Crystal fields of dilute Tb, Dy, Ho, or Er in Lu obtained by magnetization measurements

International Nuclear Information System (INIS)

Touborg, P.; Hog, J.

1975-01-01

Magnetization measurements are reported on single crystals of dilute Tb, Dy, Ho, or Er in Lu. These measurements were performed in the temperature range 1.5--100 K and field range 0--6 T and include measurements of initial susceptibility, isothermal and isofield magnetization, and basal-plane anisotropy. The results show features similar to the corresponding Y-R alloys, where R is a rare earth. Crystal-field and molecular-field parameters could be unabiguously deduced from the experimental data. The effects of crystal-field level broadening were investigated and demonstrated for Ho. Comparison of the Y-R and Lu-R results makes possible an estimate of the crystal-field parameters in the pure-rare-earth metals

Energy transfer and tunable multicolor emission and paramagnetic properties of GdF3:Dy(3+),Tb(3+),Eu(3+) phosphors.

Science.gov (United States)

Guan, Hongxia; Sheng, Ye; Xu, Chengyi; Dai, Yunzhi; Xie, Xiaoming; Zou, Haifeng

2016-07-20

A series of Dy(3+), Tb(3+), Eu(3+) singly or doubly or triply doped GdF3 phosphors were synthesized by a glutamic acid assisted one-step hydrothermal method. The samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and photoluminescence (PL) spectroscopy. The results show that the synthesized samples are all pure GdF3. The obtained samples have a peanut-like morphology with a diameter of about 270 nm and a length of about 600 nm. Under UV excitation, GdF3:Dy(3+), GdF3:Tb(3+) and GdF3:Eu(3+) samples exhibit strong blue, green and red emissions, respectively. By adjusting their relative doping concentrations in the GdF3 host, the different color hues of green and red light are obtained by co-doped Dy(3+), Tb(3+) and Tb(3+), Eu(3+) ions in the GdF3 host, respectively. Besides, there exist two energy transfer pairs in the GdF3 host: (1) Dy(3+) → Tb(3+) and (2) Tb(3+) → Eu(3+). More significantly, in the Dy(3+), Tb(3+), and Eu(3+) tri-doped GdF3 phosphors, white light can also be achieved upon excitation of UV light by adjusting the doping concentration of Eu(3+). In addition, the obtained samples also exhibit paramagnetic properties at room temperature (300 K) and low temperature (2 K). It is obvious that multifunctional Dy(3+), Tb(3+), Eu(3+) tri-doped GdF3 materials including tunable multicolors and intrinsic paramagnetic properties may have potential applications in the field of full-color displays.

Optical fiber magnetic field sensors with TbDyFe magnetostrictive thin films as sensing materials.

Science.gov (United States)

Yang, Minghong; Dai, Jixiang; Zhou, Ciming; Jiang, Desheng

2009-11-09

Different from usually-used bulk magnetostrictive materials, magnetostrictive TbDyFe thin films were firstly proposed as sensing materials for fiber-optic magnetic field sensing characterization. By magnetron sputtering process, TbDyFe thin films were deposited on etched side circle of a fiber Bragg Grating (FBG) as sensing element. There exists more than 45pm change of FBG wavelength when magnet field increase up to 50 mT. The response to magnetic field is reversible, and could be applicable for magnetic and current sensing.

Development of separation process of Dy, Y, Tm and Yb from heavier rare earth residue by solvent impregnated resin

International Nuclear Information System (INIS)

Shibata, J.; Matsumoto, S.

1998-01-01

Full text: Heavier rare earth which is contained in a small amount in ores such as bastnesite and monazite has been accumulated as heavier rare earth residue without doing separation and purification due to lack of suitable methods. The heavier rare earth residue includes seven rare earth elements such as Tb, Dy, Ho, Y, Er, Tm and Yb. Separation and recovery process of Dy, Y, Tm and Yb from leached solution of the heavier rare earth residue was investigated by using a column method with a solvent impregnated resin. The solvent impregnated resin was prepared by impregnation of organophosphorous extractant whose trade name is PC-88A into a macro porous resin, Amberlite XAD-7. It was almost impossible to separate them in simple adsorption and elution steps. However, we attained to individually separate Dy, Y, Tm and Yb from the leached solution first by changing eluent concentration gradually from pH 2 to 2mol/ l HCl in the elution step, and secondly by using a development column and changing eluent concentration in the elution step. The separation process flow was proposed for heavier rare earth residue by using the solvent impregnated resin method

Tunable emission in Ln3+ (Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor synthesized by combustion method

Science.gov (United States)

Kolte, M. M.; Pawade, V. B.; Bhattacharya, A. B.; Dhoble, S. J.

2018-05-01

Ln3+ (Ln = Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor has been synthesized by Combustion method (CS) at 550° C successfully. Ln3+ (Ln = Ce3+, Dy3+, Tb3+) ions when doped in KNa3Al4Si4O16 host lattice, it shows blue and green emission band under the near Ultraviolet (NUV) excitation wavelength. The Photoluminescence excitation (PLE) and emission spectra are observed due to f-f and d-f transition of rare earth ions. Also, an effective energy transfer (ET) study from Ce3+ → Dy3+ and Ce3+ → Tb3+ ions has been studied and confirmed on the basis of Dexter-Foster theory. Further synthesized phosphor is well characterized by XRD, SEM, TEM and decay time measurement. However, the analysis of crystallite size, lattice strain has been studied by using theoretical as well as experimental techniques. Hence, the observed tunable emission in Ln3+ doped KNa3Al4Si4O16 phosphor may be applicable for solid state lighting technology.

Sol-gel syntheses of pentaborate β-LaB5O9 and the photoluminescence by doping with Eu3+, Tb3+, Ce3+, Sm3+, and Dy3+

Science.gov (United States)

Yang, Ruirui; Sun, Xiaorui; Jiang, Pengfei; Gao, Wenliang; Cong, Rihong; Yang, Tao

2018-02-01

Rare earth (RE) borates have been extensively studied as good photoluminescent materials, however, the target hosts were limited to "RE3BO6", REBO3, and REB3O6 in the RE2O3-B2O3 phase diagram until the recent discovery of rare earth pentaborate. For the first time, the sol-gel method was employed to synthesize β-LaB5O9 doped with Eu3+, Tb3+, Ce3+, Sm3+, Dy3+. In comparison to the previous synthetic methods, the sol-gel method possesses superiorities including easily-controllable doping concentration, high yield and emission efficiency. Solid solutions of phosphors were prepared and carefully analyzed by powder X-ray diffraction. Concentration quenching or saturation was observed in Eu3+, Tb3+ and Ce3+ doped phosphors at round 10 at%. Eu3+, Tb3+, Sm3+, and Dy3+ emit red, green, orange, and close-to-white light, respectively. The absolute emission efficiency of Ce3+ is high and in the UV range, suggesting the function of being sensitizer once combined with other activators.

Host-sensitized luminescence properties in CaNb2O6:Ln(3+) (Ln(3+) = Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+)) phosphors with abundant colors.

Science.gov (United States)

Li, Kai; Liu, Xiaoming; Zhang, Yang; Li, Xuejiao; Lian, Hongzhou; Lin, Jun

2015-01-05

A series of Ln(3+) (Ln(3+) = Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+)) ion doped CaNb2O6 (CNO) phosphors have been prepared via the conventional high-temperature solid-state reaction route. The X-ray diffraction (XRD) and structure refinement, diffuse reflection, photoluminescence (PL), and fluorescent decay curves were used to characterize the as-prepared samples. Under UV radiation, the CNO host present a broad emission band from about 355 to 605 nm centered around 460 nm originating from the NbO6 octahedral groups, which has spectral overlaps with the excitation of f-f transitions of Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) in CNO:Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) samples. They show both host emission and respective emission lines derived from the characteristic f-f transitions of activators, which present different emission colors owing to the energy transfer from the NbO6 group in the host to Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) with increasing activator concentrations. The decreases of decay lifetimes of host emissions in CNO:Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) demonstrate the energy transfer from the hosts to Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+). The energy transfer mechanisms in CNO:Eu(3+)/Tb(3+)/Dy(3+) phosphors have been determined to be a resonant type via dipole-dipole mechanisms. For CNO:Sm(3+), the metal-metal charge transfer transition (MMCT) might contribute to the different variations of decay lifetimes and emission intensity from CNO:Eu(3+)/Tb(3+)/Dy(3+) samples. The best quantum efficiency is 71.2% for CNO:0.01/0.02Dy(3+). The PL properties of as-prepared materials indicate the promising application in UV-pumped white-emitting lighting diodes field.

Characterization, electrical transport and magnetic properties of the rare earth misfit layer compounds (TbS)(1.21)NbS2, (TbS)(1.20)TaS2, (DyS)(1.22)NbS2 and (DyS)(1.21)TaS2

NARCIS (Netherlands)

Zhou, W.Y.; Meetsma, A.; deBoer, J.L.; Wiegers, G.A

1996-01-01

X-ray powder and single-crystal X-ray diffraction of the title compounds showed that they are planar intergrowth compounds, built of alternating sandwiches TS2 (T=Nb, Ta) and double layers LnS (Ln=Tb, Dy), present in three orientational variants related by rotations of 120 degrees around the c axis

Induced assembly and photoluminescence of lanthanum (Tb, Eu, Dy) complexes/ZnO/polyethylene glycol hybrid phosphors

Energy Technology Data Exchange (ETDEWEB)

Yan Bing [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China)]. E-mail: byan@tongji.edu.cn; Chen Xi [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China); Wu Jianhua [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China)

2007-08-31

Some novel kinds of hybrid phosphors were assembled with lanthanum (Tb, Eu, Dy) complexes (with four kinds of terbium complexes is 2,4-dihydroxybenzonic acid (DHBA), 1,10-phenanthroline (phen), acetylacetone (AA) and nicotinic acid (Nic), respectively) doped ZnO/PEG particles by co-precipitation approach derived from Zn(CH{sub 3}COO){sub 2} (Zn(AC){sub 2}), NaOH, PEG as precursors at room temperature. The characteristic luminescence spectra for f-f transitions of Tb{sup 3+}, Eu{sup 3+}, Dy{sup 3+} were observed. It is worthy to point out that ZnO is the excellent host for lanthanum ions by the assembly of PEG matrices.

Progress in sintered NdFeB magnets with Dy/Tb grain boundary diffusion%晶界扩散Dy/Tb烧结NdFeB研究进展

Institute of Scientific and Technical Information of China (English)

刘涛; 周磊; 张昕; 程星华; 林德; 喻晓军; 李波

2011-01-01

由于汽车和电子应用领域对节能电动机的需求,在VCM、电动机、信号发生器、手机和MRI等领域中得到广泛应用的烧结钕铁硼在电动机市场应用会进一步扩展.剩磁和矫顽力等磁性能的提高有利于烧结磁体在电动机市场快速增长.通常,烧结磁体一些性能的改善总是以牺牲其他性能为代价.而晶界扩散Dy/Tb烧结磁体与传统的同类磁体相比较,其矫顽力和剩磁可同时得以改善,本文对晶界扩散Dy/Tb钕铁硼的一些研究成果进行了综述和总结.晶界扩散Dy/Tb过程中烧结磁体晶界的成份和微观组织的变化对烧结磁体磁性能改善至为重要.%Many new applications of Nd-Fe-B magnets, such as voice coil motor (VCM) in hard disc drive, motors, generators, mobile phone, MRI, etc, are expected to expand in future because of strong energy saving requirements from the automobile and electric appliances markets. Magnetic property improvement in residual (Br) and coercive force (Hcj) helps the rapid growth of the motor market. In many instances, an improvement of some characteristics of sintered magnet is achieved but only at the expense of other characteristics. It has been found that Dy/Tb grain boundary diffusion processed Nd-Fe-B sintered magnets have improvement in both the highest remanence and cocercivity among conventional rare-earth permanent mgnets, which have been introduced in this paper. The influence of Dy/Tb grain boundary diffusion on composition and microstructure of grain boundaries phase is a key point for magnetic property improvement of sintered magnet.

Family of defect-dicubane Ni4Ln2 (Ln = Gd, Tb, Dy, Ho) and Ni4Y2 complexes: rare Tb(III) and Ho(III) examples showing SMM behavior.

Science.gov (United States)

Zhao, Lang; Wu, Jianfeng; Ke, Hongshan; Tang, Jinkui

2014-04-07

Reactions of Ln(III) perchlorate (Ln = Gd, Tb, Dy, and Ho), NiCl2·6H2O, and a polydentate Schiff base resulted in the assembly of novel isostructural hexanuclear Ni4Ln2 complexes [Ln = Gd (1), Tb (2), Dy (3), Ho (4)] with an unprecedented 3d-4f metal topology consisting of two defect-dicubane units. The corresponding Ni4Y2 (5) complex containing diamagnetic Y(III) atoms was also isolated to assist the magnetic studies. Interestingly, complexes 2 and 3 exhibit SMM characteristics and 4 shows slow relaxation of the magnetization. The absence of frequency-dependent in-phase and out-of-phase signals for the Ni-Y species suggests that the Ln ions' contribution to the slow relaxation must be effectual as previously observed in other Ni-Dy samples. However, the observation of χ″ signals with zero dc field for the Ni-Tb and Ni-Ho derivatives is notable. Indeed, this is the first time that such a behavior is observed in the Ni-Tb and Ni-Ho complexes.

Isothiocyanato complexes of Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl)benzimidazole

Energy Technology Data Exchange (ETDEWEB)

Mishra, A; Singh, V K

1982-01-01

Six-coordinated complexes of the type (Ln(PyBzH)/sub 2/NCS.H/sub 2/O) (NCS)/sub 2/.nH/sub 2/O/mC/sub 2/H/sub 5/OH (Ln = Gd(III), Tb(III), Dy(III) and Ho(III), n=1-2; m=1) have been prepared from Ln(NCS)/sub 6//sup 3 -/. The room temperature magnetic moment values confirm the terpositive state of the lanthanide ions. Infrared spectra suggest the N-coordination of thiocyanate group. Electronic spectral studies of Tb(III), Dy(III) and Ho(III) complexes have been made in terms of LSJ term energies. 13 refs.

New intermetallic compounds Ln(Ag, AL)4 (Ln-Y, Gd, Tb, Dy) and their structure

International Nuclear Information System (INIS)

Kuz'ma, Yu.B.; Stel'makhovich, B.M.

1990-01-01

By the methods of X-ray analysis crystal structure of compounds Ln(Ag,Al) 4 , where Ln-Y, Gd, Tb, Dy, posessing rhombic structure, is determined. The intermetallics have been prepared for the first time. Ways of atom distribution and their coordinates in DyAg 0.55 Al 3.45 structure (a=0.4296(1), b=04179(1), c=0.9995(3), R=0.093) are specified. Other compounds are formed in case of LnAgAl 3 compositions. Interatomic distances in Dy(Ag,Al) 4 structure are considered. A supposition is made on the formation in Ln-Ag-Al systems of a greater number of intermetallic compounds

Ln3+ (Ln=Ce, Tb, Dy) and Hf doping of LuI3 powders – A material and spectroscopic study

International Nuclear Information System (INIS)

Wiatrowska, Aneta; Keur, Wilco; Ronda, Cees

2016-01-01

The moisture sensitivity of LuI 3 :Ce,Hf and luminescent properties of undoped LuI 3 and LuI 3 :M (M=Ce 3+ , Tb 3+ , Dy 3+ ) powders were investigated. The possibility of improving the air and moisture stability of LuI 3 :Ce by Hf doping was tested. It was proven that the Hf contribution to the LuI 3 :Ce stability is very limited and is insignificant to render LuI 3 :Ce scintillator powders suitable for applications. Photoluminescence results of LuI 3 without dopants added on purpose showed luminescence due to a plurality of rare-earth elements' impurities. Two types of self-trapped luminescence were found. Energy transfer between host lattice, self-trapped excitons and rare-earth ions was investigated.

Photoluminescence properties of aeschynite-type LaNbTiO6:RE3+ (RE = Tb, Dy, Ho) down-converting phosphors.

Science.gov (United States)

Ma, Qian; Lu, Mengkai; Yang, Ping; Zhang, Aiyu; Cao, Yongqiang

2014-06-01

In this study, a series of LaNbTiO6:RE(3+) (RE = Tb, Dy, Ho) down-converting phosphors were synthesized using a modified sol-gel combustion method, and their photoluminescence (PL) properties were investigated as a function of activator concentration and annealing temperature. The resultant particles were characterized using X-ray diffraction, transmission electron microscopy, scanning electron microscopy, UV/Vis diffuse reflectance spectroscopy and PL spectra. The highly crystalline LaNbTiO6:RE(3+) (RE = Tb, Dy, Ho) phosphors with an average size of 200-300 nm obtained at 1100°C have an orthorhombic aeschynite-type structure and exhibit the highest luminescent intensity in our study range. The emission spectra of LaNbTiO6:RE(3+) (RE = Tb, Dy, Ho) phosphors under excitations at UV/blue sources are mainly composed of characteristic peaks arising from the f-f transitions of RE(3+), including 489 nm ((5) D4 → (7) F6) and 545 nm ((5) D4 → (7) F5) for Tb(3+), 476 and 482 nm ((4) F9/2 → (6) H15/2) and 571 nm ((4) F9/2 → (6) H13/2) for Dy(3+), and 545 nm ((5) F4 + (5) S2 → (5) I8) for Ho(3+), respectively. The luminescent mechanisms were further investigated. It can be expected that these phosphors are of intense interest and potential importance for many optical applications. Copyright © 2013 John Wiley & Sons, Ltd.

KCa4(BO33:Ln3+ (Ln = Dy, Eu, Tb phosphors for near UV excited white–light–emitting diodes

Directory of Open Access Journals (Sweden)

Allu Amarnath Reddy

2013-02-01

Full Text Available A series of doped KCa4(BO33:Ln3+ (Ln: Dy, Eu and Tb compositions were synthesized by solid–state reaction method and their photoluminescent properties were systematically investigated to ascertain their suitability for application in white light emitting diodes. The X–ray diffraction (XRD and nuclear magnetic resonance (MAS–NMR data indicates that Ln3+–ions are successfully occupied the non–centrosymmetric Ca2+ sites, in the orthorhombic crystalline phase of KCa4(BO33 having space group Ama2, without affecting the boron chemical environment. The present phosphor systems could be efficiently excitable at the broad UV wavelength region, from 250 to 350 nm, compatible to the most commonly available UV light–emitting diode (LED chips. Photoluminescence studies revealed optimal near white–light emission for KCa4(BO33 with 5 wt.% Dy3+ doping, while warm white–light (CIE; X = 0.353, Y = 0.369 is obtained at 1wt.% Dy3+ ion concentration. The principle of energy transfer between Eu3+ and Tb3+ also demonstrates the potential white–light from KCa4(BO33:Eu3+,Tb3+ phosphor. Whereas, single Tb3+ and Eu3+–doped systems showed bright green (Tb3+ and red (Eu3+ emissions, respectively. Having structural flexibility along with remarkable chemical/thermal stability and suitable quantum efficiency these phosphors can be promising candidates as white–light–emitter for near UV LEDs.

Síntesis hidrotermal de monocristales LnMn2O5 (Ln= Y, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho y Er

Directory of Open Access Journals (Sweden)

Señarís Rodríguez, M. A.

2008-08-01

Full Text Available Ten single crystals of the series LnMn2O5 (Ln= Y, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho and Er were synthesized by hydrothermal synthesis in a single step and without subsequent thermal treatments from aqueous solutions of metals salts at 240 ºC. The obtained single crystals have a size of various micrometers and their morphology changes throughout the serie: they are polygonal in the case of the compounds with Ln= Pr, Nd, Sm, Eu and Gd and needle-like in the case of the compounds with Ln= Y, Tb, Dy, Ho and Er. After the analysis of the obtained products employing different conditions of synthesis we attributed the different morphology to a greater growth rate along the c axis when the smaller ions (Y, Tb, Dy, Ho y Er are involved, due to their better adaptation to the compound’s crystal structure.Se han conseguido preparar monocristales de 10 óxidos mixtos de la serie LnMn2O5 (Ln= Y, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho y Er mediante síntesis hidrotermal optimizada, en un único paso y sin tratamientos térmicos posteriores partiendo de las correspondientes sales metálicas en disolución acuosa a 240 ºC. Los monocristales obtenidos son relativamente grandes, de varias micras y su morfología varía a lo largo de la serie: es poligonal en el caso de los compuestos de los lantánidos del inicio de la serie (Ln= Pr, Nd, Sm, Eu y Gd y acicular en el caso de los compuestos de Y y de los lantánidos del final de la serie (Ln= Tb, Dy, Ho y Er. Tras el análisis de los productos obtenidos empleando distintas condiciones de síntesis atribuimos la diferente morfología a una mayor velocidad de crecimiento cristalino a lo largo del eje c cuando intervienen los iones más pequeños (Y, Tb, Dy, Ho y Er debido a la mejor adaptación de éstos últimos a la estructura cristalina del compuesto.

Hydrothermal synthesis, characterization, and luminescence of Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers

International Nuclear Information System (INIS)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin; Chen, Cuili; Seo, Hyo Jin

2016-01-01

Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca_2B_2O_5:Eu"3"+ nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca_2B_2O_5:Tb"3"+ nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy"3"+-doped Ca_2B_2O_5 nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu"3"+-, Tb"3"+-, Dy"3"+-doped Ca_2B_2O_5 nanofibers, respectively. It is suggested that Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers could be an efficient phosphor for lighting and display.

Structural and magnetic properties of two branches of the tripod-kagome-lattice family A2R3Sb3O14 (A = Mg, Zn; R = Pr, Nd, Gd, Tb, Dy, Ho, Er, Yb)

Science.gov (United States)

Dun, Z. L.; Trinh, J.; Lee, M.; Choi, E. S.; Li, K.; Hu, Y. F.; Wang, Y. X.; Blanc, N.; Ramirez, A. P.; Zhou, H. D.

2017-03-01

We present a systematic study of the structural and magnetic properties of two branches of the rare-earth tripod-kagome-lattice (TKL) family A2R3Sb3O14 (A = Mg, Zn; R = Pr, Nd, Gd, Tb, Dy, Ho, Er, Yb; here, we use abbreviation A-R, as in MgPr for Mg2Pr3Sb3O14 ), which complements our previously reported work on MgDy, MgGd, and MgEr [Z. L. Dun et al., Phys. Rev. Lett. 116, 157201 (2016), 10.1103/PhysRevLett.116.157201]. The present susceptibility (χdc, χac) and specific-heat measurements reveal various magnetic ground states, including the nonmagnetic singlet state for MgPr, ZnPr; long-range orderings (LROs) for MgGd, ZnGd, MgNd, ZnNd, and MgYb; a long-range magnetic charge ordered state for MgDy, ZnDy, and potentially for MgHo; possible spin-glass states for ZnEr, ZnHo; the absence of spin ordering down to 80 mK for MgEr, MgTb, ZnTb, and ZnYb compounds. The ground states observed here bear both similarities as well as striking differences from the states found in the parent pyrochlore systems. In particular, while the TKLs display a greater tendency towards LRO, the lack of LRO in MgHo, MgTb, and ZnTb can be viewed from the standpoint of a balance among spin-spin interactions, anisotropies, and non-Kramers nature of single-ion state. While substituting Zn for Mg changes the chemical pressure, and subtly modifies the interaction energies for compounds with larger R ions, this substitution introduces structural disorder and modifies the ground states for compounds with smaller R ions (Ho, Er, Yb).

Investigation on the formation of the preferred orientations in a TbDyFe alloy with directional solidification

International Nuclear Information System (INIS)

Jiang Chengbao; Xu Huibin

1999-01-01

The formation of the preferred orientations in a TbDyFe alloy was studied by transmission electron microscopy (TEM). It was found that there were several different preferred orientations in the experimental TbDyFe alloy with directional solidification. left angle 110 right angle, left angle 112 right angle and left angle 113 right angle preferred orientations were observed in this alloy solidified by our self-made super high gradient temperature directional solidification device. The preferred orientations changed with the variation of the solidification conditions. Two {111} twinning systems resulted in the left angle 110 right angle preferred orientation and a single {111} twinning system resulted in the left angle 112 right angle preferred orientation. The twinning displacement was observed and this formatted the left angle 113 right angle preferred orientation. (orig.)

Influence of strain and polycrystalline ordering on magnetic properties of high moment rare earth metals and alloys

International Nuclear Information System (INIS)

Scheunert, G; Ward, C; Hendren, W R; Bowman, R M; Lapicki, A A; Hardeman, R; Mooney, M; Gubbins, M

2014-01-01

Despite being the most suitable candidates for solenoid pole pieces in state-of-the-art superconductor-based electromagnets, the intrinsic magnetic properties of heavy rare earth metals and their alloys have gained comparatively little attention. With the potential of integration in micro and nanoscale devices, thin films of Gd, Dy, Tb, DyGd and DyTb were plasma-sputtered and investigated for their in-plane magnetic properties, with an emphasis on magnetization versus temperature profiles. Based on crystal structure analysis of the polycrystalline rare earth films, which consist of a low magnetic moment fcc layer at the seed interface topped with a higher moment hcp layer, an experimental protocol is introduced which allows the direct magnetic analysis of the individual layers. In line with the general trend of heavy lanthanides, the saturation magnetization was found to drop with increasing unit cell size. In situ annealed rare earth films exceeded the saturation magnetization of a high-moment Fe 65 Co 35 reference film in the cryogenic temperature regime, proving their potential for pole piece applications; however as-deposited rare earth films were found completely unsuitable. In agreement with theoretical predictions, sufficiently strained crystal phases of Tb and Dy did not exhibit an incommensurate magnetic order, unlike their single-crystal counterparts which have a helical phase. DyGd and DyTb alloys followed the trends of the elemental rare earth metals in terms of crystal structure and magnetic properties. Inter-rare-earth alloys hence present a desirable blend of saturation magnetization and operating temperature. (paper)

Crystal Fields in Dilute Rare-Earth Metals Obtained from Magnetization Measurements on Dilute Rare-Earth Alloys

DEFF Research Database (Denmark)

Touborg, P.; Høg, J.

1974-01-01

Crystal field parameters of Tb, Dy, and Er in Sc, Y, and Lu are summarized. These parameters are obtained from magnetization measurements on dilute single crystals, and successfully checked by a number of different methods. The crystal field parameters vary unpredictably with the rare-earth solute....... B40, B60, and B66 are similar in Y and Lu. Crystal field parameters for the pure metals Tb, Dy, and Er are estimated from the crystal fields in Y and Lu....

Levels and transitions in 160Dy following the decay of 160Tb

International Nuclear Information System (INIS)

Noordin bin Ibrahim; Stewart, N.M.

1989-01-01

The level scheme of 160 Dy has been established from γ-γ coincidence measurement following the β-decay of 160 Tb. Ge(Li) detectors were coupled to a Dual Parameter Spectrometer for data collection. A total of fifteen new gamma transitions were observed. Two energy levels at 1285 and 1288 keV were confirmed while four levels at 1349, 1670, 1694 and 1804 keV were found to be populated for the first time from β-decay of 160 Tb: Three levels at 1230, 1338 and 1507 keV are newly suggested. Relative intensities for the transitions and branching ratios of the energy levels were determined. Comparisons are made with theoretical predictions of IBA calculations, two considerations were taken: normal shell closure (Z 50/82) and subshell closure (Z = 64). (author)

Magnetostriction-strain-induced enhancement and modulation of photovoltaic performance in Si-p-n/Tb{sub x}Dy{sub 1-x}Fe{sub 2} composite

Energy Technology Data Exchange (ETDEWEB)

Wu, Zheng [School of Materials Science and Technology, China University of Geosciences, Beijing (China); Department of Physics and College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua (China); Zhang, Yihe [School of Materials Science and Technology, China University of Geosciences, Beijing (China); Fang, Cong; Ma, Ke; Lin, He; Jia, Yanmin; Chen, Jianrong [Department of Physics and College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua (China); Wang, Yu; Chan, Helen Lai Wa [Department of Applied Physics, The Hong Kong Polytechnic University (China)

2014-03-15

High photovoltaic efficiency is a key index in the application of silicon (Si) solar cells. In this study, a composite of a photovoltaic Si p-n junction solar cell and a magnetostrictive Tb{sub x}Dy{sub 1-x}Fe{sub 2} alloy was fabricated. By utilizing the magnetostrictive strain to modulate the energy bandgap of Si, the open-circuit voltage and the maximum photovoltaic output power of the Si p-n junction solar cell could be enhanced by ∝12% and 9.1% under a dc magnetic field of ∝250 mT, respectively. The significantly enhanced photovoltaic performance and the simple fabrication process make the Si-p-n/Tb{sub x}Dy{sub 1-x}Fe{sub 2} composite a promising material for high-efficiency solar cell devices. The structure of the proposed Si-p-n/Tb{sub x}Dy{sub 1-x}Fe{sub 2} laminated composite. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Magnetic Properties of Dy in Pb2Sr2DyCu3O8

International Nuclear Information System (INIS)

Skanthakumar, S.; Soderholm, L.; Movshovich, R.

1999-01-01

Superconductivity can be induced at high temperatures in Pb 2 Sr 2 RCu 3 O 8 (R - rare earth) by partially doping Ca 2+ for R 3+ . In order to understand the interplay between magnetism and superconductivity, the magnetic properties of the parent compounds, Pb 2 Sr 2 RCu 3 O 8 , have been studied. The work presented here includes magnetic susceptibility and specific heat measurements on R=Dy and extends the previous studies on R=Ce, Pr, Tb, Ho and Er. Specific heat experiments suggest that the Dy ions order antiferromagnetically with an ordering temperature of 1.3K. The magnetic susceptibility data are in good agreement with the susceptibility calculated using crystal field parameters that are extrapolated from previous modeling of the R=Er and Ho analogs of this series

Thermal decomposition of RE(C2H5CO2)3·H2O (RE = Dy, Tb, Gd, Eu and Sm)

DEFF Research Database (Denmark)

Grivel, Jean-Claude

2014-01-01

The thermal decomposition of Dy(III), Tb(III), Gd(III), Eu(III), and Sm(III) propionate monohydrates was studied in argon by means of simultaneous differential thermal analysis and thermogravimetry, infrared-spectroscopy, X-ray diffraction, and optical microscopy. After dehydration, which takes......, an intermediate stage involving a RE2O(C2H5CO2)4 composition was evidenced in the case of the Eu- and Sm-propionates. For all compounds, further decomposition of RE2O2CO3 into the corresponding sesquioxides (RE2O3) is accompanied by the release of CO2. The thermal decomposition of Dy- and Tb-propionates occurs...

Separation and recovery of high grade Dy2O3 by solvent extraction process with DEHPA in kerosene

International Nuclear Information System (INIS)

Mishra, S.L.; Thakur, N.V.; Koppiker, K.S.

1993-01-01

During the solvent extraction (SX) fractionation of rare earths chloride obtained from monazite, a heavy RE (HRE) fraction assaying 60% Y 2 O 3 is produced. This is purified further to 93% Y 2 O 3 by another SX cycle. During this step most of Dy and Tb get separated to yield a concentrate assaying >50% Dy 2 O 3 . An attempt has been made to process this Dy rich concentrate to obtain a high grade Dy 2 O 3 by a SX route using DEHPA in kerosene. The distribution data (D vs H i + ) of Dy have been generated experimentally at various metal concentrations and similar data for other metals present (Gd, Tb, Y, Er and Ho) have been derived using a mathematical expression developed in our laboratory. Based on this information mathematical models for extraction behaviour of these HRE have been derived and used in a computer program developed for multicomponent system. This program has been utilised to optimise the process parameters to obtain 95-97% pure Dy 2 O 3 at about 90% recovery. The parameters have been experimentally confirmed and Dy 2 O 3 95.5% pure w.r.t. Tb was obtained at about 90% recovery, thus confirming the validity of the program. This paper presents data obtained during these investigations. (author). 6 refs., 5 tabs

Magnetoelectric effect in two-layered self-biased composites Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68}/epoxy - PbZr{sub 0.53}Ti{sub 0.47}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Kalgin, A.V.; Gridnev, S.A.; Popov, I.I. [Voronezh State Technical University, Voronezh (Russian Federation)

2017-03-15

Direct magnetoelectric (ME) effect in two-layered Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68}/Epoxy - PbZr{sub 0.53}Ti{sub 0.47}O{sub 3} composites containing magnetostrictive layers of the epoxy with distributed in it Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68} granules and piezoelectric layers of the PbZr{sub 0.53}Ti{sub 0.47}O{sub 3} ceramics was studied. It was found, that the gradient distribution of Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68} granules in magnetostrictive layers induces the internal (self-biased) magnetic field. This field leads to the increase in ME responses in composites with the gradient distribution of Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68} granules in magnetostrictive layers as compared with ME responses in composites with the random distribution of Tb{sub 0.12}Dy{sub 0.2}Fe{sub 0.68} granules in magnetostrictive layers, which does not induce the internal magnetic field. We revealed the possibility of controlling and determining values of the internal magnetic field in composites and conditions for obtaining optimal ME responses. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Subsolidus Phase Relations of the CaO-REOx-CuO Systems (RE = Eu, Tb, Dy, Ho, Er, Lu and Sc) at 900 °C in Air

DEFF Research Database (Denmark)

Grivel, Jean-Claude

2016-01-01

The subsolidus phase relations of the CaO-REOx-CuO systems (RE = Eu, Tb, Dy, Ho, Er, Lu and Sc) were investigated in air at 900 °C. The pseudo-ternary sections with RE = Tb, Dy, Ho, Er and Lu have a similar structure. They have in common with the RE = Eu system a solid solution of Ca0.833−xRExCuO2......+y composition but the system with RE = Eu differs by the presence of an Eu2CuO4 phase instead of RE2Cu2O5 for RE = Tb, Dy, Ho, Er and Lu. In contrast, the CaO-ScO1.5-CuO section does not contain a Ca0.833−xScxCuO2+y solid solution and is dominated by the CaSc2O4 phase, which has no equivalent...... in the other systems at 900 °C in air....

General synthesis and structural evolution of a layered family of Ln8(OH)20Cl4 x nH2O (Ln = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Y).

Science.gov (United States)

Geng, Fengxia; Matsushita, Yoshitaka; Ma, Renzhi; Xin, Hao; Tanaka, Masahiko; Izumi, Fujio; Iyi, Nobuo; Sasaki, Takayoshi

2008-12-03

The synthesis process and crystal structure evolution for a family of stoichiometric layered rare-earth hydroxides with general formula Ln(8)(OH)(20)Cl(4) x nH(2)O (Ln = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Y; n approximately 6-7) are described. Synthesis was accomplished through homogeneous precipitation of LnCl(3) x xH(2)O with hexamethylenetetramine to yield a single-phase product for Sm-Er and Y. Some minor coexisting phases were observed for Nd(3+) and Tm(3+), indicating a size limit for this layered series. Light lanthanides (Nd, Sm, Eu) crystallized into rectangular platelets, whereas platelets of heavy lanthanides from Gd tended to be of quasi-hexagonal morphology. Rietveld profile analysis revealed that all phases were isostructural in an orthorhombic layered structure featuring a positively charged layer, [Ln(8)(OH)(20)(H(2)O)(n)](4+), and interlayer charge-balancing Cl(-) ions. In-plane lattice parameters a and b decreased nearly linearly with a decrease in the rare-earth cation size. The interlamellar distance, c, was almost constant (approximately 8.70 A) for rare-earth elements Nd(3+), Sm(3+), and Eu(3+), but it suddenly decreased to approximately 8.45 A for Tb(3+), Dy(3+), Ho(3+), and Er(3+), which can be ascribed to two different degrees of hydration. Nd(3+) typically adopted a phase with high hydration, whereas a low-hydration phase was preferred for Tb(3+), Dy(3+), Ho(3+), Er(3+), and Tm(3+). Sm(3+), Eu(3+), and Gd(3+) samples were sensitive to humidity conditions because high- and low-hydration phases were interconvertible at a critical humidity of 10%, 20%, and 50%, respectively, as supported by both X-ray diffraction and gravimetry as a function of the relative humidity. In the phase conversion process, interlayer expansion or contraction of approximately 0.2 A also occurred as a possible consequence of absorption/desorption of H(2)O molecules. The hydration difference was also evidenced by refinement results. The number of coordinated water

161Dy Moessbauer spectroscopy of the intermetallic compounds DyNi2Si2, DyNi2Ge2 and DyAg2Si2

International Nuclear Information System (INIS)

Onodera, Hideya; Murata, Akifumi; Koizuka, Masaaki; Ohashi, Masayoshi; Yamaguchi, Yasuo

1994-01-01

161 Dy Moessbauer spectroscopic study has been performed on DyNi 2 Si 2 , DyNi 2 Ge 2 and DyAg 2 Si 2 in order to clarify microscopic properties of antiferromagnets with incommensurate and sinusoidally moment-modulated structure. The experiments were done using the standard 161 Tb Moessbauer sources prepared by neutron irradiation at the Japan Material Testing Reactor. The Moessbauer spectra of DyNi 2 Si 2 are analyzed satisfactorily by a single set of hyperfine parameters, and hence the sinusoidal moment-modulation is considered to be realized through a distribution of spin relaxation rate. The broadened spectra of DyNi 2 Ge 2 are fitted tentatively by three subspectra. It seems for DyNi 2 Ge 2 that the incommensurate arrangement of Dy moments differed in magnitude as well as the distribution of spin relaxation rate originates the moment modulation. The fact that the spectrum of DyAg 2 Si 2 at 3 K consists of two distinct subspectra ensures the complicated antiferromagnetic structure where two kinds of Dy moments differed in magnitude are arranged noncollinearly. (author)

Synthesis and photoluminescence characteristics of (Y,Gd)BO3:RE (RE = Eu(3+), Ce(3+), Dy(3+) and Tb(3+)) phosphors for blue chip and near-UV white LEDs.

Science.gov (United States)

Rangari, V V; Singh, V; Dhoble, S J

2016-03-01

A series of Eu(3+)-, Ce(3+)-, Dy(3+)- and Tb(3+)-doped (Y,Gd)BO3 phosphors was synthesized by a solid-state diffusion method. X-Ray diffraction confirmed their hexagonal structure and the scanning electron microscopy results showed crystalline particles. The excitation spectra revealed that (Y,Gd)BO3 phosphors doped with Eu(3+), Ce(3+), Dy(3+) and Tb(3+) are effectively excited with near UV-light of 395 nm/blue light, 364, 351 and 314 nm, respectively. Photoluminescence spectra of Eu(3+)-, Ce(3+)- and Tb(3+)/Dy(3+)-doped phosphor showed intense emission of reddish orange, blue and white light, respectively. The phosphor Y0.60Gd0.38BO3:Ce0.02 showed CIE 1931 color coordinates of (0.158, 0.031) and better color purity compared with commercially available blue BAM:Eu(2+) phosphor. The phosphor (Y,Gd)BO3 doped with Eu(3+), Dy(3+) and Tb(3+) showed CIE 1931 color coordinates of (0.667, 0.332), (0.251, 0.299) and (0.333, 0.391) respectively. Significant photoluminescence characteristics of the prepared phosphors indicate that they might serve as potential candidates for blue chip and near-UV white light-emitting diode applications. Copyright © 2015 John Wiley & Sons, Ltd.

Magnetic domain structure, crystal orientation, and magnetostriction of Tb{sub 0.27}Dy{sub 0.73}Fe{sub 1.95} solidified in various high magnetic fields

Energy Technology Data Exchange (ETDEWEB)

Gao, Pengfei [Key Laboratory of Electromagnetic Processing of Materials (Ministry of Education), Northeastern University, Shenyang 110819 (China); Liu, Tie, E-mail: liutie@epm.neu.edu.cn [Key Laboratory of Electromagnetic Processing of Materials (Ministry of Education), Northeastern University, Shenyang 110819 (China); Dong, Meng [Key Laboratory of Electromagnetic Processing of Materials (Ministry of Education), Northeastern University, Shenyang 110819 (China); Yuan, Yi [School of Materials and Metallurgy, Northeastern University, Shenyang 110819 (China); Wang, Qiang [Key Laboratory of Electromagnetic Processing of Materials (Ministry of Education), Northeastern University, Shenyang 110819 (China)

2016-03-01

In this paper, we studied how applying a high magnetic field during solidification of Tb{sub 0.27}Dy{sub 0.73}Fe{sub 1.95} alloys affected their magnetic domain structure, crystal orientation, and magnetostriction. We observed the morphology of the magnetic domain during solidification, finding it change with the applied field: from fiber like (0 T) to dot like and closure mixed (4.4 T) to fiber like (8.8 T) to fishbone like (11.5 T). The alloy solidified at 4.4 T showed the best contrast of light and dark in its domain image, widest magnetic domain, fastest magnetization, and highest magnetostriction; this alloy is followed in descending order by the alloys solidified at 11.5 T, 8.8 T, and 0 T. The orientation of the (Tb, Dy)Fe{sub 2} phase changed with magnetic field from random (0 T) to 〈111〉 (4.4 T) to 〈113〉 (8.8 T) to 〈110〉 (11.5 T). The improvement in magnetostriction was likely caused by modification of both the magnetization process and the alloy microstructure. - Highlights: • We present how magnetic field affects magnetic domain structure of Tb{sub 0.27}Dy{sub 0.73}Fe{sub 1.95}. • Morphology and width of magnetic domain change with increasing magnetic field. • Magnetization and magnetostriction of alloy change with increasing magnetic field. • A transformation of random–〈111〉–〈113〉–〈110〉 for (Tb, Dy)Fe{sub 2} orientation forms.

Production of 149Tb in deep inelastic transfer reactions: an approach to the angular momentum of fragments

International Nuclear Information System (INIS)

Rivet, M.F.; Bimbot, R.; Gardes, D.; Fleury, A.; Hubert, F.; Llabador, Y.

1978-01-01

The excitation functions for deep inelastic reactions in which two to six charges are transferred from 40 Ar and 63 Cu ions to rare earth targets have been measured using activation techniques, the observed radionuclides being 150 Dy, 151 Dy and 149 gTb. From the comparison of the curves relative to 149 gTb and those relative to 150 Dy, 151 Dy, it was deduced that the low spin isomer 149 gTb was produced with significant probability for low incident energies. Using data from (heavy ions, xn) reactions, it was possible to attribute this production to the deexcitation of Tb fragments formed in deep inelastic transfers with angular momenta lower than 9n. This result is in good agreement with the angular momentum calculations performed under the hypothesis that the initial angular momentum window leading to deep inelastic reactions is situated between the critical angular momentum for fusion and that corresponding to grazing collisions. As far as Cu induced reactions are concerned, both hypothesis of rolling and sticking are consistent with the experimental data. For Ar induced reactions, the results indicate that the stage of sticking is not reached when the incident energy is lower than 200 MeV

Tunable luminescence and energy transfer properties in Na{sub 3}Bi(PO4){sub 2}:Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}, Sm{sup 3+} phosphors with high thermal stability

Energy Technology Data Exchange (ETDEWEB)

Zhu, Zizhong; Fu, Guangsheng; Yang, Yong; Yang, Zhiping, E-mail: yangzp2005@sohu.com; Li, Panlai, E-mail: li_panlai@126.com

2017-04-15

Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+}/Tb{sup 3+}/Dy{sup 3+}/Sm{sup 3+} phosphors were synthesized via a high-temperature solid-state reaction method. The X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), diffuse reflection, photoluminescence (PL) and fluorescent decay curves were utilized to characterize the obtained phosphors. Under n-UV excitation, Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+}/Tb{sup 3+}/Dy{sup 3+}/Sm{sup 3+} samples show the characteristic f-f emissions and present red, green, yellow and orange emission, respectively. When Tb{sup 3+}, Dy{sup 3+} and Sm{sup 3+} were co-doped into the Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+} phosphors, tunable emission colors can be obtained and can be efficiently adjusted by varying the doping ions and the doping concentration. The energy transfer mechanisms were investigated in detail and demonstrated that there is an efficient energy transfer from Tb{sup 3+}, Dy{sup 3+} and Sm{sup 3+} to Eu{sup 3+} via a dipole-dipole interaction mechanism. Additional, as the temperature increases from RT to 150 °C, the PL intensity of Tb{sup 3+}-Eu{sup 3+}, Dy{sup 3+}-Eu{sup 3+} and Sm{sup 3+}-Eu{sup 3+} co-doped phosphors decreased to 86%, 85% and 88%, respectively, which prove good thermal stability. All the CIE coordinates of as-prepared phosphors are displayed and show abundant colors, making these materials have potential applications for n-UV-excited white-LEDs.

Fiber-optic thermometer application of thermal radiation from rare-earth end-doped SiO2 fiber

International Nuclear Information System (INIS)

Katsumata, Toru; Morita, Kentaro; Komuro, Shuji; Aizawa, Hiroaki

2014-01-01

Visible light thermal radiation from SiO 2 glass doped with Y, La, Ce, Pr, Nd, Eu, Tb, Dy, Ho, Er, Tm, Yb, and Lu were studied for the fiber-optic thermometer application based on the temperature dependence of thermal radiation. Thermal radiations according to Planck's law of radiation are observed from the SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu at the temperature above 1100 K. Thermal radiations due to f-f transitions of rare-earth ions are observed from the SiO 2 fibers doped with Nd, Dy, Ho, Er, Tm, and Yb at the temperature above 900 K. Peak intensities of thermal radiations from rare-earth doped SiO 2 fibers increase sensitively with temperature. Thermal activation energies of thermal radiations by f-f transitions seen in Nd, Dy, Ho, Er, Tm, and Yb doped SiO 2 fibers are smaller than those from SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu. Thermal radiation due to highly efficient f-f transitions in Nd, Dy, Ho, Er, Tm, and Yb ions emits more easily than usual thermal radiation process. Thermal radiations from rare-earth doped SiO 2 are potentially applicable for the fiber-optic thermometry above 900 K

Tunable-color luminescence via energy transfer in NaCa13/18Mg5/18PO4:A (A = Eu2+/Tb3+/Mn2+, Dy3+) phosphors for solid state lighting.

Science.gov (United States)

Li, Kai; Fan, Jian; Mi, Xiaoyun; Zhang, Yang; Lian, Hongzhou; Shang, Mengmeng; Lin, Jun

2014-11-17

A series of NaCa13/18Mg5/18PO4(NCMPO):A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) phosphors have been prepared by the high-temperature solid-state reaction method. The X-ray diffraction (XRD) and Rietveld refinement, X-ray photoelectron spectroscopy (XPS), photoluminescence (PL), cathodoluminescence (CL), decay lifetimes, and PL quantum yields (QYs) were utilized to characterize the phosphors. The pure crystalline phase of as-prepared samples has been demonstrated via XRD measurement and Rietveld refinements. XPS reveals that the Eu(2+)/Tb(3+)/Mn(2+) can be efficiently doped into the crystal lattice. NCMPO:Eu(2+)/Tb(3+)/Mn(2+) phosphors can be effectively excited under UV radiation, which show tunable color from purple-blue to red including white emission based on energy transfer from Eu(2+) to Tb(3+)/Mn(2+) ions. Under low-voltage electron beam bombardment, the NCMPO:A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) display their, respectively, characteristic emissions with different colors, and the CL spectrum of NCMPO:0.04Tb(3+) has the comparable intensity to the ZnO:Zn commercial product. In addition, the calculated CIE coordinate of NCMPO:0.04Tb(3+) (0.252, 0.432) is more saturated than it (0.195, 0.417). These results reveal that NCMPO:A (A = Eu(2+)/Tb(3+)/Mn(2+), Dy(3+)) may be potential candidate phosphors for WLEDs and FEDs.

Hydrothermal synthesis, characterization, and luminescence of Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers

Energy Technology Data Exchange (ETDEWEB)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin, E-mail: huang@suda.edu.cn [Soochow University, State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science (China); Chen, Cuili; Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

2016-04-15

Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca{sub 2}B{sub 2}O{sub 5}:Eu{sup 3+} nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca{sub 2}B{sub 2}O{sub 5}:Tb{sup 3+} nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu{sup 3+}-, Tb{sup 3+}-, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers, respectively. It is suggested that Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers could be an efficient phosphor for lighting and display.

Magnetism of cyano-bridged Ln3+-M3+ complexes. Part II: one-dimensional complexes (Ln3+ = Eu, Tb, Dy, Ho, Er, Tm; M3+ = Fe or Co) with bpy as blocking ligand.

Science.gov (United States)

Figuerola, Albert; Ribas, Joan; Casanova, David; Maestro, Miguel; Alvarez, Santiago; Diaz, Carmen

2005-10-03

The reaction of Ln(NO3)3(aq) with K3[Fe(CN)6] or K3[Co(CN)6] and 2,2'-bipyridine in water/ethanol led to 13 one-dimensional complexes: trans-[M(CN)4(mu-CN)2Ln(H2O)4(bpy)]n.4nH2O.1.5nbpy (Ln = Eu3+, Tb3+, Dy3+, Ho3+, Er3+, Tm3+, Lu3+; M = Fe3+, Co3+). The structures for [EuFe]n (1), [TbFe]n (2), [DyFe]n (3), [HoFe]n (4), [ErFe]n (5), [TmFe]n (6), [LuFe]n (7), [EuCo]n (8), [TbCo]n (9), [DyCo]n (10), [HoCo]n (11), [ErCo]n (12), and [TmCo]n (13) have been solved: they crystallize in the triclinic space group P and are isomorphous. They exhibit a supramolecular architecture created by the interplay of coordinative, hydrogen bonding, and pi-pi interactions. A stereochemical study of the eight-vertex polyhedra of the lanthanide ions, based on continuous shape measures, is presented. The Ln3+-Fe3+ interaction is antiferromagnetic in [DyFe]n and [TbFe]n. For [EuFe]n, [HoFe]n, [ErFe]n, and [TmFe]n, there is no sign of any significant interaction. The magnetic behavior of [DyFe]n suggests the onset of weak long-range ferromagnetic ordering at 2.5 K.

Optical anisotropy of quasi-1D rare-earth silicide nanostructures on Si(001)

Energy Technology Data Exchange (ETDEWEB)

Chandola, S., E-mail: sandhya.chandola@isas.de [Leibniz-Institut für Analytische Wissenschaften – ISAS – e.V., Schwarzschildstraße 8, 12489 Berlin (Germany); Speiser, E.; Esser, N. [Leibniz-Institut für Analytische Wissenschaften – ISAS – e.V., Schwarzschildstraße 8, 12489 Berlin (Germany); Appelfeller, S.; Franz, M.; Dähne, M. [Institut für Festkörperphysik, Technische Universität Berlin, Hardenbergstraße 36, 10623 Berlin (Germany)

2017-03-31

Highlights: • Reflectance anisotropy spectroscopy (RAS) is capable of distinguishing optically between the semiconducting wetting layer and the metallic nanowires of rare earth (Tb and Dy) silicide nanostructures grown on vicinal Si(001). • The spectra of the wetting layer show a distinctive line shape with a large peak appearing at 3.8 eV, which is assigned to the formation of 2 × 3 and 2 × 4-like subunits of the 2 × 7 reconstruction. The spectra of the metallic nanowires show peaks at the E{sub 1} and E{sub 2} transitions of bulk Si which is assigned to strong substrate strain induced by the nanowires. • The optical anisotropy of the Tb nanowires is larger than for the Dy nanowires, which is related to the preferential formation of more strained bundles as well as larger areas of clean Si surfaces in the case of Tb. • RAS is shown to be a powerful addition to surface science techniques for studying the formation of rare-earth silicide nanostructures. Its surface sensitivity and rapidity of response make it an ideal complement to the slower but higher resolution of scanning probes of STM and AFM. - Abstract: Rare earth metals are known to interact strongly with Si(001) surfaces to form different types of silicide nanostructures. Using STM to structurally characterize Dy and Tb silicide nanostructures on vicinal Si(001), it will be shown that reflectance anisotropy spectroscopy (RAS) can be used as an optical fingerprint technique to clearly distinguish between the formation of a semiconducting two-dimensional wetting layer and the metallic one-dimensional nanowires. Moreover, the distinctive spectral features can be related to structural units of the nanostructures. RAS spectra of Tb and Dy nanostructures are found to show similar features.

Synthesis, luminescence, and energy-transfer properties of β-Na2Ca4(PO4)2(SiO4):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors.

Science.gov (United States)

Li, Kai; Shang, Mengmeng; Geng, Dongling; Lian, Hongzhou; Zhang, Yang; Fan, Jian; Lin, Jun

2014-07-07

A series of β-Na2Ca4(PO4)2(SiO4) (β-NCPS):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors were prepared via a high-temperature solid-state reaction route. The X-ray diffraction, Fourier transform infrared, photoluminescence (PL), cathodoluminescence (CL) properties, fluorescent lifetimes, and absolute quantum yield were exploited to characterize the samples. Under UV radiation, the β-NCPS:Eu(2+) phosphors present bright green emissions, and the β-NCPS:Ce(3+) phosphors show strong blue emissions, which are attributed to their 4f(6)5d(1) → 4f(7) and 5d-4f allowed transitions, respectively. The β-NCPS:Ce(3+), Tb(3+) phosphors display intense tunable color from blue to green and high absolute quantum yields (81% for β-NCPS:0.12Ce(3+) and 83% for β-NCPS:0.12Ce(3+), 0.08Tb(3+)) when excited at 365 nm. Simultaneously, the energy transfer from Ce(3+) to Tb(3+) ions is deduced from the spectral overlap between Ce(3+) emission and Tb(3+) excitation spectra and demonstrated by the change of emission spectra and decay lifetimes. Moreover, the energy-transfer mechanism from Ce(3+) to Tb(3+) ions is confirmed to be exchange interaction according to the discussion of expression from Dexter and Reisfeld. Under a low-voltage electron-beam excitation, the β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors exhibit their characteristic emissions, and the emission profiles of β-NCPS:Ce(3+),Tb(3+) phosphors are obviously different from those of the PL spectra; this difference might be ascribed to their different luminescence mechanisms. These results in PL and CL properties suggest that β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors are potential candidates for solid-state lighting and field-emission displays.

Isomerization of butene-1 on rare earth oxides. [Rare earths: La, Nd, Dy

Energy Technology Data Exchange (ETDEWEB)

Khodakov, Yu S; Nesterov, V K; Minachev, Kh M [AN SSSR, Moscow. Inst. Organicheskoj Khimii

1975-09-01

A study has been made into the isomerization of butene-1 on oxides of rare-earth elements. The dependence of the reaction rate at 20/sup 0/C on the baking temperature of La and Nd oxides have the maximum at 700/sup 0/C. A decrease in the activity of these oxides after bakinq at 800/sup 0/C is observed, as well as during experiments at -30 deq C. In the case of Dy/sub 2/O/sub 3/, the activity at 20/sup 0/C increases gradually with Tsub(bak)=500 to 800/sup 0/C Zeolite 0.57LaNaY exhibits maximum activity at Tsub(bak)=500/sup 0/C Similar data as to the effect of the baking temperature on the catalyst activity were obtained earlier for hydrogenation of ethylene. According to their maximum activity, oxides of rare-earth elements, in the isomerization as well as hydrogenation reactions, can be arranged as follows: La/sub 2/O/sub 3/>Nd/sub 2/O/sub 3/<Dy/sub 2/O/sub 3/. LaNaY has a lower activity, with respect to La/sup 3 +/ cation, than La/sub 2/O/sub 3/. The Na-form of zeolite Y was not active. The regularities of variation in the catalytic activity of La, Nd, Dy oxides and zeolite 0.57LaNaY in the reactions of double bond shift in butenes and hydroqenation of ethylene are similar.

Thermochemical properties of lanthanoid-iron-perovskite at high temperatures. [La, Nd, Sm, Eu, Gd, Tb, Dy

Energy Technology Data Exchange (ETDEWEB)

Katsura, T; Kitayama, K; Sugihara, T [Tokyo Inst. of Tech. (Japan). Faculty of Science; Kimizuka, N

1975-06-01

The standard Gibbs energy of formation of C/sup -/FeO/sub 3/(C/sup -/=La, Nd, Sm, Eu, Gd, Tb, and Dy) from metallic iron, C/sub 2//sup -/O/sub 3/, and oxygen has been determined at temperatures from 1473 to 1673 K. Based on the free-energy data, the heat of reaction and the entropy change resulting from the reaction have been calculated. The values of the heat of reaction of LaFeO/sub 3/, NdFeO/sub 3/, SmFeO/sub 3/, EuFeO/sub 3/, and GdFeO/sub 3/ (the first group) were identical, - 107 kcal/mol, at the present temperature interval. However, the values of the heat of reaction of TbFeO/sub 3/ and DyFeO/sub 3/ (the second group) decreased with an increase in the temperature. The entropy change of each reaction in the first group was constant, independent of the temperature, and each value decreased in the sequence from LaFeO/sub 3/ to GdFeO/sub 3/. The entropy change of the second group decreased with an increase in the temperature. The change of the standard Gibbs energy was intimately related to the ionic radii of C/sup -/-ions, and the relationship between the Gibbs energy and the tolerance factor has been clarified.

Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

Energy Technology Data Exchange (ETDEWEB)

Mishra, A; Singh, M P; Singh, V K

1982-05-01

The nitrato-complexes, (Y(PyBzH)/sub 2/(NO/sub 3/)/sub 2/)NO/sub 3/.H/sub 2/O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole) are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm/sup -1/cm/sup 2/mol/sup -1/) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the positive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C/sub 2/v) and uncoordinated (D/sub 3/h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms.

Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

International Nuclear Information System (INIS)

Mishra, A.; Singh, M.P.; Singh, V.K.

1982-01-01

The nitrato-complexes, [Y(PyBzH) 2 (NO 3 ) 2 ]NO 3 .H 2 O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole] are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm -1 cm 2 mol -1 ) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the terpositive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C 2 v) and uncoordinated (D 3 h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms. (author)

Predictable self-assembled [2×2] Ln(III)4 square grids (Ln = Dy,Tb)-SMM behaviour in a new lanthanide cluster motif.

Science.gov (United States)

Anwar, Muhammad Usman; Thompson, Laurence Kenneth; Dawe, Louise Nicole; Habib, Fatemah; Murugesu, Muralee

2012-05-14

The ditopic carbohydrazone ligand (L1) produces the square, self-assembled [2×2] grids [Dy(4)(L1)(4)(OH)(4)]Cl(2) (1) and [Ln(4)(L1)(4)(μ(4)-O)(μ(2)-1,1-N(3))(4)] (Ln = Dy (2), Tb (3)), with 2 exhibiting SMM behaviour. Two relaxation processes occur with U(eff) = 51 K, 91 K in the absence of an external field, and one with U(eff) = 270 K in the presence of a 1600 Oe optimum field. This journal is © The Royal Society of Chemistry 2012

Fluorination of chlorocomplexes of some rare earths by xenon difluoride. [None

Energy Technology Data Exchange (ETDEWEB)

Kiselev, Yu.M.; Goryachenkov, S.A.; Martynenko, L.I. (Moskovskij Gosudarstvennyj Univ. (USSR))

1984-01-01

The results of studying the XeF/sub 2/ reaction with anhydrous hexachlorocomplexes of some RE(3) (Ce, Pr, Nd, Tb, Dy, Er, Yb) are presented. It is shown that cesium rare earth hexachlorocomplexes react with xenon difluoride at 100-400 deg C with complex formation of the Cs/sub 3/M/sup 4/F,L7 (M=Ce, Pr, Tb, Nd, Dy) composition. In case of Er and Yb under the same conditions only flouride RE derivatives corresponding to the Cs/sub 3/MF/sub 6/ formula are obtained. Possible mechanism of the process is discussed.

Theoretical investigations on magnetic entropy change in amorphous and crystalline systems: Applications to RAg (R=Tb, Dy, Ho) and GdCuAl

Energy Technology Data Exchange (ETDEWEB)

Ranke, P.J. von, E-mail: von.ranke@uol.com.br [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil); Nóbrega, E.P. [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil); Caldas, A. [Sociedade Unificada de Ensino Superior e Cultura, SUESC, 20211-351 Rio de Janeiro, RJ (Brazil); Alho, B.P. [Instituto de Aplicação Fernando Rodrigues da Silveira, Universidade do Estado do Rio de Janeiro, Rua Santa Alexandrina, 288, 20260-232 RJ (Brazil); Ribeiro, P.O.; Alvarenga, T.S.T.; Lopes, P.H.O.; Sousa, V.S.R. de [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil); Carvalho, A. Magnus G. [Laboratório Nacional de Luz Síncrotron, CNPEM, 13083-970 Campinas, SP (Brazil); Oliveira, N.A. de [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil)

2014-11-15

We report theoretical investigations on the magnetic entropy changes in amorphous systems through two different assumptions. In the first assumption, the HPZ-anisotropic model is considered to deal with the random direction of magnetic moments, where the amorphous RAg (R=Tb, Dy and Ho) were used as prototypes systems. In the second assumption, the amorphisation is parameterized through the exchange interaction distribution and GdCuAl, in amorphous and crystalline structures, were considered as prototypes systems. Comparisons between the magnetic entropy changes under amorphisation and under the usual magnetic field variation were performed. The model reveals the dependence of refrigerant capacity on the amorphisation parameter, and an optimum amorphisation parameter was calculated. - Highlights: • Theoretical investigation on RAg (R=Tb, Dy and Ho) and GdCuAl amorphous alloys. • Magnetic entropy changes in GdCuAl in both amorphous and crystalline structures. • The refrigerant capacity was compared in both amorphous and crystalline phases.

A single crystal study of RE{sub 14}Co{sub 3}In{sub 3} (RE = Y, Tb, Dy, Ho, Er)

Energy Technology Data Exchange (ETDEWEB)

Zaremba, V.I.; Kalychak, Y.M.; Dzevenko, M.V. [Inorganic Chemistry Dept., Ivan Franko National Univ. of Lviv (Ukraine); Rodewald, U.Ch.; Heying, B.; Poettgen, R. [Inst. fuer Anorganische und Analytische Chemie, Westfaelische Wilhelms-Univ. Muenster (Germany)

2006-01-01

The rare earth-cobalt-indides RE{sub 14}Co{sub 3}In{sub 3} (RE = Y, Tb, Dy, Ho, Er) were prepared in polycrystalline form from the elements by arc-melting. Small single crystals were grown through a special annealing sequence. The compounds were investigated on the basis of X-ray powder and single crystal data: Lu{sub 14}Co{sub 2}In{sub 3} (Gd{sub 14}Co{sub 3}In{sub 2.7}) type, P4{sub 2}/nmc, Z = 4, a = 959.0(1), c = 2319.1(5) pm, wR2 = 0.055, 2289 F{sup 2} values, 65 variables for Y{sub 13.90}Co{sub 2.99}In{sub 3.02}, a = 953.8(1), c = 2315.8(5) pm, wR2 = 0.108, 2357 F{sup 2} values, 65 variables for Tb{sub 13.92}Co{sub 3.01}In{sub 2.92}, a = 949.24(3), c = 2296.5(1) pm, wR2 = 0.129, 2518 F{sup 2} values, 65 variables for Dy{sub 13.90}Co{sub 2.97}In{sub 2.95}, a = 946.3(1), c = 2289.0(5) pm, wR2 = 0.099, 2297 F{sup 2} values, 64 variables for Ho{sub 14}Co{sub 2.80}In{sub 2.89}, and a = 941.0(1), c = 2274.2(5) pm, wR2 = 0.140, 2450 F{sup 2} values, 65 variables for Er{sub 13.83}Co{sub 2.88}In{sub 3.10}. All RE{sub 14}Co{sub 3}In{sub 3} indides show a small degree of In/Co mixing (between 7 and 16% Co) on the 4c In1 site and defects on the 8g Co1 positions (between 84 and 95% Co). Except for the holmium compound, the RE{sub 14}Co{sub 3}In{sub 3} intermetallics also reveal RE/In mixing on the 4c RE1 sites, leading to the refined compositions. The seven crystallographically independent RE sites have between 9 and 10 nearest RE neighbors. The RE{sub 14}Co{sub 3}In{sub 3} structures consist of a complex intergrowth of rare earth based polyhedra. Both cobalt sites have a distorted trigonal-prismatic rare earth coordination. An interesting feature is the In2-In2 dumb-bell with an In2-In2 distance of 300 pm (for Ho{sub 14}Co{sub 2.80}In{sub 2.89}). The crystal chemistry of the RE{sub 14}Co{sub 3}In{sub 3} indides is discussed. (orig.)

Magnetostriction of rare earth-Fe2 Laves phase compounds

International Nuclear Information System (INIS)

Clark, A.E.; Abbundi, R.; Savage, H.T.

1977-01-01

Single crystal magnetostriction measurements were made as a function of temperature on TbFe 2 and DyFe 2 . From these, the intrinsic magnetoelastic coupling coefficients were determined for the rare earth-Fe 2 compounds. Employing X-ray techniques, certain multicomponent rare earth-Fe 2 compounds were identified to maximize the magnetostriction to anisotropy ratio. (Auth.)

Effect of Al-R (R = Dy or Tb) master alloys addition on the properties of magnets made of Nd14.7R1.3Fe75Co2B7

International Nuclear Information System (INIS)

Savchenko, A.G.; Ryazantsev, V.A.; Skuratovskij, Yu.E.; Lileev, A.S.; Menushenkov, V.P.

2000-01-01

The hysteresis characteristics of caked constant magnets of the (Nd, R)-(Fe, Co)-B system alloys with the Al-R master easily-melting additions, wherein R is Dy or Tb, are studied. High efficiency of the mixture method by obtaining highly-coercive constant magnets on the basis of the studied systems alloys is shown. The hysteresis properties of the caked constant magnets may be changed within sufficiently wide limits by varing the number and composition of the alloys mixture components. The effect of the Al-Dy and Al-Tb additions on properties of constant magnets of uniform nominal composition is compared. Higher efficiency of master alloys on the Tb basis is noted; the coercive force and energy characteristics of this series of caked constant magnets is higher [ru

A family of rare-earth-based single chain magnets: playing with anisotropy.

Science.gov (United States)

Bernot, Kevin; Bogani, Lapo; Caneschi, Andrea; Gatteschi, Dante; Sessoli, Roberta

2006-06-21

The first family of rare-earth-based single chain magnets is presented. Compounds of general formula [M(hfac)3(NITPhOPh)], where M = Eu, Gd, Tb, Dy, Ho, Er, or Yb, and PhOPh is the nitronyl-nitroxide radical (2,4'-benzoxo-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide), have been structurally characterized and found to be isostructural. The characterization of both static and dynamic magnetic properties of the whole family is reported. Dy, Tb, and Ho compounds display slow relaxation of the magnetization, and ac susceptibility shows a thermally activated regime with energy barriers of 69, 45, and 34 K for Dy, Tb, and Ho compounds, respectively, while only a frequency-dependent susceptibility is observed for Er below 2.0 K. In Gd and Yb derivatives, antiferromagnetic interactions dominate. The pre-exponential factors differ by about 4 orders of magnitude. Finite size effects, due to naturally occurring defects, affect the static and dynamic properties of the compounds differently.

Structure and spectroscopy of rare earth – Doped lead phosphate glasses

International Nuclear Information System (INIS)

Pisarski, Wojciech A.; Żur, Lidia; Goryczka, Tomasz; Sołtys, Marta; Pisarska, Joanna

2014-01-01

Highlights: • Lead phosphate glasses doped with rare earth ions were prepared. • The local structure was examined using X-ray diffraction and spectroscopic methods. • Different structural phosphate groups are present in lead phosphate glasses. • The electron–phonon coupling strength and phonon energy of the glass host was determined. • Several observed emission bands are due to 4f–4f electronic transitions of rare earth ions. -- Abstract: Lead–gallium phosphate glasses doped with rare the earth ions (Eu 3+ , Dy 3+ , Tb 3+ , Er 3+ ) were synthesized. The structure of obtained glasses was examined by means of use: X-ray diffraction (XRD), nuclear magnetic resonance ( 207 Pb and 31 P NMR), fourier transform infrared (FT-IR) and Raman spectroscopy. In contrast to fully amorphous Ln-doped samples (Ln = Eu, Dy, Tb), in Er-doped sample the GaPO 4 crystalline phase was identified. It was found from the NMR, FT-IR and Raman spectroscopic techniques that, different structural phosphate groups were present in lead phosphate glasses. Based on absorption measurements, the UV–VIS cut-off wavelength for lead phosphate glass was determined and its value is close to 305 nm. Excitation and emission spectra of rare earths were also detected. From excitation spectra of Eu 3+ the electron–phonon coupling strength and phonon energy of the glass host were determined. Due to 4f 6 –4f 6 (Eu 3+ ), 4f 8 –4f 8 (Tb 3+ ), 4f 9 –4f 9 (Dy 3+ ) and 4f 11 –4f 11 (Er 3+ ) electronic transitions of trivalent rare earth ions several luminescence bands were stated

Measurement of formation cross sections of short-lived nuclei by 14 MeV neutron. Nd, Sm, Dy, Er, Yb

Energy Technology Data Exchange (ETDEWEB)

Sakane, H.; Yamamoto, H.; Kawade, K. [Nagoya Univ. (Japan). School of Engineering; Iida, T.; Takahashi, A.

1997-03-01

Eight neutron activation cross sections producing the nuclei with half-lives between 3 min and 24 min were obtained at the energy range between 13.4 and 14.9 MeV by activation method. The cross sections were {sup 146}Nd(n,p){sup 146}Pr, {sup 154}Sm(n,{alpha}){sup 151}Nd, {sup 162}Dy(n,p){sup 162}Tb, {sup 163}Dy(n,np){sup 162}Tb, {sup 163}Dy(n,p){sup 163}Tb, {sup 164}Dy(n,p){sup 164}Tb, {sup 170}Er(n,{alpha}){sup 167}Dy, {sup 174}Yb(n,p){sup 170}Tm. {sup 163}Dy(n,np){sup 162}Tb (T{sub 1/2}=7.7 min) was obtained for the first time. Present results are compared with previous results and the evaluated data of JENDL-3 and ENDF/B-VI. There are some discrepancies between present results and the JENDL-3 and ENDF/B-VI. (author)

Microstructural, magnetic and magnetostrictive properties of Tb0.3Dy0.7Fe1.95 prepared by solidification in a high magnetic field

International Nuclear Information System (INIS)

Liu Tie; Liu Yin; Wang Qiang; Gao Pengfei; He Jicheng; Iwai, Kazuhiko

2013-01-01

The microstructure evolution and magnetization and magnetostriction properties of Tb 0.3 Dy 0.7 Fe 1.95 alloy solidified in a high magnetic field were investigated. A cellular microstructure was produced, with the grains highly aligned along the direction of the magnetic field. The (Tb,Dy)Fe 2 phase was highly oriented, with its 〈1 1 1〉 axis along the magnetic field direction. The easy magnetization direction of the alloy lay along the magnetic field direction. The magnetostriction at room temperature significantly increased to double that of the sample prepared without high magnetic field; in addition, a sharp rise in the initial magnetostriction at low fields was observed. Applying a high magnetic field during the solidification process is proposed as an effective route for fabricating 〈1 1 1〉 oriented Tb–Dy–Fe compounds, and improving their magnetic and magnetostrictive properties. (paper)

Journal of Earth System Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

The rare earth elements like La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and the heavy metals like Mg, V, Cr, Mn, Fe, Cu, Zn, U, Th were analysed by using standard analytical methods. The Post-Archean Australian Shale composition was used to normalise the rare earth elements. It was found that the sediments ...

Search for excited superdeformed bands in {sup 151}Dy

Energy Technology Data Exchange (ETDEWEB)

Nisius, D.; Janssens, R.V.F.; Crowell, B. [and others

1995-08-01

Following the first report of superdeformed (SD) bands with identical transition energies in the pairs ({sup 151}Tb*,{sup 152}Dy), ({sup 150}Gd*, {sup 151}Tb) and ({sup 153}Dy*, {sup 152}Dy) (where * denotes an excited SD band), it was proposed by Nazarewicz et al. that the observations could be understood in a strong-coupling approach if pseudo SU(3) symmetry were invoked. In this model there are three limiting values of the decoupling parameter; i.e. a = 0, {plus_minus}1. In the first two cases mentioned above the pairs of bands have nearly identical transition energies and are interpreted as proton excitations involving the [200]1/2 pseudospin orbital coupled to the {sup 152}Dy core, for which the value of the decoupling parameter is calculated to be a =+1.

Crystal structure of RCoIn5 (R - Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Y) and R2CoIn8 (R - Ce, Pr, Nd, Sm, Gd, Dy, Ho, Er, Tm, Y) compounds

International Nuclear Information System (INIS)

Kalychak, Ya.M.; Zaremba, V.I.; Baranyak, V.M.; Bruskov, V.A.; Zavalij, P.Yu.

1989-01-01

Usng X-ray diffraction method of monocrystal, crystal structure of HoCoIn 5 compound belonging to the HoCoGa 5 structural type is determined. Using the method of powder belonging of CeCoIn 5 structure to the HoCoGa 5 structural type is confirmed. Isostructural compounds with Y, Pr, Nd, Sm, Gd, Tb, Dy are detected. Their lattice periods are determined. Using the method of powder belonging of Ce 2 CoIn 8 compound structure to Ho 2 CoGa 8 structural type is determined. Isostructural compounds with Y, Pr, Nd, Sm, Gd, Dy, Ho, Er, Tm are detected and their lattice periods are determined

HfO2 - rare earth oxide systems in the region with high content of rare earth oxide

International Nuclear Information System (INIS)

Shevchenko, A.V.; Lopato, L.M.

1982-01-01

Using the methods of annealing and hardenings (10 2 -10 4 deg/s cooling rate) and differential thermal analysis elements of state diagrams of HfO 2 - rare earth oxide (rare earths-La, Pr, Nd, Sm, Gd, Tb, Dy, Y, Er, Yb, Lu, Sc) systems from 1800 deg C up to melting in the range of 60-100 mol% rare earth oxide concentration were constructed. Regularities of HfQ 2 addition effect on high-temperature polymorphic transformations of rare earth oxides were studied. Results of investigation were discussed from viewpoint of crystal chemistry

Competing exchange interactions and their relevance for the magnetisation process in RMn6-xCrxSn6 powders (R=Y, Gd, Tb, Dy, Ho, Er)

International Nuclear Information System (INIS)

Brabers, J.H.V.J.; Zhou, G.F.; Colpa, J.H.P.; Buschow, K.H.J.; De Boer, F.R.

1994-01-01

The free-powder magnetisation of RMn 6-x Cr x Sn 6 compounds has been measured for compounds with R=Y, Gd, Tb, Dy, Ho, Er in fields up to 38 T, and interpreted in terms of a simple model, which is also outlined in this paper. From the measurements, estimates for the R-3d mean-field coupling constant (n RT ) could be derived for the cases where R=Gd, Tb, Dy, Ho, Er. In turn, the n RT values can be related to the microscopic spin-coupling constant (J RT ). In the case of YMn 6 Sn 6 the high-field measurement presents evidence for a very weak antiferromagnetic coupling between the Mn layers. Furthermore, values for the Mn moments (μ Mn ) were also derived from the magnetisation measurements. The estimated μ Mn values are of the order of 2.0 μ B . ((orig.))

On the single-ion Magnetic Anisotropy of the Rare-Earth Metals

DEFF Research Database (Denmark)

Kolmakova, N.P.; Tishin, A.M.; Bohr, Jakob

1996-01-01

The temperature dependences of the single-ion magnetic anisotropy constants for Tb and Dy metals are calculated in terms of the multipole moments of the rare-earth ions utilizing the available crystal-field parameters. The results are compared with the existing experimental data....

The Rare Earth Magnet Industry and Rare Earth Price in China

Directory of Open Access Journals (Sweden)

Ding Kaihong

2014-07-01

Full Text Available In the past four years, the price of rare earth metal fluctuates sharply for many reasons. Currently, it has become more stable and more reasonable. This presentation is focused on the effect about the rare earth metal price. Some motor manufacturers have shifted from rare earth permanent magnet to ferrite magnet. Many motor manufacturers changed the design for the motor cooling system to make the motor function at a lower temperature. Thus the consumption of Dy can be markedly reduced. As for manufacturer of NdFeB magnet, we are also trying to optimize our process to reduce to dependence of HREE such as Dy and Tb. HS process have been introduced to solve the problem. With more and more people focusing and engaging on the REE industry, the price of REE will be more transparent without too many fluctuations. China is considering the problems of balancing the environment, energy sources, and labor sources. The application field about NdFeB such as wind turbine generator, HEV/EV, FA /OA is flourishing.

The Rare Earth Magnet Industry and Rare Earth Price in China

Science.gov (United States)

Ding, Kaihong

2014-07-01

In the past four years, the price of rare earth metal fluctuates sharply for many reasons. Currently, it has become more stable and more reasonable. This presentation is focused on the effect about the rare earth metal price. Some motor manufacturers have shifted from rare earth permanent magnet to ferrite magnet. Many motor manufacturers changed the design for the motor cooling system to make the motor function at a lower temperature. Thus the consumption of Dy can be markedly reduced. As for manufacturer of NdFeB magnet, we are also trying to optimize our process to reduce to dependence of HREE such as Dy and Tb. HS process have been introduced to solve the problem. With more and more people focusing and engaging on the REE industry, the price of REE will be more transparent without too many fluctuations. China is considering the problems of balancing the environment, energy sources, and labor sources. The application field about NdFeB such as wind turbine generator, HEV/EV, FA /OA is flourishing.

Transmission electron microscopic study of pyrochlore to defect-fluorite transition in rare-earth pyrohafnates

Energy Technology Data Exchange (ETDEWEB)

Karthik, Chinnathambi, E-mail: Karthikchinnathambi@boisestate.edu [Department of Materials Science and Engineering, Boise State University, 1910 University drive, Boise, ID 83725 (United States); Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 83415 (United States); Anderson, Thomas J. [Department of Materials Science and Engineering, Boise State University, 1910 University drive, Boise, ID 83725 (United States); Gout, Delphine [Oak Ridge National Lab, Neutron Scattering Science Division, Oak Ridge, TN (United States); Ubic, Rick [Department of Materials Science and Engineering, Boise State University, 1910 University drive, Boise, ID 83725 (United States); Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 83415 (United States)

2012-10-15

A structural transition in rare earth pyrohafnates, Ln{sub 2}Hf{sub 2}O{sub 7} (Ln=Y, La, Pr, Nd, Tb, Dy, Yb and Lu), has been identified. Neutron diffraction showed that the structure transforms from well-ordered pyrochloric to fully fluoritic through the lanthanide series from La to Lu with a corresponding increase in the position parameter x of the 48f (Fd3{sup Macron }m) oxygen site from 0.330 to 0.375. As evidenced by the selected area electron diffraction, La{sub 2}Hf{sub 2}O{sub 7}, Pr{sub 2}Hf{sub 2}O{sub 7} and Nd{sub 2}Hf{sub 2}O{sub 7} exhibited a well-ordered pyrocholoric structure with the presence of intense superlattice spots, which became weak and diffuse (in Dy{sub 2}Hf{sub 2}O{sub 7} and Tb{sub 2}Hf{sub 2}O{sub 7}) before disappearing completely as the series progressed towards the Lu end. High resolution electron microscopic studies showed the breakdown of the pyrochlore ordering in the form of antiphase domains resulting in diffused smoke-like superlattice spots in the case of Dy{sub 2}Hf{sub 2}O{sub 7} and Tb{sub 2}Hf{sub 2}O{sub 7}. - Graphical abstract: Transmission electron microscopic studies showed the ordered pyrochlore to defect fluorite transition in rare-earth pyrohafnates to occur via the formation of anti-phase domains to start with. Highlights: Black-Right-Pointing-Pointer Pyrochlore to fluorite structural transition in rare earth pyrohafnates. Black-Right-Pointing-Pointer La{sub 2}Hf{sub 2}O{sub 7}, Pr{sub 2}Hf{sub 2}O{sub 7} and Nd{sub 2}Hf{sub 2}O{sub 7} showed well ordered pyrochlore structure. Black-Right-Pointing-Pointer Short range ordering in Dy{sub 2}Hf{sub 2}O{sub 7} and Tb{sub 2}Hf{sub 2}O{sub 7}. Black-Right-Pointing-Pointer Break down of pyrochlore ordering due to antiphase boundaries. Black-Right-Pointing-Pointer Rest of the series showed fluoritic structure.

Rare earth-rich cadmium compounds RE{sub 10}TCd{sub 3} (RE = Y, Tb, Dy, Ho, Er, Tm, Lu; T = Rh, Pd, Ir, Pt) with an ordered Co{sub 2}Al{sub 5}-type structure

Energy Technology Data Exchange (ETDEWEB)

Block, Theresa; Klenner, Steffen; Heletta, Lukas; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2018-04-01

Eighteen new rare earth-rich intermetallic phases RE{sub 10}TCd{sub 3} (RE = Y, Tb, Dy, Ho, Er, Tm, Lu; T = Rh, Pd, Ir, Pt) were obtained by induction melting of the elements in sealed niobium ampoules followed by annealing in muffle furnaces. All samples were characterized by X-ray powder diffraction. The structures of four representatives were refined from single-crystal X-ray diffractometer data: ordered Co{sub 2}Al{sub 5} type, P6{sub 3}/mmc, a = 951.2(1), c = 962.9(2) pm, wR = 0.0460, 595 F{sup 2} values, 20 parameters for Er{sub 10}RhCd{sub 3}; a = 945.17(4), c = 943.33(4), wR = 0.0395, 582 F{sup 2} values, 21 parameters for Lu{sub 9.89}PdCd{sub 3.11}; a = 964.16(6), c = 974.93(6) pm, wR = 0.0463, 614 F{sup 2} values, 21 parameters for Y{sub 10}Ir{sub 1.09}Cd{sub 2.91}; a = 955.33(3), c = 974.56(3) pm, wR = 0.0508, 607 F{sup 2} values, 22 refined parameters for Dy{sub 9.92}IrCd{sub 3.08}. Refinements of the occupancy parameters revealed small homogeneity ranges resulting from RE/Cd, respectively T/Cd mixing. The basic building units of the RE{sub 10}TCd{sub 3} phases are transition metal-centered RE{sub 6} trigonal prisms (TP) that are condensed with double-pairs of empty RE{sub 6} octahedra via common triangular faces. A second type of rods is formed by slightly distorted RE3 rate at Cd{sub 6}RE{sub 6} icosahedra which are condensed via Cd{sub 3} triangular faces. The shortest interatomic distances occur for RE-T, compatible with strong covalent bonding interactions. Temperature dependent magnetic susceptibility measurements were performed for RE{sub 10}RhCd{sub 3} (RE = Dy-Tm, Lu), RE{sub 10}IrCd{sub 3} (RE = Er, Tm, Lu) and RE{sub 10}PtCd{sub 3} (RE = Y, Lu). While Y{sub 10}PtCd{sub 3} and Lu{sub 10}TCd{sub 3} (T = Rh, Ir, Pt) show Pauli paramagnetic behavior, the compounds containing paramagnetic rare earth elements show Curie-Weiss behavior (the experimental magnetic moments indicate stable trivalent RE{sup 3+}) and magnetic ordering at low temperatures

Effects of rare earth oxide addition on NdFeB magnets

International Nuclear Information System (INIS)

Ohashi, K.; Yokoyama, T.; Tawara, Y.

1988-01-01

The effects of addition of rare-earth oxides on the magnetic properties of Nd-Fe-B sintered magnets are studied. The addition of Dy 2 O 3 and Tb 4 O 7 leads to an increase in intrinsic coercivity. For addition of Dy 2 O 3 , the optimum conditions for powder mixing and the optimum Dy 2 O 3 particle size were determined. A mixing time of more than 10 minutes, and a Dy 2 O 3 particle size of less than 3 μm, are required to obtain a high intrinsic coercivity. EPMA measurements of NdFeBAl magnets with Dy 2 O 3 added reveal an inhomogeneous distribution of Dy in the Nd 2 Fe 14 B matrix: the material is Dy-rich near grain boundaries, but Dy-poor within the matrix. The appearance of such an inhomogeneous distribution of Dy is attributed to the reduction of Dy 2 O 3 in the Nd-rich phases, followed by diffusion of the resulting Dy atoms into the matrix

Oxygen stabilized rare-earth iron intermetallic compounds

International Nuclear Information System (INIS)

Dariel, M.P.; Malekzadeh, M.; Pickus, M.R.

1975-10-01

A new, oxygen-stabilized intermetallic compound was identified in sintered, pre-alloyed rare-earth iron powder samples. Its composition corresponds to formula R 12 Fe 32 O 2 and its crystal structure belongs to space group Im3m. The presence of these compounds was observed, so far, in several R--Fe--O systems, with R = Gd, Tb, Dy, Ho, Er, and Y

Structural, spectral, dielectric and magnetic properties of Tb–Dy doped Li-Ni nano-ferrites synthesized via micro-emulsion route

Energy Technology Data Exchange (ETDEWEB)

Junaid, Muhammad, E-mail: junaid.malik95@yahoo.com [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Khan, Muhammad Azhar, E-mail: azhar.khan@iub.edu.pk [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Iqbal, F. [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Murtaza, Ghulam [Centre for Advanced Studies in Physics, Government College University, Lahore 54000 (Pakistan); Akhtar, Majid Niaz; Ahmad, Mukhtar [Department of Physics, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Shakir, Imran [Deanship of scientific research, College of Engineering, King Saud University, PO Box 800, Riyadh 11421 (Saudi Arabia); Warsi, Muhammad Farooq [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan)

2016-12-01

Terbium (Tb) and dysprosium (Dy) doped lithium-nickel nano-sized ferrites (Li{sub 0.2}Ni{sub 0.8}Tb{sub 0.5x}Dy{sub 0.5x}Fe{sub 2−x}O{sub 4} where x=0.00−0.08) were prepared by micro-emulsion technique. The X-ray diffraction (XRD) patterns confirmed the single phase cubic spinel structure. The lattice constant was increased due to larger ionic radii of Tb{sup 3+} and Dy{sup 3+} cations. The crystallite size was found in the range 30–42 nm. The FTIR (Fourier transform infrared spectroscopy) spectra revealed two significant absorption bands (~400–600 cm{sup −1}) which indicate the formation of cubic spinel structure. The peaking behavior of dielectric parameters was observed beyond 1.5 GHz. The dielectric constant and dielectric loss were found to decrease by the increase of Tb–Dy contents and frequency. The doping of Tb and Dy in Li–Ni ferrites led to increase the coercive field (120–156 Oe). The smaller magnetic and dielectric parameters suggested the possible utility of these nano-materials in switching and microwave devices applications. - Highlights: • Li{sub 0.2}Ni{sub 0.8}Tb{sub 0.5x}Dy{sub 0.5x}Fe{sub 2-x}O{sub 4} ferrites were synthesized by micro-emulsion route. • Tb and Dy addition improves coercivity while decreased saturation magnetization. • These nanomaterials can be useful in microwave and switching devices applications.

Rare earth niobate coordination polymers

Science.gov (United States)

Muniz, Collin N.; Patel, Hiral; Fast, Dylan B.; Rohwer, Lauren E. S.; Reinheimer, Eric W.; Dolgos, Michelle; Graham, Matt W.; Nyman, May

2018-03-01

Rare-earth (RE) coordination polymers are infinitely tailorable to yield luminescent materials for various applications. Here we described the synthesis of a heterometallic rare-earth coordination compound ((CH3)2SO)3(RE)NbO(C2O4)3((CH3)2SO) = dimethylsulfoxide, DMSO, (C2O2= oxalate), (RE=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb). The structure was obtained from single crystal X-ray diffraction of the La analogue. The Nb˭O and DMSO terminal-bonding character guides assembly of an open framework structure with noncentrosymmetric RE-coordination geometry, and large spacing between the RE centers. A second structure was observed by PXRD for the smaller rare earths (Dy, Ho, Er, Yb); this structure has not yet been determined. The materials were further characterized using FTIR, and photoluminescence measurements. Characteristic excitation and emission transitions were observed for RE = Nd, Sm, Eu, and Tb. Quantum yield (QY) measurements were performed by exciting Eu and Tb analoges at 394 nm (QY 66%) and 464 nm (QY 71%) for Eu; and 370 nm (QY=40%) for Tb. We attribute the high QY and bright luminescence to two main structure-function properties of the system; namely the absence of water in the structure, and absence of concentration quenching.

Magnetic interactions in rhenium-containing rare earth double perovskites Sr{sub 2}LnReO{sub 6} (Ln=rare earths)

Energy Technology Data Exchange (ETDEWEB)

Nishiyama, Atsuhide; Doi, Yoshihiro; Hinatsu, Yukio, E-mail: hinatsu@sci.hokudai.ac.jp

2017-04-15

The perovskite-type compounds containing both rare earth and rhenium Sr{sub 2}LnReO{sub 6} (Ln=Y, Tb-Lu) have been prepared. Powder X-ray diffraction measurements and Rietveld analysis show that Ln{sup 3+} and Re{sup 5+} ions are structurally ordered at the B site of the perovskite SrBO{sub 3}. Magnetic anomalies are found in their magnetic susceptibility and specific heat measurements at 2.6–20 K for Ln=Y, Tb, Dy, Yb, Lu compounds. They are due to magnetic interactions between Re{sup 5+} ions. The results of the magnetic hysteresis and remnant magnetization measurements for Sr{sub 2}YReO{sub 6} and Sr{sub 2}LuReO{sub 6} indicate that the antiferromagnetic interactions between Re{sup 5+} ions below transition temperatures have a weak ferromagnetic component. The analysis of the magnetic specific heat data for Sr{sub 2}YbReO{sub 6} shows that both the Yb{sup 3+} and Re{sup 5+} ions magnetically order at 20 K. For the case of Sr{sub 2}DyReO{sub 6}, magnetic ordering of the Re{sup 5+} moments occurs at 93 K, and with decreasing temperature, the moments of Dy{sup 3+} ferromagnetically order at 5 K from the measurements of magnetic susceptibility and specific heat. - Graphical abstract: Crystal structure of double perovskite Sr{sub 2}LnReO{sub 6}. Red and black lines show cubic and monoclinic unit cells, respectively. - Highlights: • Double perovskites Sr{sub 2}LnReO{sub 6} (Ln=rare earths) were prepared. • They show an antiferromagnetic transition at 2.6–20 K. • In Sr{sub 2}DyReO{sub 6}, Dy and Re moments magnetically order at 5 and 93 K, respectively.

Microhardness of epitaxial layers of GaAs doped with rare earths

International Nuclear Information System (INIS)

Kulish, U.M.; Gamidov, Z.S.; Kuznetsova, I.Yu.; Petkeeva, L.N.; Borlikova, G.V.

1989-01-01

Results of the study of microhardness of GaAS layer doped by certain rare earths - Gd, Tb, Dy - are presented. The assumption is made that the higher is the value of the first potential of rare earth impurity ionization (i.e. the higher is the filling of 4f-shell), the lower is the effect of the element on electric and mechanical properties of GaAs epitaxial layers

Morphology and luminescence characteristics of combustion synthesized Y{sub 2}O{sub 3}: (Eu, Dy, Tb) nanoparticles with various amino-acid fuels

Energy Technology Data Exchange (ETDEWEB)

Mukherjee, S.; Sudarsan, V. [Chemistry Division Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Sastry, P.U.; Patra, A.K. [Solid State Physics Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Tyagi, A.K., E-mail: aktyagi@barc.gov.in [Chemistry Division Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India)

2014-01-15

Y{sub 2}O{sub 3} nanoparticles doped with Dy{sup 3+}, Eu{sup 3+} and Tb{sup 3+} together were prepared by the gel combustion method using a variety of amino acids namely, glycine, phenyl alanine, arginine, glutamic and aspartic acids. Number of carboxylate groups present in the amino acids used for combustion reaction was found to have strong influence on powder characteristics as well as luminescence from the samples. Based on small angle X-ray scattering studies, it is inferred that the nanoparticles prepared by using glycine and arginine as the fuels have smooth surface compared to those prepared using other amino acids. For the nanoparticles prepared using glutamic and aspartic acids, there exist a diffused pore-grain interface due to the lesser extent of heat generated in the reaction which leads to smaller particle size, poor crystallinity and improper burning of the organic materials. Lower surface area and smooth surface of the nanoparticles prepared using glycine leads to their improved luminescence properties. -- Highlights: • Surface smoothness of Y{sub 2}O{sub 3} (Dy, Eu, Tb) nanoparticles vary with amino acids. • Optimum luminescence intensity is observed when glycine is used as the fuel. • Diffused pore grain interface when glutamic and aspartic acids are used as fuels.

Rhodium-rich silicides RERh{sub 6}Si{sub 4} (RE=La, Nd, Tb, Dy, Er, Yb)

Energy Technology Data Exchange (ETDEWEB)

Vosswinkel, Daniel; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2017-07-01

Polycrystalline RERh{sub 6}Si{sub 4} (RE=La, Nd, Tb, Dy, Er, Yb) samples can be synthesized by arc-melting of the elements. Single crystals of LaRh{sub 6}Si{sub 4}, NdRh{sub 6}Si{sub 4} and YbRh{sub 6}Si{sub 4} were synthesized from the elements in bismuth fluxes (non-reactive flux medium). The structures were refined on the basis of single-crystal X-ray diffractometer data: LiCo{sub 6}P{sub 4} type, P anti 6m2, a=700.56(3), c=380.55(1) pm, wR2=0.0257, 317 F{sup 2} values, 19 variables for LaRh{sub 6}Si{sub 4}, a=698.4(5), c=377.7(2) pm, wR2=0.0578, 219 F{sup 2} values, 19 variables for NdRh{sub 6}Si{sub 4} and a=696.00(3), c=371.97(1) pm, wR2=0.0440, 309 F{sup 2} values, 19 variables for YbRh{sub 6}Si{sub 4}. The rhodium and silicon atoms build up three-dimensional, covalently bonded [Rh{sub 6}Si{sub 4}]{sup δ-} polyanionic networks with Rh-Si distances ranging from 239 to 249 pm. The rare earth atoms fill larger cavities within channels of these networks and they are coordinated by six silicon and twelve rhodium atoms in the form of hexa-capped hexagonal prisms.

Structural relative stabilities and pressure-induced phase transitions for lanthanide trihydrides REH{sub 3} (RE=Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu)

Energy Technology Data Exchange (ETDEWEB)

Kong Bo, E-mail: kong79@yeah.net [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China); College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Zhang Lin, E-mail: zhanglinbox@263.net [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China); Chen Xiangrong [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Zeng Tixian [College of Physics and Electronic Information, China West Normal University, Nanchong 637002 (China); Cai Lingcang [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China)

2012-06-15

The structures, structural relative stabilities, pressure-induced phase transitions, and equations of state for lanthanide trihydrides REH{sub 3} (RE=Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu) are systematically studied using ab initio calculations under a core state model (CSM). The obtained ground-state parameters, such as lattice constants and bulk modulus, agree well with the available data. Among the P6{sub 3}/mm, P3-bar c1, and P6{sub 3}cm structures, the P6{sub 3}cm structure is found to be the most stable structure for lanthanide trihydride via the comparison of the calculated total energies. With the help of Birch-Murnaghan equation of state, the structural transitions from hexagonal to cubic for REH{sub 3} (RE=Sm, Gd, Ho, Er, and Lu) under pressure are affirmed; especially, the similar behavior of REH{sub 3} (RE= Tb, Dy, and Tm) is reasonably predicted for the first time by this means. For the transitions, the repulsive interactions of H-H atoms may play an important role in terms of the analysis of the structures in the vicinity of the theoretical phase transition.

Production of a tracer packet of heavier rare earth elements

International Nuclear Information System (INIS)

Lahiri, S.; Nayak, D.; Maji, S.

2004-01-01

Production of a tracer packet of heavier rare earth elements containing carrier-free radionuclides of 153,155 Tb, 153,155,157 Dy, 159 Ho, 159,161 Er, 161 Tm produced by medium energy 7 Li and 12 C irradiation on an europium oxide target and the subsequent separation of bulk europium from the carrier-free products is described. (author)

Critical evaluation and thermodynamic optimisation of the Si-RE systems: Part II. Si-RE system (RE = Gd, Tb, Dy, Ho, Er, Tm, Lu and Y)

International Nuclear Information System (INIS)

Kim, Junghwan; Jung, In-Ho

2015-01-01

Highlights: • The (Si-RE) (RE = Gd, Tb, Dy, Ho, Er, Tm, Lu and Y) systems have been reviewed. • The thermodynamic optimization of the (Si-RE) systems have been performed. • Systematic changes and similarities in the (Si-RE) systems were found. • The systematic approach resolved inconsistencies in the experimental data. • The systematic approach was used to assess the unexplored phase diagrams. - Abstract: A critical evaluation and optimisation of all available phase diagrams and thermodynamic data of the (Si-RE) (RE = Gd, Tb, Dy, Ho, Er, Tm, Lu and Y) systems was conducted to obtain reliable thermodynamic functions of all the phases in the system. In the thermodynamic modelling, a systematic analysis involving the similarity and periodicity observed in the lanthanide series was applied to resolve inconsistencies in the experimental data and to estimate the unknown thermodynamic properties and phase equilibria data. In particular, the phase diagrams and thermodynamic properties of (Si-Tm) and (Si-Lu) systems which are rarely investigated can be predicted from this approach. Systematic trends in thermodynamic properties of solid and liquid phases and phase diagram of the entire (Si-RE) systems were summarized

Static magnetic susceptibility, crystal field and exchange interactions in rare earth titanate pyrochlores

NARCIS (Netherlands)

Malkin, B. Z.; Lummen, T. T. A.; van Loosdrecht, P. H. M.; Dhalenne, G.; Zakirov, A. R.

2010-01-01

The experimental temperature dependence (T = 2-300 K) of single crystal bulk and site susceptibilities of rare earth titanate pyrochlores R2Ti2O7 (R = Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) is analyzed in the framework of crystal field theory and a mean field approximation. Analytical expressions for the

Transferred hyperfine interaction between the rare-earth ions and the fluorine nuclei in rare-earth trifluorides

DEFF Research Database (Denmark)

Hansen, P. E.; Nevald, Rolf; Guggenheim, H. G.

1978-01-01

The isotropic and anisotropic transferred hyperfine interactions between F ions in the two chemically inequivalent sites and the rare-earth ions (R) have been derived from 19F NMR measurements in the temperature region 100-300 K on single crystals of TbF3 and DyF3. The isotropic interactions are ...... to vary only slightly with temperature. They are further assigned to definite R's in the unit cell, which cannot be done from macroscopic magnetic measurements....

Ion-irradiation resistance of the orthorhombic Ln_2TiO_5 (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) series

International Nuclear Information System (INIS)

Aughterson, Robert D.; Lumpkin, Gregory R.; Ionescu, Mihail; Reyes, Massey de los; Gault, Baptiste; Whittle, Karl R.; Smith, Katherine L.; Cairney, Julie M.

2015-01-01

The response of Ln_2TiO_5 (where Ln is a lanthanide) compounds exposed to high-energy ions was used to test their suitability for nuclear-based applications, under two different but complementary conditions. Eight samples with nominal stoichiometry Ln_2TiO_5 (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy), of orthorhombic (Pnma) structure were irradiated, at various temperatures, with 1 MeV Kr"2"+ ions in-situ within a transmission electron microscope. In each case, the fluence was increased until a phase transition from crystalline to amorphous was observed, termed critical dose D_c. At certain elevated temperatures, the crystallinity was maintained irrespective of fluence. The critical temperature for maintaining crystallinity, T_c, varied non-uniformly across the series. The T_c was consistently high for La, Pr, Nd and Sm_2TiO_5 before sequential improvement from Eu to Dy_2TiO_5 with T_c's dropping from 974 K to 712 K. In addition, bulk Dy_2TiO_5 was irradiated with 12 MeV Au"+ ions at 300 K, 723 K and 823 K and monitored via grazing-incidence X-ray diffraction (GIXRD). At 300 K, only amorphisation is observed, with no transition to other structures, whilst at higher temperatures, specimens retained their original structure. The improved radiation tolerance of compounds containing smaller lanthanides has previously been attributed to their ability to form radiation-induced phase transitions. No such transitions were observed here. - Highlights: • First ion-irradiation studies on a number of novel compounds including Pr_2TiO_5, Eu_2TiO_5 and Tb_2TiO_5. • Systematic in-situ ion-irradiation study of almost complete Ln_2TiO_5 series (Ln = lanthanides) with orthorhombic crystal structure type. • The first grazing incidence study of bulk irradiated Dy_2TiO_5 looking for irradiation induced phase transition.

Magnetic order of Y{sub 3}NiSi{sub 3}-type R{sub 3}NiSi{sub 3} (R=Gd–DY) compounds

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@tech.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Faculty of Geology, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Nirmala, R. [Indian Institute of Technology Madras, Chennai 600036 (India); Malik, S.K.; Quezado, S. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59082-970 (Brazil); Yao, Jinlei; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada); Nigam, A.K. [Tata Institute of Fundamental Research, Mumbai 400005 (India); Isnard, O. [Université Grenoble Alpes, Inst NEEL, BP166, F-38042 Grenoble (France); CNRS, Institut NEEL, 25 rue des martyrs, F-38042 Grenoble (France)

2016-01-15

Magnetic measurements and neutron powder diffraction investigations on the Y{sub 3}NiSi{sub 3}-type R{sub 3}NiSi{sub 3} compounds (R=Gd, Tb, Dy) reveal their complex antiferromagnetic ordering. Magnetic measurements on Gd{sub 3}NiSi{sub 3}, Tb{sub 3}NiSi{sub 3} and Dy{sub 3}NiSi{sub 3} indicate antiferromagnetic-like transition at temperatures 260 K, 202 K and 140 K, respectively. Also, the Tb{sub 3}NiSi{sub 3} and Dy{sub 3}NiSi{sub 3} compounds show spin-reorientation transition at 132 K and 99 K, respectively. Below the spin-reorientation transition, the isothermal magnetization curves indicate the metamagnetic-like behavior of Tb{sub 3}NiSi{sub 3} and Dy{sub 3}NiSi{sub 3}. The magnetocaloric effect of Dy{sub 3}NiSi{sub 3} is calculated in terms of isothermal magnetic entropy change and it reaches a maximum value of −1.2 J/kg K and −1.1 J/kg K for a field change of 50 kOe near 146 K and 92 K, respectively. The neutron diffraction studies of Tb{sub 3}NiSi{sub 3} suggest the magnetic ordering of the Tb2 4j sublattice and no magnetic ordering of the Tb1 2a sublattice. Tb{sub 3}NiSi{sub 3} transforms from the high temperature paramagnetic state to the commensurate high-temperature a- and c-axis antiferromagnet of I′2/m magnetic space group below 250 K. Below 150 K, the high-temperature antiferromagnet transforms into the low-temperature a-, b- and c-axis antiferromagnet of I′i magnetic space group. At 1.5 K, the terbium magnetic moment in Tb2 sublattice and its a-, b- and c-axis components reach the values of M{sub Tb2}=8.2(1) μ{sub B}, M{sub aTb2}=5.9(1) μ{sub B}, M{sub bTb2}=4.3(2) μ{sub B} and M{sub cTb2}=3.7(2) μ{sub B}, respectively. - Highlights: • Gd{sub 3}NiSi{sub 3}, Tb{sub 3}NiSi{sub 3} and Dy{sub 3}NiSi{sub 3} have Neel points of 260. 202 and 140 K. • Tb{sub 3}NiSi{sub 3} and Dy{sub 3}NiSi{sub 3} show spin-reorientation transition at 132 and 99 K. • Tb{sub 3}NiSi{sub 3} exhibits the commensurate magnetic ordering of Tb2 4j sublattice

Electrical Conductivity of Molten DyCl3-NaCl and DyCl3-KCl Systems: An Approach to Structural Interpretations of Rare Earth Chloride Melts

Science.gov (United States)

Iwadate, Yasuhiko; Ohkubo, Takahiro

2017-11-01

Electrical conductivities (κs) of molten DyCl3-NaCl and DyCl3-KCl systems were estimated by measuring the impedances of each mixture melt at any temperature and/or frequency. The molar volumes (Vms) were measured by dilatometry and represented as a polynomial empirical equation of temperature and composition. Due to both the properties, the molar conductivities (Λms) were calculated and their temperature and/or composition dependences were discussed from the standpoint of structural features as well. The κs increased curvilinearly with increasing temperature across the whole composition ranges. This trend was also applied to the Λms which was fitted by an Arrhenius-type equation. The relationship of Λms with melt composition was studied and the Λms were found to decrease with increasing composition of DyCl3. These findings were interpreted based on the results of structural science so far reported, and finally, the relationship between Λms and the structures of pure rare earth chloride melts was discussed.

Investigation of chemical bond characteristics, thermal expansion coefficients and bulk moduli of alpha-R2MoO6 and R2Mo2O7 (R = rare earths) by using a dielectric chemical bond method.

Science.gov (United States)

Li, Huaiyong; Zhang, Siyuan; Zhou, Shihong; Cao, Xueqiang

2009-09-01

Theoretical researches are performed on the alpha-R2MoO6 (R = Y, Gd, Tb Dy, Ho, Er, Tm and Yb) and pyrochlore-type R2Mo2O7 (R = Y, Nd, Sm, Gd, Tb and Dy) rare earth molybdates by using chemical bond theory of dielectric description. The chemical bonding characteristics and their relationship with thermal expansion property and compressibility are explored. The calculated values of linear thermal expansion coefficient (LTEC) and bulk modulus agree well with the available experimental values. The calculations reveal that the LTECs and the bulk moduli do have linear relationship with the ionic radii of the lanthanides: the LTEC decreases from 6.80 to 6.62 10(-6)/K and the bulk modulus increases from 141 to 154 GPa when R goes in the order Gd, Tb Dy, Ho, Er, Tm, and Yb in the alpha-R2MoO6 series; while in the R2Mo2O7 series, the LTEC ranges from 6.80 to 6.61 10(-6)/K and the bulk modulus ranges from 147 to 163 GPa when R varies in the order Nd, Sm, Gd, Tb and Dy. Copyright 2008 Wiley Periodicals, Inc.

Investigation of local magnetism in RZn (R = Ce, Gd, Tb, Dy) and GdCu intermetallic compounds using perturbed angular correlation gamma-gamma spectroscopy; Investigacao do magnetismo local em compostos intermetalicos do tipo RZn (R = Ce, Gd, Tb, Dy) e GdCu pela espectroscopia de correlacao angular gama-gama perturbada

Energy Technology Data Exchange (ETDEWEB)

Santos, Brianna Bosch dos

2010-07-01

This work presents, from a microscopic point of view, a systematic study of the local magnetism in RZn (R = Ce, Gd, Tb, Dy) and GdCu intermetallic compounds through measurements of hyperfine interactions using the Perturbed Angular Correlation Gamma- Gamma Spectroscopy technique with {sup 111}In {yields} {sup 111}Cd and {sup 140}La {yields} {sup 140}Ce as probe nuclei. As the magnetism in these compounds originates from the 4f electrons of the rare-earth elements it is interesting to observe in a systematic study of RZn compounds the behavior of the magnetic hyperfine field with the variation of the number of 4f electrons in the R element. The use of probe nuclei {sup 140}La {yields} {sup 140}Ce is interesting because Ce{sup +3} ion posses one 4f electron which may contribute to the total hyperfine field, and the results showed anomalous behavior. The results for {sup 111}Cd probe showed that the temperature dependence of the magnetic hyperfine field follows the Brillouin function, and the magnetic hyperfine field decreases linearly with increase of the atomic number of rare earth when plotted as a function of the rare-earth J spin projection, showing that the main contribution to the magnetic hyperfine field in RZn compounds comes from the polarization of the conduction electrons. The results for the electric field gradient measured with {sup 111}Cd for all compounds showed a strong decrease with the atomic number of the rare-earth element. We have therefore assumed that the major contribution to the electric field gradient originates from the 4f electrons of the rare-earths. The measurements of the electric field gradient for GdCu with {sup 111}Cd, after temperature decreases and increases again showed that two different structures, CsCl-type cubic and FeB-type orthorhombic structures co-exist. Finally, it is the first time that measurements of hyperfine parameters have been carried out with theses two probe nuclei in the studied RZn. (author)

Cross sections of (n, α) reactions on rare-earth elements from Tb through Lu at En ∼ 14 MeV

International Nuclear Information System (INIS)

Kadenko, A.O.; Gorbachenko, O.M.; Primenko, G.I.; Kadenko, I.M.; Plujko, V.A.

2012-01-01

The cross sections of the neutron reactions at E n = 14.6 MeV on the isotopes of Tb-159, Dy-164, Er-168, Er-170, Yb-174, Yb-176, Lu-175, and Lu-176 with alpha-particle emission were studied by the use of new experimental data and different theoretical approaches. New and improved experimental data were obtained with the neutron-activation technique. The samples of natural composition of rare earth elements were irradiated with d-t neutrons from the neutron generator NG-300. Gamma-ray spectra of the induced activities of irradiated samples were measured with HPGe spectrometer. The uncertainties of the experimental cross sections were thoroughly estimated. Available experimental results and evaluated nuclear data from the EXFOR, TENDL, ENDF data libraries were compared with different systematics and calculations with the EMPIRE 3.0 and TALYS 1.2 codes. Contribution of pre-equilibrium decay was analyzed. Different systematics for estimations of the investigated cross-sections have been tested

High coercivity rare earth-transition metal magnets

International Nuclear Information System (INIS)

Croat, J.J.

1982-01-01

Ferromagnetic compositions having intrinsic magnetic coercivities at room temperature of at least 1,000 Oersteds are formed by the controlled quenching of molten rare earth-transition metal alloys. Hard magnets may be inexpensively formed from the lower atomic weight lanthanide elements and iron. The preferable compositions lie within: at least one of Fe, Ni, Co; 20 - 70 atomic percent: at least one of Ce, Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, Y; 80 - 30 atomic percent. (author)

Synthesis and investigation of rare earth tris-acetylacetonates addUcts with acetylaceoneimine

International Nuclear Information System (INIS)

Trembovetskij, G.V.; Smirnov, E.V.; Murav'eva, I.A.; Martynenko, L.I.

1983-01-01

Adducts of tris-acetylacetonates of pare earths With acetylacetonimine of the composition MA 3 x2L (M=La, Pr, Nd, Eu, Gd, Tb) and MA 3 XL (M=Dy, Ho, Er, Tm, Yb, LU) have been synthesized. The compounds prepared are studied using the methods of elemental analysis, IR spectroscopy, PMR spectroscopy, X-ray phase analysis. Volatile tris-acetylacetonates of the yttrium subgroUp rare earths have been prepared by thermal decomposition of MA 3 xL in vacuum

RNi2B2C (R = Ho, Dy, Tb and Pr) single crystals grown by the cold copper crucible method

Science.gov (United States)

Durán, A.; Munoz, E.; Bernès, S.; Escudero, R.

2000-08-01

Single crystals of RNi2B2C (R = Ho, Dy, Tb, Pr) have been grown on cold copper crucibles in a high-frequency induction furnace. As a result, shiny metallic and brittle platelike single crystals were obtained. They were examined by x-ray and scanning electron microscopy with WDX/EDX for local composition analysis and show a very good crystallographic structure and compositions. Resistivity and dc magnetic measurements were performed to study superconducting and magnetic properties. Besides known electronic properties of the RNi2B2C family, we report for the first time results for PrNi2B2C single crystals successfully obtained by this technique.

Simulation of the magnetocaloric effect in Tb nanofilms

Energy Technology Data Exchange (ETDEWEB)

Anselmo, Dory Hélio A. L., E-mail: doryh@dfte.ufrn.br [Departamento de Física Teórica e Experimental (DFTE), Universidade Federal do Rio Grande do Norte (UFRN), Natal-RN (Brazil); Mello, Vamberto D. [Departamento de Física,Universidade do Estado do Rio Grande do Norte (UERN), Mossoró-RN (Brazil); Vasconcelos, Manoel S. [Escola de Ciência e Tecnologia (ECT), Universidade Federal do Rio Grande do Norte (UFRN), Natal-RN (Brazil)

2014-03-31

Rare-earth (RE) metals have different magnetic structures resulting from the competition between the crystal-field and exchange interactions. When a magnetic field is applied it creates a third interaction and the magnetic structures are more complicated. In thin films, it is expected that even the magnetic arrangement itself can be strongly modified. Rare-earth helimagnets such as Terbium (Tb), Holmium (Ho) and Dysprosium (Dy) represent the best candidates to evidence such finite-size effects. This finite-size effect is caused by the reduced number of atoms in the direction perpendicular to the film plane that leads to a decrease of the total magnetic exchange energy. We report this contribution to the investigation of magnetocaloric effect (MCE) of thin Terbium films in the helimagnetic temperature range, from T{sub C} = 219 K to T{sub N} = 231 K, for external fields of the order of 1 kOe. We find that for strong fields, H = 50 kOe, the adiabatic temperature change ΔT near the Néel temperature is around 15 K for any thickness of Tb films. However large thickness effects are found for small values of the magnetic field. For field strength of the order of a few kOe, the thermocaloric efficiency increases significantly for ultrathin (nanomagnetic) films.

High coercivity rare earth-transition metal magnets

International Nuclear Information System (INIS)

Croat, J.J.

1982-01-01

Ferromagnetic compositions having intrinsic magnetic coercivities at room temperature of at least 1,000 Oersteds are formed by the controlled quenching of molten rare earth -transition metal alloys. Hard magnets may be inexpensively formed from the lower atomic weight lanthanide elements and iron. The preferable compositions lie within: at least one of Fe, Ni, Co (20 to 70 atomic percent); and at least one of Ce, Pr, Na, Sm, Eu, Tb, Dy, Ho, Er, Tm, Y (80 to 30 atomic percent). (author)

Transition rates in {sup 161}Dy

Energy Technology Data Exchange (ETDEWEB)

Berg, V; Malmskog, S G

1969-06-15

The decay of {sup 161}Tb has been studied using a high resolution Ge(Li)-detector. Five new transitions were observed and fitted into the earlier proposed decay scheme. The half-life of the 131.8 keV level in {sup 161}Dy was determined in a delayed coincidence measurement to be 145 {+-} 15 psec. The low level scheme in {sup 161}Dy is discussed within a quasi-particle model allowing for Coriolis mixing. Special attention is given to the strongly retarded, K-allowed 131.8 keV E1 transition with a retardation factor F{sub W} > 1.5 x 10{sup 8}.

Isopiestic determination of the activity coefficients of some aqueous rare earth electrolyte solutions at 250C. I. The rare earth chlorides

International Nuclear Information System (INIS)

Spedding, F.H.; Weber, H.O.; Saeger, V.W.; Petheram, H.H.; Rard, J.A.; Habenschuss, A.

1976-01-01

The osmotic coefficients of the aqueous trichlorides of La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y were determined from 0.1 M to saturation at 25 0 C. Semiempirical least-squares equations were obtained for the osmotic coefficients as a function of molality and these equations were used to calculate water activities and mean molal activity coefficients. The water activities of the light rare earth chlorides at constant molalities are higher than for the heavy rare earths, while the mean molal activity coefficients are larger for the heavy rare earths than for the light ones. The above effects are discussed in terms of changes in the cationic radii and hydration of the rare earth ions

Influence of Dy in solid solution on the degradation behavior of binary Mg-Dy alloys in cell culture medium.

Science.gov (United States)

Yang, Lei; Ma, Liangong; Huang, Yuanding; Feyerabend, Frank; Blawert, Carsten; Höche, Daniel; Willumeit-Römer, Regine; Zhang, Erlin; Kainer, Karl Ulrich; Hort, Norbert

2017-06-01

Rare earth element Dy is one of the promising alloying elements for magnesium alloy as biodegradable implants. To understand the effect of Dy in solid solution on the degradation of Mg-Dy alloys in simulated physiological conditions, the present work studied the microstructure and degradation behavior of Mg-Dy alloys in cell culture medium. It is found the corrosion resistance enhances with the increase of Dy content in solid solution in Mg. This can be attributed to the formation of a relatively more corrosion resistant Dy-enriched film which decreases the anodic dissolution of Mg. Copyright © 2017 Elsevier B.V. All rights reserved.

Complexes of o-Vanillin oxime with La(III), Ce(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III), Ho(III) and Yb(III)

International Nuclear Information System (INIS)

Dhar, M.L.; Gupta, V.K.; Singh, Onkar

1988-01-01

Ten complexes of lanthanides with o-vanillin oxime have been swynthesised and characterised. The composition of the complexes as determined by elemental and thermal analyses, infrared electronic spectral and magnetic moment studies is [Ln(C 8 H 8 NO 3 ) 3 .XH 2 O], where X=2 when Ln=La, Ce, Pr, Nd, Sm and X=3 when Ln=Gd, Dy, Tb, Ho, Yb; C 8 H 8 NO 3 - represents the anion of the ligand. (author). 16 refs., 2 figs., 2 tables

Neutron scattering studies of the coexistence of long-range magnetic order and superconductivity in Dy12Mo6S8 and Tb12Mo6S8

International Nuclear Information System (INIS)

Thomlinson, W.; Shirane, G.; Moncton, D.E.; Ishikawa, M.; Fischer, O.

1978-10-01

Both Dy 1 2 Mo 6 S 8 and Tb 1 2 Mo 6 S 8 are superconducting below T/sub c/ = 2.05 K. Neutron scattering studies show that these compounds in zero applied magnetic field develop long-range antiferromagnetic order (greater than 300 A) at T/sub M/ = 0.4 K and T/sub M/ = 1.0 K, respectively, which does not destroy the superconducting state. Magnetization measurements at temperatures below T/sub M/ suggest the development of ferromagnetic order as the applied magnetic field increases. In the case of Tb 1 2 Mo 6 S 8 the neutron data show long-range ferromagnetic order developing for H greater than or equal to H/sub c2/ = 1.9 kOe where H/sub c2/ is the upper critical field for superconductivity. However, for Dy 1 2 Mo 6 S 8 long-range ferromagnetic order begins to develop at H = 200 Oe, a field much less than H/sub c2/ = 1.2 kOe. As the ferromagnetic intensity increases, the antiferromagnetic intensity decreases. Between H = 200 Oe and H = 1.2 kOe both ferromagnetic and antiferromagnetic order occur with the sample in the superconducting state

Strong broad green UV-excited photoluminescence in rare earth (RE = Ce, Eu, Dy, Er, Yb) doped barium zirconate

Energy Technology Data Exchange (ETDEWEB)

Borja-Urby, R. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Diaz-Torres, L.A., E-mail: ditlacio@cio.mx [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A.P. 1-1010, Queretaro, Qro. 76000 (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Ciudad de Mexico, D. F. 07730 (Mexico); Meza, O. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico)

2011-10-25

Highlights: > Trivalent rare earth (RE) substitution on Zr{sup 4+} sites in BaZrO{sub 3} lead to band gap narrowing. > RE substitution lead to enhanced blue-green intrinsic emission of nanocrystalline BaZrO{sub 3} > Blue-green hue of BaZrO3:RE depends on RE dopant and excitation UV wavelength > BaZrO3: Dy{sup 3+} PL chromatic coordinates correspond to pure white color coordinates of CIE 1931 model - Abstract: The wet synthesis hydrothermal method at 100 deg. C was used to elaborate barium zirconate (BaZrO{sub 3}) unpurified with 0.5 mol% of different rare earth ions (RE = Yb, Er, Dy, Eu, Ce). Morphological, structural and UV-photoluminescence properties depend on the substituted rare earth ionic radii. While the crystalline structure of RE doped BaZrO{sub 3} remains as a cubic perovskite for all substituted RE ions, its band gap changes between 4.65 and 4.93 eV. Under 267 nm excitation the intrinsic green photoluminescence of the as synthesized BaZrO{sub 3}: RE samples is considerably improved by the substitution on RE ions. For 1000 deg. C annealed samples, under 267 nm, the photoluminescence is dominated by the intrinsic BZO emission. It is interesting to notice that Dy{sup 3+}, Er{sup 3+} and Yb{sup 3+} doped samples present whitish emissions that might be useful for white light generation under 267 nm excitation. CIE color coordinates are reported for all samples.

Antiferromagnetic coupling between rare earth ions and semiquinones in a series of 1:1 complexes.

Science.gov (United States)

Caneschi, Andrea; Dei, Andrea; Gatteschi, Dante; Poussereau, Sandrine; Sorace, Lorenzo

2004-04-07

We use the strategy of diamagnetic substitution for obtaining information on the crystal field effects in paramagnetic rare earth ions using the homologous series of compounds with the diamagnetic tropolonato ligand, Ln(Trp)(HBPz(3))(2), and the paramagnetic semiquinone ligand, Ln(DTBSQ)(HBPz(3))(2), (DTBSQ = 3,5-di-tert-butylsemiquinonato, Trp = tropolonate, HBPz(3)= hydrotrispyrazolylborate) for Ln = Sm(iii), Eu(iii), Gd(iii), Tb(iii), Dy(iii), Ho(iii), Er(iii) or Yb(iii). The X-ray crystal structure of a new form of tropolonate derivative is presented, which shows, as expected, a marked similarity with the structure of the semiquinonate derivative. The Ln(Trp)(HBPz(3))(2) derivatives were then used as a reference for the qualitative determination of crystal field effects in the exchange coupled semiquinone derivatives. Through magnetisation and susceptibility measurements this empirical diamagnetic substitution method evidenced for Er(iii), Tb(iii), Dy(iii) and Yb(iii) derivatives a dominating antiferromagnetic coupling. The increased antiferromagnetic contribution compared to other radical-rare earth metal complexes formed by nitronyl nitroxide ligands may be related to the increased donor strength of the semiquinone ligand.

Study of hyperfine interactions in intermetallic compounds Gd(Ni,Pd,Cu)In, Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In; Estudo de interacoes hiperfinas em compostos intermetalicos Gd(Ni,Pd,Cu)In, Tb(Ni,Pd)In, Dy(Ni,Pd)In e Ho(Ni,Pd)In

Energy Technology Data Exchange (ETDEWEB)

Lapolli, Andre Luis

2006-07-01

Systematic behavior of magnetic hyperfine field (B{sub hf}) in the intermetallic compounds Gd(Ni,Pd,Cu)In Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In was studied by Perturbed Gamma-Gamma Angular Correlation spectroscopy. The measurements of B{sub hf} were carried out at the rare earth atom and in sites using the nuclear probes {sup 140}Ce and {sup 11}'1Cd respectively. The variation of hyperfine field with temperature, in most cases, follows the Brillouin function predicted from the molecular field theory. The hyperfine field values at rare earth atom sites obtained from {sup 140}Ce probe as well as at in sites obtained from {sup 111}Cd probe for each series of compounds were extrapolated to zero Kelvin B{sub hf}(T=0) from these curves. These values were compared with the values of the literature for other compounds containing the same rare earth element and all of them show a linear relationship with the ordering temperature. This indicates that the main contribution to B{sub hf} comes from the conduction electron polarization (CEP) through Fermi contact interaction and the principal mechanism of magnetic interaction in these compounds can be described by the RKKY type interaction. The values of B{sub hf}(T=0) for each family of intermetallic compounds RNiIn and RPdIn when plotted as a function of 4f spin projection of rare earth element also shows a linear relationship. Exceptions are the results for the compounds RNiIn obtained with {sup 111}Cd probe where a small deviation from linearity is observed. The results of the measurements carried out with the {sup 111}Cd probe were also analyzed to obtain the hyperfine parameters of the quadrupole interaction as a function of temperature for RPdln and GdNiIn compounds. The results show that for the compound GdPdIn there might be some Gd-In disorder at high temperature. (author)

Study of hyperfine interactions in intermetallic compounds Gd(Ni,Pd,Cu)In, Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In; Estudo de interacoes hiperfinas em compostos intermetalicos Gd(Ni,Pd,Cu)In, Tb(Ni,Pd)In, Dy(Ni,Pd)In e Ho(Ni,Pd)In

Energy Technology Data Exchange (ETDEWEB)

Lapolli, Andre Luis

2006-07-01

Systematic behavior of magnetic hyperfine field (B{sub hf}) in the intermetallic compounds Gd(Ni,Pd,Cu)In Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In was studied by Perturbed Gamma-Gamma Angular Correlation spectroscopy. The measurements of B{sub hf} were carried out at the rare earth atom and in sites using the nuclear probes {sup 140}Ce and {sup 11}'1Cd respectively. The variation of hyperfine field with temperature, in most cases, follows the Brillouin function predicted from the molecular field theory. The hyperfine field values at rare earth atom sites obtained from {sup 140}Ce probe as well as at in sites obtained from {sup 111}Cd probe for each series of compounds were extrapolated to zero Kelvin B{sub hf}(T=0) from these curves. These values were compared with the values of the literature for other compounds containing the same rare earth element and all of them show a linear relationship with the ordering temperature. This indicates that the main contribution to B{sub hf} comes from the conduction electron polarization (CEP) through Fermi contact interaction and the principal mechanism of magnetic interaction in these compounds can be described by the RKKY type interaction. The values of B{sub hf}(T=0) for each family of intermetallic compounds RNiIn and RPdIn when plotted as a function of 4f spin projection of rare earth element also shows a linear relationship. Exceptions are the results for the compounds RNiIn obtained with {sup 111}Cd probe where a small deviation from linearity is observed. The results of the measurements carried out with the {sup 111}Cd probe were also analyzed to obtain the hyperfine parameters of the quadrupole interaction as a function of temperature for RPdln and GdNiIn compounds. The results show that for the compound GdPdIn there might be some Gd-In disorder at high temperature. (author)

Synthesis, structures, and luminescent properties of sodium rare-earth metal(III) chloride oxotellurates(IV), Na{sub 2}Ln{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4} (Ln = Sm, Eu, Gd, Tb, Dy, and Ho)

Energy Technology Data Exchange (ETDEWEB)

Charkin, Dmitri O.; Dorofeev, Sergey G.; Berdonosov, Peter S.; Dolgikh, Valery A. [Department of Chemistry, Lomonosov Moscow State University (Russian Federation); Zitzer, Sabine; Greiner, Stefan; Schleid, Thomas [Institut fuer Anorganische Chemie, Universitaet Stuttgart (Germany); Olenev, Andrei V. [Department of Chemistry, Lomonosov Moscow State University (Russian Federation); Sine Theta Ltd., Moscow (Russian Federation)

2017-11-17

Six sodium rare-earth metal(III) chloride oxotellurates(IV), Na{sub 2}Ln{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4}, isostructural to Na{sub 2}Y{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4}, were synthesized by flux techniques and characterized by single-crystal XRD. The compounds crystallize in the monoclinic space group C2/c with lattice constants a = 23.967(1), b = 5.6342(3), c = 16.952(1) Aa, β = 134.456(5) for Ln = Sm, a = 23.932(2), b = 5.6044(5), c = 17.134(1) Aa, β = 135.151(6) for Ln = Eu, a = 23.928(1), b = 5.5928(1), c = 17.1133(8) Aa, β = 135.366(3) for Ln = Gd, a = 23.907(1), b = 5.569(3), c = 16.745(1) Aa, β = 134.205(3) for Ln = Tb, a = 23.870(1), b = 5.547(3), c = 16.665(1) Aa, β = 134.102(3) for Ln = Dy, and a = 23.814(1), b = 5.526(3), c = 16.626(1) Aa, β = 134.016(3) for Ln = Ho and Z = 4. Their crystal structure can be considered as a framework built of intergrowing Ln-O and Na-(O,Cl) slabs with channel walls decorated by tellurium atoms of [TeO{sub 3}]{sup 2-} groups. The luminescent properties of the new compounds due to the Ln{sup 3+} cations are described and discussed. We also discuss the crystal chemistry of various alkali-metal rare-earth metal(III) halide oxochalcogenates(IV). (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Room temperature synthesis of hydrophilic Ln(3+)-doped KGdF4 (Ln = Ce, Eu, Tb, Dy) nanoparticles with controllable size: energy transfer, size-dependent and color-tunable luminescence properties.

Science.gov (United States)

Yang, Dongmei; Li, Guogang; Kang, Xiaojiao; Cheng, Ziyong; Ma, Ping'an; Peng, Chong; Lian, Hongzhou; Li, Chunxia; Lin, Jun

2012-06-07

In this paper, we demonstrate a simple, template-free, reproducible and one-step synthesis of hydrophilic KGdF(4): Ln(3+) (Ln = Ce, Eu, Tb and Dy) nanoparticles (NPs) via a solution-based route at room temperature. X-Ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) and cathodoluminescence (CL) spectra are used to characterize the samples. The results indicate that the use of water-diethyleneglycol (DEG) solvent mixture as the reaction medium not only allows facile particle size control but also endows the as-prepared samples with good water-solubility. In particular, the mean size of NPs is monotonously reduced with the increase of DEG content, from 215 to 40 nm. The luminescence intensity and absolute quantum yields for KGdF(4): Ce(3+), Tb(3+) NPs increase remarkably with particle sizes ranging from 40 to 215 nm. Additionally, we systematically investigate the magnetic and luminescence properties of KGdF(4): Ln(3+) (Ln = Ce, Eu, Tb and Dy) NPs. They display paramagnetic and superparamagnetic properties with mass magnetic susceptibility values of 1.03 × 10(-4) emu g(-1)·Oe and 3.09 × 10(-3) emu g(-1)·Oe at 300 K and 2 K, respectively, and multicolor emissions due to the energy transfer (ET) process Ce(3+)→ Gd(3+)→ (Gd(3+))(n)→ Ln(3+), in which Gd(3+) ions play an intermediate role in this process. Representatively, it is shown that the energy transfer from Ce(3+) to Tb(3+) occurs mainly via the dipole-quadrupole interaction by comparison of the theoretical calculation and experimental results. This kind of magnetic/luminescent dual-function materials may have promising applications in multiple biolabels and MR imaging.

Faraday effect in rare-earth ferrite garnets located in strong magnetic fields

International Nuclear Information System (INIS)

Valiev, U.V.; Zvezdin, A.K.; Krinchik, G.S.; Levitin, R.Z.; Mukimov, K.M.; Popov, A.I.

1983-01-01

The Faraday effect is investigated experimentally in single crystal specimens of rare earth iron garnets (REIG) R 3 Fe 5 O 12 (R=Y, Gd, Tb, Dy, Er, Tm, Yb, Eu, Sm and Ho) and also in mixed iron garnets Rsub(x)Ysub(3-x)Fesub(5)Osub(12) (R=Tb, Dy). The m.easurements are carried out in pulsed magnetic fields of intensity up to 200 kOe, in a temperature range from 4.2 to 300 K and at a wavelength of the light lambda=1.15 μm. The field dependence of the Faraday effect observed in the REIG cannot be explained if only the usually considered ''paramagnetic'' contribution to the Faraday effect is taken into account. A theory is developed which, besides the paramagnetic mechanism, takes into account a diamagnetic mechanism and also the mixing of the wave functions of the ground and excited multiplets. The contributions of each of these three mechanisms to the angle of rotation of the plane of polarization by the rare earth sublattice of the iron garnet are estimated theoretically. It is concluded that the mixing mechanism contributes significantly to the field and temperature dependences of the Faraday effect in REIG

Strong luminescence of rare earth compounds in ionic liquids: Luminescent properties of lanthanide(III) iodides in the ionic liquid 1-dodecyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide

International Nuclear Information System (INIS)

Mudring, Anja-Verena; Babai, Arash; Arenz, Sven; Giernoth, Ralf; Binnemans, K.; Driesen, Kris; Nockemann, Peter

2006-01-01

Purposely designed ionic liquids can be excellent solvents for spectroscopic studies of rare earth compounds. Absorption, excitation and emission spectra of LnI 3 (Ln = Nd, Dy and Tb) in the ionic liquid 1-dodecyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide are presented. Electronic transitions were assigned from the energy level diagrams for Ln(III). Emission lifetimes for DyI 3 in [C 12 mim][Tf 2 N] are discussed. Traces of water dramatically reduce the otherwise long lifetimes and comparatively high quantum yields

Studies on the decay of 160Tb to levels in 160Dy by Ge (Li)-Ge(Li)-coincidence system

International Nuclear Information System (INIS)

Hassan, A.M.; Abou-Zeid, M.A.; Mekamer, M.

1981-01-01

This work concerned with the study of the energy levels and the properties of gamma-ray transitions in 160 Dy resulting from the B-decay of the parent radioactive isotope 160 Tb (72 d.). These studies have been done by means of, single and gamma-gamma coincidence measurements. Log(ft). Internal Conversion Coefficient (ICC) values and the branching ratios have been calculated. The construction and testes of the Ge(Li)-Ge(Li) gamma-gamma coincidence spectrometer are presented. In addition to the previously reported transitions in three new transitions of energies 203, 420 and 1048 keV have been observed for the first time. The energy level at 1288.60 keV is confirmed, due to the presence of the 246 keV and 1005 keV gamma-ray transitions in the singles and gamma-gamma coincidence spectra. Furthermore the B-intensity feeding this level was calculated for the first time to be 0.08%. The log(ft) values of the energy level at 1288.6 keV was calculated for the first time to be 10.79. The energy level diagram of 160 Dy as summerised in the present work consists of 12 excited states, the levels at 581(6 + ) and 1391 keV reported by some authors were not encluded, since no transitions populated or depopulated these levels could be observed

Reaction kinetics of H{sub 2}, O{sub 2}, and H{sub 2}O with rare earths (Y, La, Ce, Pr, Nd, Gd, Tb, Dy, and Er) at 298 K

Energy Technology Data Exchange (ETDEWEB)

Enomoto, M.; Ohata, Y. [Course of Applied Science, Graduate School of Engineering, Tokai University, 4-1-1 Kita-Kaname, Hiratsuka, Kanagawa 259-1292 (Japan); Uchida, H., E-mail: huchida@keyaki.cc.u-tokai.ac.jp [Course of Applied Science, Graduate School of Engineering, Tokai University, 4-1-1 Kita-Kaname, Hiratsuka, Kanagawa 259-1292 (Japan)

2013-12-15

Highlights: ► H{sub 2} molecules react with a clean surface of each RE sample at the highest reactivity even at 298 K. ► The H{sub 2} reactivity becomes reduced by the formation of dihydrides of each RE sample. ► The RE with a clean surface adsorb O{sub 2} more than one monolayer of O{sub 2} even at 298 K. ► The quantitative reactivity of the H atoms dissociated from H{sub 2}O was calculated. -- Abstract: High reactivity of rare earths (RE) with H{sub 2}, O{sub 2} and H{sub 2}O is well known even at room temperature. The formation of stable surface oxides/hydroxides on the surface is the one of serious problems in the production and use of materials containing RE. We have investigated the quantitative reactivities of H{sub 2}, O{sub 2}, and H{sub 2}O with the surface of Y, La, Ce, Pr, Nd, Gd, Tb, Dy, and Er under ultra high vacuum condition. The H{sub 2}, O{sub 2} and H{sub 2}O gases exhibited the highest reactivity on the clean surface of the RE at 298 K. This means that all gas molecules impinging the surface dissociate and chemisorbed. The O atoms dissociated from O{sub 2} adsorb to for oxides layers of the metals. The H atoms dissociated from H{sub 2} diffuse into the metals to form hydrides which were found to decrease the H{sub 2} reactivity. The H atoms dissociated form H{sub 2}O diffuse into the metals or form hydroxides of the metals. With increasing coverage of each gas molecules, the reactivity of each gas was decreased by several orders of magnitude.

Local rhombohedral symmetry in Tb0.3Dy0.7Fe2 near the morphotropic phase boundary

International Nuclear Information System (INIS)

Ma, Tianyu; Liu, Xiaolian; Pan, Xingwen; Li, Xiang; Jiang, Yinzhu; Yan, Mi; Li, Huiying; Fang, Minxia; Ren, Xiaobing

2014-01-01

The recently reported morphotropic phase boundary (MPB) in a number of giant magnetostrictive materials (GMMs) has drawn considerable interest to the local symmetry/structure near MPB region of these materials. In this letter, by in-situ X-ray diffraction and AC magnetic susceptibility measurements, we show that Tb 0.3 Dy 0.7 Fe 2 , the typical composition of Terfenol-D GMMs, has coexistence of rhombohedral and tetragonal phases over a wide temperature range in the vicinity of MPB. High resolution transmission electron microscopy provides direct evidence for local rhombohedral symmetry of the ferromagnetic phase and reveals regular-shaped nanoscale domains below 10 nm. The nano-sized structural/magnetic domains are hierarchically inside a single micron-sized stripe-like domain with the same average magnetization direction. Such domain structures are consistent with the low magnetocrystalline anisotropy and easy magnetic/structural domain switching under magnetic field, thus generating large magnetostriction at low field

Hyperfine interaction studies of the perovskite oxides of the type RCrO3 (R = Gd, Tb e Dy)

International Nuclear Information System (INIS)

Silva, Renilson Adriano da

2009-01-01

ABO 3 perovskite oxides have ideal cubic structure, however, some distortions in this type of structure may induce changes from cubic to orthorhombic or rhombroedric symmetry. The larger atoms A are located at the center of a cube, the B atoms are on 8 vertices and oxygen atoms occupy 12 positions in the middle of each side of the cube. Distortions in this structure may lead to new magnetic and electrical properties, with great scientific and technological interest. In this work RCrO 3 (R = Gd, Tb, Dγ) compounds (also known as orthocromites) were studied. The samples were produced by means of sol-gel chemical procedure and analyzed by X-Ray Diffraction. The results showed a single phase with Pbnm space group. The perturbed gamma-gamma angular correlation (PAC) measurements were carried out using 181 Hf( 181 Ta) and 111 In( 111 Cd) nuclear probes, which substitute 'A' and 'B' positions respectively. The probe nuclei were introduced in the samples during the chemical procedures for preparation. One of the objectives of this work's was to study the hyperfine magnetic field and its variation as a function of temperature, crystallographic structure as well as the antiferromagnetic transition temperature (T N ). The PAC Measurements were carried out in the temperature range of 20 to 300 K for R = Gd, Tb and 20 to 800 K in the case of R = Dγ from. Electric field gradient was also measured as a function of temperature. It was possible to observe the expected transition as well as the alignment of Cr spins, as found in literature. The Neel temperatures (TN) for investigated samples are ∼170 K, ∼164 K and ∼148 K for GdCrO 3 , TbCrO 3 and DyCrO 3 respectively. (author)

Hydrothermal synthesis, structure, and optical properties of two nanosized Ln{sub 26} rate at CO{sub 3} (Ln=Dy and Tb) cluster-based lanthanide-transition-metal-organic frameworks (Ln MOFs)

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yu; Huang, Lian; Miao, Hao; Wan, Hong Xiang; Mei, Hua; Liu, Ying [State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University (China); Xu, Yan [State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University (China); State Key Laboratory of Coordination Chemistry, Nanjing Tech University (China)

2015-02-16

Two Ln{sub 26} rate at CO{sub 3} (Ln=Dy and Tb) cluster-based lanthanide-transition-metal-organic frameworks (Ln MOFs) formulated as [Dy{sub 26}Cu{sub 3}(Nic){sub 24}(CH{sub 3}COO){sub 8}(CO{sub 3}){sub 11}(OH){sub 26}(H{sub 2}O){sub 14}]Cl . 3 H{sub 2}O (1; HNic=nicotinic acid) and [Tb{sub 26}NaAg{sub 3}(Nic){sub 27}(CH{sub 3}COO){sub 6}(CO{sub 3}){sub 11}(OH){sub 26}Cl(H{sub 2}O){sub 15}] . 7.5 H{sub 2}O (2) have been successfully synthesized by hydrothermal methods and characterized by IR, thermogravimetric analysis (TGA), elemental analysis, and single X-ray diffraction. Compound 1 crystallizes in the monoclinic space group Cc with a=35.775(12) Aa, b=33.346(11) Aa, c=24.424(8) Aa, β=93.993(5) , V=29065(16) Aa{sup 3}, whereas 2 crystallizes in the triclinic space group P anti 1 with a=20.4929(19) Aa, b=24.671(2) Aa, c=29.727(3) Aa, α=81.9990(10) , β=88.0830(10) , γ=89.9940(10) , V=14875(2) Aa{sup 3}. Structural analysis indicates the framework of 1 is a 3D perovskite-like structure constructed out of CO{sub 3} rate at Dy{sub 26} building units and Cu{sup +} centers by means of nicotinic acid ligand bridging. In 2, however, nanosized CO{sub 3} rate at Tb{sub 26} units and [Ag{sub 3}Cl]{sup 2+} centers are connected by Nic{sup -} bridges to give rise to a 2D structure. It is worth mentioning that this kind of 4d-4f cluster-based MOF is quite rare as most of the reported analogous compounds are 3d-4f ones. Additionally, the solid-state emission spectra of pure compound 2 at room temperature suggest an efficient energy transfer from the ligand Nic{sup -} to Tb{sup 3+} ions, which we called the ''antenna effect''. Compound 2 shows a good two-photon absorption (TPA) with a TPA coefficient of 0.06947 cm GM{sup -1} (1 GM = 10{sup -50} cm{sup 4} s photon{sup -1}), which indicates that compound 2 might be a good choice for third-order nonlinear optical materials. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Magnetostriction-strain-induced enhancement and modulation of photovoltaic performance in Si-p-n/TbxDy1-xFe2 composite

International Nuclear Information System (INIS)

Wu, Zheng; Zhang, Yihe; Fang, Cong; Ma, Ke; Lin, He; Jia, Yanmin; Chen, Jianrong; Wang, Yu; Chan, Helen Lai Wa

2014-01-01

High photovoltaic efficiency is a key index in the application of silicon (Si) solar cells. In this study, a composite of a photovoltaic Si p-n junction solar cell and a magnetostrictive Tb x Dy 1-x Fe 2 alloy was fabricated. By utilizing the magnetostrictive strain to modulate the energy bandgap of Si, the open-circuit voltage and the maximum photovoltaic output power of the Si p-n junction solar cell could be enhanced by ∝12% and 9.1% under a dc magnetic field of ∝250 mT, respectively. The significantly enhanced photovoltaic performance and the simple fabrication process make the Si-p-n/Tb x Dy 1-x Fe 2 composite a promising material for high-efficiency solar cell devices. The structure of the proposed Si-p-n/Tb x Dy 1-x Fe 2 laminated composite. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Application of 241Am EDXRF in detecting and controlling of rare earth separation process by solvent extraction

International Nuclear Information System (INIS)

Yan Chunhua; Jia Jiangtao; Liao Chunsheng; Wang Mingwen; Li Biaoguo; Xu Guangxian

1996-01-01

The article investigated a fast EDXRF analysis method by radioisotope excited ( 241 Am) employing a high-purity germanium detector in rare earth separation process by solvent extraction. Applying the method, hydrochloride aqueous samples of SeEuGd/Tb/Dy separation processes were off-line analyzed. Comparative results measured by ICP were also given out. The results show that the method can be used for a wide rare earth concentration range with low error. Being fast, effective, precise and non-destructive, it can be used for on-line analysis to detect and control rare earth separation process by solvent extraction

Grain boundary engineering in sintered Nd-Fe-B permanent magnets for efficient utilization of heavy rare earth elements

Energy Technology Data Exchange (ETDEWEB)

Loewe, Konrad

2016-10-18

The first part of the thesis investigates the diffusion of rare-earth (RE) elements in commercial sintered Nd-Fe-B based permanent magnets. A strong temperature dependence of the diffusion distance and resulting change in magnetic properties were found. A maximum increase in coercivity of ∼+350 kA/m using a Dy diffusion source occurred at the optimum annealing temperature of 900 C. After annealing for 6 h at this temperature, a Dy diffusion distance of about 4 mm has been observed with a scanning Hall probe. Consequently, the maximum thickness of grain boundary diffusion processed magnets with homogeneous properties is also only a few mm. The microstructural changes in the magnets after diffusion were investigated by electron microscopy coupled with electron probe microanalysis. It was found that the diffusion of Dy into sintered Nd-Fe-B permanent magnets occurs along the grain boundary phases, which is in accordance with previous studies. A partial melting of the Nd-Fe-B grains during the annealing process lead to the formation of so - called (Nd,Dy)-Fe-B shells at the outer part of the grains. These shells are μm thick at the immediate surface of the magnet and become thinner with increasing diffusion distance towards the center of the bulk. With scanning transmission electron microscopy coupled with electron probe analysis a Dy content of about 1 at.% was found in a shell located about 1.5 mm away from the surface of the magnet. The evaluation of diffusion speeds of Dy and other RE (Tb, Ce, Gd) in Nd-Fe-B magnets showed that Tb diffuses significantly faster than Dy, and Ce slightly slower than Dy, which is attributed to differences in the respective phase diagrams. The addition of Gd to the grain boundaries has an adverse effect on coercivity. Exemplary of the heavy rare earth element Tb, the nano - scale elemental distribution around the grain boundaries after the diffusion process was visualized with high resolution scanning transmission electron microscopy

UV induced thermoluminescence in rare earth oxide doped phosphors: possible use for UV dosimetry

International Nuclear Information System (INIS)

Yeh, S.-M.; Su, C.-S.

1996-01-01

UV induced thermoluminescent (TL) phenomena in some phosphors doped with rare earth oxides (Gd 2 O 3 :Eu, Gd 2 O 3 :Tb, Gd 2 O 3 :Dy and Y 2 O 3 :EU) have been investigated. Gd 2 O 3 :Eu and Y 2 O 3 :Eu have been found to possess prominent TL phenomena. A stable high temperature glow peak has been found at 345 o C in the cubic (C type) crystalline structure of Gd 2 O 3 :Eu. A more stable high temperature glow peak has also been found at about 380 o C in Y 2 O 3 :Eu. The sensitivity is high enough to be used as UV sensors. TL phenomena in Gd 2 O 3 :Tb and Gd 2 O 3 :Dy have also been investigated, but their TL intensities are much weaker than that of Gd 2 O 3 :Eu or Y 2 O 3 :Eu. On the other hand, all glow peaks of Gd 2 O 3 :Tb and Gd 2 O 3 :Dy are unstable at room temperature, therefore, Gd 2 O 3 :Tb and Gd 2 O 3 :Dy are not suitable for use as UV detectors. According to the above properties, the C type (cubic) crystalline structure of the Gd 2 O 3 :Eu phosphor seems to possess the potential of being the TL material for UV measurement. The position of the high temperature glow peak depends on the total UV exposure. It locates at about 380 o C when this phosphor was irradiated by 302 nm UV at 2.4 mJ.cm -2 exposure, but it shifts to 345 o C at 19.2 mJ.cm -2 or higher exposure. The response curves of this phosphor for various wavelengths, e.g. 253.7 nm, 302 nm, and 365 nm, were also measured. This phosphor is sensitive enough to measure background UV radiations, such as sunlight, bulb light etc. (author)

Measurement of cross sections producing short-lived nuclei by 14 MeV neutron. Br, Te, Dy, Ho, Yb

Energy Technology Data Exchange (ETDEWEB)

Sakane, H.; Matsumoto, T.; Yamamoto, H.; Kawade, K. [Nagoya Univ. (Japan); Iida, T.; Takahashi, A.

1997-03-01

Nine neutron activation cross sections producing the nuclei with half-lives between 2 min and 57 min have been measured at energy range between 13.4 and 14.9 MeV for Br, Te, Dy, Ho, Yb. The cross sections of {sup 81}Br(n,p){sup 81m}Se, {sup 128}Te(n,p){sup 128m}Sb, {sup 128}Te(n,{alpha}){sup 125m}Sn, {sup 164}Dy(n,p){sup 164}Tb, {sup 165}Ho(n,{alpha}){sup 162}Tb, {sup 176}Yb(n,p){sup 176}Tm were newly obtained at the six energy points between 13.4-14.9 MeV, although the previous results have been obtained at one energy point. {sup 79}Br(n,2n){sup 78}Br, {sup 164}Dy(n,p){sup 164}Tb are compared with evaluated data of JENDL-3.2. The evaluations for these reactions agree reasonably well with experimental results. The cross sections of (n,p) reaction are compared with systematics by Kasugai et. al. The systematics agrees with experimental results. (author)

Luminescence and magnetic behaviour of almond like (Na0.5La0.5)MoO4:RE3+ (RE = Eu, Tb, Dy) nanostructures

International Nuclear Information System (INIS)

Krishnan, Rajagopalan; Thirumalai, Jagannathan; Thomas, Sabu; Gowri, Mahasampath

2014-01-01

Graphical abstract: Monodispersed almond-like (Na 0.5 La 0.5 )MoO 4 :RE 3+ nanostructures synthesized by employing ethylene-diamine tetra acetic acid (EDTA) using hydrothermal route at 200 °C for 24 h. These nanoparticles were found to be novel bi-functional candidates suitable for high-quality luminescence and magnetic applications. - Highlights: • Almond like structures of (Na 0.5 La 0.5 )MoO 4 :RE 3+ were synthesized by hydrothermal method. • Time dependent self-assembly could be the dominant process for the formation of 3D networks. • Luminescence properties of nanosamples were studied in comparison with bulk sample. • Room temperature magnetic properties of bulk and nanophosphors were investigated. - Abstract: Tetragonal phase (Na 0.5 La 0.5 )MoO 4 :RE 3+ (RE = Eu, Tb, Dy) with almond like hierarchical structures assembled from nanosheets building blocks were successfully synthesized by employing disodium ethylenediaminetetraacetic acid (Na 2 EDTA) using hydrothermal route at 200 °C for 24 h. Field emission scanning electron microscope, transmission electron microscope, and X-ray diffraction patterns were used to characterize the morphology, size, and crystal structure with good resolution. The sequestering agent EDTA acts as quadridentate ligand coordinated with metal ions [Na + , La 3+ /RE 3+ ] facilitating the formation of self-organized 3D networks. The growth mechanism for the formation of almond like nanostructures is explicated in four paths: dissolution, adsorption, in situ transformation in acidic and basic media and the effective collision. Photoluminescence excitation and emission spectra reveals a spectral blue shift which was observed in the nanosamples towards shorter wavelengths compared with the bulk sample. Upon UV irradiation, both bulk and nanostructure show strong luminescence in the red region due to the 5 D 0 → 7 F 2 transition in Eu 3+ . Also, Tb 3+ and Dy 3+ doped (Na 0.5 La 0.5 )MoO 4 phosphor exhibit green and yellow

Syntheses of rare-earth metal oxide nanotubes by the sol-gel method assisted with porous anodic aluminum oxide templates

International Nuclear Information System (INIS)

Kuang Qin; Lin Zhiwei; Lian Wei; Jiang Zhiyuan; Xie Zhaoxiong; Huang Rongbin; Zheng Lansun

2007-01-01

In this paper, we report a versatile synthetic method of ordered rare-earth metal (RE) oxide nanotubes. RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM, and X-ray diffraction (XRD) have been employed to characterize the morphology and composition of the as-prepared nanotubes. It is found that as-prepared RE oxides evolve into bamboo-like nanotubes and entirely hollow nanotubes. A new possible formation mechanism of RE oxide nanotubes in the AAO channels is proposed. These high-quantity RE oxide nanotubes are expected to have promising applications in many areas such as luminescent materials, catalysts, magnets, etc. - Graphical abstract: A versatile synthetic method for the preparation of ordered rare-earth (RE) oxide nanotubes is reported, by which RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates

Magnetic properties and structural transitions of fluorite-related rare earth osmates Ln3OsO7 (Ln=Pr, Tb)

International Nuclear Information System (INIS)

Hinatsu, Yukio; Doi, Yoshihiro

2013-01-01

Ternary rare-earth osmates Ln 3 OsO 7 (Ln=Pr, Tb) have been prepared. They crystallize in an ortho-rhombic superstructure of cubic fluorite with space group Cmcm. Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). These compounds show complex magnetic behavior at low temperatures. Pr 3 OsO 7 exhibits magnetic transitions at 8 and 73 K, and Tb 3 OsO 7 magnetically orders at 8 and 60 K. The Os moments become one-dimensionally ordered, and when the temperature is furthermore decreased, it provokes the ordering in the Ln 3+ sublattice that simultaneously becomes three-dimensionally ordered with the Os sublattice. - Graphical abstract: Ternary rare-earth osmates Ln 3 OsO 7 (Ln=Pr, Tb) have been prepared. They crystallize in an orthorhombic superstructure of cubic fluorite with space group Cmcm. Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). These compounds show complex magnetic behavior at low temperatures. Pr 3 OsO 7 exhibits magnetic transitions at 8 and 73 K, and Tb 3 OsO 7 magnetically orders at 8 and 60 K. Highlights: ► Ternary rare-earth osmates Ln 3 OsO 7 (Ln=Pr, Tb) with an ordered defect-fluorite structure have been prepared. ► Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). ► These compounds show complex magnetic behavior at low temperatures due to magnetic ordering of Ln and Os.

Adducts of rare earth tris-acetylacetonates with dimethyl sulfoxide

International Nuclear Information System (INIS)

Dzyubenko, N.G.; Kalenichenko, Yu.V.; Martynenko, L.I.

1988-01-01

Adducts of rare earth and yttrium (r.e.e., M) acetylacetonates with dimethyl sulfoxide (DMSO), MA 3 xnDMSO are synthesized. The acetylacetonates of light r.e.e. (M=La-Tb) are shown by different physico-chemical methods to form diadducts of the MA 3 x2DMSOxH 2 O composition, where A - -acetylacetonate-ion, and the acetyl-acetonates of heavy r.e.e. (M=Dy-Lu, Y)-monoadducts MA 3 xDMSO. The estimation of adduct thermal stability is carried out using the values of seeming activation energy of their thermal degradation. Monoadducts are shown to give volatile forms of rare earth acetylacetonates during heating in vacuum, and diadducts do not form volatile forms of acetylacetonates

Study of hyperfine interactions in intermetallic compounds Gd(Ni,Pd,Cu)In, Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In

International Nuclear Information System (INIS)

Lapolli, Andre Luis

2006-01-01

Systematic behavior of magnetic hyperfine field (B hf ) in the intermetallic compounds Gd(Ni,Pd,Cu)In Tb(Ni,Pd)In, Dy(Ni,Pd)In and Ho(Ni,Pd)In was studied by Perturbed Gamma-Gamma Angular Correlation spectroscopy. The measurements of B hf were carried out at the rare earth atom and in sites using the nuclear probes 140 Ce and 11 '1Cd respectively. The variation of hyperfine field with temperature, in most cases, follows the Brillouin function predicted from the molecular field theory. The hyperfine field values at rare earth atom sites obtained from 140 Ce probe as well as at in sites obtained from 111 Cd probe for each series of compounds were extrapolated to zero Kelvin B hf (T=0) from these curves. These values were compared with the values of the literature for other compounds containing the same rare earth element and all of them show a linear relationship with the ordering temperature. This indicates that the main contribution to B hf comes from the conduction electron polarization (CEP) through Fermi contact interaction and the principal mechanism of magnetic interaction in these compounds can be described by the RKKY type interaction. The values of B hf (T=0) for each family of intermetallic compounds RNiIn and RPdIn when plotted as a function of 4f spin projection of rare earth element also shows a linear relationship. Exceptions are the results for the compounds RNiIn obtained with 111 Cd probe where a small deviation from linearity is observed. The results of the measurements carried out with the 111 Cd probe were also analyzed to obtain the hyperfine parameters of the quadrupole interaction as a function of temperature for RPdln and GdNiIn compounds. The results show that for the compound GdPdIn there might be some Gd-In disorder at high temperature. (author)

Effect of Dy additions on microstructure and magnetic properties of Fe-Nd-B magnets

International Nuclear Information System (INIS)

Ramesh, R.; Thomas, G.; Ma, B.M.

1987-05-01

It is shown that increasing additions of Dy causes the remanence B/sub r/ to decrease linearly. The intrinsic coercivity, iHc, increases sharply for small additions of Dy, but the increase is not proportional for higher Dy contents. The iHc increases almost linearly with the effective anisotropy field of the RE 2 Fe 14 B phase until the Dy content is about 10% of the total rare earth content. Above this concentration, there is strong deviation from linearity. Various types of possible concentration profiles of the substituted rare earth are suggested. It is also argued that preferential segregation of Dy to the interfaces could be beneficial in increasing the nucleation field. Morphologically there is no apparent effect of Dy on the microstructure. However, in the 5 atomic % Dy sample, Dy rich oxides were observed. It is shown through Energy Dispersive Xray Spectroscopy (EDXS) line profiling that Dy partitions preferentially into the RE 2 Fe 14 B phase in all the cases. No segregation of Dy to the interphase interfaces has been detected

94 β-Decay Half-Lives of Neutron-Rich _{55}Cs to _{67}Ho: Experimental Feedback and Evaluation of the r-Process Rare-Earth Peak Formation.

Science.gov (United States)

Wu, J; Nishimura, S; Lorusso, G; Möller, P; Ideguchi, E; Regan, P-H; Simpson, G S; Söderström, P-A; Walker, P M; Watanabe, H; Xu, Z Y; Baba, H; Browne, F; Daido, R; Doornenbal, P; Fang, Y F; Gey, G; Isobe, T; Lee, P S; Liu, J J; Li, Z; Korkulu, Z; Patel, Z; Phong, V; Rice, S; Sakurai, H; Sinclair, L; Sumikama, T; Tanaka, M; Yagi, A; Ye, Y L; Yokoyama, R; Zhang, G X; Alharbi, T; Aoi, N; Bello Garrote, F L; Benzoni, G; Bruce, A M; Carroll, R J; Chae, K Y; Dombradi, Z; Estrade, A; Gottardo, A; Griffin, C J; Kanaoka, H; Kojouharov, I; Kondev, F G; Kubono, S; Kurz, N; Kuti, I; Lalkovski, S; Lane, G J; Lee, E J; Lokotko, T; Lotay, G; Moon, C-B; Nishibata, H; Nishizuka, I; Nita, C R; Odahara, A; Podolyák, Zs; Roberts, O J; Schaffner, H; Shand, C; Taprogge, J; Terashima, S; Vajta, Z; Yoshida, S

2017-02-17

The β-decay half-lives of 94 neutron-rich nuclei ^{144-151}Cs, ^{146-154}Ba, ^{148-156}La, ^{150-158}Ce, ^{153-160}Pr, ^{156-162}Nd, ^{159-163}Pm, ^{160-166}Sm, ^{161-168}Eu, ^{165-170}Gd, ^{166-172}Tb, ^{169-173}Dy, ^{172-175}Ho, and two isomeric states ^{174m}Er, ^{172m}Dy were measured at the Radioactive Isotope Beam Factory, providing a new experimental basis to test theoretical models. Strikingly large drops of β-decay half-lives are observed at neutron-number N=97 for _{58}Ce, _{59}Pr, _{60}Nd, and _{62}Sm, and N=105 for _{63}Eu, _{64}Gd, _{65}Tb, and _{66}Dy. Features in the data mirror the interplay between pairing effects and microscopic structure. r-process network calculations performed for a range of mass models and astrophysical conditions show that the 57 half-lives measured for the first time play an important role in shaping the abundance pattern of rare-earth elements in the solar system.

Stability of rare earth complexes with 2-(o-hydroxyphenyl)benzimidazole in aqueous-dioxane medium. Ustojchivost' kompleksnykh soedinenij RZEh s 2-(o-oksifenil)benzimidazolom v vodno-dioksanovoj srede

Energy Technology Data Exchange (ETDEWEB)

Akhrimenko, Z M; Panyushkin, V T; Fedorova, M V [Kubanskij Gosudarstvennyj Univ., Krasnodar (USSR)

1990-01-01

Method of potentiometric titration was used to determine protonation constants of 2-(-hydroxyphenyl)benzimidazole (pK{sub 1}=4.5; pK{sub 2}=11.30) and stability constants of Pr,Nd,Sm,Eu,Tb,Dy complexes with this ligand. Nonmonotonous change of lgK{sub 1} with increase of ordinal number of rare earth element was revealed.

Static magnetic susceptibility, crystal field and exchange interactions in rare earth titanate pyrochlores.

Science.gov (United States)

Malkin, B Z; Lummen, T T A; van Loosdrecht, P H M; Dhalenne, G; Zakirov, A R

2010-07-14

The experimental temperature dependence (T = 2-300 K) of single crystal bulk and site susceptibilities of rare earth titanate pyrochlores R(2)Ti(2)O(7) (R = Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) is analyzed in the framework of crystal field theory and a mean field approximation. Analytical expressions for the site and bulk susceptibilities of the pyrochlore lattice are derived taking into account long range dipole-dipole interactions and anisotropic exchange interactions between the nearest neighbor rare earth ions. The sets of crystal field parameters and anisotropic exchange coupling constants have been determined and their variations along the lanthanide series are discussed.

Effects of pressure and magnetic field on transport properties of Y1-xRxCo2 alloys (R=Gd, Tb, Dy, Ho and Er)

International Nuclear Information System (INIS)

Takaesu, Y; Nakama, T; Kinjyo, A; Yonamine, S; Hedo, M; Yagasaki, K; Uchima, K; Uwatoko, Y; Burkov, A T

2010-01-01

Electrical resistivity ρ and thermopower S of Y 1-x R x Co 2 (R=Gd, Tb, Dy, Ho and Er) Laves phase alloy systems were measured at temperatures from 1.5 K to 300 K in magnetic fields up to 15 T and under hydrostatic pressure up to 2 GPa. We show that there is a universal linear relation between the pressure and magnetic field derivatives of the resistivity, dρ/dP and dρ/dB, with gradient, determined by pressure derivative of the critical metamagnetic field of the cobalt 3d electron system. A similar scaling behavior was found for the thermopower dependencies on pressure and alloy composition.

Hetero-metallic {3d-4f-5d} complexes: preparation and magnetic behavior of trinuclear [(L(Me2)Ni-Ln){W(CN)(8)}] compounds (Ln = Gd, Tb, Dy, Ho, Er, Y; L(Me2) = Schiff base) and variable SMM characteristics for the Tb derivative.

Science.gov (United States)

Sutter, Jean-Pascal; Dhers, Sébastien; Rajamani, Raghunathan; Ramasesha, S; Costes, Jean-Pierre; Duhayon, Carine; Vendier, Laure

2009-07-06

Assembling bimetallic {Ni-Ln}(3+) units and {W(CN)(8)}(3-) is shown to be an efficient route toward heteronuclear {3d-4f-5d} compounds. The reaction of either the binuclear [{L(Me2)Ni(H(2)O)(2)}{Ln(NO(3))(3)}] complexes or their mononuclear components [L(Me2)Ni] and Ln(NO(3))(3) with (HNBu(3))(3){W(CN)(8)} in dmf followed by diffusion of tetrahydrofuran yielded the trinuclear [{L(Me2)NiLn}{W(CN)(8)}] compounds 1 (Ln = Y), 2a,b (Gd), 3a,b (Tb), 4 (Dy), 5 (Ho), and 6 (Er) as crystalline materials. All of the derivatives possess the trinuclear core resulting from the linkage of the {W(CN)(8)} to the Ni center of the {Ni-Ln} unit. Differences are found in the solvent molecules acting as ligands and/or in the lattice depending on the crystallization conditions. For all the compounds ferromagnetic {Ni-W} and {Ni-Ln} (Ln = Gd, Tb, Dy, and Er} interactions are operative resulting in high spin ground states. Parameterization of the magnetic behaviors for the Y and Gd derivatives confirmed the strong cyano-mediated {Ni-W} interaction (J(NiW) = 27.1 and 28.5 cm(-1)) compared to the {Ni-Gd} interaction (J(NiGd) = 2.17 cm(-1)). The characteristic features for slow relaxation of the magnetization are observed for two Tb derivatives, but these are modulated by the crystal phase. Analysis of the frequency dependence of the alternating current susceptibility data yielded U(eff)/k(B) = 15.3 K and tau(0) = 4.5 x 10(-7) s for one derivative whereas no maxima of chi(M)'' appear above 2 K for the second one.

Peculiarity of component interaction in {l_brace}Y, Dy{r_brace}-Mn-Sn ternary systems

Energy Technology Data Exchange (ETDEWEB)

Romaka, V.V. [Department of Materials Engineering and Applied Physics, Lviv Polytechnic National University, Ustyyanovycha Str. 5, 79013 Lviv (Ukraine); Konyk, M. [Inorganic Chemistry Department, Ivan Franko Lviv National University, Kyryla and Mefodiya Str. 6, 79005 Lviv (Ukraine); Romaka, L., E-mail: romakal@franko.lviv.ua [Inorganic Chemistry Department, Ivan Franko Lviv National University, Kyryla and Mefodiya Str. 6, 79005 Lviv (Ukraine); Pavlyuk, V. [Inorganic Chemistry Department, Ivan Franko Lviv National University, Kyryla and Mefodiya Str. 6, 79005 Lviv (Ukraine); Jan Dlugosz University, Institute of Chemistry, Environmental Protection and Biotechnology, al. Armii Krajowej 13/15, 42200 Czestochowa (Poland); Ehrenberg, H. [Institute for Complex Materials, IFW Dresden, Helmholtzstrasse 20, D-01069 Dresden (Germany); Tkachuk, A. [Inorganic Chemistry Department, Ivan Franko Lviv National University, Kyryla and Mefodiya Str. 6, 79005 Lviv (Ukraine)

2011-07-14

Highlights: > {l_brace}Y, Dy{r_brace}-Mn-Sn ternary systems at 770 K are characterized by formation of stannides with general compositions RMn{sub 6}Sn{sub 6} and R{sub 4}Mn{sub 4}Sn{sub 7}. > The crystal structure of YMn{sub 6}Sn{sub 6} was determined by single crystal and powder diffraction methods. > Structural analysis showed that Dy{sub 4}Mn{sub 4}Sn{sub 7} compound is disordered. > Isostructural R{sub 4}Mn{sub 4}Sn{sub 7} compounds were also found with Gd, Tb, Ho, Er, Tm(confirmed), Yb, and Lu. - Abstract: The phase equilibria in the Y-Mn-Sn and Dy-Mn-Sn ternary systems were studied at 770 K by means of X-ray and metallographic analyses in the whole concentration range. Both Y-Mn-Sn and Dy-Mn-Sn systems are characterized by formation of two ternary compounds RMn{sub 6}Sn{sub 6} (MgFe{sub 6}Ge{sub 6}-type, space group P6/mmm) and R{sub 4}Mn{sub 4}Sn{sub 7} (Zr{sub 4}Co{sub 4}Ge{sub 7}-type, space group I4/mmm). The disorder in Dy{sub 4}Mn{sub 4}Sn{sub 7} compound was found by single crystal method. Compounds with the same type of structure were also found with Gd, Tb, Ho, Er, Tm (confirmed), Yb, and Lu and their lattice parameters were determined.

Carbonato-bridged Ni(II)2Ln(III)2 (Ln(III) = Gd(III), Tb(III), Dy(III)) complexes generated by atmospheric CO2 fixation and their single-molecule-magnet behavior: [(μ4-CO3)2{Ni(II)(3-MeOsaltn)(MeOH or H2O)Ln(III)(NO3)}2]·solvent [3-MeOsaltn = N,N'-bis(3-methoxy-2-oxybenzylidene)-1,3-propanediaminato].

Science.gov (United States)

Sakamoto, Soichiro; Fujinami, Takeshi; Nishi, Koshiro; Matsumoto, Naohide; Mochida, Naotaka; Ishida, Takayuki; Sunatsuki, Yukinari; Re, Nazzareno

2013-06-17

Atmospheric CO2 fixation of [Ni(II)(3-MeOsaltn)(H2O)2]·2.5H2O [3-MeOsaltn = N,N'-bis(3-methoxy-2-oxybenzylidene)-1,3-propanediaminato], Ln(III)(NO3)3·6H2O, and triethylamine occurred in methanol/acetone, giving a first series of carbonato-bridged Ni(II)2Ln(III)2 complexes [(μ4-CO3)2{Ni(II)(3-MeOsaltn)(MeOH)Ln(III)(NO3)}2] (1Gd, 1Tb, and 1Dy). When the reaction was carried out in acetonitrile/water, it gave a second series of complexes [(μ4-CO3)2{Ni(II)(3-MeOsaltn)(H2O)Ln(III)(NO3)}2]·2CH3CN·2H2O (2Gd, 2Tb, and 2Dy). For both series, each Ni(II)2Ln(III)2 structure can be described as two di-μ-phenoxo-bridged Ni(II)Ln(III) binuclear units bridged by two carbonato CO3(2-) units to form a carbonato-bridged (μ4-CO3)2{Ni(II)2Ln(III)2} structure. The high-spin Ni(II) ion has octahedral coordination geometry, and the Ln(III) ion is coordinated by O9 donor atoms from Ni(II)(3-MeOsaltn), bidentate NO3(-), and one and two oxygen atoms of two CO3(2-) ions. The NO3(-) ion for the first series roughly lie on Ln-O(methoxy) bonds and are tilted toward the outside, while for the second series, the two oxygen atoms roughly lie on one of the Ln-O(phenoxy) bonds due to the intramolecular hydrogen bond. The temperature-dependent magnetic susceptibilities indicated a ferromagnetic interaction between the Ni(II) and Ln(III) ions (Ln(III) = Gd(III), Tb(III), Dy(III)) for all of the complexes, with a distinctly different magnetic behavior between the two series in the lowest-temperature region due to the Ln(III)-Ln(III) magnetic interaction and/or different magnetic anisotropies of the Tb(III) or Dy(III) ion. Alternating-current susceptibility measurements under the 0 and 1000 Oe direct-current (dc) bias fields showed no magnetic relaxation for the Ni(II)2Gd(III)2 complexes but exhibited an out-of-phase signal for Ni(II)2Tb(III)2 and Ni(II)2Dy(III)2, indicative of slow relaxation of magnetization. The energy barriers, Δ/kB, for the spin flipping were estimated from the Arrhenius

Rare-earth doped gadolinia based phosphors for potential multicolor and white light emitting deep UV LEDs.

Science.gov (United States)

Bedekar, Vinila; Dutta, Dimple P; Mohapatra, M; Godbole, S V; Ghildiyal, R; Tyagi, A K

2009-03-25

Gadolinium oxide host and europium/dysprosium/terbium doped gadolinium oxide nanoparticles were synthesized using the sonochemical technique. Gadolinium oxide nanocrystals were also co-doped with total 2 mol% of Eu(3+)/Dy(3+),Eu(3+)/Tb(3+),Dy(3+)/Tb(3+), and also Eu(3+)/Dy(3+)/Tb(3+) ions, by the same method. The nanoparticles obtained were characterized using powder x-ray diffraction (XRD), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) techniques. The size of the particles ranged from 15 to 30 nm. The triple doped samples showed multicolor emission on single wavelength excitation. The photoluminescence results were correlated with the lifetime data to get an insight into the luminescence and energy transfer processes taking place in the system. On excitation at 247 nm, the novel nanocrystalline Gd(2)O(3):RE (RE = Dy, Tb) phosphor resulted in having very impressive CIE chromaticity coordinates of x = 0.315 and y = 0.316, and a correlated color temperature of 6508 K, which is very close to standard daylight.

The ternary systems Sc-Sm(Dy)-Si at 870 K

International Nuclear Information System (INIS)

Kotur, B.Ya.; Mokra, I.Ya.; Toporinskij, A.Ya.

1991-01-01

Isothermal cross sections of the ternary systems Sc-Sm-Si and Sc-Dy-Si at 870 K have been plotted. Investigation of scandium and disprosium in ternary systems have been examined by X-ray diffraction and microstructure analysis. Besides literary data on binary systems Sc-Si, Sm-Si, Dy-Si have been used. Formation of limited (Sc-Sm-Si, Sc-Dy-Si) and continuous (Sc-Dy-Si) solid solutions based on bisilicides of Sc and Sm(Dy) is discovered. Two and five ternary compounds in Sc-Sm-Si and Sc-Dy-Si systems have been determined and their crystal structure has been established. When investigating of Sc-(rare earth element)-Si ternary systems and should take into account the specific interaction of scandium and samarium with REE

Determination of the cross section for (n,p) reaction with producing short-lived nuclei on the 162,163Dy isotopes at 13.5 and 14.8 MeV

International Nuclear Information System (INIS)

Luo, Junhua; Feng, Zhifu; An, Li; Jiang, Li; He, Long

2016-01-01

Activation cross-sections for the 162 Dy(n,p) 162 Tb and 163 Dy(n,p) 163 Tb reactions have been measured by means of the activation technique and a coaxial HPGe γ-ray detector at 13.5 and 14.8 MeV. The fast neutrons were produced via the 3 H(d,n) 4 He reaction on Pd-300 neutron generator. The natural high-purity Dy 2 O 3 powder was used as target material. Theoretical excitation functions were calculated using the nuclear-reaction codes EMPIRE-3.2 Malta and TALYS-1.6 with default parameters, at neutron energies varying from the reaction threshold to 20 MeV. The results were also discussed and compared with some corresponding values found in the literature, with the comprehensive evaluation data in ENDF/B-VII.1 and JENDF-4.0 libraries, and with the estimates obtained from a published empirical formula based on the statistical model with Q-value dependence and odd–even effects taken into consideration. - Highlights: • The cross sections for the 162 Dy(n,p) 162 Tb and 163 Dy(n,p) 163 Tb have been measured. • 93 Nb(n,2n) 92m Nb was used as a monitor for neutron fluence. • Codes TALYS-1.6 and EMPIRE-3.2 Malta were used to model the reactions. • The results were compared with previous data. • Inconsistency with previous data and with model calculations are noted.

Some kinetic properties of DySnSe2 combination

International Nuclear Information System (INIS)

Murguzov, M.I.; Mammadova, E.R.

2008-01-01

Recently, to the acquisition of multi-component alloys and combination in the presence of rare-earth metals (REM) interest has grown considerably. According to preliminary data, in the presence of rare-earth metals you can obtain perspective semiconductor materials which are of practical importance, and can be used in various fields of microelectronics in a complex system of chalcogenides. DySnSe 2 combination is also includes to this system. Physical peculiarities of these combinations have been studied in wide interval. DySnSe 2 combination crystallizes in ortho rhombic crystal system and is an indemnification n-type semiconductor material. The mechanism of electrical conductivity in DySnSe 2 semiconductor combination is complicated and cargo carrier scattering changes at low temperatures. That is why, the mixed type conductivity occurs

Magnetocrystalline anisotropy in a (110) (Tb0.27Dy0.73)Fe2 thin-film

International Nuclear Information System (INIS)

Fuente, C de la; Arnaudas, J I; Benito, L; Ciria, M; Moral, A del; Dufour, C; Dumesnil, K

2004-01-01

Magnetic anisotropy measurements performed in a (110) (Tb 0.27 Dy 0.73 )Fe 2 (Terfenol-D) film epitaxially grown on a sapphire substrate are presented. The magnetic torque curves have been determined by using a vectorial vibrating sample magnetometer, which allows us to measure the angular dependence of magnetization components parallel, M parallel , and perpendicular, M perp , to the applied field up to 2 T. The fourfold symmetry associated with the cubic structure within the (110) plane is clearly observed. The analysis of the experimental torque has been carried out considering magnetocrystalline anisotropy up to sixth order and magnetoelastic energy up to second order; so, the magnetocrystalline anisotropy constants in the (110) plane of the film, K 1 and K 2 , have been obtained. This allows us to determine the direction of the magnetization easy axis for (110) Terfenol-D thin-film: it is [1bar12] at RT, passes through [3bar34] at 140 K and then changes to [1bar20] at 40 K. It was completely impossible to explain the angular dependence of the experimental magnetic torque without including shear and tetragonal magnetoelastic stress parameters, b 2 and b 1 , respectively. This confirms the paramount role of the strain in the determination of the magnetic properties in this kind of Terfenol-D thin film

An ICP AES method for determination of dysprosium and terbium in high purity yttrium oxide

International Nuclear Information System (INIS)

Rupawate, V.H.; Hareendran, K.N.; Roy, S.B.

2011-01-01

High purity yttrium finds interesting application in astronavigation, luminescence, nuclear energy and metallurgical industries. Most of these applications require yttrium oxide of highest purity. Consequently there is a need for production of high purity yttrium oxide. Separation and purification of yttrium from other rare earths is a challenging task due to their close chemical properties. Liquid-liquid extraction and ion exchange have been widely used in the production of yttrium oxide of highest purity. Determination of impurities, especially other rare earths, in ppm level is required for process development and chemical characterization of the high purity Y 2 O 3 . Many methods have been described in literature. However since the advent of ICP AES much work in this area has been carried out by this technique. This paper describes the work done for determination of dysprosium (Dy) and terbium (Tb) in yttrium oxide using a high resolution sequential ICP AES. Emission spectra of rare earth elements are very complex and due to this complexity it is important to select spectral interference free analyte lines for determination of rare earths in rare earth matrix. For the determination of Dy and Tb in Y 2 O 3 , sensitive lines of Dy and Tb are selected from the instrument wavelength table and spectral interference free emission lines for the determination is selected by scanning around the selected wavelengths using 5 g/L Y solution and 5 mg/L standard solutions of Dy and Tb prepared in 4% nitric acid. It is found 353.170 nm line of Dy and 350.917 nm line Tb is suitable for quantitative determination. The signal to background ratio increases with increase in matrix concentration, i.e. from 1 to 5 mg/L. The optimum forward power is determined and it is found to be 1100W for Dy and 1000W for Tb. The instrument is calibrated using matrix matched standards containing 5g/L of Y matrix. Samples are dissolved in nitric acid and Y concentration is maintained at 5g/L. Two

Local rhombohedral symmetry in Tb{sub 0.3}Dy{sub 0.7}Fe{sub 2} near the morphotropic phase boundary

Energy Technology Data Exchange (ETDEWEB)

Ma, Tianyu, E-mail: maty@zju.edu.cn [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Key Laboratory of Novel Materials for Information Technology of Zhejiang Province, Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University, Hangzhou 310027 (China); Ferroic Physics Group, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba 305-0047, Ibaraki (Japan); Liu, Xiaolian; Pan, Xingwen; Li, Xiang; Jiang, Yinzhu; Yan, Mi, E-mail: mse-yanmi@zju.edu.cn [State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering, Key Laboratory of Novel Materials for Information Technology of Zhejiang Province, Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University, Hangzhou 310027 (China); Li, Huiying; Fang, Minxia [Multi-disciplinary Materials Research Center, Frontier Institute of Science and Technology, Xi' an Jiaotong University, Xi' an 710049 (China); Ren, Xiaobing, E-mail: ren.xiaobing@nims.go.jp [Ferroic Physics Group, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba 305-0047, Ibaraki (Japan); Multi-disciplinary Materials Research Center, Frontier Institute of Science and Technology, Xi' an Jiaotong University, Xi' an 710049 (China)

2014-11-10

The recently reported morphotropic phase boundary (MPB) in a number of giant magnetostrictive materials (GMMs) has drawn considerable interest to the local symmetry/structure near MPB region of these materials. In this letter, by in-situ X-ray diffraction and AC magnetic susceptibility measurements, we show that Tb{sub 0.3}Dy{sub 0.7}Fe{sub 2}, the typical composition of Terfenol-D GMMs, has coexistence of rhombohedral and tetragonal phases over a wide temperature range in the vicinity of MPB. High resolution transmission electron microscopy provides direct evidence for local rhombohedral symmetry of the ferromagnetic phase and reveals regular-shaped nanoscale domains below 10 nm. The nano-sized structural/magnetic domains are hierarchically inside a single micron-sized stripe-like domain with the same average magnetization direction. Such domain structures are consistent with the low magnetocrystalline anisotropy and easy magnetic/structural domain switching under magnetic field, thus generating large magnetostriction at low field.

Synthesis and characterization of heterobinuclear (La-Zn, Pr-Zn, Nd-Zn, Sm-Zn, Eu-Zn, Gd-Zn, Tb-Zn, Dy-Zn) azine-bridged complexes

International Nuclear Information System (INIS)

Singh, Bachcha; Srivastav, A.K.; Singh, P.K.

1997-01-01

Zinc(II) complex of 2-acetylpyridine salicyl aldazine (Haps) of the type Zn(aps) 2 (H 2 O) 2 has been synthesised. The reaction of Zn(aps) 2 (H 2 O) 2 with lanthanide chlorides, LnCl 3 (where Ln=La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) yields azine-bridged heterobinuclear complexes of the formulae LnCl 3 Zn(aps) 2 (H 2 O) 2 . These complexes have been characterized by elemental analyses, molecular weight, conductance (solid and solution) and magnetic susceptibility measurements, mass, IR and electronic spectral data. X-ray powder diffraction data indicate the tetragonal unit lattice for Zn(aps) 2 (H 2 O) 2 and PrCl 3 Zn(aps) 2 (H 2 O) 2 . (author)

Magnetic properties and structural transitions of fluorite-related rare earth osmates Ln{sub 3}OsO{sub 7} (Ln=Pr, Tb)

Energy Technology Data Exchange (ETDEWEB)

Hinatsu, Yukio, E-mail: hinatsu@sci.hokudai.ac.jp [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan); Doi, Yoshihiro [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan)

2013-02-15

Ternary rare-earth osmates Ln{sub 3}OsO{sub 7} (Ln=Pr, Tb) have been prepared. They crystallize in an ortho-rhombic superstructure of cubic fluorite with space group Cmcm. Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). These compounds show complex magnetic behavior at low temperatures. Pr{sub 3}OsO{sub 7} exhibits magnetic transitions at 8 and 73 K, and Tb{sub 3}OsO{sub 7} magnetically orders at 8 and 60 K. The Os moments become one-dimensionally ordered, and when the temperature is furthermore decreased, it provokes the ordering in the Ln{sup 3+} sublattice that simultaneously becomes three-dimensionally ordered with the Os sublattice. - Graphical abstract: Ternary rare-earth osmates Ln{sub 3}OsO{sub 7} (Ln=Pr, Tb) have been prepared. They crystallize in an orthorhombic superstructure of cubic fluorite with space group Cmcm. Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). These compounds show complex magnetic behavior at low temperatures. Pr{sub 3}OsO{sub 7} exhibits magnetic transitions at 8 and 73 K, and Tb{sub 3}OsO{sub 7} magnetically orders at 8 and 60 K. Highlights: Black-Right-Pointing-Pointer Ternary rare-earth osmates Ln{sub 3}OsO{sub 7} (Ln=Pr, Tb) with an ordered defect-fluorite structure have been prepared. Black-Right-Pointing-Pointer Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). Black-Right-Pointing-Pointer These compounds show complex magnetic behavior at low temperatures due to magnetic ordering of Ln and Os.

Luminescence behaviors of Eu- and Dy-codoped alkaline earth metal aluminate phosphors through potassium carbonate coprecipitation

Energy Technology Data Exchange (ETDEWEB)

Liang, Chen-Jui, E-mail: cjliang@fcu.edu.tw; Siao, Hao-Yi

2016-07-01

An electronic energy mechanism of activator and sensitizer was established to describe the luminescence behaviors of Eu- and Dy-codoped M(II)Al{sub 2}O{sub 4} (M(II) = Ba, Sr, Ca, Mg) phosphors through potassium carbonate coprecipitation. Experimental results demonstrated that the prepared phosphors exhibited superior crystallinity at a temperature lower than 950 °C. The phosphors are ordered according to emission intensity as follows Ca- > Ba- > Sr- > Mg-containing phosphors. The energy level for Eu{sup 2+} 4f{sup 6}5d{sup 1} → 4f{sup 7}, Eu{sup 3+4}D{sub 0} → {sup 7}F, and Dy{sup 3+4}F{sub 9/2} → {sup 6}H transitions and the effects of nephelauxetic and crystal field in Ba-, Sr-, and Ca-containing phosphors were discussed. The energy gap, (hv){sub em}, between 5d and 4f of Eu{sup 2+} ion is strongly affected by host composition, crystal field strength, and nephelauxetic effect. The infrared emission of 4f{sub 9/2} → 6h for Dy{sup 3+} is merely depend on the transfer of energy from Eu{sup 2+} upon excited. Ca-containing phosphor with maximum (hv){sub em} is attributed to the lowest bond length of Ca−O and highest ionization potential of Ca{sup 2+} ion, which leads to the effects of crystal field and nephelauxetic greater than that in the other phosphors. - Highlights: • The list of the collected figure captions: • Develop a new coprecipitation method to prepare high efficiency phosphors. • Obtain superior crystallinity with lower calcination temperature. • Luminescence behavior of Eu- and Dy-codoped on aluminate phosphors is discussed. • Investigate the effects of alkaline earth metal containing on crystal field and nephelauxetic.

β-γ and isomeric decay spectroscopy of 168Dy

Directory of Open Access Journals (Sweden)

Zhang G.X.

2018-01-01

Full Text Available This contribution will report on the experimental work on the level structure of 168Dy. The experimental data have been taken as part of the EURICA decay spectroscopy campaign at RIBF, RIKEN in November 2014. In the experiment, a 238U primary beam is accelerated up to 345 MeV/u with an average intensity of 12 pnA. The nuclei of interest are produced by in-flight fission of 238U impinging on Be target with a thickness of 5 mm. The excited states of 168Dy have been populated through the decay from a newly identified isomeric state and via the β decay from 168Tb. In this contribution, scientific motivations, experimental procedure and some preliminary results for this study are presented.

β-γ and isomeric decay spectroscopy of 168Dy

Science.gov (United States)

Zhang, G. X.; Watanabe, H.; Kondev, F. G.; Lane, G. J.; Regan, P. H.; Söderström, P.-A.; Walker, P. M.; Kanaoka, H.; Korkulu, Z.; Lee, P. S.; Liu, J. J.; Nishimura, S.; Wu, J.; Yagi, A.; Ahn, D. S.; Alharbi, T.; Baba, H.; Browne, F.; Bruce, A. M.; Carroll, R. J.; Chae, K. Y.; Dombradi, Zs.; Doornenbal, P.; Estrade, A.; Fukuda, N.; Griffin, C.; Ideguchi, E.; Inabe, N.; Isobe, T.; Kanaya, S.; Kojouharov, I.; Kubo, T.; Kubono, S.; Kurz, N.; Kuti, I.; Lalkovski, S.; Lee, C. S.; Lee, E. J.; Lorusso, G.; Lotay, G.; Moon, C.-B.; Nishizuka, I.; Nita, C. R.; Odahara, A.; Patel, Z.; Phong, V. H.; Podolyák, Zs.; Roberts, O. J.; Sakurai, H.; Schaffner, H.; Shand, C. M.; Shimizu, Y.; Sumikama, T.; Suzuki, H.; Takeda, H.; Terashima, S.; Vajta, Zs.; Valiente-Dóbon, J. J.; Xu, Z. Y.

2018-05-01

This contribution will report on the experimental work on the level structure of 168Dy. The experimental data have been taken as part of the EURICA decay spectroscopy campaign at RIBF, RIKEN in November 2014. In the experiment, a 238U primary beam is accelerated up to 345 MeV/u with an average intensity of 12 pnA. The nuclei of interest are produced by in-flight fission of 238U impinging on Be target with a thickness of 5 mm. The excited states of 168Dy have been populated through the decay from a newly identified isomeric state and via the β decay from 168Tb. In this contribution, scientific motivations, experimental procedure and some preliminary results for this study are presented.

Synthesis and luminescence properties of BaTiO3:RE (RE = Gd , Dy ...

Indian Academy of Sciences (India)

thermoluminescence (TL) properties of BaTiO3 samples doped with Gd3+, Dy3+, Tb3+ and Lu3+ were investigated. ... electron microscope using an accelerating voltage of 20 kV. .... doping of 1% mole Gd3+ ion into the BaTiO3 compound.

Biographical Sources in the Sciences--Life, Earth and Physical Sciences (1989-2006). LC Science Tracer Bullet. TB 06-4

Science.gov (United States)

Freitag, Ruth, Comp.; Bradley, Michelle Cadoree, Comp.

2006-01-01

This guide offers a systematic approach to the wide variety of published biographical information on men and women of science in the life, earth and physical sciences, primarily from 1989 to 2006, and complements Library of Congress Science Tracer Bullet "TB88-3" ("Biographical Sources in the Sciences," compiled 1988 [ED306074]) and "TB06-7"…

Phase transitions of rare earth compounds during immobilization by foamed corundum

International Nuclear Information System (INIS)

Potemkina, T.I.; Zakharov, M.A.; Plotnikova, T.E.

1992-01-01

Expansion of work on the environmentally safe handling of radioactive materials has become very important in recent years. The proposed method for immobilizing radionuclides by injection into a porous matrix and subsequent fixation has a definite advantage over other techniques, because of its simplicity and low cost. This raises a number of problems that require careful study. The authors can distinguish the following: choice of porous matrix materials; thermal decomposition of nitrates directly in the matrix itself, which determines the minimum firing temperature; behavior and properties of oxides produced in nitrate decomposition; conditions for compound formation between injected solutions and matrix material; processes occurring during immobilizer storage. The rare earth nitrate series can be divided into two groups on the basis of behavior during thermal decomposition: the elements preceding and following Gd. The first group includes La, Pr, And Eu, for which decomposition begins simultaneously with conclusion of dehydration; the second includes Dy, Tb, and Yb, for which nitrate group decomposition begins before dehydration is complete. The authors utilized DTA, XPA, and IR analysis to study the physicochemical properties of the immobilizer produced by a single impregnation of the foamed corundum with rare earth (La, Eu, Dy, Tb, and Yb) nitrate solutions and subsequent firing at 900 degrees C for 30 min. The choice of these rare earths was dictated by the fact that the Ln 2 O 3 -AlO 3 system can be divided into three groups on the basis of phase ratios: La-Nd, Sm-Eu, and Gd-Lu. Lanthanide monoaluminates are formed in all these groups, and the difference lies in the other reaction products generated: LnAl 11 O 18 for La-Nd, LnAl 11 O 18 and Ln 4 Al 2 O 9 for Sm-Eu, and Ln 4 Al 2 O 9 and Ln 3 Al 5 O 12 for Gd-Lu

Fusion of 6Li with 159Tb at near-barrier energies

International Nuclear Information System (INIS)

Pradhan, M. K.; Mukherjee, A.; Basu, P.; Goswami, A.; Kshetri, R.; Roy, Subinit; Chowdhury, P. Roy; Sarkar, M. Saha; Palit, R.; Parkar, V. V.; Santra, S.; Ray, M.

2011-01-01

Complete and incomplete fusion cross sections for 6 Li + 159 Tb have been measured at energies around the Coulomb barrier by the γ-ray method. The measurements show that the complete fusion cross sections at above-barrier energies are suppressed by ∼34% compared to coupled-channel calculations. A comparison of the complete fusion cross sections at above-barrier energies with the existing data for 11,10 B + 159 Tb and 7 Li + 159 Tb shows that the extent of suppression is correlated with the α separation energies of the projectiles. It has been argued that the Dy isotopes produced in the reaction 6 Li + 159 Tb at below-barrier energies are primarily due to the d transfer to unbound states of 159 Tb, while both transfer and incomplete fusion processes contribute at above-barrier energies.

Magnetic properties of ball-milled TbFe2 and TbFe2B

Indian Academy of Sciences (India)

Unknown

1. Introduction. The RFe2 (R = rare earth) Laves phase compounds are known to possess large cubic anisotropy (Clark et al 1972) and highest Curie temperature (TC) of all RT2 compounds. (T = transition metal). RFe2 ... TbFe2 and TbFe2B were prepared by arc melting the high pure elements (Tb and B, 99⋅9% purity; Fe, ...

Calculations of the magnetic entropy change in amorphous through a microscopic anisotropic model: Applications to Dy{sub 70}Zr{sub 30} and DyCo{sub 3.4} alloys

Energy Technology Data Exchange (ETDEWEB)

Ranke, P. J. von, E-mail: von.ranke@uol.com.br; Nóbrega, E. P.; Ribeiro, P. O.; Alvarenga, T. S. T.; Lopes, P. H. O.; Sousa, V. S. R. de; Oliveira, N. A. de [Instituto de Física, Universidade do Estado do Rio de Janeiro—UERJ, Rua São Francisco Xavier, 524, 20550-013 Rio de Janeiro (Brazil); Caldas, A. [Sociedade Unificada de Ensino Superior e Cultura, SUESC, 20211-351 Rio de Janeiro (Brazil); Alho, B. P. [Instituto de Aplicação Fernando Rodrigues da Silveira, Universidade do Estado do Rio de Janeiro, Rua Santa Alexandrina, 288, 20260-232 Rio de Janeiro (Brazil); Carvalho, G. [Laboratório Nacional de Luz Sincroton—LNLS, 13083-970 Campinas, São Paulo (Brazil); Magnus, A.

2014-10-14

We report theoretical investigations on the magnetocaloric effect, described by the magnetic entropy change in rare earth—transition metal amorphous systems. The model includes the local anisotropy on the rare earth ions in Harris-Plischke-Zuckermann assumptions. The transition metals ions are treated in terms of itinerant electron ferromagnetism and the magnetic moment of rare earth ions is coupled to the polarized d-band by a local exchange interaction. The magnetocaloric effect was calculated in DyCo{sub 3.4} system, which presents amorphous sperimagnetic configuration. The calculations predict higher refrigerant capacity in the amorphous DyCo{sub 3.4} than in DyCo{sub 2} crystal, highlighting the importance of amorphous magnetocaloric materials. Our calculation of the magnetocaloric effect in Dy{sub 70}Zr{sub 30}, which presents amorphous asperomagnetic configuration, is in good agreement with the experimental result. Furthermore, magnetic entropy changes associated with crystal-amorphous configurations change are estimated.

Hybrid silica nanoparticles for sequestration and luminescence detection of trivalent rare-earth ions (Dy3+ and Nd3+) in solution

Science.gov (United States)

Topel, Seda Demirel; Legaria, Elizabeth Polido; Tiseanu, Carmen; Rocha, João; Nedelec, Jean-Marie; Kessler, Vadim G.; Seisenbaeva, Gulaim A.

2014-12-01

New hybrid material-based adsorbents acting also as luminescent probes upon uptake of trivalent rare-earth (RE) ions Nd3+ and Dy3+ have been developed. SiO2 NPs functionalized by three different organic ligands, N-aminopropylen-amido-iminodiacetic acid (L1), pyridine-α,β-dicarboxylic acid bis(propylenamide) (L2), and N-propylen-iminodiacetic acid (L3), have been produced and fully characterized by 13C, 1H, and 29Si solid-state NMR, FTIR, TGA, XRD, TEM, nitrogen gas adsorption, and also by NTA and DLS in solution. The synthesized hybrid materials are well dispersible and stable in aqueous solutions according to NTA and consist of spheres with diameters less than 100 nm. Their affinities to the lanthanide ions Dy3+ and Nd3+ have been investigated in aqueous solution and characterized by SEM-EDS and complexometric titration, demonstrating that they can be successfully used as adsorbents for sequestration of trivalent RE ions. The adsorbed RE ions can efficiently be desorbed from saturated nanoadsorbents by addition of hydrochloric acid. The produced nanomaterials may also be used as luminescent probes for Dy3+ and Nd3+ ions in solution.

Studies on mixed ligand complexes of adenine and xanthine with some rare earth ions

International Nuclear Information System (INIS)

Rastogi, P.R.; Singh, Mamta; Nayan, Ram

1993-01-01

Interactions of 6-aminopurine (adenine, HA) and 2,6-dihydroxypurine (xanthine, HB) with trivalent rare earth ions Y, Tb, Dy, Ho, Er and Tm, have been studied by pH-titration methods in aqueous solution at 20 o (μ = 0.1 M KNO 3 ). The ligands in their mixtures with tripositive rare earth ions (M 3+ ) form a number of mixed ligand complexes, M 3+ -adenine-xanthine, M 3+ -(adenine) 2 -xanthine, M 3+ -adenine-(xanthine) 2 in addition to the binary complexes, M 3+ -(adenine), M 3+ -(adenine) 2 , M 3+ -(adenine) 3 , M 3+ -(xanthine), M 3+ -(xanthine) 2 and M 3+ -(xanthine) 3 . The stability constants of these complexes have been evaluated and the results discussed. (author). 13 refs., 1 fig., 1 tab

Synthesis, structure, luminescent, and magnetic properties of carbonato-bridged Zn(II)2Ln(III)2 complexes [(μ4-CO3)2{Zn(II)L(n)Ln(III)(NO3)}2] (Ln(III) = Gd(III), Tb(III), Dy(III); L(1) = N,N'-bis(3-methoxy-2-oxybenzylidene)-1,3-propanediaminato, L(2) = N,N'-bis(3-ethoxy-2-oxybenzylidene)-1,3-propanediaminato).

Science.gov (United States)

Ehama, Kiyomi; Ohmichi, Yusuke; Sakamoto, Soichiro; Fujinami, Takeshi; Matsumoto, Naohide; Mochida, Naotaka; Ishida, Takayuki; Sunatsuki, Yukinari; Tsuchimoto, Masanobu; Re, Nazzareno

2013-11-04

Carbonato-bridged Zn(II)2Ln(III)2 complexes [(μ4-CO3)2{Zn(II)L(n)Ln(III)(NO3)}2]·solvent were synthesized through atmospheric CO2 fixation reaction of [Zn(II)L(n)(H2O)2]·xH2O, Ln(III)(NO3)3·6H2O, and triethylamine, where Ln(III) = Gd(III), Tb(III), Dy(III); L(1) = N,N'-bis(3-methoxy-2-oxybenzylidene)-1,3-propanediaminato, L(2) = N,N'-bis(3-ethoxy-2-oxybenzylidene)-1,3-propanediaminato. Each Zn(II)2Ln(III)2 structure possessing an inversion center can be described as two di-μ-phenoxo-bridged {Zn(II)L(n)Ln(III)(NO3)} binuclear units bridged by two carbonato CO3(2-) ions. The Zn(II) ion has square pyramidal coordination geometry with N2O2 donor atoms of L(n) and one oxygen atom of a bridging carbonato ion at the axial site. Ln(III) ion is coordinated by nine oxygen atoms consisting of four from the deprotonated Schiff-base L(n), two from a chelating nitrate, and three from two carbonate groups. The temperature-dependent magnetic susceptibilities in the range 1.9-300 K, field-dependent magnetization from 0 to 5 T at 1.9 K, and alternating current magnetic susceptibilities under the direct current bias fields of 0 and 1000 Oe were measured. The magnetic properties of the Zn(II)2Ln(III)2 complexes are analyzed on the basis of the dicarbonato-bridged binuclear Ln(III)-Ln(III) structure, as the Zn(II) ion with d(10) electronic configuration is diamagnetic. ZnGd1 (L(1)) and ZnGd2 (L(2)) show a ferromagnetic Gd(III)-Gd(III) interaction with J(Gd-Gd) = +0.042 and +0.028 cm(-1), respectively, on the basis of the Hamiltonian H = -2J(Gd-Gd)ŜGd1·ŜGd2. The magnetic data of the Zn(II)2Ln(III)2 complexes (Ln(III) = Tb(III), Dy(III)) were analyzed by a spin Hamiltonian including the crystal field effect on the Ln(III) ions and the Ln(III)-Ln(III) magnetic interaction. The Stark splitting of the ground state was so evaluated, and the energy pattern indicates a strong easy axis (Ising type) anisotropy. Luminescence spectra of Zn(II)2Tb(III)2 complexes were observed, while those

Luminescence and magnetic behaviour of almond like (Na{sub 0.5}La{sub 0.5})MoO{sub 4}:RE{sup 3+} (RE = Eu, Tb, Dy) nanostructures

Energy Technology Data Exchange (ETDEWEB)

Krishnan, Rajagopalan [Department of Physics, B.S. Abdur Rahman University, Vandalur, Chennai, Tamil Nadu (India); Thirumalai, Jagannathan, E-mail: jthirumalai@bsauniv.ac.in [Department of Physics, B.S. Abdur Rahman University, Vandalur, Chennai, Tamil Nadu (India); Thomas, Sabu [Polymer Science and Technology, Center for Nanoscience and Nanotechnology, School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686 560, Kerala (India); Gowri, Mahasampath [Department of Chemistry, B.S. Abdur Rahman University, Vandalur, Chennai, Tamil Nadu (India)

2014-08-01

Graphical abstract: Monodispersed almond-like (Na{sub 0.5}La{sub 0.5})MoO{sub 4}:RE{sup 3+} nanostructures synthesized by employing ethylene-diamine tetra acetic acid (EDTA) using hydrothermal route at 200 °C for 24 h. These nanoparticles were found to be novel bi-functional candidates suitable for high-quality luminescence and magnetic applications. - Highlights: • Almond like structures of (Na{sub 0.5}La{sub 0.5})MoO{sub 4}:RE{sup 3+} were synthesized by hydrothermal method. • Time dependent self-assembly could be the dominant process for the formation of 3D networks. • Luminescence properties of nanosamples were studied in comparison with bulk sample. • Room temperature magnetic properties of bulk and nanophosphors were investigated. - Abstract: Tetragonal phase (Na{sub 0.5}La{sub 0.5})MoO{sub 4}:RE{sup 3+} (RE = Eu, Tb, Dy) with almond like hierarchical structures assembled from nanosheets building blocks were successfully synthesized by employing disodium ethylenediaminetetraacetic acid (Na{sub 2}EDTA) using hydrothermal route at 200 °C for 24 h. Field emission scanning electron microscope, transmission electron microscope, and X-ray diffraction patterns were used to characterize the morphology, size, and crystal structure with good resolution. The sequestering agent EDTA acts as quadridentate ligand coordinated with metal ions [Na{sup +}, La{sup 3+}/RE{sup 3+}] facilitating the formation of self-organized 3D networks. The growth mechanism for the formation of almond like nanostructures is explicated in four paths: dissolution, adsorption, in situ transformation in acidic and basic media and the effective collision. Photoluminescence excitation and emission spectra reveals a spectral blue shift which was observed in the nanosamples towards shorter wavelengths compared with the bulk sample. Upon UV irradiation, both bulk and nanostructure show strong luminescence in the red region due to the {sup 5}D{sub 0} → {sup 7}F{sub 2} transition in Eu{sup 3

Synthesis and characterization of La(III), Pr(III), Nd(III), Sm(III), Eu(III), Gd(III), Tb(III) and Dy(III) complexes of 2-acetylfuran-2-thenoylhydrazone

International Nuclear Information System (INIS)

Singh, B.; Singh, Praveen K.

1998-01-01

The reaction of 2-acetylfuran-2-thenoylhydrazone(afth) with Ln(III) trichlorides yields complexes of the type [Ln(afth)Cl 2 (H 2 O)(EtOH)]Cl, [Ln(III) = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy]. The complexes have been characterized by molar conductance, magnetic susceptibility and TGA and DTA measurements, magnetic susceptibility and TGA and DTA measurements, FAB mass, infrared, proton NMR, electronic absorption and emission spectra. The terbium complex is found to be monomer from the FAB mass spectrum. The IR and NMR spectra suggest neutral tridentate behaviour of the Schiff base. A coordination number seven is proposed around the metal ions. Emission spectra suggest C 3v , symmetry around the metal ion with capped octahedron geometry for the europium complex. (author)

Chemical Bond Parameters in Sr3MRhO6 (M=Rare earth)

Institute of Scientific and Technical Information of China (English)

无

2000-01-01

Chemical bond parameters, that is, bond covalency, bond valence, macroscopic linear susceptibility, and oxidation states of elements in Sr3MRhO6 (M=Sm, Eu, Tb, Dy, Ho, Er, Yb) have been calculated. The results indicate that the bond covalency of M-O decreases sharply with the decrease of ionic radius of M3+ from Sm to Yb, while no obvious trend has been found for Rh-O and Sr-O bonds. The global instability index indicates that the crystal structures of Sr3MrhO6 (M = Sm, Eu, Tb, Dy, Ho) have strained bonds.

Ternary rare-earth based alternative gate-dielectrics for future integration in MOSFETs

Energy Technology Data Exchange (ETDEWEB)

Schubert, Juergen; Lopes, Joao Marcelo; Durgun Oezben, Eylem; Luptak, Roman; Lenk, Steffi; Zander, Willi; Roeckerath, Martin [IBN 1-IT, Forschungszentrum Juelich, 52425 Juelich (Germany)

2009-07-01

The dielectric SiO{sub 2} has been the key to the tremendous improvements in Si-based metal-oxide-semiconductor (MOS) device performance over the past four decades. It has, however, reached its limit in terms of scaling since it exhibits a leakage current density higher than 1 A/cm{sup 2} and does not retain its intrinsic physical properties at thicknesses below 1.5 nm. In order to overcome these problems and keep Moore's law ongoing, the use of higher dielectric constant (k) gate oxides has been suggested. These high-k materials must satisfy numerous requirements such as the high k, low leakage currents, suitable band gap und offsets to silicon. Rare-earth based dielectrics are promising materials which fulfill these needs. We will review the properties of REScO{sub 3} (RE = La, Dy, Gd, Sm, Tb) and LaLuO{sub 3} thin films, grown with pulsed laser deposition, e-gun evaporation or molecular beam deposition, integrated in capacitors and transistors. A k > 20 for the REScO{sub 3} (RE = Dy, Gd) and around 30 for (RE = La, Sm, Tb) and LaLuO{sub 3} are obtained. Transistors prepared on SOI and sSOI show mobility values up to 380 cm{sup 2}/Vs on sSOI, which are comparable to such prepared with HfO{sub 2}.

Hydrothermal synthesis, characterization and up/down-conversion luminescence of barium rare earth fluoride nanocrystals

International Nuclear Information System (INIS)

Jia, Li-Ping; Zhang, Qiang; Yan, Bing

2014-01-01

Graphical abstract: Lanthanide ions doped bare earth rare earth fluoride nanocrystals are synthesized by hydrothermal technology and characterized. The down/up-conversion luminescence of them are discussed. - Highlights: • Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is used for synthesis. • Barium rare earth fluoride nanocrystals are synthesized comprehensively. • Luminescence for down-conversion and up-conversion are obtained for these systems. - Abstract: Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is developed to synthesize barium rare earth fluorides nanocrystals (OA = oleylamine, EDA = ethylenediamine, O-A = oleic acid and LO-A = linoleic acid). They are presented as BaREF 5 (RE = Ce, Pr, Nd, Eu, Gd, Tb, Dy, Y, Tm, Lu) and Ba 2 REF 7 (RE = La, Sm, Ho, Er, Yb). The influence of reaction parameters (rare earth species, hydrothermal system and temperature) is checked on the phase and shape evolution of the fluoride nanocrystals. It is found that reaction time and temperature of these nanocrystals using EDA (180 °C, 6 h) is lower than those of them using OA (220 °C, 10 h). The photoluminescence properties of these fluorides activated by some rare earth ions (Nd 3+ , Eu 3+ , Tb 3+ ) are studied, and especially up-conversion luminescence of the four fluoride nanocrystal systems (Ba 2 LaF 7 :Yb, Tm(Er), Ba 2 REF 7 :Yb, Tm(Er) (RE = Gd, Y, Lu)) is observed

Ion-irradiation-induced phase transformation in rare earth sesquioxides (Dy2O3,Er2O3,Lu2O3)

International Nuclear Information System (INIS)

Tang, M.; Lu, P.; Valdez, J.A.; Sickafus, K.E.

2006-01-01

Polycrystalline pellets of cubic C-type rare earth structure (Ia3) Dy 2 O 3 , Er 2 O 3 , and Lu 2 O 3 were irradiated at cryogenic temperature (120 K) with 300 keV Kr ++ ions to a maximum fluence of 1x10 20 Kr/m 2 . Irradiated specimens were examined using grazing incidence x-ray diffraction and transmission electron microscopy. Ion irradiation leads to different radiation effects in these three materials. First, Dy 2 O 3 begins to transform to a monoclinic B-type rare earth structure (C2/m) at a peak dose of ∼5 displacements per atom (dpa) (corresponding to a fluence of 2x10 19 Kr/m 2 ). This transformation is nearly complete at a peak dose of 25 dpa (a fluence of 1x10 20 Kr/m 2 ). Er 2 O 3 also transforms to the B-type structure, but the transformation starts at a higher irradiation dose of about 15-20 dpa [a fluence of about (6-8)x10 19 Kr/m 2 ]. Lu 2 O 3 was found to maintain the C-type structure even at the highest irradiation dose of 25 dpa (a fluence of 1x10 20 Kr/m 2 ). No C-to-B transformation was observed in Lu 2 O 3 . The irradiation dose dependence of the C-to-B phase transformation observed in Dy 2 O 3 , Er 2 O 3 , and Lu 2 O 3 is closely related to the temperature dependence of the C-to-B phase transformation found in phase diagrams for these three materials

Oxide perovskites with tetravalent dysprosium and compounds of the type Ba/sub 3/RE/sub 4/O/sub 9/ (RE = Rare Earth Element)

Energy Technology Data Exchange (ETDEWEB)

Brauer, G; Kristen, H [Freiburg Univ. (Germany, F.R.)

1980-03-01

In analogy to our investigations concerning tetravalent Nd in oxide perovskites, we also tried to stabilize dysprosium(IV) by incorporation in host-lattices with the perovskite structure. As host-lattices we used BaCeO/sub 3/, BaTbO/sub 3/, and SrTbO/sub 3/. Only in Ba(Ce, Dy)O/sub 3/ we could trace Dy(IV) with certainty. Among the prepared mixed oxides, also the phase Ba/sub 3/Dy/sub 4/O/sub 9/ occured. The lattice parameters of several phases of this latter type were redetermined.

Synthesis and magnetism of μ-oxamido-bridged Cu2IILnIII - type heterotrinuclear complexes (Ln = Ce, Nd, Sm, Eu, Gd, Tb, Dy, Er)

International Nuclear Information System (INIS)

Li, Y.T.; Yan, C.W.

2001-01-01

Eight new Cu 2 II Ln III - type (Ln = Ce, Nd, Sm, Eu, Gd, Tb, Dy, Er) heterotrinuclear complexes bridged by N,N'-bis (2-aminopropyl)oxamidocopper(II) [Cu(oxdn)], namely Cu 2 (oxdn)Ln(NO 3 ) 3 , have been synthesized and characterized by elemental analyses, molar conductivity measurements and spectroscopic (IR, UV, ESR) studies. Magnetic susceptibility measurements (4.2 ∼300 K) and studies of Cu 2 (oxdn)Gd(NO 3 ) 3 complex have revealed that the central gadolinium(III) and terminal copper(II) ions are ferromagnetically coupled with the exchange integral J (Cu-Gd) = +2.98 cm -1 , while an antiferromagnetic coupling is detected between the terminal copper(II) metal ions with the exchange integral J' (Cu-Gd) = -0.75 cm -1 , on the basis of the spin Hamiltonian operator [H -2J(S Cu1 -S Gd +S Cu2 +S Gd )-2J'(S Cu1 S Cu2 )]. (author)

Synthesis, structure, and physical properties of new rare earth ferrocenoylacetonates.

Science.gov (United States)

Koroteev, Pavel S; Dobrokhotova, Zhanna V; Ilyukhin, Andrey B; Efimov, Nikolay N; Rouzières, Mathieu; Kiskin, Mikhail A; Clérac, Rodolphe; Novotortsev, Vladimir M

2016-04-21

New ferrocenoylacetonate complexes of several rare earth elements, [Ln(fca)3(bpy)]·MeC6H5 (Ln = Pr (), Eu (), Gd (), Tb (), Dy (), Ho (), Y (); bpy - 2,2'-bipyridine; Hfca - FcCOCH2COMe) as well as scandium ferrocenoylacetonate [Sc(fca)3]·0.5MeC6H5 (), were synthesized and characterized by single crystal X-ray diffraction analysis. In the crystal lattice of the isostructural complexes , two [Ln(fca)3(bpy)] molecules form a pair due to stacking interactions between the bpy ligands. The Ln(3+) ions are coordinated in a square antiprism geometry with a coordination number of 8. The Sc(3+) ions in complex are coordinated in an octahedral geometry. Thermolysis of complexes was studied under air and argon atmospheres; in the first case, it affords perovskites LnFeO3 as one of the products. Complexes display single-molecule magnet properties, and the effective relaxation barrier for the Dy complex , was found to be Δeff/kB = 241 K, which is one of the highest values obtained for a mononuclear β-diketonate lanthanide complex.

Magnetic properties and structural transitions of fluorite-related rare earth osmates Ln3OsO7 (Ln=Pr, Tb)

Science.gov (United States)

Hinatsu, Yukio; Doi, Yoshihiro

2013-02-01

Ternary rare-earth osmates Ln3OsO7 (Ln=Pr, Tb) have been prepared. They crystallize in an ortho-rhombic superstructure of cubic fluorite with space group Cmcm. Both of these compounds undergo a structural phase transition at 130 K (Ln=Pr) and 580 K (Ln=Tb). These compounds show complex magnetic behavior at low temperatures. Pr3OsO7 exhibits magnetic transitions at 8 and 73 K, and Tb3OsO7 magnetically orders at 8 and 60 K. The Os moments become one-dimensionally ordered, and when the temperature is furthermore decreased, it provokes the ordering in the Ln3+ sublattice that simultaneously becomes three-dimensionally ordered with the Os sublattice.

Heat capacity of RFe{sub x}Mn{sub 12-x} (R = Gd, Tb and Dy) compounds: wiping out a cooperative 4f-4f exchange interaction by breaking the 3d-4f magnetic symmetry

Energy Technology Data Exchange (ETDEWEB)

Pique, C; Blanco, J A; Abad, E [Departamento de Fisica, Universidad de Oviedo, Campus de Viesques, E-33204 Gijon (Spain); Burriel, R; Artigas, M [Instituto de Ciencia de Materiales de Aragon (CSIC-Universidad de Zaragoza), E-50009 Zaragoza (Spain); Fernandez-RodrIguez, J [European Synchrotron Radiation Facility, BP 220, F-38043 Grenoble Cedex (France)], E-mail: pique@uniovi.es

2008-08-27

Using adiabatic calorimetry the heat capacity of a series of RFe{sub x}Mn{sub 12-x} (R = Gd, Tb and Dy) compounds has been measured from 3 to 350 K. The substitution of Fe for Mn in RFe{sub x}Mn{sub 12-x} influences both the magnetic interactions on the 3d sublattice and the magnetism of R (the Neel temperature doubles on going from x = 0 to 6 and the compounds become ferromagnetic for x = 8 with Curie temperatures of around 300 K). In pure TbMn{sub 12} the heat-capacity data shows a {lambda}-type anomaly associated with the independent cooperative magnetic ordering of the R sublattice ({approx}5 K), while the anomaly related to the Mn magnetic ordering ({approx}100 K) is rather smooth, as observed in other itinerant magnetic systems such as YMn{sub 12}. In contrast, the substitution of Fe for Mn leads, on the one hand, to a more localized magnetic behaviour of the 3d sublattice, and, on the other, to magnetic polarization effects between the 3d and 4f sublattices, together with the disappearance of the cooperative magnetic ordering of the R sublattice due to the breaking of the antiferromagnetic symmetry in the 3d sublattice. This is reflected in the heat-capacity curve through a smooth Schottky-like anomaly. In the case of Gd compounds the magnitude of the exchange molecular-field parameter has been deduced by fitting the magnetic contribution to the heat capacity within a simple mean-field model. From this analysis we found that this molecular field acting on the rare-earth site increases with the iron concentration, reaching values as large as 48 T for the concentration x = 6. A similar analysis of the heat capacity in the ordered phase on the Tb compounds also leads to an enhancement of the molecular field with increasing Fe content. These results allow checking the possible crystal-field parameters for these RFe{sub x}Mn{sub 12-x} compounds.

Value analysis of neodymium content in shredder feed: toward enabling the feasibility of rare earth magnet recycling.

Science.gov (United States)

Bandara, H M Dhammika; Darcy, Julia W; Apelian, Diran; Emmert, Marion H

2014-06-17

In order to facilitate the development of recycling technologies for rare earth magnets from postconsumer products, we present herein an analysis of the neodymium (Nd) content in shredder scrap. This waste stream has been chosen on the basis of current business practices for the recycling of steel, aluminum, and copper from cars and household appliances, which contain significant amounts of rare earth magnets. Using approximations based on literature data, we have calculated the average Nd content in the ferrous shredder product stream to be between 0.13 and 0.29 kg per ton of ferrous scrap. A value analysis considering rare earth metal prices between 2002 and 2013 provides values between $1.32 and $145 per ton of ferrous scrap for this material, if recoverable as pure Nd metal. Furthermore, we present an analysis of the content and value of other rare earths (Pr, Dy, Tb).

Anomalous magnetoresistance in antiferromagnetic polycrystalline materials R2Ni3Si5 (R=rare earth)

International Nuclear Information System (INIS)

Mazumdar, C.; Nigam, A.K.; Nagarajan, R.; Gupta, L.C.; Chandra, G.; Padalia, B.D.; Godart, C.; Vijayaraghaven, R.

1997-01-01

Magnetoresistance (MR) studies on polycrystalline R 2 Ni 3 Si 5 , (R=Y, rare earth) which order antiferromagnetically at low temperatures, are reported here. MR of the Nd, Sm, and Tb members of the series exhibit positive giant magnetoresistance, largest among polycrystalline materials (85%, 75%, and 58% for Tb 2 Ni 3 Si 5 , Sm 2 Ni 3 Si 5 , and Nd 2 Ni 3 Si 5 , respectively, at 4.4 K in a field of 45 kG). These materials have, to the best of our knowledge, the largest positive GMR reported ever for any bulk polycrystalline compounds. The magnitude of MR does not correlate with the rare earth magnetic moments. We believe that the structure of these materials, which can be considered as a naturally occurring multilayer of wavy planes of rare earth atoms separated by Ni endash Si network, plays a role. The isothermal MR of other members of this series (R=Pr,Dy,Ho) exhibits a maximum and a minimum, below their respective T N close-quote s. We interpret these in terms of a metamagnetic transition and short-range ferromagnetic correlations. The short-range ferromagnetic correlations seem to be dominant in the temperature region just above T N . copyright 1997 American Institute of Physics

Study of magnetic properties of TGa6 with T = Ce, Pr, Nd, Tb, Ho, Dy and of solid solutions Ce(Ga1-x Alx)2

International Nuclear Information System (INIS)

Jerjini, M.

1987-10-01

At low temperature TGa 6 compounds are ordered with a Neel temperature of about 10 K. Magnetic structures are antiferromagnetic for T = Pr or Nd or modulated for T = Tb, Ho or Dy. Ce presents an abnormal behavior in CeGa 6 . Neutron inelastic scattering allows the determination of energy levels in the crystal field of cerium ion and evidences hybridation of 4f and valence electrons. Three magnetic transitions for T 6 . Study of CeGa 6 and solid solutions. Ce(Ga (1-x) Al x ) 2 shows that aluminium insertion reinforces the Kondo effect. For x = O.1 an incommensurable structure subsists at very low temperature. CeGa 2 is ordered with 3 magnetic structures. Magnetic moment is reduced with Al. The study of crystal field by neutron scattering shows that hybridation effects are more important for the compound with x = 0.1 [fr

Rare Earth Chalcogels NaLnSnS4 (Ln = Y, Gd, Tb) for Selective Adsorption of Volatile Hydrocarbons and Gases

KAUST Repository

Edhaim, Fatimah

2017-06-28

The synthesis and characterization of the rare earth chalcogenide aerogels NaYSnS4, NaGdSnS4, and NaTbSnS4 is reported. Rare earth metal ions like Y3+, Gd3+, and Tb3+ react with the chalcogenide clusters [SnS4]4– in aqueous formamide solution forming extended polymeric networks by gelation. Aerogels obtained after supercritical drying have BET surface areas of 649 m2·g–1 (NaYSnS4), 479 m2·g–1 (NaGdSnS4), and 354 m2·g–1 (NaTbSnS4). Electron microscopy and physisorption studies reveal that the new materials have pores in the macro (above 50 nm) and meso (2–50 nm) regions. These aerogels show higher adsorption of toluene vapor over cyclohexane vapor and CO2 over CH4 or H2. The notable adsorption capacity for toluene (NaYSnS4: 1108 mg·g–1; NaGdSnS4: 921 mg·g–1; and NaTbSnS4: 645 mg·g–1) and high selectivity for gases (CO2/H2: 172 and CO2/CH4: 50 for NaYSnS4, CO2/H2: 155 and CO2/CH4: 37 for NaGdSnS4, and CO2/H2: 75 and CO2/CH4: 28 for NaTbSnS4) indicate potential future use of chalcogels in adsorption-based gas or hydrocarbon separation processes.

A binuclear Fe(III)Dy(III) single molecule magnet. Quantum effects and models.

Science.gov (United States)

Ferbinteanu, Marilena; Kajiwara, Takashi; Choi, Kwang-Yong; Nojiri, Hiroyuki; Nakamoto, Akio; Kojima, Norimichi; Cimpoesu, Fanica; Fujimura, Yuichi; Takaishi, Shinya; Yamashita, Masahiro

2006-07-19

The binuclear [FeIII(bpca)(mu-bpca)Dy(NO3)4], having Single Molecule Magnet (SMM) properties, belonging to a series of isostructural FeIIILnIII complexes (Ln = Eu, Gd, Tb, Dy, Ho) and closely related FeIILnIII chain structures, was characterized in concise experimental and theoretical respects. The low temperature magnetization data showed hysteresis and tunneling. The anomalous temperature dependence of Mössbauer spectra is related to the onset of magnetic order, consistent with the magnetization relaxation time scale resulting from AC susceptibility measurements. The advanced ab initio calculations (CASSCF and spin-orbit) revealed the interplay of ligand field, spin-orbit, and exchange effects and probed the effective Ising nature of the lowest states, involved in the SMM and tunneling effects.

Enhanced luminescence of rare-earth complexes Tb(1-x)Eu(x)(m-NBA)3Phen in ZnS.

Science.gov (United States)

Lv, Yuguang; Zhang, Jingchang; Cao, Weiliang; Song, Lin; Xu, Zheng

2008-07-01

Rare-earth ternary complexes Tb(1-x)Eu(x)(m-NBA)(3)Phen (X=1, 0.25, 0.5, 0.75, 1.0) were synthesized and characterized by IR, DTA-TG, UV, fluorescent spectra and elemental analysis. It was found that luminescence of Eu(3+) complex was enhanced by doped with Tb(3+). It is proved by TG curve that the complexes are stable, ranging from ambient temperature to 360 degrees C in air. The organic-inorganic combined structural device was fabricated, and the electroluminescence intensity of the combined structural device was improved compared with the device of the purely organic components.

Enhanced luminescence of rare-earth complexes Tb 1- xEu x( m-NBA) 3Phen in ZnS

Science.gov (United States)

Lv, Yuguang; Zhang, Jingchang; Cao, Weiliang; Song, Lin; Xu, Zheng

2008-07-01

Rare-earth ternary complexes Tb 1- xEu x( m-NBA) 3Phen ( X = 1, 0.25, 0.5, 0.75, 1.0) were synthesized and characterized by IR, DTA-TG, UV, fluorescent spectra and elemental analysis. It was found that luminescence of Eu 3+ complex was enhanced by doped with Tb 3+. It is proved by TG curve that the complexes are stable, ranging from ambient temperature to 360 °C in air. The organic-inorganic combined structural device was fabricated, and the electroluminescence intensity of the combined structural device was improved compared with the device of the purely organic components.

Optimisation of the magnetic properties of mechanically milled R5.5Fe73.5-xCoxCr3B18 nanocomposites

International Nuclear Information System (INIS)

O'Sullivan, J.F.; Smith, P.A.I.; Coey, J.M.D.

1998-01-01

Mechanical milling and subsequent annealing of R 4.5 R'Fe 73.5-x Co x Cr 3 B 18 (R=Nd,Pr and R'=Tb,Dy) ingots has been found to produce hard magnetic nanocomposites of (R,R') 2 (Fe,Co) 14 B, (Fe,Cr) 2 B and α-(Fe,Co) phases. Here we report on the optimisation of the composition of such nanocomposites. Substituting different rare-earth metals has a significant effect on the magnetic properties. The replacement of Nd with Pr produces higher coercivity and remanence, and better loop squareness. However, the replacement of Tb with Dy produced inferior properties when the main rare-earth component was Nd. Improved properties were obtained with the combination of Pr and Dy or Tb. Substitution of Co for Fe was found to lower coercivity but increase the remanence. The best combination of properties measured was for Pr 4.5 Dy 1 Fe 68.5 Co 5 Cr 3 B 1x , where H c =0.41 MA/m, J r =1 T, and (BH) max for the powder was 100 kJ/m 3 . These results will be discussed in terms of the grain size and the intrinsic properties of the hard and soft magnetic phases identified using X-ray diffraction. (orig.)

Preparation, thermodynamic property and antimicrobial activity of some rare-earth (III) complexes with 3-bromo-5-iodobenzoic acid and 1,10-phenanthroline

Energy Technology Data Exchange (ETDEWEB)

Liu, Jing-Yu [Testing and Analysis Center, Hebei Normal University, Shijiazhuang 050024 (China); College of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024 (China); Ren, Ning [Department of Chemistry, Handan College, Handan 056005 (China); Zhang, Jian-Jun, E-mail: jjzhang6@126.com [Testing and Analysis Center, Hebei Normal University, Shijiazhuang 050024 (China); College of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024 (China); Zhang, Cun-Ying [No.1 High School of Shijiazhuang, Shijiazhuang 050011 (China)

2013-10-20

Graphical abstract: Four new rare-earth complexes of general formula [Ln(3-Br-5-IBA){sub 3}phen]{sub 2} [Ln = Er (1), Tb (2), Dy (3) and Ho (4); 3-Br-5-IBA = 3-bromo-5-iodobenzoate; phen = 1,10-phenanthroline] were synthesized and characterized by elemental analysis, IR, UV and TG/DSC-FTIR technology. Heat capacities of the four complexes were measured by differential scanning calorimetry (DSC). The antimicrobial activity against Escherichia coli, Staphylococcus aureus and Candida albicans were tested using disc diffusion method. - Highlights: • Four new complexes [Ln(3-Br-5-IBA){sub 3}phen]{sub 2} were synthesized and characterized. • The non-isothermal kinetics of the first stage for the complexes was studied. • The heat capacities of the complexes were measured by differential scanning calorimeter. • The antimicrobial activities for these complexes were tested. • The fluorescence properties of the complexes 2 and 3 were studied. - Abstract: Four new rare-earth complexes of general formula [Ln(3-Br-5-IBA){sub 3}phen]{sub 2} (Ln(III) = Er (1), Tb (2), Dy (3) and Ho (4); 3-Br-5-IBA = 3-bromo-5-iodobenzoate; phen = 1,10-phenanthroline) were synthesized by solution-precipitation method, and investigated using elemental analysis, infrared spectra, ultraviolet spectra and TG/DSC-FTIR technology. The non-isothermal kinetics of the first stage for the complexes was studied by using non-linear integral isoconversional method and double equal-double steps method. The heat capacities of the complexes were measured between 263.15 and 485.55 K by means of differential scanning calorimeter, and the values of the experimental heat capacities were fitted to a polynomial equation with the least-squares method. And the thermodynamic functions [H{sub T} − H{sub 298.15}], [S{sub T} − S{sub 298.15}] and [G{sub T} − G{sub 298.15}] were also derived based on the fitted polynomials and thermodynamic relationships with temperature interval of 10 K. Moreover, the

Extraordinarily large intrinsic magnetodielectric coupling of the Tb member within the Haldane spin-chain family R2BaNiO5

Science.gov (United States)

Upadhyay, Sanjay Kumar; Paulose, P. L.; Sampathkumaran, E. V.

2017-07-01

The Haldane spin-chain compound Tb2BaNiO5 has been known to order antiferromagnetically below (TN= )63 K . The present magnetic studies on the polycrystals bring out that there is another magnetic transition at a lower temperature (T2=)25 K with pronounced magnetic-field-induced metamagnetic and metaelectric behaviors. Multiferroic features are found below T2 only and not at TN. The most intriguing observation is that the observed change in dielectric constant (Δɛ') is intrinsic and largest (e.g., ˜18% at 15 K) within this Haldane spin-chain family R2BaNiO5 . Taking into account the fact that this trend (that is, the largest value of Δɛ' for the Tb case within this family) correlates well with a similar trend in TN (with the values of TN being ˜55, 58, 53, and 32 K for Gd, Dy, Ho, and Er cases), we believe that the explanation usually offered for this TN behavior in rare-earth systems is applicable for this Δɛ' behavior as well. That is, single-ion anisotropy following crystal-field splitting is responsible for the extraordinary magnetodielectric effect in this Tb case. This work provides a pathway in the field of multiferroics to promote magnetoelectric coupling.

Rare earth element patterns in nigerian coals

International Nuclear Information System (INIS)

Ewa, I.O.B.; Elegba, S.B.

1996-01-01

Rare Earth Elements (REE's) retain group coherence in their environment and are therefore useful geochemical markers. We report the pattern of ten REE's (La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Lu) determined by Instrumental Neutron Activation Analysis (INAA) for coals obtained from eight mines in Nigeria, namely, Okaba, Enugu, Ogbete, Onyeama, Gombe, Lafia, Asaba and Afikpo. Our results show the existence of fractionations with the highest index of 13.19 for Lafia coal, depletion in HREE, negative Eu anomaly for most of the coals, REE patterns that are consistent with chondritic trends; prominent (Eu/Eu * ) cn for Okaba and Gombe coals. Variations in geochemical data observed could suggest strong departures from band metamorphism during the coalification events of the Benue Trough geosynclines, where the coal deposits are all located. (author) 14 refs., 2 figs., 3 tabs

Search for and study of linking transitions between super- and normal deformed wells in the {sup 151}Tb nucleus; Recherche et etude de transitions de liaison entre les puits super- et normalement deformes dans le noyau {sup 151}Tb

Energy Technology Data Exchange (ETDEWEB)

Robin, J

2003-12-01

While the superdeformation phenomenon has been observed many times in different mass regions, the excitation energy and angular momentum are not known for most of the superdeformed bands, mainly in the A {approx} 150 mass region. We have thus undertaken the search for and study of linking transitions between super and normal deformed potential wells in the Tb{sup 151} nucleus with the EUROBALL-IV spectrometer based at the subatomic research institute of Strasbourg. This nucleus presents the peculiarity of having an excited superdeformed band identical to the yrast one of Dy{sup 152}, which has recently been linked to normal deformed states. As the Dy{sup 152} nucleus exhibits a shape coexistence in the first potential well, we have also searched for collective rotational bands with prolate but moderate shape, coexisting with the oblate structure of Tb{sup 151}. The discovery of new superdeformed bands in the Tb{sup 151,152} isotopes, the extension to lower and higher spins of the previously known bands, and mean field calculations with a deformed Woods-Saxon potential have contributed to improve our knowledge as well as raise new questions on the orbitals configuration assignments of these bands. (author)

Bulk study of a DyNiAl single crystal

Czech Academy of Sciences Publication Activity Database

Prchal, J.; Andreev, Alexander V.; Javorský, P.; Honda, F.; Jurek, Karel

272-276, - (2004), e419-e420 ISSN 0304-8853 R&D Projects: GA ČR GA106/02/0943 Keywords : rare-earth * DyNiAl * magnetic anisotropy * single crystal Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.031, year: 2004

Towards the development of new phosphors with reduced content of rare earth elements: Structural and optical characterization of Ce:Tb: Al{sub 2}SiO{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Chiriu, D.; Stagi, L.; Carbonaro, C.M.; Corpino, R. [Dipartimento di Fisica, Università degli Studi di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy); Casula, M.F. [Dipartimento di Scienze Chimiche e Geologiche and INSTM, Università di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy); Ricci, P.C., E-mail: carlo.ricci@dsf.unica.it [Dipartimento di Fisica, Università degli Studi di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy)

2016-05-15

Highlights: • A new promising inert matrix as host of luminescent ions is proposed. • Al2SiO5 matrix is free from Rare earths (critical raw materials). • Doping the matrix with Ce and Tb we obtain an efficient green emitter. • Cerium acts as sensitizer for Terbium emission. - Abstract: A new promising inert matrix as host of luminescent ions is proposed. Al2SiO5 samples, doped with rare earths (Ce, Tb single doped and co-doped) are proposed as good prospect for the development of new UV–vis converter with reduced content of rare earths elements. Structural characterization by Raman, XRD spectroscopy and TEM imaging reveals the sillimanite phase and nano sized dimension of the investigated powders. Optical characterization by steady time and time resolved emission spectroscopy for the single doped and co-doped samples allows to identify an efficient energy transfer from Ce to Tb ions under near UV excitation wavelength. The intense green emission observed in the Ce:Tb co-doped Al2SiO5 system suggests its potential application as efficient blue pumped green emitter phosphor to be exploited for white LED: to this purpose we tested the compound in combination with a red emitting doping ion recording for Ce:Tb:Cr:ASO system a correlated color temperature of 6720 K.

Distribution of rare earths in liver of mice administered with chloride compounds of 12 rare earths

International Nuclear Information System (INIS)

Shinohara, A.; Chiba, M.; Inaba, Y.

1998-01-01

Full text: Rare earths are used in high technology field, however, the information on their biological effects are not sufficient. The behaviour of rare earths in biology is of interest in connection with their toxicity. In the present study, the distribution of rare earths in liver of mice administered with these elements was investigated. The effects on Ca and other biological essential elements were also determined. Male mice (5 weeks old) were injected with one of 12 kinds of rare earths (chlorides of Y, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er and Yb) at the dose of 25 mg/KXg body weight. After 20 hours of administration, mice were sacrificed, then liver and other organs were taken out. Liver was homogenized and separated by centrifugation. The concentrations of rare earths administered were measured by microwave-induced plasma-mass spectrometry (MIP-MS) after acid digestion. The concentrations of administered elements in whole liver were about 100μg/g (wet weight), where the difference between elements was few. Distribution amounts of elements administered in four fractions were following order; 700μg precipitate > mitocondrial fraction > microsomal fraction > cytosol. The relative contents in these fractions, however, was different depending on the element administered. Calcium concentrations in liver of administered mice were higher than those of control mice. Increase of Ca concentrations were observed in all four fractions and the increase ratio was also dependent on the elements administered

Magnetic and Moessbauer studies on GdCo3B2 and DyCo3B2

International Nuclear Information System (INIS)

Malik, S.K.; Umarji, A.M.; Shenoy, G.K.

1984-10-01

Magnetization and Moessbauer studies have been carried out on GdCo 3 B 2 and DyCo 3 B 2 . These compounds are magnetically ordered with Curie temperatures of 56 0 and 21 0 K respectively. The Co atoms are either nonmagnetic or carry a small moment in these compounds. The saturation moment of DyCo 3 B 2 at 5 0 K is smaller than the Dy 3+ free-ion value. From 161 Dy Moessbauer studies, the measured hyperfine magnetic field at the Dy site is also observed to be smaller than the free-ion value. 155 Gd Moessbauer measurements in GdCo 3 B 2 reveal the presence of large crystalline electric fields at the rare earth site. This causes the moment and the hyperfine field at the Dy site in DyCo 3 B 2 to be reduced from its free-ion value

Search for and study of linking transitions between super- and normal deformed wells in the 151Tb nucleus

International Nuclear Information System (INIS)

Robin, J.

2003-12-01

While the superdeformation phenomenon has been observed many times in different mass regions, the excitation energy and angular momentum are not known for most of the superdeformed bands, mainly in the A ∼ 150 mass region. We have thus undertaken the search for and study of linking transitions between super and normal deformed potential wells in the Tb 151 nucleus with the EUROBALL-IV spectrometer based at the subatomic research institute of Strasbourg. This nucleus presents the peculiarity of having an excited superdeformed band identical to the yrast one of Dy 152 , which has recently been linked to normal deformed states. As the Dy 152 nucleus exhibits a shape coexistence in the first potential well, we have also searched for collective rotational bands with prolate but moderate shape, coexisting with the oblate structure of Tb 151 . The discovery of new superdeformed bands in the Tb 151,152 isotopes, the extension to lower and higher spins of the previously known bands, and mean field calculations with a deformed Woods-Saxon potential have contributed to improve our knowledge as well as raise new questions on the orbitals configuration assignments of these bands. (author)

Crystallographic and magnetic properties of (Nd,Dy)3Fe27.5(Ti,Mo)1.5 compounds

International Nuclear Information System (INIS)

Han, S.B.; Liu, X.F.; Lv, J.Y.; Peng, J.; Hao, Y.M.; Li, X.J.; Chen, D.F.; Xue, Y.J.; Li, J.H.; Hu, Z.B.

2006-01-01

A systematic study of the formation, structure and magnetic properties of (Nd,Dy) 3 Fe 27.5 (Ti,Mo) 1.5 compounds has been performed. Rietveld analyses of the X-ray patterns of the samples indicate that the concentrations of Ti and Mo affect the formation and structural properties slightly, whereas different rare-earth (Nd and Dy) contents influence them significantly. It is found that high Dy contents make it difficult to form the 3:29-type structures. The Curie temperatures of Nd 2.1 Dy 0.9 Fe 27.5 Ti 1.5- x Mo x decrease monotonically as more Ti was replaced by Mo but their saturation magnetizations remain almost unchanged; in contrast, for Nd 3- y Dy y Fe 27.5 TiMo 0.5 , their saturation magnetizations decrease monotonically with increasing Dy contents while their Curie temperatures are constant

The phase transition of the incommensurate phases β-Ln(PO3)3(Ln=Y,Tb...Yb), crystal structures of α-Ln(PO3)3(Ln=Y,Tb...Yb) and Sc(PO3)3

International Nuclear Information System (INIS)

Hoeppe, Hennig A.

2009-01-01

The incommensurately modulated room-temperature phases β-Ln(PO 3 ) 3 (Ln=Y,Tb...Yb) undergo a topotactic phase transition monitored by vibrational spectroscopy below 180 K leading to α-Ln(PO 3 ) 3 (Ln=Y,Dy...Yb), above 200 K the incommensurate phases are reobtained. The low-temperature phases exhibit a new structure type (α-Dy(PO 3 ) 3 ,P2 1 /c,Z=12,a=14.1422(6),b=20.0793(9),c=10.1018(4)A, β=127.532(3) 0 ). α-Tb(PO 3 ) 3 is isotypic with Gd(PO 3 ) 3 (α-Tb(PO 3 ) 3 ,I2/a,Z=16,a=25.875(6),b=13.460(3),c=10.044(2)A, β=119.13(3) 0 ). The symmetry relations between the involved phases of the phase transition are discussed. The crystal structure of Sc(PO 3 ) 3 is isotypic with that of Lu(PO 3 ) 3 and C-type phosphates. The polyphosphates consist of infinite zig-zag chains of corner-sharing PO 4 tetrahedra, the cations are coordinated sixfold in an almost octahedral arrangement. To confirm the quality of the determined crystal structures the deviation of the phosphate tetrahedra from ideal symmetry was determined and discussed. - Abstract: Basic structure from which all crystal structures of the late lanthanoids' polyphosphates at room temperature and below can be derived.

Antiferromagnetic domains in rare earth metals and alloys

Energy Technology Data Exchange (ETDEWEB)

Palmer, S B [Hull Univ. (UK). Dept. of Applied Physics

1975-12-01

Anomalies in the c-axis elastic properties of antiferromagnetic Dy, 50% Tb-Ho and 60% Gd-Y are reported. The anomalies are only present when the sample is cycled from the ferromagnetic to the antiferromagnetic state and are attributed to domains in the helical regime.

Isomer spectroscopy of neutron-rich 168 Tb 103

Energy Technology Data Exchange (ETDEWEB)

Gurgi, L. A.; Regan, P. H.; Söderström, P. -A.; Watanabe, H.; Walker, P. M.; Podolyák, Zs.; Nishimura, S.; Berry, T. A.; Doornenbal, P.; Lorusso, G.; Isobe, T.; Baba, H.; Xu, Z. Y.; Sakurai, H.; Sumikama, T.; Catford, W. N.; Bruce, A. M.; Browne, F.; Lane, G. J.; Kondev, F. G.; Odahara, A.; Wu, J.; Liu, H. L.; Xu, F. R.; Korkulu, Z.; Lee, P.; Liu, J. J.; Phong, V. H.; Yag, A.; Zhang, G. X.; Alharbi, T.; Carroll, R. J.; Chae, K. Y.; Dombradi, Zs.; Estrade, A.; Fukuda, N.; Griffin, C.; Ideguchi, E.; Inabe, N.; Kanaoka, H.; Kojouharov, I.; Kubo, T.; Kubono, S.; Kurz, N.; Kuti, I.; Lalkovski, S.; Lee, E. J.; Lee, C. S.; Lotay, G.; Moon, C. -B.; Nishizuka, I.; Nita, C. R.; Patel, Z.; Roberts, O. J.; Schaffner, H.; Shand, C. M.; Suzuki, H.; Takeda, H.; Terashima, S.; Vajta, Zs.; Yoshida, S.; Valiente-Dòbon, J. J.

2017-11-01

In-flight fission of a 345 MeV per nucleon 238U primary beam on a 2 mm thick 9Be target has been used to produce and study the decays of a range of neutron-rich nuclei centred around the doubly mid-shell nucleus 170Dy at the RIBF Facility, RIKEN, Japan. The produced secondary fragments of interest were identified event-by-event using the BigRIPS separator. The fragments were implanted into the WAS3ABI position sensitive silicon active stopper which allowed pixelated correlations between implants and their subsequent β-decay. Discrete γ-ray transitions emitted following decays from either metastable states or excited states populated following beta decay were identified using the 84 coaxial high-purity germanium (HPGe) detectors of the EURICA spectrometer, which was complemented by 18 additional cerium-doped lanthanum bromide (LaBr3) fast-timing scintillation detectors from the FATIMA collaboration. This paper presents the internal decay of a metastable isomeric excited state in the odd-odd nucleus 168Tb, which corresponds to a single proton-neutron hole configuration in the valence maximum nucleus 170Dy. These data represent the first information on excited states in this nucleus, which is the most neutron-rich odd-odd isotope of terbium (Z=65) studied to date. Nilsson configurations associated with an axially symmetric, prolate-deformed nucleus are proposed for the 168Tb ground state the observed isomeric state by comparison with Blocked BCS-Nilsson calculations.

Magnetoresistance anomaly in DyFeCo thin films

International Nuclear Information System (INIS)

Wu, J. C.; Wu, C. S.; Wu, Te-ho; Chen, Bing-Mau; Shieh, Han-Ping D.

2001-01-01

Microstructured rare-earth - transition-metal DyFeCo films have been investigated using magnetoresistance and extraordinary Hall-effect measurements. The Hall loops reveal variation of coercive fields depending on the linewidth and the composition of the films. The magnetoresistance curves, with changes up to as high as 1.3%, show positive/negative magnetoresistance peaks centered on the coercive fields depending on the linewidth of the films only. The variation of the coercivity can be attributed to the magnetic moment canting between the Dy and FeCo subcomponents and the existence of the diverged magnetization on the edges, and the anomalous magnetoresistance peaks observed are discussed with the existing theories. [copyright] 2001 American Institute of Physics

Cut-off frequency of magnetostrictive materials based on permeability spectra

International Nuclear Information System (INIS)

Meng Hao; Zhang Tianli; Jiang Chengbao

2012-01-01

The loss behavior and cut-off frequency of TbDyFe alloy and TbDyFe/epoxy composite have been investigated by measuring their permeability spectra. The loss factor of TbDyFe alloy increases exponentially as the frequency goes up, while it is almost unchanged for the TbDyFe/epoxy composite. The loss factor value for the TbDyFe composite is only 4.3% of that for the monolithic TbDyFe alloy at high frequency of 10 kHz under the peak magnetic induction of 10 mT. The cut-off frequency of TbDyFe/epoxy composite is 6800 kHz, 3 orders of magnitude larger than that of TbDyFe alloy. The cut-off frequency is found to be the ferromagnetic resonance frequency and can be calculated from Snoek's law. - Highlights: ► The cut-off frequency of TbDyFe alloy and TbDyFe/epoxy composite has been investigated. ► Permeability spectra are used to study loss behavior and cut-off frequency. ► A mathematic formula is deduced to predict the cut-off frequency. ► TbDyFe/epoxy composite presents high cut-off frequency of 6800 kHz.

Rare earth and precious elements in the urban sewage sludge and lake surface sediments under anthropogenic influence in the Republic of Benin.

Science.gov (United States)

Yessoufou, Arouna; Ifon, Binessi Edouard; Suanon, Fidèle; Dimon, Biaou; Sun, Qian; Dedjiho, Comlan Achille; Mama, Daouda; Yu, Chang-Ping

2017-11-09

Nowadays, sewage sludge and water bodies are subjected to heavy pollution due to rapid population growth and urbanization. Heavy metal pollution represents one of the main challenges threatening our environment and the ecosystem. The present work aims to evaluate the contamination state of the sewage sludge and lake sediments in the Republic of Benin. Twenty metallic elements including 15 rare earth elements (Eu, Sb, Cs, Nd, Pr, Gd, La, Ce, Tb, Sm, Dy, Ho, Eu, Yb, and Lu) and five precious elements (Ag, Au, Pd, Pt, and Ru) were investigated using inductive plasma-mass spectrometry. Results showed broad range concentrations of the elements. Ce, La, and Nd were present in both sediments and sewage sludge at concentrations ranging 5.80-41.30 mg/kg dry matter (DM), 3.23-15.60 mg/kg DM, and 2.74-19.26 mg/kg DM, respectively. Pr, Sm, Gd, Tb, Dy, Eu, Er, Yb, Cs, Ho, and Tm concentrations were lower (0.02-5.94 mg/kg DM). Among precious elements, Ag was detected at the highest concentration in all sites (0.43-4.72 mg/kg DM), followed by Pd (0.20-0.57 mg/kg DM) and Au (0.01-0.57 mg/kg DM). Ru and Pt concentrations were sewage sludge. This revealed a growing anthropogenic input which was also implied by principal component analysis. The evaluation of pollution loading index (PLI) indicated a moderate to strong contamination (0.12 ≤ PLI ≤ 0.58; 37 ≤ PLI ≤ 114, respectively, for rare earth elements and precious elements), while the degree of contamination indicated a moderate polymetallic contamination for rare earth elements and significant contamination for precious elements.

Substitution disorder and photoluminescent property of a new rare-earth borate: K{sub 3}TbB{sub 6}O{sub 12}

Energy Technology Data Exchange (ETDEWEB)

Zhao, Dan; Ma, Fa-Xue; Huang, Min; Chen, Peng-Fei; Zhang, Rong-Hua [Henan Polytechnic Univ., Jiaozuo (China). College of Chemistry and Chemical Engineering; Zhang, Rui-Juan [Henan Polytechnic University, Jiaozuo (China). Academic Affairs Office; Wei, Wei [Capital Normal Univ., Beijing (China). Dept. of Chemistry

2016-11-01

A new rare-earth borate K{sub 3}TbB{sub 6}O{sub 12} has been prepared using the high temperature molten salt method and was structurally determined by single crystal X-ray diffraction analyses. The structure features a three-dimensional (3D) framework which is composed of isolated B{sub 5}O{sub 10}, KO{sub 6}, KO{sub 8} and TbO{sub 6} groups. An atom site in the 3{sub 2} screw axis is shared by K and Tb atoms with the molar ratio of 1:1. The self-activated photoluminescence (PL) property of K{sub 3}TbB{sub 6}O{sub 12} was studied. Under the excitation of 378 nm, the emission spectrum exhibits an intense green emission centered at 543-548 nm with the chromaticity coordinates (0.342, 0.590), which can be assigned to the {sup 5}D{sub 4} → {sup 7}F{sub 5} transition of Tb{sup 3+}. The excitation spectra cover a wide range from 330 to 385 nm, which suggests that the K{sub 3}TbB{sub 6}O{sub 12} phosphors can be effectively excited by a near-UV light source. One may expect that compound K{sub 3}TbB{sub 6}O{sub 12} can be used as a green phosphor pumped by near-UV LED chips.

Spin reorientation phenomena in (R{sub 1-x}R`{sub x}){sub 2}Co{sub 14}B (R = La, R` = Dy and Ho)

Energy Technology Data Exchange (ETDEWEB)

Myojin, T. [Takamatsu Nat. Coll. of Technol. (Japan); Ohno, T. [Tokushima Univ. (Japan). Faculty of Engineering; Mizuno, K. [Tokushima Univ. (Japan). Faculty of Integrated Arts and Sciences; Tsujimura, A. [Faculty of Engineering, Tokushima Bunri Univ., Kagawa Shido (Japan); Kojima, K. [Hiroshima Univ. (Japan). Faculty of Integrated Arts and Sciences

1997-07-01

The variations of magnetization with temperature in (La{sub 1-x}R`{sub x}){sub 2}Co{sub 14}B (R` = Dy and Ho) have been measured to determine spin reorientation temperature T{sub SR} of these compounds. The phase diagrams of spin arrangement thus obtained indicate monotonous increase in T{sub SR} with R` concentration x. Also, T{sub SR}`s of R{sub 2}Co{sub 14}B(R = Tb, Dy and Ho) are found to vary linearly with the Stevens factor {alpha} of R. (orig.). 4 refs.

New features in the spectrum of {sup 152}Dy

Energy Technology Data Exchange (ETDEWEB)

Galindo-Uribarri, A; Andrews, H R; Ball, G C; Radford, D C; Janzen, V P; Ward, D [Atomic Energy of Canada Ltd., Chalk River, ON (Canada). Chalk River Nuclear Labs.; Kuehner, J A; Mullins, S; Persson, L; Prevost, D; Waddington, J C [McMaster Univ., Hamilton, ON (Canada). Dept. of Physics; Drake, T E [Toronto Univ., ON (Canada). Dept. of Physics; Wyss, R [Joint Inst. for Heavy Ion Research, Oak Ridge, TN (United States)

1992-08-01

One of the most important recent developments in nuclear structure physics has been the prediction and observation of superdeformed (SD) shapes at high angular momentum in several nuclei in the rare earth region. The first experimental observation was a ridge-valley structure in a {gamma}-{gamma} coincidence matrix for the {sup 152}Dy nucleus. The ridge was found to be generated by sequences of stretched E2 transitions and corresponded to a moment of inertia J{sup (2)} of 85 {Dirac_h}{sup 2}MeV{sup -1}. Subsequently a discrete SD band was discovered in {sup 152}Dy and the lifetimes were measured. More recently the discovery of SD bands in several nuclei in the neighbourhood of {sup 152}Dy, the discovery of multiple SD bands in some nuclei, and the discovery of new SD regions at mass A {approx} 190 and A {approx} 140 have stimulated intense research activity in this area of nuclear physics. (author). 15 refs., 4 figs.

Rare earth chalcogels NaLnSnS{sub 4} (Ln = Y, Gd, Tb) for selective adsorption of volatile hydrocarbons and gases

Energy Technology Data Exchange (ETDEWEB)

Edhaim, Fatimah; Rothenberger, Alexander [Physical Science and Engineering Division, King Abdullah University of Science and Technology, Thuwal (Saudi Arabia)

2017-08-16

The synthesis and characterization of the rare earth chalcogenide aerogels NaYSnS{sub 4}, NaGdSnS{sub 4}, and NaTbSnS{sub 4} is reported. Rare earth metal ions like Y{sup 3+}, Gd{sup 3+}, and Tb{sup 3+} react with the chalcogenide clusters [SnS{sub 4}]{sup 4-} in aqueous formamide solution forming extended polymeric networks by gelation. Aerogels obtained after supercritical drying have BET surface areas of 649 m{sup 2}.g{sup -1} (NaYSnS{sub 4}), 479 m{sup 2}.g{sup -1} (NaGdSnS{sub 4}), and 354 m{sup 2}.g{sup -1} (NaTbSnS{sub 4}). Electron microscopy and physisorption studies reveal that the new materials have pores in the macro (above 50 nm) and meso (2-50 nm) regions. These aerogels show higher adsorption of toluene vapor over cyclohexane vapor and CO{sub 2} over CH{sub 4} or H{sub 2}. The notable adsorption capacity for toluene (NaYSnS{sub 4}: 1108 mg.g{sup -1}; NaGdSnS{sub 4}: 921 mg.g{sup -1}; and NaTbSnS4: 645 mg.g{sup -1}) and high selectivity for gases (CO{sub 2}/H{sub 2}: 172 and CO{sub 2}/CH{sub 4}: 50 for NaYSnS{sub 4}, CO{sub 2}/H{sub 2}: 155 and CO{sub 2}/CH{sub 4}: 37 for NaGdSnS{sub 4}, and CO{sub 2}/H{sub 2}: 75 and CO{sub 2}/CH{sub 4}: 28 for NaTbSnS{sub 4}) indicate potential future use of chalcogels in adsorption-based gas or hydrocarbon separation processes. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Photoluminescence of trivalent rare earths in perovskite stacking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/, Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/, and Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/

Energy Technology Data Exchange (ETDEWEB)

Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1981-12-01

Rhombohedral 12 L staking polytypes Ba/sub 2/Lasub(2-x)REsub(x)/sup 3 +/MgW/sub 2/vacantO/sub 12/ show with RE/sup 3 +/ = Pr, Sm, Eu, Tb, Dy, Ho, Er, Tm; the 18 L stacking polytypes Ba/sub 6/Ysub(2-x)REsub(x)/sup 3 +/W/sub 3/vacantO/sub 18/ and the polymorphic perovskites Sr/sub 8/SrGdsub(2-x)REsub(x)/sup 3 +/W/sub 4/vacantO/sub 24/ with RE/sup 3 +/ = Sm, Eu, Dy, Ho, Er visible photoluminescence. The concentration dependence and the influence of the coordination number of the rare earth are reported.

Magnetostrictive effects in ferromagnetic Dy break-junctions

Energy Technology Data Exchange (ETDEWEB)

Mueller, Marc; Suergers, Christoph; Montbrun, Richard [Karlsruher Institut fuer Technologie, Physikalisches Institut, 76131 Karlsruhe (Germany); Loehneysen, Hilbert v. [Karlsruher Institut fuer Technologie, Physikalisches Institut, 76131 Karlsruhe (Germany); Karlsruher Institut fuer Technologie, Institut fuer Festkoerperphysik, 76021 Karlsruhe (Germany)

2011-07-01

A characteristic property of the rare-earth metals are their large magnetostrictive strains which are related to the magnetocrystalline anisotropy through the elastic energy. We have investigated the electrical conductance G of mechanical break-junctions of a dysprosium wire at 4.2 K where Dy is in the ferromagnetic state. In zero magnetic field we find the usual variation of the conductance G vs. electrode distance x while breaking the wire mechanically, with a sequence of steps and more or less prominent plateaus. The behavior G(x) is modified in magnetic fields {mu}{sub 0} H up to 1 T due to the large magnetostriction of Dy. In addition, the conductance can be changed reproducibly by variation of H. For a number of contacts we observe discrete changes in G(H) in the range of several G{sub 0} = 2 e{sup 2}/h. The behavior of G(H) and its angular dependence can be quantitatively understood by taking into account the magnetostrictive properties of Dy. This first realization of a magnetostrictive atomic switch demonstrates the possibility of reproducibly tuning the conductance of magnetic nanocontacts by a magnetic field.

Syntheses, crystal structures and photoluminescence properties of two rare-earth molybdates CsLn(MoO{sub 4}){sub 2} (Ln=Eu, Tb)

Energy Technology Data Exchange (ETDEWEB)

Zhao, Dan; Ma, Fa-Xue; Liu, Bao-Zhong; Fan, Yun-Chang; Han, Xue-Feng; Zhang, Lei; Nie, Cong-Kui [Henan Polytechnic Univ. (China). College of Chemistry and Chemical Engineering

2018-04-01

Single crystals of two cesium rare-earth molybdates CsLn(MoO{sub 4}){sub 2} (Ln=Eu, Tb) have been prepared using the high temperature molten salt (flux) method. Single-crystal X-ray diffraction analyses reveal that they crystallize in the orthorhombic space group Pccm (No. 49) and features a 2D layer structure that is composed of [Ln(MoO{sub 4}){sub 2}]{sub ∞} and [Cs]{sub ∞} layers. Under near-UV light excitation, emission spectrum of CsEu(MoO{sub 4}){sub 2} consists of several sharp lines due to the characteristic electronic transitions of Eu{sup 3+} ions, whereas CsTb(MoO{sub 4}){sub 2} exhibits characteristic green emission of Tb{sup 3+} ions.

Prospective analysis of the flows of certain rare earths in Europe at the 2020 horizon.

Science.gov (United States)

Rollat, Alain; Guyonnet, Dominique; Planchon, Mariane; Tuduri, Johann

2016-03-01

This paper proposes a forecast of certain rare earth flows in Europe at the 2020 horizon, based on an analysis of trends influencing various actors of the rare earth industry along the value chain. While 2020 is indicated as the forecast horizon, the analysis should be considered as more representative of the next decade. The rare earths considered here are used in applications that are important for a low-carbon energy transition and/or have a significant recycling potential: NdFeB magnets (Pr, Nd, Dy), NiMH batteries (Pr, Nd) and fluorescent lamp phosphors (Eu, Tb, Y). An analysis of major trends affecting the rare earth industry in Europe along the value chain (including extraction, separation, fabrication, manufacture, use and recycling), helps to build a scenario for a material flow analysis of these rare earths in Europe. The scenario assumes in particular that during the next decade, there exists a rare earth mine in production in Europe (with Norra Kärr in Sweden as a most likely candidate) and also that recycling is in line with targets proposed in recent European legislation. Results are presented in the form of Sankey diagrams which help visualize the various flows for the three applications. For example, calculations forecast flows from extraction to separation of Pr, Nd and Dy for magnet applications in Europe, on the order of 310 tons, 980 tons and 80 tons rare earth metal resp., while recycled flows are 35 tons, 110 tons and 30 tons resp. Calculations illustrate how the relative contribution of recycling to supply strongly depends on the situation with respect to demand. Considering the balance between supply and demand, it is not anticipated any significant shortage of rare earth supply in Europe at the 2020 horizon, barring any new geopolitical crisis involving China. For some heavy rare earths, supply will in fact largely outweigh demand, as for example Europium due to the phasing out of fluorescent lights by LEDs. Copyright © 2016 Elsevier Ltd

Series of isostructural planar lanthanide complexes [Ln(III)4(mu3-OH)2(mdeaH)2(piv)8] with single molecule magnet behavior for the Dy4 analogue.

Science.gov (United States)

Abbas, Ghulam; Lan, Yanhua; Kostakis, George E; Wernsdorfer, Wolfgang; Anson, Christopher E; Powell, Annie K

2010-09-06

A series of five isostructural tetranuclear lanthanide complexes of formula [Ln(4)(mu(3)-OH)(2)(mdeaH)(2)(piv)(8)], (mdeaH(2) = N-methyldiethanolamine; piv = pivalate; Ln = Tb (1), Dy (2), Ho (3), Er (4), and Tm (5)) have been synthesized and characterized. These clusters have a planar "butterfly" Ln(4) core. Magnetically, the Ln(III) ions are weakly coupled in all cases; the Dy(4) compound 2 shows Single Molecule Magnet (SMM) behavior.

The significant role of the rare earth ions on the elastic and thermodynamic parameters of LiCoDy- and ZnCoCe-ferrites

International Nuclear Information System (INIS)

Bishay, Samiha T.

2006-01-01

Two types of rare earth ferrites [Li 0.6 Co 0.1 Dy x Fe 2.3-x O 4 ; 0.0= 0.5 Co 0.5 Ce y Fe 2-y O 4 ; 0.0= L ) and shear (V S ) velocities, Young's modulus (E), Debye temperature (θ D ) and specific heat capacity (C v ) have been evaluated for all the investigated samples. The rare earth content as well as its ionic radius plays a significant role in the evaluated parameters. According to the experimental results, the two investigated types of rare earth ferrite are considered as insulator magnetic solids. It was found that for each composition there exists a characteristic temperature, down to which the resonance frequency of the investigated samples drops smoothly, but above this temperature the resonance frequency stays constant. Accordingly, these samples seem to be of importance in industrial applications especially in the field of electronics

Theory of Magnetic Properties of Heavy Rare Earth Metals:

DEFF Research Database (Denmark)

Lindgård, Per-Anker; Danielsen, O.

1975-01-01

results are given for the magnetization agreeing with experiment for Gd, Tb, and Dy. For Tb and Dy the zero-point deviations were found to be 0.05μB and 0.08μB, respectively, and the ratio [b(T)-b(0)]/[ΔM(T)-ΔM(0)] is approximately 1/3 for all temperatures below 100 K. This gives rise to large corrections......The contributions to the macroscopic-anisotropy constants and resonance energy from crystal-field anisotropy, magnetoelastic effects in the frozen and flexible lattice model, and two-ion interactions have been found for all terms allowed in a crystal of hexagonal symmetry. The temperature...... dependence is expressed as expansions of thermal averages of the Stevens operators 〈Olm〉. A systematic spin-wave theory, renormalized in the Hartree-Fock approximation, is developed and used to find the temperature dependence of the Stevens operators and the resonance energy in terms of the magnetization...

Size-dependent structure and magnetic properties of DyMnO3 nanoparticles

International Nuclear Information System (INIS)

Cai, Xuan; Shi, Lei; Zhou, Shiming; Zhao, Jiyin; Guo, Yuqiao; Wang, Cailin

2014-01-01

The structure and magnetic properties of orthorhombic DyMnO 3 nanoparticles with different particle sizes are investigated in this paper. With decreasing particle size, all the lattice parameters a, b, and c gradually decrease, whereas the orthorhombic distortion increases. Magnetic measurements reveal that the antiferromagnetic interaction of Mn ions is weakened due to the decrease in Mn-O-Mn bond angle. Above a critical field H*, DyMnO 3 undergoes a field-induced metamagnetic transition at 4 K, which is related to the spin reversal of Dy moments. The critical field H* increases monotonically with size reduction, indicating an enhancement of the antiferromagnetic interaction of Dy ions due to the decreased distance between rare earth ions. The magnetization at 4 K and 5 T, i.e., M(4 K, 5 T) shows a non-monotonic variation with particle size d, i.e., M(4 K, 5 T) initially increases with size reduction but decreases again for d < 68 nm. A modified core-shell model, in which the ferromagnetic ordering (Dy magnetic structure) and antiferromagnetic ordering (Mn magnetic structure) coexist in the core, is proposed to explain this behavior.

Solid Oxide Galvanic Cell to determine thermochemical data of Dy6UO12(s)

International Nuclear Information System (INIS)

Sahu, Manjulata; Dash, Smruti; Sen, B.K.; Venugopal, V.

2010-01-01

The rare earth elements such as Sm, Eu, Gd, and Dy have very high thermal neutron absorption cross sections and their oxides are utilized as burnable poisons in nuclear reactor to maintain constant reactivity of the core. These oxides form solid solution with urania as their ionic radii are within 20% of that of urania. Rare earth oxides-urania solid solutions are also beneficial in preventing oxidation of UO 2 (s). RE 6 UO I2 (s) (RE = rare earth) type of compounds are known to exist in RE-U-O system and their formation cannot be ruled out under transient conditions. The data on Gibbs energy of formation of compounds in RE-U-O system is therefore essential to predict the feasibility. Theoretically, the measurement of the e.m.f. of a suitable galvanic cell is one of the most accurate methods to obtain Gibbs energy of formation of compounds if e.m.f cell operates reversibly. In this study, the standard molar Gibbs energy of formation of Dy 6 UO I2 (s) was determined using solid oxide galvanic cell technique. The Gibbs energy of formation of Dy 6 UO 12 (s) is reported for the first time

Inductively coupled plasma optical emission spectrometry analysis of lanthanum, samarium and gadolinium oxides for rare earths impurities

International Nuclear Information System (INIS)

Reino, L.C.P.; Lordello, A.R.

1990-09-01

An inductively coupled plasma optical emission spectrometry method is described for the determination of Sm, Eu, La, Gd, Dy, Pr, Ho, Nd, Tb and Y in purified oxides of lanthanum, samarium and gadolinium. The method enables a simple, precise and readily available determination. Dissolution of the samples is achieved with diluted hydrochloric acid (1:1). The solutions are diluted to volume for a concentration of 1mg/ml. The lowest determination limit is 0,01% for most elements and 0,05 or 0,1% for a few rare earths in samarium and gadolinium matrices. Lanthanum, Samarium and Gadolinium concentrates with purity grade of 99,9%, 99,6% and 99,8%, respectively, can be analysed by this procedure. (author)

Molecular assembly and magnetic dynamics of two novel Dy6 and Dy8 aggregates.

Science.gov (United States)

Guo, Yun-Nan; Chen, Xiao-Hua; Xue, Shufang; Tang, Jinkui

2012-04-02

Complexation of dysprosium(III) with the heterodonor chelating ligand o-vanillin picolinoylhydrazone (H(2)ovph) in the presence of a carbonato ligand affords two novel Dy(6) and Dy(8) clusters, namely, [Dy(6)(ovph)(4)(Hpvph)(2)Cl(4)(H(2)O)(2)(CO(3))(2)]·CH(3)OH·H(2)O·CH(3)CN (2) and [Dy(8)(ovph)(8)(CO(3))(4)(H(2)O)(8)]·12CH(3)CN·6H(2)O (3). Compound 2 is composed of three petals of the Dy(2) units linked by two carbonato ligands, forming a triangular prism arrangement, while compound 3 possesses an octanuclear core with an unprecedented tub conformation, in which Dy(ovph) fragments are attached to the sides of the carbonato core. The static and dynamic magnetic properties are reported and discussed. In the Dy(6) aggregate, three Dy(2) "skeletons", having been well preserved (see the scheme), contribute to the single-molecule-magnet behavior with a relatively slow tunneling rate, while the Dy(8) cluster only exhibits a rather small relaxation barrier.

Magnetic moments of high spin rotational states in 158Dy and 164Dy+

International Nuclear Information System (INIS)

Seiler-Clark, G.

1983-09-01

For the study of their magnetic moments yrast states in 158 Dy and 164 Dy were excited via the multiple-Coulomb excitation by a 4.7 MeV/u 208 Pb beam. Hereby especially the question was of interest, how the one-particle effects in the nuclear structure in the region of the backbending anomaly in 158 Dy take effects on the g-factors of the high spin states in this region. The particle-γ angular correlations perturbed in the transient magnetic field during the passing of the excited Dy ions through a thin magnetized iron foil were measured. By the selective position-sensitive detection of Dy recoil ions and Pb projectiles under forward angles it was possible to determine additionally to the g-factors in the backbending region also g-factors in the spin region I 158 Dy and 164 Dy by detection of the particle-γ correlations precessing in the static hyperfine field after implantation in iron. The static hyperfine field was at the 4 + state in 164 Dy determined to B (Dy,Fe) = 245+-25 T. The g-factors were determined by comparison of the experimental results with calculations of the perturbed angular correlations by time-differential regarding of the population and de-excitation of the yrast states as well as by precession and hyperfine-relaxation effects during the flight of the Dy ions in the vacuum. (orig./HSI) [de

Effect of rapid quenching on the magnetism and magnetocaloric effect of equiatomic rare earth intermetallic compounds RNi (R = Gd, Tb and Ho)

Energy Technology Data Exchange (ETDEWEB)

Rajivgandhi, R. [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India); Arout Chelvane, J. [Defence Metallurgical Research Laboratory, Hyderabad 500 058 (India); Quezado, S.; Malik, S.K. [Departamento de F’ısica Teorica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59072-970 (Brazil); Nirmala, R., E-mail: nirmala@physics.iitm.ac.in [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India)

2017-07-01

Highlights: • Melt-spinning yields microcrystalline RNi (R = Gd, Tb and Ho) samples with texture. • The texture-induced anisotropy affects magnetic and magnetocaloric properties. • Melt-spinning helps one engineer magnetocaloric effect in rare-earth compounds. - Abstract: Magnetocaloric effect (MCE) in RNi (where R = Gd, Tb and Ho) compounds has been studied in their arc-melted and melt-spun forms. The compound GdNi has the orthorhombic CrB-type structure (Space group Cmcm, No. 63) and the compound HoNi has the orthorhombic FeB-type structure (Space group Pnma, No. 62) at room temperature regardless of their synthesis condition. However, arc-melted TbNi orders in a monoclinic structure (Space group P2{sub 1}/m, No. 11) and when it is rapidly quenched to a melt-spun form, it crystallizes in an orthorhombic structure (Space group Pnma, No. 62). The arc-melted GdNi, TbNi and HoNi compounds order ferromagnetically at ∼69 K, ∼67 K and ∼36 K (T{sub C}) respectively. While the melt-spun GdNi shows about 6 K increase in T{sub C}, the ordering temperature of TbNi remains nearly the same in both arc-melted and melt-spun forms. In contrast, a reduction in T{sub C} by about 8 K is observed in melt-spun HoNi, when compared to its arc-melted counterpart. Isothermal magnetic entropy change, ∆S{sub m}, calculated from the field dependent magnetization data indicates an enhanced relative cooling power (RCP) for melt-spun GdNi for field changes of 20 kOe and 50 kOe. A lowered RCP value is observed in melt-spun TbNi and HoNi. These changes could have resulted from the competing shape anisotropy and the granular microstructure induced by the melt-spinning process. Tailoring the MCE of rare earth intermetallic compounds by suitably controlled synthesis techniques is certainly one of the directions to go forward in the search of giant magnetocaloric materials.

Luminescence properties of pure and doped CaSO4 nanorods irradiated by 15 MeV e-beam

International Nuclear Information System (INIS)

Salah, Numan; Alharbi, Najlaa D.; Enani, Mohammad A.

2014-01-01

Calcium sulfate (CaSO 4 ) doped with proper activators is a highly sensitive phosphor used in different fields mainly for radiation dosimetry, lighting and display applications. In this work pure and doped nanorods of CaSO 4 were produced by the co-precipitation technique. Samples from this material doped with Ag, Cu, Dy, Eu and Tb were exposed to different doses of 15 MeV e-beam and studied for their thermoluminesence (TL) and photoluminescence (PL) properties. Color center formation leading to PL emissions were investigated before and after e-beam irradiation. The samples doped with rare earths elements (i.e. Dy, Eu and Tb) were observed to have thinner nanorods than the other samples and have higher absorption in the UV region. The Ag and Tb doped samples have poor TL response to e-beam, while those activated by Cu, Dy and Eu have strong glow peaks at around 123 °C. Quite linear response curves in the whole studied exposures i.e. 0.1–100 Gy were also observed in Cu and Dy doped samples. The PL results show that pure CaSO 4 nanorods have active color centers without irradiation, which could be enriched/modified by these impurities mainly rare earths and further enhanced by e-beam irradiation. Eu 3+ → Eu 2+ conversion is clearly observed in Eu doped sample after e-beam irradiation. These results show that these nanorods might be useful in lighting and display devices development

Thermoluminescence of CaCO3:Dy and CaCO3:Mn

International Nuclear Information System (INIS)

Bapat, V.N.; Nambi, K.S.V.

1976-01-01

CaCO 3 samples doped with Dy and Mn were prepared in the laboratory by co-precipitation techniques. Thermoluminescence and emission spectra of these phosphors were studied and were compared with those of the naturally occuring calcite and undoped CaCO 3 samples. Dy-doping seems to give a more efficient phosphor and indicates a possibility of getting a better phosphor by a judicious choice of a rare earth doping of CaCO 3 . Interesting result have been obtained on the TL glow curve variations of these phosphors with different temperature treatments prior to irradiation. (author)

Temperature-dependent structure of Tb-doped magnetite nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Rice, Katherine P.; Russek, Stephen E., E-mail: stephen.russek@nist.gov; Shaw, Justin M.; Usselman, Robert J.; Evarts, Eric R.; Silva, Thomas J.; Nembach, Hans T. [National Institute of Standards and Technology, Boulder, Colorado 80305 (United States); Geiss, Roy H. [Colorado State University, Fort Collins, Colorado 80523 (United States); Arenholz, Elke [Lawrence Berkeley National Laboratory, Advanced Light Source, Berkeley, California 94720 (United States); Idzerda, Yves U. [Department of Physics, Montana State University, Bozeman, Montana 59717 (United States)

2015-02-09

High quality 5 nm cubic Tb-doped magnetite nanoparticles have been synthesized by a wet-chemical method to investigate tailoring of magnetic properties for imaging and biomedical applications. We show that the Tb is incorporated into the octahedral 3+ sites. High-angle annular dark-field microscopy shows that the dopant is well-distributed throughout the particle, and x-ray diffraction measurements show a small lattice parameter shift with the inclusion of a rare-earth dopant. Magnetization and x-ray magnetic circular dichroism data indicate that the Tb spins are unpolarized and weakly coupled to the iron spin lattice at room temperature, and begin to polarize and couple to the iron oxide lattice at temperatures below 50 K. Broadband ferromagnetic resonance measurements show no increase in magnetic damping at room temperature for Tb-doped nanoparticles relative to undoped nanoparticles, further confirming weak coupling between Fe and Tb spins at room temperature. The Gilbert damping constant, α, is remarkably low for the Tb-doped nanoparticles, with α = 0.024 ± 0.003. These nanoparticles, which have a large fixed moment, a large fluctuating moment and optically active rare-earth elements, are potential high-relaxivity T1 and T2 MRI agents with integrated optical signatures.

Temperature-dependent structure of Tb-doped magnetite nanoparticles

International Nuclear Information System (INIS)

Rice, Katherine P.; Russek, Stephen E.; Shaw, Justin M.; Usselman, Robert J.; Evarts, Eric R.; Silva, Thomas J.; Nembach, Hans T.; Geiss, Roy H.; Arenholz, Elke; Idzerda, Yves U.

2015-01-01

High quality 5 nm cubic Tb-doped magnetite nanoparticles have been synthesized by a wet-chemical method to investigate tailoring of magnetic properties for imaging and biomedical applications. We show that the Tb is incorporated into the octahedral 3+ sites. High-angle annular dark-field microscopy shows that the dopant is well-distributed throughout the particle, and x-ray diffraction measurements show a small lattice parameter shift with the inclusion of a rare-earth dopant. Magnetization and x-ray magnetic circular dichroism data indicate that the Tb spins are unpolarized and weakly coupled to the iron spin lattice at room temperature, and begin to polarize and couple to the iron oxide lattice at temperatures below 50 K. Broadband ferromagnetic resonance measurements show no increase in magnetic damping at room temperature for Tb-doped nanoparticles relative to undoped nanoparticles, further confirming weak coupling between Fe and Tb spins at room temperature. The Gilbert damping constant, α, is remarkably low for the Tb-doped nanoparticles, with α = 0.024 ± 0.003. These nanoparticles, which have a large fixed moment, a large fluctuating moment and optically active rare-earth elements, are potential high-relaxivity T1 and T2 MRI agents with integrated optical signatures

Heterogeneous bilayer films NiFe (Fe)-Dy: magnetic circular dichroism and Dy spin ordering

Energy Technology Data Exchange (ETDEWEB)

Markov, V.V. E-mail: ise@iph.krasn.ruise@iph.krasnoyarsk.su; Kesler, V.G.; Khudyakov, A.E.; Edelman, I.S.; Bondarenko, G.V

2001-08-01

Results of the magnetic circular dichroism (MCD) and Auger electron spectroscopy (AES) investigations in the 3d transition metal-Dy bi-layer films are presented. It is shown that even at room temperature the Dy layer makes a contribution to MCD of the bi-layer film, which corresponds to the MCD value in the single-layer Dy film measured below T{sub C}=85 K. According to the AES data there is no sharp interface between 3d and Dy layers in these films. Some amount of Ni and Fe atoms is dispersed in the Dy layer and some amount of Dy atoms is dispersed in the 3d layer. The comparison of the MCD and AES data allows one to suppose the Dy layer in the bi-layer films to be magnetically ordered at room temperature under the influence of the 3d-layer spin system. The influence spreads to long distances inside Dy layer through the 3d-ions dispersed in it.

Heterogeneous bilayer films NiFe (Fe)-Dy: magnetic circular dichroism and Dy spin ordering

International Nuclear Information System (INIS)

Markov, V.V.; Kesler, V.G.; Khudyakov, A.E.; Edelman, I.S.; Bondarenko, G.V.

2001-01-01

Results of the magnetic circular dichroism (MCD) and Auger electron spectroscopy (AES) investigations in the 3d transition metal-Dy bi-layer films are presented. It is shown that even at room temperature the Dy layer makes a contribution to MCD of the bi-layer film, which corresponds to the MCD value in the single-layer Dy film measured below T C =85 K. According to the AES data there is no sharp interface between 3d and Dy layers in these films. Some amount of Ni and Fe atoms is dispersed in the Dy layer and some amount of Dy atoms is dispersed in the 3d layer. The comparison of the MCD and AES data allows one to suppose the Dy layer in the bi-layer films to be magnetically ordered at room temperature under the influence of the 3d-layer spin system. The influence spreads to long distances inside Dy layer through the 3d-ions dispersed in it

Luminescence and magnetic properties of novel nanoparticle-sheathed 3D Micro-Architectures of Fe0.5R0.5(MoO4)1.5:Ln3+ (R = Gd3+, La3+), (Ln = Eu, Tb, Dy) for bifunctional application

Science.gov (United States)

Krishnan, Rajagopalan; Thirumalai, Jagannathan; Kathiravan, Arunkumar

2015-01-01

For the first time, we report the successful synthesis of novel nanoparticle-sheathed bipyramid-like and almond-like Fe0.5R0.5(MoO4)1.5:Ln3+ (R = Gd3+, La3+), (Ln = Eu, Tb, Dy) 3D hierarchical microstructures through a simple disodium ethylenediaminetetraacetic acid (Na2EDTA) facilitated hydrothermal method. Interestingly, time-dependent experiments confirm that the assembly-disassembly process is responsible for the formation of self-aggregated 3D architectures via Ostwald ripening phenomena. The resultant products are characterized by x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), photoluminescence (PL), and magnetic measurements. The growth and formation mechanisms of the self-assembled 3D micro structures are discussed in detail. To confirm the presence of all the elements in the microstructure, the energy loss induced by the K, L shell electron ionization is observed in order to map the Fe, Gd, Mo, O, and Eu components. The photo luminescence properties of Fe0.5R0.5(MoO4)1.5 doped with Eu3+, Tb3+, Dy3+ are investigated. The room temperature and low temperature magnetic properties suggest that the interaction between the local-fields introduced by the magnetic Fe3+ ions and the R3+ (La, Gd) ions in the dodecahedral sites determine the magnetism in Fe0.5R0.5(MoO4)1.5:Eu3+. This work provides a new approach to synthesizing the novel Fe0.5R0.5(MoO4)1.5:Ln3+ for bi-functional magnetic and luminescence applications.

Effect of Dy addition on mechanical and magnetic properties of Mn-rich Ni–Mn–Ga ferromagnetic shape memory alloys

International Nuclear Information System (INIS)

Gao, L.; Dong, G.F.; Gao, Z.Y.; Cai, W.

2012-01-01

Highlights: ► The Dy addition significantly improves the compressive properties of Ni–Mn–Ga alloy. ► The mechanism of the improved mechanical properties by adding Dy is discussed. ► Dy doping results in a change of the fracture type of Ni–Mn–Ga alloy. ► Curie temperature almost remained unchanged at low Dy content and then decreases. - Abstract: The effects of partial substitution of rare earth Dy for Ga on the mechanical and magnetic properties of Mn-rich Ni 50 Mn 29 Ga 21−x Dy x (0 ≤ x ≤ 5) ferromagnetic shape memory alloys were investigated in detail. The results show that an appropriate amount of Dy addition significantly improves the mechanical properties of Ni–Mn–Ga alloy. With an increase in Dy content, the compressive strength enhances rapidly at first and then becomes stable when the Dy content is more than 1 at.%. However, the compressive strain increases dramatically and reaches a maximum value with 1 at.% Dy addition. Further increase in Dy content makes the compressive strain of the alloys decrease gradually. The mechanism of the improved mechanical properties is also discussed. Moreover, Dy doping changes the fracture type from intergranular fracture of Ni–Mn–Ga alloy to transgranular cleavage fracture of Ni–Mn–Ga–Dy alloys. The Curie temperature remains almost unchanged at low Dy content and subsequently decreases.

Photoluminescence and absorption spectra of various common TL phosphors - interpretation of TL mechanisms

International Nuclear Information System (INIS)

Nagpal, J.S.

1980-01-01

Photoluminescence and absorption spectra of TL phosphors TLD-100, CaF 2 :Dy, CaSO 4 :Dy(0.05%wt), CaSO 4 :Tm(0.05%wt) and Mg 2 SiO 4 :Tb have been measured. The absorption spectra are typical of RE 2+ in rare earth doped irradiated phosphors. On heating RE 2+ yields RE 3+ and emission from the excited states of RE 3+ is observed. (author)

Apparent and partial molal heat capacities of aqueous rare earth nitrate solutions at 250C

International Nuclear Information System (INIS)

Spedding, F.H.; Baker, J.L.; Walters, J.P.

1979-01-01

Specific heats of aqueous solutions of the trinitrates of La, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu were measured from 0.1 m to saturation at 25 0 C. Apparent molal heat capacities, phi/sub cp/, were calculated for these solutions, and empirical polynomial equations were obtained which expressed phi/sub cp/ as a function of m/sup 1/2/ for each salt. The partial molal heat capacities of the solvent, anti C 1 /sub p/, and solute, anti C 2 /sub p/, were calculated from these equations. Unlike chloride and perchlorate data reported earlier, values of anti C 1 /sub p/ for nitrate solutions across the rare earth series did not show a two series effect. Instead, anti C 1 /sub p/ values at lower concentrations (0.5 and 1.0 m) appear correlated with reported first formation constants for rare earth-nitrate complexes. 31 references, 9 figures, 2 tables

Equilibrium studies on interactions of rare earth ions with phytic acid

International Nuclear Information System (INIS)

Siddiqi, K.S.; Shah, S.A.; Aqra, F.M.A.M.; Tabassum, S.; Zaidi, S.A.A.; Benlian, D.

1993-01-01

The interaction between phytic acid and trivalent rare earth metal ions, viz., Ce 3+ , Pr 3+ , Nd 3+ , Sm 3+ , Gd 3+ , Tb 3+ , Dy 3+ and HO 3+ has been investigated potentiometrically at 25degC. The proton-ligand stability constants (pK Y H ) of phytic acid and the stability constants (logK) of metal complexes formed in aqueous medium (μ = 0.1 M NaClO 4 ) have been evaluated. The results indicate that eight protons of phytic acid are highly acidic, two are weakly acidic and two very weakly acidic, titrable in the pH ranges 1.2-4.9, 5.0-8.15 and 8.3-11.0 respectively. The stability of each phytic acid-lanthanide ion complex decreases with an increase in pH and follows the usual trend through the series. (author). 11 refs., 2 tabs

Photoluminescence and thermoluminescence characterization of Eu3+- and Dy3+ -activated Ca3(PO4)2 phosphor

International Nuclear Information System (INIS)

Nagpure, I.M.; Saha, Subhajit; Dhoble, S.J.

2009-01-01

Rare-earth-doped polycrystalline Ca 3 (PO 4 ) 2 :Eu, Ca 3 (PO 4 ) 2 :Dy and Ca 3 (PO 4 ) 2 :Eu,Dy phosphors prepared by a modified solid-state synthesis has been studied for its X-ray diffraction, thermoluminescence (TL) and photoluminescence (PL) characteristics. The PL emission spectra of the phosphor suggest the presence of Eu 3+ ion in Ca 3 (PO 4 ) 2 :Eu and Dy 3+ ion in Ca 3 (PO 4 ) 2 :Dy lattice sites. The TL glow curve of the Ca 3 (PO 4 ) 2 :Eu compounds has a simple structure with a prominent peak at 228 deg. C, while Ca 3 (PO 4 ) 2 :Dy peaking at 146 and 230 deg. C. TL sensitivity of phosphors are compared with CaSO 4 : Dy and found 1.52 and 1.20 times less in Ca 3 (PO 4 ) 2 :Eu and Ca 3 (PO 4 ) 2 :Dy phosphors, respectively. The Ca 3 (PO 4 ) 2 :Eu,Dy phosphors shows switching behavior under two different excitation wavelengths and enhancement in PL intensity of Dy 3+ ions were reported. The paper discusses the photoluminescence and thermoluminescence behavior of Eu 3+ and Dy 3+ ion in Ca 3 (PO 4 ) 2 hosts, it may be applicable to solid-state lighting as well as thermoluminescence dosimetry applications.

Blue–green afterglow of BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zhai, Bao-gai [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China); Ma, Qing-lan [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China); School of Electronics and Information, Nantong University, Jiangsu 226019 (China); Xiong, Rui [School of Physics and Technology, Wuhan University, Hubei 430072 (China); Li, Xiazhang [Analysis and Testing Center, Changzhou University, Jiangsu 213164 (China); Huang, Yuan Ming, E-mail: dongshanisland@126.com [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China)

2016-03-15

Highlights: • Afterglow can be achieved when Eu{sup 2+} is absent in the DyAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors. • The afterglow of DyAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors is discernible to naked eyes for minutes. • Dy{sup 3+} introduced trap centers are believed to be responsible for the afterglow. - Abstract: Dy{sup 3+} doped barium aluminate (BaAl{sub 2}O{sub 4}:Dy{sup 3+}) phosphors were prepared via the sol–gel combustion route at the ignition temperature of 600 °C. The phosphors were characterized with X-ray diffractometry, scanning electron microscopy, transmission electron microscopy, photoluminescence spectroscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Regardless of the absence of Eu{sup 2+} luminescent centers, broadband blue–green afterglow with its peak at about 490 nm was recorded in the BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors. The decay profile of the blue–green afterglow can be best fitted into a two-component exponential function with the two lifetime decay constants to be 8.81 and 45.25 s, respectively. The observation of blue–green afterglow from BaAl{sub 2}O{sub 4}:Dy{sup 3+} in the absence of Eu{sup 2+} provides unique opportunity in unveiling the afterglow mechanisms of rare-earth doped alkaline-metal aluminates. Possible mechanisms on the blue–green afterglow in BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors are discussed in terms of the Dy{sup 3+} ions introduced trap centers as well as luminescent centers in the crystal lattice.

Determination of rare earth contents in plant and soil by neutron activation analysis (NAA)

International Nuclear Information System (INIS)

Krafka, B.; Lin, X.L.; Henkelmann, R.

1998-01-01

Full text: The results presented are typical analytical results for Bavarian soils and plants. Plants and soils collected from identical sites are used to quantify the ratios of rare earth contents. This work has been in close cooperation with several governmental institutions, who are responsible for the protection and surveillance of agricultural sites and wooded areas. Routine sampling takes place on selected areas in the federal state of Bavaria, and the samples (soil and plants as wheat, corn or needles) are analysed with use of AAS, ICP-OES or ICP-MS techniques. INAA as an alternative method is in this context very interesting because it does not involve any sample pretreatment, prior to irradiation. It could be shown for chosen elements (K, Cr, Zn etc.), that incomplete digestion can lead to results which are remarkably lower than the total content in the sample. INAA also is an excellent technique to analyse rare earth elements. The advantage of analysing the original material, which only needs to be dried and homogenized, allows the determination of total values for most of the elements, independent of the chemical binding state of the atoms. Due to this reason, INAA is often called 'independent of matrix'. Only when the g-spectroscopy after activation is carried out, the main components may disturb the determination of trace elements. In soils, the matrix allows the pure instrumental determination of 9 rare earth elements (Ce, Dy, Eu, La, Lu, Nd, Sm, Tb, Yb). In plant material, the rare earth concentrations are much lower, so a chemical separation is needed in order to remove or reduce the main interferences like Na, K, Br etc. This combination of NAA with radiochemical separation is called Radiochemical Neutron Activation Analysis (RNAA) and allows to determine the same elements as in soils, except Dy

Easy and General Synthesis of Large-Sized Mesoporous Rare-Earth Oxide Thin Films by 'Micelle Assembly'.

Science.gov (United States)

Li, Yunqi; Bastakoti, Bishnu Prasad; Imura, Masataka; Dai, Pengcheng; Yamauchi, Yusuke

2015-12-01

Large-sized (ca. 40 nm) mesoporous Er2O3 thin films are synthesized by using a triblock copolymer poly(styrene-b-2-vinyl pyridine-b-ethylene oxide) (PS-b-P2VP-b-PEO) as a pore directing agent. Each block makes different contributions and the molar ratio of PVP/Er(3+) is crucial to guide the resultant mesoporous structure. An easy and general method is proposed and used to prepare a series of mesoporous rare-earth oxide (Sm2O3, Dy2O3, Tb2O3, Ho2O3, Yb2O3, and Lu2O3) thin films with potential uses in electronics and optical devices. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Characterization of element and mineral content in Artemisia annua ...

African Journals Online (AJOL)

Dr DIALLO

2013-06-26

Jun 26, 2013 ... The mineral elements are present in different kinds of herbal leaves in various proportions .... rare earth elements (Dy, Eu, Gd, Sm, Tb and Yb) were not detected in ..... behaviour of leached aluminum in tea infusions. The Sci.

Structure, electronic properties, luminescence and chromaticity investigations of rare earth doped KMgBO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zheng, Jianghui; Cheng, Qijin [School of Energy Research, Xiamen University, Xiamen 361005 (China); Wu, Shunqing [Department of Physics, Xiamen University, Xiamen, 361005 (China); Zhuang, Yixi [College of Materials, Xiamen University, Xiamen 361005 (China); Guo, Ziquan; Lu, Yijun [Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China); Chen, Chao, E-mail: cchen@xmu.edu.cn [School of Energy Research, Xiamen University, Xiamen 361005 (China); Department of Physics, Xiamen University, Xiamen, 361005 (China); Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China)

2015-09-01

In this work, the optimization of the geometry and the electronic properties of the host matrix KMgBO{sub 3} were investigated using density functional theory, and the comprehensive photoluminescence and chromaticity properties on five rare earth ion-doped (RE = Ce{sup 3+}, Tm{sup 3+}, Tb{sup 3+}, Eu{sup 3+}, Dy{sup 3+}) KMgBO{sub 3} phosphors were also studied. By introducing RE ions into the KMgBO{sub 3} host, excellent purple, blue, green, red and white emitting light could be obtained under the near-ultraviolet light excitation. The results suggest that rare earth doped KMgBO{sub 3} phosphors are potential luminescence materials for the application in the near-ultraviolet white light-emitting diodes. - Highlights: • The electronic properties of the host matrix KMgBO{sub 3} were investigated. • The PL properties on rare earth ions doped KMgBO{sub 3} phosphors were studied. • The chromaticity properties on rare earth ions doped KMgBO{sub 3} samples were studied. • Tm{sup 3+} and Eu{sup 3+} doped KMgBO{sub 3} samples show higher color purity than commercial phosphors.

Evolution of the orbitals Dy-4f in the DyB2 compound using the LDA, PBE approximations, and the PBE0 hybrid functional

Science.gov (United States)

Rasero Causil, Diego; Ortega López, César; Espitia Rico, Miguel

2018-04-01

Computational calculations of total energy based on density functional theory were used to investigate the structural, electronic, and magnetic properties of the DyB2 compounds in the hexagonal structure. The calculations were carried out by means of the full-potential linearized augmented plane wave (FP-LAPW) method, employing the computational Wien2k package. The local density approximation (LDA) and the generalized gradient approximation (GGA) were used for the electron-electron interactions. Additionally, we used the functional hybrid PBE0 for a better description the electronic and magnetic properties, because the DyB2 compound is a strongly-correlated system. We found that the calculated lattice constant agrees well with the values reported theoretically and experimentally. The density of states (DOS) calculation shows that the compound exhibits a metallic behavior and has magnetic properties, with a total magnetic moment of 5.47 μ0/cell determined mainly by the 4f states of the rare earth elements. The functional PBE0 shows a strong localization of the Dy-4f orbitals.

Crystal structure, magnetization, {sup 125}Te NMR, and Seebeck coefficient of Ge{sub 49}Te{sub 50}R{sub 1} (R = La, Pr, Gd, Dy, and Yb)

Energy Technology Data Exchange (ETDEWEB)

Levin, E.M., E-mail: levin@iastate.edu [Division of Materials Sciences and Engineering, US Department of Energy Ames Laboratory, Ames, IA 50011 (United States); Department of Physics and Astronomy, Iowa State University, Ames, IA 50011 (United States); Cooling, C. [Division of Materials Sciences and Engineering, US Department of Energy Ames Laboratory, Ames, IA 50011 (United States); Bud’ko, S.L. [Division of Materials Sciences and Engineering, US Department of Energy Ames Laboratory, Ames, IA 50011 (United States); Department of Physics and Astronomy, Iowa State University, Ames, IA 50011 (United States); Straszheim, W.E. [Division of Materials Sciences and Engineering, US Department of Energy Ames Laboratory, Ames, IA 50011 (United States); Lograsso, T.A. [Division of Materials Sciences and Engineering, US Department of Energy Ames Laboratory, Ames, IA 50011 (United States); Department of Materials Sciences and Engineering, Iowa State University, Ames, IA 50011 (United States)

2017-05-01

GeTe, a self-doping semiconductor, is a well-known base compound for thermoelectric and phase-change materials. It is known, that replacement of Ge in Ag{sub 6.5}Sb{sub 6.5}Ge{sub 37}Te{sub 50} (TAGS-85) material by rare earth Dy significantly enhances both the power factor and thermoelectric figure of merit. Here we demonstrate how replacement of Ge in GeTe by rare earths with different atomic size and localized magnetic moments affect XRD patterns, magnetization, {sup 125}Te NMR spectra and spin-lattice relaxation, and the Seebeck coefficient of the alloys with a nominal composition of Ge{sub 49}Te{sub 50}R{sub 1} (R = La, Pr, Gd, Dy, and Yb). SEM, EDS and WDS data show that rare earth atoms in the matrix are present at smaller extent compared to a nominal composition, whereas rare earth also is present in inclusions. Rare earths affect the Seebeck coefficient, which is a result of interplay between the reduction due to higher carrier concentration and enhancement due to magnetic contribution. The effect of replacement of Ge in GeTe by Dy on the Seebeck coefficient is smaller than that observed in Ag{sub 6.5}Sb{sub 6.5}Ge{sub 36} Te{sub 50}Dy{sub 1}. This can be explained by larger amount of rare earth, which can be embedded into the lattice of materials containing [Ag + Sb] atomic pairs and possible effect from these pairs. - Highlights: • The effects of rare earth in Ge{sub 49}Te{sub 50}R{sub 1} (R = La, Pr, Gd, Dy, and Yb) are studied. • Rare earth atoms in the matrix are present at smaller extent compared to a nominal composition. • The effect on the Seebeck coefficient is a result from carrier concentration and magnetic contribution.

Transferred hyperfine interaction at 295 K between the rare-earth ions and the fluorine and lithium nuclei in lithium rare-earth fluorides

DEFF Research Database (Denmark)

Hansen, P. E.; Nevald, Rolf

1977-01-01

The nuclear-magnetic-resonance rotation spectra for the fluorine and lithium nuclei in LiTbF4, LiDyF4, LiHoF4, and LiErF4 have been obtained at 295 K. They are separated in contributions from the dipole and the transferred hyperfine interactions. In general, the latter consists of an isotropic part...

Luminescence properties of pure and doped CaSO{sub 4} nanorods irradiated by 15 MeV e-beam

Energy Technology Data Exchange (ETDEWEB)

Salah, Numan, E-mail: nsalah@kau.edu.sa [Center of Nanotechnology, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Alharbi, Najlaa D. [Sciences Faculty for Girls, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Enani, Mohammad A. [Dept. of Nuclear Engineering, Faculty of Engineering, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

2014-01-15

Calcium sulfate (CaSO{sub 4}) doped with proper activators is a highly sensitive phosphor used in different fields mainly for radiation dosimetry, lighting and display applications. In this work pure and doped nanorods of CaSO{sub 4} were produced by the co-precipitation technique. Samples from this material doped with Ag, Cu, Dy, Eu and Tb were exposed to different doses of 15 MeV e-beam and studied for their thermoluminesence (TL) and photoluminescence (PL) properties. Color center formation leading to PL emissions were investigated before and after e-beam irradiation. The samples doped with rare earths elements (i.e. Dy, Eu and Tb) were observed to have thinner nanorods than the other samples and have higher absorption in the UV region. The Ag and Tb doped samples have poor TL response to e-beam, while those activated by Cu, Dy and Eu have strong glow peaks at around 123 °C. Quite linear response curves in the whole studied exposures i.e. 0.1–100 Gy were also observed in Cu and Dy doped samples. The PL results show that pure CaSO{sub 4} nanorods have active color centers without irradiation, which could be enriched/modified by these impurities mainly rare earths and further enhanced by e-beam irradiation. Eu{sup 3+} → Eu{sup 2+} conversion is clearly observed in Eu doped sample after e-beam irradiation. These results show that these nanorods might be useful in lighting and display devices development.

Structure and luminescence properties of Dy2O3 doped bismuth-borate glasses

International Nuclear Information System (INIS)

Mugoni, Consuelo; Gatto, C.; Pla-Dalmau, A.; Siligardi, C.

2017-01-01

In this study heavy bismuth-borate glasses were studied as host matrices of Dy 2 O 3 rare earth, for potential application as scintillator materials in high energy physics experiments and in general radiation detection systems. Glass matrices were prepared from 20BaO-xBi 2 O 3 -(80-x)B 2 O 3 (x = 20, 30, 40 mol%) ternary systems and synthesized by the melt-quenching method at different temperatures in order to obtain high density and high transparency in the UV/Vis range. Particularly, the glass manifesting the higher transparency and with sufficiently high density was doped with Dy 2 O 3 (2.5 and 5 mol%) in order to induce the luminescence characteristics. The effects of Bi 2 O 3 and Dy 2 O 3 on density, thermal behaviour, transmission as well as luminescence properties under UV excitation, were investigated. The experimental results show that the synthesized glasses can be considered promising candidate materials as dense scintillators, due to the Dy 3+ centres emission.

Size-dependent structure and magnetic properties of DyMnO{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Cai, Xuan; Shi, Lei, E-mail: shil@ustc.edu.cn; Zhou, Shiming; Zhao, Jiyin; Guo, Yuqiao; Wang, Cailin [Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026 (China)

2014-09-14

The structure and magnetic properties of orthorhombic DyMnO{sub 3} nanoparticles with different particle sizes are investigated in this paper. With decreasing particle size, all the lattice parameters a, b, and c gradually decrease, whereas the orthorhombic distortion increases. Magnetic measurements reveal that the antiferromagnetic interaction of Mn ions is weakened due to the decrease in Mn-O-Mn bond angle. Above a critical field H*, DyMnO{sub 3} undergoes a field-induced metamagnetic transition at 4 K, which is related to the spin reversal of Dy moments. The critical field H* increases monotonically with size reduction, indicating an enhancement of the antiferromagnetic interaction of Dy ions due to the decreased distance between rare earth ions. The magnetization at 4 K and 5 T, i.e., M(4 K, 5 T) shows a non-monotonic variation with particle size d, i.e., M(4 K, 5 T) initially increases with size reduction but decreases again for d < 68 nm. A modified core-shell model, in which the ferromagnetic ordering (Dy magnetic structure) and antiferromagnetic ordering (Mn magnetic structure) coexist in the core, is proposed to explain this behavior.

X-ray Absorption Spectroscopy of the Rare Earth orthophosphates

International Nuclear Information System (INIS)

Shuh, D.K.; Terminello, L.J.; Boatner, L.A.; Abraham, M.M.

1993-06-01

X-ray Absorption Spectroscopy (XAS) of the Rare Earth (RE) 3d levels yields sharp peaks near the edges as a result of strong, quasi-atomic 3d 10 4f n → 3d- 9 4f n+1 transitions and these transitions exhibit a wealth of spectroscopic features. The XAS measurements of single crystal REPO 4 (RE = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Er) at the 3d edge were performed in the total yield mode at beam line 8-2 at the Stanford Synchrotron Radiation Laboratory (SSRL). The XAS spectra of the RE ions in the orthophosphate matrix generally resemble the XAS of the corresponding RE metal. This is not unexpected and emphasizes the major contribution of the trivalent state to the electronic transitions at the RE 3d edges. These spectra unequivocally identify the transitions originating from well-characterized RE cores and correlate well with previous theoretical investigations

Observation of room temperature saturated ferroelectric polarization in Dy substituted BiFeO3 ceramics

KAUST Repository

Zhang, Shuxia

2012-04-06

High quality Bi1− x Dy x FeO3 (0 ≤ x ≤ 0.15) ceramics have been fabricated by sintering Dy-doped BiFeO3 (BFO) precursor powders at a low temperature of 780 °C. The magnetic properties of BFO were improved by the introduction of Dy on the Bi-site. More importantly, well saturated ferroelectric hysteresis loops and polarization switching currents have been observed at room temperature. A large remnant polarization (2P r) value of 62 μC/cm2 is achieved, which is the highest value reported so far for rare-earth-doped BFO ceramics. Moreover, mechanisms for improved multiferroic properties depending on chemical doping-caused structure evolutions have also been discussed.

Observation of room temperature saturated ferroelectric polarization in Dy substituted BiFeO3 ceramics

KAUST Repository

Zhang, Shuxia; Wang, Lei; Chen, Yao; Wang, Dongliang; Yao, Yingbang; Ma, Yanwei

2012-01-01

High quality Bi1− x Dy x FeO3 (0 ≤ x ≤ 0.15) ceramics have been fabricated by sintering Dy-doped BiFeO3 (BFO) precursor powders at a low temperature of 780 °C. The magnetic properties of BFO were improved by the introduction of Dy on the Bi-site. More importantly, well saturated ferroelectric hysteresis loops and polarization switching currents have been observed at room temperature. A large remnant polarization (2P r) value of 62 μC/cm2 is achieved, which is the highest value reported so far for rare-earth-doped BFO ceramics. Moreover, mechanisms for improved multiferroic properties depending on chemical doping-caused structure evolutions have also been discussed.

n-aminobenzoates of rare earths

International Nuclear Information System (INIS)

Efremova, G.I.; Buchkova, R.T.; Lapitskaya, A.V.; Pirkes, S.B.

1977-01-01

N-aminobenzoates of r.e.e. have been synthesized. Their composition corresponds to the general formula Me(C 6 H 4 NH 2 COO) 3 xnH 2 O, where Me stands for La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu; n=1.2. The compounds obtained are identified by chemical analysis and roentgenographically. Their solubility products, which are values of the order of 10 -9 -10 -10 , are determined

Reaction of xenon difluoride with certain rare earth fluorocomplexes of Cs/sub 3/MF/sub 6/ composition

Energy Technology Data Exchange (ETDEWEB)

Kiselev, Yu.M.; Goryachenkov, S.A.; Martynenko, L.I. (Moskovskij Gosudarstvennyj Univ. (USSR))

1983-05-01

By thermographic method in a specially manufactured nickel cell for thermal analysis the reaction of XeF/sub 2/ with Cs/sub 3/M/sup 3/F/sub 6/ (M=Ce, Pr, Tb, Nd, Dy, Er) is studied. Temperatures of thermal effects (Ts) corresponding to Cs/sub 3/M/sup 4/F/sub 7/ formation regularly increase in the series Ce-Tb-Pr-Dy-Nd (115-382 deg C). Cs/sub 3/M/sup 4/F/sub 7/ compounds are characterized by the methods of chemical analysis, X-ray diffraction and oscillating spectroscopy (IR and CS spectroscopy). Experimental data are best of all interpreted on assumption of the presence in Cs/sub 3/M/sup 4/F/sub 7/ crystals statistically oriented MF/sub 7/ fragments of the Dsub(5h) symmetry.

Spectrofluorimetric characterization and study for the determination of rare earth carbonate complexes

International Nuclear Information System (INIS)

Dantas, E.S.K.; Abrao, A.

1982-01-01

Some rare earths exhibit fluorescence in acid solution (HC1, H 2 SO 4 or HC10 4 ) when irradiated with ultraviolet radiation; however, analytical application of this property has not been proposed due to the lack of sensitivity resulted from the weakness of the fluorescence transitions. The rare earths are soluble in alkali carbonate solutions, forming anionic carbonate complexes (TR(CO 3 ) sup(n-) sub(x)); some of them have stronger absorption bands than those obtained in acid media. Using this property, the characterization and determination of the six rare earths which fluoresce in carbonate solution has been studied. The excitation and emission wavelengths are (in nm): Sm (406, 596); Eu (280,612); Gd (272,312); Tb (240,542); Dy (350, 576) and Tm (360, 450). Although Ce-III is highly fluorescent in acid media, when in carbonate solution it is easily oxidized to Ce-IV which does not fluoresce neither in acid nor in carbonate solutions. The other rare earths, although soluble in carbonate solution, do not fluoresce in this medium. A comparison is made, between the fluorescence of the fluorescing lanthanides, in acid and carbonate media. The precision and accuracy of this method, the detection limit of all rare earths studied and the mutual interference of some of them is also discussed. The method will be applied to the analytical control of the separation and purification of individual rare earths, now under development. (Author) [pt

Effect of separated layer thickness on magnetoresistance and magnetic properties of Co/Dy/Co and Ni/Dy/Ni film systems

Science.gov (United States)

Shabelnyk, T. M.; Shutylieva, O. V.; Vorobiov, S. I.; Pazukha, I. M.; Chornous, A. M.

2018-01-01

Co(5 nm)/Dy(tDy)/Co(20 nm)/S and Ni(5 nm)/Dy(tDy)/Ni(20 nm)/S trilayer films are prepared by electron-beam sputtering to investigate the influence of dysprosium layer thickness (tDy) and thermal annealing on the crystal structure, magnetoresistance (MR) and magnetic properties of thin films. The thickness of Dy layer changed in the range from 1 nm to 20 nm. The samples annealed for 20 min at 700 K. Electron diffraction patterns reveal that the as-deposited and annealed systems Co/Dy/Co and Ni/Dy/Ni had fcc-Co + hcp-Dy and fcc-Ni + hcp-Dy phase state, respectively. It is also shown that at the tDy = 15 nm the transition from amorphous to crystalline structures of Dy layer is observed. An increase in the Dy layer thickness results in changes in the MR and magnetic properties of the trilayer systems. It is shown that MR is most thermally stable against annealing to 700 K at tDy = 15 nm for Co/Dy/Co as well as for Ni/Dy/Ni. For tDy = 15 nm the, value of MR for both system increases by two times compared to those of pure ferromagnetic (FM) samples. The coercivity (Bc), remanent (Mr) and saturation (Ms) magnetization of the in-plain magnetization hysteresis loops are related to the Dy layer thickness too. The coercivity depends on the FM materials type and diffusion processes at the layer boundary. Accordingly, Mr and Ms are reduced with tDy increasing before and after annealing for both trilayer systems.

Combustion synthesis of Eu and Dy activated Sr3(VO4)2 phosphor ...

Indian Academy of Sciences (India)

phosphor as well as Sr3(VO4)2:Dy is blue and yellow emitting phosphor for solid state lighting i.e. white LEDs. The ... 2004; Pang et al 2004) doped with rare earth has expanded ... controlled since the LED light output (intensity and colour).

Plasma emission spectroscopy (DCP) for rare earths determination in waters from Morro do Ferro (MG) Brazil, after chromatographic preconcentration

International Nuclear Information System (INIS)

Figueiredo, A.M.R. de.

1987-01-01

Rare earth determinations in surface and well waters from Morro do Ferro was studied using chemical preconcentration methods of the group and plasma emission spectroscopy excited by direct current are - DCP. A method that combines retention in alumina is HF medium with ion exchange for the preconcentration of the group was developed in semi micro scale. DCP determination, in the sequencial mode by using mixed standards containing, Y, La, Ce, Nd, Pr, Sm, Eu, Ga, Tb, Dy, Er, Yb and Al, principal concentrate componentes was studied by analysis of the profile of each spectral line. Principal cations, anions, ph and Eh were determined. Semi-micro techniques were developed for anions preconcentration and for determination of sulphate, phosphate and carbonate. (M.J.C.) [pt

Coercivity enhancements of Nd–Fe–B sintered magnets by diffusing DyHx along different axes

International Nuclear Information System (INIS)

Ma, Tianyu; Wang, Xuejiao; Liu, Xiaolian; Wu, Chen; Yan, Mi

2015-01-01

Diffusing heavy rare earth elements along the grain boundaries (GBs) for Nd 2 Fe 14 B-type sintered magnets serves as an effective method to enhance coercivity and to minimize remanence loss simultaneously. Considering the texture anisotropy of Nd-rich GB phases, the coercivity incremental difference by diffusing DyH x fine powders along or perpendicular to the  <0 0 1 >  easy axis (c-axis) has been investigated. The coercivity increases more rapidly to 20.61 kOe (5.76 kOe higher than that of the as-sintered state) when diffusing along the c-axis than that diffusing perpendicular to c-axis (18.85 kOe, 4.00 kOe higher than the as-sintered state). Microstructural investigation reveals that Dy diffuses more easily towards the magnet inner part when treating along the c-axis than that for the perpendicular case due to the anisotropic distribution of the Nd-rich phase. This is verified by a higher Dy content at equivalent diffusing depth and a much deeper final diffusion distance. The local Dy-containing fractions with a stronger anisotropy field are richer for the magnet treated along the c-axis, leading to the much rapider coercivity enhancement. This work reveals that diffusion heavy rare earth along the c-axis is more effective to enhance coercivity for aligned Nd–Fe–B sintered magnets. (paper)

Oxygen-perovskites with fourvalent rare earth metals

Energy Technology Data Exchange (ETDEWEB)

Kristen, H R

1978-01-01

The quadrivalent oxidation stage of the elements praseodymium and terbium can be easily prepared as oxides BaPrO/sub 3/ and BaTbO/sub 3/ crystallizing with the Perovskite structure. From this observation one has tried to stabilize the elements neodymium and dysprosium in the lanthanide series by including a host lattice with Perovskite structure. BaCeO/sub 3/, BaPrO/sub 3/, BaZrO/sub 3/, BaThO/sub 3/, BaTbO/sub 3/, SrCeO/sub 3/ and SrTbO/sub 3/ are used as host lattices. The preparation was carried out by simple annealing of the corresponding oxides with BaCO/sub 3/ or SrCO/sub 3/ in air at 1350/sup 0/C. X-ray and analytical characterization showed that Nd(IV) and Dy(IV) were partly taken up by a few host lattices.

Oxygen-perovskites with fourvalent rare earth metals

Energy Technology Data Exchange (ETDEWEB)

Kristen, H R

1978-01-01

The quadrivalent oxidation stage of the elements praseodymium and terbium can be easily prepared as oxides BaPrO/sub 3/ and BaTbO/sub 3/ crystallizing with the Perovskite structure. From this observation one has tried to stabilize the elements neodymium and dysprosium in the lanthanide series by including a host lattice with Perovskite structure. BaCeO/sub 3/, BaPrO/sub 3/, BaZrO/sub 3/, BaThO/sub 3/, BaTbO/sub 3/, SrCeO/sub 3/ and SrTbO/sub 3/ are used as host lattices. The preparation was carried out by simple annealing of the corresponding oxides with BaCO/sub 3/ or SrCO/sub 3/ in air at 1350/sup 0/C. X-ray and analytical characterization showed that Nd(IV) and Dy(IV) were partly taken up by a few host lattices. (orig./HBR).

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

DEFF Research Database (Denmark)

Xu, H; Christmas, P; Wu, X R

1994-01-01

-linked Duchenne and Becker muscular dystrophies. We have examined M-laminin expression in mice with autosomal recessive muscular dystrophy caused by the mutation dy. The heavy chain of M-laminin was undetectable in skeletal muscle, heart muscle, and peripheral nerve by immunofluorescence and immunoblotting......M-laminin is a major member of the laminin family of basement membrane proteins. It is prominently expressed in striated muscle and peripheral nerve. M-laminin is deficient in patients with the autosomal recessive Fukuyama congenital muscular dystrophy but is normal in patients with the sex...... tissue from dy/dy mice, suggesting that M-laminin heavy-chain mRNA may be produced at very low levels or is unstable. Information about the chromosomal localization of the M heavy-chain in human and mouse suggests that a mutation in the M-chain gene causes the muscular dystrophy in dy/dy mice. The dy...

Extraction of Tb(III with N,N,N’,N’-tetrabutylmalonamide

Directory of Open Access Journals (Sweden)

XU RONGQI

2002-10-01

Full Text Available The study on the extraction and separation of rare earths with new extractants is important in rare earth hydrometallurgy and nuclear fuel reprocessing. In this work, a new synthesis method of N,N,N’,N’-tetrabutylmalonamide (TBMA is described with a yield higher than 80 %. The extraction behavior of TBMA employing n-hexane-20 % n-octanol, benzene and toluene as diluents toward Tb(III was investigated. The effect of the concentrations of nitric acid, lithium nitrate and extractant as well as the temperature on the extraction distribution ratio was studied in different diluents. The stoichiometry of the extracted species of Tb(III conforms to Tb(NO33·3TBMA. An attempt was made to determine the structure of the extracted species from IR and mol conductance data.

Effect of concentration on the photoluminescence properties of Sm3+ and Dy3+: cadmium lithium boro tellurite glasses.

Science.gov (United States)

Raju, K Vemasevana; Sailaja, S; Reddy, M Bhushana; Giridhar, P; Raju, C Nageswara; Reddy, B Sudhakar

2012-02-01

Rare-earth (Sm3+ or Dy3+) ions doped cadmium lithium boro tellurite glasses have been prepared by melt quenching method for their spectral studies. From X-ray diffraction (XRD) patterns the glass amorphous nature has been confirmed. Vis-NIR absorption, excitation and emission spectra of these glasses have been analyzed systematically and also rare earth ion concentration is optimised Sm3+: CLiBT glasses have shown strong orange-reddish emission at 598 nm (4G5/2-->6H7/2) with an excitation wavelength lambda(exci) = 401 nm and Dy3+: CLiBT glasses have shown strong yellow emission at 574 nm (6F9/2-->6H13/2) with lambda(exci) = 451 nm.

Construction of Polynuclear Lanthanide (Ln = Dy(III), Tb(III), and Nd(III)) Cage Complexes Using Pyridine-Pyrazole-Based Ligands: Versatile Molecular Topologies and SMM Behavior.

Science.gov (United States)

Bala, Sukhen; Sen Bishwas, Mousumi; Pramanik, Bhaskar; Khanra, Sumit; Fromm, Katharina M; Poddar, Pankaj; Mondal, Raju

2015-09-08

Employment of two different pyridyl-pyrazolyl-based ligands afforded three octanuclear lanthanide(III) (Ln = Dy, Tb) cage compounds and one hexanuclear neodymium(III) coordination cage, exhibiting versatile molecular architectures including a butterfly core. Relatively less common semirigid pyridyl-pyrazolyl-based asymmetric ligand systems show an interesting trend of forming polynuclear lanthanide cage complexes with different coordination environments around the metal centers. It is noteworthy here that construction of lanthanide complex itself is a challenging task in a ligand system as soft N-donor rich as pyridyl-pyrazol. We report herein some lanthanide complexes using ligand containing only one or two O-donors compare to five N-coordinating sites. The resultant multinuclear lanthanide complexes show interesting magnetic and spectroscopic features originating from different spatial arrangements of the metal ions. Alternating current (ac) susceptibility measurements of the two dysprosium complexes display frequency- and temperature-dependent out-of-phase signals in zero and 0.5 T direct current field, a typical characteristic feature of single-molecule magnet (SMM) behavior, indicating different energy reversal barriers due to different molecular topologies. Another aspect of this work is the occurrence of the not-so-common SMM behavior of the terbium complex, further confirmed by ac susceptibility measurement.

Theory of Random Anisotropic Magnetic Alloys

DEFF Research Database (Denmark)

Lindgård, Per-Anker

1976-01-01

A mean-field-crystal-field theory is developed for random, multicomponent, anisotropic magnetic alloys. It is specially applicable to rare-earth alloys. A discussion is given of multicritical points and phase transitions between various states characterized by order parameters with different...... spatial directions or different ordering wave vectors. Theoretical predictions based on known parameters for the phase diagrams and magnetic moments for the binary rare-earth alloys of Tb, Dy, Ho, and Er, Tb-Tm, Nd-Pr, and pure double-hcp Nd agree qualitatively with the experimental observations...... fluctuation corrections in the mean-field results is also discussed....

Spectroscopic study of magnetic phase transitions and magnetic structures in rare earth ferroborates RFe3(BO3)4 (R = Y, Er, Tb, Gd)

International Nuclear Information System (INIS)

Popova, M.N.; Chukalina, E.P.; Stanislavchuk, T.N.; Bezmaternykh, L.N.

2006-01-01

One investigated into the absorption spectra of RFe 3 (BO 3 ) 4 , R=Y, Er, Tb, Gd rare earth borate single crystals containing erbium (1%) introduced to serve as a probe. On the basis of the temperature dependences of Er 3+ ion spectral line splittings one determined the values of the magnetic ordering temperatures of Er, Tb and Gd ferroborates and the temperatures of the spin reoriented first order phase transition in GdFe 3 (BO 3 ) 4 :Er 3+ (1%). On the basis of comparison of the splitting values of Er 3+ ion ground state in RFe 3 (BO 3 ) 4 (R=Y, Er, Tb) and in GdFe 3 (BO 3 )4 compounds the magnetic structure of which is known one makes a concussion about the orientation of iron magnetic moments in the magneto-ordered state: a lightly planar structure is observed for YFe 3 (BO 3 ) 4 and ErFe 3 (BO 3 ) 4 and a lightly axial one - for TbFe 3 (BO 3 ) 4 . One discusses the role of R 3+ ion single ion anisotropy when determining the magnetic structure type in RFe 3 (BO 3 ) 4 [ru

Effect of rare-earth ion size on local electron structure in RBa2Cu3O7-δ (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors: A positron study

International Nuclear Information System (INIS)

Chen Zhenping; Zhang Jincang; Su Yuling; Xue Yuncai; Cao Shixun

2006-01-01

The effects of rare-earth ionic size on the local electron structure, lattice parameters and superconductivity have been investigated by positron annihilation technique (PAT) and related experiments for RBa 2 Cu 3 O 7-δ (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors. The local electron density n e is evaluated as a function of the rare-earth radius. The results show that both the bulk-lifetime τ B and the defect lifetime τ 2 increase with increasing rare-earth ionic radius, while the local electron density n e decrease with increasing rare-earth ionic radius. These results prove that the changes of n e , the degree of orthorhombic distortion and the coupling between the Cu-O chains and the CuO 2 planes all have an effect on the superconductivity of RBa 2 Cu 3 O 7-δ systems

Analysis of the crystal lattice instability for cage–cluster systems using the superatom model

Energy Technology Data Exchange (ETDEWEB)

Serebrennikov, D. A., E-mail: dserebrennikov@innopark.kantiana.ru, E-mail: dimafania@mail.ru; Clementyev, E. S. [I. Kant Baltic Federal University, “Functional Nanomaterials” Scientific–Educational Center (Russian Federation); Alekseev, P. A. [“Kurchatov Institute” National Research Center (Russian Federation)

2016-09-15

We have investigated the lattice dynamics for a number of rare-earth hexaborides based on the superatom model within which the boron octahedron is substituted by one superatom with a mass equal to the mass of six boron atoms. Phenomenological models have been constructed for the acoustic and lowenergy optical phonon modes in RB{sub 6} (R = La, Gd, Tb, Dy) compounds. Using DyB{sub 6} as an example, we have studied the anomalous softening of longitudinal acoustic phonons in several crystallographic directions, an effect that is also typical of GdB{sub 6} and TbB{sub 6}. The softening of the acoustic branches is shown to be achieved through the introduction of negative interatomic force constants between rare-earth ions. We discuss the structural instability of hexaborides based on 4f elements, the role of valence instability in the lattice dynamics, and the influence of the number of f electrons on the degree of softening of phonon modes.

Antiferroquadrupolar ordering and anisotropic magnetic phase diagram of dysprosium palladium bronze, DyPd3S4

International Nuclear Information System (INIS)

Matsuoka, Eiichi; Tayama, Takashi; Sakakibara, Toshiro; Hiroi, Zenji; Takeda, Naoya; Ishikawa, Masayasu; Shirakawa, Naoki

2007-01-01

From the measurements of magnetization and specific heat, we constructed B-T phase diagrams of single-crystalline DyPd 3 S 4 which is known to exhibit antiferroquadrupolar (AFQ) and antiferromagnetic (AFM) ordering at low temperatures. The phase diagrams are found to be highly anisotropic and re-entrant, which are typical of rare-earth compounds exhibiting multipolar ordering. The crystalline electric field (CEF) scheme of Dy 3+ in DyPd 3S4 was deduced from the specific heat and magnetization measurements of the Y-diluted compounds Dy 1-x Y x Pd 3 S 4 (0.1≤x≤0.9) and discussed in detail. The CEF ground state was determined to be the orbitally-degenerated quartet Γ 67 (1) , and the overall splitting width was estimated to be about 104 K. No correlation was found between the anisotropy of T Q and that of the Zeeman splitting width of the ground quartet Γ 67 (1) . (author)

Coercivity enhancement of Nd–Fe–B sintered magnets with intergranular adding (Pr, Dy, Cu)−H{sub x} powders

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yujing; Ma, Tianyu, E-mail: maty@zju.edu.cn; Liu, Xiaolian; Liu, Pan; Jin, Jiaying; Zou, Junding; Yan, Mi, E-mail: mse_yanmi@zju.edu.cn

2016-02-01

Forming Nd{sub 2}Fe{sub 14}B/(Nd, Dy){sub 2}Fe{sub 14}B core–shell structure by intergranular adding Dy-containing sources into Nd–Fe–B sintered magnets is effective to improve coercivity and to minimize remanence loss simultaneously. However, the excessive Dy located in the intergranular regions has nearly no hard magnetic contribution, causing its low utilization efficiency. In this work, diluted Dy powders (Pr{sub 37}Dy{sub 30}Cu{sub 33})–H{sub x} were prepared and incorporated into Nd–Fe–B sintered magnets via a dual-alloy approach. The coercivity increases rapidly from 15.0 to 18.2 kOe by 21.3% with 2.0 wt% (Pr, Dy, Cu)–H{sub x} addition (the equivalent Dy is only 0.32 at%). The deduced coercivity incremental ratio is 10.0 kOe per unit Dy at%. Dehydrogenation reaction of (Pr, Dy, Cu)–H{sub x} occurs during sintering, which favors Dy diffusion towards the 2:14:1 phase grains as well as smoothing the grain boundaries (GBs). The enhanced local anisotropic field and the well decoupled 2:14:1 phase grains contribute to such rapid coercivity enhancement. This work suggests that adding diluted Dy hydrides is promising for fabricating high coercivity Nd–Fe–B sintered magnets with less heavy rare-earth consumption. - Highlights: • (Pr, Dy, Cu)–H{sub x} hydride powders were introduced into Nd–Fe–B sintered magnets. • Rapid coercivity enhancement from 15.0 kOe to 18.2 kOe with only 0.32 at% Dy was realized. • High utilization efficiency of Dy was achieved due to its promoted diffusion process. • Wettability and mobility of grain boundary phase was improved.

The interplay of long-range magnetic order and single-ion anisotropy in rare earth nickel germanides

International Nuclear Information System (INIS)

Islam, Z.

1999-01-01

This dissertation is concerned with the interplay of long-range order and anisotropy in the tetragonal RNi 2 Ge 2 (R = rare earth) family of compounds. Microscopic magnetic structures were studied using both neutron and x-ray resonant exchange scattering (XRES) techniques. The magnetic structures of Tb, Dy, Eu and Gd members have been determined using high-quality single-crystal samples. This work has correlated a strong Fermi surface nesting to the magnetic ordering in the RNi 2 Ge 2 compounds. Generalized susceptibility, χ 0 (q), calculations found nesting to be responsible for both incommensurate ordering wave vector in GdNi 2 Ge 2 , and the commensurate structure in EuNi 2 Ge 2 . A continuous transition from incommensurate to commensurate magnetic structures via band filling is predicted. The surprisingly higher T N in EuNi 2 Ge 2 than that in GdNi 2 Ge 2 is also explained. Next, all the metamagnetic phases in TbNi 2 Ge 2 with an applied field along the c axis have been characterized with neutron diffraction measurements. A mixed phase model for the first metamagnetic structure consisting of fully-saturated as well as reduced-moment Tb ions is presented. The moment reduction may be due to moment instability which is possible if the exchange is comparable to the low-lying CEF level splitting and the ground state is a singlet. In such a case, certain Tb sites may experience a local field below the critical value needed to reach saturation

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Permanent link: https://www.ias.ac.in/article/fulltext/boms/039/03/0603-0611. Keywords. Predominance area diagram; Kellogg diagram; lanthanide oxychloride; rare-earth mineral processing; thermodynamic properties. Abstract. Isothermal stability field diagrams for Ln−O−Cl systems (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, ...

Optical spectroscopy of rare-earth ions doped KY(WO4)2 thin films

NARCIS (Netherlands)

García-Revilla, S.; Valiente, R.; Romanyuk, Y.E.; Utke, I.; Pollnau, Markus

KY(WO4)2 thin films doped with Dy3+, Tb3+, Yb3+, were grown onto KY(WO4)2 substrates using liquid-phase epitaxy. Spectroscopic investigations of the grown layers were performed. Obtained results were compared with spectra given for bulk crystals. Upconversion experiments after direct Yb3+ excitation

Equilibrium studies on interactions of rare earth ions with phytic acid

Energy Technology Data Exchange (ETDEWEB)

Siddiqi, K S; Shah, S A; Aqra, F M.A.M.; Tabassum, S; Zaidi, S A.A. [Aligarh Muslim Univ. (India). Dept. of Chemistry; Benlian, D [Centre de St Jerome, Cedex (France). Laboratoire de Chimie de Coordination

1993-05-01

The interaction between phytic acid and trivalent rare earth metal ions, viz., Ce[sup 3+], Pr[sup 3+], Nd[sup 3+], Sm[sup 3+], Gd[sup 3+], Tb[sup 3+], Dy[sup 3+] and HO[sup 3+] has been investigated potentiometrically at 25degC. The proton-ligand stability constants (pK[sub Y][sup H]) of phytic acid and the stability constants (logK) of metal complexes formed in aqueous medium ([mu] = 0.1 M NaClO[sub 4]) have been evaluated. The results indicate that eight protons of phytic acid are highly acidic, two are weakly acidic and two very weakly acidic, titrable in the pH ranges 1.2-4.9, 5.0-8.15 and 8.3-11.0 respectively. The stability of each phytic acid-lanthanide ion complex decreases with an increase in pH and follows the usual trend through the series. (author). 11 refs., 2 tabs.

White lines at the Lsub(I), Lsub(II), and Lsub(III) absorption edges of some rare earth compounds

Energy Technology Data Exchange (ETDEWEB)

Garg, K B; Sharma, B K; Jain, D C [Rajasthan Univ., Jaipur (India). Dept. of Physics; Sinha, A I.P. [Banasthali Vidyapeeth (India). Dept. of Chemistry

1980-11-01

The paper reports the appearance of white lines (WLS) at all the three L-absorption edges of the sulfur coordinated thiosalicylic acid compounds of Sm, Tb, and Dy. The profiles of the observed WLS are presented and discussed.

Rare earth elements determination and distribution patterns in sediments of polluted marine environment by instrumental neutron activation analysis

International Nuclear Information System (INIS)

Akyil, S.; Yusof, A.M.; Wood, A.K.H.

2001-01-01

Results obtained from the analysis of sediment core samples taken from a fairly polluted marine environment were analyzed for the REE contents to determine the concentrations of La, Ce, Sm, Eu, Tb, Dy and Yb using instrumental neutron activation analysis. Core samples were divided into strata of between 2 to 3 cm intervals and prepared in the powdered form before irradiating them in a TRIGA Mk.II reactor. Down-core concentration profiles of La, Ce, Sm, Eu, Tb, Dy and Yb in 3 core sediments from three sites are obtained. The shale-normalized REE pattern from each site was examined and later used to explain the history of sedimentation by natural processes such as shoreline erosion and weathering products deposited on the seabed and furnishing some baseline data and/or pollution trend occurring within the study area

CaSO4:Dy and/or Tm: study of its properties for dosimetry application

International Nuclear Information System (INIS)

Ferreira, M.M.

1979-01-01

In order obtain in practical and cheap solid state dosimeter with high sensitivity, a technique initially developed to cold press a mixture of suitable materials in their powder form sensitive to radiation. The material initially used was natural CaF 2 (fluorite) for this salt was extensively studied in radiation dosimetry since it shows a thermoluminescent (TL) effect after radiation. However, natural calcium fluorite shows two main disadvantages: its high senstivity to room light and the impossibility to control its impurity content due to its natural origin. Calcium sulphate was thus used as a good substitute of fluorite. Rare earths doped calcium sulphate shows a high TL sensitivity and is not disturbed by light. It is also easily obtained in the laboratory under controlled conditions so to get reproducible impurity content. The best dosimeters that can be produced with rare earth doped calcium sulphate are CaSO 4 :Dy and CaSO 4 :Tm. Calcium sulphate, simultaneously doped with Tm and Dy was produced and 100% increase was obtained in the TL sensitivity when compared with the individually are earth doped calcium sulphate. (Author) [pt

Yb3+ can be much better than Dy3+: SMM properties and controllable self-assembly of novel lanthanide 3,5-dinitrobenzoate-acetylacetonate complexes.

Science.gov (United States)

Gavrikov, Andrey V; Efimov, Nikolay N; Ilyukhin, Andrey B; Dobrokhotova, Zhanna V; Novotortsev, Vladimir M

2018-05-01

The first representatives of the binuclear lanthanide 3,5-dinitrobenzoate-acetylacetonate complexes, namely isostructural compounds [Ln(dnbz)(acac)2(H2O)(EtOH)]2 (Ln = Eu (1), Gd (2), Tb (3), Dy (4), Ho (5), Er (6), Tm (7), and Yb (8); dnbz - 3,5-dinitrobenzoate anion; acac - acetylacetonate (pentane-2,4-dionate) anion) were prepared and characterized. The SMM behavior of the Yb compound 8 was shown to be surprisingly less sensitive to the composition of the Yb3+ coordination environment in comparison with that of the Dy derivative. For Yb compound 8, the anisotropy barrier is Δeff/kB = 26 K under the dc field of 2000 Oe. This value is the highest one currently known for binuclear Yb complexes.

Inter-band B(E2) transitions strengths in 160-170Dy nuclei

International Nuclear Information System (INIS)

Vargas, Carlos E; Lerma, Sergio; Velázquez, Víctor

2015-01-01

The rare earth region of the nuclear landscape is characterized by a large collectivity observed. The microscopic studies are difficult to perform in the region due to the enormous size of the valence spaces. The use of symmetries based models avoids that problem, because the symmetry allows to choose the most relevant degrees of freedom for the system under consideration. We present theoretical results for electromagnetic properties in 160-168 Dy isotopes employing the pseudo-SU(3) model. In particular, we study the B(E2) inter-band transition strengths between the ground state, γ and, β-bands. The model succesfully describes in a systematic way rotational features in these nuclei and allows to extrapolate toward the midshell nucleus 170 Dy

Optical properties of Sr3B2O6:Dy3+/PMMA polymer nanocomposites

Science.gov (United States)

Khursheed, Sumara; Kumar, Vinay; Singh, Vivek K.; Sharma, Jitendra; Swart, H. C.

2018-04-01

The paper presents a facile way to synthesize luminescent polymer nanocomposite (PNC) films consisting of nanophosphors (NPs) of rare earth ions doped alkaline earth borates (Sr3B2O6:Dy3+) dispersed in a polymer (PMMA) matrix via a solution casting method and the results of their detailed structural and optical properties measurements. The PNC films were characterized using X-ray diffraction (XRD), Photoluminescence (PL), and differential scanning calorimetry (DSC). The crystallinity of the dispersed NPs did not suffer on account of being dispersed in the PMMA. The Rhombohedral structure and the formation of a single phase of Sr3B2O6:Dy3+ were confirmed by the XRD data of both the NP powders and the PNC films with an average particle size of 43 nm. Also, the observed PL emission and excitation spectra of the PNC films amply suggested that embedding of the nanophosphors in the PMMA matrix preserves their typical luminescence emission. The chromaticity coordinates (x = 0.37, y = 0.39) of the PNC films also validated the yellowish white emission of the nanophosphor. DSC scans on the PMMA only and the Sr3B2O6:Dy3+/PMMA films suggested an increase in the thermal stability of the PNC films as compared to pure PMMA although no significant change in the glass transition temperature was observed.

Synthesis and characterization of BaAl{sub 2}O{sub 4}:Eu{sup 2+} co-doped with different rare earth ions

Energy Technology Data Exchange (ETDEWEB)

Lephoto, M.A. [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Pitale, Shreyas S.; Swart, H.C. [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Botha, J.R. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth, ZA 6031 (South Africa); Mothudi, B.M. [Department of Physics, University of South Africa, P.O Box 392, Pretoria, ZA 6031 (South Africa)

2012-05-15

Combustion method was used in this study to prepare BaAl{sub 2}O{sub 4}:Eu{sup 2+} phosphors co-doped with different trivalent rare-earths (Re{sup 3+}=Dy{sup 3+}, Nd{sup 3+}, Gd{sup 3+}, Sm{sup 3+}, Ce{sup 3+}, Er{sup 3+}, Pr{sup 3+} and Tb{sup 3+}) ions at an initiating temperature of 600 Degree-Sign C. The phosphors were annealed at 1000 Degree-Sign C for 3 h. As confirmed from the X-ray diffraction (XRD) data, both as prepared and post annealed samples crystallized in the well known hexagonal structure of BaAl{sub 2}O{sub 4}. All samples exhibited bluish-green emission associated with the 4f{sup 6}5d{sup 1}{yields}4f{sup 7} transitions of Eu{sup 2+} at {approx}500 nm. Although the highest intensity was observed from Er{sup 3+} co-doping, the longest afterglow (due to trapping and detrapping of charge carriers) was observed from Nd{sup 3+} followed by Dy{sup 3+} co-doping. The traps responsible for the long afterglow were studied using thermoluminescence (TL) spectroscopy.

Solubility and superconductivity in RE(Ba2-xREx)Cu3O7+δ (RE = Nd, Sm, Eu, Gd, Dy)

International Nuclear Information System (INIS)

Zhang, K.; Dabrowski, B.; Segre, C.U.; Hinks, D.G.; Schuller, I.K.; Jorgensen, J.D.; Slaski, M.

1987-10-01

Solid solutions of RE(Ba 2-x RE x )Cu 3 O 7- δ (RE=Nd,Sm,Eu,Gd,Dy) for x=0 to x=0.5 have been investigated. X-ray and resistivity measurements show that there exists a solid solution region, through which, the structure changes from orthorhombic to tetragonal and the superconducting properties are depressed. The solubility limits depend strongly on the size of the rare-earth ion, with the smallest (Dy) showing no appreciable solubility. The superconducting transition temperature versus x for all of the rare-earth ion substitutions falls on a universal curve, indicating that the Ba sites are extremely ionic and magnetically isolated. 20 refs., 4 figs

High purity neodymium acetate from mixed rare earth carbonates

International Nuclear Information System (INIS)

Queiroz, Carlos A. da Silva; Rocha, Soraya M. Rizzo da; Vasconcellos, Mari E. de; Lobo, Raquel M.; Seneda, Jose A.; Pedreira, Walter dos R.

2011-01-01

A simple and economical chemical process for obtaining high purity neodymium acetate is discussed. The raw material in the form rare earth carbonate is produced industrially from the chemical treatment of Brazilian monazite. Ion exchange chromatography technique with a strong cationic resin, proper to water treatment, and without the use of retention ions was used for the fractionating of the rare earth elements (REE). In this way, it was possible to obtain 99.9% pure Nd 2 O 3 in yields greater than or equal 80%, with the elution of the REE using ammonium salt of ethylenediaminetetraacetic acid (EDTA) solution in pH controlled. The complex of EDTA-neodymium was transformed into neodymium oxide, which was subsequently dissolved in acetic acid to obtain the neodymium acetates. Molecular absorption spectrophotometry was used to monitor the neodymium content during the process and sector field inductively coupled plasma mass spectrometry was used to certify the purity of the neodymium acetates. The typical neodymium acetates obtained contain the followings contaminants in μg g -1 : Sc(5.1); Y (0.9); La (1.0); Ce (6.1); Pr (34,4); Sm (12.8); Eu (1.1); Gd (15.4); Tb (29.3); Dy (5.2), Ho(7.4); Er (14.6); Tm (0.3); Yb (2.5); Lu (1.0). The high purity neodymium acetates obtained from this procedure have been applied, replacing the imported product, in research and development area on rare earth catalysts. (author)

Thermal, optical and structural properties of Dy3+ doped sodium aluminophosphate glasses

Science.gov (United States)

Kaur, Manpreet; Singh, Anupinder; Thakur, Vanita; Singh, Lakhwant

2016-03-01

Trivalent Dysprosium doped sodium aluminophosphate glasses with composition 50P2O5-10Al2O3-(20-x)Na2O-20CaO-xDy2O3 (x varying from 0 to 5 mol%) were prepared by melt quench technique. The density of the prepared samples was measured using Archimedes principle and various physical properties like molar volume, rare earth ion concentration, polaron radius, inter nuclear distance and field strength were calculated using different formulae. The differential scanning calorimetry (DSC) was carried out to study the thermal stability of prepared glasses. The UV Visible absorption spectra of the dysprosium doped glasses were found to be comprised of ten absorption bands which correspond to transitions from ground state 6H15/2 to various excited states. The indirect optical band gap energy of the samples was calculated by Tauc's plot and the optical energy was found to be attenuated with Dy3+ ions. The photoluminescence spectrum revealed that Dy3+ doped aluminophosphate glasses have strong emission bands in the visible region. A blue emission band centred at 486 nm, a bright yellow band centred at 575 nm and a weak red band centred at 668 nm were observed in the emission spectrum due to excitation at 352 nm wavelength. Both FTIR and Raman spectra assert slight structural changes induced in the host glass network with Dy3+ ions.

Spin canting in a Dy-based single-chain magnet with dominant next-nearest-neighbor antiferromagnetic interactions

Science.gov (United States)

Bernot, K.; Luzon, J.; Caneschi, A.; Gatteschi, D.; Sessoli, R.; Bogani, L.; Vindigni, A.; Rettori, A.; Pini, M. G.

2009-04-01

We investigate theoretically and experimentally the static magnetic properties of single crystals of the molecular-based single-chain magnet of formula [Dy(hfac)3NIT(C6H4OPh)]∞ comprising alternating Dy3+ and organic radicals. The magnetic molar susceptibility χM displays a strong angular variation for sample rotations around two directions perpendicular to the chain axis. A peculiar inversion between maxima and minima in the angular dependence of χM occurs on increasing temperature. Using information regarding the monomeric building block as well as an ab initio estimation of the magnetic anisotropy of the Dy3+ ion, this “anisotropy-inversion” phenomenon can be assigned to weak one-dimensional ferromagnetism along the chain axis. This indicates that antiferromagnetic next-nearest-neighbor interactions between Dy3+ ions dominate, despite the large Dy-Dy separation, over the nearest-neighbor interactions between the radicals and the Dy3+ ions. Measurements of the field dependence of the magnetization, both along and perpendicularly to the chain, and of the angular dependence of χM in a strong magnetic field confirm such an interpretation. Transfer-matrix simulations of the experimental measurements are performed using a classical one-dimensional spin model with antiferromagnetic Heisenberg exchange interaction and noncollinear uniaxial single-ion anisotropies favoring a canted antiferromagnetic spin arrangement, with a net magnetic moment along the chain axis. The fine agreement obtained with experimental data provides estimates of the Hamiltonian parameters, essential for further study of the dynamics of rare-earth-based molecular chains.

Spectroscopic studies of Dy3 + ion doped tellurite glasses for solid state lasers and white LEDs

Science.gov (United States)

Himamaheswara Rao, V.; Syam Prasad, P.; Mohan Babu, M.; Venkateswara Rao, P.; Satyanarayana, T.; Luís F., Santos; Veeraiah, N.

2018-01-01

Rare earth ion Dy3 +-doped tellurite glasses were synthesised in the system of (75-x)TeO2-15Sb2O3-10WO3-xDy2O3 (TSWD glasses). XRD and FTIR characterizations were used to find the crystalline and structural properties. The intensities of the electronic transitions and the ligand environment around the Dy3 + ion were determined using the Judd-Ofelt (J-O) theory on the absorption spectra of the glasses. The measured luminescence spectra exhibit intense emissions at 574 and 484 nm along with less intense emissions around 662 and 751 nm. Various radiative properties of the 4F9/2 excited level of Dy3 + ion were calculated for the glasses. Decay profiles were measured to find the life times and quantum efficiencies. Yellow to blue intensity ratio (Y/B), CIE chromaticity coordinates and correlated color temperature (CCT) values are calculated using the emission spectra to evaluate the emitted light. The obtained results suggest the utility of the glasses for potential yellow laser and white LED's applications.

Magnetic properties of Dy/Zr multilayers

International Nuclear Information System (INIS)

Luche, M.C.; Boyer, P.

1992-01-01

[Dy(xA)/Zr(30A)] n superlattices (x ≤ 30), were evaporated under ultra-high vacuum on Si(100) substrates. Magnetization measurements indicate that the antiferromagnetic transition occurring at 178K in bulk Dy is suppressed in the multilayers. This phenomenon is attributed to magnetoelastic effects induced by strains at Zr/Dy interfaces. A perpendicular magnetic anisotropy takes place for x ≤ 15. However, the magnetic anisotropy is found to depend markedly on the technique used for Dy deposition. (author). 11 refs., 4 figs

Melting temperature and structural transformation of some rare-earth metals

International Nuclear Information System (INIS)

Vu Van Hung; Hoang Van Tich; Dang Thanh Hai

2009-01-01

the pressure dependence of the melting temperatures of rare-earth metals is studied using the equation of states derived from the statistical moment (SMM). SMM studies were carried out order to calculate the Helmholtz free energy of hcp, bcc Dy and fcc, bcc Ce metals at a wide range of temperatures. the stable phase of Dy and Ce metals can be determined by examining the Helmholtz free energy at a given temperature, i, e. the phase that gives the lowest free energy will be stable. For example, we found that at T lower than 1750 K the hcp Dy metal is stable. At T higher than 1750 K the bcc Dy metal is also stable. Thus 1750 K marks the phase transition temperature of Dy metal. These findings are in agreement with previous experiments. (author)

Quadrupolar frustration in shastry-sutherland lattice of DyB4 studied by resonant x-ray scattering

International Nuclear Information System (INIS)

Okuyama, Daisuke; Matsumura, Takeshi; Nakao, Hironori; Murakami, Youichi

2005-01-01

We have observed geometrical frustration of quadrupolar and magnetic moments in dysprosium tetraboride, DyB 4 , where the rare-earth sites form a Shastry-Sutherland lattice. Resonant X-ray scattering at the L III absorption edge of Dy was utilized. Analysis of the energy, polarization, temperature, and azimuthal-angle dependences of the E1 resonance of the (100) forbidden reflection show that the magnetic and quadrupolar components within the frustrated c plane have a short-range correlation, suggesting that the moments are fluctuating. In contrast, the basic antiferromagnetic component along the c-axis has a long-range order. (author)

Synthesis, structural, thermal and optical studies of rare earth coordinated complex: Tb(Sal){sub 3}Phen

Energy Technology Data Exchange (ETDEWEB)

Kaur, Gagandeep; Dwivedi, Y. [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Rai, S.B., E-mail: sbrai49@yahoo.co.in [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India)

2011-11-01

Highlights: {yields} RE coordinated complex of Tb(Sal){sub 3}Phen in crystalline phases were synthesized. {yields} Enhancement in luminescence of Tb{sup 3+} was observed in complex on 355 nm excitation. {yields} Fluorescence enhancement is due to the efficient energy transfer from Sal to Tb{sup 3+}. {yields} An observed increase in lifetime of Tb{sup 3+} is due to encapsulation in Sal/Phen network. {yields} The present system is a deserving candidate for LSC when coupled with solar cells. - Abstract: Complexes of salicylic acid (Sal) and 1,10-phenanthroline (Phen) were synthesized coordinated with terbium ion (Tb{sup 3+}) in crystalline phases. The structural characterizations of the lanthanide complex were made using FT-IR, NMR ({sup 1}H and {sup 13}C) and XRD techniques. These measurements confirm the formation of Tb(Sal){sub 3}Phen complex structure. The thermal aspects of the complex were examined using DTA and TGA techniques. An enhancement in luminescence intensity of Tb{sup 3+} ion bands were observed in Tb(Sal){sub 3}Phen complex as compared to TbCl{sub 3} crystals on 355 nm laser excitation. Enhancement is reported due to the efficient energy transfer process from Sal to Tb{sup 3+} ions. This is also confirmed by the time resolved photoluminescence spectroscopy with increase in lifetime of Tb{sup 3+} ions due to encapsulation in Sal/Phen network. Our system in itself can be a deserving candidate for luminescent solar collector material when coupled with solar cells.

Treatment: Latent TB Infection (LTBI) and TB Disease

Science.gov (United States)

... Adverse Events TB Treatment of Persons Living with HIV TB Treatment and Pregnancy TB Treatment for Children Drug-Resistant TB Research TB Epidemiologic Studies Consortium Research Projects Publications TB Trials Consortium Study ...

1,3-thiazole as suitable antenna ligand for lanthanide photoluminescence in [LnCl{sub 3}(thz){sub 4}].0.5thz, Ln = Sm, Eu, Gd, Tb, Dy

Energy Technology Data Exchange (ETDEWEB)

Dannenbauer, Nicole; Mueller-Buschbaum, Klaus [Wuerzburg Univ. (Germany). Inst. for Inorganic Chemistry; Kuzmanoski, Ana; Feldmann, Claus [Karlsruhe Institute of Technology (KIT), Karlsruhe (Germany). Inst. for Inorganic Chemistry

2014-02-15

The series of luminescent monomeric lanthanide thiazole complexes [LnCl{sub 3}(thz){sub 4}].0.5thz (Ln = Sm, Eu, Gd, Tb, Dy; thz = 1,3-thiazole) has been synthesised and characterised by powder and single-crystal X-ray diffraction, IR and photoluminescence spectroscopy, DTA/TG as well as elemental analysis. The colourless compounds exhibit photoluminescence in the visible region with varying quantum efficiencies up to QY = 48 % for [LnCl{sub 3}(thz){sub 4}].0.5thz. Both, the lanthanide ions as well as the thiazole ligand contribute to the luminescence. Excitation can be achieved via intra-4f transitions and by exciting the ligand, emission is observed mainly from the lanthanide ions again by 4f transitions. Thiazole can transfer energy to the lanthanide ions, which further feeds the lanthanide emission by an efficient antenna effect even at room temperature. The lanthanide ions show pentagonal-bipyramidal coordination by three chloride anions and four N atoms of 1,3-thiazole, which leads to a strong {sup 5}D{sub 0} → {sup 7}F{sub 4} transition for europium. Significant differences arise as compared to thiophene complexes because no sulphur atom is involved in the metal coordination, as the thiazole ligand is solely coordinated via its nitrogen function. (orig.)

Thermoluminescence of rare earth doped BaSO/sub 4/ phosphors and its applications

Energy Technology Data Exchange (ETDEWEB)

Nagpal, J.S.; Varadharajan, G. (Bhabha Atomic Research Centre, Bombay (India). Div. of Radiological Protection)

1982-03-01

Thermoluminescence of synthetic BaSO/sub 4/ samples individually doped with Y, La, Ce, Pr, Nd, Sm, Eu, Tb, Dy and Tm has been studied after ..gamma..- and microwave irradiations. BaSO/sub 4/:Eu has the highest response for ..gamma..-radiation while BaSO/sub 4/:Tb exhibits highest reduction in its ..gamma..-induced TL after exposure to microwave radiation (2425 +- 25 MHz). The reduction depends on the microwave radiant exposure and is independent of the irradiance level in the range 25-200 mW . cm/sup -2/ and hence can be useful for microwave dosimetry.

Addition compounds between same phosphinoxides and hexafluorophosphates of rare earths (III)

International Nuclear Information System (INIS)

Silva, A.M. da; Melo, S.M.; Souza, E.F. de; Almeida, M.A. de

1984-01-01

Coordination compounds were prepared from salts of lanthanide hexafluorophosphates and three different phosphine oxides: methyldiphenylphosphine oxide (MDPPO), diphenylcyclohexylphosphine oxide (DPcHPO) and phosphoric acid trimethylester (TMxPO). The analytical results indicated the following general formulae : Ln(PF 6 ) 3 .5DPChPO where Ln = La, Eu, Gd, Tb and Dy; Ln(PF 6 ) 3 6MDPPO, where Ln = La, Ce, Nd, Eu, Gd, and Tm; Ln(PF 6 ) 3 .7TMxPO, where Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm and Yb. The vibrational studies in the infrared region showed that all the phosphine oxides coordination are through the oxygen of the phosphoryl group and confirmed the non-coordination character of the PF - 6 ion. Fluorescence spectra in the visible region for the Eu (III) compounds, at the liquid nitrogen temperature indicated the microsymmetry C sub(3v) as the most probable for the Eu (III) in the compounds Eu (PF 6 ) 3 .5DPChPO and Eu (PF 6 ) 3 .7TMxPO. The symmetry site of the Eu (PF 6 ) 3 .6MDPPO compound is octahedral with tetragonal distortion. (Author) [pt

The significant role of the rare earth ions on the elastic and thermodynamic parameters of LiCoDy- and ZnCoCe-ferrites

Energy Technology Data Exchange (ETDEWEB)

Bishay, Samiha T. [Physics Department, Faculty of Girls for Science, Art and Education Ain Shams University, Asma Fahmi Street, Heliopolis, Cairo (Egypt)]. E-mail: dr_samiha@hotmail.com

2006-06-15

Two types of rare earth ferrites [Li{sub 0.6}Co{sub 0.1}Dy{sub x}Fe{sub 2.3-x}O{sub 4}; 0.0=earth content as well as its ionic radius plays a significant role in the evaluated parameters. According to the experimental results, the two investigated types of rare earth ferrite are considered as insulator magnetic solids. It was found that for each composition there exists a characteristic temperature, down to which the resonance frequency of the investigated samples drops smoothly, but above this temperature the resonance frequency stays constant. Accordingly, these samples seem to be of importance in industrial applications especially in the field of electronics.

The low-energy β(-) and electron emitter (161)Tb as an alternative to (177)Lu for targeted radionuclide therapy.

Science.gov (United States)

Lehenberger, Silvia; Barkhausen, Christoph; Cohrs, Susan; Fischer, Eliane; Grünberg, Jürgen; Hohn, Alexander; Köster, Ulli; Schibli, Roger; Türler, Andreas; Zhernosekov, Konstantin

2011-08-01

The low-energy β(-) emitter (161)Tb is very similar to (177)Lu with respect to half-life, beta energy and chemical properties. However, (161)Tb also emits a significant amount of conversion and Auger electrons. Greater therapeutic effect can therefore be expected in comparison to (177)Lu. It also emits low-energy photons that are useful for gamma camera imaging. The (160)Gd(n,γ)(161)Gd→(161)Tb production route was used to produce (161)Tb by neutron irradiation of massive (160)Gd targets (up to 40 mg) in nuclear reactors. A semiautomated procedure based on cation exchange chromatography was developed and applied to isolate no carrier added (n.c.a.) (161)Tb from the bulk of the (160)Gd target and from its stable decay product (161)Dy. (161)Tb was used for radiolabeling DOTA-Tyr3-octreotate; the radiolabeling profile was compared to the commercially available n.c.a. (177)Lu. A (161)Tb Derenzo phantom was imaged using a small-animal single-photon emission computed tomography camera. Up to 15 GBq of (161)Tb was produced by long-term irradiation of Gd targets. Using a cation exchange resin, we obtained 80%-90% of the available (161)Tb with high specific activity, radionuclide and chemical purity and in quantities sufficient for therapeutic applications. The (161)Tb obtained was of the quality required to prepare (161)Tb-DOTA-Tyr3-octreotate. We were able to produce (161)Tb in n.c.a. form by irradiating highly enriched (160)Gd targets; it can be obtained in the quantity and quality required for the preparation of (161)Tb-labeled therapeutic agents. Copyright © 2011 Elsevier Inc. All rights reserved.

Separation of Rare Earths from Uranium and Thorium

International Nuclear Information System (INIS)

Krebs, Damien

2014-01-01

Greenland Minerals and Energy - Key Highlights – A unique world class mining project: 1. World-class, large scale development project: • Economically robust, proven technology, large-scale, long life production of rare earths concentrate and uranium; • Large JORC resource base to produce ~7kt HREO, 37kt LREO & 3Mlbs U_3O_8 per annum over 30 year mine life; • Ideally located near international airport, existing towns and potential hydro-electric power source. 2. Very attractive commodity portfolio: • Heavy rare earths and uranium are both recognised as strategically important commodities for the future; • Rare earths market characterised by limited capacity and increasing demand (particularly Dy, Nd, Tb, Eu and Y). 3. Strong management and technical team: • Experienced management team with proven track record; • Well-respected and knowledgeable technical/project team in place with exceptional local expertise. 4. Highly advantageous ore-type, makes for simple cost-effective processing, highly scalable production: • High upgrade through beneficiation brings optionality to Kvanefjeld project; • Leaching can be done in Greenland, or owing to the high-grade concentrate, can be shipped to other locations; • Allows to single concentrator in Greenland, multiple refineries/partners globally. 5. Globally significant, long life, low cost, multi-commodity asset: • Company to become one of the largest producers of rare earths globally and a significant U_3O_8 mine; • Potential to supply >20% of global critical (including heavy) rare earth element demand; • Company has low cost of production due to multiple by-product opportunities. 6. Low political risk: • Stable, low-risk operating environment with government looking to develop new industries and employment; • GME fully permitted to evaluate the project, exploration licence now includes radioactive elements; • Management and board have a solid working relationship with the government and are

Magnetooptic effects and Auger electron spectroscopy of two-layer NiFe-Dy and Fe-Dy films with nonuniform layers

International Nuclear Information System (INIS)

Ehdel'man, I.S.; Markov, V.V.; Khudyakov, A.E.; Ivantsov, R.D.; Bondarenko, G.V.; Ovchinnikov, S.G.; Kesler, V.G.; Parshin, A.S.; Ronzhin, I.P.

2001-01-01

Magneto-optical effects (magnetic circular dichroism and meridional Kerr effect) and element distribution with layer thickness in two-layer NiFe-Dy and Fe-Dy films, prepared by thermal sputtering of component in ultrahigh vacuum, are investigated. It is shown, that Dy in a two-layer film in the temperature range of 80-300 K makes constant contributions to both effects investigated which are approximately equal to the values of the effects observed in an isolated Dy film only at temperatures below the temperature T c of Dy transition into a ferromagnetic state (T c ∼ 100 K for the films under study). This behaviour of magneto-optical effects is assumed to be due to the influence of a NiFe layer spin system on magnetic state of a Dy layer, this influence is enhanced by the deep penetration of Ni and Fe ions into Dy layer as it follows from the data obtained using Auger electron spectroscopy [ru

Crystal chemistry and magnetic properties of ternary rare earth sulfides

International Nuclear Information System (INIS)

Plug, C.M.; Rijksuniversiteit Leiden

1977-01-01

The results of magnetic measurements on two groups of ternary rare earth sulphides are described, the MLnS 2 (M=Li, Na, K) type of compounds and the series Ln 2 ZrS 5 , where Ln denotes one of the rare earths. None of these compounds is metallic, excluding the possibility of RKKY-interaction. In chapter II a survey of the relevant theory on magnetic properties and crystal field splitting is given. In spite of the similarity in chemical properties of the rare earths, the crystal chemistry of their compounds is rather complex. This is due to the lanthanide contraction. The third chapter deals with the description and classification of the numerous crystal structures of both ternary and binary rare earth sulphides that have been observed. Rather simple relations between various structures are presented using a new method of structure classification. The magnetic interactions expected to be based on superexchange via the anions, which is usually very structure dependent. Experiments to study the crystallographic ordering, applying both X-ray and electron diffraction methods and the results of the magnetic measurements on the compounds MLnS 2 are reported in chapter IV. The compounds Ln 2 ZrS 5 are candidates for a systematic study of the variation of the magnetic properties along the rare earth series. The results of magnetic measurements on these compounds are presented in chapter V, combined with the results of specific heat measurements. Also the magnetic structure of two representatives, Tb 2 ZrS 5 and Dy 2 ZrS 5 , determined by neutron diffraction experiments below the ordering temperature, is reported

The interplay of long-range magnetic order and single-ion anisotropy in rare earth nickel germanides

Energy Technology Data Exchange (ETDEWEB)

Islam, Z.

1999-05-10

This dissertation is concerned with the interplay of long-range order and anisotropy in the tetragonal RNi{sub 2}Ge{sub 2} (R = rare earth) family of compounds. Microscopic magnetic structures were studied using both neutron and x-ray resonant exchange scattering (XRES) techniques. The magnetic structures of Tb, Dy, Eu and Gd members have been determined using high-quality single-crystal samples. This work has correlated a strong Fermi surface nesting to the magnetic ordering in the RNi{sub 2}Ge{sub 2} compounds. Generalized susceptibility, {chi}{sub 0}(q), calculations found nesting to be responsible for both incommensurate ordering wave vector in GdNi{sub 2}Ge{sub 2}, and the commensurate structure in EuNi{sub 2}Ge{sub 2}. A continuous transition from incommensurate to commensurate magnetic structures via band filling is predicted. The surprisingly higher T{sub N} in EuNi{sub 2}Ge{sub 2} than that in GdNi{sub 2}Ge{sub 2} is also explained. Next, all the metamagnetic phases in TbNi{sub 2}Ge{sub 2} with an applied field along the c axis have been characterized with neutron diffraction measurements. A mixed phase model for the first metamagnetic structure consisting of fully-saturated as well as reduced-moment Tb ions is presented. The moment reduction may be due to moment instability which is possible if the exchange is comparable to the low-lying CEF level splitting and the ground state is a singlet. In such a case, certain Tb sites may experience a local field below the critical value needed to reach saturation.

Magnetic properties of rare earth oxides with perovskite structure

International Nuclear Information System (INIS)

Hinatsu, Yukio

2008-01-01

A perovskite composite oxide is represented by the general formula of ABO 3 . Cations at the B site characterize magnetic properties of the oxide. Many studies have been accumulated for transition metal elements at the B sites. In this report the studies of rare earth elements at the B sites are reviewed. In rare elements, tetravalent ions such as Ce 4+ , Pr 4+ and Tb 4+ can occupy the B sites with Ba and Sr ions at the A sites. Both the SrTbO 3 and BaTbO 3 have an orthorhombic structure and show the antiferromagnetic transition at about 33 K, which is originated from terbium ions coupled antiferromagnetically with the six neighboring terbium ions. A tetravalent praseodymium perovskite SrPrO 3 shows no existence of the magnetic ordering down to 2.0 K. This is in contrast to the result of isomorphous BaPrO 3 , which shows an antiferromagnetic transition at 11.5 K. A double perovskite structure is represented by the formula A 2 LnMO 6 (A=Ba, Sr, Ca; M=Ru, Ir). In a double perovskite compound Ba 2 PrRuO 6 , the Pr 3+ and Ru 5+ ions are arranged with regularity over the six-coordinate B sites. This compound transforms to an antiferromagnetic state below 117 K. Antiferromagnetic transition temperatures T N for isomorphous Sr and Ca show a clear tendency, T N (A=Ba)>T N (Sr)>T N (Ca), in the compounds with the same rare earth elements (Ln). The 6H-perovskite structure Ba 3 LnRu 2 O 9 consists of linkages between LnO 6 octahedra and Ru 2 O 9 dimers made from face-shared RuO 6 octahedra. The 6H-perovskite structure Ba 3 MRu 2 O 9 (M=Sc, Y, La, Nd-Gd, Dy-Lu) have the valence state of Ba 3 M 3+ Ru 2 4.5+ O 9 . The magnetic susceptibilities show a broad maximum at 135-370 K. This magnetic behavior is ascribed to the antiferromagnetic coupling between two Ru ions in a Ru 2 O 9 dimer and to the magnetic interaction between the Ru 2 O 9 dimers. (author)

Superdeformed bands in /sup 150/Gd and /sup 151/Tb: Evidence for the influence of high-N intruder states at large deformations

Energy Technology Data Exchange (ETDEWEB)

Fallon, P.; Alderson, A.; Bentley, M.A.; Bruce, A.M.; Forsyth, P.D.; Howe, D.; Roberts, J.W.; Sharpey-Schafer, J.F.; Twin, P.J.; Beck, F.A.

1989-02-16

Rotational bands, characteristic of a superdeformed prolate shape (epsilon approx. = 0.6) and extending to above spin 60 Planck constant, have been observed in both /sup 150/Gd and /sup 151/Tb. The magnitudes of the moments of inertia I/sup (2)/ were found to vary with frequency and the variation greatly exceeded that seen in /sup 148,149/Gd and /sup 151,152/Dy. The differences in the I/sup (2)/'s are attributed to the occupation of particular high-N orbitals. Moreover, contrary to the previous examples the bands in both /sup 150/Gd and /sup 151/Tb de-excited at a much higher rotational frequency of Planck constant..omega.. approx. = 0.4 MeV and this may indicate that the pair gap extends to higher frequencies in /sup 150/Gd and /sup 151/Tb.

Isothermal sections of phase equilibria diagrams for systems (terbium, dysprosium, holmium)-molybdenum-boron at 1273 K

International Nuclear Information System (INIS)

Kuz'ma, Yu.B.; Zakharchuk, N.P.; Maksimova, L.T.

1988-01-01

The methods of X-ray analysis are used to study the R-Mo-B (R-Tb, Dy, Ho) systems and isothermal sections of phase equilibria diagrams at 1273 K are plotted. A formation of RMoB 4 (structure of the YCrB 4 type) is confirmed and borides R 3 MoB 7 (structure of the Er 3 CrB 7 type) and ∼ RMo 4 B 8 (of the unknown structure) are obtained for the first time. Borides DyMoB 3 and HoMoB 3 are of the ErMoB 3 structure. Lattice periods of new compounds are indicated. Diffractogrammes of borides Dy 3 MoB 7 and DyMoB 3 are calculated. A peculiarity of components interaction in the systems rare-earth metal-molybdenum-boron is considered

High-field magnetization of dilute rare earths in yttrium

DEFF Research Database (Denmark)

Touborg, P.; Høg, J.; Cock, G. J.

1974-01-01

Magnetization measurements have been performed on single crystals of Y containing small amounts of Tb, Dy, or Er at 4.2 K in fields up to 295 × 105 A/m (370 kOe). Crystal-field and molecular-field parameters obtained from measurements of the initial susceptibility versus temperature give a satisf...... a satisfactory quantitative account of the high-field magnetization. This includes characteristic features due to the crossing and mixing of crystal-field levels....

Thermoluminescence properties of Al2O3:Tb nanoparticles irradiated by gamma rays and 85 MeV C6+ ion beam

International Nuclear Information System (INIS)

Salah, Numan; Alharbi, Najlaa D.; Habib, Sami S.; Lochab, S.P.

2015-01-01

Carbon ions beam is recently recognized as an ideal cancer treatment modality, because of its excellent local tumor control. These ions have a high relative biological effectiveness resulting from high linear energy transfer (LET) and their sharp Bragg peak. However, the dose of those energetic ions needs to be measured with great precision using a proper dosimeter. Aluminum Oxide (Al 2 O 3 ) is a highly luminescent phosphor widely used for radiation dosimetry using thermoluminesence (TL) technique. In this work nanoparticles of this material activated by different elements like Eu, Tb, Dy, Cu and Ag were evaluated for their TL response to gamma rays irradiation. Tb doped sample is found to be the most sensitive sample, which could be selected for exposure to 85 MeV C 6+ ion beam in the fluence range 10 9 –10 13 ions/cm 2 . The obtained result shows that C ion beam irradiated sample has a simple glow curve structure with a prominent glow peak at around 230 °C. This glow curve has a dosimetric peak better than those induced by gamma rays. This glow peak exhibits a linear response in the range 10 9 –10 11 ions/cm 2 , corresponding to the equivalent absorbed doses 0.285–28.5 kGy. The absorbed doses, penetration depths and main energy loss were calculated using TRIM code based on the Monte Carlo simulation. The wide linear response of Al 2 O 3 :Tb nanoparticles along with the low fading makes this low cost nanomaterial a good candidate for C ion beam dosimetry. - Highlights: • Nanoparticles of Al 2 O 3 doped with Eu, Tb, Dy, Cu and Ag were synthesised. • They were evaluated for their TL response to gamma rays and C ion beam irradiation. • Tb doped sample is the most sensitive sample to gamma rays. • Al 2 O 3 :Tb was exposed to 85 MeV C 6+ ion beam in the fluence range 10 9 -10 13 ions/cm 2 . • The glow peak induced by C ions has a linear response in the range 10 9 -10 11 ions/cm 2

High purity samarium oxide from mixed rare earth carbonates

International Nuclear Information System (INIS)

Queiroz, Carlos A. da S.; Seneda, Jose A.; Vasconcellos, Mari E. de; Pedreira Filho, Walter dos R.

2013-01-01

A simple and economical chemical process for the production of highly pure samarium oxides is discussed. The raw material, which was used in the form of rare earth carbonates was produced industrially from the chemical treatment of Brazilian monazite. Ion exchange chromatography was performed using a strong cationic resin that is typically employed in water treatment processes to fractionate rare earth elements (REE) without the use of retention ions. Under these conditions, 99.9% pure Sm 2 O 3 was eluted using the ammonium salt of ethylenediaminetetraacetic acid (EDTA) at a controlled pH. The EDTA-samarium complex was separated from EDTA and then precipitated as oxalate and fired to samarium oxide. Molecular absorption spectrophotometry was used to monitor the samarium content during the proposed process, and sector field inductively coupled plasma mass spectrometry was used to certify the purity of the samarium oxide. Typical samarium oxide obtained from the proposed procedure contained the following contaminants in micrograms per gram: Sc (20.90); Y (11.80); La (8.4); Ce (4.3); Pr (2.5); Nd (5.1); Eu (94); Gd (114); Tb (3.6); Dy (2.5), Ho (2.3); Er (3.0); Tm (2.3); Yb (38,2); Lu (25.6). The high-purity samarium oxides produced in the present study can be used as an alternative to imported products in research and development applications. (author)

Proceedings of the national conference on rare earth processing and utilization - 2014: abstracts

International Nuclear Information System (INIS)

Anitha, M.; Dasgupta, Kinshuk; Singh, D.K.

2014-01-01

The rare earth elements (REEs) are becoming increasingly important in the transition to a low-carbon, circular economy, considering their essential role in permanent magnets, lamp phosphors, rechargeable nickel metal hydride batteries and catalysts and other green applications. The increasing popularity of hybrid and electric cars, wind turbines and compact fluorescent lamps is causing an increase in the demand and price of REEs. The European Commission considers the REEs as the most critical raw materials group, with the highest supply risk. According to the medium-term criticality matrix of the U.S. Department of Energy (DOE), the five most critical REEs are neodymium (Nd), europium (Eu), terbium (Tb), dysprosium (Dy) and yttrium (Y). China is presently producing more than 90% of all rare earths, although they possess less than 40% of the proven reserves. Due to large and increasing domestic demands, China tightened its REE export quota from 2012 onwards. These export quotas caused serious problems for REE users outside of China. To tackle the REE supply challenge, several approaches have been proposed. Fortunately India is blessed with large resources of rare earths in the form of monazite found in the beach sands of Kerala, Tamil Nadu and Odisha. Indian Rare Earths Limited at Aluva near Kochi used to produce mainly mixed rare earths chloride and export to USA, UK, France, Japan, etc. During the 1990s and early 2000s this plant exported pure oxides of samarium, neodymium, etc. to developed countries. This national conference has expanded its canvas by including newer emerging areas in rare earths recycling, environmental issues, recent advances in rare earth material science, rare earth research and development initiatives around the world which provide a platform for the growth of rare earth Industry. Papers relevant to INIS are indexed separately

Effects of 3d-4f magnetic exchange interactions on the dynamics of the magnetization of Dy(III)-M(II)-Dy(III) trinuclear clusters.

Science.gov (United States)

Pointillart, Fabrice; Bernot, Kevin; Sessoli, Roberta; Gatteschi, Dante

2007-01-01

[{Dy(hfac)(3)}(2){Fe(bpca)(2)}] x CHCl(3) ([Dy(2)Fe]) and [{Dy(hfac)(3)}(2){Ni(bpca)(2)}]CHCl(3) ([Dy(2)Ni]) (in which hfac(-)=1,1,1,5,5,5-hexafluoroacetylacetonate and bpca(-)=bis(2-pyridylcarbonyl)amine anion) were synthesized and characterized. Single-crystal X-ray diffraction shows that [Dy(2)Fe] and [Dy(2)Ni] are linear trinuclear complexes. Static magnetic susceptibility measurements reveal a weak ferromagnetic exchange interaction between Ni(II) and Dy(III) ions in [Dy(2)Ni], whereas the use of the diamagnetic Fe(II) ion leads to the absence of magnetic exchange interaction in [Dy(2)Fe]. Dynamic susceptibility measurements show a thermally activated behavior with the energy barrier of 9.7 and 4.9 K for the [Dy(2)Fe] and [Dy(2)Ni] complexes, respectively. A surprising negative effect of the ferromagnetic exchange interaction has been found and has been attributed to the structural conformation of these trinuclear complexes.

Contribution to the study of magnetic properties of rare-earth iron intermetallic compounds

International Nuclear Information System (INIS)

Morariu, M.

1976-01-01

The intermetallic binary compounds Ysub(x)Fesub(y)(YFe 2 ,YFe 3 ,Y 6 Fe 23 ,Y 2 Fe 17 ), RFe 2 (R=Gd,Tb,Dy,Ho,Er and Tm) and the intermetallic pseudobinary compounds (Gdsub(x)Ysub(1-x))Fe 2 and Dy(Fesub(x)Nisub(1-x)) 3 were studied, using magnetic measurements and Moessbauer spectroscopy, in order to obtain information on their magnetic behaviour. The different models which describe magnetic interactions in rare-earths with 3d transition element compounds are reviewed. The magnetic hyperfine field Hsub(n) at the Fe 57 nucleus, measured by Moessbauer spectroscopy, depends on the atom position in the lattice, being sensitive to magnetic interactions with neighbouring atoms. The mean value of the magnetic hyperfine field, average Hsub(n) is proportional to the mean magnetic moment of the iron atom: average Hsub(n)/average μsub(Fe) approximately 150 kOe. The comparative study of the temperature dependence of average Hsub(n) and average μsub(Fe) values shows that this relation is valid for the whole range of magnetic ordering (T>Tsub(c)). The mean magnetic hyperfine fields at the Fe 57 nucleus in RFe 2 compounds depend on the rare-earth partner and vary approximative linearly with the Gennes factor. The spin reorientation diagram for the (Gdsub(x)Ysub(1-x))Fe 2 system is obtained. All results on Moessbauer spectroscopy are in good agreement with the magnetic measurements. The magnetic behaviour of iron atoms is justified using a model in which the most electrons are in a narrow band, so they could be considered localized, and the magnetic interactions between these atoms take place through a fraction (<5%) of 3d itinerant electrons. (author)

Magnetic rare earth superlattices

DEFF Research Database (Denmark)

Majkrzak, C.F.; Kwo, J.; Hong, M.

1991-01-01

Advances in molecular beam epitaxy deposition techniques have recently made it possible to grow, an atomic plane at a time, single crystalline superlattices composed of alternating layers of a magnetic rare earth, such as Gd, Dy, Ho, or Er, and metallic Y, which has an identical chemical structure...

Slow magnetic relaxation and single-molecule toroidal behaviour in a family of heptanuclear {Cr"I"I"ILn"I"I"I_6} (Ln=Tb, Ho, Er) complexes

Energy Technology Data Exchange (ETDEWEB)

Vignesh, Kuduva R. [IITB-Monash Research Academy, IIT Bombay, Powai, Mumbai (India); Langley, Stuart K. [School of Science and the Environment, Division of Chemistry, Manchester Metropolitan University, Manchester (United Kingdom); Swain, Abinash; Rajaraman, Gopalan [Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai (India); Moubaraki, Boujemaa; Murray, Keith S. [School of Chemistry, Monash University, Clayton, VIC (Australia); Damjanovic, Marko; Wernsdorfer, Wolfgang [Institute Neel, CNRS, Universite Grenoble Alpes, Grenoble (France); Institute of Nanotechnology (INT), Karlsruhe Institute of Technology (KIT), Eggenstein-Leopoldshafen (Germany)

2018-01-15

The synthesis, magnetic properties, and theoretical studies of three heterometallic {Cr"I"I"ILn"I"I"I_6} (Ln=Tb, Ho, Er) complexes, each containing a metal topology consisting of two Ln{sub 3} triangles connected via a Cr{sup III} linker, are reported. The {CrTb_6} and {CrEr_6} analogues display slow relaxation of magnetization in a 3000 Oe static magnetic field. Single-crystal measurements reveal opening up of the hysteresis loop for {CrTb_6} and {CrHo_6} molecules at low temperatures. Ab initio calculations predict toroidal magnetic moments in the two Ln{sub 3} triangles, which are found to couple, stabilizing a con-rotating ferrotoroidal ground state in Tb and Ho examples and extend the possibility of observing toroidal behaviour in non Dy{sup III} complexes for the first time. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

Calculation of the magnetic properties of pseudo-ternary R2M14B intermetallic compounds (R = rare earth, M = Fe, Co

Directory of Open Access Journals (Sweden)

Gabriel Gómez Eslava

2016-06-01

Full Text Available The extrinsic properties of NdFeB-based magnets can be tuned through partial substitution of Nd by another rare-earth element and Fe by Co, as such substitution leads to a modification in the intrinsic properties of the main phase. Optimisation of a magnet's composition through trial and error is time consuming and not straightforward, since the interplay existing between magnetocrystalline anisotropy and coercivity is not completely understood. In this paper we present a model to calculate the intrinsic magnetic properties of pseudo-ternary Nd2Fe14B-based compounds. As concrete examples, which are relevant for the optimisation of NdFeB-based high-performance magnets used in (hybrid electric vehicles and wind turbines, we consider partial substitution of Nd by Dy or Tb, and Fe by Co.

Application of the Instrumental Neutron Activation Analysis and High Performance Liquid Chromatography (HPLC) in the rare earth elements determination in reference geological materials

International Nuclear Information System (INIS)

Figueiredo, Ana M.G.; Moraes, Noemia M.P. de; Shihomatsu, Helena M.

1997-01-01

Instrumental Neutron Activation Analysis (INAA) and High Performance Liquid Chromatography (HPLC) were applied to the determination of rare earth elements (REE) in the geological reference materials AGV-1, G-2 and GSP-1 (USGS). Results obtained by both techniques showed good agreement with certified values, giving relative errors less than 10%. The La, Ce, Nd, Sm, Eu, Tb, Yb and Lu REE elements were determined. All the REE except Dy and Y were determined by HPLC. The reference material G94, employed in the International Proficiency Test for Analytical Geochemistry Laboratories (GeoTP1) was analysed. The results obtained are a contribution to REE contents in this sample. The INAA and HPLC application to the determination of REE in this kind of matrix is also discussed. (author). 10 refs., 1 fig., 5 tabs

Utility of Lithium in Rare-Earth Metal Reduction Reactions to Form Nontraditional Ln2+ Complexes and Unusual [Li(2.2.2-cryptand)]1+ Cations.

Science.gov (United States)

Huh, Daniel N; Darago, Lucy E; Ziller, Joseph W; Evans, William J

2018-02-19

The utility of lithium compared to other alkali metals in generating Ln 2+ rare-earth metal complexes via reduction of Ln 3+ precursors in reactions abbreviated as LnA 3 /M (Ln = rare-earth metal; A = anionic ligand; M = alkali metal) is described. Lithium reduction of Cp' 3 Ln (Cp' = C 5 H 4 SiMe 3 ; Ln = Y, Tb, Dy, Ho) under Ar in the presence of 2.2.2-cryptand (crypt) forms new examples of crystallographically characterizable Ln 2+ complexes of these metals, [Li(crypt)][Cp' 3 Ln]. In each complex, lithium is found in an N 2 O 4 donor atom coordination geometry that is unusual for the cryptand ligand. Magnetic susceptibility data on these new examples of nontraditional divalent lanthanide complexes are consistent with 4f n 5d 1 electronic configurations. The Dy and Ho complexes have exceptionally high single-ion magnetic moments, 11.35 and 11.67 μ B , respectively. Lithium reduction of Cp' 3 Y under N 2 at -35 °C forms the Y 2+ complex (Cp' 3 Y) 1- , which reduces dinitrogen upon warming to room temperature to generate the (N 2 ) 2- complex [Cp' 2 Y(THF)] 2 (μ-η 2 :η 2 -N 2 ). These results provide insight on the factors that lead to reduced dinitrogen complexes and/or stable divalent lanthanide complexes as a function of the specific reducing agent and conditions.

Determination of slip systems and their relation to the high ductility and fracture toughness of the B2 DyCu intermetallic compound

International Nuclear Information System (INIS)

Cao, G.H.; Shechtman, D.; Wu, D.M.; Becker, A.T.; Chumbley, L.S.; Lograsso, T.A.; Russell, A.M.; Gschneidner, K.A.

2007-01-01

DyCu single crystals with CsCl-type B2 structure were tensile tested at room temperature. Slip trace analysis shows that the primary slip system in DyCu with a tensile axis orientation of is {1 1 0} and the critical resolved shear stress for {1 1 0} slip is 18 MPa. Slip traces were also observed from a secondary slip system, {1 1 0} , and this slip system appears to be a key contributor to the previously reported high ductility and high fracture toughness of polycrystalline DyCu. Transmission electron microscopy determinations of the Burgers vectors of dislocations in tensile tested specimens revealed and dislocations, with -type dislocations being more abundant. The implications of these findings for the understanding of the mechanical properties of DyCu and the large family of ductile rare earth B2 intermetallics are discussed

Isothermal sections at 500 deg C of the Dy-V-Al and Dy-Cr-Al systems in the aluminium rich regions

International Nuclear Information System (INIS)

Rykhal', R.M.; Zarechnyuk, O.S.; Mats'kiv, O.P.

1979-01-01

X-ray diffraction and microscopic analyses have been used to investigate the ternary system dysprosium-vanadium-aluminium in the aluminium rich region. In the system Dy-V-Al two ternary compounds have been found: DyV 2 Al 20 (cubic structure, CeCr 2 Al 20 type, a=14.54 A and approximately DyVAl 8 (hexagonal crystal system, structure unknown, a=10.86, c=17.71 A, c/a=1.631). In the system dysprosium-chromium-aluminium three ternary compounds have been found: DyCr 2 Al 20 (cubic structure, CeCr 2 Al 20 type, a=14.39), approximately equal to DyCrAl 8 ) hexagonal crystal system, structure type unkown a=10.75, c=17.60 A, c/a=1.637) and DyCr 4 Al 8 (tetragonal structure, CeMn 4 Al 8 type, a=8.87, c=5.04 A, c/a=0.568). Isothermal sections of the systems Dy-V-Al and Dy-Cr-Al have been plotted at 500 deg C

Inelastic Neutron Scattering and Magnetisation Investigation of an Exchange-Coupled Dy2 SMM

Science.gov (United States)

Baker, Michael L.; Zhang, Qing; Sarachik, Myriam P.; Kent, Andrew D.; Chen, Yizhang; Butch, Nicholas; Pineda, Eufemio M.; McInnes, Eric

The strong spin orbit coupling and weak crystal field energies of simple exchange-coupled rare earth SMMs makes the precise evaluation of their magnetic properties nontrivial. Here we report a detailed investigation of the single molecule magnet hqH2Dy2(hq)4(NO3)3MeOH. Inelastic neutron scattering is used to obtain direct access to several low energy crystal field excitations. The INS results display several features that are not found in earlier FIR absorption experiments, while other features found in the latter are absent. Based on the effective point charge model, numerical calculations are currently underway to resolve these apparent discrepancies using complementary magnetisation measurements to resolve the exchange between Dy ions. Work supported by ARO W911NF-13-1-1025 (CCNY) and NSF-DMR-1309202 (NYU).

Extension of the energy range of the experimental activation cross-sections data of longer-lived products of proton induced nuclear reactions on dysprosium up to 65MeV.

Science.gov (United States)

Tárkányi, F; Ditrói, F; Takács, S; Hermanne, A; Ignatyuk, A V

2015-04-01

Activation cross-sections data of longer-lived products of proton induced nuclear reactions on dysprosium were extended up to 65MeV by using stacked foil irradiation and gamma spectrometry experimental methods. Experimental cross-sections data for the formation of the radionuclides (159)Dy, (157)Dy, (155)Dy, (161)Tb, (160)Tb, (156)Tb, (155)Tb, (154m2)Tb, (154m1)Tb, (154g)Tb, (153)Tb, (152)Tb and (151)Tb are reported in the 36-65MeV energy range, and compared with an old dataset from 1964. The experimental data were also compared with the results of cross section calculations of the ALICE and EMPIRE nuclear model codes and of the TALYS nuclear reaction model code as listed in the latest on-line libraries TENDL 2013. Copyright © 2015. Published by Elsevier Ltd.

Effect of trivalent transition metal ion substitution in Dy2O3 system

International Nuclear Information System (INIS)

Dhilip, M.; Saravana Kumar, K.; Anbarasu, V.

2015-01-01

One of the very promising approaches to create novel materials is to combine different physical properties in one material to achieve rich functionality. Magnetoelectric multiferroics are attracting attention for fundamental physics due to their unique coupling behaviour between ferroelectricity, ferromagnetism and ferroelasticity and also because of their promising applications for devices in spintronics, information storage, sensing and actuation. The existence of spontaneous magnetization in the perovskite like phase (layer of perovskite) has encouraged exploring the possibility of fabrication of a multiferroic material for multifunctional devices using the concept of magnetoelectric effect. The rare earth orthoferrites (LnFeO 3 where, Ln = La, Sm, Gd, Dy, Er and Yb) are a class of materials having potential for various applications. These compounds and metal ion substituted ferrites crystallising in perovskite structure show promise as catalysts gas separators, cathodes in solid oxide fuel cells, sensor materials, magneto-optic materials and as spin valves. In this present work, Fe substituted in Dysprosium Oxide compounds were prepared by standard solid state reaction at a temperature of 1300℃. The structural analysis of the prepared samples was characterized with powder X-Ray Diffraction technique and the lattice parameters were calculated with PodwerX indexing software. The structural analysis reveals that the substitution of Fe in Dy 2 O 3 system leads to change of crystalline structure from Cubic to Tetragonal. Further, decreasing trend of volume of the unit cell confirms the occupation of smaller ionic radii element Fe in the Dy site of Dy 2 O 3 system. Hence the possibilities of incorporation of trivalent transition metal ion in to the host Dy 2 O 3 site were analyzed. (author)

Tetracyanidoborates with triply charged rare earth metal cations and their optical properties

International Nuclear Information System (INIS)

Hackbarth, Liisa

2015-01-01

The aim of this thesis is the description of the synthesis and characterization of a new group of tetracyanidoborates: tetracyanidoborates with trivalent rare earth metal cations. Their optical properties in the ultraviolet and visible range are also discussed. Common synthetic routes for tetracyanidoborates are adapted and applied to the preparation of the rare earth tetracyanidoborate hydrates. They are accessible with high yields and high purity through a reaction between the tetracyanidoboronic acid and rare earth hydroxides. It is shown that the rare earth tetracyanidoborates form isostructural groups, like the [LRE(H_2O)_5][B(CN)_4]_3.0.5 H_2O, where LRE"3"+ is La, Ce, Pr, Nd, Sm, Eu and Gd, the [HRE(H_2O)_7][B(CN)_4]_3 and the [HRE(H_2O)_8][B(CN)_4]_3.3 H_2O, where HRE"3"+ is Tb, Dy, Ho, Er, Tm, Yb, Lu and Y. Furthermore, the coordination number 9 is noticed to be common among the light rare earth cations, whereas the minor coordination number 8 is prevalent for the heavy rare earth cations in their tetracyanidoborates. This different construction of the coordination spheres between light and heavy rare earth cations leads to different structures depending on the energetic efficiency of the structural arrangement. Generally, the rare earth tetracyanidoborate hydrates are found to crystallize in the monoclinic crystal system. Moreover, other different crystal structures are observed depending on the crystallization temperature and the type of coordinated ligands and co-crystallized solvent molecules. The tetracyanidoborate hydrates with triply charged rare earth cations are characterized comprehensively by X-ray diffraction, vibrational spectroscopy, NMR-spectroscopy as well as by thermal analysis. Furthermore, the optical properties of some dehydrated rare earth tetracyanidoborates are investigated by UV-spectroscopy and luminescence measurements. The results of the optical measurements indicate that the tetracyanidoborates with rare earth metal cations

Double Solvent for Extracting Rare Earth Concentrate

International Nuclear Information System (INIS)

Bintarti, AN; Bambang EHB

2007-01-01

An extraction process to rare earth concentrate which contain elements were yttrium (Y), lanthanum (La), cerium (Ce), neodymium (Nd), samarium (Sm), gadolinium (Gd) and dysprosium (Dy) which were dissolved in to nitric acid has been done. The experiment of the extraction by double solvent in batch to mix 10 ml of the feed with 10 ml solvent contained the pair of solvent was TBP and TOA, D2EHPA and TOA, TBP and D2EHPA in cyclohexane as tinner. It was selected a right pairs of solvent for doing variation such as the acidity of the feed from 2 - 6 M and the time of stirring from 5 - 25 minutes gave the good relatively extraction condition to Dy element such as using 10 % volume of TOA in D2EHPA and cyclohexane, the acidity of the feed 3 M and the time stirring 15 minutes produced coefficient distribution to dysprosium = 0.586 and separation factor Dy-Ce = ∼ (unlimited); Dy-Nd = 4.651. (author)

Phase equilibria in Dy-Cu-Al system at 500 deg C

International Nuclear Information System (INIS)

Kuz'ma, Yu.B.; Milyan, V.V.

1989-01-01

Using the methods of X-ray diffraction analysis a diagram of phase equilibria in Dy-Cu-Al system at 500 deg C is plotted. Boundaries of solid solutions on the basis of DyCu 2 , DyCu and DyAl 2 compounds are determined and homogeneity regions of ternary compounds Dy 2 (Cu, Al) 7 and Dy(CuAl) 5 are ascertained. Compounds DyCuAl 3 , Dy 4 Cu 4 Al 11 and Dy 5 Cu 6 Al 9 have been detected for the first time

X ray topographic study of defects and magnetic domains in rare earth iron garnets

International Nuclear Information System (INIS)

Mathiot, Alain.

1975-11-01

X ray topographs allow simultaneous observations of crystalline defects and magnetic domain walls (except 180 deg ones). The easy magnetization directions of rare earth iron garnets are and the equilibrium texture of (110) silices is limited by a rectangular array of 71 deg and 109 deg walls. Since the anisotropy and magnetostriction of the choosen compounds (TbIG and DyIG) increase sharply when the temperature is lowered, the influence of these parameters has been studied between 300K and 4.2K. Because of the increase of spontaneous magnetization and anisotropy, the domain number increases at low temperatures and the texture becomes less sensitive to the crystal imperfections. Besides the 109 deg walls disappear almost completely from the pattern; this has been shown to be due to the respective values of the wall energies, and particularly to the influence of the K 2 anisotropy constant. The contrasts observed on the topographs increase also sharply, because of the high values of the lambda 111 coefficient of spontaneous magnetostriction at low temperatures. A splitting of the Brugg reflection peak into two, below 60K for TbIG, each part corresponding to one family of domains, allowed a direct of lambda 111 . The garnets are materials chosen to study domain walls because of the large range of the anisotropy and magnetostriction values obtained in those compounds [fr

Mechanoluminescence of Dy doped strontium aluminate nanophosphors

Energy Technology Data Exchange (ETDEWEB)

Sharma, Ravi, E-mail: rvsharma65@gmail.com [Department of Physics, Govt. Arts and Commerce Girls College, Raipur, C.G. 492001 (India); Bisen, D.P. [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G. 492010 (India); Chandra, B.P. [Department of Postgraduate Studies and Research in Physics and Electronics, Rani Durgavati University, Jabalpur 482001 (India)

2015-12-15

Nanosized strontium aluminate phosphors activated with Dy{sup 3+} were prepared by a combustion method. Nanophosphor was prepared by this method at reaction temperatures as low as 600 °C. Powder X-ray diffraction (XRD), scanning electron microscope analysis was used to characterize the prepared product. The monoclinic phase was observed in the XRD pattern. The particle size of the samples was calculated around 35 nm. The SEM images show irregular shape of the prepared nanophosphor. Two peaks were found in the mechanoluminescence (ML) response curve plotted between time and ML intensity. The H{sub 3}BO{sub 3} added strontium aluminate phosphors activated with Dy show more bright ML peak as compared to the powders of SrAl{sub 2}O{sub 4}:Dy{sup 3+} without H{sub 3}BO{sub 3.} It was found that the PL and ML intensity increases with increasing concentration of Dy, it becomes maximum for 3% of Dy. The photoluminescence emission shows two intense fluorescence transitions peaks at 498 nm and 583 nm, {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} in the blue and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} in the yellow-orange wavelength region. - Highlights: • Combustion synthesis route is used to prepare the SrAl{sub 2}O{sub 4}: Dy {sup 3+} nanophosphors. • The size of the synthesized sample was found to be in the nano-meter range. • The mechanoluminescence of SrAl{sub 2}O{sub 4}:Dy {sup 3+} nanophosphors is studied. • The photoluminescence of SrAl{sub 2}O{sub 4}: Dy {sup 3+} nanophosphors showed blue-shift as compared to bulk. • Effect of H{sub 3}BO{sub 3} on the mechanoluminescence of SrAl{sub 2}O{sub 4}:Dy{sup 3+} was studied.

Cytotoxic and genotoxic effect of the [166Dy]Dy/166Ho-EDTMP in vivo generator system in mice

International Nuclear Information System (INIS)

Pedraza-Lopez, Martha; Ferro-Flores, Guillermina; Arteaga de Murphy, Consuelo; Morales-Ramirez, Pedro; Piedras-Ross, Josefa; Murphy-Stack, Eduardo; Hernandez-Oviedo, Omar

2004-01-01

Multiple myeloma and other hematological malignancies have been treated by myeloablative radiotherapy/chemotherapy and subsequent stem cell transplantation. [ 166 Dy]Dy/ 166 Ho-ethylenediaminetetramethylene phosphonate (EDTMP) forms a stable in vivo generator system with selective skeletal uptake in mice; therefore, it could work as a potential and improved agent for marrow ablation. Induced bone marrow cytotoxicity and genotoxicity are determined by the reduction of reticulocytes (RET) and elevation of micronucleated reticulocyte (MN-RET) in peripheral blood and ablation by bone marrow histological studies. The aim of this study was to determine the bone marrow cytotoxic and genotoxic effect of the [ 166 Dy]Dy/ 166 Ho-EDTMP in vivo generator system in mice and to evaluate by histopathology its myeloablative potential. Enriched 166 Dy 2 O 3 was irradiated and [ 166 Dy]DyCl 3 was added to EDTMP in phosphate buffer (pH 8.0) in a molar ratio of 1:1.75. QC was determined by TLC. Dy-EDTMP complex was prepared the same way with nonirradiated dysprosium oxide. A group of BALB/c mice were intraperitoneally injected with the radiopharmaceutical and two groups of control animals were injected with the cold complex and with 0.9% sodium chloride, respectively. A blood sample was taken at the beginning of the experiments and every 48 h for 12 days postinjection. The animals were sacrificed, organs of interest taken out and the radioactivity determined. The femur was used for histological studies. Flow cytometry analysis was used to quantify the frequency of RET and MN-RET in the blood samples. The MCNP4B Monte Carlo computer code was used for dosimetry calculations. Radiochemical purity was 99% and the mean specific activity was 1.3 MBq/mg. The RET and MN-RET frequency were statistically different in the treatment at the end of the 12-day period demonstrating cytotoxicity and genotoxicity induced by the in vivo generator system. The histology studies show that there was

Asteroids Dynamic Site-AstDyS

Science.gov (United States)

Knezevic, Zoran; Milani, Andrea

2012-08-01

The AstDyS online information service (http://hamilton.dm.unipi.it/astdys/) contains data on numbered and multi - opposition asteroids, including orbital elements, their uncertainty, proper elements, ephemerides with uncertainty, and more. AstDyS also provides additional scientific output computed from the raw observational data. This value added currently includes: more accurate orbits computed with advanced dynamical and observational error model s; their uncertainty, as expressed by the covariance matrix formalism; ephemerides computed on request for each observer, with uncertainty; mean and proper orbital elements (for this output, AstDyS is the primary source worldwide); statistical quality control, providing a rigorous observational error model. All this is available with a sophisticated web interface, providing multiple search functions and online computations as well as complete orbital and residual files. There are several ways in which the A stDyS service could be expanded and improved in the next future, like the explicit classification of asteroids into asteroid families, the classification of resonant asteroids, and an updated self - consistent population model (to be used, e.g., for survey simulations). The IAU Division I endorsed the proposal for AstDyS to become an IAU (permanent) service, which would include the IAU supervision of the AstDyS system, keeping under control the quality of the work and the continuous update under conditions of scientific competition.

The Ras antagonist, farnesylthiosalicylic acid (FTS, decreases fibrosis and improves muscle strength in dy/dy mouse model of muscular dystrophy.

Directory of Open Access Journals (Sweden)

Yoram Nevo

Full Text Available The Ras superfamily of guanosine-triphosphate (GTP-binding proteins regulates a diverse spectrum of intracellular processes involved in inflammation and fibrosis. Farnesythiosalicylic acid (FTS is a unique and potent Ras inhibitor which decreased inflammation and fibrosis in experimentally induced liver cirrhosis and ameliorated inflammatory processes in systemic lupus erythematosus, neuritis and nephritis animal models. FTS effect on Ras expression and activity, muscle strength and fibrosis was evaluated in the dy(2J/dy(2J mouse model of merosin deficient congenital muscular dystrophy. The dy(2J/dy(2J mice had significantly increased RAS expression and activity compared with the wild type mice. FTS treatment significantly decreased RAS expression and activity. In addition, phosphorylation of ERK, a Ras downstream protein, was significantly decreased following FTS treatment in the dy(2J/dy(2J mice. Clinically, FTS treated mice showed significant improvement in hind limb muscle strength measured by electronic grip strength meter. Significant reduction of fibrosis was demonstrated in the treated group by quantitative Sirius Red staining and lower muscle collagen content. FTS effect was associated with significantly inhibition of both MMP-2 and MMP-9 activities. We conclude that active RAS inhibition by FTS was associated with attenuated fibrosis and improved muscle strength in the dy(2J/dy(2J mouse model of congenital muscular dystrophy.

Exchange interaction in the heavy rare-earth metals calculated from energy bands

International Nuclear Information System (INIS)

Lindgard, P.A.; Liu, S.H.

1973-01-01

The exchange interaction in the ordered phases was calculated and found to be significantly influenced by the magnetic perturbation of the conduction electron states. The exchange interaction is intrinsically temperature dependent and is anisotropic. The effect explains how it is possible to have a spiral phase of Tb, although spin wave measurements show no maximum in J/sub q/ for q not equal to 0. The energy difference between the ferromagnetic and spiral phases is of correct order of magnitude to be counterbalanced by the magnetoelastic energy. The wave vector dependent matrix element is found to be similar for Gd, Tb, Dy, and Er with a narrow central conduction electron contribution and a flat region. (U.S.)

Effect of rare-earth ion size on local electron structure in RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors: A positron study

Energy Technology Data Exchange (ETDEWEB)

Chen Zhenping [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China)]. E-mail: czhping@zzuli.edu.cn; Zhang Jincang [Department of Physics, Shanghai University, Shanghai 200436 (China); Su Yuling [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China); Xue Yuncai [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China); Cao Shixun [Department of Physics, Shanghai University, Shanghai 200436 (China)

2006-02-15

The effects of rare-earth ionic size on the local electron structure, lattice parameters and superconductivity have been investigated by positron annihilation technique (PAT) and related experiments for RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors. The local electron density n {sub e} is evaluated as a function of the rare-earth radius. The results show that both the bulk-lifetime {tau} {sub B} and the defect lifetime {tau} {sub 2} increase with increasing rare-earth ionic radius, while the local electron density n {sub e} decrease with increasing rare-earth ionic radius. These results prove that the changes of n {sub e}, the degree of orthorhombic distortion and the coupling between the Cu-O chains and the CuO{sub 2} planes all have an effect on the superconductivity of RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} systems.

Effect of rare earth substitution on properties of barium strontium titanate ceramic and its multiferroic composite with nickel cobalt ferrite

International Nuclear Information System (INIS)

Pahuja, Poonam; Kotnala, R.K.; Tandon, R.P.

2014-01-01

Highlights: • Rare earth ions Dy 3+ , Gd 3+ and Sm 3+ have been substituted in Ba 0.95 Sr 0.05 TiO 3 (BST). • Ni 0.8 Co 0.2 Fe 2 O 4 has been used as ferrimagnetic phase to obtain composites. • Substitution of these ions increases dielectric constant of BST and composites. • Magnetoelectric coefficient of composites increases on substitution of these ions. - Abstract: Effect of substitution of rare earth ions (Dy 3+ , Gd 3+ and Sm 3+ ) on various properties of Ba 0.95 Sr 0.05 TiO 3 (BST) i.e. the composition Ba 0.95−1.5x Sr 0.05 R x TiO 3 (where x = 0.00, 0.01, 0.02, 0.03 and R are rare earths Dy, Gd, Sm) and that of their multiferroic composite with Ni 0.8 Co 0.2 Fe 2 O 4 (NCF) has been studied. Shifting of peaks corresponding to different compositions in the X-ray diffraction pattern confirmed the substitution of rare earth ions at both Ba 2+ and Ti 4+ sites in BST. It is clear from scanning electron microscopy (SEM) images that rare earth substitution in BST increases its grain size in both pure and composite samples. Substitution of rare earth ions results in increase in value of dielectric constant of pure and composite samples. Sm substitution in BST significantly decreases its Curie temperature. Dy substituted pure and composite samples possess superior ferroelectric properties as confirmed by polarization vs electric field (P–E) loops. Composite samples containing Dy, Gd and Sm substituted BST as ferroelectric phase possess lower values of remanent and saturation magnetizations in comparison to composite sample containing pure BST as ferroelectric phase (BSTC). Rare earth substituted composite samples possess higher value of magnetoelectric coefficient as compared to that for BSTC

DTA AND MOSSBAUER STUDIES IN RARE EARTH ORTHOFERRITES

Energy Technology Data Exchange (ETDEWEB)

Eibschuetz, M.; Gorodetsky, G.; Shtrikman, S.; Treves, D.

1963-11-15

Curie temperatures of 14 different orthoferrites with the chemical formula RFeO/sub 3/ (R = Y, La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) were measured by differential thermal analysis. Hyperfine interactions of the Fe/ sup 57/ nucleus in the same materials were determined from their Mossbauer spectra. It is found that the quadrupole splitting with the exception of the case of Sm, isomer shift, Curie temperature, and internal field vary regularly with the ionic size of R. (auth)

Synthesis and photoluminescence properties of microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors

Energy Technology Data Exchange (ETDEWEB)

Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur 441111 (India); Park, K. [Faculty of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul 143-747 (Korea, Republic of); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur 440033 (India)

2014-12-25

Graphical abstract: CIE chromaticity coordinate diagram (1931) indicating different colors of Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu (a), Dy (b and c), Sm (d–f) and Pr (g and h)) phosphor under different excitation 466 nm (a), 312 nm (b), 454 nm (c), 313 nm (d), 408 nm (e), 482 nm (f), 315 nm (g) and 450 nm (h). - Highlights: • Microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid state method. • Photoluminescence properties of phosphor were investigated. • Color of the phosphor for different excitation has been verified by chromaticity diagram. • The host absorption and energy transfer were investigated. - Abstract: The novel microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid-state reaction method at 1250 °C and their photoluminescence properties were investigated. The Eu{sup 3+} and Dy{sup 3+} activated phosphors show intense red (616 nm) and yellow (574 nm) emission respectively; which indicate that the rare earth ions are substituted at non-centrosymmetric site in the host lattice. Near white (Dy{sup 3+}) and reddish-orange (Sm{sup 3+}) emissions of rare earth ions in the host lattice show strong host absorption and energy transfer from the host to activator ion. Pr{sup 3+} activated phosphor shows a series of emission peaks in the visible region with the most intense peak in the blue region at 491 and 499 nm.

High-field magnetization of rare-earth ions in scandium

DEFF Research Database (Denmark)

Roeland, L. W.; Touborg, P.

1978-01-01

The magnetic moments of Tb, Dy, or Er ions in dilute Sc single-crystal alloys have been measured in fields up to 280 × 105 A/m (350 kOe). The Zeeman energies in this high field are comparable to the total crystal-field splittings. This gives rise to characteristic features in the magnetization cu...... curves. The crystal-field parameters obtained previously from experiments in low fields and the Zeeman interaction give a satisfactory quantitative acount of the experimental results....

Magnetic field-induced elastic bending in bilayers of Tb{sub 1−x}Dy{sub x}Fe{sub 2−y} and Pb(Zr{sub 1−z}Ti{sub z})O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Jin, Tao; Qichao, Wu; Ning, Zhang, E-mail: zhangning@njnu.edu.cn

2014-09-01

Magnetic field-induced strain in the magnetoelectric bilayers of Tb{sub 1−x}Dy{sub x}Fe{sub 2−y} and Pb(Zr{sub 1−z}Ti{sub z})O{sub 3} was studied. A butterfly shaped strain curve was observed on the surface of Pb(Zr{sub 1−z}Ti{sub z})O{sub 3}. The shape of the strain curve was found to be related to the sample thickness and the volume fraction occupied by the ferroelectrics in the bilayer. Theoretical analysis and experimental results showed that magnetoelastic bending in the bilayer composites was largely responsible for the butterfly strain curve. - Highlights: • Butterfly strain curves were observed on the PZT surface for bilayers of TDF and PZT. • The strain curve is related to the sample thickness and the volume fraction of the PZT. • A physics model depicting the field-controlled bending of the bilayers was developed. • The magnetoelastic bending was found to account for the butterfly strain curve.

The Dy–Ni–Si system as a representative of the rare earth–Ni–Si family: Its isothermal section and new rare-earth nickel silicides

Energy Technology Data Exchange (ETDEWEB)

Yuan, Fang; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada); Morozkin, A.V., E-mail: morozkin@general.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, Moscow GSP-2, 119992 (Russian Federation); Knotko, A.V. [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, Moscow GSP-2, 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Geological Faculty, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Pani, M.; Provino, A.; Manfrinetti, P. [Institute SPIN-CNR and Dipartimento di Chimica e Chimica Industriale, Università di Genova, Via Dodecaneso 31, 16146 Genova (Italy)

2014-11-15

}Si{sub 24}, ∼Dy{sub 16}Ni{sub 62}Si{sub 22}, DyNi{sub 7}Si{sub 6}, Dy{sub 3}Ni{sub 8}Si, DyNi{sub 2}Si, ∼Dy{sub 40}Ni{sub 47}Si{sub 13} and ∼Dy{sub 5}Ni{sub 2}Si{sub 3}. Quasi–binary solid solutions were detected for Dy{sub 2}Ni{sub 17}, DyNi{sub 5}, DyNi{sub 7}, DyNi{sub 3}, DyNi{sub 2}, DyNi, DySi{sub 2} and DySi{sub 1.67}. The crystal structures and magnetic properties of new phases RNi{sub 7}Si{sub 6} (GdNi{sub 7}Si{sub 6}-type), R{sub 3}Ni{sub 8}Si (Ce{sub 3}Co{sub 8}Si-type), RNi{sub 2}Si (YPd{sub 2}Si-type) and R{sub 3}Ni{sub 12}Si{sub 4} (Gd{sub 3}Ru{sub 4}Al{sub 12}-type), with R=Y, Gd–Tm, are also reported. - Highlights: • Dy–Ni–Si isothermal section was obtained at 870 K/1070 K. • Twelve known ternary dysprosium nickel silicides were confirmed in Dy–Ni–Si. • Nine new dysprosium nickel silicides were detected in Dy–Ni–Si. • Seventeen new rare earth nickel silicides were detected in (Y, Gd–Tm)–Ni–Si. • Tb{sub 3}Ni{sub 8}Si, Dy{sub 3}Ni{sub 8}Si, Ho{sub 3}Ni{sub 12}Si{sub 4} and DyNi{sub 2}Si show ferromagnetic-like ordering.

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Abstract. Elastic moduli (, ), Poisson's ratio (), microhardness () and some thermodynamical parameters such as Debye temperature (), diffusion constant (), latent heat of melting ( ) etc of PbO–Al2O3–B2O3 glasses doped with rare earth ions viz. Pr3+, Nd3+, Sm3+, Eu3+, Tb3+, Dy3+, Ho3+, Er3+ and Yb3+, ...

NdFeB Residue to Be Recycled

Institute of Scientific and Technical Information of China (English)

无

2006-01-01

@@ NdFeB is a permanent magnetic material with excellent performances. It is widely used in electronics and communications. Around 30% of rare earth elements (among which 90% is Nd, others are Tb and Dy) and 2-3% of Co element are contained in the material. NdFeB plays an important role in the development of our society and our economy.

Raman scattering of rare earth hexaborides

International Nuclear Information System (INIS)

Ogita, Norio; Hasegawa, Takumi; Udagawa, Masayuki; Iga, Fumitoshi; Kunii, Satoru

2009-01-01

Raman scattering spectra were measured for the rare-earth hexaborides RB 6 (R = Ce, Gd, or Dy). All Raman-active phonons due to B 6 vibrations were observed in the range 600 - 1400 cm -1 . Anomalous peaks were detected below 200 cm -1 , which correspond to vibrations of rare-earth ion excited by second-order Raman scattering process. The intensity and energy of the rare-earth mode decrease with decreasing temperature. This suggests that the rare-earth ion vibrates in a shallow and anharmonic potential due to the boron cage. Using the reported values of mean square displacement of rare-earth ion, we estimated the anharmonic contribution for the rare-earth vibrations.

Superdeformation studies in {sup 150}Tb and {sup 153}Ho

Energy Technology Data Exchange (ETDEWEB)

Nisius, D.; Janssens, R.V.F.; Crowell, B. [and others

1995-08-01

There are now over 40 superdeformed (SD) bands known in the A {approximately} 150 region and in most cases the properties of these bands are understood in terms of single-particle excitations in the absence of pairing. By continuing the search for new SD bands we hope to gain insight into (1) the ordering of the proton and neutron orbitals near the Fermi surface in the SD well, (2) the effects that the alignment of those orbitals has on the moments of inertia, and (3) the collective excitations in the SD well. For {sup 150}Tb, which is one proton and one neutron away from the SD doubly-magic nucleus {sup 152}Dy, it should be possible to study SD bands based on both proton and neutron hole excitations. By adding one proton to the {sup 152}Dy nucleus (i.e. {sup 153}Ho) proton excitations above the Z = 66 shell gap can be studied. These excitations are important as calculations suggested that the proton intruder orbital N = 7 might become occupied. Interactions between this orbital and a N = 5 level may result in softness towards octupole vibrations. High spin states in {sup 150}Th and {sup 153}Ho were populated using the {sup 124}Sn({sup 31}P,5n) and {sup 120}Sn({sup 37}Cl,4n) reactions, respectively. In both cases the early implementation phase of Gammasphere was used to detect the decay gamma rays and over 1 x 10{sup 9} triple and higher fold coincidence events were recorded. In {sup 150}Tb, the data analysis is complete and two new SD bands were identified. The fact that Im{sup (2)} moments of inertia are sensitive to the specific high-N intruder content of the SD bands was used to suggest configurations for the two new bands. A paper reporting these results is being prepared. For {sup 153}Ho, data analysis is still in its early stages.

Thermoelectric properties, crystal and electronic structure of semiconducting RECuSe2 (RE = Pr, Sm, Gd, Dy and Er)

International Nuclear Information System (INIS)

Esmaeili, Mehdi; Tseng, Yu-Chih; Mozharivskyj, Yurij

2014-01-01

Highlights: • Crystal and electronic structure of monoclinic and trigonal RECuSe 2 phases. • Thermoelectric properties of the RECuSe 2 phases. • Temperature stability of the RECuSe 2 phases. - Abstract: The ternary RECuSe 2 phases have been prepared and structurally characterized. They adopt either a monoclinic structure (P2 1 /c, z = 4) for lighter rare earths (RE = Pr, Sm and Gd) or Cu-disordered trigonal structure for heavier rare-earths (P3 ¯ m1, z = 1, RE = Dy and Er). The resistivity and Seebeck coefficient measurements on GdCuSe 2 , DyCuSe 2 and ErCuSe 2 indicate that the studied phases are p-type semiconductors with relatively small activation energies (0.045–0.11 eV). However, their electrical resistivities are too high (0.45–220 Ω cm at room temperature) to make them competitive thermoelectric materials. Electronic structure calculations indicate presence of a band gap in the RECuSe 2 phases

Genotoxic and cytotoxic damage by the therapeutic radiopharmaceutical [{sup 166}Dy]Dy/{sup 166}Ho-EDTMP as in vivo generator system; Dano genotoxico y citotoxico por el radiofarmaco terpeutico [{sup 166}Dy]Dy/{sup 166}Ho-EDTMP como sistema de generador in vivo

Energy Technology Data Exchange (ETDEWEB)

Pedraza L, M; Piedras R, J [Instituto Nacional de Ciencias Medicas y Nutricion, Salvador Zubiran. Vasco. de Quiroga 15, 14000 Mexico D.F. (Mexico); Ferro F, G; Morales R, P [ININ, Km. 36.5 Carretera Mexico-Toluca, Ocoyoacac, 52045 Estado de Mexico (Mexico); Murphy S, E [Hospital Santaelena, Mexico D.F. (Mexico); Hernandez O, O [Escuela Superior de Fisica y Matematicas, IPN, Mexico D.F. (Mexico)

2005-07-01

In patients with leukemias and multiple myeloma, the cure can be obtained to inclination of a bone marrow transplant (m.o.), for that which one is used a combination of external radiotherapy and chemotherapy with the consequent toxicity to healthy organs. The complex [{sup 166}Dy]Dy/{sup 166}Ho-ethylenediaminetetramethylenephosphonate ([{sup 166}Dy]Dy/{sup 166}Ho-EDTMP) it forms a generator system in vivo stable with bony selective likeness in mice therefore, this it could work as a therapeutic radiopharmaceutical for bone marrow ablation. The objective of this original work was to determine the genotoxic and cytotoxic damage produced by the [{sup 166}Dy]Dy/{sup 166}Ho-EDTMP like a generator system in vivo by means of the reticulocytes reduction (RET) and micronucleus elevation in reticulocytes (RET-MN) in peripheral blood and to evaluate its myeloablative potential for histopathologic studies. It was irradiated {sup 166}Dy{sub 2}O{sub 3} enriched and it was add in form {sup 166}DyCI{sub 3} to the EDTMP in a softening media of phosphates (pH 8), the optimal molar relationship {sup 166}Dy: EDTMP was 1.7:1 and the radiochemical purity was evaluated by ITLC. The Dy:EDTMP complexes, non radioactive, its were prepared in the same way with non irradiated dysprosium oxide. A group of BALB/c mice was injected intraperitoneally with the radiopharmaceutical and two groups of control mice were injected with the non radioactive complex and with sodium chloride 0.9% respectively. Before injecting each one of the solutions it was take a basal sample of peripheral blood of the mouse tail and each 48 h post-injection during 12 d. The animals were sacrificed to obtain the organs of interest and to determine the radioactivity in each one. The femur was used for the histopathologic studies. The quantification of the frequency of RET and RET-MN was carried out by flow cytometry of the sanguine samples and the Monte Carlo code MCNP4B for the dosimetry calculations was used. The

Synthesis, characterization and thermal decomposition of tetramethylammonium rare earth double selenates

Science.gov (United States)

Divekar, Sandesh K.; Achary, S. Nagabhusan; Ajgaonkar, Vishnu R.

2018-06-01

A series of double selenates, as (CH3)4NLn(SeO4)2rad 4H2O (Ln = Rare earth ion like La, Pr, Nd, Sm, Gd, Tb, Dy) was crystallized from mixed solution and characterized in detail for their structure, vibrational and optical properties as well as thermal stabilities. The crystal structure of the praseodymium compound was obtained by single crystal X-ray diffraction (XRD) and revealed a monoclinic (C2/c) lattice with chains formed by PrO8 and SeO4 units. The chains with compositions [Pr(SeO4)4(H2O)4]- are stacked in three dimensions and the (CH3)4N+ ions located in between them provide charge neutrality to the structure. The characterization of other compounds were carried out from powder XRD data and revealed that they all are isostructural to Pr-compound. All the functional groups were identified by Raman and IR spectroscopic studies. Solid state 77Se NMR revealed noticeable changes in selenium environment in these compounds. The optical absorption studies on the compounds show strong band edge absorptions in UV region. Thermal stabilities of the compounds, as investigated by simultaneous TG-DTA techniques indicate their sequential decompositions due to loss of H2O, (CH3)4N+ group, SeO2 and finally leaving their corresponding rare earth oxides.

TB Terms

Science.gov (United States)

... sputum can also be used to do a culture. TB blood test – a test that uses a blood sample to find out if you are infected with TB bacteria. The test measures the response to TB proteins when they are mixed with a small amount of blood. Examples of these TB blood tests include QuantiFERON ® -TB ...

Magnetic properties of the ternary carbide DyCoC2 studied by magnetization measurements, neutron diffraction and 161Dy Moessbauer spectroscopy

International Nuclear Information System (INIS)

Amanai, H.; Onodera, H.; Ohashi, M.; Matsuo, S.; Yamauchi, H.

1995-01-01

The magnetic properties of DyCoC 2 have been investigated by means of magnetization measurements, powder neutron diffraction and 161 Dy Moessbauer spectroscopy. The magnetization versus temperature curves of a single-crystalline sample reveal that the magnetic structure of DyCoC 2 is a simple collinear ferromagnetic one below T C =10.0 K. At 4.2 K, the magnitude of the Dy moment is 8.7(1)μ B , whose direction is defined by an angle of 38.0(5) from the a-axis toward the c-axis. The magnetic structure and the magnitude of the moment are also confirmed by the results of powder neutron diffraction experiments and 161 Dy Moessbauer spectroscopy, respectively. ((orig.))

Genotoxic and cytotoxic damage by the therapeutic radiopharmaceutical [166Dy]Dy/166Ho-EDTMP as in vivo generator system

International Nuclear Information System (INIS)

Pedraza L, M.; Piedras R, J.; Ferro F, G.; Morales R, P.; Murphy S, E.; Hernandez O, O.

2005-01-01

In patients with leukemias and multiple myeloma, the cure can be obtained to inclination of a bone marrow transplant (m.o.), for that which one is used a combination of external radiotherapy and chemotherapy with the consequent toxicity to healthy organs. The complex [ 166 Dy]Dy/ 166 Ho-ethylenediaminetetramethylenephosphonate ([ 166 Dy]Dy/ 166 Ho-EDTMP) it forms a generator system in vivo stable with bony selective likeness in mice therefore, this it could work as a therapeutic radiopharmaceutical for bone marrow ablation. The objective of this original work was to determine the genotoxic and cytotoxic damage produced by the [ 166 Dy]Dy/ 166 Ho-EDTMP like a generator system in vivo by means of the reticulocytes reduction (RET) and micronucleus elevation in reticulocytes (RET-MN) in peripheral blood and to evaluate its myeloablative potential for histopathologic studies. It was irradiated 166 Dy 2 O 3 enriched and it was add in form 166 DyCI 3 to the EDTMP in a softening media of phosphates (pH 8), the optimal molar relationship 166 Dy: EDTMP was 1.7:1 and the radiochemical purity was evaluated by ITLC. The Dy:EDTMP complexes, non radioactive, its were prepared in the same way with non irradiated dysprosium oxide. A group of BALB/c mice was injected intraperitoneally with the radiopharmaceutical and two groups of control mice were injected with the non radioactive complex and with sodium chloride 0.9% respectively. Before injecting each one of the solutions it was take a basal sample of peripheral blood of the mouse tail and each 48 h post-injection during 12 d. The animals were sacrificed to obtain the organs of interest and to determine the radioactivity in each one. The femur was used for the histopathologic studies. The quantification of the frequency of RET and RET-MN was carried out by flow cytometry of the sanguine samples and the Monte Carlo code MCNP4B for the dosimetry calculations was used. The radiochemical purity was 99% and in average the specific

Mobility of rare earth element in hydrothermal process and weathering product: a review

Science.gov (United States)

Lintjewas, L.; Setiawan, I.

2018-02-01

The Rare Earth Element (REE), consists of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Lu, Ho, Er, Tm, Yb, are important elements to be used as raw materials of advanced technology such as semiconductors, magnets, and lasers. The research of REE in Indonesia has not been done. Several researches were conducted on granitic rocks and weathering product such as Bangka, Sibolga, West Kalimantan, West Sulawesi and Papua. REE can be formed by hydrothermal processes such as Bayan Obo, South China. The REE study on active hydrothermal system (geothermal) in this case also has the potential to produce mineral deposits. The purpose of this review paper is to know the mobility of REE on hydrothermal process and weathering products. Mobility of REE in the hydrothermal process can change the distribution patterns and REE content such as Ce, Eu, La, Lu, Nd, Sm, and Y. Another process besides the hydrothermal is weathering process. REE mobility is influenced by weathering products, where the REE will experience residual and secondary enrichment processes in heavier minerals.

Magnetic nanosized rare earth iron garnets R_3Fe_5O_1_2: Sol–gel fabrication, characterization and reinspection

International Nuclear Information System (INIS)

Opuchovic, Olga; Kareiva, Aivaras; Mazeika, Kestutis; Baltrunas, Dalis

2017-01-01

The magnetic nanosized rare earth iron garnets (R_3Fe_5O_1_2, where R=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) were prepared by an aqueous sol–gel method. Herein we present, that all these garnets can be obtained by this effective synthesis method simply by changing the temperature of the final annealing. It was also demonstrated, that a different annealing temperature leads to a different particle size distribution of the final product. The SEM analysis results revealed that the smallest particles were formed in the range of 75–130 nm. The phase purity and structure of the rare earth iron garnets were estimated using XRD analysis and Mössbauer spectroscopy. Magnetic properties were determined by magnetization measurements. The relation between the particle size, composition and magnetic properties of the sol-gel derived garnets were also discussed in this study. - Highlights: • First time series of R_3Fe_5O_1_2 (R=from Sm to Lu) are prepared by sol–gel process. • Different sintering temperature leads to the different particle size distribution. • Correlation between microstructure, composition and magnetic properties is shown.

Syntheses, structures, and magnetic properties of a family of heterometallic heptanuclear [Cu5Ln2] (Ln = Y(III), Lu(III), Dy(III), Ho(III), Er(III), and Yb(III)) complexes: observation of SMM behavior for the Dy(III) and Ho(III) analogues.

Science.gov (United States)

Chandrasekhar, Vadapalli; Dey, Atanu; Das, Sourav; Rouzières, Mathieu; Clérac, Rodolphe

2013-03-04

Sequential reaction of the multisite coordination ligand (LH3) with Cu(OAc)2·H2O, followed by the addition of a rare-earth(III) nitrate salt in the presence of triethylamine, afforded a series of heterometallic heptanuclear complexes containing a [Cu5Ln2] core {Ln = Y(1), Lu(2), Dy(3), Ho(4), Er(5), and Yb(6)}. Single-crystal X-ray crystallography reveals that all the complexes are dicationic species that crystallize with two nitrate anions to compensate the charge. The heptanuclear aggregates in 1-6 are centrosymmetrical complexes, with a hexagonal-like arrangement of six peripheral metal ions (two rare-earth and four copper) around a central Cu(II) situated on a crystallographic inversion center. An all-oxygen environment is found to be present around the rare-earth metal ions, which adopt a distorted square-antiprismatic geometry. Three different Cu(II) sites are present in the heptanuclear complexes: two possess a distorted octahedral coordination sphere while the remaining one displays a distorted square-pyramidal geometry. Detailed static and dynamic magnetic properties of all the complexes have been studied and revealed the single-molecule magnet behavior of the Dy(III) and Ho(III) derivatives.

Faraday effect in γ-Dy2S3 and c-Dy2O3 paramagnetic crystals

International Nuclear Information System (INIS)

Shelykh, A.I.

1987-01-01

Studies of spectral and temperature dependences of Faraday effect in γ-Dy 2 S 3 and C-Dy 2 O 3 paramagnetic crystals are conducted. Paramagnetism of these crystals is brought about by Dy 3+ ions. Estimation of the effect of such factors as the value of paramagnetic ion concentration, width of the forbidden band, crystallochemical composition on magnetooptical effect in the considered compounds of dysprosium is carried out on the basis of the obtained experimental data and theoretical analysis. It is shown, that the Faraday effect in the considered compounds of dysprosium as well as the value of paramagnetic moment may be regarded rather accurately in free ion approximation

Room-temperature ferromagnetism in Dy films doped with Ni

International Nuclear Information System (INIS)

Edelman, I.; Ovchinnikov, S.; Markov, V.; Kosyrev, N.; Seredkin, V.; Khudjakov, A.; Bondarenko, G.; Kesler, V.

2008-01-01

Temperature, magnetic field and spectral dependences of magneto-optical effects (MOEs) in bi-layer films Dy (1-x) Ni x -Ni and Dy (1-x) (NiFe) x -NiFe were investigated, x changes from 0 to 0.06. Peculiar behavior of the MOEs was revealed at temperatures essentially exceeding the Curie temperature of bulk Dy which is explained by the magnetic ordering of the Dy layer containing Ni under the action of two factors: Ni impurities distributed homogeneously over the whole Dy layer and atomic contact of this layer with continues Ni layer. The mechanism of the magnetic ordering is suggested to be associated with the change of the density of states of the alloy Dy (1-x) Ni x owing to hybridization with narrow peaks near the Fermi level character for Ni

Rare earths refining by vacuum sublimation method

International Nuclear Information System (INIS)

Rytus, N.N.

1983-01-01

The process of rare earths refining by the sUblimation; method in high and superhigh oil-free vacuum, is investigated. The method is effective for rare earths obtaining and permits to prepare metal samples with a high value of electric resistance ratio γ=RsUb(298 K)/Rsub(4.2 K). The estimation of general purity is performed for Sm, Eu, Yb, Tm, Dy, Ho, Er and Se

DySectAPI: Scalable Prescriptive Debugging

DEFF Research Database (Denmark)

Jensen, Nicklas Bo; Karlsson, Sven; Quarfot Nielsen, Niklas

We present the DySectAPI, a tool that allow users to construct probe trees for automatic, event-driven debugging at scale. The traditional, interactive debugging model, whereby users manually step through and inspect their application, does not scale well even for current supercomputers. While...... lightweight debugging models scale well, they can currently only debug a subset of bug classes. DySectAPI fills the gap between these two approaches with a novel user-guided approach. Using both experimental results and analytical modeling we show how DySectAPI scales and can run with a low overhead...

Effect of Ligand Substitution around the Dy(III) on the SMM Properties of Dual-Luminescent Zn-Dy and Zn-Dy-Zn Complexes with Large Anisotropy Energy Barriers: A Combined Theoretical and Experimental Magnetostructural Study.

Science.gov (United States)

Costes, Jean Pierre; Titos-Padilla, Silvia; Oyarzabal, Itziar; Gupta, Tulika; Duhayon, Carine; Rajaraman, Gopalan; Colacio, Enrique

2016-05-02

The new dinuclear Zn(II)-Dy(III) and trinuclear Zn(II)-Dy(III)-Zn(II) complexes of formula [(LZnBrDy(ovan) (NO3)(H2O)](H2O)·0.5(MeOH) (1) and [(L(1)ZnBr)2Dy(MeOH)2](ClO4) (3) (L and L(1) are the dideprotonated forms of the N,N'-2,2-dimethylpropylenedi(3-methoxysalicylideneiminato and 2-{(E)-[(3-{[(2E,3E)-3-(hydroxyimino)butan-2-ylidene ]amino}-2,2-dimethylpropyl)imino]methyl}-6-methoxyphenol Schiff base compartmental ligands, respectively) have been prepared and magnetostructurally characterized. The X-ray structure of 1 indicates that the Dy(III) ion exhibits a DyO9 coordination sphere, which is made from four O atoms coming from the compartmental ligand (two methoxy terminal groups and two phenoxido bridging groups connecting Zn(II) and Dy(III) ions), other four atoms belonging to the chelating nitrato and ovanillin ligands, and the last one coming to the coordinated water molecule. The structure of 3 shows the central Dy(III) ion surrounded by two L(1)Zn units, so that the Dy(III) and Zn(II) ions are linked by phenoxido/oximato bridging groups. The Dy ion is eight-coordinated by the six O atoms afforded by two L(1) ligands and two O atoms coming from two methanol molecules. Alternating current (AC) dynamic magnetic measurements of 1, 3, and the previously reported dinuclear [LZnClDy(thd)2] (2) complex (where thd = 2,2,6,6-tetramethyl-3,5-heptanedionato ligand) indicate single molecule magnet (SMM) behavior for all these complexes with large thermal energy barriers for the reversal of the magnetization and butterfly-shaped hysteresis loops at 2 K. Ab initio calculations on 1-3 show a pure Ising ground state for all of them, which induces almost completely suppressed quantum tunnelling magnetization (QTM), and thermally assisted quantum tunnelling magnetization (TA-QTM) relaxations via the first excited Kramers doublet, leading to large energy barriers, thus supporting the observation of SMM behavior. The comparison between the experimental and theoretical

Synthesis, structure and magnetic properties of DyAl2 nanoparticles

International Nuclear Information System (INIS)

Zhang, W.S.; Brueck, E.; Zhang, Z.D.; Tegus, O.; Li, W.F.; Si, P.Z.; Geng, D.Y.; Klaasse, J.C.P.; Buschow, K.H.J.

2006-01-01

DyAl 2 nanoparticles have been prepared by means of arc discharge in a mixture of argon and hydrogen gas. The structure of DyAl 2 nanoparticles is studied by means of X-ray diffraction, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy. X-ray photoelectron spectroscopy shows that the as-prepared DyAl 2 nanoparticles are coated with a layer of Al 2 O 3 phase on the surface, and their sizes vary from 20 nm to about 100 nm. The DyAl 2 nanoparticles exhibit ferromagnetic properties that are different from bulk DyAl 2 compound. The gradual decrease of the magnetization with increasing temperature in a wide temperature range reveals the size distribution of the DyAl 2 nanoparticles. The magnetic-entropy changes are derived from the isothermal magnetization curves measured at different temperatures. The magnetic-entropy change of the DyAl 2 nanoparticles is lower than that of the bulk DyAl 2 material but has a broadened peak

Search for superdeformed bands in {sup 154}Dy

Energy Technology Data Exchange (ETDEWEB)

Nisius, D.; Janssens, R.V.F.; Khoo, T.L. [and others

1995-08-01

The island of superdeformation in the vicinity of the doubly magic {sup 152}Dy yrast superdeformed (SD) band is thought to be well understood in the framework of cranked mean field calculations. In particular, the calculations suggested that in {sup 154}Dy there should be no yrast or near yrast SD minimum in the 40-60 h spin range, where SD bands in this mass region are thought to be {sup 153}Dy nucleus, it is populated. However, with the presence of five SD bands in the neighboring necessary to ascertain if the addition of one single neutron diminishes the importance of shell effects to the extent that superdeformation can no longer be sustained. In an experiment utilizing the increased resolving power of the early implementation phase of Gammasphere, the reaction {sup 122}Sn({sup 36}S,4n) at 165 MeV was employed to populate high spin states in {sup 154}Dy. In a four-day run with 36 detectors, over one billion triple and higher fold coincidence events were recorded. One new SD band was identified and was assigned to {sup 154}Dy. From comparisons with the Im{sup (2)} moments of inertia of the SD bands in {sup 152}Dy and {sup 153}Dy, a configuration based on (514)9/2{sup 2} neutrons coupled to the {sup 152}Dy SD core was proposed. One unexpected and as yet unexplained feature of this new SD band is that the transition energies are almost identical to those of an excited SD band in {sup 153}Dy. It is also worth noting that the feeding of the yrast states is similar to that achieved by the deexcitation from the ensemble of all entry states in the reaction. This observation emphasizes the statistical nature of the decay-out process. A paper reporting these results was accepted for publication.

Energy transfer mechanism between Ce and Tb ions in sol–gel synthesized YSO crystals

International Nuclear Information System (INIS)

Chiriu, Daniele; Stagi, Luigi; Carbonaro, Carlo Maria; Corpino, Riccardo; Ricci, Pier Carlo

2016-01-01

The luminescence properties of Tb and Ce in Rare Earth Doped crystalline oxides largely depend on their relative concentrations: by increasing the dopant concentration, the luminescence profile changes from blue to green because of the energy transfer among centers. The kinetic properties of the luminescence of optically excited Terbium–Cerium co-doped Y_2SiO_5 sol–gel synthesized crystal powders have been investigated as a function of the Tb dopant concentration (Ce content fixed at 1% atomic). The interaction among different Tb emitting centers and their relation with Ce centers was explained within the Inokuti-Hirayama model for a dipole–dipole energy transfer mechanism in the low-middle Tb concentration range whilst the Forster–Dexter model was applied in the middle-high Tb concentration range. The kinetic model allows elucidating the role of sensitizer and activator ion as a function of Tb concentration, successfully estimating the energy transfer mechanism efficiency and calculating the critical Tb concentration. - Highlights: • The kinetic properties of Ce, Tb recombination in YSO matrix were studied. • The Inokuti-Hirayama and Forster–Dexter models were applied. • At high Tb content, the Ce to Tb energy transfer acts through the dipole−quadrupole. • At low Tb content, the Ce to Tb energy transfer acts through the dipole−dipole. • The presence of Ce reduces the critical Tb concentration (at low Tb content).

Energy transfer mechanism between Ce and Tb ions in sol–gel synthesized YSO crystals

Energy Technology Data Exchange (ETDEWEB)

Chiriu, Daniele; Stagi, Luigi; Carbonaro, Carlo Maria; Corpino, Riccardo; Ricci, Pier Carlo, E-mail: carlo.ricci@dsf.unica.it

2016-03-01

The luminescence properties of Tb and Ce in Rare Earth Doped crystalline oxides largely depend on their relative concentrations: by increasing the dopant concentration, the luminescence profile changes from blue to green because of the energy transfer among centers. The kinetic properties of the luminescence of optically excited Terbium–Cerium co-doped Y{sub 2}SiO{sub 5} sol–gel synthesized crystal powders have been investigated as a function of the Tb dopant concentration (Ce content fixed at 1% atomic). The interaction among different Tb emitting centers and their relation with Ce centers was explained within the Inokuti-Hirayama model for a dipole–dipole energy transfer mechanism in the low-middle Tb concentration range whilst the Forster–Dexter model was applied in the middle-high Tb concentration range. The kinetic model allows elucidating the role of sensitizer and activator ion as a function of Tb concentration, successfully estimating the energy transfer mechanism efficiency and calculating the critical Tb concentration. - Highlights: • The kinetic properties of Ce, Tb recombination in YSO matrix were studied. • The Inokuti-Hirayama and Forster–Dexter models were applied. • At high Tb content, the Ce to Tb energy transfer acts through the dipole−quadrupole. • At low Tb content, the Ce to Tb energy transfer acts through the dipole−dipole. • The presence of Ce reduces the critical Tb concentration (at low Tb content).

IUPAC-NIST Solubility Data Series. 100. Rare Earth Metal Fluorides in Water and Aqueous Systems. Part 3. Heavy Lanthanides (Gd–Lu)

Energy Technology Data Exchange (ETDEWEB)

Mioduski, Tomasz [Institute of Nuclear Chemistry and Technology, 03195 Warszawa (Poland); Gumiński, Cezary, E-mail: cegie@chem.uw.edu.pl [Department of Chemistry, University of Warsaw, 02093 Warszawa (Poland); Zeng, Dewen, E-mail: dewen-zeng@hotmail.com [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

2015-06-15

This is the third part of the volume devoted to solubility data for the rare earth metal (REM) fluorides in water and in aqueous ternary and multicomponent systems. It covers experimental results of trivalent fluorides of Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu (so-called heavy lanthanides), since no quantitative data on solubilities of TbF{sub 4} and YbF{sub 2} (the most stable compounds at these valencies) are available. The related literature has been covered through the end of 2014. Compilations of all available papers with the solubility data are introduced for each REM fluoride with a corresponding critical evaluation. Every such assessment contains a collection of all solubility results in aqueous solution, a selection of suggested solubility data, a solubility equation, and a brief discussion of the multicomponent systems. Only simple fluorides (no complexes or double salts) are treated as the input substances in this report. General features of the systems, such as nature of the equilibrium solid phases, solubility as a function of temperature, influence of ionic strength, solution pH, mixed solvent medium on the solubility, quality of the solubility results, and the solubility as a function of REM atomic number, have already been presented in Part 1 of the volume.

Room-temperature ferromagnetism in Dy films doped with Ni

Energy Technology Data Exchange (ETDEWEB)

Edelman, I. [Kirensky Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036 (Russian Federation)], E-mail: ise@iph.krasn.ru; Ovchinnikov, S. [Kirensky Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036 (Russian Federation); Siberian Federal University, Av. Svobodnyi 71, Krasnoyarsk 660074 (Russian Federation); Markov, V.; Kosyrev, N.; Seredkin, V.; Khudjakov, A.; Bondarenko, G. [Kirensky Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036 (Russian Federation); Kesler, V. [Institute of Semiconductor Physics, Siberian Division, Russian Academy of Sciences, Av. Akademika Lavrent' eva 13, Novosibirsk 630090 (Russian Federation)

2008-09-01

Temperature, magnetic field and spectral dependences of magneto-optical effects (MOEs) in bi-layer films Dy{sub (1-x)}Ni{sub x}-Ni and Dy{sub (1-x)}(NiFe){sub x}-NiFe were investigated, x changes from 0 to 0.06. Peculiar behavior of the MOEs was revealed at temperatures essentially exceeding the Curie temperature of bulk Dy which is explained by the magnetic ordering of the Dy layer containing Ni under the action of two factors: Ni impurities distributed homogeneously over the whole Dy layer and atomic contact of this layer with continues Ni layer. The mechanism of the magnetic ordering is suggested to be associated with the change of the density of states of the alloy Dy{sub (1-x)}Ni{sub x} owing to hybridization with narrow peaks near the Fermi level character for Ni.

Determination of the Earth's pole tide Love number k2 from observations of polar motion using an adaptive Kalman filter approach

Science.gov (United States)

Seitz, F.; Kirschner, S.; Neubersch, D.

2012-09-01

The geophysical interpretation of observed time series of Earth rotation parameters (ERP) is commonly based on numerical models that describe and balance variations of angular momentum in various subsystems of the Earth. Naturally, models are dependent on geometrical, rheological and physical parameters. Many of these are weakly determined from other models or observations. In our study we present an adaptive Kalman filter approach for the improvement of parameters of the dynamic Earth system model DyMEG which acts as a simulator of ERP. In particular we focus on the improvement of the pole tide Love number k2. In the frame of a sensitivity analysis k2 has been identified as one of the most crucial parameters of DyMEG since it directly influences the modeled Chandler oscillation. At the same time k2 is one of the most uncertain parameters in the model. Our simulations with DyMEG cover a period of 60 years after which a steady state of k2 is reached. The estimate for k2, accounting for the anelastic response of the Earth's mantle and the ocean, is 0.3531 + 0.0030i. We demonstrate that the application of the improved parameter k2 in DyMEG leads to significantly better results for polar motion than the original value taken from the Conventions of the International Earth Rotation and Reference Systems Service (IERS).

Heightened vulnerability to MDR-TB epidemics after controlling drug-susceptible TB.

Directory of Open Access Journals (Sweden)

Jason D Bishai

2010-09-01

Full Text Available Prior infection with one strain TB has been linked with diminished likelihood of re-infection by a new strain. This paper attempts to determine the role of declining prevalence of drug-susceptible TB in enabling future epidemics of MDR-TB.A computer simulation of MDR-TB epidemics was developed using an agent-based model platform programmed in NetLogo (See http://mdr.tbtools.org/. Eighty-one scenarios were created, varying levels of treatment quality, diagnostic accuracy, microbial fitness cost, and the degree of immunogenicity elicited by drug-susceptible TB. Outcome measures were the number of independent MDR-TB cases per trial and the proportion of trials resulting in MDR-TB epidemics for a 500 year period after drug therapy for TB is introduced.MDR-TB epidemics propagated more extensively after TB prevalence had fallen. At a case detection rate of 75%, improving therapeutic compliance from 50% to 75% can reduce the probability of an epidemic from 45% to 15%. Paradoxically, improving the case-detection rate from 50% to 75% when compliance with DOT is constant at 75% increases the probability of MDR-TB epidemics from 3% to 45%.The ability of MDR-TB to spread depends on the prevalence of drug-susceptible TB. Immunologic protection conferred by exposure to drug-susceptible TB can be a crucial factor that prevents MDR-TB epidemics when TB treatment is poor. Any single population that successfully reduces its burden of drug-susceptible TB will have reduced herd immunity to externally or internally introduced strains of MDR-TB and can experience heightened vulnerability to an epidemic. Since countries with good TB control may be more vulnerable, their self interest dictates greater promotion of case detection and DOTS implementation in countries with poor control to control their risk of MDR-TB.

Measurement of 160Tb and 161Tb in nuclear forensics samples

International Nuclear Information System (INIS)

Jiang, J.; Davies, A.V.; Britton, R.E.

2017-01-01

160 Tb and 161 Tb are important radionuclides to measure when analysing a Nuclear Forensics sample. An analytical method for the measurement of both 160 Tb and 161 Tb was developed in this study. Terbium was separated and purified using exchange resin and TrisKem LN Resin. The purified fraction containing 160 Tb and 161 Tb was measured by gamma spectrometry and liquid scintillation counting. The counting efficiencies of 160 Tb and 161 Tb were determined using the CIEMAT/NIST efficiency tracing method. The LSC count rate ratio, R160 Tb /R161 Tb , on the reference date was determined by sequential counting and calculated using a custom script based on their half-lives. (author)

Rare earth octacyanomolybdates(4)

International Nuclear Information System (INIS)

Zubritskaya, D.I.; Sergeeva, A.N.; Pisak, Yu.V.

1980-01-01

Optimal conditions for synthesis of rare-earth octacyanomolybdates(4) of the Ln 4 [Mo(CN) 8 ] 3 xnH 2 O composition (where Ln is a rare-earth element, other than Pr, Pm, Lu, Tb) have been worked out. The synthesis has been accomplished by neutralization with octacianomolybdic acid with rare-earth carbonates. The composition and structure of the compounds synthesized have been studied by infrared-spectroscopy. It has been established that rare-earth octacyanomolybdates(4) form three isostructural groups

An Operationally Simple Method for Separating the Rare-Earth Elements Neodymium and Dysprosium.

Science.gov (United States)

Bogart, Justin A; Lippincott, Connor A; Carroll, Patrick J; Schelter, Eric J

2015-07-06

Rare-earth metals are critical components of electronic materials and permanent magnets. Recycling of consumer materials is a promising new source of rare earths. To incentivize recycling there is a clear need for simple methods for targeted separations of mixtures of rare-earth metal salts. Metal complexes of a tripodal nitroxide ligand [{(2-(t) BuNO)C6 H4 CH2 }3 N](3-) (TriNOx(3-) ), feature a size-sensitive aperture formed of its three η(2) -(N,O) ligand arms. Exposure of metal cations in the aperture induces a self-associative equilibrium comprising [M(TriNOx)thf]/ [M(TriNOx)]2 (M=rare-earth metal). Differences in the equilibrium constants (Keq ) for early and late metals enables simple Nd/Dy separations through leaching with a separation ratio SNd/Dy =359. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Separation and Recycling for Rare Earth Elements by Homogeneous Liquid-Liquid Extraction (HoLLE Using a pH-Responsive Fluorine-Based Surfactant

Directory of Open Access Journals (Sweden)

Shotaro Saito

2015-08-01

Full Text Available A selective separation and recycling system for metal ions was developed by homogeneous liquid-liquid extraction (HoLLE using a fluorosurfactant. Sixty-two different elemental ions (e.g., Ag, Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Co, Cr, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Hf, Hg, Ho, In, Ir, La, Lu, Mg, Mn, Mo, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Re, Rh, Ru, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Te, Ti, Tl, Tm, V, W, Y, Yb, Zn, and Zr were examined. By changing pH from a neutral or alkaline solution (pH ≥ 6.5 to that of an acidic solution (pH < 4.0, gallium, zirconium, palladium, silver, platinum, and rare earth elements were extracted at >90% efficiency into a sedimented Zonyl FSA® (CF3(CF2n(CH22S(CH22COOH, n = 6–8 liquid phase. Moreover, all rare earth elements were obtained with superior extraction and stripping percentages. In the recycling of rare earth elements, the sedimented phase was maintained using a filter along with a mixed solution of THF and 1 M sodium hydroxide aqueous solution. The Zonyl FSA® was filtrated and the rare earth elements were recovered on the filter as a hydroxide. Furthermore, the filtrated Zonyl FSA was reusable by conditioning the subject pH.

Effect of additives on lithium doped magnesium oxide catalysts used in the oxidative coupling of methane

NARCIS (Netherlands)

Korf, S.J.; Roos, J.A.; Veltman, L.J.; van Ommen, J.G.; Ross, J.R.H.

1989-01-01

It has been found that it is possible to improve the activity and stability for the oxidative coupling of methane of a Li/MgO catalyst by the addition of small amounts of the oxides of various transition and rare earth metals. A number of these additives, e.g. SnO2, TiO2, Dy2O3 and Tb4O7, caused

Powder Neutron Diffraction and Magnetic structures

International Nuclear Information System (INIS)

Vigneron, F.

1986-01-01

The determination of the magnetic structures of materials (ferromagnetic, antiferromagnetic, helimagnetic, .) can be achieved only by neutron diffraction. A general survey of the powder technique is given: 2-axis spectrometer and analysis of the magnetic data. For the REBe/sb13/ intermetallic compounds (RE = Rare Earth), commensurate and/or incommensurate magnetic structures are observed and discussed as a function of RE (Gd, Tb, Dy, Ho, Er)

Effect of rare earth doping on optical and spectroscopic characteristics of BaZrO3:Eu3+,Tb3+ perovskites

Science.gov (United States)

Katyayan, Shambhavi; Agrawal, Sadhana

2018-06-01

This paper reports structural investigations of rare earth doped BaZrO3 phosphors synthesized by Solid state reaction technique with varying concentrations of Eu3+ and Tb3+ from 0 mol% to 2 mol%. The synthesized phosphors show enhanced variable emissions in the visible region corresponding to different hypersensitive electronic transitions of Eu3+ and Tb3+ ions. With cubic structure confirmed in XRD analysis, the FESEM images show uniform grain connectivity and homogeneity of prepared samples. The TEM micrographs of the synthesized phosphors show agglomerated irregular structures. The synthesized phosphors were also subjected to FTIR, Raman, EDXS analysis along with studies of thermoluminescent and photoluminescent characteristics. On subjecting to 229 nm (UV) excitation, the phosphors show enhanced PL emissions corresponding to 571 nm (5D0-7F0), 591 nm (5D0-7F1), 615 nm (5D0-7F2) and 678 nm (5D0-7F4) hypersensitive transitions of Eu3+ ions and emission peaks at 489 nm (5D4-7F6), 539 nm (5D4-7F5), 589 nm (5D4-7F4) and 632 nm (5D4-7F3) accounting for electronic transitions of Tb3+ ions respectively. The computed average PL lifetime is 14.014 s. In the TL analysis, the second order of kinetics with the activation energy varying from 5.0 × 10‑1 eV to 6.6 × 10‑1 eV is reported. The maximum TL lifetime is estimated as 19.4985 min in the TL lifetime analysis.

Effect of alkaline earth oxides on the physical and spectroscopic properties of Dy3+- doped Li2O-B2O3 glasses for white emitting material application

Science.gov (United States)

Shamshad, L.; Rooh, G.; Kirdsiri, K.; Srisittipokakun, N.; Damdee, B.; Kim, H. J.; Kaewkhao, J.

2017-02-01

Li2O-MO-B2O3:0.5Dy2O3 glasses mixed with four different alkaline earth modifier oxides MgO, CaO, SrO and BaO were synthesized by melt quench technique. Their physical properties like density, molar volume and refractive index were measured at room temperature and the effect of alkaline earth modifier oxides were studied. Also, optical absorption and photoluminescence spectra of these glasses have been acquired at room temperature. The Judd-Ofelt theory was effectively used to characterize these spectra and spectral intensities (ƒcal), Judd-Ofelt intensity parameters (Ω2, Ω4 and Ω6) and certain radiative properties have been determined. Radiative life-times (τR), branching ratios (βcal), and emission cross-sections (σp) and optical gain parameters (σp × τR) were calculated from the Judd-Ofelt intensity parameters and the variation in these parameters with the variation of glass matrix are discussed. Yellow/Blue (Y/B) ratio and chromacity color coordinates (x,y) are calculated from the emission spectra which indicates the white light generation from all the investigated samples. The correlated color temperature (CCT) for the studied glasses is found to be 4418 K. The fluorescence decay time (τexp) of the 4F9/2 level of Dy3+ has been measured from the decay profiles and compared with calculated lifetimes (τcal). Among all the studied glass matrices, the glass containing BaO exhibits high value of branching ratio, large emission cross-section and high optical gain parameter for 6F9/2 → 6H13 at 575 nm. The results indicates the suitability of all the studied glasses for laser action and white light generation.

Major, trace and rate earth elements in sediments of the Julian Adame-Alatorre dam by instrumental neutron activation analysis

International Nuclear Information System (INIS)

Mireles, F.; Pinedo, J. L.; Davila, J. I.; Oliva, J. E.; Speakman, R. J.; Glascock, M. D.

2010-10-01

The rapid industrial development in regions of Mexico during recent years has had the side effect of introducing toxic metals, fertilizers, and pesticides into the ecosystem. Sediment cores were collected from eight locations around the Julian Adame-Alatorre dam located in Municipality of Villanueva in the Zacatecas State, Mexico. The cores were analyzed for 32 major, trace, and rare earth elements (As, La, Lu, Nd, Sm, U, Yb, Ce, Co, Cr, Cs, Eu, Fe, Hf, Rb, Sb, Sc, Sr, Ta, Tb, Th, Zn, Zr, Al, Ba, Ca, Dy, K, Mn, Na, Ti, V) in order to estimate the health risk. The samples were analyzed by instrument neutron activation analysis using thermal neutron fluxes of 8 x 10 13 and 5 x 10 13 n cm -2 s -1 for short and long irradiations, respectively. The results of the contamination levels for elements such as As, Ba, Cr, Fe, Mn, Ta, V, and Zn were compared with the Mexican regulations and the guidelines of US EPA. (Author)

Thiocarbomide coordination compounds of yttrium subgroup rare earth chlorides

International Nuclear Information System (INIS)

Sakharova, Yu.G.; Perov, V.N.; Loginov, V.I.

1978-01-01

Thiocarbamide coordination compounds of chlorides of elements of the yttrium subgroup 4MeCl 3 x5Cs(NH 2 ) 2 x2OH 2 O (where Me stands for Tb, Dy, Ho, Er, Tm, Yb, Lu, Y) were produced for the first time. The compounds obtained are stable in air, have definite melting points, are highly soluble in methyl and ethyl alcohols, and are unstable in water. They recrystallize from ethyl alcohol without changing their chemical composition. The identity of these compounds was confirmed by X-ray analysis

Some Limitations in the Use of Plastic and Dyed Plastic Dosimeters

DEFF Research Database (Denmark)

Miller, Arne; Bjergbakke, Erling; McLaughlin, W. L.

1975-01-01

Several practical plastic and dyed plastic dosimeters were examined under irradiation conditions similar to those used for radiation processing of materials. Cellulose triacetate, polymethyl methacrylate, polyvinyl chloride, dyed polymethyl methacrylate, dyed Cellophane and dyed Nylon were given...

Tetracyanidoborates with triply charged rare earth metal cations and their optical properties

Energy Technology Data Exchange (ETDEWEB)

Hackbarth, Liisa

2015-11-24

The aim of this thesis is the description of the synthesis and characterization of a new group of tetracyanidoborates: tetracyanidoborates with trivalent rare earth metal cations. Their optical properties in the ultraviolet and visible range are also discussed. Common synthetic routes for tetracyanidoborates are adapted and applied to the preparation of the rare earth tetracyanidoborate hydrates. They are accessible with high yields and high purity through a reaction between the tetracyanidoboronic acid and rare earth hydroxides. It is shown that the rare earth tetracyanidoborates form isostructural groups, like the [LRE(H{sub 2}O){sub 5}][B(CN){sub 4}]{sub 3}.0.5 H{sub 2}O, where LRE{sup 3+} is La, Ce, Pr, Nd, Sm, Eu and Gd, the [HRE(H{sub 2}O){sub 7}][B(CN){sub 4}]{sub 3} and the [HRE(H{sub 2}O){sub 8}][B(CN){sub 4}]{sub 3}.3 H{sub 2}O, where HRE{sup 3+} is Tb, Dy, Ho, Er, Tm, Yb, Lu and Y. Furthermore, the coordination number 9 is noticed to be common among the light rare earth cations, whereas the minor coordination number 8 is prevalent for the heavy rare earth cations in their tetracyanidoborates. This different construction of the coordination spheres between light and heavy rare earth cations leads to different structures depending on the energetic efficiency of the structural arrangement. Generally, the rare earth tetracyanidoborate hydrates are found to crystallize in the monoclinic crystal system. Moreover, other different crystal structures are observed depending on the crystallization temperature and the type of coordinated ligands and co-crystallized solvent molecules. The tetracyanidoborate hydrates with triply charged rare earth cations are characterized comprehensively by X-ray diffraction, vibrational spectroscopy, NMR-spectroscopy as well as by thermal analysis. Furthermore, the optical properties of some dehydrated rare earth tetracyanidoborates are investigated by UV-spectroscopy and luminescence measurements. The results of the optical

TB or not TB?: a case of isolated testicular TB with scrotal involvement.

LENUS (Irish Health Repository)

Bhargava, A

2009-06-01

Despite the genitourinary tract being the most common site affected by extrapulmonary TB, isolated testicular TB remains a rare clinical entity. In patients with co-morbidities such as hepatic impairment, treatment proves a challenge, as first-line hepatotoxic pharmaceuticals are contraindicated. Here, we report a case of isolated testicular TB with scrotal involvement, on a background of hepatic dysfunction.

Simulation of statistical γ-spectra of highly excited rare earth nuclei

International Nuclear Information System (INIS)

Schiller, A.; Munos, G.; Guttormsen, M.; Bergholt, L.; Melby, E.; Rekstad, J.; Siem, S.; Tveter, T.S.

1997-05-01

The statistical γ-spectra of highly excited even-even rare earth nuclei are simulated applying appropriate level density and strength function to a given nucleus. Hindrance effects due to K-conservation are taken into account. Simulations are compared to experimental data from the 163 Dy( 3 He,α) 162 Dy and 173 Yb( 3 He,α) 172 Yb reactions. The influence of the K quantum number at higher energies is discussed. 21 refs., 7 figs., 2 tabs

The Ho–Ni–Ge system: Isothermal section and new rare-earth nickel germanides

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@tech.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Knotko, A.V. [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Faculty of Geology, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Yuan, Fang; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1 (Canada); Pani, M.; Provino, A.; Manfrinetti, P. [Institute SPIN-CNR and Dipartimento di Chimica e Chimica Industriale, Università di Genova, Via Dodecaneso 31, 16146 Genova (Italy)

2015-05-15

}CuGe{sub 6}-type), HoNiGe{sub 3} (SmNiGe{sub 3}-type), HoNi{sub 0.2÷0.6}Ge{sub 2} (CeNiSi{sub 2}-type), Ho{sub 37÷34}Ni{sub 6÷24}Ge{sub 57÷42} (AlB{sub 2}-type), HoNiGe (TiNiSi-type), Ho{sub 3}NiGe{sub 2} (La{sub 3}NiGe{sub 2}-type), the ternary system contains four new compounds: Ho{sub 3}Ni{sub 11}Ge{sub 4} (Sc{sub 3}Ni{sub 11}Ge{sub 4}-type), HoNi{sub 3}Ge{sub 2} (ErNi{sub 3}Ge{sub 2}-type), Ho{sub 3}Ni{sub 2}Ge{sub 3} (Hf{sub 3}Ni{sub 2}Si{sub 3}-type) and ~Ho{sub 5}Ni{sub 2}Ge{sub 3} (unknown structure). Quasi-binary solid solutions were found to form at 1070 K from the binary Ho{sub 2}Ni{sub 17}, HoNi{sub 5}, HoNi{sub 7}, HoNi{sub 3}, HoNi{sub 2}, HoNi and Ho{sub 2}Ge{sub 3} compounds, while no detectable solubility was observed for the other binary compounds in the Ho–Ni–Ge system. Based on the magnetization measurements, the HoNi{sub 5}Ge{sub 3}, HoNi{sub 3}Ge{sub 2} and Ho{sub 3}Ni{sub 11}Ge{sub 4} (and isostructural (Tb, Dy){sub 3}Ni{sub 11}Ge{sub 4}) compounds have been found to show paramagnetic behavior down to 5 K, whereas Ho{sub 3}Ni{sub 2}Ge{sub 3} exhibits an antiferromagnetic transition at ~7 K. Additionally, the crystal structure of the new isostructural phases (Y, Yb)Ni{sub 3}Ge{sub 2} (ErNi{sub 3}Ge{sub 2}-type), Er{sub 3}Ni{sub 11}Ge{sub 4} (Sc{sub 3}Ni{sub 11}Ge{sub 4}-type) and (Y, Tb, Dy, Er, Tm){sub 3}Ni{sub 2}Ge{sub 3} (Hf{sub 3}Ni{sub 2}Si{sub 3}-type) has been also investigated. - Highlights: • Ho–Ni–Ge system has been investigated at 1070 K and up to ~60 at% Ho. • Eight known ternary holmium nickel germanides were confirmed in Ho–Ni–Ge. • Four new holmium nickel germanides were detected in Ho–Ni–Ge. • Eight new rare earth nickel germanides were detected in (Y, Tb, Dy, Er–Yb)–Ni–Ge. • HoNi{sub 5}Ge{sub 3}, HoNi{sub 3}Ge{sub 2},(Tb, Dy, Ho){sub 3}Ni{sub 11}Ge{sub 4} and Ho{sub 3}Ni{sub 2}Ge{sub 3} are paramagnet down to 5–7 K.

Cytotoxic and genotoxic effect of the [{sup 166}Dy]Dy/{sup 166}Ho-EDTMP in vivo generator system in mice

Energy Technology Data Exchange (ETDEWEB)

Pedraza-Lopez, Martha [Departamento de Medicina Nuclear, Instituto Nacional de Ciencias Medicas y Nutricion, Salvador Zubiran, Delegacion Tlalpan, Mexico DF 14000 (Mexico); Ferro-Flores, Guillermina [Instituto Nacional de Investigaciones Nucleares, Carretera Mexico-Toluca, Ocoyoacac, Estado de Mexico, CP 52045 (Mexico); Arteaga de Murphy, Consuelo [Departamento de Medicina Nuclear, Instituto Nacional de Ciencias Medicas y Nutricion, Salvador Zubiran, Delegacion Tlalpan, Mexico DF 14000 (Mexico)]. E-mail: consuelo_murphy@yahoo.com.mx; Morales-Ramirez, Pedro [Instituto Nacional de Investigaciones Nucleares, Carretera Mexico-Toluca, Ocoyoacac, Estado de Mexico, CP 52045 (Mexico); Piedras-Ross, Josefa [Departamento de Medicina Nuclear, Instituto Nacional de Ciencias Medicas y Nutricion, Salvador Zubiran, Delegacion Tlalpan, Mexico DF 14000 (Mexico); Murphy-Stack, Eduardo [Hospital Santaelena, Mexico DF (Mexico); Hernandez-Oviedo, Omar [Escuela Superior de Fisica y Matematicas, IPN, Mexico DF (Mexico)

2004-11-01

Multiple myeloma and other hematological malignancies have been treated by myeloablative radiotherapy/chemotherapy and subsequent stem cell transplantation. [{sup 166}Dy]Dy/{sup 166}Ho-ethylenediaminetetramethylene phosphonate (EDTMP) forms a stable in vivo generator system with selective skeletal uptake in mice; therefore, it could work as a potential and improved agent for marrow ablation. Induced bone marrow cytotoxicity and genotoxicity are determined by the reduction of reticulocytes (RET) and elevation of micronucleated reticulocyte (MN-RET) in peripheral blood and ablation by bone marrow histological studies. The aim of this study was to determine the bone marrow cytotoxic and genotoxic effect of the [{sup 166}Dy]Dy/{sup 166}Ho-EDTMP in vivo generator system in mice and to evaluate by histopathology its myeloablative potential. Enriched {sup 166}Dy{sub 2}O{sub 3} was irradiated and [{sup 166}Dy]DyCl{sub 3} was added to EDTMP in phosphate buffer (pH 8.0) in a molar ratio of 1:1.75. QC was determined by TLC. Dy-EDTMP complex was prepared the same way with nonirradiated dysprosium oxide. A group of BALB/c mice were intraperitoneally injected with the radiopharmaceutical and two groups of control animals were injected with the cold complex and with 0.9% sodium chloride, respectively. A blood sample was taken at the beginning of the experiments and every 48 h for 12 days postinjection. The animals were sacrificed, organs of interest taken out and the radioactivity determined. The femur was used for histological studies. Flow cytometry analysis was used to quantify the frequency of RET and MN-RET in the blood samples. The MCNP4B Monte Carlo computer code was used for dosimetry calculations. Radiochemical purity was 99% and the mean specific activity was 1.3 MBq/mg. The RET and MN-RET frequency were statistically different in the treatment at the end of the 12-day period demonstrating cytotoxicity and genotoxicity induced by the in vivo generator system. The

Find TB. Treat TB. Working together to eliminate TB.

Centers for Disease Control (CDC) Podcasts

2014-02-26

In this podcast, Dr. Sundari Mase, Medical Team Lead in the Field Services and Evaluation Branch in the Division of Tuberculosis Elimination, discusses World TB Day and the 2014 theme.  Created: 2/26/2014 by National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP).   Date Released: 2/26/2014.

Microstructures and mechanical properties of Mg–Zn–Zr–Dy ...

Indian Academy of Sciences (India)

Microstructures and phase compositions of as-cast and extruded ZK60–Dy ( = 0–5) alloys were analysed by optical microscope, scanning electron microscope, X-ray diffraction and differential scanning calorimetry. Meanwhile, the tensile mechanical property was tested.With increasing Dy content, Mg–Zn–Dy new phase ...

Therapeutical radiopharmaceuticals based In vivo generator system [166 Dy] Dy/166 Ho

International Nuclear Information System (INIS)

Ferro F, G.; Garcia S, L.; Monroy G, F.; Tendilla, J.I.; Pedraza L, M.; Murphy, C.A. de

2002-01-01

At the idea to administer to a patient a molecule containing in it structure a father radionuclide, with a half life enough large which allows to the radiolabelled molecule to take up position specifically in a white tissue and decaying In vivo to the daughter radionuclide with properties potentially therapeutic, it is known as In vivo generator system. In this work the preparation and the preliminary dosimetric valuations of radiopharmaceuticals based In vivo generator system 166 Dy Dy/ 166 Ho for applications in radioimmunotherapy, in the treatment of the rheumatoid arthritis and in the bone marrow ablation (m.o.) for candidates patients to bone marrow transplant are presented. (Author)

Production of thermoluminescent dosemeters based on MgB4O7: Dy and MgB4O7: Tm

International Nuclear Information System (INIS)

Souza, Luiza Freire de; Souza, Divanizia N.

2013-01-01

The thermoluminescent dosimetry (TL) is a well-established technique for the detection of ionizing radiation in hospitals, clinics, and industrial establishments where there is the need to quantify the radiation. For this practice is require the use phosphors which are sensitive to radiation. Some phosphors are already commonly used in this practice, for example, TLD-100 (LiF: Mg, Ti), CaSO 4 :Tm and CaSO 4 :Dy. A compound that was most recently introduced in dosimetry and has many advantageous features to detect neutrons, electrons and gamma is the magnesium tetraborate (MgB 4 O 7 ), but the undoped material is not good for dosimetry, since signal does not show satisfactory thermoluminescence. The present work presents the analysis of the compound MgB 4 O 7 when doped with rare earth elements, thulium (Tm) and dysprosium (Dy). The production of MgB 4 O 7 : Dy and MgB 4 O 7 : Tm occurred under acidic conditions. Following the process of crystal growth, several tests were made on phosphors produced to verify the quality of materials as TL dosimeter. Initially, was made the identification of the crystalline phases found in the material, using the technique of X-ray diffractometry, and then were evaluated and compared the TL emission curves of the crystals with two different types of dopants, to this, the samples were irradiated with different radiation sources: 137 Cs (0,66 MeV), 60 Co (1.25 MeV) and X-rays (0.41 MeV) and based on the results was evaluated the energy dependence of phosphors. Another characteristic analyzed, was the decay of TL signal for the material (fading). The results show that the material can be an excellent TL dosimeter when doped with rare earth elements Dy and Tm. (author)

An operationally simple method for separating the rare-earth elements neodymium and dysprosium

Energy Technology Data Exchange (ETDEWEB)

Bogart, Justin A.; Lippincott, Connor A.; Carroll, Patrick J.; Schelter, Eric J. [Department of Chemistry, University of Pennsylvania, Philadelphia, PA (United States)

2015-07-06

Rare-earth metals are critical components of electronic materials and permanent magnets. Recycling of consumer materials is a promising new source of rare earths. To incentivize recycling there is a clear need for simple methods for targeted separations of mixtures of rare-earth metal salts. Metal complexes of a tripodal nitroxide ligand [{(2-"tBuNO)C_6H_4CH_2}{sub 3}N]{sup 3-} (TriNOx{sup 3-}), feature a size-sensitive aperture formed of its three η{sup 2}-(N,O) ligand arms. Exposure of metal cations in the aperture induces a self-associative equilibrium comprising [M(TriNOx)thf]/[M(TriNOx)]{sub 2} (M=rare-earth metal). Differences in the equilibrium constants (K{sub eq}) for early and late metals enables simple Nd/Dy separations through leaching with a separation ratio S{sub Nd/Dy}=359. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Luminescence studies on Dy3+ and Dy3+:Eu3+ co-doped boro-phosphate glasses for WLED applications

Science.gov (United States)

Vijayakumar, M.; Uma, V.; Arunkumar, S.; Marimuthu, K.

2015-06-01

Dy3+ and Dy3+:Eu3+ co-doped boro-phosphate glasses have been prepared and optically characterized using absorption, luminescence and decay measurements. The Nephelauxetic ratios (β), Bonding parameters (δ) and Judd-Ofelt (JO) intensity parameters Ωλ (λ = 2, 4 and 6) were calculated to study the nature of the environment around the RE3+ ions in the prepared glasses. The yellow to blue (Y/B) intensity ratio and the chromaticity color coordinates were calculated from the luminescence measurements. The lifetimes of the 4F9/2 excited level were measured using decay curves and is found to decrease in the Dy3+:Eu3+ co-doped glass due to the occurrence of resonant energy transfer between Dy3+-Eu3+ ions and the non-exponential decay rates have been fitted with Inokuti-Hirayama (IH) model. The decay curves are well fitted for S= 6 suggesting that the interaction between active ions for the energy transfer is of dipole-dipole nature.

Preparation and characterization of PT-rare earth/C electrocatalysts for PEM fuel cells

International Nuclear Information System (INIS)

Santoro, Thais Aranha de Barros

2009-01-01

Pt-rare earth/C electrocatalysts (rare earth = La, Ce, Pr, Nd, Sm, Tb, Dy, Ho, Er, Tm, and Lu) were prepared (20 wt.% and Pt-to-RE atomic ratio of 50:50) by an alcohol reduction process using H 2 PtCl 6 .6H 2 O (Aldrich) and rare earth (III) chlorides (Aldrich) as metal sources, ethylene glycol as solvent and reducing agent, and Vulcan XC72 as support. The electrocatalysts were characterized by Energy Dispersive X-ray Spectroscopy (EDX), X-Ray Diffractometry (XRD) and Transmission Electron Microscopy (TEM). The energy dispersive x-ray spectroscopy analysis showed that the Pt-Rare Earth atomic ratios obtained for all electrocatalysts were similar to those used in the preparations. In all diffractograms, it was observed a broad peak at about 25 degree which was associated to the Vulcan XC72 support material and four peaks at approximately 28=40 degree, 47 degree, 67 degree and 82 degree, which were associated to the (111), (200), (220), (311), and (222) planes, respectively, of the face-centered cubic (fcc) structure characteristic of platinum and platinum alloys. For the Pt-Rare Earth/C electrocatalysts, it was also observed peaks related to the rare earth oxides on the X ray diffractograms. PtLa/C electrocatalysts were prepared at different atomic ratio. Transmission electronic microscopy micrographs of electrocatalysts showed a reasonable distribution of the Pt particles on the carbon support with some agglomerations, which is in agreement with x-ray diffractometry result. The performance for CO, methanol and ethanol oxidation was investigated by cyclic voltammetry, chronoamperometry and Fourier transform infrared spectroscopy spectroscopy. The electrocatalytic activity of the Pt-Rare Earth/C electro catalyst, specially PtLa/C, were higher than that of the Pt/C electrocatalyst. Fourier transform infrared spectroscopy studies for ethanol oxidation on Pt-Rare Earth/C electrocatalyst showed that acetaldehyde and acetic acid were the main products. The PtLa/C (30

Thermoluminescence properties of Al{sub 2}O{sub 3}:Tb nanoparticles irradiated by gamma rays and 85 MeV C{sup 6+} ion beam

Energy Technology Data Exchange (ETDEWEB)

Salah, Numan, E-mail: nsalah@kau.edu.sa [Center of Nanotechnology, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Alharbi, Najlaa D. [Sciences Faculty for Girls, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Habib, Sami S. [Center of Nanotechnology, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Lochab, S.P. [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India)

2015-11-15

Carbon ions beam is recently recognized as an ideal cancer treatment modality, because of its excellent local tumor control. These ions have a high relative biological effectiveness resulting from high linear energy transfer (LET) and their sharp Bragg peak. However, the dose of those energetic ions needs to be measured with great precision using a proper dosimeter. Aluminum Oxide (Al{sub 2}O{sub 3}) is a highly luminescent phosphor widely used for radiation dosimetry using thermoluminesence (TL) technique. In this work nanoparticles of this material activated by different elements like Eu, Tb, Dy, Cu and Ag were evaluated for their TL response to gamma rays irradiation. Tb doped sample is found to be the most sensitive sample, which could be selected for exposure to 85 MeV C{sup 6+} ion beam in the fluence range 10{sup 9}–10{sup 13} ions/cm{sup 2}. The obtained result shows that C ion beam irradiated sample has a simple glow curve structure with a prominent glow peak at around 230 °C. This glow curve has a dosimetric peak better than those induced by gamma rays. This glow peak exhibits a linear response in the range 10{sup 9}–10{sup 11} ions/cm{sup 2}, corresponding to the equivalent absorbed doses 0.285–28.5 kGy. The absorbed doses, penetration depths and main energy loss were calculated using TRIM code based on the Monte Carlo simulation. The wide linear response of Al{sub 2}O{sub 3}:Tb nanoparticles along with the low fading makes this low cost nanomaterial a good candidate for C ion beam dosimetry. - Highlights: • Nanoparticles of Al{sub 2}O{sub 3} doped with Eu, Tb, Dy, Cu and Ag were synthesised. • They were evaluated for their TL response to gamma rays and C ion beam irradiation. • Tb doped sample is the most sensitive sample to gamma rays. • Al{sub 2}O{sub 3}:Tb was exposed to 85 MeV C{sup 6+} ion beam in the fluence range 10{sup 9}-10{sup 13} ions/cm{sup 2}. • The glow peak induced by C ions has a linear response in the range 10{sup 9

Application of stochastic approach based on Monte Carlo (MC) simulation for life cycle inventory (LCI) of the rare earth elements (REEs) in beneficiation rare earth waste from the gold processing: case study

Science.gov (United States)

Bieda, Bogusław; Grzesik, Katarzyna

2017-11-01

The study proposes an stochastic approach based on Monte Carlo (MC) simulation for life cycle assessment (LCA) method limited to life cycle inventory (LCI) study for rare earth elements (REEs) recovery from the secondary materials processes production applied to the New Krankberg Mine in Sweden. The MC method is recognizes as an important tool in science and can be considered the most effective quantification approach for uncertainties. The use of stochastic approach helps to characterize the uncertainties better than deterministic method. Uncertainty of data can be expressed through a definition of probability distribution of that data (e.g. through standard deviation or variance). The data used in this study are obtained from: (i) site-specific measured or calculated data, (ii) values based on literature, (iii) the ecoinvent process "rare earth concentrate, 70% REO, from bastnäsite, at beneficiation". Environmental emissions (e.g, particulates, uranium-238, thorium-232), energy and REE (La, Ce, Nd, Pr, Sm, Dy, Eu, Tb, Y, Sc, Yb, Lu, Tm, Y, Gd) have been inventoried. The study is based on a reference case for the year 2016. The combination of MC analysis with sensitivity analysis is the best solution for quantified the uncertainty in the LCI/LCA. The reliability of LCA results may be uncertain, to a certain degree, but this uncertainty can be noticed with the help of MC method.

Structural, magnetic and electronic properties of rare earth ternary oxides Li Ln(II) 2 Ln(III)O4

International Nuclear Information System (INIS)

Malki, M.

1987-06-01

Properties of a new class of rare earth ternary oxides Li Ln(II) 2 Ln(III)O 4 where Ln(II) is a divalent metal (Sr, Eu) and Ln(III) a trivalent rare earth (Eu, Gd, Dy, Er and Y). These orthorhombic compounds (type Li Eu 3 O 4 ) allow the study of many magnetic phenomena and their evolution in function of the nature of Ln(II) and Ln(III): diamagnetic ions Sr 2+ , Y 3+ ; isotrope magnetic ions: Eu 2+ , Gd 3+ and anisotrope magnetic ions Dy 3+ , Er 3+ . Magnetic and electric properties are obtained by classical techniques and from hyperfine interaction by Moessbauer spectroscopy. The possibility to use several Moessbauer resonance (nuclei Eu 151, Gd 155, Dy 161 and Er 166) completes informations obtained by the macroscopic study [fr

CaSO4: Dy + Teflon thermoluminescent dosemeters

International Nuclear Information System (INIS)

Campos, L.L.

1986-01-01

A pellet dosemeter of CaSO 4 : Dy + Teflon was developed at IPEN. CaSO 4 : Dy thermoluminescent phosphor, grown in the Dosimetric Materials Production Laboratory was chosen, due to its high sensitivity, ease of preparation and comparatively low cost. Pellets were produced by cold pressing and sintering a mixture of CaSO 4 : Dy and Teflon powders. Extensive work was done to study in detail all CaSO 4 : Dy pellets characteristics from the point of view of dosimetry with the purpose of introducing it in the routine use. A filter combination providing an energy independent response from 20 KeV to 1,25 MeV was obtained. The dosemeter consists of three pellets sealed between two thin plastic sheets and placed under plastic and lead filters. The combination of these tree filters allows the exposure as well as the energy determination of an unknown source. (Author) [pt

Effects of Dy{sub 71.5}Fe{sub 28.5} intergranular addition on the microstructure and the corrosion resistance of Nd–Fe–B sintered magnets

Energy Technology Data Exchange (ETDEWEB)

Liang, Liping; Ma, Tianyu, E-mail: maty@zju.edu.cn; Zhang, Pei; Yan, Mi, E-mail: mse_yanmi@zju.edu.cn

2015-06-15

To satisfy high-temperature applications, heavy rare-earth (RE) Dy is commonly introduced into the Nd–Fe–B sintered magnets to improve the coercivity. In addition to forming (Nd, Dy){sub 2}Fe{sub 14}B, Dy also exists in the intergranular RE-rich phase. Hence, understanding the effect of Dy on the electrochemical characteristics of the RE-rich phase and corrosion resistance of the magnet is of importance. In this work, eutectic alloy Dy{sub 71.5}Fe{sub 28.5} powders were added into the (Pr{sub 0.2}Nd{sub 0.8}){sub 12.3}Fe{sub bal}B{sub 6.1} magnet through binary-alloy approach to investigate the corrosion resistance of the magnet in electrochemical and hot/humid environments. The results demonstrate that Dy is enriched in the intergranular phase, improving its electrode potential and stability due to the higher electrode potential of Dy than Nd or Pr. As a consequence, the electrode potential difference between the 2:14:1 phase and the RE-rich phase is reduced, improving the corrosion resistance. Furthermore, formation of (Pr, Nd, Dy){sub 2}Fe{sub 14}B shell with stronger local anisotropy surrounding the 2:14:1 phase grains improves the coercivity with a slight remanence loss. Therefore, intergranular adding Dy–Fe alloy powders can obtain both high magnetic properties and good corrosion resistance simultaneously. - Highlights: • Eutectic Dy{sub 71.5}Fe{sub 28.5} powders were intergranular added to NdFeB sintered magnets. • The doped magnet showed improved corrosion resistance compared to Dy-free magnet. • Dy enrichment in RE-rich intergranular phase improved its electrode potential. • (Nd, Dy){sub 2}Fe{sub 14}B shell was expected to form in the surface of Nd{sub 2}Fe{sub 14}B grains. • Both corrosion resistance and coercivity were improved in Dy–Fe doped magnet.

Spectrographic determination of lanthanides in high-purity uranium compounds, after chromatographic separation by alumina-hydrofluoric acid

International Nuclear Information System (INIS)

Lordello, A.R.; Abrao, A.

1979-01-01

A method is presented for the determination of fourteen rare earth elements in high-purity uranium compounds by emission spectrography. The rare earths are chromatographically separated from uranium by using alumina-hydrofluoric acid. Lanthanum is used both as collector and internal standard. The technique of excitation involves a total consumption of the sample in a 17 ampere direct current arc. The range of determination is about 0.005 to 0.5 μg/g uranium. The coefficient of variation for Pr, Ho, Dy, Er, Tm, Lu, Gd and Tb amounts to 10%. (Author) [pt

Testing for TB Infection

Science.gov (United States)

... Adverse Events TB Treatment of Persons Living with HIV TB Treatment and Pregnancy TB Treatment for Children Drug-Resistant TB Research TB Epidemiologic Studies Consortium Research Projects Publications TB Trials Consortium Study ...

Band mixing in /sup 160/Dy

Energy Technology Data Exchange (ETDEWEB)

Hasiza, M L; Singh, K; Sahota, H S [Punjabi Univ., Patiala (India). Dept. of Physics

1982-11-01

The intensities of the gamma transitions in /sup 160/Dy have been measured precisely by a 45 cc Ge(Li) detector. Unequal quadrupole moments for the ground and gamma vibrational bands have been proposed in order to remove the inconsistencies in the values of band mixing parameter Z sub(gamma) for this doubly even deformed nucleus of /sup 160/Dy.

Dy–Mn–Si as a representative of family of ‘Dy–Transition Metal–Si’ systems: Its isothermal sections, empirical rProd. Type: FTPules and new rare-earth manganese silicides

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@general.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Knotko, A.V. [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Geological Faculty, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Provino, A.; Manfrinetti, P. [INFM and Dipartimento di Chimica e Chimica Industriale, Universita di Genova, Via Dodecaneso 31, 16146 Genova (Italy); Yao, Jinlei; Yuan, Fang; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada)

2013-10-15

X-ray and microprobe analyses were employed for the investigation of Dy–Mn–Si system at 870/1070/1170 K. The Dy–Mn–Si system, contains the known DyMn{sub 2}Si{sub 2}, DyMnSi and Dy{sub 2}Mn{sub 3}Si{sub 5} compounds and DyMn{sub 4}Si{sub 2}, Dy{sub 2}MnSi{sub 2} and Dy{sub 3}Mn{sub 2}Si{sub 3} were new compounds identified first time and their structure are of the type TmCu{sub 4}Sb{sub 2}, Sc{sub 2}CoSi{sub 2} and Hf{sub 3}Ni{sub 2}Si{sub 3} respectively. The quasi-binary solid solutions were detected at 870/1070/1170 K: the ThMn{sub 12}-type Dy{sub 8}Mn{sub 87}Si{sub 5}, Th{sub 6}Mn{sub 23}-type Dy{sub 23}Mn{sub 72}Si{sub 5}, MgCu{sub 2}-type Dy{sub 33}Mn{sub 58}Si{sub 9} and AlB{sub 2}-type Dy{sub 38}Mn{sub 2}Si{sub 58}. The other binary compounds of the Dy–Mn–Si system do not show any visible solubility. New phases R{sub 2}MnSi{sub 2} and R{sub 3}Mn{sub 2}Si{sub 3} (R=Gd, Tb, Ho–Tm) were found out and their structure of the type Sc{sub 2}CoSi{sub 2} and Hf{sub 3}Ni{sub 2}Si{sub 3} respectively. The specific features of ‘Dy–Transition Metal–Si’ systems were discussed. - Graphical abstract: The isothermal section of Dy–Mn–Si contains the known DyMn{sub 2}Si{sub 2}, DyMnSi, Dy{sub 2}Mn{sub 3}Si{sub 5} and new TmCu{sub 4}Sb{sub 2}-type DyMn{sub 4}Si{sub 2}, Sc{sub 2}CoSi{sub 2}-type Dy{sub 2}MnSi{sub 2} and Hf{sub 3}Ni{sub 2}Si{sub 3}-type Dy{sub 3}Mn{sub 2}Si{sub 3} ternary compounds. The ternary solid solution based on the binary compounds of the Dy–Mn and Dy–Si systems: the ThMn{sub 12}-type Dy{sub 8}Mn{sub 87}Si{sub 5}, Th{sub 6}Mn{sub 23}-type Dy{sub 23}Mn{sub 72}Si{sub 5}, MgCu{sub 2}-type Dy{sub 33}Mn{sub 58}Si{sub 9} and AlB{sub 2}-type Dy{sub 38}Mn{sub 2}Si{sub 58}. The other binary compounds of the Dy–Mn–Si system do not show any visible solubility. New Sc{sub 2}CoSi{sub 2}-type R{sub 2}MnSi{sub 2} and Hf{sub 3}Ni{sub 2}Si{sub 3}-type R{sub 3}Mn{sub 2}Si{sub 3} phases were discovered for R=Gd, Tb, Ho–Tm. Display Omitted

Investigation of thermoluminescent response of K2YF5:Dy3+ crystals for gamma and X radiation fields

International Nuclear Information System (INIS)

Silva, E.C.; Nogueira, M.S.; Faria, L.O.; Khaidukov, N.M.

2005-01-01

K 2 YF 5 crystals doped with rare earths have been synthesized with 0 to 100% of Dy 3+ ions optically active ions and an investigation was conducted to test its thermoluminescent (TL) response due to function of Dy 3+ concentration and their response in energy. After being irradiated with gamma and X-rays, it was observed that crystals doped with 1.0% of Dy 3+ feature the best response TL. The main dosimetric peak can be decomposed into three secondary TL peaks, centered in 96.4, 104.9 and 130.7 deg C, respectively, showing a good linearity and reproducibility of the dose measurements. The sensitization process seems to improve response TL and TL peak sensitivity increase to 130, 7 deg C at the expense of TL peak to 104, 9 deg C. The linear coefficient sign TL for K 2 Y 0.09 Dy 0.01 F5 is comparable to that of the dosemeter CaSO 4 : Mn, irradiated with gamma radiation source ( 137 Cs) under the same conditions. Energy dependence measurements show that the answer for X-rays with energy of 41.1 keV is more than 30 times the response to Cs-137, when exposed to the same dose. Due to the main peak in low temperature and the TL high reply to low energy fields, the results reported indicate that the K 2 YF 5 crystals doped with Dy 3+ present great potential for radiation dosimetry in X-rays therapy, clinical dosimetry and also for applications in digital thermoluminescent images

HIV/TB co-infection:perspectives of TB patients and providers on the integrated HIV/TB pilot program in Tamilnadu, India

OpenAIRE

Lakshminarayanan, Mahalakshmi

2009-01-01

The WHO recommends routine HIV testing among TB patients as a key strategy to combat the dual HIV/TB epidemic. India has integrated its HIV and TB control programs and is offering provider initiated HIV testing for all TB patients since 2007. Using a mixed methods approach, this study aims to understand the perspectives of TB patients and providers on the integrated HIV/TB pilot program in Tamilnadu, India. A survey conducted by the Tuberculosis Research Center, India on 300 TB patients is th...

Thermoelectric properties, crystal and electronic structure of semiconducting RECuSe{sub 2} (RE = Pr, Sm, Gd, Dy and Er)

Energy Technology Data Exchange (ETDEWEB)

Esmaeili, Mehdi [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1 (Canada); Tseng, Yu-Chih [CANMET Materials, Natural Resources Canada, 183 Longwood Road South, Hamilton, Ontario L8P 0A5 (Canada); Mozharivskyj, Yurij, E-mail: mozhar@mcmaster.ca [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1 (Canada)

2014-10-15

Highlights: • Crystal and electronic structure of monoclinic and trigonal RECuSe{sub 2} phases. • Thermoelectric properties of the RECuSe{sub 2} phases. • Temperature stability of the RECuSe{sub 2} phases. - Abstract: The ternary RECuSe{sub 2} phases have been prepared and structurally characterized. They adopt either a monoclinic structure (P2{sub 1}/c, z = 4) for lighter rare earths (RE = Pr, Sm and Gd) or Cu-disordered trigonal structure for heavier rare-earths (P3{sup ¯}m1, z = 1, RE = Dy and Er). The resistivity and Seebeck coefficient measurements on GdCuSe{sub 2}, DyCuSe{sub 2} and ErCuSe{sub 2} indicate that the studied phases are p-type semiconductors with relatively small activation energies (0.045–0.11 eV). However, their electrical resistivities are too high (0.45–220 Ω cm at room temperature) to make them competitive thermoelectric materials. Electronic structure calculations indicate presence of a band gap in the RECuSe{sub 2} phases.

Coercivity enhancement in hot deformed Nd2Fe14B-type magnets by doping low-melting RCu alloys (R = Nd, Dy, Nd + Dy)

Science.gov (United States)

Lee, Y. I.; Huang, G. Y.; Shih, C. W.; Chang, W. C.; Chang, H. W.; You, J. S.

2017-10-01

Magnetic properties of the anisotropic NdFeB magnets prepared by hot pressing followed by die-upsetting NdFeB MQU-F powders doped with low-melting RCu alloy powders were explored, where RCu stands for Nd70Cu30, Dy70Cu30 and (Nd0.5Dy0.5)70Cu30, respectively. In addition, the post-annealing at 600 °C was employed to modify the microstructures and the magnetic properties of the hot deformed magnets. It is found that doping RCu alloy powders is effective in enhancing the coercivity of the hot deformed NdFeB magnets from 15.1 kOe to 16.3-19.5 kOe. For Nd70Cu30-doped magnets, the increment of coercivity is only 1.2 kOe. Meanwhile, Dy70Cu30-doped and (Nd0.5Dy0.5)70Cu30-doped magnets show an almost identical enhancement of coercivity of about 4.4 kOe. Importantly, the latter magnet shows a beneficial effect of reducing the usage of Dy from 1.6 wt% to 0.8 wt%. TEM analysis shows that nonmagnetic Nd, Dy and Cu appear at grain boundary and isolate the magnetic grains, leading to an enhancement of coercivity. Doping lower melting point Dy-lean (Nd0.5Dy0.5)70Cu30 powders into commercial MQU-F powders for making high coercivity hot deformed NdFeB magnets might be a potential and economic way for mass production.

Phase transition of intermetallic TbPt at high temperature and high pressure

Science.gov (United States)

Qin, Fei; Wu, Xiang; Yang, Ke; Qin, Shan

2018-04-01

Here we present synchrotron-based x-ray diffraction experiments combined with diamond anvil cell and laser heating techniques on the intermetallic rare earth compound TbPt (Pnma and Z  =  4) up to 32.5 GPa and ~1800 K. The lattice parameters of TbPt exhibit continuous compression behavior up to 18.2 GPa without any evidence of phase transformation. Pressure-volume data were fitted to a third-order Birch-Murnaghan equation of state with V 0  =  175.5(2) Å3, {{K}{{T0}}}   =  110(5) GPa and K{{T0}}\\prime   =  3.8(7). TbPt exhibits anisotropic compression with β a   >  β b   >  β c and the ratio of axial compressibility is 2.50:1.26:1.00. A new monoclinic phase of TbPt assigned to the Pc or P2/c space group was observed at 32.5 GPa after laser heating at ~1800 K. This new phase is stable at high pressure and presented a quenchable property on decompression to ambient conditions. The pressure-volume relationship is well described by the second-order Birch-Murnaghan equation of state, which yields V 0  =  672(4) Å3, {{K}{{T0}}}   =  123(6) GPa, which is about ~14% more compressible than the orthorhombic TbPt. Our results provide more information on the structure and elastic property view, and thus a better understanding of the physical properties related to magnetic structure in some intermetallic rare earth alloys.

Tailored white light emission in Eu3+/Dy3+ doped tellurite glass phosphors containing Al3+ ions

Science.gov (United States)

Walas, Michalina; Piotrowski, Patryk; Lewandowski, Tomasz; Synak, Anna; Łapiński, Marcin; Sadowski, Wojciech; Kościelska, Barbara

2018-05-01

Tellurite glass systems modified by addition of aluminum fluoride AlF3 have been successfully synthesized as host matrices for optically active rare earth ions RE3+ (RE3+ = Eu3+, Dy3+). Samples with different Eu3+ to Dy3+ molar ratio have been studied in order to determine possibility of white light emission via UV excitation. Structural investigations confirmed amorphous character of materials whereas spectroscopic studies brought more insight into glass network's nature. FTIR results shown presence of two features related to tellurite glass matrix (in 490-935 cm-1 spectral region) and another one (940-1250 cm-1) due to aluminum addition. Especially, Al-O and Te-O-Al bonds of AlO4 tetrahedrons have been found. AlO4 units are considered as glass formers that improve network's strength and thermal resistivity against devitrification. Based on XPS studies of Al3+ photoelectron band the existence of Al-O and also Al-F bonds have been examined. Moreover, signals originating from Eu3+ and Dy3+ have been found confirming their valence state. Luminescence results revealed possibility of simultaneous UV excitation of Eu3+ and Dy3+ ions. Excitation with λexc = 390 and 393 nm resulted in white light generation starting from warm white to neutral and cool white depending on Eu3+ concentration and used excitation wavelength. Additionally, increase of decay lifetime of Eu3+ induced by Al3+ presence have been revealed based on luminescence decay analysis. Thus, tellurite glass systems modified by AlF3 and doped with Eu3+/Dy3+ may be considered as promising candidates for white light emitting sources.

On the photo-luminescence properties of sol–gel derived undoped and Dy3+ ion doped nanocrystalline Scheelite type AMoO4 (A = Ca, Sr and Ba)

International Nuclear Information System (INIS)

Jena, Paramananda; Gupta, Santosh K.; Natarajan, V.; Padmaraj, O.; Satyanarayana, N.; Venkateswarlu, M.

2015-01-01

Nanocrystalline Scheelite type Dy doped AMoO 4 [where A = Ba, Sr and Ca] samples were prepared by acrylamide assisted sol–gel process and characterized by XRD, FT-Raman, FTIR, SEM and photoluminescence (PL). PL of undoped sample shows blue/green emission in CaMoO 4 and SrMoO 4 but multicolour visible emission leading to near white light in BaMoO 4 nanoparticles; the origin of which is explained. It was observed that on doping 0.5 mol% of Dy 3+ in molybdate samples complete energy transfer takes place in case of SrMoO 4 and BaMoO 4 , but host contributed substantially in Dy doped BaMoO 4 sample, resulting in biexponential decay. It was also observed that symmetry around Dy 3+ decreases as the size of alkaline earth ion increases. Due to combined blue, yellow and red colour emission in dysprosium doped sample; all samples showed near white light emission under UV and near UV excitation

Microscopic effects of Dy doping in the topological insulator Bi2Te3

Science.gov (United States)

Duffy, L. B.; Steinke, N.-J.; Krieger, J. A.; Figueroa, A. I.; Kummer, K.; Lancaster, T.; Giblin, S. R.; Pratt, F. L.; Blundell, S. J.; Prokscha, T.; Suter, A.; Langridge, S.; Strocov, V. N.; Salman, Z.; van der Laan, G.; Hesjedal, T.

2018-05-01

Magnetic doping with transition metal ions is the most widely used approach to break time-reversal symmetry in a topological insulator (TI)—a prerequisite for unlocking the TI's exotic potential. Recently, we reported the doping of Bi2Te3 thin films with rare-earth ions, which, owing to their large magnetic moments, promise commensurately large magnetic gap openings in the topological surface states. However, only when doping with Dy has a sizable gap been observed in angle-resolved photoemission spectroscopy, which persists up to room temperature. Although disorder alone could be ruled out as a cause of the topological phase transition, a fundamental understanding of the magnetic and electronic properties of Dy-doped Bi2Te3 remained elusive. Here, we present an x-ray magnetic circular dichroism, polarized neutron reflectometry, muon-spin rotation, and resonant photoemission study of the microscopic magnetic and electronic properties. We find that the films are not simply paramagnetic but that instead the observed behavior can be well explained by the assumption of slowly fluctuating, inhomogeneous, magnetic patches with increasing volume fraction as the temperature decreases. At liquid helium temperatures, a large effective magnetization can be easily introduced by the application of moderate magnetic fields, implying that this material is very suitable for proximity coupling to an underlying ferromagnetic insulator or in a heterostructure with transition-metal-doped layers. However, the introduction of some charge carriers by the Dy dopants cannot be excluded at least in these highly doped samples. Nevertheless, we find that the magnetic order is not mediated via the conduction channel in these samples and therefore magnetic order and carrier concentration are expected to be independently controllable. This is not generally the case for transition-metal-doped topological insulators, and Dy doping should thus allow for improved TI quantum devices.

Reddish-orange, neutral and warm white emissions in Eu3+, Dy3+ and Dy3+/Eu3+ doped CdO-GeO2-TeO2 glasses

Science.gov (United States)

Rodríguez-Carvajal, David A.; Meza-Rocha, A. N.; Caldiño, U.; Lozada-Morales, R.; Álvarez, E.; Zayas, Ma. E.

2016-11-01

Eu3+, Dy3+ and Dy3+/Eu3+ doped CdO-GeO2-TeO2 glasses were prepared using the melt-quenching process and analyzed by X-diffraction, Raman spectroscopy, excitation and emission spectra, and emission decay time profiles. The lack of X ray diffraction peaks revealed that all samples are amorphous. Vibrational modes associated with Tesbnd Osbnd Te and Gesbnd Osbnd Ge related bonds and molecular oxygen were detected by Raman spectroscopy. The luminescence characteristics were studied upon excitations that correspond with the emission of InGaN (370-420 nm) based LEDs. The Eu3+ singly doped glass displayed reddish-orange global emission, with x = 0.601 and y = 0.349 CIE1931 chromaticity coordinates, upon 393 nm excitation. Neutral emission with x = 0.373 and y = 0.412 CIE1931 chromaticity coordinates and correlated color temperature (CCT) of 4400 K, was achieved in the Dy3+ singly doped glass excited at 388 nm. The Dy3+/Eu3+ co-doped glass exhibited warm, neutral and soft warm white emissions with CCT values of 3435, 4153 and 2740 K, under excitations at 382, 388 and 393 nm, respectively, depending mainly on the Dy3+ and Eu3+ relative excitation. The Dy3+ excitation bands observed in the Dy3+/Eu3+ glass by monitoring the 611 nm Eu3+ emission, suggest that Dy3+ → Eu3+ energy transfer takes place, despite the fact that the Dy3+ emission decays in the Dy3+ and Dy3+/Eu3+ doped glass, remain without changes. The shortening of Eu3+ decay in presence of Dy3+ was attributed to an Eu3+ → Dy3+ non-radiative energy transfer process, which according with the Inokuti-Hirayama model might be dominated through an electric quadrupole-quadrupole interaction, with efficiency and probability of 5.5% and 51.6 s-1, respectively.

The association between ARV and TB drug resistance on TB treatment outcome among Kazakh TB/HIV patients.

Science.gov (United States)

Mishkin, Kathryn; Alaei, Kamiar; Alikeyeva, Elmira; Paynter, Christopher; Aringazina, Altyn; Alaei, Arash

2018-02-26

TB drug resistance poses a serious threat to the public health of Kazakhstan. This paper presents findings related to TB treatment outcome and drug resistant status among people coinfected with HIV and TB in Kazakhstan. Cohort study using data were provided by the Kazakhstan Ministry of Health's National Tuberculosis Program for 2014 and 2015. Chi-square and logistical regression were performed to understand factors associated with drug resistant TB status and TB treatment outcome. In bivariate analysis, drug resistant status was significantly associated with year of TB diagnosis (p=0.001) viral load (p=0.03). TB treatment outcome was significantly associated with age at diagnosis (p=01), ARV treatment (p <0.0001), and TB drug resistant status (p=0.02). In adjusted analysis, drug resistance was associated with increased odds of successful completion of treatment with successful result compared to treatment failure (OR 6.94, 95% CI: 1.39-34.44) CONCLUSIONS: Our results suggest that being drug resistant is associated with higher odds of completing treatment with successful outcome, even when controlling for receipt of ARV therapy. Copyright © 2018. Published by Elsevier Ltd.

Synthesis and magneto-structural studies on a new family of carbonato bridged 3d-4f complexes featuring a [CoLn(CO3)] (Ln = La, Gd, Tb, Dy and Ho) core: slow magnetic relaxation displayed by the cobalt(ii)-dysprosium(iii) analogue.

Science.gov (United States)

Majee, Mithun Chandra; Towsif Abtab, Sk Md; Mondal, Dhrubajyoti; Maity, Manoranjan; Weselski, Marek; Witwicki, Maciej; Bieńko, Alina; Antkowiak, Michał; Kamieniarz, Grzegorz; Chaudhury, Muktimoy

2018-03-06

A new family of [3 + 3] hexanuclear 3d-4f complexes [(μ 3 -CO 3 ){Co II Ln III L(μ 3 -OH)(OH 2 )} 3 ]-(ClO 4 )·mC 2 H 5 OH·nH 2 O (1-5) [Ln = La (1), Gd (2), Tb (3), Dy (4), and Ho (5)] have been prepared in moderate to high yields (62-78%) following a self-assembly reaction between the ligand 6,6',6''-(nitrilotris(methylene))tris-(2-methoxy-4-methylphenol) (H 3 L), Co(OAc) 2 ·4H 2 O and the lanthanide ion precursors in the mandatory presence of tetrabutylammonium hydroxide. During the reaction, atmospheric carbon dioxide is fixed in the product molecule as a bridging carbonato ligand which connects all the three lanthanide centers of this molecular assembly through a rare η 2 :η 2 :η 2 -μ 3 mode of bridging as revealed from X-ray crystallography. The metal centers in all these compounds, except the Gd III analogue (2), are coupled in antiferromagnetic manner while the nature of coupling in the CoGd complex is ferromagnetic. DFT calculations revealed that this ferromagnetic interaction occurs most likely by the Co II -Gd III superexchange, mediated via the bridging oxygen atoms. Only the Co II -Dy III compound (4) displayed a slow relaxation of the magnetization at a very low temperature as established by AC susceptibility measurements. The data provides an estimation of the activation energy U/k B = 9.2 K and the relaxation time constant τ 0 = 1.0 × 10 -7 s.

Magnetic properties of the Tb4 + ion in Li2TbF6

Science.gov (United States)

Guillot, M.; El-Ghozzi, M.; Avignant, D.; Ferey, G.

1993-05-01

Both oxygen and fluorine have a partiality towards the stabilization of high oxidation states of rare earths such as Ce, Pr, and Tb. During the study of the MF-M'F4 (M=alkaline metal; M' rare ion) the compound Li2TbF6 was found to constitute the only representative obtained under ambient pressure of a structural type, namely α-Li2ZrF6, known until now only through the high pressure form. Magnetic measurements were carried out over the 1.4-300 K temperature range in continuous magnetic fields up to 20 T produced by a Bitter magnet. At low temperature and in H higher than 15 T, the magnetization M was observed to be field independent and very close to the calculated Tb4+ free ion value, i.e., 7μB; on the other hand, the data do not present any departure from the Brillouin function of the pure 8S7/2 state. The reciprocal magnetic susceptibility obeys a Curie-Weiss law leading to an effective moment of 7.86μB. A very unusual behavior of the terbium ion which presents a 4+ oxidation state is concluded: to the best of our knowledge, it is the first observation of this form. The so-found spherical 4f7 electronic configuration is the most compatible with the high coordination number of eight. Finally, the discussion within the series Li2MIVF6 compounds to understand the influence of both electronic configuration and size effects is presented.

Therapeutical radiopharmaceuticals based In vivo generator system [{sup 166} Dy] Dy/{sup 166} Ho; Radiofarmacos terapeuticos basados en un sistema de generador In vivo [{sup 166}Dy] Dy/{sup 166}Ho

Energy Technology Data Exchange (ETDEWEB)

Ferro F, G.; Garcia S, L.; Monroy G, F.; Tendilla, J.I. [Gerencia de Aplicaciones Nucleares en la Salud, ININ, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Pedraza L, M.; Murphy, C.A. de [Departamento de Medicina Nuclear, Instituto Nacional de Pediatria, Mexico D.F. (Mexico)

2002-07-01

At the idea to administer to a patient a molecule containing in it structure a father radionuclide, with a half life enough large which allows to the radiolabelled molecule to take up position specifically in a white tissue and decaying In vivo to the daughter radionuclide with properties potentially therapeutic, it is known as In vivo generator system. In this work the preparation and the preliminary dosimetric valuations of radiopharmaceuticals based In vivo generator system {sup 166} Dy Dy/{sup 166} Ho for applications in radioimmunotherapy, in the treatment of the rheumatoid arthritis and in the bone marrow ablation (m.o.) for candidates patients to bone marrow transplant are presented. (Author)

Changes of fluorescent spectral features after successive rare earth doping of gadolinium oxide powders

Energy Technology Data Exchange (ETDEWEB)

Kuznik, W. [Chemical Department, Silesian University of Technology, Gliwice (Poland); Institute of Physics, University of Tartu, Riia 142, Tartu 51014 (Estonia); Brik, M.G. [Institute of Physics, University of Tartu, Riia 142, Tartu 51014 (Estonia); Cieslik, I.; Majchrowski, A.; Jaroszewicz, L. [Institute of Applied Physics, Military University of Technology, Kaliskiego 2, 00-908 Warsaw (Poland); AlZayed, N.S. [Physics and Astronomy Dept., College of Science, P.O. Box 2455, King Saud University, Riyadh 11451 (Saudi Arabia); El-Naggar, A.M. [Physics and Astronomy Dept., College of Science, P.O. Box 2455, King Saud University, Riyadh 11451 (Saudi Arabia); Permanent address: Physics department, Faculty of Science, Ain Shams University, Abassia, Cairo 11566 (Egypt); Sildos, I.; Lange, S.; Kiisk, V. [Institute of Physics, University of Tartu, Riia 142, Tartu 51014 (Estonia); Kityk, I.V., E-mail: ikityk@el.pcz.czest.pl [Electrical Engineering Department, Czestochowa University of Technology, Armii Krajowej 17, Czestochowa (Poland); Physics and Astronomy Dept., College of Science, P.O. Box 2455, King Saud University, Riyadh 11451 (Saudi Arabia)

2012-01-15

Highlights: > Principally new phosphors based on rare earth moped Gd{sub 2}O{sub 3} are obtained. > The time-resolved fluorescent spectra show drastic changes with the doping. > Temperature measurements were done. - Abstract: We present a complex fluorescence study of a series of gadolinium oxide polycrystalline powders singly, doubly and triply doped with trivalent rare earth ions (Er{sup 3+}, Tb{sup 3+}, and Dy{sup 3+}), to explore a possibility of their use as materials for white light emitting diodes. The excitation and luminescence spectra along with the decay kinetics were measured in the temperature range from 6 to 300 K. The luminescence efficiency was studied within the visible spectral range, i.e. -400 nm to 750 nm under excitation by 355 nm third harmonic Nd:YAG laser pulses. Singly doped Er{sup 3+} sample gave stronger luminescence signals, but others showed significantly larger decay lifetimes. The successive rare earths doping leads to substantial changes of the spectral positions due to the up-conversion processes. In the singly (Er{sup 3+}) doped sample, following the time resolved spectrum and decay curves, there are two different types of emissions: at 660 nm and at shorter wavelengths (below 640 nm) the red emission's lifetime is ten times longer than at shorter wavelengths. The singly doped sample shows unclear temperature-dependence of luminescence with lifetime at 550 nm (the longest at 100 K, similarly at 6 K and 300 K) and achieved luminous efficacy 73.5 lm/W.

Properties of alginate fiber spun-dyed with fluorescent pigment dispersion.

Science.gov (United States)

Wang, Ping; Tawiah, Benjamin; Tian, Anli; Wang, Chunxia; Zhang, Liping; Fu, Shaohai

2015-03-15

Spun-dyed alginate fiber was prepared by the spun-dyeing method with the mixture of fluorescent pigment dispersion and sodium alginate fiber spinning solution, and its properties were characterized by SEM, TGA, DSC, and XRD. The results indicate that fluorescent pigment dispersion prepared with esterified poly (styrene-alt maleic acid) had excellent compatibility with sodium alginate fiber spinning solution, and small amount of fluorescent pigment could reduce the viscosity of spun-dyed spinning solutions. SEM photo of spun-dyed alginate fiber indicated that fewer pigment particles deposited on its surface. TGA, DSC, and XRD results suggested that thermal properties and crystal phase of spun-dyed alginate fibers had slight changes compared to the original alginate fibers. The fluorescence intensity of spun-dyed alginate fiber reached its maximum when the content of fluorescent pigment was 4%. The spun-dyed alginate fiber showed excellent rubbing and washing fastness. Copyright © 2014 Elsevier Ltd. All rights reserved.

Domain wall conductivity in semiconducting hexagonal ferroelectric TbMnO3 thin films

International Nuclear Information System (INIS)

Kim, D J; Gruverman, A; Connell, J G; Seo, S S A

2016-01-01

Although enhanced conductivity of ferroelectric domain boundaries has been found in BiFeO 3 and Pb(Zr,Ti)O 3 films as well as hexagonal rare-earth manganite single crystals, the mechanism of the domain wall conductivity is still under debate. Using conductive atomic force microscopy, we observe enhanced conductance at the electrically-neutral domain walls in semiconducting hexagonal ferroelectric TbMnO 3 thin films where the structure and polarization direction are strongly constrained along the c-axis. This result indicates that domain wall conductivity in ferroelectric rare-earth manganites is not limited to charged domain walls. We show that the observed conductivity in the TbMnO 3 films is governed by a single conduction mechanism, namely, the back-to-back Schottky diodes tuned by the segregation of defects. (paper)

Electrical and magnetic transport properties of DyTiGe

International Nuclear Information System (INIS)

Dagula, W.; Tegus, O.; Li, X.W.; Zhang, L.; Brueck, E.; Boer, F.R. de; Buschow, K.H.J.

2004-01-01

Electrical resistivity and magnetoresistance of DyTiGe were investigated as a function of temperature and magnetic field. DyTiGe is an antiferromagnet with Neel temperature, T N , of 180 K. The electrical resistivity has an anomaly around T N . Below T N , the magnetoresistance of DyTiGe abruptly changes at a critical field. At 5 K, we observe a magnetoresistance reduction of about 20%

Synthesis and luminescent properties of trivalent rare-earth (Eu{sup 3+}, Tb{sup 3+}) ions doped nanocrystalline AgLa(PO{sub 3}){sub 4} polyphosphates

Energy Technology Data Exchange (ETDEWEB)

Krishna Bharat, L.; Jeon, Yong Il; Yu, Jae Su, E-mail: jsyu@khu.ac.kr

2014-11-25

Highlights: • AgLa(PO{sub 3}){sub 4}:Eu{sup 3+}, Tb{sup 3+} nanocrystalline phosphors were prepared by a sol–gel process. • The luminescent properties were studies by near-UV excitation. • The intense MD transition indicates the presence of high inversion symmetry site. • These results suggest that the compound is a good candidate for optical applications. - Abstract: The AgLa(PO{sub 3}){sub 4} phosphors activated with trivalent rare-earth (Eu{sup 3+}, Tb{sup 3+}) ions were prepared by a sol–gel synthesis method. The crystal structure of the compound was studied by X-ray diffraction patterns and found to be crystallized in the monoclinic system with a space group P2{sub 1}/c, indicating the calculated lattice parameters of a = 10.08 Å, b = 13.12 Å, and c = 7.314 Å. The Fourier-transform infrared spectrum, photoluminescence excitation/emission spectra, and decay curves were examined to study the optical properties. The analysis of the Eu{sup 3+} ions related emission spectrum revealed the presence of highly symmetric sites for the activator ions. The Tb{sup 3+} ions related emission spectrum exhibited a {sup 5}D{sub 3} emission due to the prolonged calcination at high temperatures, which reduces the residual hydroxyl ions. The optical properties show that this host material is suitable for phosphor materials and laser crystals.

Production of thermoluminescent dosemeters based on MgB{sub 4}O{sub 7}: Dy and MgB{sub 4}O{sub 7}: Tm; Producao de dosimetros termoluminescentes a base de MgB{sub 4}O{sub 7}: Dy e MgB{sub 4}O{sub 7}: Tm

Energy Technology Data Exchange (ETDEWEB)

Souza, Luiza Freire de; Souza, Divanizia N., E-mail: luizaf25@hotmail.com, E-mail: divanizi@ufs.br [Universidade Federal de Sergipe (UFS), Sao Cristovao, SE (Brazil). Programa de Pos-Graduacao em Fisica

2013-07-01

The thermoluminescent dosimetry (TL) is a well-established technique for the detection of ionizing radiation in hospitals, clinics, and industrial establishments where there is the need to quantify the radiation. For this practice is require the use phosphors which are sensitive to radiation. Some phosphors are already commonly used in this practice, for example, TLD-100 (LiF: Mg, Ti), CaSO{sub 4}:Tm and CaSO{sub 4}:Dy. A compound that was most recently introduced in dosimetry and has many advantageous features to detect neutrons, electrons and gamma is the magnesium tetraborate (MgB{sub 4}O{sub 7}), but the undoped material is not good for dosimetry, since signal does not show satisfactory thermoluminescence. The present work presents the analysis of the compound MgB{sub 4}O{sub 7} when doped with rare earth elements, thulium (Tm) and dysprosium (Dy). The production of MgB{sub 4}O{sub 7}: Dy and MgB{sub 4}O{sub 7}: Tm occurred under acidic conditions. Following the process of crystal growth, several tests were made on phosphors produced to verify the quality of materials as TL dosimeter. Initially, was made the identification of the crystalline phases found in the material, using the technique of X-ray diffractometry, and then were evaluated and compared the TL emission curves of the crystals with two different types of dopants, to this, the samples were irradiated with different radiation sources: {sup 137}Cs (0,66 MeV), {sup 60}Co (1.25 MeV) and X-rays (0.41 MeV) and based on the results was evaluated the energy dependence of phosphors. Another characteristic analyzed, was the decay of TL signal for the material (fading). The results show that the material can be an excellent TL dosimeter when doped with rare earth elements Dy and Tm. (author)

Emission bands of phosphorus and calculation of band structure of rare earth phosphides

International Nuclear Information System (INIS)

Al'perovich, G.I.; Gusatinskij, A.N.; Geguzin, I.I.; Blokhin, M.A.; Torbov, V.I.; Chukalin, V.I.; AN SSSR, Moscow. Inst. Novykh Khimicheskikh Problem)

1977-01-01

The method of x-ray emission spectroscopy has been used to investigate the electronic structure of monophosphides of rare-earth metals (REM). The fluorescence K bands of phosphorus have been obtained in LaP, PrP, SmP, GdP, TbP, DyP, HoP, ErP, TmP, YbP, and LuP and also the Lsub(2,3) bands of phosphorus in ErP, TmP, YbP, and LuP. Using the Green function technique involving the muffin-tin potential, the energy spectrum for ErP has been calculated in the single-electron approximation. The hystogram of electronic state distribution N(E) is compared with the experimental K and Lsub(2,3) bands of phosphorus in ErP. The agreement between the main details of N(E) and that of x-ray spectra allows to state that the model used provides a good description of the electron density distribution in crystals of REM monophosphides. In accordance with the character of the N(E) distribution the compounds under study are classified as semimetals or semiconductors with a very narrow forbidden band

Theoretical investigations on magnetocaloric effect in Er{sub 1−y}Tb{sub y}Al{sub 2} series

Energy Technology Data Exchange (ETDEWEB)

Ribeiro, P.O., E-mail: paula.ribeiro@gmail.com [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil); Alho, B.P.; Alvarenga, T.S.T.; Nóbrega, E.P.; Sousa, V.S.R. de [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil); Carvalho, A. Magnus G. [Laboratório Nacional de Luz Síncrotron, CNPEM, 13083-970 Campinas, SP (Brazil); Caldas, A. [Sociedade Unificada de Ensino Superior e Cultura, SUESC, 20211-351 Rio de Janeiro, RJ (Brazil); Oliveira, N.A. de; Ranke, P.J. von [Instituto de Física, Universidade do Estado do Rio de Janeiro – UERJ, Rua São Francisco Xavier, 524, 20550-013 RJ (Brazil)

2015-04-01

We report on the magnetic and magnetocaloric effect calculations in rare earth Er{sub 1−y}Tb{sub y}Al{sub 2} compounds (y=0.00, 0.25, 0.5, 0.75 and 1.00). Our model Hamiltonian has contributions of the crystalline electrical field anisotropy in both Er and Tb magnetic sublattices, disorder in exchange interactions among Er–Er, Tb–Tb and Er–Tb magnetic ions and the Zeeman effect. The magnetization, the isothermal entropy change (ΔS{sub T}) and the adiabatic temperature change (ΔT{sub ad}) dependence on temperature were simulated and, compared with the experimental data available. - Highlights: • Modeling Er{sub (1−y)}Tb{sub y}Al{sub 2} intermetallic compounds. • Magnetic entropy changes in Er{sub (1−y)}Tb{sub y}Al{sub 2}. • Adiabatic temperature changes in Er{sub 0.75}Tb{sub 0.25}Al{sub 2} and Er{sub 0.65}Tb{sub 0.35}Al{sub 2} compounds.

Unexpected structure in the E2 quasicontinuum spectrum of 154Dy

International Nuclear Information System (INIS)

Holzmann, R.; Khoo, T.L.; Ma, W.C.

1988-01-01

The evolution of the γ quasicontinuum spectrum with neutron number has been investigated in the sequence of dysprosium isotopes /sup 152,154,156/Dy. The three nuclei display a pronounced collective E2 component. In 154 Dy this component shows an unexpected splitting into two distinct parts, signifying a structural change along the γ cascade. The E2 and statistical components can be reproduced in simple γ cascade calculations; in 152 Dy and 156 Dy only rotational bands were included, whereas in 154 Dy additional vibration-like transitions were required to reproduce the two E2 peaks. 11 refs., 2 figs

Advances in the hydrometallurgical separation techniques of high purity rare earth elements

International Nuclear Information System (INIS)

Vijayalakshmi, R.; Kain, V.

2017-01-01

Rare Earths are a series of 15 chemically similar elements that occur together in monazite mineral found in the beach sands of Kerala, Tamil Nadu and Orissa. The rare earth elements (REE) are becoming increasingly strategically important considering their essential role in permanent magnets such as, SmCo_5, Sm_2Co_1_7 and Nd_2Fe_1_4B, phosphors for LED screens and lamps, rechargeable nickel metal hydride batteries and catalysts and other green applications. The increasing popularity of hybrid and electric cars, wind turbines and compact fluorescent lamps is causing an increase in the demand and price of REE. The European Commission considers the REE as the most critical raw materials group, with the highest supply risk. According to the medium-term criticality matrix of the U.S. Department of Energy (DOE), the five most critical REE are neodymium (Nd), europium (Eu), terbium (Tb), dysprosium (Dy) and yttrium (Y). China is presently producing more than 90% of all rare earths, although they possess less than 405 of the proven reserves. Due to large and increasing domestic demands, China tightened its REE export quota from 2012 onwards. These export quotas caused serious problems for REE users outside of China. Fortunately India is blessed with large resources of rare earths in the form of monazite found in the beach sands of Kerala, Tamil Nadu and Orissa. Indian Rare Earths Limited at Aluva near Kochi produces mainly mixed rare earths chloride and till recent past exporting to USA, UK, France, Japan, etc. They have revived their rare earth separation plant to meet the in-house demands of the strategic, defense and nuclear industry. This paper discusses the recent advances made in hydrometallurgical separation techniques based on solvent extraction technique, ion-exchange resins, hollow fibre membrane extractor, solvent encapsulated polymeric beads, etc for the production of high purity rare earth elements from both primary (Monazite, xenotime) and secondary sources

Emission spectra of phosphor MgSO4 doped with Dy and Mn

International Nuclear Information System (INIS)

Zhang Chunxiang; Chen Lixin; Tang Qiang; Luo Daling; Qiu Zhiren

2001-01-01

Emission spectra of phosphor MgSO 4 doped with Dy and Dy/Mn were measured with an optical multichannel analyzer and a linear heating system whose temperature was controlled by a microcomputer. The emission spectrum bands at 480 nm and 580 nm of phosphor MgSO 4 doped with Dy were observed in the three dimensional (3D) glow curves. Compared with the 3D spectrum of CaSO 4 :Dy and the spectrum bands of MgSO 4 :Dy shows the same wavelengths which resulted from the quantum transitions among the energy levels of Dy 3 '+ ions. The intensities of the glow peaks in both spectrum bands (480 nm and 580 nm) of phosphor MgSO 4 doped with Dy/Mn were dramatically reduced except the 380 degree C glow peak

Dielectric behaviour of (Ba0.77Ca0.23(Ti0.98Dy0.02O3 ceramics

Directory of Open Access Journals (Sweden)

Abdul Moquim

2015-06-01

Full Text Available In this study, BaTiO3 is modified with Ca2+ and in addition doped with Dy3+ at the B site lattice. The main idea is to search for new lead-free ferroelectric material and improve their properties. For this purpose, the barium calcium titanate (BCT as a host and the rare earth element Dy3+ as an activator were used to fabricate a multifunctional material. The obtained ceramics was found to be homogeneous, dense and a single phase material with no evidence of secondary phases. The dielectric study showed that TC increases with the addition of dopants and the obtained ceramics behaves like a relaxor ferroelectric. Some important structural parameters and dielectric properties of dysprosium modified barium (calcium titanate ceramics are presented.

Solvent extraction of rare earths from thiocyanate medium using N,N,N',N'-tetra-2-ethylhexyl diglycolamide

International Nuclear Information System (INIS)

Anitha, M.; Kotekar, M.K.; Singh, D.K.; Sharma, J.N.; Singh, H.

2014-01-01

TEHDGA (N,N,N',N'-tetra-2-ethylhexyl diglycolamide), a neutral extractant, has been explored for separation of Yttrium from other heavy rare earths (Er) from thiocyanate medium. Presence of 5%(v/v) isodecyl alcohol was found to be optimum to prevent third phase formation. Experimental variables such as TEHDGA concentration (0.05M-0.2M), thiocyanate concentration (0.01M-0.04M), aqueous pH, rare earth concentration (0.25g/L-5g/L), temperature (35℃-65℃), stripping reagents on extraction of rare earths were investigated. The extraction of rare earths increased with increase in TEHDGA concentration and the dependency of distribution ratio of rare earth on TEHDGA concentrations is shown. The slopes were analysed to be approximately 3 for all the rare earths. The effect of thiocyanate concentration on distribution ratio is depicted. Based on slope analysis technique, the extracted species was found to be RE(SCN) 3 .3TEHDGA. The distribution ratio values decreased, may possibly be due to decrease in free extractant concentration in the organic phase, from 8.4 to 0.1 for Y with increase in yttrium concentration in the range of 0.25g/L to 5g/L. The extraction of rare earth decreased with increase in temperature indicating exothermic in nature and the enthalpy change (ΔH) obtained for Y(III) was -14.27KJ/mol. Among stripping reagents studied, oxalic acid was efficient in quantitative stripping of rare earths from TEHDGA. The extraction efficiency for rare earths by TEHDGA increased with increase in atomic number: La< Ce< Pr< Nd< Sm< Y< Eu< Gd< Tb< Dy< Ho< Er< Tm< Lu irrespective of thiocyanate concentration. Separation factors between these metal ions were also evaluated. High separation factor of 6.4 for Er/Y pair at 0.03M thiocyanate has indicated the feasibility of using TEHDGA as extractant to separate Y from Er and other rare earths as an alternative for Aliquat 336-thiocyanate system developed in our laboratory

Preparation, characterization, and luminescence properties of dysprosium perchlorate with MABA-Si and phen or dipy complexes as well as SiO{sub 2}@Dy(MABA-Si)L core-shell structure nanometermeter luminescent composites

Energy Technology Data Exchange (ETDEWEB)

Li, Wen-Xian, E-mail: nmglwx@163.com [College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021 (China); Zheng, Yu-Shan [Inner Mongolia Autonomous Region Product Quality Inspection Institute, Hohhot 010010 (China); Cao, Xiao-fang; Bai, Juan; Fu, Zhi-Fang; Bao, Jin-Rong; Li, Yi-Lian [College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021 (China)

2016-10-15

Two novel ternary rare earth complexes Dy(MABA-Si)·L{sub 2}(ClO{sub 4}){sub 3}·2H{sub 2}O (L= Phen or Dipy) were prepared using HOOCC{sub 6}H{sub 4}N(CONH(CH{sub 2}){sub 3}Si-(OCH{sub 2}CH{sub 3}){sub 3}){sub 2} which was abbreviated or denoted as MABA-Si. MABA-Si was the first ligand, L was the second ligand. The corresponding two SiO{sub 2}@Dy(MABA-Si)L nanometermeter luminescent composites were synthesized as well, and the silica spheres is the core, and the ternary rare earth complex Dy(MABA-Si)·L{sub 2}(ClO{sub 4}){sub 3}·2H{sub 2}O was the shell layer, who was abbreviated or denoted as Dy((MABA-Si)L). The ternary complexes have been characterized by element analysis, molar conductivity, IR spectra and {sup 1}HNMR spectra. The results showed that the chemical formula of the complex was Dy(MABA-Si)·L{sub 2}(ClO{sub 4}){sub 3}·2H{sub 2}O. The fluorescent spectra illustrated that the complexes displayed its characteristic luminescence in solid state, and the luminescence was superior than Dy{sup 3+}. The core-shell structure of SiO{sub 2}@Dy(MABA-Si)L nanometermeter luminescent composite was characterized by SEM, TEM and IR spectra. Based on the SEM photographs, the core-shell structure particles showed its regular microstructure including smooth surface, and good dispersity. The ternary complex coated on the mono-dispersed SiO{sub 2} spheres by self-assembly. The fluorescent spectra illustrated that the core-shell structure of SiO{sub 2}@Dy(MABA-Si)L nanometermeter luminescent composites exhibited stronger fluorescent than the ternary complexes. The fluorescence lifetime of the complexes and core-shell structure composites was measured as well.

Yttrium interaction with iron family metals

International Nuclear Information System (INIS)

Kharchenko, O.I.; Bodak, O.I.; Gladyshevskij, E.I.

1977-01-01

X-ray and micro-structure analyses were used to study ternary systems Y-Fe-Co, Y-Fe-Ni, Y-Co-Ni and phase equilibrium diagrams were plotted. The formation of a compound YCosub(0.8-0.38)Nisub(0.2-0.62) with a type MoB structure (a=3.946, c=20.85 A) was detected. Isostructural compounds with other rare earth metals (R) were found (R-Cd, Tb, Dy, Ho, Er, Tm)

From a Dy(III) single molecule magnet (SMM) to a ferromagnetic [Mn(II)Dy(III)Mn(II)] trinuclear complex.

Science.gov (United States)

Bhunia, Asamanjoy; Gamer, Michael T; Ungur, Liviu; Chibotaru, Liviu F; Powell, Annie K; Lan, Yanhua; Roesky, Peter W; Menges, Fabian; Riehn, Christoph; Niedner-Schatteburg, Gereon

2012-09-17

The Schiff base compound 2,2'-{[(2-aminoethyl)imino]bis[2,1-ethanediyl-nitriloethylidyne]}bis-2-hydroxy-benzoic acid (H(4)L) as a proligand was prepared in situ. This proligand has three potential coordination pockets which make it possible to accommodate from one to three metal ions allowing for the possible formation of mono-, di-, and trinuclear complexes. Reaction of in situ prepared H(4)L with Dy(NO(3))(3)·5H(2)O resulted in the formation of a mononuclear complex [Dy(H(3)L)(2)](NO(3))·(EtOH)·8(H(2)O) (1), which shows SMM behavior. In contrast, reaction of in situ prepared H(4)L with Mn(ClO(4))(2)·6H(2)O and Dy(NO(3))(3)·5H(2)O in the presence of a base resulted in a trinuclear mixed 3d-4f complex (NHEt(3))(2)[Dy{Mn(L)}(2)](ClO(4))·2(H(2)O) (2). At low temperatures, compound 2 is a weak ferromagnet. Thus, the SMM behavior of compound 1 can be switched off by incorporating two Mn(II) ions in close proximity either side of the Dy(III). This quenching behavior is ascribed to the presence of the weak ferromagnetic interactions between the Mn(II) and Dy(III) ions, which at T > 2 K act as a fluctuating field causing the reversal of magnetization on the dysprosium ion. Mass spectrometric ion signals related to compounds 1 and 2 were both detected in positive and negative ion modes via electrospray ionization mass spectrometry. Hydrogen/deuterium exchange (HDX) reactions with ND(3) were performed in a FT-ICR Penning-trap mass spectrometer.

Neutron diffraction studies on GdB6 and TbB6 powders

International Nuclear Information System (INIS)

Luca, S.E.; Amara, M.; Galera, R.M.; Givord, F.; Granovsky, S.; Isnard, O.; Beneu, B.

2004-01-01

We report here the first powder neutron diffraction study of GdB 6 and TbB 6 . GdB 6 and TbB 6 order antiferromagnetically at 15 and 21 K, respectively. In both compounds the transition at T N is of the first order. Moreover GdB 6 presents a second spontaneous magnetic transition at T * =8 K. The present study shows that, in both compounds, the magnetic propagation vectors belong to the star and that the direction of the magnetic moment is perpendicular to the ((1)/(2)) component of the wave-vector in GdB 6 , while in TbB 6 the moment is parallel to it. The deduced low-temperature values of the magnetic moments agree with those of the respective rare-earth trivalent ions

Study of the structure of the transition nuclei 152Dy, 154Dy and 156Er at high angular momentum

International Nuclear Information System (INIS)

Azgui, F.

1985-01-01

Measurements of feeding times of high spin yrast states in 152 Dy, 154 Dy and 156 Er were utilized to obtain information about possible spin dependent shape changes. Feeding times as well as lifetimes were determined with the recoil distance technique. In 152 Dy only long feeding times (> 10 ps) could be identified, indicating that the aligned-particle yrast states are fed through configuration of similar character, with little direct population from collective cascade in the continuum region. In 154 Dy discrete states with I ≤ 30 have lifetimes which are characteristically collective, whereas the preyrast cascade exhibit both fast ( 10 ps) feeding components. The latter imply a change with increasing spin from collective to aligned-particle character, signalling a prolate to oblate shape transition. In 156 Er the yrast states up to spin 20 ℎ were found to be collective. These levels are fed, however, from long-lived high spin states, causing time delay up to ∼ 100 ps, the existence of which is interpreted as a signature for an oblate shape at high spin [fr

Synthesis, characterization, and thermal properties of homoleptic rare-earth guanidinates: promising precursors for MOCVD and ALD of rare-earth oxide thin films.

Science.gov (United States)

Milanov, Andrian P; Fischer, Roland A; Devi, Anjana

2008-12-01

Eight novel homoleptic tris-guanidinato complexes M[(N(i)Pr)(2)CNR(2)](3) [M = Y (a), Gd (b), Dy (c) and R = Me (1), Et (2), (i)Pr (3)] have been synthesized and characterized by NMR, CHN-analysis, mass spectrometry and infrared spectroscopy. Single crystal structure analysis revealed that all the compounds are monomers with the rare-earth metal center coordinated to six nitrogen atoms of the three chelating guanidinato ligands in a distorted trigonal prism geometry. With the use of TGA/DTA and isothermal TGA analysis, the thermal characteristics of all the complexes were studied in detail to evaluate their suitability as precursors for thin film deposition by MOCVD and ALD. The (i)Pr-Me(2)N-guanidinates of Y, Gd and Dy (1a-c) showed excellent thermal characteristics in terms of thermal stability and volatility. Additionally, the thermal stability of the (i)Pr-Me(2)N-guanidinates of Y and Dy (1a, c) in solution was investigated by carrying out NMR decomposition experiments and both the compounds were found to be remarkably stable. All these studies indicate that (i)Pr-Me(2)N-guanidinates of Y, Gd and Dy (1a-c) have the prerequisites for MOCVD and ALD applications which were confirmed by the successful deposition of Gd(2)O(3) and Dy(2)O(3) thin films on Si(100) substrates. The MOCVD grown films of Gd(2)O(3) and Dy(2)O(3) were highly oriented in the cubic phase, while the ALD grown films were amorphous.

Magnetomigration of rare-earth ions in inhomogeneous magnetic fields.

Science.gov (United States)

Franczak, Agnieszka; Binnemans, Koen; Jan Fransaer

2016-10-05

The effects of external inhomogenous (gradient) magnetic fields on the movement of the rare-earth ions: Dy 3+ , Gd 3+ and Y 3+ , in initially homogeneous aqueous solutions have been investigated. Differences in the migration of rare-earth ions in gradient magnetic fields were observed, depending on the magnetic character of the ions: paramagnetic ions of Dy 3+ and Gd 3+ move towards regions of the sample where the magnetic field gradient is the strongest, while diamagnetic ions of Y 3+ move in the opposite direction. It has been showed that the low magnetic field gradients, such the ones generated by permanent magnets, are sufficient to observe the magnetomigration effects of the ions in solution. The present work clearly establishes the behavior of magnetically different ions in initially homogeneous aqueous solutions exposed to magnetic field gradients. To this avail, a methodology for measuring the local concentration differences of metal ions in liquid samples was developed.

Modification of magnetoresistance and magnetic properties of Ni thin films by adding Dy interlayer

Science.gov (United States)

Vorobiov, S. I.; Shabelnyk, T. M.; Shutylieva, O. V.; Pazukha, I. M.; Chornous, A. M.

2018-03-01

The paper reports the influence of dysprosium (Dy) interlayer addition on structure, magnetoresistance and magnetic properties of nickel (Ni) thin films. Trilayer film systems Ni/Dy/Ni have been prepared by alternate electron-beam evaporation. It is demonstrated that all as-prepared and annealed Ni thin films have face-centered cubic structure. The composition of the samples after addition of the Dy interlayer corresponds to the combination of face-centered cubic (Ni) and hexagonal close-packed (Dy) structures. The structure of Ni/Dy/Ni film systems changes from amorphous to polycrystalline when Dy interlayer thickness (t Dy) is more than 15 nm. The value of magnetoresistance increases with the adding the Dy interlayer in both longitudinal and transverse geometries, meanwhile the anisotropic character of magnetoresistance field dependences retained. The saturation and reversal magnetizations are reduced with the increasing of the Dy thickness interlayer, while the coercivity takes the minimum value at t Dy = 15 nm. The following increasing of t Dy leads to increasing of coercivity near to three times. This result indicates the influence of the crystal structure on the magnetic properties of Ni thin films at adding Dy interlayer.

Evaluating rare earth element availability: a case with revolutionary demand from clean technologies.

Science.gov (United States)

Alonso, Elisa; Sherman, Andrew M; Wallington, Timothy J; Everson, Mark P; Field, Frank R; Roth, Richard; Kirchain, Randolph E

2012-03-20

The future availability of rare earth elements (REEs) is of concern due to monopolistic supply conditions, environmentally unsustainable mining practices, and rapid demand growth. We present an evaluation of potential future demand scenarios for REEs with a focus on the issue of comining. Many assumptions were made to simplify the analysis, but the scenarios identify some key variables that could affect future rare earth markets and market behavior. Increased use of wind energy and electric vehicles are key elements of a more sustainable future. However, since present technologies for electric vehicles and wind turbines rely heavily on dysprosium (Dy) and neodymium (Nd), in rare-earth magnets, future adoption of these technologies may result in large and disproportionate increases in the demand for these two elements. For this study, upper and lower bound usage projections for REE in these applications were developed to evaluate the state of future REE supply availability. In the absence of efficient reuse and recycling or the development of technologies which use lower amounts of Dy and Nd, following a path consistent with stabilization of atmospheric CO(2) at 450 ppm may lead to an increase of more than 700% and 2600% for Nd and Dy, respectively, over the next 25 years if the present REE needs in automotive and wind applications are representative of future needs.

Study of a new dosimetric radio-thermoluminescent systems

International Nuclear Information System (INIS)

Cazac, T.C.

1980-01-01

This is the first Romanian study to investigate conditions to obtain the radio-thermo-luminescent systems: MgB 4 O 7 :A(A-Nd,Sm,Eu,Dy,Tb,Dy+Sm and Tb+Sm) MgF 2 A (A=Mn,Dy,Tb,Sm,Li), their essential dosimetric characters, as well as the (MgF 2 =Mn) thermophosphorus mixture with a ( 6 LiF) lithium target. An investigation was developed upon a new category of radio-thermoluminescent detectors with low radiation energy dependence and fading, magnesjum boride activated by several elements of the lanthanides class (Nd,Sm,Eu,Dy,Tb). A new radio-thermoluminescent dosimetric system with high sensitivity and moderate dependence on energy radiation - (Mnsup(2+)) manganese activated magnesium fluoride - was also studied. The author explored application of investigated detectors MgF 2 =Mn, MgB 4 O 7 =Dy and MgB 4 O 7 :Tb in neutron dosimetry in complex gamma-neutron fields. It is deemed that by using the dosimetric systems reported in the thesis in order to measure gamma, beta and neutron radiation doses, dosimetric control can be ensured both in professional dosimetry and in nuclear accident dosimetry, as well as in various basic and applicative investigations. A modest contribution is thus made towards achieving the national nuclear program through an extension of the thermophosphorus range with practical applications in nuclear radiation dosimetry. (author)

Improving the SMM and luminescence properties of lanthanide complexes with LnO9 cores in the presence of ZnII: an emissive Zn2Dy single ion magnet.

Science.gov (United States)

Fondo, Matilde; Corredoira-Vázquez, Julio; Herrera-Lanzós, Antía; García-Deibe, Ana M; Sanmartín-Matalobos, Jesús; Herrera, Juan Manuel; Colacio, Enrique; Nuñez, Cristina

2017-12-12

Mononuclear complexes of stoichiometry [Ln(H 3 L)(H 2 O)(NO 3 )](NO 3 ) 2 (Ln = Tb, 1; Dy, 2, Er, 3), which crystallise with different solvates, and the heterotrinuclear compound [Zn 2 Dy(L)(NO 3 ) 3 (OH)] (4) can be obtained with the same H 3 L compartmental ligand. The single X-ray crystal structure of the mononuclear complexes shows a LnO 9 core with a muffin-like disposition while the geometry of the DyO 9 core in 4 seems to be closer to spherical capped square antiprism. The analysis of the magnetic properties of all the complexes demonstrates that the mononuclear lanthanide compounds do not show slow relaxation of the magnetization, even when the samples are diluted with a diamagnetic matrix and subjected to a dc applied field of 1000 Oe. Nevertheless, the heterotrinuclear dysprosium complex 4·3H 2 O is a field-induced single ion magnet, with an estimated U eff barrier of 59 K. The luminescence characterisation of all the metal complexes in methanol solution at 298 K also shows a notable increase in the fluorescence emission of the heterotrinuclear complex with respect to the mononuclear ones, in such a way that 4 can be defined as a fluorescent single ion magnet.

High-spin structure of neutron-rich Dy isotopes

Indian Academy of Sciences (India)

Neutron-rich Dy isotopes; high-spin states; g-factors; cranked HFB theory. ... for 164Dy marking a clear separation in the behaviour as a function of neutron ... cipal x-axis as the cranking axis) in this mass region we have planned to make a sys-.

The pressure-induced structural response of rare earth hafnate and stannate pyrochlore from 0.1-50 GPa

Science.gov (United States)

Turner, K. M.; Rittman, D.; Heymach, R.; Turner, M.; Tracy, C.; Mao, W. L.; Ewing, R. C.

2017-12-01

Complex oxides with the pyrochlore (A2B2O7) and defect-fluorite ((A,B)4O7) structure-types undergo structural transformations under high-pressure. These compounds are under consideration for applications including as a proposed waste-form for actinides generated in the nuclear fuel cycle. High-pressure transformations in rare earth hafnates (A2Hf2O7, A=Sm, Eu, Gd, Dy, Y, Yb) and stannates (A2Sn2O7, A=Nd, Gd, Er) were investigated to 50 GPa by in situ Raman spectroscopy and synchrotron x-ray diffraction (XRD). Rare-earth hafnates form the pyrochlore structure for A=La-Tb and the defect-fluorite structure for A=Dy-Lu. Lanthanide stannates form the pyrochlore structure. Raman spectra revealed that at ambient pressure all compositions have pyrochlore-type short-range order. Stannate compositions show a larger degree of pyrochlore-type short-range ordering relative to hafnates. In situ high-pressure synchrotron XRD showed that rare earth hafnates and stannates underwent a pressure-induced phase transition to a cotunnite-like (Pnma) structure that begins between 18-25 GPa in hafnates and between 30-33 GPa in stannates. The phase transition is not complete at 50 GPa, and upon decompression, XRD indicates that all compositions transform to defect-fluorite with an amorphous component. In situ Raman spectroscopy showed that disordering in stannates and hafnates occurs gradually upon compression. Pyrochlore-structured hafnates retain short-range order to a higher pressure (30 GPa vs. <10 GPa) than defect-fluorite-structured hafnates. Hafnates and stannates decompressed from 50 GPa show Raman spectra consistent with weberite-type structures, also reported in irradiated stannates. The second-order Birch-Murnaghan equation of state fit gives a bulk modulus of 250 GPa for hafnate compositions with the pyrochlore structure, and 400 GPa for hafnate compositions with the defect-fluorite structure. Stannates have a lower bulk modulus relative to hafnates (between 80-150 GPa

Evidence of Coulomb correction and spinorbit coupling in rare-earth dioxides CeO 2, PrO 2 and TbO 2: An ab initio study

KAUST Repository

Kanoun, Mohammed; Reshak, A. H.; Kanoun-Bouayed, Nawel; Goumri-Said, Souraya

2012-01-01

The current study investigates the structural, elastic, electronic and optical properties of CeO 2, PrO 2 and TbO 2 using the full potential (linearized) augmented plane wave plus local orbital method within the WuCohen generalized gradient approximation (GGA) with Hubbard (U) correction and spinorbit coupling (SOC). The GGAU implementation lead us to describe correctly the relativistic effect on 4f electrons for CeO 2. We clarify that the inclusion of the Hubbard U parameter and the spinorbit coupling are responsible for the ferromagnetic insulating of PrO 2 and TbO 2. The magnetic description is achieved by the spin-density contours and magnetic moment calculations, where we show the polarization of oxygen atoms from the rare earth atoms. The mechanical stability is shown via the elastic constants calculations. The optical properties, namely the dielectric function and the reflectivity are calculated for radiation up to 12 eV, giving interesting optoelectronic properties to these dioxides. © 2011 Elsevier B.V. All rights reserved.

Evidence of Coulomb correction and spinorbit coupling in rare-earth dioxides CeO 2, PrO 2 and TbO 2: An ab initio study

KAUST Repository

Kanoun, Mohammed

2012-04-01

The current study investigates the structural, elastic, electronic and optical properties of CeO 2, PrO 2 and TbO 2 using the full potential (linearized) augmented plane wave plus local orbital method within the WuCohen generalized gradient approximation (GGA) with Hubbard (U) correction and spinorbit coupling (SOC). The GGAU implementation lead us to describe correctly the relativistic effect on 4f electrons for CeO 2. We clarify that the inclusion of the Hubbard U parameter and the spinorbit coupling are responsible for the ferromagnetic insulating of PrO 2 and TbO 2. The magnetic description is achieved by the spin-density contours and magnetic moment calculations, where we show the polarization of oxygen atoms from the rare earth atoms. The mechanical stability is shown via the elastic constants calculations. The optical properties, namely the dielectric function and the reflectivity are calculated for radiation up to 12 eV, giving interesting optoelectronic properties to these dioxides. © 2011 Elsevier B.V. All rights reserved.

Synchrotron diffraction characterization of nanostructured KY3F10:Tb

International Nuclear Information System (INIS)

Ichikawa, Rodrigo U.; Teixeira, Maria I.; Ranieri, Izilda M.; Martinez, Luis G.; Linhares, Horacio M.S.M.D.; Turrillas, Xavier

2015-01-01

Nanostructured rare-earth fluorides materials are being intensively studied recently due to their potential applications in high-dose dosimetry. Particularly, nanostructured Tb-doped KY 3 F 10 has shown satisfactory results to be used in this area. In the present work, the structure and microstructure of KY 3 F 10 :Tb was investigated by means of X-ray synchrotron diffraction. One of the samples was analyzed as synthesized and another after a heat treatment. Rietveld refinement of synchrotron diffraction data was applied to obtain cell parameters, atomic positions and atomic displacement factors and the results were compared to values found in literature. X-ray line profile analysis methods were applied to determine mean crystallite sizes and their distribution. (author)

Mechanical and corrosion properties of binary Mg–Dy alloys for medical applications

International Nuclear Information System (INIS)

Yang Lei; Huang Yuanding; Peng Qiuming; Feyerabend, Frank; Kainer, Karl Ulrich; Willumeit, Regine; Hort, Norbert

2011-01-01

Microstructure, mechanical and corrosion properties of binary magnesium–dysprosium (Mg-5, 10, 15, 20 wt.% Dy) alloys were investigated for medical applications. In the as-cast condition, the distribution of Dy is quite inhomogeneous. Mg–10Dy alloy exhibits a moderate tensile and compression yield strength, and the best elongation and corrosion resistance. After T4 (solutionizing) treatment, the distribution of Dy becomes homogeneous. The tensile and compression yield strength of all Mg–Dy alloys decreases. The elongation remains unchanged, while the corrosion resistance is largely improved after T4 treatment.

Mechanical and corrosion properties of binary Mg-Dy alloys for medical applications

Energy Technology Data Exchange (ETDEWEB)

Yang Lei, E-mail: lei.yang@hzg.de [Helmholtz-Zentrum Geesthacht, Institute of Materials Research, Max-Planck-Str. 1, D-21502 Geesthacht (Germany); Yuanding, Huang; Qiuming, Peng; Feyerabend, Frank; Kainer, Karl Ulrich; Willumeit, Regine; Hort, Norbert [Helmholtz-Zentrum Geesthacht, Institute of Materials Research, Max-Planck-Str. 1, D-21502 Geesthacht (Germany)

2011-12-15

Microstructure, mechanical and corrosion properties of binary magnesium-dysprosium (Mg-5, 10, 15, 20 wt.% Dy) alloys were investigated for medical applications. In the as-cast condition, the distribution of Dy is quite inhomogeneous. Mg-10Dy alloy exhibits a moderate tensile and compression yield strength, and the best elongation and corrosion resistance. After T4 (solutionizing) treatment, the distribution of Dy becomes homogeneous. The tensile and compression yield strength of all Mg-Dy alloys decreases. The elongation remains unchanged, while the corrosion resistance is largely improved after T4 treatment.

Microwave-assisted Extraction of Rare Earth Elements from Petroleum Refining Catalysts and Ambient Fine Aerosols Prior to Inductively Coupled Plasma - Mass Spectrometry

Science.gov (United States)

Mittlefehldt, David W.; Kulkarni, Pranav; Chellam, Shankar

2006-01-01

In the absence of a certified reference material, a robust microwave-assisted acid digestion procedure followed by inductively coupled plasma - mass spectrometry (ICP-MS) was developed to quantify rare earth elements (REEs) in fluidized-bed catalytic cracking (FCC) catalysts and atmospheric fine particulate matter (PM2.5). High temperature (200 C), high pressure (200 psig), acid digestion (HNO3, HF, and H3BO3) with 20 minute dwell time effectively solubilized REEs from six fresh catalysts, a spent catalyst, and PM2.5. This method was also employed to measure 27 non-REEs including Na, Mg, Al, Si, K, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Zr, Mo, Cd, Cs, Ba, Pb, and U. Complete extraction of several REEs (Y, La, Ce, Pr, Nd, Tb, Dy, and Er) required HF indicating that they were closely associated with the aluminosilicate structure of the zeolite FCC catalysts. Internal standardization using 115In quantitatively corrected non-spectral interferences in the catalyst digestate matrix. Inter-laboratory comparison using ICP-optical emission spectroscopy (ICP-OES) and instrumental neutron activation analysis (INAA) demonstrated the applicability of the newly developed analytical method for accurate analysis of REEs in FCC catalysts. The method developed for FCC catalysts was also successfully implemented to measure trace to ultra-trace concentrations of La, Ce, Pr, Nd, Sm, Gd, Eu, and Dy in ambient PM2.5 in an industrial area of Houston, TX.

Microwave-assisted extraction of rare earth elements from petroleum refining catalysts and ambient fine aerosols prior to inductively coupled plasma-mass spectrometry

International Nuclear Information System (INIS)

Kulkarni, Pranav; Chellam, Shankararaman; Mittlefehldt, David W.

2007-01-01

A robust microwave-assisted acid digestion procedure followed by inductively coupled plasma-mass spectrometry (ICP-MS) was developed to quantify rare earth elements (REEs) in fluidized-bed catalytic cracking (FCC) catalysts and atmospheric fine particulate matter (PM 2.5 ). High temperature (200 deg. C), high pressure (200 psig), acid digestion (HNO 3 , HF and H 3 BO 3 ) with 20 min dwell time effectively solubilized REEs from six fresh catalysts, a spent catalyst and PM 2.5 . This method was also employed to measure 27 non-REEs including Na, Mg, Al, Si, K, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Zr, Mo, Cd, Cs, Ba, Pb and U. Complete extraction of several REEs (Y, La, Ce, Pr, Nd, Tb, Dy and Er) required HF indicating that they were closely associated with the aluminosilicate structure of the zeolite FCC catalysts. Internal standardization using 115 In quantitatively corrected non-spectral interferences in the catalyst digestate matrix. Inter-laboratory comparison using ICP-optical emission spectroscopy (ICP-OES) and instrumental neutron activation analysis (INAA) demonstrated the applicability of the newly developed analytical method for accurate analysis of REEs in FCC catalysts. The method developed for FCC catalysts was also successfully implemented to measure trace to ultra-trace concentrations of La, Ce, Pr, Nd, Sm, Gd, Eu and Dy in ambient PM 2.5 in an industrial area of Houston, TX

Identification of rare earth elements by their fluorescence complexes with tetracycline

International Nuclear Information System (INIS)

Zanotti-Cavazzoni, J.C.; Boveda V, J.C.; Abrao, A.

1994-01-01

A procedure for identification of rare earth elements (REE) based on the complex formation with tetracycline (TC) and visual observation under ultraviolet light is described. One micro drop of REE chloride is placed over the filter paper impregnated with tetracycline and previously dried before use. After dried (30-60 O C) the paper is examined under the UV light. In a second procedure for the identification of mixture of REE a drop of the analyte is added over a filter paper strip impregnated with TC followed by a chromatographic development using a 2:1:1:1 (vol/vol) ethanol, acetone, ether and 1% acetic acid mixture of pH 5,8. After dried, the strip is observed under UV light. Sc, Y, La, Dy, Ho and Lu exhibited high yellow fluorescence; Gd, Tm and Yb a weak yellow; Ce an intense violet; Pr, ND, Sm and Tb violet: Eu a high red fluorescence and Er a violet brown wish, not well defined. It is possible to identify for instance 0.3 ug Ce (concentration 6 mg/L) and 0.2 ug Er (concentration 6 mg/L). Preliminary experiments indicated that those REE-TC chelates can be used for the identification and determination of the REE by spectro fluorimetry. (author). 30 refs