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1.the stretching vibration v(C-C) of C-C bond ;
C-C键的伸缩振动v(C-C);收藏指正
2.The corresponding partially deuterated ompounds ere used to aid the assignment of OH deformation vibration δ(OH) and COO~-symmetric stretching ibration v_8(COO~-).
用氘代化合物帮助指定OH基变形振动和COO~-基对称伸缩振动v_a(COO~-)。收藏指正
3.Density functional theory study of the abnormal C = C bond stretch vibrational frequencies of cycloolefine
环烯烃双键伸缩振动频率反常现象的密度泛函理论研究收藏指正
4.THE RELATIONSHIP BETWEEN OH STRETCH VIBRATION FREQUENCY AND IMPURITY CATIONS IN MUSCOVITE OCTAHEDRON
白云母八面体位置中杂质阳离子和OH伸缩振动频率的关系收藏指正
5.With increasing of wavelength, absorption loss due to high harmonics of C-H vibrations increased and absorption loss of stretching vibration was higher one order of magnitude than that of bending vibration, and both was in proportion to quantum number respectively.
随着波长的增加 ,C -H谐波吸收损耗增加 ,而伸缩振动的吸收损耗比弯曲振动高一个数量级 ,且两者分别与量子数呈线性关系收藏指正
6.The modified UV absorbent of chitosan is synthesized. It is shown through the results of FTIR that the peaks of C=O stretching vibration around 1 720cm-1 and C-O-C symmetric stretching vibration around 1 160 cm-1 of the products are strengthened observably than that of the chitosan. This demonstrates the esterification of the chiotsan is obtained.
FTIR的表征表明:与壳聚糖相比,改性产物的红外谱图中1 720 cm-1处归属于C=O伸缩振动和 1 160 cm-1处归属于C-O-C对称伸缩振动的吸收峰显著增强,表明了酯化反应的发生。收藏指正
7.In the direction vertical to the c axis,are dominated the stretching vibration weak peaks at 3 165 cm -1 ,3 114 cm -1 and 3 031 cm -1 .The occupation of [Fe 2(OH) 4] 2+ polymeric ion in Position c 1 in the beryl channels is characterized by the stretching vibration peak at 3 234 cm -1 (∥ c axis).
在垂直 c轴方向上 ,以 3165 cm-1,3114 cm-1及 30 31cm-1伸缩振动弱吸收谱带为特征。 [Fe2 ( OH) 4 ] 2 +多聚合离子占据通道中的 C1位 ,以 32 34 cm-1伸缩振动锐吸收谱带为特征 (∥ c轴 )。收藏指正
8.In the PE spectra of NH3, three (2+2) REMPI and (2+2)+1 ATI, (2+2)+2 ATI were shown, within each peak a progression of stretching vibrations v1 were found.
氨的光电子能谱显示了(2+2)REMPI和(2+2)+1 ATI、(2+2)+2 ATI三组电子峰,每组峰又包括伸缩振动v1的带系,ATI峰的振动布居出现反转。收藏指正
9.This paper also generally concluded the assignment of the different peaks in the Raman spectra. Raman shift at 938 cm-1 wavenumber was assigned to the symmetry stretch mode of the P-O bond in the (PO4 )3- tetrahedra. It was the dominant peak in the Raman spectrum of the Na3PO4 crystal.
还确认了磷酸钠Raman光谱中各个峰的归属,938 cm-1波数处的峰属于(PO4)3-中P-O键的对称伸缩振动,是Na3PO4的特征峰,425及580 cm-1处峰属于磷氧四面体的弯曲振动收藏指正
10.The IR absorption bands of 3 373,3 471 and 3 614 cm~(-1) are resulted from the hydroxyl stretching vibration in GE synthetic jadeite jade.
在3 400~3 700 cm-1范围内,GE合成翡翠显示一组(3 373,3 471,3 614 cm-1)与天然翡翠截然不同的且由羟基伸缩振动所致的红外吸收谱带。收藏指正
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