具有初曲率板弯曲的边界元分析

由于具有初曲率板弯曲问题的控制微分方程较复杂，直接求解原问题基本解推导边界积分方程较为困难。本文通过引入等效荷载，将此问题的控制微分方程化成与普通板弯曲基本方程形式相同的微分方程，利用一般求解板弯曲问题的边界元法迭代求解，建立了分析具有初曲率板弯曲问题的边界元法。算例表明本方法理论准确、精度良好。     

叠后记录Radon变换压制干扰方法

在叠加剖面中,下伏反射界面的反射信号同相轴呈连续的或带有限个间断点的连续层状图像,各种干扰则呈无规则的图像。对此剖面的振幅数据进行 Radon 变换,即分别向各方向进行投影,层状图像将产生一定形状的光滑曲线,而干扰数据将相互抵消,其剩余数据呈高斯分布。在Radon 域中通过平滑等方法消除这些呈高斯分布的噪声数据,再经 Radon 逆变换,便可获得信噪比较高的叠加剖面。其结果不改变原叠加剖面的分辨率和信号波形特征。理论与实际剖面的处理结果表明,这是一种良好的压制干扰方法。     

镶嵌在CaF2介质中纳米Cu团簇微观结构的研究

利用磁控溅射产生金属Ｃｕ团簇，同时蒸发ＣａＦ２介质，将Ｃｕ团簇包埋在ＣａＦ２介质中，团簇大小可通过改变溅射气压控制，用ＴＥＭ研究了嵌埋团簇的结构，分析结果表明：Ｃｕ团簇呈三角状多晶结构，团簇大小为１０￣７０ｎｍ，基质ＣａＦ２晶体也为多晶结构，Ｃｕ团簇的晶格常数在包埋状态下发生了膨胀，膨胀率大约在１６％左右。     

T_C≥400°C高温PTC陶瓷的研制

利用国产原料，采用传统的陶瓷材料制备工艺，研制了居里温度ＴＣ≥４００°Ｃ的高温ＰＴＣ陶瓷，制成了居里温度ＴＣ＝４１２°Ｃ，电阻Ｒ≤１０３Ω，ｌｇ（Ｒｍａｘ／Ｒｍｉｎ）＝４的高性能ＰＴＣ热敏陶瓷材料     

优化双圆弧拟合

本文提出一种优化双圆弧拟合的新算法，它采用的方法是用改变双圆弧联结点的切线使双圆弧与样条曲线间的法向误差达到最小（或小于允许误差），与其他双圆弧拟合方法相比较，该算法计算简单，线性，并可消除拟合曲线的不稳定性，拟合效果快速，良好。可直接应用于雕塑曲面的ＣＮＣ加工中。     

用于生产甲基丙烯酸的杂多酸催化剂的研究

以异丁烯为原料的两段直接氧化生产甲基丙烯酸最新工艺有许多优点。其技术关键在于研制出高效的甲基丙烯醛选择性氧化催化剂。本文报道P-Mo-As-Cu杂多化合物催化剂的组成、制备条件对催化剂活性的影响。经优化后获得高选择性、高活性的二段氧化催化剂，其甲基丙烯酸收率达60％以上。     

Beam test of the CsI(Tl) calorimeter for the BELLE detector at the KEK-B factory

We studied the performance of a prototype electromagnetic calorimeter for the BELLE detector at the KEK proton synchrotron for an energy range of 0.25–3.5 GeV. The prototype consisted of an array of 6 × 5 CsI(Tl) crystals with 30 cm length (16.2 radiation lengths) and about 6 cm × 6 cm cross section. The scintillation light of each CsI(Tl) crystal was read out by two large-area PIN photodiodes and charge-sensitive preamplifiers attached at the rear face of the crystal. We measured the energy and position resolution for electrons and the e/π separation for two sets of matrix configurations: one corresponded to the center and the other to the edge of the barrel calorimeter. The overall performance measured by the test proves that the prototype calorimeter is satisfactory for the use in the BELLE detector.     

Fe－Cu包埋团簇的制备及其微观结构的研究

基于溅射－气体－聚集（ＳＧＡ）形成团簇的原理，提出了蒸发－气体－聚集（ＥＧＡ）共沉积方法，并在方华膜载网上成功地制备了Ｆｅ－Ｃｕ纳米磁性包理团簇样品。ＴＥＭ／ＥＤ分析表明，样品中Ｆｅ团簇被Ｃｕ原子所包裹，形成了以Ｆｅ团簇为芯，Ｃｕ膜为壳的良好的芯－壳式包埋结构。当衬底温度由２５℃变化到２００℃时，样品形貌由弥散状过渡到集团状，直至形成大的块状；其结构也相应的由Ｆｅ－Ｃｕ多晶共存变化为一种不规则的单晶形态。     

Use of subunit-specific antisense oligodeoxynucleotides to define developmental changes in the properties of N-methyl-D-aspartate receptors

Antisense oligodeoxynucleotides were used to determine whether alterations in the expression of N-methyl-D-aspartate (NMDA) receptor subunit mRNA are responsible for developmental changes in the sensitivity of receptors to agonists and antagonists. Xenopus laevis oocytes were injected with mRNA prepared from neonatal and adult rat cerebral cortex, and the effects of agonists and antagonists were determined under voltage-clamp conditions. Glycine-site antagonists like 7-chlorokynurenate and glutamate-site antagonists like CGP-39653 were more potent at NMDA receptors expressed from mRNA from adult rat cerebral cortex than those expressed from mRNA from 1-day-old rat. NMDA receptors from 1-day-old rat cerebral cortex were more sensitive to activation by glycine than were receptors from adult rat cerebral cortex. 7-Chlorokynurenate and CGP-39653 were more potent inhibitors of responses seen with heteromeric NR1/NR2A receptors than with NR1/ NR2B receptors. Conversely, heteromeric NR1/NR2B receptors were more sensitive to activation by glycine than were NR1/NR2A receptors. We previously described a delay in the expression of the NR2A subunit in developing rat brain. Anti-sense oligodeoxynucleotides were used to determine whether the delayed expression of the NR2A subunit underlies changes in pharmacological properties observed during development. The properties of receptors seen when adult brain mRNA was coinjected with antisense oligodeoxynucleotides against the NR2A subunit were similar to those found in receptors from 1-day-old rat brain. These data suggest that changes in the sensitivity of NMDA receptors to antagonists and to glycine seen during development are a result of alterations in the expression of different species of NR2 subunit mRNA.