화학공학소재연구정보센터
Journal of Applied Polymer Science, Vol.113, No.6, 4100-4115, 2009
Crystallization Kinetics of Poly(L-Lactide)/Carbonated Hydroxyapatite Nanocomposite Microspheres
Microspheres consisting of carbonated hydroxyapatite (CHAp) nanoparticles and poly(L-lactide) (PLLA) have been fabricated for use in the construction of osetoconductive bone tissue engineering scaffolds by selective. laser sintering (SLS). In SLS, PLLA polymer melts and crystallizes. It is therefore necessary to study the crystallization kinetics of PLLA/CHAp nanocomposites. The effects of 10 wt% CHAp nanoparticles on the isothermal and nonisothermal crystallization behavior of PLLA matrix were studied, using neat PLLA for comparisons. The Avrami equation was successfully applied for the analysis of isothermal crystallization kinetics. Using the Lauritzen-Hoffman theory, the transition temperature from crystallization Regime 11 to Regime III was found to be around 120 degrees C for both neat PLLA and PLLA/CHAp nanocomposite. The combined Avrami-Ozawa equation was used to analyze the nonisothermal crystallization process, and it was found that the Ozawa exponent was equal to the Avrami exponent for neat PLLA and PLLA/CHAp nano-composite, respectively. The effective activation energy as a function of the relative crystallinity and temperature for neat PLLA and PLLA/CHAp nanocomposite under the nonisothermal crystallization condition was obtained by using the Friedman differential isoconversion method. The Lauritzen-Hoffman parameters were also determined from the nonisothermal crystallization data by using the Vyazovkin-Sbirrazzuoli equation. CHAp nanoparticles in the composite acted as an efficient nucleating agent, enhancing the nucleation rate but at the same time reducing the spherulite growth rate. This investigation has provided significant insights into the crystallization behavior of PLLA/CHAp nanocomposites, and the results obtained are very useful for making good quality PLLA/CHAp scaffolds through SLS. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 113: 4100-4115, 2009