scholarly journals Contributions of individual reactive biogenic volatile organic compounds to organic nitrates above a mixed forest

2012 ◽  
Vol 12 (7) ◽  
pp. 17031-17086 ◽  
Author(s):  
K. A. Pratt ◽  
L. H. Mielke ◽  
P. B. Shepson ◽  
A. M. Bryan ◽  
A. L. Steiner ◽  
...  

Abstract. Biogenic volatile organic compounds (BVOCs) can react in the atmosphere to form organic nitrates, which serve as NOx (NO + NO2) reservoirs, impacting ozone and secondary organic aerosol production, the oxidative capacity of the atmosphere, and nitrogen availability to ecosystems. To examine the contributions of biogenic emissions and the formation and fate of organic nitrates in a forest environment, we simulated the oxidation of 57 individual BVOCs emitted from a rural mixed forest in Northern Michigan. Of the total simulated organic nitrates, monoterpenes contributed ~70% in the early morning at ~12 m above the forest canopy when isoprene emissions were low. In the afternoon, when vertical mixing and isoprene nitrate production were highest, the simulated contribution of isoprene-derived organic nitrates was greater than 90% at all altitudes, with the concentration of secondary isoprene nitrates increasing with altitude. Key BVOC-oxidant reactions were identified for future laboratory and field investigations into reaction rate constants, yields, and speciation of oxidation products. Forest succession, wherein aspen trees are being replaced by pine and maple trees, was predicted to lead to increased afternoon concentrations of monoterpene-derived organic nitrates. This further underscores the need to understand the formation and fate of these species, which have different chemical pathways and oxidation products compared to isoprene-derived organic nitrates and can lead to secondary organic aerosol formation.

2012 ◽  
Vol 12 (21) ◽  
pp. 10125-10143 ◽  
Author(s):  
K. A. Pratt ◽  
L. H. Mielke ◽  
P. B. Shepson ◽  
A. M. Bryan ◽  
A. L. Steiner ◽  
...  

Abstract. Biogenic volatile organic compounds (BVOCs) can react in the atmosphere to form organic nitrates, which serve as NOx (NO + NO2) reservoirs, impacting ozone and secondary organic aerosol production, the oxidative capacity of the atmosphere, and nitrogen availability to ecosystems. To examine the contributions of biogenic emissions and the formation and fate of organic nitrates in a forest environment, we simulated the oxidation of 57 individual BVOCs emitted from a rural mixed forest in northern Michigan. Key BVOC-oxidant reactions were identified for future laboratory and field investigations into reaction rate constants, yields, and speciation of oxidation products. Of the total simulated organic nitrates, monoterpenes contributed ~70% in the early morning at ~12 m above the forest canopy when isoprene emissions were low. In the afternoon, when vertical mixing and isoprene nitrate production were highest, the simulated contribution of isoprene-derived organic nitrates was greater than 90% at all altitudes, with the concentration of secondary isoprene nitrates increasing with altitude. Notably, reaction of isoprene with NO3 leading to isoprene nitrate formation was found to be significant (~8% of primary organic nitrate production) during the daytime, and monoterpene reactions with NO3 were simulated to comprise up to ~83% of primary organic nitrate production at night. Lastly, forest succession, wherein aspen trees are being replaced by pine and maple trees, was predicted to lead to increased afternoon concentrations of monoterpene-derived organic nitrates. This further underscores the need to understand the formation and fate of these species, which have different chemical pathways and oxidation products compared to isoprene-derived organic nitrates and can lead to secondary organic aerosol formation.


2017 ◽  
Vol 17 (17) ◽  
pp. 10743-10752 ◽  
Author(s):  
Jianfei Peng ◽  
Min Hu ◽  
Zhuofei Du ◽  
Yinhui Wang ◽  
Jing Zheng ◽  
...  

Abstract. Gasoline vehicle exhaust is an important contributor to secondary organic aerosol (SOA) formation in urban atmosphere. Fuel composition has a potentially considerable impact on gasoline SOA production, but the link between fuel components and SOA production is still poorly understood. Here, we present chamber experiments to investigate the impacts of gasoline aromatic content on SOA production through chamber oxidation approach. A significant amplification factor of 3–6 for SOA productions from gasoline exhausts is observed as gasoline aromatic content rose from 29 to 37 %. Considerably higher emission of aromatic volatile organic compounds (VOCs) using high-aromatic fuel plays an essential role in the enhancement of SOA production, while semi-volatile organic compounds (e.g., gas-phase PAHs) may also contribute to the higher SOA production. Our findings indicate that gasoline aromatics significantly influence ambient PM2. 5 concentration in urban areas and emphasize that more stringent regulation of gasoline aromatic content will lead to considerable benefits for urban air quality.


2020 ◽  
Author(s):  
Junling Li ◽  
Hong Li ◽  
Kun Li ◽  
Yan Chen ◽  
Hao Zhang ◽  
...  

Abstract. Motor vehicle exhaust is one of the important contribution sources of secondary organic aerosol (SOA) in urban areas. Long-chain alkanes and aromatic hydrocarbons are included in gaseous organic pollutants of vehicle emissions, representative for diesel and gasoline vehicles respectively. In this work, the SOA production from individual anthropogenic volatile organic compounds (AVOCs) (n-dodecane, 1,3,5-trimethylbenzene) and mixed AVOCs (n-dodecane + 1,3,5-trimethylbenzene) were studied with a large-scale outdoor smog chamber. Results showed that the SOA formation from the mixed AVOCs was enhanced compared to the predicted SOA mass concentration based on the SOA yield of individual AVOCs. According to the results of mass spectrometry analysis with electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS), interaction occurred between intermediate products from the two precursors, which could be the main reason for the enhanced SOA production from the mixed AVOCs reaction system. This study indicates that further studies on SOA chemistry from the mixed VOCs reaction system are needed, as the interactions between them and the effect on SOA formation can give us a further understanding of the SOA formed in the atmosphere.


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