9 research outputs found

    A framework to model thermomechanical coupled of fracture and martensite transformation in austenitic microstructures

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    A fully thermomechanical coupled phase-field (PF) model is presented to investigate the mechanism of austenite-to-martensite phase transformation (MPT) and crack initiation as well as its propagation in pure austenitic microstructures. The latent heat release and absorption involved in the MPT are explicitly taken into account by coupling the PF model with transient latent heat transfer. In order to consider temperature dependency in the PF model for MPT, a temperature-dependent Landau polynomial function, whose parameters are identified using molecular dynamics (MD) simulations, is proposed. Furthermore, the fracture surface energy is approximated based on the second-order PF model and then, the temporal evolution of the damage variable is given by the variational derivative of the total potential free energy of the system with respect to the damage variable. The achieved numerical results demonstrate that the model can be employed to predict the fracture mechanism of austenitic microstructures under a thermomechanical field in a multiphysics environment. The results reveal that the temperature has a tremendous impact on the growth rate of both martensitic variants and consequently on the crack growth path. The key contributions of this work are to shed light on the impact of thermal boundary conditions on the coupled process of MPT, crack initiation and growth

    EDGAR 2.0: an enhanced software platform for comparative gene content analyses.

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    The rapidly increasing availability of microbial genome sequences has led to a growing demand for bioinformatics software tools that support the functional analysis based on the comparison of closely related genomes. By utilizing comparative approaches on gene level it is possible to gain insights into the core genes which represent the set of shared features for a set of organisms under study. Vice versa singleton genes can be identified to elucidate the specific properties of an individual genome. Since initial publication, the EDGAR platform has become one of the most established software tools in the field of comparative genomics. Over the last years, the software has been continuously improved and a large number of new analysis features have been added. For the new version, EDGAR 2.0, the gene orthology estimation approach was newly designed and completely re-implemented. Among other new features, EDGAR 2.0 provides extended phylogenetic analysis features like AAI (Average Amino Acid Identity) and ANI (Average Nucleotide Identity) matrices, genome set size statistics and modernized visualizations like interactive synteny plots or Venn diagrams. Thereby, the software supports a quick and user-friendly survey of evolutionary relationships between microbial genomes and simplifies the process of obtaining new biological insights into their differential gene content. All features are offered to the scientific community via a web-based and therefore platform-independent user interface, which allows easy browsing of precomputed datasets. The web server is accessible at http://edgar.computational.bio
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