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- 01J83T3E2FA0PNTH1Q069E2FNJ classification A1.
- 01J83T3E2FA0PNTH1Q069E2FNJ date "2025".
- 01J83T3E2FA0PNTH1Q069E2FNJ language "eng".
- 01J83T3E2FA0PNTH1Q069E2FNJ type journalArticle.
- 01J83T3E2FA0PNTH1Q069E2FNJ hasPart 01J83TCNBC2VSPGMDQXTRGFHS5.pdf.
- 01J83T3E2FA0PNTH1Q069E2FNJ hasPart 01J84KQRYZSEZ3CKMYGMERJCXY.pdf.
- 01J83T3E2FA0PNTH1Q069E2FNJ subject "Earth and Environmental Sciences".
- 01J83T3E2FA0PNTH1Q069E2FNJ subject "Technology and Engineering".
- 01J83T3E2FA0PNTH1Q069E2FNJ doi "10.1016/j.fuel.2024.133173".
- 01J83T3E2FA0PNTH1Q069E2FNJ issn "0016-2361".
- 01J83T3E2FA0PNTH1Q069E2FNJ issn "1873-7153".
- 01J83T3E2FA0PNTH1Q069E2FNJ volume "380".
- 01J83T3E2FA0PNTH1Q069E2FNJ abstract "The hydrothermal technique was applied to prepare a new metal–organic framework, MIL-100(Fe), which was modified by ultrasonic impregnation with different wt % of copper. The results showed that the NOx conversion over 2.3Cu-MIL-100(Fe) was 100 % at 275 °C and maintained at ≥ 85 %, with N2 selectivity ≥ 90 % in the temperature range of 275–400 °C and high SO2 resistance. An increase in the Cu content up to 2.3 wt% showed the highest surface area (1206 m2/g) observed in N2 adsorption–desorption. The results show that the introduction of Cu increased the oxygen vacancies on the catalyst surface. Electron transfer and a synergistic effect were observed between Cu and Fe. The shift of the reduction peaks to lower temperatures after the addition of Cu confirmed that Cu improved the reducibility of the catalysts. The 2.3Cu-MIL-100(Fe) exhibited the highest Lewis content (44.97 μmol/g), which functions as an active site for the selective catalytic reduction (SCR) reaction. By precisely controlling the acid-base properties of the catalyst, the specificity for the desired products can be increased in complicated reaction systems, especially in hydrocarbon-SCR technology.".
- 01J83T3E2FA0PNTH1Q069E2FNJ author F714BB94-F0ED-11E1-A9DE-61C894A0A6B4.
- 01J83T3E2FA0PNTH1Q069E2FNJ author f1e32682-2627-11ec-9b95-c06691ecff6f.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:1464266f-a064-4295-9d4e-ca3a62873391.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:459f3015-b17b-4374-b20e-7b3ba2f715a3.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:712e67b1-efdd-43a7-830c-e9358ea88e5a.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:ec09c4c3-448a-48ea-807a-1bca57029c9d.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:f076bcf2-e09b-42f0-8716-4834cdcf1d88.
- 01J83T3E2FA0PNTH1Q069E2FNJ author urn:uuid:f48b2439-e0a3-46ed-aebe-47c415da9844.
- 01J83T3E2FA0PNTH1Q069E2FNJ dateCreated "2024-09-19T00:14:51Z".
- 01J83T3E2FA0PNTH1Q069E2FNJ dateModified "2024-11-28T00:14:27Z".
- 01J83T3E2FA0PNTH1Q069E2FNJ name "Design of Cu-based MIL-100(Fe) catalyst for propylene-selective catalytic reduction of NOx : combination of activity, characterizations and mechanism".
- 01J83T3E2FA0PNTH1Q069E2FNJ pagination urn:uuid:1c757de9-f923-4047-9758-4497486f0861.
- 01J83T3E2FA0PNTH1Q069E2FNJ sameAs LU-01J83T3E2FA0PNTH1Q069E2FNJ.
- 01J83T3E2FA0PNTH1Q069E2FNJ sourceOrganization urn:uuid:5b27bc79-c7d4-4152-bb5e-aaf251643767.
- 01J83T3E2FA0PNTH1Q069E2FNJ sourceOrganization urn:uuid:cafe7a5b-7107-4342-b8fc-bd1c634e9c76.
- 01J83T3E2FA0PNTH1Q069E2FNJ type A1.