晶粒片間的 的英文怎麼說

中文拼音 [jīnglìpiānjiānde]
晶粒片間的 英文
intercrystalline
  • 晶 : Ⅰ形容詞（光亮） brilliant; glittering Ⅱ名詞1. （水晶） quartz; （rock） crystal 2. （晶體） any crystalline substance
  • 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）
  • 片 : 片構詞成分。
  • 間 : 間Ⅰ名詞1 （中間） between; among 2 （一定的空間或時間里） with a definite time or space 3 （一間...
  • 的 : 4次方是 The fourth power of 2 is direction
  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. Moreover, the heredity of al and al alloys own structure morphologies has been discussed. block or flack - like tial and bar - like or particles tib2 can be obtained by means of fluoride salt method melting at 800 c ~ 1100c under the other same condition

    用氟鹽法制備中間合金時，在其它條件相同的情況下，改變熔煉溫度（ 800 1100 ）可以得到含有塊狀和針片狀形態的tial _ 3晶體和條狀與顆粒狀tib _ 2化合物的中間合金。
  3. Tem was used to consecutively investigate the size and appearance of dibasic lead phosphite in the reaction process. it found that nanocrystal grain of lead oxide phosphite hydrate had favorite direction in the mlps method, many nanocrystal grain in near area would aggregate and assembled as nanowire, the diameter of the nanowire was about a crystal grain size and the length of nanowire could reach hundreds of nanometers, then they would gather to needle or bar like particles

    利用tem對二鹽基亞磷酸鉛在反應過程中粒子的大小、形貌進行跟蹤觀察，並記錄下三個時間下的微粒照片，發現用微液相合成法制備的二鹽基亞磷酸鉛晶粒在生長團聚時存在取向規律，同一區域的晶粒會長成一條納米線，直徑有一個晶粒的大小，長度可以達到幾百nm 。
  4. The surface of ce02 - ti02 films were very smooth and difficulty to crystallization. the ceo2 - tio2 complex films were nanocrystalline microstructure or microcrystalline even if to heat the substrates or to anneal the films. the ceo2 and tio2 nanocrystalline were not easy congregate and bigger because of heterogeneity interface disturb and have many defect

    組成ceo _ 2 - tio _ 2混合薄膜顆粒粒徑在納米尺度范圍3 ? 50nm ，與純ceo _ 2 、 tio _ 2薄膜相比，具有更小的表面粗糙度和更難結晶，這是由於異質材料晶界的相互干擾，使同質顆粒之間難于聚集而結晶長大，薄膜處于納米晶或雛晶態，即使加熱基片或薄膜進行熱處理也無明顯變化。
  5. Xrd measurements showed that tio2 in the composites was anatase nano - crystallite with 5 - 10 nm size. sem images showed that some of the tio2 nano - crystallites coated on the surface of the mmt and some of them plugged into the gap between flakes of mmt. combining xrd result with sem images, it was clearly that the mmt and tio2 nanocrystallites formed a netlike nanocomposite structure

    用改性的溶膠凝膠法制備了一種mmt tio _ 2復合電流變顆粒， xrd ， sem分析證實tio _ 2是以納米晶的形式沉積于mmt的片層結構之間及顆粒表面，形成了一種網狀包覆的納米復合結構。
  6. The results showed that its yield was inversely proportional to the concentration of - amylase and reaction time when the maize starch was hydrolyzed by - amylase ; the granular maize starch was converted into hollow - porous starch by ct - amylase, furthermore it was cracked to the fragments, it was discovered that there were laminated growth ring structure inside starch granular shown on such cracked granular fragments ; the crystallinity of maize starch granule can not he increased by the enzyme hydrolysis ; the thermodynamic stability of the product was reduced when the hydrolysis time was long

    檢測結果表明， -澱粉酶催化水解玉米澱粉時，其收率與酶的濃度和反應時間成反比；顆粒狀玉米澱粉發生酶催化水解時， -澱粉酶首先使澱粉形成多孔狀結構，並進一步使顆粒破裂，斷裂的顆粒碎片上顯示出澱粉顆粒內部具有層狀的生長環結構；酶催化水解不能提高玉米澱粉顆粒的結晶度；酶解時間較長時，產品的熱穩定性降低。
  7. The evolution on particle morphology, microstructure, grain size and microstrain of the mixture of ti and al elemental powders during mm has been investigated. it was found that the nanocrystalline composite powders with extremely fine ti / al alternative lamellar structure ( lamella spacing about 0. 1 ~ 0. 5 m ) could be prepared by mm using proper processing parameters

    研究了ti 、 al單質元素混合粉在機械球磨過程中的顆粒形貌特徵、組織結構、晶粒尺寸以及微觀應變的變化規律，表明在適當的球磨工藝條件下可獲得具有極細層片間距（ 0 . 1 ~ 0 . 5 m ）的納米晶ti / al機械復合粉。
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