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Flow capacitive deionization is a water desalination technique that uses liquid carbon-based electrodes to recover fresh water from brackish or seawater. This is a potential second-generation water desalination process, however it is limited by parameters such as feed electrode conductivity, interfacial resistance, viscosity, and so on. In this study, titanium oxide nanofibers (TiONF) were manufactured using an electrospinning process and then blended with commercial activated carbon (AC) to create a well distributed flow electrode in this study. Field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and energy dispersive X-ray (EDX) were used to characterize the morphology, crystal structure, and chemical moieties of the as-synthesized composites. Notably, the flow electrode containing 1 wt.% TiONF (ACTiONF 1 wt.%) had the highest capacitance and the best salt removal rate (0.033 mg/min·cm) of all the composites. The improvement in cell performance at this ratio indicates that the nanofibers are uniformly distributed over the electrode's surface, preventing electrode passivation, and nanofiber agglomeration, which could impede ion flow to the electrode's pores. This research suggests that the physical mixture could be used as a flow electrode in capacitive deionization.
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http://dx.doi.org/10.3390/ma14226891 | DOI Listing |
J Colloid Interface Sci
December 2024
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, China. Electronic address:
Although aqueous organic redox flow battery (RFBs) is a highly promising energy storage device, the redox reaction kinetics of the anode organic electrolyte material, especially for phenazine derivatives, are limited by low electrochemical activity of traditional porous carbon electrodes. Herein, Co/NC composite electrocatalyst was elaborated to significantly enhance the redox reaction kinetics of phenazine derivatives, in which Co/NC electrocatalyst could improve energy efficiency of aqueous phenazine RFBs by 43.2 % compared to pure carbon felt electrodes at current density of 100 mA/cm.
View Article and Find Full Text PDFAnal Chem
December 2024
Department of Analytical Chemistry, Physical Chemistry and Chemical Engineering, University of Alcalá, E-28802 Madrid, Spain.
Here, we present three-dimensional-printed dual-channel flow-through miniaturized devices (3D) with dual electrochemical detection (ED) integrating two working electrodes each in an in-channel configuration (3D-ED). Prussian Blue (PB) shell-gold nanoparticles ((PB)AuNP) core-based electrochemistry was chosen for selective hydrogen peroxide determination. 3D-ED devices exhibited impress stability, identical intrachannel and interchannel electrochemical performances, and excellent interdevice precision with values under 9%, revealing the reliability of the design and fabrication of the devices.
View Article and Find Full Text PDFBrain
December 2024
Neuroimmunology Program, Fundació Clínic per la Recerca Biomèdica - Institut d'Investigacions Biomèdiques August Pi i Sunyer (FCRB-IDIBAPS), Barcelona 08036, Spain.
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a disorder mediated by autoantibodies against the GluN1 subunit of NMDAR. It occurs with severe neuropsychiatric symptoms that often improve with immunotherapy. Clinical studies and animal models based on patients' antibody transfer or NMDAR immunization suggest that the autoantibodies play a major pathogenic role.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
South China University of Technology, School of Chemistry and Chemical Engineering, Wushan St., 510640, Guangzhou, CHINA.
The proceeding of electrochemical CO2 reduction reaction (CO2RR) requires the formation of active hydrogen species for CO2 protonation, while traditional catalysts fail to balance the rate of hydrogen supply and CO2 protonation. Herein, we propose a "hydrogen on demand" mechanism, in which the polarity of the adsorbed CO2 is enhanced to allow the capture of hydrogen from water without forming free hydrogen species, realizing the matching rate of hydrogen supply and CO2 protonation. As a proof of concept, we construct Zn-N sites modified by Se atoms, allowing the proceeding of CO2RR under the "hydrogen on demand" mechanism with superior efficiency.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Ruhr University Bochum, Analytische Chemie, Universitätsstr 150, 44780, Bochum, GERMANY.
The direct CO2 reduction reaction (CO2RR) from simulated flue gas of various CO2 concentrations could minimize extra energy for pre-concentration processes to highly concentrated CO2 as a feed-stock. We investigate the challenges for CO2RR caused by low CO2 concentrations and provide strategies concerning the impact of the chosen electrocatalyst material and the selection of the electrolyte to attain high CO selectivity. We continuously feed CO2 mixed with N2 (the typical dilutant in flue gas) in various ratios to gas diffusion electrodes in a model flow-through electrolyzer.
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