Sol–gel synthesis of mesoporous spherical zirconia

RSC Advances ◽  
2015 ◽  
Vol 5 (127) ◽  
pp. 104629-104634 ◽  
Author(s):  
Yulei Chang ◽  
Chen Wang ◽  
Tongxiang Liang ◽  
Chunsong Zhao ◽  
Xi Luo ◽  
...  

Mesoporous spherical zirconia (ZrO2) with a surface area of 113 m2g−1and average pore size of 5.0 nm is prepared by a sol–gel method with ZrOCl2·8H2O precursors and Sodium Dodecyl Sulfonate (SDS) templates with subsequent annealing at 500 °C in air.

2018 ◽  
Vol 232 (2) ◽  
pp. 245-256 ◽  
Author(s):  
Hala K. Farag ◽  
Hussein Abbas

AbstractThe present paper shows a comparative study on the synthesis of nanostructured tin oxide in the ionic liquid 1-ethyl-3-methylimidazolium trifluoromethylsulfonate ([EMIm]TfO) by sol–gel and sonochemical methods. The XRD results of the synthesized materials revealed the formation of single tetragonal phase of SnO2by sol–gel method whereas a mixture of tetragonal SnO and orthorhombic SnO2phases was obtained by the sonochemical method. The sonochemical approach led to the formation of finer nanoparticales with a higher specific surface area than that of the sol–gel synthesized oxide. The average sizes of tin oxide nanoparticles were found to be about 30 nm and 15 nm for the particles obtained by sol–gel and sonochemical methods, respectively. The surface area of SnO2nanopowder obtained by the sol–gel method (calcined at 500 °C) was estimated to be 11.6 m2g−1, and the mean pore diameter was found to be 6.33 nm. Whereas the mixed SnO/SnO2sample (calcined at 500 °C) obtained by the sonochemical method exhibited a higher surface area of 43.11 m2g−1and an average pore diameter of 1.90 nm. The band gap of the synthesized tin oxides was estimated from the UV-vis. results to be 4.01 and 4.25 eV for the sol–gel and sonochemically synthesized samples, respectively.


Materials ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 4515
Author(s):  
Ricardo Bento ◽  
Anuraag Gaddam ◽  
José M. F. Ferreira

Sol–gel synthesis using inorganic and/or organic precursors that undergo hydrolysis and condensation at room temperature is a very attractive and less energetic method for preparing bioactive glass (BG) compositions, as an alternative to the melt-quenching process. When properly conducted, sol–gel synthesis might result in amorphous structures, with all of the components intimately mixed at the atomic scale. Moreover, developing new and better performing materials for bone tissue engineering is a growing concern, as the aging of the world’s population leads to lower bone density and osteoporosis. This work describes the sol–gel synthesis of a novel quaternary silicate-based BG with the composition 60 SiO2–34 CaO–4 MgO–2 P2O5 (mol%), which was prepared using acidified distilled water as a single solvent. By controlling the kinetics of the hydrolysis and condensation steps, an amorphous glass structure could be obtained. The XRD results of samples calcined within the temperature range of 600–900 °C demonstrated that the amorphous nature was maintained until 800 °C, followed by partial crystallization at 900 °C. The specific surface area—an important factor in osteoconduction—was also evaluated over different temperatures, ranging from 160.6 ± 0.8 m2/g at 600 °C to 2.2 ± 0.1 m2/g at 900 °C, accompanied by consistent changes in average pore size and pore size distribution. The immersion of the BG particles in simulated body fluid (SBF) led to the formation of an extensive apatite layer on its surface. These overall results indicate that the proposed material is very promising for biomedical applications in bone regeneration and tissue engineering.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Wenjie Zhang ◽  
Ruyuan Li ◽  
Hongbo He

The mesoporous TiO2-Al2O3binary oxides were prepared by sol-gel method using PEG1000 as template. The effects of PEG1000 concentration on the properties and photocatalytic activity of the materials were investigated. The binary oxides were composed of nanocrystallite anatase TiO2and amorphous Al2O3. The surfaces of the samples prepared with PEG1000 were rough and had many long grooves on the surfaces. When PEG1000 concentration increased from 0 to 0.048 mol/L, the BET specific surface area of the samples changed from 99 to 140 m2·g−1, and the average pore size decreased from 22 to 11 nm. The TiO2-Al2O3binary oxides prepared at PEG1000 concentration of 0.03 mo/L had the maximum photocatalytic activity and high adsorption capacity. Methyl orange photocatalytic degradation and adsorption rates on 600 mg/l of TiO2-Al2O3binary oxides were 36.1% and 18.6% after 30 min, respectively. Total removal of the dye was achieved after 3 h of reaction.


2013 ◽  
Vol 789 ◽  
pp. 237-241 ◽  
Author(s):  
Maya Komalasari ◽  
Bambang Sunendar

Nanotechnology is one of the key technology had been developed since in all fields including textile industries for medical, hygienic, and technical textiles. Particle size with nanohad been indicated in particular for the application of controlled release material for functional textiles. TiO2nanopowder has remarkable photo-catalytic and semiconductor as material for various advanced technology fields of application such as UV Protection. In this research the synthesis of TiO2nanoparticle and characterization had been conducted successfully by sol-gel method. The starch was used as a template to get nanoparticles structure. TiO2sol with narrow particle size distribution using TiCl4as the starting material. The sol was prepared by a process where HCl was added to a gel of hydrated titanium oxide to dissolve it. The effect of preparation parameters were investigated, by deionized water : HCl 1 M was slowly added to TiCl4at 5 °C. In this study the production of anatase or rutile TiO2nanostructured powder by forced hydrolysis of aqueous Ti (IV) chloride solution and concentration from 0,3, 0,5 then 1 M. TiO2sphere were fabricated by a facile and low cost stable starch assisted by sol-gel method. Aqueous solution of starch was added and then heated in temperature 80°C and aqueous solution of ammonium hydroxide was added to adjust pH to 8. After aging period of time, the white precipitate was filtered and then calcined in temperature 5000C. The as-obtained samples were characterize,kjnhjd by SEM (Scanning Electron Microscope), UV-vis diffuse reflectance spectroscopy, X-Ray Diffraction (XRD) and Brunauer Emmett Teller (BET) analysis. The particle size is less than 100 nm and if it uses template particle TiO2more uniform distribution and spherical shape with particle size 170 200 nm. Crystalinity particle is 4 19 nm and the phase structure of anatase and rutile. The energy band gap semiconductor TiO2synthesis is 3.1 to 3.7 eV. Surface area without template starch 40.655 m2/g, with total for volume 0.278 cm3/g and pore size of 27 nm, and used template starch surface area 35.488m2/g with total for volume 0.196 cm3/g and pore size of 22 nm. Based on this research, the best a crystal phase for UV protection application is rutile phase.


2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Sang-wook Ui ◽  
In-seok Choi ◽  
Sung-churl Choi

Over the past several years, synthesized mesoporous nanosilica (SiO2) powders have been developed by many different methods. The methods include precipitation and microemulsion, the Stöber method, chemistry, and technology. In this study, mesoporous silica powders are synthesized by the sol-gel method. The sol-gel method obtains a high purity silica powder; however, the process yields a low percentage. Past syntheses of SiO2 powder precursors are expensive, but this study needs to find a replacement precursor for low cost alternatives. A high surface area was used to form an anion surfactant sodium dodecyl sulfate, which regulates the molar concentration. The particles size variability was changed by the precursor molar ratio of the sodium silicate solution with hydrochloric acid.


2019 ◽  
Vol 964 ◽  
pp. 88-96
Author(s):  
Hariyati Purwaningsih ◽  
Slamet Raharjo ◽  
Vania Mitha Pratiwi ◽  
Diah Susanti ◽  
Agung Purniawan

Rice became the main product of agriculture in agrarian countries including Indonesia. Rice husk is a waste of rice as one of the largest silica producers. Silica from rice husks can be used as a source of silica in the manufacture of sodium silicate as an alternative to the formation of mesoporous silica at a low price. In this research, the characterization of mesoporous silica nanoparticle (MSN) MCM-41 from rice husk (rice husk) with sol-gel method followed by hydrothermal treatment. Silica extraction was performed by titrating sodium silica using HCl method until the gel was formed. The mesoporous synthesis was performed with the addition of CTAB. The titration is then carried out using a solution of acetic acid. XRD shows silica with an amorphous structure. The FTIR results show that extraction silica and MSN MCM-41 contain pure silica displayed with Si-O-Si functional groups in the sample. The SEM results show MSN MCM-41 images such as a coral-like structure of agglomerated silica and the higher temperature hydrothermal treatment then it would be the more large size of particles. The material has a hexagonal pore structure such as a honeycomb as characteristic of MCM-41 with a pore size of 2.535 nm which includes mesoporous material. The result of nitrogen adsorption-desorption isotherms shows lower hydrothermal temperature will increase the specific surface area and decrease average pore size, where the best result with surface area value is 825.365 m2/gr and average pore size is 6.10426 nm obtained from process hydrothermal at 85°C.


2018 ◽  
Vol 29 (7) ◽  
pp. 075702 ◽  
Author(s):  
Feng Qingge ◽  
Cai Huidong ◽  
Lin Haiying ◽  
Qin Siying ◽  
Liu Zheng ◽  
...  

2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit

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.</


2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Nor Hafizah ◽  
Iis Sopyan

NanosizedTiO2powder was synthesized via sol-gel method using titanium tetraisopoxide (TPT) as the precursor. Mol ratios of water to TPT were varied from 1 (Powder A), 2 (Powder B), 3 (Powder C), and 4 (Powder D) to evaluate effect of hydrolysis degree. TG/DTA curves showed that amorphous phase turned to anatase crystal structure at ca. 415, 337, 310, and339∘C for Powders A, B, C, and D, respectively. XRD analysis showed that all the synthesizedTiO2powders were 100% in anatase form with Powders B and C showing considerably higher crystallinities. The powders obtained at lower water to TPT mol ratios were spherical in shape and they became bar-like shapes higher mol ratios. The lower hydrolysis degree led to higher surface area of the Powder A (24.8 m2/g) compared to Powder B (14.6 m2/g). From phenol photocatalytic measurement, Powder B was the most efficient attributed to its higher crystallinity.


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