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In situ XPS Study of Methanol Oxidation over a Copper Catalyst Derived from Layered Double Hydroxides Научная публикация

Журнал Catalysis Science and Technology
ISSN: 2044-4753 , E-ISSN: 2044-4761
Вых. Данные Год: 2024, Том: 14, Страницы: 4986-4996 Страниц : 11 DOI: 10.1039/d4cy00675e
Ключевые слова Alumina; Aluminum oxide; Catalysis; Catalysts; Copper compounds; High resolution transmission electron microscopy; Mass spectrometry; Molar ratio; Oxidation; Photoelectrons; Photons; Synthesis (chemical); Thermoanalysis; X ray photoelectron spectroscopy
Авторы Panafidin Maxim A. 1 , Bukhtiyarov Andrey V. 1 , Fedorov Alexey Yu. 1 , Bukhtiyarova Marina V. 1 , Prosvirin Igor P. 1 , Bukhtiyarov Valerii I. 1
Организации
1 Boreskov Institute of Catalysis, Lavrentieva Ave. 5, Novosibirsk, Russia

Информация о финансировании (1)

1 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) 075-15-2022-263

Реферат: Copper nanoparticles supported on alumina have been synthesized from CuAl-layered double hydroxide by heat treatment at 450 °C and have been characterized by thermal analysis, X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy. Methanol oxidation at different molar ratios of the components of the reaction feed (CH3OH : O2 = 1 : 1, 3 : 1, 6 : 1 and 1 : 3, Ptotal = 0.012 mbar) over the prepared CuAlOx catalyst has been studied by in situ X-ray photoelectron spectroscopy and mass-spectrometry. It was revealed that methanol oxidation takes place at temperatures higher than 250 °C. The conversion of methanol and selectivities towards CH2O and CO2 were found to depend on the molar ratio of the reaction mixture components and reaction temperature. A quantitative estimation of the surface composition for the CuAlOx catalyst under different experimental conditions was performed based on the deconvolution of copper Auger spectra using a linear combination of individual components. It was shown that treatment of the as-loaded CuAlOx catalyst in hydrogen at 300 °C led to a partial reduction of Cu+ to Cu0. However, there were only Cu0 species on the surface in the CH3OH : O2 = 1 : 1 reaction mixture at 400 °C indicating the formation of active sites directly during the catalytic reaction. Metallic copper was shown to be an active component for the production of formaldehyde under the conditions of methanol excess in the reaction mixture.
Библиографическая ссылка: Panafidin M.A. , Bukhtiyarov A.V. , Fedorov A.Y. , Bukhtiyarova M.V. , Prosvirin I.P. , Bukhtiyarov V.I.
In situ XPS Study of Methanol Oxidation over a Copper Catalyst Derived from Layered Double Hydroxides
Catalysis Science and Technology. 2024. V.14. P.4986-4996. DOI: 10.1039/d4cy00675e WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 28 мая 2024 г.
Принята к публикации: 15 июл. 2024 г.
Опубликована online: 15 июл. 2024 г.
Опубликована в печати: 7 сент. 2024 г.
Идентификаторы БД:
Web of science: WOS:001276153100001
Scopus: 2-s2.0-85199704622
РИНЦ: 68992685
Chemical Abstracts: 2024:1633582
OpenAlex: W4400654251
Цитирование в БД:
БД Цитирований
Web of science 1
Scopus 1
РИНЦ 1
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