晶體間反應 的英文怎麼說

中文拼音 [jīngtǐjiānfǎnyīng]
晶體間反應 英文
crystal reaction
  • 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。
  • 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...
  • 反 : Ⅰ名詞1 （方向相背） reverse side 2 （造反） rebellion 3 （指反革命、反動派） counterrevolutionari...
  • 應 : 應動詞1 （回答） answer; respond to; echo 2 （滿足要求） comply with; grant 3 （順應; 適應） suit...
  • 晶體 : [晶體學] crystal; vitrella; crystal body; crystalloid; x-tal
  1. Through the relationship between sodium chloride and target crystal : calcium hypochlorite hydrate, the recycle of mother liquid, the principle of reactive crystallization of sodium - process bleaching power was analyzed

    從氯化鈉與目標晶體水合次氫酸鈣間的關系、母液循環等角度分析了鈉法漂粉精工藝的反應結晶原理。
  2. The effects of main process factors such as feeding mode, reaction ph values, and ratio of ammonia and nickel ion, reaction time, agitation, reaction temperature and aging et al on the crystallization course and physical properties of nickel hydroxide were studied in detail. at last, we acquired the optimal preparation parameters, the spherical nickel hydroxide with high tap density and crystalloid degree, perfect flow ability were prepared

    在研究加料方式，氨水的加入量，反應時間、體系ph值、反應溫度、攪拌、陳化等主要工藝條件對ni （ oh ） _ 2結晶過程和物理性能影響的基礎上，確定了較優的工藝參數，制備出了堆積密度和結晶緻密程度較高、流動性較好的球形ni （ oh ） _ 2 。
  3. Based the eag - i etchant, a new etchant was developed, with which the etch pit pattern on ( 110 ), ( 111 ) and ( 100 ) faces of czt crystals can emerge immediately and effectually. this pager investigated relation between the ( 110 ) faces of cutting from crystals conveniently and accurately by laser reflex method. by the surface treatment, the nuclear radiation detector was fabricated with ( 110 ) of czt crystal and strong 241am responsibility was observed

    在改變e _ （ ag ）腐蝕液的配方的基礎上，研製了新的腐蝕液，可方便、快速、有效的顯示czt不同晶面的缺陷蝕坑形貌;研究了利用激光正反射法和自然解理的不同（ 110 ）面之間的關系，方便、快速、準確的進行定向切割晶體的方法;採用生長的czt單晶體自然解理的（ 110 ）面，經過表面處理，試制了探測器元件，對24lam有較強的響應。
  4. 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。
  5. Crystal zirconium phosphate - phosphonate has the stability and regulity of interlayer floor of inorganic a - zirconium phosphate, they still have the designability of the organic group in the interlayer and adjustment of the ratio of organic and inorganic phosphorus acid, they are a kind of potential smart material, we can process molecule design and optimize filtration according to the requirement of goal reaction, we can prepare special ion - exchange, catalyst, catalyst supporters nonlinear optics compound, solid state proton conductivity and the intercalation complex precusor by introducing different active organic group or active center into the choice and stable framework of inorganic a - zirconium phosphate

    有機?無機晶態混合磷酸鋯具有無機磷酸鋯的層板穩定性和規整性，同時具有層間有機基團的可設計性和有機無機磷酸混合配比的可調節性的特點，是一類很有潛力的靈巧材料，並且可以根據目標反應的要求進行分子設計和優化篩選，在無機磷酸鋯優良穩定的骨架上引入不同的活性基團或活性中心，可以制備出性能獨特的離子篩、催化劑、催化劑載體、非線性光學物質、固態質子導體和制備插層復合物的前驅物。
  6. The results indicated that the dimension, shape and purity of base material could meet the functional demand of solid lubricant ; the thermal decomposition temperature of ptfe resin exceeds 400 c, but organic and inorganic packing filler added in ptfe made the water absorption rate of composite material increased, melting temperature and decomposition temperature decreased, in the meanwhile oxidative decomposition reaction was accompanied ; polar groups such as c = o, c - o - c and so on in the carbon fiber surface is advantageous to increase compatibility with other components and interlayer shearing strength ; uniform design experimental method could help to find the relationship between formula and frictional property by relatively small tests. the developing trend of each formula ' s friction coefficient could be showed by fitting curve ; the friction coefficient with no copper powder or graphite in formula was relatively big. this fact showed that copper powder and graphite should be used cooperatively ; it was found that when the ratio of copper powder to graphite by weight is 15 : 60, 30 : 30 - 40 and 60 : 15 - 30 respectively, the friction coefficient was relatively small. the degree of crystallinity of pure ptfe reached maximum by air cooling and the abrasion loss also reached maximum among three ones ; at the same time, the abrasion loss of solid lubricant sample was also the biggest among three ones ; when solid lubricant matched with 45 # steel axle or gcrl5 steel axle, lubricant transfer film could be formed on metal surface, thus direct contact between the surface of metal friction pair rings was reduced. their working life was elongated extremely ; there was mainly much graphite, a little ptff, moo3, feso4, cus and so on in lubricant transfer film

    試驗結果表明：所選原料的尺寸、形狀及純度可滿足固體潤滑劑的性能要求；聚四氟乙烯樹脂熱分解溫度超過400 ，但在ptfe中加入無機填料會使復合材料吸水率提高，熔融溫度及分解溫度降低，且伴有氧化分解反應；碳纖維表面含有c = o及c - o - c等極性基團，有利於提高其與其它組分的相容性，提高層間剪切強度；均勻設計試驗方法能夠用較少的試驗次數找出配方與摩擦性能間的關系，擬合曲線基本能表示各配方的摩擦系數發展趨勢；配方中不加銅粉或不加石墨，其摩擦系數均較高，說明銅粉和石墨應該配合使用；當銅粉15份、石墨60份時，銅粉30份、石墨30 - 40份時，銅粉60 、石墨15 - 30份時，摩擦系數均具有較低值；純聚四氟乙烯樹脂在空氣冷卻時結晶度最大，磨損量也是三者中最大的；同時，固體潤滑劑試樣在空氣冷卻時的磨損量也是三者中最大的：不論是固體潤滑劑與45 #鋼軸配副或是固體潤滑劑鑲嵌入銅套后與gcr15鋼軸配副，在金屬表面均可形成潤滑轉移膜，從而減少金屬摩擦副表面間的直接接觸，大大延長其使用壽命;轉移膜中主要含有較多的石墨、少量聚四氟乙烯、 moo 。
  7. The voltage of lithium - intercalation reaction, impedance and structural stability of intercalation - type cathode material were analysed and calculated. theoritical results show that the reaction voltage depends on the content of lithium and the bond energy, and that the key ways to lower the electrode impedance are to increase the electronic conductivity of the electrode and the diffusion coefficient of lithium ion in the host and to decrease the size of powder. in addition, the thermal stability of lithium - insertion structure can be improved by using crystallographic co - lattice theory and doping treatment

    本文從嵌入式陰極材料的嵌鋰反應的電壓、阻抗及結構穩定性的分析和理論計算著手，得到了電壓取決于基體中各種離子間的鍵能及鋰含量、降低電極阻抗的關鍵是提高電子型導電性和li ~ +在基體中的擴散系數及減小粉末粒度的理論依據及其利用晶體的共格原理和摻雜改性的方式來提高材料嵌鋰結構的熱穩定性的設計思路。
  8. Abstract : the affects of crystal absorption for heat radiation on crystal growth, which include : the heat loss of the hot grower, the chara - cteristic of temperature - time of crystal growth, the pattern of fluid flow and the shape of interface, the interface inversion of crystal, the temperature distribution and the thermal stress distribution, are reviewed in this paper

    文摘:本文綜述了晶體對熔體熱輻射吸收對晶體生長的影響，包括對熱腔熱耗散的影響；對晶體生長溫度時間特性的影響；對液流形態和固液界面形狀的影響；對晶體界面反轉的影響；對晶體中溫度分佈和應力分佈的影響。
  9. The electrochemical impedance spectroscopy of nickel electrodeposition indicates that nickel electrodeposition occurs in two steps, the medium frequency inductive loop is ascribed to the relaxation of the electrode coverage by an adsorbed intermediate such as niohads, the low frequency capacitive loop may be due to the inhibition of nickel electrodeposition by adsorbed hydrogen. the mechanism and equivalent circuit of nickel electrodeposition were proposed on the basis of the analysis of electrochemical impedance spectroscopy

    不銹鋼電極上電積鎳的電化學阻抗行為表明氨絡合物體系鎳電沉積過程是二次放電過程，中頻感抗弧是由於中間吸附產物nioh _ （ ads ）的弛豫現象引起，低頻容抗弧可能是由於吸附氫原子對鎳結晶的阻滯作用引起，依據實驗結果提出了氨絡合物體系鎳電沉積的反應機理和等效電路模型。
  10. Noticing that strong exothermic reaction due to large negative enthalpy of mixing can occur among major components of ti - zr - based quasicrystal alloy systems and zr - based bulk amorphous alloy systems, we developed for the first time a new technique for fabricating both ti - zr - ni systems quasicrystal materials and zr - al - ni - cu systems amorphous - based composite materials using laser - induced self - propagating reaction synthesis ( lsrs )

    注意到構成ti - zr基準晶合金體系和zr基大塊非晶合金體系的主要組元之間具有很大的負混合焓，因而能夠發生很強的放熱反應。利用這一特點，我們首次開展了激光誘導自蔓延反應合成ti - zr - ni系準晶材料和zr - al - ni - cu系非晶復合材料的探索研究。
  11. This edta route has several remarkable advantages in comparison with other method. because of the greater ability of edta anions to chelate metal cations, and forming very stable and soluble complexes, all of the starting materials are mixed at the molecular or atoms level in a solution, it is easy to control the composition and a high degree of homogeneity is achievable

    傳統的合成方法是高溫固相反應，由於灼燒溫度高、灼燒時間長，形成硬團聚體，產物粒徑較大，一般為m級，需進行球磨粉碎以減少其粒徑，很難制得均相、均一粒度分佈的氧化物粉體，在研磨過程中容易引入雜質且晶形破壞使得發光亮度減小。
  12. 7. based on our crsi and algorithm and double lcslm, an adaptive optical hardware system which c & n be used to model arbitrary complicated wavefront and the compensation of the wavefront can be accomplished was built. and according to the characteristic of a crs interferogram of a step wavefront produced by an lctv, the pixel - level calibration of this system is implemented

    七、採用已建立的空間相位調制環路徑向剪切干涉儀及其波前重建演算法，和位相調制持性已知的兩塊液晶空間光調制器，創建了一套用於模擬產生任意畸變波前並加以檢測和反饋控制的自適應光學硬體系統，並通過臺階波前對該系統實現了像素級校準。
  13. To make cds / k4nb6o17 powder on the base of the k4nb6o17 powder which by the courses of ion exchanging, amine intercalation, sulfuration etc. to obtain cds / k4nb6o17 thin film through the same course of making cds / k4nb6o17 powder on the base of k4nb3o17 thin film on the quartz which made by the spin coating and after heat treatment. to make experiments with additives ( na2so3, 0. 1mol / l ) of photocatalytically decomposing water into h2 and o2 to evaluate the photocatalytic activities of the catalyst knb6o17 powder, cds / k4nb6o17 powder, k4nb6o17 film, cds / k4nb6o17 film. the crystalline structures of the midst powder and film productions were investigated by using the x - ray diffraction ( xrd )

    本課題的主要內容是：高溫固相反應合成具有層狀結構的k _ 4nb _ 6o _ （ 17 ）晶體材料，然後以此為母體材料，通過離子交換、層間胺插入、硫化處理等過程制備出cds / h _ 4nb _ 6o _ （ 17 ）粉末形式的光催化材料；通過旋轉塗覆法在石英玻璃基片上制備了k _ 4nb _ 6o _ （ 17 ）薄膜，採用一定的熱處理制度后對薄膜分別進行離子交換、層間胺插入、硫化處理等處理過程制備了cds / h _ 4nb _ 6o _ （ 17 ）薄膜形式的光催化材料。
  14. Several liquid crystals and intermediates were synthesized with this new technique

    通過微波反應合成一系列常用的含氰類液晶單體和中間體。
  15. The properties of cn thin films such as their morphology, component, crystal structure and the bonding structure and the relation between those properties and the gas - phase reaction parameters were discussed, showing that the deposition of p - c3n4 thin film is the compete result of various reaction processes in the dynamics balance conditions ; the process of cn films depo sition is diagnosed in situ through the optical emission spectra technique, the effects of experimental parameters on the concentration of the precursors and the gas - phase reactions in the plasma have been obtained ; the main reaction precursors for film deposition identified ; the relation between the characteristics of cn thin films and the reaction process in the plasma is analyzed. the cn thin films deposition under different substrate temperatures in high pressure pe - pld shows that the si atom of the substrate has participated the cn films growth process, based on this the growth mode of cn thin films on the si substrate is proposed. the further experiment of cn thin films deposition on si substrate scratched by diamond as well as covered with fe catalyzer has been attempted, which indicates that changing the dynamics conditions of the surface reaction can alter the growth characteristic of the cn thin films and can enhance obviously the films growth rate

    採用pld技術進行了碳氮化合物薄膜沉積，得到了含氮量為21at的cn薄膜；研究了襯底溫度和反應氣體壓強對薄膜結構特性的影響，給出了cn薄膜中n含量較小、 sp ~ 3鍵合結構成分較少和薄膜中僅含有局域cn晶體的原因；引入脈沖輝光放電等離子體增強pld的氣相反應，給出了提高薄膜晶態sp ~ 3鍵合結構成分和薄膜的含n量可行性途徑；應用pe - cvd技術以ch _ 4 + n _ 2為反應氣體並引入輔助氣體h _ 2 ，得到了含n量為56at的晶態cn薄膜；探討了cn薄膜形貌、成分、晶體結構、價鍵狀態等特性及其與氣體壓強和放電電流的關系，證明了- c _ 3n _ 4薄膜沉積為滿足動力學平衡條件的各種反應過程的競爭結果；採用光學發射譜技術對cn薄膜生長過程進行了實時診斷，得到了實驗參量對等離子體中活性粒子相對濃度和氣相反應過程的影響規律，給出了cn薄膜沉積的主要反應前驅物，揭示了cn薄膜特性和等離子體內反應過程之間的聯系；採用高氣壓pe - pld技術研究了不同襯底溫度條件下cn化合物薄膜的結構特性，揭示了si原子對薄膜生長過程的影響，給出了si基表面碳氮薄膜的生長模式；在金剛石研磨和催化劑fe處理的si襯底上進行cn薄膜沉積，證明了通過控制材料表面動力學條件可以改變碳氮薄膜結構特性，並可顯著提高晶態碳氮材料的生長速率。
  16. The formation process of w - type ferrite underwent from oxide of metal, the m - type transition phase to final w - phase. when the heating rate was 5 / min, at 900 for 3 hrs and 1200 for 4 hrs, pure m - type and w - type ferrites were formed in air respectively. with heat treatment temperature increasing, crystal structure was more intact, the saturation magnetization increased and the coercive force decreased

    熱處理過程表明， m型鐵氧體直接由金屬氧化物反應形成，未經歷尖晶石中間相； w型鐵氧體形成由金屬氧化物到m相過渡相最終向w相的轉變；當升溫速率為5 min ，溫度在900 ，保溫3小時和1200保溫4小時，就分別形成單相m相和w相鐵氧體；隨著熱處理溫度的升高和保溫時間的延長，衍射峰變尖銳，結晶更完整，空心微球的飽和磁化強度增大，矯頑力減小。
  17. It was found that the interfacial bonding of 93w - ofc was both the joining action of ofc / w grains and that of ofc / ni - fe binders, whereas the joining of ofc to tc4 could be seen as the mutual intense diffusion effect between ofc / tc4 and as a result cu - ti intermetallic compounds were formed at the joint. the joining of tc4 - a1 and a1 - mb2 were also attributed to the result of diffusion between elements ti - al and al - mg respectively. on the other hand, residual thermal stress and stress - induced distortion were produced at the joint simultaneously due to the difference in thermal expansion coefficient of different welding " materials

    研究表明， 93w與ofc的界面連接是ofc與93w中w晶粒的連接以及ofc與93w中ni - fe粘接劑的連接共同作用的結果； ofc與tc _ 4連接界面的形成是由於ofc與tc _ 4之間發生反應擴散，並由此在二者接頭處生成了cu - ti金屬間化合物的中間相； tc _ 4 - al的連接與al - mb _ 2的連接則分別是其基體元素ti 、 al之間和al 、 mg之間元素互擴散的結果，另外，由於熱膨脹系數的差異，擴散焊接后在不同焊件的接頭處存在殘余熱應力並由此引起接頭的形變。
  18. The forming - nucleus drive power could form numerous little crystal nucleus under natural melting temperature. the formation of tic particles in the melt could be divided into two phases which was forming - nucleus and growth. the forming mechanism of tic was : melting ti first surrounded c, then ti melting in the alloy and c formed a complicated reaction mesosphere on the carbon surface

    根據熱力學及動力學分析，認為在碳顆粒界面處tic的形核率很高，形核驅動力足以在正常的熔煉溫度下形成眾多的小晶核；熔體中tic顆粒的合成可分為形核與長大兩個階段，其形核機制為：首先活性ti原子包圍c ，溶入合金中的ti與c在碳表面形成一復雜反應中間層，隨著反應進行， ti和c顆粒不斷減少，生成的tic不斷彌散分佈於熔體中；其長大過程伴隨著tic顆粒的相互堆砌、聚集和形態規則化。
  19. Cosb3 micrometer powder has been synthesized by solid - state reaction. cosb3 nano - powders were prepared by high - energy ball - milling respectively. the influence of mass ratio of big balls and small balls, milling speed and time on particles size of cosb3 powder, were investigated

    採用固相反應法合成了平均晶徑約為3 m單相cosb _ 3粉體，採用高能球磨法制備了納米cosb _ 3化合物粉體，研究了球磨參數（球料比、級配、轉速和時間）對粉體顆粒尺寸的影響。
  20. Abstract : new progress of raman technique in the research on macromolecule science recent years was summarized in this paper including the miscibility of polymer blends, the mechanism of surface plasticization, the monitoring of stress and strain relaxation process, raman imaging, the monitoring of polymerization, determination of curing process, the monitoring of crystal process in polymer and the study on the structure of water and intra - and inter molecular interactions in the solution of polymer and gelatin. a great deal of research of raman technique in this aspects were also summarized

    文摘:綜述了拉曼技術在高分子科學研究中近年來的最新進展，包括聚合物共混物的相容性、表面增塑機理、應力鬆弛和應變過程的監測以及拉曼成像、聚合反應監控、固化過程監測、聚合物結晶過程監控、聚合物水溶液和凝膠體系中水的結構及分子間、分子內相互作用力的研究。
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