<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rashed AE</submitter><funding>Academy of Scientific Research and Technology</funding><funding>Ministry of Higher Education</funding><pagination>8403-8419</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8928532</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(10)</volume><pubmed_abstract>The design of a highly active Fe-supported catalyst with the optimum particle and pore size, dispersion, loading, and stability is essential for obtaining the desired product selectivity. This study employed a solvothermal method to prepare two Fe-MIL-88B metal-organic framework (MOF)-derived catalysts using triethylamine (TEA) or NaOH as deprotonation catalysts. The catalysts were analyzed using X-ray diffraction, N&lt;sub>2&lt;/sub>-physisorption, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, H&lt;sub>2&lt;/sub> temperature-programed reduction, and thermogravimetric analysis and were evaluated for the Fischer-Tropsch synthesis performance. It was evident that the catalyst preparation in the presence of TEA produces a higher MOF yield and smaller crystal size than those produced using NaOH. The pyrolysis of MOFs yielded catalysts with different Fe particle sizes of 6 and 35 nm for the preparation in the presence of TEA and NaOH, respectively. Also, both types of catalysts exhibited a high Fe loading (50%) and good stability after 100 h reaction time. The smaller particle size TEA catalyst showed higher activity and higher olefin yield, with 94% CO conversion and a higher olefin yield of 24% at a lower reaction temperature of 280 °C and 20 bar at H&lt;sub>2&lt;/sub>/CO = 1. Moreover, the smaller particle size TEA catalyst exhibited higher Fe time yield and CH&lt;sub>4&lt;/sub> selectivity but with lower chain growth probability (α) and C&lt;sub>5+&lt;/sub> selectivity.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Fe Nanoparticle Size Control of the Fe-MOF-Derived Catalyst Using a Solvothermal Method: Effect on FTS Activity and Olefin Production.</pubmed_title><pmcid>PMC8928532</pmcid><funding_grant_id>7825</funding_grant_id><pubmed_authors>El-Moneim AA</pubmed_authors><pubmed_authors>Nasser A</pubmed_authors><pubmed_authors>Elkady MF</pubmed_authors><pubmed_authors>Rashed AE</pubmed_authors><pubmed_authors>Matsushita Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fe Nanoparticle Size Control of the Fe-MOF-Derived Catalyst Using a Solvothermal Method: Effect on FTS Activity and Olefin Production.</name><description>The design of a highly active Fe-supported catalyst with the optimum particle and pore size, dispersion, loading, and stability is essential for obtaining the desired product selectivity. This study employed a solvothermal method to prepare two Fe-MIL-88B metal-organic framework (MOF)-derived catalysts using triethylamine (TEA) or NaOH as deprotonation catalysts. The catalysts were analyzed using X-ray diffraction, N&lt;sub>2&lt;/sub>-physisorption, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, H&lt;sub>2&lt;/sub> temperature-programed reduction, and thermogravimetric analysis and were evaluated for the Fischer-Tropsch synthesis performance. It was evident that the catalyst preparation in the presence of TEA produces a higher MOF yield and smaller crystal size than those produced using NaOH. The pyrolysis of MOFs yielded catalysts with different Fe particle sizes of 6 and 35 nm for the preparation in the presence of TEA and NaOH, respectively. Also, both types of catalysts exhibited a high Fe loading (50%) and good stability after 100 h reaction time. The smaller particle size TEA catalyst showed higher activity and higher olefin yield, with 94% CO conversion and a higher olefin yield of 24% at a lower reaction temperature of 280 °C and 20 bar at H&lt;sub>2&lt;/sub>/CO = 1. Moreover, the smaller particle size TEA catalyst exhibited higher Fe time yield and CH&lt;sub>4&lt;/sub> selectivity but with lower chain growth probability (α) and C&lt;sub>5+&lt;/sub> selectivity.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-26T03:51:17.405Z</modification><creation>2025-04-06T10:58:44.314Z</creation></dates><accession>S-EPMC8928532</accession><cross_references><pubmed>35309432</pubmed><doi>10.1021/acsomega.1c05927</doi></cross_references></HashMap>