journal article·2024-04-09

Basic Zeolites as Efficient Adsorbents for Removing Trace Amounts of Acetylene from Ethylene

Yejee Ha, Younghwan Park, Kyunglim Hyun, Seyeon Lim, Minkee Choi

Chemistry of Materials· Volume 36· Issue 7
Publisher page

Abstract

Adsorptive separation of acetylene (C 2 H 2 ) from ethylene (C 2 H 4 ) using porous materials has emerged as an energy-efficient process for obtaining polymer-grade C 2 H 4 . Numerous microporous organometallic and organic materials have recently been developed to selectively adsorb C 2 H 2 over C 2 H 4 . In contrast, zeolites, widely used commercial adsorbents due to their stability and synthesis scalability, have rarely been explored for C 2 H 2 /C 2 H 4 separation. In this study, we synthesized faujasite (FAU) zeolite adsorbents with different basic properties by controlling Si/Al ratios, charge-balancing cations (Na + and K + ), and the amount of excess alkali oxides and investigated their performance in the C 2 H 2 /C 2 H 4 separation. The results demonstrate that zeolites with higher basicity (or with more negatively charged O atoms) exhibit a stronger interaction with C 2 H 2 through C δ− –H δ+ ···O δ− Lewis acid–base interactions. Meanwhile, larger K + extraframework cations located in more accessible supercages provide additional interactions with the abundant π-electrons of C 2 H 2 . Therefore, the KX zeolite supported with 3 wt % K 2 O clusters within its micropore (3K 2 O/KX) exhibited a high IAST C 2 H 2 /C 2 H 4 selectivity of 20.2 as well as a remarkable dynamic selectivity of 121.8 at 298 K and 1 bar for a 1/99 (v/v) C 2 H 2 /C 2 H 4 mixture. The adsorbent enabled the efficient production of high-purity C 2 H 4 (>99.9995%) from a mixture of C 2 H 2 /C 2 H 4 (1/99) with a high productivity (758.2 L kg –1 ). These findings hold promise for the development of efficient, stable, and scalable inorganic adsorbents in C 2 H 2 /C 2 H 4 separation.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Zeolite Catalysis and Synthesis · Gas Sensing Nanomaterials and Sensors · Metal-Organic Frameworks: Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical and Biomolecular Engineering (BK21 Four), Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea

Funding

Korea Environmental Industry and Technology Institute

References (50)

Show source-provided references
1. 10.1016/J.ENG.2017.02.00610.1016/J.ENG.2017.02.006 ↗
2. 10.1080/0161494050036490910.1080/01614940500364909 ↗
3. 10.1126/sciadv.abb736910.1126/sciadv.abb7369 ↗
4. 10.1002/anie.20210081410.1002/anie.202100814 ↗
5. 10.1016/j.jcat.2021.09.01710.1016/j.jcat.2021.09.017 ↗
6. 10.1016/j.jcat.2022.11.00810.1016/j.jcat.2022.11.008 ↗
7. 10.1038/s41467-019-12460-710.1038/s41467-019-12460-7 ↗
8. 10.1021/acscatal.1c0475810.1021/acscatal.1c04758 ↗
9. 10.1021/acscatal.3c0144210.1021/acscatal.3c01442 ↗
10. 10.1007/s11705-015-1516-410.1007/s11705-015-1516-4 ↗
11. 10.1002/cjce.545069011810.1002/cjce.5450690118 ↗
12. 10.1039/C7CS00153C10.1039/C7CS00153C ↗
13. 10.1016/j.trechm.2019.02.01210.1016/j.trechm.2019.02.012 ↗
14. 10.1038/ncomms120610.1038/ncomms1206 ↗
15. 10.1021/ja302380x10.1021/ja302380x ↗
16. 10.1038/nchem.211410.1038/nchem.2114 ↗
17. 10.1038/ncomms832810.1038/ncomms8328 ↗
18. 10.1126/science.aaf245810.1126/science.aaf2458 ↗
19. 10.1021/jacs.7b0385010.1021/jacs.7b03850 ↗
20. 10.1002/adma.20170421010.1002/adma.201704210 ↗
21. 10.1021/jacs.0c0259410.1021/jacs.0c02594 ↗
22. 10.1021/acs.iecr.8b0095010.1021/acs.iecr.8b00950 ↗
23. 10.1038/s41467-020-20101-710.1038/s41467-020-20101-7 ↗
24. 10.1002/ange.20200768110.1002/ange.202007681 ↗
25. 10.1002/anie.20180673210.1002/anie.201806732 ↗
26. 10.1126/science.121754410.1126/science.1217544 ↗
27. 10.1021/jacs.8b1346310.1021/jacs.8b13463 ↗
28. 10.1021/acsami.1c2053310.1021/acsami.1c20533 ↗
29. 10.1021/acs.chemmater.9b0169110.1021/acs.chemmater.9b01691 ↗
30. 10.1021/jacs.8b0817410.1021/jacs.8b08174 ↗
31. 10.1002/marc.20170046810.1002/marc.201700468 ↗
32. 10.1002/adma.20190744910.1002/adma.201907449 ↗
33. 10.1002/adma.20190760110.1002/adma.201907601 ↗
34. Pässler, P.; Hefner, W.; Buckl, K.; Meinass, H.; Meiswinkel, A.; Wernicke, H. J.; Ebersberg, G.; Müller, R.; Bässler, J.; Behringer, H.; Mayer, D.Acetylene. Ullmann’s Encyclopedia of Industrial Chemistry 2000; Vol. 1, pp 277–326 10.1002/14356007.a01_097.pub2.10.1002/14356007.a01_097.pub2 ↗
35. 10.1021/cr500258910.1021/cr5002589 ↗
36. 10.1039/C7CS00109F10.1039/C7CS00109F ↗
37. 10.1126/science.aay844710.1126/science.aay8447 ↗
38. 10.1021/j100155a04010.1021/j100155a040 ↗
39. 10.1039/FT993890184310.1039/FT9938901843 ↗
40. 10.1016/0021-9517(78)90200-210.1016/0021-9517(78)90200-2 ↗
41. 10.1021/j150645a01010.1021/j150645a010 ↗
42. 10.1016/0021-9517(88)90157-110.1016/0021-9517(88)90157-1 ↗
43. Sanderson R. T. · 1976 · 77
44. 10.1016/j.jcat.2019.03.02710.1016/j.jcat.2019.03.027 ↗
45. 10.1016/S0167-2991(06)81230-910.1016/S0167-2991(06)81230-9 ↗
46. 10.1039/a802189i10.1039/a802189i ↗
47. 10.1021/j100876a02610.1021/j100876a026 ↗
48. 10.1039/F197672025710.1039/F1976720257 ↗
49. 10.1039/F1976720259210.1039/F19767202592 ↗
50. 10.1021/ar300265y10.1021/ar300265y ↗