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HOMER SIGNED

Hydrocarbon Oxidation Mechanisms Elucidated from Radical scavenging

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 HOMER project word cloud

Explore the words cloud of the HOMER project. It provides you a very rough idea of what is the project "HOMER" about.

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Project "HOMER" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF BRISTOL 

Organization address
address: BEACON HOUSE QUEENS ROAD
city: BRISTOL
postcode: BS8 1QU
website: www.bristol.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2016
 Duration (year-month-day) from 2016-04-04   to  2018-04-03

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF BRISTOL UK (BRISTOL) coordinator 195˙454.00

Map

 Project objective

Oxidation reactions of hydrocarbons are of central importance to both atmospheric and combustion chemistry, where they play a pivotal role in determining the capacity of a hydrocarbon to persist in the air or burn as a fuel. However, quantitative and complete measurements of the mechanisms by which oxidation occurs are very uncommon. Yet it is these mechanisms that ultimately determine the chemistry, influencing such diverse processes as tropospheric ozone production, secondary organic aerosol formation, soot formation and autoignition of fuels. Conventional approaches typically involve mimicking atmospheric or combustion conditions within a chemical reactor. Common to both of these chemical regimes are the phenomena of radical chain propagation, radical–radical reactions and multiple reaction pathways, leading to complex reaction mixtures that evolve rapidly with time. Subsequent gas samples are subjected to detailed and often ambiguous interpretation, placing high demands on detailed chemical models in which only a small proportion of the reactions described within underwent direct experimental measurement. This fellowship seeks to challenge these existing approaches with an alternative methodology in which the short-lived initial products of oxidation, the alkyl radicals, are rapidly converted into stable halogenated species before reaction mixtures become complex, providing crucial information on the fundamental reaction steps at work in these systems. These mixtures will be analyzed by conventional, low cost gas-chromatography methodologies, where the inherent sensitivity and discriminating power of the electron-capture detector towards halocarbons will be exploited. By combining this technique with recent insights into radical scavenging using molecular halogens, a unique and diverse apparatus emerges, which will be used to interrogate several classes of reaction.

 Publications

year authors and title journal last update
List of publications.
2017 Max R. McGillen, Basile F.E. Curchod, Rabi Chhantyal-Pun, Joseph M. Beames, Nathan Watson, M. Anwar H. Khan, Laura McMahon, Dudley E. Shallcross, Andrew J. Orr-Ewing
Criegee Intermediate–Alcohol Reactions, A Potential Source of Functionalized Hydroperoxides in the Atmosphere
published pages: 664–672, ISSN: 2472-3452, DOI: 10.1021/acsearthspacechem.7b00108
ACS Earth and Space Chemistry 1 2019-06-13
2017 Rabi Chhantyal-Pun, Max R. McGillen, Joseph M. Beames, M. Anwar H. Khan, Carl J. Percival, Dudley E. Shallcross, Andrew J. Orr-Ewing
Temperature-Dependence of the Rates of Reaction of Trifluoroacetic Acid with Criegee Intermediates
published pages: 9044-9047, ISSN: 1433-7851, DOI: 10.1002/anie.201703700
Angewandte Chemie International Edition 56/31 2019-06-13

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