Mesostructured Zirconium Oxide

1996 ◽  
Vol 431 ◽  
Author(s):  
P. Liu ◽  
J. S. Reddy ◽  
A. Adnot ◽  
A. Sayari

AbstractThe supramolecular templating technique was used to synthesize both hexagonal (Hx- ZrO2) and lamellar (L-ZrO2) phases of zirconium oxide. Under the conditions used in this work, the use of long chain primary amines and quaternary ammonium surfactants resulted in the exclusive formation of lamellar and hexagonal phases, respectively. The use of long chain cetyldimethylamine afforded a mixture of a hexagonal and a lamellar phases. Effects of synthesis parameters such as the ZrO2/surfactant ratio, ZrO2/water ratio, the nature of surfactant, the crystallization temperature and time on the formation of mesostructured ZrO2 were also studied. Addition of 1,3,5-trimethylbenzene (TMB) as a swelling agent led, in the presence of cetyltrimethylammonium bromide, to the formation of a lamellar phase rather than to pore enlargement. These materials were characterized by XRD, FTIR, XPS and EDX techniques. Regardless of their structure, the as-synthesized materials collapsed upon calcination. Treatment with monobasic potassium phosphate followed by calcination at 350 °C led to the formation of a stable porous Zr–P oxide with a surface area as high as 540 m2/g.

Langmuir ◽  
1998 ◽  
Vol 14 (18) ◽  
pp. 4987-4996 ◽  
Author(s):  
J. Gustafsson ◽  
G. Orädd ◽  
M. Nyden ◽  
P. Hansson ◽  
M. Almgren

1970 ◽  
Vol 9 (12) ◽  
pp. 2800-2801 ◽  
Author(s):  
S. F. Pavkovic ◽  
B. Rapp

2021 ◽  
Vol 2086 (1) ◽  
pp. 012042
Author(s):  
M G Volkova ◽  
V Yu Storozhenko ◽  
V V Petrov ◽  
E M Bayan

Abstract Nanoscale TiO2-SnO2 films with the Ti:Sn ratio 1:99, 3:97 and 5:95 mol%, respectively, were obtained by solid-phase low-temperature pyrolysis method. The synthesized materials were studied by X-ray phase analysis and scanning electron microscopy (SEM) analysis. Regardless of the modified agents’ concentration, the structure of cassiterite was observed for all synthesized materials. When studying the effect of synthesis parameters on the materials properties, it was shown that both an increase in the Ti4+ concentration and in the calcination temperature leads to an increase in the particle size.


1990 ◽  
Vol 269 (1) ◽  
pp. 223-226 ◽  
Author(s):  
J M Kilponen ◽  
P M Palosaari ◽  
J K Hiltunen

Isoproteins of delta 3,delta 2-enoyl-CoA isomerase (EC 5.3.3.8), an auxiliary enzyme in the beta-oxidation of unsaturated fatty acids having double bonds at odd-numbered positions, were studied in livers of control and clofibrate-treated rats. When liver extracts were applied to a hydroxyapatite column at pH 7.0, the previously characterized peroxisomal trifunctional hydratase-dehydrogenase-isomerase enzyme and the mitochondrial isomerase, which shows a preference for short-chain substrates, were eluted almost in parallel. In addition to these activities, a separate isomerase was observed to elute at a lower potassium phosphate concentration in the gradient. Experiments with extracts of purified mitochondria and peroxisomes demonstrated the mitochondrial origin of this third activity. Studies on the kinetic properties of the third isomerase showed that it has a preference for C10-C12 substrates. An Mr of 200,000 was obtained for the native protein by gel-filtration chromatography. Antibodies to mitochondrial short-chain isomerase and peroxisomal trifunctional enzyme did not recognize this novel mitochondrial isoenzyme. The immunological non-cross-reactivity can be interpreted as suggesting that the different isomerases are not closely related at the level of the primary structure of the polypeptide chain. The present data demonstrate that, similar to many other enzymes of beta-oxidation, delta 3,delta 2-enoyl-CoA isomerase has at least three isoenzymes in rat liver: mitochondrial short- and long-chain isomerases and an additional peroxisomal isoenzyme, which in this case is a part of a multifunctional protein.


2007 ◽  
Vol 46 (3) ◽  
pp. 295-300 ◽  
Author(s):  
J.S. Laskowski ◽  
M. Pawlik ◽  
A. Ansari

1982 ◽  
Vol 13 (1) ◽  
pp. 56-62 ◽  
Author(s):  
A. M. Amorim da Costa ◽  
C. F. G. C. Geraldes ◽  
J. J. C. Teixeira-Dias

Solubilization of water in common organic solvents by fatty acid salts of long-chain (C 12 —C 18 ) aliphatic primary amines was studied. It was found that, of all the salts from formate to palmitate and oleate, dodecylamine- n -butyrate and octadecylamine propionate solubilize most in xylene, the figure reaching about 29 molecules of H 2 O /mole of soap. Additions of free amine enhanced solubilization, while free butyric acid decreased the intake. Our viscosity and freezing-point measurements of the same systems indicated that the additive is most likely to form a complex with soap micelles, and that their solubilizing power is modified thereby. Freezing-point measurements of detergent solutions with and without the solubilized phase showed, surprisingly enough, that the dissolved water elevates the freezing-points considerably, showing that solubilized water acts as a binding agent between micelles and probably promotes micelle formation. The results are discussed and correlated on Winsor’s theory of solubilization.


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