Preparation and Characterization of Poly(lactic acid) with Different Molecular Weights by Thermal Hydrolysis

Article Preview

Abstract:

A feasible and effective method of thermal hydrolysis to prepare poly (lactic acid) (PLA) oligomers with different controlled molecular weight from PLA is presented in this paper. The thermal hydrolytic reaction was carried out by immerging PLA resin pellets in boiling distilled water for a certain period of time. Ester groups in PLA chains are hydrolytically degraded in the presence of water and thermal, so PLA oligomers with different molecular weight were prepared. The structures and properties of PLA oligomers were characterized by FT-IR, GPC, DSC, etc. The results showed that thermal hydrolytic reaction could effectively reduce the molecular weight of PLA, which declines with the increase of the thermal hydrolytic reaction time. Meanwhile, the content of terminal hydroxyl group, glass transition temperature, melting point of PLA oligomers prepared from thermal hydrolytic reactions exhibit gradual changes with the extension of the thermal hydrolytic time.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

19-24

Citation:

Online since:

October 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2014 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] R A Auras, L T Lim, S E M Selke., et al. Poly(lactic acid): Synthesis, Structures, Properties, Processing, and Applications. John Wiley & Sons, (2011).

DOI: 10.1002/9780470649848

Google Scholar

[2] R E Drumright, P R Gruber, D E Henton. Advanced Materials Research, Vol. 12(2000), p.1841.

Google Scholar

[3] F Pavia, C La, V Brucato. Journal of Cellular Plastics, Vol. 48(2012), p.399.

Google Scholar

[4] R Antel, J Boyce, N Gano, et al. Society of Plastics Engineers - Global Plastics Environmental Conference, Vol. 4(2009), p. (2067).

Google Scholar

[5] C Danyluk, R Erickson, S Burrows, et al. Journal of Testing and Evaluation, Vol. 38(2010), p.1.

Google Scholar

[6] C Guo, X Sheng, C Chu, et al. Advanced Materials Research, Vol. 2011 (2011), p.1741.

Google Scholar

[7] M Viljanmaa, R Mattila, et al. Polymer Degradation and Stability, Vol. 78(2002), p.269.

Google Scholar

[8] B Linnemann, M Sri Harwoko, T Gries. Chemical Fibers International, Vol. 53(2003), p.426.

Google Scholar

[9] L Fambri, A Pegoretti, R Fenner, et al. Polymer, Vol. 38(1997), p.79.

Google Scholar

[10] N J Mamouzelos, C S Proikakis, P A Tarantili, et al. Release of propranolol and diclofenac from low Mw DL-poly(lactic acid). Journal of Biomaterials Applications, Vol. 16(2002), p.177.

DOI: 10.1177/0885328202016003174

Google Scholar

[11] A G Andreopoulos, E C Hatzi, M Doxastakis. Journal of Materials Science: Materials in Medicine, Vol. 11(2000), p.393.

DOI: 10.1023/a:1008990109419

Google Scholar