Functional biocompatible magnetite–cellulose nanocomposite fibrous networks: Characterization by fourier transformed infrared spectroscopy, X-ray powder diffraction and field emission scanning electron microscopy analysis

2015 ◽  
Vol 136 ◽  
pp. 1450-1453 ◽  
Author(s):  
Neda Habibi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Infrared Spectroscopy ◽  
Field Emission ◽  
Powder Diffraction ◽  
X Ray ◽  
Fourier Transformed Infrared Spectroscopy ◽  
Electron Microscopy Analysis ◽  
Microscopy Analysis ◽  
Scanning Electron

Crystallization of Aragonite from Vaterite Precursor during Various Refluxing Times

2015 ◽  
Vol 1119 ◽  
pp. 466-470 ◽  
Author(s):  
Radek Ševčík ◽  
Petra Mácová ◽  
Marta Pérez-Estébanez
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Powder Diffraction ◽  
X Ray ◽  
Gradual Transformation ◽  
Scanning Electron

CaCO3 polymorphs are intensively studied due to their importance in the nature and the widespread use in the industry as well. This work is dealing with the crystallization of aragonite from vaterite dispersion during the refluxation at 100°C. The characterization of CaCO3 polymorphs during vaterite transformation was performed with Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and X-ray powder diffraction (XRPD). The influence of the different refluxing times on the aragonite crystallization was discussed. The purest aragonite, 70.7(2) wt.%, was synthetized in the sample refluxed for 60 minutes. Prolonged refluxation strongly affected aragonite crystals with gradual transformation into calcite.

Production of 3Y-PSZ Powders by Co-Precipitation and Milling

2008 ◽  
Vol 54 ◽  
pp. 50-55
Author(s):  
Erika Furlani ◽  
Eleonora Aneggi ◽  
Stefano Maschio
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Amorphous Powder ◽  
X Ray Diffraction ◽  
X Ray ◽  
Attrition Milling ◽  
Electron Microscopy Analysis ◽  
Microscopy Analysis ◽  
Co Precipitation ◽  
Scanning Electron

The present research compares properties and behaviour of co-precipitated 3Y-PSZ powders submitted, after co-precipitation, to different milling treatments. The characteristics of the different products were evaluated by measurement of particle size distribution, thermogravimetric analysis, X-ray diffraction, specific surface area and scanning electron microscopy analysis. It has been demonstrated that 1h of attrition milling enables the production of powders with micrometric particles: the dispersing liquid used on milling has little influence. Crystallization of the amorphous powder is achieved after 1h of high energetic milling, without any thermal treatment.

scholarly journals Synthesis of silver doped hydroxyapatite nanospheres using Ouzo effect

2016 ◽  
Vol 10 (3) ◽  
pp. 169-174 ◽  
Author(s):  
Marija Prekajski ◽  
Bojan Jokic ◽  
Ana Kalijadis ◽  
Jelena Maletaskic ◽  
Nadezda Stankovic ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Raman Spectroscopy ◽  
Single Phase ◽  
Simple Technique ◽  
Calcium Hydroxyapatite ◽  
X Ray ◽  
Electron Microscopy Analysis ◽  
Microscopy Analysis ◽  
Scanning Electron

Nanoemulsion technique, based on Ouzo effect, was applied for synthesis of the pure and silver doped (2.5 and 5mol%) calcium hydroxyapatite (HAp). After calcination at 500?C fully crystallized powders were obtained. X-ray powder diffraction analysis accompanied with Rietveld refinement revealed that the synthesized powders were single-phase hydroxyapatite. Raman spectroscopy also confirmed that the synthesized powders were single-phase. The obtained HAp particles were spherical in shape and their sizes were in the nanometer range which was revealed by field emission scanning electron microscopy analysis (FESEM). The successful synthesis of the single-phase Ag doped HAp showed that nanoemulsion method is a simple technique for obtaining pure and doped hydroxyapatite nanospheres.

Preparation of Borosilicate Xerogel and Research on its Mineralization

2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Ph Value ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Changes ◽  
Scanning Electron

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.

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