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Influence of the Organoclay Content on the Structure, Morphology, and Surface Related Properties of Novel Poly(dimethylsiloxane)-Based Polyurethane/Organoclay Nanocomposites
Novel poly(dimethylsiloxane)-based polyurethane nanocomposites (TPU-NCs) were synthesized using in situ polymerization with the nanoclay Cloisite 30B. Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical thermal analysis showed that TPU-NCs with an organoclay conten...
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Published in: | Industrial & engineering chemistry research 2017-05, Vol.56 (17), p.4970-4983 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Novel poly(dimethylsiloxane)-based polyurethane nanocomposites (TPU-NCs) were synthesized using in situ polymerization with the nanoclay Cloisite 30B. Differential scanning calorimetry, thermogravimetric analysis, and dynamic mechanical thermal analysis showed that TPU-NCs with an organoclay content of ≤5 wt % exhibited increased thermal stability, storage modulus, and hard-segment melt temperatures but decreased degrees of crystallinity. TPU-NCs displayed increased surface hydrophilicity and enhanced surface free energy with increasing organoclay content. Small- and wide-angle X-ray scattering confirmed intercalated formations of organoclays in the nanocomposites. Individual clay particles on the surfaces of TPUs with lower organoclay loadings (1 or 3 wt %) or organoclay agglomerates in TPUs with higher amounts of organoclay (≥5 wt %) were detectable using scanning electron microscopy. The relatively smooth and homogeneous character of pure TPU and the distinctly heterogeneous and rough surfaces of TPU-NCs were detected via atomic force microscopy. Among the nanomaterials prepared, TPU-NCs with 1 wt % organoclay provided the best balance between the organoclay concentration and the functional properties desired in biomedical applications. |
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ISSN: | 0888-5885 1520-5045 |
DOI: | 10.1021/acs.iecr.6b04913 |