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[Characterization of greenhouse gas emissions and stable isotopic composition of ammonia during industrial composting process]. | LitMetric

AI Article Synopsis

  • The study investigates the emissions of greenhouse gases (CO, CH, NO, and NH) from industrial composting of livestock and poultry waste, noting a lack of prior research on this scale.
  • Emission rates were measured over 19 days, revealing that methane (CH) contributed the most to global warming potential at 65%, followed by carbon dioxide (CO), ammonia (NH), and nitrous oxide (NO).
  • The isotopic composition of ammonia emitted was characterized, with a mean δN value of -11.6‰±1.2‰, offering insights into greenhouse gas emission dynamics and ammonia sources specific to livestock and poultry areas.

Article Abstract

Carbon dioxide (CO), nitrous oxide (NO), methane (CH) and ammonia (NH) emitted during the composting of livestock and poultry waste are important gaseous atmospheric pollutants. However, most previous studies on compost-related anthropogenic emissions of these gases were based on small reactor composting. Our understanding of their emissions during industrial composting remains extremely limited. In order to explore the influence of gas produced by industrial composting on regional environment, we monitored CO, CH, NO and NH emissions during industrial composting for 19 days and characterized the isotopic composition of emitted NH. On average, the emission rates of CO, CH, NO, and NH during the composting cycle were 86.8 g CO-C·d·m, 9.8 g CH-C·d·m, 3.7 mg NO-N·d·m and 736.6 mg NH-N·d·m, respectively. The contribution of CH to daily global warming potential (GWP) was the highest (65%), followed by CO, NH(indirect), and NO. Moreover, ammonia emitted from industrial compost had a mean δN value of -11.6‰±1.2‰ (range: -21.8‰--7.2‰). Overall, this study provided useful information for understanding greenhouse gas emission dynamics and characterizing atmospheric NH sources during composting process in livestock and poultry breeding areas.

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Source
http://dx.doi.org/10.13287/j.1001-9332.202206.009DOI Listing

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