RESUMO
As global effects of water scarcity raise concerns and environmental regulations evolve, contemporary wastewater treatment plants (WWTPs) face the challenge of effectively removing a diverse range of contaminants of emerging concern (CECs) from municipal effluents. This study focuses on the assessment of advanced oxidation processes (AOPs), specifically UV-C/H2O2 and UV-C/Chlorine, for the removal of 14 target CECs in municipal secondary effluent (MSE, spiked with 10 µg L-1 of each CEC) or in the subsequent MSE nanofiltration retentate (NFR, no spiking). Phototreatments were carried out in continuous mode operation, with a hydraulic retention time of 3.4 min, using a tube-in-tube membrane photoreactor. For both wastewater matrices, UV-C photolysis (3.3 kJ L-1) exhibited high efficacy in removing CECs susceptible to photolysis, although lower treatment performance was observed for NFR. In MSE, adding 10 mg L-1 of H2O2 or Cl2 enhanced treatment efficiency, with UV-C/H2O2 outperforming UV-C/Chlorine. Both UV-C/AOPs eliminated the chronic toxicity of MSE toward Chlorella vulgaris. In the NFR, not only was the degradation of target CECs diminished, but chronic toxicity to C. vulgaris persisted after both UV-C/AOPs, with UV-C/Chlorine increasing toxicity due to potential toxic by-products. Nanofiltration permeate (NFP) exhibited low CECs and microbial content. A single chlorine addition effectively controlled Escherichia coli regrowth for 3 days, proving NFP potential for safe reuse in crop irrigation (<1 CFU/100 mL for E. coli; <1 mg L-1 for free chlorine). These findings provide valuable insights into the applications and limitations of UV-C/H2O2 and UV-C/Chlorine for distinct wastewater treatment scenarios.
Assuntos
Cloro , Filtração , Peróxido de Hidrogênio , Fotólise , Raios Ultravioleta , Eliminação de Resíduos Líquidos , Águas Residuárias , Poluentes Químicos da Água , Peróxido de Hidrogênio/química , Águas Residuárias/química , Poluentes Químicos da Água/química , Poluentes Químicos da Água/análise , Eliminação de Resíduos Líquidos/métodos , Cloro/química , Filtração/métodos , Purificação da Água/métodos , Chlorella vulgaris/efeitos dos fármacos , Escherichia coli/efeitos dos fármacos , OxirreduçãoRESUMO
A tubular porous stainless steel membrane contactor was characterized in terms of ozone-water mass transport, as well as its application in removing 23 pharmaceuticals (PhACs) detected in the secondary-treated municipal wastewater, under continuous mode operation. The volumetric mass transfer coefficient (KLa) was evaluated based on liquid flow rate, gas flow rate, and ozone gas concentration. The KLa values were substantially improved with an increment in liquid flow rate (1.6 times from 30 to 70 dm3 h-1) and gas flow rate (3.6 times from 0.30 to 0.85 Ndm3 min-1) due to the improved mixing in the gas-liquid interface. For the lowest liquid flow rate (30 dm3 h-1), the water phase boundary layer (82%) exhibited the major ozone transfer resistance, but it became almost comparable with membrane resistance for the highest liquid flow rate (70 dm3 h-1). Additionally, the influence of the specific ozone dose (0.39, 0.53, and 0.69 g O3 g DOC-1) and ozone inlet gas concentration ( [Formula: see text] = 27, 80, and 134 g Nm-3) were investigated in the elimination of 23 PhACs found in secondary-treated municipal wastewater. An ozone dose of 0.69 g O3 g DOC-1 and residence time of 60 s resulted in the removal of 12 out of the 23 compounds over 80%, while 17 compounds were abated above 60%. The elimination of PhACs was strongly correlated with kinetic reaction constants values with ozone and hydroxyl radicals (kO3 and kHOâ¢), leading to a characteristic elimination pattern for each group of contaminants. This study demonstrates the high potential of membrane contactors as an appealing alternative for ozone-driven wastewater treatment.
Assuntos
Ozônio , Poluentes Químicos da Água , Purificação da Água , Águas Residuárias , Eliminação de Resíduos Líquidos/métodos , Aço Inoxidável , Poluentes Químicos da Água/análise , Purificação da Água/métodos , Água , Preparações FarmacêuticasRESUMO
This study aims the development of photoelectrodes to be incorporated in a photoelectrocatalytic ozonation (PECO) process for tertiary treatment of urban wastewaters, targeting the removal of contaminants of emerging concern (CEC). PECO tests were performed using urban wastewater after secondary treatment fortified with Cefadroxil (CFX, C16H17N3O5S), as target model CEC. Three Nitrogen and Carbon doped TiO2 (CN-TiO2) electrodes were synthesized by anodizing at 50, 70, and 90 V, and calcined. These materials were characterized by X-Ray diffraction and Rietveld refinement, Scanning Electron Microscopy, Diffuse Reflectance Spectroscopy, X-ray photoelectron spectroscopy, chronoamperometry, and electrochemical impedance spectroscopy, to correlate defects with photoactivity. All photoanodes considerably reduced their main bandgaps by the incorporation of C and N species, to enable absorption capacities in the UV region using a Xe lamp. The lowest oxygen vacancy content and largest crystallite size were found for CN-TiO2-70, favoring the reduction of bulk defects that could act as recombination of charge carriers. Therefore, oxygen vacancies affect more the TiO2 photoactivity compared to the crystallite size or the light absorption capacity, confirming that a lower content of vacancies in the material bulk and surface doping significantly influence the activity as detected by Rietveld refinement, DRS, and XPS. The electrochemical techniques confirm that the highest photocurrent was obtained for CN-TiO2-70, whence this photoanode was chosen to carry out the CFX degradation. A point defect model simulating Nyquist plot reveals that the photoactivity depends on the speed to diffuse oxygen vacancies through the TiO2 coating. All abatement processes were followed by high-performance liquid chromatography, and Total Organic Carbon (TOC). At neutral and alkaline conditions, CFX is eliminated to levels below the analytical detection limit after 90 min of treatment (TOC removals of 87 and 91%, respectively), indicating that the coupling between the CN-TiO2-70 photocatalyst and ozone is effective in eliminating the contaminant due to parallel routes forming â¢OH species. Lower CFX degradation observed at acidic pH (TOC removal of 70%) is assigned to the difficulty of oxidizing protonated CFX species.
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Luz , Oxigênio , Microscopia Eletrônica de Varredura , Titânio/química , Carbono/químicaRESUMO
The in-situ removal of lindane from spiked soil was studied using cork barriers combined with electrokinetic and ohmic heating soil remediation processes. Both vertical and horizontal cork barriers have been evaluated to retain pollutants mobilized by electro-osmotic flow or volatilized by ohmic heating. Moreover, the addition of surfactant solutions in electrolyte wells has been evaluated to promote the dragging of lindane by electrokinetic fluxes. Results indicated that the drag of lindane by liquid flows is not as important as expected, opposite to what happened with the dragging by gaseous flows. The retention of gaseous lindane was also confirmed in adsorption tests carried out in a column packed with cork granules. The addition of surfactant had a very limited effect on the mobility of lindane, and dragging of this species to the electrode wells or to a permeable reactive barrier. On the contrary, the reactivity of lindane during the electrochemical treatments is relevant due to the electrokinetic basic front promoting the in-situ conversion of lindane into less chlorinated pollutants.
RESUMO
A membrane ozone contactor, operated under continuous mode, was applied to promote the tertiary treatment of urban wastewater (UWW), targeting the removal of contaminants of emerging concern (CECs), bacterial disinfection, and toxicity reduction. This system relies on the homogeneous radial distribution of ozone (O3) in the reaction zone by "titration" through a microfiltration borosilicate tubular membrane, while the UWW swirls around the membrane and drags the O3 microbubbles generated in the membrane shell-side. The membrane is coated with titanium dioxide (TiO2-P25) and radiation can be externally supplied via four UV lamps. The ozonation tests were carried out with secondary-treated UWW collected in different seasons (winter and summer) and spiked with a mix of 19 CECs (10 µg L-1 each). For an O3 dose of 18 g m-3, the best performance was obtained by increasing the O3 concentration (maximum [O3]G,inlet of 200 g Nm-3) and decreasing the gas flow rate (minimum QG of 0.15 Ndm3 min-1), providing the highest ozone transfer yield (88 %) and, thus higher specific ozone dose (g O3 per g dissolved organic carbon). Under these conditions, removals >80 % or concentrations below the limit of quantification were obtained for up to 13 of the 19 CECs and reductions up to 5 log units for total heterotrophs and below the limit of detection for enterobacteria and enterococci. Tests including a UVC dose of 0.10 kJ L-1 enhanced disinfection ability but had no impact on CECs oxidation. After ozonation, the abundance of antibiotic resistant bacteria was reduced but not eliminated, and microbial regrowth after 3-day storage was observed. No toxic effect was detected on zebrafish embryos using a dilution factor of 4 for the ozonized UWW and when granular activated carbon adsorption was subsequently applied the dilution factor decreased to 2.
Assuntos
Ozônio , Poluentes Químicos da Água , Purificação da Água , Animais , Águas Residuárias , Peixe-Zebra , Poluentes Químicos da Água/análise , Bactérias , OxirreduçãoRESUMO
Mill scale is the metallurgical waste produced by the rolling mill in the steel hot rolling process. This hazardous waste is mainly composed of oxide iron, such as hematite, magnetite and wustite. It may have a different and alternative final destination by becoming a catalyst for wastewater treatment. In this work, the catalytic potential of mill scale (MS) from a steel plant was evaluated for hexavalent chromium reduction from synthetic and real matrices under slurry conditions (MS particles dispersed in the solution) or immobilized in Raschig rings. Experiments were conducted in an annular photoreactor irradiated by UVA light. Raschig rings were coated with MS by electrostatic link with polyethylene-grafted-maleic anhydride copolymer (PEGMA) film, and further packed in the annular zone of the UV photoreactor. SEM, XRD and FTIR analysis showed a homogeneous film of MS firmly attached on Raschig rings surface. In this way, the iron-rich industrial steel waste acted as both source of iron and photocatalyst, allowing the reduction of Cr(VI) to Cr(III) in the bulk solution and MS surface, respectively, in the presence of tartaric acid as hole and hydroxyl scavenger and Fe-complexing agent. The Raschig rings (248 g) coated with MS (23 g) achieved total Cr(VI) reduction (below detection limit) after 45 min of reaction (k = 2.0 × 10-2 mg L-1 min- 1) under UVA radiation, considering the following initial conditions: [Cr(VI)]0 = 10 mg L-1, [tartaric acid]0/[Cr(VI)]0 molar ratio = 6:1, pH = 3.0, T = 25 °C. The same system was tested for the treatment of a real effluent from a galvanic industry containing 6 mg L-1 of Cr(VI). Using the same tartaric acid/Cr(VI) molar ratio (6:1) and pH 3.0, the Cr(VI) present in the effluent was totally reduced (below detection limit) in 360 min (k = 1.93 × 10-2 mg L- 1 min- 1), showing similar kinetic behavior as the process with the synthetic matrix. In all experiments, the concentrations of dissolved iron (Fe(II) and Fe(total)) were below the disposal limit established by Brazilian legislation, and total chromium removal was achieved by Cr(III) precipitation after the photocatalytic reaction.
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Resíduos Industriais , Poluentes Químicos da Água , Cromo , Concentração de Íons de Hidrogênio , Ferro , Oxirredução , AçoRESUMO
This work provides a screening of organic contaminants and characterization of the dissolved organic matter in the sewer network until the municipal wastewater treatment plant (WWTP), identifying the network areas with a higher degree of contamination and their impact on the WWTP performance, particularly in the activated sludge reactor. Three monitoring campaigns were carried out at six selected locations of the sewage system (PVZ-1, PVZ-2, PS-F, PS-VC, CP-VC, and PS-T), influent (WWTPINF) and effluent (WWTPEFF) of the WWTP. Advanced analytical techniques were employed, namely excitation/emission matrix fluorescence-parallel factor analysis (EEM-PARAFAC), size exclusion chromatography with organic carbon detector (SEC-OCD), and liquid chromatography with high-resolution-mass spectrometric detection (LC-HRMS). EEM-PARAFAC showed higher fluorescence intensity for the protein-like component (C2), particularly at CP-VC (near seafood industries) associated with the presence of surfactants (~50 mg/L). SEC-OCD highlighted the WWTP efficiency in removing low molecular weight acids and neutrals. LC-HRMS tentatively identified 108 compounds of emerging concern (CEC) and similar detection patterns were obtained for all wastewater samples, except for PVZ-2 (lower detection), many of which occurred in the effluent. Eight CECs included on relevant Watch-Lists were detected in all WWTPEFF samples. Furthermore, 111 surfactants were detected, the classes more frequently found being alcohol ethoxylates (AEOs), nonylphenol polyethoxylates (NPEOs) and linear alkylbenzene sulphonates (LAS). The continuous presence of LAS and NPEOs allied to surfactants concentrations in the WWTPINF of 15-20 mg/L, with CP-VC location (linked with food industries) as an important contributor, explain the morphological changes in the activated sludge and high LAS content in the dewatered sludge, which may have impacted WWTP performance.
Assuntos
Poluentes Ambientais , Poluentes Químicos da Água , Purificação da Água , Poluentes Ambientais/análise , Esgotos/química , Águas Residuárias/química , Poluentes Químicos da Água/análise , Purificação da Água/métodosRESUMO
This work aims to integrate several hydrogen peroxide (H2O2) activation mechanisms, photolysis (UVC irradiation), chemical electron transfer (TiO2-P25 photocatalysis), and reaction with TiO2-P25 in dark conditions, for reactive oxygen species (ROS) generation towards the removal of contaminants of emerging concern (CECs), in a single unit operated in continuous-flow mode. An H2O2 stock solution is fed by the lumen side of a tubular ceramic membrane, delivering the oxidant to the (i) catalyst immobilized in the membrane shell-side and (ii) annular reaction zone (ARZ, space between membrane shell-side and outer quartz tube) where CECs contaminated water flows with a helix trajectory, being activated by UV light provided by four lamps placed symmetrically around the reactor. First, the effect of several parameters in the removal of a CEC target molecule, amoxicillin (AMX), was evaluated using a synthetic solution ([AMX]inlet = 2.0 mg L-1): (i) light source (UVA or UVC radiation), (ii) H2O2 dose, (iii) H2O2 injection method (radial permeation vs. upstream injection), and (iv) number of TiO2-P25 layers deposited on the membrane. The UVC/H2O2/TiO2 system with radial addition of H2O2 (20 mg L-1) and 9-TiO2-P25 layers provided the highest AMX removal efficiency (72.2 ± 0.5%) with a UV fluence of 45 mJ cm-2 (residence time of 4.6 s), due to the synergic effect of four mechanisms: (i) AMX photolysis, (ii) H2O2 photocleavage, (iii) TiO2-P25 photoactivation, and (iv) chemical reactions between H2O2 and TiO2-P25. The urban wastewater matrix showed a negative effect on AMX removal (~44%) due to the presence of ROS scavengers and light-filtering species.
Assuntos
Águas Residuárias , Poluentes Químicos da Água , Amoxicilina , Cerâmica , Peróxido de Hidrogênio/química , Oxirredução , Espécies Reativas de Oxigênio , Titânio/química , Raios Ultravioleta , Águas Residuárias/química , Poluentes Químicos da Água/análiseRESUMO
This work highlights the performance of an ultrafiltration ceramic membrane as photocatalyst support and oxidant-catalyst/water contactor to promote sulfate radical advanced oxidation processes (SR-AOPs). Peroxydisulfate (PDS) activation mechanisms include photolysis (UVC irradiation) and chemical electron transfer (TiO2-P25 photocatalysis). The photoreactor is composed of an outer quartz tube (the "window"-radiation entrance to the reactor) and an inner tubular ceramic ultrafiltration membrane, where the catalyst particles (TiO2-P25) are immobilized on the membrane shell-side. PDS stock solution is fed by the lumen side of the membrane, delivering the oxidant to the catalyst particles and to the annular reaction zone (ARZ), being the catalyst and PDS activated by UV light. The design facilitates controlled radial slip of PDS into the catalyst surface and to concurrent water to be treated, flowing with a helix trajectory in the ARZ. Under continuous mode operation, with an UV fluence of 45 mJ cm-2 (residence time of 4.6 s), the UVC/PDS/TiO2 system showed the best removal efficiency for two specific endocrine disrupting chemicals, 17ß-estradiol (E2) and 17α-ethinylestradiol (EE2), spiked (100 µg L-1 each) in demineralized water and urban wastewater after secondary treatment.
Assuntos
Poluentes Químicos da Água , Purificação da Água , Cerâmica , Estradiol/análise , Etinilestradiol/análise , Oxidantes , Oxirredução , Sulfatos , Ultrafiltração , Raios Ultravioleta , Água , Poluentes Químicos da Água/análiseRESUMO
The photocatalytic activity of TiO2 nanoparticles (NPs) supported on mesoporous silica SBA-15 (TiO2/SBA-15) was evaluated for the photodegradation of sulfadiazine (SDZ), as target contaminant of emerging concern (CEC), using either pure water solutions (PW) or a real secondary urban wastewater (UWW) spiked with SDZ. For this purpose, TiO2/SBA-15 samples with 10, 20 and 30% TiO2 (w/w) were prepared by the sol-gel post synthetic method on pre-formed SBA-15, using titanium (IV) isopropoxide as a precursor. The TiO2/SBA-15 materials were characterized by HRTEM, SAXS and XRD, nitrogen adsorption isotherms and UV-vis diffuse reflectance spectroscopy. TiO2 NPs were shown to be attached onto the external surface, decorating the SBA-15 particles. The TiO2/SBA-15 catalysts were active in SDZ photodegradation using the annular FluHelik photoreactor, when irradiated with UVA light. The 30% TiO2/SBA-15 sample presented the best performance in optimization tests performed using PW, and it was further used for the tests with UWW. The photocatalytic activity of 30% TiO2/SBA-15 was higher (56% SDZ degradation) than that of standard TiO2-P25 (32% SDZ degradation) in the removal of SDZ spiked in the UWW ([SDZ] = 2 mg L-1). The photodegradation of SDZ with 30% TiO2/SBA-15 eached 90% for UWW spiked with a lower SDZ concentration ([SDZ] = 40 µg L-1). Aside of SDZ, a suit of 65 other CECs were also identified in the UWW sample using LC-MS spectrometry. A fast-screening test showed the heterogeneous photocatalytic system was able to remove most of the detected CECs from UWW, by either adsorption and/or photocatalysis.
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Dióxido de Silício , Águas Residuárias , Espalhamento a Baixo Ângulo , Difração de Raios XRESUMO
The main goal of this work is to evaluate the usage of ozone (O3) as a pre-treatment or simultaneously combined with UVC/H2O2 process for the polishing stage treatment of real bio-treated slaughterhouse wastewater. Two different treatment strategies were tested: i) pre-ozonation of the wastewater followed by an UVC/H2O2 process (two-step treatment); ii) simultaneous application of O3/UVC/H2O2 combined process (one-step treatment). For the two-step strategy, the pre-treatment with 30 mg O3/min for 10 min reduces significantly total suspended solids (TSS), turbidity and colour, reducing light filtering effects and increasing the efficiency of the following UVC/H2O2 process. In turn, the one-step treatment strategy (O3/UVC/H2O2) allows a more efficient use of injected O3 by reducing the amount of O3 required (from 273 to 189 mg O3/Leffluent) to achieve similar mineralization levels. The real bio-treated slaughterhouse wastewater treated by O3/UVC/H2O2 process achieved final colour values of 20 Pt/Co, TSS of 35 mg/L and COD of 61 mg O2/L, allowing its direct discharge into water compartments according to European Council Directive 91/271/EEC.
Assuntos
Ozônio , Poluentes Químicos da Água , Purificação da Água , Matadouros , Peróxido de Hidrogênio , Oxirredução , Águas Residuárias , Poluentes Químicos da Água/análiseRESUMO
In this study, O3 and O3/UVC processes were evaluated for the treatment of landfill leachate after biological nitrification/denitrification, coagulation, or their combinations. The O3-driven stage efficiency was assessed by the removal of color, organic matter (dissolved organic carbon (DOC) and chemical oxygen demand (COD)), and biodegradability increase (Zahn-Wellens test). Also, fluorescence excitation-emission matrix (EEM) and size exclusion chromatography coupled with OC detector (SEC-OCD) analysis were carried out for each strategy. The bio-nitrified-leachate (LN) was not efficiently mineralized during the O3-driven processes since the high nitrites content consumed ozone rapidly. In turn, carbonate/bicarbonate ions impaired the oxidation of the bio-denitrified-leachate (LD), scavenging hydroxyl radicals (HOâ¢) and inhibiting the O3 decomposition. For both bio-leachates, only O3/UVC significantly enhanced the effluent biodegradability (>70%), but COD legal compliance was not reached. EEM and SEC-OCD results revealed differences in the organic matter composition between the nitrified-coagulated-leachate (LNC) and denitrified-coagulated-leachate (LDC). Nonetheless, the amount of DOC and COD removed per gram of ozone was similar for both. Cost estimation indicates the O3-driven stage as the costliest among the treatment processes, while coagulation substantially reduced the cost of the following ozonation. Thus, the best treatment train strategy comprised LDC (with methanol addition for denitrification and coagulated with 300 mg Al3+/L, without pH adjustment), followed by O3/UVC (transferred ozone dose of 2.1 g O3/L and 12.2 kJUVC/L) and final biological oxidation, allowed legal compliance for direct discharge (for organic and nitrogen parameters) with an estimated cost of 8.9 /m3 (O3/UVC stage counting for 6.9 /m3).
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Ozônio , Poluentes Químicos da Água , Radical Hidroxila , Nitrificação , Oxirredução , Poluentes Químicos da Água/análiseRESUMO
This work proposes a tube-in-tube membrane photoreactor, operated in a continuous-mode, to boost the efficiency of peroxydisulfate (PDS), through the photolytic (UV-C radiation) and photocatalytic (TiO2-P25) processes. This new technology can efficiently facilitate the transportation of PDS to the catalyst surface and water to be treated. The ultrafiltration tubular ceramic membrane was used as support for the TiO2-P25 and oxidant-catalyst/water contactor. Tests were performed using a synthetic solution and a municipal secondary effluent, both spiked with a pharmaceutical mix solution (paracetamol (PCT), furosemide (FRS), nimesulide (NMD), and diazepam (DZP); 200 µg L-1 of each). At steady-state regime, the UVC/S2O82-/TiO2 system, with radial PDS addition, showed the highest removal of pharmaceuticals in both matrices. Furthermore, twenty-two transformation products (TPs) were identified by applying LC-QTOF MS technique. Hence, the transformation pathways including hydroxylation in aromatic moiety by an electrophilic attack, electron transfer reactions, cleavage of C-O, C-N bond, H-abstraction and ring opening were proposed. TPs chemical structures were evaluated by in silico (Q)SAR approach using TOXTREE and EPI Suite™ software.
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Peróxido de Hidrogênio , Poluentes Químicos da Água , Oxirredução , Sulfatos , Tecnologia , Raios Ultravioleta , Poluentes Químicos da Água/análiseRESUMO
This paper presents the synthesis of a hybrid material through the use of natural pozzolan and titanium(IV) isopropoxide using the sol-gel method and its application in the photocatalytic hexavalent chromium reduction. The characterization data indicated a mesoporous material possessing a surface area of 271.7 m2 g-1. The morphology studies (SEM and TEM) showed nanosheet hybrid structures. The analysis of DRUV, FTIR, XRD, and Mössbauer spectroscopy provides a different electronic structure of the synthetized material when compared with the originals, proving the hybridization process between pozzolan and titanium(IV) isopropoxide. The photocatalytic reduction of Cr(VI) to Cr(III) using the hybrid material showed a better performance than conventional photocatalysts (precursor and TiO2-P25). Operational conditions such as chromium initial concentration (0.02-0.20 mM), solution pH (3-6), and type of scavenger (citric or tartaric acid) were evaluated in order to determine the best experimental conditions for the Cr(VI) photoreduction. At their optimum (catalyst load of 15 mg L-1, tartaric acid as scavenger, [scavenger]0/[Cr(VI)]0 M ratio = 3:1, pH 3, and 25 °C), the total photoreduction of 0.20 mM Cr(VI) was achieved in 180 min. The novel hybrid materials synthesized from pozzolan and titanium(IV) isopropoxide showed to be a potential catalyst for the Cr(VI) reduction in aqueous solution. Graphical abstract.
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Compostos Organometálicos , Titânio , Catálise , CromoRESUMO
In this study, silver molybdate was used as a catalyst in different oxidation processes to degrade pantoprazole (PAN) from aqueous suspension. The catalyst was synthesized using a controlled precipitation method and characterized by XRD, FTIR spectroscopy, BET analysis, Zeta potential, FEG-SEM/EDS, DRS and EPR. The α- and ß-phases of Ag2MoO4 were identified as crystalline structure of the butterfly-shaped particles. The metastable α-phase could be completely converted into ß-Ag2MoO4 by thermal treatment at 300 °C. The band gap energy of ß-Ag2MoO4 (Eg = 3.25 eV) is slightly higher than for as-prepared catalyst (α-Ag2MoO4 + ß-Ag2MoO4) (Eg = 3.09 eV), suggesting that as-prepared catalyst should be active under visible light. PAN is sensible to UV light irradiation, and the addition of H2O2 as electron acceptor enhanced the mineralization rate. In the catalytic UV-based reactions, high PAN oxidation efficiencies were obtained (>85%) but with low mineralization (32-64%). Catalytic peroxidation and photo-catalytic peroxidation under visible light showed the highest PAN oxidation efficiency, leading to its almost complete mineralization (>95%), even under dark conditions (98% in 120 min). Several degradation byproducts were identified and three mechanistic routes of PAN decomposition were proposed. The identified byproducts are less toxic than the parent compound. EPR coupled with the spin trapping method identified â¢OH radicals as the main ROS species in both photocatalytic and catalytic peroxidation reactions. Ag2MoO4 showed to be a promising catalyst to promote the decomposition of hydrogen peroxide into ROS.1.
Assuntos
Pantoprazol/química , Catálise , Peróxido de Hidrogênio/química , Luz , Molibdênio , Oxirredução , Prata , Soluções , Raios UltravioletaRESUMO
This work presents a disruptive approach to promote highly-efficient photo-Fenton process at neutral pH under continuous mode operation. The system consists of a tube-in-tube membrane reactor designed for continuous-flow titration of low iron doses to the annular reaction zone (ARZ). A concentrated acidic ferrous ion (Fe2+) solution is fed by the lumen-side of the membrane, permeating through the membrane pores (inside-out mode), being dosed and uniformly delivered to the membrane shell-side. Polluted water, containing amoxicillin (AMX) and oxidant (H2O2), flows continuously in the reactor annulus (space between the membrane shell-side and an outer quartz tube). The catalyst radial dispersion is enhanced by the helicoidal movement of water around the membrane shell-side, efficiently promoting its contact with H2O2 and UV light. The efficiency of photochemical and photocatalytic oxidation was evaluated as a function of catalyst dose, catalyst injection mode (radial permeation vs injection upstream from the reactor inlet), light source (UVA vs UVC) and aqueous solution matrix (synthetic vs real wastewater). At steady-state, photo-Fenton reaction with Fe2+ radial addition, driven by UVC light, showed the highest AMX removal for synthetic (â¼65%, removal rate of 44 µMAMX/min, using [Fe2+]ARZ = 2 mg/L and [H2O2]inlet = 10 mg/L) and real municipal wastewaters (â¼45%, removal rate of 31 µMAMX/min, with [Fe2+]ARZ = 5 mg/L and [H2O2]inlet = 40 mg/L), with a residence time of only 4.6 s.
Assuntos
Águas Residuárias , Poluentes Químicos da Água , Peróxido de Hidrogênio , Concentração de Íons de Hidrogênio , Ferro , Oxirredução , Poluentes Químicos da Água/análiseRESUMO
This study focuses on the influence of major dissolved constituents naturally found in waters intended for human consumption on bromate (BrO3-) reduction by heterogeneous photocatalysis. The individual and combined effect of chloride (Cl-), bicarbonate/carbonic acid (HCO3-/H2CO3), nitrate (NO3-), sulphate (SO42-) and humic acids (HAs) on BrO3- reduction was evaluated in synthetic waters (SWs). Additionally, freshwaters (FWs) from a drinking water treatment plant (DWTP) were tested and directly compared to SWs. Cl- was beneficial for contents in the range 0.47-1.4 mM, with negligible influence for lower and higher contents. NO3- had a null effect regardless of its content (0.024-0.81 mM). HCO3-/H2CO3 (0.061/0.45 mM), SO42- (0.12-2.6 mM) and HAs (0.11-1.0 mM C) had a negative effect in the tested contents. The BrO3- reduction rate was 2.8 times lower in SW with a mixture of water constituents compared to SW without constituents addition. This decline on BrO3- reduction rate corresponded to the sum of the individual species contribution and so there was no evidence of synergetic effects. By contrast, the use of FWs provided BrO3- reduction rates only slightly lower than that found for SW without constituents addition (â¼1.2-fold), which can be attributed to: (i) the distinct characteristics of the organic matter of FWs (HAs, fulvic acids and humins with distinct molecular weights and functional groups) compared to that of SW (pure HAs), and/or (ii) the presence in FWs of other inorganics in addition to those here addressed. The heterogeneous TiO2 photocatalysis proved to be a promising process for BrO3- reduction in DWTPs.
Assuntos
Poluentes Químicos da Água , Purificação da Água , Bromatos , Humanos , Nitratos , Água , Poluentes Químicos da Água/análiseRESUMO
This study aims to investigate the applicability of a hybrid electrochemical sensor composed of cork and graphite (Gr) for detecting caffeine in aqueous solutions. Raw cork (RAC) and regranulated cork (RGC, obtained by thermal treatment of RAC with steam at 380 °C) were tested as modifiers. The results clearly showed that the cork-graphite sensors, GrRAC and GrRGC, exhibited a linear response over a wide range of caffeine concentration (5-1000 µM), with R2 of 0.99 and 0.98, respectively. The limits of detection (LOD), estimated at 2.9 and 6.1 µM for GrRAC and GrRGC, suggest greater sensitivity and reproducibility than the unmodified conventional graphite sensor. The low-cost cork-graphite sensors were successfully applied in the determination of caffeine in soft drinks and pharmaceutical formulations, presenting well-defined current signals when analyzing real samples. When comparing electrochemical determinations and high performance liquid chromatography measurements, no significant differences were observed (mean accuracy 3.0%), highlighting the potential use of these sensors to determine caffeine in different samples.