Heterogeneous catalytic ozonation of aniline-contaminated waters: A three-phase modelling approach using TiO2/GAC

This work aims to study the sustainable catalytic ozonation of aniline promoted by granular active carbon (GAC) doped with TiO2. Aniline was selected as a model compound for the Accelerator manufacturing industries used in the manufacture of rubber due to its environmental impact, low biodegradability, and harmful genotoxic effects on human health. Based on the evolution of total organic carbon (TOC), aniline concentration measured using high performance liquid chromatography (HPLC), pH and ozone concentration in liquid and gas phase, and catalyst loading, a three-phase reaction system has been modelled. The proposed three-phase model related the ozone transfer parameters and the pseudo-first order kinetic constants through three coefficients that involve the adsorption process, oxidation in the liquid, and the solid catalyst. The interpretation of the kinetic constants of the process allowed the predominance of the mechanism of Langmuir–Hinshelwood or modified Eley–Rideal to be elucidated. Seven intermediate aromatic reaction products, representative of the direct action of ozone and the radical pathway, were identified and quantified, as well as precursors of the appearance of turbidity, with which two possible routes of degradation of aniline being proposed.The authors are grateful to the University of the Basque Country for their financial support of this study through the PPGA19/63 project and C. Ferreiro’s predoctoral PIF grant (PIF16/367)

Turbidity Changes during Carbamazepine Oxidation by Photo-Fenton

The objective of this study is to evaluate the turbidity generated during the Fenton photo-reaction applied to the oxidation of waters containing carbamazepine as a function of factors such as pH, H2O2 concentration and catalyst dosage. The results let establish the degradation pathways and the main decomposition byproducts. It is found that the pH affects the turbidity of the water. Working between pH = 2.0 and 2.5, the turbidity is under 1 NTU due to the fact that iron, added as a catalyst, is in the form of a ferrous ion. Operating at pH values above 3.0, the iron species in their oxidized state (mainly ferric hydroxide in suspension) would cause turbidity. The contribution of these ferric species is a function of the concentration of iron added to the process, verifying that the turbidity increases linearly according to a ratio of 0.616 NTU L/mg Fe. Performing with oxidant concentrations at (H2O2) = 2.0 mM, the turbidity undergoes a strong increase until reaching values around 98 NTU in the steady state. High turbidity levels can be originated by the formation of coordination complexes, consisting of the union of three molecules containing substituted carboxylic groups (BaQD), which act as ligands towards an iron atom with Fe3+ oxidation state.Authors are grateful to the University of the Basque Country UPV/EHU for the financial support to carry out this research study through the scholarship Student Movility for Traineeships in the Erasmus + Programme between the Anadolu University in Eskisehir (Turkey) and the Faculty of Engineering Vitoria-Gasteiz (Spain)

Kinetic modelling for concentration and toxicity changes during the oxidation of 4-chlorophenol by UV/H2O2

This work develops a kinetic model that allow to predict the water toxicity and the main degradation products concentration of aqueous solutions containing 4-chlorophenol oxidised by UV/H2O2. The kinetic model was developed grouping degradation products of similar toxicological nature: aromatics (hydroquinone, benzoquinone, 4-chlorocatechol and catechol), aliphatics (succinic, fumaric, maleic and malonic acids) and mineralised compounds (oxalic, acetic and formic acids). The degradation of each group versus time was described as a mathematical function of the rate constant of a second-order reaction involving the hydroxyl radical, the quantum yield of lump, the concentration of the hydroxyl radicals and the intensity of the emitted UV radiation. The photolytic and kinetic parameters characterising each lump were adjusted by experimental assays. The kinetic, mass balance and toxicity equations were solved using the Berkeley Madonna numerical calculation tool. Results showed that 4-chlorophenol would be completely removed during the first hour of the reaction, operating with oxidant molar ratios higher than R=200 at pH6.0 and UV=24 W. Under these conditions, a decrease in the rate of total organic carbon (TOC) removal close to 50% from the initial value was observed. The solution colour, attributed to the presence of oxidation products as p-benzoquinone and hydroquinone, were oxidised to colourless species, that resulted in a decrease in the toxicity of the solutions (9.95 TU) and the aromaticity lost.The authors are grateful to the University of the Basque Country (UPV/EHU) for their financial support of this study through the PPGA20/33 project, and C. Ferreiro's predoctoral PIF grant (PIF16/367). Documen

Colour Changes during the Carbamazepine Oxidation by Photo-Fenton

The oxidation of aqueous solutions of carbamazepine is conducted using the Fenton reagent, combined with the photolytic action of a 150 W medium pressure UV lamp, operating at T = 40 °C. The effect of acidity is analysed at an interval pH = 2.0–5.0, verifying that operating at pH = 5.0 promotes colour formation (Colour = 0.15 AU). The effect of iron is studied, finding that the colour of the water increases in a linear way, Colour = 0.05 + 0.0075 [Fe]0. The oxidising action of hydrogen peroxide is tested, confirming that when operating with [H2O2]0 = 2.0 mM, the maximum colour is generated (Colourmax = 0.381 AU). The tint would be generated by the degradation of by-products of carbamazepine, which have chromophoric groups in their internal structure, such as oxo and dioxocarbazepines, which would produce tint along the first minutes of oxidation, while the formation of acridones would slowly induce colour in the water.Authors are grateful to the University of the Basque Country UPV/EHU the financial support to carry out this research study through the scholarship Student Movility for Traineeships in the Erasmus + Programme between the Anadolu University in Eskisehir (Turkey) and the Faculty of Engineering Vitoria-Gasteiz (Spain), and the research Project PPGA20/33

Water Reuse Study from Urban WWTPs via c-Ultrafiltration and Ozonation Technologies: Basis for Resilient Cities and Agriculture

The water–development nexus is essential for the advancement and progress of cities in the face of problems such as climate change, water security and increasing environmental stress in the agricultural sector. Aiming for a circular economy and, at the same time, improving the resilience of water supply alternatives and achieving a goal of zero waste, this work presents a technical–economic study of a novel continuous ultrafiltration (c-UF) system with self-cleaning capacity coupled to an ozonation process, for the treatment of urban WWTP effluent. The removal efficiencies achieved were analysed both through macroscopic parameters (suspended solids, turbidity) and for the most frequently occurring contaminants of emerging concern (CECs). Consequently, an effluent suitable for irrigation was obtained, with a total recovery factor of 97.92%, a concentration of suspended solids (SS) below 1 mg L−1, 0.06 NTU turbidity and toxicity free, complying with the new European Regulation on Water Reuse (EU 2020/741). A comparative analysis of the proposed process with regard to conventional tertiary treatment revealed that the proposed process was 39.1% more economic, with a cost of 0.0325 € m−3. This alternative treatment will be of great interest because of its favourable technical–economic characteristics, being postulated as a basic process for implementation in modern water reuse plants.The authors are grateful to the University of the Basque Country (UPV/EHU) for their financial support of this study through the PPGA20/33 project, and C. Ferreiro’s predoctoral PIF grant (PIF16/367)

Analysis of a hybrid suspended-supported photocatalytic reactor for the treatment of wastewater containing benzothiazole and aniline

In this work, a study of the main operating variables affecting TiO2/UV photocatalysis was carried out. The treatment of an industrial effluent containing aniline and benzothiazole from the manufacture of accelerants for vulcanization was performed in a TiO2-supported commercial photoreactor. The degradation of both contaminants was monitored by GC-MS analysis. The proposed experiments were able to properly identify the phenomenon of adsorption, as well as to improve the performance of the commercial photoreactor by adding small amounts of TiO2 in suspension. The removal performance, durability of the photocatalytic material, and energy costs were analysed. The results showed that the use of suspensions intensifies the degradation obtaining an improvement of 23.15% with respect to the use of the supported catalyst. For an aniline and benzothiazole solution, the best operating conditions were found at pH = 12.0, introducing 60.0 mg L−1 of suspended TiO2 together with the existing supported catalyst

Removal of aniline and benzothiazole wastewaters using an efficient MnO2/GAC catalyst in a photocatalytic fluidised bed reactor

This work presents an efficient method for treating industrial wastewater containing aniline and benzothiazole, which are refractory to conventional treatments. A combination of heterogeneous photocatalysis operating in a fluidised bed reactor is studied in order to increase mass transfer and reduce reaction times. This process uses a manganese dioxide catalyst supported on granular activated carbon with environmentally friendly characteristics. The manganese dioxide composite is prepared by hydrothermal synthesis on carbon Hydrodarco® 3000 with different active phase ratios. The support, the metal oxide, and the composite are characterised by performing Brunauer, Emmett, and Teller analysis, transmission electron microscopy, X-ray diffraction analysis, X-ray fluorescence analysis, UV–Vis spectroscopy by diffuse reflectance, and Fourier transform infrared spectroscopy in order to evaluate the influence of the metal oxide on the activated carbon. A composite of MnO2/GAC (3.78% in phase α-MnO2) is obtained, with a 9.4% increase in the specific surface of the initial GAC and a 12.79 nm crystal size. The effect of pH and catalyst load is studied. At a pH of 9.0 and a dose of 0.9 g L−1, a high degradation of aniline and benzothiazole is obtained, with an 81.63% TOC mineralisation in 64.8 min

Application of a Combined Adsorption−Ozonation Process for Phenolic Wastewater Treatment in a Continuous Fixed-Bed Reactor

This work studied the removal of phenol from industrial effluents through catalytic ozonation in the presence of granular activated carbon in a continuous fixed-bed reactor. Phenol was chosen as model pollutant because of its environmental impact and high toxicity. Based on the evolution of total organic carbon (TOC) and phenol concentration, a kinetic model was proposed to study the effect of the operational variables on the combined adsorption–oxidation (Ad/Ox) process. The proposed three-phase model expressed the oxidation phenomena in the liquid and the adsorption and oxidation on the surface of the granular activated carbon in the form of two kinetic constants, k1 and k2 respectively. The interpretation of the constants allow to study the benefits and behaviour of the use of activated carbon during the ozonisation process under different conditions affecting adsorption, oxidation, and mass transfer. Additionally, the calculated kinetic parameters helped to explain the observed changes in treatment efficiency. The results showed that phenol would be completely removed at an effective contact time of 3.71 min, operating at an alkaline pH of 11.0 and an ozone gas concentration of 19.0 mg L−1. Under these conditions, a 97.0% decrease in the initial total organic carbon was observed.The authors are grateful to the University of the Basque Country for their financial support of this study through the GIU20/56 project and C. Ferreiro’s predoctoral PIF grant (PIF16/367)

Peritumoral adipose tissue promotes lipolysis and white adipocytes browning by paracrine action

Background: Stromal adipocytes and tumor breast epithelial cells undergo a mutual metabolic adaptation within tumor microenvironment. Therefore, browning and lipolysis occur in cancer associated adipocytes (CAA). However, the paracrine effects of CAA on lipid metabolism and microenvironment remodeling remain poorly understood. Methods: To analyze these changes, we evaluated the effects of factors in conditioned media (CM) derived from explants of human breast adipose tissue from tumor (hATT) or normal (hATN) on morphology, degree of browning, the levels of adiposity, maturity, and lipolytic-related markers in 3T3-L1 white adipocytes by Western blot, indirect immunofluorescence and lipolytic assay. We analyzed subcellular localization of UCP1, perilipin 1 (Plin1), HSL and ATGL in adipocytes incubated with different CM by indirect immunofluorescence. Additionally, we evaluated changes in adipocyte intracellular signal pathways. Results: We found that adipocytes incubated with hATT-CM displayed characteristics that morphologically resembled beige/brown adipocytes with smaller cell size and higher number of small and micro lipid droplets (LDs), with less triglyceride content. Both, hATT-CM and hATN-CM, increased Pref-1, C/EBPβ LIP/LAP ratio, PPARγ, and caveolin 1 expression in white adipocytes. UCP1, PGC1α and TOMM20 increased only in adipocytes that were treated with hATT-CM. Also, hATT-CM increased the levels of Plin1 and HSL, while decreased ATGL. hATT-CM modified the subcellular localization of the lipolytic markers, favoring their relative content around micro-LDs and induced Plin1 segregation. Furthermore, the levels of p-HSL, p-ERK and p-AKT increased in white adipocytes after incubation with hATT-CM. Conclusions: In summary, these findings allow us to conclude that adipocytes attached to the tumor could induce white adipocyte browning and increase lipolysis as a means for endocrine/paracrine signaling. Thus, adipocytes from the tumor microenvironment exhibit an activated phenotype that could have been induced not only by secreted soluble factors from tumor cells but also by paracrine action from other adipocytes present in this microenvironment, suggesting a “domino effect”.Fil: Pagnotta, Priscila Ayelén. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Gantov, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Fletcher, Sabrina Johanna. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Lombardi, Antonella. Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Crosbie, María Lujan. Complejo Medico Policial Bartolome Churruca Andres Visca; ArgentinaFil: Santiso, Natalia. Complejo Medico Policial Bartolome Churruca Andres Visca; ArgentinaFil: Ursino, Anabela. Complejo Medico Policial Bartolome Churruca Andres Visca; ArgentinaFil: Frascarolli, Celeste. Complejo Medico Policial Bartolome Churruca Andres Visca; ArgentinaFil: Amato, Alicia. Complejo Medico Policial Bartolome Churruca Andres Visca; ArgentinaFil: Dreszman, Rubén. No especifíca;Fil: Calvo, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Toneatto, Judith. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentin

Interaction of intestinal bacteria with human rotavirus during infection in children

The gut microbiota has emerged as a key factor in the pathogenesis of intestinal viruses, including enteroviruses, noroviruses and rotaviruses (RVs), where stimulatory and inhibitory effects on infectivity have been reported. With the aim of determining whether members of the microbiota interact with RVs during infection, a combination of anti-RV antibody labeling, fluorescence-activated cell sorting and 16S rRNA amplicon sequencing was used to characterize the interaction between specific bacteria and RV in stool samples of children suffering from diarrhea produced by G1P[8] RV. The genera Ruminococcus and Oxalobacter were identified as RV binders in stools, displaying enrichments between 4.8- and 5.4-fold compared to samples nonlabeled with anti-RV antibodies. In vitro binding of the G1P[8] Wa human RV strain to two Ruminococcus gauvreauii human isolates was confirmed by fluorescence microscopy. Analysis in R. gauvreauii with antibodies directed to several histo-blood group antigens (HBGAs) indicated that these bacteria express HBGA-like substances on their surfaces, which can be the target for RV binding. Furthermore, in vitro infection of the Wa strain in differentiated Caco-2 cells was significantly reduced by incubation with R. gauvreauii. These data, together with previous findings showing a negative correlation between Ruminococcus levels and antibody titers to RV in healthy individuals, suggest a pivotal interaction between this bacterial group and human RV. These results reveal likely mechanisms of how specific bacterial taxa of the intestinal microbiota could negatively affect RV infection and open new possibilities for antiviral strategies