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- Fracture toughness (22) (entfernen)
Organisationseinheit der BAM
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- 9.6 Additive Fertigung metallischer Komponenten (2)
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Eingeladener Vortrag
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Welding is one of the most common methods in industrial practice for joining components. Its main advantages are high speed in manufacturing combined with low costs and, usually, a high degree of flexibility, integrity and reliability. Nevertheless, welding is a highly complex metallurgical process and, therefore, weldments are susceptible to material discontinuities, flaws and residual stresses which may lead to structural failure and life time reduction. As a consequence weldments are an important field of fracture mechanics methods although its application is more complex than for homogeneous or non-welded structures. The aim of the paper is to provide an overview on the current state of fracture mechanics application to weldments. It starts by discussing the specific features which any fracture mechanics analysis of weldments has to take into account. Then, the experimental determination of fracture toughness, fatigue crack propagation and tensile properties of weldments is addressed. Finally, the analytical determination of the crack driving force in components and structural integrity assessment approaches for weldments are presented.
The two-part paper provides an overview on the state-of-the-art in the application of engineering fracture mechanics to weldments. This, of course, cannot be exhaustive but is limited to butt and fillet welds with crack initiation at weld toes. In the present first pari, the authors briefly focus on the susceptibility of welds to cracks and other defects. Following this, they discuss in more detail the consequences of material inhomogeneity across the weld for fracture mechanics. Inhomogeneity causes scatter in fracture toughness and strength mis-match effects which both have to be considered in fracture toughness testing, crack driving force determination and fracture assessment of welded components. Part 2 of the paper series will add a discussion of welding residual stresses and questions of applying fracture mechanics to residual as well as total lifetime estimation of welds under cyclic loading.
Although the slow crack growth in glass is dominated by stress-corrosion phenomena, it also should reflect the underlaying intrinsic fracture behavior controlled by glass chemistry and structure. To investigate such underlaying phenomena, crack growth velocity in alkali silicate glasses was measured in vacuum across 10 orders of magnitude with double cantilever beam technique. Measured and literature crack growth data were compared with calculated intrinsic fracture toughness data obtained from Young’s moduli and theoretical fracture surface energy. Data analysis reveals slight correlation with the packing density and significant deviations from the intrinsic brittle fracture behavior. These deviations do not follow simple compositional trends. Two opposing processes may explain this finding: a decrease in the apparent fracture surface energy due to stress-induced chemical changes at the crack tip and its increase due to energy dissipation during fracture.
Fracture mechanics approaches are increasingly applied for the characterization of epoxy resin and adhesive mechanical properties. Therefore, the fracture toughness and crack resistance under static load ISO 13586 [1] are often regarded as state of the art to analyse material improvements. However, experimental investigations on fatigue behaviour, thus the crack propagation according to ISO 15850 [2], seem to be much more sensitive to characterize the materials for in service loading conditions. Firstly, an efficient testing concept was developed at BAM. In this framework, the geometry for a modified single edge notched tensile specimen (SET) was developed in order to assure appropriate resolution in measuring the crack length via a CCD-camera [3]. In the next step, the influence of the cure temperature on the fracture-mechanical properties was investigated.
The crack propagation rate of environmental stress cracking was studied on high-density polyethylene compact tension specimens under static loading. Selected environmental liquids are distilled water, 2 wt% aqueous Arkopal N100 solution, and two model liquid mixtures, one based on solvents and one on detergents, representing stress cracking test liquids for commercial crop protection products. The different surface tensions and solubilities, which affect the energetic facilitation of void nucleation and craze development, are studied. Crack growth in surface-active media is strongly accelerated as the solvents induce plasticization, followed by strong blunting significantly retarding both crack initiation and crack propagation. The crack propagation rate for static load as a function of the stress intensity factor within all environments is found to follow the Paris–Erdogan law. Scanning electron micrographs of the fracture surface highlight more pronounced structures with both extensive degrees of plasticization and reduced crack propagation rate, addressing the distinct creep behavior of fibrils. Additionally, the limitations of linear elastic fracture mechanisms for visco-elastic polymers exposed to environmental liquids are discussed.
The fracture toughness in the fiber-matrix composite by means of the single fiber pull-out test can be achievable, if it is possible to measure the compliance of partial debonded fiber, which necessitates a stable crack propagation and the determination of the corresponding crack length. A combination of high stiff test equipment and a simultaneous monitoring of the photo-elastic pattern of the embedded fibers with the help of polarization microscope enables to measure crack length and determination of Gc [Hampe, A and Marotzke, C. (1997). The Energy Release Rate of the Fiber/Polymer Matrix Interface: Measurement and Theoretical Analysis, J. Reinf. Plast. and Compo., 16: 341-352.]. This method is well-known for glass fiber-amorphous polymer composite. In this investigation, we tried to implement the same technique to C-fiber with amorphous and semi-crystalline polymer composites. The energy release rate (ERR) of the fiber-matrix interface was evaluated for the carbon fiber-reinforced in polycarbonate (PC) by interfacial crack propagation arising in the single fiber pullout test. Further, the crack propagation at the fiber-matrix interface with different matrix morphology was discussed with the use of photo-elastic pattern observed with the aid of polarization microscope.
Brittle materials, such as oxide glasses, are usually very sensitive to flaws, giving rise to a macroscopic fracture strength that is much lower than that predicted by theory. The same applies to metallic glasses (MGs), with the important difference that these glasses can exhibit certain plastic strain prior to catas- trophic failure. Here we consider the strongest metallic alloy known, a ternary Co 55 Ta 10 B 35 MG. We show that this macroscopically brittle glass is flaw-insensitive at the micrometer scale. This discovery emerges when testing pre-cracked specimens with self-similar geometries, where the fracture stress does not de- crease with increasing pre-crack size. The fracture toughness of this ultra-strong glassy alloy is further shown to increase with increasing sample size. Both these findings deviate from our classical under- standing of fracture mechanics, and are attributed to a transition from toughness-controlled to strength- controlled fracture below a critical sample size.
A novel phosphorus-modified polysulfone (P-PSu) was employed as a combined toughness modifier and a source of flame retardancy for a DGEBA/DDS thermosetting system. In comparison to the results of a commercially available polysulfone (PSu), commonly used as a toughness modifier, the chemorheological changes during curing measured by means of temperature-modulated DSC revealed an earlier occurrence of mobility restrictions in the P-PSu-modified epoxy. A higher viscosity and secondary epoxy-modifier reactions induced a sooner vitrification of the reacting mixture; effects that effectively prevented any phase separation and morphology development in the resulting material during cure. Thus, only about a 20% increase in fracture toughness was observed in the epoxy modified with 20 wt.% of P-PSu, cured under standard conditions at 180 °C for 2 h. Blends of the phosphorus-modified and the standard polysulfone (PSu) were also prepared in various mixing ratios and were used to modify the same thermosetting system. Again, no evidence for phase separation of the P-PSu was found in the epoxy modified with the P-PSu/PSu blends cured under the selected experimental conditions. The particular microstructures formed upon curing these novel materials are attributed to a separation of PSu from a miscible P-PSuepoxy mixture. Nevertheless, the blends of P-PSu/PSu were found to be effective toughness/flame retardancy enhancers owing to the simultaneous microstructure development and polymer interpenetration.