二氢卟吩P6醚类衍生物的合成

以蚕沙糊状叶绿素经酸碱降解制得的二氢卟吩P6三甲酯(2)为关键中间体,设计合成了9个二氢卟吩P6醚类衍生物3a～3e和4b～4e,用UV、IR、^1H、NMR、FAB-MS和元素分析确证了它们的结构。     

In situ observation of interfacial debonding process induced by matrix crack propagation in two-dimensional unidirectional model composites

Interfacial debonding behavior is studied for unidirectional fiber reinforced composites from both experimental and analytical viewpoints. A new type of two-dimensional unidirectional model composite is prepared using 10 boron fibers and transparent epoxy resin with two levels of interfacial strength. In situ observation of the internal mesoscopic fracture process is carried out using the single edge notched specimen under static loading. The matrix crack propagation, the interfacial debonding growth and the interaction between them are directly observed in detail. As a result, the interfacial debonding is clearly accelerated in specimens with weakly bonded fibers in comparison with those with strongly bonded fibers. Secondary, three-dimensional finite element analysis is carried out in order to reproduce the interfacial debonding behavior. The experimentally observed relation between the mesoscopic fracture process and the applied load is given as the boundary condition. We successfully evaluate the mode II interfacial debonding toughness and the effect of interfacial frictional shear stress on the apparent mode II energy release rate separately by employing the present model composite in combination with the finite element analysis. The true mode II interfacial debonding toughness for weaker interface is about 0.4 times as high as that for a stronger interface. The effect of the interfacial frictional shear stress on the apparent mode II energy release rate for the weak interface is about 0.07 times as high as that for the strong interface. The interfacial frictional shear stress and the coefficient of friction for weak interface are calculated as 0.25 and 0.4 times as high as those for strong interface, respectively.     

Thermal behavior of chemically treated and untreated sisal fiber reinforced composites fabricated by resin transfer molding

Using thermogravimetric analysis (TGA), the thermal behavior of sisal fibers and sisal/polyester composites, fabricated by resin transfer molding (RTM), has been followed. Chemical treatments have been found to increase the thermal stability, which has been attributed to the resultant physical and chemical changes. Scanning electron microscopy (SEM) and infrared (FT-IR) studies were also performed to study the structural changes and morphology in the sisal fiber during the treatment. The kinetic studies of thermal degradation of untreated and treated sisal fibers have been performed using Broido method. In the composites, as the fiber content increases, the thermal stability of the matrix decreases. The treated fiber reinforced composites have been found to be thermally more stable than the untreated derivatives. The increased thermal stability and reduced moisture behavior of treated composites have been correlated with fiber/matrix adhesion.     

A Numerical Investigation on the Influence of Steel Fiber Shape and Interface Strength in Reinforced Concrete

Not all steel fiber reinforced concrete composites are equally effective in enhancing structural performance. Their mechanical behaviour strongly depends upon the reinforcement morphology as well as the properties of the interface lying between steel reinforcement and concrete matrix. Using bone-shaped short (BSS) steel fibers, instead of conventional straight short (CSS) steel fibers, to reinforce concrete has demonstrated their potential in improving toughness, ductility and energy absorbing capacity under impact significantly and simultaneously. Accomplishing a strong steel–concrete interface leads to a slight increase in composite strength but simultaneously to a significant decrease in its toughness. Due to the sensitivity of steel reinforced concrete performance on these complex geometric and material parameters, the development of a numerical tool capable of simulating accurately the composite mechanical behaviour and thus leading to optimized design solutions is desirable. The physical problem of the present work involves a typical concrete composite uniformly reinforced with steel fibers subjected to tensional loading. A micromechanical non-linear finite element formulation is utilized in order to predict the load transfer characteristics and the failure process. A linear material behaviour is assumed for the steel component; a non-linear multi-crack material response is used to describe concrete while a mix-mode bilinear behaviour is utilized for the interface providing separation of primary material phases. Numerical results are presented in terms of the global design parameters. The influence of the fiber end shape, the interface strength and the fiber volume fraction on the composite strength and toughness is addressed and consequently optimized design preferences arise.     

Physical and mechanical characterization of nanocomposites with carbon nanotubes functionalized with the matrix polymer

Single wall carbon nanotubes (SWNT) are functionalized with poly(vinyl alcohol) (PVA). The functionalized nanotubes are homogeneously dispersed in a PVA solution. Nanocomposite films with low SWNT content (0.1 to 1%) are produced by the wet-casting method. X-ray diffraction shows that the PVA crystallinity was not affected by the presence of the SWNT. The improvement in tensile modulus and strength at such low reinforcement loadings is indicative of good interfacial bonding between the functionalized nanotubes and the polymer matrix.     

1,1'-(六甲基三硅撑)双环戊二烯基二(对氯苯氧基)钛的合成及晶体结构

以1,3-二氯六甲基三硅烷相继与环戊二烯基钠、正丁基锂和四氯化钛作用合成了1,1'-(六甲基三硅撑)双环戊二烯基二氯化钛(1),1在氨基钠的存在下与对氯苯酚作用制得题目化合物(2)。通过元素分析、^1HNMR和MS鉴定了1与2的结构,并对2进行X射线结构分析确证了其结构。2的晶体属单斜晶系的P21/c空间群。晶胞参数:a=1.0746(3),b=2.4865(7),c=1.2568(2)nm; β=113.42(2)°;V=3.08137nm^3;Z=4,D0=1.305g·cm^-3。化合物中三个硅原子的桥链发生明显扭曲。通过氧原子中心原钛与苯环发生共轭,使整个分子形成共轭体系。     

荧光黄的示波极谱特性研究及其在催化反应-示波极谱分析中的应用

在pH4.9HOAc-NaOAc缓冲溶液中, 荧光黄于-0.50V(vs.SCE)产生一灵敏的单扫描示波极谱波。在100℃弱碱性介质中, 铱(IV)对KIO~4氧化荧光黄这一反应具有强烈催化作用。本文研究了荧光黄的示波极谱行为及利用该催化反应测定痕量铱的各种影响因素,拟定了铱的催化反应-示波极谱分析新方法, 它们的检出限和测定范围分别为0.04ng/mL和0.08-8.0ng/mL。     

K4H2[PMo9V3O40]·10H2O的合成及其晶体结构

采用低温技术,用X射线单晶衍射法测定了标题化合物的结构。晶体属P4/mnc空间群,=12.515(3),c=17.636(7)A,Z=2.用788个独立可观测反射精修所有结构参数得R=0.061.钼钒磷杂多酸阴离子中,PO4四面体是无序的,P-O键长1.54A.M(Mo,V)是6配位,M-O键长1.62-2.48A,K是7配位,K-O键长2.84-3.10A。     

KINETIC ANALYSIS OF CO-CONDENSATION POLYMERIZATION OF AB2 AND AB MONOMERS

This work deals with the kinetics of co-condensation polymerization of AB2 and AB monomers, giving expressions of the two-dimensional molecular weight distribution function and the number/weight average molecular weights of the resulting copolymers. The two-dimensional molecular weight distribution depends on two indices, n and l, which are the respective numbers of AB2 and AB units in a copolymer species. The evolution of the two-dimensional weight and z distributions during the co-condensation polymerization has been evaluated systematically. Finally, the two-dimensional distribution was transformed into a one-dimensional molecular weight distribution with only one variable (the molecular weight of the products instead of the degree of polymerization). The calculated results show that the highly branched copolymer has a very broad molecular weight distribution when the co-condensation polymerization approaches completion.     

胺类化合物与4，4’-二氟苯偶酰的亲核取代反应研究

应用胺类化合物与4,4'-二氟苯偶酰的亲核取代反应合成了多种对称或不对称的4,4'-双(二烷氨基)苯偶酰.结构经元素分析,IR,1H NMR和MS确定.其中伯胺与4,4'-二氟苯偶酰的反应得到了一边取代、另外一边形成亚胺结构的产物,并对此反应机理进行了探讨.