Abstracts - faqs.org

Abstracts

Chemicals, plastics and rubber industries

Search abstracts:
Abstracts » Chemicals, plastics and rubber industries

Identification of the adsorption mode of thiophene on sulfided Mo catalysts

Article Abstract:

The adsorption and reactions of thiophene on sulfided Mo/Al2O3 catalysts were investigated over wide ranges of pressure and temperature using infrared spectroscopy and temperature-programmed desorption. Thiophene was observed to become reactive on the catalysts only in the presence of gas-phase hydrogen and at high temperatures. Temperature-programmed desorption in ultrahigh vacuum following heating of a sulfided 9.4 wt % Mo/Al2O3 catalyst to 693 K in a thiophene/H2 mixture results in desorption of C4 hydrocarbons, H2S and H2 from the catalyst surface.

Author: Logan, John W., Tarbuck, Teresa L., Bussell, Mark E., McCrea, Keith R., Heiser, Jeffrey L.
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 1998
Research, Catalysts, Organosulfur compounds, Organic sulfur compounds, Thiols, Molybdenum disulfide

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Infrared spectroscopic investigation of thiophene adsorption on silica-supported nickel phosphide catalysts

Article Abstract:

The surface chemistry of thiophene on reduced and sulfided Ni/SiO2 and Ni2P/SiO2 catalysts is investigated by using infrared (IR) spectroscopy. The increased reactivity of thiophene on Ni2P/SiO2 catalysts in UHV may explain the high turnover frequency previously reported for Ni2P/SiO2 catalysts relative to sulfided Ni/SiO, Mo/SiO2, and Ni-Mo/SiO2 catalysts.

Author: Layman, Kathryn A., Bussell, Mark E.
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2004
Surface chemistry, Thiophene

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Reflection absorption infrared spectroscopy and temperature-programmed desorption studies of the adsorption and desorption of amorphous and crystalline water on a graphite surface

Article Abstract:

Reflection absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD) are used to perform a detailed investigation of the adsorption of water on highly oriented pyrolytic graphite (HOPG) at 90 K. Isothermal TPD studies are also done and it is observed that the desorption of water does not obey perfect zero-order kinetics.

Author: Brown, Wendy A., Bolina, Amandeep S., Wolff, Angela J.
Publisher: American Chemical Society
Publication Name: Journal of Physical Chemistry B
Subject: Chemicals, plastics and rubber industries
ISSN: 1520-6106
Year: 2005
Water, Graphite

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Adsorption, Analysis, Usage, Infrared spectroscopy, Chemical properties
Similar abstracts:
  • Abstracts: Theoretical study of the adsorption of acetylene on the (111) surfaces of Pd, Pt, Ni, and Rh. Low-temperature synthesis of amorphous carbon nanocoils via acetylene coupling on copper nanocrystal surfaces at 468K: A reaction mechanism analysis
  • Abstracts: Experimental verification of the through-bond mechanisms of electron transfer in bridged donor-acceptor complexes
  • Abstracts: Characterization and reactivity of niobia supported copper oxide catalysts. Modeling experimental oscillations in liquid membranes with delay equations
  • Abstracts: Investigation of the structural and electrochemical properties of size-controlled SnO2 Nanoparticles. New biphenyl derivative with planar phenyl-phenyl conformation in crystal at room temperature exhibits highly efficient UV light-emitting
  • Abstracts: Solvent triggered change of the electron excitation route of KI in supercritical NH3. Influence of the anion on lone pair formation in Sn(II) monochalcogenides: A DFT study
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.