Monolayer V205/Ti02 and MoO,/TiO, catalysts prepared by different methods

نویسندگان

  • Tadeusz Machej
  • Jerzy Haber
  • Israel E. Wachs
چکیده

Two series of supported V,O,/TiO, and MoO,/TiO, catalysts were synthesized using different preparation methods to determine the possible influence of the preparation procedures upon the final molecular structures of the catalysts. It has been found by means of ambient and in situ Raman spectroscopy that all the employed preparation methods lead to the same types of surface metal oxide species on the titania support. The hydrated surface metal oxide species of both series of the catalysts undergo, after heating in flowing dry air, reversible conversion into the dehydrated analogues. The preparation methods appear to have no influence on the final surface metal oxide structures, but can affect (delay) the process of their formation, as in the case of dry impregnation (thermal spreading) of the V,O,/TiO, system, due to the thermodynamic and diffusion factors involved.

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

Photo-oxidation of Methanol Using Mo03/Ti02: Catalyst Structure and Reaction Selectivity

Laser Raman spectra, UV-visible spectra, and photo-catalytic activity measurements are described which show that supported MoO,iTiOr catalysts prepared by impregnation possess a layer of surface molybdate species coordinated to the titania support. The saturation coverage of this surface molybdate monolayer corresponds to a surface density of ca. 4 x lOI MO atoms per cm2 of TiO*. The properties...

متن کامل

The molecular structures and reactivity of V <Subscript>2 </Subscript>O <Subscript>5 </Subscript>/TiO <Subscript>2 </Subscript>/SiO <Subscript>2 </Subscript> catalysts

A series of V205/TiO 2/SiO 2 catalysts were structurally investigated by in situ Raman spectroscopy and chemically probed by methanol oxidation in order to determine the molecular structure-reactivity relationships of the V205/TiO 2/SiO 2 catalysts. Only surface TiO,. species are present on the 3% TiO 2 /S iO 2 catalysts, and the surface TiO x species as well as bulk TiO 2 (anatase) particles c...

متن کامل

The Interaction of V205 with Ti02(Anatase) II. Comparison of Fresh and Used Catalysts for o-Xylene Oxidation to Phthalic Anhydride Two types of vanadia are present in fresh V20JIi02(anatase) catalysts calcined at 450°C: surface vanadia coordinated to the TiOz

Two types of vanadia are present in fresh V20JIi02(anatase) catalysts calcined at 450°C: surface vanadia coordinated to the TiOz support and small crystallites of V205 (1, 2). The surface vanadia is the active site for the oxidation of o-xylene to phthalic anhydride (I, 3, 4). The surface vanadia is more active and selective than the VZOfi crystallites for the o-xylene oxidation reaction (I). T...

متن کامل

The Oxidation of Toluene on Various Molybdenum-Containing Catalysts

The activities for the vapour-phase oxidation of toluene of various molybdenum-containing catalysts have been measured in a flow microreactor operating at 1 atm pressure. The catalysts comprised (a) unsupported crystalline MOO,, (b) MO oxide monolayers on A&O,, CeO,, TiO,, and ZrO, supports, and (c) Al-, Ce-, and Zr-molybdate salts. The rates of oxidation of toluene per unit surface area on the...

متن کامل

An ESR Study on Oxygen Adsorption and Illumination of Vacuum Treated V205 /Ti02

für Naturforschung in cooperation with the Max Planck Society for the Advancement of Science under a Creative Commons Attribution 4.0 International License. Dieses Werk wurde im Jahr 2013 vom Verlag Zeitschrift für Naturforschung in Zusammenarbeit mit der Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. digitalisiert und unter folgender Lizenz veröffentlicht: Creative Commons Namen...

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 2000