Catalytic partial oxidation and CO2-reforming on Rh- and Ni-based catalysts obtained from hydrotalcite-type precursors

Applied Clay Science

Volumn 13, Issue 5-6, 1998, Pages 329-345

  Basile, F ^a   Fornasari, G ^a   Poluzzi, E ^a   Vaccari, A ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Catalytic partial oxidation; CO2 reforming; Hydrotalcites; Methane; Nickel catalyst; Rhodium catalyst; Synthesis gas

Indexed keywords

CALCINATION; CARBON DIOXIDE; CATALYSIS; CLAY MINERALS; HEAT TREATMENT; METHANE; NICKEL ALLOYS; OXIDATION; REDUCTION; REFORMING REACTIONS; RHODIUM ALLOYS; SYNTHESIS GAS;

CATALYTIC PARTIAL OXIDATION; HYDROTALCITE;

CATALYST ACTIVITY;

CARBON DIOXIDE; CATALYSIS; HYDROTALCITE; METHANE; OXIDATION;

EID: 0032215147     PISSN: 01691317     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-1317(98)00031-3     Document Type: Article

References (35)

1. Basile, F., Basini, L., Fornasari, G., Matteuzzi, D., Trifirò, F., Vaccari, A., 1996a. Syngas production by partial oxidation of methane. Role of catalyst composition and reaction parameters. In: Herrero, E., Annunziata, O., Perez, C. (Eds.), Actas XV Simp. Iberoam. Catal., Vol. 3. Univ. Nac. Cordoba, Cordoba, Argentina, pp. 1843-1848.
2. Basile, F., Basini, L., Fornasari, G., Gazzano, M., Trifirò, F., Vaccari, A., 1996b. New hydrotalcite-type anionic clays containing noble metals. J. Chem. Soc., Chem. Commun., pp. 2435-2436.
3. Basile F., Basini L., D'Amore M., Fornasari G., Guarinoni A., Matteuzzi D., Del Piero G., Trifirò F., Vaccari A. Ni/Mg/Al anionic clay derived catalysts for the catalytic partial oxidation of methane: contact time dependence of the reactivity features. J. Catal. 173:1998;247-256.
4. Beller M., Cornils B., Frohning C.D., Kohlpainter C.W. Progress in hydroformylation and carbonylation. J. Mol. Catal. A. 104:1991;17-85.
5. Brown M.J., Parkyns N.D. Progress in the partial oxidation of methane to methanol and formaldehyde. Catal. Today. 8:1991;305-335.
6. Cavani F., Trifirò F., Vaccari A. Hydrotalcite-type anionic clays. Catal. Today. 11:1991;173-301. and references therein.
7. Charlot, G., 1974. Chimie Analitique Quantitative. Masson, Paris.
8. 2 over Ni/MgO at low temperatures. Angew. Chem. Int. Ed. (Engl.). 31:1992;1189-1190.
9. 3. J. Phys. Chem. 96:1992;8686-8688.
10. 3 at low temperatures. J. Catal. 139:1993;326-328.
11. Claridge J.B., Green M.L.H., Tsang S.C., York A.P.E., Ashcroft A.T., Battle P.D. A study of the carbon deposition on catalysts during the partial oxidation of methane to synthesis gas. Catal. Lett. 22:1993;299-305.
12. 3 catalyst. J. Catal. 132:1991;117-127.
13. Edwards, J.H., Maitra, A.M., 1994. The reforming of methane with carbon dioxide - current status and future applications. In: Curry-Hyde, H.E., Howe, R.F. (Eds.), Studies in Surface Science and Catalysis, Vol. 81. Elsevier, Amsterdam, pp. 291-296.
14. Elvers, B., Hawkins, S., Ravenscroft, M., Rousanville, J.F., Schulz, G. (Eds.), 1989. Ullman's Encyclopedia of Industrial Chemistry, Vol. A12. VCH, Weinheim, pp. 186-214.
15. Fornasari G., Gazzano M., Matteuzzi D., Trifirò F., Vaccari A. Structure and reactivity of high-surface-area Ni/Mg/Al mixed oxide. Appl. Clay Sci. 10:1995;69-82.
16. Foulds, G.A., Lapszewicz, J.A., 1994. Catalytic partial oxidation of methane to synthesis gas. In: Spivey, J.J., Agarwal, S.K. (Eds.), Catalysis, Vol. 11. Royal Society of Chemistry, London, pp. 413-440.
17. Fox J.M. The different catalytic routes for methane valorization: an assessment of processes for liquid fuels. Catal. Rev. Sci. Eng. 35:1993;169-212.
18. Gazzano M., Kagunya W., Matteuzzi D., Vaccari A. Neutron diffraction studies of polycrystalline Ni/Mg/Al mixed oxide obtained from hydrotalcite-like precursors. J. Phys. Chem. B. 101:1997;4514-4519.
19. Hickman D.A., Schmidt L.D. Synthesis gas formation by direct oxidation of methane over Pt monoliths. J. Catal. 138:1992;267-282.
20. Hickman D.A., Schmidt L.D. Production of syngas by direct catalytic oxidation of methane. Science. 259:1993;343-346.
21. Hickman D.A., Haupfear E.A., Schmidt L.D. Synthesis gas formation by direct oxidation of methane over Rh monoliths. Catal. Lett. 17:1993;223-237.
22. 1 to acetyls: catalysis and process. Catal. Today. 18:1993;325-354.
23. Huff M., Schmidt L.D. Ethylene formation by oxidative dehydrogenation of ethane over monoliths at very short contact times. J. Phys. Chem. 97:1993;11815-11822.
24. Prettre M., Eichner C., Perrin M. The catalytic oxidation of methane to carbon monoxide and hydrogen. Trans. Faraday Soc. 43:1946;335-339.
25. Rebours B., d'Espinose de la Caillerie J.B., Clause O. Decoration of nickel and magnesium oxide crystallites with spinel-type phases. J. Am. Chem. Soc. 116:1994;1707-1717.
26. Reichleet al. The nature of the thermal decomposition of a catalytically active anionic clay mineral. J. Catal. 101:1986;352-359.
27. Ridler, D.E., Twigg, M.W., 1989. Steam reforming. In: Twigg, M.W. (Ed.), Catalysts Handbook, 2nd edn. Wolfe, London, pp. 225-282.
28. Rostrup-Nielsen, J.R., 1984. Catalytic steam reforming. In: Anderson, J.R., Boudart, M. (Eds.), Catalysis Science and Technology, Vol. 5. Springer-Verlag, Berlin, pp. 1-118.
29. Rostrup-Nielsen J.R. Production of synthesis gas. Catal. Today. 18:1993;305-324.
30. 4 to syngas over Ni catalysts. J. Catal. 162:1996;230-238.
31. Solbakken, A., 1991. Synthesis gas production. In: Holmen, A., Jens, K.-J., Kolboe, S. (Eds.), Studies in Surface Science and Catalysis, Vol. 61. Elsevier, Amsterdam, pp. 447-455.
32. Sundset T., Sogge J., Strøm T. Evaluation of natural gas based synthesis gas production technologies. Catal. Today. 21:1994;269-278.
33. Trifirò, F., Vaccari, A., 1996. Hydrotalcite-like anionic clays (layer double hydroxides). In: Atwood, J.L., Davies, J.E.D., MacNicol, D.D., Vögtle, F. (Eds.), Comprehensive Supramolecular Chemistry, Vol. 7. Pergamon, Oxford, pp. 251-291 and references therein.
34. Tsang S.C., Claridge J.B., Green M.L.H. Recent advances in the conversion of methane to synthesis gas. Catal. Today. 23:1995;3-15.
35. Vogel, A., 1978. Textbook of Quantitative Inorganic Analysis. Longman, London.