scholarly journals Preparation of Soft Magnetic Fe-Ni-Pb-B Alloy Nanoparticles by Room Temperature Solid-Solid Reaction

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Guo-Qing Zhong ◽  
Qin Zhong

The Fe-Ni-Pb-B alloy nanoparticles was prepared by a solid-solid chemical reaction of ferric trichloride, nickel chloride, lead acetate, and potassium borohydride powders at room temperature. The research results of the ICP and thermal analysis indicate that the resultants are composed of iron, nickel, lead, boron, and PVP, and the component of the alloy is connected with the mole ratio of potassium borohydride and the metal salts. The TEM images show that the resultants are ultrafine and spherical particles, and the particle size is about a diameter of 25 nm. The largest saturation magnetization value of the 21.18 emu g−1is obtained in the Fe-Ni-Pb-B alloy. The mechanism of the preparation reaction for the Fe-Ni-Pb-B multicomponent alloys is discussed.

Sensors ◽  
2018 ◽  
Vol 18 (10) ◽  
pp. 3283 ◽  
Author(s):  
Masanobu Matsuguchi ◽  
Shinnosuke Fujii

Poly(N-isopropylacrylamide) (PNIPAM) nanoparticles formed in water-methanol binary solvent were successfully deposited on a resonator surface at room temperature by exploiting the cononsolvency effect on the phase transition of PNIPAM aqueous solutions. Scanning electron microscopic observation revealed that the nanoparticles were secondary and made up of agglomerated primary spherical particles of about 10-nm diameter, buried in the film. The magnitude of the sensor response toward HCl gas was larger than that of the nanoparticle sensor prepared from pure water solvent, and the sensitivity to 1 ppm of HCl of sensor-coated nanoparticles based on the present method was 3.3 Hz/ppm. The recovery of the sensors was less than 90% at first cycle measurement, but had improved to almost 100% at the third cycle.


2003 ◽  
Vol 775 ◽  
Author(s):  
Jeffrey Anderson ◽  
Rubi Garcia ◽  
Weilie L. Zhou

AbstractSubmicron KMnF3 cubic and spherical nanoparticles were synthesized using the reverse micelle method. The nanostructures of the nanocrystals were studied by field emission electron microscopy and transmission electron microscopy. KMnF3 nanocrystals synthesized at room temperature started with cubic submicron particles (∼100 nm) and consisted of KMnF3 nanocrystallites (10-15 nm). As the reaction continued, the nanocrystals fused together and transformed into perfect cubic nanocrystals. Spherical beads composed of KMnF3 nanocrystallites were observed at low temperature synthesis. As the reaction continued, the spherical particles grew larger, however, no characteristic cubic shape of KMnF3 nanoparticles were observed. Even as they grew larger, there was no evidence of homogeneous crystal morphology as seen in the room temperature samples. Cubic shape KMnF3 nanocrystals were self-assembled into large area self-assembling patterns.


2020 ◽  
Vol 11 (1) ◽  
pp. 107-112
Author(s):  
A Said Sikder ◽  
SD Nath ◽  
SS Sikder

Amorphous soft magnetic materials have significant potential applications in specialist power transformers and in inductive devices. With the composition of Fe82Si8B10, 82% of the transition metals Fe and about 18% of metalloid or glass-former elements like B and Si are strongly magnetic at room temperature and offer dynamic opportunities for engineering applications. The crystallization kinetics has been studied by differential thermal analysis (DTA). The sample was annealed in a controlled way in the temperature range of 350-450°C at constant annealing time one hour. The kinetics of primary crystallization α-Fe(Si) phase and secondary crystallization Fe2B phase was studied as affected due to temperature. The sample annealed at 350oC temperature is almost unchanged which is still lower than that of primary crystallization temperature but the same condition when sample annealed at 450°C completely shows that the primary crystallization α-Fe(Si) phase has vanished and crystallization event took place to a good extent. Journal of Engineering Science 11(1), 2020, 107-112


2006 ◽  
Vol 11-12 ◽  
pp. 595-598
Author(s):  
Dong Liang Peng ◽  
K. Sumiyama ◽  
H. Yamada ◽  
Takehiko Hihara ◽  
T. Uchida

Highly-densified Fe cluster-assembled films were obtained at room temperature by an energetic cluster deposition. Fe clusters were produced using a plasma-gas-condensation (PGC)-type cluster deposition apparatus with a high cluster productivity. Ionized clusters in a cluster beam were electrically accelerated and directly deposited onto a substrate together with neutral clusters from the same cluster source. By increasing the impact energy of the ionized clusters up to about 1 eV/atom, the obtained cluster-assemblies have packing fractions higher than 0.8 without any serious size change, and result in a soft magnetic behavior up to a frequency range of few hundred MHz.


2006 ◽  
Vol 510-511 ◽  
pp. 286-289
Author(s):  
Hao Wang ◽  
Wei Min Wang ◽  
Zheng Yi Fu ◽  
Tohru Sekino ◽  
Koichi Niihara

Mullite-based nanocomposites with embedded FeCr alloy nanoparticles were synthesized by reduction of sol-gel prepared Al5.4(Fe0.8Cr0.2)0.6Si2O13 solid solution in hydrogen. The feature of the formation of FeCr alloy is characterized by XRD analysis. Structural characterization revealed that the intragranular FeCr alloy nanoparticles along with inter-granular iron grains were obtained in as reduced sample. After acid washing, the intergranular metal grains were eliminated. The static magnetic properties of nanocomposite powders were studied using Magnetic Property Measurement System. It is found that part of the intra-granular metal nanoparticles have superparamagnetic behavior at room temperature.


1958 ◽  
Vol 13 (1) ◽  
pp. 19-27 ◽  
Author(s):  
Karl-Wolfgang Mundry

Crude leaf sap of plants suffering from sugar beet yellows was partially purified by density gradient centrifugation in the cold at different values of pʜ (6,2-9,0). After standing over night at 2° C the material was dialysed against buffer of pʜ 6,8 at room temperature. - As estimated by electron microscopy the most frequent length of the threadlike particles (Fig. 2) which were believed to be the infectious agent of sugar beet yellows shows a gradual shift from longer to shorter ones with rising pʜ (Fig. 1 a-e). The infectivity of the suspensions depends upon the pʜ of the preparation too. From the distribution curve of the particle lengths the relative concentrations of particles with different given minimal lengths were estimated. The dependence from the pʜ of the preparation of these relative concentrations was compared with that of the infectivity. Best agreement was observed with particles of 12 700 - 12 800 A minimal length (Fig. 3). This length seems to be identical with the “normal length” of the particles found in exsudates (12 400 -12 500 A). From these results it was concluded that a) particles which possess the normal length as found in exsudates are the infective entities of this disease, b) shorter particles are non-infectious, c) the infectious entities of the sugar beet yellows virus are of the threadlike type. There is no evidence that spherical particles are necessary for starting an infection with the sugar beet yellows virus.


2015 ◽  
Vol 228 ◽  
pp. 269-272 ◽  
Author(s):  
Magdalena Popczyk ◽  
B. Łosiewicz

The Ni-Mo alloy coatings with a high content of Mo up to 44.5 at.%, were prepared by galvanostatic electrodeposition in the range of deposition current density, jdep, from-30 to-240 mA cm-2 from the nickel plating bath containing potassium pyrophosphate, nickel chloride, sodium molybdate, and sodium bicarbonate. Investigations of hydrogen evolution reaction (HER) were carried out in 5 M KOH solution at room temperature using steady-state polarization and electrochemical impedancy spectroscopy (EIS) measurements. It was found that for the Ni-Mo alloy coatings, the increase in their catalytic properties towards the HER with the increase in the value of jdep of the coatings, was due to the intrinsic activity.


1996 ◽  
Vol 49 (1) ◽  
pp. 87 ◽  
Author(s):  
AF Waters ◽  
AH White

In the course of synthesizing oligodentate aliphatic nitrogen base adducts of Group 2 metal salts, a number of mixed- ligand species have been isolated with oxygen ligands , and characterized by room-temperature single-crystal X-ray studies. BaCl2.4en.H2O ≡[(en)4Ba(OH2)] Cl2 (1) is monoclinic, P 21/c, a 9.456(4), b 14.953(6), c 14.82(1) Ǻ, β 100.78(6)°, Z = 4 f.u ., R 0.043 for No 1862 independent 'observed' (I > 3σ(I)) diffractometer reflections. Ba -N range between 2.900(9) and 2.97(1) Ǻ, and Ba-O is 2.779(8) Ǻ in the nine-coordinate BaN8O environment. CaCl2.2dien.H2O ≡ [( dien )2Ca(OH2) Cl ] Cl (2) is monoclinic, P 21/c, a 10.808(4), b 11.999(4), c 15.71(1) Ǻ, β 123.58(4)°, Z = 4 f.u ., R 0.050 for No 3134; CaBr2.2dien.2H2O ≡ [( dien )2Ca(OH2)2] Br2 (3) is monoclinic, P 21/c, a 18.001(3), b 11.983(6), c 21.562(5) Ǻ, β 124.97(2)°, Z = 8 f.u ., R 0.045 for No 2858; CaBr2.2dien.2MeOH ≡ [( dien )2Ca( HOMe )2] Br2 (4) is orthorhombic, P212121, a 16.620(8), b 12.78(1), c 9.765(4) Ǻ, Z = 4 f.u ., R 0.073 for No 878. In (2)-(4), the cation configurations are similar, being of the form [L2Ca( dien )2], L (L') being the unidentate ligand, with the eight-coordinate calcium environments [L2Ca(N3)2] in a common isomeric configuration, the two ligands L being cis in an array of quasi-2 symmetry. Ca- Cl in (2) is 2.834(1) Ǻ; Ca-N generally range between 2.52(5) and 2.64(1) Ǻ; Ca-O(H2O) is 2.418(2) in (2), 2.434(7)-2.496(7) Ǻ in (3), while Ca-O( MeOH ) in (4) are 2.43(2) and 2.43(2) Ǻ. [Mg(HOMe)6] I2.2tmeda (5) ( tmeda = Me2N(CH2)2NMe2), orthorhombic, Pbca, a 23.423(8), b 15.306(4), c 9.345(1) Ǻ, Z = 4 f.u ., R 0.052 for No 1928, provides a usefully precise description for the centrosymmetric cation, Mg-O being 2.069(4), 2.080(4), 2.096(5) Ǻ, with Mg-O-C 128.4(4) l28.9(4), l29.7(4)°. [( tmeda )SrI2 ( HOMe )3].½tmeda (6), monoclinic, P 21/c, a 7.730(1), b 35.493(9), c 11.081(2) Ǻ, β 126.49(1)°, R 0.042 for No 3161, has a seven-coordinate, quasi-pentagonal bipyramidal SrN2I2O3 array about the metal with trans-iodines.


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