FTIR and mass spectrometric studies on the interaction of formaldehyde with TiO2 supported Pt and Au catalysts

نویسندگان

  • T. Kecskés
  • J. Raskó
  • J. Kiss
چکیده

The interaction of formaldehyde with Pt/TiO2 and Au/TiO2 catalysts was investigated at 300–473 K by Fourier transform infrared spectroscopy and mass spectrometry. The effects of the pretreatments and the metal content of the catalysts, as well as the effects of the reaction temperature on the formation of the surface species and on the gas phase products were studied. Molecularly adsorbed formaldehyde, formic acid, formate, dioxymethylene and polyoxymethylene surface species are formed during formaldehyde adsorption at 300–473 K. The main gas phase products were H2 and CO; their amounts increased with the increase of the metal content of the catalysts and with the increase of the reaction temperature. Gas phase ethylene, acetylene, as well as formic acid were detected on pure TiO2. On metal-containing TiO2 no ethylene, acetylene and formic acid were observed, which could be connected with the limited surface concentration of oxygen vacancies on these surfaces. © 2004 Elsevier B.V. All rights reserved.

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

Formaldehyde formation in the interaction of HCOOH with Pt supported on TiO2

The interaction between HCOOH and TiO2-supported Pt catalysts was investigated at 300–473 K. The formation of surface species was studied by FTIR and the simultaneous monitoring of the gas phase revealed the formation of the products during the interaction. Besides the dissociative adsorption of HCOOH and the derivatives of this process, the formation of formaldehyde both in the adsorbed layer ...

متن کامل

Highly Sensitive Detection of H2S Molecules Using a TiO2-Supported Au Overlayer Based Nanosensors: A Van Der Waals Corrected DFT Study

The adsorption of the H2S molecule on the undoped and N-doped TiO2 anatase supported Au nanoparticles were studied using density functional theory calculations. The adsorption of H2S on both Au and TiO2 sides of the nanoparticle was examined. On the TiO2 side, the fivefold coordinated titanium site was found to be the most favorable binding site, giving rise to the strong interaction of H2S wit...

متن کامل

Adsorption of CO and NO on Ceria- and Pt-Supported TiO2: In Situ FTIR Study

Pt/TiO2, Ce/TiO2 and binary system PtCe/TiO2 catalysts were prepared by impregnation method and the structural properties of these catalysts were investigated by means of XRD, CO-TPD and UV-vis diffuse reflectance spectroscopy. As investigated by XRD, the composition of the prepared samples anatase and rutile phases with higher amount of anatase phase and its particle size was in the range of 1...

متن کامل

Active Sites and Mechanism for the Water-Gas Shift Reaction on Metal and Metal/Oxide Catalysts

Current industrial catalysts for the water-gas shift reaction are commonly mixtures of Fe-Cr and Zn-Al-Cu oxides, used at temperatures between 350-500oC and 180250oC, respectively. These oxide catalysts are pyrophoric and normally require lengthy and complex activation steps before usage. Improved catalysts are being sought, particularly for lower temperature (e.g., at T<150oC, equilibrium lowe...

متن کامل

FTIR study of CO adsorption and electrical characterization of novel Pt/TiO2 Nanowire Catalysts fabricated using Electron Beam Lithography

Introduction Model supported catalysts on flat surfaces form an important link between single crystal surfaces and real world supported catalysts. The use of nanofabrication techniques to prepare such model catalysts has received a lot of attention in recent years [1]. In the present study Pt/TiO2 catalysts have been fabricated using e-beam lithography (EBL) and used to characterize the electri...

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 2004