The effect of dealumination on the apparent and actual rates of aromatization of methane over MFI-supported molybdenum catalysts

2004 ◽  
Vol 226 (1) ◽  
pp. 210-214 ◽  
Author(s):  
A SARIOLAN
2007 ◽  
Vol 246 (1) ◽  
pp. 35-39 ◽  
Author(s):  
A SARIOGLAN ◽  
O SAVASCI ◽  
A ERDEMSENATALAR ◽  
A TUEL ◽  
G SAPALY ◽  
...  

2004 ◽  
Vol 228 (1) ◽  
pp. 114-120 ◽  
Author(s):  
A SARIOGLAN ◽  
A ERDEMSENATALAR ◽  
O TUNCSAVASCI ◽  
Y BENTAARIT

1980 ◽  
Vol 45 (3) ◽  
pp. 783-790 ◽  
Author(s):  
Petr Taras ◽  
Milan Pospíšil

Catalytic activity of nickel-molybdenum catalysts for methanation of carbon monoxide and hydrogen was studied by means of differential scanning calorimetry. The activity of NiMoOx systems exceeds that of carrier-free nickel if x < 2, and is conditioned by the oxidation degree of molybdenum, changing in dependence on the composition in the region Mo-MoO2. The activity of the catalysts is adversely affected by irradiation by fast neutrons, dose 28.1 Gy, or by γ rays using doses in the region 0.8-52 kGy. The system is most susceptible to irradiation in the region of low concentrations of the minor component (about 1 mol.%). The dependence of changes in catalytic activity of γ-irradiated samples on the dose exhibits a maximum in the range of 2-5 kGy. The changes in catalytic activity are stimulated by the change of reactivity of the starting mixed oxides, leading to different kinetics of their reduction and modification of their adsorption properties. The irradiation of the catalysts results in lowered concentration of the active centres for the methanation reaction.


1980 ◽  
Vol 45 (3) ◽  
pp. 697-702 ◽  
Author(s):  
Vlastimil Vyskočil ◽  
Miroslav Zdražil

Kinetics of isomerisation of cyclohexene to methylcyclopentene proceeding as parallel reaction to hydrogenation of cyclohexene to cyclohexane on cobalt-molybdenum catalysts of different composition has been measured. The surface acidity of these catalysts was estimated from the difference in the adsorption of toluene and heptane which was measured by chromatographic method. In a series of catalysts containing molybdenum the acidity parallels isomerisation activity. Cobalt on alumina catalysts and alumina itself have greater acidity but exhibit lower isomerisation activity compared to the catalysts containing molybdenum.


Forests ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 73
Author(s):  
Maurizio D’Auria ◽  
Marisabel Mecca ◽  
Maria Roberta Bruno ◽  
Luigi Todaro

Improvements in the yield and solubility of chestnut wood extractives, by using different extraction methods and molybdenum catalysts as support, have rarely been reported in literature. Many studies focus on the different parts of trees, except for the chemical characteristics of the remaining extractives achieved from thermally modified (THM) chestnut (Castanea sativa Mill) wood. This research seeks to better understand the effects of extraction techniques and catalysts on the yield and solubility of extractives. GC-MS analysis of the chloroform soluble and insoluble fractions was also used. Accelerated Solvent Extraction (ASE) 110 °C, Soxhlet, and autoclave extraction techniques were used to obtain extractives from untreated and thermally modified (THM) chestnut wood (170 °C for 3 h). Ethanol/H2O, ethanol/toluene, and water were the solvents used for each technique. A polyoxometalate compound (H3PMo12O40) and MoO3 supported on silica were used as catalysts. The THM induced a change in the wood’s surface color (ΔE = 21.5) and an increase in mass loss (5.9%), while the equilibrium moisture content (EMC) was reduced by 17.4% compared to the control wood. The yields of the extractives and their solubility were always higher in THM and mainly used ASE as the technique. GC-MS analysis of the extractives, without catalyst support, showed different results for each extraction technique and type of wood (untreated and THM). Ultimately, the amount of extractive compound dissolved in each solvent will differ, and the choice of extraction technique will depend on the intended final application of the extracted chemical product.


1989 ◽  
Vol 53 (2-3) ◽  
pp. 217-231 ◽  
Author(s):  
J.M. Bonnier ◽  
J. Court ◽  
P.T. Wierzchowski ◽  
S. Hamar-Thibault

ChemInform ◽  
2010 ◽  
Vol 22 (21) ◽  
pp. no-no
Author(s):  
M. GHAZI ◽  
J. BARRAULT ◽  
J. C. MENEZO

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