Title of article :
Why ozonolysis may not increase the hydrophilicity of particles
Author/Authors :
McIntire، نويسنده , , T.M. and Ryder، نويسنده , , O.S. and Gassman، نويسنده , , P.L. and Zhu، نويسنده , , Z. and Ghosal، نويسنده , , S. and Finlayson-Pitts، نويسنده , , B.J.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2010
Pages :
6
From page :
939
To page :
944
Abstract :
It is commonly assumed that atmospheric oxidation of hydrocarbon particles or hydrocarbon coatings on particles leads to polar products and increased water uptake, altering atmospheric visibility and increasing the likelihood they will act as cloud condensation nuclei (CCN). We show here through laboratory experiments that increased water uptake depends on the 3-dimensional structure of the particles. Laboratory studies of particles formed during ozonolysis of surface-bound alkenes, present as terminally unsaturated self-assembled monolayers (C8= SAM) on a silica substrate, were carried out at room temperature and 1 atm pressure. SAMs were exposed to ∼1013 O3 molecules cm−3 for 40 min and resultant particles were analyzed using single particle Fourier transform infrared micro-spectroscopy (micro-FTIR) and secondary ion mass spectroscopy (SIMS). Spectroscopy results show that –COOH and other polar groups are formed but are buried inside a hydrophobic shell, consistent with earlier observations (McIntire et al., 2005; Moussa et al., 2009) that water uptake does not increase after reaction of the terminal alkene with O3. These insights into the 3-D structure of particles formed on oxidation have important implications for the ability of secondary organic aerosols to act as CCN. In addition, the nature of the surface of the particles is expected to determine their uptake into biological systems such as the surface of the lungs.
Keywords :
secondary organic aerosol , Ozonolysis , Organic oxidation , water uptake , NanoSIMS , FTIR , Self-assembled monolayer
Journal title :
Atmospheric Environment
Serial Year :
2010
Journal title :
Atmospheric Environment
Record number :
2235955
Link To Document :
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