This paper reports an exhaustive review of recent research progress in the development of millimeter-wave absorbers. With the advancement in technologies, microwave absorbers have shown their evolution in several applications such as defense, security identification, stealth technology, and several more. The importance of these absorbers is increasing due to electromagnetic interference (EMI) effects. Primarily, an abundant amount of absorbers has been developed in lower frequency bands and with the increasing demand for 5G technology, the usage of millimeter-wave bands has gained attention. This in turn requires the development of millimeter-wave absorbers to provide EMI shielding in several applications. Out of several materials, polymers have grabbed attention in the mitigation of EMI. An absorber that combines carbonaceous elements with polymers offers large design flexibility and tunability per the filler concentration. This paper focuses on the classification of these absorbers based on geometry as well as that by using polymers with their design challenges, merits, and demerits with their industrial applications. Comparative studies of geometrically based absorbers and polymeric-based absorbers are also shown.

Integrating LiMn2O4(LMO) and different carbon materials to build a mixed cathode system can provide fast transport channels to improve the conduction of both electrons and ions. In this paper, our work studied in situ low-temperature hydrothermal synthesis of LMO nanocomposites based on graphene oxide (GO)/carbon nanotubes (CNTs) hydrogel. Compared with the pure LMO nanoparticles, GO/CNTs/LMO (GCLMO) composites greatly improved electrochemical performance in specific capacity, cycle performance and rate ability. The electrochemical test results showed that the specific capacitance of GCLMO nanocomposites reached 396 F/g at the current density of 0.5 A/g, which was much higher than 221 F/g of pure LMO. Even at the current density of 10 A/g, the specific capacitance was still as high as 309 F/g. Besides, after 2000 cycles, the specific capacitance retention of the composite was 93%. Electrochemical data showed that GCLMO composite is an ideal cathode material for supercapacitors.

Nanosized, well-dispersed titania particles were synthesized via a hydrothermal method using multiwalled carbon nanotubes (MWCNTs) as structural modifiers during the nucleation process to decrease aggregation. Synthesized TiO2/MWCNT composites containing different amounts of MWCNTs were characterized using N2 physisorption, XRD, spectroscopic techniques (Raman, UV-visible, and X-ray photoelectron), and electron microscopy to illuminate the morphology, crystal structure, and surface chemistry of the composites. Photocatalytic performance was evaluated by measuring the degradation of acetaldehyde in a batch reactor under UV illumination. Average rate constants decrease in the following order: TiO2/MWCNT-1% > TiO2 > TiO2/MWCNT-5%. Addition of MWCNTs beyond the optimum loading ratio of 1:100 (MWCNT:TiO2) diminishes the effectiveness of the photocatalyst and the synergistic effect between MWCNTs and TiO2. The primary mechanism for photocatalytic activity enhancement in TiO2/MWCNT-1% is thought to be due to increased porosity, hydroxyl enrichment on the surface, and high dispersion of TiO2 particles.

Valence Compton profiles (CPs) of multiwall (MWCNTs) and single-wall carbon nanotubes (SWCNTs) were obtained by recording electron energy-loss spectra at large momentum transfer in the transmission electron microscope, a technique known as electron Compton scattering from solids (ECOSS). The experimental MWCNT/SWCNT results were compared with that of graphite. Differences between the valence CPs of MWCNTs and SWCNTs were observed, and the SWCNT CPs indicate a greater delocalization of the ground-state charge density compared to graphite. The results clearly demonstrate the feasibility and potential of the ECOSS technique as a complementary tool for studying the electronic structure of materials with nanoscale spatial resolution.

Nonuniform dispersion and weak interfacial bonding between carbon nanotubes (CNTs) and Cu matrix are two critical issues for achieving high strength and good ductility of CNT/Cu composites. Here, acid-treated CNTs precoated with Ni coatings were used to enhance the dispersion uniformity of CNTs and interfacial bonding between CNTs and Cu matrix in the CNT/Cu composites fabricated through spark plasma sintering and subsequently cold rolling. Scanning electron microscopy analysis revealed the homogeneous dispersion of Ni-coated CNTs (Ni-CNTs) in the composite compared with uncoated CNTs. Transmission electron microscope observation indicated that Cu2O nanoparticles were in situ formed at the interface in Ni-CNT/Cu composite, where CNTs were uncovered by Ni coatings. After rolling, the distribution of Ni-CNTs transformed into ribbons aligning along the rolling direction. The ultimate tensile strength (UTS) of 261 MPa was achieved in rolled 1 vol% Ni-CNT/Cu composite, which was 24.3% higher than that before rolling. The UTS of 2 vol% Ni-CNT/Cu composite obviously decreased, which could be attributed to the agglomeration of Ni-CNTs in the Cu matrix due to the increased volume content.

Flat products of carbon nanotubes (CNTs) reinforced Al matrix composites were fabricated using flake powder metallurgy via shift-speed ball milling and hot-rolling. The evolution of CNTs during preparation and the final distribution in the Al matrix were investigated, and the effect of CNT content on mechanical properties were discussed. Due to the combined effect of uniform dispersion of CNTs, structural integrity, interfacial bonding and directional alignment, the balance between high strength and ductility was successfully achieved in the annealed rolled composites with 1.5 wt% CNT addition, with the value of 382.6 MPa in tensile strength and 9.8% in fracture ductility. The load transfer strengthening was the main mechanism of the strength enhancement with CNTs addition. In addition, a strong rotated cube {001}〈110〉 texture was found in the final flat product of rolled composites. This study provides an effective route to produce and improve the mechanical properties of CNT/Al flat products.

In this work, carbon nanotubes (CNTs)-templated binuclear metallophthalocyanines (MTAPcCF3)2C (M = Mn, Fe, Co, Ni, Cu, Zn) assemblies (MTAPcCF3)2C–COOH–CNTs are designed and obtained. Whereafter, the structure and morphology of target products are analyzed by many means such as infrared, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. The electrocatalytic performances of lithium-thionyl chloride battery catalyzed by (MTAPcCF3)2C–COOH–CNTs were carried out. The result shows that all catalysts can improve the battery performance including the discharge time and the initial voltage. The catalytic performance of (MTAPcCF3)2C–COOH–CNTs is ordered following the central metal: Mn > Fe > Ni > Co > Cu > Zn. The cell capacity catalyzed by optimal catalyst (MnTAPcCF3)2C–COOH–CNTs can expand to 28.08 mAˑh, with increase by 142.07%, and the (MnTAPcCF3)2C–COOH–CNTs can extend the discharge time to 551.6 s. Besides, the reaction mechanism is presented on the basis of cyclic voltammetry measurements.

In this paper, in situ Al4C3 and carbon nanotubes (CNTs) hybrid-reinforced aluminum matrix composites were prepared by a two-step ball milling (TSBM), consisting of a 24-h long-time ball milling (LTBM) and a 6-h short-time ball milling (STBM). During LTBM, most of the CNTs were seriously damaged, and many amorphous carbon atoms derived from these damaged defects would react with Al powder to form in situ Al4C3 nanorods. Subsequently, 1 wt% CNTs were added into the composite powders for STBM to uniformly disperse CNTs into the composite powders. Compared with that of the composite prepared by one-step ball milling, the comprehensive mechanical properties of the composite prepared by the TSBM are improved obviously due to the synergistic effects of in situ Al4C3 and CNTs, and the tensile strength and elongation reached 258 MPa and 19.5%, respectively. The strengthening mechanisms of TSBM composite include fine-grained strengthening, dispersion strengthening by in situ Al4C3, and load transfer from matrix to CNTs.

Carbon nanotubes (CNTs) were added to carbon nanofibers (CNFs) as additives to improve their electrochemical properties. In the present work, CNFs were prepared by using pressurized gyration with polyacrylonitrile as the precursor. The microstructure and electrochemical properties of samples were investigated by scanning electron microscopy and electrochemical workstation, respectively. The results showed that the network structure formed in the fiber, and the fiber diameter decreased with the increase of working pressure. The integral area of cyclic voltammetry curve reached the maximum and the charge/discharge time of constant current charge/discharge curve reached the longest in the case of the CNT concentration is 0.50 wt% and working pressure is 0.2 MPa. At the same time, it exhibited the best electrochemical performance with a specific capacitance of 79 F/g at a current density of 100 mA/g. Compared with the specific capacitance of pure CNFs, the specific capacitance of CNFs with the concentration of CNTs 0.50 wt% increased by about 40%.

This research focuses on the microstructural characterization of nickel matrix composites reinforced by carbon nanotubes (CNTs). The nanocomposites were produced by a conventional powder metallurgy process and the dispersion of CNTs and mixture with nickel powders was performed in a single step by ultrasonication. Microstructural characterization of Ni–CNT nanocomposites was performed by scanning and transmission electron microscopy, electron backscattered diffraction, high-resolution transmission electron microscopy, selected area electron diffraction, and fast Fourier transform analyses. This characterization revealed CNTs embedded in the nickel grains and mainly presented as clusters at the grain boundaries. CNTs hinder recrystallization during sintering, and dislocation cells and subgrains form as a result of the recovery process.

Carbon-based nanomaterials of different dimensions (1–3D, tubes, bundles, films, papers and sponges, graphene sheets) have been created and their characteristic properties have been discussed intensively in the literature. Due to their unique advantageous, tunable properties these materials became promising candidates in new generations of applications in many research laboratories and, recently, in industries as well. Protein-based bio-nanocomposites are referred to as materials of the future, which may serve as conceptual revolution in the development of integrated optical devices, e.g. optical switches, microimaging systems, sensors, telecommunication technologies or energy harvesting and biosensor applications. In our experiments, we designed various carbon-based nanomaterials either doped or not doped with nitrogen or sulfur during catalytic chemical vapor deposition synthesis. Radio- and isotope analytical studies have shown that the used starting materials, precursors and carriers have a strong influence on the geometry and physico-/chemical characteristics of the carbon nanotubes produced. After determining the 14C isotope constitution 53 m/m% balance was found in the reaction center protein/carbon nanotubes complex in a sensitive way that was prepared in our laboratory. The result is essential in determining the yield of conversion of light energy to chemical potential in this bio-hybrid system.

To eliminate the toxic effect of chemotherapy drug of lobaplatin (LBP) on body tissue in liver cancer therapy, this work prepared a nanodrug carrier based on polyethylene glycol-modified carbon nanotubes (PEG–CNTs) and then constructed a targeted drug delivery system (LBP–PEG–CNTs) by loading LBP on PEG–CNTs. Fluorescein isothiocyanate (FITC) was used to label PEG–CNTs to observe the cellular uptake of PEG–CNTs. In addition, the inhibitions of LBP–PEG–CNTs on HepG2 cells were investigated. The results show that the FITC-labeled PEG–CNTs have good cell penetrability; meanwhile, LBP–PEG–CNTs have good stability, pH-controlled release property, and high inhibition rate on HepG2 cells. To be specific, 80% of LBP is released under physiological conditions of liver cancer cells at pH 5.0, and LBP–PEG–CNTs show a high inhibition rate of 77.86% on HepG2 cells, demonstrating that they have targeted, pH-controlled release and inhibition properties on HepG2 cells.

Carbon nanotubes (CNTs) and silicon carbide nanoparticle (nano-SiCp)-reinforced magnesium (Mg) matrix hybrid composites were prepared through a three-step melt spinning process (ball milling, mechanical stirring, and ultrasonic vibration processing). The hybrid nanoreinforcements showed high strengthening efficiency by which the yield and tensile strength of the hybrid composites experienced 46.7 and 15.2% increment, respectively, compared with the matrix alloy. Obviously, the mixed ball-milling process of SiC nanoparticles and CNTs promoted the dispersion of each other, and both the uniformly distributed SiC nanoparticles and CNTs contributed to the enhanced mechanical performance of the hybrid composites. Besides, the addition of the hybrid nanoreinforcements induced the precipitation of nanosized rod-like MgZn2 phases in the as-extruded composites which also made a contribution to the enhanced performance of the composites. Investigations on the strengthening mechanisms of the hybrid composites show that it originates from grain refinement, load transfer, precipitation enhancement, and Orowan reinforcing. More importantly, the contribution made by each part was analyzed in detail.

The new processing method of spark plasma sintering (SPS) followed by hot extrusion was developed to produce Mg–1Al–xCNTs composites. Microstructural characterization revealed that the reinforcement particles were distributed uniformly in Mg matrix. The results of mechanical properties indicated a fact that compared with monolithic Mg, all Mg–1Al–xCNTs composites, especially the Mg–1Al–0.15CNTs composite, fabricated by SPS followed by hot extrusion exhibited better tensile and compressive properties. Under tension, Mg–1Al–0.15CNTs composite exhibited higher 0.2% tensile yield strength (TYS) (157 MPa versus 98 MPa, increased by ∼60%) and ultimate tensile strength (271 MPa versus 188 MPa, increased by ∼44%) than monolithic Mg. In compression, Mg–1Al–0.15CNTs composite also obtained a great enhancement in 0.2% compressive yield strength (118 MPa versus 81 MPa, increased by ∼46%) and ultimate compressive strength (321 MPa versus 255 MPa, increased by ∼26%) compared to monolithic Mg. Meanwhile, Mg–1Al–0.15CNTs composite maintained a high tensile failure strain of ∼8.8% and a high compressive failure strain of ∼17.9%.

Different volume fractions (0.5–4.5 vol%) of carbon nanotubes (CNTs) were used to reinforce a binary Fe50Co soft magnetic alloy. The first method for dispersion involved dry mixing and ball milling of the powder, while the second included wet mixing in dimethylformamide under ultrasonic agitation, drying and then dry ball milling. The powders were consolidated using spark plasma sintering. Tensile test and SEM analyses were performed to characterize the mechanical properties and the fracture surface of the sintered materials. The best magnetic and mechanical properties were achieved using the first method. A maximum enhancement in tensile strength of around 20% was observed in the 0.5 vol% CNT composite with improved elongation compared to the monolithic Fe50Co alloy. In addition, the magnetic properties were enhanced by adding CNTs up to 1 vol%, and an improvement in densification was observed in composites up to 1.5 vol% CNT with respect to monolithic Fe50Co alloy.

The paper presents the size-dependant behaviors of the carbon nanotubes under electrostatic actuation using the modified couple stress theory and homotopy perturbation method. Due to the less accuracy of the classical elasticity theorems, the modified couple stress theory is applied in order to capture the size-dependant properties of the carbon nanotubes. Both of the static and dynamic behaviors under static DC and step DC voltages are discussed. The effects of various dimensions and boundary conditions on the deflection and pull-in voltages of the carbon nanotubes are to be investigated in detail via application of the homotopy perturbation method to solve the nonlinear governing equations semi-analytically.

This research focuses on characterization of the impact of dispersion methods on aluminum-carbon nanotubes (Al-CNTs) nanocomposite structure. Nanocomposites were produced by a conventional powder metallurgy process after the dispersion of the CNTs on the Al powders, using two approaches: (1) the dispersion of CNTs and mixture with Al powders were performed in a single step by ultrasonication; and (2) the CNTs were previously untangled by ultrasonication and then mixed with Al powders by ball milling. Microstructural characterization of Al-CNT nanocomposites was performed by optical microscopy, scanning and transmission electron microscopy, electron backscatter diffraction, and high-resolution transmission electron microscopy (HRTEM). Microstructural characterization revealed that the use of ball milling for mixing CNTs with Al powders promoted the formation of CNT clusters of reduced size, more uniformly dispersed in the matrix, and a nanocomposite of smaller grain size. However, the results of HRTEM and Raman spectroscopy show that ball milling causes higher damage to the CNT structure. The strengthening effect of the CNT is attested by the increase in hardness and tensile strength of the nanocomposites.