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It acquired the interference signal of He-Ne laser whose wavelength is 632.8nm by this FMI. Fourier Transform algorithm is used to calculate the spectrum. The difference between the spectrum acquired by our experiment and by traditional grating spectrometer are also analyzed which can present helpful reference to develop FFTS further.

使用该干涉仪测量了632.8nm He-Ne激光光源的干涉信号,采用傅里叶变换算法计算了其光谱图,并与传统光栅光谱仪测量的光谱图进行了比较,分析了两者存在的差异及其原因,为FFTS的后续研制工作提供了有益参考。

Its IR spectrogram performed by potassium bromide showed characteristic absorption peaks in the wavelength of 2917, 2849, 1716, 1463, 1382 and 720cm~(-1), respectively.

EZR_(2002)外观为黄色或黄绿色粉末,熔点在74~79℃之间;经溴化钾压片后的红外光谱图显示在2917、2849、1716、1463、1382和720cm~(-1)处有特征性吸收峰;溶于二氯甲烷后的紫外光谱图显示在412nm处有强吸收,在665nm处有次强吸收,还分别在505、535和605nm附近有弱吸收。

The content of the composition of polysaccharides was determined by anthranone-sulfuric acid method. Result There was no absorption at 240 nm and 260 nm. The IR spectrum graph of the polysaccharides was similar to Polygonatum odoratum, Radix Ranunculi Ternati and Agrimonia pilosa Ledeb.

结果 该有效多糖组分在240 nm和260 nm处无吸收,其红外光谱图与组方药玉竹、猫爪草和仙鹤草的红外光谱图有很大的相似性,周氏克金岩方中该多糖组分含量为1.41%。

A method of qualitative identification of compounds with thin layer scanning spectrogram is introduced.

介绍了用薄层扫描光谱图对化合物进行定性鉴定的方法,讨论了光谱图的各种影响因素,探讨了用光谱图和Rf 值相结合的定性方法。

These include IR, NMR, UV-visible spectroscopy and X-ray spectrography in molecular structure determination.

它们包括红外光谱学、核磁共振学、紫外光,可视光谱学及X-射线光谱图应用於分子结构之判定。

Interference images are produced by a Michelson interferometer, which used a bromine tungsten lamp as the light source. A Kretschmann prism configuration is used to stimulate SPR. The reflected biochip images are recorded by a CCD camera. Spectral images which are obtained through Fourier transform of the interference images, are analyzed and processed to get SPR curves.

系统以溴钨灯为迈克尔逊干涉仪的光源产生干涉图像,采用Kreschmann棱镜耦合结构激励SPR,由CCD摄像机采集传感芯片干涉图,对干涉图进行信息提取和傅里叶变换得到光谱图,再对光谱图进行分析处理得到SPR曲线。

Resuit:Spectra of the majority of products are diferent from the standard spectrum,but the improved method can get the spectra identical with the standard spectrum.

结果:大多数厂家的甲睾酮片按药典法预处理样品后绘制光谱图与标准光谱图存在差异,改进预处理方法后可得到与标准光谱图一致的光谱图

Through taken the measurements of pH, TOC, UV-Vis spectra and high-performance liquid chromatograph in the degrading process of solution ,it was found that the COD of dye solution increased, pH continuing declined and TOC reduced gradually. The UV-Vis spectra and high-performance shown that though dye molecules had been destroyed, Strong Chromophore Azo Double Bond of dye was certainly under attack, the big conjugated system was vandalized and dye molecules were decolorized degradation, but they were not completely changed into carbon dioxide and other inorganic matter by mineralization, it appeared accumulation of aromatic ring and double benzene nucleus, so it is thus evident that complete destruction of aromatic ring is more difficult than the double benzene.

通过测定直接大红染料脱色过程中的溶液pH、TOC、紫外可见光谱图和高效液相色谱图可知,在脱色处理时间(6h)范围内,染料溶液的COD值增大, pH值持续下降,TOC值逐渐降低,结合紫外可见光谱图和高效液相色谱图,说明染料分子虽然已经遭到破坏,染料分子内强生色基团偶氮双键确实遭到攻击,大的共轭体系被破坏,染料分子被脱色,却没有完全被彻底矿化成二氧化碳等无机物,出现了芳环和萘环结构的累积现象,可见完全破坏芳环比破坏偶氮双键发色团更困难。

By analyzing the methods of imaging spectrometer image data compression, the key point of interference figure compression is found out, and the corresponding relationship between interferogram matching and spectrogram matching is analyzed using the basic principle of several spectral matching models.

文章通过分析目前常用的成像光谱仪图像数据压缩方法,确立了决定干涉图压缩的问题关键,在分析实际应用中常用的几种光谱匹配模型的基本原理的基础上,探讨了干涉图匹配和光谱图匹配之间存在的对应关系。

The FTIR spectrum of DTC-TETA showed strong absorption peaks at 1 461-1 388 cm-1 and 1 174-996 cm-1 which were attributed to partly double bonds of C and C,respectively.The UV spectrum of DTC-TETA had two absorption peaks at 265 and 290 nm,assigned to π—π* transition of N…C…S radical and nonbonding electron n—π* transition of S…C…S radical to conjugated system,respectively.

在DTC-TETA的红外光谱图中,在1461-1388cm-1处和1174-996cm-1处分别出现含有部分双键性质的〖JGC〖ZJXS,YN键和键的特征吸收峰;在紫外光谱图中,分别在265和290 nm处出现两个最大吸收峰,分别对应于N…C…S基团的π—π*跃迁和S…C…S基团中硫原子上非键电子向共轭体系的n—π*跃迁;元素分析结果表明该化合物中碳、氢、氮、硫的摩尔比近似为

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