Organic Nitrate Contribution to New Particle Formation and Growth in Secondary Organic Aerosols from α-Pinene Ozonolysis

被引:44
|
作者
Berkemeier, Thomas [1 ]
Ammann, Markus [2 ]
Mentel, Thomas F. [3 ]
Poeschl, Ulrich [1 ]
Shiraiwa, Manabu [1 ]
机构
[1] Max Planck Inst Chem, Multiphase Chem Dept, D-55128 Mainz, Germany
[2] Paul Scherrer Inst, Environm Chem Lab, CH-5232 Villigen, Switzerland
[3] Forschungszentrum Julich, Inst Energy & Climate Res, IEK 8, D-52425 Julich, Germany
基金
瑞士国家科学基金会;
关键词
BETA-PINENE; TROPOSPHERIC DEGRADATION; MASS-SPECTROMETRY; KINETIC REGIMES; NO3; OXIDATION; OH RADICALS; PHASE; CHEMISTRY; MECHANISM; ISOPRENE;
D O I
10.1021/acs.est.6b00961
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The chemical kinetics of organic nitrate production during new particle formation and growth of secondary organic aerosols (SOA) were investigated using the short-lived radioactive tracer N-13 in flow-reactor studies of a-pinene oxidation with ozone. Direct and quantitative measurements of the nitrogen content indicate that organic nitrates accounted for similar to 40% of SOA mass during initial particle formation, decreasing to similar to 15% upon particle growth to the accumulation-mode size range (>100 nm). Experiments with OH scavengers and kinetic model results suggest that organic peroxy radicals formed by a-pinene reacting with secondary OH from ozonolysis are key intermediates in the organic nitrate formation process. The direct reaction of a-pinene with NO3 was found to be less important for particle-phase organic nitrate formation. The nitrogen content of SOA particles decreased slightly upon increase of relative humidity up to 80%. The experiments show a tight correlation between organic nitrate content and SOA particle-number concentrations, implying that the condensing organic nitrates are among the extremely low volatility organic compounds (ELVOC) that may play an important role in the nucleation and growth of atmospheric nanoparticles.
引用
收藏
页码:6334 / 6342
页数:9
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