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of these materials, including: - Synthesis of MIL-100 and SBA-15 via hydrothermal and sol-gel routes, respectively. Surface modification. Structural characterization (N₂ sorption, SAXS, XRD, SEM with EDX, X-ray
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physicochemical characterization (SEM, SAXS, DLS, DSC, TGA, DMA, rheology, adhesion testing, FTIR, Raman, XPS) Quantify adhesion, cohesion, rheological, thermal, mechanical properties Establish structure–property
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with tailored morphology Develop processing routes Perform advanced structural and physicochemical characterization (SEM, SAXS, DLS, DSC, TGA, DMA, rheology, adhesion testing, FTIR, Raman, XPS) Quantify
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morphological, strucutral and chemical analysis techniques will be used, including: cryo-FIB/SEM, cryo-TEM, in-situ and liquid-cell TEM, EC-AFM, XCT, SAXS, XAS, XRS, XPS, etc. Correlate materials characterization
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crystallization. Solvent-free reactive extrusion in line with methods following green chemistry principles will pe prioritized • Their structural characteristics will be examined using X-ray scattering (WAXS, SAXS
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techniques of cryo-electron microscopy (cryo-EM), small angle X-ray scattering (SAXS), single-molecule force spectroscopy (SMFS), biochemistry, mutational analysis, cell culture, activity assays, et cetera
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and intercellular transport using X-ray crystallography, cryo-electron microscopy (cryo-EM), microcrystal electron diffraction (microED), and small-angle X-ray scattering (SAXS). The Postdoctoral
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protein engineering, characterization of protein interactions by various methods, de novo design of protein binders, integrative structural biology using NMR, SAXS and/or single molecule FRET. Your profile
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scattering (SAXS & SANS), and cryo-EM. The work will involve the study of wild-type TTR (which is intrinsically amyloidogenic) and also a range of other mutants that are typically associated with early onset