粒度晶粒大小 的英文怎麼說
中文拼音 [lìdùjīnglìdàxiǎo]
粒度晶粒大小
英文
grain size-
Beryllium powders with the same particle size and various contents of beo were prepared by pre - sintering - acid washing processes initiatively and the influence of beo alone on o mys of beryllium was observed and some new results have been obtained - compared with the content of beo, the distribution of beo in beryllium has more critical influence on mys ; finely dispersed beo along the grain boundaries and in the matrix results in the dispersion strengthening of beryllium matrix and thereby the higher mys value ; on the contrary, the coarser beo particles clustering on the grain boundaries results in negative influence on o mys
開創性地用預燒結? ?酸洗工藝制備了相同粒度、不同beo含量的鈹粉，從而開展了beo含量單獨對鈹材_ （ mys ）影響的研究，得出一些新的結果：與beo含量相比， beo在鈹中的分佈狀態對_ （ mys ）的影響更大。沿晶界、晶內彌散分佈的較細小beo對基體鈹有彌散強化作用，使_ （ mys ）即較高；如果beo較粗大地成簇狀聚集在晶界，反而對_ （ mys ）有不良的影響。Effect of ti content on coarsening temperature and austenite grain size of ah
36粗化溫度和奧氏體晶粒大小的影響Fe - ni alloy fiber were first prepared in a mixed solution of ferrous and nickelous salts, using kbh4 as a reducing agent. conditions, such as quantity of naoh, concentration of salts, and species of surfactants, of preparation of fe - ni alloy were studied. the result show that fe - ni alloy were soft magnetic materials and they exhibited superparamagnetization at room temperature that have been widely used in industry
本文用液相還原法首次制備出纖維狀的fe - ni合金、球形的fe - co 、 co - ni合金、 fe - co - ni合金粉體材料，並對其性能進行了分析和測試，結果表明：這些合金粒徑小，比飽和磁化強度較大，矯頑力為零，呈現超順磁性，是非晶態的軟磁材料。W - cu composites prepared from the precipitation w - cu powder have higher sintered density, better mechanical and physical property, more homogeneous and finer microstructure than those prepared from w - cu powder by the balling - reduction method. in chapter 5, a combination of homogeneous precipitation and ball - milling process, namely the mechano - thermochemical process was employed to prepare ultra - fine w - cu powder
其中，球磨w一cu復合粉（ hp一m ）壓坯在1150下燒結30min后，可獲得相對密度大於99 %的幾乎全緻密的超細晶粒w一cu復合材料， w的顆粒度小於0 . 5林m 。The crystalline structure changes of pp induced by pan - milling were characterized by x - ray diffraction and raman spectroscopy. xrd analyses show that when pp was co - milled with uhmwpe, crystal transformation of pp occurred, its crystallinity and crystallite size decreased, whereas, only slight reduction of crystallinity and crystallite size were observed and no crystal transformation was found when pp was co - milled with wtr chips, and amorphization of pp was strongly enhanced by co - milling pp with iron
採用x -射線衍射研究了聚丙烯碾磨粉碎過程微觀結構變化， uhmwpe存在下pp發生晶型轉變、結晶度降低和晶粒尺寸減小；彈性材料wtr抑制pp塑性變形，碾磨導致分子堆積有序區域膨脹，晶面間距增大，結晶度下降；剛性材料金屬鐵與pp產生強烈摩擦，加快晶粒細化，晶格破裂導致非晶化。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。It is shown from results that increasing carburizing time further in the normal technology can not obviously deep the carburizing layer, but can cause nonmartensite microstructure at the bottom of the gear and coarse grain across the gear, these will heavily decrease the fatigue life of the gear
結果表明：在正常滲碳淬火工藝基礎上再延長滲碳淬火1小時，齒輪滲碳層深度變化不大，但其齒根局部表面處有非馬組織，且晶粒尺寸易產生異常長大現象，從而致使臺架疲勞壽命明顯下降。The adding of nano - particles and antioxidant ca n ' t affect the crystalline morphology of uhmwpe, but with the adding of antioxidant, the crystallinity increases and the average crystal size decreases, while the adding of nano - particles, the crystallinity decreases and crystal size increases
納米粒子和抗氧劑的添加對uhmwpe的結晶形態都沒有影響，但加入抗氧劑后uhmwpe的結晶度變大，晶粒尺寸變小，而納米粒子的加入使uhmwpe的結晶度變小，晶粒尺寸變大。Sol - gel method was used for preparing the nano - tio2 photocatalytic film on general glas slid and ito conductive glass. the spectrum property, surface image, crystlal type, particle size, thickness and other properties of this film were measured by uv - vis, afm, xrd and other apparatus
採用溶膠-凝膠法在普通玻璃載波片和ito導電玻璃上制備出負載型納米tio _ 2薄膜，並用uv - vis ， afm ， xrd等對納米tio _ 2薄膜的光譜特性、表面形貌、晶型及粒子大小、薄膜厚度等進行了表徵。Research into factors affectiong grain size during austenite grain test for steel
鋼的奧氏體晶粒度試驗中影響晶粒大小因素的研究Due to different combinations of temperature and grain size and strain rate, materials show quite novel mechanical behavior
溫度、晶粒大小、應變速率的不同組合下，材料會呈現復雜的力學行為。From the analysis of the microstructure of the modified epf30r, it indicated that the crystallinity, crystalline size, and the dimension of the filler particles of. the ppbc3b were all inferior to the epf30r ' s, which also verified the effect of the nucleator - dicpk
對改性epf30r的微觀結構分析結果表明ppbc3b的結晶度、晶體大小、所用填充粒子大小都要低於epf30r及相關材料，同時證實了成核劑dicpk的成核作用。The x - ray diffraction, scanning electronic microscope and the squid were used to characterize the properties of the mgb2 core in mgb2 / fe tapes and wires. the effect of the proportion of mg, b and sic as well as the sintering parameters on the phase formation, microstructure and the critical current densities of mgb2 / fe tapes and wires was discussed in details. the results showed that the high purity of mgb2 core could be synthesized by both the traditional vacuum sintering and the sparking plasma sintering and the vacuum sintering environment restrained the oxidation of mg effectively
相對于傳統真空燒結， sps燒結方式成相速度快、樣品晶粒細小均勻、 mgb2超導芯緻密性好、晶間連接優良，因而sps燒結樣品的臨界電流密度明顯高於傳統真空燒結樣品，其中未摻雜的帶材樣品經過sps800 ， 15分鐘燒結后，自場下的臨界電流密度jc值在10k時達到8 . 64 105a / cm2 ，而且隨著測量溫度和外加磁場的增加， sps燒結樣品的臨界電流密度下降率比傳統真空燒結樣品緩慢，在20k ，自場時為5 . 97 105a / cm2 ， 20k ， 3t時，臨界電流密度值仍大於104a / cm2 。Both of them are added to the reactor by way in turn at lower temperature to control the over - saturation of k2feo4, adoption of the lower reaction temperature as well as suitable reaction time, removing alkaline be done before disposing water and impurity in the purification procedure of k2feo4 cake
，其形貌呈長而薄的板條狀；該晶體的某些晶面與水氯法所得kj 。樣品相比出現了生長發育程度上的差異：本方法所得樣品的熱穩定性較高，隨著晶粒由小到大，固態凡eo 。的熱分解溫度為536 557k ，Using continuous compacting progress dy2o3 / zro2 materials can be sintered at low temperature. 98. 8 % of theory density was obtained for ultrafine dy2o3 / zro2 ceramic power sintering at 1200, which is 400 lower than the sintering temperature of the common ceramic power. it studied the influence of sintering temperature on the crystalline grain of power by sem
採用二次成型常壓燒結法對氧化鋯/氧化鏑的納米粉體進行燒結，在1200左右燒結得到燒結密度為理論密度的98 . 8的陶瓷體，其燒結溫度比常規陶瓷粉末的燒結溫度低四百度左右，通過掃描電鏡研究了燒結溫度對燒結體晶粒大小的影響。The results show that a certain extent, the other parameters constant, increasing power, increasing scanning speed, small grains become more dense ; the good and bad of metallurgical belt, the cellular crystal thickness and the availability and distribution of inclusions are affected by the parameters
結果表明：在一定范圍內，其它工藝參數不變，增加功率，增大掃描速度，晶粒更趨緻密細小；工藝參數影響冶金結合帶的優劣、胞狀晶區的厚薄以及夾雜物的有無和分佈。With frame gather card and ccd, metallographic image which can be processed by computer is acquired after a serials of the applications of digital image technique such as gray level transformation, dichotomy, noise eliminating, dilation and erosion, image enhancement, boundary detection, etc. an automatic quantitative metallographic analysis system is developed with visual c + + 6. 0 to realize the measuring of the size of the metal crystalline grain, evaluation the proportion of the second tissue of the metal, micro hardness. with three - level browser / server mode and active server technology, the system gives the remote user the applying service through network to communicate and analyze the image information
利用數字圖像處理技術，對圖像採集卡或ccd攝像頭採集到的金相圖像進行灰度轉換、二值化、噪音消除、圖像增強、邊緣提取等一系列圖像預處理，獲得計算機可以處理的數字圖像；並利用visualc + + 6 . 0開發定量金相分析系統，以實現對晶粒大小、金相組織第二相相對含量、顯微硬度等參量的自動測量；採用基於browser server的三層體系結構，通過網路訪問，並利用activeserver技術給遠程用戶提供應用服務，以便於根據圖像分析結果，給出專家分析意見，實現異地分析及交流。Vanadyl phthalocyanine ( vopc ) films prepared by vacuum deposition were annealed under magnetic field. uv - visible absorption results showed that the films annealed under magnetic field showed a q - band red - shift. x - ray diffraction study ( xpj ) ) indicated enhancement in diffraction intensity and shift of peak position
分析表明酞菁氧釩分子uv - vis吸收譜q帶峰值發生較大的紅移； xrd測試中衍射峰強度明顯增強，峰位變化，但峰寬變化不大；原子力顯微鏡（ afm ）分析發現晶粒大小無明顯變化。Thin films with thickness of 0. 31m and 0. 36m respectively on si substrate, have been successfully prepared by a sol - gel spin coating method. cubic nanocrystals can be obtained at relatively low sintering temperature with an average grain size of about 47 nm and 51 nm respectively. the aluminia - doped scsz thins film are the same dense as the scsz thin films. however, there are a small amount of pinholes found in the microstructure of the titania - doped scsz films
0 . 70固體電解質納米晶薄膜。燒結實驗結果表明，兩種薄膜均在650以上開始晶化，溫度越高，晶化越完全，在800可完全晶化所得納米晶顆粒呈純的螢石結構立方相鋁和鈦摻雜的納米晶顆粒的平均大小分別為47和51nm 。Results show that zro2 - ni cermet has clear crystalline interface and uniform distribution. its crystal size is 0. 3 p m. through analyzing the data of specific heat of zro2 - ni cermet, it reveals that adulterating cobalt can enhance the wetting quality of ni and zro2
用xrd 、 sem研究了zro _ 2 - ni - co金屬陶瓷的相結構和形貌，確定了合適的燒結溫度，結果表明，材料的晶粒大小和分佈十分均勻，晶界清晰，粒度在0 . 3 m左右。分享友人