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Cross-examining Polyurethane Nanodomain Formation and Internal Structure
Author(s) -
Maxwell W. Terban,
Karsten Seidel,
Elmar Pöselt,
Marc Malfois,
RoelfPeter Baumann,
Ralf Sander,
Dirk Paulus,
Bernd Hinrichsen,
Robert E. Dinnebier
Publication year - 2020
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.0c01557
Subject(s) - small angle x ray scattering , bridging (networking) , chemical physics , materials science , pair distribution function , polymerization , scattering , nanoscopic scale , polymer , crystallography , chemistry , nanotechnology , physics , composite material , optics , computer network , quantum mechanics , computer science
Structural and morphological interplay between hard and soft phases determine the bulk properties of thermoplastic polyurethanes. Commonly employed techniques rely on different physical or chemical phenomena for characterizing the organization of domains, but detailed structural information can be difficult to derive. Here, total scattering pair distribution function (PDF) analysis is used to determine atomic-scale insights into the connectivity and molecular ordering and compared to the domain size and morphological characteristics measured by AFM, TEM, SAXS, WAXS, and solid-state NMR 1 H- 1 H spin-diffusion. In particular, density distribution functions are highlighted as a means to bridging the gap from the domain morphology to intradomain structural ordering. High real-space resolution PDFs are shown to provide a sensitive fingerprint for indexing aromatic, aliphatic, and polymerization-induced bonding characteristics, as well as the hard phase structure, and indicate that hard phases coexist in both ordered and disordered states.

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