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On the other hand,interface reaction is weakened drasticallyon the interface between Co with sulfur-passivated GaAs(100)by CH3CSNH2 treatment,astable interface forms at the coverage of 8〓Ga atoms bonded with S at the surface exchangewith Co atoms and diffuse into Co matrix,which causes the formation of Co-S bonding.

另一方面,对于Co与CH3CSNH2处理的S硫化GaAs(100)表面形成的界面,界面反应大为减弱。当Co覆盖层达到〓时,形成稳定的界面。

The results were as follow: At fine, cloudlet and cloud weather in rainy season,the mean value of CO 2 content varied in a range of 349 to 350ml/m\+3 at 2.8m above the canopy, 346 to 348ml/m\+3 at 0.8m above the canopy, 345 to 349ml/m\+3 at 16m inner the forest and 352 to 357ml/m\+3 at 5m above ground in the period from 9:00 to 18:00.The CO 2 content in rainy season was lower than that in dry season. At the same weather and space-time, CO 2 content in rainy season was higher than that of CO 2 in dry season at both day and night. According to the grads calculation, there were the CO 2 flux from atmosphere to canopy with 0.61×10 -6 and 0.71×10 -6kg/(m 2·s) during day time in dry and rainy seasons respectively.

采用梯度法及CI-301PS CO2系统,实现了海南尖峰岭热带山地雨林近冠层CO 2、微气象因子梯度观测研究,结果表明:雨季晴、晴间少云及多云天气,9:00~18:00CO 2浓度平均值分别在349~350ml/m3(冠上2.8m)、346~348ml/m3(冠上0.8m)、345~349ml/m3(林内16m)、352~357ml/m3(林内5m),较旱季相应天气分别小14~17.5、10.1~23.7、1 6.4~35.7和18.1~36.1ml/m3;1:00~8:00,则雨季CO2浓度大于旱季;梯度浓度廓变量和实时动力计算反映出,8:00~18:00CO2通量由大气向林冠层,旱、雨季平均CO2通量分别为0.61×10-6kg/(m2·s和0.71×10-6kg/(m 2·s),19:00通量甚微,20:00~7:00CO2通量则由林冠向大气,平均CO2通量分别为0.36×10-6kg/(m2·s)和0.32×10-6kg/(m2·s);雨季昼夜大气流向冠层的净CO2通量是相应旱季的1.56倍。

The local ordered CoPt〓 Ll〓 phase with good FCC (111) crystalline orientation, which exists at the interfaces of multilayers and in alloy films, was considered to contribute to the PMA in Co/Pt multilayer and Co-Pt alloy films. But the appearance of large amount of ordered CoPt〓 Ll〓 phase or completely disordered Co-Pt phase will result in the decrease in PMA.

Co/Pt多层膜界面处或Co-Pt合金膜中具有FCC(111)织构特征的局部有序CoPt〓 Ll〓合金相的形成被认为可能会对多层膜和合金膜中的垂直磁各向异性作出贡献,但大量CoPt〓 Ll〓有序相或大量完全无序Co-Pt合金相的生成都会导致垂直各向异性的下降。

NO elimination reactions are much complicated in the system of NO-CO-CO2-N2 with the existence of metallic oxides. Homogeneous reaction between NO and CO, reduction of NO by the lower valued metallic oxides, direct decomposition of NO as a catalytic reaction and catalytic reaction of NO/CO may all contribute in NO elimination.

金属氧化物存在条件下NO-CO-CO2-N2体系中,NO去除反应较为复杂,NO/CO气相直接反应、低价氧化物对NO的还原作用、金属氧化物对NO分解反应的催化作用及金属氧化物对NO/CO反应的催化作用等都可能存在。

The exchange field is found to change in an exponential function of 1/|t〓-t〓| in two wedged synthetic antiferromagnets FeMn/Co (t〓=12. 0nm)/Ru (0.7nm)/Co and FeMn/Co /Ru (0.7nm)/Co (t〓=12. 0nm). It has opposite signs and different magnitudes in above two series.

实验上制备了两个系列的楔形样品FeMn/Co/Ru(0.7nm)/Co,其中t〓=12.0nm及t〓变化和t〓=12.0nm及t〓变化,发现交换偏置场与厚度呈〓关系,而且这两系列样品交换场的符号相反。

Aortic NOS/NO and HO/CO system are impaired significantly in atherosclerotic rabbits induced by high cholesterol diet. Decreases of endogenous NO and CO production are associated with atherosclerotic progression. Both L-arginine and heme-L-lysinate inhibit atherosclerotic progression by increasing NO or CO production.

高胆固醇饮食诱导的AS显著损害了主动脉NOS/NO及HO/CO系统,内源性NO及CO生成量减少与AS的发生发展密切相关。L-精氨酸及血红素-L-赖氨酸盐分别通过增加主动脉NO及CO生成量而抑制AS进展。

It is found that the nature of the interaction between CO and Pd(110) surface by population analysis and DOS analysis what the 5σ orbital of CO and the d orbital of metal formed electron donation; and the 2π* orbital of CO and 4s and 3d orbital of metal formed electron back- donation.

通过布居数分析和态密度分析发现, CO 和 Pd(110)表面的相互作用,主要是 CO 的5σ轨道和金属原子的 d 轨道形成5σ-d 配位键;同时 CO 的2π*轨道和金属原子的4s 和3d 轨道形成反馈键。

When SiO〓-NH〓-Rh-Co complex was used to catalyze the hydroformylation of methyl methacrylate, an optimal conversion of 93.4% and optimal selectivity of 84.4% for the normal aldehyde were both obtained at Rh/Co ratio of 2/1, which were both higher than that catalyzed by SiO〓-SiNH〓-Rh and SiO〓-Si-NH〓-Co momometallic catalysts. Clearly a synergistic action between Rh and Co atoms presented in the complex.

我们以SiO〓-Si-NH〓-Rh-Co催化甲基丙烯酸甲酯的醛化反应,当催化剂中Rh/Co比为2/1时,催化活性最高,可达93.4%,对正构产物β-甲酰异丁酸酯的选择性达到84.4%,都高于单金属催化剂,表明了金属间存在相互作用。

Therefore, in order to trace the origin of contribution of the various Co sites to the magnetocrystalline anisotropy of the Co-sublattice, a special attention is paid to the relationship between the evolution of anisotropy of the compounds and the preferred site occupation of non-magnetic atoms over the four available crystallographic sites in the Co sublattice.

因此,本文重点讨论了Co次晶格各向异性演化与非磁性替代原子浓度的关系,以探讨非磁性替代原子在Co次晶格四个不同晶位择优占位对Co次晶格各向异性的影响。

The δ〓C values of soil CO〓 become gradually light with depth increasing and are stable at certain depth; The δ〓C values of soil respired CO〓 are within the δ〓C values of soil CO〓; The δ〓C values of soil respired have same changing pattern with that of plants.

土壤剖面上CO〓的δ〓C值自地表向下逐渐变轻,在一定深度后大致趋于稳定;土壤呼吸CO〓δ〓C值位于土壤CO〓δ〓C值的变化范围;土壤呼吸CO〓δ〓C值的变化规律和植被δ〓C值的变化在空间上具有一致性。

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