Facile and Environmentally Friendly Synthesis of Ga2O3/MFI Catalysts for Propane Dehydrogenation
Source abstract
Abstract
A GaO x -based catalyst is recognized as a promising catalyst for dehydrogenation of light alkanes. Conventionally, impregnation and calcination are necessary processes for the loading of GaO x . However, the incomplete impregnation of gallium salt solution would generate wastewater, and the calcination for the dissociation of gallium salt would release harmful gases, such as SO x, NO x, and HCl. Meanwhile, the high temperature results in an excessive energy cost and undesired GaO x particle aggregation. Here, we report a facile and environmentally friendly method for the synthesis of GaO x -based catalysts. The gallium salt solution was replaced directly with liquid gallium (LG). Through a simple physical mixing method at room temperature, uniform GaO x nanoparticles with diameters of around 3.5 nm were loaded onto the surface of silicalite-1 (S-1). With the optimal GaO x /MFI catalyst, the propane conversion and propylene selectivity reached 22.9 and 90.1%, respectively, in the propane dehydrogenation reaction. The work offers a clean and economical strategy utilizing liquid metal (LM) as an impregnation solution for the preparation of GaO x -based catalysts.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalysis and Oxidation Reactions · Catalytic Processes in Materials Science · Zeolite Catalysis and Synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Innovation Center for Chemical Sciences, College of Chemistry, Chemical Engineering and Materials Science
Soochow University
Jiangsu Key Laboratory of Advanced Negative Carbon Technologies
Dental Clinic of Xuhui District
Funding
National Key Research and Development Program of China · Jiangsu Shuangchuang Doctor Program
References (33)
Show source-provided references
1. 10.1134/S207005041503008310.1134/S2070050415030083 ↗
2. 10.1007/s13203-015-0104-310.1007/s13203-015-0104-3 ↗
3. 10.1021/acscatal.5b0000710.1021/acscatal.5b00007 ↗
4. 10.1021/cs400343610.1021/cs4003436 ↗
5. 10.1039/D0CS00814A10.1039/D0CS00814A ↗
6. 10.1039/D0CS01260B10.1039/D0CS01260B ↗
7. 10.1039/D1CS00357G10.1039/D1CS00357G ↗
8. 10.1038/s41563-019-0412-610.1038/s41563-019-0412-6 ↗
9. 10.1038/s41586-020-2671-410.1038/s41586-020-2671-4 ↗
10. 10.1126/science.abg789410.1126/science.abg7894 ↗
11. 10.3390/catal1211137110.3390/catal12111371 ↗
12. 10.3390/molecules2608223410.3390/molecules26082234 ↗
13. 10.1016/j.jcat.2005.03.00110.1016/j.jcat.2005.03.001 ↗
14. 10.1038/s41557-023-01392-x10.1038/s41557-023-01392-x ↗
15. 10.1021/acscatal.1c0262110.1021/acscatal.1c02621 ↗
16. 10.1039/D2CY00074A10.1039/D2CY00074A ↗
17. 10.1039/C6RA27204E10.1039/C6RA27204E ↗
18. 10.1016/j.jcat.2006.02.01710.1016/j.jcat.2006.02.017 ↗
19. 10.1021/acscatal.3c0100210.1021/acscatal.3c01002 ↗
20. 10.1021/jacs.7b1290110.1021/jacs.7b12901 ↗
21. 10.1016/j.apcata.2022.11877810.1016/j.apcata.2022.118778 ↗
22. 10.1007/s10562-007-9232-410.1007/s10562-007-9232-4 ↗
23. 10.1021/jacs.2c0381010.1021/jacs.2c03810 ↗
24. 10.1021/jacs.2c0394110.1021/jacs.2c03941 ↗
25. 10.1002/ange.20140446010.1002/ange.201404460 ↗
26. 10.1016/j.apcata.2015.03.02010.1016/j.apcata.2015.03.020 ↗
27. 10.1002/cctc.20150091610.1002/cctc.201500916 ↗
28. 10.1002/smtd.20220024610.1002/smtd.202200246 ↗
29. 10.1038/s41467-024-46232-910.1038/s41467-024-46232-9 ↗
30. 10.1002/adma.20200554410.1002/adma.202005544 ↗
31. 10.1039/C7CS00043J10.1039/C7CS00043J ↗
32. Ertl G. · 199710.1002/9783527619474 ↗
33. Lloyd L. · 201110.1007/978-0-387-49962-8 ↗