Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Minsung | - |
dc.contributor.author | Kim, Sang Hoon | - |
dc.contributor.author | Kim, Jongsik | - |
dc.date.accessioned | 2025-08-20T08:31:19Z | - |
dc.date.available | 2025-08-20T08:31:19Z | - |
dc.date.created | 2025-08-20 | - |
dc.date.issued | 2025-12 | - |
dc.identifier.issn | 1383-5866 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/153005 | - |
dc.description.abstract | FeOCl and FeOOH are iso-structural and impart defective [Fe3+(O2-)4(Cl-)2]7-and [Fe3+(O2-)4(OH-)2]7-subunits on their surfaces, respectively, where Fe delta+ and Fe3+ defects can evolve center dot OH/FeIV=O and center dot OOH/O2 center dot-/1O2 in H2O2-containing aqueous media, respectively. FeOCl surface can incur marked Fe delta+/3+ leaching or rigid coordination to aqueous organics, thereby limiting its use as a reactive oxygen species (ROS) evolver and/or reservoir in aqueous phases. Conversely, FeOOH surface can avoid Fe delta+/3+ leaching by eliminating OH-ligands or their protonated analogs (H2O/H3O+) from Fe delta+/3+ in defective [Fe3+(O2-)4(OH-)2]7-sub-units. This was enabled by extensive exposure of FeOOH to supercritical CO2, producing hydrophobic FeOOH-CO2 that offered bunched merits over hydrophilic FeOOH. The number of Fe delta+ defects and their electron affinity were greater and lower, respectively, in FeOOH-CO2 than in FeOOH, resulting in higher center dot OH productivity for the former and higher 1O2 productivity for the latter, alongside with FeIV=O evolution for FeOOH-CO2. Moreover, FeOOH and FeOOH-CO2 exploited center dot OH/1O2 and FeIV=O as their primary ROS for disintegrating aqueous organics, respectively, whose inclusion of e--donating groups made FeIV=O particularly effective in initiating or propagating the destabilization of hard-to-dissociate organics via electron transfer. Furthermore, despite minimized Fe delta +/3+ leaching across FeOOH/FeOOH-CO2 surfaces, FeOOH-CO2 outcompeted FeOOH in providing higher H2O2/center dot OOH/O2 center dot- accessibility to Fe delta+/3+ defects and in avoiding their coordination to fragmented organics in H2O2-and organic-containing aqueous media. Consequently, FeOOH-CO2 was more active in, selective to, and reusable for degrading e--donating group-bearing contaminant or mineralizing textile wastewater than FeOOH, Fe2O3/Fe3O4, and FeOCl. | - |
dc.language | English | - |
dc.publisher | Pergamon Press Ltd. | - |
dc.title | Supercritical CO2-assisted regulation of FeOOH hydrophilicity for FeIV=O deployment in aqueous waste disintegration | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.seppur.2025.134563 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | Separation and Purification Technology, v.378 | - |
dc.citation.title | Separation and Purification Technology | - |
dc.citation.volume | 378 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 001546267000001 | - |
dc.identifier.scopusid | 2-s2.0-105012293612 | - |
dc.relation.journalWebOfScienceCategory | Engineering, Chemical | - |
dc.relation.journalResearchArea | Engineering | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | ENHANCED CATALYTIC-ACTIVITY | - |
dc.subject.keywordPlus | COUPLED ELECTRON-TRANSFER | - |
dc.subject.keywordPlus | IRON OXYCHLORIDE FEOCL | - |
dc.subject.keywordPlus | GOETHITE ALPHA-FEOOH | - |
dc.subject.keywordPlus | HYDROGEN-PEROXIDE | - |
dc.subject.keywordPlus | IN-SITU | - |
dc.subject.keywordPlus | HYDROXYL RADICALS | - |
dc.subject.keywordPlus | ATOM TRANSFER | - |
dc.subject.keywordPlus | WATER | - |
dc.subject.keywordPlus | DEGRADATION | - |
dc.subject.keywordAuthor | FeOOH | - |
dc.subject.keywordAuthor | supercritical CO2 extraction | - |
dc.subject.keywordAuthor | center dot OH | - |
dc.subject.keywordAuthor | O-1(2) | - |
dc.subject.keywordAuthor | Fe-IV=O | - |
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