浅谈校园网大规模移动自组的网络安全技术

随着社会经济与科技的迅速发展,移动通信技术与人们生活及工作之间的联系越发紧密,移动通信技术也得到其应有的发展.在整个环境背景下,移动自组网络技术也开始出现于人们的生活中.移动自组网络技术开始应用于如军事、医疗以及电子商务等多个领域,在校园网中的应用也较为广泛.文章首先对移动自组网络进行了阐述说明,之后对校园网移动自组网络安全技术进行了深入的分析研究,以此提升人们对校园网大规模移动自组网络安全技术的认识.     

Pore structure of bulk tungsten carbide powder catalysts

Bulk tungsten carbide catalysts are prepared by direct carburization/reduction of tungsten trioxide in methane-hydrogen mixtures. The catalytic properties of such catalysts have been studied by several authors. The porous structure of these catalysts is studied by adsorption of N₂, Kr, CF₄ and neohexane. Adsorption isotherms and hysteresis loops for the catalysts suggest the presence of a microporous structure made of parallel plates distant approximately by 20 Å. These results are compared to those obtained using such catalysts for hydrogen oxidation and where condensation in the porous structure was observed.     

高支化度酯类增塑剂的结构鉴定

利用AV50 0核磁共振波谱仪鉴定了一种从聚氨酯材料中分离出的增塑剂。这是一种新型的性能优良的耐迁移性脂肪族增塑剂。使用的手段有红外光谱 ,1 H NMR ,1 3C NMR ,1 3C 1 HCOSY ,1 H 1 HCOSY以及DEPT等技术。     

无分流换热网络合成和控制的集成研究

提出了无分流换热网络合成和控制集成的策略和方法、步骤,建立了合成和控制同步优化的数学模型,使得换热网络的合成和控制的集成研究从试探法向数学规划方法发展,从理论研究向实用性方向发展,实现了同时考虑控制要求的换热网络的自动合成。通过示例说明了本文所提方法的有效性和实用前景。     

多层结构隐身涂层附着力测试探讨

优选了多层结构隐身涂层附着力的测定方法,研究了多层结构隐身涂层在自然环境中附着力的变化规律,指出了树脂耐低温和耐温变的重要性。     

SE-I型混凝剂在水处理中的应用

利用透射电镜和微孔滤膜超滤法研究了SE -I和PAC混凝剂的结构形貌和相对分子质量分布情况 ;比较了SE -I和PAC混凝处理油田含油废水、煤矿矿井废水和水库水的效果。实验结果表明 ,SE -I较PAC具有更大的枝化度和相对分子质量 ,体现在水处理效果上是SE -I较PAC有更好的除油、除浊、去除COD和脱色效果。SE -I型混凝剂是一种高效水处理剂     

大型常压锥顶贮罐的设计

以工程实例为依据，论述国内以往较少采用的大型梁柱式支承锥顶贮罐的结构，介绍了国内外相关设计标准，给出了贮罐的典型结构－斜椽，横梁和立柱的计算公式，并用Excel电子表格编制了计算书。     

A variable gap penalty function and feature weights for protein 3-D structure comparisons

We have developed a variable gap penalty function for use inthe comparison program COMPARER which aligns protein sequenceson the basis of their 3-D structures. For deletions and insertions,components are a function of structural features of individualamino acid residues (e.g. secondary structure and accessibility).We have also obtained relative weights for different featuresused in the comparison by examining the equivalent residuesin weight matrices and in alignments for pairs of 3-D structureswhere the equivalences are relatively unambiguous. We have usedthe new parameters and the varible gap penalty function in COMPARERto align protein structures in the Brookhaven Data Bank. Thevariable gap penalty function is useful especially in avoidinggaps in secondary structure elements and the new feature weightsgive improved alignments. The alignments for both azurins andplastocyanins and N- and C-terminal lobes for aspartic proteinasesare discussed     

国内互穿网络结构阻尼涂料的研究进展

在总结了国内聚合物基阻尼涂料的研究基础上,详细综述了互穿网络(IPN)结构、乳液互穿网络(LIPN)结构聚合物基阻尼涂料的种类及研究现状,并展望了聚合物基阻尼涂料研究的发展趋势和前景。     

Influence of polymerization conditions on the structure and properties of polyethylene/polypropylene in‐reactor alloy synthesized in the gas phase with a spherical Ziegler–Natta catalyst

A spherical TiCl₄/MgCl₂‐based catalyst was used in the synthesis of in‐reactor polyethylene/polypropylene alloys by polyethylene homopolymerization and subsequent homopolymerization of propylene in the gas phase. Different conditions in the ethylene homopolymerization stage, such as monomer pressure and polymerization temperature, were investigated, and their influences on the structure and properties of in‐reactor alloys were studied. Raising the polymerization temperature is the most effective way of speeding up polymerization and regulating the ethylene content of polyethylene (PE)/polypropylene (PP) alloys, but it will cause a greater increase in the PE‐b‐PP block copolymer fraction (named fraction D) than in the fraction of PP‐block‐PE in which the PP segments have low or medium isotacticity (named fraction A). Although changing ethylene monomer pressure could influence the ethylene content of PE/PP alloys slightly, it is an effective way of regulating the structural distribution. Reducing the monomer pressure will evidently increase fractions A and D. The mechanical properties of the alloys, including impact strength and flexural modulus, can be regulated in a broad range with changes in polymerization conditions. These properties are highly dependent on the amount, distribution, and chain structure of fractions A and D. The impact strength is affected by both fraction A and fraction D in a complicated way, whereas the flexural modulus is mainly determined by the amount of fraction A. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2136–2143, 2006