Outperformance of CaO-Incorporated Alumina-Supported Pd Catalysts in Methanol Decomposition

dc.contributor.author Eryildirim, Busra
dc.contributor.author Oktar, Nuray
dc.contributor.author Dogu, Doruk
dc.contributor.other Metallurgical and Materials Engineering
dc.date.accessioned 2025-08-05T17:15:56Z
dc.date.available 2025-08-05T17:15:56Z
dc.date.issued 2025
dc.description.abstract This study aimed to investigate the impact of CaO incorporation to alumina-supported Pd catalysts on the methanol decomposition reaction. For this purpose, mayenite, alumina and/or calcium oxide-supported Pd catalysts were synthesized. The synthesized catalysts were characterized by XRD, FTIR, Laser Raman spectroscopy, N2 adsorption-desorption, pyridine adsorbed DRIFTS, CO2-TPD, XPS, SEM-EDS, and ICP-OES techniques. Catalytic activity tests were carried out over a 6 h reaction period in the range of 100-400 degrees C. The results of the characterization and activity tests showed that the addition of CaO had significant effects on the physicochemical properties of the catalyst as well as on the catalytic activity. By adding CaO to the alumina support material, the acidity was reduced, thus reducing the selectivity for dimethyl ether (DME) formation, which is significantly high for the 1Pd@Al2O3 catalyst, and increasing the H2 and CO selectivity. The mayenite-supported catalyst (1Pd@SGM), which contains alumina and calcium oxide in its unique crystal structure, showed an excellent catalytic performance close to complete methanol conversion with DME selectivity below 1% at 400 degrees C. In the stability test carried out at 350 degrees C for 6 h with 1Pd@Al2O3, 1Pd@SGM, and 1Pd@48CaO@Al2O3 catalysts used in the temperature scan, it was concluded that all catalysts were stable and 1Pd@SGM catalyst showed higher catalytic activity than the others. en_US
dc.description.sponsorship Scientific and Technological Research Council of Turkiye (TUBITAK) BIDEB-2232 Program [118C237]; Gazi University Research Fund [FDK-2023-8907]; TUBITAK en_US
dc.description.sponsorship This work was supported by the Scientific and Technological Research Council of Turkiye (TUBITAK) BIDEB-2232 Program (118C237), Gazi University Research Fund (FDK-2023-8907), TUBITAK-2211 PhD Scholarship Program, and TUBITAK-2250 Performance-Based Scholarships Program for PhD. The authors thank the Central Laboratory of METU, Central Laboratory of AYBU, and Atilim University Metal Forming Center of Excellence for the characterization results of the synthesized materials. en_US
dc.identifier.doi 10.1007/s11164-025-05652-y
dc.identifier.issn 0922-6168
dc.identifier.issn 1568-5675
dc.identifier.scopus 2-s2.0-105009028402
dc.identifier.uri https://doi.org/10.1007/s11164-025-05652-y
dc.identifier.uri https://hdl.handle.net/20.500.14411/10723
dc.language.iso en en_US
dc.publisher Springer en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Hydrogen en_US
dc.subject Methanol Decomposition en_US
dc.subject Mayenite en_US
dc.subject Alumina en_US
dc.subject Calcium Oxide Addition en_US
dc.subject Palladium en_US
dc.title Outperformance of CaO-Incorporated Alumina-Supported Pd Catalysts in Methanol Decomposition en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Doğu, Doruk
gdc.author.scopusid 57220119443
gdc.author.scopusid 6603868769
gdc.author.scopusid 56835629300
gdc.author.wosid Dogu, Doruk/P-5978-2016
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department Atılım University en_US
gdc.description.departmenttemp [Eryildirim, Busra] Gazi Univ, Grad Sch Nat & Appl Sci, Dept Chem Engn, Ankara, Turkiye; [Oktar, Nuray] Gazi Univ, Fac Engn, Dept Chem Engn, Ankara, Turkiye; [Dogu, Doruk] Atilim Univ, Dept Met & Mat Engn, Ankara, Turkiye en_US
gdc.description.endpage 4176 en_US
gdc.description.issue 8 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.startpage 4149 en_US
gdc.description.volume 51 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.wos WOS:001518284400001
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