scholarly journals One-Step Method for Preparation of Magnetic Nanoparticles Coated with Chitosan

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Karla M. Gregorio-Jauregui ◽  
Ma. Guadalupe Pineda ◽  
Jorge E. Rivera-Salinas ◽  
Gil Hurtado ◽  
Hened Saade ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Magnetic Measurements ◽  
Average Diameter ◽  
Superparamagnetic Nanoparticles ◽  
Step Method ◽  
Simple Method ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
One Step ◽  
Heavy Metal Ions Removal

Preparation of magnetic nanoparticles coated with chitosan in one step by the coprecipitation method in the presence of different chitosan concentrations is reported here. Obtaining of magnetic superparamagnetic nanoparticles was confirmed by X-ray diffraction and magnetic measurements. Scanning transmission electron microscopy allowed to identify spheroidal nanoparticles with around 10-11 nm in average diameter. Characterization of the products by Fourier transform infrared spectroscopy demonstrated that composite chitosan-magnetic nanoparticles were obtained. Chitosan content in obtained nanocomposites was estimated by thermogravimetric analysis. The nanocomposites were tested in Pb2+removal from a PbCl2aqueous solution, showing a removal efficacy up to 53.6%. This work provides a simple method for chitosan-coated nanoparticles obtaining, which could be useful for heavy metal ions removal from water.

scholarly journals Chitosan-Coated Magnetic Nanoparticles with Low Chitosan Content Prepared in One-Step

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Yolanda Osuna ◽  
Karla M. Gregorio-Jauregui ◽  
J. Gerardo Gaona-Lozano ◽  
Iliana M. de la Garza-Rodríguez ◽  
Anna Ilyna ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Weight Ratio ◽  
Average Diameter ◽  
High Yield ◽  
Infrared Spectrometry ◽  
Amino Groups ◽  
Step Method ◽  
Low Weight ◽  
One Step ◽  
Chitosan Content

Chitosan-coated magnetic nanoparticles (CMNP) were obtained at 50°C in a one-step method comprising coprecipitation in the presence of low chitosan content. CMNP showed high magnetization and superparamagnetism. They were composed of a core of 9.5 nm in average diameter and a very thin chitosan layer in accordance with electron microscopy measurements. The results from Fourier transform infrared spectrometry demonstrated that CMNP were obtained and those from thermogravimetric analysis allowed to determine that they were composed of 95 wt% of magnetic nanoparticles and 5 wt% of chitosan. 67% efficacy in the Pb+2removal test indicated that only 60% of amino groups on CMNP surface bound to Pb, probably due to some degree of nanoparticle flocculation during the redispersion. The very low weight ratio chitosan to magnetic nanoparticles obtained in this study, 0.053, and the high yield of the precipitation reactions (≈97%) are noticeable.

scholarly journals Hydrothermal Synthesis of Iridium-Substituted NaTaO3 Perovskites

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1537
Author(s):  
David L. Burnett ◽  
Christopher D. Vincent ◽  
Jasmine A. Clayton ◽  
Reza J. Kashtiban ◽  
Richard I. Walton
Keyword(s):  
Significant Proportion ◽  
Edge Length ◽  
Perovskite Oxide ◽  
Hydrogen Yield ◽  
Orthorhombic Space Group ◽  
X Ray ◽  
Profile Fitting ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
One Step

Iridium-containing NaTaO3 is produced using a one-step hydrothermal crystallisation from Ta2O5 and IrCl3 in an aqueous solution of 10 M NaOH in 40 vol% H2O2 heated at 240 °C. Although a nominal replacement of 50% of Ta by Ir was attempted, the amount of Ir included in the perovskite oxide was only up to 15 mol%. The materials are formed as crystalline powders comprising cube-shaped crystallites around 100 nm in edge length, as seen by scanning transmission electron microscopy. Energy dispersive X-ray mapping shows an even dispersion of Ir through the crystallites. Profile fitting of powder X-ray diffraction (XRD) shows expanded unit cell volumes (orthorhombic space group Pbnm) compared to the parent NaTaO3, while XANES spectroscopy at the Ir LIII-edge reveals that the highest Ir-content materials contain Ir4+. The inclusion of Ir4+ into the perovskite by replacement of Ta5+ implies the presence of charge-balancing defects and upon heat treatment the iridium is extruded from the perovskite at around 600 C in air, with the presence of metallic iridium seen by in situ powder XRD. The highest Ir-content material was loaded with Pt and examined for photocatalytic evolution of H2 from aqueous methanol. Compared to the parent NaTaO3, the Ir-substituted material shows a more than ten-fold enhancement of hydrogen yield with a significant proportion ascribed to visible light absorption.

Structural, Morphological, Magnetic and Self-Heating Studies of One-Step Polyol Synthesized Manganese Ferrite (MnFe2O4) Nanoparticles

2019 ◽  
Vol 19 (01) ◽  
pp. 1950003
Author(s):  
P. R. Ghutepatil ◽  
S. H. Pawar
Keyword(s):  
Room Temperature ◽  
Synthesis Method ◽  
Average Crystallite Size ◽  
Superparamagnetic Nanoparticles ◽  
Polyol Synthesis ◽  
X Ray Diffraction ◽  
Self Heating ◽  
Transmission Electron ◽  
One Step ◽  
Mnfe2o4 Nanoparticles

In this paper, uniform and superparamagnetic nanoparticles have been prepared using one-step polyol synthesis method. Structural, morphological and magnetic properties of obtained MnFe2O4 nanoparticles have been investigated by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA) techniques. Structural investigation showed that the average crystallite size of obtained nanoparticles was about 10[Formula: see text]nm. Magnetic study revealed that the nanoparticles were superparamagnetic at room temperature with magnetization 67[Formula: see text]emu/g at room temperature. The self-heating characteristics of synthesized MnFe2O4 nanoparticles were studied by applying external AC magnetic field of 167.6 to 335.2[Formula: see text]Oe at a fixed frequency of 265[Formula: see text]kHz. The SAR values of MnFe2O4 nanoparticles were calculated for 2, 5, 10[Formula: see text]mg[Formula: see text]mL[Formula: see text] concentrations and it is observed that the threshold hyperthermia temperature is achieved for all concentrations.

scholarly journals Characterization and Functionality of Immidazolium Ionic Liquids Modified Magnetic Nanoparticles

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Ying Li ◽  
Ning Tang ◽  
Fuyuhiko Inagaki ◽  
Chisato Mukai ◽  
Kazuichi Hayakawa
Keyword(s):  
Ionic Liquids ◽  
Magnetic Nanoparticles ◽  
Extraction Efficiency ◽  
Alkyl Chain ◽  
Organic Pollutant ◽  
High Adsorption ◽  
Transmission Electron ◽  
Polycyclic Aromatic ◽  
One Step ◽  
Modified Magnetic Nanoparticles

1,3-Dialkylimidazolium-based ionic liquids were chemically synthesized and bonded on the surface of magnetic nanoparticles (MNPs) with easy one-step reaction. The obtained six kinds of ionic liquid modified MNPs were characterized with transmission electron microscopy, thermogravimetric analysis, magnetization, and FTIR, which owned the high adsorption capacity due to the nanometer size and high-density modification with ionic liquids. Functionality of MNPs with ionic liquids greatly influenced the solubility of the MNPs with organic solvents depending on the alkyl chain length and the anions of the ionic liquids. Moreover, the obtained MNPs showed the specific extraction efficiency to organic pollutant, polycyclic aromatic hydrocarbons, while superparamagnetic property of the MNPs facilitated the convenient separation of MNPs from the bulks water samples.

Synthesis and Structural Characterization of Ferromagnetic Au/Co Nanoparticles

2014 ◽  
Vol 1708 ◽  
Author(s):  
Nabraj Bhattarai ◽  
Subarna Khanal ◽  
Daniel Bahena ◽  
Robert L. Whetten ◽  
Miguel Jose-Yacaman
Keyword(s):  
Quantum Interference ◽  
Magnetic Measurements ◽  
Ferromagnetic Behavior ◽  
Contrast Imaging ◽  
Uniform Size ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Co Nanoparticles ◽  
Z Contrast

ABSTRACTThe synthesis of bimetallic magnetic nanoparticles is very challenging because of the agglomeration and non-uniform size. In this paper, we present the synthesis of monodispersed 3-5 nm sized thiolated bimetallic alloyed Au/Co nanoparticles with decahedral and icosahedral shape, their characterization using Cs-corrected scanning transmission electron microscopy (STEM) and magnetic measurements using superconducting quantum interference device (SQUID) magnetometer. The Z-contrast imaging and energy dispersive X-ray spectroscopy (EDS) mapping showed an inhomogeneous alloying with minor segregation between Au and Co at nanoscale and the SQUID measurement exhibited the ferromagnetic behavior.

scholarly journals A novel nano zero-valent iron@chitosan for effective removal of Microcystin-LR: Kinetics and adsorption mechanism

2018 ◽  
Vol 53 ◽  
pp. 04004 ◽  
Author(s):  
Xiaofan Yang ◽  
Xueyu Wei ◽  
Xiaoping Xu ◽  
Zhigang Liu
Keyword(s):  
Low Cost ◽  
Spherical Shape ◽  
Step Method ◽  
Variable Parameters ◽  
Transmission Electron ◽  
Effective Removal ◽  
Initial Ph ◽  
Nano Zero Valent Iron ◽  
One Step ◽  
Kinetics Of

Microcystin-LR (MC-LR) is one of the most notorious toxins liberated from cyanobacteria in drinking water sources. In this study, a skillful method access to new nanozero-valent iron @chitosan (nZVIMC) was synthesized by a facile one step method. The as-prepared nZVIMC was employed as an adsorbent for the effective removal MC-LR from aqueous solution. Transmission electron microscopy (TEM) demonstrates that nZVIMC is in quasi-spherical shape with size of around 50 nm, effect of variable parameters such as pH, contact time, initial concentration of MC-LR and adsorption properties of nZVIMC on MC-LR was further investigated. Scanning electron microscope (SEM) reveals that the particles are nearly spherical in shape with agglomeration. The results indicated that good adsorption performance was achieved at an initial pH of 5. The adsorption kinetics of nZVIMC was better fitted by pseudo-secondorder kinetics. The adsorption isotherm data was fitted well to Langmuir isotherm and then to Freundlich model, with an adsorption capacity of 68.9 mg/g at 300K. Thus, we believe that nZVIMC can be used as a low cost material for efficient removal of MC-LR from water.

scholarly journals Efficient adsorption of Hg(II) from aqueous solution by N, S co-doped MnFe2O4@C magnetic nanoparticles

2020 ◽  
Vol 81 (6) ◽  
pp. 1273-1282 ◽  
Author(s):  
Hangdao Qin ◽  
Hao Cheng ◽  
Chenggui Long ◽  
Xiaogang Wu ◽  
Yanhong Chen ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Chemical Properties ◽  
Point Of Zero Charge ◽  
Simple Method ◽  
Transmission Electron ◽  
Pseudo Second Order ◽  
Enhanced Adsorption ◽  
Adsorption Desorption ◽  
Physical And Chemical ◽  
Co Doped

Abstract N, S co-doped MnFe2O4@C magnetic nanoparticles were successfully synthesized by a simple method involving the preparation of MnFe2O4 nanoparticles and subsequent pyrolysis treatment. The physical and chemical properties of MnFe2O4, MnFe2O4@C and MnFe2O4@C–NS nanoparticles were characterized by X-ray diffraction (XRD), vibrating sample magnetometry (VSM), transmission electron microscopy (TEM), N2 adsorption–desorption and the pH at the point of zero charge. Their performances in the adsorption of Hg(II) from water were investigated. The adsorption process followed pseudo-second-order kinetics and the experimental data of equilibrium isotherms fitted well with the Langmuir model. MnFe2O4@C–NS showed the highest adsorption capacity of 108.56 mg/g, increasing more than 1.7 times compared to MnFe2O4. The enhanced adsorption performance was attributed to the larger specific surface area as well as the complexation of N and S ligands on the surface. The thermodynamic parameters of ΔH°, ΔS° and ΔG° at 30 °C were −24.39 kJ/mol, −0.046 kJ/mol K and −10.45 kJ/mol, respectively, which indicated that the adsorption of Hg(II) on MnFe2O4@C–NS was exothermic and spontaneous in nature. Moreover, MnFe2O4@C–NS showed superior selectivity towards Hg(II) compared with other metal ions generally present in mercury-containing industrial wastewater.

scholarly journals A Study On Dispersion Stability Of Nickel Nanoparticles Synthesized By Wire Explosion In Liquid Media

2015 ◽  
Vol 60 (2) ◽  
pp. 1379-1382 ◽  
Author(s):  
C.K. Kim ◽  
G.-J. Lee ◽  
M.K. Lee ◽  
C.K. Rhee
Keyword(s):  
Nickel Nanoparticles ◽  
Spherical Shape ◽  
Physical Method ◽  
Average Diameter ◽  
Dispersion Stability ◽  
Wire Explosion ◽  
Transmission Electron ◽  
One Step ◽  
Polymer Surfactant ◽  
Microscopy Images

Abstract In this study, nickel nanoparticles were synthesized in ethanol using portable pulsed wire evaporation, which is a one-step physical method. From transmission electron microscopy images, it was found that the Ni nanoparticles exhibited a spherical shape with an average diameter of 7.3 nm. To prevent aggregation of the nickel nanoparticles, a polymer surfactant was added into the ethanol before the synthesis of nickel nanoparticles, and adsorbed on the freshly synthesized nickel nanoparticles during the wire explosion. The dispersion stability of the prepared nickel nanofluids was investigated by zeta-potential analyzer and Turbiscan optical analyzer. As a result, the optimum concentration of polymer surfactant to be added was suggested for the maximized dispersion stability of the nickel nanofluids.

scholarly journals Allylamine PECVD Modification of PDMS as Simple Method to Obtain Conductive Flexible Polypyrrole Thin Films

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2108
Author(s):  
Robert Texidó ◽  
Salvador Borrós
Keyword(s):  
Thin Films ◽  
Step Method ◽  
Great Stability ◽  
Simple Method ◽  
Pdms Surface ◽  
Polymeric Chains ◽  
Plasma Grafting ◽  
One Step ◽  
Different Shapes ◽  
Amine Groups

In this paper, we report a one-step method to obtain conductive polypyrrole thin films on flexible substrates. To do this, substrates were modified through allylamine plasma grafting to create a high amount of reactive amine groups on PDMS surface. These groups are used during polypyrrole particle synthesis as anchoring points to immobilize the polymeric chains on the substrate during polymerization. Surface morphology of polypyrrole thin films are modified, tailoring the polyelectrolyte used in the polypyrrole synthesis obtaining different shapes of nanoparticles that conform to the film. Depending on the polyelectrolyte molecular weight, the shape of polypyrrole particles go from globular (500 nm diameter) to a more constructed and elongated shape. The films obtained with this methodology reflected great stability under simple bending as well as good conductivity values (between 2.2 ± 0.7 S/m to 5.6 ± 0.2 S/cm).

scholarly journals One-Step Synthesis of Copper and Cupric Oxide Particles from the Liquid Phase by X-Ray Radiolysis Using Synchrotron Radiation

2016 ◽  
Vol 2016 ◽  
pp. 1-16 ◽  
Author(s):  
Akinobu Yamaguchi ◽  
Ikuo Okada ◽  
Takao Fukuoka ◽  
Mari Ishihara ◽  
Ikuya Sakurai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synchrotron Radiation ◽  
Cupric Oxide ◽  
Oxide Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
One Step ◽  
Oxide Particles

The deposition of copper (Cu) and cupric oxide (Cu4O3, Cu2O, and CuO) particles in an aqueous copper sulfate (CuSO4) solution with additive alcohol such as methanol, ethanol, 2-propanol, and ethylene glycol has been studied by X-ray exposure from synchrotron radiation. An attenuated X-ray radiation time of 5 min allows for the synthesis of Cu, Cu4O3, Cu2O, and CuO nano/microscale particles and their aggregation into clusters. The morphology and composition of the synthesized Cu/cupric oxide particle clusters were characterized by scanning electron microscopy, scanning transmission electron microscopy, and high-resolution transmission electron microscopy with energy dispersive X-ray spectroscopy. Micro-Raman spectroscopy revealed that the clusters comprised cupric oxide core particles covered with Cu particles. Neither Cu/cupric oxide particles nor their clusters were formed without any alcohol additives. The effect of alcohol additives is attributed to the following sequential steps: photochemical reaction due to X-ray irradiation induces nucleation of the particles accompanying redox reaction and forms a cluster or aggregates by LaMer process and DLVO interactions. The procedure offers a novel route to synthesize the Cu/cupric oxide particles and aggregates. It also provides a novel additive manufacturing process or lithography of composite materials such as metal, oxide, and resin.

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