Search Results (183)

Petrochemical complexes are spatially expansive and host diverse emission sources, making accurate monitoring of volatile organic compounds (VOCs) challenging using conventional two-dimensional methods. This study introduces Mobile-extraction Differential Optical Absorption Spectroscopy (Me-DOAS), a real-time, three-dimensional remote sensing technique for assessing benzene emissions in the Ulsan petrochemical complex, South Korea. A vehicle-mounted Me-DOAS system conducted monthly measurements throughout 2024, capturing data during four daily intervals to evaluate diurnal variation. Routes included perimeter loops and grid-based transects within core industrial zones. The highest benzene concentrations were observed in February (mean: 64.28 ± 194.69 µg/m³; geometric mean: 5.13 µg/m³), with exceedances of the national annual standard (5 µg/m³) in several months. Notably, nighttime and early morning sessions showed elevated levels, suggesting contributions from nocturnal operations and meteorological conditions such as atmospheric inversion. A total of 179 exceedances (≥30 µg/m³) were identified, predominantly in zones with benzene-handling activities. Correlation analysis revealed a significant relationship between high concentrations and specific emission sources. These results demonstrate the utility of Me-DOAS in capturing spatiotemporal emission dynamics and support its application in exposure risk assessment and industrial emission control. The findings provide a robust framework for targeted management strategies and call for integration with source apportionment and dispersion modeling tools. Full article

Rapid industrialization and urbanization have progressed in Korea, yet public attention to hazardous pollutants emitted from industrial complexes remains limited. With the increasing coexistence of industrial and residential areas, there is a growing need for real-time monitoring and management plans that account for the rapid dispersion of hazardous air pollutants (HAPs). In this study, we conducted spatiotemporal data collection and analysis for the first time in Korea using real-time measurements obtained through mobile extractive differential optical absorption spectroscopy (Me-DOAS) mounted on a solar occultation flux (SOF) vehicle. The measurements were conducted in the Saha Sinpyeong–Janglim Industrial Complex in Busan, which comprises the Sasang Industrial Complex and the Sinpyeong–Janglim Industrial Complex. BTEX compounds were selected as target volatile organic compounds (VOCs), and real-time measurements of both BTEX and fine particulate matter (PM) were conducted simultaneously. Correlation analysis revealed a strong relationship between PM₁₀ and PM_2.5 (r = 0.848–0.894), indicating shared sources. In Sasang, BTEX levels were associated with traffic and localized facilities, while in Saha Sinpyeong–Janglim, the concentrations were more influenced by industrial zoning and wind patterns. Notably, inter-compound correlations such as benzene–m-xylene and p-xylene–toluene suggested possible co-emission sources. This study proposes a GIS-based, three-dimensional air quality management approach that integrates variables such as traffic volume, wind direction, and speed through real-time measurements. The findings are expected to inform effective pollution control strategies and future environmental management plans for industrial complexes. Full article

Herein, electrospun nanofibers composed of polyaniline (PANI), polyethylene oxide (PEO), and Luffa cylindrica (LC) cellulose, reinforced with titanium dioxide (TiO₂) nanoparticles, were synthesized via electrospinning to investigate the effect of TiO₂ nanoparticles on PANI/PEO/LC nanocomposites and the effect of conductivity on nanofiber morphology. Cellulose extracted from luffa was added to the PANI/PEO copolymer solution, and two different ratios of TiO₂ were mixed into the PANI/PEO/LC biocomposite. The morphological, vibrational, and thermal characteristics of biocomposites were systematically investigated using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). As anticipated, the presence of TiO₂ enhanced the electrical conductivity of biocomposites, while the addition of Luffa cellulose further improved the conductivity of the cellulose-based nanofibers. FTIR analysis confirmed chemical interactions between Luffa cellulose and PANI/PEO matrix, as evidenced by the broadening of the hydroxyl (OH) absorption band at 3500–3200 cm⁻¹. Additionally, the emergence of characteristic peaks within the 400–1000 cm⁻¹ range in the PANI/PEO/LC/TiO₂ spectra signified Ti–O–Ti and Ti–O–C vibrations, confirming the incorporation of TiO₂ into the biocomposite. SEM images of the biocomposites reveal that the thickness of nanofibers decreases by adding Luffa to PANI/PEO nanofibers because of the nanofibers branching. In addition, when blending TiO₂ nanoparticles with the PANI/PEO/LC biocomposite, this increment continued and obtained thinner and smother nanofibers. Furthermore, the incorporation of cellulose slightly improved the crystallinity of the nanofibers, while TiO₂ contributed to the enhanced crystallinity of the biocomposite according to the XRD and DCS results. Similarly, the TGA results supported the DSC results regarding the increasing thermal stability of the biocomposite nanofibers with TiO₂ nanoparticles. These findings demonstrate the potential of PANI/PEO/LC/TiO₂ nanofibers for advanced applications requiring conductive and structurally optimized biomaterials, e.g., for use in humidity or volatile organic compound (VOC) sensors, especially where flexibility and environmental sustainability are required. Full article

We investigated a novel natural dye-sensitized solar cell (DSSC) utilizing gadolinium ruthenate pyrochlore oxide Gd₂Ru₂O₇ (GRO) as a photoanode and compared its performance to the TiO₂-Gd₂Ru₂O₇ (TGRO) combined-layer configuration. The films were fabricated using the spin-coating technique, resulting in spherical grains with an estimated mean diameter of 0.2 µm, as observed via scanning electron microscopy (SEM). This innovative photoactive gadolinium ruthenate pyrochlore oxide demonstrated strong absorption in the visible range and excellent dye adhesion after just one hour of exposure to natural dye. X-ray diffraction confirmed the presence of the pyrochlore phase, where Raman spectroscopy identified various vibration modes characteristic of the pyrochlore structure. Incorporating Gd₂Ru₂O₇ as the photoanode significantly enhanced the overall efficiency of the DSSCs. The device configuration FTO/compact-layer/Gd₂Ru₂O₇/Hibiscus-sabdariffa/electrolyte(I⁻/I₃⁻)/Pt achieved a high efficiency of 9.65%, an open-circuit voltage (Voc) of approximately 3.82 V, and a current density of 4.35 mA/cm² for an active surface area of 0.38 cm². A mesoporous TiO₂-based DSSC was fabricated under the same conditions for comparison. Using impedance spectroscopy and cyclic voltammetry measurements, we provided evidence of the mechanism of conductivity and the charge carrier’s contribution or defect contributions in the DSSC cells to explain the obtained Voc value. Through cyclic voltammetry measurements, we highlight the redox activities of hibiscus dye and electrolyte (I⁻/I₃⁻), which confirmed electrochemical processes in addition to a photovoltaic response. The high and unusual obtained Voc value was also attributed to the presence in the photoanode of active dipoles, the layer thickness, dye concentration, and the nature of the electrolyte. Full article

In this study, a terahertz microfluidic multi-band sensor was designed. Unlike previous microfluidic absorption sensors that rely on dipole resonance, the proposed sensor uses a physical mechanism for absorption by exciting higher-order lattice resonances in microfluidic structures. With a Fabry–Perot cavity, the sensor can form an absorption peak with a high quality factor (Q) and narrow full width at half maximum (FWHM). A high Q value and a narrow FWHM are valuable in the field of sensing and provide strong support for high-precision sensing. On this basis, the sensing performance of the device was investigated. The simulation results clearly show that the absorption sensor has ultra-high sensitivity, which reaches 400 GHz/Refractive Index Unit (RIU). In addition, the sensor generates three absorption peaks, overcoming the limitations of a single frequency band in a composite resonance mode and multidimensional frequency response, which has potential application value in the field of volatile organic compound (VOC) sensing. Full article

To overcome the shortcomings of traditional polyurethane, such as poor weather resistance and susceptibility to hydrolysis, this study systematically explores the preparation techniques of organic silicon-modified polyurethane and its application in intelligent sports fields. By introducing siloxane into the polyurethane matrix through copolymerization, physical blending, and grafting techniques, the microphase separation structure and interfacial properties of the material are effectively optimized. In terms of synthesis processes, the one-step method achieves efficient preparation by controlling the isocyanate/hydroxyl molar ratio (1.05–1.15), while the prepolymer chain extension method optimizes the crosslinked network through dual reactions. The modified material exhibits significant performance improvements: tensile strength reaches 60 MPa, tear resistance reaches 80 kN/m, and the elastic recovery rate ranges from 85% to 92%, demonstrating outstanding weather resistance. In sports field applications, the 48% impact absorption rate meets the requirements for athletic tracks, wear resistance of <15 mg suits gym floors, and the impact resistance for skate parks reaches 55%–65%. Its environmental benefits are notable, with volatile organic compounds (VOC) <50 g/L and a recycling rate >85%, complying with green building material standards. However, its development is still constrained by multiple factors: insufficient material interface compatibility, a comprehensive cost of 435 RMB/m², and the lack of a quality evaluation system. Future research priorities include constructing dynamic covalent crosslinked networks (e.g., self-healing systems), adopting bio-based raw materials to reduce carbon footprint by 30%–50%, and integrating flexible sensing technologies for intelligent responsiveness. Through multidimensional innovation, this material is expected to evolve toward multifunctionality and environmental friendliness, providing core material support for the intelligent upgrading of sports fields. Full article

To utilize a huge amount of oil palm trunk (Elaeis guineensis) biomass as wall insulation, its dimensional stability and insulation properties need to be improved. Thermal modification (TM) (without compression or densification) is one of the efficient methods widely used for improving insulation properties and dimensional stability of wood material, but such an existing method requires a complex system. In this work, the TM of oil palm wood with an initial density of 219 ± 34 kg/m³ was performed at 200 °C using a hot press machine. The optimum heat-treatment durations (2 h, 4 h, and 6 h) for their potential for insulation wall applications were explored. TM improved dimensional stability, sound-absorption coefficient, and thermal conductivity by approximately 66.7%, 26.7%, and 24.6%, respectively, but increased volatile organic compound (VOCs) emission compared with the control. Heat-treatment duration notably affected mass loss, density, and thermal conductivity. Compared with available natural material-based insulation walls, TM oil palm showed better insulation performance for all treatment durations. Thus, the heat-treatment duration of 2 h is suggested to save the energy consumption in the heat-treatment process while still achieving the same level of sound absorption, dimensional stability, and VOC emission performance as that of the long heat-treatment duration. Full article

The growing volume of plastic waste from end-of-life vehicles presents environmental concerns, driving efforts to integrate recycled plastics. This study investigates the possibility of using recycled plastic from automotive parts (painted and unpainted bumpers, fuel tanks) as a 10% filler in the core layer of three-layer particleboards (P) and evaluates its impact on physical properties (water absorption—WA and thickness swelling—TS), mechanical properties (internal bonding strength—IB, modulus of rupture—MOR, modulus of elasticity—MOE and screw driving torque—SDT) and volatile organic compounds—VOC emissions. The boards were produced using conventional hot-pressing technology and analyzed according to applicable standards. Based on the results, the density of the reference (P) was 0.72 g·cm⁻³, while wood–plastic composites ranged from 0.70 g·cm⁻³ to 0.72 g·cm⁻³. After 24 h, WA reached 40% for reference (P) and from 36.9% (for (P) containing unpainted bumpers) to 41.9% (for (P) containing fuel tanks). TS reached 18% for (P) and from 16.8% (for (P) containing unpainted bumpers and fuel tanks) to 18.1% (for (P) containing painted bumpers). Plastic is a hydrophobic material and it is assumed that by increasing the proportion of plastic filler in the particleboards, the WA and TS of prepared boards will decrease. From the point of view of mechanical properties, values for (P) containing plastic filler were slightly lower compared to reference (P). The lowest value of IB (0.39 MPa) were reached for (P) containing painted bumpers. Plastic surface treatment could interfere with adhesion between the plastic and adhesive, weakening the bond in the core layer. For this reason, is preferable to use unpainted fillers, which provide better adhesive properties and higher structural integrity. VOC emissions from wood components consisted primarily of monoterpenes such as α-pinene, 3-carene and limonene. Adding 10% plastic to the particleboard did not increase overall VOC emissions. On the other hand, combining wood and plastic particles resulted in a reduction in overall VOC emissions. The findings confirm that recycled automotive plastics can be effectively incorporated into particleboards, maintaining standard performance while reducing reliance on virgin wood materials, making them a viable and sustainable alternative for furniture and interior applications. Full article

The tungsten (W)-modified TiO₂ films were fabricated on the fluorine-doped TiO₂ substrates using the sol–gel process. The influences of W dopant on the photovoltaic properties of the tungsten-modified TiO₂ DSSC were analyzed, too. The crystallization and dye absorption of tungsten-modified TiO₂ thin films increased more than those of the undoped TiO₂ thin films. Furthermore, the optimal performances of the V_oc, J_sc, fill factor, and efficiency of the DSSC with tungsten-modified TiO₂ thin films were 0.68 V, 16.28 mA/cm², 65.5%, and 7.03%, respectively. The enhancement was mainly due to the improved crystallinity and increased dye adsorption of the tungsten-modified TiO₂ thin films, which contributed to improving the efficiency of the dye-sensitized solar cell. Full article

This study presents an effective strategy to enhance the efficiency and stability of perovskite solar cells (PSCs) by integrating neodymium-doped upconversion nanoparticles (UCNPs) coated with a TiO₂ shell into the mesoporous electron transport layer. The incorporation of neodymium (Nd³⁺) as a novel sensitizer shifts the near-infrared (NIR) absorption band away from the water vapor absorption region in the solar spectrum. This modification enables UCNPs to efficiently convert NIR light into ultraviolet (UV) and blue wavelengths, which are readily absorbed by TiO₂, generating additional charge carriers and improving photovoltaic performance. The optimized PSCs, fabricated by blending 30% UCNPs@TiO₂ with commercial TiO₂ paste, achieved a peak power conversion efficiency (PCE) of 21.71%, representing a 20.4% improvement over the control (18.04%). This enhancement included a 0.9% increase in the open-circuit voltage (V_oc), a 6.6% rise in the short-circuit current density (J_sc), and an 11.9% boost in the fill factor (FF). Additionally, the optimized PSCs exhibited remarkable stability, retaining over 90% of their initial PCE after 900 h in humid conditions, compared to only 70% for the control. These improvements result from enhanced light absorption, reduced moisture infiltration, and lower defect-related recombination. This approach provides a promising pathway for developing highly efficient and durable PSCs. Full article

Formaldehyde is the most abundant carbonyl globally and the biggest driver of cancer risk in the United States among hazardous air pollutants. Ambient formaldehyde concentration measurements are generally sparse due to high measurement costs and limited measurement infrastructure. Recent studies have used low-cost air quality sensors to affordably improve spatial coverage and provide real-time measurements. Our previous research evaluated the laboratory performance of a low-cost electrochemical formaldehyde sensor (Sensirion SFA30) over formaldehyde concentrations ranging from 0 to 76 ppb. The sensors exhibited good linearity of response, a low limit of detection, and good accuracy in detecting formaldehyde. This study evaluated the cross-sensitivity of the SFA30 and the Gravity sensors (electrochemical formaldehyde sensors) over formaldehyde concentrations ranging from 0 to 326 ppb in a laboratory evaluation system, with broadband cavity-enhanced absorption spectroscopy used to obtain the reference measurements. We evaluated the sensors in a mixture of formaldehyde with five outdoor trace gases (CO, NO, NO₂, O₃, and isobutylene) and two indoor VOCs (methanol and isopropyl alcohol). The results suggest that the Gravity sensors may be useful for outdoor formaldehyde measurements when formaldehyde levels are well above background levels and that the SFA30 sensors may be useful screening tools for indoor environments, if properly calibrated. Full article

In this study, we present a sponge-like lipophilic gel crosslinked with a branched crosslinker as an absorbent for VOC removal. The gel was synthesized by crosslinking the monomer 3-(trimethoxysilyl)propyl methacrylate (TMSPMA) with the branched crosslinker poly(2-propyl aspartamide) grafted methacrylate (PPA-g-MA). The grafted crosslinker, PPA-g-MA, was prepared by introducing acrylate groups as crosslinking moieties to the poly(succinimide) precursor for poly(2-propyl aspartamide) (PPA), which serves as a hydrophobic backbone. Lipophilic gels were synthesized with varying TMSPMA monomer concentrations and freeze-dried to form a porous structure. To evaluate VOC absorption, the toluene removal efficiency of the sponge-like lipophilic gel was tested in a continuous gas flow system. As a result, the optimal TMSPMA monomer content for maximizing toluene removal efficiency was determined. This result suggests that while an increase in silicon content generally enhances VOC removal efficiency, the porous structure of sponge-like lipophilic gels plays a more crucial role in absorption capacity. The collapse of the porous structure, caused by excessive silicon content making the material more rubber-like, explains why there exists an optimal monomer content for effective VOC absorption. Overall, these findings provide valuable insights for developing high-performance VOC absorbents. Full article

In this study, four various titanium dioxide/cuprum oxide (TiO₂/Cu_xO) photovoltaic structures deposited on glass/indium tin oxide (ITO) substrates using the direct-current (DC) reactive magnetron sputtering technique were annealed in air. In our previous work, the deposition parameters for different buffer layer configurations were first optimized to enhance cell fabrication efficiency. In this paper, the effects of post-deposition annealing at 150 °C in air on the optical properties and I-V characteristics of the prepared structures were examined. As a result, significant changes in optical properties and a meaningful improvement in performance in comparison to unannealed cells were observed. Air annealing led to an increase in the reflection coefficient of the TiO₂ layer for three out of four structures. A similar increase in the reflection of the Cu_xO layer occurred after heating for two out of four structures. Transmission of the TiO₂/Cu_xO photovoltaic structures also increased after heating for three out of four samples. For two structures, changes in both transmission and reflection resulted in higher absorption. Moreover, annealing the as-deposited structures resulted in a maximum relative increase in open-circuit voltage (V_oc) by 294% and an increase in short-circuit current (I_sc) by 1200%. The presented article gives some in-depth analysis of these reported changes in character and origin. Full article

Diagnosing ozone (O₃) formation sensitivity using tropospheric observations of O₃ and its precursors is important for formulating O₃ pollution control strategies. Photochemical reactions producing O₃ occur at the earth’s surface and in the elevated layers, indicating the importance of diagnosing O₃ formation sensitivity at different layers. Synchronous measurements of tropospheric O₃ and its precursors nitrogen dioxide (NO₂) and formaldehyde (HCHO) were performed in urban Hefei to diagnose O₃ formation sensitivity at different atmospheric layers using multi-axis differential optical absorption spectroscopy observations. The retrieved surface NO₂ and O₃ were validated with in situ measurements (correlation coefficients (R) = 0.81 and 0.80), and the retrieved NO₂ and HCHO vertical column densities (VCDs) were consistent with TROPOMI results (R = 0.81 and 0.77). The regime transitions of O₃ formation sensitivity at different layers were derived using HCHO/NO₂ ratios and O₃ profiles, with contributions of VOC-limited, VOC-NO_x-limited, and NO_x-limited regimes of 74.19%, 7.33%, and 18.48%, respectively. In addition, the surface O₃ formation sensitivity between HCHO/NO₂ ratios and O₃ (or increased O₃, ΔO₃) had similar regime transitions of 2.21–2.46 and 2.39–2.71, respectively. Moreover, the O₃ formation sensitivity of the lower planetary boundary layer on polluted and non-polluted days was analyzed. On non-polluted days, the contributions of the VOC-limited regime were predominant in the lower planetary boundary layer, whereas those of the NO_x-limited regime were predominant in the elevated layers during polluted days. These results will help us understand the evolution of O₃ formation sensitivity and formulate O₃ mitigation strategies in the Yangtze River Delta region. Full article

This paper explores a novel group of D-π-A configurations that has been specifically created for organic solar cell applications. In these material compounds, the phenothiazine, the furan, and two derivatives of the thienyl-fused IC group act as the donor, the π-conjugated spacer, and the end-group acceptors, respectively. We assess the impact of substituents by introducing bromine atoms at two potential substitution sites on each end-group acceptor (EG1 and EG2). With the donor and π-bridge held constant, we have employed density functional theory and time-dependent DFT simulations to explore the photophysical and optoelectronic properties of tailored compounds (M1–M6). We have demonstrated how structural modifications influence the optoelectronic properties of materials for organic solar cells. Moreover, all proposed compounds exhibit a greater V_oc exceeding 1.5 V, a suitable HOMO-LUMO energy gap (2.14–2.30 eV), and higher dipole moments (9.23–10.90 D). Various decisive key factors that are crucial for exploring the properties of tailored compounds—frontier molecular orbitals, transition density matrix, electrostatic potential, open-circuit voltage, maximum absorption, reduced density gradient, and charge transfer length (D_index)—were also explored. Our analysis delivers profound insights into the design principles of optimizing the performance of organic solar cell applications based on halogenated material compounds. Full article