Two-pass reverse osmosis (RO) process is prevailing in seawater desalination, but each process must consume considerable amounts of chemicals to secure product water quality. Caustic soda is used to raise the pH of the first-pass RO permeate (also the second-pass RO feed) to ensure adequate removal of boron in the subsequent second-pass RO, while antiscalants and disinfectants such as hypochlorite are added in the feed seawater for scaling and biofouling control of the first-pass RO membranes. Here, we report for the first time a flow-through electrochemically assisted reverse osmosis (FT-EARO) module system used in the first-pass RO, aiming to dramatically reduce or even eliminate chemical usage for the current RO desalination. This novel system integrated an electroconductive permeate carrier as cathode and an electroconductive feed spacer as anode on each side of the first-pass RO membrane. Upon applying an extremely low-energy (< 0.005 kWh/m) electrical field, the FT-EARO module could (1) produce a permeate with pH >10 with no alkali dosage, ensuring sufficient boron removal in the second-pass RO, and (2) generate protons and low-concentration free chlorine near the membrane surface, potentially discouraging membrane scaling and biofouling while maintaining satisfactory desalination performance. The current study further elucidated the high scalability of this novel electrified high-pressure RO module design. The low-chemical manner of FT-EARO presents an attractive practical option towards green and sustainable seawater desalination.
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http://dx.doi.org/10.1016/j.watres.2023.120982 | DOI Listing |
Anal Chim Acta
February 2025
Department of Chemistry and Applied Biosciences, Laboratory of Inorganic Chemistry, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, Zürich, CH-8093, Switzerland; Laboratory of Radiochemistry, Centre for Nuclear Engineering and Sciences, Paul Scherrer Institute, Forschungsstrasse 111, Villigen PSI, CH-5232, Switzerland. Electronic address:
Background: The direct and accurate measurement of low-level γ-emitters in samples from nuclear facilities is a challenging task due to the presence of high activities of dominant radionuclides. In this case a complex chemical separation is required to remove interfering radionuclides prior to γ-spectrometric analysis. Several radionuclides such as, Ag, Sb, Sn and Te are of relevance for radioanalytical analysis in nuclear facilities.
View Article and Find Full Text PDFWater Res
December 2024
Department of Global Smart City, Sungkyunkwan University (SKKU), 2066, Seobu-ro, Jangan-gu, Suwon, Gyeonggi-do, 16419, Republic of Korea. Electronic address:
J Am Chem Soc
January 2025
Department of Inorganic Spectroscopy, Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr, Germany, 45470.
Molybdenum nitrogenase plays a crucial role in the biological nitrogen cycle by catalyzing the reduction of dinitrogen (N) to ammonia (NH) under ambient conditions. However, the underlying mechanisms of nitrogenase catalysis, including electron and proton transfer dynamics, remain only partially understood. In this study, we covalently attached molybdenum nitrogenase (MoFe) to gold electrodes and utilized surface-enhanced infrared absorption spectroscopy (SEIRA) coupled with electrochemistry techniques to investigate its catalytic mechanism.
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 PDFAngew Chem Int Ed Engl
December 2024
Analytical Chemistry-Center for Electrochemical Sciences (CES), Faculty of Chemistry and Biochemistry, Ruhr University Bochum, Universitätsstr. 150, 44780, Bochum, Germany.
The direct CO reduction reaction (CORR) from simulated flue gas of various CO concentrations could minimize extra energy for pre-concentration processes to highly concentrated CO as a feedstock. We investigate the challenges for CORR caused by low CO 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 CO mixed with N (the typical dilutant in flue gas) in various ratios to gas diffusion electrodes in a model flow-through electrolyzer.
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