journal article·2019-08-28

Exceptionally High CO2 Capture in an Amorphous Polymer with Ultramicropores Studied by Positron Annihilation

Junjie Liu, Ning Qi, Bo Zhou, Zhiquan Chen

ACS Applied Materials & Interfaces· Volume 11· Issue 34
Publisher page

Abstract

A series of amorphous melamine-based polymer networks synthesized by Schiff base chemistry (SNW) were successfully prepared by varying the strut length. The pore structure was analyzed by gas adsorption and positron annihilation methods. Positron lifetime measurements indicate the existence of ultramicropores and also larger mesopores in the SNW materials. The sizes of micropores and mesopores are almost the same in these samples, which are about 0.7 and 16.5 nm, respectively. The relative number of micropores increases in the order of SNW-1 < SNW-2 < SNW-3, while the number of mesopores increases in the reverse order. N2 adsorption/desorption measurements also reveal micropores and mesopores in these materials. However, it gives an underestimation of the micropore volume. Benefiting from the abundant nitrogen content and high microporosity, the SNW materials exhibit exceptionally high CO2 capture ability, which reaches a maximum value of 18.3 wt % in SNW-3 at 273 K and 1 bar, followed by SNW-2 and SNW-1. This order is exactly the same as the order of micropore volume revealed by positron annihilation measurement, suggesting that micropores play a crucial role in the CO2 uptake. Our results show that positron can provide more precise information about the structure of micropores and thus can offer an accurate prediction for the adsorption capacity of complex porous materials.
Source: openalex_inverted_index · Quality: baseline

Research context

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

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

Affiliations

Hubei Nuclear Solid Physics Key Laboratory, Department of Physics, Wuhan University, Wuhan 430072, People’s Republic of China

Funding

Natural Science Foundation of Hubei Province · National Natural Science Foundation of China

References (56)

Show source-provided references
1. 10.1515/pac-2014-111710.1515/pac-2014-1117 ↗
2. 10.1021/acs.chemrev.7b0069110.1021/acs.chemrev.7b00691 ↗
3. 10.1021/jacs.7b0264810.1021/jacs.7b02648 ↗
4. 10.1021/jacs.6b0771410.1021/jacs.6b07714 ↗
5. 10.1021/jacs.6b1031610.1021/jacs.6b10316 ↗
6. 10.1021/jacs.6b1288510.1021/jacs.6b12885 ↗
7. 10.1021/acsami.7b0803210.1021/acsami.7b08032 ↗
8. 10.1039/c7cs00071e10.1039/c7cs00071e ↗
9. 10.1016/j.carbon.2013.03.01210.1016/j.carbon.2013.03.012 ↗
10. 10.1039/c5ta05230k10.1039/c5ta05230k ↗
11. 10.1039/c1sc00100k10.1039/c1sc00100k ↗
12. 10.1002/adma.20110175910.1002/adma.201101759 ↗
13. 10.1039/c1ee01222c10.1039/c1ee01222c ↗
14. 10.1002/anie.20090463710.1002/anie.200904637 ↗
15. 10.1039/c1ee01971f10.1039/c1ee01971f ↗
16. 10.1039/c7ee02110k10.1039/c7ee02110k ↗
17. 10.1039/c1ee01176f10.1039/c1ee01176f ↗
18. 10.1002/adma.20170022910.1002/adma.201700229 ↗
19. 10.1021/jacs.7b0570210.1021/jacs.7b05702 ↗
20. 10.1021/jp070148610.1021/jp0701486 ↗
21. 10.1021/la991011c10.1021/la991011c ↗
22. 10.1016/j.ccr.2016.11.00410.1016/j.ccr.2016.11.004 ↗
23. 10.1039/c8qi00240a10.1039/c8qi00240a ↗
24. Rouquerol J. · 2013
25. 10.1021/la402630s10.1021/la402630s ↗
26. 10.1021/ja801017610.1021/ja8010176 ↗
27. 10.1021/ja055052910.1021/ja0550529 ↗
28. Jean Y. C. · 200310.1142/5086 ↗
29. 10.1002/adma.20090361810.1002/adma.200903618 ↗
30. 10.1021/ja205593510.1021/ja2055935 ↗
31. 10.1007/978-3-642-81316-010.1007/978-3-642-81316-0 ↗
32. 10.1002/polb.2160210.1002/polb.21602 ↗
33. 10.1134/s001814391503004210.1134/s0018143915030042 ↗
34. 10.1021/ja902116f10.1021/ja902116f ↗
35. 10.1039/c1ee01720a10.1039/c1ee01720a ↗
36. 10.1021/ma401309x10.1021/ma401309x ↗
37. 10.1016/0010-4655(74)90070-810.1016/0010-4655(74)90070-8 ↗
38. 10.1016/0168-9002(90)90358-d10.1016/0168-9002(90)90358-d ↗
39. 10.1126/science.112041110.1126/science.1120411 ↗
40. 10.1021/acs.accounts.5b0036910.1021/acs.accounts.5b00369 ↗
41. 10.1126/science.106720810.1126/science.1067208 ↗
42. 10.1002/anie.20070159510.1002/anie.200701595 ↗
43. 10.1039/b711509a10.1039/b711509a ↗
44. 10.1016/j.progpolymsci.2017.07.00110.1016/j.progpolymsci.2017.07.001 ↗
45. 10.1021/ma201324k10.1021/ma201324k ↗
46. 10.1016/0301-0104(81)80307-210.1016/0301-0104(81)80307-2 ↗
47. 10.1021/jp983184110.1021/jp9831841 ↗
48. 10.1088/1742-6596/443/1/01200310.1088/1742-6596/443/1/012003 ↗
49. 10.1002/adma.20140002010.1002/adma.201400020 ↗
50. 10.1002/smll.20170356910.1002/smll.201703569 ↗
51. 10.1016/j.memsci.2016.09.05510.1016/j.memsci.2016.09.055 ↗
52. 10.1021/ja901576510.1021/ja9015765 ↗
53. 10.1021/acsami.8b0302310.1021/acsami.8b03023 ↗
54. 10.1021/jp305358y10.1021/jp305358y ↗
55. 10.1038/ncomms581310.1038/ncomms5813 ↗
56. 10.1016/s1387-1811(99)00060-810.1016/s1387-1811(99)00060-8 ↗