Use of by-products from integrated steel plants as catalysts for the removal of trichloroethylene from groundwater.

The removal of tricholoroethylene (TCE) has been investigated in this work through the Fenton-like process using different catalytic materials obtained from metallic by-products of the steel industry. These materials are the slag produced during the transformation of molten pig iron produced in a blast furnace into liquid steel (SLD), the dry particles (or dust) obtained from the bag filters installed in the coking installations to minimize diffuse emissions (POCA) and the dry particles obtained from the liquid sludge from the scrubber (LHA). This study aims to explore the potential of these materials for being used as permeable catalytic barriers to treat groundwater polluted with trichloroethylene (TCE). The wastes used as catalysts were chemically and physically characterized to determine their composition and porosity. The results of this study point out that among the different catalysts used LHA showed the highest catalytic activity to degrade TCE using hydrogen peroxide. Moreover, LHA was the most efficient catalyst using hydrogen peroxide due to its higher stoichiometric efficiency. It is thus concluded that LHA has a high potential to be combined with hydrogen peroxide in permeable catalytic barriers to remove organic compounds from groundwater.

Elimination study of the chemotherapy drug tamoxifen by different advanced oxidation processes: Transformation products and toxicity assessment.

Tamoxifen is a chemotherapy drug considered as recalcitrant contaminant (with low biodegradability in conventional activated sludge wastewater treatment), bioaccumulative, ubiquitous, and potentially hazardous for the environment. This work studies the removal of Tamoxifen from water by advanced oxidation processes, paying special attention to the formation of transformation products (TPs) and to the evolution of toxicity (using the Microtox® bioassay) during the oxidation processes. Five types of treatments were evaluated combining different technologies based on ozone, hydrogen peroxide and UV radiation: i) O3, ii) O3/UV, iii) O3/H2O2 (peroxone), iv) UV and v) UV/H2O2. Complete removal of tamoxifen was achieved after 30 min for all the treatments carried out with O3 while a residual concentration (about 10% of initial one) was observed in the treatments based on UV and UV/H2O2 after 4 h of reaction. Eight TPs were tentatively identified and one (non-ionizable molecule) was suspected to be present by using ultra high performance liquid chromatography coupled to high resolution mass spectrometry. An increase of toxicity was observed during all the oxidation processes. In the case of ozone-based treatments that increase was attributed to the presence of some of the TPs identified, whereas in the case of UV-based treatments there was no clear correlation between toxicity and the identified TPs.

UV/H2O2degradation of the antidepressants venlafaxine and O-desmethylvenlafaxine: Elucidation of their transformation pathway and environmental fate.

The aim of the present work is to investigate the removal and transformation of the antidepressants venlafaxine (VFX) and its main metabolite O-desmethylvenlafaxine (DVFX) upon advanced oxidation with UV/H2O2 under lab conditions. High-resolution mass spectrometry (HRMS) analyses were carried out by means of ultra-high pressure liquid chromatography (UHPLC)-linear ion trap high resolution Orbitrap instrument (LTQ-Orbitrap-MS) in order to elucidate the different transformation products (TPs) generated. The depletion of both VFX and DVFX was very significant, with the 99.9% of both compounds eliminated after 5 and 30 min of reaction, respectively. Eleven TPs for VFX and six for DVFX were detected and their molecular structures elucidated by means of MS(2) and MS(3) scans, and the corresponding degradation pathways were proposed. The combined ecotoxicity at different treatment times was evaluated by means of bioluminescence inhibition assays with the marine bacteria Vibrio fischeri. Results showed an increase in the ecotoxicity during the UV/H2O2 experiment, especially at those reaction times where the total abundance of TPs was higher.

Advanced oxidation of the antibiotic sulfapyridine by UV/H2O2: Characterization of its transformation products and ecotoxicological implications.

The aim of the present work is to investigate, under lab-scale conditions, the removal and transformation of the antibiotic sulfapyridine (SPY) upon advanced oxidation with UV/H2O2. High resolution mass spectrometry (HRMS) analyses by means of an ultra-high pressure liquid chromatography (UHPLC)-linear ion trap high resolution Orbitrap instrument (LTQ-Orbitrap-MS) were carried out in order to elucidate the different transformation products (TPs) generated. The abatement (>99%) of the antibiotic was only achieved after 180 min, highlighting its resilience to elimination and its potential persistence in the environment A total of 10 TPs for SPY were detected and their molecular structures elucidated by means of MS(2) and MS(3) scans. Finally, the combined ecotoxicity at different treatment times was evaluated by means of bioluminescence inhibition assays with the marine bacteria Vibrio fischeri.

Adsorption of volatile sulphur compounds onto modified activated carbons: effect of oxygen functional groups.

The effect of physical and chemical properties of activated carbon (AC) on the adsorption of ethyl mercaptan, dimethyl sulphide and dimethyl disulphide was investigated by treating a commercial AC with nitric acid and ozone. The chemical properties of ACs were characterised by temperature programme desorption and X-ray photoelectron spectroscopy. AC treated with nitric acid presented a larger amount of oxygen functional groups than materials oxidised with ozone. This enrichment allowed a significant improvement on adsorption capacities for ethyl mercaptan and dimethyl sulphide but not for dimethyl disulphide. In order to gain a deeper knowledge on the effect of the surface chemistry of AC on the adsorption of volatile sulphur compounds, the quantum-chemical COSMO-RS method was used to simulate the interactions between AC surface groups and the studied volatile sulphur compounds. In agreement with experimental data, this model predicted a greater affinity of dimethyl disulphide towards AC, unaffected by the incorporation of oxygen functional groups in the surface. Moreover, the model pointed out to an increase of the adsorption capacity of AC by the incorporation of hydroxyl functional groups in the case of ethyl mercaptan and dimethyl sulphide due to the hydrogen bond interactions.

H2O2-based oxidation processes for the regeneration of activated carbons saturated with volatile organic compounds of different polarity.

This study reports the sequential regeneration treatment of activated carbons (ACs) saturated with volatile organic compounds (VOCs) of different polarity using H(2)O(2) as oxidizing agent. In this process, VOCs were adsorbed onto the AC and further oxidized by H(2)O(2). A commercial AC was selected and saturated with three different VOCs: two non-polar and hydrophobic VOCs, toluene and limonene, and one polar and hydrophilic VOC, methyl ethyl ketone (MEK). The saturated AC was regenerated with H(2)O(2), and the Fenton reagent for comparison. It was found that regeneration efficiencies obtained with the H(2)O(2) treatment were equal to or even higher than those obtained with the Fenton treatment. The fate of the pre-adsorbed VOCs, once the regeneration process is completed was studied. It was found that this regeneration treatment is limited for non-polar VOCs such as toluene and limonene, as they tend to remain adsorbed onto the ACs after regeneration treatment. Contrarily, MEK tend to be transferred to the bulk phase and react with the generated oxidant species.