Effect of sol–gel conditions on BET surface area, pore volume, mean pore radius, palladium dispersion, palladium particle size, and catalytic CO oxidation activity of Pd/Al2O3 cryogels

2017 ◽  
Vol 25 (3) ◽  
pp. 697-711 ◽  
Author(s):  
Toshihiko Osaki
1997 ◽  
Vol 15 (6) ◽  
pp. 465-476 ◽  
Author(s):  
G.A. El-Shobaky ◽  
A.M. Ghozza ◽  
G.M. Mohamed

Two samples of Cr2O3/Al2O3 were prepared by mixing a known mass of finely powdered Al(OH)3 with a calculated amount of CrO3 solid followed by drying at 120°C and calcination at 400°C. The amounts of chromium oxide employed were 5.66 and 20 mol% Cr2O3, respectively. The calcined solid specimens were then treated with different doses of γ-rays (20–160 Mrad). The surface and catalytic properties of the different irradiated solids were investigated using nitrogen adsorption at −196°C and the catalysis of CO oxidation by O2 at 300–400°C. The results revealed that γ-rays brought about a slight decrease in the BET surface area, SBET (15%), and in the total pore volume, Vp (20%), of the adsorbent containing 5.66 mol% Cr2O3. The same treatment increased the total pore volume, Vp (36%), and the mean pore radius, r̄ (43%), of the other adsorbent sample without changing its BET surface area. The catalytic activities of both catalyst samples were found to increase as a function of dose, reaching a maximum value at 80–160 Mrad and 40 Mrad for the solids containing 5.66 and 20 mol% Cr2O3, respectively. The maximum increase in the catalytic activity measured at 300°C was 59% and 100% for the first and second catalyst samples, respectively. The induced effect of γ-irradiation on the catalytic activity was an increase in the concentration of catalytically active sites taking part in chemisorption and in the catalysis of CO oxidation by O2 without changing their energetic nature. This was achieved by a progressive removal of surface hydroxy groups during the irradiation process.


2011 ◽  
Vol 399-401 ◽  
pp. 625-628 ◽  
Author(s):  
Juan Tan ◽  
Xu Ying Li ◽  
Fei Yang ◽  
Jing Liu

Mesostructured nickel phosphate was synthesized with urea as alkali by sol-gel method. The obtained material nominated as NiPO-3 was characterized by means of XRD, ICP, FT-IR, TEM, and N2 adsorption. In contrast to mesoporous nickel phosphate NiPO-1 and NiPO-2 we reported before, NiPO-3 exhibits relatively longer nanotubes reached up to 400~600 nm. N2 adsorption shows that NiPO-3 possesses high BET surface area (345.8 m2g-1) and pore volume (0.46 cm3g-1). The catalytic performance of NiPO-3 showed that the total selectivity of epoxycyclohexane and hexadienol was as high as 83.38%.


2019 ◽  
Vol 2019 ◽  
pp. 1-14 ◽  
Author(s):  
Mohammad Hossein Nateq ◽  
Riccardo Ceccato

Titania nanocrystalline particles were synthesized by hydrolysis-condensation of titanium tetraisopropoxide in water-in-oil micellar solutions of water/cyclohexane/Triton X-100 system, and the effects of reflux time and water-to-surfactant molar ratio on the particle uniformity, crystallinity, and surface area were studied. Several characterization techniques including TEM and SEM, as well as X-ray diffraction and FT-IR spectroscopy, helium pycnometry, and nitrogen physisorption, were employed to evaluate the particle density and dimensions, crystallite size, surface area value, and the porosity features in the as-prepared condition and also after thermal treatment at 500°C. The results show that all treated samples are dense nanocrystalline anatase particles with BET surface area values over 100 m2·g−1 and primary particle size of 10–15 nm. However, for the as-prepared samples, as the reflux time increases, a better purification of particles from the synthesis environment is resulted, leading to denser and more crystalline powders with smaller particle size and higher BET surface area values culminating in 179 m2·g−1 for 24 hours of refluxing. Moreover, decreasing the water-to-surfactant molar ratio from 10 to 5 and 2 increases the particles surface area to 239 and 224 m2·g−1, respectively, at the expense of slight density and crystallinity degradation and considerable prolongation of surfactant removal step. Supportively, the comparison between photocatalytic activities of as-prepared samples also evidences the effectiveness of reflux time extension on improving the sample features and enhancing their functionality. This study can highlight how the earlier synthesis steps can influence the evolution of the structure of the final products.


Nanoscale ◽  
2011 ◽  
Vol 3 (3) ◽  
pp. 974 ◽  
Author(s):  
Pengna Li ◽  
Xianluo Hu ◽  
Lei Zhang ◽  
Hongxing Dai ◽  
Lizhi Zhang

2018 ◽  
Vol 5 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Amit Kumar ◽  
Shailey Singhal ◽  
Shilpi Aggarwal ◽  
Rajendra Prasad Badoni ◽  
Amit Kumar Sharma

Abstract In the present manuscript, the effect of the synthetic route on the properties of SiO2-ZrO2 has been evaluated. Co-precipitation, sol-gel and microwave methods were adopted for synthesizing the structured oxide. The properties of the final products such as surface morphology, crystallinity, surface area, pore volume and size, particle size and total acidity were examined using standard instrumentation like Fe-SEM, XRD, BET and TPD. The results revealed that the mixed oxides were mesoporous in nature with a high BET surface area (315- 435m2/g). Among various methods, the microwave route achieved the highest surface area (433m2/g), pore volume (0.70cc/g) and pore size (6.50nm). The total acidity of the sample synthesized by the microwave reactor was also higher (0.296mmol/g) than that resulting from other methods. Results conclude that microwave method is a suitable choice for synthesizing the structured oxides with desirable properties.


2017 ◽  
Vol 11 (5) ◽  
pp. 47 ◽  
Author(s):  
Heman A. Smail ◽  
Kafia M. Shareef ◽  
Zainab H. Ramli

The adsorption of lead (Pb II) ion on different types of synthesized zeolite was investigated. The BET surface area, total pore volume & average pore size distribution of these synthesized zeolites were determined by adsorption isotherms for N2, the surface area & total pore volume of their sources were found by adsorption isothermN2.The adsorption equilibrium was measured after 24h at room temperature (RT) & concentration 10mg.L-1 of Pb (II) was used. The adsorption of heavy metal Pb (II) on four different prepared zeolites (LTA from Montmorillonite clay, FAU(Y)-B.H (G2) from Barley husk, Mordenite (G1) from Chert rock, FAU(X)-S.C (G3) from shale clay & modified Shale clay by oxalic acid (N1) & sodium hydroxide (N2)), were compared with the adsorption of their sources by using static batch experimental method. The major factors affecting the heavy metal ion sorption on different synthesized zeolites & their sources were investigated. The adsorption equilibrium capacity (Qm) of Pb (II) ion for different synthesized zeolites ordered from (N1>N2>LTA>G3>G2>G1&for their sources ordered Shale clay >Montmorilonite> Barley husk>Chert rock. The atomic absorption spectrometry was used for analysis of lead heavy metal ion, the obtained results in this study showed that the different synthesized zeolites were efficient ion exchanges for removing heavy metal, in particular, the modified zeolite from shale clay by oxalic acid.


2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit

In this present study, the spherical silica support was synthesized from tetraethyloxysilane (TEOS), water, sodium hydroxide, ethylene glycol and n-dodecyltrimethyl ammonium bromide (C12TMABr). The particle size was controlled by variation of the ethylene glycol co-solvent weight ratio of a sol-gel method preparation in the range of 0.10 to 0.50. In addition, the particle size apparently increases with high weight ratio of co-solvent, but the particle size distribution was broader. The standard deviation of particle diameter is large when the co-solvent weight ratio is more than 0.35 and less than 0.15. However, the specific surface area was similar for all weight ratios ranging from 1000 to 1300 m2/g. The synthesized silica was spherical and has high specific surface area. The cobalt was impregnated onto the obtained silica to produce the cobalt catalyst used for CO2 hydrogenation.</


2008 ◽  
Vol 47 (26) ◽  
pp. 4762-4762
Author(s):  
Hanne Falsig ◽  
Britt Hvolbæk ◽  
Iben S. Kristensen ◽  
Tao Jiang ◽  
Thomas Bligaard ◽  
...  

2020 ◽  
Vol 56 (49) ◽  
pp. 6715-6718 ◽  
Author(s):  
Zi-Jian Li ◽  
Yu Ju ◽  
Bowen Yu ◽  
Xiaoling Wu ◽  
Huangjie Lu ◽  
...  

Isoreticular expansion of Th-MOFs via modulated synthesis yielded seven hierarchical complexes with superior quality single crystals, record high void space and BET surface area among Th materials, and exceptional iodine adsorption capacities.


1999 ◽  
Vol 566 ◽  
Author(s):  
Uday Mahajan ◽  
Marc Bielmann ◽  
Rajiv K. Singh

In this study, we have characterized the effects of abrasive properties, primarily particle size, on the Chemical Mechanical Polishing (CMP) of oxide films. Sol-gel silica particles with very narrow size distributions were used for preparing the polishing slurries. The results indicate that as particle size increases, there is a transition in the mechanism of material removal from a surface area based mechanism to an indentation-based mechanism. In addition, the surface morphology of the polished samples was characterized, with the results showing that particles larger than 0.5 μm are detrimental to the quality of the SiO2 surface.


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