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Zr-based bulk metallic glass matrix composites with the composition of Zr56.2Ti13.8Nb5.0Cu6.9Ni5.6Be12.(5) were synthesized by the copper-mould suction casting and the Bridgman solidification. The composite, containing a well-developed flowery beta-Zr dendritic phase, was obtained by the Bridgman solidification with the withdrawal velocity of 0.8 mm/s and the temperature gradient of 45 K/mm, and the ultimate strength of 2050 MPa and fracture plastic strain of 14.6% of the composite were achieved, which was mainly interpreted by the homogeneous dispersion of bcc beta-Zr phase in the glass matrix. Crown Copyright (C) 2008 Published by Elsevier B.V. All rights reserved.

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一、 △nifZ MoFe蛋白的纯化、特性及晶体生长 从缺失nifZ的棕色因氮菌突变种DJ194中,经离子交换层析和凝胶过滤提纯得到△nifZ MoFe蛋白,其纯度可达SDS凝胶电泳纯。它的Fe、Mo含量分别为野生型OP MoFe蛋白的56.6%和75.0%左右;C_2H_2、H~+还原活性和△H_2均只有OP MoFe蛋白的14.6%、21.7%和21.7%;其可见吸收光谱、CD及AR谱都与OP MoFe蛋白有较大差异,其中,可以反应P-cluster氧还状态和含量的ε_(450nm)、ε_(700nm)及△ε_(450nm)均要比OP MoFe蛋白低;由紫外CD谱反映的△nifZ MoFe蛋白的构象也与OP MoFe蛋白有所不同。由此我们推测,nifZ可能与固氮酶MoFe蛋白中P-cluster的合成或组装有关。为进一步阐明△nifZ MoFe蛋白的结构和功能特性,我们对△nifZ MoFe蛋白的晶体生长进行了研究,通过对沉淀剂浓度、缓冲体系和pH、蛋白浓度以及温度等条件的不断优化组合,目前我们已获得棕色短斜四棱柱形△nifZ MoFe蛋白的最大晶体为0.15 * 0.09mm。 二、 MoFe(C,O)与含Mo、Mn和Cr重组液重组的比较研究 MoFe(R)经O_2和o-phen共同处理后,成为部分缺失FeMoco和P-cluster的不全蛋白(MoFe(C,O)),其C_2H_2还原活性降至MoFe(R)的40%左右,将其分别与含Mo、Cr和Mn的重组液进行保温重组,其C_2H_2还原活性及光谱学特征都得到明显恢复。通过对不同重组液及与MoFe(C,O)形成的重组蛋白的比较,我们认为:1)MoFe(R)中的Fe和Mo原子可能是逐步被鳌合除去的,且不同蛋白中的Fe和Mo原子的缺失程度不同,因而MoFe(C,O)会以多种状态存在;2)在重组液配制过程中,发生的一系列颜色变化及沉淀反应与其是否具有重组激活能力具有相关性,重组液中可能已合成一些简单的含M(M=Mo或Cr或Mn或V)的铁硫化物,但不可能形成完整的金属原子簇;3)含M(M=Mo或Cr或Mn)的重组液均能使MoFe(C,O)中遭到破坏的FeMoco和P-cluster及其连接部分得以重新组装和修复,进而恢复其底物还原活性和光谱学特征。 三、 含锰固氮酶的初步探索 棕色固氮菌突变种UW_3(nifH~-)不能在含钼的培养中固氮生长,但能在含MnSO_4的无氮培养基中固氮生长。用含MnSO_4的无钼无氮培养基培养该突变种从中纯化得到的固氮酶组分1蛋白,其C_2H_2及H~+还原活性约相当于MoFe(R)的20%左右,Mn元素含量测定表明,其中已经含有Mn元素,Fe/Mn比值比OP MoFe蛋白中的Fe/Mo低。这些结果表明:UW_3突变种在该种条件下可能已表达了不同于已发现的三种固氮酶的新的固氮酶组分1蛋白,并且其中含有Mn元素。

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克隆得到 2种缘毛类纤毛虫———钟形钟虫 (Vorticellacampanula)和螅状独缩虫 (Carchesiumpolyp inum)的胞质Hsp70基因部分序列 ,长度均为 4 38bp ,编码 14 6个氨基酸。以细菌为外类群 ,利用最大似然法和邻接法构建包括其他 5种纤毛虫在内的共 2 6个物种的Hsp70基因氨基酸序列系统发育树 ,其拓扑结构显示 :V campanula和C polypinum聚在一起 ,并与另 2种寡膜纲的嗜热四膜虫 (Tetrahymenathermophila)及草

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本文以冶炼厂和张士灌区土壤为修复对象,以镉、铅、锌、铜为目标污染物,在室内模拟实验条件下,利用自养菌-嗜酸性氧化亚铁硫杆菌和异养菌-黑曲霉淋滤技术修复重金属污染土壤。在考察自养菌和异养菌对重金属污染土壤修复效果的基础上,重点研究了溶解性有机质和耐酸性异养菌对淋滤修复的影响和机制,同时筛选确定替代蔗糖黑曲霉发酵产酸的廉价碳源。结果发现: 自养菌-氧化亚铁硫杆菌淋滤修复过程中,筛选鉴定嗜酸性氧化亚铁硫杆菌R2对甲酸、乙酸、丙酸、草酸、苹果酸和柠檬酸的耐受浓度分别为0.1、0.4、0.4、2.0、20和40 mmol/L,而高效液相色谱测定沈阳冶炼厂土壤和张士灌区土壤中低分子量有机酸浓度很低,其中草酸含量最高,分别仅为0.04mmol/L和0.149mmol/L,远低于氧化亚铁硫杆菌能耐受的有机酸浓度。同时土壤中溶解性有机质对氧化亚铁硫杆菌R2氧化Fe2+未产生抑制作用,而耐酸性异养微生物H1(红酵母菌)和H2(头孢霉)的加入对氧化亚铁硫杆菌R2淋滤去除重金属效果未产生明显促进作用,本研究中分离筛选的嗜酸性氧化亚铁硫杆菌R2可直接应用于污染土壤的生物淋滤修复。经过5d的生物淋滤,冶炼厂土壤中Cu、Zn和Cd的最高去除率分别为30.6%、58.4%和72%。 在一步黑曲霉生物淋滤过程中,当固液比5%(w/v)、接种量3%(v/v)和淋滤修复7d时,对冶炼厂土壤来说,Cu、Cd、Pb和Zn去除率分别为75.8%,100%,30.6%和26.1%;张士灌区土壤中分别为54%,71.8%,9.5%,18.7%。在二步黑曲霉生物淋滤过程中,当固液比10%(w/v)、接种量为2%(v/v)和黑曲霉发酵时间7d,淋滤2d时,冶炼厂土壤中四种重金属去除率分别为Cu 84%,Cd 75.5%,Pb30.5%和Zn10%;张士灌区土壤中Cu、Cd、Pb和Zn的去除率分别达到57%,94.8%,20.4%和17.5%。 异养菌-黑曲霉淋滤修复重金属污染土壤效果优于有机酸淋滤。与黑曲霉淋滤相比,在直接添加有机酸淋滤修复中,冶炼厂土壤中重金属去除率分别为Cu 46.4%,Cd 61.8%,Pb 30.2%和Zn 43.3%,张士灌区土壤中重金属去除率分别为Cu 44%,Cd 0%,Pb 0%和Zn 26.2%。 淋滤前后土壤中重金属形态分级结果表明,黑曲霉一步和二步淋滤修复能有效去除污染土壤中交换态、碳酸盐结合态部分重金属,并能显著降低氧化物结合态部分重金属,但对有机态和残余态部分重金属离子去除效果并不明显。 以树木落叶和农作物副产品作为廉价碳源实施黑曲霉淋滤实验表明:杨树叶、桃树叶、土豆皮和玉米芯产酸和去除重金属效果较好。杨树叶对冶炼厂土壤中重金属去除率分别为63.5% Cu、100% Cd、16.8% Pb和Zn 27%;桃树叶去除效果分别为Cu61.8%、Cd100%、14.6%Pb和28.5%Zn;土豆皮去除效果分别为61%Cu、100%Cd、10.6%Pb和34%Zn。这些廉价碳源的利用可降低污染土壤生物淋滤修复成本。 研究生物淋滤修复技术为重金属污染土壤处理与处置开辟了新途径。

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An organic integrated pixel with organic light-emitting diodes (OLEDs) driven by organic thin film transistors (OTFTs) is fabricated by a greatly simplified processing. The OTFTs are based on copper phthalocyanine as the active medium and fabricated on indium-tin-oxide (ITO) glass with top-gate structure, thus an organic integrated pixel is easily made by integrating OLED with OTFT. The OTFTs show field-effect mobility of 0.4 cm(2) /Vs and on/off ratio of 10(3) order. The OLED is driven well and emits the brightness as large as 2100cd/m(2) at a current density of 14.6 mu A/cm(2) at -19.7 V gate voltage. This simple device structure is promising in the future large-area flexible OLED displays.

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In this contribution, we for the first time report the synthesis of raspberry-like hierarchical Au/Pt nanoparticle (NP) assembling hollow spheres (RHAHS) with pore structure and complex morphology through one in situ sacrificial template approach without any post-treatment procedure. This method has some clear advantages including simplicity, quickness, high quality, good reproducibility, and no need of a complex post-treatment process (removing templating). Furthermore, the present method could be extended to other metal-based NP assembling hollow spheres. Most importantly, the as-prepared RHAHS exhibited excellent electrocatalytic activity for oxygen reduction reaction (ORR). For instance, the present RHAHS-modified electrode exhibited more positive potential (the half-wave potential at about 0.6 V), higher specific activity, and higher mass activity for ORR than that of commercial platinum black (CPB). Rotating ring-disk electrode (RRDE) voltarnmetry demonstrated that the RHAHS-modified electrode could almost catalyze a four-electron reduction of O-2 to H2O in a 0.5 M air-saturated H2SO4 solution.

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In this study, electrode responses to a large number of electroactive species with different standard potentials at the molybdenum oxide-modified carbon fibre microdisk array (CFMA) electrode were investigated. The results demonstrated that the electrochemical behavior for those redox species with formal potentials more positive than similar to 0.0 V at the molybdenum oxide-modified CFMA electrode were affected by the range and direction of the potential scan, which were different from that at a bare CFMA electrode. If the lower limit of the potential scan was more positive than the reduction potential of the molybdenum oxide film, neither the oxidation nor the reduction peaks of the redox species tested could be observed. This indicates that electron transfer between the molybdenum oxide film on the electrode and the electroactive species in solution is blocked due to the existence of a high resistance between the film and electrolyte in these potential ranges. If the lower limit of the potential scan was more negative than the reduction potential of the molybdenum oxide film (similar to - 0.6 V), the oxidation peaks of these species occurred at the potentials near their formal potentials. In addition, the electrochemical behavior of these redox species at the molybdenum oxide-modified CFMA electrode showed a diffusionless electron transfer process. On the other hand, the redox species with formal potentials more negative than similar to - 0.2 V showed similar reversible voltammetric behaviors at both the molybdenum oxide-modified CFMA electrode and the bare electrode. This can be explained by the structure changes of the film before and after reduction of the film. In addition we also observed that the peak currents of some redox species at the modified electrode were much larger than those at a bare electrode under the same conditions, which has been explained by the interaction between these redox species and the reduction state of the molybdenum oxide film. (C) 2000 Elsevier Science Ltd. All rights reserved.

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系统地综述了压力 -温度 -体积 ( p- V- T)性质在高聚物及其共混物中的应用 ,展示了 p- V- T在研究高聚物实际应用中的重要作用

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A sample of the marine brown alga D. divaricata collected off the coast of Yantai (P. R. China) was dried, powdered, and extracted with the mixture of CHCl3 and MeOH (1: 1, v/v). By a combination of silica gel and Sephadex LH-20 column chromatography and preparative TLC, a new cadinane sesquiterpene 1,4-epoxymuurolan-5 beta-ol (1) was isolated from this species. Its structure was established by detailed MS and NMR spectroscopic analysis, as well as comparison with literature data.

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采用物理图象鲜明,而数学处理简捷、严格的方法导出用内聚力场和附着力场分布来表示的表面张力、附着层张力和固-液接触角公式,并指出传统的润湿性判据的错误根源.

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全书以命令行方式通过大量教学实例和工程应用实例,介绍了建立模型、求解和结果后处理的全过程。

目 录

前言

第1篇教学实例篇

第1章简单拉压杆结构

1.1铰接杆在外力作用下的变形

1.2人字形屋架的静力分析

1.3超静定拉压杆的反力计算

1.4平行杆件与刚性梁连接的热应力问题

1.5端部有间隙的杆的热膨胀

第2章梁的弯曲问题

2.1等截面简单超静定梁的平面弯曲分析

2.2工字形截面外伸梁的平面弯曲

2.3矩形截面梁的纵横弯曲分析

2.4悬臂梁的双向弯曲

2.5 圆形截面悬臂杆的弯扭组合变形

2.6悬臂等强度梁的弯曲

2.7弹性地基半无限长梁在端部力和力偶作用下的变形

2.8偏心受压杆的大变形分析

第3章杆系稳定性计算

3.1利用梁单元计算压杆稳定性

3.2利用实体单元计算压杆稳定性

3.3悬臂压杆的过曲屈分析

3.4平面钢架的平面外失稳

第4章实体模型应力分析

4.1 均布荷载作用下深梁的变形和应力

4.2一对集中力作用下的圆环

4.3用实体单元分析变截面杆的拉伸

4.4用二维实体单元分析等截面悬臂梁的平面弯曲

4.5变截面悬臂梁在端部集中力作用下的平面静力分析

4.6纯弯曲悬臂曲梁的二维静力分析

4.7端部集中力作用的悬臂圆环曲梁平面弯曲的三维分析

4.8均匀拉力作用下含圆孔板的孔边应力集中

4.9两端固定的厚壁管道在自重作用下的变形和应力

第5章膜和薄壳问题

5.1含椭圆孔的椭圆薄膜在外部张力作用下的静力分析

5.2圆形薄膜大变形静力分析

5.3柱形容器在内压作用下的静力分析

5.4圆柱形薄壳在均匀内压作用下的静力分析

第6章板的弯曲和壳体计算

6.1简支和固支圆板的在不同荷载作用下的弯曲

6.2悬臂长板的大挠度弯曲

6.3用壳体单元分析受均布荷载作用的固支圆板大挠度弯曲

6.4利用拉伸操作建立膨胀弯管模型

6.5两端简支开口柱壳在自重作用下的静力分析

6.6圆筒在一对横向集中力作用下的变形

6.7两边简支开口柱壳在集中力作用下的大变形曲屈

第7章简单振动系统

7.1单自由度弹簧质量系统的频率计算

7.2悬索自由振动的频率

7.3用弹簧单元连接的圆盘的扭转振动

7.4圆杆连接圆盘的扭转振动

7.5钻杆的扭转自由振动

第8章梁的振动分析

8.1简支梁的自振频率计算

8.2 自由―自由梁的纵向自由振动

8.3有轴向压力作用的简支梁的自由振动

8.4用壳体单元计算悬臂等强度梁的自由振动

8.5矩形截面薄壁悬臂梁的自由振动

第9章膜板和实体振动

9.1 圆形张紧薄膜的自由振动

9.2薄膜二维非轴对称自由振动分析

9.3薄膜三维非轴对称振动分析

9.4悬臂长板的自由振动频率

9.5悬臂宽板的模态分析

9.6固支圆板的自由振动

9.7用实体单元分析圆环的振动

9.8机翼模型的振动分析

第1 0章平面建模分析和三维实体建模

10.1 带三个圆孔的平面支座分析

10.2角支座应力分析

10.3 体斜支座的实体建模

10.4四分之一车轮的实体建模

10.5轴承支座的实体建模

第1 1章最优化设计

11.1概述

11.2最优化问题框架

11.3 ANSYS优化设计流程

11.4变截面悬臂梁的外形形状优化

11.5平面刚架的优化设计

第12章层合板和断裂力学

12.1 四边简支方形层合板在均布外载作用下的变形

12.2均布拉力作用下含裂纹板的应力强度因子计算

第2篇工程应用篇

第13章用APDL实现空间网壳结构参数化建模

13.1 K系列球面网壳结构的特点和建模

13.1.1 K系列球面网壳的特点

13.1.2几何描述

13.1.3杆件连接关系

13.2参数化设计语言APDL介绍

13.2.1参数和表达式

13.2.2 ANSYS 中的基本指令

13.2.3分支和循环

13.3用户界面设计语言UIDL介绍

13.3.1 单行参数输入

13.3.2多行参数输入

13.4网壳建模程序设计

13.4.1模型建立的步骤

13.4.2节点坐标计算

13.4.3单元连接

13.4.4变量说明

13.4.5节点坐标计算公式

13.4.6主框图说明

13.4.7单元连接关系定义

13.4.8源程序

13.5程序使用说明

13.5.1加载程序

13.5.2界面说明

13.5.3注意事项

13.6应用举例

13.6.1基本参数

13.6.2输入数据并生成模型

13.6.3输入单元参数和荷载后开始计算

13.6.4选择结果输出方式

第14章塔式起重机静动力分析

14.1塔式起重机基本概念

14.2塔式起重机拓扑模型

14.3塔机模型受力分析

14.3.1部件受力特征分析

14.3.2截面参数定义

14.3.3自重荷载和配重

14.3.4选用合适的分析模型。

14.3.5 固定塔身底部的4个节点

14.4塔机建模程序设计

14.4.1塔身节点计算和单元连接

14.4.2塔顶建模

14.4.3塔臂建模

14.4.4平衡臂和斜拉索建模

14.5塔机静力分析

14.6塔机模态分析

14.7塔机静动力分析程序

第15章长柱形天然气罐在内压作用下的静力分析

15.1概述

15.2建立模型

15.3利用轴对称壳单元SHELL51计算

15.3.1单元基本性质和约定

15.3.2求解过程

15.3.3源程序

15.3.4计算结果

15.3.5简体部分理论解

15.3.6结果讨论

15.4利用8节点2D实体单元PLANE82单元计算

15.4.1建立模型

15.4.2计算过程

15.4.3计算结果及讨论

15.4.4源程序

15.5用20节点3D实体单元solid95计算1/4模型

15.5.1建立1/4三维模型

15.5.2计算步骤

15.5.3计算结果分析

15.5.4与弹性力学解答的对比

15.5.5计算程序

附录

附录A常用结构单元参考

附录B结构分析命令速查

参考文献

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Using an unperturbed scattering theory, the characteristics of H atom photoionization are studied respectively by a linearly- and by a circularly- polarized one-cycle laser pulse sequence. The asymmetry for photoelectrons in two directions opposite to each other is investigated. It is found that the asymmetry degree varies with the carrier-envelope (CE) phase, laser intensity, as well as the kinetic energy of photoelectrons. For the linear polarization, the maximal ionization rate varies with the CE phase, and the asymmetry degree varies with the CE phase in a sine-like pattern. For the circular polarization, the maximal ionization rate keeps constant for various CE phases, but the variation of asymmetry degree is still in a sine-like pattern.