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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]

As to MNa-ZSM-5, the order is CuNa-ZSM-5〓AgNa-ZSM-5>CeNa-ZSM-5> CoNa-ZSM-5〓FeNa-ZSM-5>Na-ZSM-5. Among the samples tested, CoHZSM-5 shows the highest activity, the conversion of NO is about 60%, and the activity is higher than that of CoNa-ZSM-5 with the same exchanged level. Suggests that the exist of some Bronsted acidity is benefited for this reaction. For Fe-ZSM-5, the activity are changed obviously with the various of preparation condition. It was also found that mordenite zeolite is a good support for this reaction.

其中,Co-HZSM-5表现出最佳的反应活性,NO的最高转化率达60%以上,并且活性明显高于具有相同交换度的CoNa-ZSM-5,表明适量的酸中心存在有利于该反应的进行;对于Fe-ZSM-5,制备条件不同Fe-ZSM-5的反应活性影响很大,反应的活性中心应是处在交换位上的铁离子;另外,通过考察不同载体对铁离子交换分子筛催化剂反应性能的影响,发现丝光分子筛也是较好的催化剂载体。

In addition,the mechanism isdiscussed on the prevention of interface diffusion via S-passivation.The FexS-dominateinterface reaction layer,is considered to prevent the reaction of Fe with As further meanwhilestabilizes the interface,therefore inhibits the diffusion from the substrate into Fe overlayer,which is different from the model of Anderson.

并且提出了S钝化阻止界面扩散的内在机制,认为在钝化层基底上形成的界面反应层,阻止了Fe和衬底As的反应并稳定了界面,从而阻止衬底元素向薄膜层的扩散,这与Anderson提出的模型不同。

During the cooling to room temperature,β-phase layer with higher Fe content remained, whereas β-phase layer with lower Fe content transformed into α'-Ti martensite. The β-transformed layer and intermetallic compound layer grew parabolically with time at 1223K and 1273K.

在此基础上得出的TA2/A3复合材的工业生产和应用控制在TA2的α-Ti→β-TI转变温度以下进行,从而避免Fe〓Ti,FeTi的形成,保证界面优良性能的结论可指导TA2/A3复合材的工业生产和应用。

It is researched the influence of cooling rate and the content of silicon and manganese alloy on peritectic reaction and position of peritectic point in Fe-C alloy.

研究了冷却速率和硅、锰合金元素含量对Fe-C合金的包晶反应和包晶点位置的影响;由于CSP薄板坯冷却速率快,Fe-C相图向左下方移动,包晶反应区域的碳含量为0。

Sulphonated carbon materials made from glucose were used as the solid acid and the support of Fe(superscript 2+) in the Fenton reaction, and the effects of the structure of carbon materials prepared by different methods on the Fe(superscript 2+) loading and the degradation efficiency of methyl orange were measured.

以葡萄糖为原料制备的磺化碳材料作为Fenton反应过程中固体酸及载体,研究了磺化碳材料结构对Fe(上标 2+)的负载能力及其对甲基橙降解反应的催化性能。

This article mainly deals with Cr's pollution affecting the content of Cr,K,Mg,Fe,Mn,Zn,Cu,Mo in floating and underwater leaves of Trapa bispinosa .

研究 Cr6 +污染后菱浮水叶和沉水叶中 Cr、K、Mg、Fe、Mn、Zn、Cu、Mo元素的含量,结果显示:Cr含量随培养浓度的上升而上升,K、Mg随培养浓度的上升而下降,Fe含量随培养浓度的上升而出现先上升后下降,Mn、Zn、Cu、Mo与 Cr6 +的培养浓度无明显的相关关系。

Low concentration of Fe〓 and Mn〓 could enhance photocatalytic degradation of trichloromethane、Aroclor1260 and humic acid, but when the concentration of Fe〓 and Mn〓 was high, it could prevent photocatalytic degradation.

研究发现当溶液中Fe〓及Mn〓浓度较低时,对光催化降解三氯甲烷、Aroclor1260及腐殖酸有一定的促进作用,但当浓度逐渐增加时,这些离子又对光催化降解起阻碍作用。

Due to the B4C, the Fe+B4C composite coating with different freezing character was composed of the homogeneous and unoriented primary rod-shaped solid solution of α-Fe and the eutectics, consisting of Fe2B, CrB, Cr23C6, Cr7C3 and Fe3.

Fe杆状枝晶固溶体与其间的共晶组织组成,共晶化合物相明显增多,主要有Fe2B,CrB,Cr23C6,Cr7C3,Fe3等。

The catalytic activity is much higher than that of the unpromoted sample Fe/Zr, while light olefins selectivity decreases and methane formation increases.

催化剂的催化活性比Fe/Zr及Fe/La催化剂都大大提高,甲烷选择性也有所增加,烯烃选择性降低。

Nutrient composition of Vallisneria natans was analyzed. Results show that V. natans contained 218.4 gkg^(-1) of protein, 51.4 gkg^(-1) of crude fat, 37.6 gkg^(-1) of polysaccharides, 265.7 gkg^(-1) of ash; and 147.6 gkg^(-1) of total amino acids, 55.0 gkg^(-1) of essential amino acid; and a number of mineral elements, such as 60.5 gkg^(-1) of K, 10.9 gkg^(-1) of Ca, 16.3 gkg^(-1) of Fe, 12.7 gkg^(-1) of Na.

沉水植物苦草的营养成分分析结果表明,其蛋白质含量为218.4gkg^(-1),脂肪含量为51.4 gkg^(-1),多糖含量为37.6 gkg^(-1),灰分含量为265.7 gkg^(-1);氨基酸总量为147.6 gkg^(-1),必需氨基酸为55.0 gkg^(-1);含有K、Ca、Cu、Fe、Zn、Mn、Na、Al、Ba等多种矿质元素,其中K、Ca、Fe、Na含量分别高达60.5、10.9、16.3、12.7gkg^(-1)。

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