Gold-Iron Oxide Catalyst for CO Oxidation: Effect of Support Structure

نویسندگان

  • Hui-Zhen Cui
  • Yu Guo
  • Xu Wang
چکیده

Gold-iron oxide (Au/FeOx) is one of the highly active catalysts for CO oxidation, and is also a typical system for the study of the chemistry of gold catalysis. In this work, two different types of iron oxide supports, i.e., hydroxylated (Fe_OH) and dehydrated iron oxide (Fe_O), have been used for the deposition of gold via a deposition-precipitation (DP) method. The structure of iron oxide has been tuned by either selecting precipitated pH of 6.7–11.2 for Fe_OH or changing calcination temperature of from 200 to 600 ̋C for Fe_O. Then, 1 wt. % Au catalysts on these iron oxide supports were measured for low-temperature CO oxidation reaction. Both fresh and used samples have been characterized by multiple techniques including transmission electron microscopy (TEM) and high-resolution TEM (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), X-ray absorption near edge structure (XANES) and temperature-programmed reduction by hydrogen (H2-TPR). It has been demonstrated that the surface properties of the iron oxide support, as well as the metal-support interaction, plays crucial roles on the performance of Au/FeOx catalysts in CO oxidation.

برای دانلود 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

Optimization of Preparation Factors for Cerium Oxide Synthesis as a Support for CO PrOx Catalyst

Nanocrystalline ceria has been considered as support for carbon monoxide preferentially oxidation. In this study ceria was prepared by precipitation method and the effects of preparation conditions, such as pH of solution (8-10), aging time (1-12 hr), drying temperature (80-120 °C), calcination time (2-6 hr) and temperature (400-600 °C) were investigated on ceria synthesized powders properties....

متن کامل

Comparison of the activity of Au/CeO2 and Au/Fe2O3 catalysts for the CO oxidation and the water-gas shift reactions

We compare the activity and relevant gold species of nanostructured gold–cerium oxide and gold–iron oxide catalysts for the CO oxidation by dioxygen and water. Well dispersed gold nanoparticles in reduced form provide the active sites for the CO oxidation reaction on both oxide supports. On the other hand, oxidized gold species, strongly bound on the support catalyze the water-gas shift reactio...

متن کامل

Optimization of reaction conditions and effect of catalyst type on product distribution in Cyclooctene oxidation

Oxidation of cyclooctene was studied in presence aqueous hydrogen peroxide (30%, v/v) over nano iron oxide. The catalyst prepared by microemulsion method and characterized using various techniques including XRD, TEM and BET techniques for evaluating phase, structure and morphology and surface area. In this study, we investigated the effects of varying the catalyst content, reaction temperature,...

متن کامل

Characterization and Catalytic Behaviour of Nanostructured Iron Oxide Powder from Waste Pickle Liquor of Steel Industry

Nanostructured iron oxide powder that has been recovered from waste pickling liquor unit of steel industry was studied for oxidation catalytic applications. In this research, the powder was characterized by X-ray diffraction (XRD) and transition electron microscopy (TEM) for determination of phase structure, morphology and particle size. Furthermore, the specific surface area of the powder was ...

متن کامل

Low-temperature CO oxidation on multicomponent gold based catalysts

In this work the development of gold catalysts, essentially based on γ-alumina with small superficial fraction of Ce-Fe mixed oxides as support for the low temperature CO oxidation is proposed. Characterization results obtained by means of TEM, OSC, XPS, UV-Vis spectroscopy and H2-TPR are employed to correlate the activity data with the catalysts composition. The bare γ-alumina supported gold 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

برای دانلود 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

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016