scholarly journals Calcination Temperature Effects on Pd/Alumina Catalysts: Particle Size, Surface Species and Activity in Methane Combustion

2021 ◽  
Author(s):  
Domenica R. Fertal ◽  
Matteo Monai ◽  
Laura Proaño ◽  
Maxim P. Bukhovko ◽  
Jihyeon Park ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Temperature Effects ◽  
Methane Combustion ◽  
Surface Species ◽  
Alumina Catalysts

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.

Effect of the Synthesis Method on the Properties of Ultrafine YAG Powder

2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Hydrothermal Reaction ◽  
Synthesis Method ◽  
Particle Morphology ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Synthesis Process ◽  
Powder Materials ◽  
Co Precipitation

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.

Influence of Calcination Temperature on Particle Size and Photocatalytic Activity of Nanosized NiO Powder

2018 ◽  
Vol 92 (9) ◽  
pp. 1777-1781 ◽  
Author(s):  
Pranwadee Kaewmuang ◽  
Titipun Thongtem ◽  
Somchai Thongtem ◽  
Sila Kittiwachana ◽  
Sulawan Kaowphong
Keyword(s):  
Particle Size ◽  
Photocatalytic Activity ◽  
Calcination Temperature

The Influence of Calcination Temperature on Quantitative Phase of Hematite from Iron Stone Tanah Laut

2015 ◽  
Vol 1112 ◽  
pp. 489-492
Author(s):  
Ali Mufid ◽  
M. Zainuri
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Thermo Gravimetric Analysis ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Co Precipitation

This research aims to form particles of hematite (α-Fe2O3) with a basis of mineral iron ore Fe3O4 from Tanah Laut. Magnetite Fe3O4 was synthesized using co-precipitation method. Further characterization using X-ray fluorescence (XRF) to obtain the percentage of the elements, obtained an iron content of 98.51%. Then characterized using thermo-gravimetric analysis and differential scanning calorimetry (TGA-DSC) to determine the calcination temperature, that at a temperature of 445 °C mass decreased by 0.369% due to increase in temperature. Further Characterization of X-ray diffraction (XRD) to determine the phases formed at the calcination temperature variation of 400 °C, 445 °C, 500 °C and 600 °C with a holding time of 5 hours to form a single phase α-Fe2O3 hematite. Testing with a particle size analyzer (PSA) to determine the particle size distribution, where test results indicate that the α-Fe2O3 phase of each having a particle size of 269.7 nm, 332.2 nm, 357.9 nm, 412.2 nm. The best quantity is shown at a temperature of 500 °C to form the hematite phase. This result is used as the calcination procedure to obtain a source of Fe ions in the manufacture of Lithium Ferro Phosphate.

An X-Ray Photoelectron Spectroscopic Study of Copper Chromite Catalysts

1979 ◽  
Vol 33 (4) ◽  
pp. 380-384 ◽  
Author(s):  
J. A. Schreifels ◽  
A. Rodero ◽  
W. E. Swartz
Keyword(s):  
Spectroscopic Study ◽  
Calcination Temperature ◽  
Photoelectron Spectroscopy ◽  
Copper Chromite ◽  
Oxidation States ◽  
Surface Species ◽  
Catalytic Surface ◽  
X Ray

A series of copper chromite catalysts have been studied by x-ray photoelectron spectroscopy. The data indicate that in the as-received form the copper is present as a mixture of Cu(OH)2 and CuO. After calcination at 500 °C only CuO is present. The chromium is present as Cr+3 and Cr+4 when no promoter is added. When a BaO promoter is added, the Cr+6 is stabilized. Calcination at 500°C for varying periods of time alter the relative amounts of Cr+3 and Cr+6 on the catalytic surface. In addition, the relative amounts of the various oxidation states are a function of calcination temperature. At a calcination temperature of 240°C a Cr+5 surface species is reproducibly observed in one of the catalysts.

Fabrication and Characterization of Nanospinel ZnCr2O4 Using Thermal Treatement Method

2015 ◽  
Vol 1107 ◽  
pp. 301-307 ◽  
Author(s):  
Salahudeen A. Gene ◽  
Elias B. Saion ◽  
Abdul Halim Shaari ◽  
Mazliana A. Kamarudeen ◽  
Naif Mohammed Al-Hada
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Average Particle Size ◽  
Treatment Method ◽  
Esr Spectra ◽  
Resonance Spectroscopy ◽  
Average Particle ◽  
Face Centered Cubic ◽  
X Ray ◽  
Xrd Patterns

The fabrication of nanospinel zinc chromite (ZnCr2O4) crystals by the means of thermal treatment method from an aqueous solution containing metal nitrates, polyvinyl pyrrolidone (PVP), and deionized water was described in this study. The samples were calcined at various temperatures ranging from 773 to 973 K for the decomposition of the organic compounds and crystallization of the nanocrystals. PVP was used as capping agent to control the agglomeration of the particles. The characterization studies of the fabricated samples were carried out by X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM), energy dispersed X-ray spectroscopy (EDX) and electron spin resonance spectroscopy (ESR). The corresponding peaks of Zn, Cr and O were observed in the EDX spectrum of the sample which confirms the formation of ZnCr2O4. The XRD patterns also confirmed the formation of the single faced nanocrystallines of spinel ZnCr2O4 with a face-centered cubic structure. The average particle size of the synthesized crystals was also determined from the XRD patterns using the Scherers formula which shows that the crystallite sizes increases with increase in calcination temperature and was in good agreement with the TEM images which shows cubical ZnCr2O4 nanocrystals with uniform morphology and particle size distributions. The ESR spectra confirmed the existence of unpaired electron in the fabricated samples and the increase in g-factor and decreases in resonant magnetic field (Hr) were observed as the calcination temperature increases.

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