کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
40414 45852 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Activity of KNbO3 as catalyst for soot combustion: Effect of the preparation method
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Activity of KNbO3 as catalyst for soot combustion: Effect of the preparation method
چکیده انگلیسی

The effect of the preparation method and calcination temperature on the stability and activity of KNbO3 as catalysts for soot oxidation is reported. The solids were prepared by three different procedures: (i) by a citrate method using NbCl5 as niobium precursor; (ii) by a citrate method using NbF5 as niobium precursor; and (iii) by an autocombustion method using Nb2O5 as niobium precursor. The powders were calcined at 600 °C and 700 °C and characterized by N2 physisorption, oxygen desorption profiles, XRD and SEM. The catalytic activity is discussed in terms of both the Tm value, the temperature at which combustion of carbon black occurs at the maximum rate, and the apparent activation energy. It is found that KNbO3 calcined at 600 °C shows the higher catalytic activity. Also, a strong dependence on the preparation method is observed. The solids prepared by the citrate method show the higher catalytic activities, being the most active the one that use NbCl5 as niobium precursor. This highest catalytic activity is discussed in terms of nanosized perovskite structure and rough interfaces associated to the oxygen's vacancies. Moreover, lower apparent activation energies were obtained for the solids prepared by the citrate method. In addition, it is observed that no deactivation by metal loss after consecutive soot combustion cycles because of the stabilization of the alkaline metal inside the perovskite structure.

Figure optionsDownload high-quality image (106 K)Download as PowerPoint slideHighlights
► The effect of the synthesis method on the KNbO3 structure.
► The activity of KNbO3 catalysts depends strongly on the preparation method and the calcination temperature.
► No deactivation by potassium loss is observed due to the stabilization of the alkaline metal inside the perovskite structure.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 453, 26 February 2013, Pages 341–348
نویسندگان
, , , , ,