Effects of interphase on tensile strength of polymer/CNT nanocomposites by Kelly–Tyson theory

The micromechanics models for composites usually underpredict the tensile strength of polymer nanocomposites. This paper establishes a simple model based on Kelly–Tyson theory for tensile strength of polymer/CNT nanocomposites assuming the effect of interphase between polymer and CNT. In addition, Pukanszky model is joined with the suggested model to calculate the interfacial shear strength (τ), interphase strength (σ_i) and critical length of CNT (L_c).The proposed approach is applied to calculate τ, σ_i and L_c for various samples from recent literature. It is revealed that the experimental data are well fitted to calculations by new model which confirm the important effect of interphase on the properties of nanocomposites. Moreover, the derived equations demonstrate that dissimilar correlations are found between τ and B (from Pukanszky model) as well as L_c and B. It is shown that a large B value obtained by strong interfacial adhesion between polymer and CNT is adequate to reduce L_c in polymer/CNT nanocomposites.     

L~∞（0，1）上一个WeakL~P（0，1）有关的格半范数

本文引进一个定义在Ｌ~∞（０，１）上格半范数ρｐ与一个熟知的格半范数ρ０关系，证明了在Ｌ~∞（０，１）中的序区间上，ρ０－拓扑与ρｐ－拓扑等价，从而证明了（Ｌ~∞（０，１），ρｐ）′的闭单位球是（Ｌ~∞（０，１），ρｐ）′的某个子集的弱－闭包，本文还证明了（Ｌ~∞（０，１），ρｐ）′可看作ＷｅａｋＬｐ（０，１）对偶空间的奇异部一个理想，而且这奇异部可由（Ｌ~∞（０，１），ρｐ）′与一算子族生成．（ｆ）ａｌｌ（ｌ．＼ｎ，ｏｏ（ｊ．）＝ｈｉｌｌｓｉｌｌ）ｔ￣．，ｉｆｆ￣＊（ｔ）ｒｅｓｐｅｃｔｉｖｅｌｙａｌｌ＇ｌ，Ｌ（ｑ，１）ｉｓｔｈｅｐｒｅｄｌｓｌａｌｏｆｔｙｒｅａｋＬＩ＇，ａｌｌｌｌｈ，ｒｌｌｏｌｌ－－ａｔ（，ｌｌｌｉ（＇ｌｌｌｅａｓｌｌｒｅａｌｇａ（ｌ￣ｓ，ａｒｅｐｒｅｓｅｌｌｔａ＇ｔｉｏｌｌｔｌｌｅｏｒｅｎｌｆｆ，ｒｅｌｅｌｌｌｅｌｌｔｓｉｌｌＳａｃ，ａｌｌ（ｌＳ，，．ｉｓｏｆ）ｔａｉｌｌｅ（ｌ．Ｈｏｗｅｖｅｒ，ｉｌｌ［２］，ｉｔｉｓｓｌｌｄｗｎｔｈａｔｔｉｌｅｒｅｐｒｅｓｅｌｌｔａｔｉｏｌｌｔｉｌｅｓｆ）ｒｅｌｌｌｏｆ）ｔａｉｌｌｅ（ｌｉｌｌ［．５］ｉｓｉｌｌ（ｔｏｒｒｅ（？ｔ．Ｉｎｔｈｉｓｎｏｔｅ，ｗｅｄｅ     

Analysis of run-in process for PC manufacturing

This paper gives a review of the methodology used to tune the run-in process of a PC manufacturing line. It shows in some detail the analysis carried-out on the test data gathered on the manufacturing line and presents a clear picture of the run-in process in order to choose the best compromise between process efficiency and costs.     

TIC: A timed calculus

TIC is a timed algebraic calculus which combines ideas from asynchronous and synchronous calculi. Time is introduced by assigning explicit time restrictions to the events of an asynchronous calculus. The semantics is defined in an operational way. Interleaving of behaviours is defined in such a way that a proper merge of events in time is achieved. Weak timed bisimulation is also defined. Examples are presented to show the applicability of the calculus to the study of timed behaviours.This work was partially supported by CICYT under the TIC program (MEDAS project)     

Asbestos replacement aspects: Modification of the fibre-matrix interphase in lonomer based composites

Asbestos fibres, of the chrysotile variety, and chopped carbon fibres were pretreated by an in-situ polycondensation technique eventually resulting in a polyamide coating on the fibre surface. Ionomer based composites containing either carbon or asbestos fibres in random in plane fibre orientation were prepared, and the influence of this coating process on the tensile properties was investigated. It was found that for the asbestos-filled composites the presence of the nylon 6,6 interlayer improves the tensile performance, especially at moderate polyamide depositions. This is not the case with the pretreated carbon-filled composites for which carbon fibres with higher polyamide contents are preferred. Combinations of the treated asbestos fibres with carbon and/or aramid fibres may be used to reduce the asbestos content in asbestos-only based engineering plastics.     

An anti-plane crack perpendicular to the weak/micro-discontinuous interface in a bi-FGM structure with exponential and linear non-homogeneities

Treated was an anti-plane crack perpendicular to the interface of an exponential-type FGM strip bonded to another linear-type FGM substrate with infinite thickness. Through Fourier integral transform, the problem was reduced as a Cauchy singular integral equation, which was further solved numerically by the Lobatto–Chebyshev collocation method. Based on the numerical solution, the effects of the geometrical and physical parameters on the stress intensity factor (SIF) were analyzed and the following conclusions were obtained: (a) A notable discrepancy between the interface-perpendicular crack and the interfacial one is that, to reduce the weak-discontinuity of interface or to make the interface micro-discontinuous will not necessarily decrease the SIF of the former, but will surely decrease that of the latter. (b) When a crack tip is situated very near to the interface (or free surface), its SIF will be high and totally dominated by the interface (or free surface). (c) To increase the stiffness of the FGM on one side of the interface is beneficial to preventing the crack on the other side from growing toward the interface. Besides, some practical suggestions were further given for material design in the field of composites.     

Adhesion Mechanisms of Polyurethanes to Glass Surfaces. III. Investigation of Possible Physico-Chemical Interactions at the Interphase

Surface free energies of polyurethanes made from toluene diisocyanate and 1, 4 butanediol-based hard segments and caprolactone polyol-based soft segments were calculated using additive functions. Good agreement was found between the calculated values based on additive functions and the calculated values based on contact angle measurements. The phase-separated polyurethanes were found to have a higher polar surface free energy component (γ^P). This was linked to the preferential segregation of butanediol/butanediol-derived moieties to the polyurethane surfaces due to phase separation. The adhesion values of these polyurethanes to soda-lime glass were correlated with their respective γ^P values and a linear relationship was found. It was also shown that the adhesion values of the low γ^P polyurethanes improved substantially when the glass surfaces were coated with a thin layer of butanediol prior to the bonding. The modulus of the interphase region rich in butanediol was evaluated. Although a modulus increase was found at the interface, this increase was found to play a secondary role in the adhesion. The chemical interactions at the polyurethane/glass interphase were investigated by pre-treating the glass surfaces with methyl-trimethoxysilane and trimethylchlorosilane prior to adhesion testing. The adhesion data showed no significant difference between the uncoated and the silane-treated glass substrates. Based on this experimental evidence, the possibility of any covalent or ionic bonding at the polyurethane/glass interphase was assumed negligible. It was determined that the mechanism of adhesion between the polyurethanes and the glass surface could be through the formation of an interphase region in which hydrogen bonding between the butanediol-rich interphase region and the hydroxylated glass surface plays a key role.     

In Situ FTIR Study of the Formation of an Organosilane Layer at the Silica/Solution Interface

An FTIR experiment especially designed to study the growth of an organosilane layer at the interface between a solution and a flat silica surface is presented. High sensitivity is achieved by using the attenuated total reflection (ATR) technique in a liquid flow cell. The ATR crystal, either silicon or germanium, is covered with a very thin silica layer. Chemical reactions of a mono-and a di-hydrolyzable silane with the silica substrate have been investigated. The grafting of a submonolayer of the first reagent has been monitored by following the C-H and SiO-H vibrations. The density of grafted molecules has been estimated and information on the nature of the chemical bonding has been achieved. Evidence for the chain-polymerization of the dihydrolyzable silane at the substrate/solution interface has been inferred from the appearance of a Si-O-Si absorption band.     

外磁场激励下管道弱磁应力内检测特性研究

弱磁应力检测技术支持非接触在线应力损伤检测,在长输油气管道应力内检测技术领域具有巨大的应用潜力。但弱磁信号微弱,易受外界环境干扰,检测结果易出现偏差。为加强弱磁信号的检测能力,基于铁磁材料的微观特性,建立了外磁场弱磁应力检测模型,获得了弱磁信号强度随外磁场强度与施加应力的变化规律,描述了外磁场对弱磁应力检测信号的激励特性,并进行了系统的实验研究。结果表明,弱磁信号的切向峰值与法向零点均位于应力集中区的中心位置,且不随应力与外磁场的变化而发生波动;弱磁信号切向峰值与法向峰峰值随外磁场与应力的增加而增大;外磁场对弱磁应力检测信号的激励作用随外磁场的增加先增大后减小。     

A panoramic view of Li7P3S11 solid electrolytes synthesis,structural aspects and practical challenges for all-solid-state lithium batteries

The development of an inorganic electrochemical stable solid-state electrolyte is essentially responsible for future state-of-the-art all-solid-state lithium batteries (ASSLBs). Because of their advantages in safety, working temperature, high energy density, and packaging, ASSLBs can develop an ideal energy storage system for modern electric vehicles (EVs). A solid electrolyte (SE) model must have an economical synthesis approach, exhibit electrochemical and chemical stability, high ionic conductivity, and low interfacial resistance. Owing to its highest conductivity of 17 mS·cm^-1, and deformability, the sulfide-based Li₇P₃S₁₁ solid electrolyte is a promising contender for the high-performance bulk type of ASSLBs. Herein, we present a current glimpse of the progress of synthetic procedures, structural aspects, and ionic conductivity improvement strategies. Structural elucidation and mechanistic approaches have been extensively discussed by using various characterization techniques. The chemical stability of Li₇P₃S₁₁ could be enhanced via oxide doping, and hard and soft acid/base (HSAB) concepts are also discussed. The issues to be undertaken for designing the ideal solid electrolytes, interfacial challenges, and high energy density have been discoursed. This review aims to provide a bird's eye view of the recent development of Li₇P₃S₁₁-based solid-state electrolyte applications and explore the strategies for designing new solid electrolytes with a target-oriented approach to enhance the efficiency of high energy density all-solid-state lithium batteries.