journal article·2023-01-13

Porous Hybrid Triazine-Functionalized Polymers with High Capture Ability for I2 and Dyes

Mengshuang Zhang, Yajing Du, Hongzhi Liu

ACS Applied Polymer Materials· Volume 5· Issue 1
Publisher page

Abstract

Porous hybrid polymers have a vast range of prospects in the field of environmental restoration because of their excellent comprehensive performances in recent years. Two types of porous silsesquioxane/triazine hybrid polymers (PCS-TPH-1, PCS-TPH and PCS-TSA-1, PCS-TSA) were prepared by the Friedel–Crafts reaction with different ratios of phenyl- or thiophene-substituted triazine monomers and octavinylsilsesquioxane (OVS). PCS-TPH and PCS-TSA with higher specific surface areas were selected to probe their adsorption capacities for dyes and iodine vapor. Relative to PCA-TSA, PCS-TPH with a large specific surface area and a high mesoporous ratio preferred to adsorb large-sized Congo Red (CR) and rhodamine (RB) with absorption capacities of 935 and 1180 mg g–1, respectively. Under the combined action of heteroatoms and specific surface areas, PCS-TPH and PCA-TSA showed a similar I2 adsorption amount of ∼2.4 g g–1. In addition, due to the effect of charge transfer, the resulting materials can specifically respond to I2 among many other different types of anions.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Metal-Organic Frameworks: Synthesis and Applications · Luminescence and Fluorescent Materials

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

Affiliations

International Centre for Interdisciplinary Research and Innovation of Silsesquioxane Science, Key Laboratory of Special Functional Aggregated Materials, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, P. R. China

Shandong Institute of Advanced Technology, 250100 Jinan, P. R. China

Funding

Ministry of Science and Technology of the People's Republic of China · Shandong Province · Shandong University · National Natural Science Foundation of China · Natural Science Foundation of Shandong Province

References (51)

Show source-provided references
1. 10.1016/j.cej.2010.07.01410.1016/j.cej.2010.07.014 ↗
2. 10.1016/j.eurpolymj.2021.11075310.1016/j.eurpolymj.2021.110753 ↗
3. Wang, G.; Zhu, F.; Li, S.; Xie, K.; Huang, Z.; Geng, Y.; Dong, Y. Tetrathiafulvalenyl Covalent Organic Framework Material and Its Preparation Method and Application in Radionuclide Iodine Adsorption, CN113083235A 2021.
4. 10.1039/C8TA07109H10.1039/C8TA07109H ↗
5. 10.1016/j.envpol.2020.11549810.1016/j.envpol.2020.115498 ↗
6. 10.1002/chem.20180054810.1002/chem.201800548 ↗
7. 10.1016/j.cej.2009.10.02910.1016/j.cej.2009.10.029 ↗
8. 10.1039/C5EE02843D10.1039/C5EE02843D ↗
9. 10.1021/jacs.5b0911010.1021/jacs.5b09110 ↗
10. 10.1039/C7TA10538J10.1039/C7TA10538J ↗
11. 10.1039/C7CS00653E10.1039/C7CS00653E ↗
12. 10.1002/chem.20170208710.1002/chem.201702087 ↗
13. 10.1039/D0PY00249F10.1039/D0PY00249F ↗
14. 10.1021/acsami.6b0656910.1021/acsami.6b06569 ↗
15. 10.1016/j.scitotenv.2019.13507010.1016/j.scitotenv.2019.135070 ↗
16. 10.1021/acscatal.7b0171910.1021/acscatal.7b01719 ↗
17. 10.1002/adsu.20200028510.1002/adsu.202000285 ↗
18. 10.1021/acs.jced.6b0035810.1021/acs.jced.6b00358 ↗
19. 10.1016/j.chemosphere.2019.12537810.1016/j.chemosphere.2019.125378 ↗
20. 10.1002/anie.20171116910.1002/anie.201711169 ↗
21. 10.1038/s41467-021-26817-410.1038/s41467-021-26817-4 ↗
22. 10.1016/j.chemosphere.2021.12962210.1016/j.chemosphere.2021.129622 ↗
23. 10.1039/D1QM00686J10.1039/D1QM00686J ↗
24. Liu, H.; Du, Y. Triazine Functionalized Silsesquioxane-based Hybrid Porous Polymer For Detection Of Catalytic Degradation Of Dye Pollutants Or Nitroarenes And Preparation Method Thereof, CN112851944A 2021.
25. 10.1002/chem.20180449610.1002/chem.201804496 ↗
26. 10.1039/c2jm31248d10.1039/c2jm31248d ↗
27. 10.1002/ejic.20140215610.1002/ejic.201402156 ↗
28. 10.1039/C6TA06656A10.1039/C6TA06656A ↗
29. 10.1002/slct.20170313310.1002/slct.201703133 ↗
30. 10.1016/S1872-2067(20)63603-810.1016/S1872-2067(20)63603-8 ↗
31. 10.1021/cm101788210.1021/cm1017882 ↗
32. 10.1021/acsami.7b0391010.1021/acsami.7b03910 ↗
33. 10.1021/ja980885310.1021/ja9808853 ↗
34. 10.1039/C9NJ05509F10.1039/C9NJ05509F ↗
35. 10.1007/s11356-019-06534-810.1007/s11356-019-06534-8 ↗
36. 10.1039/C6RA02963A10.1039/C6RA02963A ↗
37. 10.1016/j.materresbull.2016.06.02910.1016/j.materresbull.2016.06.029 ↗
38. 10.1039/C5RA21130A10.1039/C5RA21130A ↗
39. 10.1039/c1jm12142a10.1039/c1jm12142a ↗
40. 10.1021/acs.iecr.5b0076110.1021/acs.iecr.5b00761 ↗
41. 10.1016/j.apsusc.2013.05.03110.1016/j.apsusc.2013.05.031 ↗
42. 10.1002/app.4610610.1002/app.46106 ↗
43. 10.1016/j.cej.2019.12242010.1016/j.cej.2019.122420 ↗
44. 10.1016/j.matchemphys.2019.12232810.1016/j.matchemphys.2019.122328 ↗
45. 10.1039/C9TA11982E10.1039/C9TA11982E ↗
46. 10.1016/j.chempr.2018.05.02010.1016/j.chempr.2018.05.020 ↗
47. 10.1016/j.jhazmat.2017.10.06510.1016/j.jhazmat.2017.10.065 ↗
48. 10.1021/acsapm.9b0112010.1021/acsapm.9b01120 ↗
49. 10.1016/j.snb.2021.12983710.1016/j.snb.2021.129837 ↗
50. 10.1021/acsami.0c0134210.1021/acsami.0c01342 ↗
51. 10.1002/asia.20210044410.1002/asia.202100444 ↗