In this study, we report a green, one-step synthesis of fluorescent carbon quantum dots (PET-FCQDs) derived from polyethylene terephthalate (PET) waste using an environmentally friendly pyrolytic method. The PET-FCQDs were systematically characterized using techniques such as UV-Vis spectroscopy, fluorescence spectroscopy, ATR-FTIR, TGA, and fluorescence microscope, confirming their nanoscale size (2–50 nm), rich functional groups and thermal stability. Thermal stability and dynamics evaluated by the Coats–Redfern method showed endothermic reactions with an activation energy of 88.84–125.05 kJ/mol. Density functional theory studies showed a binding energy, highest occupied molecular orbital, lowest unoccupied molecular orbital, and energy gap of −675.39, −5.23, −5.07, and 0.17 eV, respectively. The as-synthesized PET-FCQDs demonstrated excellent optical properties with quantum yield ($\Phi$) of 49.6% and were applied as a dual-mode fluorescent sensing probe for the detection of Pd²⁺, ciprofloxacin (CIP), and fluoxetine (FLX) in aqueous systems via fluorescence quenching and enhancement mechanisms. For Pd²⁺, the fluorescence emission intensity at 470 nm was quenched proportionally to the increasing concentration, while CIP and FLX induced fluorescence enhancement. The Stern–Volmer analysis confirmed strong interaction between the analytes and PET-FCQDs, distinguishing dynamic quenching for Pd²⁺ and static interactions for CIP and FLX. The method exhibited linear detection ranges of 1–10 mg/L for Pd²⁺, 50–150 µg/L for CIP, and 100–400 ng/L for FLX, with corresponding limits of detection (LOD) of 1.26 mg/L, 3.3 µg/L, and 134 ng/L, respectively. Recovery studies in spiked tap water and river water samples demonstrated the practical applicability of PET-FCQDs, although matrix effects were observed, particularly for FLX. This work not only highlights a sustainable route for PET waste upcycling but also demonstrates the potential of PET-FCQDs as cost-effective, sensitive, and versatile fluorescent probes for environmental monitoring of heavy metal ions and pharmaceutical pollutants. Further optimization of the sensing platform could enhance its selectivity and performance in real-world applications.

During the manufacturing of wooden musical instruments, offcut wood pieces are inevitably generated. This study explores the potential of utilizing three types of these small offcut wood pieces, mahogany, maple, and rosewood, by converting them into polyurea through liquefied wood technology by proposing a novel approach to synthesizing bio-based polyurea. This polyurea is a durable polymer, offering long-term carbon fixation and thereby contributing to environmental sustainability. In this study, various liquefaction conditions as parameters, including the temperature, sulfuric acid content, mix solvent ratio, and liquefaction time, were investigated in relation to polyurea film properties. The relationship between the mechanical and thermal properties of the resulting films and the characteristics of the liquefied product was investigated. Notably, when the hydroxyl value of the liquefied product exceeded 300, the resulting polyurea derived from the liquefied product exhibited a high tensile strength of 25 MPa. In contrast, when the hydroxyl value was below 300, the polyurea derived from the liquefied product displayed a strain value of up to 150%, alongside an increased thermal decomposition temperature. These findings suggest that the properties of polyurea can be effectively tuned by manipulating the characteristics of the liquefied product, offering a promising approach to enhancing the value of offcut wood in instrument manufacturing.

Nanobubbles have emerged as a novel technology, yet their applications remain largely limited to cleaning and oxidation. This study explores the potential of ozone nanobubbles as a pretreatment method for liquefied wood. Wood meal was treated with ozone nanobubbles in tap water under three different conditions: room temperature, 50 °C, and room temperature followed by ultrasonic treatment. The treated samples were then compared with untreated wood meal through component analysis, FT-IR functional group evaluation, and X-Ray diffraction (XRD) analysis of cellulose crystallinity. In the liquefaction process, residue rates, FT-IR analysis, hydroxyl numbers, and viscosity were examined. Additionally, the mechanical properties of synthesized polyurea films were evaluated via tensile testing. The results showed a reduction in amorphous cellulose from 62.3% to 56.6% and hemicellulose from 42.8% to 35.9%, leading to liquefied wood with a high hydroxyl value from 341 KOH/mg to 387 KOH/mg and significantly lower viscosity from 684 cP to 264 cP. Furthermore, the polyurea films synthesized from the treated liquefied wood exhibited no deterioration in physical properties. These findings highlight ozone nanobubble pretreatment as a promising and industrially valuable process for producing low-residue, low-viscosity liquefied wood without compromising material performance.

Nowadays, climate change has become a serious concern, and more attention has been drawn to utilizing biomass sources instead of fossil sources and how petroleum chemical plastics should be reduced or replaced with bio-based materials. In this study, the optimized condition of liquefaction of driftwood was examined. There was a concern that driftwood might have some decay and chemical change. However, according to the Organic Micro Element Analyzer (CHN analyzer) test and Klason lignin and Wise methods, the results proved that lignin content (37.5%), holocellulose content (66.9%), and CHN compositions were very similar to regular wood. The lowest residue content of bio-polyols was produced using liquefaction conditions of 150 °C, reaction time of 180 min, catalyst content of 10%w/w, and 12.5%w/w driftwood loading. Polyurethane foam (PUF) derived from the liquefaction of driftwood and bio-based cyanate was prepared. The PUF prepared from the liquefaction of the driftwood exhibited slightly decreased thermal durability but was superior in terms of 3-time faster biodegradation and 2.8-time increased water adsorption rate compared to pure petroleum-based PUF. As a result, it was shown that driftwood can be identified as a biomass resource for biodegradable PUF.

Although bamboo is widely distributed in Japan, its applications are very limited due to its poor combustion efficiency for fuel. In recent years, the expansion of abandoned bamboo forests has become a social issue. In this research, the possibility of a liquefaction process with fast and efficient liquefaction conditions using moso bamboo as raw material was examined. Adding 20 wt% ethylene carbonates to the conventional polyethylene glycol/glycerol mixed solvent system, the liquefaction time was successfully shortened from 120 to 60 min. At the same time, the amount of sulfuric acid used as a catalyst was reduced from 3 wt% to 2 wt%. Furthermore, polyurethane foam was prepared from the liquefied product under these conditions, and its physical properties were evaluated. In addition, the filler effects of rice husk biochar and moso bamboo fine meals for the polyurethane foams were characterized by using scanning electron microscopy (SEM) and thermogravimetry and differential thermal analysis (TG-DTA), and the water absorption and physical density were measured. As a result, the water absorption rate of bamboo fine meal-added foam and the thermal stability of rice husk biochar-added foam were improved. These results suggested that moso bamboo meals were made more hydrophilic, and the carbon content of rice husk biochar was increased.

Recycled carbon fibres frequently exhibit degraded surface functionality owing to prior matrix removal processes, limiting their compatibility with contemporary epoxy resin systems. This study proposes a nanobubble-based surface treatment route designed to restore and enhance the surface characteristics of recycled carbon fibres without aggressive chemical oxidation. The study generated ozone and carbon dioxide nanobubbles in aqueous media and experimentally investigated the effects of nanobubble treatment on the surface properties and adhesive behaviour of recycled carbon fibres. Surface chemical changes were examined using X-ray photoelectron spectroscopy, which revealed an increase in oxygen-containing functional groups due to the nanobubble treatment, indicating improved surface polarity and potential for chemical interaction with epoxy networks. The practical effectiveness of the treatment was assessed via a pinhole pull-out test that served as an indirect measure of interfacial adhesion with epoxy resin, especially the combination of ozone nanobubbles and recycled carbon fibres. Notably, the nanobubble-treated recycled carbon fibres exhibited an increase in the adhesion compared with untreated recycled carbon fibres, rising from 84.5 ± 11.5 MPa to 138.5 ± 14.8 MPa, reflecting enhanced wetting behaviour and stronger fibre–matrix interfacial bonding. Overall, the proposed nanobubble processing route offers a mild, scalable, and environmentally favourable method for restoring surface reactivity in recycled carbon fibres, supporting their reintegration into high-performance composite applications.