Coaxial electrospinning has been considered a straightforward and convenient method for producing hollow nanofibers. Therefore, the objective of this study was to develop hollow activated carbon nanofibers (HACNFs) for CO2 capture in order to reduce emissions of CO2 to the atmosphere and mitigate global warming. Results showed that the sacrificing core could be decomposed at carbonization temperatures above 900 °C, allowing the formation of hollow nanofibers. The average outer diameters of HACNFs ranged from 550 to 750 nm, with a shell thickness of 75 nm. During the carbonization stage, the denitrogenation reactions were significant, while in the CO2 activation process, the release of carbon oxides became prominent. Therefore, the CO2 activation could increase the percentages of N=C and quaternary N groups. The major nitrogen functionalities on most samples were O=C-NH and quaternary N. However, =C and quaternary N groups were found to be crucial in determining the CO2 adsorption performance. CO2 adsorption on HACNFs occurred due to physical adsorption and was an exothermic reaction. The optimal CO2 adsorption performance was observed for HACNFs carbonized at 900 °C, where 3.03 mmol/g (1 atm) and 0.99 mmol/g (0.15 atm) were measured at 25 °C. The degradation of CO2 uptakes after 10 adsorption-desorption cyclic runs could be maintained within 8.9%.

Lithium iron phosphate (LiFePO4, LFP) is the most promising cathode material for use in safe electric vehicles (EVs), due to its long cycle stability, low cost, and low toxicity, but it suffers from low conductivity and ion diffusion. In this work, we present a simple method to obtain LFP/carbon (LFP/C) composites with different types of NC: cellulose nanocrystal (CNC) and cellulose nanofiber (CNF). Microwave-assisted hydrothermal synthesis was used to obtain LFP with nanocellulose inside the vessel, and the final LFP/C composite was achieved by heating the mixture under a N2 atmosphere. The resulting LFP/C indicated that the NC in the reaction medium not only acts as the reducing agent that aqueous iron solutions need (avoiding the use of other chemicals), but also as a stabiliser of the nanoparticles produced in the hydrothermal synthesis, obtaining fewer agglomerated particles compared to synthesis without NC. The sample with the best coating-and, therefore, the best electrochemical response-was the sample with 12.6% carbon derived from CNF in the composite instead of CNC, due to its homogeneous coating. The utilisation of CNF in the reaction medium could be a promising method to obtain LFP/C in a simple, rapid, and low-cost way, avoiding the waste of unnecessary chemicals.

3D printable, flexible, and conductive composites are prepared by incorporating a thermoplastic elastomer and electrically conductive carbon fillers. The advantageous printability, workability, chemical resistance, electrical conductivity, and biocompatibility components allowed for an enabling of 3D-printed electronics, electromagnetic interference (EMI) shielding, static elimination, and biomedical sensors. Carbon-infused thermoplastic polyurethane (C/TPU) composites have been demonstrated to possess right-strained sensing abilities and are the candidate in fields such as smart textiles and biomedical sensing. Flexible and conductive composites were prepared by a mechanical blending of biocompatible TPU and carbons. 3D structures that exhibit mechanical flexibility and electric conductivity were successfully printed. Three different types of C/TPU composites, carbon nanotube (CNT), carbon black (CCB), and graphite (G) were prepared with differentiating sizes and composition of filaments. The conductivity of TPU/CNT and TPU/CCB composite filaments increased rapidly when the loading amount of carbon fillers exceeded the filtration threshold of 8%-10% weight. Biocompatible G did not form a conductive pathway in the TPU; resistance to indentation deformation of the TPU matrix was maintained by weight by 40%. Adding a carbon material to the TPU improved the mechanical properties of the composites, and carbon fillers could improve electrical conductivity without losing biocompatibility. For the practical use of the manufactured filaments, optimal printing parameters were determined, and an FDM printing condition was adjusted. Through this process, a variety of soft 3D-printed C/TPU structures exhibiting flexible and robust features were built and tested to investigate the performance of the possible application of 3D-printed electronics and medical scaffolds.

Activated carbon (AC) with a very high surface area of over 2000 m2/g was produced from low sulfur acid hydrotropic lignin (AHL) from poplar wood using H3PO4 at a moderate temperature of 450 °C (AHL-AC6). ACs with similar surface areas were also obtained under the same activation condition from commercial hardwood alkali lignin and lignosulfonate. Initial evaluation of AC performance was carried out using nitrogen adsorption-desorption and dye adsorption. AHL-AC6 exhibited the best specific surface area and dye adsorption performance. Furthermore, the adsorption results of congo red (CR) and methylene blue (MB) showed AHL-AC6 had greater adsorption capacity than those reported in literature. The dye adsorption data fit to the Langmuir model well. The fitting parameter suggests the adsorption is nearly strong and near irreversible, especially for MB. The present study for the first time provided a procedure for producing AC from lignin with Brunauer-Emmett-Teller (BET) surface area >2000 m2/g using low cost and low environmental impact H3PO4 at moderate temperatures.

The progress observed in 'soft robotics' brought some promising research in flexible tactile, pressure and force sensors, which can be based on polymeric composite materials. Therefore, in this paper, we intend to evaluate the characteristics of a force-sensitive material-polyethylene-carbon composite (Velostat®) by implementing this material into the design of the flexible tactile sensor. We have explored several possibilities to measure the electrical signal and assessed the mechanical and time-dependent properties of this tactile sensor. The response of the sensor was evaluated by performing tests in static, long-term load and cyclic modes. Experimental results of loading cycle measurements revealed the hysteresis and nonlinear properties of the sensor. The transverse resolution of the sensor was defined by measuring the response of the sensor at different distances from the loaded point. Obtained dependencies of the sensor's sensitivity, hysteresis, response time, transversal resolution and deformation on applied compressive force promise a practical possibility to use the polyethylene-carbon composite as a sensitive material for sensors with a single electrode pair or its matrix. The results received from experimental research have defined the area of the possible implementation of the sensor based on a composite material-Velostat®.

The paper considers the development of fillers representing mixtures of carbon nanotubes and graphene materials (graphene oxide and graphene nanoplatelets) in different mass ratios to modify epoxy resin. The graphene type and content effect on the dispersed phase particle effective sizes-both in aqueous suspensions and the resin-was analyzed. Hybrid particles were characterized by Raman spectroscopy and electron microscopy. The composites containing 0.15-1.00 wt.% CNTs/GO and CNTs/GNPs were thermogravimetrically analyzed, and their mechanical characteristics were determined. SEM images of the composite fracture surfaces were acquired. Optimal dispersions containing 75-100 nm particles were obtained at the CNTs:GO mass ratio of 1:4. It was shown that the CNTs can be located between the GO layers and on the GNP surface. The samples containing up to 0.2 wt.% CNTs/GO (at 1:1 and 1:4 ratios) were stable when heated in air up to 300 °C. For 0.15-0.20 wt.% CNTs/GO (at 1:1 ratio), the tensile strength and modulus of the composite increased by 84-88 and 40%, respectively. The increase in the strength characteristics was found to occur due to the interaction of the filler layered structure with the polymer matrix. The obtained composites can be used as structural materials in different fields of engineering.

High loadings of carbon black (CB) are usually used to achieve the properties demanded of rubber compounds. In recent years, distinct nanoparticles have been investigated to replace CB in whole or in part, in order to reduce the necessary filler content or to improve performance. Multilayer graphene (MLG) is a nanoparticle made of just 10 graphene sheets and has recently become commercially available for mass-product nanocomposites. Three phr (part for hundred rubbers) of MLG are added to chlorine isobutyl isoprene rubber (CIIR)/CB composites in order to replace part of the CB. The incorporation of just 3 phr MLG triples the Young's modulus of CIIR; the same effect is obtained with 20 phr CB. The simultaneous presence of three MLG and CB also delivers remarkable properties, e.g. adding three MLG and 20 phr CB increased the hardness as much as adding 40 phr CB. A comprehensive study is presented, showing the influence on a variety of mechanical properties. The potential of the MLG/CB combination is illustrated to reduce the filler content or to boost performance, respectively. Apart from the remarkable mechanical properties, the CIIR/CB/MLG nanocomposites showed an increase in weathering resistance.

This work aimed to investigate the effect of hybrid carbon nanofillers (e.g., carbon nanotubes/carbon nanofibers in the ratio 1:1 by mass) over the electrical and flexural properties for an epoxy matrix and corresponding basalt fibre reinforcing composite (BFRC) subjected to full-year seasonal water absorption. Hydrothermal ageing was performed by full immersion of the tested materials into distilled water according to the following model conditions (seasons). The mechanical properties were measured in three-point bending mode before environmental ageing and after each season. Upon environmental ageing, the relative change of flexural strength and elastic modulus of the epoxy and NC was within 10-15%. For nanomodified BFRCs, the slightly higher effect (approx. by 10%) of absorbed moisture on flexural characteristics was found and likely attributed to higher defectiveness (e.g., porosity, the formation of agglomerates etc.). During flexural tests, electrical resistance of the nanocomposites (NC) and BFRC/NC samples was evaluated. The electrical conductivity for UD BFRC/NC, before and after hydrothermal ageing, was by 2 and 3 times higher than for the NC, accordingly, revealing the orientation of electrically conductive nanoparticles and/or their agglomerates during lay-up manufacturing which was evaluated by the rules of the mixture. Based on all results obtained it can be concluded that the most potentially applicable for damage indication was UD BFRC/NC along fibres since full-year hydrothermal ageing improved its electrical conductivity by approx. 98% and, consequently, the ability to monitor damages was also enhanced.

The design of a unipole and a dual band F-shaped antenna was conducted to find the best parameters of prepared antenna. Antenna radiator part is fully made of polymer and nonmetal base composite. Thermoplastic polyurethane (PU) was chosen as a matrix and multi-wall carbon nanotubes (MWCNT) as an electrical conductive filler, which creates conductive network. The use of the composite for the antenna has the advantage in simple preparation through dip coating technique. Minor disadvantage is the usage of solvent for composite preparation. Composite structure was used for radiator part of antenna. The antenna operates in 2.45 and 5.18 GHz frequency bands. DC conductivity of our PU/MWCNT composite is about 160 S/m. With this material, a unipole and a dual band F antenna were realized on 2 mm thick polypropylene substrate. Both antenna designs were also simulated using finite integration technique in the frequency domain (FI-FD). Measurements and full wave simulations of S11 of the antenna showed good agreement between measurements and simulations. Except for S11, the gain and radiation pattern of the antennas were measured and simulated. Maximum gain of the designed unipole antenna is around -10.0 and -5.5 dBi for 2.45 and 5.18 GHz frequency bands, respectively. The manufactured antennas are intended for application in wearable electronics, which can be used to monitor various activities such as walking, sleeping, heart rate or food consumption.

Management of waste from carbon fibre composites has become a significant societal issue as the application of composite grows across many industries. In this study, carbon fibres (CF) were successfully recovered from cured carbon fibre/epoxy (CF/EP) prepreg under microwave pyrolysis at 450, 550 and 650 °C followed by oxidation of any residual char. The recovered fibres were investigated for their tensile properties, surface morphologies and the elements/functional groups presented on the surface. The chemical compositions of gaseous and oil pyrolysis products were also analysed. The microwave pyrolysis effectively pyrolyzed the epoxy (EP) resin. Char residue remained on the fibre surface and the amount of char reduced as the pyrolysis temperature increased. Compared to virgin fibres, the recovered fibre suffered from a strength reduction by less than 20%, and this reduction could be mitigated by reducing the pyrolysis temperature. The surface of recovered fibre remained clean and smooth, while the profile of elements and functional groups at the surface were similar to those of virgin fibres. The main gaseous products were CO, H2, CO2 and CH4, whilst the liquid product stream included phenolic and aromatic compounds.

In order to meet the needs of constantly advancing technologies, fabricating materials with improved properties and predictable behavior has become vital. To that end, we have prepared polydimethylsiloxane (PDMS) polymer samples filled with carbon nanofibers (CFs) at 0, 0.5, 1.0, 2.0, and 4.0 CF loadings (w/w) to investigate and optimize the amount of filler needed for fabrication with improved mechanical properties. Samples were prepared using easy, cost-efficient mechanical mixing to combine the PDMS and CF filler and were then characterized by chemical (FTIR), mechanical (hardness and tension), and physical (swelling, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and coefficient of thermal expansion) analyses to determine the material properties. We found that hardness and thermal stability increased predictably, while the ultimate strength and toughness both decreased. Repeated tension caused the CF-filled PDMS samples to lose significant toughness with increasing CF loadings. The hardness and thermal degradation temperature with 4 wt.% CF loading in PDMS increased more than 40% and 25 °C, respectively, compared with the pristine PDMS sample. Additionally, dilatometer measurements showed a 20% decrease in the coefficient of thermal expansion (CTE) with a small amount of CF filler in PDMS. In this study, we were able to show the mechanical and thermal properties of PDMS can be tuned with good confidence using CFs.

We prepared electrically conductive polystyrene (PS) nanocomposites by incorporating non-covalently surface-modified carbon nanotubes (CNTs) with hydrophilic polymers such as polydopamine (PDA) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). Further, ethylene glycol (EG) was introduced as a second dopant to improve the electrical properties of the nanocomposites prepared with PEDOT:PSS-wrapped CNTs. All conductive PS nanocomposites were prepared through latex-based process, and the morphology and properties of the nanocomposites were investigated. The electrical properties of the nanocomposites with PEDOT:PSS-wrapped CNTs were better than those of the nanocomposites with PDA-coated CNTs owing to the conducting nature of PEDOT:PSS, although the dispersions of both types of modified CNTs in the PS matrix were excellent, as evidenced by morphology and rheology. In the case of PEDOT:PSS modification, the electrical properties of the nanocomposites with EG-doped PEDOT:PSS-wrapped CNTs were superior to those of the nanocomposites without EG treatment.

This work studied the impact of three types of styrene-butadiene (SB and SBS) block copolymers on the morphology, electrical, and rheological properties of immiscible blends of polypropylene:polystyrene (PP:PS)/multi-walled carbon nanotubes (MWCNT) with a fixed blend ratio of 70:30 vol.%. The addition of block copolymers to PP:PS/MWCNT blend nanocomposites produced a decrease in the droplet size. MWCNTs, known to induce co-continuity in PP:PS blends, did not interfere with the copolymer migration to the interface and, thus, there was morphology refinement upon addition of the copolymers. Interestingly, the addition of the block copolymers decreased the electrical resistivity of the PP:PS/1.0 vol.% MWCNT system by 5 orders of magnitude (i.e., increase in electrical conductivity). This improvement was attributed to PS Droplets-PP-Copolymer-Micelle assemblies, which accumulated MWCNTs, and formed an integrated network for electrical conduction. Molecular simulation and solubility parameters were used to predict the MWCNT localization in the immiscible blend. The simulation results showed that diblock copolymers favorably interact with the nanotubes in comparison to the triblock copolymer, PP, and PS. However, the interaction between the copolymers and PP or PS is stronger than the interaction of the copolymers and MWCNTs. Hence, the addition of copolymer also changed the localization of MWCNT from PS to PS-PP-Micelles-Interface, as observed by TEM images. In addition, in the last step of this work, we investigated the effect of the addition of copolymers on inter- and intra-cycle viscoelastic behavior of the MWCNT incorporated polymer blends. It was found that addition of the copolymers not only affects the linear viscoelasticity (e.g., increase in the value of the storage modulus) but also dramatically impacts the nonlinear viscoelastic behavior under large deformations (e.g., higher distortion of Lissajous-Bowditch plots).].

Cisplatin (Cp), a chemotherapeutic agent, interacts with purines on tumor DNA, causing tumor cell apoptosis. However, cisplatin has the characteristics of non-specific distribution and lack of selectivity, resulting in systemic toxicity. Moreover, it cannot maintain the drug's high concentration in the tumor-weak acid environment. These flaws of cisplatin restrict its use in clinical applications. Therefore, a pH-responsive carbon nanotube-modified nano-drug delivery system (CNTs/Gel/Cp) was constructed in this study using gelatin (Gel)-modified carbon nanotubes (CNTs/Gel) loaded with cisplatin to release drugs precisely and slowly, preventing premature inactivation and maintaining an effective concentration. When MCp:MCNTs/Gel = 1:1, the drug reaches the highest loading rate and entrapment efficiency. To achieve the sustained-release effect, CNTs/Gel/Cp can release the medicine steadily for a long time in a pH environment of 6.0. Additionally, CNTs/Gel/Cp display antitumor properties comparable to cisplatin in a manner that varies with the dosage administered. These findings indicate that CNTs/Gel/Cp have an effective, sustained release of cisplatin and a good antitumor effect, providing a theoretical and experimental basis for the clinical application of modified carbon nanotubes (CNTs) as a new drug delivery system.

The heart is a fundamental organ of the human circulatory system and the continuous measurement of electrocardiogram (ECG) signals is of great importance for pre-detection of heart diseases. Dry electrodes that do not require electrolyte gel have been developed for wearable ECG monitoring applications. However, this kind of electrode often introduces motion artifacts because of the high contact impedance between the electrode and skin. We propose a wearable ECG monitoring garment that employs electrodes made of conductive carbon-based paste. This paste is directly applied to the skin and after drying for 5 min, it forms a patch electrode that is detachable and flexible. The contact impedance between the patch electrode and the skin is very low because the paste covers the skin in a conformal manner. The experimental results show that the contact area of the carbon-based paste on the skin replica is almost 100%. At frequencies under 10 Hz, the contact impedance of the patch electrode is of 70.0 kΩ, much lower than the typical 118.7 kΩ impedance of a Ag/AgCl electrode. We also demonstrate that the ECG signals measured using the custom-designed garment and the patch electrodes are very stable even during actions such as walking and running.

Agglomeration and restacking can reduce graphene oxide (GO) activity in a wide range of applications. Herein, GO was synthesized by a modified Hummer's method. To minimize restacking and agglomeration, in situ chemical oxidation polymerization was carried out to embed polyaniline (PANI) chains at the edges of GO sheets, to obtain GO-PANI nanocomposite. The GO-PANI was tested for the adsorptive removal of brilliant green (BG) from an aqueous solution through batch mode studies. Infrared (FT-IR) analysis revealed the dominance of hydroxyl and carboxylic functionalities over the GO-PANI surface. Solution pH-dependent BG uptake was observed, with maximum adsorption at pH 7, and attaining equilibrium in 30 min. The adsorption of BG onto GO-PANI was fit to the Langmuir isotherm, and pseudo-second-order kinetic models, with a maximum monolayer adsorption capacity (qm) of 142.8 mg/g. An endothermic adsorption process was observed. Mechanistically, π-π stacking interaction and electrostatic interaction played a critical role during BG adsorption on GO-PANI.

Three-dimensionally printed carbon-fiber-reinforced polymer (3DP-CFRP) has become an important contributor to commercialized additive manufacturing. Due to carbon fiber infills, the 3DP-CFRP parts can enjoy highly intricate geometry, enhanced part robustness, heat resistance, and mechanical properties. With the rapid growth of 3DP-CFRP parts in the aerospace, automobile, and consumer product sectors, evaluating and reducing their environmental impacts has become an urgent yet unexplored issue. To develop a quantitative measure of the environmental performance of 3DP-CFRP parts, this paper investigates the energy consumption behavior of a dual-nozzle fused deposition modeling (FDM) additive manufacturing process which includes melting and deposition of the CFRP filament. An energy consumption model for the melting stage is first defined using the heating model for non-crystalline polymers. Then, the energy consumption model for the deposition stage is established through the design of experiments approach and regression by investigating six influential parameters comprising the layer height, infill density, number of shells, travel speed of gantry, and speed of extruders 1 and 2. Finally, the energy consumption models are combined and experimentally tested with two different CFRP parts. The results show that the developed energy consumption model demonstrated over 94% accuracy in predicting the energy consumption behavior of 3DP-CFRP parts. The developed model could potentially be used to find a more sustainable CFRP design and process planning solution.

The addition of nano- and microfillers to carbon-fiber-reinforced polymers (CFRPs) to improve their static mechanical properties is attracting growing research interest because their introduction does not increase the weight of parts made from CFRPs. However, the current understanding of the high strain rate deformation behaviour of CFRPs containing nanofillers/microfillers is limited. The present study investigated the dynamic impact properties of carbon-fiber-reinforced phenolic composites (CFRPCs) modified with microfillers. The CFRPCs were fabricated using 2D woven carbon fibers, two phenolic resole resins (HRJ-15881 and SP-6877), and two microfillers (colloidal silica and silicon carbide (SiC)). The amount of microfillers incorporated into the CFRPCs varied from 0.0 wt.% to 2.0 wt.%. A split-Hopkinson pressure bar (SHPB), operated at momentums of 15 kg m/s and 28 kg m/s, was used to determine the impact properties of the composites. The evolution of damage in the impacted specimens was studied using optical stereomicroscope and scanning electron microscope. It was found that, at an impact momentum of 15 kg m/s, the impact properties of HRJ-15881-based CFRPCs increased with SiC addition up to 1.5 wt.%, while those of SP-6877-based composites increased only up to 0.5 wt.%. At 28 kg m/s, the impact properties of the composites increased up to 0.5 wt.% SiC addition for both SP-6877 and HRJ-15881 based composites. However, the addition of colloidal silica did not improve the dynamic impact properties of composites based on both phenolic resins at both impact momentums. The improvement in the impact properties of composites made with SiC microfiller can be attributed to improvement in crystallinity offered by the α-SiC type microfiller used in this study. No fracture was observed in specimens impacted at an impact momentum of 15 kg m/s. However, at 28 kg m/s, edge chip-off and cracks extending through the surface were observed at lower microfiller addition (≤1 wt.%), which became more pronounced at higher microfiller loading (≥1.5 wt.%).

A suitably modified resin film infusion (RFI) process was used for manufacturing carbon fiber-reinforced composites (CFRCs) impregnated with a resin containing nanocages of glycidyl polyhedral oligomeric silsesquioxane (GPOSS) for enhancing flame resistance and multi-wall carbon nanotubes (MWCNTs) to contrast the electrical insulating properties of the epoxy resin. The effects of the different numbers (7, 14 and 24) of the plies on the equivalent direct current (DC) and alternating current (AC) electrical conductivity were evaluated. All the manufactured panels manifest very high values in electrical conductivity. Besides, for the first time, CFRC strings were analyzed by tunneling atomic force microscopy (TUNA) technique. The electrical current maps highlight electrically conductive three-dimensional networks incorporated in the resin through the plies of the panels. The highest equivalent bulk conductivity is shown by the seven-ply panel characterized by the parallel (σ//0°) in-plane conductivity of 16.19 kS/m. Electrical tests also evidence that the presence of GPOSS preserves the AC electrical stability of the panels.

Appropriate selection of suitable materials and methods is essential for scaffolds fabrication in tissue engineering. The major challenge is to mimic the structure and functions of the extracellular matrix (ECM) of the native tissues. In this study, an optimized 3D structure containing poly(3-hydroxybutyrate) (P3HB), multiwalled carbon nanotubes (MCNTs) and curcumin (CUR) was created by electrospinning a novel biomimetic scaffold. CUR, a natural anti-inflammatory compound, has been selected as a bioactive component to increase the biocompatibility and reduce the potential inflammatory reaction of electrospun scaffolds. The presence of CUR in electrospun scaffolds was confirmed by 1H NMR and Fourier-transform infrared spectroscopy (FTIR). Scanning electron microscopy (SEM) revealed highly interconnected porosity of the obtained 3D structures. Addition of up to 20 wt% CUR has enhanced mechanical properties of the scaffolds. CUR has also promoted in vitro bioactivity and hydrolytic degradation of the electrospun nanofibers. The developed P3HB-MCNT composite scaffolds containing 20 wt% of CUR revealed excellent in vitro cytocompatibility using mesenchymal stem cells and in vivo biocompatibility in rat animal model study. Importantly, the reduced inflammatory reaction in the rat model after 8 weeks of implantation has also been observed for scaffolds modified with CUR. Overall, newly developed P3HB-MCNTs-CUR electrospun scaffolds have demonstrated their high potential for tissue engineering applications.