An investigation into the hydrogen bond of poly (p‐phenylene benzobisoxazole)/carboxylic carbon nanotube composites, insight from quantum mechanics/molecular mechanics simulation
Source abstract
Abstract
Poly (p‐phenylene benzobisoxazole)/carbon nanotube (PBO/CNTs) composites have already been experimentally synthesized with the outstanding mechanical and electrical properties. Carboxylic carbon nanotubes (CNT‐COOH), obtained by acid treatment, can better disperse than pristine nanotubes in PBO matrix, which is estimated due to hydrogen bonds between them and investigated by Quantum Mechanics/Molecular mechanics (QM/MM) calculation. In the dynamic simulation, the N atoms in PBO and H atoms in carboxyl can be close enough to form hydrogen bond and the angle of oxygen–hydrogen–nitrogen (OHN) is obtuse, suitable for hydrogen bond. Further more, the electrostatic potential (ESP) and ESP fit charge of N and O atoms in PBO has been measured by Density Functional Theory (DFT) calculation to prove that hydrogen bonds can be formed only by N atoms in the heterocycle of PBO and H atoms in carboxyl of the CNT‐COOH. POLYM. COMPOS., 36:1454–1461, 2015. © 2014 Society of Plastics Engineers
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Research context
OpenAlex topics: Carbon Nanotubes in Composites · Graphene research and applications · Polymer crystallization and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory for Specially Functional Polymers and Related Technology of Ministry of Education, School of Materials Science and Engineering East China University of Science and Technology Shanghai China
Funding
National Natural Science Foundation of China · Innovation Program of Shanghai Municipal Education Commission · Basic Innovation Research Program of Science and Technology Commission of Shanghai Municipality · Shanghai Natural Science Foundation
References (40)
Show source-provided references
1. 10.1021/ma50005a00410.1021/ma50005a004 ↗
2. Wolfe J.F. · 1988
3. 10.1038/354056a010.1038/354056a0 ↗
4. 10.1038/363603a010.1038/363603a0 ↗
5. 10.1126/science.277.5334.197110.1126/science.277.5334.1971 ↗
6. 10.1038/386474a010.1038/386474a0 ↗
7. 10.1021/ma020505510.1021/ma0205055 ↗
8. 10.1126/science.280.5367.125310.1126/science.280.5367.1253 ↗
9. 10.1016/j.carbon.2008.05.00510.1016/j.carbon.2008.05.005 ↗
10. 10.1016/j.polymer.2008.04.00310.1016/j.polymer.2008.04.003 ↗
11. 10.1126/science.282.5386.9510.1126/science.282.5386.95 ↗
12. 10.1016/j.polymer.2011.09.01310.1016/j.polymer.2011.09.013 ↗
13. 10.1002/pc.2225510.1002/pc.22255 ↗
14. 10.1002/jcc.54011060510.1002/jcc.540110605 ↗
15. 10.1007/128_2006_08410.1007/128_2006_084 ↗
16. 10.1007/s00214-006-0143-z10.1007/s00214-006-0143-z ↗
17. 10.1002/1096-987X(200012)21:16<1442::AID-JCC3>3.0.CO;2-O10.1002/1096-987X(200012)21:16<1442::AID-JCC3>3.0.CO;2-O ↗
18. 10.1016/j.molliq.2005.06.00210.1016/j.molliq.2005.06.002 ↗
19. 10.1021/jp970041q10.1021/jp970041q ↗
20. 10.1002/(SICI)1096-987X(199703)18:4<463::AID-JCC2>3.0.CO;2-R10.1002/(SICI)1096-987X(199703)18:4<463::AID-JCC2>3.0.CO;2-R ↗
21. 10.1039/a701492i10.1039/a701492i ↗
22. 10.1063/1.48129610.1063/1.481296 ↗
23. 10.1016/S0166-1280(03)00285-910.1016/S0166-1280(03)00285-9 ↗
24. 10.1063/1.152013410.1063/1.1520134 ↗
25. 10.1021/bk-1998-071210.1021/bk-1998-0712 ↗
26. 10.1021/jp953651410.1021/jp9536514 ↗
27. 10.1021/jp980939v10.1021/jp980939v ↗
28. 10.1016/S1089-3156(98)00042-710.1016/S1089-3156(98)00042-7 ↗
29. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
30. 10.1063/1.45845210.1063/1.458452 ↗
31. 10.1002/jcc.2049510.1002/jcc.20495 ↗
32. 10.1021/j100389a01010.1021/j100389a010 ↗
33. 10.1063/1.276806010.1063/1.2768060 ↗
34. 10.1080/0892702041233130853910.1080/08927020412331308539 ↗
35. 10.1063/1.44811810.1063/1.448118 ↗
36. Hansen J.P. · 1990
37. 10.1002/polb.2176710.1002/polb.21767 ↗
38. 10.1016/S0032-3861(98)00344-910.1016/S0032-3861(98)00344-9 ↗
39. 10.1021/ma981282e10.1021/ma981282e ↗
40. 10.1002/jcc.54005020410.1002/jcc.540050204 ↗