scholarly journals Optimization of Particle Size and Specific Surface Area of Pellet Feed in Dry Ball Mill using Central Composite Design

2016 ◽  
Vol 9 (44) ◽  
Author(s):  
Armin Abazarpoor ◽  
Mohammad Halali
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Central Composite Design ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ball Mill ◽  
Pellet Feed ◽  
Central Composite

scholarly journals Process improvement approach to the acid activation of smectite using factorial and orthogonal central composite design methods

2008 ◽  
Vol 73 (4) ◽  
pp. 487-497 ◽  
Author(s):  
Ljiljana Rozic ◽  
Tatjana Novakovic ◽  
Srdjan Petrovic
Keyword(s):  
Specific Surface ◽  
Central Composite Design ◽  
Surface Area ◽  
Specific Surface Area ◽  
Design Methods ◽  
Optimum Operating ◽  
Acid Activation ◽  
Liquid Ratio ◽  
Stirring Rate ◽  
Central Composite

The purpose of this study was to determine the effective operating parameters and the optimum operating conditions of an acid activation process within the framework of improvement of the process. Full two-level factorial and orthogonal central composite design methods were used successively. The examined parameters were the main and interaction effects of temperature, leaching time, acid normality, solid-to-liquid ratio and stirring rate. The selected process response was the leaching yield of the MgO content because Mg is the element most readily removed from the octahedral sheet, which affects the tendency for activation. Statistical regression analysis and analysis of variance were applied to the experimental data to develop a predictive model, which revealed that temperature, leaching time and acid normality exert the strongest influence on the specific surface area of smectite, whilst the solid-to-liquid ratio and the stirring rate have a secondary effect. Furthermore, the highest leaching yield of MgO was found to be 41.86 %, which is responsible for the increase in the specific surface area of up to 221 m2 g-1.

Physical Properties Variability of Zinc Powders Obtained by Electrochemical Method

2021 ◽  
Vol 316 ◽  
pp. 689-693
Author(s):  
K.D. Naumov ◽  
V.G. Lobanov
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Bulk Density ◽  
Surface Area ◽  
Specific Surface Area ◽  
Current Density ◽  
Zinc Concentration ◽  
Regulatory Change ◽  
Average Particle ◽  
Zinc Powders

The aim of this paper is to establish a regulatory change of zinc powders key physicochemical properties with varying electroextraction conditions. It was studied influence zinc concentration, alkali concentration and current density. Quantitative dependencies of zinc powders particle size and specific surface area from mentioned electroextraction parameters are shown. At increasing of zinc concentration, decreasing of NaOH concentration and decreasing of current density of powders particle size growth, correspondingly specific surface area is declined. It is indicated, that electrolytic zinc powders bulk density varies from 0.61 g/cm3 to 0.75 g/cm3 with a decrease of average particle size from 121 μm to 68 μm. In comparison, spherical powders bulk density used in various industries is currently 2.45-2.6 g/cm3. In all experiments, metal zinc content varied in the range of 91.1-92.5%, the rest - ZnO. To a greater extent, this indicator depends on powder washing quality from alkali and storage conditions.

scholarly journals Synthesis of Spherical Silica by Sol-Gel Method and Its Application as Catalyst Support

2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit
Keyword(s):  
Particle Size ◽  
Ethylene Glycol ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Weight Ratio ◽  
Gel Method ◽  
Sol Gel Method ◽  
Spherical Silica

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.</

Influence of Powder Particle Size of Slurries on Mechanical Properties of Porous Hydroxyapatite Ceramics

2005 ◽  
Vol 284-286 ◽  
pp. 365-368 ◽  
Author(s):  
Yin Zhang ◽  
Yoshiyuki Yokogawa ◽  
Tetsuya Kameyama
Keyword(s):  
Particle Size ◽  
Flexural Strength ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Particle Sizes ◽  
Wet Milling ◽  
Median Particle Size ◽  
Powder Characteristics ◽  
Median Particle

The effect of different particle sizes on the flexural strength and microstructure of three different types of hydroxyapatite (HAp) powders was studied. The powder characteristics of laboratory synthesized HAp powder (Lab1 and Lab2) were obtained through a wet milling method, and the median particle size and the specific surface area of powders are different with the dryness period. The median particle sizes of Lab1 and Lab2 are 0.34 µm and 0.74 µm, and the specific surface areas of Lab1 and Lab2 are 38.01 m2/g and 19.77 m2/g. The commercial HAp had median particle size of 1.13 µm and specific surface area of 11.62m2/g. The different powder characteristics affected the slip characteristics, and the flexural strength and microstructure of the sintered porous HAp bodies are also different. The optimum value for the minimum viscosity in these present HAp slip with respect to its solid loading and the optimum amount of the deflocculant were investigated. The flexural strengths of the porous HAp ceramics prepared by heating at 1200°C for 3 hrs in air were 17.59 MPa for Lab1 with a porosity of 60.48％, 10.51 MPa for Lab2 with a porosity of 57.75％, and 3.92 MPa for commercial HAp with a porosity of 79.37％.

Study on Comparison among Papermaking Powder Properties

2012 ◽  
Vol 512-515 ◽  
pp. 2434-2438
Author(s):  
Quan Xiao Liu ◽  
Wen Cai Xu
Keyword(s):  
Particle Size ◽  
Chemical Composition ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Preparation Method ◽  
Powder Properties

In this paper the comparison among some papermaking powder properties are studied. It shows that the properties of different powders are different because of different chemical composition and different preparation method and their particle size is different for different purpose such as filler and pigment. The particle size of powder for pigment powder is smaller than that for filler. The specific surface area of papermaking filler is lower than 20m2/g, the absorption value of DBP is about 45cm3/100g, the whiteness is up to 90%, and the particle size is about 3µm. The specific surface area of papermaking pigment is lower than 25m2/g, the absorption value of DBP is from 40 cm3/100g to100cm3/100g, the whiteness of clay is up to 50%, the whiteness of GCC and PCC is up to 90%, and the particle size is lower than 2µm. The specific surface area of silica is up to 100m2/g, the absorption value of DBP is up to 100cm3/100g, the whiteness is up to 97%, and the particle size is around 5µm.

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