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231225s2022 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.1c02833
|2 doi
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|a DE-627
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|a eng
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|a Jocz, Jennifer N
|e verfasserin
|4 aut
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|a Characterization of Surface Species during Benzene Hydroxylation over a NiO-Ceria-Zirconia Catalyst
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Revised 11.01.2022
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a NiO/ceria-zirconia (CZ) is a promising catalyst for the selective oxidation of benzene, as the Lewis-acidic NiO clusters can activate C-H bonds and the redox-active CZ support can activate O2 and supply active oxygen species for the reaction. In this study, we used transmission in situ infrared (IR) spectroscopy to examine surface species formed from benzene, water, oxygen, phenol, and catechol on a NiO/CZ catalyst. The formation of surface species from benzene and phenol was compared at different temperatures in the range of 50-200 °C in the presence and absence of water vapor. We also examined the role of the NiO clusters and the CZ support during benzene activation by comparing the surface species formed on NiO-CZ with those formed on a Ni-free CZ support and on a NiO/SiO2 catalyst. The spectrum of surface species from dosing benzene at 180 °C provides evidence for C-H bond activation. Specifically, the observation of C-O stretching vibrations indicates the formation of phenolate species. Introduction of water enhances these IR signals and introduces several additional peaks, indicating that a variety of different surface species are formed. These results show that NiO/CZ could catalyze direct conversion of benzene to phenol
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|a Journal Article
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|a Lyu, Yimeng
|e verfasserin
|4 aut
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|a Hare, Bryan J
|e verfasserin
|4 aut
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|a Sievers, Carsten
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 38(2022), 1 vom: 11. Jan., Seite 458-471
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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|g volume:38
|g year:2022
|g number:1
|g day:11
|g month:01
|g pages:458-471
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|u http://dx.doi.org/10.1021/acs.langmuir.1c02833
|3 Volltext
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|d 38
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