scholarly journals Insight into the Degradation of Two Benzophenone-Type UV Filters by the UV/H2O2 Advanced Oxidation Process

Water ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1238 ◽  
Author(s):  
Erdeng Du ◽  
Jiaqi Li ◽  
Siqi Zhou ◽  
Miao Li ◽  
Xiang Liu ◽  
...  
Keyword(s):  
Emerging Contaminants ◽  
Advanced Oxidation Process ◽  
Uv Light ◽  
Degradation Products ◽  
Ring Cleavage ◽  
Contaminant Concentration ◽  
Unique Contribution ◽  
Uv Filters ◽  
Positive Effects ◽  
Rsm Model

Environmental problems caused by UV filters, a group of emerging contaminants, have attracted much attention. The removal of two typical UV filters benzophenone (BP) and 4,4′-dihydroxy-benzophenone (HBP) in water was investigated by the UV/H2O2 process. The response surface methodology (RSM) and central composite design (CCD) were applied to investigate the effects of the process parameters on the degradation rate constants, including the initial contaminant concentration, H2O2 dose, and UV light intensity. BP is more easily degraded by the UV/H2O2 process. Both processes followed pseudo-first-order kinetics. The results obtained with the built RSM model are in accordance with the experimental results (adjusted coefficients R2(adj)= 0.9835 and 0.9778 for BP and HBP, respectively). For both processes, the initial contaminant concentration (exerting a negative effect) were the most important factors controlling the degradation, followed by H2O2 dose and UV intensity (exerting positive effects). A total of 15 BP degradation products and 13 HBP degradation products during the UV/H2O2 process were identified by LC/MS and GC/MS. A series of OH radical irritated reactions, including hydroxylation, carboxylation, and ring cleavage, led to the final degradation of BP and HBP. Degradation pathways of BP and HBP were also proposed. On the whole, this work is a unique contribution to the systematic elucidation of BP and HBP degradation by the UV/H2O2 process.

scholarly journals Biodegradation of two organic UV-Filters by single bacteria strains

2021 ◽  
Author(s):  
Florentina Laura Chiriac ◽  
Catalina Stoica ◽  
Iuiana Paun ◽  
Florinela Pirvu ◽  
Toma Galaon ◽  
...  
Keyword(s):  
Staphylococcus Aureus ◽  
Emerging Contaminants ◽  
Degradation Products ◽  
Aquatic Organisms ◽  
Uv Filters ◽  
Bacterial Strains ◽  
Gram Negative ◽  
Biodegradation Process ◽  
Salmonella Thyphimurium ◽  
Organic Uv Filters

Abstract Organic UV-filters, including 4-hydroxybenzophenone (4-HBP) and 2,4-dihydroxybenzophenone (BP-1), are persistent emerging contaminants whose presence in the environment poses a threat to aquatic organisms due to their endocrine disruptor’s properties. For this reason, finding suitable technological processes for their safety and efficient removal from the environment represent a priority for the scientific community. To the author’s knowledge, until now, there are no studies reporting the biodegradation of 4-HBP and BP-1 by a single bacteria strain. In this paper, there were tested the 4-HBP and BP-1 biodegradation potential of two Gram-positive (Staphylococcus aureus and Enterococcus faecalis) and two Gram-negative (Salmonella typhimurium and Serratia rubidae). The 4-HPB biodegradation process was observed only in the presence of Gram-negative bacterial strains. Thus, the biodegradation rates of 4-HBP reached up to 12.7% after 24h of incubation in presence of Salmonella thyphimurium and up to 24.0% after 24h of incubation with Serratia rubidae. Staphylococcus aureus was able to biodegrade 26.7% of BP-1, while Salmonella thiphymurium was able to biodegrade 14.7% of BP-1 after 24h of incubation. Their biodegradation products generated during the 4-HBP biodegradation process by Serratia rubidae were analyzed through LC-MS/MS analysis. The (bio)degradation products were benzophenone and a multi-hydroxylated derivative of 4-HBP and the degradation pathways were proposed. The data obtained in this study gave important information regarding the 4-HBP and BP-1 potential biodegradation by single bacterial strains.

UV Based Advanced Oxidation Process for Degradation of Ciprofloxacin: Reaction Kinetics, Effects of Interfering Substances and Degradation Product Identification

2021 ◽  
Author(s):  
Bijoli Mondal ◽  
Shib Sankar Basak ◽  
Arnab Das ◽  
Sananda Sarkar ◽  
Asok Adak
Keyword(s):  
Organic Compounds ◽  
Advanced Oxidation Process ◽  
Oxidation Process ◽  
Uv Light ◽  
Degradation Products ◽  
Irradiation Time ◽  
Advanced Oxidation ◽  
Quantum Yields ◽  
Photon Flux ◽  
First Order

Abstract In the photochemical UV-H2O2 advanced oxidation process, H2O2 absorbs UV light and is decomposed to form hydroxyl radicals (OH·), which are highly excited and reactive for electron-rich organic compounds and hence can degrade organic compounds. In the present work, the UV-H2O2 process was investigated to degrade ciprofloxacin (CIP), one of India's widely used antibiotics, from aqueous solutions using a batch type UV reactor having photon flux = 1.9 (± 0.1) ×10-4 Einstein L-1 min-1. The effects of UV irradiation time on CIP degradation were investigated for both UV and UV-H2O2 processes. It was found that about 75% degradation of CIP was achieved within 60 s with initial CIP concentration and peroxide concentration of 10 mg L-1 and 1 mol H2O2/ mol CIP, respectively, at pH of 7(±0.1) and fluence dose of 113 mJ cm-2. The experimental data were analyzed by the first-order kinetics model to find out the time- and fluence-based degradation rate constants. Under optimized experimental conditions (initial CIP concentration, pH and H2O2 dose of 10 mg L-1, 7(±0.1) and 1.0 mol H2O2 / mol CIP, respectively), the fluence-based pseudo-first-order rate constant for the UV and UV-H2O2 processes were determined to be 1.28(±0.0) ×10-4 and 1.20(±0.04) ×10-2 cm2 mJ-1 respectively. The quantum yields at various pH under direct UV were calculated. The impacts of different process parameters such as H2O2 concentration, solution pH, initial CIP concentration, and wastewater matrix on CIP degradation were also investigated in detail. CIP degradation was favorable in acidic conditions. Six degradation products of CIP were identified. Results clearly showed the potentiality of the UV-H2O2 process for the degradation of antibiotics in wastewater.

scholarly journals Efficient Degradation of Acesulfame by Ozone/Peroxymonosulfate Advanced Oxidation Process

Molecules ◽  
2019 ◽  
Vol 24 (16) ◽  
pp. 2874 ◽  
Author(s):  
Yu Shao ◽  
Zhicheng Pang ◽  
Lili Wang ◽  
Xiaowei Liu
Keyword(s):  
Hydroxyl Radical ◽  
Active Sites ◽  
Emerging Contaminants ◽  
Water Solubility ◽  
Advanced Oxidation Process ◽  
Negative Impact ◽  
Degradation Products ◽  
Electrical Energy ◽  
Sulfate Radical ◽  
Electrical Energy Per Order

Artificial sweeteners (ASWs), a class of emerging contaminants with good water solubility, have attracted much attention recently because of their wide use and negative impact on the aquatic environment and drinking water. Efficient technologies for removing ASWs are in urgent need. This study investigated degradation of typical ASW acesulfame by ozone-activated peroxymonosulfate process (O3/PMS) in prepared and real waters. O3/PMS can degrade >90% acesulfame in prepared water within 15 min at a low dosage of O3 (60 ± 5 µg∙min−1) and PMS (0.4 mM). Ozone, hydroxyl radical (HO•), and sulfate radical (SO4•−) were identified as contributors for ACE degradation and their contribution proportion was 27.1%, 25.4%, and 47.5% respectively. O3/PMS showed the best degradation performance at neutral pH and were sensitive to constituents such as chloride and natural organic matters. The qualitative analysis of degradation products confirmed the involvement of hydroxyl radical and sulfate radical and figured out that the active sites of ACE were the C=C bond, ether bond, and C-N bond. The electrical energy per order ACE degradation were calculated to be 4.6 kWh/m3. Our findings indicate that O3 is an efficient PMS activator and O3/PMS is promising due to its characteristic of tunable O3−HO• SO4•− ternary oxidant involving.

scholarly journals Photo-degradation ibuprofen by UV/H2O2 process: response surface analysis and degradation mechanism

2017 ◽  
Vol 75 (12) ◽  
pp. 2935-2951 ◽  
Author(s):  
Mingguo Peng ◽  
Huajie Li ◽  
Xu Kang ◽  
Erdeng Du ◽  
Dongdong Li
Keyword(s):  
Aqueous Solution ◽  
Response Surface ◽  
Ph Value ◽  
Uv Light ◽  
Degradation Products ◽  
Degradation Mechanism ◽  
Oh Radical ◽  
Initial Ph ◽  
Rsm Model ◽  
Degradation Intermediates

The removal of ibuprofen (IBP) in aqueous solution using UV/H2O2 process was evaluated. The response surface methodology (RSM) and Box–Behnken design were employed to investigate the effects of process parameters on IBP removal, including the initial IBP concentration, H2O2 dosage, UV light intensity, and initial pH value of solution. The RSM model developed herein fits well with the experiments, and provides a good insight into the OH radical irritated degradation mechanisms and kinetics. High resolution accurate mass spectrometry coupled with liquid chromatography was used to identify the degradation intermediates. A total of 23 degradation products were identified, including mono-hydroxylated products and dihydroxylated products. A series of OH radical-initiated reactions, including hydroxylation, dihydroxylation, decarboxylation, demethylation, ring break, lead to the final mineralization of IBP to CO2 and H2O. UV/H2O2 technology could be a promising technology for IBP removal in aqueous solution.

scholarly journals In VitroActivity of Glucosinolates and Their Degradation Products against Brassica-Pathogenic Bacteria and Fungi

2014 ◽  
Vol 81 (1) ◽  
pp. 432-440 ◽  
Author(s):  
T. Sotelo ◽  
M. Lema ◽  
P. Soengas ◽  
M. E. Cartea ◽  
P. Velasco
Keyword(s):  
Pseudomonas Syringae ◽  
Xanthomonas Campestris ◽  
Pathogenic Bacteria ◽  
Degradation Products ◽  
Allyl Isothiocyanate ◽  
Leaf Extracts ◽  
Soil Pathogens ◽  
Content Type ◽  
Positive Effects

ABSTRACTGlucosinolates (GSLs) are secondary metabolites found inBrassicavegetables that confer on them resistance against pests and diseases. Both GSLs and glucosinolate hydrolysis products (GHPs) have shown positive effects in reducing soil pathogens. Information about theirin vitrobiocide effects is scarce, but previous studies have shown sinigrin GSLs and their associated allyl isothiocyanate (AITC) to be soil biocides. The objective of this work was to evaluate the biocide effects of 17 GSLs and GHPs and of leaf methanolic extracts of different GSL-enrichedBrassicacrops on suppressingin vitrogrowth of two bacterial (Xanthomonas campestrispv. campestris andPseudomonas syringaepv. maculicola) and two fungal (AlternariabrassicaeandSclerotiniascletoriorum)Brassicapathogens. GSLs, GHPs, and methanolic leaf extracts inhibited the development of the pathogens tested compared to the control, and the effect was dose dependent. Furthermore, the biocide effects of the different compounds studied were dependent on the species and race of the pathogen. These results indicate that GSLs and their GHPs, as well as extracts of differentBrassicaspecies, have potential to inhibit pathogen growth and offer new opportunities to study the use ofBrassicacrops in biofumigation for the control of multiple diseases.

Sanitization of Chicken Frames by a Combination of Hydrogen Peroxide and UV Light To Reduce Contamination of Derived Edible Products

2019 ◽  
Vol 82 (11) ◽  
pp. 1896-1900
Author(s):  
A. M. JONES-IBARRA ◽  
C. Z. ALVARADO ◽  
CRAIG D. COUFAL ◽  
T. MATTHEW TAYLOR
Keyword(s):  
Hydrogen Peroxide ◽  
Salmonella Enterica ◽  
Advanced Oxidation Process ◽  
Uv Light ◽  
Disease Outbreaks ◽  
Aerobic Bacteria ◽  
Chicken Carcass ◽  
Serovar Typhimurium ◽  
Uv C ◽  
Water Rinse

ABSTRACT Chicken carcass frames are used to obtain mechanically separated chicken (MSC) for use in other further processed food products. Previous foodborne disease outbreaks involving Salmonella-contaminated MSC have demonstrated the potential for the human pathogen to be transmitted to consumers via MSC. The current study evaluated the efficacy of multiple treatments applied to the surfaces of chicken carcass frames to reduce microbial loads on noninoculated frames and frames inoculated with a cocktail of Salmonella enterica serovar Enteritidis and Salmonella enterica serovar Typhimurium. Inoculated or noninoculated frames were left untreated (control) or were subjected to treatment using a prototype sanitization apparatus. Treatments consisted of (i) a sterile water rinse, (ii) a water rinse followed by 5 s of UV-C light application, or (iii) an advanced oxidation process (AOP) combining 5 or 7% (v/v) hydrogen peroxide (H2O2) with UV-C light. Treatment with 7% H2O2 and UV-C light reduced numbers of aerobic bacteria by up to 1.5 log CFU per frame (P < 0.05); reductions in aerobic bacteria subjected to other treatments did not statistically differ from one another (initial mean load on nontreated frames: 3.6 ± 0.1 log CFU per frame). Salmonella numbers (mean load on inoculated, nontreated control was 5.6 ± 0.2 log CFU per frame) were maximally reduced by AOP application in comparison with other treatments. No difference in Salmonella reductions obtained by 5% H2O2 (1.1 log CFU per frame) was detected compared with that obtained following 7% H2O2 use (1.0 log CFU per frame). The AOP treatment for sanitization of chicken carcass frames reduces microbial contamination on chicken carcass frames that are subsequently used for manufacture of MSC.

Optimization of zinc oxide nanoparticle-catalyzed in vitro bilirubin photolysis and in vivo treatment of hyperbilirubinemia

Nanomedicine ◽  
2021 ◽  
Author(s):  
Haq Nawaz ◽  
Iqra Naseem ◽  
Tanzila Rehman ◽  
Mubashir Nawaz
Keyword(s):  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Uv Light ◽  
Uv Exposure ◽  
Uv Treatment ◽  
Blood Samples ◽  
Positive Effects ◽  
Oxide Nanoparticle

Aim: To optimize the Zinc oxide nanoparticles (ZnONPs)-catalyzed in vitro photolysis of bilirubin and to test their effect on bilirubin clearance in vivo. Materials & methods: ZnONPs, synthesized in an alkaline medium, were characterized. Response surface methodology was used to optimize the in vitro photolysis catalyzed by the nanoparticles (NPs). Blood samples from phenylhydrazine-induced hyperbilirubinemic rabbits which had been administered ZnONPs and UV light were analyzed to assess in vivo clearance of bilirubin. Results: The ZnONP-assisted UV treatment showed the linear and quadratic positive effects on the in vitro bilirubin photolysis with an optimal photolysis of bilirubin at 225 mg dl-1 concentration of ZnONPs and a UV exposure of 1.80 h. The ZnONP-assisted phototherapy of hyperbilirubinemic animals was also found to be more effective for in vivo clearance of bilirubin than phototherapy alone. Conclusion: After further trials, ZnONP-assisted phototherapy could be a potential treatment for hyperbilirubinemia in humans.

scholarly journals UV-LED Combined with Small Bioreactor Platform (SBP) for Degradation of 17α-Ethynylestradiol (EE2) at Very Short Hydraulic Retention Time

Materials ◽  
2021 ◽  
Vol 14 (20) ◽  
pp. 5960
Author(s):  
Oran Fradkin ◽  
Hadas Mamane ◽  
Aviv Kaplan ◽  
Ofir Menashe ◽  
Eyal Kurzbaum ◽  
...  
Keyword(s):  
Retention Time ◽  
Hydraulic Retention Time ◽  
Advanced Oxidation Process ◽  
Oxidation Process ◽  
Light Emission ◽  
Degradation Products ◽  
Secondary Effluent ◽  
Direct Photolysis ◽  
Indirect Photolysis ◽  
Uv Led

Degradation of 17α-ethynylestradiol (EE2) and estrogenicity were examined in a novel oxidative bioreactor (OBR) that combines small bioreactor platform (SBP) capsules and UV-LED (ultraviolet light emission diode) simultaneously, using enriched water and secondary effluent. Preliminary experiments examined three UV-LED wavelengths—267, 279, and 286 nm, with (indirect photolysis) and without (direct photolysis) H2O2. The major degradation wavelength for both direct and indirect photolysis was 279 nm, while the major removal gap for direct vs. indirect degradation was at 267 nm. Reduction of EE2 was observed together with reduction of estrogenicity and mineralization, indicating that the EE2 degradation products are not estrogens. Furthermore, slight mineralization occurred with direct photolysis and more significant mineralization with the indirect process. The physical–biological OBR process showed major improvement over other processes studied here, at a very short hydraulic retention time. The OBR can feasibly replace the advanced oxidation process of UV-LED radiation with catalyst in secondary sedimentation tanks with respect to reduction ratio, and with no residual H2O2. Further research into this OBR system is warranted, not only for EE2 degradation, but also to determine its capabilities for degrading mixtures of pharmaceuticals and pesticides, both of which have a significant impact on the environment and public health.

scholarly journals Kinetics, Mechanism, and Toxicity of Amlodipine Degradation by the UV/Chlorine Process

Water ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 3150
Author(s):  
Jianye Xu ◽  
Siqi Zhou ◽  
Erdeng Du ◽  
Yongjun Sha ◽  
Lu Zheng ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Advanced Oxidation Process ◽  
High Resolution Mass Spectrometry ◽  
Ph Value ◽  
Degradation Products ◽  
Degradation Mechanism ◽  
Complete Removal ◽  
Ammonia Concentration ◽  
Ammonia Nitrogen ◽  
Toxicity Tests

The UV/chlorine process, as a new type of AOP (Advanced Oxidation Process), was utilized to treat amlodipine (AML)-containing water. The influencing factors, including chlorine dose, UV intensity, solution initial pH value, and ammonia concentration, were investigated. The degradation of AML in real water and the relative contributions of OH• and Cl• were also studied. Finally, high-resolution mass spectrometry (HRMS) and GC-MS were used to identify the possible degradation products. The results demonstrated that the AML degradation process was fitted with apparent first-order kinetics. AML degradation had a positive correlation with UV intensity and chlorine dose, and a negative correlation with ammonia concentration. In the presence of ammonia nitrogen and DOM, the removal of AML from real water was reduced. OH• made a dominant percentage contribution of 55.7% to the degradation of AML. Sixteen intermediates were detected and identified. A possible degradation mechanism was also proposed. Acute toxicity tests and risk prediction both illustrated that the complete removal of AML does not guarantee the reduction of acute toxicity, but a prolonged degradation promoted the detoxification of toxic intermediates. The UV/chlorine process can be regarded to be an effective method to remove AML and reduce ecological risk.

scholarly journals Advanced Oxidation Process for Degradation of Carbamazepine from Aqueous Solution: Influence of Metal Modified Microporous, Mesoporous Catalysts on the Ozonation Process

Catalysts ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 90 ◽  
Author(s):  
Soudabeh Saeid ◽  
Matilda Kråkström ◽  
Pasi Tolvanen ◽  
Narendra Kumar ◽  
Kari Eränen ◽  
...  
Keyword(s):  
Heterogeneous Catalysts ◽  
Advanced Oxidation Process ◽  
Degradation Products ◽  
Degradation Kinetics ◽  
Removal Rate ◽  
Influence Of Temperature On ◽  
Two Temperatures ◽  
Kinetics Of ◽  
Ozonation Process ◽  
Mcm 41

Carbamazepine (CBZ), a widely used pharmaceutical compound, is one of the most detected drugs in surface waters. The purpose of this work was to identify an active and durable catalyst, which, in combination with an ozonation process, could be used to remove CBZ and its degradation products. It was found that the CBZ was completely transformed after ozonation within the first minutes of the treatment. However, the resulting degradation products, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM) and 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD), were more resistant during the ozonation process. The formation and degradation of these products were studied in more detail and a thorough catalytic screening was conducted to reveal the reaction kinetics of both the CBZ and its degradation products. The work was performed by non-catalytic ozonation and with six different heterogeneous catalysts (Pt-MCM-41-IS, Ru-MCM-41-IS, Pd-H-Y-12-EIM, Pt-H-Y-12-EIM, Pd-H-Beta-300-EIM and Cu-MCM-41-A-EIM) operating at two temperatures 20 °C and 50 °C. The influence of temperature on degradation kinetics of CBZ, BQM and BQD was studied. The results exhibited a notable difference in the catalytic behavior by varying temperature. The higher reactor temperature (50 °C) showed a higher activity of the catalysts but a lower concentration of dissolved ozone. Most of the catalysts exhibited higher removal rate for BQM and BQD compared to non-catalytic experiments in both temperatures. The Pd-H-Y-12-EIM catalyst illustrated a higher degradation rate of by-products at 50 °C compared to other catalysts.

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