Texture Evaluation of Sol-Gel Derived Mesoporous Bioactive Glass

2013 ◽  
Vol 284-287 ◽  
pp. 230-234
Author(s):  
Yu Jen Chou ◽  
Chi Jen Shih ◽  
Shao Ju Shih
Keyword(s):  
Surface Area ◽  
Calcination Temperature ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Nitrogen Adsorption ◽  
Bioactive Glasses ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Adsorption Desorption

Recent years mesoporous bioactive glasses (MBGs) have become important biomaterials because of their high surface area and the superior bioactivity. Various studies have reported that when MBGs implanted in a human body, hydroxyl apatite layers, constituting the main inorganic components of human bones, will form on the MBG surfaces to increase the bioactivity. Therefore, MBGs have been widely applied in the fields of tissue regeneration and drug delivery. The sol-gel process has replaced the conventional glasses process for MBG synthesis because of the advantages of low contamination, chemical flexibility and lower calcination temperature. In the sol-gel process, several types of surfactants were mixed with MBG precursor solutions to generate micelle structures. Afterwards, these micelles decompose to form porous structures after calcination. Although calcination is significant for contamination, crystalline and surface area in MBG, to the best of the authors’ knowledge, only few systematic studies related to calcination were reported. This study correlated the calcination parameters and the microstructure of MBGs. Microstructure evaluation was characterized by transmission electron microscopy and nitrogen adsorption/desorption. The experimental results show that the surface area and the pore size of MBGs decreased with the increasing of the calcination temperature, and decreased dramatically at 800°C due to the formation of crystalline phases.

Preparation and characterization of high-surface-area titanium dioxide by sol-gel process

2006 ◽  
Vol 13 (3-4) ◽  
pp. 251-258 ◽  
Author(s):  
Chaochin Su ◽  
Kuei-Fen Lin ◽  
Ya-Hui Lin ◽  
Bor-Hou You
Keyword(s):  
Titanium Dioxide ◽  
Surface Area ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Sol Gel Process

Preparation of monolithic titania aerogels with high surface area by a sol–gel process combined surface modification

RSC Advances ◽  
2014 ◽  
Vol 4 (62) ◽  
pp. 32934-32940 ◽  
Author(s):  
Hui Yang ◽  
Wenjun Zhu ◽  
Sai Sun ◽  
Xingzhong Guo
Keyword(s):  
Surface Modification ◽  
Surface Area ◽  
Ambient Pressure ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Ambient Pressure Drying ◽  
Sol Gel Process

Monolithic titania (TiO2) aerogels with high surface area were successfully synthesized by the sol–gel process combined surface modification, followed by ambient pressure drying.

Synthesis and Characterization of ZrO2/Graphene Nanocomposite Materials

2012 ◽  
Vol 531 ◽  
pp. 161-164 ◽  
Author(s):  
Zong Hua Wang ◽  
Fu Qiang Zhu ◽  
Jan Fei Xia ◽  
Fei Fei Zhang ◽  
Yan Zhi Xia ◽  
...  
Keyword(s):  
High Surface ◽  
High Surface Area ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
Simple Method ◽  
Transmission Electron ◽  
Ft Ir ◽  
Graphene Nanocomposite ◽  
Adsorption Desorption

Zirconia/graphene (ZrO2/graphene) nanocomposite has been successfully synthesized by a simple method. The as-prepared nanocomposite was characterized using transmission electron microscopy (TEM), FT-IR spectroscopy, power X-ray diffraction (XRD) and nitrogen adsorption-desorption. It was found that tetragonal ZrO2was uniformly deposited on graphene, which resulted in the formation of two-dimensional nanocomposite, it showed a high surface area of 165 m2/g.

Synthesis of High Surface Area Porous Silicon Carbide by Employing Soft Template in the Sol-Gel Process

2010 ◽  
Vol 148-149 ◽  
pp. 1629-1633
Author(s):  
Dong Hua Wang ◽  
Xin Fu
Keyword(s):  
Silicon Carbide ◽  
Porous Silicon ◽  
Surface Area ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Silica Xerogel ◽  
Porous Silicon Carbide ◽  
Gel Method ◽  
Sol Gel Process

High surface area porous silicon carbide was synthesized by a modified sol-gel method. In the sol-gel method, furfuryl alcohol and tetraethoxysilane were used respectively as carbon and silicon precursors for preparing a carbonaceous silica xerogel. Polymethylhydrosiloxane (PMHS) was employed as pore-adjusting agent in the sol-gel process. SiC was obtained by the carbothermal reduction of the carbonaceous silica xerogel at 1300 oC in argon flow and then purified by removing excess silica, carbon and other impurities. XRD、FTIR、SEM、HRTEM and BET were used to characterize the SiC samples. The results show that the SiC products are found to have high specific surface area of 135 m2 /g. PMHS has important effect on the surface area, pore volume of the SiC products. It is therefore suggested that PMHS plays the role of structure-directing agent that enhances the production of mesoporous pores in the SiC products.

scholarly journals High Surface Area Ceria Nanoparticles via Hydrothermal Synthesis Experiment Design

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Stanislav Kurajica ◽  
Iva Minga ◽  
Martina Guliš ◽  
Vilko Mandić ◽  
Ivan Simčić
Keyword(s):  
Hydrothermal Synthesis ◽  
Surface Area ◽  
Fine Particles ◽  
High Surface ◽  
High Surface Area ◽  
Soot Oxidation ◽  
Nitrogen Adsorption ◽  
Synthesis Temperature ◽  
Oxidation Catalyst ◽  
Adsorption Desorption

Hydrothermal synthesis of CeO2was optimized on two reactant concentrations and synthesis temperature and duration, in order to achieve material having the greatest specific surface area (SSA). Taguchi method of experimental design was employed in evaluation of the relative importance of synthesis parameters. CeO2nanoparticles were characterized using X-ray diffraction, nitrogen adsorption-desorption isotherms, and scanning electron microscopy. Optimum conditions for obtaining particles with greater SSA were calculated according to Taguchi’s model “the-higher-the-better.” Synthesis temperature was found to be the only parameter significant for enabling nanoparticles with greater SSA. Mesoporous nanocrystalline ceria with SSA as great as 226 m2 g−1was achieved, which is unprecedented for the hydrothermally synthesized ceria. The reason for this achievement was found in temperature dependence of the diffusion coefficient which, when low, favors nucleation yielding with fine particles, while when high it favors crystal growth and formation of one-dimensional structures. The occurrence of 1D-structure in sample exhibiting the smallest SSA was confirmed. Very fine crystallites with crystallite size as low as 5.9 nm have been obtained being roughly inverse proportional to SSA. Selected samples were tested as catalyst for soot oxidation. Catalyst morphology turned out to be decisive factor for catalytic activity.

Hydrophobic Silica Aerogels by Ambient Pressure Drying

2015 ◽  
Vol 830-831 ◽  
pp. 476-479
Author(s):  
Srinivasan Nagapriya ◽  
M.R. Ajith ◽  
H. Sreemoolanadhan ◽  
Mariamma Mathew ◽  
S.C. Sharma
Keyword(s):  
Surface Area ◽  
Atmospheric Pressure ◽  
Polar Solvent ◽  
Ambient Pressure ◽  
High Surface ◽  
Sol Gel ◽  
High Surface Area ◽  
Silica Aerogels ◽  
Ambient Pressure Drying ◽  
Sol Gel Process

Silica aerogels have been prepared through sol-gel process by polymerization of TEOS in the presence of NH4F and NH4OH as catalysts. The solvent present in the gel is replaced by ethanol followed by a non-polar solvent such as n-hexane prior to solvent modification step. Gels are made hydrophobic by treating them with HMDZ to prevent rupture during drying, which has been confirmed by FTIR. Gels are then washed and dried carefully in a PID controlled oven at atmospheric pressure. The ageing duration and solvent exchange combinations are optimized to yield crack-free gels prior to drying. Aerogels are characterized for density, specific surface area, pore volume, pore size, thermal stability and contact angle. Hydrophobic, high surface area (570 m2/g), low density (0.07 g/cm3) silica aerogels are synthesized by using optimized mole ratio of precursors and catalysts. Silica aerogel granules (1-3 mm) as well as monoliths (Ф~35 mm) could be produced through ambient pressure drying of gels.

Preparation and Characterization of Silica-Alumina-Pillared Montmorillonites with High Surface Area

2008 ◽  
Vol 368-372 ◽  
pp. 1712-1715
Author(s):  
Hong Yan Xu ◽  
Xiao Jun Bao ◽  
Ting Hai Wang ◽  
Yong Gang Wang
Keyword(s):  
Surface Area ◽  
Layer Structure ◽  
High Surface ◽  
High Surface Area ◽  
Nitrogen Adsorption ◽  
Bet Specific Surface Area ◽  
Silica Alumina ◽  
Novel Method ◽  
Pore Properties ◽  
Adsorption Desorption

The silica-alumina-pillared montmorillonite materials (SiAl-MMT) were developed by a novel method, which combined several techniques such as ion-exchange, intercalation and surfactant modification. The morphology, composite structure and pore properties of such composite materials, were investigated by X-ray powder diffraction (XRD), Scanning Electronic Microscopy (SEM), Fourier-transform infra-red (FTIR) spectra, as well as Nitrogen Adsorption-Desorption Isotherms. The layer structure of the prepared materials retained and their pore structures were found to be slit-shaped pores located between plate-like particles. The prepared SiAl-MMT materials had a BJH pore volume of 0.63cm3 g-1, a remarkably high BET specific surface area beyond 1000 m2 g-1, and a narrow pore size distribution in the mesoporous region 3.5-4 nm after thermal treatment at 600 °C.

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