黄铜选择性溶解固相扩散机理的研究

采用恒电位暂态和旋转盘环电极等方法研究了α、α＋β以及β黄铜在硫酸钠、硫酸以及氯化钠的稀溶液中的阳极溶解过程．结果表明，在黄铜阳极溶解的初始阶段测得的ｉ－ｔ曲线遵循抛物线定律，求得ｉ－ｔ为一通过坐标原点的直线，证明了黄铜中锌的选择性溶解受固相扩散控制，计算出在上述溶液中黄铜中锌的扩散系数值在１０－１５～１０－１３ｃｍ２·ｓ－１数量级，介质成分和微量合金元素砷对扩散系数值有明显的影响．     

水稻三系及其杂种F1的核组蛋白研究

本文提取了杂交水稻COryza Sativa L.)的三系及其F,代的组蛋白，采用聚丙烯酞胺凝胶电泳及SDS-聚丙烯酞胺凝胶电泳进行分析，并与小牛胸腺组蛋白进行了比较.水稻和小牛胸腺的H,,H‘在两种凝胶电泳中都显示了相同的泳动率.水稻H:. , H:、比小牛胸腺中的相应组份在两种凝胶电泳中皆显示较低的泳动率，具较大的分子量.在我们的研究范围中，H,表现出种的特异性，而且杂种F:的H,含量高于亲本，这提供了一种从分子遗传学角度来研究杂种优势的可能性.     

关于“交换环上赋值的完全性”一文的两则注记

将上述论文中之某些结论予以推广。1)设R为一有赋值v的环,v的核是R中一极大理理想φ。于是(R,v)成为完全赋值环,当且仅当(F,v)是完全赋值域,此处F=R/p,v是由v所导出。2)设v是环R的一个赋值,其核为R中极大理想;又设S为R的整扩环,且又是R上的有限R-模。于是(1)v在S上有拓展,设为w,它的核是S中一极大理想(2)(S,w)是个完全赋值环。3)前文定理4中关于S的条件可简化为:S是R的一个整扩张,且为R上的有限R-模。     

环戊烯分子内价轨道1a′的电子动量谱学研究

报道了环戊烯（C₅H₈）分子1a′轨道的电子动量谱，并且给出了价 轨道的电离能谱信息 .实验在非共面对称几何条件下用能量多道型电子动量谱仪完成，入射电子的能量为1200 eV 加结合能.通过Hartree-Fock 和密度泛函方法计算得到了C₅H₈分子 1a′轨道的动量谱. 对1a′轨道的电子动量谱的实验值和理论计算进行了比较，得到了该轨道的极强度（pole s trength）的信息.     

Physical implication of two problems in transition prediction of boundary layers based on linear stability theory

Up to now,the most widely used method for transition prediction is the one based on linear stability theory.When it is applied to three-dimensional boundary layers,one has to choose the direction,or path,along which the growth rate of the disturbance is to be integrated.The direction given by using saddle point method in the theory of complex variable function is seen as mathematically most reasonable.However,unlike the saddle point method applied to water waves,here its physical meaning is not so obvious,as the frequency and wave number may be complex.And on some occasions,in advancing the integration of the growth rate of the disturbance,up to a certain location,one may not be able to continue the integration,because the condition for specifying the direction set by the saddle point method can no longer be satisfied on the basis of continuously varying wave number.In this paper,these two problems are discussed,and suggestions for how to do transition prediction under the latter condition are provided.     

一种大视场相位测量轮廓术系统标定方法

在进行大视场相位测量轮廓术系统参量标定时需要大的标定平面和精密移动台,由于携带不方便,不易进行现场标定。提出了一种用于相位测量轮廓术系统参量的高精度、现场标定方法,采用一块较小的平面标定靶在有效测量体积内不同位置多次摆放,以获取密集的数据点。先标定出摄像机的内参量和外参量,再指定一个全局参考平面和若干辅助参考平面,然后在图像平面上分区计算出每个位置标定靶上每点相对辅助参考平面的高度差和相位差,最后应用极大似然估计法估计出相位高度映射参量。实验中平面高度测量的标准偏差达到0.0433 mm。这种方法只需要较小的平面标定靶,标定过程方便、精度高,完全适合大视场三维测量相位测量轮廓术系统现场标定要求。     

First-principles investigation of chemical modification on two-dimensional iron–phthalocyanine sheet

Successful synthesis of single iron–phthalocyanie(FePc) framework layer on substrate and its transferrable properties open the door for decorating the separately distributed transition metals for exploring the diverse properties. We have studied the effects of chemical modification on two-dimensional FePc organometallic framework with density functional theory. For simplicity, the non-metal atoms with variant valence electrons are used as prototypes to estimate the effects from chemical modifications with different functional groups. The thermo-stabilities of the non-metal atom decorated complex sheet materials have been estimated by the first-principles constant energy molecular dynamic simulations. Upon the nonmetal atom adsorption, the magnetic moment could be changed from 2 μBto 0, 1, 2, and 3 μBper unit cell for the case of tetra-, penta-, hexa-, and hepta-valent non-metal modifications, respectively, showing interesting promise to tailor its magnetic properties for potential applications.