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dc.contributor.advisorPeñuela Mesa, Gustavo Antonio
dc.contributor.advisorChica Arrieta, Edwin Lenin
dc.contributor.authorRubio Clemente, Ainhoa
dc.date.accessioned2023-03-17T12:42:57Z
dc.date.available2023-03-17T12:42:57Z
dc.date.created2018
dc.date.issued2018
dc.date.submitted2018-12-21
dc.identifier.urihttp://hdl.handle.net/10952/6108
dc.description.abstractNowadays, polycyclic aromatic hydrocarbons (PAHs) are a group of chemical substances that deserves a great attention. PAHs consist of two or more condensed benzene rings, bonded in linear, cluster or angular arrangements that are ubiquitous in the environment. Due to their low solubility and high affinity for particulate matter, PAHs are found in water in extreme low concentrations, in the range of ng L-1 or µg L-1. However, even at these ultra-trace or trace levels, they exhibit harmful effects on living beings and humans, especially when present as mixtures. That is the case of anthracene (AN), which has been reported as an acute phototoxic compound, and benzo[a]pyrene (BaP), which is a carcinogenic and mutagenic pollutant. Therefore, their presence in the environment and, specifically in aquatic resources must be monitored. For this purpose, the chromatographic behavior of AN and BaP was studied, and three models were found describing the identification of AN and BaP, the quantification of AN and that of BaP. The factors influencing each of the models or indexes were also optimized and a new and fast analytical method allowing the determination of the analytes of interest at ultra-trace concentrations in surface water samples was developed. In addition to monitor the target pollutants, they must be also eliminated from water because of the adverse health effects associated. However, conventional processes water treatment facilities are operating with are not efficient in tackling the problem of AN and BaP pollution in water. In this regard, the implementation of alternative treatments, including advanced oxidation processes (AOPs), provides a very attractive option. AOPs have demonstrated to be highly interesting technologies for water remediation, particularly the combination of ultraviolet radiation in the UV-C range (UV-C) and hydrogen peroxide (H2O2). This Thesis addresses the evaluation of the efficiency of the UV-C/H2O2 oxidation system to treat water sampled from a natural reservoir polluted with AN and BaP. For this purpose, initially, the removal profiles of AN and BaP were investigated, as well as the organic matter mineralization capacity of the oxidation system and the production of innocuous degradation by-products. The system allowed obtaining very positive results in terms of the degradation of the pollutants of interest and the organic matter mineralization, avoiding the production of dangerous reactive intermediates. Furthermore, after the application of this treatment process, a residual H2O2 was observed in the reaction solution, which can be used for additional microbial load removal. The residual H2O2 found within the bulk after the application of the oxidation treatment was analyzed using an analytical method proposed here. Moreover, the oxidation potential of the UV-C/H2O2 process was assessed for the inactivation of wild total coliforms naturally contained in the water of study and the results were compared with the findings obtained from other photochemical technologies based on sonochemical reactions. It was found that the technology achieving the highest microorganism elimination in the shortest time and with the lowest electrical costs results was the UV-C/H2O2 process. Nevertheless, in spite of that, it is worth noting that the implementation of the UV-C/H2O2 oxidation process still requires high electrical needs, which increases the operating costs of the process. Therefore, in order to reduce such as costs, a photovoltaic (PV) array was sized and installed for supplying the energy requirements of the selected water treatment system. The installed PV system allows for the use of renewable energy both in developing and non-developing countries. In this regard, the treatment of water to be drinkable was observed to be plausible in countries with lack of economical resources and in communities far from the electrical grid, which exist in a high number in countries such as Colombia. In the second stage of the research, and taking into account the necessity of having kinetic models for finding out the optimal operating conditions without the necessity of conducting extensive experimentation, a kinetic model for the performance of the UV-C/H2O2 oxidation process was constructed and validated using a model compound. The kinetic model allows calculating the optimal level of H2O2 for efficiently degrading the pollutant of interest, as well as the effective level of HO• to be maintained throughout the reaction time of the UV-C/H2O2 system for achieving an efficient pollutant degradation, contributing to save costs and time.es
dc.language.isoenes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectContaminación del Aguaes
dc.subjectCinética Químicaes
dc.subjectEnergía Solares
dc.titleDegradation of polycyclic aromatic hydrocarbons in water: Alternative treatments to conventional processes.es
dc.typedoctoralThesises
dc.rights.accessRightsopenAccesses
dc.description.disciplineIngeniería, Industria y Construcciónes


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