scholarly journals Source-specific light absorption by carbonaceous components in the complex aerosol matrix from yearly filter-based measurements

2021 ◽  
Vol 21 (17) ◽  
pp. 12809-12833
Author(s):  
Vaios Moschos ◽  
Martin Gysel-Beer ◽  
Robin L. Modini ◽  
Joel C. Corbin ◽  
Dario Massabò ◽  
...  
Keyword(s):  
Light Absorption ◽  
Radiation Absorption ◽  
Rural Site ◽  
Total Absorption ◽  
Biomass Smoke ◽  
Enhanced Absorption ◽  
Mass Absorption ◽  
Aerosol Absorption ◽  
Wide Range ◽  
Lensing Effect

Abstract. Understanding the sources of light-absorbing organic (brown) carbon (BrC) and its interaction with black carbon (BC) and other non-refractory particulate matter (NR-PM) fractions is important for reducing uncertainties in the aerosol direct radiative forcing. In this study, we combine multiple filter-based techniques to achieve long-term, spectrally resolved, source- and species-specific atmospheric absorption closure. We determine the mass absorption efficiency (MAE) in dilute bulk solutions at 370 nm to be equal to 1.4 m2 g−1 for fresh biomass smoke, 0.7 m2 g−1 for winter-oxygenated organic aerosol (OA), and 0.13 m2 g−1 for other less absorbing OA. We apply Mie calculations to estimate the contributions of these fractions to total aerosol absorption. While enhanced absorption in the near-UV has been traditionally attributed to primary biomass smoke, here we show that anthropogenic oxygenated OA may be equally important for BrC absorption during winter, especially at an urban background site. We demonstrate that insoluble tar balls are negligible in residential biomass burning atmospheric samples of this study and thus could attribute the totality of the NR-PM absorption at shorter wavelengths to methanol-extractable BrC. As for BC, we show that the mass absorption cross-section (MAC) of this fraction is independent of its source, while we observe evidence for a filter-based lensing effect associated with the presence of NR-PM components. We find that bare BC has a MAC of 6.3 m2 g−1 at 660 nm and an absorption Ångström exponent of 0.93 ± 0.16, while in the presence of coatings its absorption is enhanced by a factor of ∼ 1.4. Based on Mie calculations of closure between observed and predicted total light absorption, we provide an indication for a suppression of the filter-based lensing effect by BrC. The total absorption reduction remains modest, ∼ 10 %–20 % at 370 nm, and is restricted to shorter wavelengths, where BrC absorption is significant. Overall, our results allow an assessment of the relative importance of the different aerosol fractions to the total absorption for aerosols from a wide range of sources and atmospheric ages. When integrated with the solar spectrum at 300–900 nm, bare BC is found to contribute around two-thirds of the solar radiation absorption by total carbonaceous aerosols, amplified by the filter-based lensing effect (with an interquartile range, IQR, of 8 %–27 %), while the IQR of the contributions by particulate BrC is 6 %–13 % (13 %–20 % at the rural site during winter). Future studies that will directly benefit from these results include (a) optical modelling aiming at understanding the absorption profiles of a complex aerosol composed of BrC, BC and lensing-inducing coatings; (b) source apportionment aiming at understanding the sources of BC and BrC from the aerosol absorption profiles; (c) global modelling aiming at quantifying the most important aerosol absorbers.

scholarly journals Source-specific light absorption by carbonaceous components in the complex aerosol matrix from yearly filter-based measurements

2020 ◽  
Author(s):  
Vaios Moschos ◽  
Martin Gysel-Beer ◽  
Robin L. Modini ◽  
Joel C. Corbin ◽  
Dario Massabò ◽  
...  
Keyword(s):  
Light Absorption ◽  
Rural Site ◽  
Urban Background ◽  
Biomass Smoke ◽  
Enhanced Absorption ◽  
Mass Absorption ◽  
Aerosol Absorption ◽  
Lensing Effect ◽  
Spectrally Resolved

Abstract. Understanding the sources of light-absorbing organic (brown) carbon (BrC) and its interaction with black carbon (BC) and other non-refractory particulate matter (NR-PM) fractions is important for reducing uncertainties in the aerosol direct radiative forcing. In this study, we combine multiple filter-based techniques to achieve long-term, spectrally-resolved, source- and species-specific atmospheric absorption closure. We determine the total aerosol absorption at seven wavelengths based on the Aethalometer attenuation measurements, calibrated with the multi-wavelength absorption analyzer. We measure the spectrally-resolved imaginary part of the refractive index, k, for methanol extracts and determine the source-specific k for organic aerosol (OA) fractions using positive matrix factorization. The average k at 370 nm is found to be 0.06 for fresh biomass smoke, 0.03 for winter-oxygenated OA, and 0.006 for other less absorbing OA, which translates to corresponding mass absorption efficiencies (MAE) in dilute bulk solutions of 1.4, 0.7 and 0.13 m2 g−1. We apply Mie calculations to estimate the contributions of these fractions to total aerosol absorption. While enhanced absorption in the near-UV has been traditionally attributed to primary biomass smoke, here we show that anthropogenic oxygenated OA may be as important for BrC absorption during winter, especially at an urban background site. We demonstrate the absence of tar-balls in residential biomass burning particles of this study, and attribute the totality of the NR-PM absorption at shorter wavelengths to methanol-extractable BrC. As for BC, we show that the mass absorption cross-section (MAC) of this fraction is independent of its source, while we observe evidence for a lensing effect associated with the presence of NR-PM components. We find that bare BC has a MAC of 6.3 m2 g−1 at 660 nm and an absorption Ångström exponent (AAE) of 0.93 ± 0.16, while in the presence of coatings its absorption is enhanced by a factor of ~1.4. This falls within the global average enhancement factor of 1.5 ± 0.3 from filter-based techniques. Based on Mie-calculations of closure between observed and predicted total light absorption, we provide the first experimental evidence for a suppression of the lensing effect by BrC. The total absorption suppression remains modest, ~10–20 % at 370 nm, and is restricted to shorter wavelengths where BrC absorption is significant. Our long-term observations at locations representative of European urban background and rural Alpine sites show that extractable particulate BrC accounts for ~30 % of the absorption in the near-UV range (370 nm) on a yearly basis. However, if lensing suppression occurred due to internal mixing of BC and BrC as apparently the case for many samples in our study, then the additional absorption by BrC (vs transparent OA) would be partially compensated by a concurrent BC lensing factor reduction, which manifests as lower than expected total aerosol AAE values. Overall, when integrated with the solar spectrum at 300–900 nm, bare BC is found to contribute around two thirds of the solar radiation absorption by total carbonaceous aerosols, amplified by the lensing effect (with an interquartile range, IQR, of 8–27 %), while the IQR of yearly average contributions by particulate BrC is 6–13 % (13–20 % at the rural site during winter).

scholarly journals Relative importance of black carbon, brown carbon, and absorption enhancement from clear coatings in biomass burning emissions

2017 ◽  
Vol 17 (8) ◽  
pp. 5063-5078 ◽  
Author(s):  
Rudra P. Pokhrel ◽  
Eric R. Beamesderfer ◽  
Nick L. Wagner ◽  
Justin M. Langridge ◽  
Daniel A. Lack ◽  
...  
Keyword(s):  
Black Carbon ◽  
Combustion Efficiency ◽  
Absorption Enhancement ◽  
Total Absorption ◽  
Brown Carbon ◽  
Aerosol Absorption ◽  
Wide Range ◽  
Visible Wavelengths ◽  
Aerosol Emissions ◽  
Modified Combustion Efficiency

Abstract. A wide range of globally significant biomass fuels were burned during the fourth Fire Lab at Missoula Experiment (FLAME-4). A multi-channel photoacoustic absorption spectrometer (PAS) measured dry absorption at 405, 532, and 660 nm and thermally denuded (250 °C) absorption at 405 and 660 nm. Absorption coefficients were broken into contributions from black carbon (BC), brown carbon (BrC), and lensing following three different methodologies, with one extreme being a method that assumes the thermal denuder effectively removes organics and the other extreme being a method based on the assumption that black carbon (BC) has an Ångström exponent of unity. The methodologies employed provide ranges of potential importance of BrC to absorption but, on average, there was a difference of a factor of 2 in the ratio of the fraction of absorption attributable to BrC estimated by the two methods. BrC absorption at shorter visible wavelengths is of equal or greater importance to that of BC, with maximum contributions of up to 92 % of total aerosol absorption at 405 nm and up to 58 % of total absorption at 532 nm. Lensing is estimated to contribute a maximum of 30 % of total absorption, but typically contributes much less than this. Absorption enhancements and the estimated fraction of absorption from BrC show good correlation with the elemental-carbon-to-organic-carbon ratio (EC ∕ OC) of emitted aerosols and weaker correlation with the modified combustion efficiency (MCE). Previous studies have shown that BrC grows darker (larger imaginary refractive index) as the ratio of black to organic aerosol (OA) mass increases. This study is consistent with those findings but also demonstrates that the fraction of total absorption attributable to BrC shows the opposite trend: increasing as the organic fraction of aerosol emissions increases and the EC ∕ OC ratio decreases.

scholarly journals Optical-chemical relationships for carbonaceous aerosols observed at Jeju Island, Korea with a 3-laser photoacoustic spectrometer

2010 ◽  
Vol 10 (4) ◽  
pp. 9369-9389 ◽  
Author(s):  
B. A. Flowers ◽  
M. K. Dubey ◽  
C. Mazzoleni ◽  
E. A. Stone ◽  
J. J.. Schauer ◽  
...  
Keyword(s):  
Optical Properties ◽  
Chemical Composition ◽  
Radiative Forcing ◽  
Optical Model ◽  
Index Of Refraction ◽  
Enhanced Absorption ◽  
Aerosol Absorption ◽  
Photoacoustic Spectrometer ◽  
Wide Range ◽  
Pollution Plumes

Abstract. Transport of aerosols in pollution plumes from the mainland Asian continent was observed in situ at Jeju, South Korea during the Cheju Asian Brown Cloud Plume-Asian Monsoon Experiment (CAPMEX) field campaign throughout August and September 2008 using a 3-laser photoacoustic spectrometer. Transport of mixed sulfate, carbonaceous, and nitrate aerosols from various Asian pollution plumes to Jeju accounted for 76% of the deployment days, showing large variations in their measured chemical and optical properties. Our analysis of eight distinct episodes, spanning a wide range of chemical composition, optical properties, and source regions, reveals that at episodes with higher OC/SO2−4 and NO−3/SO2−4 composition ratios exhibit lower single scatter albedo at shorter wavelengths (ω405); significantly lower [ω405meas = 0.79±0.06, ω405calc = 0.86±0.01] than predicted by an optical model that assumes constant complex index of refraction with wavelength (an optical model of soot). We attribute this discrepancy to enhanced absorption by organic material. Organic carbon absorption accounts for up to 50% of the measured aerosol absorption at 405 nm for the high OC/SO2−4 episode. Coatings of elemental carbon aerosol cores are hypothesized to increase absorption by factors up to 6 at visible wavelengths. Carbonaceous aerosol absorption can alter global radiative forcing estimates substantially, underscoring the need to understand and predict chemical composition effects on optical properties.

scholarly journals Estimation of the mass absorption cross section of the organic carbon component of aerosols in the Mexico City Metropolitan Area (MCMA)

2008 ◽  
Vol 8 (3) ◽  
pp. 10189-10225 ◽  
Author(s):  
J. C. Barnard ◽  
R. Volkamer ◽  
E. I. Kassianov
Keyword(s):  
Organic Carbon ◽  
Black Carbon ◽  
Mexico City ◽  
Cross Section ◽  
Light Absorption ◽  
Absorption Cross Section ◽  
Trace Gases ◽  
Absorption Cross ◽  
Enhanced Absorption ◽  
Mass Absorption

Abstract. Data taken from the MCMA-2003 and the 2006 MILAGRO field campaigns are used to examine the absorption of solar radiation by the organic component of aerosols. Using irradiance data from a Multi-Filter Rotating Shadowband Radiometer (MFRSR) and an actinic flux spectroradiometer (SR), we derive aerosol single scattering albedo, π0,λ, as a function of wavelength, λ. We find that in the near-UV spectral range (250 to 400 nm) π0,λ is much lower compared to π0,λ at 500 nm indicating enhanced absorption in the near-UV range. Absorption by elemental carbon, dust, or gas cannot account for this enhanced absorption leaving the organic part of the aerosol as the only possible absorber. We use data from a surface deployed Aerodyne Aerosol Mass Spectrometer (AMS) along with the inferred π0,λ to estimate the Mass Absorption Cross section (MAC) for the organic carbon. We find that the MAC is about 10.5 m2/g at 300 nm and falls close to zero at about 500 nm; values that are roughly consistent with other estimates of organic carbon MAC. These MAC values can be considered as "radiatively correct" because when used in radiative transfer calculations the calculated irradiances/actinic fluxes match those measured at the wavelengths considered here. For an illustrative case study described here, we estimate that the light absorption by the "brown" (organic) carbonaceous aerosol can add about 40% to the light absorption of black carbon in Mexico City. This contribution will vary depending on the relative abundance of organic carbon relative to black carbon. Furthermore, our analysis indicates that organic aerosol would slow down photochemistry by selectively scavenging the light reaching the ground at those wavelengths that drive photochemical reactions. Finally, satellite retrievals of trace gases that are used to infer emissions currently assume that the MAC of organic carbon is zero. For trace gases that are retrieved using wavelengths shorter then 420 nm (i.e. SO2, HCHO, halogenoxides, NO2), the assumption of non-zero MAC values will induce an upward correction to the inferred emissions. This will be particularly relevant in polluted urban atmospheres and areas of biomass burning where organic aerosols are particularly abundant.

scholarly journals Relative Importance of Black Carbon, Brown Carbon and Absorption Enhancement from Clear Coatings in Biomass Burning Emissions

2016 ◽  
Author(s):  
Rudra P. Pokhrel ◽  
Eric R. Beamesderfer ◽  
Nick L. Wagner ◽  
Justin M. Langridge ◽  
Daniel A. Lack ◽  
...  
Keyword(s):  
Black Carbon ◽  
Combustion Efficiency ◽  
Absorption Enhancement ◽  
Total Absorption ◽  
Brown Carbon ◽  
Aerosol Absorption ◽  
Wide Range ◽  
Visible Wavelengths ◽  
Aerosol Emissions ◽  
Modified Combustion Efficiency

Abstract. A wide range of globally significant biomass fuels were burned during the fourth Fire Lab at Missoula Experiment (FLAME-4). A multi-channel photoacoustic absorption spectrometer (PAS) measured dry absorption at 405, 532, and 660 nm and thermally denuded (250 °C) absorption at 405 and 660 nm. Absorption coefficients were broken into contributions from black carbon (BC), brown carbon (BrC) and lensing following three different methodologies, with one extreme being a method that assumes the thermal denuder effectively removes organics and the other extreme being a method based on the assumption that black carbon (BC) has an angstrom exponent of unity. The methodologies employed provide ranges of potential importance of BrC to absorption but, on average, there was a factor of 2 difference in the ratio of the fraction of absorption attributable to brown carbon estimated by the two methods. BrC absorption at shorter visible wavelengths is of equal or greater importance to that of BC with maximum contributions of up to 92 % of total aerosol absorption at 405 nm and up to 58 % of total absorption at 532 nm. Lensing is estimated to contribute a maximum of 30 % of total absorption, but typically contributes much less than this. Absorption enhancements and the estimated fraction of absorption from BrC show good correlation with the elemental to organic carbon ratio (EC/OC) of emitted aerosols and weaker correlation with the modified combustion efficiency (MCE). Previous studies have shown that brown carbon grows darker (larger imaginary refractive index) as the ratio of black to organic aerosol (OA) mass increases. This study is consistent with those findings but also demonstrates that the fraction of total absorption attributable to BrC shows the opposite trend: increasing as the organic fraction of aerosol emissions increases and the EC/OC ratio decreases.

scholarly journals Single particle dual plasmonic effect for efficient organic solar cells

2021 ◽  
Author(s):  
Adi Prasetio ◽  
Soyeon Kim ◽  
Muhammad Jahandar ◽  
Dong Chan Lim
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Light Absorption ◽  
Resonance Effect ◽  
Localized Surface Plasmon ◽  
Main Role ◽  
Charge Generation ◽  
One Pot ◽  
Wide Range ◽  
Light Reflectance

AbstractIncorporating localized surface plasmon resonance (LSPR) into organic solar cells (OSCs) is a popular method for improving the power conversion efficiency (PCE) by introducing better light absorption. In this work, we designed a one-pot synthesis of Ag@SiO2@AuNPs dual plasmons and observed an immense increase in light absorption over a wide range of wavelengths. Ag@SiO2 plays the main role in enhancing light absorption near the ultraviolet band. The silica shell can also further enhance the LSP resonance effect and prevent recombination on the surface of AgNPs. The AuNPs on the Ag@SiO2 shell exhibited strong broad visible-light absorption due to LSP resonance and decreased light reflectance. By utilizing Ag@SiO2@AuNPs, we could enhance the light absorption and photoinduced charge generation, thereby increasing the device PCE to 8.57% and Jsc to 17.67 mA cm−2, which can be attributed to the enhanced optical properties. Meanwhile, devices without LSPR nanoparticles and Ag@SiO2 LSPR only showed PCEs of 7.36% and 8.18%, respectively.

Enhanced Absorption of Single Silicon Nanowire with Si3N4 Shell for Photovoltaic Applications

2015 ◽  
Vol 1090 ◽  
pp. 173-177 ◽  
Author(s):  
Wen Fu Liu ◽  
Hua Li Hao
Keyword(s):  
Light Scattering ◽  
Light Absorption ◽  
Calculated Result ◽  
Scattering Theory ◽  
Enhancement Factor ◽  
Shell Thickness ◽  
Silicon Nanowire ◽  
Enhanced Absorption ◽  
Photovoltaic Applications

Based on the Lorenz-Mie light scattering theory, we have calculated the light absorption of single silicon nanowire with Si3N4coating, and compared with pure single silicon nanowire. The calculated result indicates that there exists an enhanced absorption in the Si3N4-coated silicon nanowire and shows a great photocurrent enhancement factor (~70%) for the coaxial NW with the shell thickness of ~70 nm. For a special shell thickness (175 nm) in the Si3N4-coated silicon nanowire forr= 150 nm, the enhancement comes up to ~98.45%.

Radiation absorption, growth and yield of cereals

1978 ◽  
Vol 91 (1) ◽  
pp. 47-60 ◽  
Author(s):  
J. N. Gallagher ◽  
P. V. Biscoe
Keyword(s):  
Dry Matter ◽  
Growing Season ◽  
Growth Efficiency ◽  
Growth And Yield ◽  
Radiation Absorption ◽  
Exponential Equation ◽  
Crop Cover ◽  
Crop Growth Rate ◽  
Wide Range ◽  
Total Crop

SummaryAnalysis of measurements of absorbed radiation and leaf area indices of wheat and barley crops showed that throughout most of growth the fraction of absorbed solar radiation could be described by a simple exponential equation.For several of these crops grown under a wide range of weather and husbandry at Sutton Bonington and Rothamsted, 2-weekly values of crop growth rate (C) were closely related to radiation absorbed until ear emergence and about 3·0 g of dry matter (D.M.) were produced by each MJ of photosynthetically active radiation (PAR) absorbed. Final crop weight was closelyrelated to total PAR absorbed during growth (SA); on average about 2·2 g D.M. were produced per MJ absorbed, equivalent to a growth efficiency (Eg) of approximately 3·9%. Unfertilized and drought-stressed crops had a smaller Eg.The fraction of total crop D.M. harvested as grain (harvest index) varied more for wheat than for barley. Calculations of a maximum realizable grain yield made using the largest values of Eg and SA for the crops measured and assuming a harvestindex of 0.53 (achieved in an experimental crop) showed a grain D.M. yield of 10·3 t D.M./ha to be possible. To achieve such a yield would require full crop cover from the beginning of April until the end of July in a typical English growing season.

A Review on Meropenem

2021 ◽  
pp. 5034-5038
Author(s):  
Mohsina Abed ◽  
Sara Yousuf
Keyword(s):  
Intravenous Administration ◽  
Wide Spectrum ◽  
Gastrointestinal Haemorrhage ◽  
The Body ◽  
Antibacterial Drug ◽  
Bacterial Strains ◽  
Enhanced Absorption ◽  
Bacterial Cell Death ◽  
Wide Range ◽  
Synthetic Derivative

Meropenem is a new Carbapenem antibacterial agent with wide spectrum of activity for intravenous administration. It is synthetic derivative of Thienamycin. Three analogues of Meropenem are evaluated and active against 18 bacterial strains. Meropenem causes rapid bacterial cell death by covalently binding to penicillin binding proteins (PBS). Structural modification at C-2 position, produced double promoiety prodrug of Meropenem and increases bioavailability of oral administration. Other forms of drug such as liposome and nanoparticles are also available with enhanced absorption. 14C labelled Meropenem prepared from 14C Dimethylamine hydrochloride is used for the analysis of M. tuberculosis transpeptidase. ICI213,689 is the only metabolite of Meropenem and it is inactive. Meropenem penetrates well into the body fluids and tissues including cerebrospinal fluid. Its bioavailability is 100% on intravenous administration. Hence it is used in the treatment of meningitis, febrile neutropenia, anthrax and various other skin and skin structure infections. Dosage reduction is required in patient with reduced renal function but not in hepatic impairment. Seizures, gastrointestinal haemorrhage are observed in patients. Vabmoere is the combination of Meropenem and Vaborbactam which is active against the Carbapenem resistant Enterobacteriacea. Meropenem is an effective broad-spectrum antibacterial drug for the treatment of wide range of infection including polymicrobial infection in both children and adult.

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