화학공학소재연구정보센터
Journal of Industrial and Engineering Chemistry, Vol.19, No.4, 1340-1349, July, 2013
Characterizations and properties of oligoazomethines (including CH3 and NO2 groups) char composites
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In this research, the oligomers were synthesized by the polycondensation of diamins (1,4-diamino-2-nitrobenzene and 2,5-diaminotoluene sulfate) with dialdehydes (terephtaldehyde 4,40-diformylbiphenyl, bis(4-formylphenyl) ether and p-phenylene diacrolein). In this study, the oligoazomethines (OAMs) were studied using IR and UV.visible spectra and X-ray diffraction. The initial degradation temperatures (IDT) determined from TGA of OAMs were in the range of 225.2708C indicating their good thermal stability. The conductivity measurements of OAMs were carried out with an electrometer using fourpoint probe technique. The highest conductivity increase among all the oligoazomethine/char composites was observed for the OAMs composites formed with 30% char ratio.
  1. Yang CJ, Jenekhe SA, Chemistry of Materials., 3, 878 (1991)
  2. Wang CG, Shieh S, Legoff E, Kanatzidis MG, Macromolecules, 29(9), 3147 (1996)
  3. Thomas O, Inganas O, Andersson MR, Macromolecules, 31(8), 2676 (1998)
  4. El-Shekeil AG, Khalid MA, Al Yusufy FA, Macromolecular Chemistry and Physics., 202, 2971 (2001)
  5. Hyun JS, L TW, Chul KY, Hack SD, Nam CH, Optical Materials., 21, 169 (2002)
  6. Takahashi Y, Iijima M, Oishi Y, Kakinma M, Imai Y, Macromolecules., 24, 3543 (1991)
  7. Weaver MS, Bradley DC, Synthetic Metals., 8, 61 (1996)
  8. Iwan A, Sek D, Progress in Polymer Science., 33, 289 (2008)
  9. McElvain J, Tatsuura S, Wudl F, Heeger AJ, Synthetic Metals., 95, 101 (1998)
  10. Choi EJ, Ahn HK, Lee JK, Jin JI, Polymer, 41(21), 7617 (2000)
  11. Talati JD, Desai MN, Shah NK, Mater. Chem. Phys., 93(1), 54 (2005)
  12. Kim DJ, Kim SH, Jin SH, Park DK, Cho HN, Zyung T, Cho I, Choi SK, European Polymer Journal., 35, 227 (1999)
  13. Colon I, Kelsey DR, Journal of Organic Chemistry., 51, 2627 (1986)
  14. Kaya I, Bilici A, Sac¸ak M, Synthetic Metals., 159, 1414 (2009)
  15. Li W, Wan M, Solid State Communications., 92, 629 (1994)
  16. Ahmetli G, Sen N, Pehlivan E, Durak S, Progress in Organic Coatings., 55, 262 (2006)
  17. Ahmetli G, Deveci H, Altun A, Kurbanli R, Progress in Organic Coatings., 70, 9 (2011)
  18. Deveci H, Ahmetli G, Ersoz M, Kurbanli R, Progress in Organic Coatings., 73, 1 (2012)
  19. Kamura M, Kuzumoto Y, Aomori S, Houjou H, Kitamura M, Arakawa Y, Thin Solid Films, 518(18), 5115 (2010)
  20. Kaya I, Koyuncu S, Culhaoglu S, Polymer, 49(3), 703 (2008)
  21. More AS, Sane PS, Patil AS, Wadgaonkar PP, Polymer Degradation and Stability., 95, 1727 (2010)
  22. Luzny W, Stochmal-Pomarzanska E, Pron A, Polymer, 40(23), 6611 (1999)
  23. Matsumoto T, Yamada F, Kurosaki T, Macromolecules, 30(12), 3547 (1997)
  24. Liu Y, Zhao YL, Zhang HY, Xiao YL, Liang P, Zhang XZ, Jun XJ, Macromolecules., 37, 6369 (2004)
  25. Jarzabek B, Weszka J, Domanski M, Jurusik J, Cisowski J, Journal of Non-Crystalline Solids., 354, 856 (2008)
  26. El-Shekeil AG, Al-Saady HA, Al-Yusufy AF, Polymer International., 44, 78 (1997)
  27. Palewicza M, Iwan A, Sikora A, Doskocz J, Strek W, Sek D, Mazurek B, Acta Physiologica Polonica., 121, 16 (2012)
  28. Diaz FR, Moreno J, Tagle LH, East GA, Radic D, Synthetic Metals., 100, 187 (1999)
  29. El-Shekeil A, Al-Aghbari S, Polymer International., 53, 777 (2004)
  30. Hajduk B, Weszka J, Cozan V, Kaczmarczyk B, Jarzabek B, Domanski M, Archives of Materials Science and Engineering., 32, 85 (2008)
  31. Li X, Li C, Li S, Synthetic Metals., 60, 285 (1993)
  32. Moon KS, Choi HD, Lee AK, Cho KY, Yoon HG, Journal of Applied Polymer Science., 77, 294 (2001)