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New Routes of Valorization of Recycled and Bio-sourced Polyamides with a Low Toxicity Process

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Abstract

The aim of the present work is the development of new materials from renewable resources mixed with recycled polymers. The article focuses on the studies of (PAX/PA6) and (PAX/PA66) blends using three coupling agents: PBO, DGEBA, Lotader 3210. Blends of various compositions were prepared in a corotating twin-screw extruder. PA6 (PA66) acts as the polymer matrix and PAX as the dispersed phase. The morphology of the compatibilized PAX/PA6/DGEBA (25/75) and PAX/PA66/DGEBA (25/75) blends shows lower diameters and a decrease in the size of the dispersed PAX particles. The addition of DGEBA not only leads to a much finer phase domain size, but also improves the interphase between PA6 (PA66) and PAX phases. Moreover, rheological analysis indicates that the increase in viscosity was much more pronounced with DGEBA than with Lotader 3210 and PBO especially for PAX/PA6 (25/75) and PAX/PA66 (25/75) blends, which can be indicative of good reactivity of the terminal −NH2 groups of PA6 or PA66 with the epoxy groups of DGEBA. The improvement of interphase between phases induced an increase in tensile properties. VOC from PA66 were recovered and found not to modify the viability of human macrophages, which can be a sign of a low toxicity of the process.

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Abbreviations

PA6 and PA66:

Recycled polyamides

PAX:

Bio-sourced polyamide

DGEBA:

Diglycidyl ether of bisphenol A

PBO:

1, 4-phenylene bis (2-oxazoline)

LOTADER 3210:

Terpolymer of ethylene, acrylic ester and maleic anhydride

ELV:

End of life vehicles

VOC:

Volatile organic compounds

References

  1. Ellis, T.S.: Miscibility of polyamide blends: effects of configuration. Polymer 36, 3919–3926 (1995)

    Article  Google Scholar 

  2. Liu, Y., Donovan, J.A.: Miscibility and crystallization of semicrystalline nylon 6 and amorphous nylon 6IcoT blends. Polymer 36, 4797–4803 (1995)

    Article  Google Scholar 

  3. Zhang, G.Z., Yoshida, H., Kawai, T.: Miscibility of nylon 66 and nylon 48 blend evaluated by crystallization dynamics. Thermochim. Acta 416, 79–85 (2004)

    Article  Google Scholar 

  4. Khanna, Y.P., Murthy, N.S., Kuhn, W.P., Day, E.D.: Pseudo super-miscibility: blends of semi-crystalline nylon pairs exhibiting a single T, and a single T. Polym. Eng. Sci. 39, 2222–2232 (1999)

    Article  Google Scholar 

  5. Brisson, J.: Miscibility of polyamide blends. I, molecular modeling of poly(n-methyleneisophthalamide)-poly(m-phenyleneisophthalamide) blends. Macromolecules 24, 495–504 (1991)

    Article  Google Scholar 

  6. Persyn, O., Miri, V., Lefebvre, J.M., Ferreiro, V., Brink, T., Stroeks, A.: Mechanical behavior of films of miscible polyamide 6/polyamide 6I-6T blends. J. Polym. Sci. Part B Polym. Phys. 44, 1690–1701 (2006)

    Article  Google Scholar 

  7. Shibayama, M., Uenoyama, K., Oura, J.I., Nomura, S., Iwamoto, T.: Miscibility and crystallinity control of nylon-6 and poly (m-xylene adipamide). Polymer 36, 4811–4816 (1995)

    Google Scholar 

  8. Endo, M., Morishima, Y., Yano, S., Tadano, K., Murata, Y., Tsunashima, K.: Miscibility in binary blends of aromatic and alicyclic polyamides. J. Appl. Polym. Sci. 101, 3971–3978 (2006)

    Article  Google Scholar 

  9. Ellis, T.S.: Aromatic polyamide blends: enthalpy relaxation and its correlation with phase phenomena. Macromolecules 23, 1494–1503 (1990)

    Article  Google Scholar 

  10. Ellis, T.S.: Influence of structure on phase behavior of polyamide blends. Macromolecules 24, 3845–3852 (1991)

    Article  Google Scholar 

  11. Ellis, T.S.: Miscibility and immiscibility of polyamide blends. Macromolecules 22, 742–754 (1989)

    Article  Google Scholar 

  12. Ellis, T.S.: Mixing relationships in aliphatic polyamide blends. Polymer 33, 1469–1476 (1992)

    Article  Google Scholar 

  13. Xie, T.X., Yang, G.S.: The effect of maleated SEBS on the morphology and properties of nylon 1212/nylon 6 blends. Polym. Sin. 5, 700–704 (2004)

    Google Scholar 

  14. Kyotani, M.: Solution crystallization of blends of nylon 6 and nylon 12. J. Macromol. Sci., Phys. 21, 219–230 (1982)

    Article  Google Scholar 

  15. Ong, E.S., Kim, Y., Williams, H.L.: Dynamic mechanical properties of some nylons and their blends. J. Appl. Polym. Sci. 31, 367–383 (1986)

    Article  Google Scholar 

  16. Wei, M., Shin, I.D., Urban, B., Tonelli, A.E.: Partial miscibility in a nylon-6/nylon-66 blend coalesced from their common-cyclodextrin inclusion complex. J. Polym. Sci. Part B Polym. Phys. 42, 1369–1378 (2004)

    Article  Google Scholar 

  17. Ellis, T.S.: On the miscibility of blends of nylon 66 and poly(hexamethylene isophthalamide), nylon 6I. Macromolecules 29, 1836–1838 (1996)

    Article  Google Scholar 

  18. Brisson, J., Cote, P.: Factors affecting the miscibility of nylon-6i/nylon-6, 6. Macromolecules 29, 1839–1841 (1996)

    Article  Google Scholar 

  19. Kim, B.K., Baek, S.H., Kim, M.S.: Reactive blends of polyamide 6 with polyester elastomer using coupling agents. J. Appl. Polym. Sci. 91, 3966–3973 (2004)

    Article  Google Scholar 

  20. Jaziri, M., Barhoumi, N., Massardier, V., Mélis, F.: Blending PP with PA6 industrial wastes: effect of the composition and the compatibilization. J. Appl. Polym. Sci. 107(6), 3451–3458 (2008)

    Article  Google Scholar 

  21. Sonnier, R., Massardier, V., Cassagnau, P.: Compatibilization of hiPP/HDPE blends by a metallocene copolymer. Int. J. Mater. Form. 1, 657–660 (2008)

    Article  Google Scholar 

  22. Mnif, N., Massardier, V., Kallel, T., Elleuch, B.: Effects of nanoparticle treatment and compatibilizers on the properties of (PP/EPR)/nano-CaCO3 blends. Int. J. Mater. Form. 1, 639–643 (2008)

    Article  Google Scholar 

  23. Visakh, P.M., Sabu, Th.: Preparation of bionanomaterials and their polymer nanocomposites from waste and biomass. Waste Biomass Valor 1, 121–134 (2010)

    Article  Google Scholar 

  24. Bezati, F., Massardier, V., Froelich, D., Maris, E., Balcaen, J.: Elaboration and characterization of traced polypropylene with rare earth oxides for automatic identification and sorting of end-of-life plastics. Waste Biomass Valor 1, 357–365 (2010)

    Article  Google Scholar 

  25. Carmichael, J., DeGraff, W.G., Gazdar, A.F., Minna, J.D., Mitchell, J.B.: Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res. 47, 936–942 (1987)

    Google Scholar 

  26. Lemarie, A., Morzadec, C., Bourdonnay, E., Fardel, O., Vernhet, L.: Human macrophages constitute targets for immunotoxic inorganic arsenic. J. Immunol. 177, 3019–3027 (2006)

    Google Scholar 

  27. Vernhet, L., Allain, N., Payen, L., Anger, J.-P., Guillouzo, A., Fardel, O.: Resistance of human multidrug resistance-associated protein 1-overexpressing lung tumor cells to the anticancer drug arsenic trioxide. Biochem. Pharmacol. 61, 1387–1391 (2001)

    Article  Google Scholar 

  28. Wilkinson, A.N., Laugel, L., Clemens, M.L., Harding, V.M., Marin, M.: Phase structure in polypropylene/PA6/SEBS blends. Polymer 40(17), 4971–4975 (1999)

    Article  Google Scholar 

  29. Davis, R.D., Gilman, J.W., VanderHart, D.L.: Processing degradation of polyamide 6/montmorillonite clay nanocomposites and clay organic modifier. Polymer Degrad. Stab. 79, 111–121 (2003)

    Article  Google Scholar 

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Correspondence to Valérie Massardier.

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Louizi, M., Massardier, V., Taha, M. et al. New Routes of Valorization of Recycled and Bio-sourced Polyamides with a Low Toxicity Process. Waste Biomass Valor 4, 47–54 (2013). https://doi.org/10.1007/s12649-012-9133-7

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