English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
 
 
DownloadE-Mail
  Using total OH reactivity to assess isoprene photooxidation via measurement and model

Nölscher, A. C., Butler, T., Auld, J., Veres, P., Muñoz, A., Taraborrelli, D., et al. (2014). Using total OH reactivity to assess isoprene photooxidation via measurement and model. Atmospheric Environment, 89, 453-463. doi:10.1016/j.atmosenv.2014.02.024.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Nölscher, A. C.1, Author           
Butler, T.2, Author
Auld, J.1, Author           
Veres, P.1, Author           
Muñoz, A.2, Author
Taraborrelli, D.1, Author           
Vereecken, L.1, Author           
Lelieveld, J.1, Author           
Williams, J.1, Author           
Affiliations:
1Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              
2external, ou_persistent22              

Content

show
hide
Free keywords: -
 Abstract: The Tropics provide a reactive atmospheric environment with high levels of biogenic emissions, rapidly growing anthropogenic influence, high solar radiation and temperature levels. The major reactive biogenic emission is isoprene which reacts rapidly with the primary daytime oxidant OH, the hydroxyl radical. This key photooxidation process has recently been the focus of several experimental and computational studies. A novel isoprene degradation mechanism was recently proposed (MIME) supplementing the commonly used MCM 3.2 scheme. This study examined the photooxidation of isoprene in the controlled conditions of the Valencia atmospheric reaction chamber, EUPHORE (EUropean PHOtoREactor). Besides the detection of isoprene and its major oxidation products formaldehyde, methyl vinyl ketone (MVK) and methacrolein (MACR), the total loss rate of OH (total OH reactivity) was measured. The total OH reactivity was compared to the individual measurements of isoprene and its oxidation products to assess the significant contributors to the overall OH loss rate. Measured total OH reactivity showed excellent agreement to the calculation based on individual compounds detected by a Proton-Transfer-Reaction-Time-Of-Flight-Mass-Spectrometer (PTR-TOF-MS). On average 97% of the measured total OH reactivity could be explained by isoprene and its major oxidation products. Total OH reactivity was also compared to various isoprene degradation schemes to evaluate known mechanisms. The MCM 3.2 isoprene mechanism reproduced the temporal degradation of total OH reactivity (and isoprene) reasonably well with a 57% (and 95%) agreement within the model uncertainties and a linear curve fit slope of 0.69 (and 1.02) for a model to measurement correlation. Large discrepancies between modeled values and all observed compounds were found for the recent isoprene oxidation scheme in MIME. Possible mechanistic reasons are discussed and improvements proposed. The subsequently modified version of MIME differed from the measured total OH reactivity only about 12% at the end of the experiment and represented best the overall temporal profile (linear curve fit slope of correlation: 0.95). (C) 2014 Elsevier Ltd. All rights reserved.

Details

show
hide
Language(s):
 Dates: 2014-06
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Atmospheric Environment
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Oxford [England] : Pergamon
Pages: - Volume / Issue: 89 Sequence Number: - Start / End Page: 453 - 463 Identifier: ISSN: 1352-2310
CoNE: https://pure.mpg.de/cone/journals/resource/958480288336