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Structure development in silica-filled polyacrylate rubber composites during mixing

✍ Scribed by Shigeyuki Ono; Masayoshi Ito; Hideyuki Tokumitsu; Kazuhiko Seki


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
342 KB
Volume
74
Category
Article
ISSN
0021-8995

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✦ Synopsis


The structure of bound rubber in the composites from fumed silica (A200, Nippon Aerosil Co., Japan) and polyethylacrylate rubber (PEA) was studied as a function of mixing temperature. The fraction of bound rubber in the composites increased gradually with increasing the mixing temperature from 80 to 120°C, followed by saturation above 120°C. High-resolution solid-state NMR results revealed that there was no chemical bonding between silanol groups and PEA molecules. Scanning electron microscope and optical microscope observation of the composites indicated that, with increasing mixing temperature, the size of agglomerates formed by silica particles decreased. Further, the molecular weight retention of PEA dropped abruptly above 120°C. Dynamic viscoelastic measurements of the composites suggest that the development of network structure in the composites was greatly affected by the mixing temperature. Based on these data, structure development in composites is discussed.


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Structure development in silica ®lled polyisoprene composites was investigated by wide line pulsed NMR and high-resolution solid-state NMR combined with transmission electron microscopy. The rubber phase in the composites was composed of so-called bound rubber and free rubber. Furthermore, the bound