Is it possible to remediate a BTEX contaminated chalky aquifer by in situ chemical oxidation?

• Published in: Chemosphere (Oxford) 2011-08, Vol.84 (9), p.1181-1187
• Main Authors: Lemaire, Julien, Croze, Véronique, Maier, Joachim, Simonnot, Marie-Odile
• Format: Article
• Language: English
• Subjects: Applied sciences; Benzene - chemistry; Benzene - isolation & purification; Benzene Derivatives - chemistry; Benzene Derivatives - isolation & purification; BTEX; Calcium Carbonate - chemistry; Carbonates - chemistry; Chemical and Process Engineering; Cities; Drinking; Engineering Sciences; Exact sciences and technology; Industrial Waste - analysis; ISCO; Manganese Compounds - chemistry; Oxidants - chemistry; Oxidation-Reduction; Oxides - chemistry; Percarbonate; Permanganate; Persulfate; Pollution; Sulfates - chemistry; Time Factors; Toluene - chemistry; Toluene - isolation & purification; Water Pollutants, Chemical - chemistry; Water Pollutants, Chemical - isolation & purification; Water Purification - methods; Xylenes - chemistry; Xylenes - isolation & purification
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2011.06.052

► ISCO feasibility was studied for a chalky aquifer contaminated by xylenes. ► Percarbonate did not degrade xylenes in chalk slurry because of radical scavenging. ► Permanganate and Fe(II) activated persulfate were efficient. ► They induced precipitation reactions (MnO 2/siderite). ► Persulfate activation was not mandatory. An industrial coating site in activity located on a chalky plateau, contaminated by BTEX (mainly xylenes, no benzene), is currently remediated by in situ chemical oxidation (ISCO). We present the bench scale study that was conducted to select the most appropriate oxidant. Ozone and catalyzed hydrogen peroxide (Fenton’s reaction) were discarded since they were incompatible with plant activity. Permanganate, activated percarbonate and activated persulfate were tested. Batch experiments were run with groundwater and groundwater-chalk slurries with these three oxidants. Total BTEX degradation in groundwater was reached with all the oxidants. The molar ratios [oxidant]:[Fe 2+]:[BTEX] were 100:0:1 with permanganate, 100:100:1 with persulfate and 25:100:1 with percarbonate. Precipitation of either manganese dioxide or iron carbonate (siderite) occurred. The best results with chalk slurries were obtained with permanganate at the molar ratio 110:0:1 and activated persulfate at the molar ratio 110:110:1. To avoid precipitation, persulfate was also used without activation at the molar ratio 140:1. Natural Oxidant Demand measured with both oxidants was lower than 5% of initial oxidant contents. Activated percarbonate was not appropriate because of radical scavenging by carbonated media. Permanganate and persulfate were both effective at oxidant concentrations of ca 1 g kg −1 with permanganate and 1.8 g kg −1 with persulfate and adapted to site conditions. Activation of persulfate was not mandatory. This bench scale study proved that ISCO remediation of a chalky aquifer contaminated by mainly xylenes was possible with permanganate and activated or unactivated persulfate.