scholarly journals Template-Assisted Sol-Gel Synthesis of Nanocrystalline BaTiO3

2010 ◽  
Vol 7 (3) ◽  
pp. 894-898 ◽  
Author(s):  
T. V. Anuradha

Nanocrystalline perovskite barium titanate with an average particle size less than ∼10 nm is produced using sol-gel route involving ligand-assisted templating. BaTiO3is obtained by the controlled hydrolysis and condensation reaction of barium acetate (Ba(CH3COO)2) with titanium tetra chloride (TiCl4) in the reverse micelles of dodecylamine (DDA) which is used as the template. Our attempts to produce mesoporous BaTiO3have resulted in the formation of nanocrystalline BaTiO3. The synthesis of nanostructured BaTiO3is carried out using the ligand-assisted templating approach which proceeds through the sol-gel route. Dodecylamine is used as the template. The sol-gel process in general presents inherent advantages because the nanostructure of the desired materials can be controlled together with their porous structure. Ligand-assisted templating approach involves the formation of covalent bond between the inorganic analogue and the template. Ba(CH3COO)2and TiCl4are used as barium-source and titanium-source respectively. The reaction between Ba(CH3COO)2and TiCl4is found to take place deliberately on the pre-assembled species which acts as the template or occurring with in them which in turn will lead to the generation of the desired nanoscale structure (nanopores or nanoparticles).

2018 ◽  
Vol 762 ◽  
pp. 408-412
Author(s):  
Raivis Eglītis ◽  
Gundars Mežinskis

In this work two different hydrosols were used to impregnate a commercially available cotton fabric with anatase nanoparticles to give it photocatalytic activity. To increase the activity, different pre-treatment methods were applied. The nanoparticle size was determined using dynamic light scattering and x-ray diffraction and the fabrics were examined using scanning electron microscopy. Photocatalytic activity was measured using the degradation of methyl-orange while irradiating the samples with UV light. The synthesis method allowed to produce anatase with an average particle size of 32 to 37 nm depending on the synthesis method used.


2011 ◽  
Vol 412 ◽  
pp. 271-274
Author(s):  
Ying Li ◽  
Qiang Xu ◽  
Ling Dai

In order to prepare ultrafine La3NbO7 powder, a potential material for thermal barrier coatings, the calcination process of La3NbO7 was studied in this paper.The precursor of La3NbO7 was synthesized by using a citric acid complex method. A calcination process had been systematically investigated. The reaction temperature was determined by differential scanning calorimetry (DSC). The phase composition of powders was characterized by X-ray diffraction (XRD), and the morphology was obtained by scanning electron microscope (SEM). The results revealed that the single-phase La3NbO7 powder could be successfully prepared while the calcination temperature exceeded 800°C and a better morphology could be maintained at 800°C for 4 hours. Considering all above, an optimum calcination scheme was adopted at 800°C for 4 hours. The as-prepared La3NbO7 powders had a grain size of about 50nm and an average particle size of about 300nm.


2011 ◽  
Vol 287-290 ◽  
pp. 1731-1734 ◽  
Author(s):  
Han Sheng Li ◽  
Hang Xu ◽  
Shi Ying Wang ◽  
Ya Lin Pan ◽  
Qin Wu ◽  
...  

Anatase nano-titania (nano-TiO2) was prepared by using a sol-gel process mediated in reverse microemulsion combined with a solvent thermal technique. The results show that the anatase structure appears in the calcination temperature range of 400-510°C, while the transformation of anatase into rutile takes place above 510°C. The average particle size (dP) of the nano-TiO2 increases with the rise of water/Triton X-100 molar ratio (ω) but decreases with the rise of acetyl acetone/n-TBT molar ratio (p) and n-hexanol/Triton X-100 molar ratio (m). The obtained TiO2 particles with a small size have high photocatalytic activity.


2008 ◽  
Vol 23 (8) ◽  
pp. 2053-2060 ◽  
Author(s):  
S. Smitha ◽  
P. Shajesh ◽  
P. Mukundan ◽  
K.G.K. Warrier

A new organic–inorganic hybrid synthesized through a sol-gel process starting from alkoxysilane and chitosan is reported. Functionalization of the hybrid was effected through in situ hydrolysis–condensation reaction of methyltrimethoxysilane (MTMS) and vinyltrimethoxysilane (VTMS) in the reaction medium. The process yields highly transparent and hydrophobic silica–chitosan hybrids. The hybrid gel was investigated with respect to chemical modification, thermal degradation, hydrophobicity, and transparency under the ultraviolet-visible region. The extent of hydrophobicity had been tailored by varying the precursor ratio. SiO2–chitosan–MTMS hybrids showed a higher thermal stability than SiO2–chitosan–VTMS (SCV) hybrids with respect to hydrophobicity. Condensation of silsesquioxanes generated from the hydrolysis of MTMS and VTMS over the silica-chitosan particles impart hydrophobicity to the hybrid. The coatings of functionalized SiO2–chitosan precursor sol on glass substrates showed nearly 100% optical transmittance in the visible region. The present hybrid material may find application in optics and other industries.


2014 ◽  
Vol 925 ◽  
pp. 233-237 ◽  
Author(s):  
Mohamad Azani Jalani ◽  
Leny Yuliati ◽  
Salasiah Endud ◽  
Hendrik Oktendy Lintang

Gold nanoparticles (AuNPs) having particle size less than 10 nm can exhibit enhancement of surface area to give high activity such as in catalytic reaction. However, it is hard to synthesize AuNPs with small particle size due to the strong agglomeration. Herein we report that channels of mesoporous silica synthesized via the template sol-gel synthesis can be used to prepare AuNPs by calcination method. Mesoporous silica with an interpore distance of 4.1 nm was successfully fabricated as transparent thin film by using an amphiphilic trinuclear gold (I) pyrazolate complex as a template for the sol-gel synthesis. Upon calcination at 450 °C for 3 h, silica film nanocomposites showed red-shifting of surface plasmon resonance (SPR) bands from 518 (AuNPs from the bulk) to 544 nm owing to decreasing of the average particle size. The formation of AuNPs was also supported by the appearance of diffraction peaks of d111 at 2θ = 38.20° having a cubic phase. Moreover, transmission electron microscope (TEM) images and X-ray diffraction (XRD) peaks also showed smaller and more homogenous distribution of AuNPs.


2020 ◽  
Vol 21 (2) ◽  
pp. 219-226
Author(s):  
B. K. Ostafiychuk ◽  
H. M. Kolkovska ◽  
I. P. Yaremiy ◽  
B. I. Rachiy ◽  
P. I. Kolkovskyi ◽  
...  

In this work, the perovskite LaMnO3 material has been prepared based on the sol-gel process of synthesis with the participation of combustion. According to the X-ray phase analysis, it was determined that the obtained material consists of LaMnO3 one phase (space group Pm-3m). Nevertheless, it has been determined that the average size of the coherent scattering region of the obtained material is about 24 nm. Moreover, the average particle size is 40-60 nm in case the approximation that the particles are spherical shape. Thus, it has been determined that the specific surface area of the material is 42.1 m2/g. The electrochemical investigations have been performed using nanosized LaMnO3 powder as a cathode material for electrochemical capacitors. The LaMnO3 material under research showed a specific capacity of 40 F/g at a discharge of up to 1V.


2021 ◽  
Vol 10 (1) ◽  
pp. 74-78
Author(s):  
Nhan Dang Thi Thanh ◽  
Don Truong Thi ◽  
Thang Le Quoc ◽  
Tien Tran Dong ◽  
Son Le Lam

Presently, biopolymer materials have been given more attention for their outstanding properties, high efficiencies and promising applications in various fields. In this study, Fe2O3/chitosan aerogel-like spheres were successfully prepared from chitosan and FeCl3 by sol–gel process and freeze-drying to provide high-surface area materials. The factors affecting the material synthesis have been studied. The asprepared Fe2O3/chitosan material was characterized by Infrared Spectroscopy (IR), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) methods. The results showed that the aerogel spheres have a hollow structure made of chitosan nanofibril networks. Fe2O3 nanoparticles get high crystallinity and have an average particle size of 33 nm.


2020 ◽  
Vol 234 (2) ◽  
pp. 233-253 ◽  
Author(s):  
Muhammad Asif Tahir ◽  
Haq Nawaz Bhatti ◽  
Irshad Hussain ◽  
Ijaz Ahmad Bhatti ◽  
Muhammad Asghar

AbstractMesoporous silica (MPS) and MPS-Fe composite was prepared via sol–gel technique and characterized by BET, FTIR, XRD, SEM and pZc. The MPS and MPS-Fe adsorption efficiencies were evaluated for a cationic dye Turquoise-blue X-GB. The MPS-Fe composite showed pore size and BET values of 9.52 nm and 309 m2/g, respectively. XRD and SEM analysis revealed the amorphous nature and uniform distribution of spherical partciles with average particle size of 50 nm of MPS-Fe composite. The points of zero (pZc) charge found to be 2.3 and 6.3 for MPS and MPS-Fe, respectively. The MPS and MPS-Fe showed promising efficiency for the adsorption of Turquoise-blue X-GB as a function of medium pH, contact time, dye initial concentration and temperature. Among, Freundlich, Langmuir, Harkins–Jura, Temkin, Doubinin–Radushkevich isotherms, the Turquoise-blue X-GB followed Langmuir isothermal model with adsorption capacities of 83.34 mg/g and 74.07 mg/g for MPS and MPS-Fe composite, respectively. Among kinetics models, pseudo second order kinetic model fitted to the dye adsorption with R2 values of 0.998 and 0.988 for MPS and MPS-Fe composite, respectively. The negative values of enthalpy (ΔH) and free energy (ΔG) revealed exothermic and spontaneous adsorption of dye at room temperature. Results revealed that MPS and MPS-Fe composite have promising potential for Turquoise-blue X-GB dye adsorption and could possibly be extended for the adsorption of dyes from textile effluents.


2017 ◽  
Vol 748 ◽  
pp. 403-407
Author(s):  
Jia Yuan Min ◽  
Long Long Yu ◽  
Pei Song Tang ◽  
Hai Feng Chen

Using samarium (III) nitrate hexahydrate, manganese nitrate and citric acid as main raw materials, the SmMnO3 gel was prepared by sol-gel process. The gel was kept at 100 °C for 24 h to get the xerogel. Then, the xerogel was respectively calcined in muffle furnace at 600 °C, 700 °C, 800 °C and 900 °C. The structure and morphology of samples were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier Transform Infrared (FT-IR) spectroscopy. The UV photocatalytic activities of SmMnO3 were investigated by methyl orange which was used as simulated sewage. The results show that the pure SmMnO3 can be obtained through calcination between 700 °C and 800 °C, and the SmMnO3 have an average particle size of 80 nm. The SmMnO3 samples calcined at 700 °C and 800 °C show high photocatalytic activity for decomposition of methyl orange under UV-light irradiation. The SmMnO3 samples are consistent with first-order kinetics for the degradation of methyl orange. And the apparent rate constants are respectively k700 =0.01206 min-1and k800=0.01088 min-1.


2011 ◽  
Vol 1306 ◽  
Author(s):  
Christian Hörtz ◽  
Danielle M. Ladd ◽  
Dong-Kyun Seo

ABSTRACTNanoporous MgAl2O4 particulates with high porosities were successfully prepared from sol-gel reactions, solvent exchange with castor oil and subsequent combustion and calcination at 700 °C. The products were crystalline and semitransparent. Changes in the metal precursor concentrations allowed control of pore volumes from 0.7 to 1.1 cm3/g and average pore sizes from 14 to 19 nm. The specific surface areas are about 200 m2/g regardless of the precursor concentrations. After heating at 1000 °C for 10 hours, the products kept about 70% of their original pore volume and about 60% of the original surface area. Heating at 1100 °C caused a drastic reduction of pore volume and surface area to 40 and 36%, respectively, as the average particle size increased to 23 nm.


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