INTENTIONAL SYNTHESIS OF BINARY RADICAL THAT BEARING NITRONYL AND IMINO NITROXIDES: X-RAY ANALYSIS AND MAGNETIC MEASUREMENT

Heterocycles ◽  
2013 ◽  
Vol 87 (10) ◽  
pp. 2031
Author(s):  
Fumiyasu Iwahori ◽  
Takayuki Suzuki ◽  
Kosuke Kato
Keyword(s):  
2018 ◽  
Vol 25 (3) ◽  
pp. 686-705 ◽  
Author(s):  
M. Calvi ◽  
C. Camenzuli ◽  
R. Ganter ◽  
N. Sammut ◽  
Th. Schmidt

Within the SwissFEL project at the Paul Scherrer Institute (PSI), the hard X-ray line (Aramis) has been equipped with short-period in-vacuum undulators, known as the U15 series. The undulator design has been developed within the institute itself, while the prototyping and the series production have been implemented through a close collaboration with a Swiss industrial partner, Max Daetwyler AG, and several subcontractors. The magnetic measurement system has been built at PSI, together with all the data analysis tools. The Hall probe has been designed for PSI by the Swiss company SENIS. In this paper the general concepts of both the mechanical and the magnetic properties of the U15 series of undulators are presented. A description of the magnetic measurement equipment is given and the results of the magnetic measurement campaign are reported. Lastly, the data reduction methods and the associated models are presented and their actual implementation in the control system is detailed.


2010 ◽  
Vol 177 ◽  
pp. 673-676 ◽  
Author(s):  
Jun Xue ◽  
Hou Kui Xiang ◽  
Hong Qiao Ding ◽  
Shu Li Pang ◽  
Xue Hua Wang ◽  
...  

Carbon encapsulated Fe-Cu alloys nanoparticles were synthesized by using ferric nitrate, copper nitrate as metal sources and using sucrose as carbon source. The synthesis process involved a step of hydrazine hydrate reduction in alcohol solution and a step of annealing carbonization. The as-prepared samples were characterized by X-ray diffraction technique, X-ray energy dispersion spectrograph, trans- mission electron microscopy and Raman spectroscopy. The results showed the sample was core / shell structure, the metalic core was crystalline FeCu4 alloy, the shell was amorphous carbon, and the average particle size was about 51nm. The magnetic measurement by using a vibrating sample magnetometer revealed that the sample has ultra-soft magnetic property with the saturation magnetization Ms of 13.01 emu/g, residual magnetization Mr of 0.37 emu/g and coercive forces Hc of 54.43 Oe at room temperature.


2019 ◽  
Vol 966 ◽  
pp. 363-369
Author(s):  
Utami Widyaiswari ◽  
Budhy Kurniawan ◽  
Agung Imaduddin ◽  
Isao Watanabe

Mixed valence manganite materials have been studied due to their interesting physical properties such as their magnetoresistance (MR) effect. The change of Mn3+/Mn4+ ratio affects the possible bonds between anion and cation and their spin structure that may occur in the samples. The aim of this research is to study the change of magnetoresistance effect and magnetic properties of La0.67Sr0.33MnO3 (LSMO) by doping the Mn site with Ni ion. La0.67Sr0.33Mn1-xNixO3 samples were synthesized by using sol-gel method and characterized by using X-ray diffractometer (XRD) and Energy Dispersive X-ray spectroscopy (EDX) to confirm whether Ni has been doped successfully to the parental compound or not. XRD results showed that the samples have a single phase and Ni peak has been detected in the EDX result of Ni-doped LSMO. Resistivity and magnetic measurement showed that LSMO material has ferromagnetic metallic behavior, while x = 0.20 Ni-doped LSMO sample showed paramagnetic insulator behavior. The absolute value of the MR for un-doped sample is higher than the doped sample when the low field is applied, while under the influence of the high magnetic field, it become smaller than the doped sample.


2015 ◽  
Vol 33 (1) ◽  
pp. 100-106 ◽  
Author(s):  
Atieh Aliakbari ◽  
Majid Seifi ◽  
Sharareh Mirzaee ◽  
Hoda Hekmatara

AbstractIn the present paper, iron oxide nanoparticles coated by oleic acid have been synthesized in different conditions by coprecipitation method. For investigating the effect of time spent on adding the oleic acid to the precursor solution, two different processes have been considered. The as synthesized samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FT-IR). Magnetic measurement was carried out at room temperature using a vibrating sample magnetometer (VSM). The results show that the magnetic nanoparticles decorated with oleic acid decreased the saturation of magnetization. From the data, it can also be concluded that the magnetization of Fe3O4/oleic acid nanoparticles depends on synthesis conditions.


2001 ◽  
Vol 66 (10) ◽  
pp. 1490-1498 ◽  
Author(s):  
Zdeněk Smékal ◽  
Jiří Kameníček ◽  
Ingrid Svoboda ◽  
Albert Escuer

The novel complex [μ-(NC)-Fe(CN)3(NO)-μ-(CN)-Cu(ept)]n·4nH2O (ept = N-(2-aminoethyl)- propane-1,3-diamine) was obtained by the reaction of Cu(ClO4)2·6H2O with N-(2-amino- ethyl)propane-1,3-diamine and Na2[Fe(CN)5NO]·2H2O in water. This compound was characterized by IR, UV-VIS and EPR spectroscopies and magnetic measurement. Single-crystal X-ray structure analysis revealed that the title complex has a one-dimensional polymeric structure containing hexacoordinate iron(II) with five cyanide ligands (two of them, in trans position, bridging) and one nitrosyl group, and pentacoordinate copper(II) with N-(2-aminoethyl)propane-1,3-diamine and two sites occupied by bridging cyanide ligands. Magnetic investigation revealed a very weak antiferromagnetic interaction between the copper atoms (superexchange interaction parameter J = -1.7(1) cm-1; H = -JSiSi+1) within the chain through the diamagnetic [Fe(CN)5NO]2- ions.


1996 ◽  
Vol 11 (11) ◽  
pp. 2717-2724 ◽  
Author(s):  
J. Y. Huang ◽  
Y. D. Yu ◽  
Y. K. Wu ◽  
H. Q. Ye ◽  
Z. F. Dong

A ferromagnetic and supersaturated fcc Fe60Cu40 solid solution was prepared by mechanical alloying (MA). The phase transformations of the as-milled Fe60Cu40 powder upon heating to 1400 °C and subsequently cooling to room temperature were characterized by differential thermal analysis (DTA) and thermal magnetic measurement. The fcc Fe60Cu40 solid solution decomposes into α–Fe(Cu) + γ–Fe(Cu) + Cu(Fe) upon heating from 300 to 460 °C, and on further heating, α–Fe(Cu) transforms to γ–Fe(Cu) at 640 → 760 °C; during cooling, the reverse transformation occurs from 800 → 640 °C (obtained from thermomagnetic measurement) or from 700 → 622 °C (obtained from DTA). The γ ⇆ α transformation in mechanically alloyed Fe60Cu40 nanocrystalline occurs in a wide temperature range; the transformation temperature is higher than that of the martensite transformation in as-cast Fe–Cu alloys, but is much lower than that of the allotropic transformation of pure Fe. These differences may be caused by the different fabrication process, the nonequilibrium microstructure of MA, as well as the inhomogeneous grain size in α–Fe(Cu). High resolution transmission electron microscope (HRTEM) observations carried out in the specimen after the DTA run show that N-W or K-S orientation relationships exist between α–Fe(Cu) and Cu(Fe), which also represent the orientation relationship between α–Fe(Cu) and γ–Fe(Cu) due to excellent coherency between γ–Fe(Cu) and Cu(Fe). The grain size of the α–Fe(Cu) is inhomogeneous and varies from 50–600 mm. Energy dispersive x-ray spectroscopy (EDXS) result shows that the Cu content in these α–Fe(Cu) grains reaches as high as 9.5 at. % even after DTA heating to 1400 °C, which is even higher than the maximum solubility of Cu in γ–Fe above 1094 °C. This may be caused by the small grain size of α–Fe(Cu).


2016 ◽  
Vol 852 ◽  
pp. 346-348
Author(s):  
Hong Cai ◽  
Qing Bo Du ◽  
Ji Gui Xu ◽  
Hong Wei Shi ◽  
Jun Zhu

a-Fe2O3 nanorods over large areas were successfully synthesized by hydrothermal method, using FeCl3 as iron source and PVP as surfactant. The as-synthesized a-Fe2O3 nanorods were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and magnetic measurement system (SQUID-VSM) . The results show that the nanorods prepared by hydrothermal method with the diameter of about 70 nm and the length of about 300 nm. The magnetic properties of the synthesized nanorods were studied, and the remnant magnetization and coercivity of the α-Fe2O3 nanorods at 300K are found to be 0.07emu/g and 2300Oe, respectively. The a-Fe2O3 nanorods reported here may have opportunities for both fundamental research and technological applications.


2009 ◽  
Vol 155 ◽  
pp. 155-162 ◽  
Author(s):  
Kinnari Parekh ◽  
R.V. Upadhyay ◽  
V.K. Aswal

Magnetite and Co ferrite particles were synthesized with control of particle size distribution via non-aqueous route. The XRD pattern shows the formation of single phase spinel structure with the particle size of 96 Å and 80 Å respectively for magnetite and cobalt ferrite. TEM image of the same shows the particles are nearly spherical with the size matches with that obtained from X-ray and the size distribution is less than 5%. Magnetic measurement also shows the particles of uniform size with high value of saturation magnetization at room temperature compared to that obtained by other route. SANS study confirms our results of monodispersed particles with spherical shape.


2005 ◽  
Vol 19 (15n17) ◽  
pp. 2550-2555
Author(s):  
MINGZAI WU ◽  
YING XIONG ◽  
NAN JIANG ◽  
HAI PING QI ◽  
QIANWANG CHEN

Anatase Ti 1-x Co x O 2 nanoparticles were prepared by a hydrothermal process at 180 °C. Ferromagnetic hysteresis loops of the as-prepared samples were measured at room temperature. The Ti 1-x Co x O 2 ( x = 0.0376) powder shows coercivity up to 700 Oe, which is the highest value reported for anatase Ti 1-x Co x O 2. X-ray diffraction (XRD), transmission electron microscopy (TEM) and magnetic measurement results provided evidence that Co was incorporated into TiO 2 lattice. Combined with the fact that the preparation was carried out in an oxidized environment starting from cobalt (II) in the oxidized state, it is suggested that the homogeneous doping of Co into the lattice of anatase should be responsible for the improvement of coercivity in anatase Ti 1-x Co x O 2 nanoparticles.


2019 ◽  
Vol 26 (4) ◽  
pp. 1037-1044 ◽  
Author(s):  
Wolfgang Freund ◽  
Lars Fröhlich ◽  
Suren Karabekyan ◽  
Andreas Koch ◽  
Jia Liu ◽  
...  

Hard X-ray free-electron lasers (XFELs) generate intense coherent X-ray beams by passing electrons through undulators, i.e. very long periodic magnet structures, which extend over hundreds of meters. The SASE1 and SASE2 undulator systems of the European XFEL consist of 35 segments with variable-gap planar undulators which are initially tuned to precise on-axis magnetic field strengths in a magnetic measurement laboratory to keep an important quality parameter – the K-value variation from segment to segment – below a certain limit (3 × 10−4 for 12 keV photon energy). After tunnel installation only photon-based methods can determine the K-values of undulator segments with a similar accuracy. The synchrotron radiation from a single or a few segments can be spectrally filtered by a dedicated crystal monochromator (K-monochromator) and recorded with a photodiode or with an imager that provides 2D information, tuned for high sensitivity to detect low photon densities from distant single undulator segments. This instrumentation is applied for electron orbit analysis and optimization, and adjustment of individual undulators in terms of their central magnetic axis with respect to the electron beam. Single undulator segments were analysed by scanning the monochromator crystal angle and detecting the steepest slope of a photodiode signal. Alternatively, in the imaging method, an imager recorded the radiation cone of electrons passing through the undulator segment. From the spatial distribution of the radiation, the K-parameter was determined with a sufficiently high relative accuracy.


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