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IN SITU MEASUREMENT OF ADSORPTION AND BIOTRANSFORMATION AT A HAZARDOUS WASTE SITE 1
Author(s) -
Borden Robert C.,
Bedient Philip B.
Publication year - 1987
Publication title -
jawra journal of the american water resources association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.957
H-Index - 105
eISSN - 1752-1688
pISSN - 1093-474X
DOI - 10.1111/j.1752-1688.1987.tb00837.x
Subject(s) - naphthalene , biotransformation , environmental chemistry , chemistry , groundwater , tracer , hazardous waste , adsorption , limiting , environmental science , chloride , contamination , environmental engineering , waste management , organic chemistry , geology , geotechnical engineering , mechanical engineering , ecology , physics , nuclear physics , engineering , biology , enzyme
ABSTRACT: A three well injection‐production test was performed at the United Creosoting Company (UCC) site in Conroe, Texas, to estimate the effective in situ retardation factors for adsorption and to evaluate the significance of biotransformation in limiting the transport of polycydic aromatics present in the shallow aquifer. The field test was also used as a model to determine if this type of testing would be feasible at other hazardous waste sites. During the test, chloride, a non‐reactive tracer and two organic compounds, naphthalene and paradichlorobenzene (pDCB), were injected into a center well for 24 hours followed by clean ground water for six days. Ground water was continuously produced from two adjoining wells and monitored to observe the breakthrough of these compounds. Data from the test were analyzed by comparing the statistical moments of the chloride and organics distributions. Retardation factors for naphthalene and pDCB were estimated to be 1.03 and 0.97 by comparison of the statistical moments. A significant loss of naphthalene and pDCB was also observed during the three well test, apparently due to biotransformation. These results suggest that biotransformation is the major process limiting the transport of naphthalene and similar compounds at the UCC site.