scholarly journals Slowing the Kinetics of Alumina Sol-Gel Chemistry for Controlled Catalyst Overcoating and Improved Catalyst Stability and Selectivity

Small ◽  
2018 ◽  
Vol 14 (34) ◽  
pp. 1801733 ◽  
Author(s):  
Yuan-Peng Du ◽  
Florent Héroguel ◽  
Jeremy S. Luterbacher
1986 ◽  
Vol 73 ◽  
Author(s):  
Bruce D. Kay ◽  
Roger A. Assink

ABSTRACTHigh resolution 1H NMR spectroscopy at high magnetic fields is employed to study the reaction kinetics of the Si(OCH3)4:CH3OH:H2O sol-gel system. Both the overall extent of reaction as a function of time and the equilibrium distribution of species are measured. In acid catalyzed solution, condensation is the rate limiting step while in base catalyzed solution, hydrolysis becomes rate limiting. A kinetic model in which the rate of hydrolysis is assumed to be independent of the adjacent functional groups is presented. This model correctly predicts the distribution of product species during the initial stages of the sol-gel reaction.


2013 ◽  
Vol 684 ◽  
pp. 7-11
Author(s):  
Sergey Krutovertsev ◽  
Alla Tarasova ◽  
Olga Ivanova ◽  
Larisa Krutovertseva

The sensor behavior of nanostructured doped silica films produced by sol-gel way were examined. Hygroscopic substances and polyoxometalates were used as additives to make more significant sensitive characteristics of initial matrix. Factors that have effect on sol preparation and films forming were investigated. Adsorption activity of the sensitive films was studied and it was shown that the films had a highly developed surface with nano-size pores. Change of initial conditions of sol-gel process gives opportunity to influence on kinetics of gel formation and consequently, on structure and properties of final materials. The study showed that the conditions of the environment affected the sensors characteristics markedly, which can be improved by choosing of the right procedure of forming and treatment. Influence of type and additive substances quantity into doped films was discussed in the paper


Author(s):  
Tran Thi Thu Huyen ◽  
Dang Thi Minh Hue ◽  
Nguyen Thi Tuyet Mai ◽  
Tran Thi Luyen ◽  
Nguyen Thi Lan

Gases of m-xylene is one of the popurlar toxic pollutants in the exhaust gases, it is emitted into the environment from factories and engines because the fuel in the engine does not burn completely. The best solution in order to remove this toxic gases of m-xylene to protect the environment is transforming them completely into CO2 and H2O by catalysts. Perovskite of LaMnO3 is one of the catalysts that was synthesized and studied the catalytic properties in total oxidation of m-xylene in our previous report. Obtained results showed that the LaMnO3 perovskite has good catalytic characterizations such as large surface area and the amount of α-oxygen adsorbed on the catalyst is large too. So, it exhibits a good catalytic activity in total oxidation of m-xylene at relatively low reaction temperature. In present work, the reaction order  and kinetics of this reaction are determined. The obtained results demonstrated that the reaction order value with respect to m-xylene is equal to about 1, to oxygene is proximately equal to 0 and the order of reaction is equal to about 1. Based on reaction order data, it was thought that the pathway of m-xylene oxidation by air oxygen  over LaMnO3 may be followed through which the Langmuir - Hinshelwood mechanism. Keywords Catalyst, perovskite, oxidation, m-xylene, kinetics References [1] Penã M.A and Fierro J.L.G (2001), << Chemical Stuctures and Performance of Perovskite Oxide>>, Chem. Rev, 101, pp 1981-2018. [2] Seiyama T., Yamazoe N. and Eguchi K. (1985), <<Characterization and Activity of some Mixed Metal Oxide Catalysts>>, Ind. Eng. Chem. Prod. Res. Dev., 24, pp. 19-27.[3] [3] Van Santen R. A., Neurock M. (2006), Molecular Heterogeneous catalysis, Wiley – VCH, pp.62-244. [4] Petrovics, Terlecki - Baricevic A., Karanovic Lj., Kirilov - Stefanov P. , Zdujic M., Dondur V., Paneva D., Mitov I., Rakic V. (2008), <<LaMO3 (M = Mg, Ti, Fe) perovskite type oxides : Preparation, Characterization and Catalytic Properties in Methane deep Oxidation>>, Appl. Catal. B, Env., 79, pp. 186-198. [5] Spinicci R., Tofanari A., Faticanti M., Pettiti I. and Porta P. (2001), <<Hexane Total Oxidation on LaMO3 (M = Mn, Co, Fe) perovskite-type oxides>>, J. Mole. Catal., 176, pp. 247-252. [6] Trần Thị Thu Huyền, Nguyễn Thị Minh Hiền, Nguyễn Hữu Phú (2006), <<Study on the preparation of perovskite oxides La1-xSrxMnO3 (x = 0; 0,3; 0,5) by sol - gel citrate method and their catalytic activity for m-xylene toltal oxidation>>, Hội nghị xúc tác và hấp phụ toàn quốc lần thứ IV, Tp. Hồ Chí Minh, Tr. 477-482.[7] Trần Thị Thu Huyền, Nguyễn Thị Minh Hiền, Nguyễn Hữu Phú (2009), <<Nghiên cứu động học của phản ứng oxi hóa hoàn toàn m-xylen trên các xúc tác perovskit LaMnO3 và La0,7A0,3MnO3 (A = Sr, Ca, Mg)>>, Tạp chí Hóa học, T.47 (6A), Tr 132-136.[8] Geoffrey C. Bond, Catherine Louis, David T. Thompson (2006), <<Catalysis by Gold>>, Catalytic Science Series-Vol.6.


2007 ◽  
Vol 3 (1) ◽  
pp. 133-142 ◽  
Author(s):  
Ishaq Abdullah Zaafarany

Abstract          The kinetics of sol-gel transformation between A13+, La 3+ and Th4+ metal ion electrolytes and sodium alginate sol have been studied complexometrically at various  temperatures. In the presence of a large excess of sodium alginate sol concentration over that of metal ion electrolyte, the pseudo first–order plots of exchange showed sigmoidal curves with two distinct stages. The initial part was relatively fast and curved significantly at early times, followed by a slow decrease in the rates of exchange over longer time periods. The rate constants of gelation showed second-order overall kinetics which was first order in the concentration of both reactants. The thermodynamic parameters have been evaluated and tentative gelation mechanisms consistent with the kinetic results of gelation are suggested. The stability of these ionotropic metal-alginate complexes has been discussed in terms of the coordination geometry and strength of chelated bonds.


2014 ◽  
Vol 185 ◽  
pp. 86-91 ◽  
Author(s):  
Alexandre R. Bueno ◽  
Renata F.M. Oman ◽  
Paula M. Jardim ◽  
Nicolás A. Rey ◽  
Roberto R. de Avillez

2005 ◽  
Vol 31 (2) ◽  
pp. 219-228 ◽  
Author(s):  
T. G. Movchan ◽  
N. B. Ur’ev ◽  
T. V. Khamova ◽  
E. V. Tarasyuk ◽  
A. N. Potapov ◽  
...  

1980 ◽  
Vol 38-39 ◽  
pp. 45-50 ◽  
Author(s):  
L.C Klein ◽  
G.J Garvey

1994 ◽  
Vol 9 (8) ◽  
pp. 2102-2108 ◽  
Author(s):  
E. Haro-Poniatowski ◽  
R. Rodríguez-Talavera ◽  
Heredia M. de la Cruz ◽  
O. Cano-Corona ◽  
R. Arroyo-Murillo

Sols of titania were obtained by the sol-gel method and their size profile was followed by dynamical light scattering. In the early stages of the reaction an unstable behavior was detected. After this unstable regime the particle size reaches a steady state where the sols have a constant size while increasing in number. Once the sol concentration reaches its overlap value, the gelation regime takes place. For samples prepared in this way Raman spectra and x-ray diffractometry were used to characterize the kinetics of crystallization of the material.


Sign in / Sign up

Export Citation Format

Share Document