WGS and CO - PrOx reactions using gold promoted copper - ceria catalysts : “ bulk CuO - CeO 2 vs . CuO - CeO 2 / Al 2 O 3 with low mixed oxide content ”

نویسندگان

  • T. R. Reina
  • S. Ivanova
  • J. A. Odriozola
چکیده

A copper-ceria bulk catalyst has been compared to a series of catalysts designed according to the as called “supported approach”, corresponding to the dispersion of low content mixed copper-ceria oxide on alumina matrix. The principal characteristics of both types of catalysts are contemplated and the differences in their electronic and redox properties discussed in details. As a plus, the gold metal promotion of the catalysts is also envisaged. The advantages of the systems in the CO clean up reactions, WGS and CO-PrOx are commented. While the WGS activity appears to be ruled especially by the Cu/Ce surface to volume ratio, the CO-PrOx reaction is governed by the CuO loading. Gold addition provides benefits only at the low temperature WGS regime. Very importantly, the supported systems are always superior to the bulk configuration in terms of specific activity, a key factor from the catalyst’s design perspective. 1 Corresponding author present address: Department of Chemical and Process Engineering, University of Surrey Guildford, GU2 7XH, United Kingdom.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Flame synthesis of nanosized Cu-Ce-O, Ni-Ce-O, and Fe-Ce-O catalysts for the water-gas shift (WGS) reaction.

A flame synthesis method has been used to prepare nanosized, high-surface-area Cu-Ce-O, Ni-Ce-O, and Fe-Ce-O catalysts from aqueous solutions of metal acetate precursors. The particles were formed by vaporization of the precursors followed by reaction and then gas to particle conversion. The specific surface areas of the synthesized powders ranged from 127 to 163 m(2)/g. High-resolution transmi...

متن کامل

Novel embedded Pd@CeO(2) catalysts: a way to active and stable catalysts.

1-wt% Pd-CeO(2) catalysts were prepared by co-precipitation of Pd nanoparticles with ceria (Pd@CeO(2)-CP), by a microemulsion procedure (Pd@CeO(2)-ME), and by normal impregnation of Pd salts (Pd/CeO(2)-IMP) in order to test the concept that Pd-CeO(2) catalysts could be more stable for the water-gas-shift (WGS) reaction when the Pd is embedded in CeO(2). Initial WGS rates measured at 250 degrees...

متن کامل

Low-temperature water-gas shift reaction over Cu- and Ni-loaded cerium oxide catalysts

In this paper we report on the activity of Cuand Ni-containing cerium oxide catalysts for low-temperature water-gas shift (WGS). Bulk catalysts were prepared in nanocrystalline form by the urea co-precipitation–gelation method. Lanthanum dopant (10 at.%) was used as a structural stabilizer of ceria, while the content of Cu or Ni was in the range of 5–15 at.% (2–8 wt.%). At low metal loadings, C...

متن کامل

The characteristics of wet air oxidation of phenol over CuOx/Al2O3 catalysts: effect of copper loading.

The nature of active copper species is well-known to vary with copper loading, i.e., isolated Cu(2+) to bulk CuO. In this work, however, the effect of copper loading on the activity and the selectivity was investigated for the wet oxidation of phenol over CuO(x)/Al(2)O(3) catalysts. The activity and the mineralization selectivity of the catalysts increased with copper loading up to 7wt% and rem...

متن کامل

Low-content gold-ceria catalysts for the water–gas shift and preferential CO oxidation reactions

Low-content (<0.6 at.%) gold-ceria samples were prepared by one-pot synthesis by the urea gelation/co-precipitation method, and by sodium cyanide leaching of high-content (5 at.%) gold-ceria materials prepared by deposition–precipitation. These catalysts, containing cationic gold in ceria, are active for both the low-temperature water–gas shift (WGS) reaction and the preferential oxidation of C...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016