Mechanical Engineering / Makina Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/4129

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  • Article
    Citation - WoS: 14
    Citation - Scopus: 15
    Electrochemical Performance of La0.6sr0.4co0.2fe0.8o3-Ce0.9gd0.1o2 Composite Sofc Cathodes Fabricated by Electrocatalyst And/Or Electrocatalyst-Ionic Conductor Infiltration
    (Springer, 2019) Sındıraç, Can; Büyükaksoy, Aligül; Akkurt, Sedat
    Infiltration of electrocatalyst precursor solutions into previously sintered porous ionic conductor scaffolds has been used recently as an alternative method to the conventional co-sintering route to fabricate electrocatalyst-ionic conductor composites for solid oxide fuel cell (SOFC) cathode applications. However, the aqueous nitrate solutions generally used to perform the infiltration process results in electrocatalyst precipitates that are disconnected from each other, yielding poor electrode performance. In this work, polymeric electrocatalyst (La0.6Sr0.4Co0.2Fe0.8O3-LSCF) precursors that produce interconnected thin films upon heat treatment were used to infiltrate porous ionic conductor Ce0.9Gd0.1O2-delta (GDC) scaffolds to overcome these issues. In addition, for the first time in the literature, a mixture of LSCF and GDC polymeric precursors, which would yield LSCF-GDC nanocomposite coatings on the grains of the porous GDC scaffold were used as the infiltration solution. Thus, further enhancement of the electrocatalyst/ionic conductor interfacial area and achievement of improved electrode performance was aimed. As a result of the optimization studies, the lowest measured area specific polarization resistance (ASR(cathode)) values of 0.47 and 0.73 omega.cm(2) were obtained for polymeric LSCF+GDC and LSCF precursor infiltrations respectively at 700 degrees C, in air. In addition, LSCF+GDC infiltration yielded electrodes with much improved long-term stability in comparison to those obtained by LSCF infiltration. [GRAPHICS] .
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    Effects of Catalyst Precursor Type and Preparation Conditions, and Solvent Type on Activity and Selectivity of Pt/Sio2 Catalyst in Citral Hydrogenation
    (Walter de Gruyter GmbH, 2011) Depboylu, Can Okan; Yılmaz, Selahattin; Akkurt, Sedat
    In this study, citral hydrogenation reaction in liquid phase over silica gel supported Pt catalysts was investigated. It was desired to hydrogenate carbonyl group selectively to produce valuable unsaturated alcohols, namely geraniol and nerol. Pt/SiO2 catalysts were prepared by impregnation method. The effects of parameters investigated in the present study included Pt precursor type (hexachloroplatinic acid (HCLPA), platinum II acetylacetonate (PAA)), catalyst activation temperature (350°C and 450°C), catalyst activation without calcination, catalyst washing with 0.1 M NaOH and solvent type (ethanol, 2-pentanol). The catalysts activities and selectivities were affected by the type of precursor and activation temperature. The maximum citral conversion (89.50 percent) was achieved at lower activation temperature (350°C) with PAA precursor based catalyst. It was observed that higher activation temperature provided lower citral conversion but higher selectivity to unsaturated alcohols; increasing the activation temperature to 450°C decreased citral conversion to 26.10 percent. But selectivity to unsaturated alcohols, geraniol and nerol, increased from 7.06 to 54.60 percent. Catalyst washing and 2-pentanol prevented acetal formation. Catalyst activation without calcination gave lower citral conversion (20.84 percent) and selectivity to unsaturated alcohols (30.00 percent). Copyright © 2011 The Berkeley Electronic Press. All rights reserved.