Το έργο με τίτλο A comparison between electrochemical and conventional catalyst promotion: The case of N2O reduction by alkanes or alkenes over K-modified Pd catalysts από τον/τους δημιουργό/ούς Pekridis Georgios, Kaklidis Nikolaos, Konsolakis Michail, Athanasiou Costas, Yentekakis Ioannis V. , Marnellos George E. διατίθεται με την άδεια Creative Commons Αναφορά Δημιουργού 4.0 Διεθνές
Βιβλιογραφική Αναφορά
G.Pekridis, N.Kaklidis, M. Konsolakis, C. Athanasiou, I.V. Yentekakis,
G.E.Marnellos, "A comparison between electrochemical and conventional catalyst promotion: The case of N2O reduction by alkanes or alkenes over K-modified Pd catalysts, " Solid State Ionics, vol. 192, no. 1, pp. 653–658, Jun. 2011. doi: 10.1016/j.ssi.2010.03.024
https://doi.org/10.1016/j.ssi.2010.03.024
In the present work, two different methods of catalyst promotion, the electrochemical promotion (EP) and the conventional promotion (CP), were comparatively applied on a catalytic system of significant environmental and practical importance: the N2O reduction by hydrocarbons (alkanes and alkenes), in the presence or absence of O2, over Pd catalysts. A galvanic cell of the type Pd/K+-conducting β″-Al2O3/Au was constructed for the application of the EP concept whereas the CP concept was investigated via a series of highly dispersed Pd/γ-Al2O3 catalysts, conventionally promoted (by impregnation) with K modifier. Given that EP is a straightforward, efficient and in situ way for investigating the effect of a promoter on a catalytic system, the present study is dealing with its prior use as a rapid “research tool” for exploring the effect of K promoter on the catalytic system under consideration. Subsequently, the insight obtained from EP studies is applied to the design of conventional catalysts' composites, i.e. Pd/γ-Al2O3 catalysts conventionally promoted by K at loadings indicated from EP studies. For the system investigated, the optimal promoter loading was in the range of ∼ 0.45–0.55, in terms of K-coverage. In this range of K-loadings significant enhancement on de-N2O activity was obtained under reducing conditions using both methods of K-promotion. However, in the presence of excess oxygen in the reaction mixture the effect of K-promotion was less pronounced, independently of the reducing agent used.