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Degradation of TCE with Iron: The Role of Competing Chromate and Nitrate Reduction
Author(s) -
Schlicker Oliver,
Ebert Markus,
Fruth Margit,
Weidner Markus,
Wüst Wolfgang,
Dahmke Andreas
Publication year - 2000
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.1745-6584.2000.tb00226.x
Subject(s) - chromate conversion coating , nitrate , chemistry , passivation , zerovalent iron , metal , environmental chemistry , sulfate , inorganic chemistry , chromium , adsorption , organic chemistry , layer (electronics)
This study evaluates the potential of using granular iron metal for the abiotic removal of the organic ground water pollutant trichloroethene (TCE) in the presence of the common inorganic co‐contaminants chromate and nitrate, respectively. Our long‐term column experiments indicate a competitive process between TCE dechlorination and reductive transformation of chromate and nitrate, which is reflected in a significantly delayed onset of TCE dechlorination. Delay times and therefore the ranges of the nonreactive flowpaths increased with increasing experimental duration, resulting in a migration of the contaminants through the iron metal treatment zone. The present investigation also indicates that the calculated migration rates of TCE and the added cocontaminants chromate and nitrate are linearly related to the initial content of the cocontaminants. With an average pore water velocity of 0.6 m/d and a surface area concentration of 0.55 m2/mL in the column, the calculated migration rates varled between 0.10 cm/d and 5.86 cm/d. The particular similarity between the values of TCE migration and the migration of the strong oxidants chromate and nitrate and the long‐term steady state of the TCE dechlorination in the absence of the chromate and nitrate indicates that these competitive transformations are the driving force for the gradual passivation of the granular iron due to the buildup of an electrically insulating Fe(III)‐oxyhydroxide. Based on these passivation processes, general formulae were developed that allow a simplified approximation of breakthrough times for the contaminants TCE, chromate, and nitrate.