This site is using cookies to collect anonymous visitor statistics and enhance the user experience.  OK | Find out more

Skip to content
Natural Environment Research Council
Grants on the Web - Return to homepage Logo

Details of Award

NERC Reference : NE/G009031/1

Artifical Chemical Ageing of Ambient Atmospheric Aerosol

Grant Award

Principal Investigator:
Professor W Bloss, University of Birmingham, Sch of Geography, Earth & Env Sciences
Co-Investigator:
Professor R Harrison, University of Birmingham, Sch of Geography, Earth & Env Sciences
Science Area:
Atmospheric
Overall Classification:
Atmospheric
ENRIs:
Pollution and Waste
Global Change
Environmental Risks and Hazards
Science Topics:
Pollution
Environment & Health
Atmospheric Kinetics
Tropospheric Processes
Abstract:
Atmospheric aerosol, or suspended condensed phase material, is a pollutant which is harmful to health and ecosystems, provides a reaction medium for gas phase species, and affects visibility and climate, both through direct interaction with atmospheric radiation, and by providing a nucleation site for the condensation of water vapour. The magnitude of these effects depends upon the nature (physical characteristics such as number concentration, size and volatility; chemical characteristics such as composition and hygroscopicity) of the aerosol particles. Aerosol particles are produced both as primary emissions, from a range of natural processes (e.g. dust, sea salt, biomass burning) and anthropogenic activities (primarily related to fossil-fuel combustion and resuspension in urban areas). A substantial secondary source also exists, from the condensation of inorganic species and semi-volatile organic compounds. The composition of aerosol particles changes with time in the atmosphere; low-volatility vapours condense to form new or augment pre-existing particles, notably secondary organic aerosol (SOA) in the case of organic compounds. Particle constituents may also undergo chemical processing, both internally and driven by external reagents, gas-phase oxidants such as OH radicals and ozone. Such oxidation or chemical ageing may change particle physical characteristics (size, volatility) and chemical composition; this in turn may affect particle lifetime, heterogeneous reactivity, interaction with solar radiation and potential to act as cloud condensation nuclei. An understanding of the potential changes ambient particles may undergo is essential to understand their atmospheric role. We aim to investigate these changes by artificially ageing ambient atmospheric aerosol - we will construct a small reactor, in which we will subject ambient aerosol samples to greatly elevated levels of oxidants such as OH, achieving exposures equivalent to several days in the atmosphere, in a matter of minutes. We will then measure the changes in aerosol characteristics using a range of instruments, notably an Aerosol Time-of-Flight Mass Spectrometer, which will permit us to determine changes in specific particle types, and in specific compounds within the particle phase. In this application we aim to demonstrate the application of a chemical ageing reactor coupled to an ATOFMS to investigate the ageing of ambient atmospheric aerosol, and to begin to assess the range of changes in aerosol nature which result. Future application of the technique will allow us to begin to address a range of questions over the fate and evolution of atmospheric aerosol, from general issues such as what are the likely final properties of the particles emitted by a given source or in a given environment, to more specific questions over the fate of particular compounds in the particulate phase - for example, polycyclic aromatic hydrocarbons (PAH) such as benzo(a)pyrene are well-known carcinogenic pollutants, but the processes removing them from the atmosphere are not well understood - as they are strongly partitioned to the condensed phase, removal from the atmospheric system may be driven by gas-phase oxidation, limited by desorption, or by processing in the condensed phase; interpretation of previous laboratory studies of such systems is hindered by the possibility of the PAH being both adsorbed onto particles and being incorporated into the liquid phase within particles: assessment of the oxidation rate using real ambient particles would resolve this issue.
Period of Award:
14 Aug 2009 - 13 Feb 2011
Value:
£35,832
Authorised funds only
NERC Reference:
NE/G009031/1
Grant Stage:
Completed
Scheme:
Small Grants (FEC)
Grant Status:
Closed
Programme:
Small Grants

This grant award has a total value of £35,832  

top of page


FDAB - Financial Details (Award breakdown by headings)

DI - Other CostsIndirect - Indirect CostsDA - InvestigatorsDI - EquipmentDA - Estate CostsDI - T&SDA - Other Directly Allocated
£9,480£3,293£5,729£9,757£1,707£411£5,455

If you need further help, please read the user guide.