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Matsushita Carbon Resistors as Thermometers for Use at Low Temperatures and in High Fields(Physics) 松下碳电阻在低温和高磁场中用作温度计(物理)
S. Saito, Takashi Sato
A survey has been made of the properties of 1/8 W composite resistors made by the Matsushita Electric Ind. Co. Ltd. to determine whether they might be suitable as secondary thermometers in the low‐temperature region. From the measurements of resistance vs temperature, between 105 °C and 40 mK, it is confirmed that the grade ERC‐18SGJ resistors in various nominal room‐temperature resistance values from 20 to 510 Ω are suitable in very low ‐temperature work, and that resistors in the nominal resistance range 20–100 Ω are the most suitable for work down to several tens of mK. An advantage of Matsushita resistors as thermometers in the low‐temperature region is that they are available in 1/8 W size, and we can choose their nominal resistances from 10 Ω to several hundreds of ohms in steps of a few ohms. The magnetoresistance of Matsushita resistors having nominal resistances of 30 to 510 Ω has been measured in fields up to about 80 kG at temperatures between ∼4.2 and ∼1.5 K. It is shown that the percentage ch...
对松下电器有限公司生产的1/ 8w复合电阻器的性能进行了调查,以确定它们是否适合作为低温地区的二次温度计。测量的电阻与温度、105°C到40可,这是证实了年级ERC 18 sgj应承担的房间里各种名义电阻量温度从20到510Ω电阻值适合高工作温度很低,电阻的标称电阻范围20 - 100Ω是最适合工作到几可优势的松下低电阻温度计的温度区域应承担的是他们可以在1/8 W大小,我们可以选择它们的标称电阻从10 Ω到几百欧姆,以几欧姆为步骤。标称电阻为30至510 Ω的松下电阻器的磁电阻已在高达约80 kG的磁场中在~ 4.2至~ 1.5 K之间进行了测量。可以看出……的百分比。
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引用次数: 15
Internal Friction Peaks of Cold-Worked Dilute Copper-Aluminium Alloys(Metallurgy) 冷加工稀释铜铝合金的内摩擦峰(冶金)
M. Koiwa, T. Onozuka, M. Hirabayashi
Abstract The internal friction of cold-worked Cu-Al alloys is measured with an inverted torsion pendulum in the temperature range between − 180°C and + 100°C. Among 10 specimens with different contents of aluminium ranging from 0·01 to 2 at.%, distinct peaks are observed for the two compositions, 0·13 and 0·18 at. % Al, the peak height being larger for the former; detailed studies are made on 0·13 at. % Al specimens. The peak is introduced by plastic deformation and disappears on annealing at temperatures around + 150°C. For a specimen annealed in an oxidizing atmosphere prior to the final deformation, the peak is no longer observed. The peak is considered to be a combined effect of dislocations and aluminium atom-vacancy complexes.
摘要:用倒立摆测量了冷加工Cu-Al合金在- 180 ~ + 100℃温度范围内的内摩擦。在铝含量为0.01 ~ 2 at的10个试样中。%,在0·13和0·18 at两种成分中观察到明显的峰。% Al,前者峰高较大;对0·13 at进行了详细的研究。% Al标本。峰值是由塑性变形引起的,在+ 150℃左右退火时消失。对于在最终变形之前在氧化气氛中退火的试样,不再观察到峰值。该峰被认为是位错和铝原子-空位配合物的共同作用。
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引用次数: 8
Polarity in Bending Deformation in InSb Crystals : II. Theory and Supplementary Experiments(Physics) InSb晶体弯曲变形中的极性:II。理论与辅助实验(物理)
K. Sumino, H. Shimizu
Abstract A geometrical consideration of the configuration of {111} tetrahedra in a bent crystal having the sphalerite structure shows that the type of bending is reversed between the primary slip plane and some of the secondary slip planes. This explains why the secondary slip is activated and the primary slip plane becomes forest-rich in β-bending. Two types of experiments establish the origin of the higher flow stress in β-bending compared with α-bending. It is concluded that the difference in the flow stress between the two types of bending in the deformation stage after the lower yield point originates mainly from the difference in the activity of the secondary slip system, while that in the early stage of deformation originates from the difference in the rate of increase in the density of screw dislocations due to the difference in the mobility between α-dislocations and β-dislocations moving on the primary slip plane.
对具有闪锌矿结构的弯曲晶体中{111}四面体的几何形态进行了研究,结果表明,弯曲类型在主要滑移面和某些次要滑移面之间是相反的。这就解释了为什么次级滑动被激活,而初级滑动面在β弯曲中变得富含森林。两种类型的实验建立了β-弯曲比α-弯曲更高的流动应力的来源。结果表明:低屈服点后变形阶段两种弯曲的流变应力差异主要源于次级滑移体系活动性的差异,而变形早期则是由于α-位错与β-位错在初级滑移面上的迁移率不同导致螺位错密度的增加速率差异。
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引用次数: 15
Polarity in Bending Deformation of InSb Crystals : I. Experiments(Physics) InSb晶体弯曲变形中的极性:1 .实验(物理)
H. Shimizu, K. Sumino
Deformation characteristics of InSb crystals subjected to α-bending or β-bending are observed as a function of the strain rate and the temperature. Difference in the characteristics between the two types of bending is demonstrated. Higher flow stresses are observed in β-bending as compared with α-bending. No difference is found between the two types of bending in the magnitudes of parameters which characterize the strain rate and the temperature sensitivities of the yield stresses. Observations on slip bands as well as those of dislocation etch-pits show that dislocations on the secondary slip system are activated in β-bending. It is suggested that this is the cause of the observed higher flow stresses. It is shown that the motion of screw dislocations of the primary slip system controls the deformation rate in both types of bending.
观察了InSb晶体α-弯曲和β-弯曲变形特性与应变速率和温度的关系。论证了两种弯曲形式在特性上的差异。与α-弯曲相比,β-弯曲的流变应力更高。两种类型的弯曲在表征应变速率和屈服应力的温度敏感性的参数的大小上没有差异。对滑移带和位错蚀坑的观察表明,二次滑移系统的位错在β-弯曲过程中被激活。这可能是观察到较高流动应力的原因。结果表明,主滑移系统的螺位错运动控制了两种弯曲的变形速率。
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引用次数: 25
Criterion for the Appearance of Critical Attenuation of Shear Waves in Magnetic Materials(Physics) 磁性材料中横波临界衰减的出现准则(物理学)
M. Tachiki, S. Maekawa, R. A. Treder, M. Levy
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引用次数: 8
The Chemistry of Americium : III. The Coprecipitation of Am(III), Am(V), and Am(VI) by Some Fluorides and Phosphates(Chemistry) 镅的化学性质:3。某些氟化物和磷酸盐对Am(III)、Am(V)和Am(VI)的共沉淀(化学)
M. Hara, Shin Suzuki
The radiochemical behavior of americium in the coprecipitation process involving a precipitate such as lanthanum, thorium, and ceric fluorides, zirconium, and bismuth phosphates was investigated at the tracer concentrations of americium. All the precipitates except zirconium phosphate completely carried the Am(III), leaving the Am(VI) in the supernatant. The lanthanum and thorium fluorides carried portions of the Am(V) in proportion to the amounts of the metal ion of the carrier added under any given conditions. Then, the analytical conditions were established for determining the distributions of the oxidation states of americium.
在示踪剂浓度下,研究了镅在共沉淀过程中的放射化学行为,共沉淀包括镧、钍、氟化铈、锆和磷酸铋。除磷酸锆外,其余沉淀物均完全携带Am(III), Am(VI)留在上清液中。在任何给定条件下,氟化镧和氟化钍携带的部分Am(V)与载体中添加的金属离子的量成比例。然后,建立了测定镅氧化态分布的分析条件。
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引用次数: 14
Zeeman Effect of an Induced Absorption Line in Highly Excited CuCl(Physics) 高激发CuCl中诱导吸收线的塞曼效应(物理学)
T. Anzai, T. Goto, M. Ueta
Zeeman effect is studied for a narrow absorption line at 390.89 nm in CuCl crystal induced by a nitrogen laser excitation, the appearance of which was reported previously as a possible evidence for the Bose condensation of excitons. From the Zeeman splitting, it is concluded that this absorption corresponds to the formation of an exciton bound to a transiently generated neutral donor.
研究了氮激光激发下CuCl晶体在390.89 nm处的窄吸收线的塞曼效应,该效应的出现曾被报道为激子玻色凝聚的可能证据。从塞曼分裂,我们得出结论,这种吸收对应于一个激子结合到一个瞬态生成的中性供体的形成。
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引用次数: 12
A General Treatment of the Distribution of Vacancies to Solute Atoms in a Ternary Solid Solution and its Application to Low Temperature Aging in Al-Cu-Sn Alloys(Metallurgy) 三元固溶体中溶质原子空位分布的一般处理及其在Al-Cu-Sn合金低温时效中的应用(冶金)
H. Kimura, R. Hasiguti
A general treatment to calculate the concentration of vacancy-solute atom pairs in a ternary dilute solid solution is presented. This treatment is applicable to a wide range of vacancy concentration relative to the concentration of one kind of solute atoms. The treatment is applied to explain the effect of tin addition on the rates of low temperature aging in Al-Cu alloys. The difference in the activation energy for aging between Al-Cu alloys and an Al-Cu-Sn alloy is analyzed to find the binding energy of a vacancy-tin atom pair to be about 0.3eV larger than that of a vacancy-copper atom pair. The experimental result that the retardation of aging due to tin addition is appreciable only for tin concentrations larger than the vacancy concentration is also explained satisfactorily.
给出了计算三元稀固溶体中空位-溶质原子对浓度的一般处理方法。这种处理方法适用于相对于一种溶质原子浓度的较大空位浓度范围。应用该处理解释了添加锡对Al-Cu合金低温时效速率的影响。分析了Al-Cu合金和Al-Cu- sn合金的时效活化能差异,发现空位-锡原子对的结合能比空位-铜原子对的结合能大0.3eV左右。实验结果表明,只有当锡浓度大于空位浓度时,锡的加入才有明显的延缓老化的作用。
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引用次数: 4
Structure of Liquid Gallium and Rubidium by Pulsed Neutron Diffraction Using Electron Linac(Physics) 用电子直线加速器脉冲中子衍射研究液态镓和铷的结构(物理)
Kenji Suzuki, M. Misawa, Y. Fukushima
The static structure factors of liquid gallium and rubidium were measured at several temperatures above their melting points using the time of flight neutron diffractometer installed on the 300MeV Tohoku University electron linac as a pulsed neutron source. The characteristic oscillation of the structure factor of liquid gallium in a high momentum transfer region has been shown to be well understood in terms of a diatomic molecule-like atomic association with the bond
利用安装在日本东北大学300MeV电子直线加速器上的飞行时间中子衍射仪作为脉冲中子源,测量了液态镓和铷在熔点以上若干温度下的静态结构因子。在高动量传递区,液态镓结构因子的特征振荡已被证明可以很好地理解为双原子类分子原子与键的结合
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引用次数: 9
Plasticity of β-brass Single Crystals at Low Temperatures(Metallurgy) β-黄铜单晶低温塑性研究(冶金)
S. Hanada, M. Mohri, O. Izumi
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引用次数: 29
期刊
Science reports of the Research Institutes, Tohoku University. Ser. A, Physics, chemistry and metallurgy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
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