Search Results (161)

The rapid increase in polystyrene (PS) production has led to substantial growth in plastic waste, posing serious environmental and waste management challenges. Current disposal techniques are unsustainable, relying heavily on harsh conditions, high energy input, and generating environmentally harmful byproducts. This review critically discusses alternative green approaches for PS treatment through photocatalytic and non-photocatalytic upcycling methods. Photocatalytic methods utilize light energy (UV, visible, or broad-spectrum irradiation) to initiate radical reactions that cleave the inert carbon backbone of PS. In contrast, non-photocatalytic strategies achieve backbone degradation without direct light activation, often employing catalysts and thermal energy. Both approaches effectively transform PS waste into higher-value compounds, such as benzoic acid and acetophenone, though yields remain moderate for most reported methods. Current limitations, including catalyst performance, low yields, and impurities in real-world PS waste, are highlighted. Future directions toward enhancing the efficiency, selectivity, and scalability of PS upcycling processes are proposed to address the growing plastic waste crisis sustainably. Full article

A comparison of two synthesis methods for depositing Au nanoparticles onto TiO₂ was performed: (1) impregnation with HAuCl₄ followed by thermal treatment in argon, and (2) magnetron sputtering from a Au disc. The obtained materials were used for acetaldehyde decomposition in a high temperature reaction chamber and ch aracterised by UV-Vis/DR, XPS, XRD, SEM, and photoluminescence measurements. The process was carried out using an air/acetaldehyde gas flow under UV or UV-Vis LED irradiation. The mechanism of acetaldehyde decomposition and conversion was elaborated by in situ FTIR measurements of the photocatalyst surface during the reaction. Simultaneously, concentration of acetaldehyde in the outlet gas was monitored using gas chromatography. All the Au/TiO₂ samples showed absorption in the visible region, with a maximum around 550 nm. The plasmonic effect of Au nanoparticles was observed under UV-Vis light irradiation, especially at elevated temperatures such as 100 °C, for Au/TiO₂ prepared by the magnetron sputtering method. This resulted in a significant increase in the conversion of acetaldehyde at the beginning, followed by gradual decrease over time. The collected FTIR spectra indicated that, under UV-Vis light, acetaldehyde was strongly adsorbed onto Au/TiO₂ surface and formed crotonaldehyde or aldol. Under UV, acetaldehyde was mainly adsorbed in the form of acetate species. The plasmonic effect of Au nanoparticles increased the adsorption of acetaldehyde molecules onto TiO₂ surface, while reducing their decomposition rate. The increased temperature of the process enhanced the decomposition of the acetaldehyde. Full article

Microbial contamination of food can lead to faster spoilage and infections. Therefore, disinfection processes are required that have a low detrimental effect on the nutritional content. Concerning radiation disinfection, two spectral ranges have recently become important. The Far-UVC spectral range, with a wavelength below 230 nm and visible violet light. In this study, leaf spinach was used to investigate the extent to which these radiations inactivate Escherichia coli, but also to determine if the vitamin C or chlorophyll content was reduced. Frozen spinach leaves (Spinacia oleracea) were contaminated with E. coli × pGLO and irradiated with either a 222 nm krypton chloride lamp or 405 nm LEDs. The achieved bacterial reduction was determined by plating the irradiated samples on agar plates and subsequent colony counting. The vitamin C concentration was determined by means of redox titration, and the concentrations of chlorophyll a and chlorophyll b were determined using spectrometry. Both irradiations exhibited a strong antimicrobial impact on E. coli. The average log reduction doses were about 19 mJ/cm² (222 nm) and 87 J/cm² (405 nm), respectively. The vitamin C concentration decreased by 30% (222 nm) or 20% (405 nm), and the chlorophyll concentrations decreased by about 25%. Both irradiation approaches are able to substantially reduce microorganisms on spinach leaves by two orders of magnitude, but this is associated with a reduction in the nutrient content. Full article

In this study, chromium ferrite (FeCr; CrFe₂O₄) nanoparticles supported on activated carbon (AC), obtained from agricultural olive mill solid waste, were synthesized via a simple hydrothermal process. The structural, morphological, optical, and chemical properties of the FeCr/AC composite were characterized using XRD, SEM, EDX, DRS, BET, and FTIR techniques. The FeCr/AC composite was applied as a heterogeneous photo-Fenton catalyst for the degradation of methylene blue (MB) dye in an aqueous solution under 25 W visible-light LED irradiation. Critical operational factors, such as FeCr/AC dosage, pH, MB concentration, and H₂O₂ levels, were optimized. Under optimal conditions, 97.56% of MB was removed within 120 min of visible-light exposure, following pseudo-first-order kinetics. The composite also exhibited high efficiency in degrading methyl orange dye (95%) and tetracycline antibiotic (88%) within 180 min, with corresponding first-order rate constants of 0.0225 min⁻¹ and 0.0115 min⁻¹, respectively. This study highlights the potential of FeCr/AC for treating water contaminated with dyes and pharmaceuticals, in line with the Sustainable Development Goals (SDGs) for water purification. Full article

Recently, the urgency of combating antibiotic-resistant bacteria, viruses, and other pathogens has dramatically increased. With the development of nanotechnology, significant hopes are placed on nanoparticles with antimicrobial properties. The efficiency of such materials can be significantly enhanced through light-activated processes. In this study, we prepared composite ZnO-Ag nanoparticles and tested their ability to inhibit Staphylococcus aureus bacteria. The composite ZnO-Ag nanoparticles were fabricated using pulsed laser ablation of Zn and Ag targets in water using a nanosecond pulsed laser. During antibacterial tests, light-enhanced activation of the nanoparticles was achieved using low-power near UV (375 nm) and blue visible (410 nm) LED irradiation. For comparison, similar laser-fabricated ZnO nanoparticles were also tested. The combined use of nanoparticles and LED irradiation significantly increased the generation of reactive oxygen species. As a result, low nanoparticle concentrations (0.05 g/L) and low-power LED irradiation (0.17–0.22 W) significantly reduced the concentration of Staphylococcus aureus bacteria, including experiments with visible light irradiation. Compared to their ZnO counterparts, the use of ZnO-Ag composite particles led to an additional increase in antimicrobial activity. Full article

The sterility of ophthalmic drugs is a fundamental requirement for ensuring patient safety, and as such, it is subject to stringent regulatory standards. However, significant gaps remain regarding the effect of sterilization techniques on the impurity profile and relative content of active pharmaceutical ingredients (API). Previous research involving a set of five APIs used in ophthalmic preparations (dexamethasone, methylprednisolone, aciclovir, tetracycline hydrochloride, and triamcinolone) demonstrated that gamma irradiation led to the formation of specific impurities in the corticosteroids, dexamethasone and methylprednisolone. This study aims to further explore the effect of both gamma and electron beam (E-beam) irradiation on the impurity profiles of these APIs under varying conditions, with and without dry ice. The analyses were conducted using high-performance liquid chromatography with ultraviolet/visible light (UV/VIS) detection and the effect of sterilization conditions was assessed in accordance with the assay and related substances test outlined in the European Pharmacopoeia (Ph. Eur.). Additionally, this study investigated whether exposure in a controlled atmosphere with reduced oxygen or water content could mitigate the formation of impurities and influence the stability of the compounds. The results indicated a protective effect of low-temperature and low-oxygen environments during both gamma and E-beam irradiation but no effect of dry conditions. Full article

Thermoplasmonic heat generation by silver (Ag) nanoparticles can harness visible light to efficiently produce localized heating. Flame spray pyrolysis (FSP) is a powerful one-step synthesis technology for fabricating plasmonic Ag-based nanostructures. In the present study, we employed FSP to engineer core@shell Ag@SiO₂ nanoparticles coated with an ultrathin (1–2 nm) silica (SiO₂) nanolayer in a single step in tandem with their deposition as films onto solid substrates. Accordingly, we engineered a library of Ag@SiO₂ nanofilms with precisely controlled thicknesses in the range of 1–23 μm. A systematic study of the thermoplasmonic heat-generation efficiency (ΔT) of the films under visible-light irradiation (LED, λ = 405 nm) revealed that the films’ compactness and thickness are key parameters governing the heat-generation efficiency and thermal response rate. Moreover, we show that the substrate type can also play a key role; Ag@SiO₂ films on glass-fiber filters (PGFFs) enabled faster temperature increase (dT/dt) and a higher maximum temperature gain (ΔT_max) compared with Ag@SiO₂ films on glass substrates (PGSs). The photothermal conversion efficiencies were approximately 60%, with the highest efficiency (η = 65%) observed in the thinner impinged film. This study demonstrates that FSP-derived Ag@SiO₂ nanofilms provide a versatile and scalable platform for thermoplasmonic heat generation applications with significant industrial potential. Full article

Visible-light photoredox catalysis using biacetyl (BA) as a low-cost photosensitizer enables the efficient formation of triarylethylenes (TAEs) via a Mizoroki–Heck-type coupling. The reaction proceeds efficiently in acetonitrile upon blue LED irradiation under anaerobic conditions. Alternatively, supramolecular viscoelastic gels have also been explored as reaction media, allowing the possibility of working under aerobic atmosphere. Mechanistic investigations by means of transient absorption spectroscopy and quenching experiments support a charge-separated intermediate pathway. Reaction quantum yield measurements further validate the efficiency of BA, demonstrating its potential as an alternative to transition-metal catalysts. Overall, this work presents a sustainable and scalable strategy for TAEs synthesis, integrating photoredox catalysis with soft material engineering. These findings pave the way for broader applications in green chemistry and functional materials. Full article

Male infertility is a growing global concern, with asthenozoospermia being an important contributing factor. Mitochondrial dysfunction and changes in the metabolism of nitric oxide (NO) are key determinants of reduced sperm motility. This study investigates the effects of photobiomodulation (PBM) with visible and near-infrared (NIR) laser light on sperm of asthenozoospermic patients, focusing on mitochondrial energetic status, oxidative stress, and NO dynamics. Semen samples were irradiated at 450 nm, 635 nm, 810 nm, 940 nm, and 1064 nm at different power levels (0.25, 0.50, 1.00, and 2.00 W) for 60 s on a spot area of 1 cm². ATP and AMP levels, oxidative stress markers, and NO concentrations were assessed at 10 and 60 min after irradiation, with the ATP/AMP ratio calculated as an index of cellular energy balance. The results show that the PBM modulates the energetic status of spermatozoa in a way dependent on wavelength and dose. Irradiation at 810 nm produced the most marked improvement in energetic status, whereas 635 nm exposure led to a significant decrease in cellular energy levels. NO levels showed a biphasic response, correlated with the visible range and with energy metabolism at 810 nm. Irradiation with 635 nm induced higher NO production with respect to the other wavelengths. Our findings suggest that PBM mainly involves mitochondrial photoreceptors and potentially the heme and flavin groups of nitric oxide synthases, facilitating electron transitions, enhancing the effectiveness of oxidative phosphorylation, and optimizing enzymatic activity. At longer wavelengths (940 nm and 1064 nm), interactions with water and lipids may introduce additional variables that affect membrane fluidity and mitochondrial function differently from shorter wavelengths. Full article

This study introduces a visible light-mediated synthesis of 2,3-chalcogenil-dihydrobenzofuran through the oxyselenocyclization of 2-allylphenols in the presence of chalcogenides. Emphasizing sustainability, this method is notably enhanced by proceeding under mild conditions, facilitated by a straightforward I₂/SnCl₂ as a promoter and blue LED irradiation to activate the process. A variety of functional groups were effectively tolerated under our developed approach, leading to the desired products with yields ranging from good to excellent, demonstrating in this way the versatility of the method. In addition, the synthesized compounds were characterized using ¹H and ¹³C NMR techniques. Full article

The introduction of oxygen vacancies (OVs) is a promising strategy to enhance the hydrogen (H₂) evolution efficiency of photocatalysts. Sodium borohydride (NaBH₄) is widely used as a reducing agent to introduce OVs, particularly in composite materials. However, its impact on H₂ evolution remains underexplored. In this study, by employing various mass ratios of NaBH₄ to P/Ag/Ag₂O/Ag₃PO₄/TiO₂ (PAgT), OVs modified PAgT (R-PAgT) composites, which were synthesized and systematically characterized by XRD, FT-IR, and XPS. R-PAgT-10 with an optimal mass ratio exhibited a superior H₂ evolution efficiency and stability, maintaining its performance over 20 cycles under visible light irradiation, while the higher mass ratio of NaBH₄/PAgT led to the disruption of the crystal structure with excessive OVs amounts, resulting in poor stability. This study highlighted the importance of utilizing the optimal mass ratio of NaBH₄ to prepare OVs-PAgT for successful and stable H₂ evolution under visible light irradiation, which holds promise for developing efficient and durable photocatalysts for renewable energy applications. Full article

Nanoparticles of ZnFe₂O₄ and hematite with varied sizes and distributions were synthesized using the two-solvent method (cyclohexane, water) on SBA-15 silica batches. Calcination is performed in air at 700 °C (2 °C/min) with rapid quenching produced catalysts with distinct nanoparticle configurations, namely, internal zinc ferrite and external hematite. The choice of precursor was critical, and nitrate salts yielded only zinc ferrite nanoparticles, while chloride salts produced a mixture of hematite and zinc ferrite. The photocatalytic activity of these materials was evaluated under visible light irradiation from an LED lamp, using O₂ from air as an oxidizing agent without the addition of H₂O₂. Samples enriched with external hematite nanoparticles from chloride precursors achieved the highest activity, decomposing 30% of AMX in 225 min. In contrast, nitrate-derived samples with predominantly internal zinc ferrite nanoparticles exhibited lower catalytic activity. Characterization via TEM, XRD, N2 sorption, and Mössbauer spectroscopy confirmed the structural and magnetic properties of the nanoparticles. Mössbauer spectra, particularly at 12K and under a magnetic field, demonstrated the presence of hematite nanoparticles, distinguishing them from isolated Fe (III) cations. Zinc ferrite nanoparticles exhibited specific magnetic ordering, with Fe ions occupying tetrahedral and octahedral sites. The results demonstrate the critical role of nanoparticle, composition, and positioning in optimizing photocatalytic efficiency for water decomposition. Full article

Herein, a WO₃@TCN photocatalyst was successfully synthesized using a self-assembly method, which demonstrated effectiveness in degrading organic dyestuffs and photocatalytic evolution of H₂. The synergistic effect between WO₃ and TCN, along with the porous structure of TCN, facilitated the formation of a heterojunction that promoted the absorption of visible light, accelerated the interfacial charge transfer, and inhibited the recombination of photogenerated electron–hole pairs. This led to excellent photocatalytic performance of 3%WO₃@TCN in degrading TC and catalyzing H₂ evolution from water splitting under visible-light irradiation. After modulation, the optimal 3%WO₃@TCN exhibited a maximal degradation rate constant that was twofold higher than that of TCN alone and showed continuous H₂ generation in the photocatalytic hydrogen evolution. Mechanistic studies revealed that •O₂⁻ constituted the major active species for the photocatalytic degradation of tetracycline. Experimental and DFT results verified the electronic transmission direction of WO₃@TCN heterojunction. Overall, this study facilitates the structural design of green TCN-based heterojunction photocatalysts and expands the application of TCN in the diverse photocatalytic processes. Additionally, this study offers valuable insights into strategically employing acid regulation modulation to enhance the performance of carbon nitride-based photocatalysts by altering the topography of WO₃@TCN composite material dramatically. Full article

In this study we report on the efficiency of a furane-indole-chromenone-based organic derivative (FIC) as a photocatalyst in the α-arylation of enol acetate upon LED irradiation at 405 nm, and as a photoinitiator/photocatalyst in the free radical polymerization of an acrylate group in the presence of bis-(4-tert-butylphenyl)iodonium hexafluorophosphate (Iod) as an additive, or in the presence of both Iod and ethyl-4-(dimethyl amino) benzoate (EDB) under LED irradiation at 365 nm. The photochemical properties of this new light-sensitive compound are described, and the wide redox window (3.27 eV) and the high excited-state potentials FIC*/FIC^●− (+2.64 V vs. SCE) and FIC^●+/FIC* (−2.41 V vs. SCE) offered by this photocatalyst are revealed. The chemical mechanisms that govern the radical chemistry are discussed by means of different techniques, including fluorescence-quenching experiments, UV-visible absorption and fluorescence spectroscopy, and cyclic voltammetry analysis. Full article

Background/Objectives: Photoimmunotherapy (PIT) is an innovative approach for the targeted therapy of cancer. In PIT, photosensitizer dyes are conjugated to tumor-specific antibodies for targeted delivery into cancer cells. Upon irradiation with visible light, the photosensitizer dye is activated and induces cancer-specific cell death. In the present article, we describe the PIT of prostate cancer (PC) as a therapeutic option for the targeted treatment of localized prostate cancer. Methods: We conjugated the silicon phthalocyanine dye WB692-CB2 to recombinant cysteine-modified anti-CD44 and anti-EpCAM antibodies via a maleimide linker and tested the antibody dye conjugates for PIT on PC cells and prostate cancer stem cell (PCSC)-like cells. Results: The anti-CD44 and anti-EpCAM antibody dye conjugates showed specific binding and high cytotoxicity against PC and PCSC-like cells following irradiation with red light. Combined treatment with both conjugates led to enhanced cytotoxic effects. Conclusions: PIT with our dye WB692-CB2 can serve as an effective focal therapy against prostate cancer, preserving the prostate gland and minimizing side effects. It can be employed during radical prostatectomy (RP) to treat residual tumor cells or lymph node metastases in areas where further surgical intervention is not feasible. Utilizing multiple conjugates against antigens expressed on differentiated PC and PCSC-like cells, such as CD44 and EpCAM, could be an effective method to eradicate residual cancer cells in heterogeneous tumors. This approach could reduce the risk of local recurrence after RP and thus increase the therapeutic outcome of PC patients. Full article