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Fe相关的网络例句
与 Fe 相关的网络例句 [注:此内容来源于网络,仅供参考]

Sb can combine with Cu and P to form a low melting point compound which lowers the melting point of binary Cu-8P eutectic alloy by nearly 200℃. Bi and Cu can create compounds with low melting point(270℃) distributing at the boundaries and that is the reason why the melting point of (Cu-8P)-Bi is lower than that of binary Cu-8P eutectic alloy. The eutectic cluster can be refined with the addition of Fe, and that is the reason why the addition of Fe can decrease the melting point of Cu-8P alloy. Two means of decreasing the melting point of Cu-8P are found.

一定量的Sb与Cu, P形成低熔点相,从而大幅降低了Cu-8P合金的熔点,使其熔点降低近200℃;加入少量Bi后, Bi与Cu在共晶团晶界上形成熔点为270℃左右的低熔点化合物,且Bi的加入明显细化Cu-8P合金共晶团,从而使Cu-8P合金的熔点降低;加入Fe能明显细化Cu-8P合金的共晶团,使层片间距由8μm减为2μm以下,并使共晶团由层片状向短棒状转变,虽然Fe与Cu形成熔点为806℃的高温相,但Fe的细化作用使得Cu-8P合金的熔点降低,但降低幅度不大。

After comparison of 30 and 50℃ treatments, AQDS were added into 3 kinds of microorganism biocoenosis from Jiling, Tianjin and Sichuan paddy soil, and it showed that AQDS could accelerate the reduction of Fe 10%-288%, meanwhile, temperature could accelerate the reduction of Fe 6%-17%. In axenic culture treatment of 6 kinds of bacterial strains from Sichuan and Jiangxi paddy soil, the maximum accumulation amount of Fe reduction rate was constant, the maximum reaction rate and ferric reduction rate of ferric strain JX-a08 all increased as temperature rose, which showed that bacterial strain JX-a08 were suitable to 50℃.

在30和50℃培养温度下,来源于吉林、天津和四川的3种水稻土微生物群落添加AQDS可使Fe还原的反应速率常数增加10%~288%,而温度变化的增加幅度仅为6%~17%;对分离自四川和江西水稻土中的6株铁还原菌的纯培养试验发现,菌株JX-a08的Fe最大累积量、还原速率常数、最大反应速率及铁还原率均随培养温度的升高明显增加,表明菌株JX-a08更适于在50℃下生长。

Subsequently, comparing the reductive dechlorination performance between the different bemetallic systems, such as Cu/Fe, Ag/Fe, Pd/Fe, and so on, for halogenated methane, 2,4-D, HCH and chlordane.

实验结果表明,Pd/Fe双金属催化体系对高浓度高卤代甲烷系列污染物并没有表现出优于Cu/Fe还原体系的还原脱卤性能。

Firstly, the reaction thermodynamics was analyzed. Then, the reaction mechanism was studied, and the results are as following:① Ca moves to the surface of Dy〓O〓 by vapor phase;② Dy〓O〓 reduced to Dy by Ca is fast;③ Dy moves to the Fe surface mainly by vapor and various Dy-Fe alloys are produced gradually;④ The forming process of DyFe〓 may be described by Contracting Core Model;⑤ The rate-controlling step of the reaction is the Dy diffusing toward contracted and nonreaction nuclear center Fe.

首先考察反应的热力学可能性;其次探讨反应机理;通过实验确定:①Ca主要以气态形式迁移到Dy〓O〓表面参与反应;②Dy〓O〓被Ca还原为Dy的速度很快;③Dy主要以气态形式迁移到Fe表面逐级生成Dy-Fe合金;④DyFe〓的形成过程可以应用收缩核模型来描述;⑤Dy通过DyFe〓产物层向缩小的未反应核中心Fe的扩散是反应的控速步骤,通过动力学计算确定:还原扩散反应的表观活化能E〓=45kJ/mol。

The structure of the compound 〓(1) consists of a pentanuclear molecule which is center-symmetric. One W atom is coordinated by four S atoms and two Cu atom. As expected, the Fe atoms are sandwiched between two staggered pentadiene rings. The most interesting aspect of the structure is that Fe-C-P-Cu-P-Cconstitutes a distorted hexagon and Fe-Cu-W-Cu-Fe is nearly in a line.

结构是以W原子为对称中心含有五个金属原子的线型结构,W原子与四个μ〓-S和两个Cu原子配位;Fe原子在两个戊二烯环中间形成一个三明治夹心结构;Fe〓-C〓-P〓-Cu〓-P〓-C〓-构成扭曲的六边形,由于两边1,1'-双二茂铁配体的作用导致Cu-S键的拉长。

In addition,the activity of the putadiene polymerization catalyzed by SAAC.Nd.Fe-AlEt Cl-Al in the presence of phenanthroline and the relationship bet-ween the polybutadiene microstructure obtained with the content of Fe in SAAC.Nd.Fe were studied.

此外,初步考察了在邻啡绕啉存在下SAAC·Nd·Fe体系聚合丁二烯的活性以及所得产物的微观结构与络合物SAAC·Nd·Fe中Fe的含量关系。

The results show that dynamic leaching of heavy metals increases with decreasing pH values on the whole, but the relativity is not significant. The leaching concentration is negatively correlated with time. The calculation results show that the elements with the largest cumulative leaching amount are Fe, Mn, Zn and As, and those with the smallest amount are Pb, Sn, Hg and Cd. The elements with the highest stage lixiviating rate are Ni, Co, Cr, Mn, Cd and Cu, and that with the lowest rate is Fe. The elements with the highest values of cumulative lixiviating rate and cumulative lixiviating intensity are Cr, Mn, Co, Ni and Zn, and that with the lowest ones is Fe.

结果表明,重金属元素的动态浸出整体随pH值下降而升高,但相关性不明显,浸出浓度与时间整体上呈负相关关系;浸出总量效果较好的元素为Fe、Mn、Zn、As,较差的为Pb、Sn、Hg、Cd,其他元素中等;阶段浸出率较高的元素有Ni、Co、Cr、Mn、Cd、Cu,较低的元素有Fe,Sn、Zn介于中间水平;累积浸出率和累积浸出强度较高的元素有Cr、Mn、Co、Ni、Zn,较低的元素为Fe,Cu、Cd、Sn居于中间水平。

Based on features of ELNES of L3 edges, EELS spectra can also provide quantitative information regarding oxidati on states of Fe in Fe-bearing amphiboles, Fe-bearing pyroxenes, and other sili ca te minerals.

基于Fe-L3边之ELNES的特征,EELS也能提供关于含Fe的闪石、辉石及其他硅酸盐矿物中Fe的氧化态的定量信息。

Different from Ni70Mn25Co5(suitable for growing (100)crystal plate), Fe is suitable for growing (111) crystal plate. It may be related to that (100)growing area of Fe is very narrow. In diamond research with medium of Fe, most crystals are octahedron or six-eight body. It is very hard to synthesize hexahedron diamond.

与Ni70Mn25Co5触媒生长特性(适合于(100)晶面生长)不同,Fe作触媒适合于(111)晶面生长,这可能跟Fe触媒的(100)生长区非常窄有关,因为在Fe触媒粉末金刚石研究中,晶体基本为八面体或六八面体,很难合成六面体金刚石。

The results showed that there existed Lewis base sites (M=O and M-O-Fe) and Lewis acid sites on the surface of these catalysts.

研究表明,Fe-V-O、Fe-Mo-O、Fe-P-O和Fe-Al-P-O催化剂表面活性基元都是由Lewis碱位(M=O键的端氧和M-O-Fe键的桥氧位)和Lewis酸位组成。

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