journal article·2018

Catalytic degradation of phenols by recyclable CVD graphene films

Je Min Yoo, Baekwon Park, Sang Jin Kim, Yong Seok Choi, Sungmin Park, Eun Hye Jeong, Hyukjin Lee, Byung Hee Hong

Nanoscale· Volume 10· Issue 13
Publisher page

Abstract

Ferrous ion-based catalysts have been widely employed to oxidatively destruct the major industrial pollutants such as phenolic compounds through advanced oxidation processes (AOPs). These agents, however, inevitably show several drawbacks including the need for pH adjustment and further purification steps to remove residual salts. Here we report the use of a chemical vapour deposition (CVD) graphene film as a novel metal-free catalyst for the AOP-based degradation of phenols in aqueous solution, which does not require additional steps for salt removal nor external energy to activate the process. We have also verified that the catalytic activity is strongly dependent on the surface area of the graphene film and the degradation efficiency can be markedly improved by exploiting an array of multiple graphene films. Finally, the recyclability of the graphene film has been validated by performing repetitive degradation tests to ensure its practical use.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Graphene research and applications · TiO2 Photocatalysis and Solar Cells · Graphene and Nanomaterials Applications

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

Affiliations

Department of Chemistry

Seoul National University

Seoul 151-747

Korea

Applied Quantum Composites Research Centre

Korea Institute of Science and Technology

Jeonnbuk 55324

College of Pharmacy

Ewha Womans University

Seoul 120-750

Funding

National Research Foundation of Korea

References (30)

Show source-provided references
1. Halfon · Environ. Sci. Technol. · 1986 · 20 · 117310.1021/es00153a014 ↗
2. Pera-Titus · Appl. Catal., B · 2004 · 47 · 21910.1016/j.apcatb.2003.09.010 ↗
3. Gogate · Adv. Environ. Res. · 2004 · 8 · 50110.1016/S1093-0191(03)00032-7 ↗
4. Zazo · Environ. Sci. Technol. · 2005 · 39 · 929510.1021/es050452h ↗
5. Pignatello · Crit. Rev. Environ. Sci. Technol. · 2006 · 36 · 110.1080/10643380500326564 ↗
6. Andreozzia · Catal. Today · 1999 · 53 · 5110.1016/S0920-5861(99)00102-9 ↗
7. Nidheesh · RSC Adv. · 2015 · 5 · 4055210.1039/C5RA02023A ↗
8. Soltani · Chem. Eng. J. · 2014 · 251 · 20710.1016/j.cej.2014.04.021 ↗
9. Winterbourn · Toxicol. Lett. · 1995 · 82–83 · 96910.1016/0378-4274(95)03532-X ↗
10. Kremer · J. Phys. Chem. A · 2003 · 107 · 173410.1021/jp020654p ↗
11. Ragoussi · J. Am. Chem. Soc. · 2014 · 136 · 459310.1021/ja411830x ↗
12. Sun · ACS Nano · 2014 · 8 · 620210.1021/nn501640q ↗
13. Levesque · Nano Lett. · 2011 · 11 · 13210.1021/nl103015w ↗
14. Hu · J. Phys. Chem. C · 2013 · 117 · 241110.1021/jp311584r ↗
15. Kim · Nano Lett. · 2015 · 15 · 323610.1021/acs.nanolett.5b00440 ↗
16. Bae · Nat. Nanotechnol. · 2010 · 5 · 57410.1038/nnano.2010.132 ↗
17. Oyama · Brain Res. · 1994 · 635 · 11310.1016/0006-8993(94)91429-X ↗
18. Setsukinai · J. Biol. Chem. · 2003 · 278 · 317010.1074/jbc.M209264200 ↗
19. Amirfakhri · J. Power Sources · 2014 · 257 · 35610.1016/j.jpowsour.2014.01.114 ↗
20. Wu · Phys. Chem. Chem. Phys. · 2013 · 15 · 692010.1039/c3cp50900a ↗
21. Tachikawa · Jpn. J. Appl. Phys. · 2013 · 52 · 01AH0110.7567/JJAP.52.01AH01 ↗
22. Akca · PLoS One · 2011 · 6 · e1844210.1371/journal.pone.0018442 ↗
23. Martinez · Chem. Sci. · 2012 · 3 · 219110.1039/c2sc20045g ↗
24. Virendra · Prog. Mater. Sci. · 2011 · 56 · 117810.1016/j.pmatsci.2011.03.003 ↗
25. Velicky · ACS Nano · 2014 · 8 · 1008910.1021/nn504298r ↗
26. Kütt · J. Org. Chem. · 2008 · 73 · 260710.1021/jo702513w ↗
27. Harris · Am. J. Optom. Physiol. Opt. · 1988 · 65 · 52710.1097/00006324-198807000-00002 ↗
28. Wilke · Open J. Phys. Chem. · 2013 · 3 · 9710.4236/ojpc.2013.32012 ↗
29. Kiss · Bull. Soc. Chim. Fr. · 1949 · 16 · 275
30. Dewar · J. Chem. Soc. · 1958 · 307610.1039/jr9580003076 ↗