Detecting and sourcing GHGs and atmospheric trace gases in a municipal waste treatment plant using coupled chemistry and isotope compositions

Landfill operations and waste processing facilities are important and highly heterogeneous sources of both greenhouse gases (GHGs) and non-GHG air pollutants in the atmosphere. This arises the need for detailed apportionment of waste sources in order to locate and subsequently reduce emissions from landfills. Here, a time series of in situ measurements of atmospheric trace gases and spatial allocation of specific emission source types under different processing phases and environmental conditions were conducted in and in the surroundings of a Municipal Solid Waste Treatment Plant (MSWTP) in south-western Poland. Results revealed that several individual GHG sources dominated across the waste processing facility and that GHGs concentrations displayed spatial seasonality. An increase in the ground-level CH<sub>4</sub> concentrations, from ∼ 30.3 to 56.3 ppmv, was observed close (∼5 - 10 m) to the major emission sources within the MSWTP. While hotspot areas generally yielded elevated CH<sub>4</sub> concentrations near the soil surface, these were relatively low (2.4 to 8.9 ppmv) along the facility's fence line. The study of the corresponding δ<sup>13</sup>C delineated the extent of dispersion plumes downwind emission hotspots, characterized by a <sup>13</sup>C depletion (around 4.0 ‰) in the atmospheric CH<sub>4</sub> and CO<sub>2</sub>. For CH<sub>4</sub>, emissions were isotopically discriminated between the extraction wells at active quarters/cells (δ<sup>13</sup>C = -58.3 ± 1.1 ‰) and biogas produced in the biological waste treatment installation (δ<sup>13</sup>C = -62.7 ± 0.7 ‰). Most of the trace compounds (non-methane hydrocarbons, halocarbons, oxygen-bearing organic gases, ketones, nitrogenous and sulphurous gases, and other admixture compounds) detected at the ground surface were linked to the CH<sub>4</sub>- and CO<sub>2</sub>-rich spots. Despite the relatively high variability in the concentrations of organic and inorganic compounds observed at the MSWTP active zones, our results suggest that they do not have a meaningful impact on the surrounding air quality.

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Publication Details

Journal
Waste Management
Published
2024-10-10
DOI
https://doi.org/10.1016/j.wasman.2024.10.003
Citations
1
Primary Topic
Atmospheric and Environmental Gas Dynamics
Type
article
Field-Weighted Citation Impact
0.28
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article

Detecting and sourcing GHGs and atmospheric trace gases in a municipal waste treatment plant using coupled chemistry and isotope compositions

David Wîdory, Izabela Sówka, Justyna Jońca, Yaroslav Bezyk et al.
1 citations
Waste Management
Atmospheric and Environmental Gas Dynamics
0.28
article

Detecting and sourcing GHGs and atmospheric trace gases in a municipal waste treatment plant using coupled chemistry and isotope compositions

David Wîdory, Izabela Sówka, Justyna Jońca, Yaroslav Bezyk, Łukasz Kruszewski, Paweł Jagoda, Jarosław Nęcki, Maciej Górka
article en
1 citations

Abstract

Landfill operations and waste processing facilities are important and highly heterogeneous sources of both greenhouse gases (GHGs) and non-GHG air pollutants in the atmosphere. This arises the need for detailed apportionment of waste sources in order to locate and subsequently reduce emissions from landfills. Here, a time series of in situ measurements of atmospheric trace gases and spatial allocation of specific emission source types under different processing phases and environmental conditions were conducted in and in the surroundings of a Municipal Solid Waste Treatment Plant (MSWTP) in south-western Poland. Results revealed that several individual GHG sources dominated across the waste processing facility and that GHGs concentrations displayed spatial seasonality. An increase in the ground-level CH<sub>4</sub> concentrations, from ∼ 30.3 to 56.3 ppmv, was observed close (∼5 - 10 m) to the major emission sources within the MSWTP. While hotspot areas generally yielded elevated CH<sub>4</sub> concentrations near the soil surface, these were relatively low (2.4 to 8.9 ppmv) along the facility's fence line. The study of the corresponding δ<sup>13</sup>C delineated the extent of dispersion plumes downwind emission hotspots, characterized by a <sup>13</sup>C depletion (around 4.0 ‰) in the atmospheric CH<sub>4</sub> and CO<sub>2</sub>. For CH<sub>4</sub>, emissions were isotopically discriminated between the extraction wells at active quarters/cells (δ<sup>13</sup>C = -58.3 ± 1.1 ‰) and biogas produced in the biological waste treatment installation (δ<sup>13</sup>C = -62.7 ± 0.7 ‰). Most of the trace compounds (non-methane hydrocarbons, halocarbons, oxygen-bearing organic gases, ketones, nitrogenous and sulphurous gases, and other admixture compounds) detected at the ground surface were linked to the CH<sub>4</sub>- and CO<sub>2</sub>-rich spots. Despite the relatively high variability in the concentrations of organic and inorganic compounds observed at the MSWTP active zones, our results suggest that they do not have a meaningful impact on the surrounding air quality.

Waste ManagementVol. 190
Wrocław University of Science and Technology (PL), Université du Québec à Montréal (CA), University of Wrocław (PL), Instytut Nauk Geologicznych (PL), AGH University of Krakow (PL), Polish Academy of Sciences (PL)
Clean water and sanitation
Openalex Percentile: Top 41%
Atmospheric and Environmental Gas Dynamics
0.28
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