Development of Bi(Pb)-2223/Ag pancake-shaped and solenoidal coils

High temperature superconducting (HTSC) multifilamentary (MT) Bi(Pb)-2223/Ag tapes with reproducible critical current density of between 15000 and 20000 A/cm² at 77 K in self field have been achieved using the standard flat-rolling method as the intermediate deformation between sintering periods. Long lengths of Bi(Pb)-2223/Ag MT tapes up to 43 m prepared by the conventional method of powder-in-tube (PIT) have been successfully produced on a laboratory scale. Several coils have been fabricated from sections of the long length tape, using the co-wound wind-and-react (W&R) procedure for the pancake-shaped and the singly-wound W&R as well as R&W procedure for the solenoidal coils. A novel W&R solenoidal coil (reaching ~973 ampere-turns) wound on an alumina ceramic tube generates a DC field of ~19 mT at 77 K and has been fabricated together with five pancake-shaped coils, each generating an average of ~5 mT at 77 K. These are destined for magnet construction with a possible combined calculated field of ~0.04 T at 77 K (with liquid nitrogen as a coolant)     

四川盆地中部上三叠统香溪群岩性油气藏圈闭类型及其特征

四川盆地川中地区构造平缓,大型断裂欠发育,已发现的油气藏与背斜关系并不十分密切。研究认为,川中地区香溪群主要发育岩性圈闭,根据圈闭形成主控因素,结合香溪群沉积前的古地貌特征和裂缝发育特点,将川中香溪群岩性圈闭划分为4种类型:①与地层尖灭相关的地层—岩性圈闭;②与沉积—成岩相变密切相关的成岩—岩性圈闭;③与古地貌有关的差异压实作用形成的岩性圈闭;④与断层转化调节相关的裂缝—岩性复合圈闭。其中成岩—岩性圈闭和地层—岩性圈闭,是川中香溪群最重要的、分布最广泛的圈闭类型。     

A force modulation study on crystallization process in ferroelectric vinylidene fluoride and trifluoroethylene copolymer films

This paper introduces the Force Modulation technique to the study of crystallization process in ferroelectric vinylidene fluoride and trifluoroethylene copolymer films. Using this technique we have successfully visualized ferroelectric crystalline domains and observed that these ferroelectric domains grow out from amorphous phase, unite into strip-like structures, and finally congregate into a union. Force Modulation can weaken the influence of topography on imaging of ferroelectric domains, and reveal more details, which are difficult to be observed in topographical image.     

FBOLES—outline of a frequency-based on-line expert system approach for fault diagnoses in nuclear power plants

The basic concept of a novel frequency-based on-line expert system (FBOLES) approach for on-line fault diagnoses in nuclear power plants has been presented previously. This paper reports further progress, and includes how to express the uncertainties of expert opinion in knowledge-bases and propagate then in inferences, and how to deal with imperfect knowledge-bases. It also describes the main elements of FBOLES and outlines how the system works under complex conditions including the dynamic behavior of signals during accidents, multiple failures, and on-line changes of plant operation mode. Its ability to diagnose root causes of accidents has been tested using the main steam and feedwater condensate systems of a full-scale, three-loop, 950 MW nuclear power plant simulated by the Tsinghua simulator. So far the results seem good.     

Synthesis of p‐aminophenol from the hydrogenation of nitrobenzene over metal–solid acid bifunctional catalyst

BACKGROUND: A single‐step conversion of nitrobenzene (NB) to p‐aminophenol (PAP) through catalytic hydrogenation is a widely used synthesis route for PAP. The main shortcoming of this route is the use of sulfuric acid for rearrangement of the phenylhydroxylamine (PHA) intermediate. In this paper, S₂O₈^2?/ZrO₂ (PSZ) solid acid and Pt‐S₂O₈^2?/ZrO₂ (Pt‐PSZ) bifunctional catalysts were prepared for the synthesis of PAP in non‐acid medium. RESULTS: Calcination temperature has a substantial effect on the acidity, structure and activity for PHA rearrangement of PSZ. The highest PAP yield was 33.8% over PSZ calcined at 823 K when the reaction was carried out in water at 423 K. A high PAP yield of 23.9% was achieved by a single‐step reaction of nitrobenzene over Pt‐PSZ bifunctional catalysts. CONCLUSION: PSZ solid acid exhibits high activity for PHA rearrangement. Perfect tetragonal ZrO₂ and much stronger acid sites play important roles in catalytic activity. Inhibiting the hydrogenation activity by reducing the amount of Pt loading on Pt‐PSZ can improve the competition of PHA rearrangement on acid sites with hydrogenation of PHA on metal active sites, resulting in better selectivity to PAP. Copyright © 2008 Society of Chemical Industry     

电子工业用高纯氮的生产

生产电子工业用高纯氮的制氮装置 ,其要点和难点是一氧化碳和氢的清除。采用一氧化碳转换炉和特殊的冷箱内流程组织 ,可以生产纯度为 99 9999%以上的高纯氮。对制取电子工业用高纯氮制氮装置与常规制氮装置加氮终端净化器两种流程进行了比较。     

Modeling Multiterminal Spintronic Devices

We are encountering tremendous opportunities and challenges in combining emerging nanotechnology for developing nanoelectronic devices. Researchers are designing nanoelectronic circuits based on newly discovered nanoscale building blocks, such as spintronic devices. In this paper, we calculate conductance in spintronic gates using the nonequilibrium Green's function and show useful operations for "multiterminal" logic gates. These spintronic devices can be used to design complicated spin circuits     

CO毒化AB5型合金分形特征研究

研究了三种贮氢合金 L a Ni5、L a Ni4 .7Al0 .3、Ml Ni4 .5Al0 .5被 10 0× 10 - 6 CO毒化后的分形特征 ,求出这三种合金在含 10 0× 10 - 6 CO的氢中循环 ,分维分别为 0 .2 5 4 7、0 .170 9、0 .0 72 5。可以较好的解释合金被毒化的宏观现象。     

Self-assembly of highly oriented palladium-based nanowires on mica surface

The self-assembly of various nanostructures is recently attracting a great deal of research attention. In this paper, we demonstrate that a palladium chloride aqueous solution, mixed with a proper ammonia solution, can produce Tetra-amminepalladous chloride (Pd(NH₃)₄Cl₂·H₂O) nanowires. These nanowires can spontaneously form the two-dimensional hexagon-oriented Pd(NH₃)₄Cl₂·H₂O arrays on mica surfaces. We can control the length and height of these nanowires by adjusting their deposit time on the mica substrate. This method can be potentially used in making sensors or in making templates to wire and position nanodevices.     

钾基CO2吸收剂的碳酸化反应特性

对钾基CO2吸收剂的碳酸化反应机理进行研究.利用热重分析、XRD、扫描电镜和氮吸附仪进行试验.结果表明:分析纯碳酸钾的组分为K2CO3·1.5H2O,碳酸化反应速率缓慢;先将分析纯碳酸钾样品脱除结晶水后再进行碳酸化反应时,K2CO3与气氛中的水蒸气迅速生成K2CO3·1.5H2O,不利于碳酸化反应的进行;由KHCO3分解产生的K2CO3却表现出优越的碳酸化反应性能,20 min内转化率高达85%以上,经过多次循环试验后吸收剂仍保持很高的活性.从微观角度分析了两种改性钾基CO2吸收剂碳酸化反应机理差异的原因,通过拟合计算得到了这3种钾基吸收剂的碳酸化反应速率常数,为干法K2CO3/KHCO3循环脱除CO2的研究提供了一定的基础数据.