PHOTOOXIDATION OF SELECTED CARBONYL COMPOUNDS IN AIR: METHYL ETHYL KETONE, METHYL VINYL KETONE, METHACROLEIN AND METHYLGLYOXAL

Author(s):  
Waltraud H. Raber ◽  
Geert K. Moortgat
Atmosphere ◽  
2020 ◽  
Vol 11 (8) ◽  
pp. 793
Author(s):  
Akira Tani ◽  
Kana Muramatsu ◽  
Tomoki Mochizuki

Methacrolein (MACR) and methyl vinyl ketone (MVK) are key intermediate compounds in isoprene-initiated reactions, and they cause the formation of secondary organic aerosols and photochemical ozone. The importance of higher plants as a sink of these compounds and as a source of volatiles converted from these compounds was addressed in the present study. We exposed four non-isoprene-emitting plant species to MACR and MVK at concentrations of several to several hundred ppb, measured their uptake rates, and analyzed the volatiles converted from MACR and MVK by these plants. We used a flow-through chamber method to determine the exchange rates. Both MACR and MVK were absorbed by all plants via stomata. Two metabolites, methyl ethyl ketone (MEK) and 2-butanol, were detected when MVK was fumigated. The conversion ratio was 26–39% for MEK and 33–44% for all volatiles. Combined with the results of two previous relevant reports, our results suggest that MEK conversion from MVK normally occurs in a wide range of plant species, but the conversion ratio may depend on plant type, i.e., if plant species are isoprene-emitting or non-emitting, as well as on the fumigation concentrations. This finding also emphasizes the importance of bilateral exchange measurements of these compounds at lower concentrations close to ambient levels.


2009 ◽  
Vol 6 (5) ◽  
pp. 389 ◽  
Author(s):  
Hongli Wang ◽  
Xuan Zhang ◽  
Zhongming Chen

Environmental context. Carbonyl compounds, a class of oxygenated organic matter, are crucial participants in atmospheric processes. Recently, studies have shown that the aqueous-phase processes of carbonyls have an important contribution to the formation of secondary organic aerosol (SOA), which is considered to have a significant impact on global climate change and human health. We developed the classical DNPH/HPLC method to characterise the aqueous-phase carbonyls, especially methacrolein, methyl vinyl ketone, glyoxal, and methylglyoxal, which are important precursors of SOA, in order to better understand the pathways of SOA formation in the atmosphere. Abstract. The DNPH/HPLC method for characterising monocarbonyls and dicarbonyls in the aqueous phase has been developed. A series of experiments have been carried out using eight atmospheric ubiquitous carbonyl compounds as model dissolved compounds in both acetonitrile and water solution to obtain the optimal derivatisation and analysis qualifications. Compared with the analysis of carbonyls dissolved in acetonitrile, the influence of acidity on the derivatisation efficiency should be carefully considered in determining carbonyls in water and the optimal acidity is pH 2.0. We find that methyl vinyl ketone (MVK) transforms to crotonaldehyde during the derivatisation reaction. This transformation can be controlled to a minor degree by increasing the mixing ratio of DNPH to MVK up to 100 : 1. This improved method has been satisfactorily applied to laboratory simulations and field measurements for better understanding the carbonyl chemistry in the atmosphere.


2018 ◽  
Vol 20 (29) ◽  
pp. 19373-19381 ◽  
Author(s):  
Arkke J. Eskola ◽  
Malte Döntgen ◽  
Brandon Rotavera ◽  
Rebecca L. Caravan ◽  
Oliver Welz ◽  
...  

Reactions of Criegee intermediate CH2OO with unsaturated carbonyl compounds form secondary ozonide products.


1991 ◽  
Vol 47 (1) ◽  
pp. 329-336 ◽  
Author(s):  
Seizo Masuda ◽  
Keiji Minagawa ◽  
Masami Tanaka ◽  
Yutaka Asahi

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