TY - JOUR
T1 - Polyamide 6-polycaprolactone multiblock copolymers : synthesis, characterization, and degradation
AU - Cakir, S.
AU - Kierkels, R.
AU - Koning, C.E.
PY - 2011
Y1 - 2011
N2 - This work describes the synthesis and characterization of polyamide 6 (PA 6)-polycaprolactone (PCL) multiblock copolymers. Low molar mass, fully amine end-capped PA 6 was prepared by the addition of a diamine monomer during e-caprolactam polymerization. A low molar mass PCL was selected to be incorporated as the biodegradable block and was fully end-capped with toluene 2,4-diisocyanate. End group
analysis and molecular weight characterizations were performed for both end-functionalized polymers by SEC, NMR and titration analysis. Incorporation of PCL into PA 6 was mainly achieved by solution mixing of the two end-functional blocks and, was continued after the removal of the solvent with solid state polymerization (SSP) by gradual heating until about 40 ??C below the melting temperature of the PA 6. Molecular weights
started to grow immediately during solution mixing and only increased marginally during the SSP treatment. FTIR and SEC studies confirmed the reaction between the two components. DSC data, in combination with the enhanced molar mass during
solution mixing pointed to a blocky microstructure, for which distinct melting and crystallization temperatures were observed for the PCL and the PA 6 blocks. Hydrolytic and enzymatic degradation studies were performed at 25 ??C where the degree of degradation was followed by weight loss analysis, SEM and SEC.
AB - This work describes the synthesis and characterization of polyamide 6 (PA 6)-polycaprolactone (PCL) multiblock copolymers. Low molar mass, fully amine end-capped PA 6 was prepared by the addition of a diamine monomer during e-caprolactam polymerization. A low molar mass PCL was selected to be incorporated as the biodegradable block and was fully end-capped with toluene 2,4-diisocyanate. End group
analysis and molecular weight characterizations were performed for both end-functionalized polymers by SEC, NMR and titration analysis. Incorporation of PCL into PA 6 was mainly achieved by solution mixing of the two end-functional blocks and, was continued after the removal of the solvent with solid state polymerization (SSP) by gradual heating until about 40 ??C below the melting temperature of the PA 6. Molecular weights
started to grow immediately during solution mixing and only increased marginally during the SSP treatment. FTIR and SEC studies confirmed the reaction between the two components. DSC data, in combination with the enhanced molar mass during
solution mixing pointed to a blocky microstructure, for which distinct melting and crystallization temperatures were observed for the PCL and the PA 6 blocks. Hydrolytic and enzymatic degradation studies were performed at 25 ??C where the degree of degradation was followed by weight loss analysis, SEM and SEC.
U2 - 10.1002/pola.24716
DO - 10.1002/pola.24716
M3 - Article
SN - 0887-624X
VL - 49
SP - 2823
EP - 2833
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 13
ER -