x ray crystal structure 中文意思是什麼

x ray crystal structure 解釋
晶體x射線結構
  • x : X2＝ （羅馬數字）10 XX ＝ 20 IX ＝ 9 XV ＝ 15 XL ＝ 40 LX ＝ 60 XC ＝ 90 DXL ＝ 540 MX ＝ 1010 ＝...
  • ray : n 雷〈姓氏，男子名， Raymond 的昵稱〉。n 1 光線，射線，熱線；〈詩〉光輝，閃爍，曙光，一線光明。2 ...
  • crystal : n 1 結晶，（結）晶體；晶粒；水晶（＝rock crystal）；石英。2 【無線電】晶體。3 結晶玻璃；雕玻璃；...
  • structure : n. 1. 構造，結構；組織；石理，石紋。2. 建造物。3. 【化學】化學結構。4. 【心理學】（直接經驗中顯現的）結構性，整體性；整體結構。adj. -d ,-less adj.
  1. Consisting of the protracting graph of hydrogen - like atom ' s angle distributing, computer simulation of the symmetry of molecular orbital and chemical reaction mechanism, showing the molecular point group and symmetry element, computer simulation of molecular vibration, bravias ' s crystal lattice and their transforming, extracting of plane periodic lattice, extracting of solid periodic lattice, close packing of isometrical pellet and the structure of simple mental substance, close packing of unequal pellet and crystal structure of representative ionic crystal, computer simulation of phase analysis by x - ray diffraction

    內容包括類氫原子角度分布圖的繪制，分子軌道對稱性和反應機理的微機模擬，分子點群和對稱元素顯示，分子振動運動的微機模擬，布拉維晶格和晶格轉化，平面點陣抽取，立體點陣抽取，等徑網球的密堆積和金屬單質結構，不等徑圓球密堆積和典型離子晶體結構， x射線多晶衍射的微機模擬十個子模塊。
  2. Bipy 2, 2 - bipyridine has been synthesized. x - ray crystal structure analysis shows the complex crystallizes in monoclinic system, space group

    X -射線晶體結構分析表明配合物為單斜晶系，空間群
  3. Components, structure and surface morphology of the resulted films were identified by fourier transform infrared ( ftir ) spectroscopy, x - ray diffraction ( xrd ) and scanning electronic microscopy ( sem ). the analyses showed the content of cubic boron nitride in the resultant films on substrates was rather high and crystal particles of c - bn with uniform size, smooth crystal plane and regular shapes ( quadrangle and hexagon ) densely arrayed on the substrate

    傅里葉轉換紅外吸收（ ftir ）光譜儀、 x射線衍射（ xrd ）儀和掃描電鏡（ stm ）的測量結果顯示，基底上的bn膜中立方相含量很高，且晶粒大小均勻、排列緻密，晶形呈規則的四角和六角形。
  4. Meanwhile, based on the magnetic material theory, a complete analysis and summary are carried out on the three crystal structure and technology theory ; especially the ingredient analysis is made on the microscopical morphology and x - ray diffraction and its mixtures existence and relevant metallurgy about the typical second resource such as coldrolling iron and oxide red, steelmaking sludge and feso4 based on the practeal investigation of the pre - burning materials in domestic products plant, especially the analysis on the domestic markets and components, and connecting with reality and material characters in panzhihua iron and steel ( group ) cmpany, we established the product orientation and developing direction in panzhihua iron and steel ( group ) company ; after carrying out the technology reform on the old no. 1 magnetic product plant of enterprise company, making a detailed study on the various conditions for establishing a plant, the feasible research report is formed of 1400 tons ( per year ) feo preburning material and 3000 tons ( per year ) middle and high quality magnetic products ; so a necessary and reliable supports are provided both theoretically and practically for the development of the magnetic industry in panzhihua iron and s teel ( group ) cmpany

    同時，對磁性材料的理論基礎，尖晶石、磁鉛石、石榴石三大晶系結構以及其工工藝理論進行了較為全面的歸納、分析和總結；尤其針對攀鋼產生的二次資源如冷軋鐵紅、煉鋼污泥、硫酸亞鐵等三種典型原料分別作了成分分析、微觀物理形態以及x光衍射分析、其夾雜物的存在形式及相應的金相分析。對國內鐵氧體磁性材料的預燒料及磁件生產廠家的工藝、設備、技術、成本、質量狀況進行了實地的調研，特別是對國內磁性材料的市場及競爭對手進行了詳盡的分析，在此基礎上，結合攀鋼實際及原料特點確立了攀鋼發展磁材產業的產品定位及發展方向；對企業公司原有磁件一廠進行了技術工藝改造，對建廠各項條件進行了詳細的分析，形成了了年產14000噸年鐵氧體預燒料以及3000噸年中高檔磁件產品的可行性研究報告，從理論上和實踐上為攀鋼磁性產業的發展提供了必要的可靠的依據。
  5. Thirty - one crystals of polyoxometalates ( 1d, 2d, 3d ) were prepared by means of middle hydrothermal technique, molecular design and self - assembly, and characterized structurally by single crystal x - ray diffraction. the thermal stability, activity of catalysis and magnetism of some compounds were systematically studied. the continuous appearance of p - v - o, p - mo - o, v - mo - o, v - o system with novel structure enrich polyoxometalate chemistry, the reaction characterization and the synthesis law of molybdates, tungstates and vanadates under hydrothermal conditions were explored

    由於p - v - o 、 p - mo - o 、 v - mo - o 、 v - o體系新結構不斷出現，豐富了多金屬氧酸鹽化學，探討水熱條件下釩、鉬、鎢物種的反應特性和生成規律，研究原料的選擇、配比、加料順序、濃度、酸度、反應溫度、反應時間等因素對產物的生成及結構的影響，為新的催化劑、導電材料、磁性材料的研製與開發積累經驗。
  6. 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。
  7. Finally build the foundation to prepare the composites of structure and m - type ferrite with structure and function properties. the constituent phases, microstructure and crystal dimension and crystal coalescence, mechanical properties, magnetic properties of the composites were investigated by means of x - ray diffraction ( xrd ), scanning electron micrograp h ( sem ) and transmission electron micrograph ( tem ), mechanical testing instrument, vibrating sample magnetometer ( vsm ) respectively

    採用xrd技術鑒定復合材料的物相，利用sem ， tem來分析srfe12o19及其復合材料的結構形貌，顆粒大小及結合情況，使用伺服材料實驗機、洛氏硬度計及振動樣品磁強計（ vsm ）測試了復合陶瓷的抗彎強度、硬度及其磁性能，並探討它們之間關系。
  8. The epitaxial growths of ingaas / gaas / algaas fundamental material and the fabrication of 45 - deflector are extensively studied in our work. some measuring methods are used to evaluate the growth quality of our grown structure by pl, cv, x - ray double crystal diffraction, sem etc. property analysis are provided for it

    利用高能電子衍射、電化學c - v 、掃描電鏡（ sem ） 、 x射線雙晶衍射儀、光熒光譜儀（ pl ） 、原子力顯微鏡等多種方法對制備的器件進行了檢測，同時對實驗結果進行了必要的分析。
  9. And then, we measured x - ray diffractive spectrum of samples and investigated the crystal lattice structure of samples treated under different annealing temperature and different implantation condition comparing the diffraction peaks

    然後，通過x射線衍射測量了樣品的衍射譜，通過比較不同樣品衍射峰的形狀，了解了不同退火溫度及注入條件下樣品的晶格結構情況。
  10. Molar ratio of 111 in methanol - dmf mixed solution. single - crystal x - ray diffraction analysis shows that it consists of a cyano - bridged chain structure. the nd atom is eight - coordinate with a distorted square antiprism geometry. each cr

    摩爾比為111在甲醇- dmf混合溶劑中自組裝得到。由x -射線單晶衍射結構分析得知其屬于單斜晶系，空間群為
  11. The phase structure, the lattice constant, crystal grain diameter of the samples was obtained by the x - ray diffractions ( xrd ) spectra. their relations are showed respectively. influence of grain size on the lattice constant of several kind of phase structure was studied theoretically by interaction energy between atoms in nanocrystallites

    其次，從結合能的角度出發，研究了nacl結構和cscl結構的離子晶體，面心立方（ fcc ） 、體心立方（ bcc ）金屬晶體以及簡立方（ scc ） 、面心立方（ fcc ） 、體心立方（ bcc ）結構分子晶體的晶粒線度對晶格常數的影響。
  12. Sem, transmission electron microscopy ( tem ), x - ray energy - dispersion analysis ( edax ), xrd, electron diffraction ( ed ) and high - resolution electron microscopy ( hrem ) were used to investigate the morphology, atomic composition and crystal structure of the nanowires. the hexagonal cdse nanowires with single crystal structure have been obtained in dmso under 140. ( 3 ) semiconductor te and cdte nanowires embedded in aao templates were fabricated for the first time by dc < wp = 7 > electrodeposition in ethylene glycol

    Sem 、 tem 、 edax 、 xrd 、 ed 、 hrem分析的結果表明，所得cdse納米線為六方晶型，晶體的（ 001 ）晶面沿平行於基底的方向擇優生長，且隨沉積溫度的降低，這種擇優生長的趨勢越來越強；納米線晶體在生長時，由於受aao模板孔徑的限制，形成c軸方向拉長的晶粒，其長徑比達5 1以上；晶體的大小和完善程度隨沉積溫度的降低而增大， 185沉積得到多晶六方cdse納米線，而140沉積時可得到六方cdse單晶納米線。
  13. We use the basic theory of the x - ray diffraction for crystal to research the structure design of tcecs

    本論文主要利用x射線受晶體衍射的基本理論，對整個雙通道橢圓彎晶譜儀的結構設計進行研究。
  14. Main curricula : thermodynamic of material, crystal structure and the technology of x - ray, the principle of the solid state phase transition, the force behavior of material, metal material science, surface engineering, mate and engineering, the application of computer in material science

    主要課程:材料熱力學，晶體結構和x射線學，固態相變原理，材料力學性質，金屬材料學，表面工程，材料成型原理與工藝，計算機在材料科學中的應用
  15. The crystal structure of the martensite as quenching state, the variation of the structure of the martensite during non - isothermal aging in the martensite and parent state, under successive deformation condition and under thermal cycling condition in the cu - based shape memory alloys are studied by the x - ray diffraction

    摘要運用x -射線衍射分析技術研究了不同成分銅基形狀記憶合金淬火態馬氏體結構、馬氏體狀態非等溫時效過程中結構的變化規律、母相狀態時效和連續變形過程中馬氏體及母相結構的變化規律以及熱循環過程中馬氏體結構的變化情況。
  16. The investigation of structure by x - ray diffraction shows that crystal parameters changes clearly when percenting ca and la into pbtio _ 3, it was caused by the ca ion and la ion replaced the pb ion of a position in perovskite compound, that bring lattice mismatch and asymmetrical replace

    在pbtio _ 3中摻入la和ca可以有效改變薄膜的晶格常數，這是因為在abo _ 3型化合物中，鈣離子、鑭離子取代了a位的鉛離子，造成晶格失配和不對稱取代。
  17. Crystal structure analysis by x - ray

    射線晶體結構分析
  18. For adapting to the need of industrialization and improving the properties of materials, the method of mechanical activation has introduced on the basis of traditional calcinations at high temperature. the stardard spinel limn204 is prepared by the mechanical activation - high temperature solid synthesis method. the thermodynamic property, the physical - chemistry performance and the producing techniques of. battery have been studied by means of thermogravimetry ( tg ), differential scanning calorimetry ( dsc ), x - ray diffraction ( xrd ), scanning electric microscopy ( sem ) as well as various electrochemical analysis methods. studies show that synthesis temperature, calcinations time, recipe of raw materials, heat treatment and particle size of products are main factors affecting the performances of limn204 cathode materials. with the increment of synthesis temperature and time, the structure and crystal of products are getting to perfect

    隨著合成溫度和時間的增加，產物的結構和晶型越趨于完善，但在1100得到的產物有燒結和晶粒增大的現象，恆溫時間超過24h后對材料的性能影響不是很大； li mn比在0 . 95 1 . 05 2的條件下都可得到標準的尖晶石limn _ 2o _ 4 ，尤其當li mn比為1 . 05 2時，所合成的材料具有較好的電化學性能；通過兩段合成法制備的產物性能要比一段合成法法制備的產物性能好，而兩段間隔合成法比兩段連續合成法處理的材料性能更佳；顆粒的粒度隨著球磨時間的延長而減小，比表面昆明理工大學碩士學位論文摘要卻增大，粒度小且分佈范圍窄的材料有利於鏗離子的擴散。
  19. X - ray diffraction analysis and mult - peak separation applied software procedure analysis were used to determine the crystal phase and amounts of each sample. the influences of dipping time of dipping two kinds of phosphate saturable solution on the structure and the properties of kiln furniture were studied

    探討浸漬兩種磷酸鹽飽和溶液的浸漬機理，並用掃描電鏡的分析結果加以驗證；採用x -射線粉末衍射分析與多峰分離應用軟體程序分析、確定各試樣的晶相，計算各晶相的含量。
  20. 2. the chosen nanometer cacoj particles have been tested and analyzed through advanced instruments. 1 ) the crystal structure and average size of the nanometer cacos particles have been tested by rotatory anode harrow x - ray diffractometer

    2 、採用先進的儀器對所選擇的納米碳酸鈣粒子進行了測定： （ 1 ）使用旋轉陽極靶多晶x射線衍射儀測定其晶體結構和平均粒徑大小。
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