Abstract

Photochemical production is usually considered to be the main source of H2O2 in freshwater systems; here we show that significant dark production also occurs. We used isotope-labeled H2O2 as a tracer to simultaneously determine H2O2 production and decay rates in incubations of unfiltered water samples. Our new technique for H2(18)O2 analysis, requiring only small sample volumes and simple field equipment, allows for preservation of samples in remote locations, followed by gas chromatography mass spectrometry (GCMS) analysis up to six days later. Dark H2O2 production rates of 29-122 nM/h were observed in several lakewater samples. Measured production and decay rates were consistent with pseudo steady-state, early morning [H2O2] measurements made in each water body. Dark H2O2 production is likely to be more important than photochemical production for the total H2O2 budget over 24 h in the freshwater systems we examined. Our results imply that processes usually assumed to be photochemically induced in freshwaters, such as metal redox cycling mediated by H2O2 and O2(-), and production of strong oxidants from the reaction of H2O2 with Fe(II) (Fenton's reaction) could also be occurring at significant rates in the absence of light.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call