Morphological,mechanical, and electromagnetic interference shielding effectiveness characteristics of glass fiber/epoxy resin/MWCNT buckypaper composites

Glass fiber/epoxy resin composites (GF/EP) using one and three multi-walled carbon nanotube buckypapers (BP) were obtained and their complex parameters, reflectivity, and electromagnetic interference (EMI) shielding effectiveness (SE) at X-band (8.2–12.4 GHz) and Ku-band (12.4–18 GHz) were evaluated. The preparation of BP used polyacrylonitrile (PAN) nanofibers (PF These composites show both large storage and energy loss capacity in both bands revealing promising results related to EMI SE applications. Besides, a high attenuation of around 67% and 72% were achieved for BP based composites. The cross-section view of the buckypaper and the laminates was analyzed by scanning electron microscopy (SEM). The incorporation of the CNT film into the laminates showed no improvements in the elastic properties through dynamic mechanical analyses (DMA). Nevertheless, a decrease in the shear properties by the compression shear test (CST) and interlaminar shear strength (ILSS) has been observed. GF/EP/BP/PF composite presented a reduction of 29 and 39% in its ILSS properties compared to the base laminate (GF/EP). Also, the decrease was even more significant, revealing a steep reduction in its CST properties. On the other hand, the removal of the pan nanofiber (PF) led to better mechanical properties for GF/EP/BP/RPF composites. Results have shown ILSS values of 47.4 ± 2.2 MPa which are close to the base laminate (52.4 ± 3.1 MPa). The removal of the PF provided larger porous in the CNT network, making the impregnation by epoxy easier in the BP/RPF which resulted in improved shear properties compared to GF/EP/BP/PF samples.     

Thermo-mechanical and mechanical behavior of hybrid isotactic polypropylene glass fiber reinforced composites (GFRC) modified with calcium carbonate (CaCO3)

The study investigates the thermo-mechanical properties of isotactic polypropylene (iPP) hybrid composites in reference to various amounts of particle- and fiber-shaped inorganic fillers. Three grades of hybrid composites were prepared as a function of filler amount: 5, 10, and 20 wt% and different ratios of glass fiber (GF) and calcium carbonate (CaCO₃). The main objective is to describe the relationship between the hybridization efficiency and mechanical performance of polypropylene-based composites. The analysis of the thermo-mechanical properties of the composites shows that both the total amount of the filler and the ratio of GF and CaCO₃ clearly influence the properties of the composites. Hybrid composites with the highest amount of the GF display improved thermo-mechanical stability. The presence of well-dispersed CaCO₃ in the composites was found to improve elongation at break and Vicat softening temperature values. Even though it is glass fiber, which shows higher filler effectiveness and visibly reinforces the composite samples, causing an increase in tensile strength or reinforcing efficiency, replacing up to 50% of this filler with calcium carbonate does not result in a considerable deterioration of the properties of the material.     

Effect of amine functionalization of CNF on electrical, thermal, and mechanical properties of epoxy/CNF composites

This paper presents experimental results of the effect of amine functionalization of carbon nanofibers (CNF) on the electrical, thermal, and mechanical properties of CNF/epoxy composites. The functionalized and non-functionalized CNFs (up to 3 wt%) were dispersed into epoxy using twin screw extruder. The specimens were characterized for electrical resistivities, thermal conductivity (K), UTS, and Vicker’s microhardness. The properties of the nanocomposites were compared with that of neat epoxy. The volume conductivity of the specimens increased by E12 S/cm and E09 S/cm in f-CNF/epoxy and CNF/epoxy, respectively, at 3 wt% filler loading. The increase in K for former was 106% at 150 °C, while for the latter it was only 64%. Similarly, UTS increased by 61% vs. 45% and hardness 65% vs. 43%. T _g increased with increase in filler content. SEM examinations showed that functionalization resulted in better dispersion of the nanofibers and hence greater improvement in the studied properties of the nanocomposites.     

Blended Epoxy/Polyester Polymer Nanocomposites: Effect of “Nano” on Mechanical Properties

The inter-cross-linked networks of unsaturated polyester (UP) toughened epoxy blends were developed. Montmorillonite (MMT) clay was dispersed into the same system to prepare blended epoxy/UP/clay nanocomposites in different weight ratios viz. 0%, 1%, 2%, 3% and 5%. Mechanical properties like tensile strength (TS), impact strength (IS) and interlaminar shear strength (ILSS) were characterized for the above nanocomposites. Blended nanocomposites were fabricated by high shear mechanical mixing followed by ultra-sonication process to get homogeneous mixing under the aid of in situ polymerization. Mechanical properties were studied as per ASTM standards. Data obtained from mechanical property studies indicated that the introduction of UP into epoxy resin improved the impact strength to an appreciable extent. Impact strength (IS) and tensile strength (TS) were significantly improved and optimized at 3 wt. % clay content when compared with neat blend (0 wt. % clay) composites. The homogeneous morphologies of the UP toughened epoxy and epoxy/UP/clay nanocomposite systems were ascertained using scanning electron microscope (SEM) studies.     

Mechanical and morphological properties for sandwich composites of wood/PVC and glass fiber/PVC layers

This work manufactured sandwich composites from glass fiber/poly(vinyl chloride) (GF/PVC) and wood/PVC layers, and their mechanical and morphological properties of the composites in three GF orientation angles were assessed. The effects of K value (or viscosity index) of PVC and Dioctyl phthalate (DOP) loading were of our interests. The GF/PVC was used as core layer whereas wood/PVC was the cover layers. The experimental results indicated that PVC with low K value was recommended for the GF/PVC core layer for fabrication of GF/WPVC sandwich composites. The improvement of PVC diffusion at the interface between the GF and the PVC core layer was obtained when using PVC with K value of 58. This was because it could prevent de‐lamination between composite layers which would lead to higher mechanical properties of the sandwich composites, except for the tensile modulus. The sandwich composites with 0° GF orientation possessed relatively much higher mechanical properties as compared with those with 45° and 90° GF orientations, especially for the impact strength. Low mechanical properties of the sandwich composites with 45° and 90° GF orientation angles could be overcome by incorporation of DOP plasticizer into the GF/PVC core layer with the recommended DOP loadings of 5–10 parts per hundred by weight of PVC components. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

The excellent gas barrier properties and unique mechanical properties of poly(propylene carbonate)/organo-montmorillonite nanocomposites

Intercalated nanocomposites comprised of poly(propylene carbonate) (PPC) and organo-montmorillonite (OMMT) were prepared via a direct melt blending method. The morphological, thermal, rheological, mechanical, and gas barrier properties of composites were carried out in detail. Results of XRD, TEM, and SEM revealed that OMMT dispersed homogeneously in the polymer matrix, and were intercalated by PPC macromolecules. Compared with neat PPC, the PPC/OMMT nanocomposites showed an enhancement in the 5 wt% weight loss temperature (T _?5%) by near 20 °C with 3 phr OMMT concentration. With the percolation threshold formed, the rheological properties of composites translated from a liquid-like behavior to a solid-like one. Interestingly, PPC/OMMT nanocomposites revealed a concurrent improvement in the modulus, yield strength, and toughness with the addition of homogeneously dispersed clay. The oxygen permeability of well-dispersed PPC/OMMT nanocomposites reduced significantly compared with that of neat PPC. Consequently, this convenient and effective method, which facilitates to prepare PPC/OMMT nanocomposites with superior mechanical properties and excellent gas barrier performances, can be considered to broaden the application of PPC.     

An Innovative Approach to the Synthesis of PMMA/PEG/Nanobifiller Filled Nanocomposites with Enhanced Mechanical and Thermal Properties

A facile route was adopted to blend the matrix. The PMMA/PEG blend was reinforced with three types of nanofillers, i.e., pristine MWCNT (P-CNT), amine functionalized MWCNT (PDA-EA-CNT) and nanobifiller i.e. nanodiamond functional MWCNT (PDA-EA-CNT-ND) to yield three different types of nanocomposites i.e. PMMA/PEG/P-CNT, PMMA/PEG/PDA-EA-CNT and PMMA/PEG/PDA-EA-CNT-ND. These nanocomposites were reinforced with nanofiller loading (1 wt. %, 3 wt. %, 5 wt. %, 10 wt. %, 30 wt. % and 50 wt. %) by solution casting method. Structure of composite and nanofillers was confirmed by FTIR. FESEM imaging revealed that nanocomposites have micro porous morphology. At high magnification, distribution of functionalized CNT/ND appears to be protruding out of the polymeric matrix. The TGA result suggests that the thermal stability of the nanocomposites was enhanced in comparison to PMMA due to grafting of filler molecules with PMMA/PEG macromolecules. The DTG results showed that the bifiller nanocomposites (PMMA/PEG/PDA-EA-CNT-ND) exhibited improved thermal stability with T_max (431^°C) as compared to P-CNT and amine functionalized CNT (PMMA/PEG/PDA-EA-CNT) with T_max of 395^°C and 418^°C respectively. XRD results showed fine interaction between filler and the polymeric matrix. As the filler loading was increased the composites showed pronounced XRD peak at 25.9^°, corresponding to (002) reflection of nanotubes. Significant improvement in the mechanical properties of composites was recorded with the reinforcement of fillers as compared to the neat matrix. The most significant improvement in tensile strength and elastic modulus was observed for the bifiller nanocomposites with 5 wt. % PDA-EA-CNT-ND. They showed a tensile strength and elastic modulus of 29.9 MPa and 1474.31 MPa respectively as compared to amine functionalized CNT with tensile strength (25.7) and elastic modulus (1466.99 MPa)and P-CNT with tensile strength(25 MPa) and elastic modulus (1155.75 MPa).     

Influence of Multiwalled Carbon Nanotubes on Mechanical,Thermal and Electrical Behavior of Polybenzoxazine-Epoxy Nanocomposites

Multiwalled carbon nanotubes (MWCNT)-reinforced polybenzoxazine-epoxy nanocomposites were prepared via the solvent method and were investigated for their thermal, thermo-mechanical, mechanical, electrical and morphological properties. Epoxy resin (DGEBA) was modified with 5, 10 and 15 wt.% of benzoxazines using 4,4′-diaminodiphenylmethane as a curing agent at appropriate conditions. Epoxy and benzoxazines-modified epoxy systems were further reinforced with 0.25, 0.50 and 0.75 wt.% of surface-modified MWCNT. MWCNT-reinforced polybenzoxazine-epoxy nanocomposites exhibited better thermal, mechanical and dielectric properties. Dispersion of MWCNT in benzoxazine-epoxy resins and nanostructure of the composites was confirmed by transmission electron microscopy analysis.     

Crosslinked carboxylated SBR composites reinforced with chitin nanocrystals

This study aims to develop and characterize the nanocomposites using sulfur cross-linked carboxylated styrene-butadiene rubbers (S-xSBR) as the matrix and chitin nanocrystals (CNCs) as nanofillers. The composites’ morphology and properties were examined by light transmittances, fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), X-ray diffraction (XRD), dynamic mechanical analysis (DMA), thermo gravimetric analyzer (TGA), and tensile properties determination. The addition of CNCs has slight effect on transparency of the composite films. FTIR data confirm the interfacial interactions between CNCs and S-xSBR via hydrogen bonds. CNCs are uniformly dispersed in the matrix from SEM result. The addition of CNCs can significantly improve the tensile strength and modulus both in static and dynamic states. The tensile modulus and tensile strength of S-xSBR/CNCs composites with the 4 wt.% CNCs is 62.5 % and 97.6 % higher than that of pure S-xSBR. The storage modulus, glass transition temperature, and the thermal stability of the composites are higher than those of the neat S-xSBR. The mechanical properties of the composite films are water-responsive, as the swollen samples exhibit obviously decreased strength and modulus. The greatest mechanical contrast is shown in the S-xSBR/CNCs composites with 2 wt.% CNCs loading whose tensile modulus decrease from 60.4 to 6.1 MPa after swelling equilibrium. The significant reinforcement effect of CNCs on S-xSBR is attributed to the unique structure of CNCs and the interfacial interactions in the composite.     

Influence of alumina content and thermal treatment on the thermal conductivity of UPE/Al2O3 composite

Ultra high molecular weight polyethylene/alumina (UPE/Al₂O₃) microcomposites with high loading micro alumina (Al₂O₃, 20 to 100 phr) were prepared by casting method. The composites were thermal treated (cooled slowly) and then the thermal properties were studied at temperatures from 25 to 125°C. Thermogravimetric analysis (TGA) and scanning electron microscopic (SEM) proves the homodispersion of Al₂O₃ microparticles in UPE. TGA indicates that the temperature of 5% weight loss of UPE/Al₂O₃ (100 phr) composite is 467.0°C, 10.5°C higher than that of pure UPE. Differential scanning calorimetry (DSC) shows that the melting point and the real degree of crystal (X_rc) of treated UPE/Al₂O₃ composite (100 phr) are 141.4°C and 65.7%, respectively, all higher than that of untreated composite, which can be described by crystal bridge mechanism. The density of the composite is also be enhanced because of crystal volume shrinkage induced by thermal treatment. The thermal conductivity of the treated UPE/Al₂O₃ composite (100 phr) is 1.920 W (m K)^?1 at 25°C, 23.6% higher than that of the untreated composite. Crystal bridge thermal conduction mechanism is proposed. The thermal conductivity of UPE/Al₂O₃ composite has some dependency on the increasing Al₂O₃ content and also thermal treatment. These results can give some advice to design formulations for practical applications in pipe area and other wear area. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40528.     

Binary and ternary nanocomposites based on PVDF,PMMA, and PVDF/PMMA blends: polymorphism,thermal, and rheological properties

Binary and ternary nanocomposites based on poly(vinylidene fluoride) (PVDF), poly(methyl methacrylate) (PMMA), and PVDF/PMMA blends were successfully prepared through a melt-mixing process, using a commercial organoclay (15A) as the nanofiller. The 15A was more finely dispersed (intercalated/partially exfoliated) within the PVDF matrix compared with the PMMA matrix. A higher PVDF content in the ternary composite essentially led to a superior degree of 15A dispersion. The 15A addition induced the polar β-form PVDF crystals, whereas the presence of PMMA in ternary composites reduced the efficiency in promoting β-form formation by 15A. Adding 15A also enhanced the nucleation of PVDF, but the enhancement was inferior while PMMA was present. Conversely, the crystal growth of PVDF was retarded with the existence of 15A, and the PVDF/15A binary composite exhibited the greatest retardation. The equilibrium melting temperature (T_m°) of PVDF in the neat state and in the blends increased after 15A addition. The PVDF/15A binary composite possessed an evidently higher β-form T_m° than the α-form T_m° of neat PVDF (~20.1 °C rise). Similar effects on the individual components, 15A declined the thermal stability of PVDF but increased that of PMMA in the ternary composites. Rheological property measurements revealed that the ternary composites performed in-between that of individual PVDF/15A and PMMA/15A binary composites. A percolation of 15A (pseudo)network structure was developed in the composites, and a more elastic behavior was observed with increasing PVDF content in the composites.     

Thermo-mechanical behaviors of epoxy resins reinforced with nano-Al2O3 particles

This study examined the thermo-mechanical behavior of epoxy resins/nano-Al₂O₃ composites including the curing behavior, thermal stability, dynamic mechanical properties and thermal mechanical properties. The DSC curve peak temperature of the composites was decreased by the addition of nano-Al₂O₃. The thermal stability of the composites was similar to that of the neat epoxy resins. Dynamic mechanical analysis (DMA) indicated the glass transition temperature of the composites to be approximately 11 °C higher than that of the neat epoxy resins. The coefficient of thermal expansion (CTE) of the composites decreased with increasing nano-Al₂O₃ content.     

Incorporation of silicon dioxide nanoparticles at the carbon fiber‐epoxy matrix interphase and its effect on composite mechanical properties

Functionalized silicon dioxide nanoparticles (nano‐fSiO₂) were uniformly deposited on the surface of carbon fibers (CFs) using a coating process which consisted of immersing the fibers directly in a suspension of nano‐fSiO₂ particles and epoxy monomers in 1‐methyl‐2‐pyrrolidinone (NMP). The 0° flexural properties, 90° flexural properties, and Interlaminar shear strength (ILSS) mechanical properties of unidirectional epoxy composites made with nano‐fSiO₂+epoxy sized carbon fibers, with control fibers, and with epoxy‐only sized fibers were measured and compared. An obvious increase of the fiber/matrix adherence strength was obtained with the nano‐fSiO₂+epoxy coating. The nano‐fSiO₂+epoxy sized CF/epoxy composites showed a relative increase of 15%, 50%, and 22% in comparison to control fibers, for the Interlaminar shear strength, the 90^° flexural strength and the 90° flexural modulus, respectively, but little e difference was measured between the different systems for the 0° flexural properties. The observation of the fracture surfaces by scanning electron microscopy of composite fracture confirmed the improvement of the interfacially dependent mechanical properties. POLYM. COMPOS., 38:1474–1482, 2017. © 2015 Society of Plastics Engineers     

ASA/graphite/carbon black composites with improved EMI SE,conductivity and heat resistance properties

Composites, comprised of acrylonitrile styrene acrylate copolymer (ASA)/graphite (GR) with high electromagnetic interference shielding effectiveness (EMI SE), were fabricated by the introduction of carbon black (CB). The effects of CB on properties such as EMI SE, morphology, heat resistance, rheological and mechanical performance of the composites were characterized using a scanning electron microscope (SEM), rotational rheometer, electromagnetic shielding measuring instruments. The graphite and carbon black exhibited positive synergistic action, which promoted the complete formation of conductive networks in ASA matrix. The EMI SE and electrical conductivity of the ASA/GR/CB composites increased with higher CB loadings. In the frequency range of 30–3000 MHz, the maximum EMI SE of ASA composites with 50 % fillers reached 40 dB, but with 40 % fillers this property reached its maximum value of 50 dB. The flexural strength of ASA/GR/CB composites started to decline as CB loading exceeded 5 %. The heat resistance of the composites was improved due to the addition of CB. In this respect, the vicar softening temperature (VST) of the composites with 40 % fillers increased from 115.1 to 132.7 °C, and the VST of the composites with 50 % fillers was elevated from 125.4 to 138.9 °C.     

The electrical and thermal properties of polyimide/boron nitride nanocomposite films

In the paper, the polyimide (PI)/boron nitride (BN) nanocomposites were prepared by in situ polymerization and exhibited enhanced electrical property and thermal stability. The structure of synthesized PI was confirmed by scanning electron microscopy, energy dispersive spectrometer, and Fourier transform infrared. The influence of doping concentrations on the relative permittivity, electrical conductivity, loss tangent, corona-resistant lifetime, and thermal stability of PI composites was investigated. Results showed that the relative permittivity of PI/BN composites increases after doping BN nanoparticles. It was noteworthy that both the electrical conductivity and loss tangent of PI composites were enhanced in low frequency (0–3000 Hz) and the situations were shifted in high frequency (>3000 Hz). It was observed that the corona-resistant lifetime of PI/BN composite with 20 wt% BN increases more than eight times. Moreover, significant improvements in the thermal stability of PI composites were achieved by addition of only a small amount of BN. The decomposition temperatures at 5 and 10% weight loss were 518.7 and 551.6 °C for 15 wt% doped PI/BN composite, respectively, which increases by 37.3 and 40.5 °C compared to those of pure PI. The resulting properties expand further the application range of polyimides.     

Utilization of Recycled Polypropylene for Production of Eco-Composites

Renewable raw materials and recyclable thermoplastic polymers provide attractive eco-friendly quality as well as environmental sustainability to the resulting natural fiber reinforced composites. We studied the possibility of using the recycled polypropylene (PP) for production of composites based on kenaf fibers (KF) and rice hulls (RH) as reinforcements. Polypropylene/rice-hulls (PP/RH/CA) and polypropylene/kenaf (PP/K/CA) composites with 30% fiber (filler) content and appropriate compatibilizing agent (CA)—a maleic anhydride grafted PP (MAPP), have been prepared by two steps procedure: melt mixing and compression molding. Flexural strength and thermal stability of the composites with recycled PP were similar to those with neat PP. The composites reinforced with kenaf fibers have shown better properties than those based on rice hulls. The flexural strength of the composite sample with recycled PP is 51.3 MPa in comparison with 51.1 MPa for the composite with neat PP. Degradation temperatures of neat and composite with recycled PP at residual weight 90% are 344.4°C and 343.5°C, respectively. The results obtained report the possibility of utilization of recycled PP for the production of natural reinforcements based composites with good mechanical characteristics for using as construction building materials in housing systems.     

Thermal conductivity and dynamic mechanical property of glycidyl methacrylate‐grafted multiwalled carbon nanotube/epoxy composites

The well dispersed multiwalled carbon nanotube (MWCNT)/epoxy composites were prepared by functionalization of the MWCNT surfaces with glycidyl methacrylate (GMA). The morphology and thermal properties of the epoxy nanocomposites were investigated and compared with the surface characteristics of MWCNTs. GMA‐grafted MWCNTs improved the dispersion and interfacial adhesion in epoxy resin, and enhanced the network structure. The storage modulus of 3 phr GMA‐MWCNTs/epoxy composites at 50°C increased from 0.32 GPa to 2.87 GPa (enhanced by 799%) and the increased tanδ from 50.5°C to 61.7°C (increased by 11.2°C) comparing with neat epoxy resin, respectively. Furthermore, the thermal conductivity of 3 phr GMA‐MWCNTs/epoxy composite is increased by 183%, from 0.2042 W/mK (neat epoxy) to 0.5781 W/mK. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A facile route for the synthesis of mechanically strong MWCNTs/NDs nanobifiller filled polyacrylate composites

ABSTRACT

We present here the synthesis of novel Nano-Bifiller filled composites with extremely promising material properties. To achieve this goal, initially, poly (methyl methacrylate) (PMMA) and poly (ethylene glycol) (PEG) blend were formed. Later, the matrix was reinforced with purified carbon (P-CNT), amino modified carbon nanotube (PDA-CNT) and amino modified carbon nanotube nanodiamond (PDA-CNT-ND). In this way, three series of nanocomposites, i.e. PMMA/PEG/P-CNT, PMMA/PEG/PDA-CNT, and PMMA/PEG/PDA-CNT-ND were synthesized with varying P-CNT, PDA-CNT and PDA-CNT-ND loading (i.e., 1 wt.%, 3 wt.%, 5 wt.%, 10 wt.%, 30 wt.% and 50 wt.%) by a solution blending route. The reinforcement and loading effect of these three types of nanofillers on the matrix was studied. Studies were performed using Fourier transform infrared spectroscopy (FTIR), mechanical testing, thermogravimetric analysis (TGA), field emission scanning electron microscopy (FE-SEM) and X-ray powder diffraction (XRD) to explore the structural, morphological, mechanical and thermal properties of nanocomposites prepared. The inter-association of poly (methyl methacrylate) and poly (ethylene glycol) (PMMA/PEG) due to hydrogen bonding and covalent attachment of matrix to the sidewalls of nanotubes was confirmed by FTIR spectra. The experimental results showed that a loading of 5 wt. % filler in matrix produced a tensile strength and modulus of 26.4 (MPa) and 1255.75 (MPa) in PMMA/PEG/P-CNT nanocomposites, while 28.8 (MPa) and 1411.04 (MPa) in PMMA/PEG/PDA-CNT nanocomposites and 29.4 (MPa) and 1419.41 (MPa) in PMMA/PEG/PDA-CNT-ND nanocomposites as compared to neat PMMA which has tensile strength and modulus of 21.79 (MPa) and 1083.84 (MPa) respectively. These results depict that bifiller nanocomposites showed better mechanical properties as compared to pristine and amine functionalized MWCNT. Scanning electron microscopy revealed granular morphology with few protruding out carbon nanotubes. Thermal stability of PMMA/PEG/PDA-CNT-ND nanocomposites was found higher than PMMA/PEG/PDA-CNT and PMMA/PEG/P-CNT nanocomposites. The T_o (369^°C) and T₁₀ (515^°C) values for PMMA/PEG/PDA-CNT-ND composites was higher than PMMA/PEG/PDA-CNT [T_o (354^°C) and T₁₀ (420^°C)] and PMMA/PEG/P-CNT composites [T_o (312^°C) and T₁₀ (390^°C)]. These results suggest that the bifiller nanocomposites were thermally more stable. The XRD spectra showed a pronounced XRD peak at 25.9^°, corresponding to (002) reflection of the nanotubes indicating that MWCNT structure was not destroyed during composite formation. The peak appeared at 75.3^° were indexed to (220) reflections due to nanodiamond structure.     

Comparative study of interphase evolution in polysiloxane resin-derived matrix containing carbon micro and nanofibers during thermal treatment

The work presents the results of research on composite materials made of silicon-containing polymer-derived ceramic matrix composites (PDC-Cs) and nanocomposites (PDC-NCs). Carbon micro and nanofibers (CFs and CNFs) were used as reinforcements. The interactions between carbon micro and nanofibers and polysiloxane matrix, as well as interphase evolution mechanism in composite samples during their heating to 1000 °C were studied. CF/resin and CNF/resin composites were prepared via liquid precursor infiltration process of unidirectionally aligned fibers. After heating to 700 °C–800 °C, decomposition of the resin in the presence of CNFs led to the formation of fiber/organic-inorganic composites with pseudo-plastic properties and improved oxidation resistance compared to as-prepared fiber/resin composites. The most favourable mechanical properties and oxidation resistance were obtained for composites and nanocomposites containing the maximum amount of carbon nanoparticles precipitated in the SiOC matrix during the heat treatment at 800 °C. The precipitated carbon phase improves fiber/matrix adhesion of composites.     

Effect of reinforcement of sustainable β‐CaSiO3 nanoparticles in bio‐based epoxy resin system

The β‐CaSiO₃ nanoparticles (NPs) were prepared using calcium carbonate from egg shells and silica as precursors. These NPs were incorporated (1–4 wt %) into bio‐based epoxy resin to fabricate nanocomposites. Thermal and mechanical tests were carried out on these composites. The results of dynamic mechanical analysis showed significant improvement in the storage modulus of 1 and 2 wt % composites. The thermomechanical analysis data revealed ～19 and 20% of reduction in coefficient of thermal expansion for 1 wt % of CaSiO₃ before and after glass transition as compared to the neat epoxy system. Thermogravimetric analysis results also showed delayed thermal degradation of the composites by significant amounts (17–35°C) for 5% of decomposition, a proportional increase in residues corresponding to the loading concentrations. The flexure tests showed significant improvements in strength (17–36%), modulus (5–33%), and toughness for 1–4 wt % of reinforcement of β‐CaSiO₃ NPs. Theoretical calculations of the reinforcement effect on the flexure modulus of the composites agree well with the experimental values. The scanning electron micrograph of the fractured surfaces revealed better interfacial interactions in the composites and enhancements in crack path deflections over the neat specimen. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40867.