The morphology of sheep wool applied as organic fertilizer biodegraded in the soil was examined. The investigations were conducted in natural conditions for unwashed waste wool, which was rejected during sorting and then chopped into short segments and wool pellets. Different types of wool were mixed with soil and buried in experimental plots. The wool samples were periodically taken and analyzed for one year using Scanning Electron Microscopy (SEM) and Energy-dispersive X-ray Spectroscopy (EDS). During examinations, the changes in the fibers' morphology were observed. It was stated that cut wool and pellet are mechanically damaged, which significantly accelerates wool biodegradation and quickly destroys the whole fiber structure. On the contrary, for undamaged fibers biodegradation occurs slowly, layer by layer, in a predictable sequence. This finding has practical implications for the use of wool as an organic fertilizer, suggesting that the method of preparation can influence its biodegradation rate. (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(SEM)(sic)(sic)(sic)(sic)(sic)X(sic)(sic)(sic)(sic)(EDS)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic). (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic), (sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic)(sic).

Plastic pollution is a universal problem, and microbial management of plastic waste represents a promising area of biotechnological research. This study investigated the ability of bacterial strains which were isolated from landfill soil to degrade Low-Density Polyethylene (LDPE). Strains obtained via serial dilution were screened for LDPE degradation on Minimal Essential Medium (MEM) with hexadecane. Nine isolates producing clearance zones on hexadecane-supplemented MEM were further tested for biofilm formation on LDPE sheets. High cell surface hydrophobicity isolates (>10%) were selected for detailed biodegradation studies. The C-8 bacterial isolate showed the highest LDPE weight loss (3.57%) and exhibited maximum laccase (0.0219 U/mL) and lipase activity (19 mm) among all bacterial isolates after 30 days. Weight loss was further validated by FTIR and SEM analysis. FTIR analysis revealed that in comparison to control, changes in peak were observed at 719 cm-1 (C-H bending), 875.67 cm-1 (C-C vibrations), 1307.07 cm-1 (C-O stretching), 1464.21 cm-1 (C-H bending), 2000-1650 cm-1 (C-H bending), 2849.85 cm-1 (C-H stretching) in microbial treated LDPE sheets. The treated LDPE also displayed increase in carbonyl index (upto 2.5 to 3 folds), double bond index (1 to 2-fold) and internal double bond index (2 to 2.5-fold) indicating oxidation and chain scission in the LDPE backbone. SEM analysis showed substantial micrometric surface damage on the LDPE film, with visible cracks and grooves. Using 16S rRNA gene sequencing, the C-8, C-11, C-15 and C-19 isolate were identified as Bacillus paramycoides, Micrococcus luteus, Bacillus siamensis and Lysinibacillus capsica, respectively.

There is currently a growing interest in biopolymers, such as bacterial cellulose and thermoplastic starch, which are renewable and abundantly available in nature. This study investigated the multilayer sandwich composite with thermoplastic starch and bacterial cellulose, using water (TPS/BC-w) and glycerol (TPS/BC-g) as coupling agents. The composites produced by compression molding resulted in a homogeneous, transparent and flexible structure. TPS/BC-w showed superior mechanical property and better adhesion compared to TPS/BC-g. Therefore, the permeability, biodegradation, hydrothermal aging and stability analyses were conducted only for TPS/ BC-w. The water vapor permeability of TPS/BC-w is 6.7 times lower than that of thermoplastic starch, indicating better barrier performance. Thermoplastic starch and bacterial cellulose degraded in about 9 days, and TPS/BCw degraded in 60 days. Biodegradation analysis by COQ release confirmed the complete biodegradation process, with COQ emissions of 57 %, 42.5 % and 39.6 % after 120 days for thermoplastic starch, bacterial cellulose and TPS/BC-w, respectively. TPS/BC-w remained intact for more than a year, in an environment without direct contact with soil or water. These results indicate that TPS/BC-w composed of natural macromolecules may exhibit functional properties and is useful for applications such as short-shelf-life packaging, particularly for dry products, due to its barrier properties and controlled biodegradability.

Pesticide contamination has become a major environmental concern with organophosphates such as chlorpyrifos emerging as major pollutants posing significant risks to both ecosystems and human health. Chlorpyrifos is widely used in agriculture to control pests, however due to its persistence, its accumulation in soils can lead to long-term environmental damage. The objective of this study was to isolate and characterize chlorpyrifos-degrading bacteria from a tobacco field exposed to intensive pesticide use in T & uuml;rkiye. To achieve this, a selective enrichment strategy was employed to promote the growth of chlorpyrifos-degrading microorganisms. Two distinct experimental setups were established to target both normally growing and slower-growing bacteria: the first involved a 4-week incubation with weekly subculturing as described in the literature, while the second applied an 8-week incubation with biweekly subculturing. At the end of the enrichment period, bacterial loads were compared between the two groups. Four of the nine bacterial isolates were obtained from the newly tested long-term setup. Among all isolates, members of the genus Pseudomonas exhibited the best adaptation to the prolonged enrichment conditions. Additionally, isolates belonging to the genera Klebsiella, Sphingobacterium, and Peribacillus were isolated from the normally growing group. Two isolates (AB4 & AB15), identified as Sphingobacterium thalpophilum, were determined to be novel chlorpyrifos degraders. This is the first reported study from T & uuml;rkiye focusing on the biodegradation of chlorpyrifos by native soil bacteria. The findings revealed that various ecological areas, constitute potential sources for new microbial metabolic processes and these bacterial strains can be used in bioremediation studies.

In this work, poly(L-lactic acid)/thermoplastic alginate (PLA/TPA) biocomposites were prepared through a melt blending method. The TPA was initially prepared using glycerol as a plasticizer. The effects of TPA content on the interactions between blend components, thermal properties, phase morphology, mechanical properties, hydrophilicity, and biodegradation properties of biocomposites were systematically investigated. Fourier transform infrared (FTIR) spectroscopy analysis corroborated the interaction between the blend components. The addition of TPA enhanced the nucleating effect for PLA, as determined by differential scanning calorimetry (DSC). Scanning electron microscopy (SEM) revealed poor phase compatibility between the PLA and TPA phases. The thermal stability and mechanical properties of the biocomposites decreased with the addition of TPA, as demonstrated by thermogravimetric analysis (TGA) and tensile tests, respectively. The hydrophilicity and soil burial degradation rate of biocomposites increased significantly as the TPA content increased. These results indicated that PLA/TPA biocomposites degraded faster than pure PLA, making them suitable for single-use packaging, but this necessitates careful optimization of TPA content to balance mechanical properties and soil burial degradation rate for practical single-use applications.

Most self-healing rubber composites are produced through hydrogen or ionic bonding. In this study, high-strength self-healing composites were prepared by using guar gum (GG) powder as a filler. The fundamental properties of GG were analyzed using various techniques, including scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and thermogravimetric analysis, before its use. After incorporating GG into epoxidized natural rubber (ENR), various properties of the rubber composites, including mechanical strength, self-healing efficiency, and biodegradability, were evaluated at different GG concentrations. The results revealed that GG has a structure similar to polysaccharides, containing hydroxy functional groups in its chemical structure. As GG was added to ENR, both hardness and tensile strength increased, with the maximum tensile strength of similar to 1.03 N/mm(2) (approximately 91.3% increase) observed at 3 parts per hundred rubber (phr) of GG. Notably, self-healing efficiency improved with increasing GG content up to 1 phr (approximately an 81.8% increase), after which it began to decrease. In biodegradability tests, the ENR/GG composites exhibited significant degradation over a 360-day soil burial period, with the formulation containing 5 phr of GG showing the highest weight loss (approximately 40.4%). The rubber composites with good self-healing and mechanical properties could have potential applications in various fields, including medical devices and food packaging. Moreover, the unique properties of the composite could be adapted for use in smart materials or flexible electronics, where self-healing and biodegradability can extend device lifetimes and reduce waste.

(1) Background: Plastic contamination is on the rise, despite ongoing research focused on alternatives such as bioplastics. However, most bioplastics require specific conditions to biodegrade. A promising alternative involves using microorganisms isolated from landfill soils that have demonstrated the ability to degrade plastic materials. (2) Methods: Soil samples were collected, and bacteria were isolated, characterized, and molecularly identified. Their degradative capacity was evaluated using the zone of clearing method, while their qualitative and structural degradative activity was assessed in a liquid medium on poly(butylene succinate) (PBS) films prepared by the cast method. (3) Results: Three strains-Bacillus cereus CHU4R, Acinetobacter baumannii YUCAN, and Pseudomonas otitidis YUC44-were selected. These strains exhibited the ability to cause severe damage to the microscopic surface of the films, attack the ester bonds within the PBS structure, and degrade lower-weight PBS molecules during the process. (4) Conclusions: this study represents the first report of strains isolated in Yucat & aacute;n with plastic degradation activity. The microorganisms demonstrated the capacity to degrade PBS films by causing surface and structural damage at the molecular level. These findings suggest that the strains could be applied as an alternative in plastic biodegradation.

Recycling paper sludge waste (PSW) into inexpensive sheets for applications in household interiors, construction, and footwear is a sustainable approach to resource utilisation and pollution reduction. A flexible recycled sheet (FRS) in board form was developed using cellulosic-based PSW from the paper industry and a styrene-butadiene rubber (SBR) binder. Various SBR concentrations were tested to determine the optimal amount for superior mechanical properties. The produced FRS was characterised using Fourier transform infrared spectroscopy, thermogravimetric analysis, high-resolution scanning electron microscopy, and energy-dispersive X-ray spectroscopy. FRS made with 1000 g of PSW:300 ml of SBR exhibited enhanced mechanical properties, including tensile strength (62.32 +/- 0.51 MPa), elongation at break (51.99 +/- 0.94%), tearing strength (17.76 +/- 0.45 N/mm), and flexibility (6.98 +/- 0.24%). A biodegradation study, conducted per ASTM D 5988-03, assessed environmental impact by measuring carbon-to-CO2 conversion in soil over 90 days. All FRS samples showed similar degradation within the first 30 days, with FRS 5 degrading significantly faster thereafter due to its higher cellulose and hemicellulose content. This highlights the potential of PSW-based FRS as an environmentally friendly and mechanically robust material for diverse applications.

The Ceibapentandra shell, a by-product of the kapok tree used in the mattress industry, is generated during fiber extraction from seed pods. The improper disposal of Ceibapentandra shells after cotton removal, such as through landfilling or burning, contributes to environmental pollution. However, their biodegradable nature and potential for bio-based applications, including reinforcement in bioplastics and composites, present sustainable solutions for waste management and enhance the sustainability of the kapok industry. This study investigates the fabrication of biofilms by reinforcing polylactic acid (PLA) with varying concentrations (5, 10, 15, 20, and 25 wt.%) of Ceibapentandra shell powder (CPSP) using the solution casting method. The incorporation of CPSP enhances the crystalline structure of the films, while the strong interfacial bonding between PLA and CPSP improves chemical interactions. Notably, the biocomposite with 20 wt.% CPSP demonstrated significant improvements in mechanical properties, achieving a 45.66% increase in tensile strength and a 40.44% increase in tensile modulus compared to pure PLA. Optical analyses revealed enhanced UV shielding, with a 61% reduction in UV transmittance and favorable values for %haze, %transparency, and % opacity. Despite the hydrophilic nature of CPSP resulting in higher water vapor absorption (up to 75.48%), biodegradation studies indicated substantial weight loss, with PLA/25 wt.% CPSP films showing 48% degradation in soil and 34% in vegetative waste. Furthermore, these biofilms exhibited robust antimicrobial activity, achieving a 94% reduction in Escherichiacoli within 24 h. Overall, the results suggest that PLA/CPSP biofilms are sustainable materials for packaging applications.

Poly(butylene adipate-co-terephthalate) (PBAT) and graphene oxide (GO) nanocomposite films were prepared by extrusion to evaluate their potential as films for food packaging. The films were prepared with contents of 0.05, 0.1, and 0.25% in mass of GO by solid-solid deposition methodology. It was verified that GO did not modify the hydrophobicity and crystallinity degree of PBAT. The reduction of molecular weight due to GO incorporation was verified, and it could be the main reason for the observed decrease in tensile strength and increase in elongation. The nanofiller permitted ultraviolet blocking, thermal stability, and oxygen barrier improvements without compromising film visibility. Compared to the neat PBAT film, the oxygen permeability coefficient was reduced by 13.6% for PBAT/GO0.25. The elongation and tenacity were also improved by 90% and 33%, respectively, for the highest concentration of GO (0.25%). Besides, GO at 0.25% accelerated the mineralization rate of PBAT in soil, probably due to the lower molecular weight of nanocomposites in relation to the neat polymer. The preliminary information obtained in this work indicates that the level of PBAT hydrolytic degradation during the extrusion process was not high enough to avoid its application in food packaging because the obtained thermal, mechanical, and ultraviolet (UV) barriers still indicate an exciting balance of properties for this purpose, which can even be improved with future research.