Chemical characterization and source apportionment of carbonaceous aerosols during post-monsoon biomass burning and Diwali at an upwind site of Delhi

Severe post-monsoon haze in Delhi-NCR poses air-quality and health risks and reflects regional and urban emissions. Sonipat lies along the principal transport corridor linking the agricultural burning regions of Punjab and Haryana with Delhi and serves as an intermediate receptor for regional pollution. However, source apportionment at upwind locations remains limited. To address this gap, we measured composition-based PM 2.5 , defined as non-refractory PM 2.5 plus equivalent black carbon, at Sonipat from 25 October to 15 November 2023 using a Time-of-Flight Aerosol Chemical Speciation Monitor and a multi-wavelength Aethalometer. Positive matrix factorization, black-carbon apportionment, and trajectory and wind analyses were used to identify carbonaceous aerosol sources and examine their evolution during haze, non-haze, and Diwali periods. Two severe haze episodes occurred, with composition-based PM 2.5 exceeding 300 µg m −3 . Organic aerosol contributed 65 % of non-refractory PM 2.5 , and its daily mean reached nearly 140 µg m −3 . Oxygenated organic aerosol accounted for approximately 57 %–60 % of total organic aerosol, with more-oxidized oxygenated organic aerosol reaching 42.8 µg m −3 during peak haze, indicating substantial secondary processing and accumulation. Under the reference absorption Ångström exponent pair, biomass- or solid-fuel-related eBC accounted for approximately 78 % of the campaign-integrated eBC burden, although the quantitative source split was sensitive to the assumed exponents. Northwestern transport signatures and co-variation of eBC bb with biomass-burning and solid-fuel organic aerosol indicate an important regional combustion influence. These findings show that carbonaceous aerosol was already present at this receptor before further interaction with Delhi emissions and support coordinated regional controls alongside sustained urban emission reductions.

Authors

Institutions

Publication Details

Journal
Atmospheric chemistry and physics
Published
2026-09-21
DOI
https://doi.org/10.5194/acp-26-13227-2026
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Chemical characterization and source apportionment of carbonaceous aerosols during post-monsoon biomass burning and Diwali at an upwind site of Delhi

Vasu Singh, Sagnik Dey, Lokesh Kumar Sahu, Jaswant Rathore et al.
Atmospheric chemistry and physics
Atmospheric chemistry and aerosols
article

Chemical characterization and source apportionment of carbonaceous aerosols during post-monsoon biomass burning and Diwali at an upwind site of Delhi

Vasu Singh, Sagnik Dey, Lokesh Kumar Sahu, Jaswant Rathore, Dilip Kumar Ganguly, Ravi Kumar Kunchala
article en

Abstract

Severe post-monsoon haze in Delhi-NCR poses air-quality and health risks and reflects regional and urban emissions. Sonipat lies along the principal transport corridor linking the agricultural burning regions of Punjab and Haryana with Delhi and serves as an intermediate receptor for regional pollution. However, source apportionment at upwind locations remains limited. To address this gap, we measured composition-based PM 2.5 , defined as non-refractory PM 2.5 plus equivalent black carbon, at Sonipat from 25 October to 15 November 2023 using a Time-of-Flight Aerosol Chemical Speciation Monitor and a multi-wavelength Aethalometer. Positive matrix factorization, black-carbon apportionment, and trajectory and wind analyses were used to identify carbonaceous aerosol sources and examine their evolution during haze, non-haze, and Diwali periods. Two severe haze episodes occurred, with composition-based PM 2.5 exceeding 300 µg m −3 . Organic aerosol contributed 65 % of non-refractory PM 2.5 , and its daily mean reached nearly 140 µg m −3 . Oxygenated organic aerosol accounted for approximately 57 %–60 % of total organic aerosol, with more-oxidized oxygenated organic aerosol reaching 42.8 µg m −3 during peak haze, indicating substantial secondary processing and accumulation. Under the reference absorption Ångström exponent pair, biomass- or solid-fuel-related eBC accounted for approximately 78 % of the campaign-integrated eBC burden, although the quantitative source split was sensitive to the assumed exponents. Northwestern transport signatures and co-variation of eBC bb with biomass-burning and solid-fuel organic aerosol indicate an important regional combustion influence. These findings show that carbonaceous aerosol was already present at this receptor before further interaction with Delhi emissions and support coordinated regional controls alongside sustained urban emission reductions.

Atmospheric chemistry and physicsVol. 26(18)
Physical Research Laboratory (IN), Indian Institute of Technology Delhi (IN)
Sustainable cities and communities
Openalex Percentile: Top 15%
Atmospheric chemistry and aerosols
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.