journal article·2022-01-11

Optimizing Host–Guest Selectivity for Ethylbenzene Capture Toward Superior Styrene Purification

Yanjun Ding, Avishek Dey, Lukman O. Alimi, Prashant M. Bhatt, Jing Du, Carine Maaliki, Mohamed Eddaoudi, Johan Jacquemin, Niveen M. Khashab

Chemistry of Materials· Volume 34· Issue 1
Publisher page

Abstract

The separation of ethylbenzene (EB) and styrene (ST) mixtures to obtain pure ST has been an enduring challenge for the petrochemical industry. So far, adsorptive separation using porous materials has mainly focused on capturing ST rather than EB, where high temperatures are needed to reactivate the sieving materials and collect the product. Here, we tuned the host–guest interactions in thienothiophene-based trianglimine (ThT-TI) macrocycles to selectively adsorb the unreacted EB over ST, after a dehydrogenation reaction, to readily provide pure ST without the need for further thermal treatments. This is the first report on the selective adsorptive separation of EB over ST using macrocycles as molecular hosts. Both crystalline and amorphous ThT-TI can be used to separate EB with 96% uptake capacity. Single-crystal and powder X-ray diffraction patterns suggest that this selective adsorption arises from a guest-induced structural reordering and involvement of the sulfur atoms in host/guest C–H···π interactions. We believe that this work paves the way for a new generation of molecular sieves that are designed to afford high-purity products by in situ capturing of the unreacted starting materials.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Membrane Separation and Gas Transport

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

Affiliations

Smart Hybrid Materials (SHMs) Laboratory, Advanced Membranes and Porous Materials Center, Department of Chemistry, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Kingdom of Saudi Arabia

Functional Materials Design, Discovery and Development Research Group, Advanced Membranes and Porous Materials Center, Division of Physical Sciences and Engineering, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Kingdom of Saudi Arabia

Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun 130024, China

Laboratoire PCM2E, Université de Tours, Parc de Grandmont, 37200 Tours, France

Funding

King Abdullah University of Science and Technology

References (47)

Show source-provided references
1. 10.1038/s41467-021-21374-210.1038/s41467-021-21374-2 ↗
2. 10.1080/0161494740807186410.1080/01614947408071864 ↗
3. 10.1021/la902276a10.1021/la902276a ↗
4. 10.1021/ja044866710.1021/ja0448667 ↗
5. 10.1039/c2ee22858k10.1039/c2ee22858k ↗
6. 10.1038/374042a010.1038/374042a0 ↗
7. 10.1021/ja305663k10.1021/ja305663k ↗
8. 10.1126/science.aaf632310.1126/science.aaf6323 ↗
9. 10.1002/anie.20170876910.1002/anie.201708769 ↗
10. 10.1038/s41563-018-0206-210.1038/s41563-018-0206-2 ↗
11. 10.1021/jacs.9b0307510.1021/jacs.9b03075 ↗
12. 10.1021/ja908837810.1021/ja9088378 ↗
13. 10.1021/acs.accounts.8b0065810.1021/acs.accounts.8b00658 ↗
14. 10.1039/b802426j10.1039/b802426j ↗
15. 10.1021/acs.inorgchem.5b0020610.1021/acs.inorgchem.5b00206 ↗
16. 10.1021/ie301526810.1021/ie3015268 ↗
17. 10.1016/j.seppur.2020.11675810.1016/j.seppur.2020.116758 ↗
18. 10.1039/C4CS00006D10.1039/C4CS00006D ↗
19. 10.1002/ejic.20100049410.1002/ejic.201000494 ↗
20. 10.1021/jp105637u10.1021/jp105637u ↗
21. 10.1021/acsami.0c1823210.1021/acsami.0c18232 ↗
22. 10.1021/acsami.9b2009210.1021/acsami.9b20092 ↗
23. 10.1002/anie.20210431810.1002/anie.202104318 ↗
24. 10.1021/ja106142x10.1021/ja106142x ↗
25. 10.1021/jacs.5b1286010.1021/jacs.5b12860 ↗
26. 10.1021/acs.langmuir.5b0036310.1021/acs.langmuir.5b00363 ↗
27. 10.1038/s41563-019-0427-z10.1038/s41563-019-0427-z ↗
28. 10.1021/acs.accounts.8b0025510.1021/acs.accounts.8b00255 ↗
29. 10.1021/acs.accounts.8b0029810.1021/acs.accounts.8b00298 ↗
30. 10.1002/anie.20191305510.1002/anie.201913055 ↗
31. 10.1002/anie.20200943610.1002/anie.202009436 ↗
32. 10.1002/anie.20200699910.1002/anie.202006999 ↗
33. 10.1002/adfm.20190984210.1002/adfm.201909842 ↗
34. 10.1002/anie.20200778210.1002/anie.202007782 ↗
35. 10.1038/nmat403510.1038/nmat4035 ↗
36. 10.1021/jacs.5b1179710.1021/jacs.5b11797 ↗
37. 10.1038/nchem.155010.1038/nchem.1550 ↗
38. 10.1021/jacs.6b1330010.1021/jacs.6b13300 ↗
39. 10.1021/jacs.0c1301910.1021/jacs.0c13019 ↗
40. 10.1039/D1SC00440A10.1039/D1SC00440A ↗
41. 10.1021/jacs.9b1242810.1021/jacs.9b12428 ↗
42. 10.1039/c004873a10.1039/c004873a ↗
43. 10.1021/jacs.0c0577610.1021/jacs.0c05776 ↗
44. 10.1021/jo000623v10.1021/jo000623v ↗
45. 10.1007/s00214005026910.1007/s002140050269 ↗
46. 10.1016/S0009-2614(98)00862-810.1016/S0009-2614(98)00862-8 ↗
47. 10.1103/PhysRevA.38.309810.1103/PhysRevA.38.3098 ↗