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Boreskov Institute of Catalysis of the Siberian Branch of Russian ...

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IntroductionHYDROGEN PRODUCTION BY STEAM REFORMING OFDIMETHYL ETHER OVER Cu-Zn/CeO 2 -ZrO 2 CATALYTICMONOLITHSCristian Ledesma, Jordi LlorcaInstitut de Tècniques Energètiques, Universitat Politècnica de CatalunyaAv. Diagonal 647, Ed. ETSEIB, 08028 Barcelona, SPAINFax : (0034)934017149, E-mail : jordi.llorca@upc.eduOP-V-11Hydrogen and fuel cells are attracting much attention as potential devices for energytransportation and transformation. Steam reforming and oxidative steam reforming <strong>of</strong> naturalgas and o<strong>the</strong>r hydrocarbons as well as alcohols as a route for producing hydrogen in a variety<strong>of</strong> environments have been addressed extensively in <strong>the</strong> last decades. Dimethyl e<strong>the</strong>r (DME)has recently become a potential fuel for hydrogen production because provides a highhydrogen to carbon ratio, has a high energy density, and can be easily handled, stored, andtransported [1-4] .Steam reforming <strong>of</strong> DME comprises two consecutive, moderately endo<strong>the</strong>rmic reactions:DME hydrolysis and methanol (MeOH) steam reforming. The overall reaction is (1) [4] :(CH 3 ) 2 O + 3 H 2 O 6 H 2 + 2 CO 2 ΔHº=135 kJ mol –1 (1)The hydrolysis reaction is known to take place actively over acidic catalysts. Since DMEhydrolysis provides low equilibrium conversion, an active catalyst to effectively reformmethanol is also <strong>the</strong> key for DME steam reforming. In general, steam reforming <strong>of</strong> MeOHproceeds over Cu-, Pt- or Pd-based catalysts [4] . As a consequence, catalyst formulationscontaining both acidic and metal sites are thus preferred.In this work, DME steam reforming has been performed over several Cu-Zn/CeO 2 -ZrO 2catalysts, which have been used for coating cordierite monolithic structures for practicalapplication [5] .Catalysts preparationCordierite monoliths were first coated with 10% w/w <strong>of</strong> ZrO 2 , CeO 2 and Ce 0.5 Zr 0.5 O 2supports, using zirconium oxychloride and cerium trichloride as precursors. Monoliths weredried under continuous rotation at 373 K for 2 h and calcined in air at 773 K for 2 h. Cu, orZn, or a mixture <strong>of</strong> Cu and Zn were <strong>the</strong>n added to each support by incipient wetnessimpregnation using copper nitrate and zinc nitrate as precursors. The total metal loading wasca. 10% w/w with respect to <strong>the</strong> support. The resulting catalytic monoliths were dried undercontinuous rotation at 373 K for 2 h and calcined in air at 773 K for 5 h.187

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