超比

基本解释 (translations)

hypergeometric

与超比相关的网络例句 [注：此内容来源于网络，仅供参考]

The Si/Al ratio of NaY molecular sieve was determined by an empirical formula of lattice constant obtained by extension function method of X-ray diffraction and framework Si/Al ratio of NaY molecular sieve determined by solid nuclear magnetic resonant spectrum method.

前言晶胞参数是决定晶体结构的重要参数之一，Na Y超稳分子筛属立方晶系，由于 Na Y超稳分子筛骨架硅铝比受许多条件的影响，如投料比、晶化温度、晶化压力和晶化时间等。通过研究发现分子筛骨架的硅铝比与其晶胞参数相关，而分子筛的硅铝比可作为合成分子筛产品质量的控制指标 [1] 。

Through electron micrograph, sepiolite is found to have net fiber structure shaped by straw bundle.

海泡石一超细水泥的实验看出，超细水泥具有粒径小、比表面积大、水化速度快的特点，在加入海泡石后，海泡石并没有对超细水泥的水化速度产生很大的影响，能够使超细水泥的一些施工性能得到更好的改善，同样对超细水泥的胶结强度、抗折强度、抗冲击韧性起到提升的作用。

With the addition of the agglomerant solution, the particle emission concentration in flue gas decreased significantly.The submicron particles agglomeration technology whose cost is cheaper can control the emissions of submicron particles and decrease the opacity of flue gas obviously without changing the operation parameters of the ESP.The particle agglomeration technique is a useful and promising method to control the emission of submicron particles from coal combustion.

结果表明，化学团聚对于超细颗粒物的脱除具有显著的作用，喷入团聚促进剂后的烟尘排放浓度远比无团聚和喷水的情况要低；团聚促进剂的高分子链对超细颗粒的吸附絮凝作用促进超细颗粒团聚，显著降低烟尘排放浓度，实现超细颗粒物经济高效脱除，达到国家新的烟尘排放标准。

SO〓〓/M〓O〓 solid superacid was applied to the photocatalytic oxidation of organic pollutants for the first time. Porous SO〓〓/TiO〓 solid superacid catalysts with high specific surface area were prepared by sol-gel method. The photocatalytic degradation of bromomethane was used as model reaction. The influence of impregnation with H〓SO〓 solution on the structure of catalysts and their photocatalytic performance was systematically studied by using X-ray diffraction, X-ray photoelectron spectroscopy, N〓 sorption analysis applying BET method, UV-Vis diffuse reflectance spectroscopy, FTIR spectroscopy, O〓-TPD and photocatalytic activity measurement. The acidity of TiO〓-based catalysts was investigated by Hammett indicator method, NH〓-TPD and IR spectra of pyridine adsorbtion. The mechanism of superacidifing effects on photocatalytic performances such as the photocatalytic degradation rate of bromomethane, apparent kinetic constant and apparent quantum efficiency was discussed.The results indicated that SO〓〓 is combined with metal ions of TiO〓 in a chelating bidentate mode.

本文首次将SO〓〓/MxOy型固体超强酸催化剂用于光催化氧化有机污染物研究，采用溶胶-凝胶法制备了具有多孔性和大比表面结构的二氧化钛基固体超强酸光催化剂SO〓〓/TiO〓，以光催化降解溴代甲烷为模型反应，系统地研究了H〓SO〓浸渍处理对催化剂表面酸性及其气相光催化性能的影响，结合XRD、BET、XPS、FTIR、Hammett指示剂法、吡啶吸附红外光谱、NH〓-TPD、O〓-TPD、紫外可见漫反射光谱等多种表征手段，深入地讨论了超强酸化对TiO〓的改性机理，阐明了引起SO〓〓/TiO〓超强酸催化剂光催化降解溴代甲烷的转化率、表观反应速率常数和表观量子效率变化的本质原因。

The structural and photocatalytic properties of TiO〓 as well as surface acidity were greatly improved by sulfation. SO〓〓/TiO〓 solid superacid with Hammett constant Ho less than -12.14 was prepared by treating the TiO〓 with 1.0mol. L〓 sulfuric acid solution and then calcining at 450℃ for 3h. When compared to unmodified TiO〓, the SO〓〓/TiO〓 superacid catalyst exhibited higher anatase content, smaller crystal size, higher specific surface area, centralized pore size distribution, and the blue-shifted band edge of uv-vis adsorption spectra. Furthermore, the SO〓〓/TiO〓 superacid also showed excellent reaction activity and stability for CH〓Br photocatalytic decomposition even under the moist reaction conditions. The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明：SO〓〓与TiO〓表面的结合为螯合式双配位结构；TiO〓光催化剂表面经H〓SO〓浸渍处理后，提高了表面酸性，改善了催化剂结构和光催化性能，当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时，可制得SO〓〓/TiO〓超强酸催化剂(H〓＜-12.14)，其结构和光催化活性得到明显改善，与TiO〓相比，SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移，具有优异的光催化氧化活性、稳定性及抗湿性能，光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级，是一种有实际应用前景的高效光催化剂；由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型，认为在SO〓〓/TiO〓超强酸催化剂表面，由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心，其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移，具有可逆吸附水的性能，是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

Their catalytic activities in the condensation reaction of cyclohexanone with ethanediol were studied.The results showed that the catalytic activity of SO_4~(2-)/ZrO_2-Ce_2O_3 in the condensation reaction ...

实验表明：(1)SO42-/ZrO2-Ce2O3在缩合反应中的催化活性比SO42-/ZrO2和SO42-/ZrO2要强；(2)引入适当数量的Ce2O3使得固体超强酸的酸强度增大；(3)当固体超强酸SO42-/ZrO2-Ce2O3的制备条件为焙烧温度550℃、焙烧时间4h、Ce2O3质量与ZrO2质量比2%时，酸对缩合反应的催化活性最高。

The structure of supersonic combustion flow field was analyzed. The effects of temperature and equivalent ratio of supersonic premixed flow on the structure of supersonic combustion flow field, ignition and flame propagation were studied.

采用普通的纹影系统实现了高温超声速燃烧流场显示；对超声速燃烧流场结构作出了分析；研究了超声速预混可燃气的温度以及当量比对超声速燃烧流场结构、点火与火焰传播特性的影响。

Using Field single ignition experiments of the four unconfined volume dispersion and small dosage solid FAE and TNT bombs experiments, we got the peak overpressures of solid FAE at different distances. Compared with TNT, The overpressure of FAE is 1.14~1.6 times higher than that of the TNT. Based on the theory of the air shock wave overpressure, the FAE relativity TNT mass is evaluated. At the edge of the explosive field, the number is 3.88. Pictures of high speed photography indicate that the duration and the most effect area of the FAE and TNT. Compared with TNT, obviously the FAE has more advantages. And, based on the theory of the critical concentration of dust explosion, the radius of dust explosive zone is evaluated. The phenomenon that the overpressure decays rapidly with distance is analyzed. It is suggested that the explosive temperature should be increased as the main approach to improve the FAE explosive capability in the condition when the over pressure is invariable.

通过四组无约束固态燃料空气炸药装置与等质量的TNT在野外开放空间的一次起爆对比实验，测得了不同配方组份FAE装置在不同距离的爆炸超压分布，FAE装置峰值超压比相同距离的TNT高1.14-1.6倍；并运用空气冲击波峰值超压公式计算出了FAE的等效爆炸TNT当量随距离的变化关系，在爆炸场边缘区，FAE装置爆炸当量达到了3.88倍TNT当量；通过高速摄影的图片得到了爆炸产生火球的持续时间和最大作用范围，与等质量TNT爆炸火球相比，FAE的优势明显；运用粉尘爆炸下极限浓度估算了云雾爆轰区半径，并分析了测量到的固态FAE爆炸场的压力分布单调衰减的原因；建议在保持超压不变的情况下，把提高爆温作为提高FAE爆炸性能的主要途径。

Therefore, the EL spectra of (Znq_2)_4 is wider than that of Znq_2. 4._2 was synthesized. The analysis of molecular spatial structure and the characterization of material performance of_2 and Liq showed that two Liq molecules and two Naq molecules were connected by Na-O-Na bond bridges to form_2. Compared with Liq,_2 exhibits stronger rigidity in planar molecular structure, larger steric hindrance and intermolecular distance, and much smaller molecular polarity, thus resulting in much longer fluorescence lifetime, much higher fluorescence quantum efficiency, wider energy bandgap and better film formability. When used as light-emitting layer in OLED,_2 shows lower formation probability of excited dimmer and exciplex formation than Liq, thus emits bluer light with higher current efficiency than Liq. When_2 ultrathin film is used as electron injection layer in OLED, it exhibits higher current density, higher luminance, lower turn-on voltage and higher current efficiency than Liq ultrathin film for the existence of sodium ions in_2 ultrathin film. 5. The summarization the relationship between molecular spatial structure and material performance of Alq_3,(Znq_2) and Liq, lead the conclusion that the molecular spatial structure of Mq_n affects its material performance in such aspects as the rigidity of planar molecular structure, intermolecular interaction, molecule stacking mode and intermolecular distance.

制备了_2，通过对_2和Liq的分子空间结构与性能进行分析与讨论，发现_2是通过两个Na-O-Na键桥将两个Liq和两个Naq连接构成的，其分子平面结构的刚性程度强于Liq，空间位阻大于Liq，分子之间的距离大于Liq，分子极性远远小于Liq；_2的荧光寿命长于Liq，荧光量子效率高于Liq，成膜性优于Liq；_2的禁带宽度比Liq大，光致发光光谱中_2的最大发射峰较Liq发生蓝移；当_2在OLED中作为发光层时，激发二聚体与激基复合物的生成几率远远小于Liq，发的光比Liq更蓝，电流效率大于Liq；_2超薄膜中有Na离子的存在，与Liq超薄膜相比，当其在OLED中作为电子注入层时，具有更大的电流密度，更高的发光强度，更低的阈值电压和更高的电流效率 5、对上述Alq_3、Znq_2和Liq的分子空间结构与材料性能之间的关系进行了归纳总结，认为Mq_n的分子空间结构主要在分子平面结构的刚性程度，相邻分子之间的相互作用，分子堆叠的方式和分子之间的距离这四个方面影响其性能。

与超比相关的网络解释 [注：此内容来源于网络，仅供参考]

confluent hypergeometric equation：合流超几何方程;合流超比方程

合流分析 confluence analysis | 合流超几何方程;合流超比方程 confluent hypergeometric equation | 合流超几何函数;合流超比函数 confluent hypergeometric function

confluent hypergeometric function：合流超几何函数;合流超比函数

合流分析 confluence analysis | 合流超几何方程;合流超比方程 confluent hypergeometric equation | 合流超几何函数;合流超比函数 confluent hypergeometric function

hypergeometric differential equation：超几何微分方程;超比微分方程

超椭圆积分 hyperelliptic integral | 超几何曲线;超比曲线 hypergeometric curve | 超几何微分方程;超比微分方程 hypergeometric differential equation

generalized hypergeometric differential equation：广义超几何微分方程;广义超比微分方程

广义高斯和 generalized Gaussian sum | 广义超几何微分方程;广义超比微分方程 generalized hypergeometric differential equation | 广义逆元 generalized inverse

hypergeometric function：超几何函数, 超比函数

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hypergeometric function：超幾何関数

hypergeometric equation 超比方程,高斯微分方程 | hypergeometric function 超幾何関数 | hypergeometric polynomial 超比多项式

hypergeometric：超比

hypergenesis 表生蚀变 | hypergeometric 超比 | hypergeometric 超几何

hypergeometric：超比 超几何

hypergenesis /表生蚀变/ | hypergeometric /超比/超几何/ | hypergeusia /味觉过敏/

hypergeometric function：超幾何関数

hypergeometric equation 超比方程,高斯微分方程 | hypergeometric function 超幾何関数 | hypergeometric polynomial 超比多项式

hypergeometric polynomial：超比多项式

hypergeometric function 超幾何関数 | hypergeometric polynomial 超比多项式 | hypergeometric tail-area probability 超几何尾区概率