Effect of microbial hydrogen consumption on the hydrogen permeation behaviour of AISI 4135 steel under cathodic protection

The feasibility of microbial hydrogen consumption to mitigate the hydrogen embrittlement (HE) under different cathodic potentials was evaluated using the Devanathan-Stachurski electrochemical test and the hydrogen permeation efficiency η. The hydrogen permeation efficiency η in the presence of strain GA-1 was lower than that in sterile medium. The cathodic potential inhibited the adherence of strain GA-1 to AISI 4135 steel surface, thereby reducing the hydrogen consumption of strain GA-1. The adherent GA-1 cells were capable of consuming ‘cathodic hydrogen’ and reducing the proportions of absorbed hydrogen, indicating that it is theoretically possible to control HE by hydrogen-consuming microbes.     

Effect of chemical phosphorylation on solubility of buffalo milk proteins

Buffalo milk proteins (casein, co-precipitate or whey protein concentrate) were phosphorylated with phosphorus oxychloride (POCl₃) at three different pH values (5.0, 7.0 and 9.0). The solubilities of phosphorylated milk proteins were examined over the pH range 3.0–9.0 in water and ionic (0.1 m NaCl or 10–70 mm Ca²⁺) systems. The solubilities of buffalo milk proteins decreased at pH 3.0, while there was an increase in the solubilities of casein and co-precipitate near their isoelectric points upon phosphorylation. Solubilities of these phosphorylated milk proteins were pH dependent in 0.1 m NaCl but there was a decrease in their solubilities with increase in calcium ion concentration. This alteration could be due to the shifting of isoionic points of phosphorylated buffalo milk proteins towards acidic pH.     

An understanding of high entropy alloys from phase diagram calculations

The concept of High Entropy Alloy (HEA) is understood from the point of view of phase diagram calculation. The role of entropy of mixing on the phase stability is discussed for both ideal and non-ideal solid solution phases. The relative stability of a solid solution phase and line compounds is illustrated using hypothetical systems. Calculated binary and multicomponent phase diagrams are used to explain the phenomena observed experimentally for HEAs. The potential of using the CALPHAD (CALculation of PHAse Diagrams) approach in aiding the design of alloys with multiple key components is also discussed.     

Effect of LiAl5O8 additions on the sintering and optical transparency of LiAlON

LiAl₅O₈ (zeta alumina) was reaction sintered with α-Al₂O₃ and AlN to produce γ-LiAlON. Zeta alumina transforms from a primitive to a face-centered cubic structure above 1290 °C with a lattice parameter similar to γ-AlON. Weight loss measurements combined with XRD suggest solubility of Li in the spinel structure at elevated temperatures. The Vickers hardness, at a 1-kg load, of the pressureless sintered LiAlON was 16.5 ± 0.5 GPa, independent of the grain size or amount of zeta alumina added, for LiAl₅O₈ additions ranging between 0 and 16 wt.%. In-line transmission in the visible and near-IR regions increased with increasing grain size, most likely due to pore coalescence.     

Near-zero-shrinkage Al2O3 ceramic foams with coral-like and hollow-sphere structures via selective laser sintering and reaction bonding

The large shrinkage that ceramics undergo during sintering is a severe challenge for high-performance porous ceramics. In this study, we report a powder-based selective laser sintering (SLS) approach to prepare Al₂O₃ ceramic foams with near-zero shrinkage, high porosity, and outstanding strength. The ceramic foams consist of specific coral-like and hollow-sphere structures derived from the raw Al₂O₃/Al composite powders via reaction bonding (RB). A near-zero shrinkage of 0.91 ± 0.15 % and a high porosity of 73.7 ± 0.2 % can be achieved based on the Kirkendall effect during the oxidation of Al particles. Meanwhile, the reinforced sintering necks and robust bond-bridge connections between hollow-sphere and coral-like structures result in a remarkable bending strength of 7.37 ± 0.37 MPa. This measured strength is more than six times higher than other fabricated samples from spherical Al₂O₃ powders, and the comprehensive performance of ceramic foams prepared by this novel SLS/RB strategy is exceptionally remarkable versus that via conventional forming methods.     

Influence of starting powder choice on structure property relations in gadolinia stabilized zirconia 3Gd-TZP manufactured from co-milled starting powders

Two 3Gd-TZP materials were manufactured from powders produced by intense mixing and milling of unstabilized zirconia starting powders and gadolinia as stabilizer oxide by hot pressing at 1250 °C – 1400 °C. The materials show a combination of high toughness and moderate strength. In detail depending on starting powder the two TZP showed distinct differences concerning transformation characteristics, sintering temperature dependence of mechanical properties and the tendency to develop R-curve related deformation features such as non-linear stress strain curves and formation of transformation bands prior to fracture.     

Effect of ultrasonic vibration on the dechromisation corrosion of a CuCr alloy in HCl solution

The effect of ultrasonic vibration on the dechromisation corrosion of a CuCr alloy in HC1 solution was studied and the corrosion mechanisms were analyzed. It is found that ultlasonic vibration reduces the dechromisation incubation time, accelerates the dechromisafion corrosion rate, decreases the temperature and concentration of HC1 solution, and when the dechromisation occurs it seriously weakens the microstmcture of dechromisation layer. It is concluded that ultrasonic vibration can accelerate destruction of the passivation film on the Cr surface and increase the activities of Cl^- and Cr.     

低温球磨制备高热稳定性纳米晶Al-Zn-Mg-Cu合金块体材料

利用液氮球磨和真空热压技术制备纳米晶Al-10Zn-3Mg-1.8Cu(质量分数,%)合金块体材料。采用X射线衍射(XRD)和透射电镜(TEM)对材料在制备过程中的固态相变、晶粒尺寸和热稳定性进行分析。结果表明,材料经过液氮球磨15 h后晶粒尺寸为37 nm,真空热压后材料晶粒保持在100 nm,热挤压后晶粒尺寸约为300 nm,热处理后晶粒尺寸保持不变。材料的高热稳定性原因在于大量合金元素和杂质元素超饱和固溶于Al基体中阻止了晶粒的长大,以及细小析出MgZn2相和Al2O3颗粒对于晶界的钉扎作用。     

Light-Responsive Programmable Shape-Memory Soft Actuator Based on Liquid Crystalline Polymer/Polyurethane Network

Liquid crystalline polymers (LCPs), especially liquid crystalline elastomers (LCEs) can generate ultrahigh shape change amplitude but has lower mechanical strength. Although some attempts have been tried to improve the mechanical performance of LCE, there are still limitations including complicated fabrication and high actuation temperature. Here, a versatile method is reported to fabricate light-driven actuator by covalently cross-linking polyurethane (PU) into LCP networks (PULCN). This new scheme is distinct from the previous interpenetrating network strategy, the hydrogen bonds and covalent bonds are used in this study to improve the miscibility of non-liquid-crystalline PU and LCP materials and enhance the stability of the composite system. This material not only possesses the shape memory properties of PU but shows shape-changing behavior of LCPs. With a shrinkage ratio of 20% at the phase transition temperature, the prepared materials reached a maximum mechanical strength of 20 MPa, higher than conventional LCP. Meanwhile, the resulting film shows diverse and programmable initial shapes by constructing crosslinking density gradient across the thickness of the film. By integration of PULCN with near-infrared light-responsive polydopamine, local and sequential light control is achieved. This study may provide a new route for the fabrication of programmable and mechanically robust light-driven soft actuator.