α钛富氧层增厚动力学模型

为了实现在工业化生产中对α钛富氧层厚度预测和控制,通过实验研究α钛富氧层在高温空气环境中的形成及增厚过程,讨论热处理温度和时间的影响作用,建立高温(750~850℃)空气环境下关于温度、时间的富氧层增厚动力学模型。结果表明:当恒温热处理温度为750~850℃时,α钛富氧层厚度x与保温时间t0.5呈正比例关系,且升高热处理温度可显著提高富氧层增厚速度。在此温度范围内,氧原子的扩散激活能约为203473 J/mol,计算曲线与实验数据吻合性较好。结合文献中已有的扩散系数方程和实验测得的富氧层厚度数据,推导得到5个富氧层增厚动力学方程,其中3个方程的计算曲线与实验数据吻合性较好,可为实际生产中预估富氧层厚度提供理论支持。     

KF-NaF-AlF3 System: Liquidus Temperature and Phase Transition

JOM - The development of low-temperature aluminum electrolysis makes it possible to reduce energy consumption and greenhouse gas emissions. The KF-NaF-AlF3-based electrolyte is a promising...     

The effect of the exposed crystal plane on the antioxidant activity of nanoceria

Previous reports have noted that exposed crystal planes could affect the antioxidant activity of nanocerias, although the synthesized nanocerias used in those studies had different exposed crystal planes, as well as different sizes and morphologies. In order to better understand the effect of the crystal planes on the antioxidant activity of the materials, two types of nanocerias with similar morphology and size distribution but different crystal planes were synthesized using the hydrothermal method (CeO₂–H) and the ultrasonic template method (CeO₂–U). The antioxidant activities of the nanocerias were further explored within different ·OH concentrations in the reaction system. The experimental results showed that there is an obvious difference in the antioxidant activity of the two types of nanocerias in the lower free radical concentration system due to the effects of exposed crystal planes. CeO₂–U, with more active crystal planes (100), had stronger antioxidant activity. However, with the increase in the ·OH concentration in the reaction system, the difference in the antioxidant activity of the two nanocerias decreased. This research will increase our understanding of the antioxidant activity of the exposed crystal planes on nanocerias.     

Highly dispersed MnO nanoparticles supported on N-doped rGO as an efficient oxygen reduction electrocatalyst via high-temperature pyrolysis

Transition metal-based compounds, due to their excellent ORR catalytic performance under alkaline condition, have recently emerged as one of the most promising alternatives to noble metal-based ORR catalysts. It is worth noting that manganese oxide can take an unique advantage for decomposition of intermediate adsorption products H₂O₂ and can effectively reduce O₂ to OH⁻. However, most research has focused on MnO₂, while attention has rarely been paid to MnO catalysts. In addition, under high-temperature pyrolysis condition, MnO is the most stable manganese oxide but MnO nanoparticles easily agglomerate. Hence, it is very difficult to obtain well-dispersed and small-sized MnO nanoparticles. Herein, on the basis of pre-synthesizing uniformly distributed manganese complexes on the reduced graphene oxide (rGO), we innovatively prepare highly dispersed and small-sized MnO nanoparticles (~3.94 nm) via high-temperature pyrolysis, which are uniformly anchored on N-doped reduced graphene oxide (NrGO) as an efficient oxygen reduction electrocatalyst. The as-obtained MnO/NrGO (1050 °C) electrocatalyst achieves satisfactory onset potential (0.942 V) and half-wave potential (0.820 V) under alkaline condition. And the limiting current density is 4.17 mA cm⁻², which is very close to that of Pt/C (20 wt%, JM). Meanwhile, MnO/NrGO (1050 °C) catalyst presents superior longstanding durability and methanol resistance than Pt/C (JM). This work indicates that high-temperature pyrolysis can improve the purity of manganese oxide, simultaneously the defects of NrGO can reduce particle size of MnO nanoparticles, which are greatly beneficial to improve ORR performance. This work provides a new idea for research of MnO catalysts for ORR in the future.     

Controllable electrodeposition synthesis of Pd/TMxOy-rGO/CFP composite electrode for highly efficient methanol electro-oxidation

A novel and high-efficiency Pd/TM_xO_y-rGO/CFP (TM_xO_y = Co₃O₄, Mn₃O₄, Ni(OH)₂) electrocatalyst for directly integrated membrane electrode was synthesized by controllable cyclic voltammetry electrodeposition combined with hydrothermal process. The results showed excellent performance towards methanol oxidation reduction. The Pd/Co₃O₄-rGO/CFP as-prepared catalyst has the best electrocatalytic activity, and mass activity is 5181 mA·mg⁻¹_Pd, which is about 40 times and 4.3 times that of the commercial Pd/C and Pt/C catalyst (JM). It can be attributed that the small size of Pd nanoparticle, uniformity of distribution, and the synergistic interaction between transition metal oxide on the support surface and Pd nanoparticles. The prepared Pd/TM_xO_y-rGO/CFP composite electrode is a promising catalyst for integrated membrane electrode assembly of proton exchange membrane fuel cells in the future.     

低碱度下高硫铅锌矿的无钙浮选分离工艺研究

为了解决高硫铅锌矿分离时石灰用量大的问题,结合工艺矿物学,对云南某高硫铅锌矿进行了选矿试验研究。试验结果表明,在低碱度的情况下(pH值=9)采用LY-2可以较好地抑制黄铁矿。闭路试验可获得铅精矿含铅61.13%,铅回收率88.40%,铅硫分离铅作业回收率91.75%,硫精矿含铅1.66%,含锌2.76%,铅回收率7.95%,锌回收率5.19%,实现了铅硫的高效分离,对该类矿山的开发提供新思路。     

某含锌锡多金属硫化矿石锌浮选试验研究

某含锌锡多金属硫化矿石Zn、Sn、Fe、S含量分别为6.04%、1.05%、29.33%、19.08%，锌主要以铁闪锌矿、闪锌矿的形式存在，锡主要以锡石的形式存在，铁主要以黄铁矿、磁黄铁矿等形式存在，其中的金属矿物共生关系密切，相互包裹现象普遍。为确保不影响后续选锡，对锌浮选流程进行了试验研究。结果表明：矿石在磨矿细度为-0.074 mm占80%的情况下，采用预先脱硫—锌硫混浮再分离流程处理，在选择硫酸铜为锌矿物活化剂、丁基黄药为捕收剂、松醇油为起泡剂、石灰为黄铁矿抑制剂的情况下，经1段脱硫、2粗1扫锌硫混浮、1粗2精锌硫分离，锌硫分离精选尾矿与锌硫混浮扫选精矿2次精选后锌硫分离，最终获得锌精矿Zn品位47.06%、回收率90.76%，试验指标良好。     

Effects of Sn doping on the manufacturing,performance and carbon deposition of Ni/ScSZ cells in solid oxide fuel cells

This work demonstrates the effect of tin (Sn) doping on the manufacturing, electrochemical performance, and carbon deposition in dry biogas-fuelled solid oxide fuel cells (SOFCs). Sn doping via blending in technique alters the rheology of tape casting slurry and increases the Ni/ScSZ anode porosity. In contrast to the undoped Ni/ScSZ cells, where open-circuit voltage (OCV) drops in biogas, Sn–Ni/ScSZ SOFC OCV increases by 3%. The maximum power densities in biogas are 0.116, 0.211, 0.263, and 0.314 W/cm² for undoped Ni/ScSZ, undoped Ni/ScSZ with 3 wt% pore former, Sn–Ni/ScSZ and Sn–NiScSZ with 1 wt% pore former, respectively. Sn–Ni/ScSZ reduces the effect of the drop in the maximum power densities by 26%–36% with the fuel switch. A 1.28–2.24-fold higher amount of carbon is detected on the Sn–Ni/ScSZ samples despite the better electrochemical performance, which may reflect an enhanced methane decomposition reaction.     

High pressure EIGA preparation and 3D printing capability of Ti—6Al—4V powder

Ti—6Al—4V alloy powder was processed by electrode induction melting gas atomization (EIGA) at high gas pressure (5.5–7.0 MPa). The effects of atomizing gas pressure on the powder characteristics and the microstructure, along with the mechanical properties of the as-fabricated block by laser melting deposition (LMD), were investigated. The results indicate that the diameters of powders are distributed in a wide range of sizes from 1 to 400 μm, and the median powder size (d₅₀) decreases with increasing gas pressure. The powders with a size fraction of 100–150 μm obtained at gas pressures of 6.0 and 6.5 MPa have better flowability. The oxygen content is consistent with the change trend of gas pressure within a low range of 0.06%–0.20%. Specimens fabricated by LMD are mainly composed of α+β grains with a fine lamellar Widmanstatten structures and have the ultimate tensile strength (UTS) and yield strength of approximately 1100 and 1000 MPa, respectively. Furthermore, the atomized powders have a favorable 3D printing capability, and the mechanical properties of Ti—6Al—4V alloys manufactured by LMD typically exceed those of their cast or wrought counterparts.     

铝空气电池废电解液生产超细氢氧化铝工艺条件研究

以铝空气电池的废电解液为原料, 采用种分法生产氢氧化铝。结果表明, 当种分时间为24 h、晶种系数为2%~4%时, 可生产出超细氢氧化铝, 且粒径分布宽度窄, 阻燃性能优良, 达到HG/T4530-2013氢氧化铝阻燃剂ATH-1一等品的要求。