In situ carbonization of a soft-template to directly synthesize crystalline mesoporous metal oxides with high surface areas

2014 ◽  
Vol 38 (12) ◽  
pp. 5846-5855 ◽  
Author(s):  
Limin Guo ◽  
Shintaro Ida ◽  
Takashi Daio ◽  
Hidehisa Hagiwara ◽  
Tatsumi Ishihara

High-surface-area crystalline mesoporous tantalum oxide has been successfully synthesized using a pluronic tri-block polymer as the template.

1982 ◽  
Vol 10 (3) ◽  
pp. 325-332 ◽  
Author(s):  
D. Scherson ◽  
S.B. Yao ◽  
E.B. Yeager ◽  
J. Eldridge ◽  
M.E. Kordesch ◽  
...  

1996 ◽  
Vol 457 ◽  
Author(s):  
Lin-chiuan Yan ◽  
Levi T. Thompson

ABSTRACTNew methods have been developed for the synthesis of high surface area cation-substituted hexaaluminates. These materials were prepared by calcining high temperature (ethanol extraction) or low temperature (CO2 extraction) aerogels at temperatures up to 1600°C. Cation-substituted hexaaluminates have emerged as promising catalysts for use in high temperature catalytic combustion. In comparing unsubstituted and cation-substituted hexaaluminates, we found that the phase transformations were much cleaner for the cation-substituted materials. BaCO3 and BaAl2O4 were intermediates during transformation of the unsubstituted materials, while the cation-substituted materials transformed directly from an amorphous phase to crystalline hexaaluminate. Moreover, the presence of substitution cations caused the transformation to occur at lower temperatures. Mn seems to be a better substitution cation than Co since the Mn-substituted materials exhibited higher surface areas and better heat resistances than the Co-substituted materials. The low temperature aerogel-derived materials possessed quite different characteristics from the high temperature aerogel-derived materials. For example, phase transformation pathways were different.


RSC Advances ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 4763-4771 ◽  
Author(s):  
Muhammad Bilal Hussain ◽  
Malik Saddam Khan ◽  
Herman Maloko Loussala ◽  
Muhammad Sohail Bashir

Cr(vi) reduction is performed by BiOCl0.8Br0.2 composite produced via a facile in situ synthetic process at room temperature while making use of PVP (Mw = 10 000).


2020 ◽  
Vol 19 ◽  
pp. 100570
Author(s):  
Wimalika R.K. Thalgaspitiya ◽  
Tharindu Kankanam Kapuge ◽  
Dinithi Rathnayake ◽  
Junkai He ◽  
William S. Willis ◽  
...  

2020 ◽  
Vol 4 (3) ◽  
pp. 851-861 ◽  
Author(s):  
Nai-hsuan Hu ◽  
Chamika U. Lenora ◽  
Timothy A. May ◽  
Nathan C. Hershberger ◽  
Joseph C. Furgal

Specific pore size distributions of synthesized methylsilsesquioxane-based network materials stem from a combination of the solvation of monomers and growing oligomers, as well as miscibility of water in tested solvents; enabling specific analyte uptake materials.


2010 ◽  
Vol 148-149 ◽  
pp. 1096-1099
Author(s):  
Gong Ming Peng ◽  
De Lian Yi ◽  
Lin Wu ◽  
Zhao Hui Ou Yang ◽  
Jian Guo Wang

Novel base catalysts were obtained by subjecting Y zeolites to nitridation. These materials were characterized by elemental analysis, X-ray diffraction, BET surface area analysis, In situ diffuse reflectance infrared fourier transform Spectroscopy (in situ DRIFTS), Pyrrole adsorption. The results indicated nitrogen-incorporated NaY zeolite was well ordered and possess high surface area and pore volume. In situ DRIFTS experiments confirmed that N atoms had been introduced into the framework by nitridation to form -NH2- or -NH- species. It was found that Lewis basicity of these oxynitride materials increased by the pyrrole adsorption. Furthmore, the basic catalytic properties of nitrogen-incorporated zeolites were evaluated by Knoevenagal condensation of benzaldehyde with diethyl malonate and enhanced yield of product was achieved.


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