Oxidation of atomic mercury by hydroxyl radicals and photoinduced decomposition of methylmercury species in the aqueous phase

• The rate constant for Hg0+.OH, kHg0+.OH=(2.4±0.3)×109 M−1 s−1, in the aqueous phase was determined using a relative rate technique with methyl mercury as reference compound. The .OH initiated mercury reaction proceeds via the molecular Hg(I) radical which is oxidised to Hg(II) by dissolved O2. The reaction can be of importance under certain atmospheric circumstances, such as when the aqueous phase capacity of forming OH radicals is significant and the gas phase concentration of ozone drops. The same end product, i.e. Hg(II) was observed from the photodegradation of methylmercury hydroxide. In this case, molecular Hg(I) radicals are again likely to be formed after photodegradation of the Hg–C bond with subsequent oxidation. A lifetime of 230 h of methylmercury at outdoor conditions was estimated due to this reaction. The action of .OH on methylmercury species also involves breaking of organometallic bonds and formation of Hg(II). Speciation of these reaction products from methylmercury is important for the estimation of biogeochemical cycling of mercury.

Subject headings

NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Meteorologi och atmosfärforskning (hsv//swe)

NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Meteorology and Atmospheric Sciences (hsv//eng)

NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Miljövetenskap (hsv//swe)

NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Environmental Sciences (hsv//eng)

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)

NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Biogeochemical cycling

Flux

Photolysis

Redox reactions

Biogeochemical cycling

Publication and Content Type

ref (subject category)

art (subject category)