资源有限网络计划的PRWI启发式优化方法

本文在综合考虑了有资源约束的网络计划结构特征、资源强度、时间约束等方面因素的基础上，提出了一种新的资源优化的启发式优化方法—ＰＲＷＩ方法，并通过分析证明了该方法处理问题的效果较现有的其它方法好。     

CexGdyTb1-x-yP5O14晶体生长及其光谱

采用蒸发溶液法从磷酸溶液中生长出一系列CexGdyTb1-x-yP5O14晶体.测定了它们的结构.它们属于单斜晶系,空间群P21/c.测定了Ce0.9Gd0.1P5O14、Ce0.9Tb0.1P5O14和La0.8Gd0.1Tb0.1P5O14等晶体的光谱.首次观察到,将Gd加入CexTb1-xP5O14晶体中形成.CexGdyTb1-x-yP5O14时阻碍了Ce3+→Tb3+的能量传递,导致Ce3+的发射峰增强,Tb3+的5D4-FJ发射峰减弱、而5D3-7FJ发射峰增强.     

Bi3+和Eu3+在Ca2SiO4中的发光和能量传递

用高温固态反应合成了Ca2SiO4:Bi3+,Ca2SiO4:Eu3+和Ca2SiO4:Eu3+,Bi3+发光体。讨论了不同掺杂量和掺杂种类时Bi3+对Eu3+的5D0-7F1,5D0-7F2发射的影响规律。实验发现,Ca2SiO4:Bi3+在紫外线激发下发出明亮的蓝色光,Ca2SiO4:Eu3+,Bi3+中的Bi3+能将激发能传递给Eu3+,使Eu3+的5D0-7F1和5D0-7F2两种跃迁都大大加强,同时,Bi3+也发出鲜艳的紫色光。     

纯锆上离子注入钇和镧后的表面分析

用金属蒸汽真空弧源，以40kV加速电压对纯锆样品分别进行了10¹⁶—10¹⁷/cm²的钇、镧离子注入，注入温度约为130℃.然后对注入样品进行表面分析.x射线光电子能谱分析表明，注入的钇以Y₂O₃形式存在，镧以La₂O₃形式存在.俄歇电子能谱表明，纯锆基体表面的氧化膜厚度随着离子注入剂量的增加而增加，当离子注入剂量达到10¹⁷/cm²时，氧化膜的厚度达到了最大值.卢瑟福背散射显示镧层的厚度约为30nm，同时直接观察到当离子注入剂量为(La+Y)10¹⁷/cm²时，纯锆样品表面发生了严重的溅射. 关键词： 纯锆 钇和镧离子共注入 卢瑟福背散射 x射线光电子能谱     

ON THE CONVERGENCE OF THE RELAXATION METHODS FOR POSITIVE DEFINITE LINEAR SYSTEMS

1.IntroductionTheclassicaliterativemethods,suchastheJacobimethod,theGauss-SeidelmethodandtheSORmethod,aswellastheirsymmetrizedvariants,playanimportantroleforsolvingthelargesparsesystemoflinearequationsInaccordancewiththebasicextrapolationprincipleofthelineariterativemethod,Hadjidimos[1]furtherproposedaclassofacceleratedoverrelaxation(AOR)methodforsolyingthelinearsystem(1.1)in1978.Thismethodincludestwoarbitraryparameters,andtheirsuitablechoicesnotonlycannaturallyrecovertheJacobi,theGauss-S…     

用超磁致伸缩调谐光纤光栅的光分/插复用器

提出并研究了一种新型多信道切换的全光分/插复用器,它主要由光纤Bragg光栅(FBG)和一对光环行器组成.采用了一种高效的超磁致伸缩材料(GMM)使FBG产生有效的Bragg波长偏移.用控制电流来调控FBG的应变和Bragg波长偏移.用4只相同的FBG与波长叠加技术相结合,可建立能提供15种不同下路信道方式的OADM.     

Synthesis and light emitting properties of polyacetylenes having pendent fluorene groups

Five novel fluorene‐containing polymers, poly[(9,9‐dimethylfluoren‐2‐yl)acetylene] ( PFA1 ), poly[(1‐pentyl‐2‐(9,9‐dimethylfluoren‐2‐yl)acetylene) ( PFA2 ), poly[1‐decyl‐2‐(9,9‐dimethylfluoren‐2‐yl)acetylene] ( PFA3 ), poly[1‐phenyl‐2‐(9,9‐dimethylfluoren‐2‐yl)acetylene] ( PFA4 ), and poly[1‐(3,4‐difluorophenyl)‐2‐(9,9‐dimethylfluoren‐2‐yl)acetylene] ( PFA5 ) were synthesized by the polymerization of the corresponding fluorene‐substituted acetylenic monomers ( M1–M5), using WCl₆, MoCl_5, and TaCl₅ as catalysts and n‐Bu₄Sn as a cocatalyst. The synthesized polymers were thermally stable and readily soluble in common organic solvents. The degradation temperatures for a 5% weight loss of the polymers were ∼352–503 °C under nitrogen. PFA1–PFA5 show emission peaks from 402 to 590 nm. Besides, their electroluminescent properties were studied in heterostructure light‐emitting diodes (LEDs), using PFA2–PFA5 as an emitting layer. The PFA5 device revealed an orange‐red emission peak at 602 nm with a maximum luminescence of 923 cd/m² at 8 V. A device with the ITO/PEDOT/ a mixture of PFA2 (98 wt %) and PFA5 (2 wt %)/Ca/Al showed near white emission. Its maximum luminance and current efficiency are 450 cd/m² at 15 V and 1.3 cd/A, respectively. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 519–531, 2006     

Chiral separation of synthetic vicinal diol compounds by capillary zone electrophoresis with borate buffer and beta-cyclodextrin as buffer additive.

The investigation on capillary electrophoretic enantioseparation of six synthetic compounds containing vicinal diol groups has been undertaken to acquire the optimum conditions using native beta-cyclodextrin (beta-CD) as chiral selector and borate as a background electrolyte. The separation was carried out in an uncoated capillary (58.5 cm x 75 microm i.d., effective length 48.5 cm) and the effects of several important factors were investigated in detail. The results showed that beta-CD as a chiral selector exhibited good enantioselectivity and that the enantioseparation was greatly influenced by the structure of the diols, the borate concentration and the buffer pH. The optimum performance was obtained for the chiral vicinal diols under the conditions of 200 mM borate buffer of pH 9.8 containing 1.7% beta-CD at an applied voltage of 15 kV and a capillary temperature of 20 degrees C. Under the conditions, four diols were baseline separated with fast analysis time and the good theoretical plate numbers (above 10 x 10(4)) and favorable migration-time reproducibilities (RSDs below 3.0%) were obtained. The separation results were satisfactory.     

4,4’-二苯甲酰基联苯构象的分子力学研究

4,4’—二苯甲酰基联苯有两个三岔点,属于二元三岔共轭体系。从结构式上看,卽可把它作为二苯甲酮骨架的取代产物,又可看作是在联苯骨架上的取代。作为系统研究三岔共轭体系结构效应的部分工作,我们用QCFF/PI+MCA(Quantum Mechanical Extension of the Consistent Force Field to PI Electron System+Molecular Crystal Analysis)程序研究了其晶态和孤立态(气态)构象。研究结果表明,在孤立态中,联苯基的二个苯环的最小二乘     

双甲基丙烯酰氧苯基丙烷与苯乙烯共聚物的光学性能

标题共聚物的耐冲击性与丙烯酸酯均聚物相比有明显改善,但随着双烯单体含量的降低,共聚物的耐热性和表面硬度有所下降。丙烯酸酯含量为70%的共聚物的吸收紫外光能力最强(<370nm全吸收),含量为5%～10%的共聚物耐吸水性、耐酸耐碱性及耐冲击性最好。