Flame-retardant effect of cross-linked phosphazene derivatives and pentaerythritol derivatives on polypropylene

Journal of Thermal Analysis and Calorimetry - A phosphazene-based flame retardant (PBFA) was synthesized by hexachlorocyclotriphosphazene and N-aminoethylpiperazine. To improve the flame retardancy...     

电化学聚对苯膜的现场ESR及其性能研究

本文用现场电化学-ESR联合测试的技术, 对电化学聚对萃膜在浓H_2SO_4中的性质进行了研究, 结果表明: 聚对苯膜具有高的电导率和相对低的自旋磁化率, 极化子与偶极化子为主要导电者, 并在一定的电位下相互转化, 自旋粒子有很大的离域性。膜中链与链之间可能存在部分的氧桥结构, 而引起体系结构的某些变化, 使聚对苯膜的电导提高以及掺杂容易进行。掺杂量受电位控制, 浓H_2SO_4中的HSO_4~-嵌入/脱嵌的电化学可逆性很好, 最大掺杂量可相当于每5个苯环单元氧化出一个正电荷, 可望将电化学聚对苯用作稳定的二次电池电极材料。     

New Photoluminescence Phenomena of Ge／SiO2 Glass Synthesized by Sol-gel Method

New Ge/SiO2 glasses have been synthesized by heating the GeO2/SiO2 dry gels under H2 gas at 700℃. The resulting fluorescence spectra show that this kind of Ge/SiO2 glasses emit strong photoluminescence at 392 nm (3.12 eV), medium strong photoluminescence at 600 nm (2.05 eV) and weak photoluminescence at 770 nm (1.60 eV) respectively. Possible photoluminescence mechanisms are also discussed based on the results of X-ray diffraction (XRD) and X-ray photoelectron spectra (XPS).     

On multi-choice TU games arising from replica of economies

In this paper we derive a multi-choice TU game from r-replica of exchange economy with continuous, concave and monetary utility functions, and prove that the cores of the games converge to a subset of the set of Edgeworth equilibria of exchange economy as r approaches to infinity. We prove that the dominance core of each balanced multi-choice TU game, where each player has identical activity level r, coincides with the dominance core of its corresponding r-replica of exchange economy. We also give an extension of the concept of the cover of the game proposed by Shapley and Shubik (J Econ Theory 1: 9-25, 1969) to multi-choice TU games and derive some sufficient conditions for the nonemptyness of the core of multi-choice TU game by using the relationship among replica economies, multi-choice TU games and their covers.     

A subwavelength MIM waveguide resonator with an outer portion smooth bend structure

We systematically investigate bends in metal–insulator–metal (MIM) subwavelength plasmonic waveguides resonator, realized in a two-dimensional (2D) plasmon polariton metal using a finite-difference time-domain (FDTD) method with perfectly matched layers (PMLs) boundary conditions. We apply the outer portion of the bend structure in resonator which can lead to remarkably good bending transmission characteristics. We discuss the existence conditions of different modes which affect the device performance, and analyze coupling efficiency of the outer portion of the bend structure resonator in detail. Meanwhile, we find that the first dip of the outer portion smooth bend resonator nearly linear shifts toward longer wavelengths with the increase of the effective waveguiding length. In addition, add/drop directional couplers are realizable using the present resonator structure.     

取代基效应(SCS)与乙烯-α-烯烃共聚物的序列结构Ⅲ.定量分析

本文在分析乙烯-α-烯烃共聚物序列结构时,把代表共单体反接单元的亚甲基(CH₂)βγ和γδ分别归属给了二元组VV和三元组EEV。与此同时,CH₂-δδ和δδ⁺归属给了二元组EE。表征乙烯长序列的CH₂-δ⁺δ⁺分属二元组EE和三元组EEE,对应峰强度在EE和EEE之间的分配是处理序列分布的关键。在本文中运用序列结构的Bovey关系和Randall统计进行演算,求得了修正值△的数学表达式,严格解和近似解。在规则链条件下得到的近似解与G.J.Ray的结果完全相同。当共单体含量较少时,谱峰强度Iδ⁺δ⁺的分配接近相等。在二元组和三元组的水平上,乙烯-α-稀烃共聚物的¹³C NMR谱中共有十三个峰,属于CH₂的有十个,属于CH的有三个。利用这些谱峰的强度数据可以建立一套计算公式,由此提供共聚物序列结构的全部信息。因此这是一个研究乙烯-α-烯烃共聚物序列结构的普适方法。     

准二维电荷密度波导体钾紫青铜KxMo6O17单晶样品的制备

采用碳酸盐替代高钼酸盐电解还原的方法成功制备出了准二维电荷密度波导体钾紫青铜单晶.通过x射线衍射、透射电子显微术等方法对单晶进行结构分析表明：晶胞参数a=b=0.5540nm，c=1.3508nm，单晶为三角晶系，对称群为P3.电阻温度关系曲线的测量显示：钾紫青铜K_xMo₆O₁₇单晶在112K附近发生金属到金属的Peierls相变. 关键词： 钾紫青铜 电荷密度波 Peierls相变     

A 3D LIF system for turbulent buoyant jet flows

A Laser-Induced Fluorescence (LIF) system for mapping the three dimensional tracer concentration field in turbulent flows is described. The system is particularly suited to studies of single or multiple buoyant jets discharged into unstratified and stratified flowing environments for conditions typical of wastewater discharges into surface water bodies. A laser beam is scanned through the flow and LIF images are obtained in parallel planes with a high-speed synchronized CCD camera. Refractive index matching is used to minimize refractive index variations due to local density gradients. An application to vertical round buoyant jets discharging into unstratified and stratified cross flows is presented. The three-dimensional system can obtain vastly more data than is possible with probe-based techniques and can yield far more insight into the flow and mixing processes.Abbreviations a Combined attenuation coefficient, cm^-1 - a_w Attenuation coefficient for fresh water, cm^-1 - B Buoyancy flux of buoyant jet, cm⁴/s³ - c Tracer concentration, g/l - C _salt, C _eth Salt and ethanol concentrations, g/l - d Port diameter, cm - g Acceleration due to gravity, cm/s² - Modified acceleration due to gravity at source, cm/s² - Q Volume flux of buoyant jet, cm³/s - I Image gray scale level, DN - l _a,l _Q , l _M , l _s, l _t Buoyant jet length scales, cm (Eq. 8) - L _y Distance from camera to image plane, cm - M Momentum flux of buoyant jet, cm⁴/s² - M _y Image scale factor - N Buoyancy frequency, s^-1 - u _a Ambient flow velocity, cm/s - u _j Jet exit velocity, cm/s - P Laser power, W - S ₀ Lowest dilution on the vertical center-plane through the nozzle - S _m Minimum dilution: lowest dilution in a vertical plane perpendicular to the flow - x, y, z Coordinates, cm - z _m Maximum rise height of buoyant jets, cm - z _e Equilibrium rise height of buoyant jets, cm - Image calibration constant - ₀ Effluent density, g/cm³ - _a Ambient density, g/cm³     

Spectrophotometric detection of tyrosinase activity based on boronic acid-functionalized gold nanoparticles

A spectrophotometric method for the detection of tyrosinase activity is developed by utilizing the product-triggered aggregation of boronic acid-functionalized gold nanoparticles. Based on the changes of absorbance in UV-visible spectra, the assay shows extremely high sensitivity and lowered limit of detection of 1 × 10(-10) u mL(-1).     

Triptycene‐Derived Calix[6]arenes: Synthesis,Structures, and Their Complexation with Fullerenes C60 and C70

Two pairs of novel triptycene‐derived calix[6]arenes 4 a , b and 5 a , b have been efficiently synthesized through both one‐pot and two‐step fragment‐coupling strategies starting from 2,7‐bis(hydroxymethyl)‐1,8‐dimethoxytriptycene 1 . Subsequent demethylation of 4 a , b and 5 a , b with BBr₃ in dry dichloromethane gave the macrocyclic compounds 6 a , b and 7 a , b . Treatment of either 4 a or 6 a with AlCl₃ resulted in the same debutylated product 8 , while 9 was similarly obtained from either 5 a or 7 a . Structural studies revealed that all of the macrocycles have well‐defined structures with fixed conformations both in solution and in the solid state owing to the introduction of the triptycene moiety with a rigid three‐dimensional (3D) structure, making them very different from their classical calix[6]arene counterparts. As a consequence, it was found that all of these the triptycene‐derived calix[6]arenes could encapsulate small neutral molecules in their cavities in the solid state. Moreover, it was also found that the macrocycles 4 b and 5 b showed highly efficient complexation abilities toward fullerenes C₆₀ and C₇₀, forming 1:1 complexes with association constants ranging from (5.22±0.20)×10⁴ to (8.68±0.30)×10⁴ M ^?1.