566 research outputs found

    Double diaphragm forming simulation using a global-to-local modelling strategy for detailed defect detection in large structures

    Get PDF
    A global-to-local modelling strategy is presented based on a sub-modelling approach to predict the formation of macroscale defects in bi-axial non-crimp fabric (NCF) during double diaphragm forming (DDF). A full-scale global simulation is initially performed using a coarse membrane element mesh (5 mm edge length) to locate areas containing potential defects. Refined local simulations are subsequently performed using high a fidelity shell-element mesh (1 mm edge length) to explicitly predict the shape of forming induced defects in these areas, using boundary conditions derived from the global simulation. The methodology is validated by forming a fabric blank over a generic geometry comprising local changes in cross-sectional shape, in order to invoke forming induced defects in a controlled manner. The defective areas predicted by the simulation agree well with the locations observed from the forming experiments, including the shape and length of surface visible defects such as fabric wrinkling and bridging. The CPU time for this two-stage approach is shown to be approximately 13% compared to the CPU time required for the high fidelity full-scale model for the same geometry

    Simulating the effect of fabric bending stiffness on the wrinkling behaviour of biaxial fabrics during preforming

    Get PDF
    A macroscopic finite element model has been established to investigate the forming-induced wrinkling behaviour for bi-axial fabrics. Results indicate that using a linear bending model with a constant bending stiffness produces unrealistic wrinkle patterns in the fabric plies. A non-linear bending model produces more accurate forming induced wrinkle patterns compared to experimental data, since the bending stiffness parameter is varied as a function of the applied forming load to account for the onset of fibre buckling. Areas of high in-plane shear are more likely to induce out-of-plane wrinkles, indicating a positive correlation between wrinkling onset and shear deformation. A new methodology has been developed to quantitatively evaluate the severity of fabric wrinkles based on the FE simulation results. The distance between the surface of the preform and the mould tool is used to locate areas with out-of-plane defects, using the principal curvature to isolate wrinkles from areas of fabric bridging (poor conformity)

    Inter-ply stitching optimisation of highly drapeable multi-ply preforms

    Get PDF
    An efficient finite element model has been developed in Abaqus/Explicit to solve highly non-linear fabric forming problems, using a non-orthogonal constitutive relation and membrane elements to model bi-axial fabrics. 1D cable-spring elements have been defined to model localised inter-ply stitch-bonds, introduced to facilitate automated handling of multi-ply preforms. Forming simulation results indicate that stitch placement cannot be optimised intuitively to avoid forming defects. A genetic algorithm has been developed to optimise the stitch pattern, minimising shear deformation in multi-ply stitched preforms. The quality of the shear angle distribution has been assessed using a maximum value criterion (MAXVC) and a Weibull distribution quantile criterion (WBLQC). Both criteria are suitable for local stitch optimisation, producing acceptable solutions towards the global optimum. The convergence rate is higher for MAXVC, while WBLQC is more effective for finding a solution closer to the global optimum. The derived solutions show that optimised patterns of through-thickness stitches can improve the formability of multi-ply preforms compared with an unstitched reference case, as strain re-distribution homogenises the shear angles in each ply

    Defect formation during preforming of a bi-axial non-crimp fabric with a pillar stitch pattern

    Get PDF
    To capture the asymmetrical shear behaviour of a bi-axial NCF with a pillar stitch, a non-orthogonal constitutive model was developed and implemented in finite element forming simulations. Preforming experiments indicate that the local distribution of defects is significantly different on both sides of each bi-axial ply, with two different defect mechanisms observed. Correlation with simulation results indicates that one defect type is caused by excessive shear, inducing out-of-plane wrinkling in regions of positive shear (macro-scale wrinkling). The other defect type is caused by fibre compression, inducing in-plane wrinkling in regions of negative shear (meso-scale wrinkling). Local distributions of shear angle and wrinkling strain were used to determine the wrinkling mode and to confirm the corresponding defect mechanism. Results indicate that simulations based on the advanced constitutive model can predict local shear angles within ±5°of experimental values and that predicted wrinkling positions and defect types correlate well with the experiments

    A novel hotspot specific isothermal amplification method for detection of the common PIK3CA p.H1047R breast cancer mutation

    Get PDF
    Breast cancer (BC) is a common cancer in women worldwide. Despite advances in treatment, up to 30% of women eventually relapse and die of metastatic breast cancer. Liquid biopsy analysis of circulating cell-free DNA fragments in the patients’ blood can monitor clonality and evolving mutations as a surrogate for tumour biopsy. Next generation sequencing platforms and digital droplet PCR can be used to profile circulating tumour DNA from liquid biopsies; however, they are expensive and time consuming for clinical use. Here, we report a novel strategy with proof-of-concept data that supports the usage of loop-mediated isothermal amplification (LAMP) to detect PIK3CA c.3140 A > G (H1047R), a prevalent BC missense mutation that is attributed to BC tumour growth. Allele-specific primers were designed and optimized to detect the p.H1047R variant following the USS-sbLAMP method. The assay was developed with synthetic DNA templates and validated with DNA from two breast cancer cell-lines and two patient tumour tissue samples through a qPCR instrument and finally piloted on an ISFET enabled microchip. This work sets a foundation for BC mutational profiling on a Lab-on-Chip device, to help the early detection of patient relapse and to monitor efficacy of systemic therapies for personalised cancer patient management

    FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

    Get PDF
    Background:Breast cancer is one of the most common malignancies in women. Genome-wide association studies have identified FGFR2 as a breast cancer susceptibility gene. Common variation in other fibroblast growth factor (FGF) receptors might also modify risk. We tested this hypothesis by studying genotyped single-nucleotide polymorphisms (SNPs) and imputed SNPs in FGFR1, FGFR3, FGFR4 and FGFRL1 in the Breast Cancer Association Consortium. Methods:Data were combined from 49 studies, including 53 835 cases and 50 156 controls, of which 89 050 (46 450 cases and 42 600 controls) were of European ancestry, 12 893 (6269 cases and 6624 controls) of Asian and 2048 (1116 cases and 932 controls) of African ancestry. Associations with risk of breast cancer, overall and by disease sub-type, were assessed using unconditional logistic regression. Results:Little evidence of association with breast cancer risk was observed for SNPs in the FGF receptor genes. The strongest evidence in European women was for rs743682 in FGFR3; the estimated per-allele odds ratio was 1.05 (95 confidence interval=1.02-1.09, P=0.0020), which is substantially lower than that observed for SNPs in FGFR2. Conclusion:Our results suggest that common variants in the other FGF receptors are not associated with risk of breast cancer to the degree observed for FGFR2. © 2014 Cancer Research UK

    Evidence of Color Coherence Effects in W+jets Events from ppbar Collisions at sqrt(s) = 1.8 TeV

    Full text link
    We report the results of a study of color coherence effects in ppbar collisions based on data collected by the D0 detector during the 1994-1995 run of the Fermilab Tevatron Collider, at a center of mass energy sqrt(s) = 1.8 TeV. Initial-to-final state color interference effects are studied by examining particle distribution patterns in events with a W boson and at least one jet. The data are compared to Monte Carlo simulations with different color coherence implementations and to an analytic modified-leading-logarithm perturbative calculation based on the local parton-hadron duality hypothesis.Comment: 13 pages, 6 figures. Submitted to Physics Letters
    corecore