Pretreatment of Chrysotile With Rare Earth Compounds Lowered Its Cytotoxicity by Lessening Surface Charges

Pathological effects of asbestos are probably dependent on the special surface properties of the fibers, such as surface charge, surface metal ions. The present study was designed to determine whether the pretreatment of chrysotile asbestos fibers (CAF) with rare earth compounds (REC) solution can reduce their pathogenicity. The results showed that REC-pretreated CAF induced less nitrogen oxide (NO) production by alveolar macrophages (AM). In addition, the pretreatment lowered the capacity of hemolysis and the methylene blue (MB) adsorption of the native CAF. These findings suggested that the pretreatment of CAF with REC solution reduced the in vitro toxicity of CAF by lessening its surface charges. Nevertheless, the pathogenicity and the carcinogenicity of REC-pretreated CAF in vivo remain to be investigated.

Rare Earth Compounds in Cemented Carbides with Trace Rare Earth Additions

The morphology,structure and distribution of the rare earth compounds in the YG8R.YT5R and YT14R cemented carbides with additions of trace light rare earths were studied with an analytical electron microscope. The particles of the rare earth compounds in these alloys are all spherical and distribute at interfaces between the Co-cement phase and WC hard phase or(TiW)C solid solution,and in the(TiW)C solid solution.In the YG8R and YTI4R alloys,the rare earth compound is RE_2O_3 with a bcc structure,while in the YT5R alloy. the rare earth compound is RE_2O_2S with a hcp structure.

Prediction of Heat of Fusion of Rare Earth Compounds from Binary Phase Diagrams

Based on the thermodynamical principle the new formula for calculation of heat of fusion and its error have been derived from binary phase diagrams which could be classified to eutectic,solid solution,degenerate eutectic and involving a compound phase diagram and so on.Using these formulae heats of fusion of some rare earth ox- ides have been predicted.

Study of the Coarse Blocky Compounds in the As－cast 7075 Aluminium Alloys Containing Rare Earth Elements

The coarse blocky compounds in the as-cast 7075 aluminium alloys containing rare earth elements, neodymium, cerium or mischmetal were investigated by means of transmission electron microscope with EDX and scanning electron microscope. The blocky compounds in these alloys were identified as rare earth compounds, (Cr, Ti)2 RE (Al, X)20 (X is magnesium, copper and zinc),body-centred cubic, with 184 atoms to the unit cell , lattice parameter 1.453￣1. 458 nm, Vickers hardness 4000￣5600 MPa and calculated density 3400 kg/m3. The results show that the amount of blocky compounds in the alloys decreases with decreasing of Ti and Cr content or with increasing of cooling rate during solidification.

Study on Simultaneous Catalytic Reduction of Sulfur Dioxide and Nitric Oxide on Rare Earth Mixed Compounds

CeO2/γ-Al2O3, La203/γ-Al2O3, CeO2-La203/γ-Al2O3 and CeO2-La2O3, which were prepared by impregnating in certain ratio, were used as the catalysts for the reduction of SO2 and NO by CO. Separate and simultaneous removal of SO2 and NO over LaEO3/γ-Al2O3, CeOE/γ-Al2O3, CeOE-LaEO3/γ-Al2O3 were investigated. The phase characteristics of catalysts were also analyzed by X-ray diffraction. The result shows that the conversions of SO2 and NO are above 98 % over CeOE/γ-Al2O3 and CeOE-LaEO3/γ-Al2O3. After SO2 is added in the NO-CO-N2 system （NO ：SO2 = 1：2 - 1 ： 3）, the conversions of SO2 and NO are both above 98%. Furthermore, it is found that CeO2-La2O3 with various ratios has different activity for the simultaneous reduction of SO2 and NO.

Review of magnetic properties and magnetocaloric effect in the intermetallic compounds of rare earth with low boiling point metals

The magnetocaloric effect （MCE） in many rare earth （RE） based intermetallic compounds has been extensively in- vestigated during the last two decades, not only due to their potential applications for magnetic refrigeration but also for better understanding of the fundamental problems of the materials. This paper reviews our recent progress on studying the magnetic properties and MCE in some binary or ternary intermetallic compounds of RE with low boiling point metal（s） （Zn, Mg, and Cd）. Some of them exhibit promising MCE properties, which make them attractive for low temperature magnetic refrigeration. Characteristics of the magnetic transition, origin of large MCE, as well as the potential application of these compounds are thoroughly discussed. Additionally, a brief review of the magnetic and magnetocaloric properties in the quaternary rare earth nickel boroncarbides RENi2B2C superconductors is also presented.

STUDY ON THE COORDINATION COMPOUNDS OF RARE EARTHS WITH DIPEPTIDE-COORDINATION OF RARE EARTHS WITH DL-ALANYL-ALANINE

In this paper protonation constants of the title lisand and stability constants of its coordination compounds with rare earths have been determined by potentiometric titration at 25±0.1℃ and ionic strength of 0.10mol.dm^(-3)NaClO_4. The coordination of rare earths with DL-alanyl-alanine has been discussed. The stability of the coordination compound shows 'tetrad effect'. The position for yttrium shifts from its usual Bo-Er region to the vicinity of Tb.

Research and Development of Rare Earth Advanced Materials in China

China is rich in resources of rare earths(REs). Based on tremendous work, China has made great achievements in research and development of REs since 1980s, and the production of RE has won the leading position in the world. The application of RE elements in advanced materials have progressed significantly during the past years. The wide range of rare earth application in China has been reviewed and discussed in this paper, including the development of advanced RE materials (RE-Al alloys, rare earth nonferrous metal alloys, rare earth luminescent materials, rare earth hydrogen storage materials, rare earth permanent magnet and rare earth compounds used in agriculture, i.e., rare earth micronutrient fertilizer etc.) End the research of new RE materials (high T-c rare earth superconductor, rare earth electronic and photonic materials, rare earth ceramics and rare earth precious metal alloys). Finally, the further development works to be required are as follow: (1) to enhance the applied fundamental research, study the intrinsic properties of rare earth elements and develop less well known uses; (2) to undertake the applied research of median and heavy rare earth and find a way out of the unbalance of RE resources in the various applications; (3) to strengthen the applied research of RE element's in energy field, solving the energy-related, energy-saved and environmental problems.

SYNTHESIS AND IDENTIFICATION OF CONDUCTING POLYANILINE DOPED WITH RARE EARTH CHLORIDE

Polyaniline doped with rare earth chloride was synthesized in organic solvent and identified by elemental analysis and infrared spectroscopy. The experimental results show that there exists both doping and complexation at the same time in the resulting product. When pH4. Moreover, polyaniline doped with rare earth chloride exhibits better thermal stability than that doped with hydrochloric acid.

Study on Nanocrystalline Rare Earth Mg-Based System Hydrogen Storage Alloys with AB_3-Type

A sort of rare earth Mg-based system hydrogen storage alloys with AB3-type was prepared by double-roller rapid quenching method. The alloys were nanocrystalline multi-phase structures composed of LaNi3 phase and LaNi5 phase by X-ray diffraction and scanning electron microscopy analyses, and the suitable absorption/desorption plateau was revealed by the measurement of P-C-I curve. Electrochemical studies indicate that the alloys exhibit good electrochemical properties such as high capacity and stable cycle life, and the discharge capacity is 369 mAh·g-1 at 0.2 C (72 mA·g-1). after 460 cycles, the capacity decay was only 19.4% at 2 C (720 mA·g-1).

STUDY ON SYNTHESIS,CHARACTERIZATION AND STRUCTURE OF A NEW RARE EARTH COORDINATION COMPOUND WITH BENZOIC ACID

In this paper,a new rare earth benzoate coordination compound,[TbL_3(HL)(H_2O)]_2 (HL=C_7H_6O_2=benzoic acid) is synthesized and characterized by elemental analysis DTA,TG,DTC,and IR spectra.The title compound crystallizes in triclinic,space.group P with a=9.148(1),b=11.460(2), c=13.506(2);α=112.76(1),β=91.83(1),γ=91.99(1)°;Z=1;V=1303.3.The final R factor is 0.0235.The rare earth ion is nine-coordinated to form a distorted monocapped square antiprism.

Synthesis and Properties of Rare Earth Complexes with p-Methoxybenzoyl-Benzoylmethane and / or Amines

p-Methoxybenzoyl-benzoylmethane(HA)and its complexes LnA_4QH and LnA_3·xH_2O(for Ln=La～ Yb,Q=n-tributyl amine,diethyl amine,hexahydropyridine)were synthesized and characterized by elemental analysis,molar conductivity measurement,infrared spectroscopy,UV-visible absorption spectroscopy,thermal analysis and ~1H NMR spectra.Possibilities of using praseodymium and europium complexes as shift reagent are also discussed.

The effect of high-temperature annealing on LaFe_(11.5)Si_(1.5) and the magneto-caloric properties of La_(1-x)Ce_xFe_(11.5)Si_(1.5) compounds

The powder X-ray diffraction patterns of LaFell.sSil.5 compounds annealed at different high temperatures from 1323 K （5 h） to 1623 K （2 h） show that a large amount of 1：13 phase begins to form in LaFell.sSiL5 compound annealed at 1423 K （5 h）. In the temperature range from 1423 to 1523 K, ^-Fe and LaFeSi phases rapidly decrease to form 1：13 phase. LaFeSi phase is rarely observed, and the most amount of 1：13 phase is obtained in the compound annealed at 1523 K （5 h）. With the annealing temperature increasing to 1573 and 1623 K, LaFeSi is detected again in the LaFell.sSil.s compound. According to the results of annealing at different high-temperatures, the Lal-xCexFelt.sSit.5 compounds are annealed at high temperatures of 1373 K （2 h） ＋ 1523 K （5 h）. The main phase is NaZn13-type phase, and the impurity is a small amount of et-Fe in Lal-xCexFexx.sSil.5 compounds with 0 〈 x 〈 0.35, and there is a large amount of CeaFe17 phase in Lao.sCeo.sFela.sSil.s. It indicates that the substitution of cerium atoms for La in LaFelLsSil.5 compounds has limit. At the same time, the substitution of Ce for La has large effect on magnetocaloric properties. With increasing Ce content from x = 0 to x = 0.35, the Curie temperature decreases linearly from 196 to 168 K, the magnetic entropy change increases from 16.5 to 57.3 J-kg-kK-1 in a low magnetic field change of 0-2 T, and the thermal hysteresis also increases from 3 K to 8 K.

Phase formation with NaZn_(13) structure in metamagnetic La(Fe_(1–x)Co_x)_(11.9)Si_(1.1) compounds

The effects of different annealing conditions on the phase formation with NaZn13 structure were investigated in La（Fe1-xCox）11.9Si1.1 （x=0.068） compounds. It was found that the 1：13 phase was not formed directly from the melt upon cooling but via a peritectic reaction between the pro-peritectic γ-Fe and the La-rich phase. Annealing temperature was very important for the formation of 1：13 phase. Ice water was confirmed to be a preferable quenching medium. La（Fe1-xCox）11.9Si1.1 （x=0.068） compounds with almost single 1：13 phase were obtained at 1473 K after 15 d.

Solution-reaction Calorimetric Study of Coordination Compounds of Rare Earth Perchlorates with Alanine and Imidazole

Two coordination compounds of rare earth perchlorates with alanine and imidazole, [RE(Ala)n(Im)(H2O)]- (ClO4)3(s) (RE=La, n=3; RE=Nd, n=2), have been prepared and characterized. The standard molar enthalpies of reaction for the following two reactions, LaCl37H2O(s)+3Ala(s)+Im(s)+3NaClO4(s)=[La(Ala)3(Im)(H2O)]- (ClO4)3(s)+3NaCl(s)+6H2O(l) (1) and NdCl36H2O(s)+2Ala(s)+Im(s)+3NaClO4(s)=[Nd(Ala)2(Im)(H2O)]- (ClO4)3(s)+3NaCl(s)+5H2O(l) (2), were determined by solution-reaction calorimetry, at T=298.15 K, as 36.168±0.642 kJmol-1 and 48.590±0.934 kJmol-1 respectively. From the results and other auxiliary quantities, the standard molar enthalpies of formation of [La(Ala)3(Im)(H2O)](ClO4)3(s) and [Nd(Ala)2(Im)(H2O)] (ClO4)3(s) were derived, fmHD!{[La(Ala)3(Im)(H2O)](ClO4)3, s}=(-2984.8±1.0) kJmol-1 and fmHD! {[Nd(Ala)2(Im)(H2O)]- (ClO4)3, s}=(-2387.8±0.8) kJmol-1 , respectively.

Dynamic performance of magneto-optical Bi-substituted rare-earth iron garnet

The dynamic performances of magneto-optical Bi-substituted rare-earth iron garnet (BIG) under different external magnetic fields and at different frequencies are experimentally studied. The measurement data indicate that the Faraday rotation angle is almost proportional to the external magnetic field when the garnet is far less saturated, while there is good switch performance when it is saturated. The higher the working frequency is, the larger the saturation magnetic field and the phase delay of Faraday angle relative to the field. The saturation fields and the phase delays at different frequencies are measured. The dynamic performance of the BIG determines the performance of BIG-based optical devices. To get the better performance of such devices, the garnets with small dampness and large stiffness should be chosen elaborately.

Crystal structure and negative thermal expansion of solid solution Lu_2W_(3-x)Mo_xO_(12)

A new series of solid solutions Lu2W3-xMoxO12 （0.5≤r≤2.5） were successfully synthesized by the solid-state method. Their crystal structure and negative thermal expansion properties were studied using high-temperature X-ray powder diffraction and the Rietveld method. All samples of rare-earth ttmgstates and molybdates are found to crystallize in the same orthorhombic structure with space group Pnca and show the negative thermal expansion phenomena related to transverse vibration of bridging oxygen atoms in the structure. Thermal expansion coefficients （TEC） of Lu2W3_xMoxO12 are determined as -20.0× 10^-6 K^-1 for x=0.5 and -16.1×10^-6 K^-1 for x=2.5 but -18.6× 10^-6 and -16.9× 10^-6K^-1 for unsubstituted Lu2W3012 and Lu2M03012 in the identical temperature range of 200 to 800℃. High-temperature X-ray diffraction （XRD） data and bond length analysis suggest that the difference between W-O and Mo-O bond is responsible for the change of TECs after the element substitution in this series of solid solutions.

Hydrothermal Synthesis of Nanostructural La_xBi_(2-x)Se_yTe_(3-y) Powders

Nanostructural monophase LaxBi2-xSeyTe3-y alloy was synthesized with a hydrothermal route using BiCl3, LaCl3, selenium and tellurium powders as the precursors, NaOH and disodium ethylenediaminetetraacetiate （EDTA） as the additives. The hydrothermally synthesized powders have a petal-like morphology self-structured by the parallel side-by-side arrangement of the nano-scales. It is found that an alkaline additive is necessary for the synthesis of a monophase Bi2Te3 based alloy.

New ternary compound La_8Al_(13)Sn_3

A new ternary compound La8Al13Sn3 was synthesized and studied by means of X-ray powder diffraction technique. The compound La8Al13Sn3 crystallizes in a hexagonal AlB2-type structure with space group P6/mmm （No. 191） and the lattice parameters a = 0.44919（1） nm and c = 0.43835（1） nm. The Smith and Snyder figure of merit for index, FN, is F30 = 197.3（30）. The Rietveld refinement for the crystal structure of the compound was carried out successfully. The liability R-factors of Rietveld refinement are Rp = 0.114 and Rwp = 0.148. The compound La8Al13Sn3 decomposes into LaAl2 with cubic structure and space group Fd 3m （227）, LaAl3 with hexagonal structure and space group P63/mmc （194）, and Sn at 720°C.

Influence of Sn substitution for Co in RCo_2 (R= Gd,Tb,Dy) alloys on the structure and magnetocaloric effect

The phases and the magnetocaloric effect in the alloys R（Co1-xSnx）2 with X = 0, 0.025, 0.050, 0.075, and 0.100 were investigated by X-ray diffraction analysis and magnetization measurement. The substitution of Sn in RCo2 is limited. The cubic MgCu2-type structure for the alloys of RCo2 was confirmed by X-ray powder diffraction and the remaining alloys mainly consisted of the RCo2 phase, along with some RCo3 and R5Sn3 impurity phases. The impurity phases increase with the increase of Sn content. The Tc of the alloys is not very sensitive to the Sn substitution for Dy（Co1-xSnx）2 and Tb（Co1-xSnx）2, whereas in Gd（Co1-xSnx）2, the Curie temperatures significantly increase. The maximum magnetic entropy changes in the alloys Dy（Co1-xSnx）2 （x = 0, 0.025, 0.050, 0.075） are 5.78, 5.43, 3.88, and 2.98 J·kg^-1·K^-1, respectively, and those in the Tb（Co1-xSnx）2 （x = 0, 0.025） are 3.44, and 2.29 J·kg^-1·K^-1 respectively in the applied field change of 0-2.0 T.