Functionalized graphene nanoplatelets/poly(ethylene oxide) nanocomposites: Correlation between crystallization behavior and mechanical performance

Poly(ethylene oxide) (PEO) nanocomposites containing pristine or functionalized graphene nanoplatelets (FGnP) prepared via solution blending and thermal and mechanical properties of nanocomposites were investigated. Chemical functionalization of graphene nanoplatelets was conducted through an amidation reaction between carboxylic acid groups of acidified graphene and hydroxyl groups of polyethylene glycol (PEG). An interfacial linkage and a good dispersion of FGnP was observed via scanning electron microscope (SEM). Differential scanning calorimetry (DSC) analysis revealed that the degree of crystallinity of samples decreased by addition of graphene nanoplatelets, while the size of spherulites increased as indicated by polarized optical microscope (POM). A lower degree of crystallinity and larger spherulites were detected in the case of FGnP. Filler/matrix interfacial adhesion was also remarkably influenced the mechanical properties of PEO as an effective reinforcement of matrix obtained upon the addition of FGnP nanosheets compared to untreated graphene.     

Effect of solvent and blended polymer on electrical conductivity of PEDOT:PSS/polymer blended nanofibers

Poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT:PSS) and polyethylene oxide (PEO) (or polyvinyl alcohol (PVA)) blended electrospun nanofibers were prepared in the presence of dimethyl sulfoxide (DMSO) and ethylene glycol (EG). The effects of added solvents (DMSO and EG) and blended polymers (PEO and PVA) on electrical conductivity and current-voltage (I-V) response were investigated. Electrical conductivity was dependent on both the additional solvent and blended polymers. PEDOT:PSS/PEO blended nanofibers showed a much higher electrical conductivity than PEDOT:PSS/PVA. EG blended PEDOT:PSS/PEO blended nanofibers showed much higher electrical conductivity than DMSO. The PEDOT:PSS/PEO/EG blended nanofibers web showed the highest value in I-V response.     

Effect of surfactant functionalization of multi-walled carbon nanotubes on mechanical,electrical and thermal properties of epoxy nanocomposites

The present paper compares the mechanical, electrical and thermal properties of epoxy nanocomposites (prepared by solution blending method) by adding four different multi-walled carbon nanotubes (MWCNTs), which are pristine, cationic, anionic and non-ionic surfactant functionalized MWCNTs, respectively. This investigation focused on the effects of dispersion of MWCNTs on the physical properties. Systematical characterization on the dispersion of MWCNTs in different solvents were did via UV-Vis spectrophotometer. The Hansen solubility parameters (HSPs) and dispersion of MWCNTs in solvent and epoxy were both changed after surfactants introduced especially for the non-ionic surfactant. Finally, mechanical, fracture toughness, electrical and thermal properties of epoxy composites were found can be improved because of good dispersion of MWCNTs (especially non-ionic surfactant).     

Effects of Chemical Functionalization of MWCNTs on the Structural and Physical Properties of Elastomeric Copolyetherester-based Composite Fibers

Elastomeric copolyetherester (CPEE)-based composite fibers incorporating various neat and functionalized multiwalled carbon nanotubes (MWCNTs) were prepared through a conventional wet-spinning and coagulation process. The influence of functionalized MWCNTs on the morphological features, and the thermal, mechanical properties and electrical conductivity of CPEE/MWCNT (80/20, w/w) composite fibers were investigated. FE-SEM images show that a composite fiber containing poly(ethylene glycol)-functionalized MWCNTs (MWCNT-PEG) has a relatively smooth surface owing to the good dispersion of MWCNT-PEGs within the fiber, whereas composite fibers including pristine MWCNTs (p-MWCNT), acid-functionalized MWCNTs (a-MWCNT), and ethylene glycol-modified MWCNTs (MWCNT-EG) have quite a rough surface morphology owing to the presence of MWCNT aggregates. As a result, the CPEE/MWCNT-PEG composite fiber exhibits noticeably increased thermal and tensile mechanical properties as well as a faster crystallization behavior, which stems from an enhanced interfacial interaction between the CPEE matrix and MWCNT-PEGs.     

Functionalized multi-walled carbon nanotubes with hyperbranched aromatic polyamide for poly(methyl methacrylate) composites

Multi-walled carbon nanotubes (MWCNTs) were functionalized with hyperbranched aromatic polyamide (HAP) by in situ polymerization and by the AB ₂ approach to enhance the mechanical properties of poly(methylmethacrylate) (PMMA) composites. Various concentrations of HAP-functionalized MWCNTs (HAP-f-MWCNTs) were used to prepare HAP-f-MWCNT-reinforced PMMA composite films. The covalent attachment of HAP to the MWCNTs, as achieved by in situ functionalization, resulted in effective dispersion of the MWCNTs in the PMMA matrix, thus enhancing the mechanical and thermal properties of the composite films. The breaking stress of the composites increased largely with the HAP-f-MWCNT loading.     

Enhanced mechanical and thermal properties of hybrid graphene nanoplatelets/multiwall carbon nanotubes reinforced polyethylene terephthalate nanocomposites

The effects of graphene nanoplatelets (GNP) and multiwall carbon nanotube (MWCNT) hybrid nanofillers on the mechanical and thermal properties of reinforced polyethylene terephthalate (PET) have been investigated. The nanocomposites were melt blended using the counter rotating twin screw extruder followed by injection molding. Their morphology, mechanical and thermal properties were characterized. Combination of the two nanofillers in composites formulation supplemented each other which resulted in the overall improvement in adhesion between fillers and matrix. The mechanical properties and thermal stability of the hybrid nanocomposites (PET/GNP1.5/MWCNT1.5) were significantly improved compared to PET/GNP3 and PET/MWCNT3 single filer nanocomposites. However, it was observed that GNP was better in improving the mechanical properties but MWCNT resulted in higher thermal stability of Nanocomposite. The transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM) revealed uniform dispersion of the hybrid fillers in PET/GNP1.5/MWCNT1.5 nanocomposites while agglomeration was observed at higher filler content. The MWCNT prevented the phenomenal stacking of the GNPs by forming a bridge between adjacent GNP planes resulting in higher dispersion of fillers. This complimentary geometrical structure is responsible for the significant improvement in the thermal stability and mechanical properties of the hybrid nanocomposites.     

Tensile,Thermal, and Electrical Conductivity Properties of Carbon Fiber Reinforced Composites Using Itaconic Acid Based Dispersants

We prepared itaconic acid based dispersants (IBDs) by the copolymerization of itaconic acid with acrylic acid, acrylamide, or vinyl sulfonic acid, and compared the efficacy of the IBDs on carbon fiber (CF) dispersion in a water-based system, against that of sodium dodecyl sulphate (SDS) which is widely used as a dispersing agent. The procedure to fabricate nonwoven CF (NCF)/PP composites using IBDs includes the following steps: the synthesis of IBDs, the dispersion of CFs in water by the IBDs, the formation of a NCF, and hot pressing of NCF with polypropylene (PP) layer. We determined the tensile, thermal properties, and the electrical conductivity of non-woven CF/PP composites. It was found that using IBDs as a CF dispersing agent led to the CF/PP composites having better tensile, thermal, and electrical properties, as compared to when SDS was used as a dispersing agent.     

Enhanced thermal conductivity for PVDF composites with a hybrid functionalized graphene sheet-nanodiamond filler

A new thermal conductive poly(vinylidene fluoride) (PVDF) composite has been developed via a hybrid functionalized graphene sheets (FGS)-nanodiamonds (NDs) filler by a simple solution method. The PVDF composite showed different thermal conductivities at different proportion of hybrid filler. The thermal conductivity of the composite was up to 0.66 W/m·K for a mixture containing 45 wt% hybrid filler, which is about 2-fold increment in comparison to the PVDF martrix. The PVDF composites consisting of 20 wt% hybrid FGS/ND filler at the weight ratio of 1:3 shows the best thermal stability. The electrical conductivity of composites was increased from 5.1×10^?15 S cm^?1 (neat PVDF) to 7.1×10^?7 S cm^?1 of the PVDF composite with 10 wt% hybrid filler.     

Fabrication and Characterization of Graphene Enriched Polysulfon Amide Nanocomposites by Electrospinning System

In this paper, we report on the fabrication and characterization of poly(sulfone amide)/graphene (PSA/G) nonwoven based nanocomposite mat assembled via electrospinning technique. Different types of nanocomposite mats were electrospun by varying the weight percentage of graphene in the polymer solution. The surface morphologies, chemical structural, thermal, and electrical properties of the nanocomposites were evaluated systematically. The morphology of the PSA/G nanocomposites exhibited that mesh-like ultrafine nanofibers were densely aligned. Thermal stability and electrical properties of the PSA/G composites could be improved obviously with the addition of graphene. And the thickness uniformity of the nanocomposite mat was improved by using an electrospinning system. Our experimental results suggested that the PSA/G nanocomposites have potential to serve in many different applications, especially in the area of electronic components.     

Composites of polyvinyl alcohol and carbon nanotubes decorated with silver nanoparticles

A simple method to decorate carbon nanotubes (CNTs) with silver nanoparticles was developed to enhance the electrical conductivity of CNTs. The acid-treated CNTs were suspended in the silver acetate solution, ammonia solution was then added, and the CNTs decorated with silver nanoparticles (Ag@CNTs) were produced. The Ag@CNTs were dispersed in polyvinyl alcohol (PVA) to fabricate electrically conducting polymer composites. The electrical, thermal and mechanical properties of the composites were measured. The electrical conductivity of the composites containing 0.8 % (o.w.f.) Ag@CNTs was more than four orders of magnitude higher than those of pristine and functionalized CNTs respectively, which confirmed the effectiveness of the Ag@CNTs as conducting filler. However, the improved electrical conductivity led to somewhat decrease of mechanical properties of PVA/Ag@CNTs composites.     

The enhanced electrical conductivity of cotton fabrics via polymeric nanocomposites

Enhanced electrical conductivity of cotton fabrics coated with polyaniline (PANI) and PANI/carbon coated Fe (Fe@C) and carbon coated Co (Co@C) metal nanoparticles (NPs) composites were investigated. PANI/metal nanoparticle (NP) composites were fabricated with a surface initialized polymerization method and silanization helped with chemical bonding to cotton. The volume resistivity of the samples and structural characterizations were assessed by relevant methods. The results showed that enhanced electrical conductivity, thermal stability and magnetization were obtained via polymeric nanocomposites (PNC) and all these findings revealed that PANI/metal NP PNC coated cotton fabrics would exhibit good level electromagnetic shielding performance as a function of combined electrical conductivity and magnetization which is the objective of our future studies.     

Surface-Modified Cellulose Nanocrystal-incorporated Poly(butylene succinate) Nanocomposites

In this work, surface acetylation of cellulose nanocrystals was performed to improve their interfacial adhesion with hydrophobic polymer matrix and to restore their thermal stability by removing the sulfate groups. The morphological, chemical, and thermal characteristics of the surface-modified cellulose nanocrystals (ACNs) were confirmed by field emission-transmission electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Furthermore, poly(butylene succinate) (PBS)/ACNs nanocomposites were also prepared via melt-mixing process, and the reinforcing effects of ACNs on the thermal, mechanical, and biodegradable properties of the nanocomposites were investigated. The Young’s modulus and tensile strength of the PBS/ACN nanocomposites increased from 115.36 and 33.67 MPa for the neat PBS to 130.55 MPa and 39.97 MPa, respectively. The thermal stability and biodegradability of the nanocomposites also increased with increasing ACN content.     

Synthesis and characterization of electrically conductive composite films of polypyrrole/poly(acrylonitrile-co-styrene)

Homogeneus Polypyrrole (PPy)/poly(acrylonitrile-co-styrene) (SAN) composite thin films were prepared by chemical polymerization of pyrrole on poly(acrylonitrile-co-styrene) matrix. Ce (IV) is used as an oxidant for in-situ polymerizion of pyrrole on SAN matrix, having an advantageous over the impregnation method. The formation and incorporation of PPy in the copolymer matrix were confirmed by FTIR-ATR and UV-Visible spectrophotometric measurements. Thermal analyses showed that after polymerization of Py in copolymer matrix, thermal behavior of SAN was changed and derivative of weight loss at this temperature was increased by increasing of PPy content. XPS and FTIR-ATR analysis of composite films indicated cerium salt with nitrate ion acted as a dopant. The increase in the AC electrical conductivity of the PPy/SAN composites over pure SAN was observed. At lower frequency up to 10⁵ Hz, conductivity was shown an independent behavior from frequency; but at high frequencies (10⁵–10⁷ Hz), dependence on frequency was explained by polaron and bipolaron formations of PPy. The dispersion of PPy particles in copolymer matrix was proven by SEM, AFM and digital camera. By the increase of PPy content in the composite films, increase in AC conductivities, and decrease in dielectric constants and loss were observed.     

Tunable functional properties on polyester fabric using simultaneous green reduction of graphene oxide and silver nitrate

Here, a novel method is introduced to create tunable properties on the polyester fabric through diverse chemical modifications. The polyester fabric was primarily modified with NaOH or ethylenediamine to enhance the surface activity. This will produce diverse chemical groups on the polyester fabric surface including carboxylate, hydroxyl and amine groups. The fabric was treated with grahene oxide through exhaustion method. The silver nitrate was then added and simultaneously reduced with grapheme oxide using ascorbic acid and ammonia to produce reduced graphen oxide/silver nanocomposites (rGO/Ag) on the fabric surface. The synthesized nanocomposites were characterized by TEM and Raman spectra. The presence and uniform distribution of the nanocomposites on the fabric surface was also confirmed by SEM images and EDX patterns. The electrical resistivity was varied on the raw and modified polyester fabric due to the diverse formation of the graphene nanosheets network on the fabric surface. More Ag particles were formed on the surface of the alkali hydrolyzed polyester whereas more graphene nanosheets deposited on the aminolyzed polyester fabric. Also the hydrolyzed polyester fabric exhibited higher antibacterial properties with the lowest silver nitrate in the processing solution. The aminolyzed fabric showed a lower electrical resistance than the hydrolyzed and raw fabrics with the same amount of GO in the procedure bath. The aminolyzed polyester fabric indicated higher affinity towards GO produced higher antibacterial properties before reduction and without silver nitrate however lower electrical resistance obtained after reduction comparing with other samples.     

Improved dispersion of carbon nanotubes in chitosan

Carbon nanotubes (CNT)/chitosan films and fibers can find use in specialized applications like the artificial muscles and other intelligent switching devices. The dispersion state of the single walled carbon nanotubes (SWCNTs) in chitosan matrix plays a major role in deciding the ultimate properties of composite. A suitable chemical treatment for purification and functionalization of SWCNTs is reported. Optimal conditions to prepare water soluble and stable, dispersion of SWCNT in chitosan are presented. The dispersion behavior of purified and functionalized SWCNT was characterized by visual observations, transmission electron microscopy (TEM), and Raman spectroscopy. The dispersion obtained using functionalized SWCNT was stable, while the purified SWCNT dispersion showed limited stability. The better stability of functionalized SWCNT dispersion in chitosan was evidenced by improved interaction between chitosan and carboxyl functional groups of SWCNT.     

Enhanced mechanical and dielectric properties of poly(vinylidene fluoride)/polyurethane/multi-walled carbon nanotube nanocomposites

Multi-walled carbon nanotubes (MWNTs) nanocomposites with the polymer matrix composed of blends of poly(vinylidene fluoride) (PVDF) and polyurethane (PU) were prepared via functionalization of 3,4,5-triflouroaniline (TFA) on MWNTs. The MWNTs/polymer nanocomposites showed a dominantly enhanced elongation due to incorporation of PU molecules in PVDF matrix and the improved MWNTs dispersion in the polymer matrix resulting from functionalization of MWNTs with TFA. The functionalization of TFA on MWNTs was confirmed by the measurements of Raman, FT-IR spectra, SEM, and TEM images. In addition, the dielectric constant of nanocomposites increased with an increase of TFA-functionalized MWNTs in PVDF/PU/MWNTs nanocomposites. The polymer blend nanocomposites incorporating MWNTs may be available as an alternative potential route for the actuator materials.     

Thermal properties of copolyetherester/silica nanocomposites

Thermal properties of copolyetherester/silica nanocomposites were examined by using DSC and TGA. The segmented block copolyetheresters with various hard segment structures and hard segment contents (HSC) were synthesized and their silica nanocomposite films were prepared by solution casting method. The nano-sized fumed silica particles were found to act as a nucleating agent of the copolyetheresters. The nanocomposites always showed reduced degree of supercooling or faster crystallization than the corresponding copolyetheresters. The nanocomposites also showed increased hard segment crystallinity except HSC 35 sample which had short hard segment length. In case of 2GT [poly(ethylene terephthalate)] copolyetheresters, which were not developed commercially because of their low crystallization rate, the hard segment crystallinity increased considerably. The copolyetherester/silica nanocomposites showed better thermal stability than copolyetheresters.     

Structural investigation of anionic functional poly(vinyl alcohol) doped polypyrrole nanospheres

This article reports on a facile route for the preparation of polypyrrole nanospheres with improved water solubility, ordering and conductivity in the presence of a polyelectrolyte, such as phosphorylated polyvinyl alcohol. The phosphorylated polyvinyl alcohol (PPVA) was used as both the stabilizer and the dopant in the chemical oxidative polymerization of pyrrole. The resulting PPVA doped polypyrrole (PPy) nanocomposites (PPy-PPVA) were characterized with FTIR, TGA, SEM and AFM techniques. The electrical conductivity of polymer was measured by four-point probe method. Our observation and results suggest a plausible formation mechanism of PPy nanospheres, PPVA micelle might have functioned as ‘template’ during the polymerization of pyrrole monomers, meanwhile, the PPy chains doped with phosphate group. It was found that the size decreased and their dispersion stability in water increased with the increasing feeding ratio of PPVA. The conductivity of PPy with different morphologies was also measured and compared. When the PPVA: pyrrole feeding ratio ranged from 20 to 50 wt%, the PPy-PPVA nanoparticles showed spherical shape with excellent uniformity, good electrical conductivity (up to 33.1 S·cm^?1), and weakly temperature dependent conductivity. It’s worth mentioning that the PPy-PPVA nanocomposite prepared in high PPVA feeding ratio has been well-dispersed for more than 24 months, which indicates its significant dispersion stability.     

Polyester-based thermoplastic elastomer/MWNT composites: Rheological, thermal, and electrical properties

Polyester-based thermoplastic elastomer (Hytrel®) was melt-compounded with multi-walled nanotubes (MWNTs) using an internal mixer and the changes in the thermal, electrical and rheological properties were investigated using a range of nanotube contents (from 0.1 to 7 wt%). Even at nanotube concentrations as low as 0.1 wt%, the crystallization temperature was remarkably elevated by 15 °C and it increased further up to 22 °C with a 5 wt% loading. On the contrary, the melting temperature increased by 2 °C with 0.1 wt% MWNTs and it was slightly decreased by further additions of MWNTs. Electrical conductivity measured by the four probe method was detected from the 1 wt% MWNTs, indicative of electrical percolation. In addition, MWNTs starting from 4 wt% and above had no significant effect on the electrical conductivity, while it rapidly increased with nanotube contents below 4 wt%. Dynamic rheological properties were measured using a strain controlled rotational rheometer. The complex viscosity increased with MWNT contents giving an abrupt increase between 0.5 and 1 wt% loadings. In addition, the storage and loss modulus increased in a different manner depending on the range of the nanotube concentration. In the Cole-Cole plot, the slope of the nanocomposites decreased from 1.63 to 0.74 with increasing nanotube contents. In the Casson plot, the addition of MWNTs up to 0.5 wt% did not show any yield behavior giving an extremely low value for the yield stress, but further additions of nanotubes increased it notably. The presence of nanotubes in the elastomer increased the relaxation time with nanotube contents and their effect became weak as the frequency increased.     

Thermal and structure properties of biobased cellulose nanowhiskers/poly (lactic acid) nanocomposites

Cellulose nanowhiskers were used to improve the performance of poly (lactic acid) (PLA). The nanocomposites mixed with three different molecular weight of poly (ethylene glycol) (PEG) were characterized by mechanical testing, thermal gravimetry and differential scanning calorimetry. The tensile test showed an increase in tensile strength and elongation at break with the addition of PEG to PLA/CNW nanocomposites, the thermal analysis results showed an increase of crystallization temperature (T _c) and crystallization compatibility (larger crystallization and melting areas), which indicated that the cellulose nanowhiskers (CNW) and PEG or CNW alone should not be considered as nucleating agents for the PLA matrix; The CNW was homo-dispersed which contributed to decreasing mobility of polymer chain segments. The compatibility between hydrophobic PLA matrix and the hydrophilic CNW was improved by the addition of different molecular weight polymeric-PEG. The thermo gravimetric analysis indicated that the thermal stability of the different composites were reflected well in the region between 25 °C and 245 oC. The structure of the PLA/CNW/PEG composites was characterized by AFM, which showed that the CNW dispersed in the PLA matrix evenly.