Preparation and Calcination Temperature Optimization of La1-xSrxCo1-yFeyO3 for Removing NOx Effectively

2017 ◽  
Vol 727 ◽  
pp. 369-373
Author(s):  
Jia Qi Zhang ◽  
Ge Gao ◽  
Zheng Ma ◽  
Zhe Jia Ji Zhu ◽  
Hui Ying Chen

The automotive emission has become the main source of the air pollution in cities. How to remove NOx effectively is the key and difficult point in the control of automobile exhaust. In this work, sol-gel was applied to prepare NOx purification catalyst, LaCoO3 which was doped with strontium (Sr) and iron (Fe). The average particle size was less than 25 nm. The optimum composition of doped LaCoO3 was determined as La0.8Sr0.2Co0.95Fe0.05O3 with a minimum particle size, 14.3nm. The denitrification rate of La0.8Sr0.2Co0.95Fe0.05O3 increased by 27.9% compared with that of LaCoO3. It was noted that the sample powder would agglomerate when doped LaCoO3 was calcinated at 800°C, the calcination temperature of LaCoO3. Therefore the calcination temperature for double doped LaCoO3 was optimized. According to results of XRD and BET, the optimum calcination temperature of La0.8Sr0.2Co0.95Fe0.05O3 is 575°C, which not only overcame the agglomeration but also reduced the particle size to 11.2nm. The denitrification rate of La0.8Sr0.2Co0.95Fe0.05O3 calcinated at 575°C is up to 95.8% which is higher 38.7% than that of it calcinated at 800 °C.

2019 ◽  
Vol 16 (4) ◽  
pp. 0910
Author(s):  
Fayyadh Et al.

In this research, titanium dioxide nanoparticles (TiO2 NPs) were prepared through the sol-gel process at an acidic medium (pH3).TiO2 nanoparticles were prepared from titanium trichloride (TiCl3) as a precursor with Ammonium hydroxide (NH4OH) with 1:3 ratio at 50 °C. The resulting gel was dried at 70 °C to obtain the Nanocrystalline powder. The powder from the drying process was treated thermally at temperatures 500 °C and 700 °C. The crystalline structure, surface morphology, and particle size were studied by using X-ray diffraction (XRD), Atomic Force Microscopy (AFM), and Scanning Electron Microscope (SEM). The results showed (anatase) phase of titanium dioxide with the average grain size of 110 nm at 500 °C calcination temperature, and (anatase- rutile) mixed phase of titanium dioxide with the average particle size of 118.1 nm at 700 °C calcination temperature. The anti-bacterial activity of the synthesis specimens was recorded through the Kirby-Bauer disc method (disc devotion method). The results displayed a pretty excellent antibacterial activity of TiO2 NPs to bacteria strains: Gram positive staphylococcus aureus, gram negative pseudomonas aeruginosa, and "gram negative escherichia coli. The sensitivity of the tested bacteria to TiO2 NPs depends on the oxidation state of the TiO2 NPs, particle size, volume, and the density of the unit cell. The small- average particle size of titanium dioxide particles showed high antibacterial activity against bacteria, while the larger- average particle size of titanium dioxide particles showed less antibacterial activity. The novelty of this production is the manufacturing of a novel kind of TiO2 NPs and achievement its best antibacterial activity.


2017 ◽  
Vol 17 (01n02) ◽  
pp. 1760012
Author(s):  
S. Gowreesan ◽  
A. Ruban Kumar

The scope of the present work is in enhancing the particle size, and dielectric properties of Mg-substituted Cobalt ferrites nanoparticles prepared by sol–gel auto combustion method. The different ratios of Mg-substituted Co Ferrites (Co[Formula: see text]MgxFe2O4([Formula: see text], 0.05, 0.10, 0.15, 0.20 and 0.30)) are calcinated at 850[Formula: see text]C. The synthesized nanoparticles were characterized by powder XRD, FTIR, FE-SEM, EDX techniques and dielectric behavior. The structural parameters were confirmed from powder XRD and the average particle size is obtained from 39 to 67 nm due to the substitution of Mg[Formula: see text] which was calculated by Debye Scherrer’s formula. FE-SEM showed the surface morphology of the different ratio of the sample. The dielectric loss has measured the frequency range of 50[Formula: see text]Hz–5[Formula: see text]MHz. From electrical modulus, conductivity relaxation and thermal activation of charge carriers has been discussed.


2006 ◽  
Vol 510-511 ◽  
pp. 786-789 ◽  
Author(s):  
Dong Sik Bae ◽  
Byung Ik Kim ◽  
Kyong Sop Han

ZnO-TiO2 nanoparticles were synthesized by a reverse micelle and sol-gel process. The average particle size of the colloid was below 30 nm and well dispersed in the solution. ZnOTiO2 composite membranes were fabricated by using the dip-coating method on a porous alumina support. ZnO-TiO2 composite membranes showed a crack-free microstructure and narrow particle size distribution even after the heat treatment up to 600°C. The average particle size of the membrane was 30-40nm, and the pore size of ZnO-TiO2 composite membrane was below 10 nm.


2016 ◽  
Vol 709 ◽  
pp. 66-69
Author(s):  
Jeyashelly Andas ◽  
Rahmah Atikah Rosdi ◽  
Nur Izzati Mohd Anuar

A series of Fe-Co nanoparticles were synthesized via sol-gel route at acidic, neutral and basic condition using rice husk as the silica source. The synthesized nanomaterials were designated as Fe-Co3, Fe-Co7 and Fe-Co9 and characterized by Fourier Transform Infrared (FTIR), Transmission Electron Microscope (TEM) and particle size analyzer. The great effect of pH was clearly evidenced from the shifting in the siloxane bond in the FTIR spectrum. TEM investigation confirmed the existence of discrete and almost sphere like nanoparticles. The particle size decreased with an increase in the pH, registering the smallest average particle size at pH 9. In brief, this study promises a fast, rapid and promising method for the conversion of silica rice husk into nanoscale bimetallic materials.


2015 ◽  
Vol 1107 ◽  
pp. 301-307 ◽  
Author(s):  
Salahudeen A. Gene ◽  
Elias B. Saion ◽  
Abdul Halim Shaari ◽  
Mazliana A. Kamarudeen ◽  
Naif Mohammed Al-Hada

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.


2004 ◽  
Vol 847 ◽  
Author(s):  
Christophe Barbé ◽  
Sandrine Calleja ◽  
Linggen Kong ◽  
Elizabeth Drabarek ◽  
Alexandra Bush ◽  
...  

ABSTRACTUsing sol-gel technology combined with water-in-oil (W/O) emulsions, we have developed an innovative method for producing ceramic particles with independent control over the release rate and particle size. The average particle size can be varied from 10 nm to 100 μm and is controlled by the emulsion chemistry. The release rate can be independently varied from mg/hours to mg/month, and is controlled by the internal microstructure of the particles and the initial sol-gel chemistry.


1996 ◽  
Vol 11 (5) ◽  
pp. 1199-1209 ◽  
Author(s):  
J. M. McHale ◽  
P. C. McIntyre ◽  
K. E. Sickafus ◽  
N. V. Coppa

An aqueous, all nitrate, solution-based preparation of BaTiO3 is reported here. Rapid freezing of a barium and titanyl nitrate solution, followed by low temperature sublimitation of the solvent, yielded a freeze-dried nitrate precursor which was thermally processed to produce BaTiO3. XRD revealed that 10 min at temperatures ≧600 °C resulted in the formation of phase pure nanocrystalline BaTiO3. TEM revealed that the material was uniform and nanocrystalline (10–15 nm). The high surface to volume ratio inherent in these small particles stabilized the cubic phase of BaTiO3 at room temperature. It was also found that the average particle size of the BaTiO3 produced was highly dependent upon calcination temperature and only slightly dependent upon annealing time. This result suggests a means of selection of particle size of the product through judicious choice of calcination temperature. The experimental details of the freeze-dried precursor preparation, thermal processing of the precursor, product formation, and product morphology are discussed.


2012 ◽  
Vol 600 ◽  
pp. 190-193 ◽  
Author(s):  
Wei Wei ◽  
Jing Yi Zhang ◽  
Li Ping Wu ◽  
Guo Tong Qin

The hydrophobic silica granular aerogels were synthesized via sol-gel synthesis followed by ambient pressure drying. The tetraethyloxylane (TEOS) was used as original precursor. The aerogels were analyzed using nitrogen adsorption, scanning electron microscopy (SEM) and laser particle size analyzer. It was found that the aerogel was mesoporous material with high surface area. The aerogels were prepared in grain form by dipping into disperse solution in order to adsorption application. The average particle size of the aerogel was controlled by pH and disperse solution volume. The pH also affected gel time. The aerogels were used to absorb phenol from water. The saturated adsorption amount could reach up to 145 mg•g-1.


2018 ◽  
Vol 279 ◽  
pp. 208-213
Author(s):  
Hua Dong Wang ◽  
Zhi Qiang Sun ◽  
Xiao Bo Yang ◽  
Tao Wu ◽  
Heng Dong ◽  
...  

Dispersed Y2O3-MgO nanopowder was synthesized by calcining the stearate. XRD, TG-DTA, FT-IR, BET and FE-SEM were employed to analyze The formation mechanism of the precursor and the Y2O3-MgO nanopowder. Pure and dispersed Y2O3-MgO nanopowder with an average particle size of 40 nm was produced by calcining the precursor at 600 °C. The particle size increases to about 70 nm with the increase of the calcination temperature to 700 °C. In the preparation of Y2O3-MgO from stearate, no water medium is involved, thus capillarity force and bridging of adjacent particles by hydrogen bonds can be avoided, resulting in good dispersion of the particles. The dispersed Y2O3-MgO nanopowder prepared in this work has potential application in infrared transparent ceramic materials.


1998 ◽  
Vol 519 ◽  
Author(s):  
Francisco Del Monte ◽  
Yuhuan Xu ◽  
John D. Mackenzie ◽  
B. Claflin ◽  
G. Lucovsky

AbstractSemiconductor PbS quantum dot-doped Ormocers were successfully prepared by the sol-gel technique. Ormocers preparation was based on the use of trifunctional silane precursors at the solution stage. Formation of PbS particles took place in the pores of the Ormocers through lead precursor reaction with H2S gas. It was observed that temperature was an important factor in the reaction leading to the first appearance of PbS particles. The dot size of PbS was controlled through chemical interaction with the non-hydrolyzed groups of the trifunctional silane precursors. These groups prevent uncontrolled nucleation and aggregation processes during the particle formation and growth. The control of particle size was studied at different conditions for nucleation and aggregation. Determination of the average particle size was done by XR-Diffraction. Optical absorption spectra were also measured at the UV-VIS wavelength range. Absorption edge blue shifts show the quantum confinement effect in these materials.


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