Journal of Thermal Analysis and Calorimetry

, Volume 87, Issue 2, pp 519–527 | Cite as

Oxidative degradation of EVA copolymers in the presence of catalysts

Comparison among different zeolites and related materials
regular

Abstract

A study of the catalytic degradation of EVA copolymers under air atmosphere has been carried out using thermogravimety (TG). Three commercial EVA copolymers and five zeolites and related materials catalysts have been selected. The degradation process in air atmosphere involves four main decomposition steps (as observed in TG), being more complex than the corresponding process in inert atmosphere. The presence of MCM-41, HY and H-β does not seem to noticeably affect to the overall degradation temperature, despite the temperature of maximum reaction rate for the second decomposition step being slightly displaced towards lower temperatures. Contrarily, the presence of HZSM-5 and HUSY zeolites seems to displace the main stage of the oxidative degradation process towards higher temperatures. Moreover, the relative importance of the second and third decomposition step is different depending on the amount and the nature of the zeolite mixed with the EVA sample. The results obtained show that the presence of the catalyst also enhances the formation of the carbonous residue.

Keywords

degradation EVA copolymers MCM-41 oxidative TG zeolites 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Gugumus, F 1996Polym. Degrad. Stab.53161CrossRefGoogle Scholar
  2. 2.
    Allen, NS, Edge, M, Rodrigues, M, Liauw, CM, Fontan, E 2001Polym. Degrad. Stab.711CrossRefGoogle Scholar
  3. 3.
    García, AN, Font, R 2004Fuel831165CrossRefGoogle Scholar
  4. 4.
    Marcilla, A, Gómez-Siurana, A, Menargues, S, Ruiz Femenia, R, García Quesada, J 2006J. Anal. Appl. Pyrolysis76138CrossRefGoogle Scholar
  5. 5.
    Marcilla, A, Gómez-Siurana, A, Menargues, S 2005Thermochim. Acta438155CrossRefGoogle Scholar
  6. 6.
    Kim, H-S, Yang, H-S, Kim, H-J, Park, H-J 2004J. Therm. Anal. Cal.76395CrossRefGoogle Scholar
  7. 7.
    Xie, W, Pan, W-P 2001J. Therm. Anal. Cal.65669CrossRefGoogle Scholar
  8. 8.
    Marcilla, A, Beltrán, M, Conesa, J 2001J. Anal. Appl. Pyrolysis58–59117CrossRefGoogle Scholar
  9. 9.
    Garforth, A, Fiddy, S, Lin, Y-H, Ghanbari, A, Sharratt, PN, Dwyer, J 1997Thermochim. Acta29465CrossRefGoogle Scholar
  10. 10.
    Marcilla, A, Gómez, A, Menargues, S, García-Martínez, J, Cazorla-Amorós, D 2003J. Anal. Appl. Pyrolysis68–69495CrossRefGoogle Scholar
  11. 11.
    Marcilla, A, Gómez, A, Menargues, S 2005Polym. Degrad. Stab.89454CrossRefGoogle Scholar
  12. 12.
    Sultan, B-A, Sörvik, E 1991J. Appl. Polym. Sci.431761CrossRefGoogle Scholar
  13. 13.
    Serrano, DP, Aguado, J, Escola, JM, Garagorri, E 2003Appl. Catal B: Environ4495CrossRefGoogle Scholar
  14. 14.
    Marcilla, A, Beltrán, M, Hernández, F, Navarro, R 2004Appl. Catal A: Gen.28737CrossRefGoogle Scholar
  15. 15.
    Marcilla, A, Gómez, A, Reyes–Labarta, JA 2001Polymer428103CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2007

Authors and Affiliations

  1. 1.Departamento Ingeniería QuímicaUniversidad de AlicanteAlicanteSpain

Personalised recommendations