Effect of tributyltin alkoxides chain length on the ring-opening polymerization of ε-caprolactone: Kinetics studies by non-isothermal DSC

• Main Authors: Wanich Limwanich, Sureerat Khunmanee, Nawee Kungwan, Winita Punyodom, Puttinan Meepowpan
• Format: Journal
• Published: 2018
• Subjects: Agricultural and Biological Sciences
• Online Access: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84949115044&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/44400
• Institution: Chiang Mai University

© 2014 Elsevier B.V. All rights reserved. The kinetics of ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) initiated by 1.0 mol% of the tributyltin alkoxides (Bu 3 SnOR; R = Me, Et, nPr and nBu) was investigated by non-isothermal DSC technique. The DSC curves showed the dependency of polymerization exotherms with the heating rate. The polymerization rate increased with increasing of heating rate for all initiating systems. The values of activation energy (E a ) obtained from the peak method of Kissinger for Bu 3 SnOMe, Bu 3 SnOEt, Bu 3 SnOnPr and Bu 3 SnOnBu initiated ROP of ε-CL were 52.4, 70.3, 75.9 and 78.0 kJ/mol, respectively. The values of E a increased with increasing of alkoxy chain length but polymerization rate decreased. The variation of E a with monomer conversion was investigated by Friedman and Starink isoconversional methods. The Bu 3 SnOnBu initiator produced the highest molecular weight and %yield of poly(ε-caprolactone) (PCL).