A mathematical model is developed to describe the dynamic behavior of mesophilic (35 +/- 5 degrees C) and thermophilic digestion (55 +/- 5 degrees C). Special emphasis is given to acetotrophic methanogenesis and propionate degradation, as the steps that determine the stability of anaerobic digestion, as well as to hydrolysis rate, which determines the degradation efficiency of particulate degradable organic carbon. Within the range of 6-20 (mesophilic) and 2-8 d (thermophilic) hydraulic retention time (HRT), the observed maximum growth rates for acetotrophic methanogens are 0.33 and 1.3 d(-1), respectively, with a 15% decay rate. Temperature and pH dependence as well as ammonia inhibition of acetate and propionate conversion are determined and included in the model, which allows us to simulate the effect of protein- and nitrogen-rich waste addition and the consequences of temporarily increased free ammonia at high pH. No inhibition of hydrogen conversion was observed in the same free ammonia range. The pH optimum is between 6.6 and 7.3. Acetotrophic methanogenesis is strongly inhibited below pH 6.2, whereas above pH 7.4 it can be inhibited by free ammonia. For digesters fed with ordinary municipal sewage sludge, free ammonia inhibition of acetate conversion leads to an increase in acetate at about 35 and 140 mg of N/L for mesophilic (HRT = 20 d) and thermophilic (HRT = 6 d) conditions, respectively. The hydrolysis rate constant is 0.25 and 0.4 d(-1) respectively for these two conditions. The model is validated with load variation experiments in laboratory and full-scale digesters for step and shock loads.
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http://dx.doi.org/10.1021/es010139p | DOI Listing |
J Phys Chem A
January 2025
Department of Mechanical Engineering, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR 999077, China.
An adequate understanding of the NO interacting chemistry is a prerequisite for a smoother transition to carbon-lean and carbon-free fuels such as ammonia and hydrogen. In this regard, this study presents a comprehensive study on the H atom abstraction by NO from C to C alkynes, dienes, and trienes forming 3 HNO isomers (i.e.
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December 2024
Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350108, China.
The nitrate reduction reaction (NORR) has emerged as a promising approach for wastewater treatment and ammonia (NH) synthesis. Poly(triazine imide)/LiCl (PTI/LiCl), a highly crystalline carbon nitride with a well-defined structure, has shown significant potential in this field. In this study, the electronic properties and catalytic performance of PTI/LiCl for NORR were investigated through theoretical calculations.
View Article and Find Full Text PDFSci Rep
December 2024
Horticulture Crops Research Department, West Azerbaijan Agricultural and Natural Resources Research and Education Centre, Agricultural Research, Education and Extension Organization (AREEO), Urmia, Iran.
Strawberry (Fragaria × ananassa) is a horticultural crop known for its sensitivity to mechanical damage and susceptibility to postharvest decay. In recent years, various strategies have been implemented to enhance both the yield and quality of strawberries, among which the application of nitric oxide-producing compounds has garnered special attention. The present study aimed to investigate the effects of varying concentrations of sodium nitroprusside (SNP), specifically 0, 200, 400, and 600 μM, on strawberries (cv.
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January 2025
Qinhuangdao Huaheng Biological Limited Company, Qinhuangdao, 066000, China.
A full-scale simultaneous partial nitrification, anaerobic ammonia oxidation (anammox), and denitrification (SNAD) reactor was initiated to address the problem of high energy consumption for the treatment of low C/N wastewater. The SNAD system achieved a nitrogen removal rate of 0.9 kg/(m·d) at an influent NH₄-N concentration of 500 mg/L after 450 days of stable operation.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
School of Physics, Henan Normal University, Xinxiang, Henan, 453007, China.
Electrochemical reduction of naturally abundant nitrogen (N) under ambient conditions is a promising method for ammonia (NH) synthesis, while the development of a highly active, stable and low-cost catalyst remains a challenge. Herein, the N reduction reaction of TM@g-BCN in electrochemical nitrogen reduction has been systematically investigated using density functional theory (DFT) calculations and compared with that of TM@g-CN. It was found that TM atoms are more stably anchored to g-BCN than to g-CN.
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