Crystallographic,morphological and photoluminescent investigations of Tb3+-doped YAlO3 perovskites for lighting applications

Terbium(III)-doped yttrium aluminate perovskite (YAP:xTb³⁺) (x = 0.01–0.08 mol) was synthesized using a simple gel-combustion method. Structural elucidations were performed using X-ray diffraction (XRD) and Rietveld analysis. Fourier-transform infrared spectral studies validated the efficient synthesis of designed doped samples. Transmission electron microscopic images showed the agglomerated irregular dimensions of the synthesized nanocrystalline materials. When excited at 251 nm, a strong emissive line attributed to ⁵D₄ → ⁷F₅ electronic transition was observed at 545 nm (green emission). The maximum luminescence was found at the optimized concentration (0.05 mol) of Tb³⁺ ions; this emission was quenched by dipolar–dipolar (d–d) interactions. Chromaticity (x and y) and correlated colour temperature parameters were obtained by analysing the emission profiles. Finally, the colour coordinates of nanophosphors were closer to the National Television Standards Committee green coordinates, which replicates their potency in the design and architecture of R-G-B-based white LEDs.     

Formation of Thick Dense Yttrium Iron Garnet Films Using Aerosol Deposition

Aerosol deposition (AD) is a thick-film deposition process that can produce layers up to several hundred micrometers thick with densities greater than 95% of the bulk. The primary advantage of AD is that the deposition takes place entirely at ambient temperature; thereby enabling film growth in material systems with disparate melting temperatures. This report describes in detail the processing steps for preparing the powder and for performing AD using the custom-built system. Representative characterization results are presented from scanning electron microscopy, profilometry, and ferromagnetic resonance for films grown in this system. As a representative overview of the capabilities of the system, focus is given to a sample produced following the described protocol and system setup. Results indicate that this system can successfully deposit 11 µm thick yttrium iron garnet films that are  > 90% of the bulk density during a single 5 min deposition run. A discussion of methods to afford better control of the aerosol and particle selection for improved thickness and roughness variations in the film is provided.     

Characteristics of rare earth (RE = Eu,Tb, Tm)‐doped Y2O3 phosphors for thermometry

The temperature‐dependent photoluminescences of Y₂O₃:Eu (6% Eu), Y₂O₃:Tb (4% Tb) and Y₂O₃:Tm (1% Tm) were investigated for high‐temperature phosphor thermometry. Two different phases, the monoclinic phase and cubic phase, were considered because the fluorescence spectra vary with the phase. To employ the intensity ratio method, we investigated their photoluminescence spectra under the excitation light of an Hg–Xe lamp as the temperature was elevated from room temperature to more than 1200 K. As a result, it was confirmed that the luminescence intensity of all of the phosphors varied with elevating temperature, i.e. thermal quenching, with the variations depending on the type of rare earth impurity and their phases. The results indicate that Y₂O₃:Eu phosphors are applicable to the intensity ratio method because they show appropriate variations in the intensity ratio of two emission lines, and they also have strong and sharp peak intensities without excessive optical noise or black body radiation over a wide range of temperatures. The intensity ratios for Y₂O₃:Tb provide such small variations with temperature that the temperature resolution is low, despite the strong emission intensities. As for Y₂O₃:Tm, the intensity ratios also have a low temperature resolution and their emission intensities are weak. Therefore, Y₂O₃:Tb and Y₂O₃:Tm are not appropriate for the intensity ratio method for phosphor thermometry. Copyright © 2010 John Wiley & Sons, Ltd.     

The effects of aluminum, iron, chromium, and yttrium on rat intestinal smooth muscle in vitro

The modification of peristaltic activity in the presence of several metal ions has been investigated in the rat intestine by the isolated organ technique. The metals tested modify the intestinal movements: aluminum, chromium, and yttrium cause a decrease of amplitude, while iron showed no effect. By use of microscopic techniques, the presence of yttrium hydroxide was observed in the intestinal tissues. Iron also appears as a precipitate outside of the intestinal serosal, which may explain why iron did not modify the peristaltism. Chromium and aluminum were not apparent to microscope, despite being detected and quantified in the tissues by means of atomic emission spectrometer. We conclude that the trivalent ions of these elements may operate differently on the mechanisms of intestinal contractions: yttrium precipitates in intercellular spaces, iron precipitates outside the intestines, and chromium and aluminum remain in solution and are distributed homogeneously in the smooth intestinal muscle.     

Fluorescence probe enhanced spectrofluorimetric method for the determination of sparfloxacin in tablets and biological fluids

Yttrium‐sensitized fluorescence was used to develop a sensitive and simple spectrofluorimetric method for the determination of sparfloxacin. The method is based on the strong fluorescence of sparfloxacin after adding the fluorescence probe yttrium in buffer solution (pH = 8), and various factors influencing fluorescence were investigated. Under optimum conditions, the enhanced fluorescence intensity of the system showed a good linear relationship with the concentration of sparfloxacin over the range 8 × 10^?7 to 1.4 × 10^?5 mol L^?1 with a correlation coefficient of 0.9997. The detection limit (S/N = 3) was determined as 9.01 × 10^?8 mol L^?1. The mechanism of the sensitizing effect of probe was discussed. This method has been successfully applied for the determination of sparfloxacin in pharmaceuticals, human urine and serum samples; the result obtained was satisfactory. Copyright © 2010 John Wiley & Sons, Ltd.     

Distribution and mobility of scandium and yttrium in selected types of soils in Poland

Abstract

This study was conducted to investigate the chemical speciation of yttrium and scandium in selected types of soils and also determined the total content and profile distribution of those elements. The research was performed on soil samples from forest areas in Puszcza Borecka (Poland) known as a non-contaminated site. Soil samples were collected from natural brown, lessive and rusty soil profiles.

The sequential extraction procedure was applied to separate fractions of scandium and yttrium according to the Tessier method. The range of total content of scandium and yttrium was respectively: 0.63-6.48 mg kg^-1 and 2.25 to 27.93 mg kg^-1. Scandium and yttrium occurred predominantly in residual fraction (F5) in each genetic horizon. Also both elements occurred mainly in fraction bound to organic matter (F4). The mean percentage content of scandium measured in mobile fractions (∑F1-F2) reached about 3% (in Bbr, Bt horizons) to 14% (in Bv horizons) in relation to the total content of the element in the analysed soils. The percentage content of yttrium measured in mobile fractions reached about 4% (in A, Bv horizons) to 28% in Bt horizons in relation to the total content of the element in forest soils of Puszcza Borecka.     

Rare earth activated yttrium aluminate phosphors with modulated luminescence

Yttrium aluminate (Y₃A₅O₁₂) was doped with different rare earth ions (i.e. Gd³⁺, Ce³⁺, Eu³⁺ and/or Tb³⁺) in order to obtain phosphors (YAG:RE) with general formula,Y_3‐x‐aGd_xRE_aAl₅O₁₂ (x = 0; 1.485; 2.97 and a = 0.03). The synthesis of the phosphor samples was done using the simultaneous addition of reagents technique. This study reveals new aspects regarding the influence of different activator ions on the morpho‐structural and luminescent characteristics of garnet type phosphor. All YAG:RE phosphors are well crystallized powders containing a cubic‐Y₃Al₅O₁₂ phase as major component along with monoclinic‐Y₄Al₂O₉ and orthorhombic‐YAlO₃ phases as the impurity. The crystallites dimensions of YAG:RE phosphors vary between 38 nm and 88 nm, while the unit cell slowly increase as the ionic radius of the activator increases. Under UV excitation, YAG:Ce exhibits yellow emission due to electron transition in Ce³⁺ from the 5d level to the ground state levels (²F_5/2, ²F_7/2). The emission intensity of Ce³⁺ is enhanced in the presence of the Tb³⁺ ions and is decreased in the presence of Eu³⁺ ions due to some radiative or non‐radiative processes that take place between activator ions. By varying the rare earth ions, the emission colour can be modulated from green to white and red. Copyright © 2015 John Wiley & Sons, Ltd.     

Synthesis and characterization of yttrium complexes bearing a bulky arylamido ancillary ligand

Reaction of anhydrous YCl₃ with 1 equiv. of arylamido lithium 2,6-ⁱPr₂C₆H₃NSiⁱPr₃Li in THF gave an anionic mono-arylamido-ligated yttrium dichloride complex {[2,6-ⁱPr₂C₆H₃NSiⁱPr₃]YCl₂(THF)}₂[LiCl(THF)₂] (1). Alkylation of 1 with 4 equiv. of LiCH₂SiMe₃ afforded an anionic arylamido-ligated yttrium tris(alkyl) complex [2,6-ⁱPr₂C₆H₃NSiⁱPr₃]Y(CH₂SiMe₃)₃Li(THF)₂ (2). Both complexes were characterized by NMR, elementary analysis, and X-ray structural determination.     

钇元素对玉米幼苗水分利用效率的调控

盆栽实验条件下,研究不同浓度钇元素对玉米幼苗水分生理特性的影响,并分析其对玉米幼苗水分利用效率(WUE)的调控。结果表明,钇用皱在干土中的浓度为0～0．05mg／g时,玉米幼苗的根长、根冠比(R／S)、WUE呈升高趋势;当钇用量在干土中的浓度为0．05～0．50mg／g时,玉米幼苗的根长、R／S、WUE呈下降趋势。随着钇用量的增加．气孔导度(Cs)始终呈下降趋势,叶水势(LWP)始终呈升高趋势。钇元素作用下玉米幼苗WUE的提高得益于根系活性的增强和适宜的Cs,使干物质的积累和水分的耗散达到最优值．干土中最佳钇用量为0．05mg／g。     

Domestic Yttrium Consumption Trends in Japan

Yttrium tends to occur in the same ore deposits as the lanthanides and exhibits similar chemical properties as rare earth elements. Yttrium sources are typically concentrated in China, and there are concerns about supply security. Yttrium is used in small, but essential, quantities in a variety of advanced industrial sectors, for example, in phosphors, advanced ceramics, optical glasses, and batteries. In terms of resource security, it is important to verify the domestic yttrium consumption trends. In order to characterize the domestic yttrium consumption trends in Japan, we tracked the historical yttrium consumption patterns from 2001 to 2011 by applying the bottom‐up approach and illustrated the recent domestic yttrium flow by using a substance flow analysis. The results showed that the total yttrium consumption has remained steady over 10 years, from 1,124 tonnes (t) in 2001 to 967 t in 2011. Recent consumption in 2011 was driven primarily by the use of yttrium in fluorescent lamps (462 t), nickel metal hydride batteries (185 t), and optic glasses (149 t).