scholarly journals The Effect of Calcium Doping on the Surface and Catalytic Properties of Cobaltic Oxide Catalysts

2003 ◽  
Vol 21 (3) ◽  
pp. 229-243 ◽  
Author(s):  
Nasr-Allah M. Deraz
Keyword(s):  
Activation Energy ◽  
Calcination Temperature ◽  
Calcium Oxide ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Peroxide Decomposition ◽  
Cobaltic Oxide ◽  
Adsorption Of Nitrogen ◽  
Activation Energy Of Sintering ◽  
Calcium Doping

The effects of calcium oxide doping (0.75, 1.5 and 3 mol% CaO) and calcination temperature (400, 500, 600 and 700°C) on different surface properties of Co3O4 were investigated. The structural properties of pure and doped oxide samples were determined by XRD methods, the textural properties were investigated via the adsorption of nitrogen at −196°C while the hydrogen peroxide decomposition activity of the investigated solids was determined by oxygen gasometric measurement of the reaction kinetics at 20–40°C. The dissolution of calcium ions in the Co3O4 lattice at temperatures in the range 400–600°C was accompanied by a marked decrease in the mean hydraulic radii (rh) and an increase in the surface area (SBET) and total pore volume (Vp) of the prepared oxide samples. In contrast, doping at 700°C brought about a decrease in the SBET and Vp values of the investigated solids. The catalytic activity for H2O2 decomposition on cobaltic oxide calcined at 400–700°C was found to decrease considerably on doping with CaO. The activation energy for sintering (ΔEs) of the pure and doped solids was determined from the variation in their SBET values as a function of the calcination temperature of these solids. Calcium oxide treatment resulted in a 50% increase in the activation energy of sintering of cobaltic oxide solid calcined at 400–600°C. This increase reflects the role of CaO doping in hindering the sintering of cobaltic oxide.

scholarly journals Characterization and Catalytic Behaviour of Co3(PO4)2–AlPO4 Catalysts

1998 ◽  
Vol 16 (4) ◽  
pp. 285-293 ◽  
Author(s):  
M.R. Mostafa ◽  
F.Sh. Ahmed
Keyword(s):  
Pore Radius ◽  
Surface Acidity ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Acid Sites ◽  
Adsorption Of Nitrogen ◽  
Amorphous Structures ◽  
Ft Ir ◽  
Catalytic Behaviour ◽  
The Mean

Co3(PO4)2, AlPO4 and the binary system Co3(PO4)2-AlPO4 with different compositions were prepared by the coprecipitation method. The structural properties of these samples were determined using XRD, DTA and FT-IR techniques. The textural properties were determined from the adsorption of nitrogen at 77 K. The surface acidity was measured by a calorimetric titration method. The samples were tested as catalysts in the dehydration of ethanol and isopropanol using a pulse microcatalytic technique. The data obtained from XRD and FT-IR indicate the amorphous structures of the prepared catalysts. An increase in Co3(PO4)2 content led to a decrease in the surface area and in the total pore volume and an increase in the mean pore radius. The surface acidity of the catalyst depends on the chemical composition; the surface acidity increased with an increase in the AlPO4 content. The dehydration temperature and the distribution of acid sites are important parameters in determining the selectivity and activity of the catalyst.

scholarly journals Chemical and Physical Properties of the Al1-xFexPO4 System Prepared by the Coprecipitation Method. II. Surface Acidity, Textural Properties and Catalytic Activity

2002 ◽  
Vol 20 (8) ◽  
pp. 741-755 ◽  
Author(s):  
F.Sh. Mohamed
Keyword(s):  
Catalytic Activity ◽  
Calcination Temperature ◽  
Pore Volume ◽  
Pore Radius ◽  
Surface Acidity ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Coprecipitation Method ◽  
Temperature Variations ◽  
Kinetics Of

A coprecipitation method for the preparation of Al1-xFexPO4 catalysts with x (or Fe/P ratio) = 0.0, 0.2, 0.4, 0.6 and 0.8 was developed. The samples were calcined at temperatures within the range 200–800°C. The surface structure, cumulative acidity, textural properties, and the catalytic activity and selectivity of the prepared samples towards isopropanol and cyclohexane conversion were studied using different techniques. The results showed that the freshly calcined samples consisted of an amorphous phase, a quartz-type and a tridymite-type phase depending on the calcination temperature. The total surface acidity decreased with FePO4 content or calcination temperature. Variations in the Fe/P ratio and the calcination temperature led to changes in both the surface area and total pore volume of the Al1-xFexPO4 samples. Increases in the Fe/P ratio and increasing calcination temperature led to increases in the pore radius. The catalytic activity and selectivity were significantly affected as the structures of the Al1-xFexPO4 catalysts varied. The kinetics of the reaction were also studied.

scholarly journals Surface Characteristics of the Pure and Li2O-doped MoO3/Al2O3 System

1998 ◽  
Vol 16 (2) ◽  
pp. 127-134 ◽  
Author(s):  
G.A. El-Shobaky ◽  
Kh.A. Khalil
Keyword(s):  
Activation Energy ◽  
Calcination Temperature ◽  
Total Pore Volume ◽  
Nitrogen Adsorption ◽  
Surface Characteristics ◽  
Ammonium Molybdate ◽  
Lithium Oxide ◽  
Sintering Process ◽  
The Mean ◽  
Nitrogen Adsorption Isotherms

Two series of MoO3/Al2O3 solids, having the nominal compositions 0.2MoO3: Al2O3 and 0.5MoO3:A12O3, were prepared by impregnating finely powdered Al(OH)3 samples with calculated amounts of ammonium molybdate solutions. The solids thus obtained were dried at 120°C and then calcined in air at temperatures varying between 400°C and 1000°C. The doped samples were prepared by treating Al(OH)3 with LiNO3 solutions prior to impregnation with ammonium molybdate. The dopant concentrations employed were 1.5 and 6.0 mol% Li2O, respectively. The surface characteristics, viz. the specific surface area (SBET), the total pore volume (VP) and the mean pore radius (r) of the various pure and doped solids were measured from nitrogen adsorption isotherms conducted at -196°C. The SBET data measured for different adsorbents calcined at various temperatures enabled the apparent activation energy for sintering (ΔE3) to be determined for all the adsorbents investigated. The results obtained reveal that the SBET value of the pure and doped solids decreased on increasing the calcination temperature in the range 400–1000°C. The decrease was, however, more pronounced when the calcination temperature increased from 500°C to 700°C due to the formation of Al2(MoO4)3. Lithium oxide doping decreased the SBET value of the solid samples investigated and also decreased the activation energy for sintering to an extent proportional to the amount of dopant present. The sintering process for the pure and doped solids proceeds, mainly, via a particle adhesion mechanism.

scholarly journals Characterization of Manganese Oxide/Alumina Catalysts

1995 ◽  
Vol 12 (3) ◽  
pp. 221-229 ◽  
Author(s):  
S.A. El-Hakam
Keyword(s):  
Manganese Oxide ◽  
Calcination Temperature ◽  
Manganese Content ◽  
Textural Properties ◽  
Catalytic Decomposition ◽  
Experimental Conditions ◽  
Surface Areas ◽  
Ft Ir ◽  
Mn Content ◽  
Alumina Catalysts

The effect of heat treatment of manganese oxide/alumina catalysts of various manganese content on the structural and textural properties and the catalytic decomposition of hydrogen peroxide were investigated. The FT-IR results have shown that depending on the calcination temperature and metal loading MnO2 and MnO3 are formed on the investigated samples. No spinel structure was detected under the experimental conditions. The surface areas were found to decrease with increasing calcination temperature and metal content up to 30 wt.% Mn. The mean pore radius increased with both calcination temperature and Mn content. The rate of catalytic decomposition of H2O2 was found to depend on the pH, the calcination temperature and the state of Mn on the catalyst surface.

scholarly journals Preparation of Apatite-Wollastonite-Phlogopite glass-ceramic composites by powder sintering method

2013 ◽  
Vol 45 (3) ◽  
pp. 331-339
Author(s):  
A. Faeghi-Nia
Keyword(s):  
Activation Energy ◽  
Particle Size ◽  
Glass Ceramic ◽  
Ceramic Composite ◽  
Ceramic Composites ◽  
Powder Sintering ◽  
Powdered Glass ◽  
Activation Energy Of Sintering ◽  
Sintering Method ◽  
Glass Ceramic Composite

An Apatite-Wollastonite-Phlogopite glass-ceramic composite, was developed by sintering and crystallization of the powdered glass. The non-isothermal and isothermal sintering kinetics were studied for this glass-ceramic. Hot-stage microscopy (HSM) measurements demonstrated that it is possible to sinter and crystallize this glass-ceramic with 80% relative density. The activation energy of sintering was analyzed using previously reported model of sintering and it was obtained Q=193.83 KjmolK-1. Also it was shown that the microstructure of sample is a function of particle size distribution.

scholarly journals Investigation of activated Al-pillared clay efficiency in vegetable oil purification

2004 ◽  
pp. 31-36 ◽  
Author(s):  
Gizela Lomic ◽  
Erne Kis ◽  
Etelka Dimic ◽  
Ranko Romanic
Keyword(s):  
Surface Area ◽  
Vegetable Oil ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Sample Surface ◽  
Pillared Clay ◽  
Acid Activation ◽  
Micropore Surface Area ◽  
Natural Clays ◽  
Oil Purification

This paper represents a contribution to the applicability of natural clays and their derivates as adsorbents in the process of purification of vegetable oil. Investigation of textural properties of raw and purified clay samples reveals that during acid activation and Al-pillaring, BET and micropore surface area increases significantly. However, bleaching capacity of clay and its derivates is not determined by using sample surface area, but rather sample total pore volume. Surface area, especially micropore surface area contributes to removal of smaller molecules. This was confirmed by successful elimination of moisture and volatile materials by samples with an appropriate micropore structure. Used samples of clay and its derivates do not significantly influence acid and peroxide values of raw sunflower oil during its treatment.

scholarly journals Influence of the Calcination Temperature on the properties of The Alumina as Catalyst Support for Catalysis

Paliva ◽  
2020 ◽  
pp. 155-161
Author(s):  
Tomáš Hlinčík ◽  
Veronika Šnajdrová ◽  
Veronika Kyselová
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Calcination Temperature ◽  
Specific Surface Area ◽  
Catalyst Support ◽  
Chemical Properties ◽  
Total Pore Volume ◽  
Temperature Range ◽  
Calcination Temperatures ◽  
Physical And Chemical

Alumina is commonly used in industrial practice as a catalyst support and it is made from boehmite. Depending on the calcination temperature, this mineral is transformed into various crystalline modifications which have different physical and chemical properties. For this reason, the following parameters were determined at different calcination temperatures: length, width, material hardness, specific surface area and total pore volume. The results show that with increasing calcination temperature there have been significant changes which may be important when using the material as a catalyst support, e.g. in the preparation of catalysts or in the design of cat-alytic reactors. The specific surface area, which decreases in the temperature range 450–800 °C, is an important parameter for the preparation of catalysts, so it is appropriate to choose a temperature of 600 °C, when the specific surface area is above 200 m2·g-1. The effect of calcination temperature on the structural transitions of boehmite was also monitored. The results showed that γ-Al2O3 has the most suitable properties as a catalyst sup-port in the temperature range 450–800 °C.

THE RATE OF ADSORPTION OF SOME LOW BOILING GASES ON A MODIFIED SARAN CHARCOAL

1955 ◽  
Vol 33 (2) ◽  
pp. 344-351 ◽  
Author(s):  
J. R. Dacey ◽  
D. G. Thomas
Keyword(s):  
Activation Energy ◽  
Pore Structure ◽  
Temperature Variation ◽  
New Method ◽  
Adsorption Experiment ◽  
Vinylidene Chloride ◽  
Adsorption Of Nitrogen

The pyrolysis at 300 °C. of vinylidene chloride monomer adsorbed on Saran charcoal alters the pore structure of the charcoal so that low boiling gases such as nitrogen are adsorbed slowly. The rates of adsorption of nitrogen, argon, and methane have been measured. They were found to vary with pressure and temperature, and from the temperature variation an activation energy may be calculated. A new method of determining this energy is described which involves changing the temperature during only one adsorption experiment.

scholarly journals Characterization and comparison of walnut shells-based activated carbons and their adsorptive properties

2020 ◽  
Vol 38 (9-10) ◽  
pp. 450-463
Author(s):  
Xiya Li ◽  
Jieqiong Qiu ◽  
Yiqi Hu ◽  
Xiaoyuan Ren ◽  
Lu He ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Activated Carbons ◽  
Low Cost ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Hydrothermal Carbonization ◽  
Bet Surface Area ◽  
Activation Process ◽  
Walnut Shells ◽  
Adsorption Desorption

The production of low-cost biologically activated carbons (BACs) is urgent need of environmental protection and ecological sustainability. Hence, walnut shells were treated by traditional pyrolysis, direct KOH impregnation and combined activation composed of hydrothermal carbonization and two-step H3PO4- and pyrolysis-activation process to obtain porous carbon with high adsorption capacity. It was found that the best adsorption capacity for iodine and organic dye methylene blue (MB) can be obtained using the KOH impregnation at impregnation ratio of 1:1 or combined activation comprising of 2 h H3PO4 activation and 1 h pyrolysis activation at 1000°C. The produced KOH, H3PO4/pyrolysis activated BACs at the optimum conditions are superior to that of commercial ACs, 9.4 and 1.3 times for MB removal, 4 and 4.5 times for iodine number respectively. Characterization results demonstrated their porous structure with very good textural properties such as high BET surface area (1689.1 m2/g, 1545.3 m2/g) and high total pore volume (0.94 cm3/g, 0.96 cm3/g). The N2 adsorption-desorption isotherm of H3PO4/pyrolysis activated hydrochar suggested the co-existence of micro and meso-pores. Moreover, they are more effective for the removal of Fe(III) and Cr(VI) from aqueous solution than the commercial AC, suggesting a promising application in the field of water treatment.

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