Search Results (41)

Contaminants of emerging concern (CECs), including pharmaceuticals and perfluorinated compounds, pose a growing threat to water quality due to their persistence and resistance to conventional treatment methods. In this context, photocatalytic processes capable of promoting both oxidative and reductive transformations have attracted increasing attention. This study explores the synthesis and performance of a SnS₂-TiO₂ heterojunction photocatalyst, designed to facilitate such reactions under solar and UV-A light. The composite was synthesized via the hydrothermal method and thoroughly characterized for its morphological, structural, surface, and semiconducting properties. The results confirmed the formation of a type-II heterojunction with improved visible-light absorption and suppressed charge recombination. Photoelectrochemical measurements indicated enhanced charge separation and favorable band-edge alignment for reductive processes. Photocatalytic experiments with amoxicillin (AMX) and perfluorooctanoic acid (PFOA) revealed distinct degradation behaviors: AMX was predominantly degraded via superoxide-mediated reductive pathways, whereas PFOA exhibited limited transformation, likely proceeding via a combination of oxidative and reductive mechanisms. While overall removal efficiencies were moderate, this study highlights the role of band structure engineering and heterojunction design in tailoring photocatalytic behavior. The SnS₂-TiO₂ system serves as a promising platform for further development of composite materials to address the challenge of CECs in water treatment. Full article

The pharmaceutical product is a powdered tablets containing bisoprolol fumarate that is used in the treatment of circulatory system diseases. They were examined by X-band (9.3 GHz) electron paramagnetic resonance spectroscopy. The aim of this work was to determine the influence of the physical conditions of storage on the properties and content of free radicals in this pharmaceutical product. The product was subjected to a temperature of 50 °C, UVA radiation, and UVA radiation and then a temperature of 50 °C. The amplitude, integral intensity, linewidth of EPR lines, and g factor, were analyzed. Free radicals were formed in all tested samples; thus, the product containing bisoprolol fumarate should not be stored at a temperature of 50 °C, and it should be protected from UVA radiation, which is in line with the manufacturer’s requirements. The content of free radicals in the examined product was highest after treatment at a temperature of 50 °C. The lowest free radical content characterized the product after the interaction of both UVA radiation and a temperature of 50 °C. EPR lines were not microwave saturated below a power of 70 mW, which indicates fast spin-lattice relaxation processes in the product. It has been demonstrated that free radical formation in the product containing bisoprolol fumarate depends on the type of physical factor. Full article

In this research, an emerging, non-metallic photocatalyst was prepared by the thermal polymerization method from three different precursors: urea, melamine, and three mixtures of melamine and cyanuric acid. Graphitic carbon nitride (g-C₃N₄) samples from urea and melamine were synthesized in a muffle furnace at three different temperatures: 450°, 500°, and 550 °C for 2 h, while the samples made of a mixture of melamine and cyanuric acid (with mass ratios of 1:1, 1:2, and 2:1) were synthesized at 550 °C for 2 h. All the samples were characterized in order to determine their chemical and physical properties, such as crystallite size and structure, and phase composition by the following techniques: Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS). Nitrogen adsorption/desorption isotherms were used to investigate the Brunauer, Emmett, and Teller (BET) specific surface area and Barrett–Joyner–Halenda (BJH) pore size distribution. Band gap values were determined by diffuse reflectance spectroscopy (DRS). Furthermore, adsorption and photocatalytic degradation of the local anesthetic drug procaine were monitored under UV-A, visible, and simulated solar irradiation in a batch reactor. Kinetic parameters, as well as photocatalytic mechanisms using scavengers, were determined and analyzed. The results of the photocatalysis experiments were compared to the benchmark TiO₂ Evonik Aeroxide P25. The results indicated that the g-C₃N₄ sample synthesized from urea at 500 °C for 2 h exhibited the highest degradation rate of procaine under visible light. Full article

Developing sustainable and green packaging products that protect foods and preserve their unique properties from UV radiation, which causes photochemical damage, is one of the extensive challenges in the food-packaging industry. Accordingly, carboxymethyl cellulose sodium (CMC)/graphene (G) nanocomposites that contained different weight percentages were prepared by a mechanical milling method. The influence of the G on the chemical composition and optical properties of the nanocomposites were studied by different techniques. SEM and FT-IR analyses confirmed the interaction between the CMC and G. The XRD spectrum showed that the crystallite size of the CMC decreased with G addition. The findings showed that changing the G concentration modified the CMC’s optical properties. The CMC’s transmittance decreased to 52%, 49%, and 57% in the UV-C (200–280), UV-B (280–320 nm), and UV-A (320–400) regions, respectively, with the addition of 2 wt.% of G. Moreover, the optical band gap decreased to 4.80 eV, while the Urbach energy increased from 0.34 to 0.94 eV as the G content increased. The density functional theory (DFT) assumption was followed to establish the electronic properties and vibrational spectrum of the CMC/G model. The theoretically determined IR and experimental FT-IR spectra of the CMC/G nanocomposites showed good agreement. The obtained results show that these nanocomposites are good candidates for food packaging. Full article

Coupling TiO₂ with various elements could enhance its photocatalytic activity. In this study, an innovative ultrasound-assisted sol–gel method was used to synthesize TiO₂/Ag(x%) by varying Ag–support mass (x = 9.3, 17.1, and 23.6%), followed by calcination at 450 °C for 30 min. The aim was to demonstrate that Ag compositing improves photoactivity under visible light (>400 nm). The synthesized photocatalysts were assessed for their effectiveness in the degradation and mineralization of Methylene Blue (MB) and Acid Orange 7 (AO7) using visible lamps emitting in the range of 400–800 nm. Characterization of the prepared photocatalysts was performed by using Raman spectroscopy, SEM/EDS, pH_pzc, and UV–visible spectroscopy. Raman spectroscopy confirmed the predominance of the anatase phase in all the photocatalysts. The photodegradation efficiencies of the selected dyes, MB and AO7, reached 99% (pH 6) and 95% (pH 3) after 180 min of irradiation, respectively. The best performance for the degradation of the two dyes was observed with TiO₂/Ag9.3%, showing optimal kinetics at this doping concentration. The improved photoactivity of the TiO₂/Ag composite is due to a decrease in the recombination rate of electron/hole (e⁻/h⁺) and a decrease in the band gap from 3.13 to 2.49 eV. The mineralization rate of both dyes under visible light is about 9.3%, indicating the presence of refractory by-products that resist complete degradation. Under UVA irradiation, complete mineralization is obtained. This study confirms the potential of TiO₂/Ag composite as a high-performance and cost-effective photocatalyst for solar environmental remediation, highlighting the role of silver in extending light absorption into the visible region and improving charge separation. Full article

Monomers of N-hydroxypyridine-2(1H)-thione were isolated in low-temperature matrices of solid normal hydrogen (n-H₂). The matrix-isolated compound was irradiated with UV-B (λ = 305 nm) or UV-A (λ > 360 nm) light. Upon such irradiation, the initial form of N-hydroxypyridine-2(1H)-thione was completely consumed and converted into photoproducts. 2-Mercaptopyridine and water were identified as the main products of these photochemical transformations. Identification of photoproduced 2-mercaptopyridine is unquestionable. It is based on the identity of two sets of IR bands: (i) the bands observed in the IR spectrum recorded (in a separate experiment) for monomers of 2-mercaptopyridine trapped in an n-H₂ matrix and (ii) a set of IR bands observed in the spectrum recorded after UV irradiation of N-hydroxypyridine-2(1H)-thione. It should be emphasized that the UV-induced processes, occurring for N-hydroxypyridine-2(1H)-thione isolated in an n-H₂ matrix, lead to products that are significantly different from those generated from the compound trapped in solid Ar or in solid N₂. Full article

Vertical-cavity surface emitting lasers in UVA band (UVA VCSELs) operating at a central wavelength of 395 nm are designed by employing PICS3D(2021) software. The simulation results indicate that the thickness of the InGaN quantum well and GaN barrier layers affect the emission efficiency of UVA VCSELs greatly, suggesting an optimal thicknesses of 2.2 nm for the well layer and 2.7 nm for the barrier layer. Additionally, an overall consideration of threshold current, series resistance, photoelectric conversion efficiency, and optical output power results in the optimized thickness of the ITO current spreading layer, ~20 nm. Furthermore, by employing a five-pair Al_0.15Ga_0.85N/GaN multi-quantum barrier electron blocking layer (EBL) instead of a single Al_0.2Ga_0.8N EBL, the device shows a ~51% enhancement in the optical output power and a ~48% reduction in the threshold current. The number of distributed Bragg reflector (DBR) pairs also plays crucial roles in the device’s photoelectric performance. The device designed in this study demonstrates a minimum lasing threshold of 1.16 mA and achieves a maximum wall plug efficiency of approximately 5%, outperforming other similar studies. Full article

Antioxidants of plant extract play an important role in the phytosynthesis of silver nanoparticles (phyto-AgNPs), providing the reduction of silver ions and capping and stabilization of nanoparticles. Despite the current progress in the studies of phytosynthesis, there is no approach to the selection of plant extract for obtaining phyto-AgNPs with desired properties. This work shows that antioxidant activity (AOA) of plant extracts is a key parameter for targeted phytosynthesis. In support of this fact, the synthesis of phyto-AgNPs was carried out using extracts of four plants with different AOA, increasing in the order Ribes uva-crispa < Lonicera caerulea < Fragaria vesca < Hippophae rhamnoides. Phyto-AgNPs have been characterized using Fourier-transform infrared spectroscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, selected area electron diffraction technique, ultraviolet–visible spectroscopy, electrochemical impedance spectroscopy and cyclic voltammetry. It was established that the change in the AOA of the plant extract is accompanied by a size-dependent change in the optical and electrochemical properties of phyto-AgNPs. In particular, an increase in the extract AOA leads to the formation of smaller phyto-AgNPs with higher electrochemical activity and low charge transfer resistance. A “blue shift” and an increase in the plasmon resonance band of silver sols are observed with an increase in the extract AOA. The obtained regularities prove the existence of the “AOA–size–properties” triad, which can be used for controlled phytosynthesis and prediction of phyto-AgNPs’ properties. Full article

Traditional optical communication systems rely on single narrow-band PDs, which can expose confidential information and data to potential eavesdropping in free space. With advancements in technology, even optical communication in the UV spectrum, invisible to the sun, faces risks of interception. Consequently, broad-band PDs that combine optical encryption with algorithmic encryption hold significant promise for secure and reliable communication. This study presents a photodetector based on TiO₂–α-Ga₂O₃ heterostructures, prepared via direct oxidation and hydrothermal reaction, demonstrating self-powered UVC/UVA broad-band detection capabilities. The PD exhibits response peaks at approximately 250 and 320 nm, with R of 42.16 and 59.88 mA/W and D* of 8.21 × 10¹³ and 9.56 × 10¹³ Jones, respectively. Leveraging the superior optical response characteristics of UVC and UVA wavelengths, this device has been employed to develop a communication system designed for data transmission. The proposed system features two independent channels: one for data transmission using UVC and another for key distribution using UVA. Secure communication is ensured through specialized encryption algorithms. In summary, this work offers a straightforward, cost-effective, and practical method for fabricating self-powered UVC/UVA broad-band PDs. This PD provides new insights into the development of multi-purpose, multi-band secure optical communication devices and holds promise for integration into multifunctional optoelectronic systems in the future. Full article

Long-term exposure to a relatively high concentration of airborne bacteria emitted from intensive livestock houses could potentially threaten the health and welfare of animals and workers. There is a dual effect of air sterilization and promotion of vitamin D synthesis for the specific bands of ultraviolet light. This study investigated the potential use of A-band ultraviolet (UVA) tubes as a clean and safe way of reducing airborne bacteria and improving calf health. The composition and emission characteristics of airborne bacteria were investigated and used to determine the correct operating regime of UVA tubes in calf houses. Intermittent exceedances of indoor airborne bacteria were observed in closed calf houses. The measured emission intensity of airborne bacteria was 1.13 ± 0.09 × 10⁷ CFU h⁻¹ per calf. Proteobacteria were the dominant microbial species in the air inside and outside calf houses. After UVA radiation, the indoor culturable airborne bacteria decreased in all particle size ranges of the Anderson sampler, and it showed the highest reduction rate in the size range of 3.3–4.7 μm. The results of this study would enrich the knowledge of the source characteristics of the airborne bacteria in intensive livestock farming and contribute to the environmental control of cattle in intensive livestock production. Full article

In this study, the optimal microwave-assisted sol-gel synthesis parameters for achieving TiO₂ nanoparticles with the highest specific surface area and photocatalytic activity were determined. Titanium isopropoxide was used as a precursor to prepare the sol (colloidal solution) of TiO₂. Isopropanol was used as a solvent; acetylacetone was used as a complexation moderator; and nitric acid was used as a catalyst. Four samples of titanium dioxide were synthesized from the prepared colloidal solution in a microwave reactor at a temperature of 150 °C for 30 min and at a temperature of 200 °C for 10, 20, and 30 min. The phase composition of the TiO₂ samples was determined by X-ray diffraction analysis (XRD) and Fourier-transform infrared spectroscopy (FTIR). Nitrogen adsorption/desorption isotherms were used to determine the specific surface area and pore size distributions using the Brunauer–Emmett–Teller (BET) method. The band-gap energy values of the TiO₂ samples were determined by diffuse reflectance spectroscopy (DRS). The distribution of Ti and O in the TiO₂ samples was determined by SEM-EDS analysis. The effects of adsorption and photocatalytic activity of the prepared TiO₂ samples were evaluated by the degradation of ciprofloxacin (CIP) as an emerging organic pollutant (EOP) under UV-A light (365 nm). The results of the photocatalytic activity of the synthesized TiO₂ nanoparticles were compared to the benchmark Degussa P25 TiO₂. Kinetic parameters of adsorption and photocatalysis were determined and analyzed. It was found that crystalline TiO₂ nanoparticles with the highest specific surface area, the lowest energy band gap, and the highest photocatalytic degradation were the samples synthesized at 200 °C for 10 min. The results indicate that CIP degradation by all TiO₂ samples prepared at 200 °C show a synergistic effect of adsorption and photocatalytic degradation in the removal process. Full article

Spinels are important materials for an application in bioimaging. The key advantage with spinel-type hosts is the presence of antisite defects, which act as charge reservoirs for trapping electrons and holes at complementary defect sites. This makes them a host system similar to a molecular system. Herein, we present a systematic approach to modulating the band gap of an inverse ${\mathrm{Zn}}_2$${\mathrm{TiO}}_4$ spinel. With a change in ZnO concentration, the absorption band at 375 nm diminishes and disappears at a ZnO:TiO₂ concentration of 1.40:1.00. The band gap of the material is modified from 3.30 to 4.40 eV. The crystal structure of the sample does not change drastically as determined using X-ray diffraction and Rietveld refinement. The ${\mathrm{Zn}}_2$${\mathrm{TiO}}_4$ emits in the UV-A region with a lifetime in the time domain of ‘ns’. The sample also shows persistent luminescence of at least 15 min upon excitation with 254 nm with prominent emission in the UV-A region (300–390 nm). The present results open a new avenue for the synthesis of spinel hosts where the band gap can be modified with ease. The UV emission thus observed is expected to find usage in interesting applications like photocatalysis, anti-counterfeiting, water disinfecting, etc. Full article

Organic UV filters have been known to generate harmful by-products and undergo photoreactive degradation, which ultimately poses a great threat to consumers using sunscreen products. Inorganic UV filters such as TiO₂ and ZnO, although considered safer options, are not without threat considering their photocatalytic nature and ability to generate reactive oxygen species. A study was conducted to identify the influence of different metal ions on the photochemical properties of layered double hydroxides (LDH), Zinc-Titanium LDH (Zn-Ti LDH), Zinc-Aluminium LDH (Zn-Al LDH), and Magnesium- Aluminium LDH (Mg-Al LDH) and their prospects in photoprotection. The photocatalytic properties of the LDH were analyzed and compared to TiO₂ and ZnO. The intermediate band gaps of Zn-Ti (3.72 eV) and Zn-Al LDH (3.3 eV) proved favorable and safer for the use of these LDH in cosmetic formulations as they offer lower photo-reactivity when compared to cosmetic grade ZnO and TiO₂. The in vitro SPF values obtained for formulations containing 2 wt% Zn-Ti and 2 wt% Zn-Al LDH showed promise, with both samples claiming “broad spectrum” protection and valid claims of UVA protection. Full article

The 70% polyvinyl alcohol/30% polyvinyl pyrrolidone (PVA/PVP) polymer blends, with different weight ratios of tetrapropylammonium iodide (TPAI) or tetrahexylammonium iodide (THAI) salt, were prepared using dimethyl sulfoxide (DMSO) as a solvent. The X-ray diffraction technique was used to trace the crystalline nature of the formed blends. The SEM and EDS techniques were applied to figure out the morphology of the blends. The variation in the FTIR vibrational bands was used to investigate the chemical composition and the effect of different salt doping on the functional groups of the host blend. The influence of the salt type (TPAI or THAI) and its ratio on the linear and nonlinear optical parameters for the doped blends were investigated in detail. Absorbance and reflectance are highly enhanced in the UV region reaching a maximum for the blend with 24% TPAI or THAI; so, it can be employed as shielding materials for UVA and UVB types. The direct (5.1 eV) and indirect (4.8 eV) optical bandgaps were reduced continuously to (3.52, 3.63 eV) and (3.45, 3.51 eV) while increasing the content of TPAI or THAI, respectively. The blend doped with 24% wt TPAI exhibited the highest refractive index (around 3.5 in 400–800 nm). The DC conductivity is affected by the content and type of salt, its dispersion, and blend-salt interaction. The activation energies of different blends were obtained by applying the Arrhenius formula. Full article

Absorbing aerosols have significant influences on tropospheric photochemistry and regional climate change. Here, the direct radiative effects of absorbing aerosols at the major AERONET sites in East Asia and corresponding impacts on near-surface photochemical processes were quantified by employing a radiation transfer model. The average annual aerosol optical depth (AOD) of sites in China, Korea, and Japan was 1.15, 1.02 and 0.94, respectively, and the corresponding proportion of absorbing aerosol optical depth (AAOD) was 8.61%, 6.69%, and 6.49%, respectively. The influence of absorbing aerosol on ultraviolet (UV) radiation mainly focused on UV-A band (315–400 nm). Under the influence of such radiative effect, the annual mean near-surface J[NO₂] (J[O¹D]) of sites in China, Korea, and Japan decreased by 16.95% (22.42%), 9.61% (13.55%), and 9.63% (13.79%), respectively. In Beijing–Tianjin–Hebei (BTH) and Yangtze River Delta (YRD) region, the annual average AOD was 1.48 and 1.29, and the AAOD was 0.14 and 0.13, respectively. The UV radiative forcing caused by aerosols dominated by black carbon (BC-dominated aerosols) on the surface was −3.19 and −2.98 W m⁻², respectively, accounting for about 40% of the total aerosol radiative forcing, indicating that the reduction efficiency of BC-dominated aerosols on solar radiation was higher than that of other types of aerosols. The annual mean J[NO₂] (J[O¹D]) decreased by 14.90% (20.53%) and 13.71% (18.20%) due to the BC-dominated aerosols. The daily maximum photolysis rate usually occurred near noon due to the diurnal variation of solar zenith angle and, thus, the daily average photolysis rate decreased by 2–3% higher than that average during 10:00–14:00. Full article