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Measurement and Interpretation of Low Levels of Dissolved Oxygen in Ground Water
Author(s) -
White Art F.,
Peterson Maria L.,
Solbau Ray D.
Publication year - 1990
Publication title -
groundwater
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 94
eISSN - 1745-6584
pISSN - 0017-467X
DOI - 10.1111/j.1745-6584.1990.tb01715.x
Subject(s) - chemistry , oxygen , absorbance , environmental chemistry , stoichiometry , titration , selenium , inorganic chemistry , detection limit , seawater , hexavalent chromium , chromium , analytical chemistry (journal) , chromatography , geology , oceanography , organic chemistry
A Rhodazine‐D colorimetric technique was adapted to measure low‐level dissolved oxygen concentrations in ground water. Prepared samples containing between 0 and 8.0 μmoles · 1 ‐1 dissolved oxygen in equilibrium with known gas mixtures produced linear spectrophotometric absorbance with a lower detection limit of 0.2 μmoles · 1 ‐1 . Excellent reproducibility was found for solutions ranging in composition from deionized water to sea water with chemical interferences detected only for easily reduced metal species such as ferric ion, cupric ion, and hexavalent chromium. Such effects were correctable based on parallel reaction stoichiometries relative to oxygen. The technique, coupled with a downhole wire line tool, permitted low‐level monitoring of dissolved oxygen in wells at the selenium‐contaminated Kesterson Reservoir in California. Results indicated a close association between low but measurable dissolved oxygen concentrations and mobility of oxidized forms of selenium in the shallow aquifer which were in general electrochemical disequilibrium.