Passivation of Fe-Cr alloys studied with ICP-AES and EQCM

The response of sputter deposited Fe-15Cr and Fe-25Cr alloys to a rapid potential increase in the passive region was studied using two in situ methods: electrochemical quartz crystal microbalance and inductive coupled plasma-atomic emission spectroscopy (ICP-AES). Both methods indicated an increase in the dissolution rate of iron following the potential change; the total amount of material dissolved being higher for the Fe-15Cr alloy. For both alloys, about 10% of the total dissolved material was Cr. This result compared well with experiments on a 430 stainless steel. ICP-AES is shown to be useful for the in situ determination of partial currents of metal dissolution using solution analysis in a flow cell.     

水量对锐钛矿溶胶制备、结构及光催化性能的影响

选择“钛酸丁酯-水-乙醇-盐酸”的溶胶．凝胶反应体系，考察反应物水的用量变化对反应过程、溶胶结构和光催化性能的影响，并获得了含有锐钛矿晶体、具有光催化性能的氧化钛溶胶。钛酸丁酯与水的摩尔比为1：2、1：4、1：8时，会逐渐形成凝胶，溶胶常温干燥后的粉体呈无定型结构，透射电镜中只能观察到细小的成膜粒子，溶胶不能使罗丹明B溶液分解褪色。钛酸丁酯与水的摩尔比为1：40、1：100、1：200时，钛酸丁酯发生充分水解，有可能形成稳定的溶胶；溶胶常温干燥后的粉体呈锐钛矿晶型，且结晶强度随水的用量的增加而增强；透射电镜中可观察到松散的团聚体、初显正方形较为紧密的结晶体和致密规则的正方形锐钛矿晶体；各溶胶均可催化降解罗丹明B使其褪色。     

CRYSTAL STRUCTURE OF γ-Li_xFe_2O_3 WITH ELECTROCHEMICAL INSERTION OF Li

Crystal structure of γ-Li_xFe_2O_3,inserted Li electrochemically,was studied by Moss-bauer spectroscopy together with X-ray diffraction,XPS and electrochemical method,Onthe insertion of Li at low current density,the crystal structure is keeping original spinel;while at higher current density or by thermal activation,owing to violent movement ofLi~+ ions,part of crystal structure transforms into rock type similar to face-centeredcubic structure of ferrous oxide.The transition channels during insertion of Li~+ ions andlimitation of Li~+ ions inserted were discussed.     

双滑移取向Cu单晶的循环形变行为──Ⅱ．滑移带和形变带SCIEI

用光学显微镜和扫描电镜研究了双滑移取向（［０３４］，［１１７］）Ｃｕ单晶循环饱和后的表面形貌，塑性分切应变幅（γｐｌ）低于１０^（－３）时，［０３４］晶体表面上要为主滑移系的驻留滑移带（ＰＳＢｓ）占据，次滑移只在边缘区域启动，其ＰＳＢｓ细窄（＜１μｍ），体积百分数在１％以下．γｐｌ＞１０^（－３）时，次滑移开始在试样的中部启动，同时，表面出现二种贯穿晶体的宏观形变带（ＤＢＩ，ＤＢＩＩ），滑移带在形变带内集中．［１１７］晶体在γｐｌ＝４．４×１０^（－４）时，双滑移现象已十分明显．γｐｌ＞１０^（－３）时，表面也形成与前者相似的形变带．ＤＢＩ的惯习面与主滑移面平行（［０３４］晶体）或接近（［１１７］晶体），ＤＢＩＩ的惯习面则与前者垂直，文章讨论了形变带形成的可能原因．     

ELECTRON MICROANALYSIS FOR LASER MELTED ZONE IN 45 STEEL WITH Fe-Ni-Cr COATING

The Fe-Ni-Cr coating laver has been alloyed with 45 steel base metal by transverse.flow typeCO_2 gas laser of maximum output 5kW.The characteristics of the melted zone and the es-sence of the“bright band”has been investigated using the electron microscopy.The resultsshow that the“bright band”belongs to the melted zone and is a vertical section of the planecrystal,The width of the“bright band”equals the height of the plane crystal,which decreaseswith the increase of laser beam scanning rate and the decrease of laser power.This has beenexplained in terms of constitutional supercooling G/R.     

共晶自生复合材料的晶形转变

自生复合材料的晶形转变受到成分过冷与曲面过冷两个因素的控制.非金属相具有较大的熔化熵且易形成小平面是改变领先相的因素,而领先相的改变则可能是晶形转变的根本原因.     

Molecular Dynamics Simulation of Micro Mechanisms in Slip Deformation Theory of Crystals

Based on the discussion that there should be a micromechanism that causes a macroscopic slip of mono-crystal copper, molecular dynamics simulations with the analytical displacement feld around a crack tip have been carried out. The result of the simulation shows that macroscopic shear slip in an f.c.c. mono-crystal copper occurs as discrete time events. This is because cross-slips occur in many places in a material such that a macroscopic shear slip is blocked until some critical state of deformation. A macroscopic shear slip then occurs suddenly at the critical state in which the area of disordered atomic arrangement has stretched from one end of a crystal to the other end. The reason why macroscopic shear slips occur in the directions of the slip planes of a crystal is attributed to the fact that the areas of disordered atomic arrangement develop only along those directions.     

DD3单晶镍基合金蠕变—疲劳及寿命预测

从应变范围区分法(SRP),应变能区分法(SEP)的有关概念出发,研究DD3单晶镍基合金拉—拉应力状态下的蠕变—疲劳性能和保持时间的影响,并对其进行了定量计算;同时,用应变能区分法的数值法(SEP—NCM)实现对拉—拉应力状态下蠕变—疲劳的寿命预测。     

Optical Investigation of the Effects of Substrate Orientation on Oxidation of Single Crystal β-NiAl

The residual stresses in -Al₂O₃ scales formed on high-purity FeCrAl and FeCrAlY during oxidation at 1200°C and subsequent cooling and reheating were studied using photostimulated luminescence spectroscopy. Systematic measurements of the stress in the oxide were made as a function of both alloy thickness and cooling rate and the development of stresses in the oxide scale during thermal cycling was investigated as a function of the temperature. Depending on the ratio of the alloy and oxide-scale thicknesses, substantial stress relaxation was observed to occur during cooling at a rate of 8 K/min. Compressive growth stresses of 1 GPa were determined by comparing the residual-stress measurements at room temperature with those calculated based on thermal-expansion mismatch. No significant differences in the growth stresses, the total residual stresses, or the stress relaxation during thermal cycling were observed between the oxides formed on the Y-doped and undoped FeCrAl samples. Stress relaxation is also shown to lead to the development of tensile stresses in the oxide scale under certain conditions, in particular, those associated with slow cooling followed by rapid heating.     

Application of an analytical phase transformation model

Employing isothermal and isochronal differential scanning calorimetry, an analytical phase transformation model was used to study the kinetics of crystallization of amorphous Mg82.3Cu17.7 and Pd40Cu30P20Ni10 alloys. The analytical model comprised different combinations of various nucleation and growth mechanisms for a single transformation. Applying different combinations of nucleation and growth mechanisms, the nucleation and growth modes and the corresponding kinetic and thermodynamic parameters, have been determined. The influence of isothermal pre-annealing on subsequent isochronal crystallization kinetics with the increase of pre-annealing can be analyzed. The results show that the changes of the growth exponent, n, and the effective overall activation energy Q, occurring as function of the degree of transformation, do not necessarily imply a change of nucleation and growth mechanisms, i.e. such changes can occur while the transformation is isokinetic.