Sulfite has been widely employed as a key agent in many industrial processes, leading to a large amount of sulfite-laden wastes generated. Given its antimicrobial function and destructive ability on cell walls, detailed mechanisms for impacts of sulfite on waste activated sludge (WAS) and outcomes of methane production after the sulfite-pretreatment have not been clear so far. In this study, the feasibility of methane production from sulfite pretreated WAS was verified and investigated. Biochemical methane potential tests demonstrated that methane production from WAS after the pretreatment at 800 mg S/L of sulfite (a typical level in sulfite-laden wastes) increased by up to 25%. Kinetic analysis of the test results indicated that sulfite pretreatment increased the sludge hydrolysis rate (k) by 1.71 times while the ultimate biochemical methane potential (B) by 1.20 times. Further study investigated the effects of sulfite on WAS from the macro-scale (i.e. sludge physicochemical properties) to the micro-scale (i.e. bacterial viability, microbial community). Sulfite concentrations of up to 800 mg S/L substantially enhanced WAS disintegration and solubilization, reducing the particle size by up to 39%, boosting substrate release by 87% and improving cell lysis by 43% through the direct destruction of gram-positive microorganisms (e.g., norank_p_Saccharibacteria) in WAS. Adverse impact on anaerobic digestion by introduction of sulfite was not observed in this study, though a long-term evaluation is needed in the future work. Based on the findings of the present study, sulfite-laden by-products or wastes from industrial processes may be co-treated with WAS when overall cost-effectiveness is concerned.
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http://dx.doi.org/10.1016/j.watres.2019.04.048 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
UESTC: University of Electronic Science and Technology of China, School of Materials and Energy, Chengdu, Sichuan, 611731, Chengdu, CHINA.
The electrochemical reduction of carbon dioxide (CO2) to methane (CH4) presents a promising solution for mitigating CO2 emissions while producing valuable chemical feedstocks. Although single-atom catalysts have shown potential in selectively converting CO2 to CH4, their limited active sites often hinder the realization of high current densities, posing a selectivity-activity dilemma. In this study, we developed a single-atom cobalt (Co) doped copper catalyst (Co1Cu) that achieved a CH4 Faradaic efficiency exceeding 60% with a partial current density of -482.
View Article and Find Full Text PDFChemSusChem
January 2025
University of Electronic Science and Technology of China, School of Material and Energy, Qingshuihe Campus:No.2006, Xiyuan Ave, West Hi-Tech Zone, 611731, Chengdu, CHINA.
Modulating the oxidation state of copper (Cu) is crucial for enhancing the electrocatalytic CO2 reduction reaction (CO2RR), particularly for facilitating deep reductions to produce methane (CH4) or multi-carbon (C2+) products. However, Cuδ+ sites are thermodynamically unstable, fluctuating their oxidation states under reaction conditions, which complicates their functionality. Incorporating interfacial metal oxides has emerged as an effective strategy for stabilizing these oxidation states.
View Article and Find Full Text PDFTransl Anim Sci
January 2025
Lethbridge Research and Development Centre, Agriculture and Agri-Food Canada, Lethbridge, Alberta T1J 4B1, Canada.
A study was conducted to assess growth performance, methane (CH) emissions, and feeding behavior of feedlot steers consuming backgrounding and finishing diets with an essential oil blend (EO), monensin (Mon), and their combination (EO + Mon). The study was structured as a 2 × 2 factorial, with two feed additive treatments (Control, EO) and two monensin treatments (no Monensin, Monensin). One hundred Angus × steers were evenly distributed across each treatment into four pens, and each dietary phase consisted of four, 28-d periods.
View Article and Find Full Text PDFSci Rep
January 2025
New materials Technology and Processing Reserearch Center, Neyshabur Branch, Islamic Azad University, Neyshabur, Iran.
The conversion of diluted CO₂ into high-energy fuels is increasingly central to renewable energy research. This study investigates the efficacy of a Gd₂NiMnO₆ dendritic nanofibrous (DNF) photocatalyst in transforming carbon dioxide to methane through photoreduction. Gd₂NiMnO₆ DNF was found to provide active adsorption sites and control the strand dimensions for metal groups, facilitating the chemical absorption of CO₂.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Chinese Academy of Sciences Dalian Institute of Chemical Physics, State Key Laboratory of Catalysis and Dalian National Laboratory for Clean Energy, CHINA.
Hydroxy radical (•OH) is a prestigious oxidant that allows the cleavage of strong chemical bonds of methane but is untamed, leading to over-oxidation of methane and waste of oxidants, especially at high methane conversion. Here, we managed to buffer •OH in an aqueous solution of photo-irradiated Fe3+, where •OH almost participates in methane oxidation. Due to the interaction between Fe3+ and SO42-, the electron transfer from OH- to excited-state Fe3+ for •OH generation is retarded, while excessive •OH is consumed by generated Fe2+ to restore Fe3+.
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