Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions

dc.bibliographicCitation.firstPage27732eng
dc.bibliographicCitation.issue47eng
dc.bibliographicCitation.journalTitleRSC Advances : an international journal to further the chemical scienceseng
dc.bibliographicCitation.lastPage27742eng
dc.bibliographicCitation.volume9eng
dc.contributor.authorWolf, Patrick
dc.contributor.authorLogemann, Morten
dc.contributor.authorSchörner, Markus
dc.contributor.authorKeller, Laura
dc.contributor.authorHaumann, Marco
dc.contributor.authorWessling, Matthias
dc.date.accessioned2022-04-14T08:17:02Z
dc.date.available2022-04-14T08:17:02Z
dc.date.issued2019
dc.description.abstractIn times of depleting fossil fuel reserves, optimizing industrial catalytic reactions has become increasingly important. One possibility for optimization is the use of homogenous catalysts, which are advantageous over heterogeneous catalysts because of mild reaction conditions as well as higher selectivity and activity. A new emerging technology, supported ionic liquid phase (SILP), was developed to permanently immobilize homogeneous catalyst complexes for continuous processes. However, these SILP catalysts are unable to form freestanding supports by themselves. This study presents a new method to introduce the SILP system into a support made from multi-walled carbon nanotubes (MWCNT). In a first step, SILP catalysts were prepared for hydroformylation as well as low-temperature water–gas shift (WGS) reactions. These catalysts were integrated into freestanding microtubes formed from MWCNTs, with silica (for hydroformylation) or alumina particles (for WGS) incorporated. In hydroformylation, the activity increased significantly by around 400% when the pure MWCNT material was used as SILP support. An opposite trend was observed for WGS, where pure alumina particles exhibited the highest activity. A significant advantage of the MWCNT composite materials is the possibility to coat them with separation layers, which allows their application in membrane reactors for more efficient processes.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8694
dc.identifier.urihttps://doi.org/10.34657/7732
dc.language.isoengeng
dc.publisherLondon : RSC Publishingeng
dc.relation.doihttps://doi.org/10.1039/c9ra04830h
dc.relation.essn2046-2069
dc.rights.licenseCC BY-NC 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/eng
dc.subject.ddc540eng
dc.subject.otherAluminaeng
dc.subject.otherAluminum oxideeng
dc.subject.otherBioreactorseng
dc.subject.otherCatalyst selectivityeng
dc.subject.otherCatalyst supportseng
dc.subject.otherChemical shifteng
dc.subject.otherFossil fuelseng
dc.subject.otherGlass ceramicseng
dc.subject.otherHydroformylationeng
dc.subject.otherIonic liquidseng
dc.subject.otherMultiwalled carbon nanotubes (MWCN)eng
dc.subject.otherNanocatalystseng
dc.subject.otherNanotubeseng
dc.subject.otherProven reserveseng
dc.subject.otherSilicaeng
dc.subject.otherTemperatureeng
dc.subject.otherCatalytic reactionseng
dc.subject.otherEmerging technologieseng
dc.subject.otherHeterogeneous catalysteng
dc.subject.otherHomogeneous catalysteng
dc.subject.otherHomogenous catalysteng
dc.subject.otherLow-temperature water-gas shifteng
dc.subject.otherMild reaction conditionseng
dc.subject.otherSupported ionic liquid-phaseeng
dc.subject.otherWater gas shifteng
dc.titleMulti-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactionseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorDWIeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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