三氨基三硝基苯材料微孔结构的小角x射线散射实验研究

应用同步辐射x射线小角散射技术研究了不同工艺制备的三氨基三硝基苯样品中的微孔状况 ，得到了样品材料有关微结构参数，包括微孔平均孔径及孔径分布、分形特征、Porod常数 及界面参数等，并分析了微孔结构参数的变化规律.结果表明，不同工艺制备的TATB样品材 料其微孔结构有较大差别，都有较显著的特征. 关键词： 小角x射线散射 TATB材料微孔分布     

用原位x射线小角散射研究块体非晶合金Zr55Cu30Al10 Ni5的结构弛豫

应用同步辐射x射线小角散射法在原位对块体非晶合金Zr₅₅Cu₃₀Al ₁₀Ni₅在等温退火过程中的微结构变化进行研究.实验表明：在等温退火过程中电子 密度涨落反映了晶化之前的结构弛豫过程；在一定的退火温度下、随退火时间的增加，拓扑短程序弛豫与化学短程序弛豫之间存在一个电子密度均匀化的过程；导致这两种弛豫过程转变的退火时间与退火温度有关，温度越高，所需的退火时间越短. 关键词： 原位x射线小角散射 块体非晶合金 等温退火 结构弛豫     

Al-Zn-Mg-Cu-Li合金时效过程微结构演化的小角x射线散射研究

应用小角x射线散射技术分析了Al-Zn-Mg-Cu-Li合金在130，150和160℃温度时效24 h析出粒子的微结构参数的变化情况. 粒子的半径随着时效温度的增高而增加，它的比内表面积和体积百分数随着时效温度的增高而减小. 对Porod曲线q³J(q)-q²的分析表明,析出粒子与基体之间有明显的界面. 关键词： 小角x射线散射 Al-Zn-Mg-Cu-Li合金 时效 析出粒子     

Al-Zn-Mg-Cu合金时效过程的小角度x射线散射研究

通过同步辐射小角度x射线散射方法（SAXS），研究了三种Al_Zn_ Mg_Cu合金沉淀析出过程显微结构参数（析出相尺寸和体积分数），随时效温度和时效时间 的演化，同时分析了Zn含量对合金沉淀析出过程的影响.结果表明，三种合金（A，B，C） 在实验条件下析出相均属于纳米尺度，析出相的最大体积分数随Zn含量的增加而增加，最大体积分数分别为0.023—0.028，0.052—0.054和0.04.在一定时效温度下，体积分数随时效时间的变化规律，符合析出相的形核、核长大和粗化动力学过程.  关键词： 小角度x射线散射 Al_Zn_Mg_Cu合金 时效 析出相尺寸 析出相体积分数     

小角x射线散射确定TiNi薄膜中晶化粒子的长大激活能

用小角x射线散射技术研究以直流磁控溅射方法制备TiNi合金薄膜其退火生成的晶化粒子的长大行为.发现在室温下溅射的TiNi合金薄膜存在小于1nm尺寸的微空洞,将退火后薄膜的小角x射线散射强度扣除退火前微空洞产生的小角x射线散射强度,用这种方法得到的散射强度遵从Porod定律;而用通常方法扣除背底得到的散射强度结果不满足Porod定律.TiNi合金薄膜在733—793K之间退火晶化粒子的长大激活能Eg=301kJmol. 关键词： TiNi薄膜 晶化粒子 长大激活能     

两亲性嵌段聚合物的同步辐射小角x射线散射研究

应用同步辐射小角x射线散射(SAXS)方法研究了不同聚合条件下苯乙烯对乙烯基苯甲酸两亲性嵌段聚合物的聚集行为,结果发现该聚合物在选择性溶液中自组装形成胶束.胶束的形态和结构取决于嵌段聚合物的组成、浓度以及溶剂的性质等因素 关键词： 小角x射线散射 两亲性嵌段聚合物 分形维数 粒径     

同步辐射小角x射线散射方法研究由城市固体垃圾制备的活性炭

应用同步辐射小角x射线散射方法研究了由不同城市固体垃圾制备而成的活性炭的孔结构-结果发现利用木类、纸张、塑料这三类典型垃圾组分的热解残余物为原料制备中孔发达的活性炭是可行的-活性炭的形态和结构取决于垃圾热解残余物的组分和热解程度等因素- 关键词： 小角x射线散射 活性炭 分形维数 平均孔径     

块体非晶合金Zr55Cu30Al10Ni5 结构弛豫的研究

应用同步辐射小角x射线散射和差示扫描量热分析对块体非晶合金Zr55₅₅Cu 30₃₀Al10₁₀Ni5₅结构弛豫进行了研究.实验结果表 明：经340℃、不同时间退火后的非晶内 部的电子密度涨落随退火时间的延长先增大而后减小；玻璃转变温度附近焓弛豫峰的表观激 活能则随退火时间的延长先减小而后增大.结果反映了随退火时间的延长，块体非晶合金内 部类液体区不断减少及类固体区不断增加的过程. 关键词： 小角x射线散射 块体非晶合金 结构弛豫     

蠕变镍基单晶高温合金微观结构与界面特征的X射线小角散射研究

利用SAXS技术对蠕变过程中不同尺度范围的微观结构变化分析表明X射线小角散射(SAXS)与中子小角散射(SANS)测量的二维散射图具有明显的差异,由散射强度曲线的变化说明了蠕变过程中二次析出γ'相形貌和不同区域尺寸特征的改变情况.分析结果表明二次析出γ'相存在两类特征尺寸,在蠕变过程中沿[100]或[010]方向的变化趋势类似,均是在第一和第二阶段有所减小,在第三阶段又有所增大,相较而言,特征尺寸较大的γ'相变化也较为显著.二次析出γ'相在蠕变第二阶段元素扩散最严重,相表面最粗糙,在第三阶段两相界面又进一 关键词： 单晶高温合金 二次析出γ'相 X射线小角散射 微观结构     

水分子凝胶中有机凝胶因子聚集体的分形结构研究

水分子凝胶是一种新型软凝聚体系.是凝胶因子在很低的浓度下在水中聚集、自组装，使水凝胶化形成的凝聚体系.透射电镜(TEM)表明凝胶因子在水中聚集、自组装成细纤维状结构.通过对TEM照片进行数字化处理，采用Sandbox法和密度-密度相关函数法计算的结果表明凝胶因子在聚集组装过程中具有典型的分形特征.根据C++程序计算出分形维数D＝1.814—1.977.以分形理论对凝胶因子的聚集过程以及由此形成的水分子凝聚体系的分形特征进行了讨论.利用小角x射线散射(SAXS)研究进一步表明，凝聚体系的分形结构存在于尺度α 关键词： 分形 凝胶因子 水分子凝聚体系 透射电镜(TEM) 小角x射线散射(SAXS)     

Compositional dependence of the deformation behaviour of ultrahigh-purity Ti–Al alloys

The present study is concerned with the effect of the O and Al concentrations on the deformation behaviour of ultrahigh-purity (UHP) Ti–(48,?50,?52)?at.%?Al alloys using UHP Ti with 30?wt?ppm?O. It has been shown that yield strength increases with increasing O content. Stoichiometric Ti–50?at.%?Al alloys had the lowest yield strength and the highest ductility when the O content was sufficiently low. It is suggested that the deformation mechanism of UHP binary Ti–Al is strongly related to the Al concentration. The deformation substructure of UHP Ti–48?at.%?Al is shown to be dominated by ordinary dislocation as well as deformation twinning and a small portion of superdislocations. The deformation substructure of UHP Ti–50?at.%?Al alloy was similar to that of Ti–48?at.%?Al, but deformation twinning was not observed. Most of dislocation structures of UHP Ti–52?at.%?Al alloy consisted of faulted dipoles. The major deformation mode of UHP Ti–48?at.%?Al and UHP Ti–50?at.%?Al alloys was ordinary dislocation in deformation orientation, which takes advantage of ordinary dislocation slip. However, the major deformation mode in this orientation for UHP Ti–52?at.%?Al alloys was superdislocation slip.     

Influence of chromate, molybdate and tungstate on pit formation in chloride medium

It has been characterized and evaluated the 2024-T351 and 7050-T7451 aluminum alloys pitting corrosion in naturally aerated chloride aqueous solutions containing chromate, molybdate and tungstate. It has been carried out electrochemical and non-electrochemical immersion corrosion tests accompanied by surface metallography analysis using an optical microscopy. Chromate for the two alloys and in molybdate for 7050 has corrosion inhibiting effects, whereas tungstate promotes the pitting corrosion for these alloys. Quantitative surface analysis upon the alloys after immersion has indicated that pits are predominantly conical or quasi-conical and irregular. In general, pits have been wider than deep and the widest have been also the deepest. Despite inhibitor presence, when pits have been nucleated, they grow with the same intensity.     

Diffusion and precipitation phenomena across layer interfaces in a roll bonding composite of Al(Si) and Al(Cu)

Layered composite structures can be generated in metallic sheets by roll bonding of dissimilar metals/alloys. In this investigation, heat treatable (Al(Cu)) and non-heat treatable (Al(Si)) aluminium alloys are roll bonded in sheet form. Large hardness differences between layers poses significant bonding challenges in the form of multiple necking within the hard Al(Cu) layers. For successful processing, it is vital to choose the candidate materials in a state of marginal hardness differences during rolling, but being capable of altering properties through subsequent heat treatments. Atomic diffusion takes place during heat treatment of the composite sheet and results in gradual hardness variation across sheet thickness. The Al(Cu) layers contribute to strength, whereas the Al(Si) layers provide protection from corrosion/wear-related degradation in the newly developed hybrid sheet. The overall mechanical properties of the heat-treated composite fall between the base alloys. The bonding interfaces are noted as the potential spots for initiating failure.     

Creep deformation of single crystals of new Co–Al–W-based alloys with fcc/L12 two-phase microstructures

The creep deformation behaviour of single crystals of Co–Al–W-based alloys with γ?+?γ′ two-phase microstructures has been investigated in tension under a constant stress of 137?MPa in air at 1000°C as a function of the γ′ solvus temperature and the volume fraction of the γ′ phase. When described by the creep strain rate versus time curve, the creep deformation of Co–Al–W-based alloys consists of transition and accelerating regions without a steady-state region, as observed in many modern nickel-based alloys. However, the creep strength of the present Co–Al–W-based alloys is comparable with nickel-based superalloys of the first generation but is much weaker than those of the second and higher generations. Unlike in nickel-based superalloys, the so-called p (parallel)-type raft structure, in which the γ′ phase is elongated along the tensile axis direction, is formed during creep in Co–Al–W-based alloys, being consistent with what is expected from the positive values of lattice misfit between the γ and γ′ phases. As a result, of the alloys investigated, the best creep properties are obtained with the alloy possessing the highest volume fraction (85%) of the γ′ phase, which is far larger than usual for nickel-based superalloys (55–60%).     

A corrosion resistant cerium oxide based coating on aluminum alloy 2024 prepared by brush plating

Cerium oxide based coatings were prepared on AA2024 Al alloy by brush plating. The characteristic of this technology is that hydrogen peroxide, which usually causes the plating solution to be unstable, is not necessary in the plating electrolyte. The coating showed laminated structures and good adhesive strength with the substrate. X-ray diffraction and X-ray photoelectron spectroscopy analysis showed that the coatings were composed of Ce(III) and Ce(IV) oxides. The brush plated coatings on Al alloys improved corrosion resistance. The influence of plating parameters on structure and corrosion resistance of the cerium oxide based coating was studied.     

Fundamental understanding of Na-induced high temperature embrittlement in Al–Mg alloys

Sodium is an undesirable impurity in aluminium–magnesium alloys. In trace amounts it leads to high temperature embrittlement (HTE), due to intergranular fracture, which results in edge cracking during hot rolling. In the present work, the results of a thermodynamic investigation to elucidate the mechanism are presented. Correlations between HTE, phase formation, temperature and composition in Al–Mg alloys were determined. It is suggested that: (i) HTE is related to the formation of an intergranular Na-rich liquid phase, which significantly weakens the strength of grain boundaries; (ii) for a given Mg content, there exists a maximum Na content above which HTE cannot be avoided; and (iii) for a given alloy, a proper hot-rolling temperature should be chosen with respect to Na and Mg contents to suppress HTE. The HTE sensitive zone and a hot-rolling safe zone of Al–Mg–Na alloys are defined as functions of processing temperature and alloy composition. The tendency of HTE formation was evaluated based on thermodynamic simulations of phase fraction of the intergranular Na-rich liquid phase.     

A model of grain refinement and strengthening of Al alloys due to cold severe plastic deformation

This paper presents a model which quantitatively predicts grain refinement and strength/hardness of Al alloys after very high levels of cold deformation through processes including cold rolling, equal channel angular pressing (ECAP), multiple forging (MF), accumulative roll bonding (ARB) and embossing. The model deals with materials in which plastic deformation is exclusively due to dislocation movement within grains, which is in good approximation the case for many metallic alloys at low temperature, for instance aluminium alloys. In the early stages of deformation, the generated dislocations are stored in grains and contribute to overall strength. With increase in strain, excess dislocations form and/or move to new cell walls/grain boundaries and grains are refined. We examine this model using both our own data as well as the data in the literature. It is shown that grain size and strength/hardness are predicted to a good accuracy.     

Microstructural evolution of SiC joints soldered using Zn–Al filler metals with the assistance of ultrasound

SiC ceramics were successfully soldered with the assistance of ultrasound. Two kinds of filler metals, namely non-eutectic Zn–5Al–3Cu and eutectic Zn–5Al alloys, were used. The effects of ultrasonic action on the microstructure and mechanical properties of the soldered joints were investigated. The results showed that ultrasound could promote the wetting and bonding between the SiC ceramic and filler metals within tens of seconds. For the Zn–5Al–3Cu solder, a fully grain-refined structure in the bond layer was obtained as the ultrasonic action time increased. This may lead to a substantial enhancement in the strength of the soldered joints. For the Zn–5Al solder, the shear strength of the soldered joints was only ∼102 MPa when the ultrasonic action time was shorter, and fractures occurred in the brittle lamellar eutectic phases in the center of the bond layer. With increasing ultrasonic action time, the lamellar eutectic phase in the bond layer of SiC joints could be completely transformed to a fine non-lamellar eutectic structure. Meanwhile, the grains in the bond layer were obviously refined. Those results led to the remarkable enhancement of the shear strength of the joints (∼138 MPa) using the Zn–5Al solder, which had approached that enhancement using the Zn–5Al–3Cu solder. The enhanced mechanical properties of the joints were attributed to the significant refinement of the grains and the change in the eutectic structure in the bond layer. Prolonged enhanced heterogeneous nucleation triggered by ultrasonic cavitation is the predominant refinement mechanism of the bond metals of the SiC joints.     

Mg-Al系工业合金牌号的成分式解析

Mg-Al系牌号是应用最广的镁基工业合金,但其牌号背后的成分根源一直未知,构成研发新合金的主要障碍.本文应用描述固溶体短程序结构特征的团簇共振模型,得到了Mg-Al二元固溶体的最理想化学结构单元[Al-Mg_(12)]Mg_1,然后对《the American Society for Testing Materials》手册中所有Mg-Al系工业合金牌号进行成分解析,得到相应团簇成分式,如AZ63A合金解析后的团簇成分式为[Al_(0.78)Zn_(0.16)-Mg_(12)]Mg_(1.04)Mn_(0.02),AZ81A合金解析后的团簇成分式为[Al_(0.97)Zn_(0.03)-Mg_(12)]Mg_(0.98)Mn_(0.02).再根据成分式与化学结构单元之间的误差,对比该牌号合金的力学性能,验证了该化学结构单元在Mg-Al体系中的准确性,揭示出看似复杂的工业合金牌号后面隐藏的简单成分规律,为发展Mg-Al体系合金指出了一个全新的途径.     

Microstructure and texture development of 7075 alloy during homogenisation

The microstructure evolution of Al–Zn–Mg–Cu alloy during homogenisation was studied by optical microscope, field emission scanning electron microscope, energy dispersive X-ray Spectroscopy, differential scanning calorimetry and X-ray diffraction in detailed. It has been found that primary cast structure consisted of primary α (Al), lamellar eutectic structure η Mg(Zn, Cu, Al)₂ and a small amount of θ (Al₂Cu) phase. A transformation of primary eutectic phase from η Mg(Zn, Cu, Al)₂ to S (Al₂CuMg) was observed after 6 h of homogenisation treatment. The volume fraction of dendrite network structure and intermetallic phase was decreased with increase in holding time and finally disappeared after 96 h of homogenisation, which is consistent with the results of homogenisation kinetic analysis. Crystallographic texture of this alloy after casting and 96 h of homogenisation was also studied. It was found that casting process led the development of strong Goss, Brass, P and CuT components, while after homogenisation Cube, S and Copper components became predominant. Mechanical tests revealed higher hardness, yield strength and tensile strength for cast materials compared to homogenised alloys due to the presence of coarse micro-segregation of MgZn₂ phase. The significant improvement of ductility was observed after 96-h homogenisation, which was attributed to dissolution of second phase particles and grain coarsening. Fracture surfaces of the cast samples indicated the presence of shrinkage porosity and consequently failure occurred in the interdendritic regions or grain boundaries with brittle mode, while homogenised alloys failed under ductile mode as evident by the presence of fine dimple surfaces.