Growth, microstructure, and failure of crazes in glassy polymers

We report on an extensive study of craze formation in glassy polymers. Molecular dynamics simulations of a coarse-grained bead-spring model were employed to investigate the molecular level processes during craze nucleation, widening, and breakdown for a wide range of temperature, polymer chain length $N$, entanglement length $N_e$ and strength of adhesive interactions between polymer chains. Craze widening proceeds via a fibril-drawing process at constant drawing stress. The extension ratio is determined by the entanglement length, and the characteristic length of stretched chain segments in the polymer craze is $N_e/3$. In the craze, tension is mostly carried by the covalent backbone bonds, and the force distribution develops an exponential tail at large tensile forces. The failure mode of crazes changes from disentanglement to scission for $N/N_e\sim 10$, and breakdown through scission is governed by large stress fluctuations. The simulations also reveal inconsistencies with previous theoretical models of craze widening that were based on continuum level hydrodynamics

Strategies for Controlled Placement of Nanoscale Building Blocks

The capability of placing individual nanoscale building blocks on exact substrate locations in a controlled manner is one of the key requirements to realize future electronic, optical, and magnetic devices and sensors that are composed of such blocks. This article reviews some important advances in the strategies for controlled placement of nanoscale building blocks. In particular, we will overview template assisted placement that utilizes physical, molecular, or electrostatic templates, DNA-programmed assembly, placement using dielectrophoresis, approaches for non-close-packed assembly of spherical particles, and recent development of focused placement schemes including electrostatic funneling, focused placement via molecular gradient patterns, electrodynamic focusing of charged aerosols, and others

Morphology and toughness of coextruded PS/PMMA multilayers

The micromechanical behaviour of multilayered tapes made of two brittle incompatible amorphous polymers PS and PMMA was studied by means of an optical and a High Voltage Electron Microscope (HVEM). Microlayers of PS and PMMA were coextruded with varying number of layers: 64, 512 and 4096 layers. Mechanical properties of the PS/PMMA tapes were also examined. An increase in layer numbers was found to lead to a decrease in layer thickness that, in turn, resulted in: a) formation of thicker and longer crazes and, therefore, increased volume of the material involved in the plastic deformation; b) a noticeable increase in strength and strain at break (i.e. of toughness) of the samples. Enhanced toughness of the multilayered tapes is accounted for by massive cooperating crazing and yielding of both PS and PMMA phases

Micromechanical deformation processes in toughened PP/PA/SEBS-g-MA blends prepared by reactive processing

Toughening mechanisms occurring in PP/PA6 (70 vol.-%/30 vol.-%) blends containing various amounts of SEBS-g-MA have been studied by in situ straining in a high voltage electron microscope (HVEM). Variation of volume fraction of compatibilizer (SEBS-g-MA) with constant PA6 content and reactive processing conditions give excellent control over morphology and toughness/stiffness balance. With increasing volume fraction of compatibilizer the blend morphology changes significantly from discrete to cluster to island-like (percolating) structures. Micromechanical deformation processes have been characterized as a function of blend morphologies. Based on experimental results, the major toughening mechanism is the fibrillized cavitation process, and the main energy dissipation during deformation is shear yielding of matrix material triggered by irreversible plastic growth of microvoids caused by the fibrillized cavitation process. Finally, schematic models for micromechanical deformation processes in the various blend morphologies are proposed

Microindentation studies at the near surface of glassy polymers: Influence of molecular weight

6 pags., 8 figs.The viscoelastic‐plastic properties of various amorphous, glassy polymers [polystyrene (PS), poly(styrene‐acrylonitrile) copolymer (SAN), poly(methyl methacrylate) (PMMA), poly(vinyl chloride) (PVC), polycarbonate (PC)] in the micron and submicron range were investigated by means of load‐displacement analysis from depth‐sensing experiments. Hardness and Young's modulus values decrease rapidly with increasing depth up to a few microns. New data on the glass transition temperature correlation with microhardness are presented. The influence of annealing below the glass transition temperature upon the microhardness for various glassy polymers is pointed out. For PS, the influence of the molecular weight variation and molecular weight distribution on the microhardness is reported. Results are discussed on the basis of an entanglement network model, recently developed to explain the fine structure of crazes in amorphous polymers.Deutscher Akademischer Austauschdienst (DAAD) Max–Buchner Forschungsstiftung Dirección General de Investigación. Grant Number: BFM2000‐1474 Dirección General de Universidades, Ministerio de Educación, Cultura y Deporte MCYT, SpainPeer reviewe

Aggregation, fracture initiation and strength of PP/CaCO3 composites

Polypropylene/CaC03 composites were homogenized in a twin-screw compounder and then injection molded into tensile bars. Six different fillers were used in a wide range of average particle sizes between 0.08 and 12 pm. Tensile and flexural properties were measured by standard techniques, while impact resistance was determined by instrumented impact testing. Structure was characterized by light and electron microscopy, while failure initiation and propagation was studied with in situ high-voltage electron microscopy. The results showed that aggregation of particulate fillers occurs when their particle size is smaller than a critical value. This critical size depends on component properties and processing conditions. Strength and impact resistance usually decrease with increasing number of aggregates. The presence of aggregation can be detected by the use of a simple semiempirical model. Comparison of samples prepared by two different technologies showed that twin-screw extrusion and injection molding leads to relatively homogeneous composites, which was indicated by smaller deviations of the properties from theoretical predictions. In spite of the accept-able dispersion, impact resistance showed a large standard deviation, probably determined by the local variation of structure. In composites containing relatively large particles, the dominating micromechanical deformation process is debonding, while in the presence of extensive aggregation of small particles, cracks are initiated inside and propagate through aggregates. Mixed-mode failure may also occur at certain intermediate particle sizes