scholarly journals Biodesulfurization of Dibenzothiophene by Microbial Cells Coated with Magnetite Nanoparticles

2005 ◽  
Vol 71 (8) ◽  
pp. 4497-4502 ◽  
Author(s):  
GuoBin Shan ◽  
JianMin Xing ◽  
HuaiYing Zhang ◽  
HuiZhou Liu

ABSTRACT Microbial cells of Pseudomonas delafieldii were coated with magnetic Fe3O4 nanoparticles and then immobilized by external application of a magnetic field. Magnetic Fe3O4 nanoparticles were synthesized by a coprecipitation method followed by modification with ammonium oleate. The surface-modified Fe3O4 nanoparticles were monodispersed in an aqueous solution and did not precipitate in over 18 months. Using transmission electron microscopy (TEM), the average size of the magnetic particles was found to be in the range from 10 to 15 nm. TEM cross section analysis of the cells showed further that the Fe3O4 nanoparticles were for the most part strongly absorbed by the surfaces of the cells and coated the cells. The coated cells had distinct superparamagnetic properties. The magnetization (δs) was 8.39 emu · g−1. The coated cells not only had the same desulfurizing activity as free cells but could also be reused more than five times. Compared to cells immobilized on Celite, the cells coated with Fe3O4 nanoparticles had greater desulfurizing activity and operational stability.

2015 ◽  
Vol 233-234 ◽  
pp. 513-516 ◽  
Author(s):  
A.P. Safronov ◽  
Galina V. Kurlyandskaya ◽  
S.M. Bhagat ◽  
I.V. Beketov ◽  
A.M. Murzakaev ◽  
...  

Spherical nickel nanoparticles were prepared by the electrical explosion of wire. The as-prepared nanoparticles were modified immediately after fabrication at room temperature in order to provide tunable surface properties with focus on the development of composites filled with nanoparticles. Following liquid modificators were used: hexane, toluene and the solution of polystyrene in toluene. In one case the surface modification by carbon was made in gas phase as a result of hydrocarbon injection. The average size of the nanoparticles was about 50 nm and unit cell parameters were close to 0.351 nm. Detailed characterization was done by X-ray diffraction, transmission electron microscopy, and magnetization measurements. Sphericity was also checked using microwave resonant absorption.


Author(s):  
R. A. Dvorikov ◽  
V. A. Vasnev ◽  
А. А. Korlukov ◽  
М. I. Buzin

New magnetic nanomaterials with magnetization up to 32 Gs·cm3/g were synthesized from highly branched ferrocene-containing polymers by thermal structural transformations in a field of 2.5 kOe. The structure and properties of the prepared polymers were studied by IR spectroscopy, transmission electron microscopy (TEM) and thermogravimetric analyses. According to IR spectroscopy the content of 1,3,5-substituted benzene rings in the ferrocene-containing polymer increases at 500°C. X-ray diffraction study showed that iron in such a sample is present exclusively in the form of Fe3O4 magnetite. As the heating temperature increased to 600°C, the composition of the samples became more complex: along with magnetite they contain cementite Fe3C and wustite FeO.97O. The magnetization of the ferrocene-containing polymer depends on the synthesis and heat treatment temperature. For a sample synthesized at 140°C the formation of a magnetically ordered phase begins at 500°C, and at 800°C the magnetization reaches a maximum value of 32 Gs·cm3/g. The average size of magnetic particles according to TEM analysis was 8-26 nm. The principal possibility of controlling the size and composition of the nanoparticles, as well as their magnetization depending on the conditions of production and the temperature of polymer structuring is shown. The obtained results provide a good basis for the directed synthesis of magnetic ferrocene-containing polymers with preset characteristics.


2020 ◽  
Vol 71 (2) ◽  
pp. 10-14
Author(s):  
Elena Vasilica Trandafir ◽  
Radu Ciocarlan ◽  
Aurel Pui ◽  
Rolf Hempelmann ◽  
Ovidiu Florin Caltun

A series of Zn ferrite nanoparticles was prepared by varying the concentration of precipitating agent (NaOH) in the range of 1 � 5 M. Carboxymethylcellulose (CMC) was used as capping agent for stabilizing the particles and to prevent agglomeration. The synthesis done at low temperature was followed by a thermal treatment at 500ºC for 6 h in air. The crystallite size determined using Scherer formula ranged between 8 - 10 nm while the nanoparticles average size observed by Transmission Electron Microscopy varied in between 7-10 nm showing that the increase of coprecipitation agent concentration influences the particles growth. Vibrating sample magnetometry confirmed the strong influence that nanoparticles morphology and size play on superparamagnetic properties of Zn ferrite.


2017 ◽  
Vol 7 (3) ◽  
Author(s):  
Mahnaz Mahdavi Shahri

Magnetic nanoparticles (MNPs) are very important systems with potential use in drug delivery systems, ferrofluids, and effluent treatment. In many situations, such as in biomedical applications, it is necessary to cover inorganic magnetic particles with an organic material, such as polymers. A superparamagnetic nanocomposite Fe3O4/poly(maleic anhydride-co-acrylic acid) P(MAH-co-AA) with a core/shell structure was successfully synthesized by a dispersion polymerization route. Iron oxide nanoparticles were used as a core, and P(MAH-co-AA) as a shell was covered on the surface of the Fe3O4 magnetic nanoparticles. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that the Fe3O4/P(MAH-co-AA) magnetic nanocomposite were highly uniform in size and cubic shape with the average size about 17.06 nm. X-ray diffraction confirmed magnetite cores and also indicated that the binding process did not change the phase of Fe3O4. Vibrational sample magnetometer (VSM) revealed the nanoparticles were superparamagnetic and the saturation magnetization was 83.6 and 46.6 emu g-1 for pure Fe3O4 and composite nanoparticles, respectively. Measurements by VSM also showed that the degree of saturation magnetization increased with increasing iron oxide concentration from 1% to 7 wt % of Fe3O4.


Author(s):  
Brian L. Rhoades

A gas reaction chamber has been designed and constructed for the JEM 7A transmission electron microscope which is based on a notably successful design by Hashimoto et. al. but which provides specimen tilting facilities of ± 15° aboutany axis in the plane of the specimen.It has been difficult to provide tilting facilities on environmental chambers for 100 kV microscopes owing to the fundamental lack of available space within the objective lens and the scope of structural investigations possible during dynamic experiments has been limited with previous specimen chambers not possessing this facility.A cross sectional diagram of the specimen chamber is shown in figure 1. The specimen is placed on a platinum ribbon which is mounted on a mica ring of the type shown in figure 2. The ribbon is heated by direct current, and a thermocouple junction spot welded to the section of the ribbon of reduced cross section enables temperature measurement at the point where localised heating occurs.


Author(s):  
D. L. Callahan ◽  
Z. Ball ◽  
H. M. Phillips ◽  
R. Sauerbrey

Ultraviolet laser-irradiation can be used to induce an insulator-to-conductor phase transition on the surface of Kapton polyimide. Such structures have potential applications as resistors or conductors for VLSI applications as well as general utility electrodes. Although the percolative nature of the phase transformation has been well-established, there has been little definitive work on the mechanism or extent of transformation. In particular, there has been considerable debate about whether or not the transition is primarily photothermal in nature, as we propose, or photochemical. In this study, cross-sectional optical microscopy and transmission electron microscopy are utilized to characterize the nature of microstructural changes associated with the laser-induced pyrolysis of polyimide.Laser-modified polyimide samples initially 12 μm thick were prepared in cross-section by standard ultramicrotomy. Resulting contraction in parallel to the film surface has led to distortions in apparent magnification. The scale bars shown are calibrated for the direction normal to the film surface only.


Author(s):  
L. D. Peachey ◽  
J. P. Heath ◽  
G. Lamprecht

Biological specimens of cells and tissues generally are considerably thicker than ideal for high resolution transmission electron microscopy. Actual image resolution achieved is limited by chromatic aberration in the image forming electron lenses combined with significant energy loss in the electron beam due to inelastic scattering in the specimen. Increased accelerating voltages (HVEM, IVEM) have been used to reduce the adverse effects of chromatic aberration by decreasing the electron scattering cross-section of the elements in the specimen and by increasing the incident electron energy.


Author(s):  
N.-H. Cho ◽  
S. McKernan ◽  
C.B. Carter ◽  
K. Wagner

Interest has recently increased in the possibility of growing III-V compounds epitactically on non-polar substrates to produce device quality material. Antiphase boundaries (APBs) may then develop in the GaAs epilayer because it has sphalerite structure (face-centered cubic with a two-atom basis). This planar defect may then influence the electrical behavior of the GaAs epilayer. The orientation of APBs and their propagation into GaAs epilayers have been investigated experimentally using both flat-on and cross-section transmission electron microscope techniques. APBs parallel to (110) plane have been viewed at the atomic resolution and compared to simulated images.Antiphase boundaries were observed in GaAs epilayers grown on (001) Ge substrates. In the image shown in Fig.1, which was obtained from a flat-on sample, the (110) APB planes can be seen end-on; the faceted APB is visible because of the stacking fault-like fringes arising from a lattice translation at this interface.


Author(s):  
H. J. Bender ◽  
R. A. Donaton

Abstract The characteristics of an organic low-k dielectric during investigation by focused ion beam (FIB) are discussed for the different FIB application modes: cross-section imaging, specimen preparation for transmission electron microscopy, and via milling for device modification. It is shown that the material is more stable under the ion beam than under the electron beam in the scanning electron microscope (SEM) or in the transmission electron microscope (TEM). The milling of the material by H2O vapor assistance is strongly enhanced. Also by applying XeF2 etching an enhanced milling rate can be obtained so that both the polymer layer and the intermediate oxides can be etched in a single step.


Author(s):  
J. Douglass ◽  
T. D. Myers ◽  
F. Tsai ◽  
R. Ketcheson ◽  
J. Errett

Abstract This paper describes how the authors used a combination of focused ion beam (FIB) microprobing, transmission electron microscopy (TEM), and data and process analysis to determine that localized water residue was causing a 6% yield loss at die sort.


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