Source apportionment using receptor model based on aerosol mass spectra and 1 h resolution chemical dataset in Tianjin, China

2019 ◽  
Vol 198 ◽  
pp. 387-397 ◽  
Author(s):  
Xing Peng ◽  
Xiaoxi Liu ◽  
Xurong Shi ◽  
Guoliang Shi ◽  
Mei Li ◽  
...  
2012 ◽  
Vol 185 (7) ◽  
pp. 5585-5593 ◽  
Author(s):  
Sarath K. Guttikunda ◽  
Ramani V. Kopakka ◽  
Prasad Dasari ◽  
Alan W. Gertler

2013 ◽  
Vol 6 (4) ◽  
pp. 6409-6443 ◽  
Author(s):  
F. Canonaco ◽  
M. Crippa ◽  
J. G. Slowik ◽  
U. Baltensperger ◽  
A. S. H. Prévôt

Abstract. Source apportionment using the bilinear model through the multilinear engine (ME-2) was successfully applied to non-refractory organic aerosol (OA) mass spectra collected during winter 2011 and 2012 in Zurich, Switzerland using the aerosol chemical speciation monitor ACSM. Five factors were identified: low-volatility oxygenated OA (LV-OOA), semivolatile oxygenated OA (SV-OOA), hydrocarbon-like OA (HOA), cooking OA (COA) and biomass burning OA (BBOA). A graphical user interface SoFi (Source Finder) was developed at PSI in order to facilitate the testing of different rotational techniques available within the ME-2 engine by providing a priori factor profiles for some or all of the expected factors. ME-2 was used to test the positive matrix factorization (PMF) model, the fully constrained chemical mass balance (CMB) model, and partially constrained models utilizing a values and pulling equations. Within the set of model solutions determined to be environmentally reasonable, BBOA and SV-OOA factor mass spectra and time series showed the greatest variability. This variability represents uncertainty in the model solution and indicates that analysis of model rotations provides a useful approach for assessing the uncertainty of bilinear source apportionment models.


2013 ◽  
Vol 6 (12) ◽  
pp. 3649-3661 ◽  
Author(s):  
F. Canonaco ◽  
M. Crippa ◽  
J. G. Slowik ◽  
U. Baltensperger ◽  
A. S. H. Prévôt

Abstract. Source apportionment using the bilinear model through a multilinear engine (ME-2) was successfully applied to non-refractory organic aerosol (OA) mass spectra collected during the winter of 2011 and 2012 in Zurich, Switzerland using the aerosol chemical speciation monitor (ACSM). Five factors were identified: low-volatility oxygenated OA (LV-OOA), semivolatile oxygenated OA (SV-OOA), hydrocarbon-like OA (HOA), cooking OA (COA) and biomass burning OA (BBOA). A graphical user interface SoFi (Source Finder) was developed at PSI in order to facilitate the testing of different rotational techniques available within the ME-2 engine by providing a priori factor profiles for some or all of the expected factors. ME-2 was used to test the positive matrix factorization (PMF) model, the fully constrained chemical mass balance (CMB) model, and partially constrained models utilizing a values and pulling equations. Within the set of model solutions determined to be environmentally reasonable, BBOA and SV-OOA factor mass spectra and time series showed the greatest variability. This variability represents the uncertainty in the model solution and indicates that analysis of model rotations provides a useful approach for assessing the uncertainty of bilinear source apportionment models.


2022 ◽  
Vol 423 ◽  
pp. 127030
Author(s):  
Ram Proshad ◽  
Tapos Kormoker ◽  
Mamun Abdullah Al ◽  
Md. Saiful Islam ◽  
Sujan Khadka ◽  
...  

2009 ◽  
Vol 9 (6) ◽  
pp. 2227-2240 ◽  
Author(s):  
A. P. Grieshop ◽  
N. M. Donahue ◽  
A. L. Robinson

Abstract. Experiments were conducted to investigate the effects of photo-oxidation on organic aerosol (OA) in dilute wood smoke by exposing emissions from soft- and hard-wood fires to UV light in a smog chamber. This paper focuses on changes in OA composition measured using a unit-mass-resolution quadrupole Aerosol Mass Spectrometer (AMS). The results highlight how photochemical processing can lead to considerable evolution of the mass, volatility and level of oxygenation of biomass-burning OA. Photochemical oxidation produced substantial new OA, more than doubling the OA mass after a few hours of aging under typical summertime conditions. Aging also decreased the volatility of the OA and made it progressively more oxygenated. The results also illustrate strengths of, and challenges with, using AMS data for source apportionment analysis. For example, the mass spectra of fresh and aged BBOA are distinct from fresh motor-vehicle emissions. The mass spectra of the secondary OA produced from aging wood smoke are very similar to those of the oxygenated OA (OOA) that dominates ambient AMS datasets, further reinforcing the connection between OOA and OA formed from photo-chemistry. In addition, aged wood smoke spectra are similar to those from OA created by photo-oxidizing dilute diesel exhaust. This demonstrates that the OOA observed in the atmosphere can be produced by photochemical aging of dilute emissions from different types of combustion systems operating on fuels with modern or fossil carbon. Since OOA is frequently the dominant component of ambient OA, the similarity of spectra of aged emissions from different sources represents an important challenge for AMS-based source apportionment studies.


2021 ◽  
Vol 14 (10) ◽  
pp. 6905-6916
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Anna Trubetskaya ◽  
Wei Xu ◽  
William Smith ◽  
...  

Abstract. Reference mass spectra are routinely used to facilitate source apportionment of ambient organic aerosol (OA) measured by aerosol mass spectrometers. However, source apportionment of solid-fuel-burning emissions can be complicated by the use of different fuels, stoves, and burning conditions. In this study, the organic aerosol mass spectra produced from burning a range of solid fuels in several heating stoves have been compared using an aerosol chemical speciation monitor (ACSM). The same samples of biomass briquettes and smokeless coal were burnt in a conventional stove and Ecodesign stove (Ecodesign refers to a stove conforming to EU Directive 2009/125/EC), while different batches of wood, peat, and smoky coal were also burnt in the conventional stove, and the OA mass spectra were compared to those previously obtained using a boiler stove. The results show that although certain ions (e.g., m/z 60) remain important markers for solid-fuel burning, the peak intensities obtained at specific m/z values in the normalized mass spectra were not constant with variations ranging from < 5 % to > 100 %. Using the OA mass spectra of peat, wood, and coal as anchoring profiles and the variation of individual m/z values for the upper/lower limits (the limits approach) in the positive matrix factorization (PMF) analysis with the Multilinear Engine algorithm (ME-2), the respective contributions of these fuels to ambient submicron aerosols during a winter period in Dublin, Ireland, were evaluated and compared with the conventional a-value approach. The ME-2 solution was stable for the limits approach with uncertainties in the range of 2 %–7 %, while relatively large uncertainties (8 %–29 %) were found for the a-value approach. Nevertheless, both approaches showed good agreement overall, with the burning of peat (39 % vs. 41 %) and wood (14 % vs. 11 %) accounting for the majority of ambient organic aerosol during polluted evenings, despite their small uses compared to electricity and gas. This study, thus, accounts for the source variability in ME-2 modelling and provides better constraints on the primary factor contributions to the ambient organic aerosol estimations. The finding from this study has significant implications for public health and policymakers considering that it is often the case that different batches of solid fuels are often burnt in different stoves in real-world applications.


2021 ◽  
Author(s):  
Chunshui Lin ◽  
Darius Ceburnis ◽  
Anna Trubetskaya ◽  
Wei Xu ◽  
William Smith ◽  
...  

Abstract. Reference mass spectra are routinely used to facilitate source apportionment of ambient organic aerosol (OA) measured by an aerosol chemical speciation monitor (ACSM). However. source apportionment of solid fuel burning emissions can be complicated by the use of different fuels, stoves and burning conditions. In this study, the organic aerosol mass spectra produced from burning a range of solid fuels in several stoves have been compared using an ACSM. The same samples of biomass briquettes and smokeless coal were burnt in a conventional and Ecodesign stove, while different batches of wood, peat, and smoky coal were also burnt in the conventional stove and the OA mass spectra compared to those previously obtained using a boiler stove. The results shows that although certain ions (e.g., m/z 60) remain important markers for solid fuel burning, the peak intensities obtained at specific m/z values were not constant with variations ranging from <5% to >100 %. Using the OA mass spectra of peat, wood and coal as anchoring profiles and the variation of individual m/z values for the upper/lower limits in ME-2 analysis (the limits approach), the respective contributions of these fuels to ambient sub-micron aerosols during a winter period in Dublin were evaluated and compared with the conventional a value approach. The ME-2 solution was stable for the limits approach with uncertainties in the range of 2–7 %, while relatively large uncertainties (8–29 %) were found for the a value approach. Nevertheless, both approaches showed good agreement overall, with the burning of peat (39 % vs 41 %) and wood (14 % vs 11 %) accounting for the majority of ambient organic aerosol during polluted evenings, despite their small uses. This study, thus, accounts for the source variability in ME-2 modelling and provides better constraints on the primary factor contributions to the ambient organic aerosol estimations. The finding from this study has significant implications for public health and policymakers considering that it is often the case that different batches of solid fuels are often burned in different stoves in real-world applications.


2017 ◽  
Author(s):  
Carlo Bozzetti ◽  
Imad El Haddad ◽  
Dalia Salameh ◽  
Kaspar Rudolf Daellenbach ◽  
Paola Fermo ◽  
...  

Abstract. We investigated the seasonal trends of OA sources affecting the air quality of Marseille (France) which is the largest harbor of the Mediterranean Sea. This was achieved by measurements of nebulized filter extracts using an aerosol mass spectrometer (offline-AMS). PM2.5 (particulate matter with an aerodynamic diameter


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