Deformation fracture properties

Molecular Composites via Ionic Interactions and Their Deformation—Fracture Properties... 

Step 3. The set of fracture properties G(t) are related to the interfaee structure H(t) through suitable deformation mechanisms deduced from the micromechanics of fracture. This is the most difficult part of the problem but the analysis of the fracture process in situ can lead to valuable information on the microscopic deformation mechanisms. SEM, optical and XPS analysis of the fractured interface usually determine the mode of fracture (cohesive, adhesive or mixed) and details of the fracture micromechanics. However, considerable modeling may be required with entanglement and chain fracture mechanisms to realize useful solutions since most of the important events occur within the deformation zone before new fracture surfaces are created. We then obtain a solution to the problem. 

The purpose of this paper is to investigate the mechanical properties (plastic deformation, micromechanisms of deformation, fracture) of several amorphous polymers considered in [1], i.e. poly(methyl methacrylate) and its maleimide and glutarimide copolymers, bisphenol A polycarbonate, aryl-aliphatic copolyamides. Then to analyse, in each polymer series, the effect of chemical structure on mechanical properties and, finally, to relate the latter to the motions involved in the secondary transitions identified in [ 1] (in most cases, the p transition). 

The goal of this investigation of the mechanical properties of amorphous polymers (plastic deformation, micromechanisms of deformation, fracture) was to analyse the influence of secondary transition motions on these properties. 

Abstract The fracture properties and microdeformation behaviour and their correlation with structure in commercial bulk polyolefins are reviewed. Emphasis is on crack-tip deformation mechanisms and on regimes of direct practical interest, namely slow crack growth in polyethylene and high-speed ductile-brittle transitions in isotactic polypropylene. Recent fracture studies of reaction-bonded interfaces are also briefly considered, these representing promising model systems for the investigation of the relationship between the fundamental mechanisms of crack-tip deformation and fracture and molecular structure. 

In terms of tonnage, polyolefins are by far the most important polymeric materials for structural applications, and there is consequently enormous interest in optimising their fracture properties. A rational approach to this requires detailed understanding of the relationships between macroscopic fracture and molecular parameters such as the molar mass, M, and external variables such as temperature, T, and test speed, v. Considerable effort is therefore also devoted to characterising the irreversible processes (crazing and shear deformation) that accompany crack initiation and propagation in these polymers, some examples of which will given. 

Methods of objective measurement of cereal foam structures are reviewed, including image analysis, confocal microscopy and x-ray tomography. The analysis of foam structures and their relationship with mechanical and rheological properties is described, and also the relationships between these structures and sensory descriptors such as crispness, crunchiness and texture. The size, shape and anisotropy of bubbles and their cell walls in foams are seen as critical in determining their fracture properties and sensory perception of crispness. Techniques for measuring crispness using acoustic emission and force-deformation profiles are discussed. 

One of the most important subjects of applied polymer science is the understanding of the deformation mechanisms and the fracture properties of semi-crystalline polymers. At the same time, it is one of the most diffictdt to study, and the amount of research in this area is high (see e.g. One of the complications experienced with semi-crystalline polymers stems from the fact that they are composed of crystalline and amorphous phases, arranged in a diversity of microstructures. These are generally... 

Finally, in the future, the fracture properties of the materials studied here will be investigated to evaluate the impact of the formulation combined to the storage conditions on the material mechanical properties at large deformations. 

While promising results have been obtained in the laboratory, significant additional work is required to establish the full magnitude of the property improvements that may be achieved by controlling reinforcement distribution and morphology. It is a specific objective to identify the maximum volume fraction that can be produced while still retaining the required fracture properties for aerospace applications. This will require extension of the present research to include physically based modeling of deformation and fracture of DRA. This, in turn, will require an improved three-dimensional description of the relevant microstructural features that control deformation and fracture. This effort on microstructural quantification will be outlined in Section 2.6. 

Many properties of materials, such as plastic deformation, fracture, diffusion, and phase transformation, require statistical averaging over many atomic events. Computer modeling of such processes is facilitated by usage of semiempirical interatomic potenhals allowing fast calculations of the total energy and classical interatomic forces. 

---