Artificial Sunlight Research Articles

A solar evaporator fabricated from corncob waste for the desalination of seawater and removal of oil/herbicides from contaminated water

Corncob (CC) based solar evaporators were employed to desalinize seawater brought from the Vallarta coast in Mexico. The pure CC produced an evaporation-rate and evaporation-efficiency of 0.63 kg m−2 h−1 and 38.4%, respectively, under natural solar light. Later, the CC was coated with carbonized CC (CCCE evaporator) or was coated with graphene (CCGE evaporator). Those evaporators were used for the desalination of seawater and obtained higher evaporation rates of 1.59–1.67 kg m−2 h−1, and higher evaporation efficiencies of 92–94% (under natural solar light). The desalination experiments were repeated under artificial solar light and the evaporation-rates/evaporation-efficiencies slightly decreased to 1.43–1.52 kg m−2 h−1/88–92%. The surface analysis of the evaporators by FTIR, XPS and Raman revealed that the CCGE evaporator had on its surface a lower content of defects and a higher amount of OH groups than the CCCE evaporator. Therefore, the CCGE evaporator had higher evaporation-rates/evaporation-efficiencies in comparison with the CCCE evaporator. Furthermore, we purified water contaminated with three different herbicides (fomesafen, 2–6 dichlorobenzamide and 4-chlorophenol at 30 ppm) by evaporation and using natural solar light. Interestingly, the CCCE and CCGE evaporators also removed the herbicides by physical adsorption with efficiencies of 12–22.5%. Moreover, the CCGE evaporator removed vegetable oil from contaminated water by adsorption and its maximum adsorption capacity was 1.72 g/g. Overall, our results demonstrated that the corncob-based evaporators studied here are a low-cost alternative to obtain clean water under natural solar light and this one was more effective for the desalination of seawater than the artificial sunlight (Xe lamp).

A polymer-Au/TiO2 nano-composite based floating catalyst for photocatalytic dye degradation under natural sunlight

Floating catalysts for photocatalytic dye degradation under sunlight is very useful for large-scale real-world application. The strategy of immobilizing semiconductor photo-catalysts to a variety of low-density floating material is demonstrated with the objective of easy recovery, low catalyst loss and long reusability. In this study a polymer-Au/TiO2 (Z@Au/TiO2) floating photo-catalyst was developed using Au/TiO2 as a visible light active photo-catalyst immobilized on Zein based low density polymer material. The synthesized floating catalyst was meticulously characterized by a range of spectroscopic, thermo gravimetric and imaging techniques to confirm its chemical identity and stability. Under either artificial or natural sunlight conditions, a variety of dye molecules (Auramine (Aur), Congo red (CR), Jakazol red (JR), and Methyl violet (MV)) could be degraded through photocatalytic degradation with floating Z@Au/TiO2. Additionally, it was demonstrated that it could be collected easily after the catalysis and can be reused for several cycles. Due to its ease of fabrication and high photocatalytic activity, Z@Au/TiO2 floating photo-catalyst may be helpful in treating water pollution for environmental remediation.

Scalable Carbon Black‐Enabled Membranes for Sustainable Solar Membrane Desalination

AbstractSolar energy is used worldwide for generating electricity or desalting seawater. Photothermal membrane distillation (PMD), an emerging thermal‐driven process for seawater desalination, combines interfacial heating with membrane distillation (MD) technology to address the energy consumption issues of conventional MD. However, it is still a great challenge to develop a cost‐effective and scalable membrane, which hampers the practical use of PMD. Herein, a dual‐layer carbon black (CB)/PVDF membrane is prepared via direct electrospraying on a commercial PVDF membrane. With the introduction of a functional layer, a photothermal effect is imparted to the bare membrane, thus significantly increasing the water production rate and solar utilization efficiency (SUE) during exposure to artificial sunlight (≈57% enhancement and 72% SUE under 1 sun). In addition to the outstanding photothermal properties, this functional layer also served as a passivation coating to synergistically reduce the crystallization rate and physical binding of inorganic salts on the modified membrane without adding hazardous chemicals or using laborious steps. This multifunctional coated membrane and fast‐growing solar desalination technology provides a promising solution to the water crisis, especially in off‐grid areas where energy and resources are both relatively insufficient.

Natural sunlight-driven oxidation of Mn2+(aq) and heterogeneous formation of Mn oxides on hematite

The oxidation of dissolved Mn2+(aq) plays a critical role in driving manganese cycles and regulating the fate of essential elements and contaminants in environmental systems. Based on sluggish oxidation rate, abiotic processes have been considered less effective oxidation pathway for manganese oxidation in environmental systems. Interestingly, a recent study (Jung et al., 2021) has shown that the rapid photochemical oxidation of Mn2+(aq) could be a feasible scenario to uncover the potential significance of abiotic Mn2+(aq) oxidation. Nevertheless, the significance of photochemical oxidation of Mn2+(aq) under natural sunlight exposure remains unclear. Here, we demonstrate the rapid photocatalytic oxidation of Mn2+(aq) and the heterogeneous growth of tunnel-structured Mn oxides under simulated freshwater and seawater conditions in the presence of natural sunlight and hematite. The natural sunlight-driven photocatalytic oxidation of Mn2+(aq) by hematite showed kinetic constants of 1.02 h−1 and 0.342 h−1 under freshwater and seawater conditions, respectively. The natural sunlight-driven photocatalytic oxidation rates are quite comparable to the results obtained from the previous laboratory test using artificial sunlight, which has ∼4.5 times stronger light intensity. It is likely because of ∼5.5 times larger light exposure area in the natural sunlight-driven photocatalytic oxidation than that of the laboratory test using artificial sunlight. We also elucidate the roles of cation species in controlling the oxidation rate of Mn2+(aq) and the crystalline structure of Mn oxide products. Specifically, in the presence of large amounts of cations, the oxidation rate of Mn2+(aq) was slower likely because of competitive adsorption. Furthermore, our findings highlight that Mg2+ contributes significantly to the formation of large-tunneled Mn oxides. These results illuminate the importance of abiotic photocatalytic processes in controlling the redox chemistry of Mn in real environmental aqueous systems on the oxidation of Mn2+(aq), and provide an environmentally sustainable approach to effectively remediate water contaminated with Mn2+(aq) using natural sunlight.

CuO/ZnO Type-II heterojunction modified by rGO nanosheets for improved photocatalytic mineralization of antibiotics

In the present work, CuO/ZnO type-II heterojunction was modified by graphene oxide nanosheets for excellent photocatalytic mineralization of antibiotics under artificial UV light and natural sunlight. For this purpose, CuO/ZnO heterojunction-graphene oxide nanocomposites were synthesized via a facile refluxing method in aqueous media. The synthesized nanocomposites were characterized through diverse characterization techniques such as XRD, FT- IR, Raman, SEM, TEM, and UV–Vis DRS to determine their structural, morphological, and optical properties. XRD analysis confirmed the monoclinic CuO and hexagonal wurtzite ZnO phase in bare CuO/ZnO heterojunction and different CuO/ZnO heterojunction-graphene oxide nanocomposites as well. The optical band gap was found in the range of 3.06–3.19 eV for different nanocomposites. The photocatalytic activity of the bare heterojunction and nanocomposites was performed against the degradation of ciprofloxacin under the irradiation of artificial UV and natural sunlight as well. The highest degradation % of ciprofloxacin was achieved at 96.27 % and 76.44 % under artificial UV and natural sunlight within 120 min, respectively over CuO/ZnO heterojunction with 3 wt% of graphene oxide. The outstanding photocatalytic performance of CuO/ZnO heterojunction-graphene oxide (3 wt%) owing to the high adsorption capacity and synergism between CuO/ZnO and graphene oxide caused the improved separation of charge species resulting higher production rate of reactive oxygen species and prompt degradation of ciprofloxacin.

Comparing the decay of human wastewater-associated markers and enteric viruses in laboratory microcosms simulating estuarine waters in a temperate climatic zone using qPCR/RT-qPCR assays

This study investigated the decay rates of wastewater-associated markers and enteric viruses in laboratory microcosms mimicking estuarine water environments in temperate Sydney, NSW, Australia using qPCR and RT-qPCR assays. The results demonstrated the reduction in concentrations of Bacteroides HF183, Lachnospiraceae Lachno3, cross-assembly phage (crAssphage), pepper mild mottle virus (PMMoV), human adenovirus (HAdV 40/41), and enterovirus (EV) over a span of 42 days under spring/summer temperatures, presence/absence of microbiota, and different light conditions. The study found that HF183, Lachno3, crAssphage, PMMoV, HAdV 40/41, and EV exhibited varying decay rates depending on the experimental conditions. The average T90 values ranged from a few days to several months, indicating the rapid decay or prolonged persistence of these markers and enteric viruses in the estuarine environment. Furthermore, the study examined the effects of indigenous microbiota and spring/summer temperatures on wastewater-associated markers and enteric viruses decay rates. It was found that the presence of microbiota and temperature significantly influenced the decay rates of HF183 and PMMoV. Additionally, the study compared the effects of artificial sunlight and spring/summer temperatures on marker decay rates. Bacterial markers decayed faster than viral markers, although among viral markers crAssphage decay rates were relatively faster when compared to PMMoV. The exposure to artificial sunlight significantly accelerated the decay rates of bacterial markers, viral markers, and enteric viruses. Temperature also had an impact on the decay rates of Lachno3, crAssphage, and HAdV 40/41. In conclusion, this study provides valuable insights into the decay rates of wastewater-associated markers and enteric viruses under different experimental conditions that mimicked temperate environmental conditions. The findings contribute to our understanding of the fate and persistence of these markers in the environment which is crucial for assessing and managing risks from contamination by untreated human wastewater.

Carbon and hydrogen isotope fractionation of phthalates during photocatalysis reactions in aqueous solution containing Fe(III) complexes or iron minerals

The hydrogen and carbon isotope fractionation factor (ε2H, ε13C) of dimethyl-, diethyl‑ and dibutyl phthalic acid ester during photosensitized degradation by artificial sunlight with Fe(III) ions and iron minerals (hematite, goethite and magnetite) in aqueous solution were examined by compound-specific isotope analysis (CSIA) in order to analyze the degradation mechanism. Hematite does not catalyze photosensitized degradation of phthalates. The correlation of 2H and 13C isotope fractionation (Λ = Δδ2H/Δδ13C) of phthalates with increasing chain length (dimethyl-; diethyl‑; and dibutyl-) were compared with values of the ∙OH radical model reaction with the aromatic ring as well as acidic and alkaline hydrolysis. The Λ values of die photosensitized reaction of diethyl phthalate with goethite (-5.1 ± 1.8) and magnetite (-18.9 ± 3.9) show a large difference compared to Fe(III) solutions (4.7 ± 0.9 to 4.8 ± 1.0) suggesting specific reaction mechanisms. The fractionation factors determined here have potential to characterize the degradation of phthalates catalyzed by photo-induced reaction of Fe(III), goethite and magnetite in natural system and in remediation approaches.

Development & Reliability Verification of Ultra-high Color Rendering White Artificial Sunlight LED Device using Deep Blue LED Light Source and Phosphor

Development & Reliability Verification of Ultra-high Color Rendering White Artificial Sunlight LED Device using Deep Blue LED Light Source and Phosphor

Experimental and DFT study of photocatalytic activity of reduced graphene oxide/copper sulfide composite for removal of organic dyes from water

In this work, successful nanocomposites composed of different ratios of reduced graphene oxide and copper sulphide (xCuS–rGO) were fabricated to aid in treating water contaminated with organic dyes. XRD, TEM, SEM, XPS, IR, EDX and BET were applied for the characterization of (CuS–rGO). The photocatalytic strength of the prepared nanocomposites was evaluated using artificial sunlight irradiation. The nanocomposites were tested for their ability to degrade both anionic and cationic organic dyes, including amaranth and rhodamine B (RhB). The excellent photocatalytic strength of our composites, relative to pristine CuS and rGO, was interpreted as rGO sheets being very porous. In addition, the charge moved efficiently from rGO to CuS. The combined properties enhanced the efficiency of photodegradation of CuS–rGO composite across the dyes under the illumination of simulated sunlight. The electron transportation from rGO sheets to the CuS conduction band enhances the charge separation and transportation. The role of superoxide radicals in photocatalytic degradation was unveiled and the interactions between the studied dyes and our catalysts were investigated by density functional theory study and scavenging investigation. This work gives new ideas about the preparation and properties of (CuS–rGO) composites and their broad application in solving environmental problems.

Accelerated aging of tire and road wear particles by elevated temperature, artificial sunlight and mechanical stress — A laboratory study on particle properties, extractables and leachables

Tire and road wear particles (TRWP) are generated in large quantity by automobile traffic on roads but their way of degradation in the environment is largely unclear. Laboratory experiments were performed on the effect of elevated temperature (simulating 2–3 years), sunlight exposure (simulating 0.5 years) and mechanical stress on the physical properties and chemical composition of TRWP and of cryo-milled tire tread (CMTT). No significant effects were observed of the applied mechanical stress on mean properties of pristine particles. After sunlight exposure up to 40 % in mass were lost from the TRWP, likely due to the loss of mineral incrustations from their surface. The chemical composition of TRWP and CMTT was characterized by determining 27 compounds, antioxidants (phenylene diamines), vulcanization agents (benzothiazoles and guanidines) and their transformation products (TPs). Extractables of TRWP (580–850 μg/g) were dominated by TPs, namely benzothiazolesulfonic acid (BTSA). CMTT showed much higher amounts of extractables (4600 μg/g) which were dominated by parent chemicals such as N-(1,3-dimethylbutyl)-N′-phenyl-1,4-phenylenediamine (6-PPD), diphenylguanidine (DPG) and mercaptobenzothiazole (MBT). Sunlight exposure affected the amount of extractables more strongly than elevated temperature, for TRWP (−45 % vs −20 %) and CMTT (−80 % vs −25 %) and provoked a clear shift from parent compounds to their TPs. After sunlight exposure extractables of TRWP were dominated by BTSA and DPG. Sunlight exposure drastically reduced the 6-PPD amount extracted from both, TRWP and CMTT (−93 %, −98 %), while its quinone (6-PPDQ) increased by around 1 % of the 6-PPD decrease, only. For many TPs, concentration in leachates were higher than in extracts, indicating ongoing transformation of their parent compounds during leaching. These results highlight that abiotic aging of TRWP leads to strong changes in their chemical composition which affect their particle properties and are of relevance for the environmental exposure to tire-related chemicals.

Potato-on-rod like of Z-scheme plasmon Ag2CrO4-Ag2Mo2O7 heterojunction nanophotocatalyst with high stability and accelerated photo-degradation evolution of organic contaminants

The shocking increase of resistant dye pollutants in the environment and their harmful effects has become a potential threat to the ecosystem. In the current work, the novel and highly efficient potato-on-rod-like Z-scheme plasmon Ag2CrO4–Ag2Mo2O7 heterojunction nano-photocatalyst was synthesized by precipitation method to photodegrade different organic dyes under artificial sunlight. The required analysises were carried out to characterize nanophotocatalysts. FESEM and TEM results showed the placement way of potato-like Ag2CrO4 between/on rod-like Ag2Mo2O7 which was leading to suitable structure and surface morphology. Besides, the morphology observations released the meso-/macroporous potato-on-rod like architecture self-assembled by nanoparticles. DRS analysis also confirmed two band gap energies of 2.55 and 1.72 eV in Ag2CrO4–Ag2Mo2O7 (3:1) resulting from forming a heterojunction structure and the plasmon Ag. Ag2CrO4–Ag2Mo2O7 (3:1) nanophotocatalyst exhibited the most remarkable activity in the photodegradation of 10 mg/L 2-naphthol orange (97.8%), 10 mg/L rhodamine B (99.7%), 10 mg/L crystal violet (98.9%), and 10 mg/L methyl orange (56.1%) with a catalyst dosage of 0.1 gr for about 90 min. The appropriate energy band gap, the formation of the heterostructure, the presence of meso (0.0038 cm3/g) and macro (0.0044 cm3/g) holes, and pore diameter at about 17.2 nm based on BET-BJH analysis that facilitated the penetration of pollutant molecules, increased pollutant adsorption and demonstrated stunning capability of efficient light harvesting, the reason was electron-hole pairs recombination rate reduction. Moreover, the fabricated samples showed tremendous catalyst constancy and reusability even after the fourth run. Results have shown the remarkable photocatalytic activity under visible light and provide an environment-friendly and green strategy to overcome the challenges of organic pollutants present in aqueous solutions.

Enhancement of photodegradation of polyethylene with adsorbed polycyclic aromatic hydrocarbons under artificial sunlight irradiation

The photodegradation of plastic waste produces microplastics (MPs) in marine environments. Plastics can adsorb hydrophobic organic pollutants such as polycyclic aromatic hydrocarbons (PAHs) and can be transported over long distances. However, the impact of adsorbed pollutants on the photodegradation remains unknown. Here, we show that adsorbed PAHs act as photocatalysts that promote the photodegradation of polyethylene. Upon light irradiation, coloration and surface degradation of the PAH-adsorbed polyethylene sheets were observed, indicating that the PAH-adsorbed polyethylene sheets are less resistant to light. Furthermore, fluorene, phenanthrene, anthracene, benzo[a]anthracene, benzo[a]pyrene, and indeno[1,2,3-cd]perylene adsorbed on polyethylene MP exhibited lower photodegradation rates than the aqueous phase. These results indicate that these PAHs can act as photocatalysts; their role of PAHs may have two adverse effects on marine environment. First, enhanced photodegradation of plastic waste increased the production of MPs. Second, the lifetime of PAHs is extended, thereby enhancing PAHs pollution in marine environments.

Kinetics and product identification of water-dissolved nitroguaiacol photolysis under artificial sunlight.

Nitroguaiacols are typical constituents of biomass-burning emissions, including absorbing aerosols which contribute to climate change. Although they are also harmful to humans and plants, their atmospheric fate and lifetimes are still very speculative. Therefore, in this work, the photolysis kinetics of aqueous-phase 4-nitroguaiacol (4NG) and 5-nitroguaiacol (5NG), and the resulting photo-formed products were investigated under artificial sunlight, observing also the effect of sunlight on the absorption properties of the solutions. We found the photolysis of 5NG slower than that of 4NG, whereas the absorbance in the visible range prevailed in the 5NG solutions at the end of experiments. Although we identified dinitroguaiacol as one of the 4NG photolysis products, which increased light absorption of 4NG-containing solutions, considerably more chromophores formed in the 5NG photolyzed solutions, implying its stronger potential for secondary BrC formation in the atmosphere. In general, denitration, carbon loss, hydroxylation, nitration, and carbon gain were characteristic of 4NG phototransformation, while carbon loss, hydroxylation, and carbon gain were observed in the case of 5NG. The photolysis kinetics was found of the first order at low precursor concentrations (<0.45mM), resulting in their lifetimes in the order of days (125 and 167h illumination for 4NG and 5NG, respectively), which suggests long-range transport of the investigated compounds in the atmosphere and proposes their use as biomass-burning aerosol tracer compounds.

Leaching of chemicals and DOC from tire particles under simulated marine conditions

Tire wear particles (TWPs) represent one of the major anthropogenic pools of particles ending up in the environment. They contain a large variety of chemicals, a part of which may be released into the environment through leaching, although the influence of sunlight and other environmental factors during this process is still unclear. This laboratory study compares the leaching of organic compounds from TWP in seawater in the dark and under artificial sunlight for 1) cryo-milled tire tread (CMTT), 2) ‘virgin’ crumb rubber (VCR) and 3) crumb rubber immersed in the sea for ≥12 months prior to the experiments (WCR). Leachates were analyzed for dissolved organic carbon (DOC) and 19 tire-derived chemicals, benzothiazoles and phenylguanidines as well as phenylendiamines by liquid chromatography-high resolution-mass spectrometry. For DOC and most chemicals, the amounts released decreased in the order CMTT &amp;gt; VCR &amp;gt; WCR and increased when leaching occurred under artificial sunlight. sunlight also led to the formation of 23 transformation processes related to 1,3-diphenylguanidine (DPG). In contrast, 4-hydroxydiphenylamine (4-HDPA) and N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine quinone (6-PPDQ) were found in lower amounts upon sunlight exposure. The 19 quantified chemicals, however, did only account for 6%–55% of the DOC in the leachates; most of the DOC, thus, remained unexplained. This study highlights that the amount of chemicals leached from tire particles depends upon their aging history and may be modulated by environmental conditions.

Cotton fabric loaded with ZnO nanoflowers as a photocatalytic reactor with promising antibacterial activity against pathogenic E. coli

Nanofinishing is the process by which ultrafine dispersion of nanomaterials is applied to a textile for the development of functionalities. The utilization of nanometal oxides as antimicrobial agents have shown a substantial antimicrobial property in cotton. In the present study, previously synthesized powder containing ZnO nanoflowers (ZnO NFs) was characterized for morphology, surface composition, roughness, and charge using Transmission electron microscopy (TEM), Scanning transmission electron microscopy (STEM), Atomic force microscopy(AFM) and Zeta potential. Optical properties of crystalline ZnO were determined by Photoluminescence (PL), Diffused reflectance Spectroscopy (DRS), and bandgap energy determination. Highly crystalline, ZnO NFs bearing crystal defects and high surface charge were loaded onto the pristine cotton by a dip coating method using Triton X-100 as dispersant and iSys MTX fabric binder. The pristine cotton fabric of 125 g/m2 was nano finished by loading 20,42 and 58 µg/cm2 (1–3 dip cycles) ZnO NFs respectively. The loading of ZnO NFs onto the surface of cotton fabric was confirmed by SEM and used for antibacterial activity against E. coli as a photocatalytic reactor. The prepared samples were irradiated with a UV lamp of λmax = 254 nm (15 min, 30 min, 45 min) and D65 artificial sunlight (60 min, 120 min, 180 min) to investigate their photocatalytic activity against pathogenic E. coli using modified Breed Smear’s method. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of ZnO NFs@ cotton were determined as 19.53 µg/ml and 39.06 µg/ml respectively after exposure to UV light. After exposure to sunlight MIC and MBC observed were higher i.e. 156.25 µg/ml and 312.5 µg/ml respectively showing lesser activity in sunlight as compared to ionizing UV radiations. To verify the photocatalytic activity, hydroxyl radicals generated by ZnO NFs@ cotton were also determinedtime-resolved PL on exposure to a UV lamp and D65 artificial sunlight. This nano-finished cotton is a promising candidate to be used as a medical textile with high antibacterial activity even after 20 washing cycles with only a 5% decrease in efficiency.

Photocatalytical transformation of fluorotelomer- and perfluorosulfonamide-based PFAS on mineral surfaces and soils in aqueous suspensions

Per- and polyfluorinated substances (PFAS) are widely used industrial and household chemicals and occur on various contaminated field sites. To better understand their behavior on soils, spike experiments were performed with 6:2 diPAP (6:2 polyfluoroalkyl phosphate diester) on pure mineral phases (titanium dioxide, goethite and silicon dioxide) in aqueous suspensions under artificial sunlight. Further experiments were performed with uncontaminated soil and four precursor PFAS. Titanium dioxide (referenced as 100 %) showed the highest reactiveness to transform 6:2 diPAP to its primary metabolite 6:2 fluorotelomer carboxylic acid, followed by goethite with the addition of oxalate (4.7 %), silicon dioxide (1.7 %) and soil (0.0024 %). Experiments with four precursors [6:2 diPAP, 6:2 fluorotelomer mercapto alkyl phosphate (FTMAP), N-ethyl perfluorooctane sulfonamide ethanol–based phosphate diester (diSAmPAP), N-ethyl perfluorooctane sulfonamidoacetic acid (EtFOSAA)] on natural soils showed a transformation of all four precursors by simulated sunlight. The production of the primary intermediate from 6:2 FTMAP (6:2 FTSA, rate constant k = 2.7∗10−3h−1) was approximately 13-times faster than from 6:2 diPAP (6:2 FTCA, rate constant k = 1.9∗10−4h−1). EtFOSAA was completely decomposed within 48 h whereas only ~7 % diSAmPAP was transformed in the same time. The primary photochemical transformation product of diSAmPAP and EtFOSAA was PFOA, PFOS was not detected. The production rate constant of PFOA varied significantly between EtFOSAA (k = 0.01h−1) and diSAmPAP (k = 1.3∗10−3h−1). Photochemically produced PFOA consisted of branched and linear isomers and can therefore be used in source tracking. Experiments with different soils suggest that the oxidation of EtFOSAA to PFOA is expected to primarily be driven by hydroxyl radicals, whereas for the oxidation of EtFOSAA to further intermediates, another mechanism instead or in addition to the oxidation by hydroxyl radicals is responsible.

Briefly Analyze the Impact of Artificial Light Sources on Human Health—Take Zhuqiang Artificial Sunlight Lamp as an Example

Briefly Analyze the Impact of Artificial Light Sources on Human Health—Take Zhuqiang Artificial Sunlight Lamp as an Example

Effect of atmosphere and relative humidity on photodegradation of clopidogrel under artificial solar and indoor light irradiation

Knowledge of the chemical stability of active pharmaceutical ingredients (APIs) is an important issue in the drug development process. This work describes a methodical approach and a comprehensive protocol for forced photodegradation studies of solid clopidogrel hydrogen sulfate (Clp) under artificial sunlight and indoor irradiation at different relative humidities (RHs) and atmospheres. The results showed that, at low RHs (up to 21%), this API was relatively resistant to simulated sunlight as well as indoor light. However, at higher RHs (between 52% and 100%), more degradation products were formed, and the degradation rate increased with rising RH. The influence of oxygen on the degradation was relatively low, and most degradation reactions proceeded even in humid argon atmosphere. The photodegradation products (DP) were analyzed with two different HPLC systems (LC-UV, LC-UV-MS) and selected impurities were separated by a semi-preparative HPLC and identified by high resolution mass spectrometry (ESI-TOF-MS) and 1H NMR techniques. Based on the obtained results, a light induced degradation pathway could be proposed for Clp in solid state.

Partial Photoluminescence Imaging for Inspection of Photovoltaic Cells: Artificial LED Excitation and Sunlight Excitation

Photovoltaic power is a crucial renewable energy source that has the potential to enhance a city’s sustainability. However, in order to identify the various issues that may occur during the lifespan of a photovoltaic module, solar module inspection techniques are crucial. One valuable technique that is commonly used is luminescence, which captures silicon emissions. This article focuses on a specific luminescence technique called partial photoluminescence. This technique involves illuminating a specific portion of the solar cell surface and recording the luminescence emission generated in the remaining area. This method has been trialed in a laboratory environment, utilizing infrared LEDs as the excitation source. An analysis of the main parameters that affect the technique is provided, where pictures have been taken under varying exposure times ranging from 50 ms to 400 ms, irradiance levels ranging from 200 W/m2 to 1000 W/m2, and a percentage of illuminated cells ranging from 10% to 40%. Furthermore, the experimental device has been modified to generate images utilizing sunlight as the excitation source. Several pictures of damaged cells were taken under an irradiance range of 340 W/m2 to 470 W/m2. The quality of the partial photoluminescence images is comparable to conventional electroluminescence images, but longer exposure times are required.

Nachhaltiger Eisen‐Photokatalysator auf Holzbasis für vielfältige Anwendungen mit Sonnenlicht: Wasseraufbereitung und radikalische Photopolymerisation

AbstractDurch Behandlung von Holz und Eisenoxid wurde ein nachhaltiger Photokatalysator für vielfältige Verwendungzwecke hergestellt, welcher demethyliertes Lignin (Fe3O4@D‐wood) enthält. Die Charakterisierung erfolgte mittels XRD, UV/Vis, Photostromunterschungen und elektrochemischen Messungen. Dieses Material wurde zum Gegenstand photokatalytischer Untersuchungen für die Wasseraufbereitung und die Materialsynthese mittels radikalischer Photopolymerisation. Die Bestrahlung vonFe3O4@D‐woodmit künstlichem Sonnenlicht zeigte eine verbesserte Aktivität bei der photochemischen Oxidation von organischen Schadstoffen in Gegenwart von H2O2. Die effiziente Erzeugung reaktiver Radikale ermöglichte bei diesem System auch die Photopolymerisation. Hier können Radikale, die auf reaktiven Sauerstoffspezies (ROS) basieren und in dem katalytischen Zyklus erzeugt werden, als die dominierenden Spezies zur Initiierung der radikalischen Polymerisation angesehen werden. Eine Mischung ausUDMAundTPGDAzeigte eine gute Reaktivität mit Cumolhydroperoxid (CHP). Der für die Wasseraufbereitung verwendete Photokatalysator ermöglicht die Wiederverwendung für die Photopolymerisation.