钽在冲击载荷下的动态力学特性

 在对称碰撞实验中,用VISAR测试系统记录了自由面粒子速度剖面。结合材料常压弹性纵波声速的测量,利用冲击加载的双波结构,测量了钽在30 GPa以内的冲击波速度,给出了线性相关性非常好的D-u_p 关系,并与高压下的测量结果作了比较。同时对由自由面粒子速度剖面来计算层裂强度的模型进行了讨论,发现模型差异对钽的层裂强度的影响超过30%。     

Agarose Sols and Gels Revisited

Agarose sols have been seen for long as solutions of flexible chains that, on cooling, produce thermoreversible gels through double-helix formation. Investigations of the chain conformation in the sol state by small-angle neutron scattering reveals instead a rigid chain with a very large persistence length (l_p > 9 nm). The chain cross-section radius and mass per unit length correspond to characteristics of helices as those described by Foord and Atkins. These results lead one to a reappraisal of the occurrence of double helices in the gelation process, as they rather suggest a transition of the type loose-single helix⇒tight single helix. Studies of gels from agarose/water/cosolvent where the cosolvent is Dimethyl Sulfoxide (DMSO), Dimethyl Formamide (DMF), and Methyl Formamide (MF) have led one to conclude on the formation of agarose/water/ cosolvent ternary complexes. The contrast variation method by neutron scattering gives further support to this assumption. Finally, determination of the gel nanostructure allows one to account for the two regimes observed for the variation of the elastic modulus vs concentration.     

Molecular Dynamics Simulation of the Fracture in Polymer‐Exfoliated Layered Silicate Nanocomposites

Summary: The MD technique was used to investigate the fracture behavior in fully exfoliated layered silicate (nanoplatelet)‐polymer nanocomposites. MD results reveal that the addition of the nanoplatelets can improve the fracture strength of polymers. The interactions between the surface of the nanoplatelets and the segments of the polymer, and the relaxation time of polymer chains have significant influences on the fracture strength of the polymer. For polymers with T_g below room temperature, such as polyurethane, or close to room temperature, such as nylon, the nanoplatelets are always working for the enhancement of the mechanical properties. However, for polymers with T_g above room temperature, such as epoxy and polystyrene, the addition of the nanoplatelets is not working well for toughening these polymers. If the nanoplatelets are to enhance the mechanical properties of these polymers, it is necessary to build up a stress relaxation interface between the polymer and the nanoplatelet in order to reduce the effect of the difference between the relaxation time of nanofillers and that of polymers.

Force per area versus distance curves as a function of the difference of the relaxation times of the nanoplatelets and polymer chains.     

畴极化转动对多晶铁电材料断裂特性的影响

主要基于细观力学方法揭示了畴极化转动对多晶铁电陶瓷的各向异性断裂特性的平均影响。首先,用Eshelby-Mori-Tanaka理论和统计模型分析了无穷大铁电材料体中一椭球夹杂的内、外电弹性场,得到畴极化转动对电弹性场的平均影响;其次,推导了等效多晶铁电陶瓷中含一钱币状裂纹的裂纹扩展力(能量释放率)G_ext,并用它估计了畴极化转动对多晶铁电陶瓷断裂特性的影响。对BaTiO₃陶瓷中裂纹扩展力的计算结果表明,对多晶铁电材料断裂特性分析必须考虑畴极化转动的影响。计算结果得出了与实验相一致的结论:在受较小的力时,外加电场对裂纹扩展产生较大的影响,而且在某种程度上能促进了裂纹扩展。     

基于断裂能的岩土节理弹性-软化塑性本构模型

基于准脆性材料的断裂力学和塑性理论,提出了用于岩土节理软化行为描述的弹性软化塑性本构模型.模型的主要特点是:1)节理材料的软化塑性和扩容特性直接与断裂失效过程相联系,所采用的材料参数比已有的弹塑性软化模型所用的参数少;2)模型可以描述混合断裂失效及相应的摩擦滑动,具有较广的适用性.     

Ductile‐to‐Semiductile Transition in PP‐MWNT Nanocomposites

A ductile‐to‐semiductile transition in the crack resistance behaviour of PP/MWNT composites is discussed, using an essential work of fracture approach based on a post yield fracture mechanics concept and its possible interrelation to the structural attributes studied by TEM, SEM, and WAXD. A maximum in the non‐essential work of fracture is observed at 0.5 wt.‐% MWNT content, which demonstrates the enhanced resistance to crack propagation compared to pure PP, followed by a sharp decline with the increase in MWNT content to 1.5 wt.‐%, which reveals a ductile‐to‐semiductile transition. Fracture kinetic studies present a qualitative picture of the nature of such a transition in terms of a) switch over from non‐steady (in pure PP) to steady‐state crack tip opening displacement rate (in nanocomposites), and b) a ductile‐to‐semiductile transition; largely as a result of delayed‐yielding of the nanocomposites.

     

Study of Adhesion and Fracture of Polymer Laminates by Imaging of Interfaces

The adhesion and fracture of styrene‐acrylonitrile random copolymer and poly(methyl methacrylate) (PMMA/SAN) laminates were studied. They showed a drastic transition from brittle to ductile on varying the acrylonitrile (AN) content in SAN, with changes in the fracture mode from interfacial failure to cohesive fracture. Energy‐filtering transmission electron microscopy (EFTEM) and scanning electron microscopy (SEM) with an in‐lens detector system were employed to study the interface and adhesion of the laminates. The effect of the AN content in SAN on the PMMA/SAN interfacial structures could be revealed by imaging of the interfaces using elemental mapping and electron energy loss spectroscopy (EELS). The in‐lens detector system in the SEM enabled the differentiation of thin interfaces with poor adhesion strength, yielding smooth and flat fracture surfaces, where numerous nanosized fibrils were formed normal to the surfaces.

     

A method for measuring bending stresses based on electromagnetic actuation and Raman spectroscopy

Bending stress and fracture strength of micromachined structures are the parameters determining the function and life span of microelectromechanical systems (MEMS) and are also indispensable data for MEMS design. This paper reports the results of a study in which a bending stress measurement method based on electromagnetic actuation and Raman spectroscopy has been examined. In this study, an eight‐cantilever mass structure is chosen as the experimental object. The results have indicated that it can accurately measure the bending stresses and fracture strength. Copyright © 2006 John Wiley & Sons, Ltd.     

Essential Work of Fracture of photo-oxidized LDPE/EVA Films

The Essential Work of Fracture approach (EWF) was used to determine how UV-C irradiation alters the fracture behaviour of LDPE/EVA films. Complementary characterization was performed by FTIR, DSC, TOM, and uniaxial tensile testing. The crosslinking reactions that govern photo-oxidation process at initial stage of exposure stiffened the amorphous phase of the polymer, leading to films with enhanced elastic modulus, yield stress and ultimate strength, but impaired strain at break. In the fracture experiments carried out on films irradiated within 0 and 5 days, EWF methodology requirements were met and the corresponding fracture toughness parameters (w_e and βw_p ) turned out to be sensitive to UV-C irradiation. Longer irradiation time triggered the development of microcracks, which not allowed further stable crack growth and invalidated the application of EWF approach.     

Application of Polyelectrolytic Temperature-Responsive Hydrogels in Chemical Sensors

Summary: A rapidly expanding field of on-line process monitoring and on-line control in biotechnology, food industry, pharmaceutical industry, process chemistry, environmental measuring technology, water treatment and sewage processing requires the development of new micro fabricated reliable chemical and biosensors that are specific for particular species and can attain the analytic information in a faster, simpler and cheaper manner. Using a functionalised polymer coating in sensors provides the possibility to detect, transmit and record the information regarding the concentration change or the presence of a specific analyte (a chemical or biological substance that needs to be measured) by producing a signal proportional to the concentration of the target analyte. However, the sensor response time and signal reproducibility are limited by the visco-elastical and hysteresis behaviour of the polymer material. We propose some methods improving the properties of the chemical sensors on the basis of thermo-shrinking N-isopropylacrylamide (NIPAAm) copolymer gels.