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结构射

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The indicator element (2) is designed as a waveguide panel, wherein light beams propagate with total reflection and get outcoupled therefrom with a diffractive outcoupling system (2u), such as a grating structure or the like, which is configured as an indicator pattern, for producing an indicator pattern (2a) activable in the indicator element (2) by the action of light, such that divergent recesses and/or grooves of various sizes and/or shapes constitute divergent local gratings of various sizes and/or shapes, such as multi-shaped and/or binary pixels and/or units, the filling factor, shape, profile and/or size thereof being optimized in such a way that the diffraction efficiency is a function of place.

把指示元件(2)设计成波导板,其中光束以全反射方式传播并且从那里通过构造成指示图案的衍射外耦合系统(2u)、如光栅结构等得到外耦合,用于在指示元件(2)中产生可由光作用激活的指示图案(2a),使得各种尺寸和/或形状的分散的凹口和/或槽纹构成各种尺寸和/或形状的发散的局部光栅、诸如多形状的和/或二元像素和/或单像素的,所述局部光栅的填充系数、形状、轮廓和/或尺寸可以以这样的方式优化,使得衍射效率是位置的函数。

The composition of Fe-Co and Fe-Co-Mn alloy is analyzed by using Electron Probe Micro Analysis and the magnetic properties of porous alumite film in which Fe-Co and Fe-Co-Mn alloy electrodeposited are measured by a Vibrating Sample Magnetometer .

本论文通过使用多种现代测试技术,如:扫描电镜、透射电镜、电子探针X射线能谱、X射线衍射、电子衍射分析和振动样品磁强测试等,对铝阳极氧化膜的形貌、纳米级微孔内Fe—Co和Fe—Co—Mn合金的晶体结构、Fe—Co和Fe—Co—Mn合金在纳米级微孔内的电沉积工艺以及纳米级微孔内Fe—Co和Fe—Co—Mn合金的磁性进行了系统的研究。

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。

The endocyclic Sn atoms exist in a distorted triginal bipyramidal geometry with the coordination number of 5. The exocyclic Sn atoms form 6 significant bonds and exist in a distorted octahedron geometry.

化合物12的X衍射单晶测定表明,化合物是以Sn2O2四元环为中心的中心对称二聚体结构、内环锡为5配位的畸变三角双锥结构、外环锡为6配位的畸变八面体结构。

TEM shows that drying by direct heating might result in hard aggregation of the tourmaline powder, while hard aggregation might be avoided by azeotropic distillation. Raman spectroscopy reveals that there are O_H and C_H on the surfaces of the tourmaline powder obtained by azeotropic distillation, which indicates that butoxy is chemically adsorbed on the surfaces of tourmaline particles, but not adsorbed on those formed by direct drying. X_ray powder diffraction shows that the intensity of diffraction peaks decreases after grinding. There is no damage to the tourmaline crystal lattice in the process of direct heating, azeotropic distillation, or ultrafine grinding.

透射电镜分析结果表明,直接加热脱去水或正丁醇会使电气石超细颗粒发生硬团聚,而共沸蒸馏法则可有效防止硬团聚的产生;拉曼光谱结果表明,共沸蒸馏法制备的电气石粉末表面存在O—H和C—H键,说明正丁醇在颗粒表面为化学吸附,而直接干燥法得到的电气石粉末表面则没有;X射线粉晶衍射结果表明,研磨过程降低了粉末衍射峰的强度,但直接加热干燥和共沸蒸馏干燥均未破坏电气石的晶格结构。

In this paper, the main work has been focused on the rare reported arsenomolybdates, and nine novel compounds have been synthesized. Sandwich arsenomolybdates:(NH_4)_(12)[Cr_2AsMo_7O_(27_2]·11H_2O (1)(NH_4)_(14)[Cu_2AsMo_7O_(27_2]·13H_2O (2) Double sandwich arsenomolybdates:(NH_4)_(12)Cu(H_2O)_4[As_2Fe_6Mo_(22)O_(85)(H_2O)]·19H_2O (3)(NH_4)_(15)[As_2CoFe_5Mo_(22)O_(85)(H_2O)]·16H_2O(4)(NH_4)_(14)Mn_(0.5)[As_2Fe_5MnMo_(22)O_(85)(H_2O)]·22H_2O(5) Cagelike arsenomolybdate:(NH_4)_(11)[AgAs_2Mo_(16)O_(54)]·9H_2O (6) Organic-inorganic molybdenum arsenate complexes:CuAs_6Mo_6O_(30{[Cu_4]_3[CuAs_6Mo_6O_(30)]}_2·6H_2O (7),[Cu_2]_3[As_3Mo_3O_(15)]_2·2H_2O (8)(NH_4)_(10){Cu(H_2O)_4}[AsMo_6O_(21)(O_2CCH_3)_3]_2·12H_2O (9)All of the above polyoxomolybdates were characterized by IR spectroscopy, TG-DSC, elemental analysis, and single-crystal X-ray analysis to identify their structures and chemical compositions.

本文选择目前报道尚少的砷钼杂多化合物为研究重点,合成了不同结构类型的九个新的杂多化合物:单夹心化合物:(NH_4)_(12)[Cr_2AsMo_7O_(27_2]·11H_2O(1)(NH_4)_(14)[Cu_2AsMo-7O_(27_2]·13H_2O(2)双夹心化合物:(NH_4)_(12)Cu(H_2O)_4[As_2Fe_6Mo_(22)O_(85)(H_2O)]·19H_2O(3)(NH_4)_(15)[As_2CoFe_5Mo_(22)O_(85)(H_2O)]·16H_2O(4)(NH_4)_(14)Mn_(0.5)[As_2Fe_5MnMo_22_O_(85(来源:AbcccBC论文网www.abclunwen.comH_2O]·22H_2O(5)笼状结构化合物:(NH_4)_(11)[AgAs_2Mo_(15)O_(54)]·9H_2O(6)有机配体修饰的化合物:CuAs_6Mo_6O_(30{[Cu_4]_3[CuAs_6Mo_6O_(30)]}_2·6H_2O(7) [Cu_2]_3[As_3Mo_3O_(15)]_2·2H_2O(8)(NH_4)_(10){Cu(H_2O)_4}[AsMo_6O_(21)(O_2CCH_3)_3]_2·12H_2O(9)对上述新化合物进行了瓜光谱分析、元素分析、热分析和X-射线单晶衍射测试,确定了它们的组成和结构,对部分化合物还进行了UV-vis及荧光光谱分析和循环伏安表征。

The crystallitic carbon was prepared from anthracite by demineralization and carbonization,then the magnesium/carbon nanocomposites for hydrogen storage were manufactured through reaction milling of the mixture of magnesium,crystallitic carbon and aluminium under hydrogen atmosphere.

将无烟煤进行脱灰和碳化,制备微晶碳,再将微晶碳和铝添加到镁中,用氢气反应球磨法制取镁/碳纳米复合储氢材料。用透射电子显微镜、选区电子衍射、X射线衍射和差示扫描量热分析对储氢材料的粒度、晶体结构和放氢温度进行了测定。

Crystallographic data at room temperature and low temperature are obtained by Rietveld analyses of powder X-ray diffraction data.

并用Rietveld全谱拟合法对X射线衍射测量所得的晶体结构衍射谱进行了拟合。

In other words, the interruption of reentry induced by RFCA does not indicate the definite histological lesion or enzym injury of the reentrant circle, but probably signifies that the change of ion channels with a large area involves the reentant circle.

也就是说射频消融终止折返性心动过速并不一定是折返环路的组织结构或代谢损伤所致,而可能是射频电流对大范围的心肌细胞膜离子流的影响累到及折返环路所致。

The results indicate that a regular diffractive facular lattice will appear in the maximum diffraction-free distance with the increase of the oblique incident angle.

结果指出,随着入射轴棱锥角度的增大,在最大无衍射距离内会形成有规则的光学点阵,这种光学点阵与三维光子晶体的结构相近,实验结果与数值模拟相吻合。

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