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Showing 4 results for Paramagnetic

N. Yazdani, J. Javadpour, B. Eftekhari Yekta, M. Hamrang,
Volume 16, Issue 1 (3-2019)
Abstract

This study focuses on the physical, magnetic, biological and antibacterial behaviour of cobalt-doped HAp powder samples. Pure and Cobalt- doped HAp nanoparticles were synthesized by hydrothermal method. Calcium nitrate, di- ammonium hydrogen phosphate and cobalt nitrate were used as precursor materials.  The synthesized powders were characterized using x-ray diffraction pattern (XRD), fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), vibrating sample magnetometer (VSM), Raman spectroscopy as well as MTT assay and cell adhesion test. Disc diffusion method was used to investigate antibacterial activity of the samples. The results confirmed the substitution of Ca by Co ions in the HAp lattice. In addition, this substitution induced size reduction and morphology change in HAp particles. All cobalt substituted HAp powder samples displayed paramagnetic properties, as opposed to the diamagnetic behaviour observed in the pure HAp samples. In addition, these nanoparticles exhibited cell adhesion, biocompatibility and antibacterial activity against S.aureus bacteria.
This study focuses on the physical, magnetic, biological and antibacterial behaviour of cobalt-doped HAp powder samples. Pure and Cobalt- doped HAp nanoparticles were synthesized by hydrothermal method. Calcium nitrate, di- ammonium hydrogen phosphate and cobalt nitrate were used as precursor materials.  The synthesized powders were characterized using x-ray diffraction pattern (XRD), fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), vibrating sample magnetometer (VSM), Raman spectroscopy as well as MTT assay and cell adhesion test. Disc diffusion method was used to investigate antibacterial activity of the samples. The results confirmed the substitution of Ca by Co ions in the HAp lattice. In addition, this substitution induced size reduction and morphology change in HAp particles. All cobalt substituted HAp powder samples displayed paramagnetic properties, as opposed to the diamagnetic behaviour observed in the pure HAp samples. In addition, these nanoparticles exhibited cell adhesion, biocompatibility and antibacterial activity against S.aureus bacteria.
Najwa Gouitaa, Lamcharfi Taj-Dine, Bouayad Lamfaddal, Abdi Farid, Mohamed Ounacer, Mohammed Sajieddine,
Volume 18, Issue 2 (6-2021)
Abstract

    The structural and dielectric properties of iron and bismuth co-substituted BaTiO3 ceramic with the formula: B0.95Bi0.05Ti1-xFexO3 for x=0.00 to 1.00, synthesis with solid state route, were characterized.     The X-ray diffraction results show a tetragonal phase for x=0.00. While for x=0.40 to 0.80 we observed a coexistence of tree phase tetragonal, hexagonal and pseudo-cubic. And at x=1.00 only the pseudo-cubic phase is present and the other phase disappeared. The Raman results indicate the existence of tetragonal band for x≤0.40, and an appearance of characteristic bands of Fe3+ ions for more than 0.40 of Fe content. The SEM micrographs show an increase in grain size with the increase of Fe content and it reaches a maximum at x=0.40.  And the Mossbauer spectroscopy indicates that our samples is paramagnetic at room temperature and that the Fe is   oxidized under Fe3+ with no existence of Fe2+ and Fe4+ ions. The temperature dependence of dielectric permittivity was investigated in the frequency range from 20 Hz to 2MHz. The results show three dielectric relaxation phase transitions from a rhombohedral ferroelectric to orthorhombic ferroelectric (TR-O) then to a tetragonal ferroelectric phase (at TO-T), and finally to cubic paraelectric at the Curie temperature (TC).  In addition, the temperature of phase transition shifted to the lower temperature with the increase of Fe content for all the phase transitions. And the maximum of dielectric permittivity increases for TR-O while for TT-O and Tm phases transitions, it reaches a maximum at x=0.60 and x=0.80 respectively and then decreases.

Salma Bessalah, Samira Jbahi, Mouldi Zagrouba, Hajji Sawsen, Amel Raoufi, Mustpha Hidouri,
Volume 19, Issue 2 (6-2022)
Abstract

Abstract
In this research, Gelatine (GEL)/ Chitosan (CH) wound dressing was prepared and irradiated with gamma rays from 60Co source for wound healing applications. GEL-CH composite characterization and functional properties were determined. The structural changes occurring after γ-irradiation at doses from 5 to 25 kGy were reported by physico-chemical techniques such as Electron Paramagnetic Resonance (EPR), Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Electrochemical Impedance Spectroscopy (EIS) studies. The antioxidant capacity was studied using DPPH (1,1-diphenyl-2-picrylhydrazyl free radical) scavenging and the antibacterial activities of Staphylococcus aureus and Escherichia coli were observed using liquid medium. Results revealed that EPR spectroscopy of un-irradiated GEL-CH showed 2 paramagnetic centers correspond to g=2.077 and g= 2.079. After irradiation, no active centre was appeared. A dose-dependent decrease in the central signal intensity was detected, then the EPR signal intensity almost disappears at 20 kGy. Gamma rays caused a slight increase in ion conductivity. FTIR suggest a slightly crosslinking phenomenon at 20 kGy. The XRD analysis does not show peak indicating crystallinity between a range of 2θ (15–30°). Moreover, γ-irradiation elevated the Scavenging DPPH radical activity (0.75 ± 0.07%). Gamma rays did not affect the antibacterial activity of GEL-CH wound dressing against pathogenic bacteria. The innovative results showed that the required γ-radiation for sterilization was ranged from 5 to 25 kGy. It permits to improve the physico-chemical and biological properties and maintain the native structural integrity of the GEL/ COL wound dressing
Amit Bandekar, Pravin Tirmali, Paresh Gaikar, Shriniwas Kulkarni, Nana Pradhan,
Volume 21, Issue 1 (3-2024)
Abstract

The Mn-Zn ferrite with a composition of Mn0.25Mg0.08Cu0.25Zn0.42Fe2O4 has been synthesized in this study using the chemical sol-gel technique at a pH of 7. The sample was prepared and subsequently annealed at a temperature of 700°C. The nanocrystalline ferrite samples were subjected to characterization using X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), Thermogravimetry (TG), and Differential thermal analysis (DTA). The findings of these observations are delineated and deliberated. The sample's phase composition was verified using X-ray diffraction examination. The crystalline size was determined using Scherrer's formula and was observed to be within the range of 20-75 nm. Two notable stretching bands were seen in the FTIR spectra within the range of 400-650 cm-1. The spinel structure of the produced nanoparticles was confirmed by these two bands. The magnetic characteristics of the powder were examined using a Vibrating Sample Magnetometer (VSM). The presence of M-H hysteresis loops suggests that the produced nanoparticles have superparamagnetic properties, as evidenced by their low coercive force, remanent magnetization, and saturation magnetization values.
 

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