ABSTRACT
Chemical foaming technology is widely used in the preparation of silicone rubber foam and is attributable to its one-step molding capability and eco-friendly production processes. The microrheological properties of silicone rubber play a pivotal role during the foaming process. In this study, Rheolaser Lab (Formulaction, Toulouse, France) was used to conduct in situ examinations for the influence of a crosslinking agent on the microrheological properties of silicone rubber foam for the first time. This study monitors the entire reaction process of silicone rubber foam from liquid to solid, as well as the matching of crosslinking and foaming reactions. Various parameters, including solid-liquid balance, elasticity index, and macroscopic viscosity index, are measured to analyze the microrheological properties of silicone rubber foam. The results show that the silicone rubber foam exhibits good microrheological properties, thereby demonstrating excellent performance at a crosslinking agent content of 2%. Through adjusting the experimental conditions, a sustainable and efficient approach was proposed for better cellular structure control in the industrial preparation of silicone rubber foam.
ABSTRACT
Recently, flexible temperature sensors have attracted significant interest due to their wide-ranging applications in areas such as biomedical monitoring, environmental monitoring, electronic skin, and intelligent robots. However, a combination of high sensitivity and high resolution remains a critical challenge. These properties depend on the synthesis techniques of the sensitive materials. In this work, we use a laser irradiation method to prepare a silver nanoparticle-modified carbon nanotube (Ag-MWCNT) which is further mixed with poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). The developed temperature sensor exhibited a high sensitivity of -0.45% °C-1 and linearity with an R2 value of 0.998 in the temperature range of 25-80 °C. Additionally, the sensor demonstrated remarkable repeatability, making it suitable for real-time temperature monitoring of the human body and environment. This temperature sensor is successfully demonstrated in practical applications such as monitoring the temperature of various parts of the human body and sensing the spatial temperature. These demonstrations highlight their significant potential in electronic skin and other related fields.
ABSTRACT
To assess the individual and synergistic effects of 2-butyne-1,4-diol (BD) and chloride ions on the microstructure and residual stress of electrodeposited nickel, various nickel layers were prepared from sulfamate baths comprising varying concentrations of BD and chloride ions by applying direct-current electrodeposition. And their surface morphologies, microstructure, and residual stress were tested using SEM, XRD, EBSD, TEM, and AFM. While the nickel layers composed of pyramid morphology were prepared from additive-free baths, the surface flattened gradually as the BD concentration of the baths was increased, and the acicular grains in the deposits were replaced with <100> oriented columnar grains or <111> oriented nanograins; additionally, the residual tensile stress of the deposits increased. The addition of chloride ions to the baths containing BD significantly increased the residual stress in the nickel layers, although it only slightly promoted surface flattening and columnar grain coarsening. The effects of BD and chloride ions on the growth mode and residual stress of nickel deposits were explained via analysis of surface morphologies and microstructure. And the results indicate that the reduction of chloride ion concentration is a feasible way to reduce the residual stress of the nickel deposits when BD is included in the baths.
ABSTRACT
In this paper, we report an in situ study regarding the microstructural evolution of a nickel-based alloy with high proportional twin boundaries by using electron backscatter diffraction techniques combined with the uniaxial tensile test. The study mainly focuses on the evolution of substructure, geometrically necessary dislocation, multiple types of grain boundaries (especially twin boundaries), and grain orientation. The results show that the Cr20Ni80 alloy can be obtained with up to 73% twin boundaries by annealing at 1100 °C for 30 min. During this deformation, dislocations preferentially accumulate near the twin boundary, and the strain also localizes at the twin boundary. With the increasing strain, dislocation interaction with grain boundaries leads to a decreasing trend of twin boundaries. However, when the strain is 0.024, the twin boundary is found to increase slightly. Meanwhile, the grain orientation gradually rotates to a stable direction and forms a Copper, S texture, and α-fiber <110>. Above all, during this deformation process, the alloy is deformed mainly by two deformation mechanisms: mechanical twinning and dislocation slip.
ABSTRACT
Zn anode is confronted with serious Zn dendrite growth and water-induced parasitic reactions, which severely hinders the rapid development and practical application of aqueous zinc metal batteries (AZMBs). Herein, inspired by sodium hyaluronate (SH) biomolecules in living organisms featured with the functions of water retention, ion-transport regulation, and film-formation, the SH working as a dynamic and self-adaptive "mask" is proposed to stabilize Zn anode. Benefiting from the abundant functional groups with high hydrophilicity and zincophilicity, SH molecule can constrain active water molecules on the Zn-electrolyte interface and participate in Zn2+ solvation structure to suppress parasitic reactions. Furthermore, the dynamical adsorption of SH with high-density negative charge on the Zn surface could serve as Zn2+ reservoirs to guide uniform Zn deposition. Consequently, stable Zn plating and an ultrahigh cumulative plating capacity (CPC) of 4.8 Ah cm-2 are achieved even at 20 mA cm-2 (20 mAh cm-2 ) in a Zn||Zn symmetric battery, reaching a record level in AZMBs. In addition, the Zn||ß-MnO2 full battery exhibits a substantially improved cycle stability. This work presents a route to realize a highly reversible and stable Zn metal anode by learning from nature.
Subject(s)
Manganese Compounds , Oxides , Electrodes , ZincABSTRACT
Developing rare-earth doped oxysulfide phosphors with diverse morphologies has significant value in many research fields such as in displays, medical diagnosis, and information storage. All of the time, phosphors with spherical morphology have been developed in most of the related literatures. Herein, by simply adjusting the pH values of the reaction solution, Gd2O2S:Tb3+ phosphors with various morphologies (sphere-like, sheet-like, cuboid-like, flat square-like, rod-like) were synthesized. The XRD patterns showed that phosphors with all morphologies are pure hexagonal phase of Gd2O2S. The atomic resolution structural analysis by transmission electron microscopy revealed the crystal growth model of the phosphors with different morphology. With the morphological change, the band gap energy of Gd2O2S:Tb3+ crystal changed from 3.76 eV to 4.28 eV, followed by different luminescence performance. The samples with sphere-like and cuboid-like microstructures exhibit stronger cathodoluminescence intensity than commercial product by comparison. Moreover, luminescence of Gd2O2S:Tb3+ phosphors have different emission performance excited by UV light radiation and an electron beam, which when excited by UV light is biased towards yellow, and while excited by an electron beam is biased towards cyan. This finding provides a simple but effective method to achieve rare-earth doped oxysulfide phosphors with diversified and tunable luminescence properties through morphology control.
ABSTRACT
Understanding the strengthening effect of niobium on ferrite grain boundaries from the perspective of valence electron structures will help to use niobium and other microalloying elements more effectively to improve the performance of steel materials. In this paper, the effect of niobium element on ferrite grain boundary strengthening is studied based on microstructure analysis at the nanometer scale. The enrichment of niobium in pipeline steel at ferrite boundary was observed by a three-dimensional atomic probe test. Segregation of Nb is observed in the ferrite grain boundaries of X70 steel, and its maximum concentration is 0.294-0.466 at.%. The charges in the occupancy of the Fe 3d state in grain and grain boundary were 7.23 and 7.37, respectively, based on quantitative analysis of electron energy loss spectra (EELS). The first-principle calculation suggests that the charges in the occupancy of 3d state for grain boundary iron are 6.57 and 6.68, respectively, before and after the Nb doping (with an increase of 1.67%), which reveals a similar trend to that of the EELS results. Through Nb alloying, the 3d valence electronic density of the state of Fe in grain boundary moves to a lower energy, which can reduce the total energy of the system and make the grain boundary more stable. Meanwhile, the charges in the occupancy of the 3d state for Fe in the grain boundary increases, providing more electrons for grain boundary bonding. These improve the strength and toughness of the material. This work provides a fundamental understanding for pipeline steel strengthening by element alloying.
ABSTRACT
Precipitates in two X80 pipeline steels were studied by transmission electron microscopy equipped with an energy filtering system. The steels are microalloyed with niobium and niobium-vanadium (Nb-V), respectively, and produced by continuous hot rolling. Besides the precipitates TiN and (Ti, Nb) (C, N), which were 10-100 nm in size, a large number of precipitates smaller than 10 nm distributed in the two steels have been observed. In the Nb-V microalloyed steel, only a few titanium nitrides covered by vanadium compounds on the surface have been observed. It is inferred that the vanadium exists mainly in the matrix as a solid solution element. The fact has been accepted that there was no contribution to the precipitation strengthening of the X80 steel by adding 0.04-0.06% vanadium under the present production process. By contrast, the toughness of the Nb-V steel is deteriorated. Therefore, a better toughness property of the Nb microalloyed X80 results from the optimum microalloying composition design and the suitable accelerating cooling after hot rolling.
ABSTRACT
Graphene oxide (GO) sheets were introduced to stabilize the melted polyethylene glycol (PEG) during the solid-liquid phase change process, which can be used as a smart heat storage system. The structural properties and phase change behaviors of the PEG-GO composites were comprehensively investigated as a function of the PEG content by means of various characterization techniques. The highest stabilized PEG content is 90 wt% in the composites, resulting in a heat storage capacity of 156.9 J g(-1), 93.9% of the phase change enthalpy of pure PEG. Notably, GO has much stronger impact on lowering of the phase change temperature of PEG compared with some other porous carbon materials (activated carbon and ordered mesoporous carbon) due to the unique thin layer structure of GO. Because of the high heat storage capacity and the moderate phase change temperature, the PEG-GO composite is a promising heat energy storage candidate at mild temperature.
ABSTRACT
In this work, pure nanostructured Mg(2)FeH(6) is successfully synthesized by sintering of a mixture of 2Mg + Fe nanoparticles. The successful preparation of pure Mg(2)FeH(6) can be attributed to the small particle sizes of Mg and Fe nanoparticles prepared by hydrogen plasma-metal reaction (HPMR), which benefits the synthesis. The hydrogen storage properties of Mg(2)FeH(6) and the synthesis mechanism of the Mg-Fe-H system are studied. The sample desorbs 5.0 wt% of hydrogen rapidly in 6 min under an initial hydrogen pressure of approximately 100 Pa at 623 K. The enthalpy and entropy of the reaction are deduced from the equilibrium plateau pressures of the desorption isotherms. The obtained Mg(2)FeH(6) shows favorable hydrogen storage properties due to the specific nanostructure of the materials.
