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high specific surfaces
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  “high specific surfaces”译为未确定词的双语例句
     This high hydrogen storage capacity under the moderate conditions was mainly attributed to the crystal structure of Ag(TCNQ) and the high specific surfaces of the aligned nanowires.
     推测其贮氢机理是由于Ag(TCNQ)疏松的晶体结构及纳米线阵列较大的比表面积.
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     Specific as:
     具体为:
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     High signal and specific probes were selected.
     采取差异选择法 ,筛选强杂交信号和高特异性的分型探针。
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     Conclusions: There were high specific in the test of ciguatoxin.
     结论:雪卡毒素检测具高度特异性。
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     High heel
     情迷高跟
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     high resolution;
     分辨率高;
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  high specific surfaces
Owing to their extremely high specific surfaces and their high surface-to-volume ratios nanosized ceramic powders show a strong tendency to agglomeration and poor flowability.
      
The geochemical importance of clay minerals stems from their ubiquity in soils and sediments, high specific surfaces, and ion-exchange properties.
      


The author's previous work indicated that the activity of granular fused iron catalysts decreased seriously with time due to the gradual plugging up of the pore volume of catalysts by the high boiling point products. In this paper, the activity data were treated with Wheeler's internal diffusion law mathematically. And the results suggest that the rate is a chemical controlling one in the initial period of the synthesis, and the coefficient of the catalysts surface is of 0.98 (with space velocity...

The author's previous work indicated that the activity of granular fused iron catalysts decreased seriously with time due to the gradual plugging up of the pore volume of catalysts by the high boiling point products. In this paper, the activity data were treated with Wheeler's internal diffusion law mathematically. And the results suggest that the rate is a chemical controlling one in the initial period of the synthesis, and the coefficient of the catalysts surface is of 0.98 (with space velocity 1000 hr~(-1), CO conversion 90% or so). When the catalysts pore volume are plugged up by the high boiling point products (whether the pore to be micro or macro), the rate becomes an internal diffusion controlling one, and the effectiveness of the catalytic surface changed into 0.082. The calculated coefficient of diffusion is of 2.4 10~(-5) cm~2/sec, which is in agreement with the magnitude of liquid-phase diffusion. Under the diffusional controlling conditions, the activity level of catalysts depends upon Deff, ks and Sg, by the rate law k∝2~(1/Deff·ks·Sg.) Where change of effective diffusivity. Deff, under the liquid phase conditions is not essential. But both the specific reaction rate, ks, and the effective surface, Sg are the major factors to the catalytic activity improvements. Therefore the precipited iron catalysts, owing to its high specific surface area and high specific activity, may be the promising one of the granular catalysts suitable for the high space velocity synthesis.

已往的工作指出,顆粒熔鉄催化剂在合成过程中活性有随时間下降的現象,认为主要是由于腊液堵塞孔隙的关系,应用成型方法构成大孔,能够有利于腊液的流出,延緩了活性下降的时間,但当腊液堵滿孔隙时,活性下降的水平仍与未成型的顆粒催化剂相近。本文根据活性方面的数据,进行了宏观动力学的分析,由动力学計算再次指明:当腊液未堵塞孔隙吋,合成反应是化学反应控制,此时表面有效利用系数达0.98(空速1000,CO轉化90%以上)。而当腊液堵塞孔隙后,轉为液相扩散控制,对362-1大顆粒催化剂言,此时表面有效利用系数为0.082,并求得气体通过液柱的扩散系数为2.4×10~(-5)厘米~2/秒。在扩散控制的情况下,由动力学分析指明,能影响活性水平的主要是Deff、Ks、Sg。有效扩散系数Deff在液相扩散情况下的改变是不大的,增大孔径并不能提高扩散控制时的活性水平。因此,孔径的增大在合成烃情况下仅起延緩腊液的积聚作用,而不能提高終活性的水平。由动力学分析指出,沉淀剂由于有大的表面积(較熔鉄剂大数倍以至数十倍),因此,可能适用于高速固定床操作而不須进行再生。实驗也驗証了这个看法。

The crystallite dimensions of a new solvay type catalyst for propylene polymerization were determined from the data of breadth of X-ray diffraction lines at half peak intensity. The crystallites have the size of about 100 A and they are smaller then those prepared by other methods. Their catalytic activity increases linearly with decreasing crystallite size.Surface area and pore structure of the catalyst were determined by elution chro-matographic method on model ST-03 analyzer. Our results showed that...

The crystallite dimensions of a new solvay type catalyst for propylene polymerization were determined from the data of breadth of X-ray diffraction lines at half peak intensity. The crystallites have the size of about 100 A and they are smaller then those prepared by other methods. Their catalytic activity increases linearly with decreasing crystallite size.Surface area and pore structure of the catalyst were determined by elution chro-matographic method on model ST-03 analyzer. Our results showed that such catalyst possess high specific surface area and large pore volume and has both large and fine pores. Therefore, active centres can be fully available.

用X射线衍射法测定了索尔维型丙烯聚合新催化剂的微晶粒大小为100A左右,比其它方法所制得的同类型催化剂微晶粒要小;并发现催化剂活性与微晶粒大小几乎成线性关系,微晶粒越小催化活性越高。 用ST-03型比表面、孔径分布测定仪研究了催化剂的孔结构。结果表明本催化剂具有较大的比表面和孔体积及粗细孔均备的优良孔结构,保证钛活性中心的充分利用,因而催化剂表现出较高的催化活性。

Titanium nickelide intermetallic compounds have been prepared by means of coprecipitation-reduction followed by diffusion processes, in order to obtain the cathodic material with improved hydrogen absorbing character.Titanium-nickel hydroxides are first precipited by NaOH from mixed solution of NiCl2 and TiCl4. After dehydration at 600℃, the mixed hydroxide is reduced by CaH2 to give hydrided TiNi and Ti2Ni.The coprecipitation-reduction and diffution process has been discussed in detail. The lattice parameters...

Titanium nickelide intermetallic compounds have been prepared by means of coprecipitation-reduction followed by diffusion processes, in order to obtain the cathodic material with improved hydrogen absorbing character.Titanium-nickel hydroxides are first precipited by NaOH from mixed solution of NiCl2 and TiCl4. After dehydration at 600℃, the mixed hydroxide is reduced by CaH2 to give hydrided TiNi and Ti2Ni.The coprecipitation-reduction and diffution process has been discussed in detail. The lattice parameters of TiNiH1.14 and TiNiH2.56 are 24.85A and 11.91A.The temperature-composition dissociation isobars at 1 atm. for the product and potential-time plots of TiNi and Ti2Ni electrodes have been drawn respectively. The discharge capacities were determined as 262.2 mAh/g for TiNiH1.14 and 169.9 mAh/g for Ti2NiH2.56.Since the product has higher specific surface and excellent electro-catalytic activity, electrodes made from the product have much important effect on decreasing the polarization and increasing the cycle life.

本文提出一种用共沉淀还原扩散法制备钛镍金属互化物的方法,详细讨论了共沉淀还原扩散过程,合成了比表面高、电催化活性良好的钛镍金属互化物。

 
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