Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate
The increase in world population and human activities are leading to an increase in water stress in many regions of the planet, coupled with a decrease in the quality of water bodies. Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; ho...
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description | The increase in world population and human activities are leading to an increase in water stress in many regions of the planet, coupled with a decrease in the quality of water bodies. Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; however, it is necessary to intensify this type of treatment in order to reduce contact times and to reach a greater number of pollutants. The generation of sulfate radicals by activation of peroxymonosulfate (PMS) by divalent iron (Fe2+) and/or titanium dioxide (TiO2) were statistically studied to understand the role of these compounds as activators, using methylene blue as target pollutant because of its ease of handling and analysis. A factorial experimental design was used to study the influence of different variables (PMS, Fe2+, and TiO2) in the presence of UV-A or UV-C. There were relevant differences in the discoloration of methylene blue when analyzing the size of the effects and significance of the experiments, when UV-A or UV-C was used, being faster with UV-C. For instance, total discoloration of methylene blue was reached after 60 min with the system PMS/UV-C, while after 90 min only the 59% of methylene blue disappeared in presence of PMS/UV-A. Both Fe2+ and TiO2 in combination with PMS and UV increased the discoloration effect. So, in the presence of Fe2+, total discoloration of methylene blue was observed after 30 min in presence of UV-A, while this yield was reached in 7.5 min under UV-C. In the case of PMS/TiO2, it required 60 min under UV-A radiation to totally remove methylene blue, and around 15 min with UV-C. Statistically, the three variables were observed to have the main effect in combination with UV. Furthermore, the PMS/Fe2+ system has a significant interaction with UV-A and UV-C radiation, while the interaction of PMS/TiO2 was significant under UV-A, but with a negative effect under UV-C, or in other words the high elimination rates observed are achieved by the oxidation potential of UV-C, and the effect of PMS and TiO2 by itself. |
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Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; however, it is necessary to intensify this type of treatment in order to reduce contact times and to reach a greater number of pollutants. The generation of sulfate radicals by activation of peroxymonosulfate (PMS) by divalent iron (Fe2+) and/or titanium dioxide (TiO2) were statistically studied to understand the role of these compounds as activators, using methylene blue as target pollutant because of its ease of handling and analysis. A factorial experimental design was used to study the influence of different variables (PMS, Fe2+, and TiO2) in the presence of UV-A or UV-C. There were relevant differences in the discoloration of methylene blue when analyzing the size of the effects and significance of the experiments, when UV-A or UV-C was used, being faster with UV-C. For instance, total discoloration of methylene blue was reached after 60 min with the system PMS/UV-C, while after 90 min only the 59% of methylene blue disappeared in presence of PMS/UV-A. Both Fe2+ and TiO2 in combination with PMS and UV increased the discoloration effect. So, in the presence of Fe2+, total discoloration of methylene blue was observed after 30 min in presence of UV-A, while this yield was reached in 7.5 min under UV-C. In the case of PMS/TiO2, it required 60 min under UV-A radiation to totally remove methylene blue, and around 15 min with UV-C. Statistically, the three variables were observed to have the main effect in combination with UV. Furthermore, the PMS/Fe2+ system has a significant interaction with UV-A and UV-C radiation, while the interaction of PMS/TiO2 was significant under UV-A, but with a negative effect under UV-C, or in other words the high elimination rates observed are achieved by the oxidation potential of UV-C, and the effect of PMS and TiO2 by itself.</description><identifier>ISSN: 2073-4441</identifier><identifier>EISSN: 2073-4441</identifier><identifier>DOI: 10.3390/w13202860</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Catalytic activity ; Decomposition ; Design of experiments ; Discoloration ; Experimental design ; Free radicals ; Iron ; Methylene blue ; Oxidation ; Photocatalysis ; Pollutants ; Potassium ; Reagents ; Titanium dioxide ; Ultraviolet radiation ; Variables ; Water quality ; Water stress ; World population</subject><ispartof>Water (Basel), 2021-10, Vol.13 (20), p.2860</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; however, it is necessary to intensify this type of treatment in order to reduce contact times and to reach a greater number of pollutants. The generation of sulfate radicals by activation of peroxymonosulfate (PMS) by divalent iron (Fe2+) and/or titanium dioxide (TiO2) were statistically studied to understand the role of these compounds as activators, using methylene blue as target pollutant because of its ease of handling and analysis. A factorial experimental design was used to study the influence of different variables (PMS, Fe2+, and TiO2) in the presence of UV-A or UV-C. There were relevant differences in the discoloration of methylene blue when analyzing the size of the effects and significance of the experiments, when UV-A or UV-C was used, being faster with UV-C. For instance, total discoloration of methylene blue was reached after 60 min with the system PMS/UV-C, while after 90 min only the 59% of methylene blue disappeared in presence of PMS/UV-A. Both Fe2+ and TiO2 in combination with PMS and UV increased the discoloration effect. So, in the presence of Fe2+, total discoloration of methylene blue was observed after 30 min in presence of UV-A, while this yield was reached in 7.5 min under UV-C. In the case of PMS/TiO2, it required 60 min under UV-A radiation to totally remove methylene blue, and around 15 min with UV-C. Statistically, the three variables were observed to have the main effect in combination with UV. Furthermore, the PMS/Fe2+ system has a significant interaction with UV-A and UV-C radiation, while the interaction of PMS/TiO2 was significant under UV-A, but with a negative effect under UV-C, or in other words the high elimination rates observed are achieved by the oxidation potential of UV-C, and the effect of PMS and TiO2 by itself.</description><subject>Catalytic activity</subject><subject>Decomposition</subject><subject>Design of experiments</subject><subject>Discoloration</subject><subject>Experimental design</subject><subject>Free radicals</subject><subject>Iron</subject><subject>Methylene blue</subject><subject>Oxidation</subject><subject>Photocatalysis</subject><subject>Pollutants</subject><subject>Potassium</subject><subject>Reagents</subject><subject>Titanium dioxide</subject><subject>Ultraviolet radiation</subject><subject>Variables</subject><subject>Water quality</subject><subject>Water stress</subject><subject>World population</subject><issn>2073-4441</issn><issn>2073-4441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpN0E1LAzEQBuAgCpbag_8g4ElkNZ-7ybEUq0KhBetNWKbZLE1pNzXJqvvv3bYizmUG5mEGXoSuKbnnXJOHL8oZYSonZ2jASMEzIQQ9_zdfolGMG9KX0EpJMkDvr6mtOuxrnNYWL9Y-eQMJtl1yBo9Ncp8uHddLN2cYmgpPLbvDrjn6I4DkfHMgCxv8d7fzjY_ttoZkr9BFDdtoR799iN6mj8vJczabP71MxrPMMMZSRrUSlbSS5wDWFCB0rgtScSMFrKhcaZtDBZwxo4Eoy-sVaKYKDrKQuqKWD9HN6e4--I_WxlRufBua_mXJpBJCkZzJXt2elAk-xmDrch_cDkJXUlIe8iv_8uM_RYxhOQ</recordid><startdate>20211013</startdate><enddate>20211013</enddate><creator>González-Quiles, Rodrigo</creator><creator>de Andrés, Juan Manuel</creator><creator>Rodríguez-Chueca, Jorge</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><orcidid>https://orcid.org/0000-0003-0268-8294</orcidid><orcidid>https://orcid.org/0000-0002-0654-5496</orcidid><orcidid>https://orcid.org/0000-0001-9050-1682</orcidid></search><sort><creationdate>20211013</creationdate><title>Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate</title><author>González-Quiles, Rodrigo ; de Andrés, Juan Manuel ; Rodríguez-Chueca, Jorge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c222t-1984d5e536aaec7a496970d3c54ab15b9e6ada322c9a08e3fba92873a5759d1e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Catalytic activity</topic><topic>Decomposition</topic><topic>Design of experiments</topic><topic>Discoloration</topic><topic>Experimental design</topic><topic>Free radicals</topic><topic>Iron</topic><topic>Methylene blue</topic><topic>Oxidation</topic><topic>Photocatalysis</topic><topic>Pollutants</topic><topic>Potassium</topic><topic>Reagents</topic><topic>Titanium dioxide</topic><topic>Ultraviolet radiation</topic><topic>Variables</topic><topic>Water quality</topic><topic>Water stress</topic><topic>World population</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>González-Quiles, Rodrigo</creatorcontrib><creatorcontrib>de Andrés, Juan Manuel</creatorcontrib><creatorcontrib>Rodríguez-Chueca, Jorge</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Water (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>González-Quiles, Rodrigo</au><au>de Andrés, Juan Manuel</au><au>Rodríguez-Chueca, Jorge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate</atitle><jtitle>Water (Basel)</jtitle><date>2021-10-13</date><risdate>2021</risdate><volume>13</volume><issue>20</issue><spage>2860</spage><pages>2860-</pages><issn>2073-4441</issn><eissn>2073-4441</eissn><abstract>The increase in world population and human activities are leading to an increase in water stress in many regions of the planet, coupled with a decrease in the quality of water bodies. Advanced oxidation processes have demonstrated great potential for the reduction of almost any organic pollutant; however, it is necessary to intensify this type of treatment in order to reduce contact times and to reach a greater number of pollutants. The generation of sulfate radicals by activation of peroxymonosulfate (PMS) by divalent iron (Fe2+) and/or titanium dioxide (TiO2) were statistically studied to understand the role of these compounds as activators, using methylene blue as target pollutant because of its ease of handling and analysis. A factorial experimental design was used to study the influence of different variables (PMS, Fe2+, and TiO2) in the presence of UV-A or UV-C. There were relevant differences in the discoloration of methylene blue when analyzing the size of the effects and significance of the experiments, when UV-A or UV-C was used, being faster with UV-C. 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subjects | Catalytic activity Decomposition Design of experiments Discoloration Experimental design Free radicals Iron Methylene blue Oxidation Photocatalysis Pollutants Potassium Reagents Titanium dioxide Ultraviolet radiation Variables Water quality Water stress World population |
title | Study of the Photocatalytic Activity of TiO2 and Fe2+ in the Activation of Peroxymonosulfate |
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