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Application of on-line FTIR methodology to study the mechanisms of heterogeneous advanced oxidation processes
[Display omitted] •FTIR spectroscopy serves as a powerful tool for on-line reaction monitoring.•Real time FTIR data contributes to the optimization of heterogeneous AOPs.•FTIR on-line methodology compared with other methods reduces analysis time.•Catalytic oxidation of an emerging water pollutant, 1...
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Published in: | Applied catalysis. B, Environmental Environmental, 2016-05, Vol.185, p.344-352 |
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container_title | Applied catalysis. B, Environmental |
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creator | Barndõk, Helen Merayo, Noemi Blanco, Laura Hermosilla, Daphne Blanco, Ángeles |
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•FTIR spectroscopy serves as a powerful tool for on-line reaction monitoring.•Real time FTIR data contributes to the optimization of heterogeneous AOPs.•FTIR on-line methodology compared with other methods reduces analysis time.•Catalytic oxidation of an emerging water pollutant, 1,4-dioxane, was studied.•Major decomposition pathways of 1,4-dioxane were established and compared.
On-line FTIR-methodology was used to study the routes of 1,4-dioxane degradation in heterogeneous photocatalysis with titanium dioxide (TiO2) and heterogeneous photo-Fenton with zero valent iron (Fe0). To determine the multiple decomposition mechanisms of this environmental pollutant, heterogeneous Fe0-catalyst was compared with a homogenous iron catalyst and different photocatalytic systems with UV radiation and solar light were studied. In addition, the influence of H2O2 addition profile was assessed to optimize of the reagent dose and reaction time. Complete removal of 1,4-dioxane and 85% mineralization of TOC were achieved by UV photo-Fenton with Fe0, while solar light could work as cost-effective alternative, achieving 65% removal of 1,4-dioxane. Although constant addition of H2O2 was crucial for the rapid oxidation of organic matter, significant degradation was reached by only half of the stoichiometric amount of H2O2. Meanwhile, apparently similar treatment efficiencies were observed in both UV-assisted and solar photocatalysis (almost 60% of 1,4-dioxane removal). The degradation routes for 1,4-dioxane in both advanced oxidation processes were established and presented based on extensive chromatography analysis, whereas FTIR monitoring served as a powerful tool for on-line reaction monitoring. Ethylene glycol diformate was detected as the major primary intermediate in TiO2-photocatalysis, whereas ethylene glycol was found as the main initial by-product in Fe0-based photo-Fenton. An alternative route of 1,4-dioxane degradation through methoxyacetic and acetic acids was observed, being more pronounced in photo-Fenton processes and accentuated further in the presence of Fe0. |
doi_str_mv | 10.1016/j.apcatb.2015.12.036 |
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•FTIR spectroscopy serves as a powerful tool for on-line reaction monitoring.•Real time FTIR data contributes to the optimization of heterogeneous AOPs.•FTIR on-line methodology compared with other methods reduces analysis time.•Catalytic oxidation of an emerging water pollutant, 1,4-dioxane, was studied.•Major decomposition pathways of 1,4-dioxane were established and compared.
On-line FTIR-methodology was used to study the routes of 1,4-dioxane degradation in heterogeneous photocatalysis with titanium dioxide (TiO2) and heterogeneous photo-Fenton with zero valent iron (Fe0). To determine the multiple decomposition mechanisms of this environmental pollutant, heterogeneous Fe0-catalyst was compared with a homogenous iron catalyst and different photocatalytic systems with UV radiation and solar light were studied. In addition, the influence of H2O2 addition profile was assessed to optimize of the reagent dose and reaction time. Complete removal of 1,4-dioxane and 85% mineralization of TOC were achieved by UV photo-Fenton with Fe0, while solar light could work as cost-effective alternative, achieving 65% removal of 1,4-dioxane. Although constant addition of H2O2 was crucial for the rapid oxidation of organic matter, significant degradation was reached by only half of the stoichiometric amount of H2O2. Meanwhile, apparently similar treatment efficiencies were observed in both UV-assisted and solar photocatalysis (almost 60% of 1,4-dioxane removal). The degradation routes for 1,4-dioxane in both advanced oxidation processes were established and presented based on extensive chromatography analysis, whereas FTIR monitoring served as a powerful tool for on-line reaction monitoring. Ethylene glycol diformate was detected as the major primary intermediate in TiO2-photocatalysis, whereas ethylene glycol was found as the main initial by-product in Fe0-based photo-Fenton. An alternative route of 1,4-dioxane degradation through methoxyacetic and acetic acids was observed, being more pronounced in photo-Fenton processes and accentuated further in the presence of Fe0.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2015.12.036</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>1,4-Dioxane ; Byproducts ; Degradation ; Ethylene glycol ; Fe0 microspheres ; Heterogeneous catalysts ; Iron ; On-line systems ; Oxidation ; Photo-Fenton ; Photocatalysis ; TiO2 photocatalysis ; Titanium dioxide</subject><ispartof>Applied catalysis. B, Environmental, 2016-05, Vol.185, p.344-352</ispartof><rights>2016 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-e72aa2145b5610564029c835f215ea6fd18edccd33f302fe713d0c3dad242c303</citedby><cites>FETCH-LOGICAL-c455t-e72aa2145b5610564029c835f215ea6fd18edccd33f302fe713d0c3dad242c303</cites><orcidid>0000-0002-0006-2397 ; 0000-0001-6820-7698</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Barndõk, Helen</creatorcontrib><creatorcontrib>Merayo, Noemi</creatorcontrib><creatorcontrib>Blanco, Laura</creatorcontrib><creatorcontrib>Hermosilla, Daphne</creatorcontrib><creatorcontrib>Blanco, Ángeles</creatorcontrib><title>Application of on-line FTIR methodology to study the mechanisms of heterogeneous advanced oxidation processes</title><title>Applied catalysis. B, Environmental</title><description>[Display omitted]
•FTIR spectroscopy serves as a powerful tool for on-line reaction monitoring.•Real time FTIR data contributes to the optimization of heterogeneous AOPs.•FTIR on-line methodology compared with other methods reduces analysis time.•Catalytic oxidation of an emerging water pollutant, 1,4-dioxane, was studied.•Major decomposition pathways of 1,4-dioxane were established and compared.
On-line FTIR-methodology was used to study the routes of 1,4-dioxane degradation in heterogeneous photocatalysis with titanium dioxide (TiO2) and heterogeneous photo-Fenton with zero valent iron (Fe0). To determine the multiple decomposition mechanisms of this environmental pollutant, heterogeneous Fe0-catalyst was compared with a homogenous iron catalyst and different photocatalytic systems with UV radiation and solar light were studied. In addition, the influence of H2O2 addition profile was assessed to optimize of the reagent dose and reaction time. Complete removal of 1,4-dioxane and 85% mineralization of TOC were achieved by UV photo-Fenton with Fe0, while solar light could work as cost-effective alternative, achieving 65% removal of 1,4-dioxane. Although constant addition of H2O2 was crucial for the rapid oxidation of organic matter, significant degradation was reached by only half of the stoichiometric amount of H2O2. Meanwhile, apparently similar treatment efficiencies were observed in both UV-assisted and solar photocatalysis (almost 60% of 1,4-dioxane removal). The degradation routes for 1,4-dioxane in both advanced oxidation processes were established and presented based on extensive chromatography analysis, whereas FTIR monitoring served as a powerful tool for on-line reaction monitoring. Ethylene glycol diformate was detected as the major primary intermediate in TiO2-photocatalysis, whereas ethylene glycol was found as the main initial by-product in Fe0-based photo-Fenton. An alternative route of 1,4-dioxane degradation through methoxyacetic and acetic acids was observed, being more pronounced in photo-Fenton processes and accentuated further in the presence of Fe0.</description><subject>1,4-Dioxane</subject><subject>Byproducts</subject><subject>Degradation</subject><subject>Ethylene glycol</subject><subject>Fe0 microspheres</subject><subject>Heterogeneous catalysts</subject><subject>Iron</subject><subject>On-line systems</subject><subject>Oxidation</subject><subject>Photo-Fenton</subject><subject>Photocatalysis</subject><subject>TiO2 photocatalysis</subject><subject>Titanium dioxide</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU1Lw0AQhhdRsFb_gYccvSTu7GaT7UUoxWpBEKSel-3upN2SZGM2LfbfmzSexdMMzLzvfDyE3ANNgEL2uE90Y3S3SRgFkQBLKM8uyARkzmMuJb8kEzpjWcx5zq_JTQh7SinjTE5INW-a0vVi5-vIF5Gv49LVGC3Xq4-owm7nrS_99hR1PgrdwfbJDvuC2enahSoMmh122Pot1ugPIdL2qGuDNvLfzo6-TesNhoDhllwVugx49xun5HP5vF68xm_vL6vF_C02qRBdjDnTmkEqNiIDKrKUspmRXBQMBOqssCDRGmM5LzhlBebALTXcastSZjjlU_Iw-vaTvw4YOlW5YLAs9XlHBZKJVMJM5P9opTLLAc6u6dhqWh9Ci4VqWlfp9qSAqgGE2qsRhBpAKGCqB9HLnkYZ9hcfHbYqGIfDi1yLplPWu78NfgClw5Rk</recordid><startdate>20160515</startdate><enddate>20160515</enddate><creator>Barndõk, Helen</creator><creator>Merayo, Noemi</creator><creator>Blanco, Laura</creator><creator>Hermosilla, Daphne</creator><creator>Blanco, Ángeles</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-0006-2397</orcidid><orcidid>https://orcid.org/0000-0001-6820-7698</orcidid></search><sort><creationdate>20160515</creationdate><title>Application of on-line FTIR methodology to study the mechanisms of heterogeneous advanced oxidation processes</title><author>Barndõk, Helen ; Merayo, Noemi ; Blanco, Laura ; Hermosilla, Daphne ; Blanco, Ángeles</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-e72aa2145b5610564029c835f215ea6fd18edccd33f302fe713d0c3dad242c303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>1,4-Dioxane</topic><topic>Byproducts</topic><topic>Degradation</topic><topic>Ethylene glycol</topic><topic>Fe0 microspheres</topic><topic>Heterogeneous catalysts</topic><topic>Iron</topic><topic>On-line systems</topic><topic>Oxidation</topic><topic>Photo-Fenton</topic><topic>Photocatalysis</topic><topic>TiO2 photocatalysis</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barndõk, Helen</creatorcontrib><creatorcontrib>Merayo, Noemi</creatorcontrib><creatorcontrib>Blanco, Laura</creatorcontrib><creatorcontrib>Hermosilla, Daphne</creatorcontrib><creatorcontrib>Blanco, Ángeles</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barndõk, Helen</au><au>Merayo, Noemi</au><au>Blanco, Laura</au><au>Hermosilla, Daphne</au><au>Blanco, Ángeles</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of on-line FTIR methodology to study the mechanisms of heterogeneous advanced oxidation processes</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2016-05-15</date><risdate>2016</risdate><volume>185</volume><spage>344</spage><epage>352</epage><pages>344-352</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>[Display omitted]
•FTIR spectroscopy serves as a powerful tool for on-line reaction monitoring.•Real time FTIR data contributes to the optimization of heterogeneous AOPs.•FTIR on-line methodology compared with other methods reduces analysis time.•Catalytic oxidation of an emerging water pollutant, 1,4-dioxane, was studied.•Major decomposition pathways of 1,4-dioxane were established and compared.
On-line FTIR-methodology was used to study the routes of 1,4-dioxane degradation in heterogeneous photocatalysis with titanium dioxide (TiO2) and heterogeneous photo-Fenton with zero valent iron (Fe0). To determine the multiple decomposition mechanisms of this environmental pollutant, heterogeneous Fe0-catalyst was compared with a homogenous iron catalyst and different photocatalytic systems with UV radiation and solar light were studied. In addition, the influence of H2O2 addition profile was assessed to optimize of the reagent dose and reaction time. Complete removal of 1,4-dioxane and 85% mineralization of TOC were achieved by UV photo-Fenton with Fe0, while solar light could work as cost-effective alternative, achieving 65% removal of 1,4-dioxane. Although constant addition of H2O2 was crucial for the rapid oxidation of organic matter, significant degradation was reached by only half of the stoichiometric amount of H2O2. Meanwhile, apparently similar treatment efficiencies were observed in both UV-assisted and solar photocatalysis (almost 60% of 1,4-dioxane removal). The degradation routes for 1,4-dioxane in both advanced oxidation processes were established and presented based on extensive chromatography analysis, whereas FTIR monitoring served as a powerful tool for on-line reaction monitoring. Ethylene glycol diformate was detected as the major primary intermediate in TiO2-photocatalysis, whereas ethylene glycol was found as the main initial by-product in Fe0-based photo-Fenton. An alternative route of 1,4-dioxane degradation through methoxyacetic and acetic acids was observed, being more pronounced in photo-Fenton processes and accentuated further in the presence of Fe0.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2015.12.036</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0006-2397</orcidid><orcidid>https://orcid.org/0000-0001-6820-7698</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 1,4-Dioxane Byproducts Degradation Ethylene glycol Fe0 microspheres Heterogeneous catalysts Iron On-line systems Oxidation Photo-Fenton Photocatalysis TiO2 photocatalysis Titanium dioxide |
title | Application of on-line FTIR methodology to study the mechanisms of heterogeneous advanced oxidation processes |
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