双晶

The X-ray diffraction patterns were calculated analogically by using Rietveld method and the phase content in rare-earth two phase Nd2Fe14B/α-Fe magnet was determined based on standardless quantitative phase analysis.

稀土双相永磁合金是基于软磁相的高饱和磁化强度和硬磁相的高各向异性的特点，通过两相晶粒在纳米尺度上交换耦合而成的一种纳米晶复合永磁材料，它具有显著的剩磁增强效应，可望获得较高的综合磁性能[1~3]。

The quantitative experimental data reveal that the scale could be reduced with the effect of magnetic treatment and the effect of the antiscale in different flow rate is different.

利用双道的实时监测系统，通过监测碳酸钙过饱和溶液中的pH和Ca2+浓度在析晶过程中的变化，系统的研究了不同流速下磁场的阻垢效果。

The bichromatic laser is also expected to induce the confined(i.e.,frequency fixed)Rabi flopping between conduction and valence bands in SSL's.

我们发现，双色激光驱动的超晶格中的导带价带之间的Rabi翻转的频率只能取分立值。

The study of structure shows that the noncrystalline network is composed of [PO_4] tetrahedron and [VO_5] trigoral bipyramid.

结构研究表明[PO_4]四面体及[VO_5]三角双锥体共同构成非晶态的网络骨架。

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。

Fe(superscript 3+) occupied both tetrahedral sites in spinel block and trigonal bipyramid sites in mirror plane for LaFeMnAl(subscript 12-x-y)O19 (x=0.5, 1) hexaaluminate.

LaFeMnAl(下标 12-x-y)O19(x=0.5， 1)中Fe以Fe(上标 3+)位于六铝酸盐尖晶石结构中的四面体位和镜面层结构中的三角双锥位，其中后者为N2O分解的主要活性中心。

The conoscopic interference pattern of wafer with optical axis parallel to the surface of a crystal is sensitive to the crystal birefractive index.

光轴平行表面的晶片的会聚偏光干涉对晶体的双折射率非常敏感。

On the basis of developing a new technology to synthesize sodium diacetate successfully without any pollution,the culture of bigger crystal in perfect shape and single crystal of small dimension suitable for X-ray diffraction was attained.

在研究成功双乙酸钠零污染合成工艺的基础上，培养成功了晶型完美的大尺寸晶体和适宜进行X光结构分析的小尺寸单晶，并进一步应用四圆衍射仪测得其晶体结构。

Other Ingredients: gelatin, dibasic calcium phosphate, microcrystalline cellulose, colloidal silicon dioxide, and magnesium stearate.

其他成分：明胶，双磷酸钙，微晶纤维素，胶体二氧化矽和硬脂酸镁。

The molecular sieve is prepared in the steps: at the room temperature, hexadecyl trimethyl ammonium bromide is mixed and dissolved with the sodium hydroxide, and is added with TEOS in dropping way, and simultaneously added with Me metal salt water solution and lanthanum nitrate solution in dropping way; the pH value of the mixed solution is adjusted by acetic acid to be 10 to 11, and is mixed for 1 to 2 hours after being stabilized; the sol is moved into a polyfluortetraethylene bottle to be heated and crystallized for 2 days in the oven at the temperature of 100 DEG C; after filtering, washing and drying for nights, and being calcined in a muffle at the temperature of 550 DEG C for 3 to 7 hours, the dual-metal-atom improved MCM-41 mesoporous molecular sieve is obtained.

该分子筛的制备为室温下，将十六烷基三甲基溴化铵和氢氧化钠混合溶解，搅拌并滴加入TEOS，同时滴加入Me金属盐水溶液和硝酸镧溶液并搅拌，用乙酸调节pH值至10～11，稳定后搅拌1～2小时，溶胶转入聚四氟乙烯瓶中在100℃下烘箱水热晶化2天，经过滤、洗涤、干燥过夜，马弗炉550℃焙烧3-7h，得双金属原子改性MCM-41介孔分子筛产品。

This paper discusses design and realizable methods of remote test output interface from logical design angle.

本文从逻辑设计的角度讨论遥测输出接口的设计及实现方法。

This also 星体投射plies to buildings, structures and geological features.

这也适用于建筑物和地质特征。