信息技术与大学数学课程整合的方式与理论探讨

信息技术与大学数学课程整合正成为当前我国信息技术教育乃至整个教育信息化进程中的一个热点问题,探讨其整合的方式及理论基础是非常必要的.本文首先结合大学数学案例探讨了整合的三种方式:动态的课堂演示型、单机的数学实验型和全交互的网络教学型,其次探讨了整合所依据的四种理论:传播理论、建构主义理论、教学设计理论和系统理论,最后提出了自己对信息技术与大学数学课程整合的一些思考.     

Half‐titanocene complexes bearing dianionic 6‐benzimidazolylpyridyl‐2‐carboximidate ligands: Synthesis,characterization, and their ethylene polymerization

6‐Benzimidazolylpyridyl‐2‐carboximidic half‐titanocene complexes, Cp′TiLCl (Cp′ = C₅H₅, MeC₅H₄, C₅Me₅, L = 6‐benzimidazolylpyridine‐2‐carboxylimidic, C1–C13 ), were synthesized and characterized along with single‐crystal X‐ray diffraction. The half‐titanocene chlorides containing substituted cyclopentadienyl groups, especially pentamethylcyclopentadienyl groups were more stable, while those without substituents on the cyclopentadienyl groups were easily transformed into their dimeric oxo‐bridged complexes, (CpTiL)₂O ( C14 and C15 ). In the presence of excessive amounts of methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), all half‐titanocene complexes showed high catalytic activities for ethylene polymerization. The substituents on the Cp groups affected the catalytic behaviors of the complexes significantly, with less substituents favoring increased activities and higher molecular weights of the resultant polyethylenes. Effects of reaction conditions on catalytic behaviors were systematically investigated with catalytic systems of mononuclear C1 and dimeric C14 . With C1 /MAO, large MAO amount significantly increases the catalytic activity, while the temperature only has a slight effect on the productivity. In the case of C14 /MAO catalytic system, temperature above 60 °C and Al/Ti value higher than 5000 were necessary to observe good catalytic activities. In both systems, higher reaction temperature and low cocatalyst amount gave the polyethylenes with higher molecular weights. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3396–3410, 2008     

Phase and shape controlling of MnS nanocrystals in the solvothermal process

MnS nanocrystals with different phases and shapes were prepared through solvothermal synthesis. The products were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), UV–vis absorption and photoluminescence (PL) spectra. The solvent and reaction time played an important role in controlling the phase and shape of MnS nanocrystals. The possible mechanism of the shape evolution was investigated, which revealed that the crystal growth along the unique c axis of γ-MnS resulted in the rod-like MnS at the primary period, and the tetrahedral crystal seed of β-MnS with zincblende structure resulted in the interlinking of MnS rods, so the zigzag and three-branched and palm-like MnS appeared; with increasing reactive time the thermodynamically stable spherical α-MnS was favored through the Ostwald ripening process. The PL results showed that the intensity of γ-MnS was much weaker than that of α-MnS, and the trap state emissions of γ-MnS at 470 and 482 nm, respectively, disappeared, which might be ascribed to the difference of the shapes between the sphere and the rod or branch.     

Formation mechanism of ethanol-water excimer

The fluorescent spectrum and the excitation spectrum were used to present the cluster molecular structure feature in ethanol-water solutions.Through analyzing the fluorescent characteristics of an excimer,it is proposed that the excimers are formed between the ethanol-water cluster molecules in the excited state and in the ground state.The fluorescent lifetime and the fluorescent intensity decay process give information about the photo-physical and photo-chemical processes of the formation and the dissociation of an excimer.The theoretical calculation and physical analysis coincide with the experimental results.The preliminary conclusion about the structure feature of ethanol-water cluster molecule is that it has a planar one like a sandwich.     

超导芯截面形状对Bi-2223/Ag带Jc的影响

磁光图像显示Ｂｉ－２２２３／Ａｇ带材中单根超导芯的宽面两侧边缘分布有较大的超导电流密度，Ｂｉ－２２２３单根超导芯的横截面是纺锤形的，单位宽度上的横截面面积之比与电流密度在横截面上不同部分的分布之比相当，高的电流密度在单根超导芯两则的分布可能是由单芯横截面的形状引起的。     

Distributional Dimension of Fraetal Sets in Local Fields

The distributional dimension of fractal sets in R^n has been systematically studied by Triebel by virtue of the theory of function spaces. In this paper, we first discuss some important properties about the B-type spaces and the F-type spaces on local fields, then we give the definition of the distributional dimension dimD in local fields and study the relations between distributional dimension and Hausdorff dimension. Moreover, the analysis expression of the Hausdorff dimension is given. Lastly, we define the Fourier dimension in local fields, and obtain the relations among all the three dimensions. Keywords local field, B-type space, F-type space, distributional dimension, Hausdorff dimension Fourier dimension     

An assessment of a parallel,finite element method for three‐dimensional,moving‐boundary flows driven by capillarity for simulation of viscous sintering

A parallel, finite element method is presented for the computation of three‐dimensional, free‐surface flows where surface tension effects are significant. The method employs an unstructured tetrahedral mesh, a front‐tracking arbitrary Lagrangian–Eulerian formulation, and fully implicit time integration. Interior mesh motion is accomplished via pseudo‐solid mesh deformation. Surface tension effects are incorporated directly into the momentum equation boundary conditions using surface identities that circumvent the need to compute second derivatives of the surface shape, resulting in a robust representation of capillary phenomena. Sample results are shown for the viscous sintering of glassy ceramic particles. The most serious performance issue is error arising from mesh distortion when boundary motion is significant. This effect can be severe enough to stop the calculations; some simple strategies for improving performance are tested. Copyright © 2001 John Wiley & Sons, Ltd.