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Dive into the research topics where Francisca C. Moreira is active.

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Featured researches published by Francisca C. Moreira.


Water Research | 2012

Biodegradability enhancement of a pesticide-containing bio-treated wastewater using a solar photo-Fenton treatment step followed by a biological oxidation process

Vítor J.P. Vilar; Francisca C. Moreira; Ana C.C. Ferreira; C. Gonçalves; M.F. Alpendurada; Rui A.R. Boaventura

This work proposes an efficient combined treatment for the decontamination of a pesticide-containing wastewater resulting from phytopharmaceutical plastic containers washing, presenting a moderate organic load (COD=1662-1960 mg O₂ L⁻¹; DOC=513-696 mg C L⁻¹), with a high biodegradable organic carbon fraction (81%; BOD₅=1350-1600 mg O₂ L⁻¹) and a remaining recalcitrant organic carbon mainly due to pesticides. Nineteen pesticides were quantified by LC-MS/MS at concentrations between 0.02 and 45 mg L⁻¹ (14-19% of DOC). The decontamination strategy involved a sequential three-step treatment: (a) biological oxidation process, leading to almost complete removal of the biodegradable organic carbon fraction; (b) solar photo-Fenton process using CPCs, enhancing the bio-treated wastewater biodegradability, mainly due to pesticides degradation into low-molecular-weight carboxylate anions; (c) and a final polishing step to remove the residual biodegradable organic carbon, using a biological oxidation process. Treatment performance was evaluated in terms of mineralization degree (DOC), pesticides content (LC-MS/MS), inorganic ions and low-molecular-weight carboxylate anions (IC) concentrations. The estimated phototreatment energy necessary to reach a biodegradable wastewater, considering pesticides and low-molecular-weight carboxylate anions concentrations, Zahn-Wellens test and BOD₅/COD ratio, was only 2.3 kJ(UV) L⁻¹ (45 min of photo-Fenton at a constant solar UV power of 30 W m⁻²), consuming 16 mM of H₂O₂, which pointed to 52% mineralization and an abatement higher than 86% for 18 pesticides. The biological oxidation/solar photo-Fenton/biological oxidation treatment system achieved pesticide removals below the respective detection limits and 79% mineralization, leading to a COD value lower than 150 mg O₂ L⁻¹, which is in agreement with Portuguese discharge limits regarding water bodies.


Water Research | 2015

Remediation of a winery wastewater combining aerobic biological oxidation and electrochemical advanced oxidation processes

Francisca C. Moreira; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar

Apart from a high biodegradable fraction consisting of organic acids, sugars and alcohols, winery wastewaters exhibit a recalcitrant fraction containing high-molecular-weight compounds as polyphenols, tannins and lignins. In this context, a winery wastewater was firstly subjected to a biological oxidation to mineralize the biodegradable fraction and afterwards an electrochemical advanced oxidation process (EAOP) was applied in order to mineralize the refractory molecules or transform them into simpler ones that can be further biodegraded. The biological oxidation led to above 97% removals of dissolved organic carbon (DOC), chemical oxygen demand (COD) and 5-day biochemical oxygen demand (BOD5), but was inefficient on the degradation of a bioresistant fraction corresponding to 130 mg L(-1) of DOC, 380 mg O2 L(-1) of COD and 8.2 mg caffeic acid equivalent L(-1) of total dissolved polyphenols. Various EAOPs such as anodic oxidation with electrogenerated H2O2 (AO-H2O2), electro-Fenton (EF), UVA photoelectro-Fenton (PEF) and solar PEF (SPEF) were then applied to the recalcitrant effluent fraction using a 2.2 L lab-scale flow plant containing an electrochemical cell equipped with a boron-doped diamond (BDD) anode and a carbon-PTFE air-diffusion cathode and coupled to a photoreactor with compound parabolic collectors (CPCs). The influence of initial Fe(2+) concentration and current density on the PEF process was evaluated. The relative oxidative ability of EAOPs increased in the order AO-H2O2 < EF < PEF ≤ SPEF. The SPEF process using an initial Fe(2+) concentration of 35 mg L(-1), current density of 25 mA cm(-2), pH of 2.8 and 25 °C reached removals of 86% on DOC and 68% on COD after 240 min, regarding the biologically treated effluent, along with energy consumptions of 45 kWh (kg DOC)(-1) and 5.1 kWh m(-3). After this coupled treatment, color, odor, COD, BOD5, NH4(+), NO3(-) and SO4(2-) parameters complied with the legislation targets and, in addition, a total dissolved polyphenols content of 0.35 mg caffeic acid equivalent L(-1) was found. Respirometry tests revealed low biodegradability enhancement along the SPEF process.


International Journal of Molecular Sciences | 2016

Nitrogen Removal from Landfill Leachate by Microalgae.

Sérgio Pereira; Ana L. Gonçalves; Francisca C. Moreira; Tânia F.C.V. Silva; Vítor J.P. Vilar; J. C. M. Pires

Landfill leachates result from the degradation of solid residues in sanitary landfills, thus presenting a high variability in terms of composition. Normally, these effluents are characterized by high ammoniacal-nitrogen (N–NH4+) concentrations, high chemical oxygen demands and low phosphorus concentrations. The development of effective treatment strategies becomes difficult, posing a serious problem to the environment. Phycoremediation appears to be a suitable alternative for the treatment of landfill leachates. In this study, the potential of Chlorella vulgaris for biomass production and nutrients (mainly nitrogen and phosphorus) removal from different compositions of a landfill leachate was evaluated. Since microalgae also require phosphorus for their growth, different loads of this nutrient were evaluated, giving the following N:P ratios: 12:1, 23:1 and 35:1. The results have shown that C. vulgaris was able to grow in the different leachate compositions assessed. However, microalgal growth was higher in the cultures presenting the lowest N–NH4+ concentration. In terms of nutrients uptake, an effective removal of N–NH4+ and phosphorus was observed in all the experiments, especially in those supplied with phosphorus. Nevertheless, N–NO3− removal was considered almost negligible. These promising results constitute important findings in the development of a bioremediation technology for the treatment of landfill leachates.


Applied Catalysis B-environmental | 2017

Electrochemical advanced oxidation processes: A review on their application to synthetic and real wastewaters

Francisca C. Moreira; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar


Applied Catalysis B-environmental | 2013

Decolorization and mineralization of Sunset Yellow FCF azo dye by anodic oxidation, electro-Fenton, UVA photoelectro-Fenton and solar photoelectro-Fenton processes

Francisca C. Moreira; Sergi Garcia-Segura; Vítor J.P. Vilar; Rui A.R. Boaventura; Enric Brillas


Applied Catalysis B-environmental | 2014

Degradation of the antibiotic trimethoprim by electrochemical advanced oxidation processes using a carbon-PTFE air-diffusion cathode and a boron-doped diamond or platinum anode

Francisca C. Moreira; Sergi Garcia-Segura; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar


Chemical Engineering Journal | 2014

Enhancement of the photo-Fenton reaction at near neutral pH through the use of ferrioxalate complexes: A case study on trimethoprim and sulfamethoxazole antibiotics removal from aqueous solutions

Isabelli Dias; Bruno S. Souza; João H.O.S. Pereira; Francisca C. Moreira; Márcia Dezotti; Rui A.R. Boaventura; Vítor J.P. Vilar


Water Research | 2015

Incorporation of electrochemical advanced oxidation processes in a multistage treatment system for sanitary landfill leachate

Francisca C. Moreira; J. Soler; Amélia Fonseca; Isabel Saraiva; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar


Applied Catalysis B-environmental | 2015

Degradation of trimethoprim antibiotic by UVA photoelectro-Fenton process mediated by Fe(III)–carboxylate complexes

Francisca C. Moreira; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar


Water Research | 2016

Tertiary treatment of a municipal wastewater toward pharmaceuticals removal by chemical and electrochemical advanced oxidation processes

Francisca C. Moreira; J. Soler; M.F. Alpendurada; Rui A.R. Boaventura; Enric Brillas; Vítor J.P. Vilar

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Márcia Dezotti

Federal University of Rio de Janeiro

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