镀锌层硅酸盐+虫胶复合转化膜的制备和表征

目的阻碍热镀锌板出现白锈,提高镀锌层的耐腐蚀性能。方法采用正交试验法优化出添加虫胶水溶液的有机无机复合钝化液。通过电化学Tafel极化曲线、交流阻抗(EIS)、乙酸铅点滴和中性盐雾试验,对比分析基体、硅酸盐+虫胶复合钝化膜与铬酸盐钝化膜的耐腐蚀性能。采用摩擦法测试对比分析基体和无铬钝化膜试样的附着性能,并通过扫描电子显微镜、X射线光电子能谱和红外光谱对形貌和结构进行分析。结果添加虫胶水溶液的复合钝化膜表面平整致密,72 h中性盐雾试验后的腐蚀面积小于10%。乙酸铅点滴试验和电化学测试显示,复合钝化膜的耐腐蚀性能较基体好。附着力试验测试显示,复合钝化膜具有良好的附着能力。结论因为复合钝化液中的虫胶与硅酸盐交织为O—Si—CH_2结构,与金属离子结合生成致密的膜层附着在镀锌层表面,使得复合钝化膜致密平整,且使腐蚀过程得到了强烈的抑制。     

核燃料用γ-U合金的成分规律

铀合金作为一种重要核燃料,其体心立方结构的高温稳定的γ-U合金具有较好的综合性能,是合金设计所追求的目标。本文引入描述稳定固溶体结构的"团簇加连接原子"模型,用于建立γ-U固溶体合金的结构模型和相应成分式,指出其结构单元为体心立方第一近邻配位多面体团簇加3个连接原子构成。进而利用该结构单元对现有合金成分进行了解析,能够稳定形成体心立方bcc结构的合金均满足上述模型,如[Mo-U14]Mo3(U-10.7Mo),[Zr-U14]Nb3(U-7.5Nb-2.5Zr,即不锈铀)等,这些合金实际上均在各自体系中具有最优良的结构稳定性,显示出优异的耐蚀性。本文证实,基于团簇加连接原子模型的成分设计方法在预测γ-U合金成分与性能上具有重要指导价值。     

NiCrAlFe精密电阻合金中的L12有序结构研究

有序结构的形成是决定NiCrAlFe精密电阻合金电学性能的关键因素。本文利用第一性原理赝势平面波方法，计算了合金处于无序固溶体结构和形成L12型有序结构时的结合能、态密度、晶格常数等参数，并利用高分辨透射电子显微镜（HRTEM）对合金进行了结构表征，还测试了固溶态和时效态的电阻率。从结合能来看，该合金形成L12有序结构时比无序固溶体更加稳定；态密度以及部分态密度计算结果则表明，在L12有序结构中，Ni、Cr、Al、Fe会强烈成键而使得整个合金体系变得稳定；HRTEM分析结果证明固溶态合金经过和时效处理后出现了L12有序结构，而且该有序结构的晶格常数与计算值基本一致。对比无序固溶体与L12型有序结构费米能级处的态密度值发现，当形成L12有序结构时合金的导电能力较无序固溶体下降，电阻率升高，与实际测试结果吻合。     

Microstructure and mechanical properties of squeeze-cast Al−5.0Mg−3.0Zn−1.0Cu alloys in solution-treated and aged conditions

The microstructure and mechanical properties at different depths of squeeze-cast, solution-treated and aged Al−5.0Mg−3.0Zn−1.0Cu alloy were investigated. For squeeze-cast alloy, from casting surface to interior, the grain size of α(Al) matrix and width of T-Mg₃₂(AlZnCu)₄₉ phase increase significantly, while the volume fraction of T phase decreases. The related mechanical properties including ultimate tensile strength (UTS) and elongation decrease from 243.7 MPa and 2.3% to 217.9 MPa and 1.4%, respectively. After solution treatment at 470 °C for 36 h, T phase is dissolved into matrix, and the grain size increases so that the UTS and elongation from surface to interior are respectively reduced from 387.8 MPa and 18.6% to 348.9 MPa and 13.9%. After further peak-aging at 120 °C for 24 h, numerous G.P. II zone and η′ phase precipitate in matrix. Consequently, UTS values of the surface and interior increase to 449.5 and 421.4 MPa, while elongation values decrease to 12.5% and 8.1%, respectively.     

Ordinary Portland Cement composition for the optimization of the synergies of supplementary cementitious materials of ternary binders in hydration processes

The synergistic effects of using several supplementary cementitious materials (SCMs), such as Blast Furnace Slags plus Limestone Filler or Fly Ashes, depend on the OPC composition. When using an OPC which is poor in C₃A and alkalis in ternary formulations, a similar initial strength gain to that of a plain OPC is detected and at longer hydration ages, the formation of monocarboaluminate, hemicarbonate and hydrotalcite instead of monosulphate can be seen. If an OPC with a higher C₃A content and alkalis is used with SCMs, the higher availability of Al causes the early formation of monocarboaluminate and a lower initial strength gain. At longer hydration times, in ternary blends with both OPCs, the mechanical strengths are higher and the C-S-H gels formed are richer in Al and poorer in C/S ratio with a subsequent lowering of the alkali content in the pore solution when compared to that in plain OPC.     

Hydrogen sorption properties of V85Ni15

An alloy with nominal composition V₈₅Ni₁₅ was prepared in a vacuum induction melting apparatus. The chemical analysis of the sample showed a V (Ni) content of 82.63 (15.68) at% and small contaminations by carbon and aluminum. XRD measurements confirmed that the bcc Ni-V solid solution phase is the main constituent of the sample. However, a minor impurity (approximately 6.5 wt%) due to the precipitation of the sigma NiV_3-x phase is present in the sample.Hydrogen sorption measurements extending from 150 °C up to 400 °C in a wide pressure range (up to 90 bar) were performed. Upon hydrogenation below 250 °C, one observes the subsequent presence of an α phase and of two hydride phases with different values of dehydrogenation enthalpy: ΔH_dehydr = 21 ± 1 kJ/mol for 0.15 ≤ H/M ≤ 0.30 and ΔH_dehydr = 26 ± 2 kJ/mol for 0.53 ≤ H/M ≤ 0.59. Above 300 °C, there is no evidence of the formation of hydrides and only an α phase is present up to the maximum measured composition, with a hydrogenation enthalpy ΔH_hydr = 10.0 ± 0.5 kJ/mol.     

多次真空固溶处理对GH1131高温合金组织和力学性能的影响

利用真空高压气淬工艺研究了GH1131高温合金经1100~1170 ℃范围内多次真空固溶处理后的组织和力学性能。结果表明,固溶态组织包含奥氏体晶粒和颗粒状碳化物,且随着固溶温度的升高,晶粒度稍有增大趋势。GH1131高温合金经多次真空固溶处理后组织均匀,常温与高温力学性能稳定,经1100 ℃+1130 ℃+1170 ℃三次真空固溶处理后,晶粒度维持了6~8级,900 ℃高温抗拉强度达到200 MPa。