Insight into selective oxidation of dual-phase steel after annealing in pure H2 atmosphere at different heating rates and temperatures

In this paper, the oxidation behaviors of DP980 advanced high strength steel (AHSS) are studied during annealing in a hydrogen atmosphere with different temperatures and heating rates. It is revealed that with the increase in holding time, the different heating rates affecting the surface oxide precipitation on the strip surface will be weakened. Mass transfer of Mn in heating, soaking, and cooling stages has been considered to illustrate the effect of heating rate on the oxide morphology of steel. And then, the Wagner model and aluminothermic reaction kinetics were performed to discuss the transition from external to internal and maximum reduction diameter of MnO oxidation.     

7055铝合金挤压材黑线缺陷分析

利用高倍组织观察,结合能谱分析,对7055铝合金挤压材阳极氧化后的“黑线”缺陷进行了分析。结果表明:“黑线”区域为AlZr聚集导致。通过严格控制原料质量,改善AlZr中间合金组织;在合金成分范围内,适当降低Zr元素的含量;熔炼过程中适当提高加热温度及时间,使Al₃Zr粒子熔解等手段,可消除“黑线”缺陷。     

综放工作面风量及采空区漏风定量检测

通过对中煤塔山煤矿30509综放工作面采空区漏风及有害气体分析的研究，总结了通过定量连续释放SF₆示踪气体，来检测工作面风量与采空区漏风的方法，测定了沿工作面采空区的漏风分布及漏风流线的深度。采用定时测量法，确定了30509工作面随工作面不断推进，与对应地表发生了导通现象；采用定量测量法，确定了内部漏风量和外部漏风量较大，对综采工作面采空区自然发火存在较大风险，同时提出了防范措施，为减少综放工作面采空区漏风、防止自然发火的发生提供了参考。     

高铁酸盐-亚硫酸盐体系氧化降解水中污染物阿特拉津

针对目前日益严峻的农药污染问题，本文以阿特拉津（ATZ）为目标污染物，利用高铁酸盐活化亚硫酸盐的方式对其进行降解。探究了亚硫酸盐浓度、高铁酸盐浓度、ATZ浓度、pH以及亚硫酸盐投加方式对ATZ去除率的影响。研究结果表明，在pH为7、高铁酸盐浓度为100μmol/L、亚硫酸盐浓度为400μmol/L、ATZ的浓度为5μmol/L的条件下，10s时间内可以去除95%的ATZ。利用自由基淬灭实验对体系中的活性物质进行鉴定，结果表明，高铁酸盐-亚硫酸盐体系中起主要作用的是硫酸根自由基（SO{}_{\mathrm{4}}^{·-}），其对ATZ降解的贡献约占53%；其次是羟基自由基（·OH），约占36%。通过改变亚硫酸盐投加方式，减少了SO{}_{\mathrm{4}}^{·-}的自我消耗，提高了高铁酸盐-亚硫酸盐降解ATZ的效率。这些实验结果有助于高铁酸盐-亚硫酸盐体系的实际水处理应用。     

超声振动光整的EDEM数值模拟与实验研究

采用EDEM离散元分析软件对普通钝化光整实验及带有超声振动辅助光整实验进行数值模拟，仿真结果为超声振动光整加工系统的提出提供了依据。使用超声振动光整设备对平头铣刀进行钝化实验，进行了不同钝化条件下的实验研究。通过扫描电镜观察了钝化前后铣刀的表面形貌及钝圆半径的变化，分析了超声振动光整对钝化效率及效果的影响。实验结果表明，增加了超声振动钝化后的钝化效率提高了约26%，表面形貌得到较大改善。     

Fabrication of in-situ self-reinforced Si3N4 ceramic foams for high-temperature thermal insulation by protein foaming method

To meet demand for lightweight and high-strength ceramic foams, in-situ self-reinforced Si₃N₄ ceramic foams, with compressive strength of 13.2–45.9 MPa, were fabricated by protein foaming method combined with sintered reaction-bonded method. For comparison, ordinary protein foamed ceramics with irregular block microstructure were fabricated via reaction-bonded method, which had compressive strength of 3.6–20.5 MPa. Physical properties of these two types of samples were systematically compared. When open porosity was about 80%, both types of Si₃N₄ ceramic foams had excellent thermal insulation properties (<0.15 W m^?1 K^?1), while compressive strength of in-situ self-reinforced samples increased by more than 158% compared with ordinary samples. Under high-temperature oxidation conditions, microstructures of both types of samples were deformed with increase in oxidation temperature. Moreover, after oxidation temperature was increased to 1400 °C, oxidation weight gain decreased from 18.07% for ordinary samples to only 2.18% for self-reinforced samples. Thus, high-temperature oxidation resistance of Si₃N₄ ceramic foams was greatly improved.     

纳米级超声造影剂的理论研究进展

为了克服超声造影剂中微米级气泡尺寸较大的局限性,大量研究人员对超声应用的替代造影剂(纳米级造影剂)进行了研究。随着生物纳米技术的飞速发展,纳米级超声造影剂在诊断与治疗领域有着广阔的发展前景。与超声造影剂中的微米级气泡相比,纳米级造影剂粒径较小,渗透能力极强,可以通过血管内皮间隙,进而可以实现血管外病变部位的显影。文中详细论述了超声造影剂在超声作用下的行为以及2种主要的纳米级造影剂:纳米气泡和纳米液滴造影剂,对其理论研究进展进行了总结,并提出了目前仍存在的一些问题及其未来的研究方向。     

Mesoporous SmMnO3/CuMnOx catalyst for photothermal synergistic degradation of gaseous toluene

Mesoporous SmMnO₃/CuMnO_x catalyst was prepared by a two-step method using flaky CuMnO_x with high specific surface and excellent catalytic ability as the carrier, which was further applied to photothermal synergistic degradation of gaseous toluene. Quantitative analysis of O₂-TPD and H₂-TPR showed that SmMnO₃/CuMnO_x exhibited abundant of the surface oxygen species and oxygen vacancies content, which enabled it to convert free oxygen to lattice oxygen more quickly during the reaction, and thus improving the reaction process. I-t and photoluminescence experiments demonstrated the improvement of photogenerated electron and hole separation ability of SmMnO₃/CuMnO_x catalyst. UV–Vis analysis manifested the full spectral range of absorption. XPS analysis verified the unequal positions of valence band of the two materials, which can facilitate the separation of photogenerated electrons from holes and improve the ability of better electron transfer. SmMnO₃/CuMnO_x catalyst has higher adsorbed oxygen content and light absorption capacity, which is beneficial to the catalytic oxidation. In situ DRIFTs proved that the oxidation reaction on the catalyst followed the Mars-van Krevelen redox cycle. The VOCs test found that SmMnO₃/CuMnOx composite catalyst is with lower onset reaction temperature (T₉₀ = 190 °C, T₉₀, corresponding to 90% conversion) and good mineralization (100% at 275 °C).     

Nonwoven Ni–NiO/carbon fibers for electrochemical water oxidation

The development of technologically efficient anodes for water oxidation is crucial to improve hydrogen production via water splitting. Electrodes based on metallic active sites dispersed in carbon matrices have been shown to be an attractive way to attain this goal. However, challenges remain to prevent catalyst agglomeration that otherwise can result in a decrease of performance over time.In this work, we report an alternative and efficient method to produce nickel-nickel oxide nanoparticles-embedded in carbon nanofibers (Ni–NiO/C), by the solution blow spinning (SBS) process. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses show the carbon nanofibrillar matrix as a robust support, with well-dispersed nickel nanoparticles on the surface. The responses of the linear scanning voltammetry, cyclic voltammetry and electrochemical impedance spectroscopy demonstrate how a small fraction of nickel on the fiber surface (≈1.2–5.3%) is enough to promote substantial improvement in performance (η = 278 and 309 mV vs RHE for 10 mA cm^?2) and a significant turnover frequency (TOF) values of 1.38 (η = 278) and 1.30 s^?1 (η = 309). These promising results are correlated with a large amount of Ni³⁺ present on the fiber surfaces, as identified by X-ray Photoelectron Spectroscopy (XPS). This work provides a low-cost and rapid preparation technique that can be extended for the manufacture of a wide variety of electrodes based on metals supported on carbon nanofibers.