Electrolytic transformation of ordinance related compounds (ORCs) in groundwater: Laboratory mass balance studies

• Published in: Chemosphere (Oxford) 2006-02, Vol.62 (5), p.689-698
• Main Authors: Wani, Altaf H., O’Neal, Brenda R., Gilbert, David M., Gent, David B., Davis, Jeffrey L.
• Format: Article
• Language: English
• Subjects: Applied sciences; Carbon Radioisotopes - chemistry; Carbon Radioisotopes - metabolism; chemical residues; e − Barrier; Earth sciences; Earth, ocean, space; electrical treatment; Electrochemistry - methods; electrodes; Electrolysis; Electrolytes - chemistry; electrolytic reactive barriers; Electrolytic treatment; Engineering and environment geology. Geothermics; Exact sciences and technology; Explosives; Fresh Water - chemistry; groundwater contamination; Groundwaters; hexahydro-1,3,5-trinitro-1,3,5-triazine; Natural water pollution; ordinance related compounds; organic nitrogen compounds; Pollution; Pollution, environment geology; porous media; RDX; remediation; sand; TNT; Triazines - chemistry; trinitrotoluene; Trinitrotoluene - chemistry; Water Pollutants, Chemical; Water treatment and pollution
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2005.06.012

Electrolytic reactive barriers (e − barriers) consist of closely spaced permeable electrodes installed across a groundwater contaminant plume in a permeable reactive barrier format. Application of sufficient potential to the electrodes results in sequential oxidation and reduction of the target contaminant. The objective of this study was to quantify the mass distribution of compounds produced during sequential electrolytic oxidation and reduction of ordinance related compounds (ORCs) in a laboratory analog to an e − barrier. In this study, a series of column tests were conducted using RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) and TNT (2,4,6-trinitrotoluene) as representative ORCs. The experimental setup consisted of a plexiglass column packed with quartz–feldspar sand to simulate aquifer conditions. A single set of porous electrodes consisting of expanded titanium-mixed metal oxide mesh was placed at the midpoint of the sand column as a one-dimensional analog to an e − barrier. Constant current of 20 mA (variable voltage) was applied to the electrode set. Initial studies involved quantification of reaction products using unlabeled RDX and TNT. Approximately 70% of the influent concentration was transformed, in one pass, through sequential oxidation–reduction for both contaminants. Following the unlabeled studies, 14C labeled RDX and TNT were introduced to determine the mass balance. An activity balance of up to 96% was achieved for both 14C-RDX and 14C-TNT. For both contaminants, approximately 21% of the influent activity was mineralized to 14CO 2. The proportion of the initial activity in the dissolved fraction was different for the two test contaminants. Approximately 30% of the initial 14C-RDX was recovered as unreacted in the dissolved phase. The balance of the 14C-RDX was recovered as non-volatile, non-nitroso transformation products. None of the 14C-RDX was sorbed to the column sand packing. For 14C-TNT approximately 51% of the initial activity was recovered in the dissolved phase, the majority was unreacted TNT. The balance of the 14C-TNT was either sorbed to the sand packing (approximately 24%) or dissolved/mineralized as unidentified ring cleavage products (∼4%).