Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2016Tertiary treatment of a municipal wastewater toward pharmaceuticals removal by chemical and electrochemical advanced oxidation processes133citations
  • 2015Incorporation of electrochemical advanced oxidation processes in a multistage treatment system for sanitary landfill leachate112citations
  • 2015Degradation of trimethoprim antibiotic by UVA photoelectro-Fenton process mediated by Fe(III)-carboxylate complexes82citations
  • 2014Degradation of the antibiotic trimethoprim by electrochemical advanced oxidation processes using a carbon-PTFE air-diffusion cathode and a boron-doped diamond or platinum anode184citations

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Chart of shared publication
Brillas, E.
4 / 5 shared
Boaventura, Rar
4 / 16 shared
Soler, J.
2 / 2 shared
Vilar, Vjp
4 / 17 shared
Alpendurada, Mf
1 / 1 shared
Fonseca, A.
1 / 9 shared
Saraiva, I.
1 / 1 shared
Garcia Segura, S.
1 / 1 shared
Chart of publication period
2016
2015
2014

Co-Authors (by relevance)

  • Brillas, E.
  • Boaventura, Rar
  • Soler, J.
  • Vilar, Vjp
  • Alpendurada, Mf
  • Fonseca, A.
  • Saraiva, I.
  • Garcia Segura, S.
OrganizationsLocationPeople

article

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

  • Brillas, E.
  • Boaventura, Rar
  • Soler, J.
  • Vilar, Vjp
  • Moreira, Fc
  • Fonseca, A.
  • Saraiva, I.
Abstract

The current study has proved the technical feasibility of including electrochemical advanced oxidation processes (EAOPs) in a multistage strategy for the remediation of a sanitary landfill leachate that embraced: (i) first biological treatment to remove the biodegradable organic fraction, oxidize ammonium and reduce alkalinity, (ii) coagulation of the bio-treated leachate to precipitate humic acids and particles, followed by separation of the clarified effluent, and (iii) oxidation of the resulting effluent by an EAOP to degrade the recalcitrant organic matter and increase its biodegradability so that a second biological process for removal of biodegradable organics and nitrogen content could be applied. The influence of current density on an UVA photoelectro-Fenton (PEF) process was firstly assessed. The oxidation ability of various EAOPs such as electro-Fenton (EF) with two distinct initial total dissolved iron concentrations ([TDI](0)), PEF and solar PEF (SPEF) was further evaluated and these processes were compared with their analogous chemical ones. A detailed assessment of the two first treatment stages was made and the biodegradability enhancement during the SPEF process was determined by a Zahn-Wellens test to define the ideal organics oxidation state to stop the EAOP and apply the second biological treatment. The best current density was 200 mA cm(-2) for a PEF process using a BDD anode, [TDI](0) of 60 mg L-1, pH 2.8 and 20 degrees C. The relative oxidation ability of EAOPs increased in the order EF with 12 mg [TDI](0) L-1 < EF with 60 mg [TDI](0) L-1 < PEF with 60 mg [TDI](0) L-1 <= SPEF with 60 mg [TDI](0) L-1, using the above-mentioned conditions. While EF process was much superior to the Fenton one, the superiority of PEF over photo-Fenton was less evident and SPEF attained similar degradation to solar photo-Fenton. To provide a final dissolved organic carbon (DOC) of 163 mg L-1 to fulfill the discharge limits into the environment after a second biological process, 6.2 kJ L-1 UV energy and 36 kWh m(-3) electrical energy were consumed using SPEF with a BDD anode at 200 mA cm(-2), 60 mg [TDI](0) L-1, pH 2.8 and 20 degrees C.

Topics
  • density
  • Carbon
  • laser emission spectroscopy
  • Nitrogen
  • precipitate
  • iron
  • current density