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Direct synthesis of vertically oriented Co-Mg-Al layered double hydroxide on spherical γ-Al2O3 for passive NOx adsorber
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Choi, Yeji | - |
| dc.contributor.author | Mun, Sungyong | - |
| dc.contributor.author | Lee, Ki Bong | - |
| dc.date.accessioned | 2025-12-30T02:30:32Z | - |
| dc.date.available | 2025-12-30T02:30:32Z | - |
| dc.date.issued | 2025-04 | - |
| dc.identifier.issn | 0169-4332 | - |
| dc.identifier.issn | 1873-5584 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210165 | - |
| dc.description.abstract | Co-Mg-Al layered double hydroxides (LDHs) are directly synthesized on spherical γ-Al2O3 using a hydrothermal treatment method with urea for low-temperature NOx adsorber, and the formation mechanism of LDHs is studied. γ-Al2O3 acts as an Al3+ source and a support, and urea provides CO32– and OH– during hydrothermal treatment. During the hydrothermal reaction, a gibbsite-like amorphous aluminum hydroxide (AOH) phase is formed on the γ-Al2O3 surface, and Co2+ and Mg2+ are dissolved into AOH layers to form LDHs. The urea concentration is a critical factor for nucleation and particle growth during LDH synthesis, affecting the properties and NOx storage/release performance of LDH-derived mixed metal oxides. Sintering of LDH-derived mixed metal oxide particles is prevented during calcination and regeneration at elevated temperatures owing to chemical bonding between the LDHs and the AOH layer, thus enhancing NOx adsorption performance. | - |
| dc.format.extent | 11 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Elsevier BV | - |
| dc.title | Direct synthesis of vertically oriented Co-Mg-Al layered double hydroxide on spherical γ-Al2O3 for passive NOx adsorber | - |
| dc.type | Article | - |
| dc.publisher.location | 네델란드 | - |
| dc.identifier.doi | 10.1016/j.apsusc.2024.162248 | - |
| dc.identifier.scopusid | 2-s2.0-85214320635 | - |
| dc.identifier.wosid | 001409602300001 | - |
| dc.identifier.bibliographicCitation | Applied Surface Science, v.687, pp 1 - 11 | - |
| dc.citation.title | Applied Surface Science | - |
| dc.citation.volume | 687 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 11 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalResearchArea | Physics | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Coatings & Films | - |
| dc.relation.journalWebOfScienceCategory | Physics, Applied | - |
| dc.relation.journalWebOfScienceCategory | Physics, Condensed Matter | - |
| dc.subject.keywordPlus | IN-SITU SYNTHESIS | - |
| dc.subject.keywordPlus | HIGHLY EFFICIENT CATALYSTS | - |
| dc.subject.keywordPlus | MIXED OXIDES | - |
| dc.subject.keywordPlus | HYDROTHERMAL SYNTHESIS | - |
| dc.subject.keywordPlus | COBALT CARBONATE | - |
| dc.subject.keywordPlus | UREA HYDROLYSIS | - |
| dc.subject.keywordPlus | HYDROTALCITE | - |
| dc.subject.keywordPlus | OXIDATION | - |
| dc.subject.keywordPlus | SOOT | - |
| dc.subject.keywordPlus | STORAGE | - |
| dc.subject.keywordAuthor | Structured monolith catalyst | - |
| dc.subject.keywordAuthor | Urea hydrolysis | - |
| dc.subject.keywordAuthor | Hydrothermal treatment | - |
| dc.subject.keywordAuthor | NOx adsorption | - |
| dc.subject.keywordAuthor | Hydrotalcite-like compound | - |
| dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0169433224029684?via%3Dihub | - |
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