Amorphous poly(3-hydroxybutyrate) films prepared by compression molding and solvent casting were degraded in aqueous media at different pH values. The time dependence of degradation was monitored by the measurement of weight loss, the extraction of the degradation products from the degrading sample, as well as by UV-Vis spectrophotometry and HPLC analysis of the aqueous solution. The results proved that degradation takes place mainly in the bulk of the samples and not on their surface. The overall rate of degradation depends strongly on pH; it increases with increasing pH values. Metabolite extraction and chromatography proved that degradation does not occur randomly, but with larger frequency at the end of the chains. By assuming that the hydrolysis of PHB is a SN2 type nucleofil substitution reaction, a kinetic model was proposed which describes the formation of various degradation products. The diffusion of metabolites was also accommodated into the model thus the concentration in the aqueous solution could also be predicted well. The correlation between prediction and experimental results is excellent. The model can be extended also for the description of the hydrolytic degradation of other aliphatic polyesters. 1 INTRODUCTION Poly(3-hydroxybutyrate) (PHB) is one of the most important biopolyesters from the family of polyhydroxyalkanoates which are produced by microorganisms from renewable resources [1-7]. Unlike in the synthetic polymerization of PHB, the production of the biopolymer by microbial fermentation excludes the presence of toxic products [8-10] and the hydrolytic degradation of PHB leads mainly to the monomer D-3-hydroxybutyric acid. This acid is a normal component of blood and is one of the three ketones which are

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