A modeling study of the formation of cloud condensation nuclei in the jet regime of aircraft plumes

被引:24
作者
Gleitsmann, G [1 ]
Zellner, R [1 ]
机构
[1] Univ Essen Gesamthsch, Inst Phys & Theoret Chem, D-45117 Essen, Germany
关键词
D O I
10.1029/98JD01733
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The formation of cloud condensation nuclei in the jet regime of a B-747 airliner at cruise has been investigated by modeling studies. Both the formation of H2O/H2SO4 clusters by homogeneous nucleation and the deposition of water vapor on soot particles activated by the adsorption of gaseous H2SO4, sulfuric acid hydrates, and H2O/H2SO4 clusters were taken into account. H2SO4 has been assumed to be formed only by OH oxidation of SO2 in the plume. Whereas at ambient temperatures between 219 and 224 K the heterogeneous condensation leads to ice particles with average diameters between 3.0 and 1.1 mu m for soot emission indices of EI(soot) = (0.05 - 0.5) g/kg, respectively, no heterogeneous condensation occurs at higher temperatures. Homogeneously nucleated H2O/H2SO4 clusters, on the other hand, have diameters of less than 7 nm and do not contribute to visible contrail formation. Assuming different sulfur emission indices (0.1 g/kg less than or equal to EI(SO2) less than or equal to 10 g/kg), we conclude that the contrail onset is essentially independent of this quantity and that a fractional H2SO4 surface coverage corresponding to a 0.1 monolayer (ML = 0.1) must be sufficient to activate the soot:particles for H2O uptake, at least for EI(SO2) greater than or equal to 0.5 g/kg fuel. Calculations based on higher threshold values (i.e., 0.1 < ML less than or equal to 0.3) lead to results which are in disagreement with the onset of contrail formation as deduced by visual observations. Moreover, the present modeling study provides an estimate of the effect of mutual coupling of homogeneous and heterogeneous condensation pathways.
引用
收藏
页码:19543 / 19555
页数:13
相关论文
共 43 条
[31]   Reactive uptake and hydration experiments on amorphous carbon treated with NO2, SO2, O-3, HNO3, and H2SO4 [J].
Rogaski, CA ;
Golden, DM ;
Williams, LR .
GEOPHYSICAL RESEARCH LETTERS, 1997, 24 (04) :381-384
[32]  
Sabinina L, 1935, Z PHYS CHEM A-CHEM T, V173, P237
[33]   In situ observations of particles in jet aircraft exhausts and contrails for different sulfur-containing fuels [J].
Schumann, U ;
Strom, J ;
Busen, R ;
Baumann, R ;
Gierens, K ;
Krautstrunk, M ;
Schroder, FP ;
Stingl, J .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D3) :6853-6869
[34]  
SEINFELD J, 1986, ATMOSPHERIC CHEM PHY, P307
[35]  
Smoluchowski M, 1917, Z PHYS CHEM, V92, P129, DOI DOI 10.1515/ZPCH-1918-9209
[36]   THE MECHANISM OF THE HO-SO2 REACTION [J].
STOCKWELL, WR ;
CALVERT, JG .
ATMOSPHERIC ENVIRONMENT, 1983, 17 (11) :2231-2235
[37]  
STRAUSS B, 1994, IMPACT EMISSIONS AIR, P396
[38]   Time lag effects on the binary homogeneous nucleation of aerosols in the wake of an aircraft [J].
Taleb, DE ;
McGraw, R ;
Mirabel, P .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (11D) :12885-12890
[39]   CHEMISTRY IN PLUMES OF HIGH-FLYING AIRCRAFT WITH H-2 COMBUSTION ENGINES - A MODELING STUDY [J].
WEIBRING, G ;
ZELLNER, R .
ANNALES GEOPHYSICAE-ATMOSPHERES HYDROSPHERES AND SPACE SCIENCES, 1994, 12 (05) :403-408
[40]  
WORLD METEOROLOGICAL ORGANIZATION, 1995, 37 WMO GLOB OZ RES M