Oxidative potential of mineral dust particles: A focus on chemical components and cell-free assay 

2021 ◽  
Author(s):  
Eduardo José dos Santos Souza ◽  
Khanneh Wadinga Fomba ◽  
Nabil Deabji ◽  
Hartmut Herrmann
Keyword(s):  
Transition Metals ◽  
Mineral Dust ◽  
Cell Damage ◽  
Evaluation Model ◽  
Respiratory Illness ◽  
Dust Particles ◽  
Chemical Components ◽  
Buffer Solution ◽  
Oxidative Potential ◽  
Chelex 100

<p>Oxidative potential (OP) assays are feasible methods to comprehensively understand how exposure to atmospheric chemical components can influence the formation of reactive oxygen species (ROS) in the human body. The increase of ROS concentration can enhance the oxidation of numerous components, such as of the DNA, proteins, and lipids, which cause mutations and cell damage, leading to respiratory illness. According to available studies, the mechanisms of PM-related health effects are not totally understood. The aim of the present study is to assess which available assays are suitable for evaluating the OP of different Mineral dust (MD) samples and what limitations may apply to either method. Cell-free assays are assessed including methods based on the interaction of ascorbic acid (AA) and dithiothreitol (DTT) with soluble aerosol chemical components.</p> <p>Oxidative potential experiments were carried out on both commercially available standard solutions, ultrapure water (DTT) and buffer solution (AA), as well as on soluble extracts of one-quarter filter samples obtained using both shaking and ultrasound procedures. Most limitations were related to high concentrations of transition metals in the buffer solution composition, which was treated using Chelex 100 sodium resin. Transition metals were strongly correlated to both methods, such as Ti, Cr, V, and Mn for DTT assays, and Fe, and Sr for AA assay. The mineral dust OP values were lower than the OP of particulate matter samples from urban metropolitan centers. Such results could be related to the fewer metal and quinone concentrations in the MD samples in comparison to the urban sample. DTT assay has shown more sensibility to the MD content compared with AA chemical procedure. These assays contribute to building an impact-evaluation model for assessing the variation of MD OP based on its different chemical composition.</p>

scholarly journals Hygroscopicity of Different Types of Aerosol Particles: Case Studies Using Multi-Instrument Data in Megacity Beijing, China

2020 ◽  
Vol 12 (5) ◽  
pp. 785 ◽  
Author(s):  
Tong Wu ◽  
Zhanqing Li ◽  
Jun Chen ◽  
Yuying Wang ◽  
Hao Wu ◽  
...  
Keyword(s):  
Enhancement Factor ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Dust Aerosol ◽  
Dust Particles ◽  
Chemical Components ◽  
Hygroscopic Growth ◽  
Microphysical Properties ◽  
Fine Mode ◽  
Fine Mode Aerosol

Water uptake by aerosol particles alters its light-scattering characteristics significantly. However, the hygroscopicities of different aerosol particles are not the same due to their different chemical and physical properties. Such differences are explored by making use of extensive measurements concerning aerosol optical and microphysical properties made during a field experiment from December 2018 to March 2019 in Beijing. The aerosol hygroscopic growth was captured by the aerosol optical characteristics obtained from micropulse lidar, aerosol chemical composition, and aerosol particle size distribution information from ground monitoring, together with conventional meteorological measurements. Aerosol hygroscopicity behaves rather distinctly for mineral dust coarse-mode aerosol (Case I) and non-dust fine-mode aerosol (Case II) in terms of the hygroscopic enhancement factor, f β ( R H , λ 532 ) , calculated for the same humidity range. The two types of aerosols were identified by applying the polarization lidar photometer networking method (POLIPHON). The hygroscopicity for non-dust aerosol was much higher than that for dust conditions with the f β ( R H , λ 532 ) being around 1.4 and 3.1, respectively, at the relative humidity of 86% for the two cases identified in this study. To study the effect of dust particles on the hygroscopicity of the overall atmospheric aerosol, the two types of aerosols were identified and separated by applying the polarization lidar photometer networking method in Case I. The hygroscopic enhancement factor of separated non-dust fine-mode particles in Case I had been significantly strengthened, getting closer to that of the total aerosol in Case II. These results were verified by the hygroscopicity parameter, κ (Case I non-dust particles: 0.357 ± 0.024; Case II total: 0.344 ± 0.026), based on the chemical components obtained by an aerosol chemical speciation instrument, both of which showed strong hygroscopicity. It was found that non-dust fine-mode aerosol contributes more during hygroscopic growth and that non-hygroscopic mineral dust aerosol may reduce the total hygroscopicity per unit volume in Beijing.

scholarly journals Aerosol optical depth retrievals at the Izaña Atmospheric Observatory from 1941 to 2013 by using artificial neural networks

2016 ◽  
Vol 9 (1) ◽  
pp. 53-62 ◽  
Author(s):  
R. D. García ◽  
O. E. García ◽  
E. Cuevas ◽  
V. E. Cachorro ◽  
A. Barreto ◽  
...  
Keyword(s):  
Neural Networks ◽  
Time Series ◽  
Artificial Neural Networks ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Mineral Dust ◽  
Dust Particles ◽  
Filter Radiometer ◽  
Artificial Neural

Abstract. This paper presents the reconstruction of a 73-year time series of the aerosol optical depth (AOD) at 500 nm at the subtropical high-mountain Izaña Atmospheric Observatory (IZO) located in Tenerife (Canary Islands, Spain). For this purpose, we have combined AOD estimates from artificial neural networks (ANNs) from 1941 to 2001 and AOD measurements directly obtained with a Precision Filter Radiometer (PFR) between 2003 and 2013. The analysis is limited to summer months (July–August–September), when the largest aerosol load is observed at IZO (Saharan mineral dust particles). The ANN AOD time series has been comprehensively validated against coincident AOD measurements performed with a solar spectrometer Mark-I (1984–2009) and AERONET (AErosol RObotic NETwork) CIMEL photometers (2004–2009) at IZO, obtaining a rather good agreement on a daily basis: Pearson coefficient, R, of 0.97 between AERONET and ANN AOD, and 0.93 between Mark-I and ANN AOD estimates. In addition, we have analysed the long-term consistency between ANN AOD time series and long-term meteorological records identifying Saharan mineral dust events at IZO (synoptical observations and local wind records). Both analyses provide consistent results, with correlations  >  85 %. Therefore, we can conclude that the reconstructed AOD time series captures well the AOD variations and dust-laden Saharan air mass outbreaks on short-term and long-term timescales and, thus, it is suitable to be used in climate analysis.

scholarly journals The Impact of Ambient Atmospheric Mineral-Dust Particles on the Calcification of Lungs

Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 125
Author(s):  
Mariola Jabłońska ◽  
Janusz Janeczek ◽  
Beata Smieja-Król
Keyword(s):  
Mineral Dust ◽  
Smoking Habit ◽  
Lower Lobe ◽  
Ambient Air ◽  
Dust Particles ◽  
Masking Effect ◽  
Amorphous Calcium Carbonate ◽  
Calcium Salts ◽  
The Impact ◽  
First Time

For the first time, it is shown that inhaled ambient air-dust particles settled in the human lower respiratory tract induce lung calcification. Chemical and mineral compositions of pulmonary calcium precipitates in the lung right lower-lobe (RLL) tissues of 12 individuals who lived in the Upper Silesia conurbation in Poland and who had died from causes not related to a lung disorder were determined by transmission and scanning electron microscopy. Whereas calcium salts in lungs are usually reported as phosphates, calcium salts precipitated in the studied RLL tissue were almost exclusively carbonates, specifically Mg-calcite and calcite. These constituted 37% of the 1652 mineral particles examined. Mg-calcite predominated in the submicrometer size range, with a MgCO3 content up to 50 mol %. Magnesium plays a significant role in lung mineralization, a fact so far overlooked. The calcium phosphate (hydroxyapatite) content in the studied RLL tissue was negligible. The predominance of carbonates is explained by the increased CO2 fugacity in the RLL. Carbonates enveloped inhaled mineral-dust particles, including uranium-bearing oxides, quartz, aluminosilicates, and metal sulfides. Three possible pathways for the carbonates precipitation on the dust particles are postulated: (1) precipitation of amorphous calcium carbonate (ACC), followed by its transformation to calcite; (2) precipitation of Mg-ACC, followed by its transformation to Mg-calcite; (3) precipitation of Mg-free ACC, causing a localized relative enrichment in Mg ions and subsequent heterogeneous nucleation and crystal growth of Mg-calcite. The actual number of inhaled dust particles may be significantly greater than was observed because of the masking effect of the carbonate coatings. There is no simple correlation between smoking habit and lung calcification.

scholarly journals Phosphate Buffer Solubility and Oxidative Potential of Single Metals or Multielement Particles of Welding Fumes

Atmosphere ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 30
Author(s):  
Manuella Ghanem ◽  
Esperanza Perdrix ◽  
Laurent Yves Alleman ◽  
Davy Rousset ◽  
Patrice Coddeville
Keyword(s):  
Transition Metals ◽  
Phosphate Buffer ◽  
Soluble Fraction ◽  
Certified Reference Materials ◽  
Health Effect ◽  
Oxidative Capacity ◽  
Pure Metal ◽  
Welding Fumes ◽  
Oxidative Potential ◽  
Potential Health

To evaluate the chemical behavior and the health impact of welding fumes (WF), a complex and heterogeneous mixture of particulate metal oxides, two certified reference materials (CRMs) were tested: mild steel WF (MSWF-1) and stainless steel WF (SSWF-1). We determined their total chemical composition, their solubility, and their oxidative potential in a phosphate buffer (PB) solution under physiological conditions (pH 7.4 and 37 °C). The oxidative potential (OPDTT) of WF CRMs was evaluated using an acellular method by following the dithiothreitol (DTT) consumption rate (µmol DTT L−1 min−1). Pure metal salts present in the PB soluble fraction of the WF CRMs were tested individually at equivalent molarity to estimate their specific contribution to the total OPDTT. The metal composition of MSWF-1 consisted mainly of Fe, Zn, Mn, and Cu and the SSWF-1 composition consisted mainly of Fe, Mn, Cr, Ni, Cu, and Zn, in diminishing order. The metal PB solubility decreased from Cu (11%) to Fe (approximately 0.2%) for MSWF-1 and from Mn (9%) to Fe (<1%) for SSWF-1. The total OPDTT of SSWF-1 is 2.2 times the OPDTT of MSWF-1 due to the difference in oxidative capacity of soluble transition metals. Cu (II) and Mn (II) are the most sensitive towards DTT while Cr (VI), Fe (III), and Zn (II) are barely reactive, even at higher concentrations. The OPDTT measured for both WF CRMs extracts compare well with simulated extracts containing the main metals at their respective PB-soluble concentrations. The most soluble transition metals in the simulated extract, Mn (II) and Cu (II), were the main contributors to OPDTT in WF CRMs extracts. Mn (II), Cu (II), and Ni (II) might enhance the DTT oxidation by a redox catalytic reaction. However, summing the main individual soluble metal DTT response induces a large overestimation probably linked to modifications in the speciation of various metals when mixed. The complexation of metals with different ligands present in solution and the interaction between metals in the PB-soluble fraction are important phenomena that can influence OPDTT depletion and therefore the potential health effect of inhaled WF.

scholarly journals On realistic size equivalence and shape of spheroidal Saharan mineral dust particles applied in solar and thermal radiative transfer calculations

2011 ◽  
Vol 11 (9) ◽  
pp. 4469-4490 ◽  
Author(s):  
S. Otto ◽  
T. Trautmann ◽  
M. Wendisch
Keyword(s):  
Land Surface ◽  
Mineral Dust ◽  
Single Scattering ◽  
Radiative Heating ◽  
Dust Particles ◽  
Axis Ratio ◽  
Solar Cooling ◽  
Prolate Shape ◽  
Spheroidal Model

Abstract. Realistic size equivalence and shape of Saharan mineral dust particles are derived from in-situ particle, lidar and sun photometer measurements during SAMUM-1 in Morocco (19 May 2006), dealing with measured size- and altitude-resolved axis ratio distributions of assumed spheroidal model particles. The data were applied in optical property, radiative effect, forcing and heating effect simulations to quantify the realistic impact of particle non-sphericity. It turned out that volume-to-surface equivalent spheroids with prolate shape are most realistic: particle non-sphericity only slightly affects single scattering albedo and asymmetry parameter but may enhance extinction coefficient by up to 10 %. At the bottom of the atmosphere (BOA) the Saharan mineral dust always leads to a loss of solar radiation, while the sign of the forcing at the top of the atmosphere (TOA) depends on surface albedo: solar cooling/warming over a mean ocean/land surface. In the thermal spectral range the dust inhibits the emission of radiation to space and warms the BOA. The most realistic case of particle non-sphericity causes changes of total (solar plus thermal) forcing by 55/5 % at the TOA over ocean/land and 15 % at the BOA over both land and ocean and enhances total radiative heating within the dust plume by up to 20 %. Large dust particles significantly contribute to all the radiative effects reported. They strongly enhance the absorbing properties and forward scattering in the solar and increase predominantly, e.g., the total TOA forcing of the dust over land.

scholarly journals Modelling Atmospheric Mineral Aerosol Chemistry to Predict Heterogeneous Photooxidation of SO<sub>2</sub>

2017 ◽  
Author(s):  
Zechen Yu ◽  
Myoseon Jang ◽  
Jiyeon Park
Keyword(s):  
Mineral Dust ◽  
Uv Light ◽  
Full Range ◽  
Saharan Dust ◽  
Dust Particles ◽  
Oh Radicals ◽  
Desorption Kinetics ◽  
So2 Oxidation ◽  
Photocatalytic Ability ◽  
Sulfate Formation

Abstract. The photocatalytic ability of airborne mineral dust particles is known to heterogeneously promote SO2 oxidation, but prediction of this phenomenon is not fully taken into account by current models. In this study, the Atmospheric Mineral Aerosol Reaction (AMAR) model was developed to capture the influence of air-suspended mineral dust particles on sulfate formation in various environments. In the model, SO2 oxidation proceeds in three phases including the gas phase, the inorganic-salted aqueous phase (non-dust phase), and the dust phase. Dust chemistry is described as the adsorption-desorption kinetics (gas-particle partitioning) of SO2 and NOx. The reaction of adsorbed SO2 on dust particles occurs via two major paths: autoxidation of SO2 in open air and photocatalytic mechanisms under UV light. The kinetic mechanism of autoxidation was first leveraged using controlled indoor chamber data in the presence of Arizona Test Dust (ATD) particles without UV light, and then extended to photochemistry. With UV light, SO2 photooxidation was promoted by surface oxidants (OH radicals) that are generated via the photocatalysis of semiconducting metal oxides (electron–hole theory) of ATD particles. This photocatalytic rate constant was derived from the integration of the combinational product of the dust absorbance spectrum and wave-dependent actinic flux for the full range of wavelengths of the light source. The predicted concentrations of sulfate and nitrate using the AMAR model agreed well with outdoor chamber data that were produced under natural sunlight. For seven consecutive hours of photooxidation of SO2 in an outdoor chamber, dust chemistry at the low NOx level was attributed to 70 % of total sulfate (60 ppb SO2, 290 μg m−3 ATD, and NOx less than 5 ppb). At high NOx (> 50 ppb of NOx with low hydrocarbons), sulfate formation was also greatly promoted by dust chemistry, but it was significantly suppressed by the competition between NO2 and SO2 that both consume the dust-surface oxidants (OH radicals or ozone). The AMAR model, derived in this study with ATD particles, will provide a platform for predicting sulfate formation in the presence of authentic dust particles (e.g. Gobi and Saharan dust).

scholarly journals Simulation of heterogeneous photooxidation of SO<sub>2</sub> and NO<sub><i>x</i></sub> in the presence of Gobi Desert dust particles under ambient sunlight

2018 ◽  
Vol 18 (19) ◽  
pp. 14609-14622 ◽  
Author(s):  
Zechen Yu ◽  
Myoseon Jang
Keyword(s):  
Urban Areas ◽  
Mineral Dust ◽  
Buffering Capacity ◽  
Dust Particles ◽  
Gobi Desert ◽  
Heterogeneous Chemistry ◽  
Desert Dust ◽  
Malachite Green Dye ◽  
Photodegradation Rate ◽  
Nitrate Salts

Abstract. To improve the simulation of the heterogeneous oxidation of SO2 and NOx in the presence of authentic mineral dust particles under ambient environmental conditions, the explicit kinetic mechanisms were constructed in the Atmospheric Mineral Aerosol Reaction (AMAR) model. The formation of sulfate and nitrate was divided into three phases: the gas phase, the non-dust aqueous phase, and the dust phase. In particular, AMAR established the mechanistic role of dust chemical characteristics (e.g., photoactivation, hygroscopicity, and buffering capacity) in heterogeneous chemistry. The photoactivation kinetic process of different dust particles was built into the model by measuring the photodegradation rate constant of an impregnated surrogate (malachite green dye) on a dust filter sample (e.g., Arizona test dust – ATD – and Gobi Desert dust – GDD) using an online reflective UV–visible spectrometer. The photoactivation parameters were integrated with the heterogeneous chemistry to predict the formation of reactive oxygen species on dust surfaces. A mathematical equation for the hygroscopicity of dust particles was also included in the AMAR model to process the multiphase partitioning of trace gases and in-particle chemistry. The buffering capacity of dust, which is related to the neutralization of dust alkaline carbonates with inorganic acids, was included in the model to dynamically predict the hygroscopicity of aged dust. The AMAR model simulated the formation of sulfate and nitrate using experimental data obtained in the presence of authentic mineral dust under ambient sunlight using a large outdoor smog chamber (University of Florida Atmospheric Photochemical Outdoor Reactor, UF-APHOR). Overall, the influence of GDD on the heterogeneous chemistry was much greater than that of ATD. Based on the model analysis, GDD enhanced the sulfate formation mainly via its high photoactivation capability. In the case of NO2 oxidation, dust-phase nitrate formation is mainly regulated by the buffering capacity of dust. The measured buffering capacity of GDD was 2 times greater than that of ATD, and consequently, the maximum nitrate concentration with GDD was nearly 2 times higher than that with ATD. The model also highlights that in urban areas with high NOx concentrations, hygroscopic nitrate salts quickly form via titration of the carbonates in the dust particles, but in the presence of SO2, the nitrate salts are gradually depleted by the formation of sulfate.

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