RESUMO
Fenton and Fenton-like processes, which could produce highly reactive species to degrade organic contaminants, have been widely used in the field of wastewater treatment. Therein, the chemistry of Fenton process including the nature of active oxidants, the complicated reactions involved, and the behind reason for its strongly pH-dependent performance, is the basis for the application of Fenton and Fenton-like processes in wastewater treatment. Nevertheless, the conflicting views still exist about the mechanism of the Fenton process. For instance, reaching a unanimous consensus on the nature of active oxidants (hydroxyl radical or tetravalent iron) in this process remains challenging. This review comprehensively examined the mechanism of the Fenton process including the debate on the nature of active oxidants, reactions involved in the Fenton process, and the behind reason for the pH-dependent degradation of contaminants in the Fenton process. Then, we summarized several strategies that promote the Fe(II)/Fe(III) cycle, reduce the competitive consumption of active oxidants by side reactions, and replace the Fenton reagent, thus improving the performance of the Fenton process. Furthermore, advances for the future were proposed including the demand for the high-accuracy identification of active oxidants and taking advantages of the characteristic of target contaminants during the degradation of contaminants by the Fenton process.
Assuntos
Peróxido de Hidrogênio , Ferro , Eliminação de Resíduos Líquidos , Ferro/química , Peróxido de Hidrogênio/química , Eliminação de Resíduos Líquidos/métodos , Poluentes Químicos da Água/química , Poluentes Químicos da Água/análise , Águas Residuárias/química , Oxirredução , Radical Hidroxila/químicaRESUMO
Innately designed to induce physiological changes, pharmaceuticals are foreknowingly hazardous to the ecosystem. Advanced oxidation processes (AOPs) are recognized as a set of contemporary and highly efficient methods being used as a contrivance for the removal of pharmaceutical residues. Since reactive oxygen species (ROS) are formed in these processes to interact and contribute directly toward the oxidation of target contaminant(s), a profound insight regarding the mechanisms of ROS leading to the degradation of pharmaceuticals is fundamentally significant. The conceptualization of some specific reaction mechanisms allows the design of an effective and safe degradation process that can empirically reduce the environmental impact of the micropollutants. This review mainly deliberates the mechanistic reaction pathways for ROS-mediated degradation of pharmaceuticals often leading to complete mineralization, with a focus on acetaminophen as a drug waste model.
Assuntos
Acetaminofen , Espécies Reativas de Oxigênio , Acetaminofen/química , Espécies Reativas de Oxigênio/metabolismo , Poluentes Químicos da Água/química , Oxirredução , Preparações Farmacêuticas/metabolismoRESUMO
Harnessing bacteria for superoxide production in bioremediation holds immense promise, yet its practical application is hindered by slow production rates and the relatively weak redox potential of superoxide. This study delves into a cost-effective approach to amplify superoxide production using an Arthrobacter strain, a prevalent soil bacterial genus. Our research reveals that introducing a carbon source along with specific iron-binding ligands, including deferoxamine (DFO), diethylenetriamine pentaacetate (DTPA), citrate, and oxalate, robustly augments microbial superoxide generation. Moreover, our findings suggest that these iron-binding ligands play a pivotal role in converting superoxide into hydroxyl radicals by modulating the electron transfer rate between Fe(III)/Fe(II) and superoxide. Remarkably, among the tested ligands, only DTPA emerges as a potent promoter of this conversion process when complexed with Fe(III). We identify an optimal Fe(III) to DTPA ratio of approximately 1:1 for enhancing hydroxyl radical production within the Arthrobacter culture. This research underscores the efficacy of simultaneously introducing carbon sources and DTPA in facilitating superoxide production and its subsequent conversion to hydroxyl radicals, significantly elevating bioremediation performance. Furthermore, our study reveals that DTPA augments superoxide production in cultures of diverse soils, with various soil microorganisms beyond Arthrobacter identified as contributors to superoxide generation. This emphasizes the universal applicability of DTPA across multiple bacterial genera. In conclusion, our study introduces a promising methodology for enhancing microbial superoxide production and its conversion into hydroxyl radicals. These findings hold substantial implications for the deployment of microbial reactive oxygen species in bioremediation, offering innovative solutions for addressing environmental contamination challenges.
Assuntos
Arthrobacter , Biodegradação Ambiental , Radical Hidroxila , Ferro , Superóxidos , Radical Hidroxila/metabolismo , Superóxidos/metabolismo , Arthrobacter/metabolismo , Ferro/metabolismo , Ligantes , Microbiologia do Solo , Poluentes do Solo/metabolismo , Desferroxamina/metabolismoRESUMO
Recently, granular activated carbon (GAC) has shown its effectiveness as a cathode material for in situ ROS generation. Here, we present an electrochemically modified GAC cathode using electrode polarity reversal (PR) approach for enhanced H2O2 decomposition via 2-electron oxygen reduction reaction (2e-ORR). The successful GAC modification using PR necessitates tuning of the operational parameters such as frequency, current, and time intervals between the PR cycles. This modification enhances the GAC hydrophilicity by increasing the density of surface oxygen functionalities. After optimization of the electrode polarity, using the 20 (No PR)-2 (PR) interval and 140 mA current intensity, the â¢OH concentration reaches 38.9 µM compared to the control (No PR) (28.14 µM). Subsequently, we evaluated the enhanced â¢OH generation for the removal of glyphosate, a persistent pesticide used as a model contaminant. The modified GAC using PR removed 67.6% of glyphosate compared to 40.6% by the unmodified GAC without PR, respectively. The findings from this study will advance the utilization of GAC for in situ ROS synthesis, which will have direct implications on increasing the effectiveness of electrochemical water treatment systems.
RESUMO
Citrinin (CIT), a mycotoxin produced by Monascus, Penicillium, and other fungies, can contaminate red yeast rice and other foods, thus constraining their application and development. Exploring efficient degradation methods of citrinin is becoming as one of the hot research topics. In this study, the degradation of citrinin, irradiated by visible (Vis) light, ultraviolet (UV) light, and simulated sunlight alone, as well as in combination with hydrogen peroxide (light/H2O2), was investigated. The research demonstrates UV, Vis, and simulated sunlight all have a degree of degradation on citrinin, and the degradation efficiency correlates with light source and light intensity. Interestingly, when combined with 100 W Vis and 0.01 M H2O2, the citrinin degradation rate increases to 32%, compared to 1% and 5% achieved by Vis and H2O2 alone. Hydroxyl radicals, arising from the uniform cracking of H2O2 under Vis, were experimentally validated by electron spin resonance measurement and could accelerate the dissociation of citrinin by nucleophilic attacking. Employing the density functional theory, we deduced nucleophilic â¢OH mainly attack onto C8 and C5 site by comparing the electrophilic Parr functions (Pk+) value of main C atom of citrinin. This research presents a rapid and efficient degradation of citrinin by combining visible light with H2O2. PRACTICAL APPLICATION: This research presents a rapid and efficient method for the degradation of citrnin in red yeast rice and other citrnin containing products by combining visible light with H2O2.
RESUMO
The extracellular degradation of antibiotics facilitated by bio-nanoparticles is significant in the field of waste valorization. Among different bio-nanoparticles, bio-FeS nanoparticles stand out for their convenient and cost-effective synthesis. Nevertheless, there is a lack of understanding regarding the extracellular degradation of pollutants driven by bio-FeS nanoparticles. Hence, this study aimed to investigate the role of bio-FeS nanoparticles in the extracellular degradation of tetracycline under aerobic and anaerobic conditions. The findings demonstrated that bio-FeS nanoparticles generated hydroxyl radical (·OH), which significantly contributes to the degradation of tetracycline in both aerobic and anaerobic environments. The production of ·OH in anaerobic conditions was primarily attributed to the limited formation of FeS2 during the biosynthesis of nanoparticles, which was very different from aerobic conditions. The bio-FeS nanoparticles facilitated extracellular electron transport by promoting electron shuttles and Fe(II)/Fe(III) cycling, resulting in the continuous production of ·OH. The degradation pathways showed differences under aerobic and anaerobic conditions, with intermediates exhibiting higher toxicity and greater cellular damage under aerobic conditions. However, in anaerobic conditions, bio-FeS nanoparticles enabled the successful integration of intracellular and extracellular degradation of tetracycline. This research proposed a new avenue for biocatalysis and environmental remediation.
RESUMO
The widespread presence and use of Bisphenol A (BPA) in aquatic environments has caused significant ecological damage. Coal gangue (CG), a byproduct of coal mining, poses a major environmental concern due to its vast land occupation and potential for pollution. A magnetic recyclable geopolymer (MnFe2O4-CGP) using coal gangue geopolymer (CGP) as the carrier was successfully synthesized and was evaluated for its ability to Fenton-like degrade BPA. The characterization techniques revealed the successful incorporation of spherical MnFe2O4 onto the CGP surface and that CGP serves as an excellent platform for the immobilization and dispersion of MnFe2O4. The degradation rate reached 100% within 60 min at pH = 5, 15 mmol/L H2O2, 0.6 g/L catalyst, and 50 mg/L BPA, significantly higher than MnFe2O4 and CGP alone. It was indicated that the degradation rate of BPA in MnFe2O4-CGP composites was 0.1121 min-1, which was consistent with the first-order kinetic model. The saturation magnetization of MnFe2O4-CGP was measured to be 10.96 emu/g, enabling convenient recovery. MnFe2O4-CGP exhibited excellent stability, as the degradation rate of BPA remained above 95% even after five reaction cycles. This efficiency may be due to the MnFe2O4-CGP induced generation of reactive radicals. Quenching and EPR radical trapping experiments unequivocally confirmed that the reactive radical was hydroxyl radical (â¢OH). These results indicate that MnFe2O4-CGP has potential application prospects as a magnetic recyclable geopolymer composite in Fenton-like catalysis.
RESUMO
Despite the vital roles of Fe0/biochar composites in the Fenton-like systems for eliminating pollutants that have been recognized, the contributions of persistent free radicals (PFRs) of carbon-based materials are typically overlooked. In this study, the high-PFR-containing biochar nanoiron composites were prepared (nZVI/500), and the in situ generation of hydroxyl radicals (·OH) and degradation of p-nitrophenol (PNP) were investigated. The results showed that nZVI/500 could effectively remove PNP in solution within the pH range of 3-8. Quantitative experiments of ·OH presented that, compared with low PFRs-containing composites, nZVI/500 could generate 64.6 µM ·OH in 60 min without any extra energy consumption. Mechanistic studies revealed that (1) both PFRs and Fe0 are able to utilize dissolved oxygen to generate H2O2 in situ; (2) PFRs can promote the cycling of Fe3+/Fe2+ in the system due to their strong electron exchange ability; and (3) PFRs directly transfer electrons to H2O2; therefore, the presence of PFRs accelerates the generation of ·OH in the system and facilitates the removal of PNP. This study provides an important theoretical basis and technical reference for expanding the application of PFR-rich carbon-based materials to remove environmental pollutants.
RESUMO
Tumor tissues are well known for their unique high hydrogen peroxide (H2O2) microenvironment. How to exploit this tumor microenvironment for tumor cell killing is a question. In this study, a Mn-doped metal-organic framework (Mn-ZIF) was constructed. It possesses good peroxidase (POD) activity, which can oxidize tumor-localized H2O2 into hydroxyl radicals (·OH), that possesses the ability to directly kill tumor cells. More surprisingly, in vivo experiments the researchers not only observed the tumor-killing effect of Mn-ZIF, but also found it changes in macrophage phenotype in the tumor region. There was an increase in macrophage polarization towards the M1 subtype. This suggests that the tumor-killing effect of Mn-ZIF not only comes from its POD activity, but also regulates the immune microenvironment in the tumor region. In conclusion, the preparation of Mn-ZIF provides a new way for comprehensive tumor therapy.
RESUMO
The presence of polyethylene terephthalate (PET) microplastics (MPs) in waters has posed considerable threats to the environment and humans. In this work, a heterogeneous electro-Fenton-activated persulfate oxidation system with the FeS2-modified carbon felt as the cathode (abbreviated as EF-SR) was proposed for the efficient degradation of PET MPs. The results showed that i) the EF-SR system removed 91.3 ± 0.9 % of 100 mg/L PET after 12 h at the expense of trace loss (< 0.07 %) of [Fe] and that ii) dissolved organics and nanoplastics were first formed and accumulated and then quickly consumed in the EF-SR system. In addition to the destruction of the surface morphology, considerable changes in the surface structure of PET were noted after EF-SR treatment. On top of the emergence of the O-H bond, the ratio of C-O/C=O to C-C increased from 0.25 to 0.35, proving the rupture of the backbone of PET and the formation of oxygen-containing groups on the PET surface. With the verified involvement and contributions of SO4â¢- and â¢OH, three possible paths were proposed to describe the degradation of PET towards complete mineralization through chain cleavage and oxidation in the EF-SR system.
RESUMO
Systemic oxidative stress stemming from increased free radical production and reduced antioxidant capacity are common characteristics of obese individuals. Using hydrogen peroxide (H2O2) to induce DNA damage in vitro, in peripheral blood mononuclear cells (PBMCs) from obese subjects and controls, the DNA protective ability of dihidroqercetin (DHQ) and biochaga (B) alone or in combination, were evaluated. The effects of DHQ and B were estimated under two experimental conditions: pre-treatment, where cells were pre-incubated with the substances prior to H2O2 exposure; and post-treatment when cells were first exposed to H2 H2O2, and further treated with the compounds. DNA damage was evaluated using the comet assay. The results of pre- and post-treatment showed a significant decrease in DNA damage produced by H2O2 in the obese group. This decrease was not significant in control group probably due to a small number of subjects in this pilot study. More prominent attenuation was noted in the pre-treatment with DHQ (250 µg/mL). Analysis of antioxidant properties revealed that DHQ's remarkable reducing power, 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenging activity, and potent âOH scavenging properties may contribute to strong attenuation of H2O2 induced DNA damage. Also, B showed strong reducing power, DPPH, and âOH scavenging ability, while reducing power and DPPH scavenger effects were increased in the presence of DHQ. Conclusively, DHQ and B may reduce H2O2-induced DNA damage in PBMCs from obese subjects when challenged in vitro, and could be valuable tools in future research against oxidative damage-related conditions.
RESUMO
Investigating the fate of persistent organic pollutants in water distribution systems (WDSs) is of great significance for preventing human health risks. The role of iron corrosion scales in the migration and transformation of organics in such systems remains unclear. Herein, we determined that hydroxyl (â¢OH), chlorine, and chlorine oxide radicals are generated by Fenton-like reactions due to the coexistence of oxygen vacancy-related Fe(II) on goethite (a major constituent of iron corrosion scales) and hypochlorous acid (HClO, the main reactive chlorine species of residual chlorine at pH â¼ 7.0). â¢OH contributed mostly to the decomposition of atrazine (ATZ, model compound) more than other radicals, producing a series of relatively low-toxicity small molecular intermediates. A simplified kinetic model consisting of mass transfer of ATZ and HClO, â¢OH generation, and ATZ oxidation by â¢OH on the goethite surface was developed to simulate iron corrosion scale-triggered residual chlorine oxidation of organic compounds in a WDS. The model was validated by comparing the fitting results to the experimental data. Moreover, the model was comprehensively applicable to cases in which various inorganic ions (Ca2+, Na+, HCO3-, and SO42-) and natural organic matter were present. With further optimization, the model may be employed to predict the migration and accumulation of persistent organic pollutants under real environmental conditions in the WDSs.
Assuntos
Poluentes Químicos da Água , Cinética , Radicais Livres/química , Poluentes Químicos da Água/química , Oxirredução , Ferro/química , Compostos de Ferro/química , Minerais/químicaRESUMO
Plasma technology as an advanced oxidation technology, has gained increasing interest to generate numerous chemically reactive species during the plasma discharge process. Such chemically reactive species can trigger a chain of chemical reactions leading to the degradation of macromolecules including polysaccharides. This review primarily summarizes the generation of various chemically reactive species during plasma treatment and their effects on the physico-chemical properties and biological activities of polysaccharides. During plasma treatment, the type of chemically reactive species that play a major role is related to equipment, working gases and types of polysaccharides. The primary chain structure of polysaccharides did not changed much during the plasma treatment, other physico-chemical properties might be changed, such as molecular weight, solubility, hydrophilicity, rheological properties, gel properties, crystallinity, elemental composition, glycosidic bonding, and surface morphology. Additionally, the biological activities of plasma-treated polysaccharides including antibacterial, antioxidant, immunological, antidiabetic activities, and seed germination promotion activities in agriculture could be improved. Therefore, plasma treatment has the potential application in preparing polysaccharides with enhanced biological activities.
Assuntos
Gases em Plasma , Polissacarídeos , Polissacarídeos/química , Polissacarídeos/farmacologia , Gases em Plasma/química , Antioxidantes/química , Antioxidantes/farmacologia , Peso Molecular , Solubilidade , Antibacterianos/química , Antibacterianos/farmacologia , HumanosRESUMO
In this work, a novel CuMn-Sb-SnO2 anode is developed by a simple, low-cost preparation process. The doping of Cu and Mn causes surface reconstruction, which optimizes its electronic structure, compared to the Sb-SnO2 anode. Experimental results demonstrate that the levofloxacin degradation kinetics constant in the CuMn-Sb-SnO2 system (0.188 min-1) was 8.5 times higher than that in the Sb-SnO2 system, which is surpassing most reported anodes. Moreover, electrochemical characterization also revealed that the CuMn-Sb-SnO2 anode possessed more active sites, higher OEP potential, and lower charge transfer resistance. Notably, electrochemical characterization and EPR experiments confirmed the formation of Cu (III), highlighting their crucial role in promoting the generation of â¢OH during the catalytic process. Additionally, theoretical calculations and XPS analysis revealed that Cu and Mn rely on self-mediated redox shuttles to act as "electron porters", significantly accelerating internal electron transfer between Sn and Sb to enhance the production of â¢OH. Furthermore, the CuMn-Sb-SnO2 anode exhibits great practicability due to its efficient degradation of various antibiotics. This study offers valuable new insights into developing novel electrodes for the efficient degradation of antibiotic wastewater.
RESUMO
Ozonation is used worldwide for drinking water disinfection and increasingly also for micropollutant abatement from wastewater. Identification of transformation products formed during the ozonation of micropollutants is challenging due to several factors including (i) the reactions of both oxidants, ozone and hydroxyl radicals with the micropollutants, as well as with intermediate transformation products, (ii) effects of the water matrix on the ozone and hydroxyl radical chemistry and (iii) the generation of oxidation by-products. In this study, a simple approach to achieve realistic ozonation conditions in the absence of dissolved organic matter has been developed. It is based on composing synthetic water matrices with low-molecular-weight scavenger compounds (phenol, methanol, acetate, and carbonate) that mimic the chemical interactions of ozone and hydroxyl radicals with real water matrices. Synthetic waters composed of only four low-molecular-weight compounds successfully replicated two lake waters and two secondary wastewater effluents, matching instantaneous ozone demand, ozone and hydroxyl radical exposures in the initial phase, as well as the ozone evolution in the second phase of the ozonation process. The synthetic water matrices also reproduced the effects of temperature and pH changes observed in real waters. The abatement of two micropollutants, bezafibrate and atrazine, and the formation of the corresponding transformation products during ozonation were in agreement for synthetic and real waters. Furthermore, the kinetics and extent of bromate formation during ozonation in synthetic water were comparable to real lake water and wastewater. This supports the robustness of the proposed approach because bromate formation is very sensitive to the interplay of ozone and hydroxyl radicals. Furthermore, with the novel reaction system, a significant effect of hydroxyl radicals scavenging by carbonate on bromate formation was demonstrated. Overall, the herein-developed approach based on synthetic water matrices allows to perform realistic ozonation studies including both oxidants, ozone and hydroxyl radicals, without the constraints of using dissolved organic matter.
Assuntos
Ozônio , Poluentes Químicos da Água , Purificação da Água , Ozônio/química , Purificação da Água/métodos , Poluentes Químicos da Água/química , Radical Hidroxila/química , Águas Residuárias/química , Sequestradores de Radicais Livres/química , Peso MolecularRESUMO
The electro-Fenton (EF) process is an advanced oxidation technology with significant potential; however, it is limited by two steps: generation and activation of H2O2. In contrast to the production of H2O2 via the electrochemical two-electron oxygen reduction reaction (ORR), the electrochemical three-electron (3e-) ORR can directly activate molecular oxygen to yield the hydroxyl radical (â OH), thus breaking through the conceptual and operational limitations of the traditional EF reaction. Therefore, the 3e- ORR is a vital process for efficiently producing â OH in situ, thus charting a new path toward the development of green water-treatment technologies. This review summarizes the characteristics and mechanisms of the 3e- ORR, focusing on the basic principles and latest progress in the in situ generation and efficient utilization of â OH through the modulation of the reaction pathway, shedding light on the rational design of 3e- ORR catalysts, mechanistic exploration, and practical applications for water treatment. Finally, the future developments and challenges of efficient, stable, and large-scale utilization of â OH are discussed based on achieving optimal 3e- ORR regulation and the potential to combine it with other technologies.
RESUMO
This study explores novel approaches to enhance photocatalysis efficiency by introducing a photonic crystal (PC)-enhanced, multi-layered sub-bandgap photocatalytic reactor. The design aims to effectively utilize sub-bandgap photons that might otherwise go unused. The device consists of three types of layers: (1) two polymeric triplet-triplet annihilation upconversion (TTA-UC) layers converting low-energy green photons (λEx = 532 nm, 2.33 eV) to high-energy blue photons (λEm = 425 nm, 2.92 eV), (2) a platinum-decorated WO3 layer (Eg = 2.8 eV) serving as a visible-light photocatalyst, and (3) a PC layer optimizing both TTA-UC and photocatalysis. The integration of the PC layer resulted in a 1.9-fold increase in UC emission and a 7.9-fold enhancement in hydroxyl radical (â¢OH) generation, achieved under low-intensity sub-bandgap irradiation (17.6 mW cm-2). Consequently, the combined layered structure of TTA/Pt-WO3/TTA/PC achieved a remarkable 38.8-fold improvement in â¢OH production, leading to outstanding degradation capability for various organic pollutants (e.g., 4-chlorophenol, bisphenol A, and methylene blue). This multi-layered sub-bandgap photocatalytic structure, which uniquely combines TTA-UC and PC layers, offers valuable insights into designing efficient photocatalytic systems for future solar-driven environmental remediation.
RESUMO
Hydroxyl radical (·OH) scavenging capacity (HOSC) estimation is essential for evaluating antioxidants, natural extracts, or drugs against clinical diseases. While nanozymes offer advantages in related applications, they still face limitations in activity and selectivity. In response, this work showcases the fabrication of laminarin-modulated osmium (laminarin-Os) nanoclusters (1.45 ± 0.05 nm), functioning as peroxidase-like nanozymes within a colorimetric assay tailored for rational HOSC estimation. This study validates both the characterization and remarkable stability of laminarin-Os. By leveraging the abundant surface negative charges of laminarin-Os and the surface hydroxyls of laminarin, oxidation reactions are facilitated, augmenting laminarin-Os's affinity for 3,3',5,5'-tetramethylbenzidine (TMB) (KM = 0.04 mM). This enables the laminarin-Os-based colorimetric assay to respond to ·OH more effectively than citrate-, albumin-, or other polysaccharides-based Os. In addition, experimental results also validate the selective peroxidase-like behavior of laminarin-Os under acidic conditions. Antioxidants like ascorbic acid, glutathione, tannic acid, and cysteine inhibit absorbance at 652 nm in the colorimetric platform using laminarin-Os's peroxidase-like activity. Compared with commercial kits, this assay demonstrates superior sensitivity (e.g., responds to ascorbic acid 0.01-0.075 mM, glutathione 1-15 µg/mL, tannic acid 0.5-5 µM, and monoammonium glycyrrhizinate cysteine 1.06-10.63 µM) and HOSC testing for glutathione, tannic acid, and monoammonium glycyrrhizinate cysteine. Overall, this study introduces a novel Os nanozyme with exceptional TMB affinity and ·OH selectivity, paving the way for HOSC estimation in biomedical research, pharmaceutical analysis, drug quality control, and beyond.
Assuntos
Benzidinas , Sequestradores de Radicais Livres , Glucanos , Radical Hidroxila , Osmio , Benzidinas/química , Colorimetria/métodos , Sequestradores de Radicais Livres/química , Sequestradores de Radicais Livres/farmacologia , Glucanos/química , Radical Hidroxila/química , Radical Hidroxila/análise , Osmio/química , Oxirredução , Peroxidase/química , Peroxidase/metabolismoRESUMO
The effectiveness of ozonation, one of the techniques known for destroying organic contaminants from wastewater, depends on the composition of the wastewater matrix. The required ozone (O3) dose is determined based on the target compounds during ozonation. Hydroxyl radicals are quantified using a probe compound. The para-chlorobenzoic acid (pCBA) is typically used as a probe compound to measure hydroxyl radicals. However, real-time measurement is impossible, as the analysis process consumes time and resources. This study aimed to evaluate the spectroscopic characteristics of various organic substances in wastewater ozonation through fluorescence excitation-emission matrix and parallel factor analysis. The study also demonstrated that real-time analyzable tryptophan-like fluorescence (TLF) can be used as a hydroxyl radical index. Importantly, the correlation between para-chlorobenzoic acid and TLF was derived, and the results showed a high correlation (R2 = 0.91), confirming the reliability of our findings. Seven trace organic compounds, classified based on their reactivity with O3 and hydroxyl radicals, were selected as target compounds and treated with O3. The TLF index was used as a model factor for the removal rate of the target compounds. The experimental and model values matched when the O3 dose was below 1.0 g O3/g DOC (RMSE: 0.0445-0.0895).
Assuntos
Radical Hidroxila , Ozônio , Triptofano , Águas Residuárias , Poluentes Químicos da Água , Ozônio/química , Ozônio/análise , Águas Residuárias/química , Poluentes Químicos da Água/análise , Triptofano/análise , Triptofano/química , Radical Hidroxila/química , Radical Hidroxila/análise , Fluorescência , Eliminação de Resíduos Líquidos/métodos , Compostos Orgânicos/análise , Compostos Orgânicos/química , Clorobenzoatos/química , Clorobenzoatos/análise , Espectrometria de Fluorescência/métodos , Purificação da Água/métodosRESUMO
We investigated the deoxyribonucleic acid (DNA) damage induced by laser filamentation, which was generated by focusing femtosecond near-infrared Ti:Sapphire laser light in water at several repetition rates ranging from 1000 Hz to 10 Hz. Using plasmid DNA (pUC19), the single-strand break, double-strand break, nucleobase lesions, and the fragmented DNA were analyzed and quantified by agarose gel electrophoresis. Additionally, the H2O2 concentration after irradiation was determined. We observed that (1) the DNA damage per laser shot and (2) the enzyme-sensitive base lesions per total DNA damage decreased as the laser repetition rate increased. Furthermore, (3) extraordinarily short DNA fragments were likely to be produced, compared with those produced using X-rays, and (4) most OH radicals could be eliminated by recombination to generate H2O2, preventing them from damaging the DNA. The Monte-Carlo simulation of the strand break formation implies that the observed dependency of strand break efficiency on the laser repetition rate is mainly due to diffusion of DNA molecules. These findings quantitatively and qualitatively revealed that an intense laser pulse induces a specific DNA damage profile that is not induced by X-rays, a sparsely ionizing radiation source.