用于纳米生物膜层厚度测试的光纤生物传感器

研制出光纤感应生物传感器,用以测试nm级的生物膜层的厚度.给出了测试的实现过程、实验结果和提高信噪比的方法,并与表面等离子体共振(SPR)技术进行了比较.     

Miscibility level and mechanical characterization of blends of two liquid‐crystalline polymers based on p‐hydroxybenzoic acid

Injection‐molded blends composed of two liquid‐crystalline polymers (LCPs) based on 60/40 p‐hydroxybenzoic acid/ethylene terephthalate (R3) and 73/27 p‐hydroxybenzoic acid/2,6‐hydroxynaphthoic acid (VA) copolymers, respectively, were obtained across the whole composition range. The two amorphous phases of the blends contained only slight amounts of the minority component, and the occurrence of some chemical reaction, mainly at high VA contents, was detected by Fourier transform infrared. Synergisms in the modulus of elasticity and in the tensile strength were seen in most of the blend compositions. The largest synergism was in the 50/50 R3/VA blend, which showed a modulus of elasticity 26% higher than that of either of the two components and a 17% positive deviation in the tensile strength with respect to the rule of mixtures. The different orientation of the LCPs in the blends explains the differences in the mechanical behavior. However, contrary to previous works on LCP blends and despite the almost complete immiscibility, the observed negative volume of mixing appears to be the main parameter that determines the synergistic mechanical behavior. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1022–1032, 2003     

The theory of non-linear molecular orientation and stress in polymer fluids

Non-linear stress, and orientation characteristics for polymer fluids (melts, solutions) composed of chain macromolecules of finite length have been derived. Freelyjointed chains with inverse Langevin statistics have been assumed, and their behaviour in potential hydrodynamic fields analyzed. Numerical calculations have been performed for uniaxial extensional flow in a wide range of flow rates (and stresses). In the range of small stresses, orientation is a linear function of stress. At higher stresses, orientation factor levels off, asymptotically approaching unity.Flow orientation characteristics significantly differ from those derived from affine deformation of polymer networks. This difference is a natural consequence of constraints imposed by network junctions on chain deformation.This work is dedicated to Professor Hanns-Georg Kilian on his 60th birthday in appreciation of his contribution to Polymer Physics.     

高分子材料注塑固化阶段的残余应力分析

在结晶性高分子材料注塑过程的固化阶段，温度分布、材料细观结构和应力应变之间相互耦合，因而其变化规律非常复杂．本文在井上等人考虑材料细观结构变化的金属热加工工艺应力分析［３～６］的基础上，发展了一套用于高分子注塑固化阶段残余应力分析的本构描述和有限元分析方法．在本构模型中，同时考虑了温度变化、结晶和“冻结取向”对变形的贡献．     

Local fracture resistance based on microstructural efficiency concept and simulation of injection molding

Local fracture resistance (FR) of short (SGF) and discontinuous long glass fibre (LGF) reinforced polypropylene (PP) was predicted using the ‘microstructural efficiency concept’ together with a simulation program for fibre orientation in injection molding. The ‘microstructural efficiency concept’ describes the relation between microstructural parameters such as the fibre content, the fibre aspect ratio and the processing (injection molding) induced layer structure taking also into account the local fibre orientation. The local fibre orientation in injection molding was predicted with the MOLDFLOW^®-software. The predicted local FR was compared with the measured one, which was determined by using compact tension samples and linear elastic fracture mechanics (LEFM). The comparison showed, that for SGF-PP good consistence between the predicted and measured FR existed, for LGF-PP the discrepancy was higher. Yet for both materials, the ‘microstructural efficiency concept’ together with the results obtained from the simulation of the fibre orientation can be used for FR prediction of an injection molded workpiece.     

一种通过改进Canny算子提取光弹条纹骨架线的方法

光弹性法是确定应力集中系数的有效手段，在实际工程中应力参数都是通过分析光弹干涉条纹图获得的，由于光弹干涉条纹图的复杂性，且影响成像质量的因素较多，因此如何从光弹干涉条纹图中撇开其复杂性，较高精度的提取骨架线，是一项较困难的工作，本文提出一种由改进的Canny算子对条纹方位图进行直接运算提取光弹条纹骨架线的算法，实验表明此方法对光弹条纹图很有效。     

Macroscopic theory of orientation transitions in the extensional flow of side-chain nematic polymers

A macroscopic continuum mechanical model for incompressible side-chain nematic polymers, under isothermal conditions is given. The model is a synthesis of a transient network model and the standard nematorheological model. Simplifications in the model yield constitutive equations that are identical to well known Theological models for polymer melts and for low molar mass nematics. A detailed analysis of four possible composite orientation modes of polymer backbone and mesogenic side groups in uniaxial extensional flow is given. It is shown that the thermal sensitivity of the viscoelastic parameters leads to thermally-induced orientation transitions. The extension rate sensitivity of the competition between elastic and flow orienting effects leads to flow-induced orientation transition. The role of smectic A fluctuations in thermally-induced transitions during uniaxial extensional nematic flow is elucidated. The model is able to predict and explain the experimentally observed orientation modes and thermally-induced orientation transitions of a side-chain nematic polymer subjected to uniaxial extensional flow.     

Revealing the Preferred Interlayer Orientations and Stackings of Two‐Dimensional Bilayer Gallium Selenide Crystals

Characterizing and controlling the interlayer orientations and stacking orders of two‐dimensional (2D) bilayer crystals and van der Waals (vdW) heterostructures is crucial to optimize their electrical and optoelectronic properties. The four polymorphs of layered gallium selenide (GaSe) crystals that result from different layer stackings provide an ideal platform to study the stacking configurations in 2D bilayer crystals. Through a controllable vapor‐phase deposition method, bilayer GaSe crystals were selectively grown and their two preferred 0° or 60° interlayer rotations were investigated. The commensurate stacking configurations (AA′ and AB stacking) in as‐grown bilayer GaSe crystals are clearly observed at the atomic scale, and the Ga‐terminated edge structure was identified using scanning transmission electron microscopy. Theoretical analysis reveals that the energies of the interlayer coupling are responsible for the preferred orientations among the bilayer GaSe crystals.     

Fabrication of microporous membranes from melt extruded polypropylene precursor films via stretching: Effect of annealing

In this work, the effects of annealing conditions on the microstructure of polypropylene(PP) precursor films and further on the porous structure and permeability of stretched membranes were investigated. Combinations of WAXD, FTIR, DSC and DMA results clearly showed the crystalline orientation and crystallinity of the precursor film increased with annealing temperature, while the molecular chain entanglements in the amorphous phase decreased. Changes in the deformation behavior suggested more lamellar separation occurred for the films annealed at higher temperatures. Surface morphologies of the membranes examined by SEM revealed more pore number and uniform porous structure as the annealing temperature increased. In accordance with the SEM results, the permeability of the membranes increased with annealing temperature. On the other hand, it was found that 10 min was almost enough for the annealing process to obtain the microporous membranes with an optimal permeability.     

Coupled Orientation and Stretching of Chains in Mesoscale Models of Polydisperse Linear Polymers in Startup of Steady Shear Flow Simulations

Polydisperse linear polymers are studied in startup of steady shear flow simulations using dissipative particle dynamics. The results show that with an increase in polydispersity the stress overshoot declines while the steady‐state stress increases. Various physical characteristics of the systems are studied including frequency of nonbonded interactions, gyration radius data, flow alignment angles, and average bond lengths. The patterns in the data suggest higher forces are necessary to orient and stretch long chain fractions in the flow direction. Relaxation modulus data prove the broad range of relaxation mechanisms in polydisperse systems. Linear viscoelasticity theory is used to quantify the relaxation spectrum. The results indicate an increase in the longest relaxation time in systems with higher polydispersity. The steady‐state shear viscosity results show higher viscosities with an increase in polydispersity at all shear‐rates. The good agreement of the characteristic behaviors of modeled polydisperse polymers with experiments is encouraging for future work.