Ultrafast degradation of micropollutants in water via electro-periodate activation catalyzed by nanoconfined Fe2O3

Herein, we developed and evaluated an electrochemical periodate (PI) activation system for the ultrafast degradation of aqueous micropollutants (τ 

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2022-07, Vol.309, p.121289, Article 121289
Hauptverfasser: Guo, Dongli, Yao, Yuan, You, Shijie, Jin, Limin, Lu, Ping, Liu, Yanbiao
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container_title Applied catalysis. B, Environmental
container_volume 309
creator Guo, Dongli
Yao, Yuan
You, Shijie
Jin, Limin
Lu, Ping
Liu, Yanbiao
description Herein, we developed and evaluated an electrochemical periodate (PI) activation system for the ultrafast degradation of aqueous micropollutants (τ 
doi_str_mv 10.1016/j.apcatb.2022.121289
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Filters constructed from carbon nanotubes (CNT) coated with Fe2O3 nanoparticles on the outer (Fe2O3-out-CNT) and inner surfaces (Fe2O3-in-CNT) were prepared to regulate the generation of reactive oxygen species (ROS) during PI activation. The activation function of the electroactive nanohybrid filters lay in their ability to facilitate the redox cycling of Fe(III)/Fe(II) assisted by an electric field. The results showed that a non-radical (i.e., 1O2) pathway dominated the degradation process in the electro/Fe2O3-in-CNT/PI system, while a contrastive radical pathway (i.e., HO• and IO3•) was identified in the electro/Fe2O3-out-CNT/PI system. The electro/Fe2O3-in-CNT/PI system exhibited enhanced catalytic activity towards the micropollutants degradation relative to its electro/Fe2O3-out-CNT/PI counterpart. Density functional theory calculations suggested that PI could be directly decomposed under the nanoconfined environment, rather than forming a stable adsorption complex in the unconfined system. [Display omitted] •An electrochemical PI activation system was developed for ultrafast water remediation.•Non-radical pathway dominated BPA degradation in the E/Fe2O3-in-CNT/PI system.•Radical pathway was identified in the E/Fe2O3-out-CNT/PI system.•Ultrafast and robust organic degradation were obtained in the E/Fe2O3-in-CNT/PI system.•IO4− were transformed into nontoxic IO3− without generation of undesired I species.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2022.121289</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Carbon nanotubes ; Catalytic activity ; Degradation ; Density functional theory ; Electric fields ; Electric filters ; Electrochemistry ; Ferric oxide ; Filters ; Iron ; Micropollutants ; Nanoconfinement effect ; Nanoparticles ; Nanotechnology ; Nanotubes ; Periodate activation ; Reactive oxygen species ; Redox properties ; Singlet oxygen ; Water remediation</subject><ispartof>Applied catalysis. 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B, Environmental</title><description>Herein, we developed and evaluated an electrochemical periodate (PI) activation system for the ultrafast degradation of aqueous micropollutants (τ &lt; 3 s). Filters constructed from carbon nanotubes (CNT) coated with Fe2O3 nanoparticles on the outer (Fe2O3-out-CNT) and inner surfaces (Fe2O3-in-CNT) were prepared to regulate the generation of reactive oxygen species (ROS) during PI activation. The activation function of the electroactive nanohybrid filters lay in their ability to facilitate the redox cycling of Fe(III)/Fe(II) assisted by an electric field. The results showed that a non-radical (i.e., 1O2) pathway dominated the degradation process in the electro/Fe2O3-in-CNT/PI system, while a contrastive radical pathway (i.e., HO• and IO3•) was identified in the electro/Fe2O3-out-CNT/PI system. The electro/Fe2O3-in-CNT/PI system exhibited enhanced catalytic activity towards the micropollutants degradation relative to its electro/Fe2O3-out-CNT/PI counterpart. Density functional theory calculations suggested that PI could be directly decomposed under the nanoconfined environment, rather than forming a stable adsorption complex in the unconfined system. [Display omitted] •An electrochemical PI activation system was developed for ultrafast water remediation.•Non-radical pathway dominated BPA degradation in the E/Fe2O3-in-CNT/PI system.•Radical pathway was identified in the E/Fe2O3-out-CNT/PI system.•Ultrafast and robust organic degradation were obtained in the E/Fe2O3-in-CNT/PI system.•IO4− were transformed into nontoxic IO3− without generation of undesired I species.</description><subject>Carbon nanotubes</subject><subject>Catalytic activity</subject><subject>Degradation</subject><subject>Density functional theory</subject><subject>Electric fields</subject><subject>Electric filters</subject><subject>Electrochemistry</subject><subject>Ferric oxide</subject><subject>Filters</subject><subject>Iron</subject><subject>Micropollutants</subject><subject>Nanoconfinement effect</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>Nanotubes</subject><subject>Periodate activation</subject><subject>Reactive oxygen species</subject><subject>Redox properties</subject><subject>Singlet oxygen</subject><subject>Water remediation</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kEFr3DAQhUVoIdu0_yAHQc_ejiSvLV0KJTRtIZBLcxZjaVy0OJIjabdsf30V3HNPw8B7b-Z9jN0K2AsQw6fjHleHddpLkHIvpJDaXLGd0KPqlNbqDduBkUOn1Kiu2btSjgAgldQ7lp-WmnHGUrmnXxk91pAiTzN_Di6nNS3LqWKshYfIf2OlzM8BOS3kak7dSjmk5iGOrobzZm6v4HL5Q55PFx4xJpfiHGLb70k-qvfs7YxLoQ__5g17uv_68-579_D47cfdl4fOKdXXzo9u8OhAenMwXpvBwwgoh3Eyws2uR3UwMx30iDD1AudpMg7MOBCAhmE8qBv2cctdc3o5Uan2mE45tpNWDn1TghG6qfpN1dqWkmm2aw7PmC9WgH2la492o2tf6dqNbrN93mzUGpwDZVtcoOjIh9zQWJ_C_wP-AsaGhpc</recordid><startdate>20220715</startdate><enddate>20220715</enddate><creator>Guo, Dongli</creator><creator>Yao, Yuan</creator><creator>You, Shijie</creator><creator>Jin, Limin</creator><creator>Lu, Ping</creator><creator>Liu, Yanbiao</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>SOI</scope></search><sort><creationdate>20220715</creationdate><title>Ultrafast degradation of micropollutants in water via electro-periodate activation catalyzed by nanoconfined Fe2O3</title><author>Guo, Dongli ; Yao, Yuan ; You, Shijie ; Jin, Limin ; Lu, Ping ; Liu, Yanbiao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-d7c6dac02d959d896d070a267b91cfc4a359fe587a0b41afbb9c0976e00806753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Carbon nanotubes</topic><topic>Catalytic activity</topic><topic>Degradation</topic><topic>Density functional theory</topic><topic>Electric fields</topic><topic>Electric filters</topic><topic>Electrochemistry</topic><topic>Ferric oxide</topic><topic>Filters</topic><topic>Iron</topic><topic>Micropollutants</topic><topic>Nanoconfinement effect</topic><topic>Nanoparticles</topic><topic>Nanotechnology</topic><topic>Nanotubes</topic><topic>Periodate activation</topic><topic>Reactive oxygen species</topic><topic>Redox properties</topic><topic>Singlet oxygen</topic><topic>Water remediation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Dongli</creatorcontrib><creatorcontrib>Yao, Yuan</creatorcontrib><creatorcontrib>You, Shijie</creatorcontrib><creatorcontrib>Jin, Limin</creatorcontrib><creatorcontrib>Lu, Ping</creatorcontrib><creatorcontrib>Liu, Yanbiao</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Dongli</au><au>Yao, Yuan</au><au>You, Shijie</au><au>Jin, Limin</au><au>Lu, Ping</au><au>Liu, Yanbiao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrafast degradation of micropollutants in water via electro-periodate activation catalyzed by nanoconfined Fe2O3</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2022-07-15</date><risdate>2022</risdate><volume>309</volume><spage>121289</spage><pages>121289-</pages><artnum>121289</artnum><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>Herein, we developed and evaluated an electrochemical periodate (PI) activation system for the ultrafast degradation of aqueous micropollutants (τ &lt; 3 s). Filters constructed from carbon nanotubes (CNT) coated with Fe2O3 nanoparticles on the outer (Fe2O3-out-CNT) and inner surfaces (Fe2O3-in-CNT) were prepared to regulate the generation of reactive oxygen species (ROS) during PI activation. The activation function of the electroactive nanohybrid filters lay in their ability to facilitate the redox cycling of Fe(III)/Fe(II) assisted by an electric field. The results showed that a non-radical (i.e., 1O2) pathway dominated the degradation process in the electro/Fe2O3-in-CNT/PI system, while a contrastive radical pathway (i.e., HO• and IO3•) was identified in the electro/Fe2O3-out-CNT/PI system. The electro/Fe2O3-in-CNT/PI system exhibited enhanced catalytic activity towards the micropollutants degradation relative to its electro/Fe2O3-out-CNT/PI counterpart. Density functional theory calculations suggested that PI could be directly decomposed under the nanoconfined environment, rather than forming a stable adsorption complex in the unconfined system. [Display omitted] •An electrochemical PI activation system was developed for ultrafast water remediation.•Non-radical pathway dominated BPA degradation in the E/Fe2O3-in-CNT/PI system.•Radical pathway was identified in the E/Fe2O3-out-CNT/PI system.•Ultrafast and robust organic degradation were obtained in the E/Fe2O3-in-CNT/PI system.•IO4− were transformed into nontoxic IO3− without generation of undesired I species.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2022.121289</doi></addata></record>
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subjects Carbon nanotubes
Catalytic activity
Degradation
Density functional theory
Electric fields
Electric filters
Electrochemistry
Ferric oxide
Filters
Iron
Micropollutants
Nanoconfinement effect
Nanoparticles
Nanotechnology
Nanotubes
Periodate activation
Reactive oxygen species
Redox properties
Singlet oxygen
Water remediation
title Ultrafast degradation of micropollutants in water via electro-periodate activation catalyzed by nanoconfined Fe2O3
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