5 research outputs found

    Element partitioning and electron backscatter diffraction analysis from feeding wire to as-deposited microstructure of wire and arc additive manufacturing with super duplex stainless steel

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    The redistribution of alloying elements and the crystallographic characterizations in wire and arc additive manufactured (WAAM) super duplex stainless steel (SDSS) was investigated from the wire to the final as-deposited structure. The results showed that elemental partitioning between austenite and ferrite was suppressed in the last layer and the solidified droplet. The high Ni content but low Cr and N contents in the initial state of the intragranular austenite (IGA) confirmed the predominance of the chromium nitrides acted as the nucleation sites. Gathering of nitrogen was found more distinct in the coarsening IGA, Widmanstätten austenite (WA) than the grain boundary austenite (GBA). The columnar epitaxial ferrite presented a strong texture in the deposition direction, while the and orientations was found in the austenite. Random orientations of the intragranular secondary austenite was revealed. The Rotated Cube texture of the austenite grains were consumed by the “recrystallization” textures (Brass, Rotated Brass, Cu, R, E, and F) caused by the austenite reformation. The low-angle interphase boundaries between austenite and ferrite were predominated in the as-deposited wall, and, at which, the K–S orientation took the crucial part. A Taylor factor analysis revealed that through fabrication via additive process, the austenite became oriented “harder” and contributed most to good mechanical properties. The textured microstructure contributed about a 2.6% higher engineering strain in the Z direction and a 27.8 MPa higher yield strength in the X direction

    Detection of Landfill Leachate Leakage Based on ERT and OCTEM

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    Leakage in the impervious layer of a domestic waste landfill seriously pollutes the soil and groundwater. Therefore, it is necessary to carry out rapid nondestructive leakage location detection. In this research, the electrical resistivity tomography (ERT) method and the opposing-coils transient electromagnetic method (OCTEM) were used to detect the leakage location. The inversion sections of both methods showed a clear low–middle–high resistivity spectrum in the longitudinal direction that could be used to speculate the distribution pattern of the upper waste body layer, the bottom impermeable layer, and the lower limestone layer. The leakage area was identified in Zone B of the landfill on the basis of inversion results and drilling verification results. The results indicate that OCTEM and ERT were both sensitive to leakage detection. However, OCTEM had higher longitudinal resolution and more refined inversion results, resulting in more effective delineation for the location of the damage and leakage of the impervious landfill layer, thereby providing a new technical basis for landfill leakage detection

    Selective inhibition of Ezh2 by a small molecule inhibitor blocks tumor cells proliferation

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    Ezh2 protein is the enzymatic component of the Polycomb Repressive Complex (PRC)-2, which represses its target genes by methylating lysine 27 of histone H3 (H3K27) and regulates cell proliferation and differentiation during embryonic development. Recently, hot-spot mutations of Ezh2 have been identified in diffused large B cell lymphomas (DLBCLs) and follicular lymphomas (FLs). To investigate if tumor growth is dependent on the enzymatic activity of Ezh2, we have developed a potent and selective small molecule inhibitor, JAD593, which inhibits the enzymatic activity of Ezh2 through direct binding and competing with the methyl group donor S-Adenosyl methionine (SAM). JAD593-treated cells exhibit genome-wide loss of H3K27 methylation. Furthermore, inhibition of Ezh2 by JAD593 in DLBCL cells carrying the Y641 mutations results in decreased proliferation, cell cycle arrest and apoptosis. These results provide strong validation of Ezh2 as a potential therapeutic target for the treatment of cancer with the Ezh2 mutation
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