scholarly journals Characterization of Magnetic Nanoparticles Coated with Chitosan: A Potential Approach for Enzyme Immobilization

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Azariel Díaz-Hernández ◽  
Jorge Gracida ◽  
Blanca E. García-Almendárez ◽  
Carlos Regalado ◽  
Rosario Núñez ◽  
...  
Keyword(s):  
Particle Size ◽  
Magnetic Nanoparticles ◽  
Size Distribution ◽  
Photoelectron Spectroscopy ◽  
Average Particle Size ◽  
Superparamagnetic Nanoparticles ◽  
Spherical Particles ◽  
Cross Linking ◽  
Average Particle ◽  
X Ray

Cross-linking of magnetic nanoparticles with proteins plays a significant role in the preparation of new materials for biotechnological applications. The aim was the maximization of the magnetic mass attracted and protein loading of magnetic iron oxide nanoparticles coated with chitosan, synthesized in a single step by alkaline precipitation. Chitosan-coated magnetite particles (Fe3O4@Chitosan) were cross-linked to a xylanase and a cellulase (Fe3O4@Chitosan@Proteins), showing a 93% of the magnetic saturation of the magnetite. X-ray diffraction pattern in composites corresponds to magnetite. Thermogravimetry and differential scanning calorimetry showed that 162 mg of chitosan was coating one gram of composite and 12 mg of protein was cross-linked to each gram of magnetic support. Cross-linking between enzymes and Fe3O4@Chitosan was confirmed by infrared spectroscopy with Fourier transform, X-ray energy, and X-ray photoelectron spectroscopy dispersion analysis. From dynamic light scattering, transmission and electron microscopy the average particle size distribution was 230 nm and 430 nm for Fe3O4@Chitosan and Fe3O4@Chitosan@Proteins, showing agglomerates of individual spherical particles, with an average diameter of 8.5 nm and 10.8 nm, respectively. The preparation method plays a key role in determining the particle size and shape, size distribution, surface chemistry, and, therefore, the applications of the superparamagnetic nanoparticles.

Synthesis and Studying Induction Heating of Mn1-xZnxFe2O4 (x=0-0.5) Magnetic Nanoparticles for Hyperthermia Treatments

2021 ◽  
Vol 882 ◽  
pp. 200-218
Author(s):  
S. Mahmood Hussein ◽  
T.H. Mubarak ◽  
S.M. Ali Ridha ◽  
Jasim Al-Zanganawee
Keyword(s):  
Particle Size ◽  
Relaxation Time ◽  
Magnetic Nanoparticles ◽  
Smart Materials ◽  
Average Particle Size ◽  
Superparamagnetic Nanoparticles ◽  
Soft Magnetic Materials ◽  
Precipitation Method ◽  
Average Particle ◽  
Co Precipitation

The recent development of the using the magnetic nanoparticles for hyperthermia treatments emphasizes the needed of smart materials to become a safety for heat therapy. Self-regulate magnetic nanoparticles of MnZnFe2O4 may be proper for thermal treatments. Structure and magnetic properties of the synthesis Mn1-xZnx Fe2O4 with x=0- 0.5 by step 0.1were studied. Superparamagnetic nanoparticles of MnZnFe2O4 were prepared by co-precipitation method, followed that heat treatment in the autoclave reactor. XRD results showed that is difficult to prepare MnZnFe2O4 directly using the co-precipitation method. Preparation method yield nanoparticles with spherical shape and there is a slight change in the particle size distribution, also observed shrinkage occurs in the particle size after heat treatments, the average particle size was estimated about 20nm as confirmed by FESEM images. FTIR spectra of samples showed two distinct absorption peaks in the range ~ 617 – 426 (cm-1) related to stretching vibrations of the (Fe-O) in the tetrahedral and octahedral side respectively. Magnetic measurements were carried out using (VSM), M-H curves indicate typical soft magnetic materials and particles so small to be identical superparamagnetic nanoparticles. Heating ability of water based colloidal dispersions of samples were studied under magnetic field strength 6.5kA/m and the frequency 190 kHz, and the results showed when increasing Zn2+ to x=0.3 or more the samples not heated up. Depending on the heating curve susceptibility, effective relaxation time and Néel relaxation time , were determined.

Synchrotron X-Ray Scattering for the Structural Characterization of Catalysts

1986 ◽  
Vol 30 ◽  
pp. 389-394
Author(s):  
R. J. De Angelis ◽  
A. G. Dhere ◽  
M. A. Maginnis ◽  
P. J. Reucroft ◽  
G. E. Ice ◽  
...  
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Profile Analysis ◽  
Average Particle Size ◽  
Initial Slope ◽  
Average Particle ◽  
Particle Size Range ◽  
Diffraction Profile ◽  
X Ray

Discussions exist in the literature concerning the application of single x-ray diffraction profile analysis to determine the average particle size, particle size distribution and root mean squared strain in catalytic systems. Nandi et al. have shown that the single order analysis can give erroneous strain results and is subject to error in the large particle size range. They further indicated that the initial slope of Stokes corrected Fourier coefficients gives more reliable average p article size than that which is calculated from single order peak shape analysis. There is apparent agreement that the average particle size and the particle size distribution measured by single order profile analysis, in small metal particle systems, are reliable.

Preparation and characterization of anatase N–F-codoped TiO2 sol and its photocatalytic degradation for formaldehyde

2007 ◽  
Vol 22 (9) ◽  
pp. 2389-2397 ◽  
Author(s):  
Donggen Huang ◽  
Shijun Liao ◽  
Shuiqing Quan ◽  
Lei Liu ◽  
Zongjian He ◽  
...  
Keyword(s):  
Particle Size ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Average Particle Size ◽  
Synergetic Effect ◽  
Tetrabutyl Titanate ◽  
Average Particle ◽  
Dielectric Relaxation Spectroscopy ◽  
X Ray

Anatase nitrogen and fluoride codoped TiO2 sol (N–F–TiO2) catalysts were fabricated by a modified sol-gel hydrothermal method, using tetrabutyl titanate as precursor. The microstructure and morphology of sol sample were characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet-visible dielectric relaxation spectroscopy (UV-VIS-DRS), x-ray photoelectron spectroscopy (XPS), etc. It was shown that N–F–TiO2 particles in sol were partly crystallized to anatase structure and dispersed in the aqueous medium homogeneously. The average particle size was ∼12.0 nm calculated from XRD patterns, and the particle size distribution was narrow. It was noteworthy that the N–F-codoped TiO2 sol particles showed strong visible-light response and high photocatalytic activity for formaldehyde degradation under irradiation by visible light (400–500 nm); we suggested that it may result from the generation of additional band of N 2p in the forbidden band and the synergetic effect of codoping nitrogen and fluorine.

scholarly journals Thermal, Structural, and Physical Properties of Freeze Dried Tropical Fruit Powder

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
K. A. Athmaselvi ◽  
C. Kumar ◽  
M. Balasubramanian ◽  
Ishita Roy
Keyword(s):  
Particle Size ◽  
Physical Properties ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Tropical Fruit ◽  
X Ray ◽  
Freeze Dried ◽  
Fruit Powder ◽  
Lcr Meter

This study evaluates the physical properties of freeze dried tropical (guava, sapota, and papaya) fruit powders. Thermal stability and weight loss were evaluated using TGA-DSC and IR, which showed pectin as the main solid constituent. LCR meter measured electrical conductivity, dielectric constant, and dielectric loss factor. Functional groups assessed by FTIR showed presence of chlorides, and O–H and N–H bonds in guava, chloride and C–H bond in papaya, and chlorides, and C=O and C–H bonds in sapota. Particle size and type of starch were evaluated by X-ray diffraction and microstructure through scanning electronic microscopy. A semicrystalline profile and average particle size of the fruit powders were evidenced by X-ray diffraction and lamellar/spherical morphologies by SEM. Presence of A-type starch was observed in all three fruits. Dependence of electric and dielectric properties on frequency and temperature was observed.

scholarly journals FORMULATION AND EVALUATION OF DOXORUBICIN CONTAINING NANOGELS FOR DELIVERY TO CANCER CELLS

2018 ◽  
Vol 8 (5) ◽  
pp. 178-183
Author(s):  
Manish Kumar ◽  
Hemant K. Sharma
Keyword(s):  
Average Particle Size ◽  
Gellan Gum ◽  
Cross Linking ◽  
Average Particle ◽  
Scanning Calorimetry ◽  
Green Method ◽  
X Ray ◽  
Oppositely Charged ◽  
Chemical Cross Linking

The objective of this study is to prepare nanogels were prepared via charged gellan gum. It was prepared by in situ cross linking reaction between two oppositely charged materials by green method without use of chemical cross linking agents. The prepared nanogels were characterized by Dynamic light scattering, scanning electron microscopy, differential scanning calorimetry and X- Ray diffractometry. The prepared formulation had average particle size of 226 nm with polydispersity index of 0.3. The doxorubicin loaded nanogel demonstrated sustained release for 20 h. The prepared nanogels were hemocompatible and cyctocompatible as revealed by hemocompatibility and MTT assay respectively. All results confirmed that these nanogels can be used for cancer treatment. Keywords: Nanogel, Chitosan, Gellan gum, Doxorubicin, Cancer.

Particle Size Distribution of ZrO2:Pr3+ – Influences of pH, High Power Ultrasound, Surfactant and Dopant Quantity

2007 ◽  
Vol 128 ◽  
pp. 97-100 ◽  
Author(s):  
Stephanie Möller ◽  
Janusz D. Fidelus ◽  
Witold Łojkowski
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
High Power ◽  
Average Particle Size ◽  
Sodium Dodecyl ◽  
Average Particle ◽  
Power Ultrasound ◽  
High Power Ultrasound ◽  
Influence Of Ph

The aim of the work was to examine the influence of pH, high power ultrasound, surfactant and dopant quantity on the particle size distribution of ZrO2:Pr3+, with praseodymium content varying between 0.05 and 10 %. The nanopowders were obtained via a hydrothermal microwave driven process. To establish if the dopant was located on the surface of the zirconia nanoparticles, the particle size distribution, as a function of pH, was measured to obtain an estimate of the isoelectric point of the samples. All results indicated that the dopant was concentrated on the surface: the measurements of the particle size distribution show that the pH corresponding to maximum average particle size changes towards higher values when the Pr content increases. Measurements of the particle size distribution dependency on the application of high power ultrasound and the addition of the sodium dodecyl sulphate surfactant show that, under certain conditions, there is a better stabilisation of the nanopowders in a dispersion and undesirable agglomeration is hindered.

scholarly journals Olive Leaves as Biotemplates for Enhanced Solar-Light Harvesting by a Titania-Based Solid

Nanomaterials ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 1057
Author(s):  
Jesús Hidalgo-Carrillo ◽  
Juan Martín-Gómez ◽  
M. Carmen Herrera-Beurnio ◽  
Rafael C. Estévez ◽  
Francisco J. Urbano ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Average Particle Size ◽  
Solar Irradiation ◽  
Bet Surface Area ◽  
Resonance Spectroscopy ◽  
Average Particle ◽  
Olive Leaves ◽  
Sem Images ◽  
X Ray

Olive leaves (by-product from olive oil production in olive mills) were used as biotemplates to synthesize a titania-based artificial olive leaf (AOL). Scanning electron microscopy (SEM) images of AOL showed the successful replication of trichomes and internal structure channels present in olive leaves. The BET surface area of AOL was 52 m2·g−1. X-ray diffraction (XRD) and Raman spectra revealed that the resulting solid was in the predominantly-anatase crystalline form (7.5 nm average particle size). Moreover, the synthesis led to a red-shift in light absorption as compared to reference anatase (gap energies of 2.98 and 3.2 eV, respectively). The presence of surface defects (as evidenced by X-ray photoelectron spectroscopy, XPS, and electron paramagnetic resonance spectroscopy, EPR) and doping elements (e.g., 1% nitrogen, observed by elemental analysis and XPS) could account for that. AOL was preliminarily tested as a catalyst for hydrogen production through glycerol photoreforming and exhibited an activity 64% higher than reference material Evonik P25 under solar irradiation and 144% greater under ultraviolet radiation (UV).

scholarly journals Preparation of ultrafine iron phosphate micro-powder from phosphate slag

2018 ◽  
Vol 238 ◽  
pp. 02002
Author(s):  
Fangjing Sun ◽  
Yi Zhang ◽  
Jiawei Zhang ◽  
Xixi Yan ◽  
Xiaoyu Liu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Electron Microscope ◽  
Average Particle Size ◽  
Iron Phosphate ◽  
Average Particle ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Phosphate Slag ◽  
Scanning Electron

In this experiment, ultrafine iron phosphate micro-powder was prepared by hydrothermal method which used phosphate slag as an iron source. The effects of reaction temperature, surfactants type and amount on its particle size were explored. The samples were characterized by using Malvern Laser Particle Size Analyzer (MS2000), X-Ray Diffractometer (XRD), Scanning Electron Microscope (SEM) and Energy Dispersive X-Ray Spectroscopy (EDX).The results showed that at 160 °C, 1 wt%CTAB, monoclinic iron phosphate micro-powder was obtained with an average particle size about 0.4 μm which also has a good dispersion in aqueous solution.

Morphology-Controlled CaCO3 Nanostructures by Modified Co-Precipitation in Pulsed Mode

2015 ◽  
Vol 752-753 ◽  
pp. 148-153
Author(s):  
M.M. Nassar ◽  
Taha Ebrahiem Farrag ◽  
M.S. Mahmoud ◽  
Sayed Abdelmonem
Keyword(s):  
Particle Size ◽  
Calcium Carbonate ◽  
Rotation Speed ◽  
Average Particle Size ◽  
Calcium Nitrate ◽  
Precipitation Method ◽  
Average Particle ◽  
X Ray ◽  
Co Precipitation ◽  
Pulsed Mixing

Calcium carbonate nanoparticles and nanorods were synthesized by precipitation from saturated sodium carbonate and calcium nitrate aqueous solutions through co precipitation method. A new rout of synthesis was done by both using pulsed mixing method and controlling the addition of calcium nitrate. The effect of the agitation speed, and the temperature on particle size and morphology were investigated. Particles were characterized using X-ray Microanalysis, X-ray analysis (XRD) and scanning electron microscopy (SEM). The results indicated that increasing the mixer rotation speed from 3425 to 15900 (rpm) decreases the average particle size to 64±7 nm. A rapid nucleation then aggregation induced by excessive shear force phenomena could explain this observation. Moreover, by increasing the reaction temperature, the products were converted from nanoparticle to nanorods. The maximum attainable aspect ratio was 6.23 at temperature of 75°C and rotation speed of 3425. Generally, temperature raise promoted a significant homoepitaxial growth in one direction toward the formation of calcite nanorods. Overall, this study can open new avenues to control the morphology of the calcium carbonate nanostructures.

Multiferroic Bismuth Ferrite Nanoparticles: Rapid Sintering Synthesis, Characterization, and Optical Properties

2010 ◽  
Vol 152-153 ◽  
pp. 81-85
Author(s):  
Xiong Wang ◽  
Yin Lin ◽  
Jin Guo Jiang
Keyword(s):  
Electron Microscopy ◽  
Phase Transition ◽  
Optical Properties ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray ◽  
Bifeo3 Nanoparticles ◽  
Rapid Sintering

The homogeneous multiferroic BiFeO3 nanoparticles with average particle size of 85 nm have been successfully synthesized by a simple sol-gel route. The prepared sample was characterized by a variety of techniques, such as X-ray diffractometry, thermogravimetric analysis and differential thermal analysis, differential scanning calorimeter analysis, scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. The obtained results shows that rapid sintering and subsequently quenching to room temperature are the two vital important factors for the preparation of pure BiFeO3. The magnetic phase transition (TN = 369 °C) and the ferroelectric phase transition (TC = 824.5 °C) were determined, revealing the antiferromagnetic and ferroelectric nature of the as-prepared BiFeO3 nanoparticles. The optical properties of the nanopowders were investigated. The strong band-gap absorption at 486 nm (2.55 eV) of the BiFeO3 nanoparticles may bring some novel applications.

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