Effects of on-line solution and off-line heat treatment on microstructure and hardness of die-cast AZ91D alloy

The effects of on-line solution, off-line solution and aging heat treatment on the microstructure and hardness of the die-cast AZ91D alloys were investigated. Brinell hardness of die-cast AZ91D alloy increases through on-line solution and off-line aging treatment but decreases after off-line solution treatment. By X-ray diffractometry, optical microscopy, differential thermal analysis, scanning electron microscopy and X-ray energy dispersive spectroscopy, it is found that the microstructures of the die-cast AZ91D magnesium alloy before and after on-line solution and off-line aging are similar, consisting of α-Mg and β-Al12Mg17. The precipitation of Al element is prevented by on-line solution so that the effect of solid solution strengthening is enhanced. The β-Al12Mg17 phases precipitate from supersaturated Mg solid solution after off-line aging treatment, and lead to microstructure refinement of AZ91D alloy, so the effect of precipitation hardening is enhanced. The β-Al12Mg17 phases dissolve in the substructure after off-line solution treatment, which leads to that the grain boundary strengthening phase is reduced significantly and the hardness of die cast AZ91D is reduced.

ASTM A240 UNS S32101双相不锈钢SMAW焊接工艺研究

针对ASTM A240 UNS S32101双相不锈钢的性能特点和焊接特性,采用手工电弧焊接(SMAW),选用合理的焊接材料,调整焊接工艺和技术措施,严格控制层间温度和焊接热输入,焊接后焊缝及热影响区获得了与母材较为相近、比例适当的铁素体和奥氏体双相组织,焊接接头具有良好的力学性能。并通过焊接工艺评定试验,验证了SMAW焊接方法的可行性和有效性,确定了ASTM A240 UNS S32101双相不锈钢合理的SMAW焊接工艺,为现场焊接提供了指导。

SnO_2-based solid solutions for CH_4 deep oxidation: Quantifying the lattice capacity of SnO_2 using an X-ray diffraction extrapolation method

A series of SnO2‐based catalysts modified by Mn, Zr, Ti and Pb oxides with a Sn/M （M=Mn, Zr, Ti and Pb） molar ratio of 9/1 were prepared by a co‐precipitation method and used for CH4 and CO oxidation. The Mn3＋, Zr4＋, Ti4＋and Pb4＋cations are incorporated into the lattice of tetragonal rutile SnO2 to form a solid solution structure. As a consequence, the surface area and thermal stability of the catalysts are improved. Moreover, the oxygen species of the modified catalysts become easier to be reduced. Therefore, the oxidation activity over the catalysts was improved, except for the one modified by Pb oxide. Manganese oxide demonstrates the best promotional effects for SnO2. Using an X‐ray diffraction extrapolation method, the lattice capacity of SnO2 for Mn2O3 was 0.135 g Mn2O3/g SnO2, which indicates that to form stable solid solution, only 21%Sn4＋cations in the lattice can be maximally replaced by Mn3＋. If the amount of Mn3＋cations is over the capacity, Mn2O3 will be formed, which is not favorable for the activity of the catalysts. The Sn rich samples with only Sn‐Mn solid solution phase show higher activity than the ones with excess Mn2O3 species.

Combinatorial Optimization of Ba/Fe-cordierite Solid Solution （Ba0.05Fe0.1Mg）2Al4Si5O18 for High Infrared Radiance Materials

A combinatorial chemistry method was employed to screen the Ba2＋ and Fe3＋ incorporated into cordierite structure （Ba0.05Fe0.1Mg）2A14Si5018 for exploring of high infrared radiance materials. A series of square-type sample array that consists of 7×7 compositions was syn- thesized by ink-jetting nitrate solutions into micro-reactor wells in a ceramic plate and then heat-treated at high temperatures. X-ray diffraction and infrared thermograph were used to analyze the effects of Ba2＋/Fe3＋ incorporating on the lattice distortion of cordierite and resultant changes in infrared radiance properties. Based on the results of X-ray phase analy- sis and radiance measurement of the scale-up prepared samples, the optimal Ba2＋ and Fe3＋ co-adding amount was determined to be 5%Ba2＋ plus 10%Fe3＋. Moreover, the infrared emissivity of the optimal composition at 100 ℃ was found to be higher than 0.8 in a wide wavelength range of 5-24μm. The research work demonstrates a promising application of Ba2＋/Fe3＋ cordierite solid solution as a kind of infrared heating materials for energy saving.

Facile synthesis of Fe/Ni bimetallic oxide solid-solution nanoparticles with superior electrocatalytic activity for oxygen evolution reaction

The sluggish oxygen evolution reaction （OER） is an important half-reaction of the electrochemical water-splitting reaction. Amorphous Fe/Ni composite oxides have high activity. In this work, we modified the aerosol spray-assisted approach and obtained amorphous Fe-Ni-Ox solid-solution nanoparticles （Fe-Ni-Ox-NPs） approximately 20 nm in size by choosing iron/nickel acetylacetonates as raw materials instead of inorganic salts. The small-sized Fe-Ni-Ox-NPs were characterized by scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, X-ray diffraction （XRD） analysis, energy-dispersive X-ray spectroscopy （EDX）, and X-ray photoelectron spectroscopy （XPS）. Furthermore, an investigation of electrochemical OER performance suggests that the small-sized Fe-Ni-Ox-NPs have higher activity than the large-sized Fe-Ni-Ox-MPs. A small overpotential of 0.315 V was demanded to obtain a working current density of 50 mA/cm2, and the Tafel slope was as low as 38 mWdec.