In situ preparation of hetero-polymers/clay nanocomposites by CUAAC click chemistry
Yazarlar (2)
Prof. Dr. Mehmet Atilla TAŞDELEN Yalova Üniversitesi, Türkiye
Çağatay Altınkök İstanbul Teknik Üniversitesi, Türkiye
| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Turkish Journal of Chemistry (Q3) | ||
| Dergi ISSN | 1300-0527 Dergi Bilgileri (2021) | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 01-2021 |
| Kabul Tarihi | – | Yayınlanma Tarihi | 17-02-2021 |
| Cilt / Sayı / Sayfa | 45 / 1 / 50–59 | DOI | 10.3906/kim-2007-62 |
| Makale Linki | http://dx.doi.org/10.3906/kim-2007-62 | ||
| UAK Araştırma Alanları |
Polimer Bilimi
Nanoteknoloji
Yüzey Kimyası
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| Özet |
| A series of polymer/clay nanocomposites containing mechanistically two different polymers, poly (ethylene glycol)(PEG) and poly (epsilon caprolactone)(PCL), were prepared by simultaneous copper (I)-catalyzed alkyne-azide cycloaddition click reactions. Both clickable polymers, PEG-Alkyne and PCL-Alkyne, were simultaneously clicked on to azide-functional montmorillonite (MMT-N3) nanoclay to get corresponding PEG-PCL/MMT nanocomposites. The chemical structures of the resulting nanocomposites were verified by following azide and silicone-oxygen bands using FT-IR and characteristic bands of PEG and PCL segments using 1H-NMR spectroscopy. The combined XRD and TEM analysis confirmed that all PEG-PCL/MMT nanocomposites had partially exfoliated/intercalated morphologies. In addition, the increase of MMT-N3 loading not only improved the onset and maximum degradation temperatures of the nanocomposites but also their char yields. Furthermore, the incorporation of MMT-N3 in the polymer matrix did not significantly influence the crystallization behavior of both PEG and PCL segments. |
| Anahtar Kelimeler |
| Clay | Click chemistry | Nanocomposite | Poly(epsilon caprolactone) | Poly(ethylene glycol) |
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| Web of Science | 5 |
| Scopus | 3 |
| Google Scholar | 5 |