Dissolved inorganic carbon (DIC) content of aqueous systems is a key function of the pH, of the total alkanility (TA), and of the partial pressure of CO2. However, common analytical techniques used to determine the DIC content in water are unable to operate under high CO2 pressure. Here, we propose to use Raman spectroscopy as a novel alternative to discriminate and quantitatively monitor the three dissolved inorganic carbon species CO2(aq), HCO3(-), and CO3(2-) of alkaline solutions under high CO2 pressure (from P = 0 to 250 bar at T = 40 °C). In addition, we demonstrate that the pH values can be extracted from the molalities of CO2(aq) and HCO3(-). The results are in very good agreement with those obtained from direct spectrophotometric measurements using colored indicators. This novel method presents the great advantage over high pressure conventional techniques of not using breakable electrodes or reference additives and appears of great interest especially in marine biogeochemistry, in carbon capture and storage and in material engineering under high CO2 pressure.
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http://dx.doi.org/10.1021/ac5025446 | DOI Listing |
Mar Environ Res
January 2025
Key Laboratory of Marine Ecosystem Dynamics, Second Institute of Oceanography, Ministry of Natural Resources, Hangzhou, 310012, China; State Key Laboratory of Satellite Ocean Environment Dynamics, Second Institute of Oceanography, Ministry of Natural Resources, Hangzhou, 310012, China.
This study examines the seasonal variations in carbonate system parameters in the East China Sea (ECS) off the Yangtze River estuary (YRE) and analyzes the contributions of anthropogenic CO₂ and eutrophication to acidification. Carbonate parameters data were collected during summer 2019 and combined winter 2011. During winter, acidification is primarily driven by rising atmospheric CO₂, with minimal impact from biological processes.
View Article and Find Full Text PDFWater Res
January 2025
Georgia Tech Shenzhen Institute (GTSI), Tianjin University, Shenzhen 518067, China. Electronic address:
Nitrogen recovery from urine and CO utilization are both vital for achieving a circular economy and mitigating climate change. Divided engineering solutions have been proposed to address either problem, but there is still a lack of integrated technologies to simultaneously tackle the two tasks. We demonstrated CO-driven ion exchange for nitrogen recovery (CIXNR) from urine and evaluated the process in Malawi.
View Article and Find Full Text PDFSci Rep
January 2025
Climate and Environmental Institute, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul, 02792, Republic of Korea.
Abiotic H and hydrocarbons are found in fluids discharged from ultramafic-hosted hydrothermal vents. Beneath the hydrothermal vents, abiotic H and hydrocarbons can be formed by serpentinization reactions and Fischer-Tropsch-type hydrocarbon-forming reactions, respectively, over ultramafic rocks. However, the source rocks that form abiotic H and hydrocarbons may extend to broader subsurface rocks.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemistry, University of Toronto, Toronto, ON, Canada.
As the global quest for sustainable energy keeps rising, exploring novel efficient and practical photocatalysts remains a research and industrial urge. Particularly, metal organic frameworks were proven to contribute to various stages of the carbon cycle, from CO capture to its conversion. Herein, we report the photo-methanation activity of three isostructural, nickel-based metal organic frameworks incorporating additional niobium, iron, and aluminum sites, having demonstrated exceptional CO capture abilities from thin air in previous reports.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
Institute for Catalysis, Hokkaido University, N-21, W-10, Sapporo 001-0021, Japan.
The effective elimination of NO from automobile exhaust at low temperatures poses significant challenges. Compared to other materials, supported RhO catalysts exhibit high NO decomposition activities, even in the presence of O, CO, and HO. Metal additives can enhance the low-temperature NO decomposition activities over supported RhO catalysts; however, the enhancement mechanism and active sites require further investigation.
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