Determination of wood burning and fossil fuel contribution of black carbon at Delhi, India using aerosol light absorption technique

2014 ◽  
Vol 22 (4) ◽  
pp. 2846-2855 ◽  
Author(s):  
S. Tiwari ◽  
A. S. Pipal ◽  
A. K. Srivastava ◽  
D.S. Bisht ◽  
G. Pandithurai
2017 ◽  
Vol 17 (6) ◽  
pp. 4229-4249 ◽  
Author(s):  
Peter Zotter ◽  
Hanna Herich ◽  
Martin Gysel ◽  
Imad El-Haddad ◽  
Yanlin Zhang ◽  
...  

Abstract. Equivalent black carbon (EBC) measured by a multi-wavelength Aethalometer can be apportioned to traffic and wood burning. The method is based on the differences in the dependence of aerosol absorption on the wavelength of light used to investigate the sample, parameterized by the source-specific absorption Ångström exponent (α). While the spectral dependence (defined as α values) of the traffic-related EBC light absorption is low, wood smoke particles feature enhanced light absorption in the blue and near ultraviolet. Source apportionment results using this methodology are hence strongly dependent on the α values assumed for both types of emissions: traffic αTR, and wood burning αWB. Most studies use a single αTR and αWB pair in the Aethalometer model, derived from previous work. However, an accurate determination of the source specific α values is currently lacking and in some recent publications the applicability of the Aethalometer model was questioned.Here we present an indirect methodology for the determination of αWB and αTR by comparing the source apportionment of EBC using the Aethalometer model with 14C measurements of the EC fraction on 16 to 40 h filter samples from several locations and campaigns across Switzerland during 2005–2012, mainly in winter. The data obtained at eight stations with different source characteristics also enabled the evaluation of the performance and the uncertainties of the Aethalometer model in different environments. The best combination of αTR and αWB (0.9 and 1.68, respectively) was obtained by fitting the Aethalometer model outputs (calculated with the absorption coefficients at 470 and 950 nm) against the fossil fraction of EC (ECF ∕ EC) derived from 14C measurements. Aethalometer and 14C source apportionment results are well correlated (r  =  0.81) and the fitting residuals exhibit only a minor positive bias of 1.6 % and an average precision of 9.3 %. This indicates that the Aethalometer model reproduces reasonably well the 14C results for all stations investigated in this study using our best estimate of a single αWB and αTR pair. Combining the EC, 14C, and Aethalometer measurements further allowed assessing the dependence of the mass absorption cross section (MAC) of EBC on its source. Results indicate no significant difference in MAC at 880 nm between EBC originating from traffic or wood-burning emissions. Using ECF ∕ EC as reference and constant a priori selected αTR values, αWB was also calculated for each individual data point. No clear station-to-station or season-to-season differences in αWB were observed, but αTR and αWB values are interdependent. For example, an increase in αTR by 0.1 results in a decrease in αWB by 0.1. The fitting residuals of different αTR and αWB combinations depend on ECF ∕ EC such that a good agreement cannot be obtained over the entire ECF ∕ EC range using other α pairs. Additional combinations of αTR  =  0.8, and 1.0 and αWB  =  1.8 and 1.6, respectively, are possible but only for ECF ∕ EC between  ∼  40 and 85 %. Applying α values previously used in the literature such as αWB of  ∼  2 or any αWB in combination with αTR  =  1.1 to our data set results in large residuals. Therefore we recommend to use the best α combination as obtained here (αTR  =  0.9 and αWB  =  1.68) in future studies when no or only limited additional information like 14C measurements are available. However, these results were obtained for locations impacted by black carbon (BC) mainly from traffic consisting of a modern car fleet and residential wood combustion with well-constrained combustion efficiencies. For regions of the world with different combustion conditions, additional BC sources, or fuels used, further investigations are needed.


2011 ◽  
Vol 4 (7) ◽  
pp. 1409-1420 ◽  
Author(s):  
H. Herich ◽  
C. Hueglin ◽  
B. Buchmann

Abstract. The contributions of fossil fuel (FF) and wood burning (WB) emissions to black carbon (BC) have been investigated in the recent past by analysis of multi-wavelength aethalometer data. This approach utilizes the stronger light absorption of WB aerosols in the near ultraviolet compared to the light absorption of aerosols from FF combustion. Here we present 2.5 years of seven-wavelength aethalometer data from one urban and two rural background sites in Switzerland measured from 2008–2010. The contribution of WB and FF to BC was directly determined from the aerosol absorption coefficients of FF and WB aerosols which were calculated by using confirmed Ångstrom exponents and aerosol light absorption cross-sections that were determined for all sites. Reasonable separation of total BC into contributions from FF and WB was achieved for all sites and seasons. The obtained WB contributions to BC are well correlated with measured concentrations of levoglucosan and potassium while FF contributions to BC correlate nicely with NOx. These findings support our approach and show that the applied source apportionment of BC is well applicable for long-term data sets. During winter, we found that BC from WB contributes on average 24–33 % to total BC at the considered measurement sites. This is a noticeable high fraction as the contribution of wood burning to the total final energy consumption is in Switzerland less than 4 %.


2018 ◽  
Vol 18 (14) ◽  
pp. 10219-10236 ◽  
Author(s):  
Athina-Cerise Kalogridis ◽  
Stergios Vratolis ◽  
Eleni Liakakou ◽  
Evangelos Gerasopoulos ◽  
Nikolaos Mihalopoulos ◽  
...  

Abstract. The scope of this study was to estimate the contribution of fossil fuel and wood burning combustion to black carbon (BC) and carbon monoxide (CO) during wintertime, in Athens. For that purpose, in situ measurements of equivalent black carbon (eBC) and CO were simultaneously conducted in a suburban and an urban background monitoring site in Athens during the 3 months of winter 2014–2015. For the deconvolution of eBC into eBC emitted from fossil fuel (BCff) and wood burning (BCwb), a method based on the spectral dependency of the absorption of pure black carbon and brown carbon was used. Thereafter, BCwb and BCff estimated fractions were used along with measured CO concentrations in a multiple regression analysis, in order to quantify the contribution of each one of the combustion sources to the ambient CO levels. For a comparative analysis of the results, we additionally estimated the wood burning and fossil fuel contribution to CO, calculated on the basis of their CO ∕ NOx emission ratios. The results indicate that during wintertime BC and CO are mainly emitted by local sources within the Athens Metropolitan Area (AMA). Fossil fuel combustion, mainly from road traffic, is found to be the major contributor to both eBC in PM2.5 and CO ambient concentrations in AMA. However, wintertime wood burning makes a significant contribution to the observed eBC (of about 30 %) and CO concentrations (on average, 11 and 16 % of total CO in the suburban and urban background sites respectively). Both BC and CO from biomass burning (BCwb and COwb, respectively) present a clear diurnal pattern, with the highest concentrations during night-time, supporting the theory of local domestic heating being their main source.


2016 ◽  
Author(s):  
Peter Zotter ◽  
Hanna Herich ◽  
Martin Gysel ◽  
Imad El-Haddad ◽  
Yanlin Zhang ◽  
...  

Abstract. Black carbon (BC) measured by a multi-wavelength Aethalometer can be apportioned to traffic and wood burning. The method is based on the differences in the dependence of aerosol absorption on the wavelength of light used to investigate the sample, parameterized by the source-specific Ångström absorption exponent (α). While the spectral dependence (defined as α values) of the traffic-related BC light absorption is low, wood smoke particles feature enhanced light absorption in the blue and near ultraviolet. Source apportionment results using this methodology are hence strongly dependent on the α values assumed for both types of emissions: traffic αTR, and wood burning αWB. Most studies use a single αTR and αWB pair in the Aethalometer model, derived from previous work. However, an accurate determination of the source specific α values is currently lacking and in some recent publications the applicability of the Aethalometer model was questioned. Here we present an indirect methodology for the determination of WB and αTR by comparing the source apportionment of BC using the Aethalometer model with 14C measurements of the EC fraction on 16 to 40 h filter samples from several locations and campaigns across Switzerland during 2005–2012, mainly in winter. The data obtained at eight stations with different source characteristics also enabled the evaluation of the performance and the uncertainties of the Aethalometer model in different environments. The best combination of αTR and αWB (0.9 and 1.68, respectively) was obtained by fitting the Aethalometer model outputs (calculated with the absorption coefficients at 470 nm and 950 nm) against the fossil fraction of EC (ECF/EC) derived from 14C measurements. Aethalometer and 14C source apportionment results are well correlated (r = 0.81) and the fitting residuals exhibit only a minor positive bias of 1.6 % and an average precision of 9.3 %. This indicates that the Aethalometer model reproduces reasonably well the 14C results for all stations investigated in this study using our best estimate of a single αWB and αTR pair. Combining the EC, 14C and Aethalometer measurements further allowed assessing the dependence of the mass absorption cross section (MAC) of BC on its source. Results indicate no significant difference in MAC at 880 nm between BC originating from traffic or wood burning emissions. Using ECF/EC as reference and constant a priori selected αTR values, αWB was also calculated for each individual data point. No clear station-to-station or season-to-season differences in αWB were observed, but αTR and αWB values are interdependent. For example, an increase in αTR by 0.1 results in a decrease in αWB by 0.1. The fitting residuals of different αTR and αWB combinations depend on ECF/EC such that a good agreement cannot be obtained over the entire ECF/EC range using other α pairs. Additional combinations of αTR = 0.8, and 1.0 and αWB = 1.8 and 1.6, respectively, are possible but only for ECF/EC between ~ 40 % and 85 %. Applying α values previously used in literature such as αWB of ~ 2 or any αWB in combination with αTR = 1.1 to our data set results in large residuals. Therefore we recommend to use the best α combination as obtained here (αTR = 0.9 and αWB = 1.68) in future studies when no or only limited additional information like 14C measurements are available. However, these results were obtained for locations impacted by BC mainly from traffic consisting of a modern car fleet and residential wood combustion with well-constrained combustion efficiencies. For regions of the world with different combustion conditions, additional BC sources or fuels used further investigations are needed.


2019 ◽  
Vol 216 ◽  
pp. 11-25 ◽  
Author(s):  
U.C. Dumka ◽  
D.G. Kaskaoutis ◽  
P.C.S. Devara ◽  
R. Kumar ◽  
S. Kumar ◽  
...  

2008 ◽  
Vol 42 (9) ◽  
pp. 3316-3323 ◽  
Author(s):  
Jisca Sandradewi ◽  
Andre S. H. Prévôt ◽  
Sönke Szidat ◽  
Nolwenn Perron ◽  
M. Rami Alfarra ◽  
...  

2020 ◽  
Vol 20 (22) ◽  
pp. 14419-14435
Author(s):  
Junjun Deng ◽  
Hao Guo ◽  
Hongliang Zhang ◽  
Jialei Zhu ◽  
Xin Wang ◽  
...  

Abstract. Black carbon (BC) is the most important light-absorbing aerosol in the atmosphere. However, sources of atmospheric BC aerosols are largely uncertain, making it difficult to assess its influence on radiative forcing and climate change. In this study, year-round light-absorption observations were conducted during 2014 using an aethalometer in Xiamen, a coastal city in Southeast China. Source apportionment of BC was performed and temporal variations in BC sources were characterized based on both light absorption measurements and a source-oriented air quality model. The annual average concentrations of BC from fossil fuel (BCff) and biomass burning (BCbb) by the aethalometer method were 2932 ± 1444 ng m−3 and 1340 ± 542 ng m−3, contributing 66.7 % and 33.3 % to total BC, respectively. A sensitivity analysis was performed with different absorption Ångström exponent (AAE) values of fossil fuel combustion (αff) and biomass burning (αbb), suggesting that the aethalometer method was more sensitive to changes in αbb than αff. BCbb contribution exhibited a clear diurnal cycle, with the highest level (37.9 %) in the evening rush hour and a seasonal pattern with the maximum (39.9 %) in winter. Conditional probability function (CPF) analysis revealed the large biomass-burning contributions were accompanied by east-northeasterly and northerly winds. Backward trajectory indicated that air masses from North and East–Central China were associated with larger biomass-burning contributions. Potential source contribution function (PSCF) and concentration-weighted trajectory (CWT) suggested that North and East–Central China and Southeast Asia were potential sources of both BCff and BCbb. The source-oriented modeling results showed that transportation, residential and open biomass burning accounting for 45.3 %, 30.1 % and 17.6 % were the major BC sources. Among the three fuel catalogs, liquid fossil fuel (46.5 %) was the largest source, followed by biomass burning (32.6 %) and coal combustion (20.9 %). Source contributions of fossil fuel combustion and biomass burning identified by the source-oriented model were 67.4 % and 32.6 %, respectively, close to those obtained by the aethalometer method. The findings provide solid support for controlling fossil fuel sources to limit the impacts of BC on climate change and environmental degradation in the relatively clean region in China.


2021 ◽  
Author(s):  
Anna Ryś ◽  
Lucyna Samek

Abstract. The evaluation of black carbon (BC) sources is very important, especially in environmental sciences. This study shows how the contributions of biomass burning and fossil fuel/traffic to PM2.5 mass can be assessed. MABI was used for this purpose and gave the possibility to measure the transmission of light at different wavelengths. Absorption coefficients were calculated from measurements data and recalculated for concentrations of eBC. The samples of PM2.5 fraction were collected from February 1, 2020 to March 27, 2021 every third day in Krakow, Poland (50°04' N, 19°54'47" E). The concentrations of equivalent BC (eBC) from fossil fuel/traffic and biomass burning were in the range 0.82–11.64 μg m−3) and 0.007–0.84 μg m−3, respectively. At the same time, PM2.5 concentrations varied from 3.14 to 55.24 μg m−3. It means that about 18 % of PM2.5 mass belongs to eBC and 11.3 % of this value comes from biomass burning. The eBC contribution is the significant part of PM2.5 mass and we observed seasonal variation of the eBC concentration during the year with the peak in winter. The contribution of biomass burning to PM2.5 mass is more stable during the whole year. The eBC concentration during workdays is a bit higher than during weekend days but biomass burning is similar for both days (work and weekend taken as the mean for the whole period).


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