Dergiler / Turkish Journal of Chemistry / 2007 / Cilt: 31 - Sayı: 6

Synhesis of piperazine based polyimide in the presence of ionic liquids

Sayfa
569–578
Yayın Tarihi
2022-11-04
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 glass transition temperatures and thermal stabilities were higher for polyimide synthesized in ionic liquids than conventional polyimides prepared in aprotic solvents.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Ionic liquids derived from imidazolium, pyridinium, and alkylammonium salts were investigated not only as catalysts but also as solvents in polymerization of 1,4-bis(3-aminopropyl) piperazine.
📊
Temel Bulgular & Veri:They are even greater than the values obtained by conventional 2-stage polymerization in organic liquids.
💡
Sonuç & Katkı:The glass transition temperatures and thermal stabilities were higher for polyimide synthesized in ionic liquids than conventional polyimides prepared in aprotic solvents.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Ionic liquids derived from imidazolium, pyridinium, and alkylammonium salts were investigated not only as catalysts but also as solvents in polymerization of 1,4-bis(3-aminopropyl) piperazine. Results were compared with the conventional polymerizations in N-methylpyrrolidone (NMP). The catalyst has not only a detectable influence on polymer solubility, but also the degrees of polymerization are notably higher. They are even greater than the values obtained by conventional 2-stage polymerization in organic liquids. Ionic liquids based on imidazolium salts seem preferable over pyridinium and alkylammonium salts due to the higher degree of polydispersity of the polyimides obtained. The glass transition temperatures and thermal stabilities were higher for polyimide synthesized in ionic liquids than conventional polyimides prepared in aprotic solvents.

🔖

Bu Makaleye Atıf Yap

SEÇKİN, T., ALICI, B., KÖYTEPE, S. (2022). Synhesis of piperazine based polyimide in the presence of ionic liquids. Turkish Journal of Chemistry, Cilt: 31 - Sayı: 6, 569–578. https://ajindex.com/articles/602186

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (13)

  1. J.S. Moulthrop, R.P. Swatloski, G. Moyna and R.D. Rogers, Chem. Commun. 1557-1559 (2005)
  2. H.M. Luo, S. Dai, P.V. Bonnesen, A.C. Buchanan, J.D. Holbrey, N.J. Bridges and R.D. Rogers, Anal. Chem. 76, 3078-3083 (2004)
  3. J.H. Li, Y.F. Shen, Y.J. Zhang and Y. Liu, Chem. Commun. 360-362 (2005). 4. (a) Z.Y. Li, H.T. Liu, Y. Liu, P. He and J.H. Li, J. Phys. Chem. B. 108, 17512-17518 (2004). (b) Y. Liu, M.J. Wang, Z.Y. Li, H.T. Liu, P. He and J.H. Li, Langmuir 21, 1618-1622 (2005). (c) M.C. Buzzeo, C. Hardacre and R.G. Compton, Anal. Chem. 76, 4583-4588 (2004). 5. (a) S. Park and R. Kazlauskas, Curr. Opin. Biotechnol. 14, 432-437 (2003). (b) M.F. Machadoand J.M. Saraiva, Biotechnol. Lett. 27, 1233-1239 (2005). (c) W.Y. Lou, M.H. Zong and H. Wu, Biocatal. Biotransform. 22, 171-176 (2004). (d) F. Zhao, X.E. Wu, M.K. Wang, Y. Liu, L.X. Gao and S. Dong, J. Anal. Chem. 76, 4960-4967 (2004). (e) Y. Liu, M. Wang, J. Li, P. He, H.T. Liu and J.H. Li, Chem. Commun. 1778-1780 (2005)
  4. H. Huang, N.F. Hu, Y.H. Zeng and G. Zhou, Anal. Biochem. 308, 141-151 (2002)
  5. R.D. Rogers, K.R. Seddon “Ionic Liquids Industrial Applications to Green Chemistry”, ACS Symposium Series 818, American Chemical Society, Washington, DC, 2002
  6. R.D. Rogers, K.R. Seddon, P. Kubisa, “Ionic Liquids as Green Solvents”, ACS Symposium Series 856, American Chemical Society, Washington, DC, 2003
  7. V. Strehmel, A. Laschewsky, H. Kraudelt, H. Wetzel, E. Gornitz, In ACS Symposium Series 913; R.D. Rogers, C.S. Brazel, Eds.; American Chemical Society, Washington, DC, pp 17-36, 2005
  8. P. Kubisa, Prog. Polym. Sci. 29, 3-12 (2004)
  9. D.A. Canelas and J.M. DeSimone, Adv. Polym. Sci. 133, 103-140 (1997)
  10. H. Zhang, L. Bu. M. Li, K. Hong, A.E. Visser, R.D. Rogers and J.W. Mays, ACS Symposium Series 818; R.D. Rogers, K.R. Seddon, Eds.; American Chemical Society: Washington, DC; pp 114-123, 2002. 13. (a) M.G. Benton and C.S. Brazel, ACS Symposium Series 818; R.D. Rogers, K.R. Seddon, Eds.; American Chemical Society: Washington, DC; pp 125-133, 2002. (b) K. Hong, H. Zhang, J.W. Mays, A.E. Visser, C.S. Brazel, J.D. Holbrey, W.M. Reichert and R. Rogers, Chem. Commun. 1368-1369 (2002). (c) H. Zhang, K. Ho ng, J.W. Mays, Macromolecules 35, 5738-5741 (2002)
  11. S. Harrison, S.R. Mackenzie and D.M. Haddleton, Chem. Commun. 2850-2851 (2002)
  12. S. Harrison, S.R. Mackenzie, D.M. Haddleton, Macromolecules 36, 5072-5075 (2003)
  13. S. Perrier, T.P. Davis, A.J. Carmichael and D.M. Haddleton, Eur. Polym. J.