Laboratory study on new particle formation from the reaction OH + SO2: influence of experimental conditions, H2O vapour, NH3 and the amine tert-butylamine on the overall process

被引:160
作者
Berndt, T. [1 ]
Stratmann, F. [1 ]
Sipilae, M. [1 ,2 ]
Vanhanen, J. [2 ]
Petaja, T. [2 ]
Mikkila, J. [2 ]
Gruener, A. [1 ]
Spindler, G. [1 ]
Mauldin, R. Lee, III [3 ]
Curtius, J. [4 ]
Kulmala, M. [2 ]
Heintzenberg, J. [1 ]
机构
[1] Leibniz Inst Tropospharenforsch eV, D-04318 Leipzig, Germany
[2] Univ Helsinki, Dept Phys, FIN-00014 Helsinki, Finland
[3] Natl Ctr Atmospher Res, Earth & Sun Syst Lab, Div Atmospher Chem, Boulder, CO 80307 USA
[4] Goethe Univ Frankfurt, Inst Atmospher & Environm Sci, D-60438 Frankfurt, Germany
关键词
SULFURIC-ACID-WATER; VOLATILE ORGANIC-COMPOUNDS; SO2; OXIDATION-PRODUCTS; TERNARY NUCLEATION; AEROSOL FORMATION; ALIPHATIC-AMINES; FORMATION EVENTS; H2SO4; AMMONIA; RATES;
D O I
10.5194/acp-10-7101-2010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nucleation experiments starting from the reaction of OH radicals with SO2 have been performed in the IfT-LFT flow tube under atmospheric conditions at 293+/-0.5K for a relative humidity of 13-61%. The presence of different additives (H-2, CO, 1,3,5-trimethylbenzene) for adjusting the OH radical concentration and resulting OH levels in the range (4-300) x 10(5) molecule cm(-3) did not influence the nucleation process itself. The number of detected particles as well as the threshold H2SO4 concentration needed for nucleation was found to be strongly dependent on the counting efficiency of the used counting devices. High-sensitivity particle counters allowed the measurement of freshly nucleated particles with diameters down to about 1.5 nm. A parameterization of the experimental data was developed using power law equations for H2SO4 and H2O vapour. The exponent for H2SO4 from different measurement series was in the range of 1.7-2.1 being in good agreement with those arising from analysis of nucleation events in the atmosphere. For increasing relative humidity, an increase of the particle number was observed. The exponent for H2O vapour was found to be 3.1 representing an upper limit. Addition of 1.2 x 10(11) molecule cm(-3) or 1.2 x 10(12) molecule cm(-3) of NH3 (range of atmospheric NH3 peak concentrations) revealed that NH3 has a measureable, promoting effect on the nucleation rate under these conditions. The promoting effect was found to be more pronounced for relatively dry conditions, i.e. a rise of the particle number by 1-2 orders of magnitude at RH = 13% and only by a factor of 2-5 at RH=47% (NH3 addition: 1.2 x 10(12) molecule cm(-3)). Using the amine tert-butylamine instead of NH3, the enhancing impact of the base for nucleation and particle growth appears to be stronger. Tert-butylamine addition of about 10(10) molecule cm(-3) at RH = 13% enhances particle formation by about two orders of magnitude, while for NH3 only a small or negligible effect on nucleation in this range of concentration appeared. This suggests that amines can strongly influence atmospheric H2SO4-H2O nucleation and are probably promising candidates for explaining existing discrepancies between theory and observations.
引用
收藏
页码:7101 / 7116
页数:16
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