Orotic acid is a natural heterocyclic compound that acts as a nucleation agent in poly(lactic acid) (PLA). PLA materials with increasing orotic acid content were prepared and characterized. It was found that crystallinity of about 28% was reached with 0.3% content of the agent. Further enhancement in the content of the agent did not provoke any additional significant increase of crystallinity. Subsequently, it was investigated whether the orotic acid content affected photodegradation of PLA and, in the next phase, its biodegradation. The results of rheological measurements showed that the compound slightly accelerates photodegradation of the material, which was accompanied by the cleavage of PLA chains. Previous photodegradation was shown to accelerate the subsequent biodegradation by shortening the lag phase of the process, where the explanation is probably in the reduction of the polymer molecular weight during the photodegradation. Moreover, the presence of orotic acid in both initial and photodegraded samples was found to influence biodegradation positively by shortening the lag phase and increasing the observed maximal rate of the biodegradation.
The present paper focuses on the effects of blending poly (ε-caprolactone) (PCL) with thermoplastic starch (TPS) on the final biodegradation rate of PCL/TPS blends, emphasizing the type of environment in which biodegradation takes place. The blends were prepared by melt-mixing the components before a two-step processing procedure, which strongly affects the degree of plasticization and therefore the final material morphology, as was detailed in the previous work, was used for the thermoplastic starch. The concentration row of pure PCL over PCL/TPS blends to pure TPS was analyzed for biodegradation in two different environments (compost and soil), as well as from a morphological, thermomechanical, rheological, and mechanical point of view. The morphology of all the samples was studied before and after biodegradation. The biodegradation rate of the materials was expressed as the percentage of carbon mineralization, and significant changes, especially after exposure in soil, were recorded. The crystallinity of the measured samples indicated that the addition of thermoplastic starch has a negligible effect on PCL-crystallization. The blend with 70% of TPS and a co-continuous morphology demonstrated very fast biodegradation, with the initial rate almost identical to pure TPS in both environments while the 30% TPS blend exhibited particle morphology of the starch phase in the PCL matrix, which probably resulted in a dominant effect of the matrix on the biodegradation course. Moreover, some molecular interaction between PCL and TPS, as well as differences in flow and mechanical behavior of the blends, was determined.
A study was conducted on the biodegradation of aromatic-aliphatic copolyester-based agricultural film in soil at 25 °C. The polymer is known to be biodegradable under composting conditions although rather recalcitrant under mesophilic conditions. The material investigated comprised of the copolyester filled with approximately 25% of starch containing biodegradable plasticizers, and its behavior was compared to the corresponding material without the filler. Mineralization followed by CO2 production merely reached the point of about 6% after 100 days of incubation in the pure copolyester film, whereas the value of around 53% was recorded for the filled copolyester film, which exceeded the readily biodegradable starch filler content in the material by more than 20% and could be accounted for biodegradation of the copolyester. It was suggested that the accelerated copolyester biodegradation in the starch-filled material was most likely explained by the increase in the active surface area of the material available for the microbial attack after biodegradation of the filler. The results were supported by changes in molecular weight distributions of the copolyester and observations made by several microscopic techniques. These findings encourage further development of biodegradable agricultural films based on this material.
During the steam explosion pretreatment of plant biomass, degradation products are generated, and some of these have inhibitory activity against biogas production. The aim of this study was to investigate and quantify the effect of selected model inhibitory compounds on methane production. The results showed no significant inhibition of methane production by furfural at concentrations below 1 g/L. In addition, the microbial community was able to restore biogas production inhibited by this compound after a certain time. 5-hydroxymethylfurfural was evaluated as a more potent inhibitor, with a significant effect above 0.2 g/L. Both compounds were more effective inhibitors with cellulose as the carbon substrate, probably reflecting higher sensitivity of the cellulolytic step in biogas production. No significant inhibition was observed for the phenolic compounds tested, gallic and tannic acids, at concentrations of up to 2 g/L. Thus, the compounds investigated should not represent a problem for the biogas production involving steam explosion preprocessed plant biomass.
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