Wide angle X-ray diffraction and Fourier transform infrared dichroism studies of stretched-recovery-restretched process of polyurethane/clay nanocomposite
Autor: | Yongmei Ma, Guangyang Xu, Jiaqi Fan, Jun Liu, Zongneng Qi, Deyan Shen, Guangming Chen, Xianjun Zheng |
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Rok vydání: | 2007 |
Předmět: |
chemistry.chemical_classification
Nanocomposite Materials science Polymers and Plastics Polymer Dichroism Condensed Matter Physics symbols.namesake chemistry.chemical_compound Fourier transform Montmorillonite Polymerization chemistry X-ray crystallography Polymer chemistry Materials Chemistry symbols Physical and Theoretical Chemistry Fourier transform infrared spectroscopy Composite material |
Zdroj: | Journal of Polymer Science Part B: Polymer Physics. 45:654-660 |
ISSN: | 1099-0488 0887-6266 |
DOI: | 10.1002/polb.21075 |
Popis: | An intercalated polyurethane (PU) /clay nanocomposite was prepared by in situ intercalative polymerization. The PU/clay nanocomposite pellet or film samples were stretched-recovery-restretched, using selfmade microstretching tools. The changes of the basal spacings of clay and the orientation of polymer chain segments during the stretched-recovery-restretched process were studied by wide angle X-ray diffraction (WAXD) and Fourier transform infrared (FTIR) dichoism techniques. The WAXD results show that the basal spacing of clay did not change obviously, indicating that no macromolecular chains entered or moved out of the interlayer space, and the orientations of both hard and soft segments inside the interlayer space did not change obviously, either. The FTIR dichroism tests suggest that outside the interlayer space, the orientation of the hard chain segment increased, decreased, and then increased again during the stretched-recovery-restretched process. However, no obvious changes of the degree of orientation of the soft segment were observed during the processes, the slightly orientation might be released during the relaxation process before the measurements. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 654–660, 2007 |
Databáze: | OpenAIRE |
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