Synergy between ozonation and GAC filtration for chlorinated ethenes-contaminated groundwater treatment

Chlorinated ethenes are among the most frequently occurring groundwater contaminants. Pump and granular activated carbon (GAC) treatment is frequently applied to limit the spreading from point contaminations. Perchloroethene (PCE) and trichloroethene (TCE) sorb well to GAC, but dichloroethene (DCE) and vinyl chloride (VC) sorb poorly, thereby defining a low efficiency seen as amounts of GAC used. On the other hand, ozone reacts fast with VC and DCE, but slowly with PCE and TCE. We utilise for the first time the synergy between ozonation and GAC to treat chlorinated ethenes-contaminated groundwater as an upgrade to an existing GAC treatment installation. Laboratory experiments confirmed that VC and trans-DCE could be >90% removed with just 0.23 g O-3/m(3), corresponding to 0.18 mg O-3/mg DOC. For cis-DCE, 1,1-DCE and TCE, ozone doses of 0.86, 0.87 and 2.8 mg O-3/mg DOC, respectively, were required to remove 90%. In full-scale, trans-DCE and 1,1-DCE were completely removed with 1.6 g O-3/m(3), while only 90% of cis-DCE and 50% TCE were removed with this ozone dose. A relationship between extinction of fluorescence from naturally occurring organic matter with ozone, was used to gauge the ozone dose delivered in the full-scale system. This approach predicted precisely the removal of chlorinated ethenes. Finally, based on the obtained results, we estimated that an optimised ozone treatment would increase the lifetime of an activated carbon filters from 1.0 years to 7.2 years.

Automated summary

Chlorinated ethenes are commonly found in groundwater and can be effectively removed through the synergy between ozonation and GAC treatment, with different ozone doses required for different chlorinated ethenes. This approach can significantly increase the lifetime of activated carbon filters in treating chlorinated ethenes-contaminated groundwater.