Study on the Preparation and Particle Size Control of Silica Sphere in a Sol-Gel Process

2013 ◽  
Vol 787 ◽  
pp. 52-57
Author(s):  
Ying Qiu ◽  
Shu Chun Hu ◽  
Jing Zhai ◽  
Zhi Jian Lin ◽  
Wen Feng Liu ◽  
...  

Silica sphere has wide applications not only in the field of physical chemistry dealing with dynamic behavior and stability of particulate systems, but also in industries including catalysts, ceramics, pigments, pharmacy, etc. However, the control on the particle size is a key factor in the preparation process of silica sphere. In this paper, silica sphere with uniform sphere morphology and amorphous structure was prepared by a sol-gel method, and the control of particle size was emphatically studied. The results showed that the particle size of the as-prepared silica sphere was obviously influenced by the raw materials concentration. The average size of the product increased from 0.66 μm to 0.90 μm when ethanol concentration increased from 7.14M to 9.55M, increased from 0.50 μm to 0.90 μm with the increase of ammonia concentration in the range of 1.88M to 2.36M, and increased from 0.47 to 0.90 μm while tetraethoxysilane concentration increased from 0.08M to 0.11M. Further study indicated that the silica particle size was also influenced by reaction temperature, it increased with the increase of temperature from 26°C to 28°C, and decreased with the further increase of temperature in the scope of 28°C to 32°C.

1999 ◽  
Vol 606 ◽  
Author(s):  
Keishi Nishio ◽  
Jirawat Thongrueng ◽  
Yuichi Watanabe ◽  
Toshio Tsuchiya

AbstructWe succeeded in the preparation of strontium-barium niobate (Sr0.3Ba0.7Nb2O6 : SBN30)that have a tetragonal tungsten bronze type structure thin films on SrTiO3 (100), STO, or La doped SrTiO3 (100), LSTO, single crystal substrates by a spin coating process. LSTO substrate can be used for electrode. A homogeneous coating solution was prepared with Sr and Ba acetates and Nb(OEt)5 as raw materials, and acetic acid and diethylene glycol monomethyl ether as solvents. The coating thin films were sintered at temperature from 700 to 1000°C for 10 min in air. It was confirmed that the thin films on STO substrate sintered above 700°C were in the epitaxial growth because the 16 diffraction spots were observed on the pole figure using (121) reflection. The <130> and <310> direction of the thin film on STO were oriented with the c-axis in parallel to the substrate surface. However, the diffraction spots of thin film on LSTO substrate sintered at 700°C were corresponds to the expected pattern for (110).


2010 ◽  
Vol 5 (6) ◽  
pp. 361 ◽  
Author(s):  
R.-J. Tan ◽  
Y.-H. Tseng ◽  
C.-H. Kuo

2022 ◽  
Author(s):  
Monika Patel ◽  
Sunita Mishra ◽  
Ruchi Verma ◽  
Deep Shikha

Abstract Nanotechnology is a completely unique branch of technology that offers with substances in a very small size between (1-100 nm) with various crystal shapes which include spherical nanoparticles, flower shaped, Nano rods, Nano ribbons, and Nano platelets. Metals have ability to produce large number of oxides. These metal oxides play an major role in many areas of chemistry, physics, material science and food science. In this research, Zinc Oxide (ZnO) and Copper (II) oxide nanoparticles were synthesized via sol-gel process using zinc nitrate and copper (II) nitrate as precursor respectively. The characterization of CuO and ZnO nanoparticles was done by using various techniques. X-ray Diffraction (XRD) indicates the crystallinity and crystal size of CuO and ZnO nanoparticle. Fourier transform infrared spectroscopy (FT-IR) was used to get the infrared spectrum of the sample indicating composition of the sample which contains various functional groups. XRD result shows the particle size of CuO at highest peak 29.40140 was 61.25 nm and the particle size of ZnO at highest peak 36.24760 was 21.82 nm. FT-IR spectra peak at 594.56 cm-1 indicated characteristic absorption bands of ZnO nanoparticles and the broad band peak at 3506.9 cm-1 can be attributed to the characteristic absorption of O-H group. The analysis of FT-IR spectrum of CuO shows peaks at 602.09, 678.39, and 730.19cm−1 which refer to the formation of CuO. A broad absorption peak noticed at 3308.2 cm−1 attributed to O–H stretching of the moisture content.


2019 ◽  
Vol 8 (1) ◽  
pp. 39 ◽  
Author(s):  
Susanto Susanto ◽  
Ricka Prasdiantika

Synthesis of Fe3O4@SiO2 modified with propyldiethylenetriamine (Fe3O4@SiO2@PDETA) with variation of synthesis routes have been investigated. Research was begun with synthesis of Fe3O4 using dispersion agent of trisodium citrate at coprecipitation system through stirring using ultrasonic wave. Coating magnetite with propyldiethylenetriamine modified silica was carried out through sol-gel process with two different mixing sequences of raw materials (two synthesis routes) with main materials of Fe3O4 synthesized, N-[3-(Trimethoxysilyl)propyl]-diethylenetriamine (TMSPDETA) and Na2SiO3. The products were characterized by fourier transform infrared (FTIR) spectrophotometer and scanning electron microscope-energy dispersive X-ray (SEM-EDX). Results indicate that Fe3O4@SiO2@PDETA has been synthesized succesfully. Fe3O4@SiO2@PDETA synthesized through route 1 (magnetite mixed with a mixture TMSPDETA and Na2SiO3) contains more propyldiethylenetriamine group than that of through route 2 (magnetite mixed with Na2SiO3 solution, then mixed with TMSPDETA)


1994 ◽  
Vol 9 (8) ◽  
pp. 2102-2108 ◽  
Author(s):  
E. Haro-Poniatowski ◽  
R. Rodríguez-Talavera ◽  
Heredia M. de la Cruz ◽  
O. Cano-Corona ◽  
R. Arroyo-Murillo

Sols of titania were obtained by the sol-gel method and their size profile was followed by dynamical light scattering. In the early stages of the reaction an unstable behavior was detected. After this unstable regime the particle size reaches a steady state where the sols have a constant size while increasing in number. Once the sol concentration reaches its overlap value, the gelation regime takes place. For samples prepared in this way Raman spectra and x-ray diffractometry were used to characterize the kinetics of crystallization of the material.


2019 ◽  
Vol 947 ◽  
pp. 82-90
Author(s):  
Pirutchada Musigapong ◽  
Sophie Marie Briffa ◽  
Iseult Lynch ◽  
Siriwat Soontaranon ◽  
N. Chanlek ◽  
...  

The information provided by different characterisation methods when measuring particle size varies depending on the chosen technique and analytical approach (e.g. light scattering, transmission electron microscopy, spectroscopy, x-ray scattering). This in turn has an impact on the accuracy of the results as well as comparability between methods and overall confidence on the analyses. The present study used a common sol-gel reaction to synthesise amorphous silica nanoparticles (aSiNPs) and characterised the product purity and homogeneity. The reaction involved hydrolysis and condensation of tetraethyl orthosilicate (TEOS) in the presence of lysine, which acted as catalyst for the silica production and also as a capping agent for particle size control in a suspension kept at pH 8-10. According to DLS data, the stock suspension was stable for at least 6 months in Milli Q water without surfactant when kept at 4°C. This study focused on multi-method size and shape characterisation of the aSiNPs, involving the following techniques: DLS, TEM, FTIR, STEM and SAXS. These techniques provided information on hydrodynamic diameter, core particle dimensions, sphere equivalent size, and radius of gyration. Our results show two particle populations, one around 2 nm and the other around 7 nm in diameter. Notably, these two populations are not resolved (i.e. “visible”) by all methods used.


2013 ◽  
Vol 860-863 ◽  
pp. 845-848 ◽  
Author(s):  
De Yi Li ◽  
Kun Peng ◽  
Ling Ping Zhou ◽  
Jia Jun Zhu

SiO2 antireflective films were prepared by two-step catalyzed sol-gel method with TEOS as the raw materials, acid and ammonia as catalyst. Effects of the ratio of acid-catalyzed and base-catalyzed silica sols on the transmittance and stability of SiO2 film were investigated. The transmittance can be adjusted by change the ratio of base-catalyzed sols, and a higher transmittance can be obtained in the higher ratio of base-catalyzed coatings. A higher stability of SiO2 film in salt spray can be obtained in higher ratio of acid-catalyzed AR coatings. AR coatings with excellent transmittance and stability can be obtained by adjusting the ratio of acid/base catalyzed silica sols.


2012 ◽  
Vol 512-515 ◽  
pp. 207-210
Author(s):  
Quan Wen ◽  
Jian Feng Huang ◽  
Li Yun Cao ◽  
Jian Peng Wu

V2O5 powders were successfully synthesized by the EDTA assistanced ultrasound sol-gel process using NH4VO3 and EDTA, NH3•H2O as raw materials. The synthesized activation energy and the influence of pH values and the calcination temperatures on the phases and microstructures of powders were particularly investigated. The precursor powders and the V2O5 powders were characterized by X-ray diffraction (XRD), fourier transform inelectron microscopy (FT-IR), scanning electron microscopy (SEM) and differential scanning calorimetry-thermal gravimetric (DSC-TG). Results show that the obtained products exhibit good crystallization under the conditions of pH=4, calcination temperature 400~500 °C and calcination time 0.5 h during the synthesizing process. The as-prepared V2O5 powders show preferred growth orientation along (001) plane at the pH=4. By DSC analysis, the ultrasonic cavitation result in the decrease in synthesized activation energy obviously than that was prepared without ultrasonic irradiation.


2014 ◽  
Vol 670-671 ◽  
pp. 113-116 ◽  
Author(s):  
Xiao Yan Zhang ◽  
Xi Wei Qi ◽  
Zhi Yuan Yang ◽  
Rui Xia Zhong

Multiferroic BiFeO3 powders were synthesized by two methods: sol-gel process and hydrothermal method. The synthesized powders were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (SEM) and particle size distribution analysis. The results obtained by XRD, which is consistent with 86-1518 JCPDS card, show that powders prepared by hydrothermal method are composed of the single phase with the trigonal structure (perovskite-type). It can be found by particle size distribution analysis that the particle size of the samples prepared by sol-gel process is finer and more uniform than that of the samples synthesized by the hydrothermal method. The SEM images of samples depicts that the synthesized BiFeO3 powders are united and the average grain size of hydrothermal processed samples is significantly large as compared to the sol-gel derived sample.


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