Influence of relative humidity on heterogeneous reactions of O 3 and O 3 /SO 2 with soot particles: Potential for environmental and health effects

2017 ◽  
Vol 165 ◽  
pp. 198-206 ◽  
Author(s):  
Xiang He ◽  
Shufeng Pang ◽  
Jiabi Ma ◽  
Yunhong Zhang
Author(s):  
Muhammad Usman Khan ◽  
Athanasios Besis ◽  
Riffat Naseem Malik

2011 ◽  
Vol 37 (6) ◽  
pp. 1131-1142 ◽  
Author(s):  
Claudia Som ◽  
Peter Wick ◽  
Harald Krug ◽  
Bernd Nowack

RSC Advances ◽  
2019 ◽  
Vol 9 (67) ◽  
pp. 39201-39229 ◽  
Author(s):  
Mohsen M. M. Ali ◽  
Hongtao Zhao ◽  
Zhongyu Li ◽  
Najeeb N. M. Maglas

Crude oil and its products and wastes are among the significant sources of naturally occurring radioactive materials (NORMs).


1986 ◽  
Vol 65 ◽  
pp. 351 ◽  
Author(s):  
Anthony V. Arundel ◽  
Elia M. Sterling ◽  
Judith H. Biggin ◽  
Theodor D. Sterling

2010 ◽  
Vol 10 (7) ◽  
pp. 3261-3272 ◽  
Author(s):  
H.-W. Wong ◽  
R. C. Miake-Lye

Abstract. Condensation trails (contrails) formed from water vapor emissions behind aircraft engines are the most uncertain components of the aviation impacts on climate change. To gain improved knowledge of contrail and contrail-induced cirrus cloud formation, understanding of contrail ice particle formation immediately after aircraft engines is needed. Despite many efforts spent in modeling the microphysics of ice crystal formation in jet regime (with a plume age <5 s), systematic understanding of parametric effects of variables affecting contrail ice particle formation is still limited. In this work, we apply a microphysical parcel modeling approach to study contrail ice particle formation in near-field aircraft plumes up to 1000 m downstream of an aircraft engine in the soot-rich regime (soot number emission index >1×1015 (kg-fuel)−1) at cruise. The effects of dilution history, ion-mediated nucleation, ambient relative humidity, fuel sulfur contents, and initial soot emissions were investigated. Our simulation results suggest that ice particles are mainly formed by water condensation on emitted soot particles. The growth of ice coated soot particles is driven by water vapor emissions in the first 1000 m and by ambient relative humidity afterwards. The presence of chemi-ions does not significantly contribute to the formation of ice particles in the soot-rich regime, and the effect of fuel sulfur contents is small over the range typical of standard jet fuels. The initial properties of soot emissions play the most critical role, and our calculations suggest that higher number concentration and smaller size of contrail particle nuclei may be able to effectively suppress the formation of contrail ice particles. Further modeling and experimental studies are needed to verify if our findings can provide a possible approach for contrail mitigation.


2011 ◽  
Vol 11 (2) ◽  
pp. 5127-5171 ◽  
Author(s):  
J. C. Kaiser ◽  
N. Riemer ◽  
D. A. Knopf

Abstract. We simulate the heterogeneous oxidation of condensed phase polycyclic aromatic hydrocarbons (PAHs) on soot particles in an urban atmosphere using the particle-resolved aerosol model PartMC-MOSAIC. We focus on the interaction of the major atmospheric oxidants (O3, NO2, OH, and NO3) with PAHs and include competitive co-adsorption of water vapour for a range of atmospheric conditions. For the first time detailed heterogeneous chemistry based on the Pöschl-Rudich-Ammann (PRA) framework is modelled on soot particles with a realistic size distribution and a continuous range of chemical ages. We find PAH half-lives τ1/2 on the order of seconds during the night, when the PAHs are rapidly oxidized by the gas-surface reaction with NO3. During the day, τ1/2 is on the order of minutes and determined mostly by the surface layer reaction of PAHs with adsorbed O3. Such short PAH half-lives may lead to efficient conversion of hydrophobic soot into more hygroscopic particles, thus increasing the particles' aerosol-cloud interaction potential. Despite its high reactivity appears to have a negligible effect on PAH degradation which can be explained by its very low concentration in the atmosphere. An increase of relative humidity from 30% to 80% increases PAH half-lives by up to 50% for daytime degradation and by up to 100% or more for nighttime degradation. Uptake coefficients, averaged over the particle population, are found to be relatively constant over time for O3 (~2×10−7 to ~2×10−6) and NO2 (~5×10−6 to ~10−5) at the different levels of NOx emissions and RH considered in this study. In contrast, those for OH and NO3 depend strongly on the surface concentration of PAhs. We do not find a significant influence of heterogeneous reactions on soot particles on the gas phase composition. The PAH half-lives presented in this paper can be used as parameterisations for the treatment of heterogeneous chemistry in large-scale atmospheric chemistry models.


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