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The crystalline structures have been studied using wide and small angle X-ray scattering (WAXS and SAXS), transmission electron microscopy (TEM) and infrared (IR) spectroscopy.
Static and real-time wide and small angle X-ray scattering (WAXS, SAXS), Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC) were used to investigate the crystalline phase of PVDF.
Thermoplastic polyurethanes prepared from succinate and adipate based polyols are compared using differential scanning calorimetry, dynamic mechanical spectroscopy, tensile measurements, wide and small angle X-ray scattering, transmission electron microscopy, atomic force microscopy, and abrasion tests.
Besides, crystalline morphology and orientation were studied by wide and small angle X-ray scattering to confirm the orientation effect of the shear in the crystalline part of the material.
Simultaneous, real-time wide and small angle X-ray scattering (WAXS, SAXS), differential scanning calorimetry, and optical ellipsometry were used to study initially isotropic, amorphous films of HIQ-40.
In this study, two complementary synchrotron X-ray diffraction techniques, wide and small angle X-ray scattering (WAXS/SAXS) were used to obtain multi-scale quantitative information about the structure and deformation response of human enamel to in situ uniaxial compressive loading.
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In Ridgewood, the front of the village hall was covered with an American flag about 30 feet high and 50 feet wide, and smaller flags flew from the utility poles in the business district on Ridgewood Avenue.
Wide and small-angle X-ray scattering (WAXS and SAXS) of synchrotron radiation, as well as solid-state nuclear magnetic resonance spectroscopy (NMR) measurements are performed.
Overall, the data indicate that both, large scale (genome wide) and small-scale duplications contributed to the evolution of the anoctamin subfamilies, which is in good agreement with previous findings demonstrating that large-scale gene duplications have occurred during chordate evolution [ 29- 31].
Secondly, the starting point of any phylogenetic analysis, identification of orthologous genes, is a major problem for plants due to abundant genome-wide and small scale duplications.
An FCS-based screen of a library of all open reading frames fused to GFP fusions in Saccharomyces cerevisiae has been reported 26 and HCS genome-wide and small molecule screens of animals has been successfully achieved.
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