Olívia Salomé G. P. Soares
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A catalytic tool for the defluorination of PFAS in drinking water into degradable organics
Open Date: 2023-03-10
Close Date: 2024-09-09
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CORK based electrodes for eco-conscious supercapacitors - towards zero emission energy storage
Open Date: 2023-03-01
Close Date: 2026-02-28
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Unravelling the role of conductive materials in the acceleration of methane production from waste in anaerobic digestion processes
Open Date: 2022-01-01
Close Date: 2024-12-31
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Carbon-based noble metal-free bifunctional electrocatalyst for renewable energy production: Improving the Unitized Regenerative Fuel Cell
Open Date: 2021-03-01
Close Date: 2024-02-01
Grant: Close
NanoCAT - Using modified carbon nanotubes to prevent biofilm formation in urinary catheters and stents
Open Date: 2021-03-01
Close Date: 2024-02-01
Articles (10)
Catalytic Hydrogenation of Nitrate over Immobilized Nanocatalysts in a Multi-Phase Continuous Reaction System: System Performance, Characterization and Optimization
Nitrate catalytic reduction in a continuous system was studied in the presence of Pd-Cu macrostructured catalysts synthesized through a novel washcoating methodology of the pre-formed bimetallic powder catalyst. The present work aims to understand the behavior of the macrostructured bimetallic catalyst in the presence of different reaction conditions in order to achieve the design of an optimized facility that can produce the best catalytic results: maximum NO3− conversion with enhanced N2 selectivity. The residence time of the inlet solution and the catalyst concentration in the reactor proved to be the parameters that most influenced the conversion and selectivity due to the important role that these parameters play in the hydrodynamic conditions of the reactor. A higher loading of catalyst and lower inlet flow rates allow promoting a higher contact time between the three phases that participate in the reaction (G-L-S). The most efficient reaction conditions (three pieces of the macrostructured catalyst, liquid flow rate of 10 mL min−1, and a total gas flow rate of 200 Ncm3 min−1 (1:1 H2:CO2)) allowed obtaining an NO3− conversion of 51% with a corresponding N2 selectivity of 23%. Also, the conversion results strongly depended on the total gas flow rate used during the reaction since this assists the mixing between the three phases and promotes a greater contact that will contribute to enhanced catalytic results.
Year:
2023
Collaborators (7)
Luis Miguel Madeira
Associate Professor
Universidade do Porto Faculdade de Engenharia
Olga Nunes
Associate Professor
Universidade do Porto Faculdade de Engenharia
Professor Kathryn A. Whitehead
Professor in Microbiology at Interfaces
Manchester Metropolitan University
Luciana C. Gomes
University of Porto
Manuel Fernando Ribeiro Pereira
University of Porto
Ana Rita Querido
University of Porto
Filipe Mergulhão
Professor Associado
Universidade do Porto Faculdade de Engenharia

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