scCO2 was used to assist in the preparation of PP/CNT composites. Two types of CNTs were used: MWNTs with and without HDPE coating (cMWNTs). The morphology of the nanocomposites and their mechanical and thermal properties were investigated and compared with samples made by traditional melt compounding. The use of cMWNT leads to better dispersion and properties in melt‐compounded nanocomposites. For systems prepared using scCO2‐assisted mixing, however, better properties were obtained using pristine MWNTs, avoiding the additional costs of nanotube modification. It was also shown that observed improvements in the mechanical properties for these materials were due to a combination of matrix modification and nanotube reinforcement, rather than a reinforcement effect caused solely by MWNTs.
The present study investigates the effect of polyphosphazene elastomer and halloysite nano tubular fillers in the blend of poly(phenylene oxide) and liquid crystalline polymer. Fabricated materials were extensively investigated with field emission scanning electron microscope, high resolution transmission electron microscope, thermogravimetric analyzer, rheometer, universal testing machine, and dynamic mechanical thermal analyzer. Significant changes in morphology were observed when fillers were added along with the compatibilizing agent polyphosphazene. Filler-matrix adhesion improves in the presence of polyphosphazene that results in the reduction in the average domain sizes of the dispersed phase where the interfacial phenomena controls the size of the dispersed phase. 相似文献
The effect of nanosilica addition on the morphology and mechanical properties of blends of isotactic PP and an ethylene/octene copolymer (EOC) is studied. TEM reveals that the well‐dispersed nanoparticles are localized exclusively in the PP phase. In the presence of a maleated PP compatibilizer addition of nanosilica leads to more finely dispersed EOC domains and a finer co‐continuous morphology. The nanoparticles reduce the rate of coalescence of the dispersed phase domains. The mechanical properties depend on the EOC and PP‐g‐MA content. Tensile and flexural properties are significantly enhanced in the presence of the silica nanoparticles, whereas impact properties are not affected. These enhancements are attributed to the favorable microstructure of the blends.
An in situ lubrication dispersion method is developed to achieve electrical conductivity in PP containing a small amount of MWCNTs. Good dispersion of the MWCNTs in PP is observed even after a short mixing time because the interactions between the entangled nanotubes are reduced. By in situ lubrication dispersion, the electrical percolation threshold of the PP nanocomposite can be as low as 0.5–0.7 wt% MWCNT. Rheological data also support percolation at 0.5 wt% MWCNT. With 0.5 wt% MWCNT, the slope of G′ at low frequency approaches unity and shows non‐terminal behavior. The proposed dispersion method enhances the wetting of MWCNTs and improves MWCNT dispersion compared to both direct mixing of MWCNT powder with a polymer melt and conventional master batch dilution.
Polymeric electromagnetic interference (EMI) shielding foaming materials are found and applied in many frontier fields such as aerospace, transportation, and portable electronics. In this paper, a foam based on a composite system of poly(vinylidene fluoride) (PVDF) filled with carbon nanotubes (CNTs) is prepared for EMI shielding properties by using a solid-state supercritical CO2 foaming strategy. PVDF is chosen as the matrix because of its excellent chemical resistance, thermal stability, and flame retardancy. The inclusion of CNTs renders this composite system enhanced complex viscosity and storage modulus by about two orders of magnitude. The electrical conductivity and EMI specific shielding effectiveness of obtained foams can be adjusted and reached the optimum value of 0.024 S m−1 and 29.1 dB cm3 g−1, respectively, originating from the gradual development of interconnected CNTs and conductive CNTs network as well as the introduction of cell structure in PVDF matrix. Interestingly, the reorientation of CNTs caused by foaming process results in electrical conductivity percolation threshold of PVDF/CNTs foams markedly decreases, in comparison to their unfoamed samples. This study provides a facile, efficient, green, and economic route for the preparation of EMI shielding foams consisted of fluorinated polymers and carbonaceous fillers. 相似文献
Summary: The crystallization of the PBT minor phase in an EEA continuous matrix has been studied by DSC and SEM. When PBT is the minor phase, PBT crystallizes at a lower temperature, as expected, near Tc,f1 = 105 °C. Introducing different CB nanoparticles into the EEA continuous phase at contents increasing from 0.02 to 5 wt.‐% leads to important modifications of the PBT crystallization. A new PBT exotherm appears at Tc,f2 = 144 °C on the addition of CB, becoming really visible at Tc,f3 = 158 °C and finally moving to Tc,n = 185 °C at high content. The areas corresponding to these new peaks were found to increase to the detriment of that of the fractionated crystallization at Tc,f1 = 105 °C. Morphological studies and interfacial tension measurements were made to understand the surprising activity of the CB. Moreover, the substitution of the EEA phase with the less polar LLDPE confirmed the importance of the strong interactions developed by EEA with CB aggregates.
Melting and recrystallization DSC curves for the PBT/EEA 60/40 blend. 相似文献
Summary: MWNT mixtures with PC were prepared in three different miniature mixers at 265 °C and 50 rpm for 6 min by the master batch dilution method. One mixer is a 4.5 cm3 DACA microcompounder (DACA Instruments) consisting of two conical co‐rotating screws with a bypass, allowing the material to circulate for defined periods. The other two miniature mixers are custom‐built in our lab: the 2.2 cm3 APAM and the 3 cm3 MBM. The volume resistivity for the nanocomposites obtained from the APAM and the MBM showed a similar trend for different MWNT compositions. The electrical percolation concentration for the nanocomposites prepared in the APAM and the MBM is between 0.50 wt.‐% (or 0.34 vol.‐%) and 0.75 wt.‐% (or 0.52 vol.‐%) MWNT, and it is between 0.75 wt.‐% (or 0.52 vol.‐%) and 1.00 wt.‐% (or 0.69 vol.‐%) for the DACA microcompounder. Rheological characterization indicates that the microstructure of PC/MWNT composites prepared from the miniature mixers changes at a concentration of 0.38 wt.‐% for the APAM and the MBM and 0.50 wt.‐% for the DACA where an interconnected network is formed. TEM micrographs show that there are some small aggregates in the nanocomposites obtained from the APAM, fewer aggregates from the MBM, and least from the DACA. AFM analysis suggests that the length of nanotubes is reduced from 0.57 µm to 0.38–0.42 µm after they were melt mixed in the three mixers.
Effect of MWNT content on volume resistivity of PC/MWNT obtained from different microcompounders. 相似文献
TPVs are prepared by dynamic vulcanization in which crosslinking of an elastomeric polymer takes place during its melt mixing with a thermoplastic polymer under high‐shear conditions. 30:70 wt% blends of PP and ethylene–octene copolymer are vulcanized using electron‐induced reactive processing (EIReP) employing a range of absorbed doses (25, 50, and 100 kGy) while keeping the electron energy and treatment time fixed. The structure/property relationships of the prepared samples are studied using various characterization techniques such as DMA, DSC, SEM, and melt rheology. The results suggest that EIReP offers a novel route to prepare TPVs without any chemical crosslinking and coupling agents.
The effect of organically modified clay on the morphology and properties of poly(propylene) (PP) and poly[(butylene succinate)‐co‐adipate] (PBSA) blends is studied. Virgin and organoclay modified blends were prepared by melt‐mixing of PP, PBSA and organoclay in a batch‐mixer at 190 °C. Scanning electron microscopy studies revealed a significant change in morphology of PP/PBSA blend in the presence of organoclay. The state of dispersion of silicate layers in the blend matrix was characterized by X‐ray diffraction and transmission electron microscopic observations. Dynamic mechanical analysis showed substantial improvement in flexural storage modulus of organoclay‐modified blends with respect to the neat polymer matrices or unmodified blends. Tensile properties of virgin blends also improved in the presence of organoclay. Thermal stability of virgin blends in air atmosphere dramatically improved after modification with organoclay. The effect of organoclay on the melt‐state liner viscoelastic properties of virgin blends was also studied. The non‐isothermal crystallization behavior of homopolymers, virgin, and organoclay‐modified blends were studied by differential scanning calorimeter. The effect of incorporation of organoclay on the cold crystallization behavior of PP/PBSA blends is also reported.
The effect of hydrophilic and hydrophobic nanosilica on the morphological, mechanical and thermal properties of polyamide 6 (PA) and poly(propylene) (PP) blends is investigated by extrusion compounding. Depending on the difference between the polymer/nanoparticle interfacial tensions, different morphologies are obtained as highlighted by TEM and SEM. Hydrophobic nanosilica migrates mainly at the PA/PP interface, which leads to a clear refinement of PP droplet size. The macroscopic properties of the hybrid blends are discussed and interpreted in relation with the blend morphology and melt‐mixing procedure. The control over coalescence allows a morphology refinement of the blends and improves mechanical properties.
Dispersion of CNTs in polymers can yield impressive property enhancements at low volume fractions, thus maintaining the inherent processability of the polymer. In particular, they can improve the electromechanical response of piezoelectric polymers by lowering the actuation voltage and increasing strain and stress response. In this work, piezoelectric PVDF and DWNTs are solution‐cast into films. SEM of fracture surfaces confirms good dispersion, and electrical conductivity measurements reveal a low percolation threshold (0.23 vol.‐%). The effect of CNTs on storage modulus, Tc, Tm and Tg of PVDF is studied. Electromechanical strain is observed at low actuation voltages, possibly due to enhanced local electric field in the presence of DWNTs.
We report a ternary system of poly(styrene‐co‐acrylonitrile) (SAN), poly(vinyl chloride) (PVC), and multi‐walled carbon nanotube (MWCNT) composites prepared by both a solution blending method and the SOAM. The MWCNT content in the composites was optimized by both TGA and mechanical characterization of binary mixtures of SAN/MWCNT and PVC/MWCNT composites. The dispersion of MWCNTs in the miscible SAN/PVC blends was characterized by FT‐Raman spectroscopy, FE‐SEM, and FE‐TEM. The distribution of MWCNTs in the SAN/PVC blends was examined in terms of their wetting coefficients and minimization of the interfacial energy. Composites prepared using the SOAM method showed superior physical properties to the SAN/PVC blends and SAN/PVC/MWCNT composites prepared using the solution blending method.
Polyhydroxyalkanoate (PHA) and poly(propylene carbonate) (PPC) are blended in order to investigate their mutual contributions in terms of functional properties. A wide range of blend composition is processed through extrusion from dry blends. Droplet‐matrix morphology is observed for all samples. Thermal investigations reveal the PPC effect on the PHA crystallization process with a decrease and broadening of the crystallization temperature window and on the depression of its glass transition temperature. This investigation also confirms the as yet un‐reported non‐miscibility of this kind of blend. However, a slight phase interaction is expected since thermal behavior of PHA is impacted. The fragile behavior of PHA is balanced by the high ductility of PPC. The weak strain at break of PHA can thus be increased by up to 200% although a significant amount of PPC is needed to start modifying this property. Stress at break and modulus are linearly decreased from pure PHA to pure PPC values. PPC also acts as an impact modifier for PHA. In terms of barrier properties, PHA brings a large contribution even at low content to the initially high oxygen and water vapor permeability of PPC.
CNF‐reinforced PP nanocomposites were fabricated from CNFs dispersed in a boiling PP/xylene solution. Their thermal properties were characterized by TGA and DSC and shown to exhibit improved thermal stability and higher crystallinity. They were further processed into thin films by compression molding. The electrical conductivity and dielectric property of the PP/CNF nanocomposite thin films were studied. Both electric conductivity and real permittivity increased with increasing fiber loading. Electrical conductivity percolation is observed between 3.0 and 5.0 wt.‐% fiber loading. The rheological behavior of the nanocomposite melts were also investigated. It was found that a small fiber concentration affects the modulus and viscosity of PP melt significantly.
The influence of talc loading on phase morphology of PLA/PCL/talc composites and improvement in resulting properties are reported. Talc‐based composites of PLA/PCL blends were prepared by melt blending. SEM analysis demonstrates that PLA appears as discrete domain phase, while PCL acts as a bulk phase in the blend. Talc addition decreases PLA domain sizes and voids in the matrix. This results in significant improvement of oxygen and water vapor barrier properties of composite by 33 and 25%, respectively, at 3 wt.‐% talc loading. DSC shows that talc acted as nucleating agent for PCL phase in the composite and improves its crystallinity. Various theoretical models based on dispersion and filler geometry are used to predict the tensile modulus and oxygen permeability.
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