Effects of volume ratio on the microstructure and mechanical properties of particle reinforced magnesium matrix composite

In the present study, the AZ91 alloy reinforced by (submicron + micron) SiCp with four kind volume ratio was fabricated by the semisolid stirring casting technology. The influence of volume ratio between submicron and micron SiCp on the microstructure and mechanical properties of Mg matrix was investigated. Results show that the submicron SiCp is more conducive to grain refinement as compared with micron SiCp. With the increase of volume ratio, the submicron particle dense regions increase and the average grain size decreases. The yield strength of bimodal size SiCp/AZ91 composite is higher than monolithic micron SiCp/AZ91composite. Both Δσ_Hall–Petch and Δσ_CTE increase as the volume ratio changes from 0:10, 0.5:9.5, 1:9 to 1.5:8.5. Among the composite with different volume ratio, the S-1.5 + 10-8.5 composite has the best mechanical properties. The interface debonding is found at the interface of micron SiCp-Mg. As the increase of volume ratio, the phenomenon of interface debonding weakens and the amount of dimples increases.     

Electroactive shape memory polymer based on optimized multi-walled carbon nanotubes/polyvinyl alcohol nanocomposites

The development of shape memory polymers (SMPs) has gained remarkable attention due to their wide range of applications, from biomedical to electromechanical. In this work, we have developed and optimized an electroactive SMP based on polyvinyl alcohol/multi-walled carbon nanotubes (PVA/MWNTs) composites. When a constant voltage of 60 V was applied to the optimized sample, the polymer shape could be recovered to the original form within 35 s. Different weight fractions of MWNT/PVA composites were prepared by using a simple solution blending and transitional solution casting method, and their microstructures, electrical conductivities, thermal conductivities, and electroactive shape memory properties were investigated. According to our systematic analysis, the enhanced performance can be attributed to the reinforcement of MWNTs that led to the improved electrical and thermal conductivities of the PVA matrix.     

Hollow structured Zn0.76Co0.24S–Co9S8 composite with two-phase synergistic effect as bifunctional catalysts

It is of great significance to develop efficient and inexpensive oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) bifunctional catalysts for the current energy crisis. But this is still a long-term and formidable challenge. In this work, a two-phase synergistic effect between transition metal sulfides is applied in the design of ORR/OER bifunctional catalysts. Co-based zeolite imidazolate framework (MOF) is used as a precursor to prepare the hollow Co₉S₈ through vulcanization and heat treatment. At the same time, the phase transformation occurs to form some Zn_0.76Co_0.24S on surface during the heat treatment due to the Zn-polydopamine coating. The hollow structure Zn_0.76Co_0.24S–Co₉S₈ composite has been verified and promotes the diffusion of reactants and products, and the interaction between two phases greatly promotes the catalytic reactions. The coating of Zn-polydopamine forms uniform carbon layer on surface, enhancing the conductivity of Zn_0.76Co_0.24S–Co₉S₈ composite. The Zn_0.76Co_0.24S–Co₉S₈ composite shows much better performance of ORR and OER compared to any of them. The overpotential of OER at a current density of 10 mA/cm² is 330 mV, and the half-wave potential of ORR is 0.83 V. Additionally, the Zn_0.76Co_0.24S–Co₉S₈ composite displays better cyclic stability. The synergistic effect of Zn_0.76Co_0.24S and Co₉S₈ can be considered as the foremost factor for the improvement of catalyst performance, which provides new possibilities for the development of non-precious metal bifunctional catalysts.     

Unique cyclic performance of post-treated carbide-derived carbon as an anode electrode

Carbide-derived carbon (CDC) is an attractive anode material for Li-ion battery applications because diverse pore textures and structures from amorphous to highly ordered graphite can be controlled by changing the synthesis conditions and precursor, respectively. To elucidate the unique cycling behavior of the post air-treated CDC anode, electrochemical performance was studied under variation of C-rates with structural changes before and after cycling. By tailoring the pore texture of CDCs as removal of amorphous phase by post air-activation, the anode electrode showed a high increase of capacity under prolonged cycling and under high C-rate conditions such as 0.3–1.0 C-rates. The discharge capacities of the treated CDC increased from 400 mAh g⁻¹ to 913 mAh g⁻¹ with increasing cycle number and were close to high initial irreversible value, 1250 mAh g⁻¹, at the 220th cycle under a 0.1C-rate condition, which are unique and unusual cyclic properties in carbon anode applications. Under high C-rate conditions, the discharge capacities started to increase from around 160 mAh g⁻¹ and values of 415 mAh g⁻¹, 372 mAh g⁻¹, and 336 mAh g⁻¹, were observed at 0.3, 0.5, and 1.0 C-rates, respectively, at 600 cycles, demonstrating stable capacity performance.     

Effect of swaging on microstructure and mechanical properties of liquid-phase sintered 93W-4.9(Ni,Co)-2.1Fe alloy

The effect of swaging on the microstructure and mechanical properties of 93W-4.9Ni-2.1Fe alloy was investigated. The alloy was prepared by liquid-phase sintering under hydrogen atmosphere followed by vacuum heat treatment and swaging at 600 °C with different area reductions (ranging from 15.0% to 84.8%). The as-swaged alloy with area reduction 84.8% exhibits the highest ultimate tensile strength (about 1490 MPa) and the lowest elongation (about 2.5%), which has been attributed to higher fraction of tungsten cleavage. For the as-sintered alloys, the fracture modes are a combination of the ductile rupture of W-Ni-Fe-Co matrix, transgranular cleavage of the tungsten particles, W-W interfacial segregation and W-M interfacial debonding, whereas transgranular cleavage of the tungsten particles is the main characteristic in the as-swaged alloy. Transmission electron microscopy images indicate that tungsten grains and W-Ni-Fe-Co matrix phase are composed of high-density dislocations. Based on the results, when running the swaging of 93W-4.9(Ni, Co)-2.1Fe alloy at 600 °C, the strengthening mechanism can be mainly due to the working-hardening.     

Vegetable waste as substrate and source of suitable microflora for bio-hydrogen production

Self-fermentation of cellulosic substrates to produce biohydrogen without inoculum addition nor pretreatments was investigated. Dark fermentation of two different substrates made of leaf-shaped vegetable refuses (V) and leaf-shaped vegetable refuses plus potato peels (VP), was taken in consideration. Batch experiments were carried out, under two mesophilic anaerobic conditions (28 and 37 °C), in order to isolate and to identify potential H₂-producing bacterial strains contained in the vegetable extracts. The effect of initial glucose concentration (at 1, 5 and 10 g/L) on fermentative H₂ production by the isolates was also evaluated.H₂ production from self-fermentation of both biomasses was found to be feasible, without methane evolution, showing the highest yield for V biomass at 28 °C (24 L/kg VS). The pH control of the culture medium proved to be a critical parameter. The isolates had sequence similarities ≥98% with already known strains, belonging to the family Enterobacteriaceae (γ-proteobacteria) and Streptococcaceae (Firmicutes). Four genera found in the samples, namely Pectobacterium, Raoultella, Rahnella and Lactococcus have not been previously described for H₂ production from glucose. The isolates showed higher yield (1.6–2.2 mol H₂/mol glucose_added) at low glucose concentration (1 g/L), while the maximum H₂ production ranged from 410 to 1016 mL/L and was obtained at a substrate concentration of 10 g/L. The results suggested that vegetable waste can be effectively used as both, substrate and source of suitable microflora for bio-hydrogen production.     

‘Two way’ shape memory composites based on electroactive polymer and thermoplastic membrane

A practical and facile strategy was proposed to fabricate composites that not only use the properties of individual components (commercial electroactive polymer and thermoplastic resin) to their advantage, but also produce synergy effect of ‘two way’ shape memory properties. In this design, electroactive polymer is treated as soft segment which provides actuation force via converting electrical energy to dynamic energy. Thermoplastic material serves as ‘hard segment’ to help with fixation of temporary shape thanks to its re-structuring and stiffness/modulus changing abilities through the reversible transitional temperature. Compared with traditional one way and two way shape memory materials, this composite material has the capability of changing shape without pre-programming. High shape recover property (99 ± 0.3%.) has been obtained due to the rubber elasticity of electroactive polymer matrix. Many features could be brought up based on this design, such as accurate control over deformation by changing strength of applied electric field as well as tailorable stimulus temperature and mechanical properties.     

Mechanical behavior and tensile/compressive strength asymmetry of ultrafine structured Ti–Nb–Ni–Co–Al alloys with bi-modal grain size distribution

Bulk ultrafine structured metallic materials with the bi-modal grain size distribution exhibit both high strength and good ductility. Here we show a new family of bi-modal Ti–Nb–Ni–Co–Al alloys. Their microstructure consists of an ultrafine structured eutectic matrix and relatively coarse β-Ti dendrites. Chemical modification of the parent Ti–Nb–Ni–Cu–Al system significantly affected type and volume fraction of matrix phases. In its turn, this influenced the deformation behavior. The unexpected “double yielding” behavior as well as tensile/compressive fracture strength asymmetry of the designed alloys are discussed in detail. For that, the microstructure alterations under compressive and tensile loading was in situ and ex situ analyzed by scanning electron microscopy.     

Functionalization of multi-wall carbon nanotubes to reduce the coefficient of the friction and improve the wear resistance of multi-wall carbon nanotube/epoxy composites

Functionalization of multi-wall carbon nanotubes (MWCNTs) was achieved by grafting carboxyl groups and amino groups. Fourier transform infrared spectroscopy was used to detect the changes produced by functional groups on the surface of the MWCNTs. Three different MWCNTs were incorporated into epoxy resin and the friction and wear behavior of MWCNT/epoxy composites was investigated using a M-2000 wear testing machine at different sliding speeds under different applied loads. Scanning electron microscopy was used to observe the worn surfaces of the samples. The results indicated that the functional groups had been grafted on the surface of MWCNTs. Compared with neat epoxy, the composites with MWCNTs showed a lower friction coefficient and wear rate, and the wear rate decreased with the increase of MWCNT loading. Combining epoxy resin with MWCNTs is an efficient method to improve the wear resistance and decrease the coefficient of friction.