Light Irradiation Time Research Articles

A study on the proliferation of Myzus persicae (sulzer) during the winter season for year-round production within a smart farm facility.

In this study, we examined the feasibility of Myzus persicae proliferation through interrelationships with host plants in a smart farm facility during winter. We investigated aphid proliferation under an LED artificial light source and attempted to interpret aphid proliferation in relation to the net photosynthetic rate of the host plant, Eutrema japonicum. We observed that aphids continuously proliferated in the smart farm facility in winter without dormancy. The average number of aphids was greater under the 1:1 red:blue light irradiation time ratio, where the photosynthetic rate of the host plant was lower than under the 5:1 and 10:1 red:blue light irradiation time ratios. These results show that it is important to maintain a low net photosynthetic rate of the host plant, E. japonicum, in order to effectively proliferate aphids under artificial light such as in the case of smart farm facilities.

Facile preparation and modification of SrTiO3 through Ni–Cd co-doping as an efficient visible-light-driven photocatalyst

Visible light-driven Ni–Cd co-doped SrTiO3 photocatalyst was prepared through a co-precipitation technique. The influence of various amounts of doped elements on the properties of the pure SrTiO3 phase has been explored. The characterization was performed employing the X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopy (XPS), field emission-scanning electron microscopy (FESEM), UV–visible diffuse reflectance spectroscopy (DRS), photoluminescence (PL), electrochemical impedance spectroscopy (EIS), and transient photocurrent experiments. By Ni–Cd co-doping, the average particle size was reduced from 100 to 65 nm, the band gap value was lowered from 3.2 to 2.78 eV, and the powder's surface area was increased by about 2.3 times compared with the pure phase. Low PL peak intensity, small EIS radius, and higher photocurrent density of the 5 wt% doped sample indicate higher charge transfer efficiency than the pure sample. The effect of different photocatalytic experiment parameters on the photodegradation performance has been studied. In this regard, a 60-min visible light irradiation time, 1 g mL−1 initial dye concentration, and 0.7 g L−1 powder dosage were found to be the best values. After 60 min of visible light irradiation, doped SrTiO3 with 5 wt% Ni–Cd thoroughly degraded methylene blue (MB) dye. Additionally, the superoxide radical and holes also play a significant role in photodegradation as determined by the scavenger trapping test. Compared with MB, the prepared sample demonstrated less degradation ability for methyl orange (MO) and Rhodamine-B (RhB) dyes.

Artificial Intelligence-Assisted Terahertz Imaging for Rapid and Label-Free Identification of Efficient Light Formula in Laser Therapy.

Photodynamic therapy (PDT) is considered a promising noninvasive therapeutic strategy in biomedicine, especially by utilizing low-level laser therapy (LLLT) in visible and near-infrared spectra to trigger biological responses. The major challenge of PDT in applications is the complicated and time-consuming biological methodological measurements in identification of light formulas for different diseases. Here, we demonstrate a rapid and label-free identification method based on artificial intelligence (AI)-assisted terahertz imaging for efficient light formulas in LLLT of acute lung injury (ALI). The gray histogram of terahertz images is developed as the biophysical characteristics to identify the therapeutic effect. Label-free terahertz imaging is sequentially performed using rapid super-resolution imaging reconstruction and automatic identification algorithm based on a voting classifier. The results indicate that the therapeutic effect of LLLT with different light wavelengths and irradiation times for ALI can be identified using this method with a high accuracy of 91.22% in 33 s, which is more than 400 times faster than the biological methodology and more than 200 times faster than the scanning terahertz imaging technology. It may serve as a new tool for the development and application of PDT.

Photocatalytic degradation of Estrone and Congo red by the magnetic antibacterial photocatalyst g-C3N4/CeO2/M-rGO under visible light and optimization by Box-Behnken statistical design (BBD)

Construction of multi-interface contact step-scheme photocatalyst is a promising pathway to achieve high-electron transfer efficiency for photodegradation Estrone and Congo red (CR). In this work, g-C3N4 was selected as the main component, CeO2 nanosheets with unique Ce4+→Ce3+ conversion property and M-rGO were loaded on the surface of g-C3N4 to construct magnetic photocatalyst, whose structure imparted reusability by magnetic retrieval and at the same time M-rGO acted as an efficient host for g-C3N4/CeO2 composite photocatalyst. The photocatalytic performances were investigated with Estrone and CR, and the results showed that the composite photocatalyst g-C3N4/CeO2/M-rGO could degrade 71% of Estrone and 92% of CR. Free radical scavenger test showed that superoxide and hydroxyl radical species played a major role in the degradation. Furthermore, it was demonstrated that the magnetic photocatalyst g-C3N4/CeO2/M-rGO possessed strong antibacterial properties against Proteus mirabilis. A three-factor-three-level Box-Behnken design (BBD) was selected to optimize three greatly influential parameters: light irradiation time (min), the mass of photocatalyst (mg) and pollution concentration (ppm) by responding surface methodology. It was expected that the g-C3N4/CeO2/M-rGO can be used as a magnetic photocatalyst to achieve its valorization, which has very broad development prospects in the field of environmental remediation or catalysis.

Influence of Factors in the Photopolymerization Process on Dental Composites Microhardness.

The aim of the present paper is to investigate the influence of factors in photopolymerization process that govern microhardness of three types of dental composites—universal (UC), bulk-fill (BC), and flowable (FC). Cylindrical specimens with different thicknesses are made and light cured. The significance of light intensity, irradiation time, and layer thickness on Vickers microhardness is evaluated by experimental design, analysis of variance, and regression analysis. It is found that the main factor influencing the microhardness on the top surface of the three composites is light intensity. The second factor is layer thickness for the UC and FC, while for BC, it is curing time. The third factor is curing time for the first two composites and layer thickness for bulk-fill. The significance of factors’ influence on the microhardness of the bottom surface is the same for the UC and FC, but different for BC. The main factor for the first two composites is layer thickness, followed by curing time and light intensity. For bulk-fill, curing time is main factor, light intensity is second, and layer thickness is last. Different significance of factors influencing the microhardness on top and bottom surfaces of investigated composites is revealed for the first time in the present study.

Photocatalytic degradation of tetracycline hydrochloride by a Fe3O4/g-C3N4/rGO magnetic nanocomposite mechanism: modeling and optimization.

The photocatalytic degradation of antibiotics requires a good separation efficiency of photogenerated electron-hole pairs and a wide visible light absorption range. Current studies have discussed the successful preparation of ferroferric oxide/graphite carbon nitride/reduced graphene oxide (Fe3O4/g-C3N4/rGO). The phase structure and morphology of the Fe3O4/g-C3N4/rGO composites were characterized by XRD, HR-TEM, SEM, and EDS. The obtained composites were used to degrade tetracycline hydrochloride (TCH) to evaluate its photocatalytic activity. The effects of four variables on the degradation of TCH were analyzed by the response surface method and artificial intelligence (gradient regression tree, random forest, artificial neural network, etc.). The results showed that the graphite carbon nitride in the catalyst maintained its original structure and that the photocatalytic activity was significantly improved. The degradation rate of TCH was 86.7% under the optimal conditions (the Fe3O4/g-C3N4/rGO dosage was 0.1g, pH = 7.0, the initial concentration of TCH was 20mg/L, and the visible light irradiation time was 60min). At the same time, the degradation rate of TCH changed little after the material was used five times, which indicates that the stability and recyclability of the Fe3O4/g-C3N4/rGO photocatalyst were excellent. Finally, a possible photocatalytic mechanism of the Fe3O4/g-C3N4/rGO photocatalyst is proposed in this paper.

Synthesis and Property Examination of Er2FeSbO7/BiTiSbO6 Heterojunction Composite Catalyst and Light-Catalyzed Retrogradation of Enrofloxacin in Pharmaceutical Waste Water under Visible Light Irradiation.

A new photocatalyst, Er2FeSbO7, was prepared by solid phase sintering using the high-temperature synthesis method for the first time in this paper. Er2FeSbO7/BiTiSbO6 heterojunction (EBH) catalyst was prepared by the solvent thermal method for the first time. Er2FeSbO7 compound crystallized in the pyrochlore-type architecture and cubelike crystal system; the interspace group of Er2FeSbO7 was Fd3m and the crystal cellular parameter a of Er2FeSbO7 was 10.179902 Å. The band gap (BDG) width of Er2FeSbO7 was 1.88 eV. After visible light irradiation of 150 minutes (VLGI-150min) with EBH as a photocatalyst, the removal rate (RR) of enrofloxacin (ENR) concentration was 99.16%, and the total organic carbon (TOC) concentration RR was 94.96%. The power mechanics invariable k toward ENR consistency and visible light irradiation (VLGI) time with EBH as a photocatalyzer attained 0.02296 min−1. The power mechanics invariable k which was involved with TOC attained 0.01535 min−1. The experimental results showed that the photocatalytic degradation (PCD) of ENR within pharmaceutical waste water with EBH as a photocatalyzer under VLGI was in keeping with the single-order reactivity power mechanics. The RR of ENR with EBH as a photocatalyzer was 1.151 times, 1.269 times or 2.524 times that with Er2FeSbO7 as a photocatalyst, BiTiSbO6 as a photocatalyst, or N-doping TiO2 (N-TO) as a photocatalyst after VLGI-150min. The photocatalytic activity, which ranged from high to low among above four photocatalysts, was as follows: EBHP > Er2FeSbO7 > BiTiSbO6 > N-TO. After VLGI-150min toward three periods of the project with EBH as a photocatalyst, the RR of ENR attained 98.00%, 96.76% and 95.60%. The results showed that the stability of EBH was very high. With appending trapping agent, it could be proved that the oxidative capability for degrading ENR, which ranged from strong to weak among three oxidic radicals, was as follows: superoxide anion > hydroxyl radicals (HRS) > holes. This work provides a scientific basis for the research and oriented leader development of efficient heterojunction catalysts.

Enhanced photo-reactivity of polyanthracene in the VIS region.

The wavelength-dependent photo-reactivity of polyanthracene was explored upon UV-C and VIS light irradiation. The material was prepared via one-pot chemical oxidation route using FeCl3 as oxidizing agent. A decrease in surface hydrophobicity of a polyanthracene-coated poly(methylmethacrylate) substrate from 109.11° to 60.82° was observed upon UV-C exposure for 48 hrs which was attributed to increase in oxygen content at the surface, as validated by energy dispersive X-ray spectroscopy. Upon exposure to ultraviolet-visible LEDs, photo-dimerization of polyanthracene in solution occurred and was monitored using UV-VIS spectroscopy. The photo-dimer product formation decreased from 381 nm to 468 nm and was found to be higher for the polyanthracene material compared to the monomer anthracene. At 381 nm, photo-dimerization of the material was found to be approx. 4x more efficient than the non-substituted monomer counterpart. Results obtained show that photo-dimerization of polyanthracene will proceed upon exposure with visible light LEDs with reduction in efficiency at longer wavelengths. To compensate, irradiation power of the light source and irradiation time were increased.

Zeolitic imidazolate framework grafted by cobalt tungstate as an efficient photocatalyst for photocatalytic oxidative desulfurization of dibenzothiophene

In this research, novel nanohybrid of zeolitic imidazolate framework supported cobalt tungstate semiconductor (ZIF-67@CoWO4) with various CoWO4 loading ratios (from 0 to 30 %wt) has been fabricated as a visible-light-driven photocatalyst for dibenzothiophene (DBT) removal from model fuel. XRD, UV-DRS, FE-SEM, EDX, BET and VSM characterizations were used to analyze the fabricated nanocomposites. At specific experimental conditions (100 mg/l DBT in model fuel, photocatalyst dosage of 2 g/l, visible light irradiation time of 2 h and H2O2/DBT mole ratio of 8:1), the ZIF-67@(1 wt%)CoWO4 sample exhibited excellent photocatalytic oxidative desulfurization (PODS) activity (96.7%) between different prepared photocatalysts, The improved reaction performance of ZIF-67@(1%wt)CoWO4 heterostructure can be attributed to the reciprocal effects of the high adsorption capacity of ZIF-67, optical properties of CoWO4 nanoparticles and the high charges separation and transfer efficiencies. Besides, the ZIF-67@CoWO4 photocatalyst possesses good stability for PODS and can be reused for five reaction cycles without a significant activity loss, indicating that it might be very useful in the deep PODS of hydrocarbon fuel.

Statistical optimization of process conditions for pyrvinium pamoate elimination using UV/zeolite‐based nanostructures/H 2 O 2

Statistical optimization of process conditions for pyrvinium pamoate elimination using UV/zeolite‐based nanostructures/H ₂ O ₂

Application of machine learning algorithms in predicting the photocatalytic degradation of perfluorooctanoic acid

ABSTRACT Perfluorooctanoic acid (PFOA) is used in a variety of industries and is highly persistent in the environment, with potential human health risks. Photocatalysis has been extensively used for the decomposition of various organic pollutants, yet its simulation and modeling are challenging. This research aimed to establish different machine learning (ML) algorithms which can simulate and predict the photocatalytic degradation of PFOA. The published results were used to estimate and predict the photocatalytic degradation of PFOA. Statistical criteria including the coefficient of determination (R2 ), mean absolute error (MAE), and mean squared error (MSE) were considered in assessing the best method of modeling. Among the seven ML algorithms pre-screened, Adaptive Boosting (AdaBoost), Gradient Boosting Machine (GBM), and Random Forest (RF) showed the best performance and were chosen for deep modeling and analysis. Grid search was used to optimize the models developed by AdaBoost, GBM, and RF; and permutation variable importance (PVI) was used to analyze the relative importance of different variables. Based on the modeling results, GBM model (R2 = 0.878, MSE = 106.660, MAE = 6.009) and RF model (R2 = 0.867, MSE = 107.500, MAE = 6.796) showed superior performances compared with AdaBoost model (R2 = 0.574, MSE = 388.369, MAE = 16.480). Furthermore, the PVI results suggested that the GBM model provided the best outcome, with the light irradiation time, type of catalyst, dosage of catalyst, solution pH, irradiation intensity, initial PFOA concentration, oxidizing agents (peroxymonosulfate, ammonium persulfate, and sodium persulfate), irradiation wavelength, and solution temperature as the most important process variables in decreasing order.

Synthesis, Performance Measurement of Bi2SmSbO7/ZnBiYO4 Heterojunction Photocatalyst and Photocatalytic Degradation of Direct Orange within Dye Wastewater under Visible Light Irradiation.

Originally, the new catalyst Bi2SmSbO7 was synthesized by the hydrothermal synthesis method or by the solid-phase sintering method at a lofty temperature. A solvothermal method was utilized to prepare a Bi2SmSbO7/ZnBiYO4 heterojunction photocatalyst (BZHP). The crystal structure of Bi2SmSbO7 belonged to the pyrochlore structure and face-centered cubic crystal system by the space group of Fd3m. The cell parameter a was equivalent to 10.835(1) Å (Bi2SmSbO7). With Bi2SmSbO7/ZnBiYO4 heterojunction (BZH) as the photocatalyst, the removal rate (RR) of direct orange (DO) and the total organic carbon were 99.10% and 96.21% after visible light irradiation of 160 min (VLI-160M). The kinetic constant k toward DO concentration and visible light irradiation time (VLI) with BZH as photocatalyst reached 2.167 min−1. The kinetic constant k, which was concerned with total organic carbon, reached 0.047 min−1. The kinetic curve that came from DO degradation with BZH as a catalyst under VLI conformed to the second-order reaction kinetics. After VLI-160M, the photocatalytic degradation (PD) removal percentage of DO with BZH as the photocatalyst was 1.200 times, 1.268 times or 3.019 times that with Bi2SmSbO7 as the photocatalyst, ZnBiYO4 as the photocatalyst or with nitrogen-doped titanium dioxide as the photocatalyst. The photocatalytic activity (PA) was as following: BZH > Bi2SmSbO7 > ZnBiYO4 > nitrogen-doped titanium dioxide. After VLI-160M for three cycles of experiments with BZH as the photocatalyst, the RR of DO reached 98.03%, 96.73% and 95.43%, respectively, which meant that BZHP possessed high stability. By using the experiment of adding a trapping agent, the oxidative purifying capability for degradation of direct orange, which was in gradual depressed order, was as following: hydroxyl radical > superoxide anion > holes. Finally, the possible degradation pathway and degradation mechanism of DO were discussed systematically. A new high active heterojunction catalyst BZHP, which could efficiently remove toxic organic pollutants such as DO from dye wastewater after VLI, was obtained. Our research was meant to improve the photocatalytic property of the single photocatalyst.

Degradation of phenol by photocatalysis using TiO2/montmorillonite composites under UV light.

Composites of titanium (IV) oxide combined with montmorillonite (MMT) with various TiO2/MMT were prepared for photocatalysis application. The prepared samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), diffuse reflectance UV-visible spectroscopy, and X-ray photoelectron spectroscopy (XPS). The main influential factors such as the TiO2/MMT dose, calcined temperature, and pH value of the solution were studied. The main intermediates of phenol degradation were determined by high performance liquid chromatography (HPLC). The results showed that the average size of TiO2 nanoparticles was decreased from 22.51 to 10.66nm through the immobilization on MMT. The components in the interlayer domain were replaced by titanium pillars, and the pillaring reaction proceeded in the interlayer domain, the basic skeleton of MMT was unchanged, and TiO2 was dispersed on the surface of the MMT. When the initial concentration of phenol is 10mg/L, the phenol solution pH is 6, and the UV light irradiation time is 240min; the phenol degradation rate of 30%TiO2/MMT composite is 89.8%, which is better than MMT (11.5%) and pure TiO2 (58.8%). It shows that TiO2 loaded on MMT improves its photocatalytic activity. The phenol reaction process detected by HPLC showed that it had undergone through hydroquinone and benzoquinone, and finally converted into maleic acid and carbon dioxide and small molecules. The possible photocatalysis mechanism is presented.

Inhibition of efflux pump encoding genes and biofilm formation by sub-lethal photodynamic therapy in methicillin susceptible and resistant Staphylococcus aureus

BackgroundPhotodynamic therapy (PDT) is an effective method to inactivate microorganisms which is based on reactive oxygen species (ROS) generated by photosensitizer and light at certain wavelength. Exposure to sub-lethal dose of PDT (sPDT) could activate the regulatory systems in the surviving bacteria in response to oxidative stress. This study aimed to evaluate the effect of sPDT on efflux pump and biofilm formation in Staphylococcus aureus (S. aureus), which are two important virulence related factors. MethodsDifferent light irradiation time and toluidine blue O (TBO) concentrations were tested to select a sPDT in methicillin-susceptible and methicillin-resistant S. aureus (MSSA and MRSA). Efflux function was evaluated with EtBr efflux experiment. Biofilm formation was evaluated by crystal violet staining. Gene expressions of norA, norB, sepA, mepA and mdeA following sPDT were analyzed with real-time PCR. ResultsSub-lethal PDT was set at 40 J/cm2 associated with 0.5 μM TBO. Efflux function was significantly inhibited in both strains. The average expression levels of mdeA and mepA in MSSA and MRSA were increased by (3.09, 1.77, 1.57) and (3,44, 1.59, 6.29) fold change respectively, norB and sepA were decreased by (3.77, 6.14) and (3.02, 3.47) fold change respectively. Expression level of norA was decreased by 5.44-fold change in MSSA but increased by 2.80-fold change in MRSA. Biofilm formation in both strains was impeded. ConclusionsTBO-mediated sPDT could inhibit efflux pump function, alter efflux pump encoding gene expression levels and retard biofilm formation in MSSA and MRSA. Therefore, sPDT is proposed as a potential adjuvant therapy for infections.

Solar Light-Assisted Oxidative Degradation of Ciprofloxacin in Aqueous Solution by Iron(III) Chelated Cross-Linked Chitosan Immobilized on a Glass Plate

The massive worldwide use of antibiotics leads to water pollution and increasing microbial resistance. Hence, the removal of antibiotic residues is a key issue in water remediation. Here, we report the solar light-assisted oxidative degradation of ciprofloxacin (CPF), using H2O2 in aqueous solution, catalyzed by iron(III) chelated cross-linked chitosan (FeIII-CS-GLA) immobilized on a glass plate. The FeIII-CS-GLA catalyst was characterized by FTIR and 57Fe-Mössbauer spectroscopies as well as X-ray diffraction, revealing key structural motifs and a high-spin ferric character of the metal. Catalytic degradation of CPF was investigated as a function of solar light irradiation time, solution pH, concentration of H2O2 and CPF, as well as cross-linker dosage and iron(III) content in FeIII-CS-GLA. The system was found to serve as an efficient catalyst with maximum CPF degradation at pH 3. The specific ·OH scavenger mannitol significantly reduces the degradation rate, indicating that hydroxyl radicals play a key role. The mechanism of catalytic CPF degradation was evaluated in terms of pseudo-first-order and Langmuir-Hinshelwood kinetic models; adsorption of CPF onto the FeIII-CS-GLA surface was evidenced by field emission scanning electron microscopy coupled with energy dispersive X-ray spectroscopy. FeIII-CS-GLA can be reused multiple times with only minor loss of catalytic efficiency. Antimicrobial activity tests performed against both Gram-negative (Escherichia coli DH5α, Salmonella typhi AF4500) and Gram-positive bacteria (Bacillus subtilis RBW) before and after treatment confirmed complete degradation of CPF. These results establish the immobilized FeIII-CS-GLA as a rugged catalyst system for efficient photo-Fenton type degradation of antibiotics in aqueous solutions.

Inactivation of Bacillus subtilis by Curcumin-Mediated Photodynamic Technology through Inducing Oxidative Stress Response.

Photodynamic sterilization technology (PDT) is widely used in disease therapy, but its application in the food industry is still at the research stage because of the limitations of food-grade photosensitizers. Curcumin exhibits photosensitivity and is widely used as a food additive for its natural color. This study aimed to determine the effect of curcumin-mediated photodynamic technology (Cur-PDT) on Bacillus subtilis and to elucidate the anti-bacterial mechanism involved. First, the effects of curcumin concentration, duration of light irradiation, light intensity, and incubation time on the inactivation of B. subtilis were analyzed. It was found that Cur-PDT inactivated 100% planktonic cells with 50 μmol/L curcumin in 15 min (120 W). Then, the cell morphology, oxidation state and the expression of membrane structure- and DNA damage-related genes of B. subtilis vegetative cells were investigated under different treatment conditions. The membrane permeability of cells was enhanced and the cell membrane structure was damaged upon treatment with Cur-PDT, which were exacerbated with increases of treatment time and curcumin concentration. Meanwhile, the production of reactive oxygen species increased and the activities of the antioxidant enzymes SOD, GPX, and CAT decreased inside the cells. Furthermore, the Cur-PDT treatment significantly downregulated the mRNA of the membrane protein TasA and upregulated the DNA damage recognition protein UvrA and repair protein RecA of B. subtilis. These results suggested that curcumin-mediated PDT could effectively inactivate B. subtilis by inducing cell redox state imbalance, damaging DNA, and disrupting membrane structures.

ZrO2–Ag2O nanocomposites encrusted porous polymer monoliths as high-performance visible light photocatalysts for the fast degradation of pharmaceutical pollutants

This work reports a unique ZrO2-Ag2O heterojunction nanocomposite uniformly dispersed on a macro-/meso-porous polymer monolithic template to serve as simple and effective visible light-driven heterogeneous plasmonic photocatalysts for water decontamination. The monolithic photocatalysts' structural properties and surface morphology are characterized using various surface and structural characterization techniques. The photocatalytic performance of the proposed photocatalysts is evaluated by optimizing multiple operational parameters. The photocatalytic properties of the fabricated monolithic nanocomposite are monitored through time-dependent photocatalytic disintegration of norfloxacin drug, a widely employed antimicrobial, with considerable aquatic persistence. The analytical results conclude that a (60:40) ZrO2-Ag2O nanocomposite embedded polymer monolith exhibits superior photocatalytic activity for the complete mineralization of norfloxacin molecules under optimized conditions of solution pH (3.0), photocatalyst quantity (100mg), pollutant concentration (15mg/L), photosensitizers (2.0mM KBrO3), visible light intensity (300W/cm2 tungsten lamp) and irradiation time (≤ 1h). The proposed new-age inorganic-organic hybrid visible light photo-catalysts with superior structural and surface properties exhibit brilliant performance and fast responsiveness for water decontamination applications, in addition to their excellent chemical stability, high durability, multi-reusability, and cost-effectiveness.

Photoresponsive Gelation of Four-Armed Poly(ethylene glycol) with Photodimerizable Groups.

Standard hydrogels prepared by free radical polymerization (FRP) have heterogeneous structures with a wide mesh size distribution, which affect their mechanical and separation properties. Recent research has identified four-armed poly(ethylene glycol) (tetra-PEG) as a solution to this problem. tetra-PEG gels with a homogeneous network can be prepared and applied as high-strength gels and cell-culture substrates by reacting two types of tetra-PEG with different reactive groups at the ends. In this study, we report a photoresponsive tetra-PEG that undergoes a phase transition from a sol to a gel state in response to light. tetra-PEGs containing cinnamoyl and maleimide groups at the ends of the four-armed chains were found to gel when exposed to light. The effects of polymer concentration and light irradiation time on the gelation of tetra-PEG containing photodimerization groups were investigated. The results showed that the elastic modulus of the gel increased with the increase in the light irradiation time.

Effect of short-term light irradiation with varying energy densities on the activities of nitrifiers in wastewater

Microalgal-bacterial consortium (MBC) process has been proposed as an alternative to conventional activated sludge process for nitrogen removal from wastewater. As one of the most influencing parameters, light irradiation effects on microalgae have been extensively investigated. However, light influence on the performance of nitrifiers in activated sludge and its mechanism remains unclear. In this study, the effects of three factors (light irradiation power, irradiation time and sludge concentration) on activities and physiological characteristics of ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB) were systematically studied through both the Design of Experiments driven response surface methodology (RSM) approach and light-nitrification kinetic modeling. Results indicated that light irradiation with the specific light energy density (Es) at 0.0203–0.1571 kJ·mg−1 VSS (80–160 W/400–1000 μmol·m−2·s−1, 2.0–5.0 h and 2750–4250 mg·L−1) stimulated the relative AOB activities (rAOB) by 120.0%. This was supported by the increased electron transport system activity, key enzyme activity (AMO) , gene expression (amoA) and energy generation (ATP consumption) in the light treatment. Moreover, further Es increasing up to 0.18 kJ·mg−1 VSS inhibited both AOB and NOB activities. The inhibition was ascribed to the joint light responses of metabolic disorders and lipid peroxidation. The findings enhance our understanding of nitrifiers’ physiological responses to short-term light irradiation, and promote the development of MBC as a sustainable approach for wastewater treatment.

Green phytoextracts as natural photosensitizers in LED-based photodynamic disinfection of multidrug-resistant bacteria in wastewater effluent

The photodynamic treatment (PDT) process is a promising technology to control emerging pollutants and antimicrobial resistance problems in the water environment. The reactive oxygen species (ROS) produced when natural and nontoxic photosensitizers (PS) are exposed to light are the key functional components of the PDT process that can effectively achieve microbial inactivation with minimal negative impact. This study examined the application of green phytoextracts from two plants, Chamaecyparis obtusa and Moringa oleifera, as natural photosensitizers for the white light-emitting diode (LED) based photodynamic disinfection of multidrug-resistant (MDR) and total coliforms (TC) from secondary effluent in full-scale municipal wastewater treatment plants. Gas chromatography–mass spectrometry and Fourier transform infrared spectroscopy showed that the phytoextracts contained 57 compounds, particularly aromatic and phenolic hydroxyl compounds. The phytoextracts showed an excellent activity as a PS compared to the intrinsic antibacterial effect. Under a light intensity of 17 mW/cm2, the complete inactivation (6.55 Log CFU/mL) was observed at an irradiation time of 100 min for Escherichia coli ART-2 and 80 min for Staphylococcus aureus, meaning that E. coli was resistant. The light intensity was an important factor influencing photodynamic disinfection. For the complete disinfection of TC satisfying the water reclamation regulation, the irradiation time requirement was 20 min under a light intensity of 80 mW/cm2. During the photodynamic reaction, a significant amount of ROS was generated from the phytoextracts as the light irradiation time was increased. The major ROS was singlet oxygen (1O2, Type II) during the initial 40 min of reaction time and hydroxyl radical (•OH, Type I) after 40 min until complete inactivation.