Jet engine exhaust chemiion measurements:: Implications for gaseous SO3 and H2SO4

被引:38
作者
Arnold, F
Stilp, T
Busen, R
Schumann, U
机构
[1] Max Planck Inst Kernphys, Atmoshper Phys Div, D-69029 Heidelberg, Germany
[2] DLR, Inst Phys Atmosphar, D-82230 Wessling, Germany
关键词
jet exhaust ions; S(VI);
D O I
10.1016/S1352-2310(97)00400-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We have made mass spectrometric measurements of negative chemiions (CI) in the exhaust of a jet engine on the ground. The measurements took place at plume ages between 6.6 and 19 ms at low- and high-fuel sulfur content (FSC). Total negative CI-number densities reached up to 1.4.10(7) cm(-3) corresponding to an emission index for negative CI of 3 x 10(15) CI per kg fuel. The most abundant negative CI species were found to be HSO4-H2SO4, HSO4-SO3, HSO4-HNO3, and NO3-(HNO3)(m). Probably HSO4--containing ions are formed from NO3--containing ions by reactions with SO3 and gaseous sulfuric acid (GSA). Hence our experiments indicate the presence of SO3 and GSA. Building on this ion reaction scheme the S(VI) number density (S(VI) = SO3 + H2SO4) was inferred from the CI-composition measurements. For low FSC one obtains (S(VI)) = 6.4 x 10(11) cm(-3) which corresponds to an efficiency for fuel sulfur conversion to gaseous S(VI) of epsilon = 0.012. Our findings have important implications for bimolecular H2SO4-H2O-nucleation in jet aircraft exhaust plumes at cruise altitudes. New aerosol particles may form via homogeneous and/or CI-induted nucleation while heterogeneous nucleation on soot particles may activate soot particles to become water vapour condensation nuclei. Our findings imply that nucleation and condensational growth are more efficient than predicted by most previous models which assumed smaller epsilon. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3073 / 3077
页数:5
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