We can't find the internet
Attempting to reconnect
Something went wrong!
Hang in there while we get back on track
Electrochemical removal of polystyrene nanoplastics in a filter-press reactor using modified Ti-felt anodes [Dataset]
Summary
This dataset accompanies a study testing an electrochemical reactor designed to destroy polystyrene nanoplastics in water. It provides the raw experimental data supporting the published findings on how different electrode designs and reactor flow configurations affect nanoplastic removal efficiency.
Ti-felt anodes, with high surface area, have been used as supports of Pt and SnO2-Sb-Pt electrocatalysts. Anodes have been applied in a filter-press electrochemical reactor for the electrooxidation of polystyrene nanoplastics (NPs) (100 mg·L-1). Two types of configurations have been used. In the first, the solution with NPs flows through the anode, taking advantage of its porosity (acting as a sort of membrane) to enhance the contact of NPs with the anode and the oxidative species generated. In the second configuration, the solution of NPs flows parallel to the anode, and the NPs flow parallel to it. Comparing both configurations at 25 mA·cm-2, for the Ti-Pt anode, the flow-through configuration decreases energy consumption by ~7-fold and treatment time by ~15-fold when compared to the flow-by configuration. For Ti-SnO2-Sb-Pt anode, ratios of ~6.5-fold and ~13-fold were obtained, respectively. Moreover, the effect of the current density (50, 25, 12.5, and 5 mA·cm-2) was studied. For the Ti-Pt electrode, a treatment time of only 40 minutes was achieved at a current density of 25 mA·cm-2 with the F-T configuration, with a faradaic efficiency of 62.09 %, and electrochemical energy per order (EEO) of 21.91 kW·h·m-3·order-1. In the case of the F-B configuration at 25 mA·cm-2 the treatment time increases until 600 min, with a faradaic efficiency of 8.27 % and EEO of 156.57 kW·h·m- 3·order-1.
Sign in to start a discussion.
More Papers Like This
Electrochemical removal of polystyrene nanoplastics in a filter-press reactor using modified Ti-felt anodes: Comparison of flow-through and flow-by configurations
Electrochemical water treatment — using electric current to break down contaminants — can remove polystyrene nanoplastics from water, and this study found that reactor design makes a dramatic difference in efficiency. A "flow-through" configuration where water passes directly through the electrode reduced treatment time by up to 15-fold and cut energy use by 7-fold compared to a side-flow design. These findings suggest that with the right reactor architecture, electrochemical treatment could be a practical tool for removing nanoplastics from contaminated water supplies.
Electrochemical and photoelectrochemical oxidation processes for polystyrene microplastic treatment: BDD anode vs Sb-doped SnO2 ceramic anode coated with a CdFe2O4 photocatalytic layer
This is a companion dataset to an electrochemical microplastic treatment study comparing a boron-doped diamond anode with a photoactive tin-oxide ceramic anode for degrading polystyrene microplastics. The data covers removal efficiency, organic carbon mineralization, and energy use under different current levels and lighting conditions. It supports research into scalable water treatment technologies for microplastic removal.
Electrooxidation of polystyrene nanoplastics by modified Ti-felt electrodes
Researchers developed Ti-felt electrodes coated with Pt and SnO2-Sb-Pt for electrochemical oxidation of polystyrene nanoplastics, finding that the high surface area electrodes achieved substantially higher current densities than boron-doped diamond electrodes for nanoplastic degradation.
Electrochemical and photoelectrochemical oxidation processes for polystyrene microplastic treatment: BDD anode vs Sb-doped SnO2 ceramic anode coated with a CdFe2O4 photocatalytic layer
Researchers tested two electrode types — a boron-doped diamond anode and a tin-oxide ceramic anode coated with a cadmium ferrite photocatalyst — for breaking down polystyrene microplastics using electrical current, with and without visible light. The study tracked removal efficiency, carbon mineralization, and energy consumption to compare the two systems. Findings help identify more sustainable and effective electrochemical methods for treating microplastic-contaminated water.
Electrochemical and photoelectrochemical oxidation processes for polystyrene microplastic treatment: BDD anode vs Sb-doped SnO2 ceramic anode coated with a CdFe2O4 photocatalytic layer
Researchers compared two electrode-based methods for breaking down polystyrene microplastics in water: a boron-doped diamond anode and a ceramic anode with a light-activated coating. Both approaches achieved over 95% removal of microplastics, with the diamond anode reaching up to 99% efficiency. The study demonstrates that electrochemical oxidation is a promising technology for removing microplastic contamination from water.