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Large greenhouse gas emissions occur via the release of carbon dioxide (CO) and methane (CH) from the surface layer of lakes. Such emissions are modeled from the air-water gas concentration gradient and the gas transfer velocity (). The links between and the physical properties of the gas and water have led to the development of methods to convert between gases through Schmidt number normalization. However, recent observations have found that such normalization of apparent estimates from field measurements can yield different results for CH and CO. We estimated for CO and CH from measurements of concentration gradients and fluxes in four contrasting lakes and found consistently higher (on an average 1.7 times) normalized apparent values for CO than CH. From these results, we infer that several gas-specific factors, including chemical and biological processes within the water surface microlayer, can influence apparent estimates. We highlight the importance of accurately measuring relevant air-water gas concentration gradients and considering gas-specific processes when estimating .
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http://dx.doi.org/10.1021/acs.est.2c09230 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, P. R. China.
Electrochemical CO capture (eCC) excels in selectivity, reversibility, low-temperature operation, and reusability, yet liquid-phase systems struggle with mass transfer limitations. In this study, a phenazine-based capture agent was chemically grafted onto carboxylated carbon nanotubes, achieving an active loading of 4.4 wt %.
View Article and Find Full Text PDFBioresour Technol
September 2025
Center for Water Cycle Research, Climate and Environmental Research Institute, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea; Division of Energy & Environment Technology, KIST School, Korea University of Science and Technology, Seoul 02792, Republic of Korea. Electronic a
This study evaluates ammonia gas recovery from high-strength anaerobic digestate using a bipolar membrane electrodialysis (BPED) and membrane contactor (MC). Ammonia is a promising carbon-neutral energy carrier, while digestates present both environmental challenges and opportunities for ammonia recovery. The BPED was tested at 2,000---10,000 mg-N/L under varying voltages and flow rates, achieving up to 87.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
School of Ecology and Environment, Zhengzhou University, Zhengzhou 450001, China; Henan Key Laboratory of Environmental Chemistry and Low Carbon Technology, Zhengzhou 450001, China. Electronic address:
Solid electrolyte cell is a novel gas purification approach, which has unique superiority in simultaneous nitrogen oxides (NO) and volatile organic compounds (VOCs) removal. The development of effective electrode materials and the comprehensive understanding of reaction mechanisms are essential to advancing this technology. In this study, LaPrBaNiO (x = 0, 0.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
College of New Energy and Materials, State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing, Changping, 102249, China.. Electronic address:
Hard carbon has emerged as the most widely studied and commercialized anode material for sodium-ion batteries (SIBs). However, improving the charge transfer kinetics within the plateau potential range of the hard carbon anode is crucial for the development of fast-charging SIBs. In this study, we prepared a novel composite material, ZAPA-1300, by uniformly mixing starch, asphalt, and zinc oxide (ZnO), followed by a two-step treatment process.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266580, PR China; Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), Qingdao 266580, PR China. Electronic address:
With the trend of heavy and inferior crude oil, the design of hydrodesulfurization (HDS) catalysts with excellent activity and high active metal utilization is an inevitable trend for the upgrading of refining technology. In this study, a highly dispersed Mo catalyst confined within nitrogen-doped porous carbon (xMo@NC) was prepared using an in situ encapsulation-pyrolysis approach and used in the HDS reaction of dibenzothiophene (DBT). The methods of XRD, HRTEM, HAADF-STEM, N physisorption, FT-IR, Raman, and XPS were used to carry out thorough microstructural characterization.
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