作者: Tz. Ivanova , I. Panaiotov , F. Boury , P. Saulnier , J.E. Proust
DOI: 10.1016/S0927-7765(99)00043-0
关键词: Aqueous solution 、 Electrostatics 、 Surface pressure 、 Organic chemistry 、 Polymer 、 Molecule 、 Chemical engineering 、 Monolayer 、 Lactide 、 Chemistry 、 Hydrolysis
摘要: Abstract The hydrolysis kinetics of insoluble poly-( d , l -lactide) monolayers spread on basic or acidic aqueous subphase were followed by measuring simultaneously the decrease in surface area at constant pressure and evolution potential. An approach to analyse role electrostatic interactions during alkaline pH, interpreting potential data was developed. theoretical predictions based idea a random fragmentation polymer molecules leading interfacial accumulation charged products solubilisation small fragments describes well experimental results. reversibility hydrolysis/esterification reaction pH is taken into account.