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The use of bioplastic, such as polycaprolactone, to substitute conventional plastic remains a problem to solve. The bioplastic degradation time is still relatively low when compared to the rate of plastic consumption by the public. Therefore, exploration of indigenous bacteria with plastic-degrading potential is needed. This study aims to reveal the potential of indigenous bacteria isolated from Wonorejo Mangrove as plastic-degrading bacteria based on their growth in selective media and biofilm formation. Bacterial isolates obtained from water bodies and sediments of Wonorejo’s mangrove were inoculated on minimum salt media with the addition of 0.25% polycaprolactone as the sole carbon source and then incubated for four weeks to determine the bacterial growth based on its total number. The total number of bacteria was calculated by the direct counting method using a hemocytometer. The results indicated a slight decrease in the number of cells for each isolate. Isolate T1A.1 obtained from mangrove water samples encountered a decrease in the total number of bacteria by 2 times the initial number. Meanwhile, isolate T2.1, which was isolated from mangrove sediments, was decreased by 1.4 times from the initial number. However, the enumeration did not cover the cells that formed the biofilm, which was observed in this study. Based on the ability of the isolates to live in the minimum media and the biofilm formation indicated their potential as plastic-degrading agents, specifically for polycaprolactone. Identification and further studies of both isolates are needed to get a better insight into their potential as polycaprolactone-degrading agents.
The use of bioplastic, such as polycaprolactone, to substitute conventional plastic remains a problem to solve. The bioplastic degradation time is still relatively low when compared to the rate of plastic consumption by the public. Therefore, exploration of indigenous bacteria with plastic-degrading potential is needed. This study aims to reveal the potential of indigenous bacteria isolated from Wonorejo Mangrove as plastic-degrading bacteria based on their growth in selective media and biofilm formation. Bacterial isolates obtained from water bodies and sediments of Wonorejo’s mangrove were inoculated on minimum salt media with the addition of 0.25% polycaprolactone as the sole carbon source and then incubated for four weeks to determine the bacterial growth based on its total number. The total number of bacteria was calculated by the direct counting method using a hemocytometer. The results indicated a slight decrease in the number of cells for each isolate. Isolate T1A.1 obtained from mangrove water samples encountered a decrease in the total number of bacteria by 2 times the initial number. Meanwhile, isolate T2.1, which was isolated from mangrove sediments, was decreased by 1.4 times from the initial number. However, the enumeration did not cover the cells that formed the biofilm, which was observed in this study. Based on the ability of the isolates to live in the minimum media and the biofilm formation indicated their potential as plastic-degrading agents, specifically for polycaprolactone. Identification and further studies of both isolates are needed to get a better insight into their potential as polycaprolactone-degrading agents.
This study investigates the modeling and experimental validation of cell morphology in microcellular-foamed polycaprolactone (PCL) using supercritical carbon dioxide (scCO2) as the blowing agent. The microcellular foaming process (MCP) was conducted using a solid-state batch foaming process, where PCL was saturated with scCO2 at 6 to 9 MPa and 313 K, followed by depressurization at a rate of −0.3 and −1 MPa/s. This study utilized the Sanchez–Lacombe equation of state and the Peng–Robinson–Stryjek–Vera equation of state to model the solubility and density of the PCL-CO2 mixture. Classical nucleation theory was modified and combined with numerical analysis to predict cell density, incorporating factors such as gas absorption kinetics, the role of scCO2 in promoting nucleation, and the impact of depressurization rate and saturation pressure on cell growth. The validity of the model was confirmed by comparing the theoretical predictions with experimental and reference data, with the cell density determined through field-emission scanning electron microscopy analysis of foamed PCL samples. This study proposes a method for predicting cell density that can be applied to various polymers, with the potential for wide-ranging applications in biomaterials and industrial settings. This research also introduces a Python-based numerical analysis tool that allows for easy calculation of solubility and cell density based on the material properties of polymers and penetrant gases, offering a practical solution for optimizing MCP conditions in different contexts.
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