Dergiler / Turkish Journal of Chemistry / 2013 / Cilt: 37 - Sayı: 2

Synthesis and characterization of thermally stable camphor-based polyimide--clay nanocomposites

Sayfa
182–194
Yayın Tarihi
2013-02-01
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The morphology and properties of PI nanocomposites greatly depend on the functional groups of the organic modifiers, synthesis procedure, and structure of polyimide because of the chemical reactions and physical interactions involved.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:A new monomer was prepared from (1R,3S)-(+)-camphoric acid.
📊
Temel Bulgular & Veri:Polyimide-montmorillonite nanocomposites were prepared from solution of polyimide and with different weight percentages (1, 5, 10 wt %) of organo-modified montmorillonite (OM-MMT) using N-methyl-2-pyrrolidone (NMP) as aprotic solvent.
💡
Sonuç & Katkı:The morphology and properties of PI nanocomposites greatly depend on the functional groups of the organic modifiers, synthesis procedure, and structure of polyimide because of the chemical reactions and physical interactions involved.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Polyimide · nanocomposites · organoclay

Özet

A new monomer was prepared from (1R,3S)-(+)-camphoric acid. Novel polyimide and polyimide--clay hybrid composites were developed from one-pot condensation reactions of this monomer and pyromellitic dianhyride. Polyimide-montmorillonite nanocomposites were prepared from solution of polyimide and with different weight percentages (1, 5, 10 wt %) of organo-modified montmorillonite (OM-MMT) using N-methyl-2-pyrrolidone (NMP) as aprotic solvent. The reactive organoclay was formed by using hexadecylpyridinium chloride as a swelling agent for silicate layers of montmorillonite. The polyimide--clay composites films (PI--MMT) were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD). All composites were subjected to differential scanning calorimetry measurements for the purpose of examining Tg from all compositions. The clay content significantly influenced the thermal behavior of the polymeric films, such as glass transition and decomposition temperatures of polyimide--clay composites. The glass transition temperatures of the composites were higher than that of the original polyimide. Their thermal decomposition temperatures (Td = temperature at 5% mass loss) were measured via thermogravimetric analysis and showed that the introduction of clay into polymer backbones increased thermal stability. SEM, XRD, and the other conventional techniques were used for structural characterization. Dispersion of the modified clay in the polyimide matrix resulted in nanostructured material containing intercalated polymer between the silicate layers. The morphology and properties of PI nanocomposites greatly depend on the functional groups of the organic modifiers, synthesis procedure, and structure of polyimide because of the chemical reactions and physical interactions involved.

Abstract

A new monomer was prepared from (1R,3S)-(+)-camphoric acid. Novel polyimide and polyimide--clay hybrid composites were developed from one-pot condensation reactions of this monomer and pyromellitic dianhyride. Polyimide-montmorillonite nanocomposites were prepared from solution of polyimide and with different weight percentages (1, 5, 10 wt %) of organo-modified montmorillonite (OM-MMT) using N-methyl-2-pyrrolidone (NMP) as aprotic solvent. The reactive organoclay was formed by using hexadecylpyridinium chloride as a swelling agent for silicate layers of montmorillonite. The polyimide--clay composites films (PI--MMT) were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD). All composites were subjected to differential scanning calorimetry measurements for the purpose of examining Tg from all compositions. The clay content significantly influenced the thermal behavior of the polymeric films, such as glass transition and decomposition temperatures of polyimide--clay composites. The glass transition temperatures of the composites were higher than that of the original polyimide. Their thermal decomposition temperatures (Td = temperature at 5% mass loss) were measured via thermogravimetric analysis and showed that the introduction of clay into polymer backbones increased thermal stability. SEM, XRD, and the other conventional techniques were used for structural characterization. Dispersion of the modified clay in the polyimide matrix resulted in nanostructured material containing intercalated polymer between the silicate layers. The morphology and properties of PI nanocomposites greatly depend on the functional groups of the organic modifiers, synthesis procedure, and structure of polyimide because of the chemical reactions and physical interactions involved.

🔖

Bu Makaleye Atıf Yap

YİĞİT, M., SEÇKİN, T., YİĞİT, B., KÖYTEPE, S. (2013). Synthesis and characterization of thermally stable camphor-based polyimide--clay nanocomposites. Turkish Journal of Chemistry, Cilt: 37 - Sayı: 2, 182–194. https://ajindex.com/articles/184696

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (24)

  1. Schmidt, D.; Shah, D.; Giannelis. E. P. Curr. Opin. Solid State Mater. Sci. 2002, 6, 205–212.
  2. Schmidt, G.; Malwitz, M. M. Curr. Opin. Colloid Interface Sci. 2003, 8, 103–108.
  3. Sanchez, C.; Ribot, F.; Lebeau, B. J. Mater. Chem. 1999, 9, 35–44.
  4. Morgan, A. B. Polym. Adv. Technol. 2006, 17, 206–217.
  5. Tobushi, H.; Hayashi, S.; Hoshio, K.; Miwa, N. Smart. Mater. Struct. 2006, 15, 1033–1038.
  6. Kawasumi, M.; Hasegawa, N.; Kato, M.; Okada, A. Macromolecules 1997, 30, 6333–6338.
  7. Peng, Z. Q.; Chen, D. J. J. Polym. Sci. B. Polym. Phys. 2006, 44, 534–540.
  8. Tian, M.; Qu, C. D.; Feng, Y. X. J. Mater. Sci. 2003, 38, 4917–4924.
  9. Shen, L.; Lin, Y. J.; Du, Q. G.; Zhong, W.; Yang, Y. L. Polymer. 2005, 46, 5758–5766.
  10. Lai, S. Q.; Yue L.; Li T. S.; Liu X. J.; Lv R. G. Macromol. Mater. Eng. 2005, 290, 195–201.
  11. Utracki, L. A. J. Nanosci. Nanotechnol. 2008, 8, 1582–1596.
  12. Carrado, K. A. Appl. Clay. Sci. 2000, 17(1–2), 1–23.
  13. Hussain, F.; Hojjati, M.; Okamoto, M.; Gorga, R. E. J. Comp. Mater. 2006, 40, 1511–1575.
  14. Carastan, D. J.; Demarquette, N. R. Int. Mater. Rev. 2007, 52, 345–380.
  15. Alexandre, M.; Dubois, P. Mater. Sci. Eng. 2000, R28, 1–63. Se¸ ckin, T.; K¨ oytepe, S.; Yi˘ git, M.; C ¸ etinkaya, E. Des. Monomers and Polym. 2004, 7, 377–390. Yi˘ git, M.; Se¸ ckin, T.; K¨ oytepe, S.; C ¸ etinkaya, E. Turk. J. Chem. 2007, 31, 113–124.
  16. Judenstein, P.; Sanchez, C. J. Mater. Chem. 1996, 6, 511–525.
  17. Laine, R.; Sanchez, C.; Brinker, C. J.; Gianellis, E. Hybrid Materials Mater. Res. Soc., Pittsburgh, 1998.
  18. Tsai, M. H.; Whang, W. T. Polymer, 2001, 42, 4197–4207.
  19. Volksen, W.; Cotts, P.; Yoon, D. Y. J. Polym. Sci. A-2. 1987, 25, 2487–2495. K¨ oytepe, S.; G¨ ok, Y.; Alıcı, B.; Se¸ ckin, T.; C ¸ etinkaya E. Polym. Int. 2004, 53, 688–697. Se¸ ckin, T.; C ¸ etinkaya, E.; K¨ oytepe, S.; Yigit, B. Polym. Bull. 2003, 50, 139-146.
  20. Yano, K.; Usuki, A.; Okada, A. J. Polym. Sci. Polym. Chem. 1997, 35, 2289-2294. ¨ Onal, M.; Sarıkaya, Y.; Alemdaro˘ glu, T.; Bozdo˘ gan, ˙I. Turk. J. Chem., 2003, 27, 683-693.
  21. Serra, M. E. S.; Murtinho, D.; Goth, A.; Gonsalves, A. R.; Abreu, P. E.; Pais, A. C. Chirality 2009, 22, 425–431.
  22. Xie, W.; Gao, Z.; Liu, K.; Pan, W. P.; Vaia, R.; Hunter, D.; Singh, A. Thermochim. Acta. 2001, 367–368, 339–350.
  23. Meszaros, L; Czvikovszky, T. Radiat. Phys. Chem. 2007, 76, 1329–1332.
  24. Mohanty, S.; Nayak, S. K. Polym. Compos. 2007, 28, 153–162.