Mechanical and thermal properties of modified kaolin clay/unsaturated polyester nanocomposites

The improvement in thermal and mechanical properties of Nanocomposites prepared with unsaturated polyester (UP) as polymer matrix and various loadings of amino‐modified nano kaolinite clay as filler has been studied. Mechanical stirring and ultrasonication resulted in better dispersion of the clay. For curing polyester resin, cobalt naphthenate was used as accelerator and MEKP as initiator. Dynamic Mechanical Analysis (DMA) was carried out to find storage and loss modulus. Thermal stability was found through thermogravimetric analysis and the evaluation of structure and morphology of the nanocomposites were done through XRD, SEM, and TEM. Nanocomposite with 3 phr of amino modified clay has shown higher storage modulus and an improved thermal stability of UP/clay nanocomposites has been established. Tensile strength and toughness of the composite have been found to achieve maximum values at 1 phr of clay and the storage modulus has had an improvement of 38% compared to neat UPR. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43245.     

PEGylated copper(II)-chelated polydopamine nanocomposites for photothermal-enhanced chemodynamic therapy against tumor cells

Photothermal-enhanced chemodynamic therapy is a novel and promising strategy for effective tumor treatment. Herein, a kind of polydopamine (PDA)-based nanoplatform is reported for photothermal-enhanced chemodynamic therapy against tumor cells. PDA nanoparticles (NPs) were prepared through the self-polymerization method, which were subsequently chelated with Cu²⁺ and linked with poly(ethylene glycol) (PEG) chains, finally obtaining PDA-Cu(II)-PEG NPs. The fabricated PDA-Cu(II)-PEG NPs were uniform in shape with a narrow polydispersity. They can firstly react with glutathione (GSH) to generate Cu⁺, inducing GSH depletion meanwhile. The formed Cu⁺ could catalyze H₂O₂ to produce hydroxyl radicals (˙OH) via a Fenton-like reaction. The formed PDA-Cu(II)-PEG NPs displayed good photothermal conversion efficiency and photothermal stability. They can be internalized by 4T1 cells effectively. Under near-infrared light irradiation, PDA-Cu(II)-PEG NPs can generate hyperthermia and ˙OH for photothermal/chemodynamic therapy against tumor cells.     

Influence of the processing parameters and composition on the thermal stability of PLA/nanoclay bio‐nanocomposites

Poly(lactic acid) (PLA) is one the most promising bio‐based and biodegradable polymer. However, its low thermal stability limits the range of applications and complicates its transformation via the most industrial common processes. The novelty of this work is studying the thermal stability of PLA and PLA/clay nanocomposites during use, as a function of the composition and using a wide range of extrusion and injection moulding processing parameters. To improve the thermal stability of the PLA, laminar silicates containing different organomodifications have been added (Cloisite 20A and Cloisite 30B). The results show that the processing conditions and composition define the morphology of the bio‐nanocomposites, which plays key role in defining final thermal properties of the material. In general, clays improve the thermal stability of the processed material, increasing the degradation temperature and decreasing the degradation rate under a wide range of processing conditions. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40747.     

Soundproofing properties of polypropylene/clay/carbon nanotube nanocomposites

In this article, polypropylene (PP)/clay/carbon nanotube (CNT) composites were prepared via a solution blending method. Sound transmission loss (STL), determined with an impedance tube, was used to characterize their soundproofing properties. The STL for the PP/4.8 wt % clay/0.5 wt % CNT composite was about 15–21 dB higher than that for pure PP at high frequencies (3200–6400 Hz) and about 8–14 dB higher at low frequencies (580–620 Hz). X‐ray diffraction (XRD) and transmission electron microscopy (TEM) were used to study the crystallinity and the microstructure. A synergistic effect on the STL was established between the structure of the homogeneous dispersion and strong interfacial adhesion. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of bone ash fillers on mechanical and thermal properties of biobased epoxy nanocomposites

In this study, the fabrication and characterization of bone ash filled biobased epoxy resin (Super SAP 100/1000, contains 37% biobased carbon content) nanocomposites are presented. Biosource bone ash was modified by size reduction and surface modification processes using a combination of ball milling and sonochemical techniques and characterized using X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The modified bone ash particles were incorporated into biobased epoxy with noncontact mixing process. The as-fabricated nanocomposites were characterized using various thermal and mechanical analyses. The nanocomposites showed significant improvement in flexural strength (41.25%) and modulus (34.56%) for 2 wt% filler loading. Dynamic mechanical analysis (DMA) results showed improvement in both storage modulus and loss modulus. Additionally, DMA results showed a slight reduction in glass transition temperature which also complies with differential scanning calorimetry results. Thermomechanical analysis results showed a reduction in the coefficient of thermal expansion. Thermogravimetric analysis results showed improved thermal stability at both onset of degradation and the major degradation. These enhanced thermal and mechanical performances of the epoxy nanocomposites allows them to be suitable for lightweight aerospace, automotive, and biomedical applications.     

Thermal and mechanical properties of PA12/C30B nanocomposites in relationship with nanostructure

This work focuses on the effect of nanoclay mass fraction on the properties of polyamide 12 matrix. Relationships between mechanical, thermal, and structural properties of polyamide 12/Cloisite^® 30B nanocomposites were studied. The material structure, previously described from XRD and TEM experiments, was more thoroughly characterized in the present work using SEM and FTIR techniques. The FTIR results clearly showed that clay galleries are intercalated by PA chains, which leads to a partially exfoliated nanostructure, confirming the TEM observations and the XRD analysis. However, a few micrometric aggregates are evidenced by SEM analysis, particularly at high clay fractions. TGA and DTA measurements showed that the thermal stability of PA12 matrix is slightly modified by the Cloisite^® 30B content. Viscoelastic properties of the nanocomposites in solid‐state were analyzed as functions of strain, frequency, and temperature. The extent of the linear response regime of the material is shown to be sensitive to the amount of clay: nonlinearities appear at lower strain values as the clay mass fraction increases. Both relative dynamical moduli also increase with increasing clay mass fraction, with frequency dependence for the viscous modulus and without frequency dependence for the elastic modulus. Finally, similarities have been pointed out between viscoelastic properties of the nanocomposites in solid and melt states. For example, the percolation threshold is highlighted at the same clay mass fraction, ～2%, in both states. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41938.     

Thermal conductivity and stability of a three‐phase blend of carbon nanotubes,conductive polymer,and silver nanoparticles incorporated into polycarbonate nanocomposites

Metallic and non‐metallic nanofillers can be used together in the design of polycarbonate (PC) nanocomposites with improved electrical properties. Here, the preparation of three‐phase blend (carbon nanotubes (CNT), silver nanoparticles, and conductive polymer) in a two‐step process before incorporation in the PC is reported. First, ethylene diamine functionalized multiwall carbon nanotubes (MWCNT‐EDA) were decorated with Ag nanoparticles. Next, the Ag‐decorated CNTs were coated with poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT : PSS). Due to the high thermal conductivity instrinsic to both metallic and non‐metallic phases, it is expected that the thermal properties of the resulting nanocomposite would largely differ from those of pristine PC. We thus investigated in detail how this hybrid conductive blend affected properties such as the glass transition temperature, the thermal stability, and the thermal conductivity of the nanocomposite. It was found that this strategy results in improved thermal conductivity and thermal stability of the material. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42281.     

Polymerization kinetics and thermal properties of dicyanate/clay nanocomposites

The polymerization kinetics and thermal properties of dicyanate/clay nanocomposites were investigated. A type of organically modified clay was used as nanometer‐size fillers for the thermosetting dicyanate resin. Differential scanning calorimetry (DSC) was used to study the curing behavior of the dicyanate/clay nanocomposite systems. The polymerization rate of the nanocomposite systems increased with increasing clay content. An autocatalytic reaction mechanism could adequately describe the polymerization kinetics of the dicyanate/clay nanocomposite systems. The polymerization kinetic parameters were determined by fitting the DSC conversion data to the proposed kinetic equation. The glass‐transition temperature of the dicyanate/clay nanocomposites increased with increasing clay content. The thermal decomposition behavior of the dicyanate/clay nanocomposites was investigated by thermogravimetric analysis. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1955–1960, 2004     

Development of biodegradable PLA/PBT nanoblends

Poly(lactic acid)/poly(butylene terephthalate) (PLA/PBT) blends with 3, 5, and 10 wt % of PBT were produced in a twin‐screw extruder, with the addition of ethylene–glycidyl methacrylate copolymer as compatibilizer. An uncompatibilized PLA/PBT blend with 5 wt % of PBT was prepared for comparison studies. The epoxy reactive groups in the compatibilizer allowed modification of the interfacial tension in the blends and reduced the PBT dimensions. The crystallinity of the blends was studied, and its influence on mechanical properties was analyzed. Tensile tests showed an increase in strain at break from 3% for neat PLA to 49% for PLA with 3 wt % PBT, while the tensile modulus dropped from 3.59 GPa to 3.35 GPa for the same samples. Izod results showed a transition from a brittle behavior of PLA to a ductile one for compatibilized blends. These results indicate that the nanometer‐size dispersed phase was effective in changing the deformation behavior of the matrix without a significant loss of modulus. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45951.     

Online ultrasonic film casting of LLDPE and LLDPE/clay nanocomposites

Transparent cast films of linear low density polyethylene (LLDPE) with nanoclay up to 10 wt % were prepared in one step process using an ultrasonically assisted compounding extruder operating at various ultrasonic amplitudes combined with film casting machine operating at various take up speeds. Thermal, rheological, morphological, and mechanical properties and gas permeability of these films were studied. Ultrasonic treatment introduced an increase in the complex viscosity and storage modulus and a reduction in the tangent loss of LLDPE/clay nanocomposite melts. Cast films prepared by ultrasonic treatment at an amplitude of 7.5 μm showed the highest mechanical properties in both the machine and transverse directions and the lowest oxygen permeability. X‐ray diffraction patterns along with the SEM and TEM images revealed the presence of the exfoliated structure due to the ultrasonic treatment for cast films containing up to 7.5 wt % of clay loading. NMR studies of LLDPE cast films showed an increase of branching due to the ultrasound treatment. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

The role of the interphase on the shear induced failure of multiwall carbon nanotubes reinforced epoxy nanocomposites

Multiwall Carbon Nanotubes (MWCNT) with an elevated aspect ratio were chemically functionalized with amines and two types of epoxide groups. Thermogravimetric analysis and Fourier Transform‐Infrared Spectroscopy (FTIR) analysis corroborated that the functionalization degree was substantial (up to 30 wt %) and the presence of a covalent bond with the MWCNT. The functionalized MWCNT (f‐CNT) were incorporated into an epoxy matrix after its dispersion in the diglycidyl ether of bisphenol A (DGEBA) precursor. To induce a shear failure mode, a short‐beam (SB) experimental setup was implemented. The SB shear strength (SBSS) proved that the functionalization had a strong influence on its value. For the case of pristine CNT, a neutral effect was obtained. A strong detrimental effect (?17.2% ± 9.5) was measured for the amine type f‐CNT and a positive effect (up to 10.9% ± 8.9) was measured of the epoxide type f‐CNT. Fractographic analysis of each formulation was correlated with SBSS performance, proving that the surface texture of the fractured samples was strongly correlated to its value. Furthermore, dynamic mechanical analysis proved that the damping factor and the crosslink molecular weight were correlated with the SBSS performance. A lower full width at half maximum of the damping factor was associated to an improvement of SBSS. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41364.     

In situ sintered silver decorated 3D structure of cellulose scaffold for highly thermoconductive electromagnetic interference shielding epoxy nanocomposites

This study presents a 3-dimensional (3D) network structure of cellulose scaffold (CS), which was in situ decorated with silver nanoparticles (AgNPs). The scaffold was then infiltrated with epoxy matrix and cured at elevated temperature to sinter the AgNPs; finally, highly thermoconductive epoxy composites (Ag@CS/epoxy) was obtained. The resultant Ag@CS20/epoxy composite reached a thermal conductivity of 2.52 W·m⁻¹·K⁻¹ at 2.2 vol% of filler loading, which shows an enhancement of over 11-folds in the thermal conductivity compared to the neat epoxy. The superb electrical conductivity value of over 53,691 S·m⁻¹ of the Ag@CS20/epoxy was achieved, which led to exceptional EMI SE values of 69.1 dB. Furthermore, surface temperatures during heating and cooling were also investigated to demonstrate the superior heat dissipating capacity of the Ag@CS/epoxy composite, which can be potentially put an application as thermal dissipating material in the next generation of electronics.     

Investigating the thermal,mechanical, and electrochemical properties of PVdF/PVP nanofibrous membranes for supercapacitor applications

Polyvinylidene fluoride and polyvinylpyrrolidone polymers incorporated with carbon black nanoparticles (50 nm) were electrospun to fabricate nanofibrous membranes for supercapacitor separators. Different weight percentages (0, 0.25, 0.5, 1, 2, and 4 wt %) of carbon black nanoparticles were dispersed in N,N‐dimethylacetamide and acetone prior to the electrospinning processes at various voltage, pump speed, and tip‐to‐collector distances. The morphology, thermal, mechanical, hydrophobic, and electrochemical characterization of nanofibrous membrane were analyzed using different techniques, such as scanning electron microscopy, differential scanning calorimetry, capacitance bridge, thermogravimetric analysis, dynamic mechanical analyzer, and water contact angle. Effects of annealing and UV irradiation exposures on the nanofibrous membranes were investigated in detail. Test results revealed that the physical properties of the nanocomposite separators were significantly enhanced as a function of carbon black inclusions in the polymeric structures, which may be useful for the applications of supercapacitor separators and other energy storage devices. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43707.     

Thermal and mechanical properties of polyamide 12/graphene nanoplatelets nanocomposites and parts fabricated by fused deposition modeling

The printable polyamide 12 (PA12) nanocomposite filaments with 6 wt % graphene nanoplatelets (GNPs) for fused deposition modeling (FDM) were prepared by melting compounding and smoothly printed via a commercial FDM three‐dimensional (3D) printer. The thermal conductivity (λ) and elastic modulus (E) of 3D printed PA12/GNPs parts along to the printing direction had an increase by 51.4% and 7% than that of compression molded parts, which is due to the GNPs preferentially aligning along to the printing direction. Along with these improved properties, ultimate tensile strength of 3D printed PA12/GNPs parts was well maintained. These results indicate that FDM is a new way to achieve PA12/GNPs parts with enhanced λ over compression moulding, which could contribute to realize efficient and flexible heat management for a wide range of applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45332.     

Modification of structural,thermal, and electrical properties of PVA by addition of silicon carbide nanocrystals

SiC‐PVA nanocomposite films, synthesized using solution‐casting technique were structurally characterized using X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. Morphological studies of the SiC‐PVA nanocomposite films were carried out using Transmission electron microscopy (TEM) and Scanning electron microscopy (SEM). TEM analysis confirms that the size of SiC nanocrystals present in PVA matrix are 23 ± 9 nm, which is consistent with size calculated using XRD. SiC‐PVA nanocomposite films were further characterized for their thermal and electrical properties. Thermogravimetric/differential thermal analysis (TG/DTA) indicates that the char yield of nanocomposite films containing 3 wt % SiC nanocrystal is ～30% more than PVA. This increase in char yield is an indication of the potency of flame retardation of SiC‐PVA nanocomposite films. I‐V analysis reveals that Schottky mechanism is the dominant conduction mechanism which is responsible for the increase in conductivity of PVA with the addition of SiC nanocrystals. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42464.     

Synchronization of thermal properties and constituents in Nanocomposite: Manufacturing,characterization, adjustable properties

This is critical to maintain better thermal properties, especially thermal conductivity as well as low particle content along with organized particle dispersion in polymer nanocomposites. Thus, this study is designed to develop a nanocomposite containing a constant reinforcing load of binary particles (carbon and alumina) in the binary matrix of polypropylene (PP)/poly ethylene-co-vinyl acetate (EVA). The samples were prepared through the melt blending and hot pressing technique. Compared to pure PP/EVA matrix, the nanocomposites showed a shift in Fourier-transform infrared spectroscopy peak and absorption intensity, which proves better interaction of nanoparticles with the matrix. The Scanning Electron Microscopy analysis showed the nanocomposite having carbon (C) and alumina (A) relative ratio 2:3 offered even structure with better distribution of nanoparticles compared to other nanocomposites. Also, Differential scanning calorimetry and Thermogravimetric analysis revealed that alumina-rich binary nanoparticles reinforced composites offer an efficient improvement in thermal behavior. Moreover, the nanocomposite containing high alumina relative ratio (C: A = 2:3) gives a sharp shift in thermal conductivity of 1.57 W/m-k from 1.2 W/m-k of carbon-rich nanocomposite (C: A = 3:2) and 0.16 W/m-k of pure PP/EVA. However, these relative properties emphasize the important role of this nanocomposite as a programmable thermal material.     

Structure,electrical, dielectric,and optical investigation on polyvinyl alcohol/metal chloride nanocomposites

Different concentrations of metal chlorides/polyvinyl alcohol nanocomposites have been prepared by the typical solvent cast technique. The prepared samples were investigated by different techniques such as X‐ray diffraction, differential scanning calorimetry, and scanning electron microscope. DC and AC conductivities are examined at different temperatures and frequencies. An activation process was found in the DC conductivity versus temperature relation and the activation energy was calculated. The AC conductivity obeyed the ω^S power law. The behavior of S with temperature was studied. Various dielectric parameters such as dielectric constant (ε′), dielectric loss (ε″) and loss tangent (tan δ) have been determined in the temperature range 303–443 K at different frequencies. The dielectric parameters were found to decrease with increasing frequency. The study of dielectric relaxation as a function of temperature at constant frequency shows two relaxation mechanisms. The optical band gaps and band tails were estimated from the measured absorption spectra. The applied photon energy found to affect the observed optical band gaps. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Creep resistance of linear low density polyethylene/carbonaceous hybrid nanocomposites: Experiments and modeling

In the present work, the creep response of nanocomposites based on metallocene linear low density polyethylene (mLLDPE), reinforced with three types of carbonaceous nanofillers, namely carbon nanotubes (CNTs), graphene oxide (GO) platelets, and carbon nanofibers (CNFs) was experimentally studied. The effect of the nanofiller loading and the hybrid character of nanocomposites on the creep resistance of the nanocompsites was analyzed. In all cases, the creep resistance of the nanocomposites examined has been postulated. To support these results, creep has been modeled by a power creep law, while the creep- recovery modeling was achieved by a viscoelastic model. The implementation of the viscoelastic model has been made by assuming that the nanocomposite's structure can be represented by a physical network, with the dispersed nanofillers participating in the molecular rearrangements, which take place upon the imposition of stress. The time dependent constitutive equation involves a relaxation function, based on a Gaussian type distribution function, associated with the energy barriers that molecular segments need to overcome, for transitions to occur. It was found that creep-recovery strain could be accurately captured with the same set of parameters, whereas the number of required model parameters was quite lower than that in the widely known viscoelastic models.     

Selective localization of organophilic clay Cloisite 30B in biodegradable poly(lactic acid)/poly(3-hydroxybutyrate) blends

The influence of selective localization of the nanoclay Cloisite 30B on the morphological, thermal and thermo-mechanical properties of biodegradable poly(lactic acid)/poly(hydroxybutyrate) blends was evaluated in this work. For this, different compounds were obtained by adding the filler in a single phase or mixed with the two matrices simultaneously by melting processing. The simultaneous processing leads to a better dispersion of nanoparticles on the blend and generates a more homogeneous polymer interface, but the properties do not increase in relation to those that were processed in separate steps. For the blends obtained in separated steps, the polymeric domains and, consequently, the superficial tension between phases are better controlled by a nanolayer. Thus, the results obtained in this work indicate that better control of the polymeric interfaces can generate a more significant effect on the thermal and thermo-mechanical properties of nanostructured blends than just a good dispersion of the fillers.     

Mechanical and thermal properties of bio‐based CaCO3/soybean‐based hybrid unsaturated polyester nanocomposites

Bio‐based calcium carbonate nanoparticles (CaCO₃) were synthesized via size reduction of eggshell powder using mechanical attrition followed by high intensity ultrasonic irradiation. The transmission electron microscopic (TEM) and BET surface area measurements show that these particles are less than 10 nm in size and a surface area of ～44 m²/g. Bio‐based nanocomposites were fabricated by infusion of different weight fractions of as‐prepared CaCO₃ nanoparticles into Polylite® 31325‐00 resin system using a non‐contact Thinky® mixing method. As‐prepared bio‐nanocomposites were characterized for their thermal and mechanical properties. TEM studies showed that the particles were well dispersed over the entire volume of the matrix. Thermal analyses indicated that the bio‐nanocomposites are thermally more stable than the corresponding neat systems. Nanocomposite with 2% by weight loading of bio‐CaCO₃ nanoparticles exhibited an 18°C increase in the glass transition temperature over the neat Polylite 31325 system. Mechanical tests have been carried out for both bio‐nanocomposites and neat resin systems. The compression test results of the 2% Bio‐CaCO₃/Polylite 31325 nanocomposite showed an improvement of 14% and 27% in compressive strength and modulus respectively compared with the neat system. Details of the fabrication procedure and thermal and mechanical characterizations are presented in this article. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1442–1452, 2013