journal article·2013-03-27

Scalable and Versatile Graphene Functionalized with the Mannich Condensate

Ruijuan Liao, Zhenghai Tang, Tengfei Lin, Baochun Guo

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Abstract

The functionalized graphene (JTPG) is fabricated by chemical conversion of graphene oxide (GO), using tea polyphenols (TP) as the reducer and stabilizer, followed by further derivatization through the Mannich reaction between the pyrogallol groups on TP and Jeffamine M-2070. JTPG exhibits solubility in a broad spectrum of solvents, long-term stability and single-layered dispersion in water and organic solvents, which are substantiated by AFM, TEM, and XRD. The paper-like JTPG hybrids prepared by vacuum-assisted filtration exhibits an unusual combination of high toughness (tensile strength of ~275 MPa and break strain of ~8%) and high electrical conductivity (~700 S/m). Still, JTPG is revealed to be very promising in the fabrication of polymer/graphene composites due to the excellent solubility in the solvent with low boiling point and low toxicity. Accordingly, as an example, nitrile rubber/JTPG composites are fabricated by the solution compounding in acetone. The resulted composite shows low threshold percolation at 0.23 vol.% of graphene. The versatilities both in dispersibility and performance, together with the scalable process of JTPG, enable a new way to scale up the fabrication of the graphene-based polymer composites or hybrids with high performance.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Graphene research and applications · Graphene and Nanomaterials Applications · Polymer Nanocomposite Synthesis and Irradiation

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

Affiliations

Department of Polymer Materials and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China

State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou, 510640, P. R. China

References (47)

Show source-provided references
1. Edwards R. S. · Nanoscale · 2013 · 5 · 3810.1039/C2NR32629A ↗
2. Luo B. · Small · 2012 · 8 · 63010.1002/smll.201101396 ↗
3. Batzill M. · Surf. Sci. Rep. · 2012 · 67 · 8310.1016/j.surfrep.2011.12.001 ↗
4. Rao C. N. R. · Angew. Chem., Int. Ed. · 2009 · 48 · 775210.1002/anie.200901678 ↗
5. Weiss N. O. · Adv. Mater. · 2012 · 24 · 578210.1002/adma.201201482 ↗
6. Potts J. R. · Polymer · 2011 · 52 · 510.1016/j.polymer.2010.11.042 ↗
7. Georgakilas V. · Chem. Rev. · 2012 · 112 · 615610.1021/cr3000412 ↗
8. Niyogi S. · Nano Lett. · 2010 · 10 · 406110.1021/nl1021128 ↗
9. Shan C. · Langmuir · 2009 · 25 · 1203010.1021/la903265p ↗
10. Xu Y. · Adv. Mater. · 2009 · 21 · 127510.1002/adma.200801617 ↗
11. Yang H. · Chem. Commun. · 2009 · 388010.1039/b905085j ↗
12. Yang H. · J. Mater. Chem. · 2009 · 19 · 463210.1039/b901421g ↗
13. Colson J. W. · Science · 2011 · 332 · 22810.1126/science.1202747 ↗
14. Reuven D. · J. Mater. Chem. · 2012 · 22 · 1568910.1039/c2jm33313a ↗
15. Reuven D. G. · ACS Nano · 2012 · 6 · 101110.1021/nn204825b ↗
16. Zhang S. · ACS Nano · 2011 · 5 · 178510.1021/nn102467s ↗
17. Xu Y. X. · J. Am. Chem. Soc. · 2008 · 130 · 585610.1021/ja800745y ↗
18. Tang Z. · J. Mater. Chem. · 2011 · 21 · 1711110.1039/c1jm13239c ↗
19. Tang Z. · Polymer · 2011 · 53 · 67310.1016/j.polymer.2011.11.056 ↗
20. Kozhemyakina N. V. · Adv. Mater. · 2010 · 22 · 548310.1002/adma.201003206 ↗
21. Zhang Y. · Energy Environ. Sci. · 2011 · 4 · 451710.1039/c1ee01400e ↗
22. Bai H. · Chem. Commun. · 2009 · 166710.1039/b821805f ↗
23. Liao R. · J. Phys. Chem. C · 2011 · 115 · 2074010.1021/jp2068683 ↗
24. Wang Y. · ACS Appl. Mater. Interfaces · 2011 · 3 · 112710.1021/am1012613 ↗
25. Hummers W. S. · J. Am. Chem. Soc. · 1958 · 80 · 133910.1021/ja01539a017 ↗
26. Wu H. · Green Chem. · 2011 · 13 · 65110.1039/c0gc00843e ↗
27. Zhu H. · Dalton Trans. · 2012 · 41 · 1046510.1039/c2dt30998j ↗
28. Bors W. · Arch. Biochem. Biophys. · 2000 · 374 · 34710.1006/abbi.1999.1606 ↗
29. Wang G. · Carbon · 2009 · 47 · 135910.1016/j.carbon.2009.01.027 ↗
30. Mladenova R. · Eur. Polym. J. · 2002 · 38 · 98910.1016/S0014-3057(01)00260-9 ↗
31. Laobuthee A. · J. Am. Chem. Soc. · 2001 · 123 · 994710.1021/ja004048o ↗
32. Sundberg P. · J. Electron Spectrosc. Relat. Phenom. · 1988 · 46 · 1910.1016/0368-2048(88)80002-1 ↗
33. Stankovich S. · Carbon · 2007 · 45 · 155810.1016/j.carbon.2007.02.034 ↗
34. Wang L. · J. Phys. D: Appl. Phys. · 2011 · 44 · 44530210.1088/0022-3727/44/44/445302 ↗
35. Kuila T. · Prog. Mater. Sci. · 2012 · 57 · 106110.1016/j.pmatsci.2012.03.002 ↗
36. Lei Y. · Green Chem. · 2011 · 13 · 165510.1039/c1gc15081b ↗
37. Dikin D. A. · Nature · 2007 · 448 · 45710.1038/nature06016 ↗
38. Chen C. · Adv. Mater. · 2009 · 21 · 300710.1002/adma.200803726 ↗
39. Gao Y. · ACS Nano · 2011 · 5 · 213410.1021/nn103331x ↗
40. Chen H. · Adv. Mater. · 2008 · 20 · 355710.1002/adma.200800757 ↗
41. Park S. · ACS Nano · 2008 · 2 · 57210.1021/nn700349a ↗
42. Park S. · J. Phys. Chem. C · 2009 · 113 · 1580110.1021/jp907613s ↗
43. Park S. · Adv. Mater. · 2010 · 22 · 173610.1002/adma.200903611 ↗
44. Chen H. · Adv. Mater. · 2008 · 20 · 355710.1002/adma.200800757 ↗
45. Park S. · ACS Nano · 2008 · 2 · 57210.1021/nn700349a ↗
46. Dikin D. A. · Nature · 2007 · 448 · 45710.1038/nature06016 ↗
47. Dang Z. M. · Adv. Mater. · 2007 · 19 · 85210.1002/adma.200600703 ↗