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thermodynamically相关的网络例句

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After the oxidative polymerization of DMP,styrene was in-situ polymerized under the initiation of dibenzoyl peroxide and dicumyl peroxide,finally thermodynamically compatible PPO/PS alloy was prepared.When styrene content was 50 wt%,for the synthesized PPO/PS alloy the yield and the weight-average molecular weight were determined to be 95%and 1.7×10~5 for PPO,93%and 2.0×10~5 for PS,respectively.The influence of the concentration of DMP and catalyst,molar ratio of N/Cu, oxygen partial pressure,NaOH concentration and temperature on the initial polymerization rate(R_0) of DMP was studied.It was found that the initial polymerization rate of DMP increased with the concentration of DMP and catalyst. The initial polymerization rate increased with the molar ratio of N/Cu at first and then decreased.

通过测定DMP氧化聚合过程中氧气吸收量随时间的变化,研究了DMP和催化剂浓度、N/Cu摩尔比、氧气分压、氢氧化钠浓度及温度对水介质中DMP氧化聚合初始速率的影响,发现DMP氧化聚合初始速率与氧气分压的0.1次方成正比;DMP氧化聚合初始速率随DMP和催化剂浓度及温度的增加而增加;随氢氧化钠浓度和N/Cu摩尔比的增加DMP氧化聚合初始速率先增加后降低。

It was found that the thermodynamically unfavourable isomerization of quadracyclane to norbornadiene could be accomplished in the presence of toluene or durene as a co-sensitizer.

首次发现在甲苯、杜苯等芳烃共敏化下,可以使原来不能进行的、热力学不利的四环烷→降冰片二烯异构化得以进行,并根据CIDNP结果提出这是由于生成了敏化剂/底物/芳烃三元基激络合物使反应的势能面改变造成的并促进单线态的系间窜跃。

By thermodynamically and dynamically calculating and analysing ,a new growth mechanism of spherical graphite has been proposed ,that is,the spherical graphite does not grow inwardly,but grow outwardly and when spherical graphite grow outwardly carbon atoms come into and fill-up the entocoele of spherical graphite by the diffusing way.

通过对石墨球最终表面的形态进行分析,可以获得气泡的表面并不是石墨球的最终表面,石墨球表面主要由于受到石墨球表面各微晶长大速度不均匀性、铁水中的三大起伏、微量元素与碳原子的竟相吸附、由于浓度梯度和温度梯度所引起铁水的对流等各种因素的综合影响结果使其表面成为凹凸起伏的形状

Experimental data are also analyzed kinetically and thermodynamically.

考察了MD-1膜驱剂溶液的电导率、粘度和其在原油中的分配。

The calculation results show that the SiH insertion reaction into HCl is thermodynamically dominant at low temperature and kinetically favored at higher temp...

该反应在研究的温度范围内是一放热、熵减少的反应,反应的速率常数随温度的升高而增大,而且服从Arrhenius定律。

Type II is more kinetically controlled, while type I is thermodynamically controlled.

加热条件下,四方形空穴结构可以完全转化成烷基链对插的结构。

Analyzed the relative stability and isomerization, it was found that Ni3BPsuperscript (3 was thermodynamically the most stable one. In addition, Ni3BPsuperscript (1, Ni3BPsuperscript (1 with singlet state and Ni3BPsuperscript (3, NiPsuperscript (3 with triplet state are kinetically stable ones.

分析各异构体的相对稳定性及异构化过程得出:Ni3BP上标(3是单、三重态中热力学最稳定的异构体;单重态的Ni3BP上标(1、Ni3BP上标(1和三重态的Ni3BP上标(3、Ni3BP上标(3具有一定的动力学稳定性。

The Diels-Alder reactions forming one C—B bond and one C—C bond are always more favorable than the corresponding Diels-Alder reactions forming two C—C bonds, both thermodynamically and kinetically, which is in agreement with experimental observation.

形成一个C—B键的杂Diels-Alder反应都比相应的Diels-Alder反应在热力学和动力学上容易进行,这与实验结果一致。

It was demonstrated thermodynamically that the initial products with respect to the uranium-hydrogen system included UH, UH2, UH3, U2H2 and U2H4. The potential energy surface analyzing results confirmed that the optimized structures and suggested, theoretically, that the main initial products were UO or linear U02 in the uranium-oxygen system, and uranium monocarbide or uranium oxycarbides in the uranium-carbon monoxide system, depending on the different interaction mode.

计算结果从热力学上证明了铀与H_2的初始反应产物可能有UH、UH_2、UH_3、U_2H_2和U_2H_4 等;随着铀与O_2相互作用的方式的不同,铀氧化的初始产物或者是UO分子,或者是直线型UO_2分子;CO在铀上的吸附属于解离吸附,并以CO的碳端与铀原子相互作用最有利,初始相互作用产物主要有碳化物和碳氧化物。

All the possibility of the nitridation reaction mentioned above was discussed thermodynamically.

以MCl〓、NH〓Cl和Na为原料,在500℃的温度和~8M Pa的压力下合成出8nm的TiN和14nm的VN纳米晶。

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