含La2O3奥氏体不锈钢堆焊合金层晶粒细化机制及对其耐腐蚀、磨损性能的影响

目的 通过在超低碳Cr19Ni10不锈钢堆焊合金中加入稀土氧化物La2O3，细化其微观组织，获得力学性能、耐腐蚀性能和耐磨性能等综合性能优良的堆焊合金层。方法 采用添加La2O3的超低碳Cr19Ni10不锈钢焊条制备了四种不锈钢堆焊合金。采用X射线荧光光谱、红外碳硫分析仪和X射线衍射分析仪，对堆焊合金层的元素组成和相组成进行了测定。采用金相显微镜和晶粒度统计软件，对堆焊合金层的微观组织形貌进行观察，并对晶粒度进行了统计分析。采用显微维氏硬度计和纳米压痕仪对堆焊合金层的硬度和杨氏模量进行了测定。采用电化学工作站和CSM摩擦磨损试验机对堆焊合金层的耐腐蚀性能和耐磨性能进行了评价，并且采用白光共聚焦显微镜对磨损后的磨痕形貌和尺寸进行了观察和测定。采用二维晶格错配度理论，对La2O3/γ-Fe界面间的晶格错配关系进行了计算。结果 在堆焊合金层中加入La2O3，随着La2O3加入量的增加，堆焊合金层奥氏体晶粒细化越明显。当La2O3的添加量由0%增加至1.5%时，奥氏体晶粒平均面积由400 μm²减少为210 μm²。堆焊合金层加入La2O3，可以明显提高其力学性能、耐腐蚀性能和耐磨损性能。当La2O3的添加量由0%增加至1.0%时，堆焊合金层的微观硬度由180HV增加到225HV，宏观硬度由125HBS增加到150HBS，杨氏模量由186 GPa左右增加到217 GPa，腐蚀电位由?0.4 V增加到?0.25 V，磨痕深度由50 μm减小到10 μm。La2O3(001)面和γ-Fe(110)面的二维晶格错配度为8.7%(<12%)，说明La2O3可以作为γ-Fe的中等有效异质形核基底，从而细化了堆焊合金层中的奥氏体晶粒。结论 La2O3可以有效地细化奥氏体晶粒，改善堆焊合金层的力学性能，提高其耐腐蚀和耐磨损性能。但是，La2O3加入量存在一个最佳值，当La2O3的加入量为1.0%时，堆焊合金层的综合性能最好。     

基于密闭爆发器试验的发射装药内弹道性能预估

为了预估发射装药的内弹道性能,建立了一种基于密闭爆发器试验检测发射药的静态燃烧性能参数进而预测其装药内弹道性能的方法,采用不同批次的单樟-5/7发射药进行了装药性能预估计算,并基于30 mm火炮对内弹道性能预估精度进行了试验验证。结果表明,采用所建立的基于密闭爆发器试验的发射装药内弹道性能预估方法计算获得的最大膛压为376.0 MPa,与试验测试的膛压平均值388.7 MPa的计算误差为3.27%;计算的炮口初速为1143.5 m/s,与试验测试的炮口初速平均值1156.3 m/s的计算误差为1.11%。所建立的基于密闭爆发器试验的发射装药内弹道性能预估方法具有较高的精度,可对发射药样品不同批次间的内弹道性能进行高效精确的预估,为长期贮存发射药使用寿命的判定及发射药产品的出厂校验提供了一种高效低成本的弹道性能评价方法。     

Crystal structure,phase compositions,and microwave dielectric properties of malayaite-type Ca1−xSrxSnSiO5 ceramics

Low-permittivity Ca_1−xSr_xSnSiO₅ (0 ≤ x ≤ 0.45) microwave dielectric ceramics were prepared via traditional state-reaction at 1400°C-1450°C for 5 hours. Moreover the microwave dielectric properties of SnO₂ ceramic were obtained for the first time. SnO₂ ceramic was difficult to densify, and SnO₂ ceramic (ρ_rel = 65.1%) that was sintered at 1525°C exhibited the optimal microwave dielectric properties of ε_r = 5.27, Q × f = 89 300 GHz (at 14.5 GHz), and τ_f = −26.7 ppm/°C. For Ca_1−xSr_xSnSiO₅ (0 ≤ x ≤ 0.15) ceramics, Sr²⁺ could be dissolved in the Ca²⁺ site of Ca_1−xSr_xSnSiO₅ to form a single phase, and the partial substitution of Ca²⁺ by Sr²⁺ could improve the microwave dielectric properties of CaSnSiO₅ ceramic. Secondary phases (SnO₂ and SrSiO₃) appeared at 0.2 ≤ x ≤ 0.45 and could adjust the abnormally positive τ_f value of CaSnSiO₅ ceramic. The highest Q × f value (60 100 GHz at 10.4 GHz) and optimal microwave dielectric properties (ε_r = 9.42, Q × f = 47 500 GHz at 12.4 GHz, and τ_f = −1.2 ppm/°C) of Ca_1−xSr_xSnSiO₅ ceramics were obtained at x = 0.05 and 0.45, respectively.     

Hydrogen promotion by Co/SiO2@HZSM-5 core-shell catalyst for syngas from plastic waste gasification: The combination of functional materials

In the present work, a core-shell structured Co/SiO₂@HZSM-5 catalyst was prepared for hydrogen production from syngas of plastic waste gasification. The cobalt catalyst was coated with HZSM-5 shell through a hydrothermal process, and the Co/SiO₂@HZSM-5, with different loadings of HZSM-5 (e.g., 10–30 wt %) exhibited excellent activity and durability for dehydrogenation reactions. The amount of HZSM-5 was found to be an important factor for hydrogen production. Temperature-programmed reduction with H₂ and temperature-programmed desorption of ammonia was applied to determine the active site and the acidity of prepared catalyst, respectively. The prepared Co/SiO₂@HZSM-5 was tested through reforming of plastic gasification syngas and shown superior hydrogen production ability (∼90%) and stability (over 15 h). The effects of reduction-oxidation behavior on the catalytic performance were also discussed.     

Insights into the long-term stability of the magnesia modified H-ZSM-5 as an efficient solid acid for steam reforming of dimethyl ether

The long-term performance of the bifunctional catalyst composed of MgO-modified H-ZSM-5 and Cu/ZnO/Al₂O₃ for steam reforming of dimethyl ether (SRD) is studied under the same conditions. Although the surface chemical state and acid property of 1.55–2.47 wt% MgO modified H-ZSM-5 are almost the same, a significant impact of MgO contents on the stability of the bifunctional catalyst is observed from the 50 h SRD results. The initial dimethyl ether conversion (around 100%) and H₂ yield (∼95%) over the optimal bifunctional catalyst with 2.17 wt% MgO modified H-ZSM-5 is still kept over 90% at 50 h. Combining the characterization data of spent catalysts and SRD results, the synergetic effect between the MgO-modified H-ZSM-5 and Cu/ZnO/Al₂O₃ is rigorously revealed as the key factor in determining the stability of the bifunctional catalyst for SRD. These results demonstrate that MgO-modified H-ZSM-5 is a promising and efficient solid acid for SRD.     

多运营商高铁隧道移动网络覆盖方案

高铁移动网络覆盖是国内三大通信运营商的一个重点,而高铁隧道内移动网络覆盖更是运营商的一大难点痛点。文章根据我国中部省份某高铁线路覆盖规划实例,采用“设备+POI+泄漏电缆”模式,即三家运营商信号源设备通过同一POI(point of interface,多系统接入平台)接入,信号输出到泄漏电缆进行隧道覆盖,隧道口场坪站安装宽频切换天线对隧道外进行延伸覆盖,通过链路预算合理布置各运营商主设备信号源,从而实现隧道到室外的无缝覆盖。最后,根据已有成熟网络覆盖解决方案,对未来5G高铁隧道移动网络覆盖方案进行了探讨。     

溶解氧变化对阴极极化下10Ni5CrMo钢氢脆敏感性的影响

摘要：为研究溶解氧质量浓度对10Ni5CrMo钢在阴极极化条件下氢脆敏感性影响规律，对10Ni5CrMo钢进行了阴极极化下的电化学交流阻抗谱测试﹑并采用慢应变速率拉伸实验和断口分析方法研究了海水中溶解氧质量浓度变化和不同阴极极化下10Ni5CrMo钢的氢脆敏感性。结果表明：溶解氧质量浓度变化对10Ni5CrMo钢强度几乎没有影响；同一溶解氧质量浓度下，随极化电位负移，断裂时间、伸长率、断面收缩率明显降低，氢脆系数增加，氢脆敏感性显著提高，极化电位达到-1000mV时，氢脆系数已超过安全区允许的最高值25%，进入危险区；同一极化电位下，随着海水中溶解氧质量浓度减少，材料塑性变差，断裂时间、伸长率和断面收缩率不断降低，氢脆系数增加，氢脆敏感性提高。     

煤矿5G分布式MIMO组网技术研究（增刊）

根据煤矿井下的安全防爆要求，天线的射频发射功率受到严格限制，导致煤矿5G的基站部署密度显著高于地面场景。为了解决由此引发的交叉覆盖问题，本文提出了煤矿5G分布式MIMO组网技术，利用分布在不同位置的天线实现对用户数据的联合并行发送，不仅避免了由交叉覆盖导致的乒乓切换等负面效应，还提升了边缘区域的信号覆盖效果。在乌兰木伦煤矿的300米采煤工作面内，利用分布式MIMO组网技术实现了5G信号的无边界覆盖，上行速率不低于500Mbps，保障了煤机数据的实时有效传输。     

Influence of T5 heat treatment on the microstructure and lubricated wear behavior of ternary ZnAl40Cu2 and quaternary ZnAl40Cu2Si2.5 alloys

A ternary ZnAl40Cu2 and a quaternary ZnAl40Cu2Si2.5 alloys were produced by permanent mold casting and subjected to T5 heat treatment at a temperature of 150 °C for 24 hours. The structural, mechanical and lubricated wear properties of these alloys were investigated in the as-cast and heat-treated conditions and the results were compared with those of SAE 65 (CuSn12) plain bearing bronze. Microstructure of the ternary alloy consisted of aluminum-rich α, eutectoid conversion product of α+η and ϵ phase located in the interdendritic channels. In addition to these phases, silicon particles were observed in the microstructure of the quaternary alloy. T5 heat treatment caused a considerable amount of reduction in the hardness, tensile strength and wear resistance of ZnAl40-based ternary and quaternary alloys, but improved their ductility and stability. These alloys in the as-cast and heat-treated conditions exhibited lower wear volume or higher wear resistance than SAE 65 bearing bronze. Among the experimental alloys, the optimum mechanical properties and wear performance were obtained from ZnAl40Cu2Si2.5 alloy in both as-cast and heat-treated conditions. Adhesion appeared to be the main wear mechanism for the ZnAl40-based alloys, but abrasion dominated the wear of SAE 65 bronze.