The oxidation of two ternary Ni-Cu-10 at.% Al alloys in 1 atm of pure O2 at 800-900 °C

The oxidation of the ternary alloys Ni-45Cu-10Al and Ni-30Cu-10Al has been studied at 800-900 °C under 1 atm O₂. The presence of 10 at.% Al reduces significantly the oxidation rate of the corresponding Cu-Ni alloys during the initial oxidation stages, even before the establishment of a complete Al₂O₃ layer. The weight of individual sample of the two ternary Ni-Cu-10Al alloys at 800 °C increases more rapidly than at 900 °C during the initial oxidation stage. As oxidation proceeds, the weight gain at 800 °C slows down to a degree that the total weight gain after 24 h oxidation at 800 °C is less than that at 900 °C. Due to a faster formation of the Al₂O₃ layer, which suppresses earlier the further oxidation of Cu and Ni, the external region of the scales grown on Ni-45Cu-10Al contain much less Cu and Ni oxides than those grown on Ni-30Cu-10Al. The transition from the internal oxidation to the selective external oxidation of the most reactive component Al in Ni-Cu-Al alloys is favored by higher values of the Al content, of temperature and of the Cu/Ni ratio.     

Cr_2O_3对矾土－尖晶石耐火材料抗渣性的影响

以高铝矾土及预合成电熔ＭＡ砂为原料，制各了矾土－尖晶石耐火材料。对其加入铬精矿后的抗渣性进行了试验。结果表明，少量铬精矿的加入能形成尖晶石固溶体，提高制品的抗渣性能。     

Cast bulk ZrTiAlCuNi amorphous alloys

Cylindrical bulk amorphous samples with diameters up to 10 mm have been prepared by casting ZrTiAlCuNi alloys in a copper mould. In order to rank glass-forming ability as a function of alloy composition, alloys were also cast into wedge-shaped moulds; to a first approximation, the thickness of the amorphous region obtained can be taken as an indication of glass-forming ability. The compositions which lead to the production of bulk glasses all have reduced glass transition temperatures in excess of 0.65 and the extremely high glass-forming ability of these compositions is discussed. We suggest that both the Al and Ti contents are determining factors for the production of bulk amorphous samples and these are believed to reduce the driving force for, and hence the rate of, crystallisation. These amorphous alloys have been found to display high thermal stability and can be annealed for several minutes in the supercooled liquid region. They are ductile at room temperature and have a high value of yield stress.     

中高频小功率电子元器件用非晶材料的开发与应用

随着电力和电子技术的飞速发展，相应的元器件向高频化，小型化，高效率和节能的方向发展，从而对元器件用材料也提出了更高要求。为此，本文概述了冶金部钢铁研究总院近年来所研究的用于开关电源，脉冲变压器，传感器，电流互感器和电感器等方面的非晶软磁合金的性能及其应用概况。     

人工神经网络在单晶合金设计中的应用

把一种新发展的功能极强的信息处理技术－计算机人工神经网络技术用于单晶合金的高温持久性能预测并和其它方法进行比较，结果表明：这种方法精度最高。     

共混合金力学性能的研究 Ⅲ.CPP对PVC共混体系力学性能的影响

将ＰＰ氯化后作为ＰＶＣ共混体系的刚性体分散相，旨在改善高分子合金的相容性，ＤＳＣ实验表明，ＣＰＰ（氯化聚丙烯）与ＰＶＣ的相容性比ＰＶＣ与ＰＰ的好。在用弹性体增韧的ＰＶＣ／ＣＰＥ和ＰＶＣ／ＡＢＳ共混体系中加入刚性体ＣＰＰ后，随着ＣＰＥ、ＡＢＳ用量的增加，共混合金的冲击强度增加，并且由刚性的ＣＰＰ的加入所产生的冲击强度最大值的幅度也有所提高，其趋势是ＣＰＥ、ＡＢＳ用量越多，共混合金冲击强度值达到最大值时所需ＣＰＰ的量越多，增加的幅度也越大。ＣＰＰ对共混合金的拉伸屈服强度和断裂伸长率的影响比较小。     

Comparison of supports for the direct synthesis of hydrogen peroxide from H2 and O2 using Au–Pd catalysts

The direct synthesis of hydrogen peroxide from H₂ and O₂ using a range of supported Au–Pd alloy catalysts is compared for different supports using conditions previously identified as being optimal for hydrogen peroxide synthesis, i.e. low temperature (2 °C) using a water–methanol solvent mixture and short reaction time. Five supports are compared and contrasted, namely Al₂O₃, -Fe₂O₃, TiO₂, SiO₂ and carbon. For all catalysts the addition of Pd to the Au only catalyst increases the rate of hydrogen peroxide synthesis as well as the concentration of hydrogen peroxide formed. Of the materials evaluated, the carbon-supported Au–Pd alloy catalysts give the highest reactivity. The results show that the support can have an important influence on the synthesis of hydrogen peroxide from the direct reaction. The effect of the methanol–water solvent is studied in detail for the 2.5 wt% Au–2.5 wt% Pd/TiO₂ catalyst and the ratio of methanol to water is found to have a major effect on the rate of hydrogen peroxide synthesis. The optimum mixture for this solvent system is 80 vol.% methanol with 20 vol.% water. However, the use of water alone is still effective albeit at a decreased rate. The effect of catalyst mass was therefore also investigated for the water and water–methanol solvents and the observed effect on the hydrogen peroxide productivity using water as a solvent is not considered to be due to mass transfer limitations. These results are of importance with respect to the industrial application of these Au–Pd catalysts.     

镇沅金精矿选择性固砷焙烧—氰化浸出新工艺研究

对云南镇沅金矿的难当金精矿进行了选择性固砷焙烧－氰化浸出的试验研究，取得了满意结果。砷固定率大于９２％，硫挥发率为７８％－８４％，金浸出率可达９１％－９３％。选择性固砷焙烧－氰化浸出新工艺可有效消除砷害，综合利用有价成分硫，特别适宜于含砷高硫，同时含碳等杂质的细粒浸染型难浸金矿石的处理，在我国有较大的发展前景。     

高碳铬铁电炉高基质干式打结料的研究

通过对组成打结料成分特性的研究，提出以优质原料生产的MgO-CaO-Fe2O3系合成砂为骨料，用MgO〉97％，粒度〈0．088mm烧结镁砂做细粉，适当添加超微粉等工艺措施，制成适当高碳铬铁电炉炉底用的高基质打结料，通过调控基质成分，实现材料相和固相的复合烧结。     

Strengths and ductility of Mo–TiC alloys after secondary recrystallization

A series of Mo–TiC alloys were heated in vacuum at 2473 K for 36 ks. First grain growth behavior was observed using a scanning electron microscope. Then effects of TiC addition on the strengths and ductility at low temperature were discussed from the viewpoints of chemical composition and grain structure.

Materials with TiC additions of not larger than 0.1% demonstrated a single-crystalline grain structure. Both yield and maximum strengths increased by TiC addition and consequently ductility was improved.