Melt Polycondensation and Analysis of Hydroxyl-Terminated Poly(L-lactic Acid) Using Small Molecular Diols as Terminating Agents

Article Preview

Abstract:

The synthesis of hydroxyl-terminated poly (L-lactic acid) (PLLA) by direct melt polycondensation of L-lactic acid and use of small molecular diols as terminating agents was investigated. L-lactic acid was dewatered to prepare the dehydrated prepolymer at first. Then PLLA was prepared through melt polycondensation in a melt with catalyst system including TSA, SnCl2 and Sn (Oct)2. Finally, ethylene glycol, 1,4-butanediol, and 1,8-octanediol, respectively, were used in hydroxyl termination of the PLLA. The molecular weights and end-group structures of all products were characterized by gel permeation chromatography (GPC) and 1H-NMR. DSC and Disc Polarimeter were used to characterize crystallinity and racemization, respectively. The results show that two kinds of hydroxyl-terminated PLLA polymers were obtained: complete hydroxyl-terminated PLLA prepared by using ethylene glycol or 1,4-butanediol, incomplete hydroxyl-terminated PLLA prepared by using 1,8-octanediol or combination of two kinds of diols. Combination of ethylene glycol or 1,4-butanediol with 1,8-octanediol can reach high hydroxyl termination of PLLA, and maintain the molecular weight by decrease of alcoholysis at the same time. 1H-NMR was found as an effective estimating way for extents of reactions. The hydroxyl-terminating reactions of PLLA by the diols reduced the crystallinity and resulted in racemization to some extent.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

890-894

Citation:

Online since:

June 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Chen G P, Ushida T and Tateishi T: Biomaterials. 22(2001) 2563-2567.

Google Scholar

[2] Kricheldorf H R: Chemosphere. 43(2001) 49-54.

Google Scholar

[3] Vert M, Schwarch G and Coudane J: J. Macromol. Sci., Pure Appl. Chem. A32(1995)787- 796.

Google Scholar

[4] Xie J X: PhD Thesis, Beijing Institute of Technology. (2007)

Google Scholar

[5] Hiki S, Miyamoto M and Kimura Y: Polymer. 41(2000) 7369-7379.

Google Scholar

[6] Hiltunen K, Harkonen M and Seppala J V, et al.: Macromolecules. 29(1996) 8677-8682.

Google Scholar

[7] Gu S, Yang M and Yu T, et al.: Polym Int. 57(2008) 982-986.

Google Scholar

[8] Wiggins J S, Hassan M K and Mauritz K A, et al.: Polymer. 47(2006) 1960-1969.

Google Scholar

[9] Wallach J A, Huang S J: Biomacromolecules. 1(2000) 174-179.

Google Scholar

[10] Cooper T R, Storey R F: Macromolecules. 41(2008) 655-662.

Google Scholar

[11] Gupta A P, Kumar V: Eur. Polym. J. 43(2007) 4053-4074.

Google Scholar

[12] Wang H, Sun X and Seib P: J. Appl. Polym. Sci. 84(2002) 1257-1262.

Google Scholar

[13] Woo S I, Kim B O and Jun H S, et al.: Polym. Bull. 35(1995) 415-421.

Google Scholar

[14] Yu H X: PhD Thesis, Dong Hua University. (2008)

Google Scholar

[15] Marega C, Marigo A and Dinoto V, et al.: Makromol Chem.193(1992) 1599-1602.

Google Scholar

[16] Jamshidi K, Hydon S H and Ikada Y: Polymer. 29(1988) 2229-2234.

Google Scholar

[17] Moon S I, Kimura Y: Ppolym Int. 52(2003) 209-303.

Google Scholar