THE EFFECT OF BETA-DECAY ON THE EXCHANGE PROPERTIES OF THE RARE EARTH–EDTA COMPLEX IONS

1961 ◽  
Vol 39 (5) ◽  
pp. 1049-1053 ◽  
Author(s):  
P. Glentworth ◽  
R. H. Betts

It is shown that the rare earth ion Yb3+ is very resistant towards ordinary thermal exchange when it is complexed with the chelating agent EDTA in aqueous solution. However, when the complexed rare earth atom, as the 1.8-h Yb-177, emits a beta-particle, the daughter atom Lu-177 escapes readily from the chelate structure. Nuclear recoil arising from the beta-particle emission is shown not to be the cause of the escape of the daughter atom. It is suggested that the observed lability of the daughter atom is a result of a high degree of chemical reactivity of the chelate ion arising from the sudden change in atomic number of the central metal ion of the chelate structure.

2012 ◽  
Vol 184 ◽  
pp. 110-115
Author(s):  
X.P. Wang ◽  
J. Hu ◽  
Zhong Zhuang ◽  
Tao Zhang ◽  
Qian Feng Fang

The relaxation and phase transition behaviors of rare-earth ion substituted fast oxide-ion conductors (La1-xRex)2Mo2O9 (Re=Nd, Gd) were investigated by internal friction (IF) measurement in the temperature range 300 K - 950 K. Three different IF peaks (labeled as PL, PH, and PG, respectively) were observed in the rare-earth ion doped La2Mo2O9 samples. Peak PL corresponds to short diffusion processes of oxygen ions among different oxygen vacancy sites. Peak PH is associated with the static/dynamic disorder transition in oxygen ion distribution. Peak PG is a newly discovered peak embodying phase transition-like characteristics and is suggested to be related to order-disorder transition associated with the rearrangement of La/ Re sub-lattice.


1964 ◽  
Vol 2 (8) ◽  
pp. iv
Author(s):  
J. Verdone ◽  
M. Veyssie ◽  
B. Dreyfus

2014 ◽  
Vol 716-717 ◽  
pp. 32-35
Author(s):  
Wen Bin Liu ◽  
Adu ◽  
Yu Guang Lv ◽  
Li Li Yu ◽  
Yong Xiang Du ◽  
...  

In this paper, a rare earth metal terbium ion as the central metal ion, a nanohydroxyapatite powder of the lanthanum doped terbium was synthesis by precipitation with hydroxyapatite as ligand. The sample was characterized by infrared spectrum, fluorescence spectrum and X ray diffraction instrument, and the thermal properties and fluorescence properties, structure of powderes were discussed. A nanohydroxyapatite powder of the lanthanum doped terbium achieves the maximum luminous intensity, when the La3+ doping concentration of Tb3+ was HAP 5% (La3+ and Tb3+ mole fraction ratio) devices. Rare earth powder of the lanthanum doped terbium hydroxyapatite has the stability chemical properties, the luminescence properties and good biological activity, the rare earth powder has good luminescent properties can be used in preparation of a good light emitting device. At the same time a nanohydroxyapatite powder of the lanthanum doped terbium has good antibacterial property, can be used as antibacterial materials.


1996 ◽  
Vol 49 (9) ◽  
pp. 997 ◽  
Author(s):  
LI Semenova ◽  
BW Skelton ◽  
AH White

Adducts [( dmso )nLn(O2NO)3], obtained by the crystallizatior , of lanthanoid (III) nitrate ( Ln (NO3)3.-xH2O) with excess dimethyl sulfoxide (' dmso ') in methanol or ethanol, have been the subject of a series of room-temperature single-crystal X-ray studies, defining more clearly the manner in which stoichiometry and structure systematically vary with change in metal ion radius. All complexes studied are mononuclear, the metal ion being complexed by three bidentate nitrate ligands and a number of dmso ligands , four for La-Sm and three beyond. The array La- Sm is monoclinic C2/c, a ≈ 14.9, b ≈ 15.5, c ≈ 15.5 Ǻ, β ≈ 108.4°, Z = 4 f.u .; the metal atom is disposed on a crystallographic 2 axis, which also passes through one of the nitrate groups. The series Eu -Tm (inclusive also of Y) is monoclinic, P21/n, a ≈ 11.5, b ≈ 12.7, c ≈ 13.6 Ǻ, β ≈ 100°, Z = 4 f.u ., while Yb and Lu are also monoclinic, P21/c, a ≈ 10.0, b ≈ 12.6, c ≈ 16 Ǻ, β ≈ 100.6°, Z = 4 f.u.


2007 ◽  
Vol 49 (1) ◽  
pp. 91-98 ◽  
Author(s):  
U. V. Valiev ◽  
J. B. Gruber ◽  
D. K. Sardar ◽  
B. Zandi ◽  
I. S. Kachur ◽  
...  

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