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Abstract: Plastics play a crucial role in our daily lives. The challenge, however, is that they become waste and contribute to a global environmental problem, increasing concerns about pollution and the urgent need to protect the environment. The accumulation and fragmentation of plastic waste, especially micro- and nanoplastics in aquatic systems, poses a significant threat to ecosystems and human health. In this study, the decomposition and fragmentation processes of conventional and biobased plastic waste in simulated water bodies (waters with different pH values) and in real water systems (tap water and seawater) are investigated over a period of one and six months. Three types of plastic were examined: thermoplastic polyethylene terephthalate and thermoset melamine etherified resin in the form of nonwovens and biobased polylactic acid (PLA) in the form of foils. Such a comprehensive study involving these three types of plastics and the methodology for tracking degradation in water bodies has not been conducted before, which underlines the novelty of the present work. After aging of the plastics, both the solid fraction and the leachate in the liquid phase were carefully examined. The parameters studied include mass loss, structural changes and alterations in functional groups observed in the aged plastics. Post-exposure assessment of the fragmented pieces includes quantification of the microplastic, microscopic observations and confirmation of composition by in situ Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy. The leachate analysis includes pH, conductivity, turbidity, total carbon and microplastic size distribution. The results highlight the importance of plastic waste morphology and the minor degradation of biobased PLA and show that microfibers contribute to increased fragmentation in all aquatic systems and leave a significant ecological footprint. This study underlines the crucial importance of post-consumer plastic waste management and provides valuable insights into strategies for environmental protection. It also addresses the pressing issue of plastic pollution and provides evidence-based measures to mitigate its environmental impact.
Keywords: polylactic acid, polyethylene terephthalate fabric, melamine etherifed resin fabric, aquatic environment, fragmentation, waste disposal
Published in DKUM: 09.09.2024; Views: 73; Downloads: 5
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Abstract: The main aim of this thesis was development of thin functional layers from hemicelluloses xylans on the polyethylene terephthalate (PET) surfaces. Hemicelluloses, xylans, as renewable polymers, were chemically modified in order to introduce anionic and cationic functional groups. Two types of chemical modifications were performed: carboxymethylation in order to increase anionic nature of xylans and improve their hydrophilic character and cationization for introducing of amino groups and antimicrobial characteristics. Both types of modifications were successful, which was proved by ATR FTIR and raman techniques, elemental analysis, total bound nitrogen determination, size exclusion chromatography and polyelectrolyte titrations. Polyelectrolyte titration results showed increased amounts of deprotonated carboxyl groups in carboxymethylated xylans as well as increased amounts of protonated groups in cationized xylans. Antimicrobial activity of xylans was investigated by the determination of minimal inhibitory concentration (MIC) against S. aureus, E. coli, and C. albicans and it was found out that the samples with higher amounts of active amino groups showed lower MIC. Cationised glucuronoxylan showed significantly higher antimicrobial activities against S. aureus in comparison to cationised arabinoxylan and nonmodified xylan samples. However, none of xylan samples was active against fungi. In order to analyze surface properties of solid surfaces, films from xylan (nonmodified and modified) water solution was formed by casting method. The surface chemical composition of films were investigated by x-ray photoelectron spectroscopy (XPS), and the results showed that films made from carboxymethylated xylans had significantly higher amounts of carbon fraction involved in O=C-O bonds, compared to nonmodified xylans. Such surface chemical structure caused higher surface free energy with higher electron-donor contribution and thus high hydrophilicity of these films. Films made by cationized xylans had higher amount of carbon involved in C-C and C-H bonds compared to nonmodified and lower surface free energy with increase of dispersive Lifshitz Van der Waals contribution. In order to thoroughly investigate the adsorption of xylans onto synthetic surfaces Quartz crystal microbalance with dissipation unit (QCM-D) was used. For these measurements model films were prepared from PET by spin coating technique. Adsorption studies were performed at different conditions, such as pH, concentration and ionic strength of xylan solutions. For all the chemically modified xylans the adsorption was improved at pH 5 and with increased ionic strength with divalent ions. The adsorption increased as well with increasing of xylan solution concentration. In order to improve binding of adsorbed xylans so-called anchoring polymers were applied. When anchoring polymers were applied, better adsorption and fixation of adsorbed layer was confirmed, thus the adsorbed masses of xylans after rinsing with water were significantly higher in comparison to the adsorption without immediate anchoring layer. On the basis of these results, real PET fabric surfaces were treated using chemically modified xylans. The xylan solutions were applied onto PET fabric samples using spray coating technique, which is the best approximate to the large-scale procedures. In the first step, PET fabric was activated by alkaline hydrolysis and after that, anchoring agents and carboxymethylated and/or cationized xylans were adsorbed. The success of these treatments was evaluated by the determination of negative and positive charge of the treated PET fabric samples by titration techniques, methylene blue and acid orange 7 adsorption methods, water contact angles and wettability determination. From the potentiometric titrations results it was clearly seen that each new adsorbed layer onto PET fabric totally screened the charge of the former one. FESEM images showed rather thick layers covering the
Keywords: hemicellulose, polyethylene terephthalate, glucuronoxylan, arabinoxylan, carboxymethylation, cationization, PET model films, quartz crystal microbalance, PET fabric, surface free energy, wettability, antimicrobial properties
Published in DKUM: 11.03.2016; Views: 2333; Downloads: 150
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