The role of tungsten oxide in the selective hydrogenolysis of glycerol to 1,3-propanediol over Pt/WOx/Al2O3

Applied Catalysis B: Environmental

Volumn 204, Issue , 2017, Pages 260-272

  García Fernández, Sara ^a   Gandarias, Inaki ^a   Requies, Jesús ^a   Soulimani, Fouad ^b   Arias, Pedro L ^a   Weckhuysen, Bert M ^b  

^a UNIVERSITY OF THE BASQUE COUNTRY UPV EHU   (Spain)

^b UTRECHT UNIVERSITY   (Netherlands)

Author keywords

1,3 Propanediol; ATR IR spectroscopy; Glycerol; Hydrogenolysis; Tungsten oxide

Indexed keywords

CATALYSTS; GLYCEROL; HYDROGENOLYSIS; HYDROLYSIS; OXIDES; PLATINUM; PRECIOUS METALS; RHENIUM; SPECTROSCOPIC ANALYSIS; TUNGSTEN COMPOUNDS; ULTRATHIN FILMS;

1 ,3 PROPANEDIOL; ATR-IR SPECTROSCOPY; ATTENUATED TOTAL REFLECTION INFRARED SPECTROSCOPY; CATALYTIC SURFACES; COMPETITIVE ADSORPTION; HETEROGENEOUS CATALYST; SPECTROSCOPIC STUDIES; TUNGSTEN OXIDE;

TUNGSTEN;

EID: 84997132409     PISSN: 09263373     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcatb.2016.11.016     Document Type: Article

References (67)

1. [1] Tendam, J., Hanefeld, U., Renewable chemicals: dehydroxylation of glycerol and polyols. ChemSusChem 4 (2011), 1017–1034.
2. [2] Pagliaro, M., Rossi, M., The Future of Glycerol: New Uses of a Versatile Raw Material. 2nd ed., 2008, The Royal Society of Chemistry, Cambridge.
3. [3] Zhou, C.-H., Beltramini, J.N., Fan, Y.-X., Lu, G.Q., Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals. Chem. Soc. Rev. 37 (2008), 527–549.
4. [4] Corma Canos, A., Iborra, S., Velty, A., Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 107 (2007), 2411–2502.
5. [5] Dumeignil, F., A new concept of biorefinery comes into operation: the EuroBioRef concept. Michele, A., Angela, D., Dumeignil, F., (eds.) Biorefinery From Biomass to Chem. Fuels, 1 st ed., 2012, De Gruyter, Berlin/Boston, 1–17.
6. [6] Nakagawa, Y., Tomishige, K., Heterogeneous catalysis of the glycerol hydrogenolysis. Catal. Sci. Technol. 1 (2011), 179–190.
7. 3 catalysts. J. Catal. 290 (2012), 79–89.
8. [8] Yuan, Z., Wang, L., Wang, J., Xia, S., Chen, P., Hou, Z., Zheng, X., Hydrogenolysis of glycerol over homogenously dispersed copper on solid base catalysts. Appl. Catal. B Environ. 101 (2011), 431–440.
9. [9] Yuan, Z., Wu, P., Gao, J., Lu, X., Hou, Z., Zheng, X., Pt/solid-base: predominant catalyst for glycerol hydrogenolysis in a base-free aqueous solution. Catal. Lett. 130 (2009), 261–265.
10. 2 Catalyst. Chem. Lett. 36 (2007), 1274–1275.
11. [11] Huang, L., Zhu, Y.-L., Zheng, H.-Y., Li, Y.-W., Zeng, Z.-Y., Continuous production of 1,2-propanediol by the selective hydrogenolysis of solvent-free glycerol under mild conditions. J. Chem. Technol. Biotechnol. 83 (2008), 1670–1675.
12. 2 catalyst for the hydrogenolysis of glycerol in water. Appl. Catal. B Environ. 94 (2010), 318–326.
13. [13] Daniel, O.M., Delariva, A., Kunkes, E.L., Datye, A.K., Dumesic, J.A., Davis, R.J., X-ray absorption spectroscopy of bimetallic Pt-Re catalysts for hydrogenolysis of glycerol to propanediols. ChemCatChem 2 (2010), 1107–1114.
14. [14] Chia, M., Pagán-Torres, Y.J., Hibbitts, D., Tan, Q., Pham, H.N., Datye, A.K., Neurock, M., Davis, R.J., Dumesic, J.A., Selective hydrogenolysis of polyols and cyclic ethers over bifunctional surface sites on rhodium–rhenium catalysts. J. Am. Chem. Soc. 133 (2011), 12675–12689.
15. [15] Nakagawa, Y., Shinmi, Y., Koso, S., Tomishige, K., Direct hydrogenolysis of glycerol into 1,3-propanediol over rhenium-modified iridium catalyst. J. Catal. 272 (2010), 191–194.
16. 2 catalyst, Appl. Catal. B Environ. 105 (2011), 117–127.
17. 2, Appl. Catal. A Gen. 433–434:433 (2012), 128––.
18. 2 for the hydrogenolysis of ethers and polyols, Appl. Catal. B Environ. 111–112:111 (2012), 27––.
19. 2 in the C-O hydrogenolysis of biomass-derived substrates. Chem. Rec. 14 (2014), 1041–1054.
20. [20] Zhang, L., Karim, A.M., Engelhard, M.H., Wei, Z., King, D.L., Wang, Y., Correlation of Pt-Re surface properties with reaction pathways for the aqueous-phase reforming of glycerol. J. Catal. 287 (2012), 37–43.
21. [21] Arundhathi, R., Mizugaki, T., Mitsudome, T., Jitsukawa, K., Kaneda, K., Highly selective hydrogenolysis of glycerol to 1,3-propanediol over a boehmite-supported platinum/tungsten catalyst. ChemSusChem 6 (2013), 1345–1347.
22. 3 catalytic system behavior for the selective glycerol hydrogenolysis to 1,3-propanediol. J. Catal. 323 (2015), 65–75.
23. 2-induced reconstruction and rurface-rnhanced absorption. J. Phys. Chem. B. 105 (2001), 3187–3195.
24. [24] Griffiths, P.R., de Haseth, J.A., The handbook of infrared and Raman characteristic frequencies of organic molecules. Lin-Vien, D., Colthup, N.B., Fateley, W.G., Grasselli, J.G., (eds.) Handb. Infrared Raman Charact. Freq. Org. Mol., 2nd ed., 1991, John Wiley & Sons, New York.
25. 3 catalysts in vapor and liquid phases. J. Phys. Chem. B. 109 (2005), 2810–2820.
26. 3 in gas and aqueous phase: promotion effects by water and pH. J. Catal. 246 (2007), 66–73.
27. 3. J. Catal. 256 (2008), 15–23.
28. [28] Ortiz-Hernández, I., Williams, C.T., In Situ Investigation of solid-liquid catalytic interfaces by attenuated total reflection infrared spectroscopy. Langmuir 19 (2003), 2956–2962.
29. [29] Mojet, B.L., Ebbesen, S.D., Lefferts, L., Light at the interface: the potential of attenuated total reflection infrared spectroscopy for understanding heterogeneous catalysis in water. Chem. Soc. Rev. 39 (2010), 4643–4655.
30. [30] NIST, Standard Reference Database, (n.d.). http://webbook.nist.gov/chemistry/name-ser.html.
31. [31] Koichumanova, K., Sai Sankar Gupta, K.B., Lefferts, L., Mojet, B.L., Seshan, K., An in situ ATR-IR spectroscopy study of aluminas under aqueous phase reforming conditions. Phys. Chem. Chem. Phys. 17 (2015), 23795–23804.
32. [32] Boga, D.A., Liu, F., Bruijnincx, P.C.A., Weckhuysen, B.M., Aqueous-phase reforming of crude glycerol: effect of impurities on hydrogen production. Catal. Sci. Technol. 6 (2015), 134–143.
33. 2 hydrogenation and in situ ATR-IR spectroscopy of catalytic solid–liquid interfaces. Phys. Chem. Chem. Phys. 4 (2002), 2667–2672.
34. [34] Ortiz-Hernández, I., Owens, D.J., Strunk, M.R., Williams, C.T., Multivariate analysis of ATR-IR spectroscopic data: applications to the solid-liquid Catalytic interface. Langmuir 22 (2006), 2629–2639.
35. [35] Silverstein, M.R., Webster, F.X., Kiemle, D.J., Spectrometric Identification of Organic Compounds. 7th ed., 2005, Wiley, New York.
36. 2. J. Catal. 318 (2014), 151–161.
37. 3 and the role of coadsorbed water. Langmuir 29 (2013), 581–593.
38. [38] Dömök, M., Tóth, M., Raskó, J., Erdohelyi, A., Adsorption and reactions of ethanol and ethanol-water mixture on alumina-supported Pt catalysts. Appl. Catal. B Environ. 69 (2007), 262–272.
39. [39] Zaki, M.I., Hasan, M.A., Pasupulety, L., In situ FTIR spectroscopic study of 2-propanol adsorptive and catalytic interactions on metal-modified aluminas. Langmuir 17 (2001), 4025–4034.
40. [40] Deo, A.V., I.G. Dalla Lana, Infrared study of the adsorption and mechanism of surface reactions of 1-propanol on γ-alumina and γ-alumina doped with sodium hydroxide and chromium oxide. J. Phys. Chem. 73 (1969), 716–723.
41. [41] Sablinskas, V., Steiner, G., Hof, M., Machán, R., Applications. Gauglitz, G., Moore, D.S., (eds.) Handb. Spectrosc., 2nd ed., 2014, Wiley-VCH, Weinheim, 95–174.
42. [42] Nakagawa, Y., Tamura, M., Tomishige, K., Catalytic materials for the hydrogenolysis of glycerol to 1,3-propanediol. J. Mater. Chem. A 2 (2014), 6688–6702.
43. [43] Stuart, B., Infrared spectroscopy. Kirk-Othmer, (eds.) Kirk-Othmer Encycl. Chem. Technol., 5th ed., 2000, Wiley, New York, 1–20.
44. [44] Ebbesen, S.D., Mojet, B.L., Lefferts, L., CO adsorption and oxidation at the catalyst-water interface: an investigation by attenuated total reflection infrared spectroscopy. Langmuir 22 (2006), 1079–1085.
45. 2 catalyst. Chem. Eng. J. 231 (2013), 103–112.
46. [46] Van Bronswijk, W., Watling, H.R., Yu, Z., A study of the adsorption of acyclic polyols on hydrated alumina. Colloids Surf. A Physicochem. Eng. Asp. 157 (1999), 85–94.
47. [47] Dasari, M.A., Kiatsimkul, P.P., Sutterlin, W.R., Suppes, G.J., Low-pressure hydrogenolysis of glycerol to propylene glycol. Appl. Catal. A Gen. 281 (2005), 225–231.
48. [48] Miyazawa, T., Kusunoki, Y., Kunimori, K., Tomishige, K., Glycerol conversion in the aqueous solution under hydrogen over Ru/C+ an ion-exchange resin and its reaction mechanism. J. Catal. 240 (2006), 213–221.
49. 3 catalyzed 1,3-propanediol formation from glycerol using tungsten additives. ChemCatChem 5 (2013), 497–505.
50. 2 in vapor phase. Catal. Lett. 131 (2009), 312–320.
51. [51] Menezes, A.O., Rodrigues, M.T., Zimmaro, A., Borges, L.E.P., Fraga, M.A., Production of renewable hydrogen from aqueous-phase reforming of glycerol over Pt catalysts supported on different oxides. Renew. Energy. 36 (2011), 595–599.
52. [52] King, D.L., Zhang, L., Xia, G., Karim, A.M., Heldebrant, D.J., Wang, X., Peterson, T., Wang, Y., Aqueous phase reforming of glycerol for hydrogen production over Pt-Re supported on carbon. Appl. Catal. B Environ. 99 (2010), 206–213.
53. 2 catalysts in a fixed-bed reactor. Green Chem. 12 (2010), 1466–1472.
54. δ++ species interacted with WOx clusters. J. Hazard. Mater. 225–226 (2012), 146–154.
55. [55] Barton, D.G., Shtein, M., Wilson, R.D., Soled, S.L., Iglesia, E., Structure and electronic properties of solid acids based on tungsten oxide nanostructures. J. Phys. Chem. B. 103 (1999), 630–640.
56. [56] Oh, J., Dash, S., Lee, H., Selective conversion of glycerol to 1,3-propanediol using Pt-sulfated zirconia. Green Chem. 13 (2011), 2004–2007.
57. 2. Catal. Lett. 142 (2012), 267–274.
58. 3. Chem. Lett. 41 (2012), 1720–1722.
59. 3 catalysts. J. Mol. Catal. A Chem. 398 (2015), 391–398.
60. [60] Zhu, S., Qiu, Y., Zhu, Y., Hao, S., Zheng, H., Li, Y., Hydrogenolysis of glycerol to 1,3-propanediol over bifunctional catalysts containing Pt and heteropolyacids. Catal. Today 212 (2013), 120–126.
61. [61] Koso, S., Furikado, I., Shimao, A., Miyazawa, T., Kunimori, K., Tomishige, K., Chemoselective hydrogenolysis of tetrahydrofurfuryl alcohol to 1,5-pentanediol. Chem. Commun., 2009, 2035–2037.
62. [62] Koso, S., Nakagawa, Y., Tomishige, K., Mechanism of the hydrogenolysis of ethers over silica-supported rhodium catalyst modified with rhenium oxide. J. Catal. 280 (2011), 221–229.
63. [63] Nimlos, M.R., Blanksby, S.J., Qian, X., Himmel, M.E., Johnson, D.K., Mechanisms of glycerol dehydration. J. Phys. Chem. A 110 (2006), 6145–6156.
64. [64] Barton, D.G., Soled, S.L., Meitzner, G.D., Fuentes, G.A., Iglesia, E., Structural and catalytic characterization of solid acids based on zirconia modified by tungsten oxide. J. Catal. 181 (1999), 57–72.
65. 2. Appl. Catal. A Gen. 250 (2003), 65–73.
66. [66] Alhanash, A., Kozhevnikova, E.F., Kozhevnikov, I.V., Gas-phase dehydration of glycerol to acrolein catalysed by caesium heteropoly salt. Appl. Catal. A Gen. 378 (2010), 11–18.
67. [67] Amada, Y., Watanabe, H., Hirai, Y., Kajikawa, Y., Nakagawa, Y., Tomishige, K., Production of biobutanediols by the hydrogenolysis of erythritol. ChemSusChem 5 (2012), 1991–1999.