Influence of the mass fraction of oxide in aluminum nanoparticles on the explosive decomposition threshold and light absorption efficiency in PETN-based compounds

2014 ◽  
Vol 50 (5) ◽  
pp. 578-581 ◽  
Author(s):  
B. P. Aduev ◽  
D. R. Nurmukhametov ◽  
A. A. Zvekov ◽  
N. V. Nelyubina
Keyword(s):  
Light Absorption ◽  
Mass Fraction ◽  
Absorption Efficiency ◽  
Aluminum Nanoparticles ◽  
Explosive Decomposition

scholarly journals Spectral- and size-resolved mass absorption efficiency of mineral dust aerosols in the shortwave: a simulation chamber study

2017 ◽  
Author(s):  
Lorenzo Caponi ◽  
Paola Formenti ◽  
Dario Massabó ◽  
Claudia Di Biagio ◽  
Mathieu Cazaunau ◽  
...  
Keyword(s):  
Remote Sensing ◽  
Light Absorption ◽  
Mass Fraction ◽  
Climate Models ◽  
Mineral Dust ◽  
Absorption Efficiency ◽  
Aerodynamic Diameter ◽  
Dust Composition ◽  
Simulation Chamber ◽  
Mass Absorption Efficiency

Abstract. This paper presents new laboratory measurements of the mass absorption efficiency (MAE) between 375 and 850 nm for mineral dust of different origin in two size classes: PM10.6 (mass fraction of particles of aerodynamic diameter lower than 10.6 µm) and PM2.5 (mass fraction of particles of aerodynamic diameter lower than 2.5 µm). Experiments have been performed in the CESAM simulation chamber using generated mineral dust from natural parent soils, and optical and gravimetric analyses. Results show that the MAE values are lower for the PM10.6 mass fraction (range 37–135 × 10−3 m2 g−1 at 375 nm) than for the PM2.5 (range 95–711 × 10−3 m2 g−1 at 375 nm), and decrease with increasing wavelength as λ-AAE, where Angstrom Absorption Exponent (AAE) averages between 3.3–3.5, regardless of size. The size-independence of AAE suggests that, for a given size distribution, the possible variation of dust composition with size would not affect significantly the spectral behavior of shortwave absorption. Because of its high atmospheric concentration, light-absorption by mineral dust can be competitive to black and brown carbon even during atmospheric transport over heavy polluted regions, when dust concentrations are significantly lower than at emission. The AAE values of mineral dust are higher than for black carbon (~ 1), but in the same range as light-absorbing organic (brown) carbon. As a result, depending on the environment, there can be some ambiguity in apportioning the AAOD based on spectral dependence, which is relevant to the development of remote sensing of light-absorption aerosols from space, and their assimilation in climate models. We suggest that the sample-to-sample variability in our dataset of MAE values is related to regional differences of the mineralogical composition of the parent soils. Particularly in the PM2.5 fraction, we found a strong linear correlation between the dust light-absorption properties and elemental iron rather than the iron oxide fraction, which could ease the application and the validation of climate models that now start to include the representation of the dust composition, as well as for remote sensing of dust absorption in the UV-VIS spectral region.

scholarly journals Spectral- and size-resolved mass absorption efficiency of mineral dust aerosols in the shortwave spectrum: a simulation chamber study

2017 ◽  
Vol 17 (11) ◽  
pp. 7175-7191 ◽  
Author(s):  
Lorenzo Caponi ◽  
Paola Formenti ◽  
Dario Massabó ◽  
Claudia Di Biagio ◽  
Mathieu Cazaunau ◽  
...  
Keyword(s):  
Remote Sensing ◽  
Light Absorption ◽  
Mass Fraction ◽  
Climate Models ◽  
Mineral Dust ◽  
Absorption Efficiency ◽  
Aerodynamic Diameter ◽  
Dust Composition ◽  
Simulation Chamber ◽  
Mass Absorption Efficiency

Abstract. This paper presents new laboratory measurements of the mass absorption efficiency (MAE) between 375 and 850 nm for 12 individual samples of mineral dust from different source areas worldwide and in two size classes: PM10. 6 (mass fraction of particles of aerodynamic diameter lower than 10.6 µm) and PM2. 5 (mass fraction of particles of aerodynamic diameter lower than 2.5 µm). The experiments were performed in the CESAM simulation chamber using mineral dust generated from natural parent soils and included optical and gravimetric analyses. The results show that the MAE values are lower for the PM10. 6 mass fraction (range 37–135  ×  10−3 m2 g−1 at 375 nm) than for the PM2. 5 (range 95–711  ×  10−3 m2 g−1 at 375 nm) and decrease with increasing wavelength as λ−AAE, where the Ångström absorption exponent (AAE) averages between 3.3 and 3.5, regardless of size. The size independence of AAE suggests that, for a given size distribution, the dust composition did not vary with size for this set of samples. Because of its high atmospheric concentration, light absorption by mineral dust can be competitive with black and brown carbon even during atmospheric transport over heavy polluted regions, when dust concentrations are significantly lower than at emission. The AAE values of mineral dust are higher than for black carbon (∼ 1) but in the same range as light-absorbing organic (brown) carbon. As a result, depending on the environment, there can be some ambiguity in apportioning the aerosol absorption optical depth (AAOD) based on spectral dependence, which is relevant to the development of remote sensing of light-absorbing aerosols and their assimilation in climate models. We suggest that the sample-to-sample variability in our dataset of MAE values is related to regional differences in the mineralogical composition of the parent soils. Particularly in the PM2. 5 fraction, we found a strong linear correlation between the dust light-absorption properties and elemental iron rather than the iron oxide fraction, which could ease the application and the validation of climate models that now start to include the representation of the dust composition, as well as for remote sensing of dust absorption in the UV–vis spectral region.

scholarly journals Development of Visible-Light-Driven Rh–TiO2–CeO2 Hybrid Photocatalysts for Hydrogen Production

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 848
Author(s):  
Jong-Wook Hong
Keyword(s):  
Hydrogen Production ◽  
Visible Light ◽  
Light Absorption ◽  
Photocatalytic Performance ◽  
Environmental Issues ◽  
Absorption Efficiency ◽  
Low Light ◽  
Practical Applications ◽  
Visible Light Driven ◽  
Poor Stability

Visible-light-driven hydrogen production through photocatalysis has attracted enormous interest owing to its great potential to address energy and environmental issues. However, photocatalysis possesses several limitations to overcome for practical applications, such as low light absorption efficiency, rapid charge recombination, and poor stability of photocatalysts. Here, the preparation of efficient noble metal–semiconductor hybrid photocatalysts for photocatalytic hydrogen production is presented. The prepared ternary Rh–TiO2–CeO2 hybrid photocatalysts exhibited excellent photocatalytic performance toward the hydrogen production reaction compared with their counterparts, ascribed to the synergistic combination of Rh, TiO2, and CeO2.

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>

Light absorption properties, chromophore composition and sources of brown carbon aerosol in Xi’an, Northwest China

2020 ◽  
Author(s):  
Ru-Jin Huang ◽  
Wei Yuan ◽  
Lu Yang ◽  
Jie Guo ◽  
Jing Duan ◽  
...  
Keyword(s):  
Light Absorption ◽  
Coal Combustion ◽  
Radiative Forcing ◽  
Northwest China ◽  
Absorption Efficiency ◽  
Vehicular Emissions ◽  
Absorption Properties ◽  
Seasonal Differences ◽  
Brown Carbon ◽  
The Impact

<p>The impact of brown carbon aerosol (BrC) on the Earth’s radiative forcing balance has been widely recognized but remains uncertain, mainly because the relationships among BrC sources, chromophores, and optical properties of aerosol are poorly understood (Feng et al., 2013; Laskin et al., 2015). In this work, the light absorption properties and chromophore composition of BrC were investigated for samples collected in Xi’an, Northwest China from 2015 to 2016. Both absorption Ångström exponent and mass absorption efficiency show distinct seasonal differences, which could be attributed to the differences in sources and chromophore composition of BrC. Three groups of light-absorbing organics were found to be important BrC chromophores, including those show multiple absorption peaks at wavelength > 350 nm (12 polycyclic aromatic hydrocarbons and their derivatives) and those show single absorption peak at wavelength < 350 nm (10 nitrophenols and nitrosalicylic acids and 3 methoxyphenols). These measured BrC chromophores show distinct seasonal differences and contribute on average about 1.1% and 3.3% of light absorption of methanol-soluble BrC at 365 nm in summer and winter, respectively, about 7 and 5 times higher than the corresponding mass fractions in total organic carbon. The sources of BrC were resolved by positive matrix factorization (PMF) using these chromophores instead of commonly used non-light absorbing organic markers as model inputs. Our results show that in spring vehicular emissions and secondary formation are major sources of BrC (~70%), in fall coal combustion and vehicular emissions are major sources (~70%), in winter biomass burning and coal combustion become major sources (~80%), while in summer secondary BrC dominates (~60%).</p><p> </p><p>References:</p><p>Feng, Y., V. Ramanathan, and V. R. Kotamarthi: Brown carbon: A significant atmospheric absorber of solar radiation?, Atmos. Chem. Phys., 13, 8607-8621, doi:10.5194/acp-13-8607-2013, 2013.</p><p>Laskin, A., J. Laskin, and S. A. Nizkorodov: Chemistry of atmospheric brown carbon, Chem. Rev., 115, 4335-4382, doi:10.1021/cr5006167, 2015.</p>

scholarly journals Mass absorption efficiency of elemental carbon and water-soluble organic carbon in Beijing, China

2011 ◽  
Vol 11 (22) ◽  
pp. 11497-11510 ◽  
Author(s):  
Y. Cheng ◽  
K.-B. He ◽  
M. Zheng ◽  
F.-K. Duan ◽  
Z.-Y. Du ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Biomass Burning ◽  
Light Absorption ◽  
Elemental Carbon ◽  
Organic Aerosol ◽  
Absorption Efficiency ◽  
Water Soluble ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon ◽  
Mass Absorption Efficiency

Abstract. The mass absorption efficiency (MAE) of elemental carbon (EC) in Beijing was quantified using a thermal-optical carbon analyzer. The MAE measured at 632 nm was 8.45±1.71 and 9.41±1.92 m2 g−1 during winter and summer respectively. The daily variation of MAE was found to coincide with the abundance of organic carbon (OC), especially the OC to EC ratio, perhaps due to the enhancement by coating with organic aerosol (especially secondary organic aerosol, SOA) or the artifacts resulting from the redistribution of liquid-like organic particles during the filter-based absorption measurements. Using a converting approach that accounts for the discrepancy caused by measurements methods of both light absorption and EC concentration, previously published MAE values were converted to the equivalent-MAE, which is the estimated value if using the same measurement methods as used in this study. The equivalent-MAE was found to be much lower in the regions heavily impacted by biomass burning (e.g., below 2.7 m2 g−1 for two Indian cities). Results from source samples (including diesel exhaust samples and biomass smoke samples) also demonstrated that emissions from biomass burning would decrease the MAE of EC. Moreover, optical properties of water-soluble organic carbon (WSOC) in Beijing were 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 MAE of WSOC (measured at 365 nm) was 1.79±0.24 and 0.71±0.20 m2 g−1 during winter and summer respectively. The large discrepancy between the MAE of WSOC during winter and summer was attributed to the difference in the precursors of SOA such that anthropogenic volatile organic compounds (AVOCs) should be more important as the precursors of SOA in winter. The MAE 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 stronger emissions of biomass burning in China.

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