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Uptake of formaldehyde by sulfuric acid solutions: Impact on stratospheric ozone
Author(s) -
Tolbert Margaret A.,
Pfaff Jeanne,
Jayaweera Indira,
Prather Michael J.
Publication year - 1993
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/92jd02386
Subject(s) - sulfuric acid , stratosphere , ozone , formaldehyde , chlorine , atmospheric chemistry , trace gas , chemistry , chemical reaction , volcanic gases , reactivity (psychology) , ozone layer , environmental chemistry , inorganic chemistry , atmospheric sciences , volcano , geology , organic chemistry , medicine , alternative medicine , pathology , seismology
Chemical reactions on sulfuric acid aerosols have recently been shown to play an important role in stratospheric chemistry. In particular, these reactions push odd‐nitrogen compounds into HNO 3 and thereby enhance the chlorine‐catalyzed destruction of ozone. It has been suggested that our current set of heterogeneous reactions may be incomplete. Indeed we show that formaldehyde, CH 2 O, is rapidly and irreversibly taken up by stirred sulfuric acid solutions (60 to 75 wt % H 2 SO 4 at −40° to −65°C) with uptake coefficients as large as γ = 0.08. If similar uptake occurs under stratospheric pressures of CH 2 O (that is, 1000 times lower than used in the present study), then the removal of CH 2 O from the gas phase can take away a significant source of odd hydrogen in the mid‐ and high‐latitude lower stratosphere. We show here that with the inclusion of this reaction, concentrations of OH and HO 2 are reduced by as much as 4% under background levels of aerosols and more than 15% under elevated (volcanic) conditions. Further, the accumulation of CH 2 O in stratospheric aerosols over a season may alter the composition and reactivity of these sulfuric acid‐water mixtures.

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