journal article·2024-08-14

Highly Selective SO2 Capture by Triazine-Functionalized Triphenylamine-Based Nanoporous Organic Polymers

Sihan Tong, Jiangli Zhu, Zefeng Wang, Jun Yan

ACS Applied Materials & Interfaces· Volume 16· Issue 32
Publisher page

Abstract

The emissions of sulfur dioxide (SO 2 ) from combustion exhaust gases pose significant risks to public health and the environment due to their harmful effects. Therefore, the development of highly efficient adsorbent polymers capable of capturing SO 2 with high capacity and selectivity has emerged as a critical challenge in recent years. However, existing polymers often exhibit poor SO 2 /CO 2 and SO 2 /N 2 selectivity. Herein, we report two triazine-functionalized triphenylamine-based nanoporous organic polymers (ANOP-6 and ANOP-7) that demonstrate both good SO 2 uptake and high SO 2 /CO 2 and SO 2 /N 2 selectivity. These polymers were synthesized through cost-effective Friedel–Crafts reactions using cyanuric chloride, 3,6-diphenylaminecarbazole, and 2,2′,7,7′-tetrakis(diphenylamino)-9,9′-spirobifluorene. The resultant ANOPs are composed of triazine and triphenylamine units and feature an ultramicroporous structure. Remarkably, ANOPs exhibit impressive adsorption capacities for SO 2, with uptakes of approximately 3.31–3.72 mmol·g –1 at 0.1 bar, increasing to 9.52–9.94 mmol·g –1 at 1 bar. The static adsorption isotherms effectively illustrate the ability of ANOPs to separate SO 2 from SO 2 /CO 2 and SO 2 /N 2 mixtures. At 298 K and 1 bar, ANOP-6 shows outstanding selectivity toward SO 2 /CO 2 (248) and SO 2 /N 2 (13146), surpassing all previously reported triazine-based nanoporous organic polymers. Additionally, dynamic breakthrough tests demonstrate the superior separation properties of ANOPs for SO 2 from an SO 2 /CO 2 /N 2 mixture. ANOPs exhibit a breakthrough time of 73.1 min·g –1 and a saturated SO 2 capacity of 0.53 mmol·g –1 . These results highlight the exceptional adsorption properties of ANOPs for SO 2, indicating their promising potential for the highly efficient capture of SO 2 from flue gas.
Source: openalex_inverted_index · Quality: baseline

Research context

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

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

Affiliations

International Scientific and Technological Cooperation Base of Industrial Solid Waste Cyclic Utilization and Advanced Materials, School of Materials Science and Engineering, North Minzu University, Yinchuan 750021, China

College of Ecology, Lishui University, Lishui 323000, China

R&D Center of Green Manufacturing New Materials and Technology of Synthetic Leather, Sichuan University-Lishui University, Lishui 323000, China

Funding

Graduate Innovation Project of North Minzu University · Natural Science Foundation of Ningxia Province · National Natural Science Foundation of China · Eighth Batch of NingXia Youth Talents Supporting Program

References (54)

Show source-provided references
1. 10.1038/nature1537110.1038/nature15371 ↗
2. 10.1080/10473289.2001.1046438710.1080/10473289.2001.10464387 ↗
3. 10.1016/j.rser.2010.11.03710.1016/j.rser.2010.11.037 ↗
4. 10.1039/C8PY01620H10.1039/C8PY01620H ↗
5. 10.1039/C6CS00851H10.1039/C6CS00851H ↗
6. 10.1016/j.progpolymsci.2011.09.00210.1016/j.progpolymsci.2011.09.002 ↗
7. 10.1039/D3CC05456J10.1039/D3CC05456J ↗
8. 10.1039/D3PY01215H10.1039/D3PY01215H ↗
9. 10.1021/acsapm.3c0216010.1021/acsapm.3c02160 ↗
10. 10.1021/acsapm.3c0146110.1021/acsapm.3c01461 ↗
11. 10.1039/D2TA10031B10.1039/D2TA10031B ↗
12. 10.1016/j.seppur.2023.12320510.1016/j.seppur.2023.123205 ↗
13. 10.1016/j.cej.2021.13248010.1016/j.cej.2021.132480 ↗
14. 10.1021/acsmacrolett.2c0032010.1021/acsmacrolett.2c00320 ↗
15. 10.1039/C6TA06089G10.1039/C6TA06089G ↗
16. 10.1039/C9TA06847C10.1039/C9TA06847C ↗
17. 10.1021/ma502071w10.1021/ma502071w ↗
18. 10.1039/D2NJ00727D10.1039/D2NJ00727D ↗
19. 10.1021/acsami.8b1341710.1021/acsami.8b13417 ↗
20. 10.1021/acsami.9b1590310.1021/acsami.9b15903 ↗
21. 10.1002/agt2.40810.1002/agt2.408 ↗
22. 10.1021/acs.iecr.2c0193110.1021/acs.iecr.2c01931 ↗
23. 10.1021/acsapm.2c0052910.1021/acsapm.2c00529 ↗
24. 10.1002/adfm.20190478110.1002/adfm.201904781 ↗
25. 10.1039/C6PY02050J10.1039/C6PY02050J ↗
26. 10.1039/C6TA00638H10.1039/C6TA00638H ↗
27. 10.1002/macp.20220003410.1002/macp.202200034 ↗
28. 10.1021/acs.macromol.1c0241310.1021/acs.macromol.1c02413 ↗
29. 10.1021/acsami.0c2174110.1021/acsami.0c21741 ↗
30. 10.1021/acsanm.1c0205310.1021/acsanm.1c02053 ↗
31. 10.1039/C4TA04429K10.1039/C4TA04429K ↗
32. 10.1021/acsami.3c0528810.1021/acsami.3c05288 ↗
33. 10.1021/jacs.3c0330910.1021/jacs.3c03309 ↗
34. 10.1038/s41598-017-00738-z10.1038/s41598-017-00738-z ↗
35. 10.1021/jacs.3c1306910.1021/jacs.3c13069 ↗
36. 10.1021/acsnano.1c0717810.1021/acsnano.1c07178 ↗
37. 10.1021/acs.inorgchem.0c0352610.1021/acs.inorgchem.0c03526 ↗
38. 10.1021/acs.inorgchem.1c0003310.1021/acs.inorgchem.1c00033 ↗
39. 10.1002/adma.20160692910.1002/adma.201606929 ↗
40. 10.1021/jacs.8b0843310.1021/jacs.8b08433 ↗
41. 10.1002/anie.20210455510.1002/anie.202104555 ↗
42. 10.1016/j.cej.2020.12485910.1016/j.cej.2020.124859 ↗
43. 10.1021/acs.inorgchem.2c0163410.1021/acs.inorgchem.2c01634 ↗
44. 10.1021/acs.macromol.1c0038510.1021/acs.macromol.1c00385 ↗
45. 10.1021/acsanm.1c0337310.1021/acsanm.1c03373 ↗
46. 10.1021/acsapm.4c0132510.1021/acsapm.4c01325 ↗
47. 10.1016/j.micromeso.2024.11320610.1016/j.micromeso.2024.113206 ↗
48. 10.1021/acs.iecr.9b0604010.1021/acs.iecr.9b06040 ↗
49. 10.1021/acs.iecr.9b0193810.1021/acs.iecr.9b01938 ↗
50. 10.1016/j.cej.2019.12357910.1016/j.cej.2019.123579 ↗
51. 10.1021/acsmaterialslett.0c0026410.1021/acsmaterialslett.0c00264 ↗
52. 10.1021/acsami.9b0142310.1021/acsami.9b01423 ↗
53. 10.1016/j.seppur.2017.11.05610.1016/j.seppur.2017.11.056 ↗
54. 10.1021/acsomega.0c0221810.1021/acsomega.0c02218 ↗