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衍射光谱

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The thermal behavior of silver behenate has been studied by infrared spectroscopy, X-ray diffraction, combined thermogravimetry-differential thermal analysis-mass spectrometry. The results indicated that complicated phase transitions took place while heating silver behenate,but there were two distinct thermal transitions. During the first transition at 138°C, the alkyl chains of silver behenate were transformed from an ordered into disordered state.

通过采用粉末X射线衍射、红外光谱、热重-差热分析与质谱联用技术,对山嵛酸银纳米晶体的热行为研究发现,山嵛酸银受热发生了一系列相转变,它有两个明显的突变:即在138℃左右,山嵛酸银的烷基链从高度有序转变为无序状态;在231℃左右,山嵛酸银发生了热分解,其主要分解产物为银纳米粒子和山嵛酸。

The structures of the two types of kaolinite and their benzamide intercalation compounds were characterized by the powder X-ray diffraction and Fourier-transformed infrared spectroscopy.

利用X射线粉末衍射和Fourier变换红外光谱实验分析了2种高岭石及其苯甲酰胺插层复合物的结构。

In our study, polyimide hybrid films containing bimetalic compounds were prepared by codoping poly with a bariumand titanium precursor prepared from Ba(CH_3COO)_2, Ti_4, and acetic acid followed by casting and thermal curing.

陶瓷粉BTL是由Ba(CH_3COO)_2,Ti_4和乙酸制成的钡钛前驱物,采用溶胶凝胶法合成,并由红外光谱和X-射线衍射图证明,在650℃BTL完全转化为BaTiO_3晶体。 3。通过两步法合成含陶瓷粉的聚酰亚胺复合材料。

Bipyridyl and 1,10-phenanthroline (L3), Cl3SnCH2CH2COORo L (L= L1, a; L2, b; L3, c), formed by low-heating solid-state reaction. The crystal structures of 1 and 2 show that the tin atom adopts a distorted trigonal bipyramid geometry via intramolecular carbonyl oxygen to tin coordination [the distances of Sn-0 bond are 0.2351(6) ran for 1 and 0.2362(3) nm for 2]. Compound 1 belongs to monoclinic with space group P2/c, a = 0.9842(2) nm, b =1. 0923(8) nm, c = 1.23948(11) nm,/?= 93.894(15)°, V= 1.3294(4) ran3, Mr = 366.23, 7 = 4. Compound2 belongs to monoclinic with space group P2{/c, a = 1.04443(9) nm, b = 1.04823(7) nm, c = 1.28113(9) nm,/= 90. 953(8)°, V= 1.40239(19) nm3, Mr = 380.25, Z = 4

利用元素分析、红外光谱、核磁共振对其结构进行了表征,并通过X射线单晶衍射测定了1和2的晶体结构,二者均为具有分子内羰基氧原子配位的畸变三角双锥结构。1属于单斜品系,空间群P21/c, a=0.9842(2)nm,b=1.0923(8)nm,c=1.23948(11)nm,β=93.894(15)°,V=1.3294(4) nm^3,Mr=366.23,Z=4.2属于单斜晶系,空间群P21/c,a=1.04443(9)nm,b=1.04823 (7)nm,c=1.28113(9)nm,β=90.953(8)°,V=1.40239(19)nm^3,Mr=380.25,Z=4。

A two-fold penetration coordination polymer n (1)(bpy=4,4'-bipyridyl) has been synthesized through hydrothermal reaction and structurally characterized by single crystal X-ray diffraction method.

利用水热反应,合成了一个具有二重穿插结构的一价铜配位聚合物n(1)(bpy=4,4'-联吡啶),并利用元素分析,X射线单晶衍射,红外光谱以及热重分析等手段对标题化合物进行了表征。

The structure of products was characterized by means of infrared spectra, wide-angle X-ray diffraction and differential scanning caloriimetry and the effect of deacetylation in course of konjac glucomannan carboxy methylation was analyzed.

运用红外光谱、广角X-射线衍射和示差扫描量热法表征产物结构并探讨脱乙酰基对KGM羧甲基改性的影响。

The chalcogenidometalates were characterized by elemental analysis, IR and X-ray crystallographic, and their thermal stability and optical properties were also investigated.

三、用元素分析、红外光谱、热重分析和单晶X射线衍射仪对合成的化合物进行了表征,测定了化合物的热稳定性和光学性质。

The mineralogical characteristics of dioctahedral micas have been studied by chemical analysis, XRD, IR, DTA, SEM and IEM.

用化学分析、X射线衍射、红外光谱、差热和热重分析、扫描电镜及透射电镜等研究了白云母、绢云母和伊利石的基本矿物学特征。

FT-IR spectra shows that the polyaniline is present primarily in the emeraldine salt form, and the polymeric chains interact with inorganic framework, most likely via V=O…HN hydrogen bonding. XRD,TG and DSC indicate that the lamellar structure of the V_2O_5 is preserved, PAn chains eliminate water form the interlamellar region and are partially inserted between the layers, and exist with extended-chain conformation owing to the confined environment.Electrochemical investigation in the range of 1.8~3.8V vs.

红外光谱表明复合物中PAn主要以导电聚苯胺盐的形式存在,PAn链与V_2O_5晶格之间可能形成了V=O…HN氢键。X射线衍射、热重和差示扫描量热证实了PAn/V_2O_5复合物保持了较规整的层间排列结构,PAn取代了V_2O_5干凝胶中的层间水而部分嵌入其片层间,由于受空间的限制,PAn分子链以比较伸展的链构象存在。

Firstly,two novel rare earth complexes(CH_2=CHO)Ln~Ⅲ[2,6-_2PhNSiMe _3]_2Li_3Ln=Y(2,Yb(3)containing arylamido and enolate mixed ligands have been synthesized by treatment of 2 equiv of of 2,6-~iPr_2PhNHSiMe_3 with exces n-BuLi at -78℃in THF for 12h,followed by reaction with 1 equiv of LnCl_3at 80℃for 24h in one-pot.All the two compounds were characterized by spectroscopic methods,elemental analyses,and a single-crystal X-ray diffraction study.

首先,-78℃下,在两当量的2,6-~iPr_2PhNHSiMe_3(1)THF溶液中加入过量的n-BuLi,反应12小时,再加入一当量的LnCl_380℃下,反应24小时,一锅法合成了含胺基、乙烯醇基混合配体的新型稀土金属配合物(CH_2=CHO)Ln~Ⅲ[2,6-_2PhNSiMe_3]_2Li_3Ln=Y(2、Yb(3),上述化合物结构经单晶X-ray衍射、光谱和元素分析表征,表明我们得到的是一类新型的三价稀土配合物。

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