Nanoscale reinforcement of polypropylene composites with carbon nanotubes and clay: Dispersion state,electromagnetic and nanomechanical properties

In the present study, the bifiller system incorporating various amount of multiwalled carbon nanotubes (MWCNTs) and 3 wt% clay in polypropylene is investigated to obtain composites with multifunctional performance. The dispersion state of two nanofillers in the polypropylene matrix was characterized by applying TEM and Raman spectroscopy. Both composites demonstrate similar rheological behavior with a rheological percolation threshold of ?_p1 = 1.5 wt% for the monofiller (MWCNTs) and ?_p2 = 2 wt% for the bifiller systems (MWCNTs and 3% clay). The effect of two nanofillers on electromagnetic and nanomechanical properties was evaluated. Above rheological percolation both type composites show considerable electromagnetic shielding efficiency at small layer thickness due mostly to the addition of MWCNTs. The nanomechanical properties improvement is strongly dependent on the structure formed by MWCNTs in the polymer. The hardness and Young's modulus, measured by nanoindentation, is higher for the bifiller systems in comparison with the monofiller one above the rheological percolation threshold. This was attributed to the continuous network structure formed by interacted MWCNTs and infiltrated fine clay stacks. POLYM. ENG. SCI., 56:269–277, 2016. © 2015 Society of Plastics Engineers     

Surface,interface and electronic properties of F8:F8BT polymeric thin films used for organic light‐emitting diode applications

Ultrathin polymeric films consisting of poly(9,9‐di‐n‐octylfluorenyl‐2,7‐diyl) (F8) blended with poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT) grown onto PEDOT:PSS/ITO/PET were investigated by X‐ray photoelectron spectroscopy (XPS), depth‐profiling XPS, reflection electron energy loss spectroscopy (REELS) and angle‐dependent X‐ray absorption spectroscopy (XAS) to gain information on the films' electronic, order and interface properties. AFM studies provide valuable information on the films' nanotopographical properties and homogeneity. Spectroscopic ellipsometry and photoluminescence spectroscopy were used also to obtain information on the optoelectronic properties. Well‐ordered films were observed from the XAS analysis, measured at the sulfur K absorption edge. XPS measurements demonstrated that the surface composition of the polymer thin films prepared by a spin‐coating wet‐chemical deposition method matches the expected F8:F8BT blend stoichiometry. The interfacial properties were studied through an argon ion sputtering process coupled to the XPS acquisition, showing an enhancement of oxygen components at the interface. The films' inhomogeneity was verified by AFM images and analysis. We obtained a value of 3.1 eV as the electronic bandgap of the F8:F8BT film from REELS data, whereas analysis of the spectroscopic ellipsometry spectra revealed that the optical bandgap of F8:F8BT has a value of 2.4 eV. A strong green emission was obtained for the produced films, which is in agreement with the expected emission due to the 1:19 ratio of the F8 and F8BT blended polymers. © 2018 Society of Chemical Industry     

Investigation of electrical,mechanical, and thermal properties of functionalized multiwalled carbon nanotubes‐reduced graphene Oxide/PMMA hybrid nanocomposites

Electrical, mechanical, and thermal properties of the poly(methyl methacrylate) (PMMA) composites containing functionalized multiwalled carbon nanotubes (f‐MWCNTs) and reduced graphene oxide (rGO) hybrid nanofillers have been investigated. The observed electrical percolation threshold of FHC is 0.8 wt% with maximum conductivity of 1.21 × 10^?3 S/cm at 4 wt% of f‐MWCNTs. The electrical transport mechanism and magneto resistance studied of hybrid composites have also been investigated. Progressive addition of f‐MWCNTs in rGO/PMMA composite results increase in mechanical (tensile strength and Young's modulus) and thermal (thermal stability) properties of f‐MWCNTs‐rGO/PMMA hybrid nanocomposites (FHC). The increased mechanical properties are due to the efficient load transfer from PMMA matrix to f‐MWCNTs and rGO through better chemical interaction. The strong interaction between PMMA and f‐MWCNTs‐rGO in FHC is the main cause for improved thermal stability. POLYM. ENG. SCI., 59:1075–1083, 2019. © 2019 Society of Plastics Engineers     

In situ polymerization,thermal, damping,and mechanical properties of multiwalled carbon nanotubes/polyisobutylene‐based polyurethane nanocomposites

Despite the development of strong, durable, and cost efficient polyisobutylene‐based polyurethane (PIB‐based PU) materials has yet to be achieved. The well dispersion and maximum interfacial interaction between the nanofiller and the PIB‐based PU at low loading have been scarcely studied. Here, the preparation of PIB‐based PU nanocomposites with Multiwalled carbon nanotubes (MWCNTs) using a simple in situ polymerization method is reported. The thermogravimetric analysis tests show that MWCNTs significantly improved the thermal stability of MWCNTs/PIB‐based PU nanocomposites. Compare to the pure PIB‐based PU the onset temperature of degradation for the nanocomposite was about 20°C higher at 0.7 wt% MWCNTs loading. Efficient load transfer is found between the nanofiller MWCNTs and PIB‐based PU and the mechanical properties of the MWCNTs/PIB‐based PU nanocomposite with well dispersion are improved. A 63% improvement of Young's modulus and slightly increased of tensile strength are achieved by addition of only 0.7 wt% of MWCNTs. The experimentally determined Young's modulus is in well agreement with the theoretical simulation. It is worth noting that the PIB‐based PU and MWCNTs/PIB‐based PU nanocomposites exhibit excellent damping properties (tan δ > 0.3) from −45°C to 8°C. POLYM. COMPOS., 36:198–203, 2015. © 2014 Society of Plastics Engineers     

Fabrication and modification of cellulose acetate based mixed matrix membrane: Gas separation and physical properties

[Cellulose acetate (CA)-blend-multi walled carbon nano tubes (MWCNTs)] mixed matrix membranes (MMMs), [CA/polyethylene glycol (PEG)/MWCNTs] and [CA/styrene butadiene rubber (SBR)/MWCNTs] blend MMMs were prepared by solution casting method for gas separation applications using Tetrahydrofuran (THF) as solvent. Both raw-MWCNTs (R-MWCNTs) and functionalized carboxylic-MWCNTs (C-MWCNTs) were used in membrane preparation. The MWCNTs loading ratio and pressure effects on the gas separation performance of prepared membranes were investigated for pure He, N₂, CH₄ and CO₂ gases. Results indicated that utilizing C-MWCNT instead of R-MWCNTs in membrane fabrication has better performance and (CO₂/CH₄) and (CO₂/N₂) selectivity reached to 21.81 and 13.74 from 13.41 and 9.33 at 0.65 wt% of MWCNTs loading respectively. The effects of PEG and SBR on the gas transport performance and mechanical properties were also investigated. The highest CO₂/CH₄ selectivity at 2 bar pressure was reached to 53.98 for [CA/PEG/C-MWCNT] and 43.91 for [CA/SBR/C-MWCNT] blend MMMs at 0.5 wt% and 2 wt% MWCNTs loading ratio respectively. Moreover, increase of feed pressure led to membrane gas permeability and gas pair selectivity improvement for almost all prepared membranes. The mechanical properties analysis exhibited tensile modules improvement with increasing MWCNTs loading ratio and utilizing polymer blending.     

Studies of the Mechanical Properties and Practical Coating Adhesion on PP Modified by Oxidized Wax

In this study, the influences of polarity and the amount of oxidized polypropylene wax (OPPW) in blends with polypropylene (PP) were investigated by studying their surface properties. OPPW was completely miscible with PP up to 10 wt%. The adhesive strength of a acrylic-based primer coating on PP sheets, containing different wt% of OPPWs, was evaluated by using a direct 'pull off' test method. The results showed that the adhesive strength of the coating improved with an increase of the amount of OPPW in the blend. However, the degree of polarity in the OPPW did not have a significant impact on its adhesive properties. These observations were also supported by the results of ATR–FT-IR spectroscopy and surface energy measurements of the substrate. Furthermore, the results of adhesion test on the coating panels showed a significant enhancement after exposing to heat in an oven prior to the application of coating, e.g., about 230% increase for the blend containing 8 wt% of OPPW. The TGA curves showed a maximum drop of about 10% in thermal stability in comparison with that of the unblended PP. The changes in the mechanical properties of the blends were explained by considering the morphology of the blends and were supported by the changes in blend crystalinity and melting behavior. The elastic modulus remained almost unchanged while elongation and stress to breakpoint experienced a sharp reduction at concentrations of wax content higher than 6 wt%. The study showed a good balance of substrate coatability with its bulk properties at a blend concentration of about 6 wt% of OPPW.     

Preparation and Characterization of Polycarbonate-Blend-Raw/Functionalized Multi-Walled Carbon Nano Tubes Mixed Matrix Membrane for CO2 Separation

Membrane composed of PC as base of polymer matrix with different ratio of multiwall carbon nano tubes (MWCNTs) as nanofillers and poly ethylene glycol (PEG) as second polymer was prepared by solution casting method. Both raw-MWCNTs (R-MWCNTs) and functionalized carboxyle-MWCNTs (C-MWCNTs) were used in membrane preparation. The MWCNTs loading ratio and pressure effects on the gas transport properties of membranes were examined in relation to pure He, N₂, CH₄, and CO₂ gases. Results showed that the use of C-MWCNT instead of R-MWCNTs in mixed matrix membranes (MMMs) fabrication with base of PC provides better performance and also it increases (CO₂/CH₄) and (CO₂/N₂) selectivities to 27.38 and 25.42 from 25.45 and 19.24, respectively (at 5 wt% of MWCNTs). PEG as the second rubbery polymer was utilized to improve the separation performance and mechanical properties. In blend MMMs, highest (CO₂/CH₄) selectivity at 2 bar pressure increased to 35.64 for PC/PEG/C-MWCNT blend MMMs which was 27.28 for PC/MWCNTs MMMs at 10 wt%. Increase of feed pressure led to gas permeability and gas pair selectivity improvement in approximately all of membranes. Analysis of mechanical properties showed improvement in tensile modules with the increase of MWCNTs loading ratio and use of PEG in prepared MMMs.     

Morphology evolution induced by carbon nanotubes on thermal and mechanical characters of semi-crystalline aromatic polyimide

A series of nanocomposites based on a new semi-crystalline polyimide (PI) and multi-walled carbon nanotubes (MWCNTs) were prepared by in situ polymerization. The TEM measurement reveals the improved dispersion of carboxylic acid-functionalized MWCNTs (COOH-MWCNTs) in semi-crystalline PI compared with pristine MWCNTs. The TGA analysis show that the concentration of carboxylic acid groups on the surface of nanotubes is about 4.34 wt%. The FT-IR spectroscopy analysis indicate that the imide rings of the PI interact non-covalently with nanotubes. The Polarized optical microscopy observation reveals significant morphology evolution in semi-crystalline PI induced by MWCNTs. The SEM micrographs suggest the strong interfacial interaction between COOH-MWCNTs and PI main chains, and significant changes in the fracture surfaces morphology. The WAXRD measurements reveal that COOH-MWCNTs promote the semi-crystalline PI crystallinity and structure change. COOH-MWCNTs can more efficiently improve the mechanical and thermal properties of resulting nanocomposites than pristine MWCNTs. COOH-MWCNT/PI nanocomposites show increases of Young’s modulus and yield strength, as high as 20–30 %, without sacrificing the elongation at break at loadings of 0.5 wt% nanotubes. Furthermore, with increasing the loadings of COOH-MWCNTs to 1.0 wt%, Young’s modulus and yield strength decrease due to nanotube aggregation, but elongation at break increase about 46 %. An abrupt increase of elongation at break in pristine MWCNT/PI nanocomposites was also registered at nanotubes loadings increasing from 0.5 to 1 wt%. These results indicate that the properties of semi-crystalline PI nanocomposites reinforced with carbon nanotubes are not only determined by the dispersion of nanotubes in the PI matrix and their interfacial interactions, but also by the crystalline phase morphology evolution in the PI matrix.     

Improvement in mechanical properties of enamel via carbon nanotube addition

Enameled metal equipment exploits the strength of metal materials and the corrosion resistance of enamel; therefore, it is widely used in the chemical industry. However, the mechanical properties of the enamel restrict its service life. Multi-walled carbon nanotubes (MWCNTs) are one-dimensional nanomaterials with high-specific surface area, C–C bond structure, and SP₂ hybrid orbital. Herein, the effect of the dosage of MWCNTs on the mechanical properties of enamel is studied by adding MWCNTs to improve the mechanical properties of the enamel. Microscopic observation showed that the toughening mechanism of MWCNTs was mainly manifested in fracture and pull out behaviors. According to three-point bending test, when 0.4 wt% carbon nanotubes were added, the reinforcing effect of enamel layer reached the best state. These results provide reference for optimizing the formulation of enamel and extending the service life of enamel.     

Synthesis and characterization of multiwalled carbon nanotube/polyurethane composites via surface modification multiwalled carbon nanotubes using silane coupling agent

Well‐dispersed multiwalled carbon nanotubes/polyurethane (MWCNTs/PU) composites were synthesized in situ polymerization based on treating MWCNTs with nitric acid and silane coupling agent. The morphology and degree of dispersion of the MWCNTs were studied using a high resolution transmission electron microscopy (HR‐TEM) and X‐ray powder diffraction (XRD). The result showed that MWCNTs could be dispersed still in the PU matrix well with the addition of 2 wt% MWCNTs. The thermal and mechanical properties of the composites were characterized by dynamic mechanical thermal analysis, thermogravimetric analysis, tensile, and impact testing. The result suggested that the glass transition temperature (T_g) of composites increased greatly with increasing MWCNTs content slightly, and the MWCNTs is also helpful to improve mechanical properties of composites. Furthermore, the composites have an excellent mechanical property with the addition of 0.5 wt% MWCNTs. The electrical property testing indicates that the MWCNTs can improve evidently the electrical properties of composites when adding 1 wt% MWCNTs to the PU matrix. The volume resistivity of composites reaches to an equilibrium value. POLYM. COMPOS., 33:1866–1873, 2012. © 2012 Society of Plastics Engineers     

Effect of strain rate on tensile properties of polyurethane/(multiwalled carbon nanotube) nanocomposite

In this research, polyurethane (PU)/(carbon nanotube) (CNT) samples, with two different contents of multiwalled carbon nanotubes (MWCNTs; i.e., 0.5 and 1.0 wt%) were fabricated through a solution casting method. To investigate the effect of strain rate on tensile properties, tensile tests were done on standard samples at constant temperature and different strain rates (2 × 10^?5 to 2 × 10^?2 s^?1). Eyring's model was performed to clarify the role of both strain rate and CNTs content on activation volume and activation enthalpy of PU. To elucidate the role of strain rate and CNTs content on fracture behavior of PU, fracture surfaces of some samples were also investigated by scanning electron microscopy. The results of tensile tests show the intense effect of strain rate on tensile properties of PU/MWCNTs nanocomposites. Also, it was proved that the dependency of tensile properties of PU nanocomposites on strain rate decreases as CNTs content increases. The microscopic observations of the samples also demonstrate that increasing the strain rate changes the behavior of the fracture surface to less a ductile fracture, and increasing CNTs content causes much surface roughness. Finally, by investigation of the activation enthalpies, it is confirmed that much higher enthalpy is needed to fracture the samples with increased MWCNTs content, as the activation enthalpy changes from 45 for neat PU to 131 kJ/mol for PU/(1% MWCNTs) samples. J. VINYL ADDIT. TECHNOL., 22:356–361, 2016. © 2014 Society of Plastics Engineers     

Comparative analysis of electric,magnetic, and mechanical properties of epoxy matrix composites with different contents of multiple walled carbon nanotubes

Epoxy composites based on aligned chemical vapor deposition–grown multiwall carbon nanotubes (MWCNTs), containing trapped iron nanoparticles, with weight fractions ranging from 0.03 to 1 wt%, were produced following a well‐known processing way. Electrical and mechanical properties as well as their densities were measured. The results are compared with previous studies investigating the magnetic percolation behavior in the same samples of composites. A percolation threshold at 0.4 wt% of MWCNTs was determined by the electrical property and it agrees with the threshold observed in the magnetic properties. A hop in the porosity and a depression of the bulk mechanical properties were also found at the threshold value. These results point out that there is an efficiency threshold related to the sonication stage of the fabrication process and the weight fraction of MWCNTs, and after this threshold, the initial nanotubes pans were not separated into individual MWCNTs or into small ropes. An optimized sonication stage is proposed and the improvement in the dispersion of the filler is shown. POLYM. COMPOS., 28:612–617, 2007. © 2007 Society of Plastics Engineers     

Enhanced Thermal Conductivity of Epoxy Composites with MWCNTs/AlN Hybrid Filler

To further improve the thermal conductivity of epoxy resin, the multi-walled carbon nanotube/aluminum nitride (MWCNTs/AlN) hybrid filler was employed to prepare thermal conductivity MWCNTs/AlN/epoxy composite by casting process, and the silane coupling reagent of γ-glycidoxy propyl trimethoxy silane(KH-560) was also used to functionalize the surface of MWCNTs and/or AlN. Results revealed that, the thermal conductivity of epoxy resin was improved remarkably with the addition of MWCNTs/AlN hybrid filler, a higher thermal conductivity of 1.04 W/mK could be achieved with 29 wt% MWCNTs/AlN hybrid filler (4 wt% MWCNTs +25 wt% AlN), about 5 times higher than that of native epoxy resin. And the epoxy composite with 29 wt% MWCNTs/AlN hybrid filler possessed better thermal conductivity and mechanical properties than those of single 5 wt% MWCNTs or 40 wt% AlN. The thermal decomposition temperature of MWCNTs/AlN/epoxy composite was increased with the addition of MWCNTs/AlN hybrid filler. For given filler loading, surface treatment of MWCNTs and/or AlN by KH-560 exhibited a positive effect on the thermal conductivity of epoxy composite.     

Nanocomposite films of poly(vinylidene fluoride) filled with polyvinylpyrrolidone‐coated multiwalled carbon nanotubes: Enhancement of β‐polymorph formation and tensile properties

To improve interactions between carbon nanotubes (CNTs) and poly(vinylidene fluoride) (PVDF) matrix, multiwalled CNTs (MWCNTs) were successfully coated with amphiphilic polyvinylpyrrolidone (PVP) using an ultrasonication treatment performed in aqueous solution. It was found that PVP chains could be attached noncovalently onto the nanotubes' surface, enabling a stable dispersion of MWCNTs in both water and N,N‐dimethylformamide. PVP‐coated MWCNTs/PVDF nanocomposite films were prepared by a solution casting method. The strong specific dipolar interaction between the PVP's carbonyl group (C?O) and the PVDF's fluorine group C?F₂ results in high compatibility between PVP and PVDF, helping PVP‐coated MWCNTs to be homogenously dispersed within PVDF. Fourier transform infrared and X‐ray diffraction characterization revealed that the as‐prepared nanocomposite PVDF films exhibit a purely β‐polymorph even at a very low content of PVP‐wrapped MWCNTs (0.1 wt%) while this phase is totally absent in the corresponding unmodified MWCNTs/PVDF nanocomposites. A possible mechanism of β‐phase formation in PVP‐coated MWCNTs/PVDF nanocomposites has been discussed. Furthermore, the tensile properties of PVDF nanocomposites as function of the content in PVP‐coated MWCNTs were also studied. Results shows that the addition of 2.0 wt% of PVP‐coated MWCNTs lead to a 168% increase in Young's modulus and a 120% in tensile strength. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Novel bioresource-based poly(3-Hydroxybutyrate-co-4-Hydroxybutyrate)/poly(LacticAcid) blend fibers with high strength and toughness via melt-spinning

Novel biodegradable blend fibers based on the biomaterials poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P3HB4HB) and poly(lacticacid) (PLA) were successfully prepared by combining melt spinning and hot drawing. The results showed that the commixture could continuous and stable spin for a P3HB4HB ratio of 30–35 wt% and winding speed of 20–30 m/min. The thermal stability of the P3HB4HB/PLA blend fiber was increased, as determined by thermogravimetric analysis. The crystallinity degree of the P3HB4HB/PLA blend fibers increased with increasing the P3HB4HB content. The addition of PLA resulted in a low cold crystallization temperature and diminutive size of the lamellar stacks, which would be favorable for the enhancement of the mechanical properties of the blend fiber, when the P3HB4HB content was 30–35 wt%. The P3HB4HB/PLA composite fiber was one type of high-strength and high-toughness fiber, with 1 GPa breaking stress and over 80% strain at break. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48956.     

Styrene butadiene rubber/epoxidized natural rubber/carbon filler nanocomposites: microstructural development and cure characterization

Microstructural development of elastomeric nanocomposites based on (50/50 wt%) styrene butadiene rubber (SBR) and epoxidized natural rubber (50 mol% epoxidation, ENR50) as the rubber matrix including two types of carbon fillers, carbon black (CB) and functionalized multiwall carbon nanotube (NH₂-MWCNT), which were prepared through melt mixing, was studied. The results from FTIR analysis show that there is interaction between functional groups on MWCNT surface and the rubber chains. The AFM analysis also indicates good dispersion of filler particles in the rubber phases. FESEM images from cryo-fractured surface of samples have revealed that nanotubes were rarely pulled out of matrix and their diameter increased, resulting from good interaction between MWCNTs and rubber chains. The DMA results confirm good interfacial interaction between them. Furthermore, the reduced difference between the two T_gs of phases (ΔT_g) shows that the incorporation of 3 phr MWCNT into the blend leads to increment in rubber phase compatibility but at higher MWCNT content (5 phr) due to lower Mooney viscosity of SBR phase, MWCNTs tend to remain in this phase. The bound rubber was adopted to characterize the polymer–filler interaction, showing that bound rubber content has an increasing trend with increasing in fillers content. The cure rheometric studies reveal that MWCNTs accelerate the cure process due to the presence of amine groups on the nanotube surface. In addition, the mechanical properties of samples show an increasing trend by increasing nano-filler content.

     

Mechanical,morphological, and thermal properties of poly(vinyl chloride)/low‐density polyethylene composites filled with date palm leaf fiber

This article investigates the mechanical, morphological, and thermal properties of poly(vinyl chloride) (PVC) and low‐density polyethylene (LDPE) blends, at three different concentrations: 20, 50, and 80 wt% of LDPE. Besides, composite samples that were prepared from PVC/LDPE blend reinforced with different date palm leaf fiber (DPLF) content, 10, 20, and 30 wt%, were also studied. The sample in which PVC/LDPE (20 wt%/80 wt%) had the greatest tensile strength, elongation at break, and modulus. The good thermal stability of this sample can be seen that T_10% and T_20% occurred at higher temperatures compared to others blends. DPLF slightly improved the tensile strength of the polymer blend matrix at 10 wt% (C10). The modulus of the composites increased significantly with increasing filler content. Ageing conditions at 80°C for 168 h slightly improved the mechanical properties of composites. Scanning electron microscopic micrographs showed that morphological properties of tensile fracture surface are in accordance with the tensile properties of these blends and composites. Thermogravimetric analysis and derivative thermogravimetry show that the thermal degradation of PVC/LDPE (20 wt%/80 wt%) blend and PVC/LDPE/DPLF (10 and 30 wt%) composites took place in two steps: in the first step, the blend was more stable than the composites. In the second step, the composites showed a slightly better stability than the PVC/LDPE (20 wt%/80 wt%) blend. Based on the above investigation, these new green composites (PVC/LDPE/DPLF) can be used in several applications. J. VINYL ADDIT. TECHNOL., 25:E88–E93, 2019. © 2018 Society of Plastics Engineers     

Selective localization of carbon nanotubes in PC/PET blends

The localization of multi‐walled carbon nanotubes (MWCNTs) in immiscible polymer blends composed of polycarbonate (PC) and poly(ethylene terephthalate) (PET) is studied. Although partial miscibility is confirmed for the blend, presumably owing to the transesterification reaction, the MWCNT addition is found to have no influence on the miscibility. Moreover, morphological investigation and solvent extraction experiments reveal that MWCNTs are preferentially localized in PET phase. Thermal behavior demonstrates that MWCNTs act as an effective nucleating agent for PET, leading to the increment in crystallization temperature and crystallinity of PET. Tensile properties of PC/PET blends, i.e., Young's modulus, yield strength, and ultimate strength, are significantly improved by the addition of MWCNTs. POLYM. COMPOS., 38:1103–1111, 2017. © 2015 Society of Plastics Engineers     

Effect of graphene nanosheets on the mechanical,electrical, and rheological properties of polyamide 6/acrylonitrile–butadiene–styrene blends

Polyamide 6 (PA6) and acrylonitrile butadiene styrene blend reinforced by graphene nanosheets (GNs) nanocomposites were prepared by batch system followed by hot compression to get samples for different tests. A low amounts of graphene were used (1, 2, 3, 4 wt%), with this selected loading range, the mechanical properties (Young's modulus) have increased linearly with GNs contents. However, it is observed stability in the tensile strength. The electrical and rheological properties are well characterized and have shown that the evolution of the properties runs through a threshold loading charge. The results are related to the blends morphology, and SEM images showed selective preferential localization in the polyamide 6 phase. Moreover, the presence of GNs in the blends has reduced the surface tension between the two polymers. POLYM. COMPOS. 37:998–1006, 2016. © 2014 Society of Plastics Engineers     

Control of carbon nanotubes at the interface of a co-continuous immiscible polymer blend to fabricate conductive composites with ultralow percolation thresholds

The concept of “double percolation”, i.e., conductive fillers are selectively located in one phase of a co-continuous polymer blend to form a percolated network in the selected phase, is widely used to reduce the percolation thresholds of conductive polymer composites to a fraction of their original values. However, it is expected that the percolation threshold can be significantly reduced further if the conductive fillers are only selectively distributed at the continuous interface of the co-continuous polymer blend, where only a very small amount of fillers are needed to build up the conductive percolated network. Multiwalled carbon nanotubes (MWCNTs) with very high aspect ratio (ca. 1000) are selectively distributed at a continuous interface of a co-continuous immiscible poly(lactic acid)/poly(ε-caprolactone) (PLA/PCL) blend at a weight ratio of 50/50 by controlling the migration process of MWCNTs from the unfavorable PLA to the favorable PCL phase. Compared to the PLA/PCL/MWCNTs composites by the traditional double percolation method (percolation threshold is ca. 0.97 wt%), the percolation threshold of PLA/MWCNTs/PCL composites (ca. 0.025 wt%) drops 2 orders of magnitude due to controlling the MWCNTs at the continuous interface between the PLA and PCL phases.