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The system may acts as a constant temperature controller in order to study the relations between luminescence characteristic and temperature.

该系统除可作一般的恒稳控制以研究样品的发光性能对温度的依赖关系,也可在0℃~160℃范围内给出不同的升温速率以研究不同升温速率下样品的陷阱深度及分布情况。

FASS(field amplified sample stacking) is a technique for oncolumn enrichment in capillary zone electrophoresis. The distribution of solute in column during injection can be divided into two parts: the stack zone in running buffer and the sample solution zone imported by electroosmosis.

直接柱头场效应进样是一种毛细管区带电泳柱内富集,其进样过程中样品在柱内的分布可分为两部分,即在运行缓冲溶液中的堆积区段和由电渗流引入的样品溶液区段。

We obtained the accurate refractive index inhomogeneity without system error. At last, in order to resolve the question of the spherometer weared out at the laboratory long-term use, we proposed the method that use the interferometer to adjust the spherometer.

研究了测量光学材料的折射率不均匀性5种方法,建立了四步测量法的数理模型,并且在所研制的CXM100-2W式干涉仪上进行了样品材料的具体测量,在消除了系统误差的情况下,准确的得到了样品材料的折射率不均匀性分布。

If the sample is insulant, it is possibleto reach zero temperature difference sintering with zero heat release rate.

重点分析了径向温度分布问题,样品内对称面上任一点与样品中心的温差为:△T=〓。

The crystal structure was perovskite-like type, as evidenced by the results of X-ray diffraction and scanning electron micrography. The distribution of K4Nb6O17 powder with particle size of less than 10 m, which would become larger as the calcining temperature grew.

通过XRD和SEM对样品进行表征,发现该法合成的K_4Nb_6O_(17)均具有钙钛矿结构,样品的颗粒大小分布不均,但大多小于10μm,且合成的温度越高,颗粒粒径越大。

Ray diffraction analysis displays that Major phases present in the sintered bodies were the BaTiO3 compounds with a perovskite structure and the BaBiO3 compounds with a monoclinal structure.

射线衍射分析表明烧结体中的相由钙钛矿结构的Ba- TiO3和单斜结构的BaBiO3组成。利用扫描电镜分析了样品的断面形貌,能谱确定了样品中相的分布规律。

Then the materials were characterized by XRD, FT-IR, SEM, thermogravimetric analysis, and N2 adsorption-desorption experiments. It turned out the sample possessed ordered hexagonal mesoporous channels, high specific surface area of 1207 m2/g, high specific pore volume of 1.03 cm3/g and narrow pore distribution between 2~3nm.

通过 X 射线衍射、傅立叶转换光谱、扫描电镜、热重及低温氮气吸附-脱附试验等测试方法对样品进行了表征,表明该条件所合成的样品具有规整有序的六方介孔孔道,较大的比表面积(1207m2/g)和比孔容(1.03cm3/g),孔径大小分布窄(2~3nm),为高质量的 MCM-41 介孔分子筛。

Based on a quantitative analysis of radiolarian in 80 surface-sediment samples from the northern area of Okinawa Trough, this paper reported the species composition and faunal assemblages characteristic of radiolarian, expounded the distribution pattern of radiolarian abundance and diversity in surface sediments from this area. In this paper, a preliminary study on the relation of the distribution and abundance of radiolarian to environmental factors, such as chemical and physical properties of the overlying masses (sea-surface temperature, salinity, nutrients and primary productivity) and the type and composition of sea-bed sediments was made. The radiolarian data was evaluated using a Q-mode factor analysis to identify different faunal assemblages and their geographic distributions, then the relationship between radiolarian assemblages and distribution of water masses, hydrographic boundaries such as frontal systems was analyzed. A new radiolarian-based transfer function to estimate mean-annual sea surface temperature and seasonal range were examined to test its success in the study area.

本文对冲绳海槽北部80个表层沉积样品中的放射虫进行了系统鉴定和定量统计,研究了放射虫的种类组成与类群特征以及其丰度和分异度的分布;分析了海水温度、盐度、营养盐以及沉积物类型、成分等环境因素对放射虫分布的影响;采用Q-型因子分析,求得放射虫的属种和组合分布特征,探讨了放射虫组合与不同水团、海洋水文结构之间的关系;并对Pisias(1997)建立的估计表层海水年平均温度和其变化范围的放射虫转换函数在研究区的适用性做了检验。

The results showed that the determined components are homogenous on different position of sample surface and in different depth of the sample, and the repeatablity of determination resuts was also good under same preparation conditions. So this way could surmount the error from the sample preparation of powder press.

试验结果表明,块状样品表面不同部位及不同深度的化学成分分布均匀,相同熔融条件下的样品重复性良好,解决了用粉末压片制样对测定结果带来的误差。

Technique details were optimized about steps from sample treatment to gel staining, and 2 - DE gels are lampros and aequalis distributed , the method of sample treatment suitable for mass spectrography analysis.

优化从样品处理到凝胶染色几个过程的技术细节,蛋白表达谱清晰且分布均匀,样品处理方法适合后期的质谱测试分析。

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