Characterization of Carbide Precipitation during Tempering for Quenched Dievar Steel.

Carbide precipitation and coarsening are investigated for quenched Dievar steel during tempering. Lath/lenticular martensite, retained austenite, lower bainite, auto-tempered, and larger spherical carbides are all observed in the as-quenched condition. The carbide precipitation sequence on tempering is ascertained to be: M8C7 + cementite → M8C7 + M2C + M7C3 → M8C7 + M7C3 + M23C6 → M8C7 + M7C3 + M23C6 + M6C; carbides become coarser on tempering, and the sizes for inter-lath carbides increase noticeably with increasing tempering temperatures due to the faster grain boundary diffusion, whereas the sizes for intra-lath carbides remain nearly constant. The rate of coarsening for carbides by tempering at 650 °C is much higher than those by tempering at 550 °C and 600 °C, due to the faster diffusion of alloying elements at higher temperatures.

Achieving a combination of decent biocompatibility and large near-linear-elastic deformation behavior in shell-core-like structural TiNb/NiTi composite.

As expected from the material design, a novel shell-core-like structural TiNb/NiTi composite possessing both decent biocompatibility and large near-linear-elastic deformation behavior (namely as near-linear elasticity accompanied by high elastic strain limit) was prepared successfully by a hot pack-rolling combined with cold rolling procedure. Non-cytotoxic TiNb outer shell obstructs the NiTi inner core from cells and provides the decent biocompatibility of TiNb/NiTi composite. Large near-linear-elastic deformation behavior for this TiNb/NiTi composite has been confirmed to be associated with intrinsic elastic deformation, two types of reversible stress-induced martensitic transformations (i.e. ß↔α'' and B2↔B19' transformations) occurring in a homogeneous manner, together with the (001) compound twin in B19' martensitic plates. Our study provides a new design approach for developing NiTi-based composites with both decent biocompatibility and large near-linear-elastic deformation behavior for biomedical or engineering applications.

Band Engineering and Morphology Control of Oxygen-Incorporated Graphitic Carbon Nitride Porous Nanosheets for Highly Efficient Photocatalytic Hydrogen Evolution.

Graphitic carbon nitride (g-C3N4)-based photocatalysts have shown great potential in the splitting of water. However, the intrinsic drawbacks of g-C3N4, such as low surface area, poor diffusion, and charge separation efficiency, remain as the bottleneck to achieve highly efficient hydrogen evolution. Here, a hollow oxygen-incorporated g-C3N4 nanosheet (OCN) with an improved surface area of 148.5 m2 g-1 is fabricated by the multiple thermal treatments under the N2/O2 atmosphere, wherein the C-O bonds are formed through two ways of physical adsorption and doping. The physical characterization and theoretical calculation indicate that the O-adsorption can promote the generation of defects, leading to the formation of hollow morphology, while the O-doping results in reduced band gap of g-C3N4. The optimized OCN shows an excellent photocatalytic hydrogen evolution activity of 3519.6 µmol g-1 h-1 for ~ 20 h, which is over four times higher than that of g-C3N4 (850.1 µmol g-1 h-1) and outperforms most of the reported g-C3N4 catalysts.

Design and fabrication of a Nb/NiTi superelastic composite with high critical stress for inducing martensitic transformation and large recoverable strain for biomedical applications.

A novel Nb/NiTi superelastic composite with a shell-core structure was designed and fabricated to achieve a combination of biocompatibility and superelasticity (large recoverable strain ε accompanied by high critical stress for inducing martensitic transformation σSIM). The good biocompatibility is mainly attributed to the outer non-cytotoxic Nb shell that prevents inner NiTi core from direct contact with cells. Meanwhile, the inner NiTi core endows the composite with superelasticity through a fully reversible stress-induced martensitic transformation between B2 parent phase and B19' martensite. These results might shed some light on design and development of novel superelastic composites for biomedical applications.

Is CuO Suitable for Improving the Electrochemical Properties of g-C3N4?

G-C3N4 has a bright application prospect as an electrode material of supercapacitors, which makes it a concern. In order to increase the specific capacitance of g-C3N4, we consider to combine it with a metal oxide with high theoretical specific capacitance and utilize the synergistic effect. As a common metal oxide, CuO has the characteristics of high theoretical capacitance, high chemical stability, simple preparation and environmental friendliness. A composite containing CuO nanobelts and graphitic C3N4 (g-C3N4) was successfully synthesized by a chemical precipitation method. Various testing methods were used to explore its composition, microstructure and electrochemical properties to discuss whether CuO is suitable for improving the electrochemical properties of g-C3N4.

Ultra-Small Fe3O4 Nanoparticles Decorated WS2 Nanosheets with Superior Electrochemical Properties for Supercapacitors.

Fe3O4 nanoparticles/WS2 nanosheets nanocomposite was successfully synthesized in this study by a one-step hydrothermal method. Three different contents of Fe3O4 in the nanocomposite were prepared by changing the quantity of FeCl3·6H2O, ascorbic acid and NaHCO3. Fe3O4 nanoparticles are about 3 nm in diameter and combined with WS2 to form stable heterojunctions, which are good for releasing the volume change of electrode materials in charge/discharge procedure. Because of the large theory capacitance of Fe3O4 nanoparticle, the specific capacitance of the Fe3O4 nanoparticles/WS2 nanosheets nanocomposites increase with increasing content of Fe3O4 nanoparticles. When the weight ratio for Fe3O4 nanoparticles to WS2 nanosheets is up to 8:10, the specific capacitances of the nanocomposite are 83.85 F g-1 and 149.25 F g-1 as the scanning rate at 20 mV s-1 and the current density at 0.5 A g-1, respectively. Both of them of Fe3O4 nanoparticles/WS2 nanosheets are as almost 7 times high as that of WS2 nanosheets under the same measurement condition. This work shows that the Fe3O4 nanoparticles/WS2 nanosheets nanocomposite will be a kind of potential electrode materials for supercapacitors.

N,S-Atom-coordinated Co9S8 trinary dopants within a porous graphene framework as efficient catalysts for oxygen reduction/evolution reactions.

The intrinsic instability and difficulty in controlling the uniform size distributions of cobalt sulfides greatly restrict their application for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as a bifunctional electrocatalyst in regenerative fuel cells and rechargeable metal-air batteries. Herein, we synthesize a stable electrocatalyst of N,S-atom-coordinated Co9S8 trinary dopants within a porous graphene framework (Co9S8@NS-3DrGO), in which Co9S8 nanoparticles show uniform sizes and distributions. The stable Co9S8-based composites are fabricated by a facile soft template-assisted strategy, and the attraction of this method is that the intermediate of melamine formaldehyde resin (MFR) plays trifunctional roles, including (i) it acts as the templated bonding material to crosslink GO sheets together, (ii) it facilitates the formation of a core-shell architecture, and (iii) it acts as the N source for doping. Catalyst composition and performance are largely dependent on the pyrolysis temperature. Extensive investigation elucidates that the mechanism of electrocatalytic activity is attributed to: (i) the unique core-shell structure of the composites, as well as uniform particle sizes and distributions of Co9S8, (ii) the active nitrogen (pyridinic N and graphitic N) contents, and (iii) the large surface area and porous architecture. The composite pyrolyzed at 850 °C exhibits the best electrocatalytic performance, which shows a positive ORR half-wave potential (0.826 V), a small OER overpotential (317 mV) at 10 mA cm-2, and high stability, comparable to the commercial noble catalysts Pt/C and RuO2 in alkaline media. Furthermore, when applied in zinc-air batteries, it also displays a comparable performance to a Pt/C + RuO2 mixture catalyst. This work provides an approach to stabilize cobalt sulfides and control their particle sizes and distributions by ingeniously employing the soft template of MFR and pyrolyzing them at various temperatures.

Liquid Exfoliation and Electrochemical Properties of WS2 Nanosheets.

Commercial WS2 powders were exfoliated in sodium dodecyl sulfate solution with a combination of ball-milling and sonication. WS2 nanosheets can be uniformly dispersed in the solution. The layers and thicknesses of WS2 nanosheets could be tailored via changing the ball-milling speed. The effects of the ball-milling speed on crystallinity and morphology of the samples were analyzed. The results show that the layer structure of WS2 nanosheets is destroyed and the crystallinity is decreased with increase of the ball-milling rate. The monolayer WS2 nanosheets at 200 rpm are obtained, which are mesoporous with the specific surface area as 5.419 m2 g-1. The specific capacitance and charge/discharge efficiency of WS2 nanosheets at 200 rpm are better than those of other samples. Its specific capacitance under the scanning rate of 20 mV s-1 and the current density of 0.5 A g-1 are 13.46 F g-1 and 22.50 F g-1, respectively. The charge/discharge curve of WS2 nanosheets at 200 rpm is a symmetrical triangle, which shows rapid charge and slow discharge. It means that WS2 nanosheets at 200 rpm has good electrochemical reversibility. The load transfer resistance and the internal series resistance of this sample are 84.60 Ω and 4.18 Ω, respectively.

Novel CsxWO3/TiO2 Microspheres as Enhanced Visible Light Photocatalysts for Dye Pollutant Treatments.

CsxWO3/TiO2 composites with different contents of CsxWO3 were successfully synthesized in this study by a facile hydrothermal process. CsxWO3/TiO2 composites were characterized by XRD, Raman, UV-visible diffuse reflectance spectra (DRS), photoluminescence spectra (PL) and SEM. TiO2 nanoparticles were distributed uniformly on the surface of the CsxWO3 microsphere in the prepared CsxWO3/TiO2 composites, and they formed heterojunctions with CsxWO3. The effect of CsxWO3 on the photoactivities of composites was investigated via DRS and PL. All CsxWO3/TiO2 catalysts showed enhanced photocatalytic activity for degrading rhodamine B under visible light irradiation. The 50% CsxWO3/TiO2 sample showed the best photocatalytic activity and its kinetic constant was 20 times larger than that of TiO2. The possible photocatalytic mechanism is also discussed from the trapping experiments of active species. The improved photocatalytic activity for the CsxWO3/TiO2 catalyst may be attributed to the synergetic effect between CsxWO3 microspheres and TiO2 nanoparticles. This novel photocatalyst can be used to degrade environmental pollutants in the future.

Newly Designed Graphene Cellular Monolith Functionalized with Hollow Pt-M (M = Ni, Co) Nanoparticles as the Electrocatalyst for Oxygen Reduction Reaction.

Newly designed graphene cellular monoliths (GCMs) functionalized with hollow Pt-M nanoparticles (NPs) (Pt-M/GCM, M = Ni, Co) have been successfully achieved by a facile and powerful method on the basis of sonochemical-assisted reduction and gelatinization processes. First, hollow Pt-M (M = Ni, Co) NPs were synthesized and distributed on graphene oxide sheets (Pt-M/GO) by sodium borohydride reduction of metal precursors in the ultrasonic environment. Second, the hollow structure was further formed by ascorbic acid (AA) reduction of Pt precursors in gelatinization process. Meanwhile, GO sheets with hollow Pt-M NPs were reduced to graphene, and were assembled into Pt-M/GCM hydrogels by gelatinization process. The Pt-M/GCM (M = Ni, Co) electrocatalysts have a factor of 9.4-18.9 enhancement in electrocatalytic activity and higher durability toward oxygen reduction reaction (ORR), compared with those of commercial Pt/C catalyst. In detail, the mass activities for Pt-Ni/GCM and Pt-Co/GCM are 1.26 A mgPt-1 and 1.79 A mgPt-1, respectively; meanwhile, the corresponding specific activities are 1.03 and 2.08 mA cm-2. The successful synthesis of such attractive materials paves the way to explore a series of porous materials in widespread applications.

Biomedical Potential of Ultrafine Ag/AgCl Nanoparticles Coated on Graphene with Special Reference to Antimicrobial Performances and Burn Wound Healing.

In recent years, researchers have proven the release of silver ions (Ag(+)) from silver nanoparticles (Ag NPs) significantly affects their toxicity to bacteria and other organisms. Due to the difficulty in maintaining a steady flux of a high concentration of Ag(+), it is still challenging to develop a highly efficient, stable, and biocompatible Ag NP-based antimicrobial material. To circumvent this issue, we developed a new Ag-based bactericide through the fabrication of sunlight-driven and ultrafine silver/silver chloride anchored on reduced graphene oxide (Ag/AgCl/rGO). This stable Ag/AgCl nanophotocatalyst with negligible release of Ag(+) generated a high amount of oxidative radicals, killing the bacteria, thus achieving both high bactericidal efficiency and stability. Moreover, functionalization of the nanomaterial with poly(diallyldimethylammonium chloride) (PDDA) gives it a highly adsorptive capacity, which allows it to capture the bacteria and possibly enhances the bactericidal activity. In vivo histopathological studies showed that the Ag/AgCl/rGO nanomaterial could obviously promote the regeneration of the epidermis, which indicated the good biomedical potential of Ag/AgCl/rGO nanomaterial in burn wound healing.

Antibacterial effect and proteomic analysis of graphene-based silver nanoparticles on a pathogenic bacterium Pseudomonas aeruginosa.

Graphene-based silver nanoparticles (Ag NPs-GE) material has been developed and demonstrated antibacterial effect against Escherichia coli and Pseudomonas aeruginosa. In this study, the antibacterial activity and mechanism on P. aeruginosa were investigated. The experiments results showed the minimum bactericidal concentration of Ag NPs-GE to P. aeruginosa is 20 µg/ml. When P. aeruginosa were exposed to 20 µg/ml Ag NPs-GE for 1 h, the cell wall was breakdown. In order to study the mechanism of antibacterial effect of Ag NPs-GE, two-dimensional electrophoresis was carried out to compare the protein expressional profiles of P. aeruginosa exposed to 5 µg/ml Ag NPs-GE or 5 µg/ml AgNO3 with the untreated bacteria. Identification of differentially expressed protein was performed by MALDI-TOF/TOF MS. The change of proteomic profile induced by Ag NPs-GE was distinct from that induced by AgNO3. Seven identified proteins were found induced and nine proteins were suppressed by Ag NPs-GE. Five identified proteins were found induced and twenty proteins were suppressed by AgNO3. In addition, either Ag NPs-GE or AgNO3 suppressed the expression of eight proteins, amidotransferase, 30S ribosomal protein S6, bifunctional proline dehydrogenase/pyrroline-5-carboxylate dehydrogenase, arginyl-tRNA synthetase, nitroreductase, acetolactate synthase 3, methionyl-tRNA synthetase and periplasmic tail-specific protease. Furthermore, gene ontology analysis and KEGG pathway analysis were used to characterize the functions of those proteins.

Highly stable and dispersive silver nanoparticle-graphene composites by a simple and low-energy-consuming approach and their antimicrobial activity.

A simple and low-energy-consuming approach to synthesize highly stable and dispersive silver nanoparticle-graphene (AgNP-GE) nanocomposites has been developed, in which the stability and dispersivity of the composites are varied greatly with the pH value and temperature of the reaction. The results demonstrate that the optimal reaction conditions are pH 11 at room temperature for 70 min. As-synthesized composites display excellent antimicrobial activity, and can completely inhibit the growth of Escherichia coli cells at a concentration of 20 mg L(-1) (20 ppm). After treatment with 10 ppm AgNP-GE composites, the cells are killed completely within 3 h. The unique structure imparts such good antimicrobial properties to the composites. Firstly, the sheetlike AgNP-GE tends to be adsorbed and accumulated onto the surface of cells, which can change the permeability and enhance the antimicrobial activity. Secondly, Ag(+) released from AgNPs can act on the cells effectively and fully, thereby resulting in cell death.

Visible-light-induced WO3/g-C3N4 composites with enhanced photocatalytic activity.

Novel WO3/g-C3N4 composite photocatalysts were prepared by a calcination process with different mass contents of WO3. The photocatalysts were characterized by thermogravimetric analysis (TG), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectrometry (EDS), high-resolution transmission electron microscopy (HRTEM), UV-vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) and electrochemical impedance spectroscopy (EIS). The photocatalytic activity of the photocatalysts was evaluated by degradation of methylene blue (MB) dye and 4-chlorophenol (4-CP) under visible light. The results indicated that the WO3/g-C3N4 composite photocatalysts showed higher photocatalytic activity than both the pure WO3 and pure g-C3N4. The optimum photocatalytic activity of WO3/g-C3N4 at a WO3 mass content of 9.7% under visible light irradiation was up to 4.2 times and 2.9 times as high as that of the pure WO3 and pure g-C3N4, respectively. The remarkably increased performance of WO3/g-C3N4 was mainly attributed to the synergistic effect between the interface of WO3 and g-C3N4, including enhanced optical absorption in the visible region, enlarged specific surface areas and the suitable band positions of WO3/g-C3N4 composites.

[Study on adductive reaction of Ni[(C4H9O)2PS2]2 with nitrogen base by spectrophotometric method(II)].

Reaction of Ni[(C4H9O)2PS2]2 with ethylamine, n-propylamine, n-butylamine, and n-amylamine have been studied by spectrophotometry in ethanol at 30 degrees C. For nitrogen base(B), the adduct formation of NiL2.B and NiL2.B2 is established, and their additive equilibrium constants (lg beta n) and molecular number (n) have been discussed. All the NiL2.B and NiL2.B2 complexes exhibit virtually the same electronic spectra arising from the five-coordinate NiNS4 and six-coordinate NiN2S4 chromophore respectively. The constants (lg beta n) increase with basicity (pKa) of nitrogen base and can be described by experimental formulas: lg beta 1 = -9.69 +1.15 pKa; lg beta 2 = -18.73 +2.28 pKa.