Mechanism of the Degradation of 1,4-Dioxane in Dilute Aqueous Solution Using the UV/Hydrogen Peroxide Process

Abstract

1,4-Dioxane is an EPA priority pollutant often found in contaminated groundwaters and industrial effluents. The common techniques used for water purification are not applicable to 1,4-dioxane, and the currently used method (distillation) is laborious and expensive. This study aims to understand the degradation mechanism of 1,4-dioxane and its byproducts in dilute aqueous solution toward complete mineralization, by using the UV/H 2 O 2 process in a UV semibatch reactor. The decay of 1,4-dioxane generated several intermediates identified and quantified as aldehydes (formaldehyde, acetaldehyde, and glyoxal), organic acids (formic, methoxyacetic, acetic, glycolic, glyoxylic, and oxalic) and the mono- and diformate esters of 1,2-ethanediol. Measurement of the total organic carbon (TOC) during the treatment indicated a good agreement between the experimentally determined TOC values and those calculated from the quantified reaction intermediates, ending in complete mineralization. A reaction mechanism, which accounts for the observed intermediate products and their time profiles during the treatment, is proposed. Considering the efficacy of the 1,4-dioxane removal from dilute aqueous solutions, as shown in this work, the present study can be regarded as a model for industrially affordable Advanced Oxidation Technologies.