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氘化

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Absorption velocity increases with initial pressure, and keeps constant at different initial composition of uranium deuteride .

增加混合气体的初始压力有利于铀吸氘速率的增加,氘化铀的初始氘量不影响铀的吸氘速率。

Deuterium containing helium absorption of unsaturated uranium deuteride with different composition at varied initial pressure is studied.

研究了不同含氦量的混合气体、吸氘初始压力以及不同组成的不饱和氘化铀对铀吸氘行为的影响。

The deuterium desorption behavior of titanium deuteride with oxide layer on the surface in a constant volume system was investigated in the temperature range of 873 to

测定了3种不同氧化层厚度的氘化钛在873~1073K范围内的热解吸反应速率常数,得到673K下氧化5、2h的氘化钛和未经氧化处理的氘化钛热解吸氘的活化能分别为29。

The deuterium thermal desorption behavior of titanium deuteride with or without anodic oxide layer on the surface in a constant volume system has been investigated in the temperature range of 600℃ to 800℃.

应用反应速率分析方法,测定了氘化钛和表面有阳极氧化层的氘化钛在恒容体系和600-800℃范围内的热解吸反应速率常数,得到氘化钛和阳极氧化的氘化钛热解吸氘的活化能分别为24。

Results show that deuterium absorption quantity and velocity decrease with helium content increase. Absorption velocity increases with initial pressure, and keeps constant at different initial composition of uranium deuteride.

结果表明,氦含量的增加会显著减少铀的吸氘量,降低铀的吸氘速率;增加混合气体的初始压力有利于铀吸氘速率的增加,氘化铀的初始氘量不影响铀的吸氘速率。

P-t curves of titanium hydride and titanium deuteride desorbing hydrogen and deuterium are investigated at 350~550 ℃ by using the method of reaction rate analysis in a constant volume system.

在高真空金属系统上测定了氢化钛和氘化钛在恒容体系中、350~550℃温度下热解吸氢和氘的P-t曲线;应用反应速率分析方法计算了各自在不同温度下的反应速率常数,得到氢化钛和氘化钛热解吸的表观活化能分别为27。

The rate-controlling steps of deuterating and dedeuterating reaction in α+β region are assumed to the nucleation-growth and diffusion in deuterium of deuteride respectively.

在α+β相域,氘化与去氘化反应的速控步骤分别为氘化物的成核-长大过程和氘化物中氘的扩散过程。

Kinetics parameters of LaNi5-xAlx (x=0, 0.1, 0.2, 0.3) alloys were measured. The influence of aluminium content on deuterating-dedeuterating kinetic function of LaNi5-xAlx was assessed under isothermal and isochoric condition.

测定了LaNi5-xAlx(x=0, 0.1, 0.2, 0.3)的氘化与去氘化的动力学参数,评价了铝含量对LaNi5-xAlx合金的氘化与去氘化动力学函数的影响。

For a deep understanding of electron screening effects, the DT reaction has been studied in a series of deuterated metal-, insulator- and semiconductor targets using the 100 kV accelerator of the Dynamitron-Tandem-Laboratorium at the Ruhr-University-Bochum.

为深入了解电子屏蔽效应的机制,在鲁尔大学DTL实验室100kV加速器上采用一系列氘化金属靶、氘化绝缘体靶和氘化半导体靶进行了DT反应的研究。

The results show that x does not change deuterating-dedeuterating reaction order. Activation energy increases while the rate constant decreases with x increasing. Deuterating and dedeuterating reaction order a (with respect to deutertium pressure) and b (with respect to deuterium content) are 2 and 1, 0.5 and 1, respectively.

研究结果表明,铝含量不改变合金的氘化与去氘化的反应级数;反应速率常数随x的增加而减少;活化能随x的增加而增加;氘化与去氘化反应级数 a和 b 分别为2和1及0.5和1。

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