journal article·2021-09-22

Efficient and Recyclable Heterogeneous Catalyst Based on PdNPs Stabilized on a Green-Synthesized Graphene-like Nanomaterial: Effect of Surface Functionalization

Samia Mahouche-Chergui, Abdallah Oun, Imane Haddadou, Clémentine Hoyez, Laurent Michely, Claudiane Ouellet-Plamondon, Benjamin Carbonnier

ACS Applied Materials & Interfaces· Volume 13· Issue 37
Publisher page

Abstract

This work reports for the first time a straightforward and efficient approach to covalent surface functionalization of a sustainable graphene-like nanomaterial with abundant carboxylic acid groups. This approach results in an efficient and robust chelatant platform for anchoring highly dispersed ultrasmall palladium particles with excellent catalytic activity in the reduction of both cationic (methylene blue, MB) and anionic (eosin-Y, Eo-Y) toxic organic dyes. The large-specific-surface-area (SBET = 266.94 m2/g) graphene-like nanomaterial (GHN) was prepared through a green and cost-effective pyrolysis process from saccharose using layered bentonite clay as a template. To introduce a high density of carboxylic acid functions, GHN was first doubly functionalized by successive grafting reaction using two different strategies: (i) in the first case, GHN was first grafted by (3-glycidyloxypropyl) trimethoxysilane (GPTMS) and then bifunctionalized by chemical grafting of tris(4-hydroxyphenyl)methane triglycidyl ether (TGE). In the second case, the grafting order of the two molecules has been reversed. GHN-GPTMS-TGE provided the highest number of grafted reactive epoxy groups, and it was selected for further functionalization with carboxylic acid functions via a ring-opening reaction through a two-step hydrolysis (H2SO4)/oxidation (KMnO4) approach. The GHN nanomaterial bearing carboxylic acid groups was then treated with sodium hydroxide to produce a deprotonated carboxylic acid-rich platform. Finally, due to a high density of accessible chelatant carboxylic acid groups, GHN–COO– binds strongly a great amount of Pd2+ ions to form stable complexes which after reduction by NaBH4 leads to highly dispersed, densely anchored, and uniformly distributed nanoscale Pd particles (d ∼ 4.5 nm) on the surface of the functionalized GHN. The GHN–COO–@PdNPs nanohybrid proved to be highly efficient for dye reduction by NaBH4 in aqueous solution at room temperature. Moreover, because of the high stability of the as-prepared graphene-like supported PdNPs, it exhibited very good reusability and could be recycled up to eight times without any significant loss in activity.
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Research context

OpenAlex topics: Nanomaterials for catalytic reactions · Graphene and Nanomaterials Applications · Advanced Photocatalysis Techniques

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

Affiliations

Univ Paris Est Creteil, CNRS, ICMPE, UMR 7182, 2 Rue Henri Dunant, Thiais 94320, France

Construction Engineering Department, École de Technologie Supérieure, 1100 Notre-Dame West, Montreal, Quebec H3C 1K3, Canada

Funding

Universit?? Paris-Est Cr??teil Val-de-Marne

References (68)

Show source-provided references
1. 10.1016/j.ceramint.2018.12.16710.1016/j.ceramint.2018.12.167 ↗
2. 10.1039/c1ra00641j10.1039/c1ra00641j ↗
3. 10.1016/j.jelechem.2017.04.00810.1016/j.jelechem.2017.04.008 ↗
4. 10.1016/j.electacta.2018.10.03910.1016/j.electacta.2018.10.039 ↗
5. 10.1021/acsami.9b1199010.1021/acsami.9b11990 ↗
6. 10.1016/j.surfcoat.2020.12574210.1016/j.surfcoat.2020.125742 ↗
7. Singla R. · 2016 · 41
8. 10.1016/j.apcatb.2014.07.00910.1016/j.apcatb.2014.07.009 ↗
9. 10.1016/j.colsurfa.2013.04.01310.1016/j.colsurfa.2013.04.013 ↗
10. 10.1016/j.jcis.2017.01.11310.1016/j.jcis.2017.01.113 ↗
11. 10.1002/adma.20180069610.1002/adma.201800696 ↗
12. 10.1016/j.jhazmat.2020.12367310.1016/j.jhazmat.2020.123673 ↗
13. 10.1016/j.jhazmat.2020.12277410.1016/j.jhazmat.2020.122774 ↗
14. 10.1021/acsami.9b1016110.1021/acsami.9b10161 ↗
15. 10.1016/j.dyepig.2018.11.02510.1016/j.dyepig.2018.11.025 ↗
16. 10.1016/j.carbon.2017.04.02510.1016/j.carbon.2017.04.025 ↗
17. 10.1021/ja107719u10.1021/ja107719u ↗
18. 10.1002/adfm.20150221410.1002/adfm.201502214 ↗
19. 10.1038/s41467-020-15782-z10.1038/s41467-020-15782-z ↗
20. 10.1073/pnas.111689710910.1073/pnas.1116897109 ↗
21. Silva M. K. L. · 2019 · 15710.1007/978-981-32-9057-0_6 ↗
22. Sinha A. · 2019 · 4910.1007/978-981-32-9057-0_2 ↗
23. 10.1021/la102801d10.1021/la102801d ↗
24. 10.1002/adsc.20160113710.1002/adsc.201601137 ↗
25. 10.1016/j.saa.2017.07.00210.1016/j.saa.2017.07.002 ↗
26. 10.1021/acsami.5b0983010.1021/acsami.5b09830 ↗
27. 10.1021/am301057610.1021/am3010576 ↗
28. 10.1021/am200523z10.1021/am200523z ↗
29. 10.1021/am402661t10.1021/am402661t ↗
30. 10.1016/j.ces.2021.11648210.1016/j.ces.2021.116482 ↗
31. 10.1021/ja044337310.1021/ja0443373 ↗
32. 10.1016/j.cej.2020.12580810.1016/j.cej.2020.125808 ↗
33. 10.1021/am300889u10.1021/am300889u ↗
34. 10.1039/c3cp53258e10.1039/c3cp53258e ↗
35. 10.1016/j.compositesb.2019.10728810.1016/j.compositesb.2019.107288 ↗
36. 10.1039/c7ta09418c10.1039/c7ta09418c ↗
37. Jorio, A.; Dresselhaus, M. S.; Saito, R.; Dresselhaus, G. Raman Spectroscopy in Graphene Related Systems; Wiley-VCH, 2011; pp 1–358.10.1002/9783527632695 ↗
38. 10.1016/j.flatc.2016.12.00210.1016/j.flatc.2016.12.002 ↗
39. 10.1039/c3ta13716c10.1039/c3ta13716c ↗
40. 10.1002/app.4424510.1002/app.44245 ↗
41. 10.1021/jp203741y10.1021/jp203741y ↗
42. Hansora, D. P.; Mishra, S. Graphene Nanomaterials Fabrication, Properties, and Applications; Jenny Stanford Publishing, 2017; pp 19–101.
43. 10.1016/j.carbon.2018.11.01210.1016/j.carbon.2018.11.012 ↗
44. 10.1080/1542140100372321910.1080/15421401003723219 ↗
45. 10.1016/j.carres.2012.04.01810.1016/j.carres.2012.04.018 ↗
46. 10.1016/j.colsurfa.2013.12.03210.1016/j.colsurfa.2013.12.032 ↗
47. 10.1016/j.arabjc.2017.04.01110.1016/j.arabjc.2017.04.011 ↗
48. 10.14314/polimery.2017.51610.14314/polimery.2017.516 ↗
49. 10.1039/c9ra00343f10.1039/c9ra00343f ↗
50. 10.1039/c6ra22788k10.1039/c6ra22788k ↗
51. 10.1021/acsami.6b0989510.1021/acsami.6b09895 ↗
52. Bhawani S. A. · 2019 · 9110.1016/B978-0-12-814548-7.00005-2 ↗
53. 10.1002/cctc.20160053210.1002/cctc.201600532 ↗
54. 10.1016/j.jhazmat.2012.02.06810.1016/j.jhazmat.2012.02.068 ↗
55. 10.1039/c4cc04454a10.1039/c4cc04454a ↗
56. 10.1016/j.matchemphys.2019.12184910.1016/j.matchemphys.2019.121849 ↗
57. 10.1016/j.apcata.2015.01.03310.1016/j.apcata.2015.01.033 ↗
58. 10.1088/0957-4484/24/12/12530110.1088/0957-4484/24/12/125301 ↗
59. 10.1088/0957-4484/19/30/30560310.1088/0957-4484/19/30/305603 ↗
60. 10.1039/c8ra03404d10.1039/c8ra03404d ↗
61. 10.1016/j.ccr.2015.12.00510.1016/j.ccr.2015.12.005 ↗
62. 10.1021/ic302608g10.1021/ic302608g ↗
63. 10.1002/slct.20170163110.1002/slct.201701631 ↗
64. 10.1039/c5ra18476b10.1039/c5ra18476b ↗
65. 10.1039/c3nr02179c10.1039/c3nr02179c ↗
66. 10.1007/s11814-016-0368-z10.1007/s11814-016-0368-z ↗
67. 10.1016/j.materresbull.2008.03.02410.1016/j.materresbull.2008.03.024 ↗
68. 10.1039/c6nj03467e10.1039/c6nj03467e ↗