脉冲条件下ITER HCCB TBS动态氚输运分析

在ITER脉冲运行条件下对中国氦冷固态增殖剂实验包层系统(HCCB TBS)动态氚输运进行了分析,利用Modelica语言开发了一套动态氚分析程序.对比了在脉冲运行工况及连续运行工况下TBS流体中的氚浓度和分压的动态变化、固体材料中氚盘存量的动态变化以及氚渗透通量的动态变化.脉冲运行下TBS系统氚变化趋势与物理分析结果...     

基于运行反馈的压水堆氚排放量研究北大核心CSCD

以压水堆核电厂中氚的产生机理和氚源项计算模型为基础,结合对国内外大量压水堆核电厂的氚排放运行数据的系统性分析,识别出冷却剂硼酸活化和次级中子源活化是压水堆氚排放量的主要来源,其中对中国广核集团运行机组,锑铍中子活化后的产氚量对氚年排放量的贡献可达到40%,而氚从完整的锆合金包壳的燃料棒中的释放是可以忽略不计的。由于优化次级中子源是降低压水堆氚排放量的唯一有效措施,通过分析建议压水堆核电厂采用双层不锈钢包壳的次级中子源或者取消次级中子源以降低压水堆氚排放。     

LiAlO_2陶瓷小球的堆外放氚行为

将LiAlO2陶瓷小球置于裂变反应堆中辐照,采用热解吸技术研究该类产氚材料的堆外放氚特性,考察了升温速率、载气组分、催化活性元素和提氚温度对氚释放行为的影响;采用电子自旋磁共振(ESR)实验技术研究了辐照缺陷的顺磁特征。结果表明:LiAlO2中氚的扩散速度慢,热解吸活化能高,氚释放主要分布在750~1000K;表面氢同位素交换反应贡献大,释氚形态受载气条件的影响较大,当氦气中添加H2时,会增大HTO转化成HT的比例;中子辐照会在LiAlO2中诱生F+,O-和O2-等缺陷色心,其退火湮灭行为与氚释放过程存在一定关系。     

Pd-Ag膜电解浓缩氚的动力学模型及理论计算

建立了模拟Pd-Ag合金膜电解浓缩氚的过程和诸多电解参数的动力学模型。采用求解数学扩散方程的方法得到理论值,并与文献报道的实验数据进行比较。计算结果表明：氚在Pd-Ag膜上的吸附、解吸、浓缩等行为受到诸多条件的制约。在保证密封性能的前提下,对Pd-Ag膜电解槽体的要求是至少应包括有含氚水路循环、阳极气体消除和阴极扩散后氚再生3个组成部分,采取相匹配的级联技术可以提高分离效果;对电解参数的要求是采取尽可能高的电解液温度和稳定的OH^-浓度,合适的电流密度,合理的膜厚度、表面特征和Pd黑结合紧密。     

化学链燃烧中Fe氧化过程产物层生长特性

利用TGA、SEM研究了化学链燃烧中Fe氧化反应过程产物层的生长机理,以及产物层形貌对化学反应动力学的影响。考虑了不同的反应条件,包括氧化时间、反应温度、O_2浓度的影响。实验结果表明,氧化产物呈三维岛状生长,反应初期产物岛较小但密度较大,随着反应的进行,产物岛不断长大,但密度先减小后增加;温度及O_2浓度对产物层生长均有影响。产物岛的成核与生长改变了产物层的表观形貌,减小了表观反应速率。     

CLAM钢表面Fe-Al合金渗层的制备

FeAl/Al2O3阻氚涂层具有高阻氚因子、耐腐蚀和耐高温等优良性能,是ITER首选的阻氚涂层.Fe-Al合金渗层对Al2O3膜层的形成质量有重要的影响.本文采用了AlCl3-EMIC离子液体电镀法在CLAM钢表面镀铝,然后利用热处理使Al与基体相互扩散制备Fe-Al合金渗层.采用X射线衍射仪、扫描电子显微镜和能量散射...     

陶瓷—金属复合体系氢同位素渗透模型

在陶瓷（玻璃或氧化物）材料中氢同位素分子扩散的１次方定律和金属材料中原子扩散的１／２次方定律的基础上建立了双层介质扩散模型，推导出氢浓度分布函数，镀膜复合体的氢渗透速率以及渗透速率对驱动氢压的幂指数表达式，讨论了稳态氢渗透速率随膜厚，测量温度，驱动氢压变化的规律，根据实验测量的镀膜复合体的渗透速率，稳态渗透速率对驱动氢压依赖关系的幂指数大小，得以了膜材本身的渗透，扩散，溶解等热力学参数，同时估算了     

LaNi4．25Al0．75合金吸放氚性能

在真空系统中对熔融法制备的LaNi4.25Al0.75合金的氘活化特性、吸放氚p-C-T曲线和不同温度下的吸放氚速率，以及材料吸附氚气与解析氚气的纯度进行了研究，以考核该合金氚操作与贮存性能。     

矩形管道载氚热磁流体输运特性的数值模拟研究

聚变堆液态金属包层矩形管道中的氚输运过程与磁流体动力学(MHD)流动传热过程耦合在一起，形成了复杂的载氚热磁流体输运特性。基于开发的MHD流动与传热数值模拟程序对矩形管道中液态金属MHD流动传热特性及其氚输运的影响进行了数值模拟。该程序首先求解了动量守恒方程，并与理论解进行了对比验证，然后与能量守恒方程耦合求解，得到了温度影响下矩形管道中的液态金属流场分布，在此基础上对强磁场高核热梯度影响下的氚浓度分布进行了数值模拟，得到了氚浓度在管道中的分布特性。结果显示，液态金属在矩形管道中的流动传热对氚输运过程产生了显著影响。     

NBT导致的深亚微米PMOS器件退化与物理机理

研究了深亚微米PMOS器件在负偏压温度(negative bias temperature, NBT) 应力前后的电流电压特性随应力时间的退化，重点分析了NBT应力对PMOS器件阈值电压漂移的影响，通过实验证明了在栅氧化层和衬底界面附近的电化学反应和栅氧化层内与氢相关的元素的扩散，是PMOS器件中NBT效应产生的主要原因.指出NBT导致的PMOS器件退化依赖于反应机理和扩散机理两种机理的平衡. 关键词： 深亚微米PMOS器件 负偏压温度不稳定性 界面态 氧化层固定正电荷     

Modeling of diffusion and absorption processes of tritium in beryllium membranes

The permeation of tritium produced in thermonuclear fusion through metallic membranes, which is a topical problem in radiation physics, is addressed. A physical model for the permeation of hydrogen through a beryllium membrane is proposed which takes into account the oxide layer on the surface of the membrane. The model is implemented in the form of a system of differential equations, which is solved by numerical methods. As a result of the computer modeling it is shown that as the temperature is raised, the oxide layer in a certain interval blocks the permeation of tritium in the membrane, and it is found that the tritium is distributed in a rather limited region of the membrane over its thickness. This circumstance will permit the use of special processing by etching or mechanical treatment. Zh. Tekh. Fiz. 69, 38–41 (July 1999) Deceased     

Adsorption behaviour of NaCl solution on the surface of MgO: a molecular dynamics study

Magnesium alloy is one of the most promising biomaterials in vascular clogging and bone injury. But it still has some defects to overcome and the key task is to control the degradation velocity. In this study, the reaction between NaCl solution and MgO is simplified as the first stage of the degradation of magnesium alloy stent, and the adsorption properties of NaCl solution on the MgO surface are investigated by MD simulation. The distribution of each component of the solution perpendicular to the MgO surface is analysed and the diffusion coefficient is calculated. Besides, a parameterised analysis is carried out. The results show that there is a solution layer formed at the surface of the MgO, and the existence of metal oxide restricts the diffusion of the solution. The adsorption capacity and the diffuse rate have an opposite variation tendency with the change of temperature, concentration and velocity. The self-diffusion coefficient of the solution increases with the increase in temperature as well as velocity, inversely adsorption capacity decreases with the increase in velocity. Besides, the influence of temperature on the adsorption capacity is small. What is more, the diffusion coefficient decreases while the adsorption capacity increases with the increase in concentration.     

CFETR氦冷固态增殖包层多物理场氚输运分析

针对中国聚变工程实验堆(CFETR)外中平面氦冷固态增殖包层模块,开展了包层热、流、氚的多物理场耦合模拟分析,获得包层模块的氚分布、氚滞留量及氚渗透量。分析结果显示,在包层球床区无因吹洗气体流动滞缓而造成的氚滞留现象,其吹洗气体流道设计合理。同时,开展了入口吹洗气体掺氢量的参数敏感性分析。分析显示吹洗气体掺氢可以降低材料表面氚浓度,从而降低结构材料中的氚浓度梯度,抑制氚渗透;入口氢气浓度从 1ppm 增加到 1000ppm 时,氚渗透量降低为 1/20。     

Possibility of Using a Multilayer Target to Reduce Losses of Tritium in a Neutron Tube

The ability of yttria layers to act as barriers to hydrogen desorption is studied. The possibility is discussed of using these layers to reduce losses of tritium from a neutron tube target. The composition of a multilayer target in which tritium desorption is reduced by an accumulator layer (zirconium) and barrier layers (yttria) is described. It is shown that deuterium losses observed in thermal desorption tests over 4 h at 623 K fell by 85–87%. A system is proposed for the renewal of an external barrier layer subjected to sputtering by a deuteron ion flux.     

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Based on the design of the 2015 version of China Fusion Engineering Test Reactor (CFETR) water cooled ceramic breeder (WCCB) blanket modules surrounding the plasma, a tritium transport model has been developed. Tritium transport analysis has been carried out for each blanket module with different breeding zones, purge gas loop, coolant loop and steam generator. The results indicate that the concentration, permeability and retention of tritium among blanket modules are different. For all of the WCCB blanket modules in CFETR, the tritium retention inside the breeder is 6.62×10^-2g, the tritium retention inside the structural materials is 2.01g, the tritium retention inside purge gas and coolant loop are 4.03×10^-4g and 0.19g respectively, the tritium permeation through the steam generator tube walls is 20mg•y^-1, the tritium permeation from the coolant pipes is 0.1mg•y^-1.     

Enhanced fatigue performance of porous coated Ti6Al4V biomedical alloy

Biofunctional coatings are necessary to improve integration of titanium implants in the host tissue but they may be detrimental for the implant fatigue properties. This study presents an attempt towards enhancement of the in vitro fatigue strength of plasma electrolytic oxidation coated Ti6Al4V alloy by applying shot peening process prior to coating. The electrolytic oxidation was performed in calcium acetate and calcium glycerophosphate electrolytes that allowed formation of porous oxide coatings with high surface free energy and apatite like ability. A deformed surface layer coupled with induced residual compressive stresses seem to affect oxide growth rate and fatigue behavior of the titanium alloy.     

Surface effect on oxygen permeation through dense membrane of mixed-conductive LSCF perovskite-type oxide

La_0.1Sr_0.9Co_0.9Fe_0.1O_3−δ (LSCF1991) dense disks with different thicknesses and surface areas were prepared to investigate the contribution of surface reactions and bulk diffusion in oxygen permeation phenomena. The bulk diffusion controlled situation became significant with increasing the membrane thickness, and the surface reaction controlled situation prevailed at smaller surface area. The increase in surface area at the low P(O₂) (anode) side was more effective to increase the oxygen permeation flux than that at the high P(O₂) (cathode) side. The coating of a porous catalyst layer below the optimum thickness was also effective in enhancing the oxygen permeability due to the increase in surface area, but the coating with too thick layer deteriorated the permeability probably due to the increase in the gas diffusion resistance.     

Improvement of hot-dip zinc coating by enriching the inner layers with iron oxide

The performance of hot-dip galvanic coating formed on steel not only depends on the alloy composition of the superficial layer but also significantly, on the composition of the inner alloy layers at the coating/substrate interface. Further, the presence of barrier oxide layers, if any can also improve the performance of galvanic coating. In the present work, the effect of inner iron oxide barrier layer formed prior to hot-dip galvanization was investigated. A continuous and adherent iron oxide layer was formed on steel by anodic oxidation of the steel substrate. Although the wettability of oxide surface by liquid zinc was initially poor, the increase in dipping time and the transition of the oxide layer to unstable form due to the presence of Cl⁻ ion in the flux facilitated localized growth of Fe-Zn alloy phases. The inhibitive nature of the oxide layer was temporary, since the presence of Cl⁻ induces micro cracks on the oxide surface thereby facilitating better zinc diffusion. The modification of the substrate structure during galvanization was found to influence the galvanizing process significantly. The present study predicts scope for application of this process for protection of rusted steel specimens too.     

Roughness simulation for thin films prepared by atomic layer deposition

The kinetic lattice Monte Carlo method for film growth simulation without taking crystallization into account was applied to study the roughness of the HfO₂ film grown by atomic layer deposition at 100–500°C from HfCl₄ and H₂O. The calculations were performed using a simplified kinetic mechanism of the growth of HfO₂ films obtained by reducing the detailed kinetic mechanism developed earlier. Ab initio quantum-chemical calculations were performed to determine the kinetic parameters of diffusion processes on the surface of hafnium oxide that could influence film roughness. Because of the special features of atomic layer deposition, the rate of film growth and film roughness were finite even if surface relaxation was ignored. It was found that, irrespective of the temperature, the diffusion of hydrogen and adsorbed HfCl₄ complexes did not change the profile of the growing film and only insignificantly increased the mean rate of growth. The results obtained were also qualitatively applicable to zirconium dioxide at fairly low (≤100°C) temperatures in the absence of crystallization.