电荷量

The primary conclusions of the present work are as following first, the charges of membrane sarface effect the rate of protein adsorption, but do not effect the amount of protein ultimately adsorbed second, the nonspecific adsorption of avidin can be detached by adding a suitable amount of bivalent alkaline-earth metal ions; third, the binding of avidin to membrane bound model receptor is astricted remarkable by the latelal steric hindrence.

实验结果表明，膜表面电荷对非特异性吸附的速率有很大的影响，而对最终的蛋白吸附量影响不大；非特异性的吸附可以通过二阶阳离子的脱附而去除；受体蛋白质与配体间的特异性结合受到侧向空间位阻效应的制约。

It can be seen that the bulk modulus depends mainly on electrons per atomic volume and mass density, while covalent structure of chemical bonding and N content make more contribution to theoretical hardness, and appropriate content N—N covalent bonding in the same direction tends to increase the shear modulus of nitrides.

说明在Tc的氮化物中，其体弹模量与材料的晶体结构、平均每个原子上的电荷密度和材料的质量密度有关；化学键的共价性结构和氮元素的含量对理论计算硬度有正作用；而剪切模量的极大值则与其层状结构及体系中一定量的方向基本一致的N—N键相关。

According to Lorentz transformation,the relativistic covariant of electromagnetic field tensor and 4-dimension forces,and the relativistic invariance of electric charge,it can be directly proved that a moving magnetic monopole will be acted- by a magnetic Lorentz force ,and that the magnetic Lorentz force has the same accuracy as the Coulomb low.

概述了磁单极概念的历史发展，从洛伦兹变换出发，利用电磁场张量和四维力的协变性以及电荷相对论不变，直接证明了运动磁单极受磁洛伦兹力，建议了一个磁洛伦兹力的验证方案，并用磁洛伦兹力公式导出狄拉克电荷量子化条件。证明了磁洛伦兹力公式具有与库仑定律相同的精确度

The results show that the major contribution to DOS of Mg and Pb are the 2p orbit of Mg and the 5d orbit of Pb, followed by the 3s orbit of Mg and the 6p orbit of Pb, the 6s orbit of Pb is the smallest one. There are a large number of charges around Mg, it has the characteristics of typical metal bond. Mg and Pb share some charges to form covalent bond, but the distortion of the charge at the junction is little; the proportion of covalent bond is less than the metal bond, Mg2Pb is semimetal. The elastic modulus and shear modulus of Mg2Pb are 68.6 and 27.9 GPa, respectively. Based on Pugh empirical criterions and Poisson's ratio, Mg2Pb is brittle in nature.

结果表明：Mg和Pb对态密度的贡献主要是Mg的2p轨道和Pb的5d轨道，其次为Mg的3s轨道和Pb的6p轨道，Pb的6s轨道贡献最小；在Mg原子周围有大量的电荷存在，呈典型的金属键特征，Mg、Pb之间存在共用的电荷，有较强的离域性，以共价键形式存在，但交界电荷的畸变不大，故共价键所占比例较少，金属键所占比例较大，Mg2Pb化合物呈半金属性；Mg2Pb的弹性模量和切变模量分别为68.6和27.9 GPa，Pugh经验判据和泊松比均表明Mg2Pb具有脆性。

It was particularly observed that, with increasing fraction of Q〓 mode Jahn-Teller distortion and decreasing of that of Q〓 mode in the CO state, the magnetic structure evolves from CE-type to C-type, orbital ordering from 3d〓/3d〓 to 3d〓, and crystal structure from tetragonally compressed to tetragonally elongated orthorhombic.

特别是，我们发现〓在电荷有序态下随着Ca〓离子掺杂量从x=0.5增大到x=0.75，合作Jahn-Teller晶格畸变的畸变模式从Q〓模式逐渐转变到Q〓模式，这种晶格畸变模式的转变直接导致了电荷有序态下的磁结构从CE-型转变到C-型，轨道序从3d〓/3d〓转变到3d〓，晶体结构从压缩的正交对称性转变到拉伸的正交对称性。

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。

However, for a femtoampere level of current, it may be better to use the coulombs function of an electrometer to measure the change in charge over time and then use those charge measurements to determine the current.

对飞安级电流，用静电计的库仑表功能测量整段时间的电荷变化量和用这些电荷测定电流更好。

The cause of the C-V curve stretch-out is interface trapped charge.The hysteresis loop direction and area can to obtain type and amount of charges. From the result of measure, clockwise hysteresis loop is negative charges.

在磁滞方面，磁滞回路方向与面积可得知缺陷捕获电荷的形态与数量，由量测结果得知，磁滞回路为顺时钟代表捕获的电荷为负电荷。

In this study, we used poly L-latcide, poly DL-latcide-co-glycolide 75:25 (PLGA7525) and poly DL-latcide-co-glycolide 50:50 (PLGA5050) during citric acid inducing ammonium bicarbonate gas forming process to form porous polymer film, and rolled the porous polymer film to make nerve conduits with pores and multi-layered. Electron Spectroscopy for Chemical Analyzer and Attenuated Total Reflectance – Fourier-Transform Infrared Spectrometer were employed for determining elements' functionabilities and chemical compounds. Charge Coupled Device camera and Scanning Electron Microscope were employed for macroscopic and microscopic morphologies and structural observation. Differential Scanning Calorimetry was employed for measuring glass-transition temperature. Nano-indentation system was employed for measuring elastic modulus and hardness. Biodegradation and water absorption ratios were measured to analyze their chemical properties and SEM was employed for microscopic morphology of the tested nerve conduit.

本研究将以聚乳酸、聚乳酸-聚甘醇酸共聚合物（75：25）、聚乳酸-聚甘醇酸共聚合物（50：50）做为研究材料，以柠檬酸诱发碳酸氢铵发泡之气泡成型法制作具有相连通孔隙之高分子薄膜，再将高分子薄膜卷制成特殊多层的导管，制作具有多层孔隙之新型神经再生导管，以电子能谱化学分析及减弱式全反射-傅立叶转换红外线光谱分析进行成份分析及化学元素测定；以电荷耦合元件摄影机、扫瞄式电子显微镜进行多层孔隙型神经导管巨观及微观形态结构观察；以示差扫瞄热量量测分析玻璃转换温度、奈米三维量测弹性模数及硬度；以及进行降解性质测定，并以扫瞄式电子显微镜进行降解后之导管微观结构形态观察。

If you are unfortunate enough to the lovelorn, please tell me, I will help you out, really, please contact me!

如果你不幸失恋了，请告诉我，我会帮助你摆脱困境，真的，请联系我啦！

China's plan to cut energy intensity by 20 percent and pollutant discharges by 10 percent between 2006 and 2010 is a case in point.

中国计划在2006年到2010间降低20%的能源强度和减少10%的主要污染物排放，就是一个这样的例子。