《打绳结》教学设计

教学目的要求: 1.让学生认识几种绳结的名称,学会几种基本的打绳结的方法。 2.在打绳结的实践中,培养学生的动手能力、观察思维能力和创造精神。 3.结合教学内容,向学生进行爱人民。

聚乙烯网线的断裂特性分析

对聚乙烯网线断裂特性进行了试验研究,结果表明:断裂强力随拉伸速度的增加而增大,断裂伸长率随拉伸速度的增加而减小,且二者与拉伸速度的变化量和网线的粗度有关;网线的干、湿状态对断裂强力有影响,湿态下可获得较大的断裂强力;网线的单线结断裂强力有所损失,损失率的大小与网线粗度有关,受干、湿状态影响较小。

Determination of Structure and Polarity of Si C Single Crystal by X-Ray Diffraction Technique

Structure and polarity of the Si C single crystal have been analyzed with the four- circle X- ray diffraction method by a double- crystal diffractom eter.The hexagonal{ 10 15 } pole figure shows that this Si C sam ple has a6 H modification.The difference between the integrated intensities m easured byω scan in the triple- axis diffraction set- up finds some convincing evidence that the surface is either a Si- terminated face or C- terminated face.The experi- mental ratios of| F( 0 0 0 L) | 2 / | F( 0 0 0 L) | 2 are in good agreem entwith the calculated ones after the dispersion cor- rections to the atomic scattering factors( L=6 ,12 and18,respectively) .Thus,this m easurem ent technique is con- venient for the application of the materials with remarkable surface polarity.

Structure of the organic crystallite unit in coal as determined by X-ray diffraction

X-ray diffraction （XRD） was used to study the structure of the organic crystallite unit （La, Lo doo2） in coals collected from Henan and Shanxi Provinces. XRD patterns of coal were collected in a step-scan mode （0.1 °/step） over an angular range of 2-90° （20）, allowing 8 s at each step. The structure of the crystallite unit was determined from the Scherrer equation and peak parameters deduced from whole pattern fitting. The results show that the structure of the crystallite unit in coal is mainly controlled by the coal rank. As the coal rank increases the average diameter of a coal crystallite unit （La） increases, the interlayer spacing （doo2） decreases slightly, and the average height of a coal crystallite unit （Lc） increases at first but then decreases. A new diffraction peak from the crystallite unit in coal was found at a low scattering angle in the XRD pattern （2-10~）. This suggests a structure with an inter-layer spacing from 1.9 to 2.8 nm exists in coal crystallites.

Effect of Crystallization Conditions on Polymorphic Diversity of Malic Acid RS-Racemate

Enantiomers （R （＋） and S（-））, RS-racemate mixture of enantiomers） of malic acid C4H605 have been （double compound） and （R ＋ S） -conglomerate （mechanical investigated by means of X-ray diffractometry and high tern- perature X-ray diffraction method. The RS-racemate was found to be able to form three polymorphic modifications, which we denominated as M1 （monoclinic, space group P21/c）, M2 （monoclinic, space group Cc）, and Tc （triclinic, space group P-l ）, the latter modification having been unknown before. Modification Tc was also described, and its X- ray diffraction characteristics, including interplanar spacings d, hkl indices, unit cell parameters, were defined. In addi- tion, X-ray diffraction characteristics for both reported earlier M1 and M2 monoclinic polymorphic modifications were measured with higher accuracy. The ability of RS-racemate to form one of the above three modifications （MI, M2, and Tc） or their mixtures containing various proportions and combinations of the components （M1 ＋ M2, M1 ＋ Tc, or M2 ＋ Tc） was found to depend on the type of crystallization medium （a melt, aqueous medium, ethanol or acetone solu- tion）, crystallization rate （from 2--3 minutes to 4 months）, and crystallization temperature. Heating S-enantiomer and M1 RS-racemate up to their respective melting points （100 ℃ and 124 ℃, correspondingly） only made them undergo thermal deformations, while heating （R ＋ S） -conglomerate in the temperature range of 96--110 ℃ resulted in its homogenization to form M2 RS-racemate, which, near the melting point （118 ℃）, namely, in the range of 112-116 ℃, was transformed into MI RS-racemate. Keywords： polvmorDhism; racemic, chiral

Synthesis and Characterization of New Palladium（ll） Complexes Containing 4,5-dimethyl-2,2＇-bipyridine： X-ray Crystal Structure of Bis（4-methyl pyrdine）-4,5- dimethyl-2,2＇-bipyridine palladium （11） Perchlorate

New heteroleptic and homoleptic complexes of the type[Pd（4,5-dmbipy）C12], [Pd（4,5-dmbipy）L2], and [Pd（4,5-dimebipy）2]2＋ （L = Pyridine or 4-methylpyridine（4-picoline）, bipy = 2,2＇-bipyridine, and 4,5-dimebipy = 4,5-dimethyl-2,2＇-bipyridine） were synthesized and characterized by IH NMR and elemental analysis. The crystal structure of bis（4-methylpyridine）-4,5- dimethyl-2,2＇-bipyridinepalladium（II）perchlorate [Pd（4,5-dmbipy）（4-pic）2]（CIO4）2 was also determined by single crystal X-ray diffraction. This complex crystallized in the triclinic crystal system and space group PI with a = 9.562 （2）, b = 11.326 （4）, c = 15.0120 （10） A°; α = 70.940°, β= 77.60 （2）, γ= 67.86 （2） and z = 4. The Pd （II） in square planar environment showed a small distortion towards tetrahedral through one coordinated bipyridine ring twisting with respect to the other.

Research on Network-on-chip Dynamic and Adaptive Algorithm and Choice Strategy

With further increase of the number of on-chip device, the bus structure has not met the requirements. In order to make better communication between each part, the chip designers need to explore a new structure to solve the interconnection of on-chip device. The paper proposes a network-on-chip dynamic and adaptive algorithm which selects NoC platform with 2-dimension mesh as the carrier, incorporates communication energy consumption and delay into unified cost function and uses ant colony optimization to realize NOC map facing energy consumption and delay. The experiment indicates that compared with random map, single objective optimization can separately saves （30% - 47 %） and （ 20% - 39%） in communication energy consumption and execution time compared with random map, and joint objective optimization can further excavate the potential of time dimension in mapping scheme dominated by the energy.

Structural and optical verification of residual strain effect in single crystalline CdTe nanowires

Single crystalline CdTe nanowires have been synthesized using Au-catalyzed chemical vapor deposition. X-ray diffraction reveals the existence of non- negligible inhomogeneous compressive strain in the nanowires along the 〈111〉 growth direction. The effect of the strain on the electronic structure is manifested by the blue-shifted and broadened photoluminescence spectra involving shallow donor/acceptor states. Such residual strain is of great importance for a better understanding of the optical and electrical behaviors of various semiconductor nanomaterials as well as for device design and applications.

IMPLICITIZATION USING UNIVARIATE RESULTANTS

Among several implicitization methods, the method based on resultant computation is a simple and direct one, but it often brings extraneous factors which are difficult to remove. This paper studies a class of rational space curves and rational surfaces by implicitization with univaxiate resultant computations. This method is more efficient than the other algorithms in finding implicit equations for this class of rational curves and surfaces.

Nonlinear optical material of a low-dimensional coordination polymer:Synthesis,structure,NLO and fluorescence properties

Employing unsymmetrical 2-mercapto-5-methyl-1,3,4-thiadiazole and 2,2′-bipyridine as mixed ligands, a new low-dimensional coordination polymer [Zn(MMTA) 2 (2,2′-bipy)] n (MMTA = 2-mercapto-5-methyl-1,3,4-thiadiazole, 2,2′-bipy = 2,2′-bipyridine), has been synthesized under solvothermal condition and characterized by single crystal X-ray diffraction. This compound crys- tallizes in the noncentrosymmetric space group Cc, with cell parameters: a = 8.291(4) , b = 15.483(9) , c = 15.620(6) , = 96.00(5)°, V = 1994.1(2) 3 , and Z = 4. The mixed ligands link the zinc center into a mononuclear unit, which is futher linked by weak C-H···N and C-H···S hydrogen bonds into a three-dimensional noncentrosymmetric framework. The compound exhibits intense photoluminescence and distinct NLO properties at room temperature. The intensity of the green light produced by the powder sample of the compound is about 3.2 times that produced by KDP powder. On the basis of the results of TG analysis, the structure is thermally stable up to ～260 °C.

One pot synthesis, crystal structures and properties of two new MOFs with imidazole-containing tripodal ligand

Two new different Cu(Ⅱ) MOFs with the same 1,3,5-tris(1-imidazolyl) benzene(tib) ligand {[Cu(tib)2]·(H2O)2·Br2}n(1) and {[Cu2(tib)·Br·Cl]·2Br}n(2) were obtained by one pot synthesized of tib with CuBr in the presences of HCl and water. X-ray single crystal diffraction analyses indicate that both complexes 1 and 2 have two dimensional frameworks containing different building blocks. Each Cu(Ⅱ) atom in complex 1 is coordinated by four N atoms from different tib ligands. However, there are two different cryptographic Cu(Ⅱ) atoms in complex 2, one is four coordinated by two bromine atoms and two N atoms from different tib ligands, the other is six coordinated by two chloride atoms and four N atoms from different tib ligands. The thermal gravimetric analysis of complexes 1 and 2 are depicted in the paper.

Microstructure and texture evolution of cold drawing <110> single crystal copper

By means of electron backscattering diffraction and transmission electron microscopy the microstructure and texture of drawn single crystal copper with initial orientation （110） parallel to axial direction have been investigated in the present work. In or- der to analyze the effect of initial orientation on microstructure and texture of drawn copper, the results of the drawn （110） sin- gle crystal copper wires have been compared with （100） and （111） single crystal copper wires. It is found that the grain subdi- vision of （110） single crystal is more evident than that of （100） and （111）, and the textures consisting of （111） and （100） abruptly form in the drawn （110） single crystal. At high strains, due to shear strain, the distribution of fiber textures is imho- mogenous along the radial direction of drawn （110） single crystal copper wires. （100） is near the surface and （111） is at the center. The microstructure results of drawn （110） single crystal show that at low strains, it can be characterized as two kinds of geometrically necessary boundaries with noncrystalline character. At medium strains, S bands can be observed. At high strains, lamellar boundaries form. Mean misofientation and average spacing of dislocation boundary are larger in drawn （110） single crystal, as compared with （111） and （100）. In drawn （110） single crystal with high strains, the bimodal distribution forms at lower strains than in drawn （100） single crystal, which is because the dislocation boundaries with high angle are contributed by not only the boundary between （111） and （100） fiber textures but also the boundary in （111） or （100） texture.

Fabrication and properties of well-ordered arrays of single-crystalline NiSi2 nanowires and epitaxial NiSi2/Si heterostructures

In this study, we reported the design, fabrication, and characterization of well- ordered arrays of vertically-aligned, epitaxial NiSi2/Si heterostructures and single- crystalline NiSi2 nanowires on （001）Si substrates. The epitaxial NiSi2 with {111} facets was found to be the first and the only silicide phase formed inside the Si nanowires after annealing at a temperature as low as 300℃. Upon annealing at 500 ℃ for 4 h, the residual parts of Si nanowires were completely consumed and the NiSi2/Si heterostructured nanowires were transformed to fully silicided NiSi2 nanowires. XRD, TEM and SAED analyses indicated that all the NiSi2 nanowires were single crystalline and their axial orientations were parallel to the [001] direction. The obtained vertically-aligned NiSi2 nanowires, owing to their well-ordered arrangement, single-crystalline structure, and low effective work function, exhibit excellent field-emission properties with a very low turn-on field of 1.1 V/m. The surface wettability of the nanowires was found to switch from hydrophobic to hydrophilic after the formation of NiSi2 phase and the measured water contact angle decreased with increasing extent of Ni silicidation. The increased hydrophilicity can be explained by the Wenzel model. The obtained results present the exciting prospect that the new approach proposed here will provide the capability to fabricate other highly-ordered, vertically-aligned fully silicided nanowire arrays and may offer potential applications in constructing vertical silicide-based nanodevices.