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      ZnO is a CO 2-selective steam reforming catalyst

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          Abstract

          Graphical abstract

          A surprisingly high CO 2-selectivity (95–99.6%) of single-phase ZnO in methanol and formaldehyde steam reforming, which helps in gaining enhanced understanding of the catalytic performance of the unsupported and supported intermetallic compound ZnPd, has been observed.

          Highlights

          ► ZnO is a CO 2-selective methanol steam reforming catalyst. ► ZnO selectively catalyzes formaldehyde via steam reforming to CO 2. ► A beneficial role of ZnO in oxidizing formyl-containing species is evident in ZnO supported systems.

          Abstract

          ZnO was tested as possible methanol and – since formaldehyde is one of the key intermediates in methanol conversion reactions – also as formaldehyde steam reforming catalyst. Catalytic experiments in a batch as well as a flow reactor resulted in highly selective steam reforming, though at low specific activities, of formaldehyde and methanol over ZnO toward CO 2 (selectivity of 95–99.6%). Comparison of the behavior of ZnPd near-surface intermetallic phases, unsupported intermetallic ZnPd and supported ZnPd/ZnO catalysts reveals that formaldehyde is formed from methanol in parallel with CO 2 on the former, while on unsupported intermetallic ZnPd and ZnO-supported ZnPd, it is efficiently reacted toward CO 2, thus, a beneficial role of ZnO in oxidizing formaldehyde-derived intermediates toward CO 2 is evident.

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          Most cited references29

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          Direct synthesis of hydrogen peroxide from H2 and O2 using TiO2-supported Au–Pd catalysts

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            Subsurface-controlled CO2 selectivity of PdZn near-surface alloys in H2 generation by methanol steam reforming.

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              'Shape effects' in metal oxide supported nanoscale gold catalysts.

              We report the activity of shape-controlled metal oxide (CeO(2), ZnO and Fe(3)O(4)) supported gold catalysts for the steam reforming of methanol (SRM) and the water gas shift (WGS) reactions. Metal oxide nanoshapes, prepared by controlled hydrolysis and thermolysis methods, expose different crystal surfaces, and consequently disperse and stabilize gold differently. We observe that similar to gold supported on CeO(2) shapes exposing the {110} and {111} surfaces, gold supported on the oxygen-rich ZnO {0001} and Fe(3)O(4) {111} surfaces shows higher activity for the SRM and WGS reactions. While the reaction rates vary among the Au-CeO(2), Au-ZnO and Au-Fe(3)O(4) shapes, the apparent activation energies are similar, indicating a common active site. TPR data further indicate that the reaction lightoff coincides with the activation of Au-O-M species on the surface of all three oxide supports evaluated here. Different shapes contain a different number of binding sites for the gold, imparting different overall activity.
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                Author and article information

                Journal
                J Catal
                J Catal
                Journal of Catalysis
                Academic Press
                0021-9517
                1090-2694
                January 2013
                January 2013
                : 297
                : C
                : 151-154
                Affiliations
                [a ]Institute of Physical Chemistry, University of Innsbruck, Innrain 52a, A-6020 Innsbruck, Austria
                [b ]Max-Planck-Institut für Chemische Physik fester Stoffe, Nöthnitzer Straße 40, D-01187 Dresden, Germany
                Author notes
                [* ]Corresponding author. simon.penner@ 123456uibk.ac.at
                Article
                YJCAT10972
                10.1016/j.jcat.2012.10.003
                3546163
                23335817
                a01ccb22-346f-4414-bf58-aa9aab2b56ec
                © 2013 Elsevier Inc.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 3 September 2012
                : 1 October 2012
                : 4 October 2012
                Categories
                Article

                Catalysis
                bi-functional synergism,formaldehyde,methanol steam reforming,oxide support,pdzn,zno,znpd
                Catalysis
                bi-functional synergism, formaldehyde, methanol steam reforming, oxide support, pdzn, zno, znpd

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