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X-ray data from a cyclic tensile study of melt-spun poly(3-hydroxybutyrate) P3HB fibers: A reversible mesophase

Wide-angle x-ray diffraction (WAXD) patterns that show mesophases in core-sheath bicomponent fibers and amorphous fibers are presented in section 1.1 of the article. Section 1.2 presents molecular dynamics simulations and scattered intensity calculations of stretched P3HB chains. Sections 1.3–1.6 su...

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Detalles Bibliográficos
Autores principales: Perret, Edith, Reifler, Felix A., Gooneie, Ali, Hufenus, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722231/
https://www.ncbi.nlm.nih.gov/pubmed/31497630
http://dx.doi.org/10.1016/j.dib.2019.104376
Descripción
Sumario:Wide-angle x-ray diffraction (WAXD) patterns that show mesophases in core-sheath bicomponent fibers and amorphous fibers are presented in section 1.1 of the article. Section 1.2 presents molecular dynamics simulations and scattered intensity calculations of stretched P3HB chains. Sections 1.3–1.6 summarize WAXD and small-angle x-ray scattering (SAXS) data analysis from a tensile study of melt-spun P3HB fibers. Azimuthal profiles are extracted from 2D WAXD patterns at various angular regions and the positions of equatorial reflections and corresponding d-spacings are summarized. Additionally, the extracted structural parameters from SAXS images are summarized. The tensile stress calculations, crystal orientation calculations, applied intensity corrections, calculations of long spacings, coherence lengths and lamellar diameters are explained in the methods subsections 2.3.1–2.3.7. WAXD and SAXS measurements of P3HB fibers were recorded on a Bruker Nanostar U diffractometer (Bruker AXS, Karlsruhe, Germany). The recorded WAXD/SAXS patterns were analyzed with the evaluation software DIFFRAC.EVA (version 4.2., Bruker AXS, Karlsruhe, Germany) and python codes. For more information see ‘Tensile study of melt-spun poly(3-hydroxybutyrate) P3HB fibers: Reversible transformation of a highly oriented phase’ (Perret et al., 2019).