442 research outputs found

    Fatigue behavior of foreign object damaged 7075 heat treated aluminum alloy coated with PVD WC/C

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    AbstractThe effect of a physically vapor deposited (PVD) WC/C coating on the fatigue behavior of as produced and foreign object damaged (FOD) solution heat treated and aged 7075 aluminum alloy was studied. Coated and uncoated samples were tested under rotating bending to determine the fatigue strengths between 104 and 106 cycles in both damaged and smooth condition. FOD was produced with single shots of small hard steel spheres impacting at 100 m/s in the minimum cross section. SEM was used to characterize the features of the fracture surfaces

    The Digital Image Correlation technique applied to the deformation behavior of welded sheet joints

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    The existence of a welded zone generally influences the local strain and stress distribution especially in case of welding defects. A method able to measure the local deformability can hence give many important information about the real stress and strain fields useful to improve the welded structure design. In this experimental work, some new generation automotive steels have been considered, because of the well known welding problems due to their unstable microstructural condition. Such materials, known as Q&P steels and available only as thin sheets, require a suitable quenching process able to give high mechanical resistance and satisfying deformability. Some sheet samples were welded by electron beam technique, because it is able to reduce the width of the heat affected zone where the main microstructural changes are concentrated. From such samples, tensile specimens were machined. During the tensile tests, the deformations were measured both by a traditional extensometer and by a 3D Digital Image Correlation (3D DIC) technique. A preliminary investigation of the melted and the heat affected zones resulted in small dimensions (about 10 mm) and hence the measuring setup has been optimized in order maximize the achievable measuring resolution minimizing the resulting uncertainty. This result can be achieved by a pattern generated by a suitable software and by an accurate preparation of the surface where the pattern will be deposited on

    Study of new heat treatment parameters for increasing mechanical strength and stress corrosion cracking resistance of 7075 Aluminium alloy

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    For many years 7075 Aluminum alloys have been widely used especially in those applications for which highmechanical performances are required. It is well known that the alloy in the T6 condition is characterized bythe highest ultimate and yield strengths, but, at the same time, by poor stress corrosion cracking (SCC)resistance. For this reason, in the aeronautic applications, new heat treatments have been introduced toproduce T7X conditions, which are characterized by lower mechanical strength, but very good SCC behavior,when compared with the T6condition. The aim of this work is to study the tensile properties and the SCCbehavior of 7075 thick plates when submitted to a single step ageing by varying the ageing times. The tests werecarried out according to the standards and the data obtained from the SCC tests were analyzed quantitatively byan image analysis software. The results show that, if compared with the T7X conditions, the single step ageingperformed in the laboratory can produce acceptable tensile and SCC properties. The data should be confirmedby experiments carried out on thick plates submitted to heat treatments in industrial furnace

    Relation between toughness, infinite fatigue life and microstructure in large blooms for automotive plastic molds.

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    Presentazione orale al European Congress on Advanced Material and Processes (Euromat 2005), Praga (R. Ceca), 5/10/2005 - 8/10/200

    Genomic analysis of the function of the transcription factor gata3 during development of the Mammalian inner ear

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    We have studied the function of the zinc finger transcription factor gata3 in auditory system development by analysing temporal profiles of gene expression during differentiation of conditionally immortal cell lines derived to model specific auditory cell types and developmental stages. We tested and applied a novel probabilistic method called the gamma Model for Oligonucleotide Signals to analyse hybridization signals from Affymetrix oligonucleotide arrays. Expression levels estimated by this method correlated closely (p<0.0001) across a 10-fold range with those measured by quantitative RT-PCR for a sample of 61 different genes. In an unbiased list of 26 genes whose temporal profiles clustered most closely with that of gata3 in all cell lines, 10 were linked to Insulin-like Growth Factor signalling, including the serine/threonine kinase Akt/PKB. Knock-down of gata3 in vitro was associated with a decrease in expression of genes linked to IGF-signalling, including IGF1, IGF2 and several IGF-binding proteins. It also led to a small decrease in protein levels of the serine-threonine kinase Akt2/PKB beta, a dramatic increase in Akt1/PKB alpha protein and relocation of Akt1/PKB alpha from the nucleus to the cytoplasm. The cyclin-dependent kinase inhibitor p27(kip1), a known target of PKB/Akt, simultaneously decreased. In heterozygous gata3 null mice the expression of gata3 correlated with high levels of activated Akt/PKB. This functional relationship could explain the diverse function of gata3 during development, the hearing loss associated with gata3 heterozygous null mice and the broader symptoms of human patients with Hearing-Deafness-Renal anomaly syndrome

    Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy.

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    Inherited retinal dystrophies present extensive phenotypic and genetic heterogeneity, posing a challenge for patients' molecular and clinical diagnoses. In this study, we wanted to clinically characterize and investigate the molecular etiology of an atypical form of autosomal recessive retinal dystrophy in two consanguineous Spanish families. Affected members of the respective families exhibited an array of clinical features including reduced visual acuity, photophobia, defective color vision, reduced or absent ERG responses, macular atrophy and pigmentary deposits in the peripheral retina. Genetic investigation included autozygosity mapping coupled with exome sequencing in the first family, whereas autozygome-guided candidate gene screening was performed by means of Sanger DNA sequencing in the second family. Our approach revealed nucleotide changes in CDHR1; a homozygous missense variant (c.1720C &gt; G, p.P574A) and a homozygous single base transition (c.1485 + 2T &gt; C) affecting the canonical 5' splice site of intron 13, respectively. Both changes co-segregated with the disease and were absent among cohorts of unrelated control individuals. To date, only five mutations in CDHR1 have been identified, all resulting in premature stop codons leading to mRNA nonsense mediated decay. Our work reports two previously unidentified homozygous mutations in CDHR1 further expanding the mutational spectrum of this gene
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