scholarly journals Hydrothermal assisted conventional sol-gel method for synthesis of bioactive glass 70S30Cы

Author(s):  
Ta Anh Tuan ◽  
Elena V. Guseva ◽  
Nguyen Anh Tien ◽  
Ha Tuan Anh ◽  
Bui Xuan Vuong ◽  
...  

Bioactive glasses (Bioglasses) are widely synthesized by the conventional sol-gel method consisting of two main steps for sol and gel formation. However, the conversion from sol to gel requires a long time (5–7 days). In this study, the hydrothermal system was used to quickly synthesize the bioactive glass by reducing the conversion time from sol to gel. The hydrothermal assisted conventional sol-gel method was applied for synthesis of the bioactive glass 70SiO2–30CaO (mol%) (noted as 70S30C). The synthetic glass was investigated by the physical-chemical techniques. The ‘‘in vitro’’ experiments in SBF (Simulated Body Fluid) solution was also performed to evaluate the bioactivity of synthetic material. The obtained results show that the bioactive glass 70S30C was successfully elaborated by using the hydrothermal assisted conventional sol-gelmethod. The consuming time was reduced compared to the conventional method. The physical-chemical characterization confirmed that the synthetic glass is amorphous material with mesoporous structure consisting of interconnected particles.The specific surface area, pore volume and average pore diameter of synthetic glass were 142.8 m2/g, 0.52 cm3/g, and 19.1 nm, respectively. Furthermore, synthetic bioactive glass exhibited interesting bioactivity when immersed in simulated body fluid (SBF) solution for 1 days and good biocompatibility when cultured in cellular media.

2015 ◽  
Vol 1107 ◽  
pp. 397-402
Author(s):  
H.J.M. Ridzwan ◽  
N.H. Jamil ◽  
S.A. Syamsyir ◽  
W.A.W. Razali

The bioactive glasses of SiO2-CaO-P2O5-SrO system have been prepared by a quick alkali mediated sol-gel method. The prepared bioactive glass of 1, 3, 5 wt% of SrO (coded: SR1, SR3, SR5, respectively) were characterized by SEM, XRD and FTIR. XRD pattern of all glasses calcined at 700°C in air confirmed that the calcined bioactive glass generally existed in amorphous state. The samples were immersed in simulated body fluid (SBF) to investigate the presence of hydroxyapatite (HA). All bioactive glass samples can induce the formation of hydroxyapatite (HA) as verified by SEM and XRD.


2007 ◽  
Vol 330-332 ◽  
pp. 777-780 ◽  
Author(s):  
Fang Fang Wang ◽  
Yun Mao Liao ◽  
Min Wang ◽  
Ping Gong ◽  
Xiao Yu Li ◽  
...  

In this study, an exclusive sodium titanate (Na2Ti6O13) coating on titanium was fabricated by sol-gel method and evaluated in vitro. The coating was characterized by SEM and XRD. The bioactivity of the Na2Ti6O13 coating was evaluated by the biomimetic growth of apatite on its surface after soaked in an acellular simulated body fluid (SBF) for a period of time. In vitro osteoblasts culture was carried out to determine cytocompatibility by the measurement of the proliferation and alkaline phosphatase (ALP) activity of the cells. XRD patterns showed that Na2Ti6O13 was well crystallized when the coating was heated at 800°C. SEM observation exhibited that the Na2Ti6O13 coated titanium had a homogeneous surface without any cracks. After immersion in SBF, the apatite layer can be formed on the coating. The cells culture showed that the osteoblasts grew well on the Na2Ti6O13 coated titanium. It can be concluded that Na2Ti6O13 coating on titanium obtained by sol-gel method is bioactive.


2005 ◽  
Vol 16 (11) ◽  
pp. 1045-1050 ◽  
Author(s):  
M. M. Pereira ◽  
J. R. Jones ◽  
R. L. Orefice ◽  
L. L. Hench

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.


2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Amanda Sayure Kasuya de Oliveira ◽  
Adriana Perpetua Figueiredo Paulista ◽  
Ana Ellen Valentim de Alencar ◽  
Tiago Pinheiro Braga

Aluminum oxide and/or silicon oxide-based supports were synthesized by proteic sol-gel method. The characterization was performed through the analysis of TG, XRD, FTIR, SEM, and N2 physisorption. The XRD diffractograms showed an amorphous material profile. TG results indicate the total liberation of the organic and inorganic material in the calcination temperature used, occurring in different mass loss range. This piece of information was reaffirmed by the FTIR spectra, which presented characteristic bands of gelatin structure before calcinations which disappear in the spectrum of the solid after calcinations, indicating the loss of organic matter from gelatin after heat treatment. The spectra exhibited M-O stretching vibration at low wavenumbers after calcinations related to metal oxides. The acquired images by SEM suggest the obtaining of a highly porous material with very different characteristics depending on the composition of the support. The N2 isotherms indicate the presence of a micro/mesoporous oxide with interesting textural properties, particularly for the supports containing aluminum and silicon oxide. The ethanol dehydration results showed greater selectivity to diethyl ether compared to ethylene. From the reaction data, the following order of acid strength was obtained: 2Si-Al > Si-2Al > Si-Al > Al, which is related to the Si-Al ratio.


RSC Advances ◽  
2014 ◽  
Vol 4 (43) ◽  
pp. 22678-22687 ◽  
Author(s):  
Qing Hu ◽  
Yuli Li ◽  
Guohou Miao ◽  
Naru Zhao ◽  
Xiaofeng Chen

Monodispersed mesoporous bioactive glass sub-micron spheres with a controllable size and good biocompatibility were fabricated by an improved sol–gel method.


2010 ◽  
Vol 64 (4) ◽  
Author(s):  
Melek Erol

AbstractIn this study, bioactivity of glass in the system SiO2-CaO-Al2O3-P2O5-Na2O-MgO-CaF2 was investigated. For this purpose, a glass sample was prepared by the traditional melting method. Crystallization behavior of bioactive glass was also investigated using differential thermal analyses. The Avrami constant of bioactive glass sample calculated according to the Ozawa equation was 3.72 ± 0.4, which indicates bulk crystallization. Using the Matusita-Sakka and the Kissinger equations, activation energy of crystal growth was determined as (394 ± 17) kJ mol−1 and (373 ± 12) kJ mol−1, respectively. These results indicate that the crystallization activation energy data of bioactive glass obtained in this study are accurate and reliable. Bioactivity of the resultant glass sample was analyzed by immersion in simulated body fluid. Scanning electron microscopy, thin film X-ray diffraction, ultraviolet spectroscopy and inductively coupled plasma techniques were used to monitor changes in the glass surface and the simulated body fluid composition. The results revealed that a hydroxyapatite layer was formed on the glass surface after 21 days of immersion in SBF. Formation of the hydroxyapatite layer confirmed the bioactivity of the glass in the system SiO2-CaO-Al2O3-P2O5-Na2O-MgO-CaF2. In addition, physical and mechanical properties of the sample were measured to determine changes in the properties with the immersion time. The results show that bioactive glass maintained its strength during the immersion in a simulated body fluid solution.


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