State-of-the-Art Review on Amorphous Carbon Nanotubes: Synthesis, Structure, and Application.

Carbon nanotubes (CNTs) have rapidly received increasing attention and great interest as potential materials for energy storage and catalyst fields, which is due to their unique physicochemical and electrical properties. With continuous improvements in fabrication routes, CNTs have been modified with various types of materials, opening up new perspectives for research and state-of-the-art technologies. Amorphous CNTs (aCNTs) are carbon nanostructures that are distinctively different from their well-ordered counterparts, such as single-walled and multi-walled carbon nanotubes (SWCNTs and MWCNTs, respectively), while the atoms in aCNTs are grouped in a disordered, crystalline/non-crystalline manner. Owing to their unique structure and properties, aCNTs are attractive for energy storage, catalysis, and aerospace applications. In this review, we provide an overview of the synthetic routes of aCNTs, which include chemical vapor deposition, catalytic pyrolysis, and arc discharge. Detailed morphologies of aCNTs and the systematic elucidation of tunable properties are also summarized. Finally, we discuss the future perspectives as well as associated challenges of aCNTs. With this review, we aim to encourage further research for the widespread use of aCNTs in industry.

Synergistic Reinforcement of Si3N4 Based Ceramics Fabricated via Multiphase Strengthening under Low Temperature and Short Holding Time.

Si3N4 ceramic as a tool material shows promising application prospects in high-speed machining fields; however, the required high mechanical properties and low-cost preparation of Si3N4 ceramic tool materials restrict its application. Herein, synergistic reinforced Si3N4 ceramic tool materials were fabricated by adding ß-Si3N4 seeds, inexpensive Si3N4 whiskers and TiC particles into coarse commercial Si3N4 powder (D50 = 1.5 µm), then sintering by hot-pressing with low temperature and short holding time (1600 °C-30 min-40 MPa). The phase assemblage, microstructure evolution and toughening mechanisms were investigated. The results reveal that the sintered Si3N4 ceramics with synergistic reinforcement, compared to those with individual reinforcement, present an enhancement in relative density (from 94.92% to 97.15%), flexural strength (from 467.56 ± 36.48 to 809.10 ± 45.59 MPa), and fracture toughness (from 8.38 ± 0.19 to 10.67 ± 0.16 MPa·m1/2), as well as a fine Vickers hardness of 16.86 ± 0.19 GPa. Additionally, the various reinforcement modes of Si3N4 ceramics including intergranular fracture, crack deflection, crack bridging and whiskers extraction were observed in crack propagation, arising from the contributions of the added ß-Si3N4 seeds, Si3N4 whiskers and TiC particles. This work is expected to serve as a reference for the production of ceramic cutting tools.

Microstructure and Properties of NiCoCrAlTi High Entropy Alloy Prepared Using MA-SPS Technique.

In this study, Ni35Co35Cr12.6Al7.5Ti5Mo1.68W1.39Nb0.95Ta0.47 high entropy alloy (HEA) was prepared using mechanical alloying (MA) and spark plasma sintering (SPS) based on the unique design concept of HEAs and third-generation powder superalloys. The HEA phase formation rules of the alloy system were predicted but need to be verified empirically. The microstructure and phase structure of the HEA powder were investigated at different milling times and speeds, with different process control agents, and with an HEA block sintered at different temperatures. The milling time and speed do not affect the alloying process of the powder and increasing the milling speed reduces the powder particle size. After 50 h of milling with ethanol as PCA, the powder has a dual-phase FCC+BCC structure, and stearic acid as PCA inhibits the powder alloying. When the SPS temperature reaches 950 °C, the HEA transitions from a dual-phase to a single FCC phase structure and, with increasing temperature, the mechanical properties of the alloy gradually improve. When the temperature reaches 1150 °C, the HEA has a density of 7.92 g cm-3, a relative density of 98.7%, and a hardness of 1050 HV. The fracture mechanism is one with a typical cleavage, a brittle fracture with a maximum compressive strength of 2363 MPa and no yield point.

Effect of Electrode Induction Melting Gas Atomization on Powder Quality: Satellite Formation Mechanism and Pressure.

Electrode induction melting gas atomization (EIGA) is a wildly applied method for preparing ultra-clean and spherical metal powders, which is a completely crucible-free melting and atomization process. Based on several experiments, we found that although the sphericity of metal powders prepared by EIGA was higher than that of other atomization methods, there were still some satellite powders. To understand the formation mechanism of the satellite, a computational fluid dynamics (CFD) approach FLUENT and a discrete particle model (DPM) were developed to simulate the gas atomization process, and several EIGA experiments with different argon pressures (2.5-4.0 MPa) were designed. A numerical simulation of the gas-flow field verified the formation trajectory of satellites, and the Hall flow rate of the powder produced under different pressures was 13.3, 13.8, 15.6, and 16.8, which were consistent with the prediction of the numerical simulation. This study provides theoretical support for understanding the satellite formation mechanism and improving powder sphericity in the EIGA process.

The Effect of Yttrium on the Solution and Diffusion Behaviors of Helium in Tungsten: First-Principles Simulations.

We systematically investigated the influence of yttrium (Y) on the evolution behavior of helium (He) in tungsten (W) by first-principles calculations. It is found that the addition of Y reduces the solution energy of He atoms in W. Interestingly, the solution energy of He decreases with decreasing distance between Y and He. The binding energies between Y and He are inversely correlated with the effective charge of He atoms, which can be attributed to the closed shell structure of He. In addition, compared with pure W, the diffusion barrier (0.033 eV) of He with Y is lower, calculated by the climbing-image nudged elastic band (CI-NEB) simulations, reflecting that the existence of Y contributes to the diffusion of He in W. The obtained results provide a theoretical direction for understanding the diffusion of He.

Effect of Ultra-High Pressure Sintering and Spark Plasma Sintering and Subsequent Heat Treatment on the Properties of Si3N4 Ceramics.

In this study, coarse Beta silicon nitride (ß-Si3N4) powder was used as the raw material to fabricate dense Si3N4 ceramics using two different methods of ultra-high pressure sintering and spark plasma sintering at 1550 °C, followed by heat treatment at 1750 °C. The densification, microstructure, mechanical properties, and thermal conductivity of samples were investigated comparatively. The results indicate that spark plasma sintering can fabricate dense Si3N4 ceramics with a relative density of 99.2% in a shorter time and promote α-to-ß phase transition. Coarse ß-Si3N4 grains were partially fragmented during ultra-high pressure sintering under high pressure of 5 GPa, thereby reducing the number of the nucleus, which is conducive to the growth of elongated grains. The UHP sample with no fine α-Si3N4 powder addition achieved the highest fracture strength (822 MPa) and fracture toughness (6.6 MPa·m1/2). The addition of partial fine α-Si3N4 powder facilitated the densification of the SPS samples and promoted the growth of elongated grains. The ß-Si3N4 ceramics SPS sintered with fine α-Si3N4 powder addition obtained the best comprehensive performance, including the highest density of 99.8%, hardness of 1890 HV, fracture strength of 817 MPa, fracture toughness of 6.2 MPa·m1/2, and thermal conductivity of 71 W·m-1·K-1.

A Study of Hot Deformation Behavior of T15MN High-Speed Steel during Thermal Compression.

The hot deformation behavior of T15MN high-speed steel during thermal compression was studied by experiment and simulation. Specifically, the hot compression test was carried out on a Gleeble-1500 thermal-mechanical simulator at temperatures from 1273 to1423 K and strain rates from 0.01 to 10 s-1 with the deformation degree of 60%. It was found that all the flow stress curves were characterized by a single peak, indicating the occurrence of dynamic recrystallization (DRX), and flow stress will increase with increasing strain rate and decreasing deformation temperature. Based on the experimental data, the constitutive equations and thermal activation energy were obtained (Qact = 498,520 J/mol). Meanwhile, a cellular automaton model was established via the MATLAB platform to simulate the dynamic recrystallization phenomenon during hot deformation. The simulation results indicate that a good visualization effect of the microstructural evolution is achieved. Both increasing deformation temperature and decreasing strain rate can promote the increase in the average size and volume fraction of recrystallized grains (R-grains). Additionally, the calculated flow stress values fit in well with the experimental ones in general, which indicates that the established CA model has a certain ability to predict the deformation behavior of metal materials at elevated temperatures.

Evaluation of cytotoxicity and biodistribution of mesoporous carbon nanotubes (pristine/-OH/-COOH) to HepG2 cells in vitro and healthy mice in vivo.

Mesoporous carbon nanotubes (mCNTs) hold great promise interests, owing to their superior nano-platform properties for biomedicine. To fully utilize this potential, the toxicity and biodistribution of pristine and surface-modified mCNTs (-OH/-COOH) should preferentially be addressed. The results of cell viability suggested that pristine mCNTs induced cell death in a concentration-dependent manner. As evidence of reactive oxygen species (ROS), malondialdehyde (MDA) and superoxide dismutase (SOD), pristine mCNTs induced noticeable redox imbalance. 99mTc tracing data suggested that the cellular uptake of pristine mCNTs posed a concentrate-dependent and energy-dependent manner via macropinocytotic and clathrin-dependent pathways, and the main accumulated organs were lung, liver and spleen. With OH modification, the ROS generation, MDA deposition and SOD consumption were evidently reduced compared with the pristine mCNTs at 24/48 h high-dose exposure. With COOH modification, the modified mCNTs only showed a significant difference in SOD consumption at 24/48 h exposure, but there was no significant difference in the measurement of ROS and MDA. The internalization mechanism and organ distribution of modified mCNTs were basically invariant. Together, our study provides evidence that mCNTs and the modified mCNTs all could induce oxidative damage and thereby impair cells. 99mTc-mCNTs can effectively trace the distribution of nanotubes in vivo.

Theoretical Predictions of the Structural and Mechanical Properties of Tungsten-Rare Earth Element Alloys.

Tungsten (W) is considered as the potential plasma facing material of the divertor and the first wall material in fusion. To further improve the ductility of W, the structural and mechanical properties of W-M (M = rare earth element Y, La, Ce and Lu) alloys are systematically investigated by first-principles calculations. Our results reveal that all the W1-xMx (x = 0.0625, 0.125, 0.1875, 0.25) alloys can form binary solid solution at the atomic level, and the alloys keep bcc lattice structures until the concentration of M increases to a certain value. Although the moduli of the alloys are reduced compared to that of pure W metal, the characteristic B/G ratio and Poisson's ratio significantly increase, implying all the four rare earth elements can efficiently improve the ductility of W metal. Considering both factors of mechanical strength and ductility, La and Ce are better alloying elements than Y and Lu.

First-Principles Studies of Adsorptive Remediation of Water and Air Pollutants Using Two-Dimensional MXene Materials.

Water and air pollution is a critical issue across the whole world. Two-dimensional transition metal carbide/nitride (MXene) materials, due to the characteristics of large specific surface area, hydrophilic nature and abundant highly active surficial sites, are able to adsorb a variety of environmental pollutants, and thus can be used for environmental remediation. First-principles method is a powerful tool to investigate and predict the properties of low-dimensional materials, which can save a large amount of experimental costs and accelerate the research progress. In this review, we summarize the recent research progresses of the MXene materials in the adsorptive remediation of environmental pollutants in polluted water and air using first-principles simulations, and try to predict the research direction of MXenes in the adsorptive environmental applications from first-principles view.

Author Correction: Nanostructured laminar tungsten alloy with improved ductility by surface mechanical attrition treatment.

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.

Nanostructured laminar tungsten alloy with improved ductility by surface mechanical attrition treatment.

A nanostructured laminar W-La2O3 alloy (WL10) with improved ductility was prepared using a surface mechanical attrition treatment (SMAT). φ1.5 mm ZrO2 WL10 balls subjected to SMAT (called φ1.5 mm ZrO2 ball SMATed WL10) samples possess the best surface profile and excellent integrated mechanical properties (the ductile-brittle transition temperature (DBTT) value decreases by approximately 200 °C, and the bending strength decreases by 100 Mpa). A highly dense group of laminates was detected near the surface of the φ1.5 mm ZrO2 ball SMATed WL10 sample. The SMATed WL10 laminates were composed of a micro-grain layer, an ultrafine-grain layer and a nanosized-grain layer. The nanostructured laminar surface layer of the φ1.5 mm ZrO2 ball SMATed WL10 sample is approximately 1-2 µm. The top surface of the WL10 plates with and without the SMAT process possesses residual compressive stress of approximately -883 MPa and -241 MPa, respectively, in the y direction and -859 MPa and -854 MPa, respectively, in the x direction. The SMAT process could be a complementary method to further improve the toughness of tungsten-based materials.

Observation of intermediate template directed SiC nanowire growth in Si-C-N systems.

SiC nanowires (NWs) are commonly prepared in a Si-C-N system, but its formation mechanism is not fully understood. High resolution transmission electron microscopy and electron energy loss spectroscopy observation recorded the growth process of how Si(3)N(4) NWs were transformed into SiC NWs, and demonstrated the validity of an intermediate template directed SiC NW growth via carbothermal reduction of intermediate Si(3)N(4) NWs in a Si-C-N system. Based on this discovery, an intermediate-template growth mechanism of SiC NWs was proposed.

Resistance sintering under ultra high pressure: a new approach to produce bulk nanocrystalline refractory metal.

Several different types of commercially available grades of W and Mo powders with nano size (50 nm) and micro size (0.2-3 microm) were sintered by a novel sintering method named as resistance sintering under ultra high pressure in the absence of additive. The sintering effect was characterized through microstructure observation and testing the mechanical properties. It is finds that as very short sintering time (less than 1 min.) is needed, this novel method is an effective technology to fabricate nanocrystalline refractory metal. Density greater than 90% theoretical density was achieved, while the grain size still remained about 50 nm, this grain size is substantially smaller than previously reported. The sintering mechanism of this sintering method is very different from the conventional sintering methods and was primarily analyzed in this paper.

Frontal polymerization synthesis of starch-grafted hydrogels: Effect of temperature and tube size on propagating front and properties of hydrogels.

The frontal polymerization process was used to produce superabsorbent hydrogels based on acrylic acid monomers grafted onto starch. Using a simple test tube which was nonadiabatic and permitted contact with air, the effects of initial temperature and tube size on the propagating front of grafting copolymerization and the properties of hydrogels were explored. The unrestricted access of the reaction mixture to oxygen delayed the formation of self-propagating polymerization front. The ignition time was markedly lengthened with the increasing of tube size attributed to the formation of large amounts of peroxy radicals. The front velocity dependence on initial temperature could be fit to an Arrhenius function with the average apparent activation energy of 24 kJ mol(-1), and on tube size to a function of higher order. The increase of the initial temperature increased the front temperature, which lead to more soluble oligomers and higher degree of crosslinking. The interplay of two opposite effects of oligomer and crosslinking determined the sol and gel content. An increase in tube size had two effects on the propagating front. One was to reduce heat loss. The other effect was to increase the number of escaping gas bubbles. The combined action of the two effects resulted in a maximum value of front temperature, an increase in sol content and a reduction in gel content with tube size. The highest swelling capacity of hydrogels was obtained when the initial temperature or tube size favored a formation of porous microstructure of hydrogels.

Frontal copolymerization synthesis and property characterization of starch-graft-poly(acrylic acid) hydrogels.

Recently, a considerable amount of research has centered on uniquely structured polymers synthesized through self-propagating frontal polymerization. The obtained polymer materials have better features than those obtained by using the classical batch route. The additional advantages are short reaction times and low cost. This work describes the first frontal polymerization synthesis of a graft copolymer superabsorbent hydrogel of acrylic acid onto starch at high monomer and initiator concentration. The effects of varying the relative amounts of the reaction components on the most relevant parameters relating to frontal polymerization were explored. The front velocity dependence on initiator concentration could be fit to a power function. The temperature profiles were found to be very sharp with a maximum temperature below 150 degrees C, which was responsible for high monomer conversion. The ultimate properties of the product appear to depend on the polymerization front velocity and the temperature. The high-temperature and rapid temperature increase at the polymerization front led to products with interconnected porous structures caused by the evaporation of water. So, a fast-swelling, highly absorbing hydrogel with respect to batch polymerization was obtained.