154 research outputs found

    Towards robust unstructured turbomachinery large eddy simulation

    Get PDF
    This is the final version of the article. It first appeared from Elsevier via http://dx.doi.org/10.1016/j.compfluid.2015.06.017Industrial legacy codes usually have had long pedigrees within companies, and are deeply embedded into design processes. As the affordability and availability of computing power has increased, these codes have found themselves pushed into service as large eddy simulation solvers. The approximate Riemann solver of Roe, which is frequently used as the core method in such legacy codes, is shown to need much user care when adopted as the discretisation scheme for large eddy simulation. A kinetic energy preserving (KEP) scheme—which retains the same advantageous stencil and communications halo as the original Roe scheme—is instead implemented and tested. The adaptations of code required to switch between the two schemes were found to be extremely straightforward. As the KEP scheme intrinsically bounds the growth of the kinetic energy, it is significantly more stable than the classical non-dissipative schemes. This means that the expensive smoothing terms of the Roe scheme are not always necessary. Instead, an explicit subgrid scale turbulence model can be sensibly applied. As such, a range of mixed linear–non-linear turbulence models are tested. The performance of the KEP scheme is then tested against that of the Roe for canonical flows and engine-realistic turbine blade cutback trailing edge cases. The new KEP scheme is found to perform better than the original in all cases. A range of mesh topologies: hexahedral; prismatic; and tetrahedral; are also tested with both schemes, and the KEP scheme is again found to perform significantly better on all mesh types for these flows.This work was supported by an iCASE studentship from the Engineering and Physical Sciences Research Council, via Rolls-Royce plc. The funding from both organisations is gratefully acknowledged

    Thermal properties comparison of hybrid CF/FF and BF/FF cyanate ester-based composites

    Full text link
    [EN] Insights within thermal expansion, conductivity, and decomposition dependencies with temperature on symmetrical and unsymmetrical layered carbon (CF) or basalt (BF) fabrics in combination with flax fibers (FF) were approached. Driven by commercial application and environmental concerns, the paper draws attention on a modified formula of cyanate ester with a common epoxy resin under an optimized ratio of 70:30 (vol%) as well as on the hybrid reinforcements stacking sequences. Synergetic effects were debated in terms of the CF and BF stacking sequences and corresponding volume fraction followed by comparisons with values predicted by the deployment of hybrid mixtures rules (RoHM/iRoHM). CF hybrid architectures revealed enhanced effective thermophysical properties over their BF counterparts and both over the FF-reinforced polymer composite considered as a reference. Thermal conductivities spread between 0.116 and 0.299 W m-1 K-1 from room temperature up to 250 C on all hybrid specimens, giving rise to an insulator character. Concerning the coefficient of thermal expansion, CF hybrid architectures disclosed values of 1.236 10-6 K-1 and 3.102 10-6 K-1 compared with BF affine exhibiting 4.794 10-6 K-1 and 6.245 10-6 K-1, respectively, with an increase in their volume fraction.The corresponding author gratefully acknowledges the financial assistance of German Academic Exchange Service-DAAD that enabled and supported the internship with Fraunhofer Research Institution for Polymeric Materials and Composites-PYCO, Germany. Many thanks go to Dr. Christian Dreyer and Dr. Maciej Gwiazda for the resin formula and access to the composite manufacturing technology.Motoc, DL.; Ferrándiz Bou, S.; Balart, R. (2018). Thermal properties comparison of hybrid CF/FF and BF/FF cyanate ester-based composites. Journal of Thermal Analysis and Calorimetry. 133(1):509-518. https://doi.org/10.1007/s10973-018-7222-yS5095181331Assarar M, Zouari W, Sabhi H, Ayad R, Berthelot J-M. Evaluation of the damping of hybrid carbon–flax reinforced composites. Compos Struct. 2015;132:148–54.Duc F, Bourban PE, Plummer CJG, Månson JAE. Damping of thermoset and thermoplastic flax fibre composites. Compos A Appl Sci Manuf. 2014;64:115–23.Saba N, Jawaid M, Alothman OY, Paridah MT. A review on dynamic mechanical properties of natural fibre reinforced polymer composites. Constr Build Mater. 2016;106:149–59.Tian H, Zhang S, Ge X, Xiang A. Crystallization behaviors and mechanical properties of carbon fiber-reinforced polypropylene composites. J Therm Anal Calorim. 2017;128(3):1495–504.Alvarez V, Rodriguez E, Vázquez A. Thermaldegradation and decomposition of jute/vinylester composites. J Therm Anal Calorim. 2006;85(2):383–9.Manfredi LB, Rodríguez ES, Wladyka-Przybylak M, Vázquez A. Thermal degradation and fire resistance of unsaturated polyester, modified acrylic resins and their composites with natural fibres. Polym Degrad Stab. 2006;91(2):255–61.Lazko J, Landercy N, Laoutid F, Dangreau L, Huguet MH, Talon O. Flame retardant treatments of insulating agro-materials from flax short fibres. Polym Degrad Stab. 2013;98(5):1043–51.Bar M, Alagirusamy R, Das A. Flame retardant polymer composites. Fibers Polym. 2015;16(4):705–17.Kollia E, Loutas T, Fiamegkou E, Vavouliotis A, Kostopoulos V. Degradation behavior of glass fiber reinforced cyanate ester composites under hydrothermal ageing. Polym Degrad Stab. 2015;121:200–7.Jawaid M, Abdul Khalil HPS. Cellulosic/synthetic fibre reinforced polymer hybrid composites: a review. Carbohyd Polym. 2011;86(1):1–18.Azwa ZN, Yousif BF, Manalo AC, Karunasena W. A review on the degradability of polymeric composites based on natural fibres. Mater Des. 2013;47:424–42.H-y Cheung, M-p Ho, K-t Lau, Cardona F, Hui D. Natural fibre-reinforced composites for bioengineering and environmental engineering applications. Compos B Eng. 2009;40(7):655–63.Dittenber DB, GangaRao HVS. Critical review of recent publications on use of natural composites in infrastructure. Compos A Appl Sci Manuf. 2012;43(8):1419–29.Faruk O, Bledzki AK, Fink H-P, Sain M. Biocomposites reinforced with natural fibers: 2000–2010. Prog Polym Sci. 2012;37(11):1552–96.Praveen RS, Jacob S, Murthy CRL, Balachandran P, Rao YVKS. Hybridization of carbon–glass epoxy composites: an approach to achieve low coefficient of thermal expansion at cryogenic temperatures. Cryogenics. 2011;51(2):95–104.Jawaid M, Abdul Khalil HPS, Alattas OS. Woven hybrid biocomposites: dynamic mechanical and thermal properties. Compos A Appl Sci Manuf. 2012;43(2):288–93.Swolfs Y, Gorbatikh L, Verpoest I. Fibre hybridisation in polymer composites: a review. Compos A Appl Sci Manuf. 2014;67:181–200.Rojo E, Alonso MV, Oliet M, Del Saz-Orozco B, Rodriguez F. Effect of fiber loading on the properties of treated cellulose fiber-reinforced phenolic composites. Compos B Eng. 2015;68:185–92.LeGault M. Natural fiber composites: market share, one part at the time. Compos World. 2016;5(2):68–75.Joshi SV, Drzal LT, Mohanty AK, Arora S. Are natural fiber composites environmentally superior to glass fiber reinforced composites? Compos A Appl Sci Manuf. 2004;35(3):371–6.Wambua P, Ivens J, Verpoest I. Natural fibres: can they replace glass in fibre reinforced plastics? Compos Sci Technol. 2003;63(9):1259–64.Bertomeu D, García-Sanoguera D, Fenollar O, Boronat T, Balart R. Use of eco-friendly epoxy resins from renewable resources as potential substitutes of petrochemical epoxy resins for ambient cured composites with flax reinforcements. Polym Compos. 2012;33(5):683–92.Alam M, Akram D, Sharmin E, Zafar F, Ahmad S. Vegetable oil based eco-friendly coating materials: a review article. Arab J Chem. 2014;7(4):469–79.Bakare FO, Ramamoorthy SK, Åkesson D, Skrifvars M. Thermomechanical properties of bio-based composites made from a lactic acid thermoset resin and flax and flax/basalt fibre reinforcements. Compos A Appl Sci Manuf. 2016;83:176–84.Pardauil JJR, de Molfetta FA, Braga M, de Souza LKC, Filho GNR, Zamian JR, et al. Characterization, thermal properties and phase transitions of amazonian vegetable oils. J Therm Anal Calorim. 2017;127(2):1221–9.Głowińska E, Datta J, Parcheta P. Effect of sisal fiber filler on thermal properties of bio-based polyurethane composites. J Therm Anal Calorim. 2017;130(1):113–22.Mosiewicki MA, Aranguren MI. A short review on novel biocomposites based on plant oil precursors. Eur Polym J. 2013;49(6):1243–56.Lligadas G, Ronda JC, Galià M, Cádiz V. Renewable polymeric materials from vegetable oils: a perspective. Mater Today. 2013;16(9):337–43.Fombuena V, Sanchez-Nacher L, Samper MD, Juarez D, Balart R. Study of the properties of thermoset materials derived from epoxidized soybean oil and protein fillers. J Am Oil Chem Soc. 2013;90(3):449–57.Pil L, Bensadoun F, Pariset J, Verpoest I. Why are designers fascinated by flax and hemp fibre composites? Compos A Appl Sci Manuf. 2016;83:193–205.Wooster TJ, Abrol S, Hey JM, MacFarlane DR. Thermal, mechanical, and conductivity properties of cyanate ester composites. Compos A Appl Sci Manuf. 2004;35(1):75–82.Mallarino S, Chailan JF, Vernet JL. Glass fibre sizing effect on dynamic mechanical properties of cyanate ester composites I. Single frequency investigations. Eur Polym J. 2005;41(8):1804–11.Sothje D, Dreyer C, Bauer M, editors. Advanced possibilities in thermoset recycling. In: The 3rd international conference on thermosets. 2013; Berlin, Germany.Yuan L, Huang S, Gu A, Liang G, Chen F, Hu Y, et al. A cyanate ester/microcapsule system with low cure temperature and self-healing capacity. Compos Sci Technol. 2013;87:111–7.Czigány T. Special manufacturing and characteristics of basalt fiber reinforced hybrid polypropylene composites: mechanical properties and acoustic emission study. Compos Sci Technol. 2006;66(16):3210–20.Marom G, Fischer S, Tuler FR, Wagner HD. Hybrid effects in composites: conditions for positive or negative effects versus rule-of-mixtures behaviour. J Mater Sci. 1978;13(7):1419–26.Torquato S. Random heterogeneous materials: microstructure and macroscopic properties. New York: Springer; 2002.Cherki A-B, Remy B, Khabbazi A, Jannot Y, Baillis D. Experimental thermal properties characterization of insulating cork–gypsum composite. Constr Build Mater. 2014;54:202–9.Bismarck A, Aranberri-Askargorta I, Springer J, Lampke T, Wielage B, Stamboulis A, et al. Surface characterization of flax, hemp and cellulose fibers; Surface properties and the water uptake behavior. Polym Compos. 2002;23(5):872–94.Motoc Luca D, Ferrandiz Bou S, Balart Gimeno R. Effects of fibre orientation and content on the mechanical, dynamic mechanical and thermal expansion properties of multi-layered glass/carbon fibre-reinforced polymer composites. J Compos Mater. 2014;49(10):1211–1221.CES EduPack. Granta Design; 2013.Monteiro SN, Calado V, Rodriguez RJS, Margem FM. Thermogravimetric behavior of natural fibers reinforced polymer composites—An overview. Mater Sci Eng, A. 2012;557:17–28

    SMI of Bcl-2 TW-37 is active across a spectrum of B-cell tumors irrespective of their proliferative and differentiation status

    Get PDF
    The Bcl-2 family of proteins is critical to the life and death of malignant B-lymphocytes. Interfering with their activity using small-molecule inhibitors (SMI) is being explored as a new therapeutic strategy for treating B-cell tumors. We evaluated the efficacy of TW-37, a non-peptidic SMI of Bcl-2 against a range spectrum of human B-cell lines, fresh patient samples and animal xenograft models. Multiple cytochemical and molecular approaches such as acridine orange/ethidium bromide assay for apoptosis, co-immunoprecipitation of complexes and western blot analysis, caspase luminescent activity assay and apoptotic DNA fragmentation assay were used to demonstrate the effect of TW-37 on different B-cell lines, patient derived samples, as well as in animal xenograft models. Nanomolar concentrations of TW-37 were able to induce apoptosis in both fresh samples and established cell lines with IC50 in most cases of 165–320 nM. Apoptosis was independent of proliferative status or pathological classification of B-cell tumor. TW-37 was able to block Bim-Bcl-XL and Bim-Mcl-1 heterodimerization and induced apoptosis via activation of caspases -9, -3, PARP and DNA fragmentation. TW-37 administered to tumor-bearing SCID mice led to significant tumor growth inhibition (T/C), tumor growth delay (T-C) and Log10kill, when used at its maximum tolerated dose (40 mg/kg × 3 days) via tail vein. TW-37 failed to induce changes in the Bcl-2 proteins levels suggesting that assessment of baseline Bcl-2 family proteins can be used to predict response to the drug. These findings indicate activity of TW-37 across the spectrum of human B-cell tumors and support the concept of targeting the Bcl-2 system as a therapeutic strategy regardless of the stage of B-cell differentiation

    The Complete Mitochondrial Genomes of Six Heterodont Bivalves (Tellinoidea and Solenoidea): Variable Gene Arrangements and Phylogenetic Implications

    Get PDF
    BACKGROUND: Taxonomy and phylogeny of subclass Heterodonta including Tellinoidea are long-debated issues and a complete agreement has not been reached yet. Mitochondrial (mt) genomes have been proved to be a powerful tool in resolving phylogenetic relationship. However, to date, only ten complete mitochondrial genomes of Heterodonta, which is by far the most diverse major group of Bivalvia, have been determined. In this paper, we newly sequenced the complete mt genomes of six species belonging to Heterodonta in order to resolve some problematical relationships among this subclass. PRINCIPAL FINDINGS: The complete mt genomes of six species vary in size from 16,352 bp to 18,182. Hairpin-like secondary structures are found in the largest non-coding regions of six freshly sequenced mt genomes, five of which contain tandem repeats. It is noteworthy that two species belonging to the same genus show different gene arrangements with three translocations. The phylogenetic analysis of Heterodonta indicates that Sinonovacula constricta, distant from the Solecurtidae belonging to Tellinoidea, is as a sister group with Solen grandis of family Solenidae. Besides, all five species of Tellinoidea cluster together, while Sanguinolaria diphos has closer relationship with Solecurtus divaricatus, Moerella iridescens and Semele scaba rather than with Sanguinolaria olivacea. CONCLUSIONS/SIGNIFICANCE: By comparative study of gene order rearrangements and phylogenetic relationships of the five species belonging to Tellinoidea, our results support that comparisons of mt gene order rearrangements, to some extent, are a useful tool for phylogenetic studies. Based on phylogenetic analyses of multiple protein-coding genes, we prefer classifying the genus Sinonovacula within the superfamily Solenoidea and not the superfamily Tellinoidea. Besides, both gene order and sequence data agree that Sanguinolaria (Psammobiidae) is not monophyletic. Nevertheless, more studies based on more mt genomes via combination of gene order and phylogenetic analysis are needed to further understand the phylogenetic relationships in subclass Heterodonta

    Malignant mixed Mullerian tumors of the uterus: histopathological evaluation of cell cycle and apoptotic regulatory proteins

    Get PDF
    <p>Abstract</p> <p>Aim</p> <p>The aim of our study was to evaluate survival outcomes in malignant mixed Mullerian tumors (MMMT) of the uterus with respect to the role of cell cycle and apoptotic regulatory proteins in the carcinomatous and sarcomatous components.</p> <p>Methods</p> <p>23 cases of uterine MMMT identified from the Saskatchewan Cancer Agency (1970-1999) were evaluated. Immunohistochemical expression of Bad, Mcl-1, bcl-x, bak, mdm2, bax, p16, p21, p53, p27, EMA, Bcl-2, Ki67 and PCNA was correlated with clinico-pathological data including survival outcomes.</p> <p>Results</p> <p>Histopathological examination confirmed malignant epithelial component with homologous (12 cases) and heterologous (11 cases) sarcomatous elements. P53 was strongly expressed (70-95%) in 15 cases and negative in 5 cases. The average survival in the p53+ve cases was 3.56 years as opposed to 8.94 years in p53-ve cases. Overexpression of p16 and Mcl-1 were observed in patients with longer survival outcomes (> 2 years). P16 and p21 were overexpressed in the carcinomatous and sarcomatous elements respectively. Cyclin-D1 was focally expressed only in the carcinomatous elements.</p> <p>Conclusions</p> <p>Our study supports that a) cell cycle and apoptotic regulatory protein dysregulation is an important pathway for tumorigenesis and b) p53 is an important immunoprognostic marker in MMMT of the uterus.</p

    Microarray analysis and scale-free gene networks identify candidate regulators in drought-stressed roots of loblolly pine (P. taeda L.)

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Global transcriptional analysis of loblolly pine (<it>Pinus taeda </it>L.) is challenging due to limited molecular tools. PtGen2, a 26,496 feature cDNA microarray, was fabricated and used to assess drought-induced gene expression in loblolly pine propagule roots. Statistical analysis of differential expression and weighted gene correlation network analysis were used to identify drought-responsive genes and further characterize the molecular basis of drought tolerance in loblolly pine.</p> <p>Results</p> <p>Microarrays were used to interrogate root cDNA populations obtained from 12 genotype × treatment combinations (four genotypes, three watering regimes). Comparison of drought-stressed roots with roots from the control treatment identified 2445 genes displaying at least a 1.5-fold expression difference (false discovery rate = 0.01). Genes commonly associated with drought response in pine and other plant species, as well as a number of abiotic and biotic stress-related genes, were up-regulated in drought-stressed roots. Only 76 genes were identified as differentially expressed in drought-recovered roots, indicating that the transcript population can return to the pre-drought state within 48 hours. Gene correlation analysis predicts a scale-free network topology and identifies eleven co-expression modules that ranged in size from 34 to 938 members. Network topological parameters identified a number of central nodes (hubs) including those with significant homology (E-values ≤ 2 × 10<sup>-30</sup>) to 9-cis-epoxycarotenoid dioxygenase, zeatin O-glucosyltransferase, and ABA-responsive protein. Identified hubs also include genes that have been associated previously with osmotic stress, phytohormones, enzymes that detoxify reactive oxygen species, and several genes of unknown function.</p> <p>Conclusion</p> <p>PtGen2 was used to evaluate transcriptome responses in loblolly pine and was leveraged to identify 2445 differentially expressed genes responding to severe drought stress in roots. Many of the genes identified are known to be up-regulated in response to osmotic stress in pine and other plant species and encode proteins involved in both signal transduction and stress tolerance. Gene expression levels returned to control values within a 48-hour recovery period in all but 76 transcripts. Correlation network analysis indicates a scale-free network topology for the pine root transcriptome and identifies central nodes that may serve as drivers of drought-responsive transcriptome dynamics in the roots of loblolly pine.</p

    Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.

    Get PDF
    Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field

    Pan-cancer analysis of whole genomes

    Get PDF
    Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
    corecore