SiC/MoSi2 based coatings for Cf/C composites by two step pack cementation

In order to improve the oxidation resistance of C_f/Cs produced by chemical vapour infiltration, a multilayer coating based on silicon carbide and molybdenum disilicide was produced by two-step pack cementation technique. The inner SiC layer with a thickness up to 25 μm was obtained without promoted reaction additives by varying the composition, and thermal treatment conditions. The SiC/SiC-MoSi₂ coating was produced with a thickness up to 80 μm by two step pack cementation, considering the effect of the inner layer characteristic. The enhancement of the oxidation resistance, observed in SiC/SiC-MoSi₂ coated C_f/Cs by means of thermal analysis in flowing air up to 1500 °C, was due to the formation of SiO₂ promoted by the passive oxidation of silicon carbide and molybdenum disilicide.     

生物氧化预处理ORP实时动态精准预测研究

提出基于相空间重构理论和学习型狼群算法优化最小二乘支持向量回归机(LSSVR)的氧化还原电位(ORP)实时动态精准预测方法。以生物氧化预处理过程中采集到的ORP数据为研究对象,采用小波分析滤除ORP数据中的噪声,以相空间重构的ORP时间序列训练LSSVR预测模型。为了提高模型的泛化能力,提出学习型狼群算法优化LSSVR模型参数,并用时间窗口平移化方法和反馈校正法分别对模型和预测输出进行更新和修正。试验结果对比表明所提方法可行有效。     

45#钢Cr-N包埋共渗涂层的组织特征及形成机理

目的研究在45~#钢表面包埋共渗沉积Cr_2N涂层提高其耐蚀性的可行性。方法采用包渗法,对在1100℃下保温不同时间,得到不同时期的氮铬共渗涂层。利用扫描电镜及能谱仪、X射线衍射仪研究氮铬共渗层的微观组织及其生长机制,利用极化曲线评估涂层耐蚀性能。结果 45~#钢氮铬包埋共渗在保温4 h时可获得最佳涂层,涂层组织为Cr_2N层(约15μm)、Cr的沉积层(约10μm)、Cr的扩散层(约15μm)。Cr_2N层呈现强烈的(002)晶面择优取向;Cr沉积层为Fe-Cr合金及铬的碳化物相(Cr_7C_3,Cr_3C_2)。在模拟燃料电池腐蚀液中,45~#钢、45涂层样品、304不锈钢自腐蚀电位和自腐蚀电流分别为-0.521 V和230.63μA·cm~(-2),-0.448 V和10.89μA·cm~(-2),-0.299 V和5.26μA·cm~(-2)。当腐蚀电位高于0.3 V时,涂层样品会二次钝化,腐蚀电流低至1.43μA·cm~(-2)。结论沉积Cr_2N的45~#钢样品相对原样其耐蚀性有很大提高,并且当腐蚀电位达到0.3 V以上时,其耐蚀性能优于304不锈钢。     

网络安全体系中防火墙技术分析

本文就目前防黑客领域中最热门的网络安全工具即网络防火墙技术做了详细的分析，并讨论了防火墙的分类，防火墙的功能，防火墙的安全防护技术等，该方案的分析对组网技术中安全方案的设计具有实际意义。     

Effect of Substrate Characteristics on Interdiffusion Coefficients of Ni and Al Atoms in β-NiAl Phase of Aluminide Coatings

Interdiffusion coefficients at 950℃ and 1050℃function of composition of β-NiAI phase. The β-NiAI phase is formed by pack cementation on surface of superalloy. Results of the calculation show that interdiffusion coefficients in β-NiAI phase strongly depend on the compositions and vary over several orders of magnitude. Compared with the interdiffusion coefficients in the stoichiometric β-NiAI phase, the interdiffusion coefficients in β-NiAI phase formed on superalloy is obviously small, probably due to the composition, complicated microstructure and precipitates. However, it could be seen clearly that the shapes of the diffusivity curves are very similar to each other. The similarity of the diffusion curves and the difference between interdiffusion coefficients imply that the compositions, microstructures and precipitates of superalloy have a distinctly adverse effect on the interdiffusion of Ni and Al atoms during aluminization, but do not change the essential characteristics of β-NiAI phase.     

CeO₂改善低温渗铝涂层抗氧化性能的研究

在Ni基体上电沉积纯Ni镀层和Ni-CeO2复合镀层并对其进行620 °C低温渗铝,制备了无CeO2和CeO2改性的铝化物涂层。将以上两种涂层在1000 °C下氧化,研究CeO2颗粒的加入对氧化膜的生长速率和粘附性能的影响。结果表明,在δ-Ni2Al3涂层中加入纳米CeO2颗粒可以推迟一层完整α-Al2O3膜的形成时间,降低氧化膜的生长速率。此外,纳米CeO2颗粒的加入提高了氧化膜的粘附性,原因是与没有CeO2掺杂的涂层相比,CeO2改性铝化物涂层在氧化膜/涂层界面上形成的空洞尺寸较小。     

Structure of Al-modified silicide coatings on an Nb-based ultrahigh temperature alloy prepared by pack cementation techniques

In order to prepare Al-modified silicide coatings on an Nb-based ultrahigh temperature alloy, both a two-stage pack cementation technique and a co-deposition pack cementation technique were employed. The two-stage process included siliconizing a specimen at 1150 °C for 4 h followed by aluminizing it at 800-1000 °C for 4 h. The coating prepared by pack siliconization was composed of a thick (Nb,X)Si₂ (X represents Ti, Cr and Hf elements) outer layer and a thin (Nb,X)₅Si₃ transitional layer; after the siliconized specimens were aluminized at or above 860 °C, a (Nb,Ti)₃Si₅Al₂ phase developed at the surface of the coating, and furthermore, when aluminizing was carried out at 860 °C, a new (Nb,Ti)₂Al layer formed in the coating between the (Nb,X)₅Si₃ layer and the substrate, but when aluminizing was performed at 900-1000 °C, the new layer formed was (Nb,Ti)Al₃. The co-deposition process was carried out by co-depositing Si and Al on specimens at 1000-1150 °C for 8 h under different pack compositions, and it was found that the structure of co-deposition coatings was more evidently affected by co-deposition temperature than pack composition. An Al-modified silicide coating with an outer layer composed of (Nb,Ti)₃Si₅Al₂, (Nb,X)Si₂ and (Nb,Ti)Al₃ was obtained by co-depositing Si and Al at 1050 °C.     

Microstructure and corrosion resistance of simultaneous Al-Fe coating on copper by pack cementation

Simultaneous Al-Fe coatings on copper were prepared by pack cementation to investigate the microstructure and corrosion resistance. The cross-section of prepared specimen was analyzed by scanning electron microscope (SEM) equipped with an energy dispersive X-ray spectrometer (EDS). Then the cross-section of specimen corroded by solution of ferric chloride in ethanol was evaluated using SEM and X-ray diffraction (XRD). The coating consists of an intermetallic layer and an interdiffusion layer, and the thickness of coating layer increases parabolically with holding temperatures from 730 °C to 900 °C. The aluminum content in the coating varies between 7.65 and 4.0% from the surface to the inside layer while the iron content varies between 2 and 0.5%. The coating layer is composed of а-Cu/Al solid solution with a small amount of iron. Alumina formed on the surface of the coating layer during corrosion provides very good protection for the coating layer in the corrosive atmosphere and enhances the corrosion resistance of the coating.     

Y对Nb基体表面包埋渗铝涂层微观组织和生长机制的影响

通过向包埋渗铝剂中添加Y₂O₃粉末在纯Nb基体表面制备了Y改性的渗铝涂层,研究了Y对涂层微观组织和生长机制的影响。结果表明,Y对涂层的相组成和NbAl₃相的晶粒形态均无明显影响。随包埋剂中Y₂O₃添加量的增加,涂层表面的Y含量升高。Y改性后,涂层的生长机制由受Al原子的沿晶扩散控制转变为受Al原子的晶内扩散控制,降低了涂层的生长速率,并使NbAl₃相的柱状晶区形成了<010>//ND和<110>//ND的2种丝织构。     

Isothermal and cyclic oxidation behavior of a sandwiched coating for C/C composites

A ZrC–SiC/TiC–SiC/SiC sandwich-structured coating is prepared on a C/C composite by pack cementation methods. The microstructures of this coating are characterized by using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), and the oxidation resistance is investigated by performing an oxidation test at 1773 K and a cyclic oxidation test. The results show that the mass losses are 7.4% and 3.8% after oxidation for 144 h and 40 cycles, respectively. The sandwich structure relaxes, releases the thermal stress caused by the mismatch in the coefficients of thermal expansion, and absorbs energy to prevent the initiation and propagation of cracks. The ZrC–SiC/TiC–SiC/SiC coating exhibits good isothermal oxidation resistance and excellent cyclic oxidation protection properties.