization containing amine end groups effectively improve the compatibility of the nano-BaTiO₃ and the epoxy matrix. Storage modulus, glass transition temperature, tensile and flexural properties of nanocomposites and dielectric properties are increased until 10% by weight of nano-BaTiO₃ loading, well dispersed in the matrix. Above 10 wt.% of nano-BaTiO₃, scanning electronic microscopy and thermal analysis showed that agglomeration of nanoparticles occurs. Rheological and mechanical nanocomposites properties were evaluated and matrix occlusion behaviors were identified. In light of the specific behavior of the occluded polymer, the dielectric properties, especially dielectric loss are discussed.     

Synergistic effect of organic and inorganic nano fillers on the dielectric and mechanical properties of epoxy composites

Titanium oxide TiO₂/epoxy and TiO₂ with detonation nano-diamond (DND)/epoxy nanocomposites were prepared by using ultrasonication method. TiO₂ and DND particles as reinforcement species and epoxy as matrix were used to produce nanocomposites. The addition of DND particles into TiO₂/epoxy composite improved the dielectric and mechanical properties of nanocomposites in significant amount. The dielectric properties of TiO₂-DND/epoxy nanocomposite demonstrated increase in permittivity and conductivity after addition of the DND particles. The maximum and minimum reflection losses of TiO₂-DND/epoxy nanocomposite for 0.6 and 0.2 wt% DND loading were detected at ?14.5 and ?1.3 dB, respectively. The flexural and tensile strength of TiO₂-DND/epoxy nanocomposites with the addition of 0.4 wt% DNDs were enhanced to 220% and 223%, respectively. Additionally, the energy to break and percent break strain were 3.9 J and 3.86, respectively for 0.4 wt% DND loading in TiO₂-DND/epoxy nanocomposite. Therefore, the present work findings claim that DND particles are well suitable to enrich the dispersion of TiO₂ nanoparticles in epoxy matrix, which develops a strong load transfer interface between the nanoparticles and epoxy matrix and consequently leads to superior properties.     

Ductile unidirectional continuous rayon fibre-reinforced hierarchical composites

Endless rayon fibres (Cordenka®) were used to reinforce polyhydroxybutyrate (PHB) nanocomposites containing 2.5 wt.% nanofibrillated cellulose (NFC) to create truly green hierarchical composites. Unidirectional (UD) composites with 50–55% fibre volume fraction were produced using a solvent-free continuous wet powder impregnation method. The composites exhibit ductile failure behaviour with a strain-to-failure of more than 10% albeit using a very brittle matrix. Improvements at a model composite level were translated into higher mechanical properties of UD hierarchical composites. The Young’s moduli of rayon fibre-reinforced (NFC-reinforced) PHB composites were about 15 GPa. The tensile and flexural strength of hierarchical PHB composites increased by 15% and 33% as compared to the rayon fibre-reinforced neat PHB composites. This suggests that incorporation of NFC into the PHB matrix binds the rayon fibres, which does affect the load transfer between the constituents resulting in composites with better mechanical properties.     

Novel polypropylene biocomposites reinforced with carbon nanotubes and hydroxyapatite nanorods for bone replacements

Multi-walled carbon nanotubes (MWNTs) of 0.1 and 0.3 wt.% and hydoxyapatite nanorods (nHAs) of 8–20 wt.% were incorporated into polypropylene (PP) to form biocomposites using melt-compounding and injection molding techniques. The structural, mechanical, thermal and in vitro cell responses of the PP/MWNT–nHA hybrids were investigated. Tensile and impact tests demonstrated that the MWNT additions are beneficial in enhancing the stiffness, tensile strength and impact toughness of the PP/nHA nanocomposites. According to thermal analysis, the nHA and MWNT fillers were found to be very effective to improve dimensional and thermal stability of PP. The results of osteoblast cell cultivation and dimethyl thiazolyl diphenyl tetrazolium (MTT) tests showed that the PP/MWNT–nHA nanocomposites are biocompatible. Such novel PP/MWNT–nHA hybrids are considered to be potential biomaterials for making orthopedic bone implants.     

Dispersion,thermal and mechanical properties of polypropylene/magnesium hydroxide nanocomposites compatibilized by SEBS-g-MA

Isotactic polypropylene (PP)/nano-magnesium hydroxide (nano-MH) composites with 10 wt.% maleic anhydride grafted styrene–ethylene-butylene–styrene tri-block copolymer (SEBS-g-MA) as a compatilizer were prepared by melt extrusion compounding and injection molding. The effects of SEBS-g-MA on dispersion of nano-MHs in PP matrix and interfacial adhesion were studied in order to prepare highly filled PP/MH nanocomposites. The results showed that SEBS-g-MA improved both dispersion of nano-MHs and interfacial adhesion in PP/MH nanocomposites with up to 40 wt.% nano-MHs. The elastic moduli of PP/SEBS-g-MA /MH nanocomposites increased marginally and tensile yield strengths were almost invariant with nano-MH loading. Significant impact toughening of these ternary nanocomposites was, however, achieved due to the cavitation of SEBS-g-MA/MH particles and expansion of voids as well as plastic deformation of the PP matrix.     

Effects of post-annealing on the microstructure and mechanical properties of friction stir processed Al–Mg–TiO2 nanocomposites

Aluminum matrix nanocomposites were fabricated via friction stir processing of an Al–Mg alloy with pre-inserted TiO₂ nanoparticles at different volume fractions of 3%, 5% and 6%. The nanocomposites were annealed at 300–500 °C for 1–5 h in air to study the effect of annealing on the microstructural changes and mechanical properties. Microstructural studies by scanning and transmission electron microscopy showed that new phases were formed during friction stir processing due to chemical reactions at the interface of TiO₂ with the aluminum matrix alloy. Reactive annealing completed the solid-state reactions, which led to a significant improvement in the ductility of the nanocomposites (more than three times) without deteriorating their tensile strength and hardness. Evaluation of the grain structure revealed that the presence of TiO₂ nanoparticles refined the grains during friction stir processing while the in situ formed nanoparticles hindered the grain growth upon the post-annealing treatment. Abnormal grain growth was observed after a prolonged annealing at 500 °C. The highest strength and ductility were obtained for the nanocomposites annealed at 400 °C for 3 h.     

Mechanical and morphological properties of fly ash/epoxy composites using conventional thermal and microwave curing methods

Conventional thermal and microwave curing methods were utilized to cure fly ash/epoxy composites, and the mechanical and morphological properties of the composites were evaluated. The conventional thermal curing was performed at 70 °C for 80 min while microwave curing was carried out at 240 W for 18 min in order to achieve the optimum cure of the composites, determined using Differential Scanning Calorimeter. The results suggested that the tensile and flexural moduli of the composites increased with increasing fly ash content while the effect became opposite for tensile, flexural and impact strengths, and tensile strain at break. Improved mechanical properties of the composite could be obtained by addition of N-2(aminoethyl)-3-aminopropyltrimethoxysilane coupling agent, the contents of 0.5 wt% being recommended for the optimum mechanical properties. Beyond these recommended contents, the mechanical properties greatly reduced, except for the flexural modulus. The comparative results indicated that the composites by the microwave cure consumed shorter cure time and had higher ultimate strengths (especially impact strength), and strain at break than those by the conventional thermal cure. The composites with higher tensile and flexural moduli could be obtained by the conventional thermal cure.     

Influence of thermal conditions on the tensile properties of basalt fiber reinforced polypropylene–clay nanocomposites

In this paper, a comparative study on the tensile properties of clay reinforced polypropylene (PP) nanocomposites (PPCN) and chopped basalt fiber reinforced PP–clay nanocomposites (PPCN-B) is presented. PP matrix are filled with 1, 3 and 5 wt.% of nanoclays. The ultimate tensile strength, yield strength, Young’s modulus and toughness are measured at various temperature conditions. The thermal conditions are included the room temperature (RT), low temperature (LT) and high temperature (HT). The basal spacing of clay in the composites is measured by X-ray diffraction (XRD). Nanoscale morphology of the samples is observed by transmission electron microscopy (TEM). Addition of nanoclay improves the yield strength and Young’s modulus of PPCN and PPCN-B; however, it reduces the ultimate tensile strength. Furthermore, the addition of chopped basalt fibers to PPCN improves the Young’s modulus of the composites. The Young’s modulus and the yield strength of both PPCN and PPCN-B are significantly high at LT (−196 °C), descend at RT (25 °C) and then low at HT (120 °C).     

In vitro study of hydroxyapatite/polycaprolactone (HA/PCL) nanocomposite synthesized by an in situ sol–gel process

Hydroxyapatite (HA) is the most substantial mineral constituent of a bone which has been extensively used in medicine as implantable materials, owing to its good biocompatibility, bioactivity high osteoconductive, and/or osteoinductive properties. Nevertheless, its mechanical property is not utmost appropriate for a bone substitution. Therefore, a composite consist of HA and a biodegradable polymer is usually prepared to generate an apt bone scaffold. In the present work polycaprolactone (PCL), a newly remarkable biocompatible and biodegradable polymer, was employed as a matrix and hydroxyapatite nanoparticles were used as a reinforcement element of the composite. HA/PCL nanocomposites were synthesized by a new in situ sol–gel process using calcium hydroxide and phosphoric acid precursors in the presence of Tetrahydrofuran (THF) as a solvent. Chemical and physical characteristics of the nanocomposite were studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and Fourier transform infrared (FTIR) analyses. The results indicated that pure HA nanoparticles were well-incorporated and homogenously dispersed in the PCL matrix. It was found that the mechanical property of PCL was improved by addition of 20 wt.% HA nanoparticles. Furthermore, the biological property of nanocomposites was investigated under in vitro condition. For this purpose, HA/PCL scaffolds were prepared through a salt leaching process and immersed in a saturated simulated body fluid (SBF) after 3 and 7 days. It was found that a uniform layer of biomimetic HA could be deposited on the surface of HA/PCL scaffolds. Therefore, the prepared HA/PCL scaffolds showed good potential for bone tissue engineering and could be used for many clinical applications in orthopedic and maxillofacial surgery.     

Effect of SiC nanoparticles on the mechanical properties of steel-based nanocomposite produced by accumulative roll bonding process

In the present work, the effect of SiC nanoparticles on the mechanical properties of steel-based nanocomposite produced by accumulative roll bonding (ARB) process was investigated. The microstructure of the fabricated nanocomposites after fourth ARB cycle was exhibited an excellent distribution of SiC nanoparticles in the interstitial free (IF) steel matrix without any porosity. The findings revealed that with increasing the number of ARB cycles, the tensile strength of the ARB-processed pure IF steel and also nanocomposites was improved, but their elongation was decreased at first step and then was increased at second step. The tensile strength of the ARB-processed pure IF steel and nanocomposites was 4.5 and 6 times higher than the same value was obtained for annealed IF steel, respectively. In addition, the ARB-processed pure IF steel and nanocomposite was exhibited a higher hardness than the annealed IF steel so that the hardness values of the pure IF steel and nanocomposite were 3.78 and 4.44 times higher than that of the annealed IF steel.     

The role of oleate-functionalized layered double hydroxide in the melt compounding of polypropylene nanocomposites

In this research, the oleate-functionalized magnesium and aluminum layered double hydroxide (LDH; Mg:Al = 3:1) o-LDH was applied as nanofiller in the melt blending of polypropylene (PP) nanocomposites, in order to understand its role in this process. o-LDH was prepared using the memory effect of the calcined carbonated LDH. Blending of PP and low o-LDH filler contents of 0.45 and 0.90 wt.% afforded the nanocomposites PP0.45 and PP0.90, respectively, which were characterized by transmission electron microscopy, X-ray diffraction, small angle X-ray scattering, thermo-gravimetric analysis, differential scanning calorimetry and dynamic mechanical analysis. The oleate LDH surface functionalization enhanced the system compatibility as a relative regular dispersion of o-LDH tactoids was observed within the matrix, together with partial PP intercalation. This o-LDH incorporation increased the PP relative crystallinity, induced crystalline orientation and decreased the glass transition temperature. Furthermore, the nanocomposites showed improved initial resistance to decomposition and stiffness. These results showed that the o-LDH acted as both nucleating agent and plasticizer, and that the presented approach can be used for the development of PP nanocomposites with distinguished properties.     

Effect of layered silicate reinforcement on the structure and mechanical properties of spent polyamide-12 nanocomposites

The aim of this work was to study the structure and mechanical properties of spent polyamide-12 and spent polyamide-12/layered silicate reinforced novel nanocomposites. Layered silicate at 1, 3, 5 and 7 wt.% was incorporated in spent polyamide-12 and its nanocomposites were prepared using single screw injection moulding technique. The interlamellar structure and surface morphology were characterised by transmission electron microscope (TEM) and scanning electron microscope (SEM). Different levels of layered silicate dispersion (as characterised by TEM and SEM) correlated strongly with improvements in mechanical performance. The results showed that the tensile and flexural properties are found to be increased with the incorporation of layered silicate into spent PA-12 matrix. Comparison of tensile and flexural test results between virgin PA-12, spent PA-12 and spent PA-12 nanocomposites showed that spent PA-12 samples have retained 70% of its tensile and 80% of its flexural properties respectively, compared to virgin PA-12.     

Preparation,morphology and properties of acid and amine modified multiwalled carbon nanotube/polyimide composite

The precursor of polyimide, polyamic acid, was prepared by reacting 4,4′-oxydianiline (ODA) with 3,3′,4,4′-benzophenone tetracarboxylic dianhydride (BTDA). Unmodified, acid-modified and amine-modified multiwall carbon nanotubes (MWCNT) were separately added to the polyamic acid and heated to 300 °C to produce polyimide/carbon nanotube composite. Scanning electron microscopic (SEM) and transmission electron microscopic (TEM) microphotographs reveal that acid-modified MWCNT and amine-modified MWCNT were dispersed uniformly in the polyimide matrix. The effect of the acid and amine-modified MWCNTs on the surface and volume electrical resistivities of MWCNT/polyimide composites were investigated . The surface electrical resistivity of the nanocomposites decreased from 1.28 × 10¹⁵ Ω/cm² (neat polyimide) to 7.59 × 10⁶ Ω/cm² (6.98 wt% unmodified MWCNT content). Adding MWCNTs influenced the glass transition temperatures of the nanocomposites. Modified MWCNTs significance enhanced the mechanical properties of the nanocomposites. The tensile strength of the MWCNT/polyimide composite was increased from 102 MPa (neat polyimide) 134 MPa (6.98 wt% acid modified MWCNT/polyimide composites).     

Effect of clay and PEO-PPO-PEO block copolymer on the microstructure and properties of cyanate ester/epoxy composite

In this study, processing, morphology and properties of poly (ethylene oxide)-block-poly (propylene oxide)-block-poly (ethylene oxide) (PEO-PPO-PEO) triblock copolymer and clay modified cyanate ester/epoxy hybrid nanocomposites were investigated. The PEO-PPO-PEO triblock copolymer preferentially reaction-induced microphase separate into spherical micelles in the cyanate ester/epoxy matrix. PEO-PPO-PEO was used as both nanostructuring agent for cyanate ester/epoxy blended resin and thus the predominantly intercalated and few exfoliated platelets of were also observed with clay, which successfully reduced the brittleness of the cyanate ester/epoxy blended resin increasing the toughness of designed materials. The stiffness and heat resistance of the neat BCE/EP resin could be retained in the BCE/EP/F68/clay hybrid nanocomposites. The optimum property enhancement was observed in the hybrid nanocomposites containing 5 wt% PEO-PPO-PEO and 3 wt% clay. The thermo/mechanical properties of the hybrid nanocomposites depend on microstructure, dispersion state and the ratio between organic and inorganic modifiers content.     

Combination effect of carbon nanotubes with graphene on intumescent flame-retardant polypropylene nanocomposites

A novel polypropylene (PP) nanocomposite was fabricated by the incorporation of intumescent flame retardant (IFR), carbon nanotubes (CNTs) and graphene into the PP matrix. Results from TEM indicate that IFR, CNTs and exfoliated graphene nanosheets are dispersed finely in the PP matrix, which is supported by the XRD analysis results. Thermogravimetric (TGA) results show that the addition of IFR, CNTs and graphene improved the thermal stability and the char yields of PP. The PP/IFR/CNTs/RGO nanocomposites, filled with 18 wt% IFR, 1 wt% CNTs and 1 wt% graphene, achieve the limiting oxygen index value of 31.4% and UL-94 V0 grade. Cone calorimeter data reveal that combustion behavior, heat release rate peak (PHRR) and average specific extinction area (ASEA) of PP decrease substantially when combination effects of IFR, CNTs and graphene intervene. For the PP/IFR/CNTs/RGO nanocomposites, the PHRR exhibits an 83% reduction and the time of ignition is delayed 40 s compared with neat PP.