La3+ 掺杂对 CeO2 红外发射性能的影响研究

随着飞行器飞行速度和发动机燃烧室温度的提高, 金属类隐身涂层材料已无法满足环境使用要求。 CeO2 具有较高熔点、 抗氧化、 较低红外发射率等特点, 被认为是红外隐身应用的候选材料, 但其发射率仍无法满足 高温红外隐身需求。 本文通过固相反应法对 CeO2 进行 La3+ 掺杂改性, 研究掺杂量对 CeO2 粉体红外发射性能的 影响规律。 结果表明, 随着掺杂量从 10 mol% 增加到 30 mol%, 粉体在 3~6 μm 波段的发射率不断降低, 其中 Ce0.7La0.3O2 的红外发射率仅为 0.1。     

An electrochemical method for the preparation of Mg–Li alloys at low temperature molten salt system

Mg–Li alloys have been prepared by electrolysis in a molten salt electrolyte of 50% LiCl–50% KCl (mass%) at low temperature of 420–510 °C. The effects of electrolytic temperature and cathodic current density on alloy formation rate and current efficiency were studied. For the deposition of metallic lithium on the cathode consisting of solid Mg and liquid Mg–Li, both electrolytic temperature and cathodic current density have no obvious influence on current efficiency; while for the deposition of metallic lithium on the solid magnesium cathode, both electrolytic temperature and cathodic current density greatly affect alloy formation rate and current efficiency. The optimum electrolysis condition is—molten salt mixture, LiCl:KCl = 1:1 (mass%), electrolytic temperature: 480 °C, cathode current density: 1.13 A cm⁻². Mg–Li alloys with low lithium content (about 25 wt% Li) were prepared via electrolysis at low temperature following by thermal treatment at higher temperature.     

纺机织轴边盘的金属型低压铸造

介绍了采用金属型低压铸造生产边盘所涉及的设备、模具、工艺 ,并对产品质量和经济效益进行了分析     

锰对低铬白口铸铁组织及硬度的影响

系统研究了Ｍｎ对水平连铸低铬白口铸铁铸态及正火态组织和硬度的影响。结果表明，Ｍｎ＞２．０％之后对组织有较大影响，由于出现（Ｍ＋Ａ）组成物，使基体硬度显著提高，这将大大改善了低铬白口铸铁中碳化物与基体硬度的相对关系。试验证实，Ｍｎ＞３％之后明显改善硬度分布均匀性。还讨论了使低铬锰白口铸铁具有最佳综合性能的合理含Ｍｎ量范围     

The effects of water pollution on the immersion corrosion of mild and low alloy steels

The short-term immersion corrosion of mild and low alloy steels in seawaters is known to be proportional to the concentration of dissolved oxygen (DO) in the bulk water. Longer-term corrosion is a function of the activity of sulphate-reducing bacteria and is influenced by the concentration of nutrients in the bulk water. These influences are examined in more detail for the corrosion of steels in the brackish waters of the River Thames and for several immersion corrosion sites on the Eastern Australian seaboard and in the North Sea. The published data sources were supplemented with plausible assumptions about environmental conditions. New interpretations of the data are provided based on the previously published model for immersion corrosion. For waters with negligible salinity and sulphate levels early corrosion loss was shown to depend on the dissolved oxygen content of the waters, and later corrosion loss was a direct function of nitrogenous nutrient (pollution) levels. This also applies to longer-term corrosion.     

Environmental effects on the stress corrosion cracking susceptibility of 3.5NiCrMoV steels in high temperature water

Constant elongation rate tests (CERTs) were carried out to investigate the effects of environmental factors of dissolved oxygen and temperature on the stress corrosion cracking (SCC) susceptibility of 3.5NiCrMoV turbine steels. Tests were conducted in pure water of various dissolved oxygen concentrations at temperatures of 50 °C-200 °C in the range of strain rates from 5 × 10⁻⁸/s to 1 ×  10⁻⁶/s. Dissolved oxygen significantly affected the SCC susceptibility of turbine steels in water. The SCC susceptibility of the turbine steels increases as the dissolved oxygen concentration in water increases. The elongation of the turbine steels tested in aerated water at 150 °C at a strain rate of 1 × 10⁻⁷/s decreased to half of that of the steels tested in deaerated water in the same test condition. And the SCC susceptibility of the steels increased with decreasing strain rate, and with increasing temperature. The increase of the SCC susceptibility of the turbine steels in the higher dissolved oxygen environment is considered to be due to the higher content of dissolved oxygen enhancing the reduction reactions of oxygen on the metal surfaces (cathode) and accelerating the dissolution rate at the crack tips (anode) by galvanic attack of an aeration cell.     

模糊控制在半固态浆料制备装置中的应用

介绍了低转速输送管半固态浆料制备装置的原理和组成，采用模糊控制技术改进了该装置的温度控制系统，并详细介绍了该控制系统的总体设计及软硬件方案。试验证明，模糊控制技术的应用提高了该装置的温度控制效果，实现了良好稳定的铝金属半固态浆料微观组织控制作用。     

低温熔体获得方式对熔体温度处理效果的影响

利用熔体温度处理工艺研究了A3 5 6铝合金低温熔体的不同获得方式对其凝固组织的影响 ,用直接炉内保温和机械搅拌 2种方式改变低温熔体的结构 ,以获得理想的凝固组织。实验结果表明 ,熔体温度处理过程中 ,对低温熔体机械搅拌可以明显改善混合后熔体的组织形貌 ,使组织形貌由树枝晶转变为等轴晶 ;在搅拌基础上选取较低的低温熔体温度 ,能够得到很好的凝固组织。     

Axial characterization of catalytic activity in close-coupled lightoff and underfloor catalytic converters

A exhaust system consisting of a close-coupled Pd technology 32 in³ lightoff converter and Pt/Rh technology 170 in³ underfloor converter was vehicle-aged for 56000 miles on a vehicle equipped with a 3.8 l engine. Following this aging, the converters were taken off the vehicle and cut into 1″ thick sections along their axis and characterized for lightoff and warmed-up activity using a laboratory reactor to simulate vehicle exhaust. Each section was also analyzed for the quantity of oil additive poisons (phosphorus and zinc) deposited. Following this initial characterization, the phosphorus and zinc deposits were removed, and the sections were characterized again for lightoff and warmed-up activity. This procedure was used to qualitatively determine the relative contribution of oil additive poisoning and thermal sintering to the total activity deterioration as a function of axial position in the catalyst monoliths.

Analysis of the lightoff converter as taken from the vehicle showed a dramatic axial gradient in the lean and stoichiometric lightoff and warmed-up (600°C) performance for HC, CO and NO_x, with most of the deterioration having taken place in the forward-most 1″ section of the converter, which was consistent with the gradient in the deposition of phosphorus (P) and zinc (Zn) in this converter. Comparison of these data sets with those obtained after removal of the P and Zn poisons indicates that most of the total deterioration of lean HC and CO activity can be attributed to P and Zn poisoning of the forwardmost 1″ section. When tested under stoichiometric conditions, most of the deterioration of HC activity is attributable to P and Zn poisoning, while most of the deterioration of CO and NO_x activity is attributable to thermal deterioration. A similar activity and poison deposition gradient was detected in the underfloor converter, but to a smaller extent.     

Characteristics of epoxy resin cured with in situ polymerized curing agent

In order to improve the heat resistance of a cured epoxy resin together with reducing the viscosity of the resin composition, an epoxy resin was cured with a curing agent formed from the radical copolymerization of vinyl monomers during the cure process of the epoxy resin. N-phenylmaleimide and p-acetoxystyrene were used as vinyl monomers of the curing agent. The epoxy resin was cured by the insertion reaction of the ester group of the in situ polymerized curing agent and the epoxy group of the epoxy resin. In the cure system of the epoxy and the phenol resins, reduction of the viscosity of the resin composition was achieved by replacing some or all of the phenol resin with these monomers. When all phenol resins were replaced by these monomers, the viscosity of resin composition (0.01 Pa s at 70 °C) decreased by about 1/2000 compared with that of the system with only phenol resin (21 Pa s at 70 °C). The glass transition temperature (T_g) of the cured resin with no phenols was 174 °C, an improvement of 17 °C compared with that of the system cured with only phenol resin. The flexural strength of the new resins remained unchanged.