晶體尺寸 的英文怎麼說

中文拼音 [jīngtǐchǐcùn]
晶體尺寸 英文
crystal-size dimension
  • 晶 : Ⅰ形容詞（光亮） brilliant; glittering Ⅱ名詞1. （水晶） quartz; （rock） crystal 2. （晶體） any crystalline substance
  • 體 : 體構詞成分。
  • 尺 : 尺名詞[音樂] （中國民族音樂音階上的一級 樂譜上用做記音符號 參看「工尺」） a note of the scale in ...
  • 寸 : Ⅰ量詞（長度單位） cun a unit of length （=1/3 decimetre）Ⅱ形容詞（極短或極小） very little; very ...
  • 晶體 : [晶體學] crystal; vitrella; crystal body; crystalloid; x-tal
  1. The quality of buffer layer and thin films was analyzed by afm, xrd, rheed and xps respectively. the effect of the experimental parameters such as carbonization time, working pressure, c source gas flow rate, carbonization temperature, different carbonization gas and substrate on the carbonization process was studied firstly. it was observed that the size of particles was increased with the increase of carbonization time and the rms was opposite, but the trend was reduced while the carbonization time was long enough ; the size of particles was increased with the increase of working pressure too, and choosing a proper working pressure could get a smooth surface ; the size of particles was unobviously changed while the gas flow rate was low, but it was notability increased with the increase of gas flow rate while the gas flow rate was high enough, and a smooth surface could be also obtained by choosing a proper gas flow rate ; with the increase of carbonization temperature, the size of particles was increased, the rms is decreased and a good single - crystalline carbonization layer could be obtained, but a rough surface was formed at a excessive high temperature ; the rms of

    對于碳化工藝，側重研究了碳化時間、反應室氣壓、 c源氣體的流量、碳化溫度以及不同種類的c源氣體、基片取向等因素對碳化層質量的影響，研究結果表明:隨著碳化時間的增長，碳化層的晶粒尺寸隨之變大，表面粗糙度隨之降低，但當碳化到一定時間之後，碳化反應減緩，碳化層的晶粒尺寸以及表面粗糙度的變化幅度變小;碳化層的晶粒尺寸隨反應室氣壓的升高而變大，適中的反應室氣壓可得到表面比較平整的碳化層;在c源氣體的流量相對較小時，碳化層的晶粒尺寸隨氣體流量的變化不明顯，但當氣體流量增大到一定程度時，碳化層的晶粒尺寸隨氣體流量的增大而明顯變大，同時，適中的氣體流量得到的碳化層表面粗糙度較低;碳化溫度較低時，碳化層的晶粒取向不明顯，隨著碳化溫度的升高，碳化層的晶粒尺寸明顯變大，且有微弱的單晶取向出現，但取向較差，同時，適中的碳化溫度可得到表面平整的碳化層;相比于c _ 2h _ 2 ，以ch _ 4作為c源氣體時得到的碳化層表面平整得多;比起si （ 100 ） ，選用si （ 111 ）作為基片生長的碳化層的晶粒取向一致性明顯更好。
  2. The corrosion behavior of nanocrystalline ( nc ) copper bulks with various grain sizes prepared from igc ( inert gas condemsation ) and vacuum annealing in comparison with conventional microcrystalline ( mc ) copper ( as - rolled and electrolytic ) in acid copper sulphate solution and neutral solution containing chlorides under free corrosion conditions and anodic polarizations has been studied using potentiodynamic polarization, potentiometric analysis, cyclic voltammetry and electrochemical impedance spectroscopy. x - ray diffraction was used to estimate the grain size of the annealed nc copper. field emission gun scanning electron microscopy and x - ray energy - dispersive spectroscopy was used to characterize the surface morphology and analyze the surface composition after the polarization and potentiometric test of both nc and mc copper

    本文研究了用igc （惰性氣體蒸發凝聚原位溫壓法）制備並真空退火到不同晶粒尺寸的納米晶銅和微米晶銅（冷軋紫銅、電解銅）在酸性硫酸銅溶液和中性含氯溶液中，在自腐蝕狀態和陽極極化狀態下的腐蝕性能。使用了動電勢極化、電位測定、循環伏安法（ cv ）和電化學阻抗譜（ eis ）等方法。 x -射線衍射（ xrd ）的方法用來估算納米晶銅晶粒尺寸。
  3. The effects of the fabrication conditions on the crystal structure, grain size, micromorphology and electrochemical performance of these materials have been studied in depth. the reaction mechanism of the low - heating solid - state reaction method has also been investigated. in addition, a novel electrochemical method ( rpg method ) based on the concept of " ratio of potentio - galvano - charge capacity " has been for the first time developed to determine the diffusion coefficient of lithium - ion within insertion - host materials on the basis of the spherical diffusion model

    本論文較系統地考察了低熱固相反應法合成鋰離子電池正極材料的可行性問題，研究了工藝條件對材料的晶體結構、晶粒尺寸、微觀形貌及電化學性能等的影響，探討了低熱固相反應的機理，並通過引進「恆壓-恆流充電容量比」的概念，給出了一種測定鋰離子嵌入脫出固相擴散系數的新方法。
  4. Numerical simulation of austenite grain size during hot deformation of q345 steel

    345鋼熱變形奧氏體晶粒尺寸的數值模擬
  5. Prediction model of recrystallized grain size of austenite in hot rolled strip

    熱軋鋼板奧氏體再結晶晶粒尺寸的預測模型
  6. The tensile and compression experiment on bulk nanocrystalline ag prepared by igc method was carried on mt810 with different grain sizes and zwick 10tn2s machine at different strain rates under normal temperature respectively. the stain rate sensitivity m was found to be 0. 025, which was extremely lower than the ordinary values. also the work hardening exponent is very low

    本文從用惰性氣體蒸發冷凝和真空原位壓結法（ igc ）制備得到的直徑80mm ，厚度7 . 6mm的大尺寸納米晶金屬ag樣品上切割得到符合力學實驗要求的拉伸和壓縮試樣，在mts810和zwick精密力學測試機上分別精確測定了拉伸和壓縮應力?應變曲線與晶粒尺寸和應變速率的關系。
  7. So far as the grain size order of magnitude is concerned, the thickness of the acicular ferrite is about 200nm, while the thickness of the austenite existing inside the ferrite is only several nm to 10 nm

    從晶粒尺寸數量級來說，針狀鐵素體的厚度約為200納米，而鐵索體內奧氏體的厚度僅為幾到10納米數量級。
  8. Results show that the grain size of all samples is below 100nm, and the lattice parameters and grain sizes are dependent on the sintering temperature

    結果表明，前驅體的焙燒溫度對樣品的晶型、晶胞參數及晶粒尺寸有很大影響。
  9. By increasing the h2 dilution ratio, it is found that atomic hydrogen can selectively etch amorphous phase and stabilize crystalline phase. from the study on the distance from substrate to catalyzer, choosing a proper distance can ensure the gas fully decomposed, while a relatively low substrate temperature can cause the nanocrystalline particles to lose mobility and keep their sizes. the pre - carbonization process can enhance the nucleation density and make the growth of high quality nanocrystalline p - sic films much easier

    實驗結果表明：隨著工作氣壓的減小，薄膜的晶粒尺寸有所減小；通過提高氫氣稀釋度，利用原子氫在成膜過程中起的刻蝕作用，可以穩定結晶相併去除雜相；選擇適當的熱絲距離能保證反應氣體充分分解，又使襯底具有較高的過冷度，是形成納米薄膜的重要條件；採用分步碳化法可以提高形核密度，有利於獲得高質量的納米- sic薄膜；襯底施加負偏壓可以明顯提高襯底表面的基團的活性，因負偏壓產生的離子轟擊還能造成高的表面缺陷密度，形成更多的形核位置。
  10. The gel c - s - h has the trend to crystallizing and transforming into low crystallized hydrates, which were similar to tobermorite. the incorporation of mineral mixtures improves greatly the orientation of ch either in interface zone or matrix zone and the crystal sizes also become small

    由於礦物摻合料的晶核作用、填充密實和二次水化作用，明顯改善了界面過渡區和基體中ch的擇優取向，並且不論是在界面區還是基體中，結晶相的晶粒尺寸都發生了明顯的細化。
  11. The versatile system is able to handle various substrate sizes ranging from 2 ” to 8 ” and can accommodate up to 75 wafers per run, depending on size

    這個多功能體能處理各種各樣晶片，尺寸范圍從2英寸到8英寸，根據晶片的尺寸大小，腔室內可容納達75片晶片每次。
  12. The results of pure cu show ecap can produce bulk material of submicrometer level indeed. as the number of passes increases, the initial structure of pure cu has been refined largely. after six passes, i. e. the equivalent true strain of 4 ~ 5, the grain size gradually becomes stable and uniform

    對純銅室溫ecap晶粒超細化行為及組織穩定性的研究表明： ecap技術的確能制備出亞微米級的塊體材料，隨著ecap道次的增加，純銅的組織被大大細化， ecap六道次（即等效真應變4 5 ）后，晶粒尺寸趨于穩定，硬度基本飽和。
  13. The results showed that there was anomalistic crystal whose size reached nanometer grade in fine pvc ; it ' s about 80nm. the crystal structure was damaged by jet - milling, which induced the melting point of nanocrystal pvc decreased from 210 " c to 128 擄 c. the nanocrystal pvc induced the decrease. of plasicizing time and equilibrium torque and the increase of maximal torque, which showed that the nanocrystal pvc had self - plasticization in pvc composites

    通過sem 、 tem 、 ftir和dsc測試表明：氣流粉碎制得的pvc微粉中具有不規則納米晶體，尺寸在80nm左右；氣流粉碎破壞了pvc的晶體結構，使納米晶pvc的熔點從210下降到128 ；納米晶pvc使體系塑化時間、平衡轉距降低、最大轉距升高，具有自增塑作用；納米晶pvc的加入使pvc的沖擊和拉伸強度都有大幅度上升。
  14. By compounding caco3 with pp, the effect of caco3 content, diameter and shape on the crystallization, dispersion morphology and properties of pp / caco3 composites was investigated. the results showed that addition of caco3 into pp decreased the apparent crystal size in perpendicular direction to the ( 110 ), ( 040 ) and ( 130 ) crystallographic planes of ppa crystal, and with similar uniform dispersion of caco3, the dominant factor influencing toughness is the diameter of caco3 particles, but not the decrease of pp crystal size. the toughening effectiveness of nano caco3 is obviously better than that of micron caco3

    將caco _ 3與pp進行填充復合，研究了caco _ 3含量、粒徑及形狀對體系的結晶，分散形態及性能的影響，發現碳酸鈣的加入使聚丙烯晶型垂直於（ 110 ） 、 （ 040 ）和（ 130 ）晶面的表觀晶體尺寸減小，揭示了在分散均勻的情況下，影響材料韌性的主導因素不是晶粒尺寸的減小，而是碳酸鈣的粒徑，納米張玲：彈性體及無機剛性粒子增韌增強聚丙烯復合材料的研究碳酸鈣的增韌效果明顯優于微米碳酸鈣。
  15. The presence of montmorillonite makes the crystal size diminish markedly and makes the integrality of crystal reduce. 4

    加入蒙脫土后，尼龍66的晶體尺寸明顯減小，結晶的完整性下降。
  16. This dissertation developed a simple and cost - effective approach to fabricate electrolyte thin films using filter - coating technique, and reported our initial results to fabricate ysz electrolyte thin films with a modified dry pressing method

    結果表明，三種方法獲得的樣品晶體尺寸為5 - 7nm 。拉曼光譜證實它們均以立方相為主，伴有少量的四方相。
  17. On the other hand, when using p ( an - mma - as ) as polymer matrix, the gradient distribution of copper in pmgcf is raisonne, the crystal is smaller and compacter than the former, the flexibility of pmgcf increase as the concentration of mma in copolymer increase, the size of copper crystal increase as as the concentration of ita in copolymer increase

    P （ an - mma - as ）為基體時金屬梯度分佈較合理，金屬晶體細小而且緻密，而且所制的pmgcf柔韌性較好，隨mma含量的增多而柔韌性增大，隨其中的as的含量的增大，所得的金屬晶體尺寸變化與p （ an ita ）相似，但變化的趨勢較緩慢。
  18. Thirdly, that an electromagnetism can not enhance the growth of a fouling crystal is proved more when the fouling water recycles and passes through an electromagnetism. at the same time, a new technics of electromagnetic anti - fouling & descaling is come up with, which combines the advanced technology of membrane and electromagnetism

    3 、在冷態循環實驗中，進一步驗證電磁是否有促進污垢晶體尺寸長大的作用，同時提出了一種將膜技術和電磁技術相結合，進行抗垢、減垢的實用新工藝。
  19. M17l - support lcd size

    M17l -支援液晶體尺寸
  20. M15l - support lcd size

    M15l -支援液晶體尺寸
分享友人
分享到 Line

分享到臉書