scholarly journals Measurement report: Long emission-wavelength chromophores dominate the light absorption of brown carbon in Aerosols over Bangkok: impact from biomass burning

2021 ◽  
Author(s):  
Jiao Tang ◽  
Jiaqi Wang ◽  
Guangcai Zhong ◽  
Hongxing Jiang ◽  
Yangzhi Mo ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Light Absorption ◽  
Linear Regression Analysis ◽  
Multiple Linear Regression Analysis ◽  
Water Soluble ◽  
Emission Wavelength ◽  
Brown Carbon ◽  
Molecular Weights ◽  
Secondary Formation ◽  
Combustion Emission

Abstract. Chromophores represent an important portion of light-absorbing species, i.e. brown carbon. Yet knowledge on what and how chromophores contribute to aerosol light absorption is still sparse. To address this problem, we examined soluble independent chromophores in a set of year-round aerosol samples from Bangkok. The water-soluble chromophores identified via excitation-emission matrix (EEM) spectroscopy and follow-up parallel factor analysis could be mainly assigned as humic-like substances and protein-like substances, which differed in their EEM pattern from that of the methanol-soluble fraction. The emission wavelength of chromophores in environmental samples tended to increase compared with that of the primary combustion emission, which could be attributed to secondary formation or the aging process. Fluorescent indices inferred that these light-absorbing chromophores were not significantly humified and comprised a mixture of organic matter of terrestrial and microbial origin, while these inferences exhibited a refutation with primary biomass burning and coal combustion results. A multiple linear regression analysis revealed that larger chromophores that were oxygen-rich and highly aromatic with high molecular weights, were the key contributors of light absorption, preferably at longer emission wavelength (λmax > 500 nm). Positive matrix factorization analysis further suggested that up to 60 % of these responsible chromophores originated from biomass burning emissions.

scholarly journals Measurement report: Long-emission-wavelength chromophores dominate the light absorption of brown carbon in aerosols over Bangkok: impact from biomass burning

2021 ◽  
Vol 21 (14) ◽  
pp. 11337-11352
Author(s):  
Jiao Tang ◽  
Jiaqi Wang ◽  
Guangcai Zhong ◽  
Hongxing Jiang ◽  
Yangzhi Mo ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Light Absorption ◽  
Linear Regression Analysis ◽  
Multiple Linear Regression Analysis ◽  
Water Soluble ◽  
Emission Wavelength ◽  
Brown Carbon ◽  
Molecular Weights ◽  
Secondary Formation ◽  
Combustion Emission

Abstract. Chromophores represent an important portion of light-absorbing species, i.e., brown carbon. Yet knowledge of what and how chromophores contribute to aerosol light absorption is still sparse. To address this problem, we examined soluble independent chromophores in a set of year-round aerosol samples from Bangkok. The water-soluble fluorescent chromophores identified via excitation–emission matrix (EEM) spectroscopy and follow-up parallel factor analysis could be mainly assigned as humic-like substances and protein-like substances, which differed in their EEM pattern from that of the methanol-soluble fraction. The emission wavelength of fluorescent chromophores in environmental samples tended to increase compared with that of the primary combustion emission, which could be attributed to secondary formation or the aging process. Fluorescent indices inferred that these light-absorbing chromophores were not significantly humified and comprised a mixture of organic matter of terrestrial and microbial origin, which exhibited a different characteristic from primary biomass burning and coal-combustion results. A multiple linear regression analysis revealed that larger fluorescent chromophores that were oxygen-rich and highly aromatic with high molecular weights were the key contributors of light absorption, preferably at longer emission wavelengths (λmax⁡ > 500 nm). Positive matrix factorization analysis further suggested that up to 50 % of these responsible chromophores originated from biomass burning emissions.

Brown carbon aerosol in urban Beijing: Significant contributions from biomass burning and secondary formation

2020 ◽  
Author(s):  
Ting Wang ◽  
Rujin Huang ◽  
Lu Yang ◽  
Wei Yuan ◽  
Yuquan Gong
Keyword(s):  
Biomass Burning ◽  
Light Absorption ◽  
Coal Combustion ◽  
Absorption Efficiency ◽  
Traffic Emission ◽  
Brown Carbon ◽  
Factorization Model ◽  
Secondary Formation ◽  
Vis Spectroscopy ◽  
The Impact

<p>Atmospheric brown carbon (BrC) has significant impact on Earth’s radiative budget. However, due to our very limited knowledge about the relationship between BrC light absorption and the associated sources, the estimation for radiative effects of BrC is still largely constrained. In this study, we combine ultraviolet−visible (UV−vis) spectroscopy measurements and chemical analyses of BrC samples collected from January to December 2015 in urban Beijing, to investigated the sources of atmospheric BrC. The multiple liner regression model was applied to apportion the contributions of individual primary and secondary organic aerosol (OA) source components to light absorption of BrC. Our results indicated that biomass burning emission and secondary formation are highly absorbing up to 500 nm, and their contributions increased with the wavelengths. In contrast, the contribution of traffic emission and coal combustion to total absorption decreased with the wavelength and the large contributions were mostly found at shorter wavelengths. Then the mass absorption efficiency (MAE) of major light-absorbing components were estimated, which can provide a support to estimate the impact of BrC from these sources on the climate. The positive matrix factorization model were also used to verify the contributions of different source components of BrC absorption at 365 nm. The results consistently demonstrate that the biomass burning and secondary formation contributes significantly to the overall absorption, followed by coal combustion and traffic emission.</p>

scholarly journals Measurement Report: Optical properties and sources of water-soluble brown carbon in Tianjin, North China: insights from organic molecular compositions

2022 ◽  
Author(s):  
Junjun Deng ◽  
Hao Ma ◽  
Xinfeng Wang ◽  
Shujun Zhong ◽  
Zhimin Zhang ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Light Absorption ◽  
Radiative Forcing ◽  
North China ◽  
Water Soluble ◽  
Formation Mechanisms ◽  
Chemical Compositions ◽  
Brown Carbon ◽  
Near Ultraviolet

Abstract. Brown carbon (BrC) aerosols exert vital impacts on climate change and atmospheric photochemistry due to their light absorption in the wavelength range from near-ultraviolet (UV) to visible light. However, the optical properties and formation mechanisms of ambient BrC remain poorly understood, limiting the estimation of their radiative forcing. In the present study, fine aerosols (PM2.5) were collected during 2016–2017 on a day/night basis over urban Tianjin, a megacity in North China, to obtain seasonal and diurnal patterns of atmospheric water-soluble BrC. There were obvious seasonal but no evident diurnal variations in light absorption properties of BrC. In winter, BrC showed much stronger light absorbing ability since mass absorption efficiency at 365 nm (MAE365) (1.54 ± 0.33 m2 g−1), which was 1.8 times larger than that (0.84 ± 0.22 m2 g−1) in summer. Direct radiative effects by BrC absorption relative to black carbon in the UV range were 54.3 ± 16.9 % and 44.6 ± 13.9 %, respectively. In addition, five fluorescent components in BrC, including three humic-like fluorophores and two protein-like fluorophores were identified with excitation-emission matrix fluorescence spectrometry and parallel factor (PARAFAC) analysis. The lowly-oxygenated components contributed more to winter and nighttime samples, while more-oxygenated components increased in summer and daytime samples. The higher humification index (HIX) together with lower biological index (BIX) and fluorescence index (FI) suggest that the chemical compositions of BrC were associated with a high aromaticity degree in summer and daytime due to photobleaching. Fluorescent properties indicate that wintertime BrC were predominantly affected by primary emissions and fresh secondary organic aerosol (SOA), while summer ones were more influenced by aging processes. Results of source apportionments using organic molecular compositions of the same set of aerosols reveal that fossil fuel combustion and aging processes, primary bioaerosol emission, biomass burning, and biogenic and anthropogenic SOA formation were the main sources of BrC. Biomass burning contributed much larger to BrC in winter and at nighttime, while biogenic SOA contributed more in summer and at daytime. Especially, our study highlights that primary bioaerosol emission is an important source of BrC in urban Tianjin in summer.

scholarly journals Atmospheric evolution of molecular-weight-separated brown carbon from biomass burning

2019 ◽  
Vol 19 (11) ◽  
pp. 7319-7334 ◽  
Author(s):  
Jenny P. S. Wong ◽  
Maria Tsagkaraki ◽  
Irini Tsiodra ◽  
Nikolaos Mihalopoulos ◽  
Kalliopi Violaki ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Biomass Burning ◽  
Light Absorption ◽  
Laboratory Experiments ◽  
Atmospheric Transport ◽  
Water Soluble ◽  
Brown Carbon ◽  
Atmospheric Lifetime ◽  
Radiative Balance ◽  
Considerable Uncertainty

Abstract. Biomass burning is a major source of atmospheric brown carbon (BrC), and through its absorption of UV/VIS radiation, it can play an important role in the planetary radiative balance and atmospheric photochemistry. The considerable uncertainty of BrC impacts is associated with its poorly constrained sources, transformations, and atmospheric lifetime. Here we report laboratory experiments that examined changes in the optical properties of the water-soluble (WS) BrC fraction of laboratory-generated biomass burning particles from hardwood pyrolysis. Effects of direct UVB photolysis and OH oxidation in the aqueous phase on molecular-weight-separated BrC were studied. Results indicated that the majority of low-molecular-weight (MW) BrC (<400 Da) was rapidly photobleached by both direct photolysis and OH oxidation on an atmospheric timescale of approximately 1 h. High MW BrC (≥400 Da) underwent initial photoenhancement up to ∼15 h, followed by slow photobleaching over ∼10 h. The laboratory experiments were supported by observations from ambient BrC samples that were collected during the fire seasons in Greece. These samples, containing freshly emitted to aged biomass burning aerosol, were analyzed for both water- and methanol-soluble BrC. Consistent with the laboratory experiments, high-MW BrC dominated the total light absorption at 365 nm for both methanol and water-soluble fractions of ambient samples with atmospheric transport times of 1 to 68 h. These ambient observations indicate that overall, biomass burning BrC across all molecular weights has an atmospheric lifetime of 15 to 28 h, consistent with estimates from previous field studies – although the BrC associated with the high-MW fraction remains relatively stable and is responsible for light absorption properties of BrC throughout most of its atmospheric lifetime. For ambient samples of aged (>10 h) biomass burning emissions, poor linear correlations were found between light absorptivity and levoglucosan, consistent with other studies suggesting a short atmospheric lifetime for levoglucosan. However, a much stronger correlation between light absorptivity and total hydrous sugars was observed, suggesting that they may serve as more robust tracers for aged biomass burning emissions. Overall, the results from this study suggest that robust model estimates of BrC radiative impacts require consideration of the atmospheric aging of BrC and the stability of high-MW BrC.

Chemical composition and light absorption of brown carbon emitted from residential coal combustion in China

2020 ◽  
Author(s):  
Jianzhong Song ◽  
Meiju Li ◽  
Xingjun Fan ◽  
Peng'an Peng
Keyword(s):  
Organic Carbon ◽  
Organic Compounds ◽  
Biomass Burning ◽  
Light Absorption ◽  
Coal Combustion ◽  
Extraction Methods ◽  
Water Soluble ◽  
Brown Carbon ◽  
Smoke Particles ◽  
Soluble Organic Carbon

&lt;p&gt;Brown carbon (BrC) is a type of light-absorbing organic compounds with a high capacity to absorb light in the low-wavelength visible and near-ultraviolet regions, which is ubiquitous in atmospheric aerosols, rainwater, and cloudwater samples. BrC can not only alter the light absorption and radiative forcing of aerosols but can also influence the formation of cloud condensation nuclei; therefore, it has a potential impact on atmospheric chemistry and climate change. Numerous studies have demonstrated that combustion processes are significant sources of atmospheric BrC, however most of these studies were focused on the emissions of biomass burning. Knowledge of primary BrC from coal combustion is still limited. In the study, smoke particles emitted from the combustion of residential coals with different geological maturity were collected in a combustion system. Then BrC fractions, including water soluble organic carbon (WSOC), water soluble humic-like substances (HULIS&lt;sub&gt;w&lt;/sub&gt;), alkaline soluble organic carbon (ASOC) and methanol soluble organic carbon (MSOC) were extracted and characterized for their abundances, chemical, and light absorption properties.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;Our results showed that the abundance and light absorption of the coal combustion-derived BrC fractions were strongly dependent on the extraction methods used and the coal maturity. The abundances of MSOC fraction was significantly higher than WSOC and ASOC fractions and even higher than the sum of WSOC and ASOC, indicating that most organic compounds in smoke particles were soluble in pure methanol. The WSOC and MSOC fractions from the combustion of low maturity coal had relatively low SUVA&lt;sub&gt;254&lt;/sub&gt; and MAE&lt;sub&gt;365&lt;/sub&gt; values, indicated that they had relatively low levels of aromatic structures and light absorption.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;The WSOC and MSOC fractions were characterized by ultrahigh-resolution mass spectrometry. The results showed that S-containing compounds (CHOS and CHONS) are found to be the dominant components of the WSOC, whereas CHO and CHON compounds make a great contribution to the MSOC samples. Noted that a greater abundance of S-containing compounds was found in the smoke produced from coal combustion compared to biomass burning and atmospheric samples, indicated that coal combustion could be an important source of atmospheric S-containing compounds in certain areas. The findings also suggest that organic molecules with a high aromaticity index and low polarity showed stronger light absorption. In summary, our study indicated that coal combustion is a potential source of atmospheric BrC and their abundance, chemical, and light absorption were strongly dependent on the extraction methods used and the coal maturity.&lt;/p&gt;

scholarly journals Water-Soluble Organic Aerosol material and the light-absorption characteristics of aqueous extracts measured over the Southeastern United States

2010 ◽  
Vol 10 (13) ◽  
pp. 5965-5977 ◽  
Author(s):  
A. Hecobian ◽  
X. Zhang ◽  
M. Zheng ◽  
N. Frank ◽  
E. S. Edgerton ◽  
...  
Keyword(s):  
Factor Analysis ◽  
Biomass Burning ◽  
Light Absorption ◽  
Fine Particle ◽  
Organic Aerosol ◽  
Water Soluble ◽  
Aqueous Extracts ◽  
Brown Carbon ◽  
Southeastern Us ◽  
Yearly Average

Abstract. Light absorption of fine particle (PM2.5) aqueous extracts between wavelengths of 200 and 800 nm were investigated from two data sets: 24-h Federal Reference Method (FRM) filter extracts from 15 Southeastern US monitoring sites over the year of 2007 (900 filters), and online measurements from a Particle-Into-Liquid Sampler deployed from July to mid-August 2009 in Atlanta, Georgia. Three main sources of soluble chromophores were identified: biomass burning, mobile source emissions, and compounds linked to secondary organic aerosol (SOA) formation. Absorption spectra of aerosol solutions from filter extracts were similar for different sources. Angstrom exponents were ~7±1 for biomass burning and non-biomass burning-impacted 24-h filter samples (delineated by a levoglucosan concentration of 50 ng m−3) at both rural and urban sites. The absorption coefficient from measurements averaged between wavelength 360 and 370 nm (Abs365, in units m−1) was used as a measure of overall brown carbon light absorption. Biomass-burning-impacted samples were highest during winter months and Abs365 was correlated with levoglucosan at all sites. During periods of little biomass burning in summer, light absorbing compounds were still ubiquitous and correlated with fine particle Water-Soluble Organic Carbon (WSOC), but comprised a much smaller fraction of the WSOC, where Abs365/WSOC (i.e., mass absorption efficiency) was typically ~3 times higher in biomass burning-impacted samples. Factor analysis attributed 50% of the yearly average Abs365 to biomass burning sources. Brown carbon from primary urban emissions (mobile sources) was also observed and accounted for ~10% of the regional yearly average Abs365. Summertime diurnal profiles of Abs365 and WSOC showed that morning to midday increases in WSOC from photochemical production were associated with a decrease in Abs365/WSOC. After noon, this ratio substantially increased, indicating that either some fraction of the non-light absorbing fresh SOA was rapidly (within hours) converted to chromophores heterogeneously, or that SOA from gas-particle partitioning later in the day was more light-absorbing. Factor analysis on the 24-h integrated filter data associated ~20 to 30% of Abs365 over 2007 with a secondary source that was highest in summer and also the main source for oxalate, suggesting that aqueous phase reactions may account for the light-absorbing fraction of WSOC observed throughout the Southeastern US in summer.

scholarly journals Optical properties of elemental carbon and water-soluble organic carbon in Beijing, China

2011 ◽  
Vol 11 (2) ◽  
pp. 6221-6258
Author(s):  
Y. Cheng ◽  
K.-B. He ◽  
M. Zheng ◽  
F.-K. Duan ◽  
Y.-L. Ma ◽  
...  
Keyword(s):  
Optical Properties ◽  
Organic Carbon ◽  
Biomass Burning ◽  
Light Absorption ◽  
Elemental Carbon ◽  
Water Soluble ◽  
Brown Carbon ◽  
Sulphate Concentration ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon

Abstract. The mass absorption cross-section (MAC) of elemental carbon (EC) in Beijing was quantified using a thermal-optical carbon analyzer and the influences of mixing state and sources of carbonaceous aerosol were investigated. The MAC measured at 632 nm was 29.0 and 32.0 m2 g−1 during winter and summer respectively. MAC correlated well with the organic carbon (OC) to EC ratio (R2 = 0.91) which includes important information about the extent of secondary organic aerosol (SOA) production, indicating the enhancement of MAC by coating with SOA. The extrapolated MAC value was 10.5 m2 g−1 when the OC to EC ratio is zero, which was 5.6 m2 g−1 after correction by the enhancement factor (1.87) caused by the artifacts associated with the "filter-based" methods. The MAC also increased with sulphate (R2 = 0.84) when the sulphate concentration was below 10 μg m−3, whereas MAC and sulphate were only weekly related when the sulphate concentration was above 10 μg m−3, indicating the MAC of EC was also enhanced by coating with sulphate. Based on a converting approach that accounts for the discrepancy caused by measurements methods of both light absorption and EC concentration, previously published MAC values were converted to the "equivalent MAC", which is the estimated value if using the same measurement methods as used in this study. The "equivalent MAC" was found to be much lower in the regions heavily impacted by biomass burning (e.g., India), probably due to the influence of brown carbon. Optical properties of water-soluble organic carbon (WSOC) in Beijing were also presented. Light absorption by WSOC exhibited strong wavelength (λ) dependence such that absorption varied approximately as λ−7, which was characteristic of the brown carbon spectra. The mass absorption efficiency (σabs) of WSOC (measured at 365 nm) was 1.83 and 0.70 m2 g−1 during winter and summer respectively. The seasonal pattern of σabs was attributed to the difference in the precursors of SOA, because WSOC in Beijing has been demonstrated to be strongly linked to SOA. Moreover, the σabs of WSOC in Beijing was much higher than results from the southeastern United States which were obtained using the same method as used in this study, perhaps due to the influence of biomass burning.

scholarly journals Sources of water-soluble Brown Carbon at a South-Eastern European Site

2021 ◽  
Author(s):  
Charalampia Baliaka ◽  
Christos Kaltsonoudis ◽  
Kalliopi Florou ◽  
Spiro Jorga ◽  
Christina Vasilakopoulou ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Light Absorption ◽  
Organic Aerosol ◽  
Water Soluble ◽  
Automated System ◽  
Urban Site ◽  
Multiple Sources ◽  
Brown Carbon ◽  
Liquid Waveguide Capillary Cell ◽  
Primary Emissions

&lt;p&gt;Atmospheric brown carbon (BrC) is a highly uncertain, but potentially important contributor to light absorption in the atmosphere. Laboratory and field studies have shown that BrC can be produced from multiple sources, including primary emissions from fossil fuel combustion and biomass burning (BB), as well as secondary formation through a number of reaction pathways. It is currently thought that the dominant source of atmospheric BrC is primary emissions from BB, but relatively few studies demonstrate this in environments with complex source profiles.&lt;/p&gt;&lt;p&gt;A field campaign was conducted during a month-long wintertime period in 2020 on the campus of the University of Peloponnese in the southwest of Patras, Greece which represents an urban site. During this time, ambient filter samples (a total of 35 filters) were collected from which the water-soluble BrC was determined using a semi-automated system similar to Hecobian et al. (2010), &amp;#160;where absorption was measured over a 1 m path length. To measure the BrC, a UV-Vis Spectrophotometer was coupled to a Liquid Waveguide Capillary Cell and the light absorption intensity was recorded at 365 and 700 nm. The latter was used as a reference wavelength. We found that the average BrC absorption in Patras at a wavelength of 365 nm was 8.5 &amp;#177; 3.9 Mm&lt;sup&gt;-1&lt;/sup&gt; suggesting that there was significant BrC in the organic aerosol during this period. Attribution of sources of BrC was done using simultaneous chemical composition data observations (primarily organic carbon, black carbon, and nitrate) combined with Positive Matrix Factorization analysis. This analysis showed that in addition to the important role of biomass burning (a contribution of about 20%) and other combustion emissions (also close to 20%), oxidized organic aerosol (approximately 40%) is also a significant contributor to BrC in the study area.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Reference&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;Hecobian, A., Zhang, X., Zheng, M., Frank, N., Edgerton, E.S., Weber, R.J., 2010. Water-soluble organic aerosol material and the light-absorption characteristics of aqueous extracts measured over the Southeastern United States. Atmos. Chem. Phys. 10, 5965&amp;#8211;5977. https://doi.org/10.5194/acp-10-5965-2010&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;

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