12 research outputs found

    Role of Stabilization Heat Treatment Inducing γ′-γ″ Co-Precipitates and η Phase on Tensile Behaviors of Inconel 706

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    Inconel 706 (IN706) alloy is commonly used in aircraft engines and power plant components that must meet very high performance requirements. The stabilization treatment has a significant effect on the precipitation and evolution of the reinforcing phases of the alloy, favoring the creep properties and adversely affecting the room-temperature tensile properties. However, the mechanism of the effect of the stabilization treatment on the mechanical properties of the alloys remains unclear. In this study, the effect of stabilization treatment time on the microstructure and tensile properties of IN706 alloy was investigated. The results showed that as the stabilization time gradually increased, the tensile strength remained basically unchanged (about 1250 MPa), the yield strength decreased from 1031 MPa to 985 MPa, and the plasticity decreased from 28.2% to 20.2%. The stabilization treatment induces the precipitation of granular, rod-shaped, and needle-like η phases at grain boundaries, accompanied by the appearance of a precipitate free zone (PFZ). Since the η phase is enriched with Ti and Nb, its precipitation along the grain boundary results in the depletion of Ti and Nb in the surrounding regions, thereby constraining the precipitation of the γ′ and γ″ phases, resulting in the appearance of PFZ. With increasing stabilization time, the size increase and volume fraction decrease in γ′-γ″ co-precipitates due to the precipitation of η-phase precipitates, leading to a decrease in their yield strength. Combined with in situ tensile tests, it was found that the decrease in the elongation of the stabilization treatment samples was due to the presence of η phase at the grain boundaries, which induced stress concentration and cracking at the grain boundaries. The results show that the mechanical properties of the material were gradually enhanced as the stabilization time decreased. This means it can help to choose the suitable process for IN706 alloy in different service conditions

    Preparation of Fluorescent Conjugated Polymer Fibrous Membranes for Rapid Recognition of Aromatic Solvents

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    Fluorescent poly­(phenylenevinylene) (PPV)/poly­(vinyl alcohol) (PVA) fibrous membrane was prepared via electrospinning of PPV precursor and PVA aqueous solution followed by thermal elimination. Further cross-linking produced the cross-linked membrane PPV/CPVA. Both PPV/PVA and PPV/CPVA membranes were found to have similar morphology and photophysics. These membranes showed a great fluorescence quenching response to aromatic solvents and a much smaller response to other organic solvents. Water also effectively quenched the fluorescence of PPV/PVA but not that of PPV/CPVA. This was attributed to un-cross-linked PVA being able to dissolve in water and the cross-linking improving the resistance of the membrane toward water. The sensing behavior was found to have good reversibility. The contact angle study showed that addition of only about 1% of PPV into the matrix reduced the hydrophilicity of the membrane significantly, suggesting that the PPV chains would be located at the surface of the fibers. X-ray photoelectron spectroscopy (XPS) investigation further confirmed such surface enrichment of PPV in the binary polymer blends. The PPV chain on the surface facilitated the π–π interaction between the polymer backbones and the aromatic molecules, thus leading to good selectivity and fast response of the two fibrous membranes toward aromatic solvents

    Fluorescence Quenching of a Conjugated Polymer by Synergistic Amine-Carboxylic Acid and π–π Interactions for Selective Detection of Aromatic Amines in Aqueous Solution

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    Fluorescence sensing of amine in aqueous solution is challenging. The various basicity and chemical structures of amines may lead to poor selectivity in aqueous solution, and selective fluorescence detection of primary aromatic amine is rarely reported. This paper presents design and synthesis of a fluorescent conjugated polymer for rapid and selective sensing of aromatic amines in aqueous solution. The fluorescent conjugated polymer, poly­[fluorenyl-<i>alt</i>-p-phenyleneethynylene] with pendant carboxylic acid groups and long alky chains, is synthesized via palladium-catalyzed Sonogashira coupling reaction. The fluorescence of the polymer is selectively quenched by the aromatic amines in aqueous solution, whereas the aliphatic amines enhance the fluorescence of the polymer. The high selectivity to the aromatic amines, particularly to the environmentally important <i>p</i>-phenylenediamine, likely originates from the amplified π–π fluorescence quenching synergized by amine and carboxylic acid interaction. Our results demonstrate an effective material design strategy that may be extended to fluorescence sensing of other aromatic compounds

    Mechanisms of Heat-Treatment-Induced Cracking in Additively Manufactured IN738 Alloy

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    The present study conducts a comprehensive study on heat-treatment-induced cracking of Inconel 738 (IN738) alloy fabricated by laser powder bed fusion (LPBF) using scanning electron microscopy (SEM), energy dispersion spectrum (EDS), and electron backscatter diffraction (EBSD). The results indicate that the macroscopic crack is dominantly triggered by the strain-age cracking mechanism and propagates along grain boundaries. The initiation of cracking is facilitated by the superimposition of residual stress induced by the LPBF process and contraction stress induced by precipitation, while the reopening of compress pores at grain boundaries weakens the grain boundaries and provides fast channels for cracking. These results revealed the coupling effects in triggering heat-treatment-induced cracking, offering a fundamental guideline for crack control during heat treatment of additively manufactured IN738 alloy

    Detection of Sudan Dyes Based on Inner-Filter Effect with Reusable Conjugated Polymer Fibrous Membranes

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    Developing effective methods for detecting illegal additives in food or seasoning is of great significance. In this study, a sensing strategy for selective detection of Sudan dyes was designed based on the fluorescence inner-filter effect (IFE) by using poly­(phenylenevinylene) (PPV) solid materials in combination with an optimized experimental protocol. Two types of fluorescent solid materials, electrospun fibrous membranes and drop-cast films, were fabricated with PPV as the fluorophore and poly­(vinyl alcohol) as the matrix, respectively. Sudan dyes greatly quenched the fluorescence of the membrane and film, whereas other food colorings or possible food ingredients displayed a much smaller or negligible quenching effect. The sensing mechanism was studied, and the selectivity was ascribed to IFE, which requires the overlap between the absorption of the analyte and absorption/emission of the sensing material. The form of materials (membrane or film), the content of PPV, and the cross-linking process did not have much influence on the selectivity and sensitivity, which is consistent with the IFE mechanism and demonstrates the advantage of not requiring strict control of the preparative process. All the cross-linked materials were found to be stable against water/humidity and displayed good reversibility in sensing and can be reused at least for 10 cycles with negligible influence on the sensing performance. A cross-linked membrane was selected for detecting Sudan dyes in chili powder because folding did not affect the mechanical stability of the membrane. Two different protocols were used to pretreat the chili samples, which allowed the detection of Sudan dyes in chili powder as well as the discrimination of Sudan dyes from synthetic food coloring such as allura red. This study provides a facile and cost-effective method for preparing reusable sensing materials for detecting some dyes in commercial foods or food seasonings

    3D Visualized Characterization of Fracture Behavior of Structural Metals Using Synchrotron Radiation Computed Microtomography

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    Synchrotron radiation computed micro-tomography (SR-&mu;CT) is a non-destructive characterization method in materials science, which provides the quantitative reconstruction of a three-dimension (3D) volume image with spatial resolution of sub-micrometer level. The recent progress in brilliance and flux of synchrotron radiation source has enabled the fast investigation of the inner microstructure of metal matrix composites without complex sample preparation. The 3D reconstruction can quantitatively describe the phase distribution as well as voids/cracks formation and propagation in structural metals, which provides a powerful tool to investigate the deformation and fracture processes. Here, we present an overview of recent work using SR-&mu;CT, on the applications in structural metals

    Receptor-Free Poly(phenylenevinylene) Fibrous Membranes for Cation Sensing: High Sensitivity and Good Selectivity Achieved by Choosing the Appropriate Polymer Matrix

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    Poly­(phenylenevinylene)/polyimide (PPV/PI) and poly­(phenylenevinylene)/ polymethylmethacrylate (PPV/PMMA) fibrous membranes without any deliberately introduced receptors were prepared as fluorescence sensing materials through electrospinning, followed by thermal treatment. Both of these membranes displayed higher sensitivity toward most cations compared to the corresponding spin-coated films. PPV/PMMA membranes were more sensitive than PPV/PI membranes toward Cu<sup>2+</sup> and Fe<sup>3+</sup>. About 4.5 fold of intensity enhancement upon 20 nM of Cu<sup>2+</sup>, 80% of quenching upon 20 nM of Fe<sup>3+</sup> with fast response and simple regeneration were realized for PPV/PMMA membrane. The preliminary investigation into the mechanism revealed that the properties of the polymer matrix and thermal treatment of the membrane played important roles in the sensing performance

    Role of layered structure in ductility improvement of layered Ti-Al metal composite

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    Layered Ti-Al metal composite (LMC) was designed and fabricated by hot-rolling and annealing of pure Ti and Al sheets. The as-prepared composite exhibits high tensile ductility, being superior to any individual Ti or Al sheets. The stress/strain evolution and fracture behavior of the LMC were analyzed by in-situ observations during the tensile deformation. Three deformation stages of LMC were clearly observed by neutron diffraction: elastic stage, elastic-plastic stage and plastic stage. It is found that stress partitioning at the elastic-plastic deformation stage improves the strain balance of LMC, but leads to an internal stress accumulated at the interface. Additionally, a strain-transfer from Ti to adjacent Al layers relieves the strain localization of Ti layers in LMC, which improves the ductility of Ti. Both stress partitioning and strain localization of Ti layers facilitate the nucleation of cracks at a low macro strain. However, the crack propagation is constrained by layered structure. In terms of the Al layers, the constrained micro-cracks relieve the stress concentration in Al layer and improve the ductility of Al layers, so that cracking indirectly affects the plastic deformation behavior of LMC, then improving its entire ductility. This work provides a new structural strategy towards simultaneously improving strength and ductility to develop high performance LMC by structural design
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