晶狀體微粒 的英文怎麼說

中文拼音 [jīngzhuàngtǐwéilì]
晶狀體微粒 英文
lens particles
  • 晶 : Ⅰ形容詞（光亮） brilliant; glittering Ⅱ名詞1. （水晶） quartz; （rock） crystal 2. （晶體） any crystalline substance
  • 狀 : Ⅰ名詞1 （形狀） form; shape 2 （情況） state; condition; situation; circumstances 3 （陳述事件或...
  • 體 : 體構詞成分。
  • 粒 : Ⅰ名 （小圓珠形或小碎塊形物） small particles; grain; granule; pellet Ⅱ量詞（用於粒狀物）
  1. Ajs20, the precursor contained 20wt % alunina sol seeding, was calcined at around 1000 to get free - aggregation nano - sized a - alaos powders with a median particle size of 70nm. and, calcining ajs2, the precursor contained 2wt % alumina sol seeding, at hoo ' c, we get a - alaos nano - sized powders with a particle size of loonm and good dispersion by tem. this paper also gives the proper mechanisms of these factors " influences on the transformation to alpha phase

    研究結果顯示，含有20wt膠體籽晶的前驅體ajs20在1000左右煅燒就可獲得平均粒徑為70nm 、無團聚的納米- al _ 2o _ 3粉體；而含有2wt膠體籽晶的前驅體ajs2在1100即可獲得粒徑在100nm左右、幾乎單顆粒分散、有少量「樹枝狀」微結構的納米- al _ 2o _ 3粉體。
  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 main results are as the following : ( 1 ) the microstructure of lamellae pearlite has evolved ultrafine cementite particles throughout the ferrite matrix uniformly after four passes. the ferrite matrix is homogeneous grains, and average grain size is - 0. 3um

    主要結果如下： （ 1 ） ecap變形四道次后，片層狀的珠光體組織演變為了超細的滲碳體顆粒均勻分佈於亞微晶鐵素體基體的組織。
  4. Xrd spectra show that the bulk gan particles are wurtzite structure, and the nc gan has small domain size and the structure of solid solution phase

    Xrd結果顯示經由氣凝法合成前後氮化鎵均為一六方晶系結構，利用塊狀氮化鎵生成的奈米粉體粒徑微細且是一種固溶相結構。
  5. Determined by dsc. whereafter, the surface micro - morphology of both sides of tini sma thin film deposited on glass was investigated by atomic force microscope ( afm ), and the difference of morphology between the two sides is observed. it has been shown that, in the growing surface of sputtered tini film, the trend of grain to accumulating along the normal direction like a column is clearly observed, and the grain is very loose which resulted in more microcavities, but in the surface facing to glass substrate, grain is so compact that there are hardly microcavities

    通過濺射法，在玻璃襯底上淀積了tini薄膜，並在600進行了真空退火， dsc法測得其馬氏體逆相變峰值溫度為75 ，利用原子力顯微鏡，對玻璃基tini形狀記憶合金薄膜的襯底面與生長面進行了表面微觀形貌分析，發現：生長面晶粒呈現出沿薄膜法線方向柱狀堆積的趨勢，晶粒緻密性差，微孔洞多；而襯底面晶粒緻密，幾乎沒有微孔洞存在。
  6. The results showed that the in - situ formed tibi particles which had a size of about 50nm, exhibited a homogenous dispersion in the copper matrix. moreover, the interface between the nanoscale particles and the copper matrix was clean, and there was no certain location relationship. due to their reinforcement, the tensile strength and hardness of the in - situ cu - tib _ 2 nanocomposite significantly improved

    通過光學顯微鏡、 tem 、 xrd等對cu - tib2原位復合材料進行了金相組織、微結構分析，原位復合材料的鑄態金相組織中彌散分佈著團簇狀的tib2顆粒；形變態金相組織中tib2顆粒呈纖維狀排列； tem觀察表明：在基體內存在著尺寸約為50nm 、彌散分佈的tib2顆粒，且tib2顆粒與基體之間界面清晰，但由於tib2結構與銅晶體結構的差別較大， tib2顆粒與基體之間無固定的位向關系；納米tib對銅基體有良好的增強作用。
  7. The analysis of microstructure of samples showed that the grain of tio2 were very small under 700, the distance of grain became small with temperature increasing, the rate and size of pore was decreasing. the relative density of sample at 900 was 97 % and the grain size of sintered body was about 200nm. when the temperature exceeded 1100, the grain size of body grew up several times ( > 2 m )

    Tio _ 2燒結體sem顯微形貌分析表明：低溫（ 700 ）時坯體內顆粒無明顯長大，燒結體緻密度不高（ 80 ）晶粒間距隨溫度升高而變小，氣孔率也隨之降低，氣孔尺寸變小；當溫度超過900時，晶粒間連接緊密，燒結體內出現大量絮狀物質，緻密度大幅度提高，達97以上，小氣孔已聚集成大孔洞且分佈均勻，晶粒長大不明顯（ 200nm左右） ；當溫度超過1100時，燒結體緻密度有所提高，但晶粒尺寸出現異常長大，長大了十幾倍（達2 m以上） 。
  8. 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。
分享友人
分享到 Line

分享到臉書