scispace - formally typeset
Open AccessJournal ArticleDOI

The role of VOC oxidation products in continental new particle formation

Reads0
Chats0
TLDR
In this article, the role of oxidation products of VOC's such as mono-and sesquiterpenes in atmospheric nucleation events was investigated using the Tandem Differential Mobility Analyzer results.
Abstract
Aerosol physical and chemical properties and trace gas concentrations were measured during the QUEST field campaign in March-April 2003, in Hyytiala, Finland. Our aim was to understand the role of oxidation products of VOC's such as mono- and sesquiterpenes in atmospheric nucleation events. Particle chemical compositions were measured using the Aerodyne Aerosol Mass Spectrometer, and chemical compositions of aerosol samples collected with low-pressure impactors and a high volume sampler were analysed using a number of techniques. The results indicate that during and after new particle formation, all particles larger than 50 nm in diameter contained similar organic substances that are likely to be mono- and sesquiterpene oxidation products. The oxidation products identified in the high volume samples were shown to be mostly aldehydes. In order to study the composition of particles in the 10-50 nm range, we made use of Tandem Differential Mobility Analyzer results. We found that during nucleation events, both 10 and 50 nm particle growth factors due to uptake of ethanol vapour correlate strongly with gas-phase monoterpene oxidation product (MTOP) concentrations, indicating that the organic constituents of particles smaller than 50 nm in diameter are at least partly similar to those of larger particles. We furthermore showed that particle growth rates during the nucleation events are correlated with the gas-phase MTOP concentrations. This indicates that VOC oxidation products may have a key role in determining the spatial and temporal features of the nucleation events. This conclusion was supported by our aircraft measurements of new 3-10 nm particle concentrations, which showed that the nucleation event on 28 March 2003, started at the ground layer, i.e. near the VOC source, and evolved together with the mixed layer. Furthermore, no new particle formation was detected upwind away from the forest, above the frozen Gulf of Bothnia.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Climate change, phenology, and phenological control of vegetation feedbacks to the climate system

TL;DR: In this paper, the authors discuss the environmental drivers of phenology, and the impacts of climate change on phenology in different biomes, and assess the potential impact on these feedbacks of shifts in phenology driven by climate change.
Journal ArticleDOI

Nucleation and Growth of Nanoparticles in the Atmosphere

TL;DR: Nucleation and Growth of Nanoparticles in the Atmosphere Renyi Zhang,* Alexei Khalizov, Lin Wang, Min Hu, and Wen Xu.
Journal ArticleDOI

Atmospheric composition change – global and regional air quality

Paul S. Monks, +68 more
TL;DR: A review of the state of scientific understanding in relation to global and regional air quality is outlined in this article, in terms of emissions, processing and transport of trace gases and aerosols.
Journal ArticleDOI

Phenology feedbacks on climate change

TL;DR: A longer growing season as a result of climate change will in turn affect climate through biogeochemical and biophysical effects, and the magnitude and sign of this effect are unknown but depend on water availability and regional characteristics.
References
More filters
Journal ArticleDOI

Development of an Aerosol Mass Spectrometer for Size and Composition Analysis of Submicron Particles

TL;DR: In this article, the authors describe an aerosol mass spectrometer (AMS) which has been developed in response to these aerosol sampling needs and demonstrate quantitative mea surement capability for a laboratory-generated pure component NH4 NO3 aerosol.
Journal ArticleDOI

Ambient aerosol sampling using the Aerodyne Aerosol Mass Spectrometer

TL;DR: The Aerodyne Aerosol Mass Spectrometer (AMS) as mentioned in this paper was designed to measure size-resolved mass distributions and total mass loadings of volatile and semivolatile chemical species in/on submicron particles.
Journal ArticleDOI

Stable sulphate clusters as a source of new atmospheric particles

TL;DR: Results from an aerosol dynamics model with a ternary nucleation scheme indicate that nucleation in the troposphere should be ubiquitous, and yield a reservoir of thermodynamically stable clusters 1–3 nm in size.
Journal ArticleDOI

A generalised method for the extraction of chemically resolved mass spectra from aerodyne aerosol mass spectrometer data

TL;DR: A generalised method for deconvolution of mass spectral data from the aerodyne aerosol mass spectrometer (AMS) is presented in this paper, which is designed to arithmetically separate the raw data into partial mass spectra for distinct chemical species.
Journal ArticleDOI

Quantitative sampling using an Aerodyne aerosol mass spectrometer 1. Techniques of data interpretation and error analysis

TL;DR: In this paper, the authors used the quadrupole mass spectrometer (AMS) during the mass spectrum (MS) mode of operation to estimate the chemical composition and size of volatile and semivolatile fine airborne particulate matter.
Related Papers (5)

Evolution of Organic Aerosols in the Atmosphere

Jose L. Jimenez, +66 more
- 11 Dec 2009 -