Homocondensation of Acetone over Cation-Exchanged Granulated Hierarchical Yh Zeolites
The catalytic performance (activity and selectivity) of a FAU-type hierarchical NaYh zeolite, as well as of a series of modified samples, was investigated in the homocondensation of acetone. The modified samples were prepared from NaYh by ion exchange of Na+ for cations of alkali (Li+, K+), alkaline-earth (Ca2+, Mg2+), transition (Co2+, Ni2+), and rare-earth (La3+) metals, as well as by decationation (H-NaYh, HYh). The predominantly acidic zeolites (Ca-NaYh, Mg-NaYh, Co-NaYh, Ni-NaYh, La-NaYh, H-NaYh, and HYh) promoted the formation of acetic acid and mesitylene even at 250°C. The zeolites that contained alkali metal cations (Na+, Li+, and K+) exhibited activity only when the temperature was elevated. Starting from 350°C, NaYh and Li-NaYh promoted the formation of acetic acid. In contrast, the performance of K-NaYh under heating was characterized by the absence of acetic acid formation and a smooth increase in the selectivity towards isophorone (up to 23%) and mesitylene (up to 18%). Over the range of 400–450°C, in the presence of K-NaYh, secondary isophorone transformations were intensified, resulting in the formation of 3,5-xylenol as the main product with a selectivity of 32%.
Authors
- Victor Yu. Kirsanov (ORCID: https://orcid.org/0000-0002-0671-6048)
- Boris Ivanovich Kutepov (ORCID: https://orcid.org/0000-0003-0745-5510)
- Н. Г. Григорьева (ORCID: https://orcid.org/0000-0001-6451-9205)
- A. N. Khazipova (ORCID: https://orcid.org/0000-0003-1206-4637)
- S. G. Karchevsky (ORCID: https://orcid.org/0000-0001-6778-4872)
- Л. Ф. Коржова (ORCID: https://orcid.org/0009-0000-6961-9790)
Institutions
- Institute of Catalysis and Petrochemistry (RU)
- Ufa Institute of Chemistry (RU)
- Bashkir Scientific Research Institute of Petroleum Refining (RU)
- Academy of Sciences of the Republic of Bashkortostan (RU)
Publication Details
- Journal
- Petroleum Chemistry
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1134/s0965544125600663
- Primary Topic
- Catalysis for Biomass Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00