Conversion of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid over Au-based catalysts: Optimization of active phase and metal-support interaction

Applied Catalysis B: Environmental

Volumn 163, Issue , 2015, Pages 520-530

  Albonetti, Stefania ^a,c   Lolli, Alice ^a,c   Morandi, Vittorio ^b   Migliori, Andrea ^b   Lucarelli, Carlo ^d   Cavani, Fabrizio ^a  

^a Dip Chimica Industriale Toso Montanari   (Italy)

^b CNR   (Italy)

^c INSTM UdR   (Italy)

^d UNIVERSITY OF INSUBRIA   (Italy)

Author keywords

2,5 Furandicarboxylic acid; CeO2; Gold copper catalysts; HMF

Indexed keywords

CATALYST SELECTIVITY; CERIUM OXIDE; COPPER COMPOUNDS; GOLD; NANOCATALYSTS; NANOPARTICLES; OXIDATION; OXIDE MINERALS; PARTICLE SIZE; SYNTHESIS (CHEMICAL); TITANIUM DIOXIDE;

2 ,5-FURANDICARBOXYLIC ACIDS; 5 HYDROXYMETHYL FURFURALS; CATALYST PREPARATION; CEO2; GOLD-COPPER CATALYSTS; METAL-SUPPORT INTERACTIONS; N-VINYL-2-PYRROLIDONE; NANOPARTICLE SYNTHESIS;

CATALYST ACTIVITY;

EID: 84908610835     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2014.08.026     Document Type: Article

References (87)

1. Chheda J.N., Huber G.W., Dumesic J.A. Angew. Chem. Int. Ed. 2007, 46:7164-7183.
2. Sheldon R.A. Green Chem. 2014, 16:950-963.
3. Vohra M., Manwar J., Manmode R., Padgilwar S., Patil S. J. Environ. Chem. Eng. 2014, 2:573-584.
4. Luque L., Westerhof R., van Rossum G., Oudenhoven S., Kersten S., Berruti F., Rehmann L. Bioresour. Technol. 2014, 161:20-28.
5. Dutta S., De S., Saha B. Biomass Bioenerg. 2013, 55:355-369.
6. Corma A., Iborra S., Velty A. Chem. Rev. 2007, 107:2411-2502.
7. Climent M.J., Corma A., Iborra S. Green Chem. 2014, 16:516-547.
8. Chheda J.N., Roman-Leshkov Y., Dumesic J.A. Green Chem. 2007, 9:342-350.
9. Werpy T., Petersen G. Top Value Added Chemicals From Biomass 2004, http://www1.eere.energy.gov/bioenergy/pdfs/35523.pdf.
10. Yang F., Liu Q., Bai X., Du Y. Bioresour. Technol. 2011, 102:3424-3429.
11. van Putten R.J., van der Waal J.C., de Jong D., Rasrendra C.B., Heeres H.J., de Vries J.G. Chem. Rev. 2013, 113:1499-1597.
12. Koopman F., Wierckx N., de Winde J.H., Ruijssenaars H.J. Bioresour. Technol. 2010, 101:6291-6296.
13. Dijkman W.P., Groothuis D.E., Fraaije M.W. Angew. Chem. Int. Ed. 2014, 53:6515-6518.
14. C. Munoz de Diego, P.W. Shammel, M.A. Dam, G.J.M. Gruter, WO Patent 2011/043660 (2011), assigned to Furanix Technologies BV.
15. M.A. Lilga, R.T. Hallen, J. Hu, J.F. White, M.J. Gray, US 2010/0152470 (2010), assigned to Battelle Memorial Institute.
16. A. Shalkh, D.R. Parker, M.E. Janka, L.R. Partin, US Patent 2014/0142328 (2014), assigned to Eastman Chemical Company.
17. Gorbanev Y.Y., Klitgaard S.K., Woodley J.M., Christensen C.H., Riisager A. ChemSusChem 2009, 2:672-675.
18. Davis S.E., Zope B.N., Davis R.J. Green Chem. 2012, 14:143-147.
19. Rosatella A.A., Simeonov S.P., Frade R.F.M., Afonso C.A.M. Green Chem. 2011, 13:754-793.
20. Moreau C., Belgacem M.N., Gandini A. Top. Catal. 2004, 27:11-30.
21. Cai J., Ma H., Zhang J., Song Q., Du Z., Huang Y., Xu J. Chem. Eur. J. 2013, 19:14215-14223.
22. Gupta N.K., Nishimura S., Takagaki A., Ebitani K. Green Chem. 2011, 13:824-827.
23. Pasini T., Piccinini M., Blosi M., Bonelli R., Albonetti S., Dimitratos N., Lopez-Sanchez J.A., Sankar M., He Q., Kiely C.J., Hutchings G.J., Cavani F. Green Chem. 2011, 13:2091-2099.
24. Villa A., Schiavoni M., Campisi S., Veith G.M., Prati L. ChemSusChem 2013, 6:609-612.
25. Semagina N., Kiwi-Minsker L. Catal. Rev. Sci. Eng. 2009, 51:147-217.
26. Yan N., Yuan Y., Dyson P.J. Chem. Commun. 2011, 47:2529-2531.
27. Ziaei-azad H., Yin C.-X., Shen J., Hu Y., Karpuzov D., Semagina N. J. Catal. 2013, 300:113-124.
28. Toshima N., Wang Y. Langmuir 1994, 10:4574-4580.
29. Rossi L.M., Vono L.L.R., Garcia M.A.S., Faria T.L.T., Lopez-Sanchez J.A. Top. Catal. 2013, 56:1228-1238.
30. Dimitratos N., Lopez-Sanchez J.A., Hutchings G.J. Chem. Sci. 2012, 3:20-44.
31. Albonetti S., Pasini T., Lolli A., Blosi M., Piccinini M., Dimitratos N., Lopez-Sanchez J.A., Morgan D.J., Carley A.F., Hutchings G.J., Cavani F. Catal. Today 2012, 195:120-126.
32. M. Blosi, S. Albonetti, M. Dondi, G. Baldi, A. Barzanti, PCT/EP2010/052534 (2010), assigned to Colorobbia.
33. Yin J., Shan S., Yang L., Mott D., Malis O., Petkov V., Cai F., Shan Ng M., Luo J., Chen B.H., Engelhard M., Zhong C.J. Chem. Mater. 2012, 24:4662-4674.
34. Bauer J.C., Mullins D., Li M., Wu Z., Pyzant E.A., Overbury S.H., Dai S. Phys. Chem. Chem. Phys. 2011, 13:2571-2581.
35. Bracey C.L., Ellis P.R., Hutchings G.J. Chem. Soc. Rev. 2009, 38:2231-2243.
36. Bauer J.C., Veith G.M., Allerd L.F., Oyola Y., Overbury S.H., Dai S. ACS Catal. 2012, 2:2537-2546.
37. Liu X., Wang A., Li L., Zhang T., Mou C.Y., Lee J.F. J. Catal. 2011, 278:288-296.
38. An K., Alayoglu S., Ewers T., Somorjai G.A. Colloid Interface Sci. J. 2012, 373:1-13.
39. Miguel-García I., Berenguer-Murcia Á., Cazorla-Amorós D. Appl. Catal. B 2010, 98:161-170.
40. Blosi M., Albonetti S., Baldi G., Gatti F., Dondi M. Dyes Pigments 2012, 4(2):355-362.
41. Albonetti S., Blosi M., Gatti F., Migliori A., Ortolani L., Morandi V., Baldi G., Dondi M. Stud. Surf. Sci. Catal. 2010, 175:621-624.
42. Blosi M., Albonetti S., Ortelli S., Costa A.L., Ortolani L., Dondi M. New J. Chem. 2014, 38:1401-1409.
43. Bayrakdar E., Gürkaynak Altinçekiç T., Faruk Öksüzömer M.A. Fuel Process. Technol. 2013, 110:167-175.
44. Kim C., Lee H. Catal. Commun. 2009, 10:1305-1309.
45. Rioux R.M., Songa H., Grass M., Habas S., Niesz K., Hoefelmeyer J.D., Yang P., Somorjai G.A. Top. Catal. 2006, 39:167-174.
46. Vuyyuru K.R., Strasser P. Catal. Today 2012, 195:144-154.
47. Patil K.R.S., Lund C.R.F. Energy Fuels 2011, 25:4745-4755.
48. Piccolo A., Conte P., Cozzolino A. Eur. J. Soil Sci. 1999, 50:687-694.
49. Casanova O., Iborra S., Corma A. ChemSusChem 2009, 2:1138-1144.
50. Si R., Flytzani-Stephanopoulos M. Angew. Chem. Int. Ed. 2008, 47:2884-2887.
51. He J.L., Xu T., Wang Z.H., Zhang Q.H., Deng W.P., Wang Y. Angew. Chem. Int. Ed. 2012, 51:2438-2442.
52. Abad A., Concepción P., Corma A., García H. Angew. Chem. Int. Ed. 2005, 44:4066-4069.
53. Mori K., Hara T., Mizugaki T., Ebitani K., Kaneda K. J. Am. Chem. Soc. 2004, 26:10657-10666.
54. Cargnello M., Fornasiero P., Gorte R.J. Catal. Lett. 2012, 142:1043-1048.
55. Lakshmanan P., Averseng F., Bion N., Delannoy L., Tatibouët J.-M., Louis C. Gold Bull. 2013, 46:233-242.
56. Pushkarev V.V., Kovalchuk V.I., d'Itry J.L. J. Phys. Chem. B 2004, 108:5341-5348.
57. Li C., Domen K., Maruya K., Onishi T. J. Catal. 1990, 123:436-442.
58. Oliva C., Termignone G., Vatti F.P., Forni L., Vishniakov A.V. J. Mater. Sci. 1996, 31:149-158.
59. Martin D., Duprez D. J. Phys. Chem. 1996, 100:9429-9438.
60. Subbiah S., Simeonov S.P., Esperança J.M.S.S., Paulo L., Rebelo N., Afonso C.A.M. Green Chem. 2013, 15:2849-2853.
61. Kundakovic L., Flytzani-Stephanopoulos M. J. Catal. 1998, 179:203-221.
62. Wang M., Wang F., Ma Ji., Li M., Zhang Z., Wang Y., Zhang X., Xu J. Chem. Commun. 2014, 50:292-294.
63. Beier M.J., Hansen T.W., Grunwaldt J.-D. J. Catal. 2009, 266:320-330.
64. Xia Y.N., Xiong Y.J., Lim B., Skrabalak S.E. Angew. Chem. Int. Ed. 2009, 48:60-103.
65. Villa A., Wang D., Su D.S., Prati L. ChemCatChem 2009, 1:510-514.
66. Somorjai G.A., Frei H., Park J.Y. J. Am. Chem. Soc. 2009, 131:16589-16605.
67. Tsunoyama H., Ichikuni N., Sakurai H., Tsukuda T. J. Am. Chem. Soc. 2009, 131:7086-7093.
68. Evangelisti C., Panziera N., D'Alessio A., Bertinetti L., Botavina M., Vitulli G. New J. Catal. 2010, 272:246-252.
69. Quintanilla A., Butselaar-Orthlieb V.C.L., Kwakernaak C., Sloof W.G., Kreutser M.T., Kapteijn F. J. Catal. 2010, 271:104-114.
70. Borodko Y., Humphrey S.M., Tilley T.D., Frei H., Somorjai G.A. J. Phys. Chem. C 2007, 111:6288-6295.
71. Chen K., Wu H., Hua Q., Chang S., Huang W. Phys. Chem. Chem. Phys. 2013, 15:2273-2277.
72. Sonstrom P., Baumer M. Phys. Chem. Chem. Phys. 2011, 13:19270-19284.
73. Blavo S.O., Qayyum E., Baldyga L.M., Castillo V.A., Sanchez M.D., Warrington K., Barakat M.A., Kuhn J.N. Top. Catal. 2013, 56:1835-1842.
74. Niu Z., Li Y. Chem. Mater. 2014, 26:72-83.
75. Baker L.R., Kennedy G., Krier J.M., Van Spronsen M., Onorato R.M., Somorjai G.A. Catal. Lett. 2012, 142:1286-1294.
76. Lopez-Sanchez J.A., Dimitratos N., Hammond C., Brett G.L., Kesavan L., White S., Miedziak P., Tiruvalam R., Jenkins R.L., Carley A.F., Knight D., Kiely C.J., Hutchings G.J. Nat. Chem. 2011, 3:551-556.
77. Fernandes S., Kim H.-S., Hatti-Kaul R. Protein Express. Purif. 2002, 24:460-469.
78. Ansar S.M., Ameer F.S., Hu W., Zou S., Pittman C.U., Zhang D. Nano Lett. 2013, 13:1226-1229.
79. Ketchie W.C., Fang Y.-L., Wong M.S., Murayama M., Davis R.J. J. Catal. 2007, 250:94-101.
80. Li F., Zhang Q.H., Wang Y. Appl. Catal. A 2008, 334:217-226.
81. Hackett S.E.J., Brydson R.M., Gass M.H., Harvey I., Newman A.D., Wilson K. Angew. Chem. Int. Ed. 2007, 46:8593-8596.
82. Guo H., Al-Hunaiti A., Kemell M., Rautiainen S., Leskela M., Repo T. ChemCatChem 2011, 3:1872-1875.
83. Ide M.S., Davis R.J. Acc. Chem. Res. 2014, 47:825-833.
84. Zope B.N., Hibbitts D.D., Neurock M., Davis R.J. Science 2010, 330:74-78.
85. Casanova O., Iborra S., Corma A. J. Catal. 2009, 265:109-116.
86. Li H.-F., Zhang N., Chen P., Luo M.-F., Lu J.-Q. Appl. Catal. B 2011, 110:279-285.
87. Zheng N.F., Stucky G.D. J. Am. Chem. Soc. 2006, 128:14278-14280.