ChemInform Abstract: Preparation of Highly Porous Silica Gel from Poly(tetramethylene oxide) /Silica Hybrids.

ChemInform ◽  
2010 ◽  
Vol 28 (48) ◽  
pp. no-no
Author(s):  
J. WEN ◽  
B. DHANDAPANI ◽  
S. T. OYAMA ◽  
G. L. WILKES
1997 ◽  
Vol 9 (9) ◽  
pp. 1968-1971 ◽  
Author(s):  
J. Wen ◽  
B. Dhandapani ◽  
S. T. Oyama ◽  
G. L. Wilkes

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 702
Author(s):  
Davyd Urbanas ◽  
Edita Baltrėnaitė-Gedienė

In this study, Mn-based catalysts supported by highly porous silica gel powder (SSA up to 470 m2·g−1 and total pore volume up to 0.8 cm3·g−1) were prepared by six different methods in liquid solutions (electroless metal deposition, stepwise addition of a reducing agent, wet impregnation, incipient wetness impregnation, urea hydrolysis, and ammonia evaporation) and tested for selective catalytic reduction of NOx with ammonia (NH3-SCR de-NOx). Prior to the activity test all the catalysts prepared were characterized by ICP-OES, SEM, EDX mapping, XPS, XRD and N2 adsorption techniques to provide the comprehensive information about their composition and morphology, investigate the dispersion of active components on the carrier surface, identify the chemical forms and structural properties of the catalytically active species of the catalysts prepared. The results revealed that all the methods applied for preparation of SCR de-NOx catalysts can ensure the uniform distribution of Mn species on the carrier surface, however as it is typical for preparation techniques in a liquid phase the significant reduction in SSA and pore volume along with increasing the loading was observed. Considering both the physicochemical properties and the catalytic performance of the catalysts the least effective preparation method was shown to be ammonia evaporation, while the most attractive techniques are incipient wetness impregnation and electroless metal deposition.


1995 ◽  
Vol 190 (3) ◽  
pp. 206-211 ◽  
Author(s):  
S. Satoh ◽  
I. Matsuyama ◽  
K. Susa

2008 ◽  
Vol 18 (24) ◽  
pp. 2833 ◽  
Author(s):  
Joanna Claire Rooke ◽  
Alexandre Léonard ◽  
Hugo Sarmento ◽  
Jean-Pierre Descy ◽  
Bao-Lian Su

1953 ◽  
Vol 31 (11) ◽  
pp. 998-1003 ◽  
Author(s):  
M. H. Waldman ◽  
J. A. Snelgrove ◽  
R. Mcintosh

The dielectric constants of ethyl chloride and n-butane adsorbed on nonporous TiO2 were measured. The plot of capacity change versus volume adsorbed was found to reveal two linear sections in the case of ethyl chloride with an abrupt change in the slope of the plot occurring at the Vm value calculated using the B.E.T. or Hüttig adsorption equations. With n-butane the plot was linear beyond Vm. For ethyl chloride on rutile a slight temperature dependence in the polarization was observed for the volume of gas adsorbed above Vm, while a negligible temperature dependence was noted for the portion below Vm. It is postulated that the observations with the polar gas on the nonporous rutile can be explained by a change from oscillatory to rotational motion of the adsorbed molecule after the monolayer is complete. It was noted that gases adsorbed on nonporous TiO2 behaved differently from gases adsorbed on porous silica gel. This appears to lead to the necessity of postulating changes of density for the adsorbed phase on silica gel.


Sign in / Sign up

Export Citation Format

Share Document