Physico-chemical properties of 3-methoxy-2-nitrobenzoates of some rare earth elements(Ⅲ)

The complexes of 3-methoxy-2-nitrobenzoates of Pr（Ⅲ）, Nd（Ⅲ）, Sm（Ⅲ）, Eu（Ⅲ）, Gd（Ⅲ）, Tb（Ⅲ）, Er（Ⅲ） and Tm（Ⅲ） with the formula： Ln（C8H6NO5）3·2H2O, where Ln=lanthanides（Ⅲ）, were synthesized and characterized by elemental analysis, Forier transform irtrared （FTIR） spectroscopy, magnetic and thermogravimetric studies and also by X-ray diffraction （XRD） measurements. The complexes had col- ours typical for Ln（Ⅲ） ions. The carboxylate groups bound as bidentate chelating. On heating to 1173 K in air they decomposed in the same way, at first, dehydrated in one step to anhydrous salts, and then decomposed to the oxides of respective metals with intermediate formation of the oxycarbonates. The enthalpy values of the dehydration process changed from 133.72 to 44.50 kJ/mol. Their solubility in water at 293 K was of the order of 10-4 mol/dm3. The magnetic moments of analysed complexes were determined by Gouy＇s method in the range of 76-303 K.

Synthesis of lanthanum ricinoleate and its effect on thermal stability and mechanical properties in PVC

The lanthanum ricinoleate（abbreviated as Lari3） of rare earth heat stabilizer was synthesized by the reaction of ricinoleic acid, lanthanum nitrate and sodium hydroxide. The IR and fluorescence spectra methods confirmed the structure of the product. The thermal stability of PVC in the presence of Lari3 was studied by the Congo method and using TG analysis. The results showed that Lari3 could be used as a thermal stabilizer for PVC. When the ratio of Lari3/pentaerythritol was 3：1, the complex exhibited better synergistic effect. Incorporation of Lari3 to PVC resulted in a marked increase of maximum and onset degradation temperature as well as elongation and impact strength of PVC. Lari3 might replace the labile chlorine atoms to interrupt the formation of conjugated double bonds in PVC chains and act as HCl scavenger to restrain the self-catalyticdehydrochlorination.

Synthesis of NaYF_4:Nd@NaLuF_4@SiO_2@PS colloids for fluorescence imaging in the second biological window

Nd doped nanoparticles is commonly used as bioimaging agents but presents poor stability. Here, a polymer coating is applied to NaYF4：Nd nanoparticles using a versatile step-by-step coating strategy. The as-synthesized NaYF_4：Nd@NaLuF_4@SiO_2@PS colloids show good stability in various polar solvent and are very stable in water at least for 6 months. These NaYF_4：Nd@NaLuF_4@SiO_2@PS colloids can exhibit strong down converting photoluminescence when excited by 808 nm lasers. Moreover, these NaYF_4：Nd@NaLuF_4@SiO_2@PS colloids accumulate in liver of mice when used as bio-imaging agents. which exhibit strong fluorescence luminescence in NIR Ⅱ window.

Lanthanum incorporated in MCM-41 and its application as a support for a stable Ni-based methanation catalyst

Herein, lanthanum was incorporated via hydrothermal synthesis into a MCM-41 framework structure with La/Si molar ratios from 0.01 to 0.1. Samples of NiO supported on LaMCM-41 were prepared using the impregnation method. The catalyst performance was evaluated using a fixed bed CO methanation reactor. A Ni/LaMCM-41 catalyst with La/Si = 0.1 shows the best catalytic performance with a CO conversion of almost 100% and a CH4 selectivity of 89.5% at 250 ℃ under a pressure of 1.5 MPa and at an airspeed of 36,000 mL/（g·h）. Compared with Ni-La/MCM-41（La/Si = 0.1） and Ni/MCM-41 prepared via the impregnation method, Ni/LaMCM-41（La/Si = 0.1） shows a higher CO conversion and CH4 selectivity.In a 100 h stability test, the Ni/LaMCM-41（La/Si = 0.1） catalyst shows excellent stability; furthermore, the CO conversion is always greater than 98.0%, which is significantly better than the results for Ni/MCM-41.We experimentally demonstrate that elemental La enters the framework of MCM-41. The Ni/LaMCM-41 catalyst performs well because the La reduces the average particle size of the NiO particles and enhances the interaction between NiO and MCM-41; moreover, the introduction of La significantly inhibits the sintering of the catalyst and the formation of carbon deposits.

Thermal stability and optical properties of a novel Tm^(3+) doped fluorotellurite glass

A series of fluorotellurite glasses based on（81–x）Te O2-（10＋x）KF-9La2O3（TKL）, where x=0 mol.%, 5 mol.%, 10 mol.%, 15 mol.%, doped with 2000 ppm Tm2O3, were prepared by the conventional melt quenching method.The influence of KF content on the thermal stability and optical spectroscopic properties of the Tm3＋ doped fluorotellurite glasses were investigated by differential scanning calorimetry（DSC）, X-ray diffraction（XRD）, density measurement, Fourier transform infrared spectroscopy（FTIR）, UV-VIS-NIR optical spectroscopy and fluorescence spectroscopy.Judd-Ofelt intensity parameters of Tm3＋ in as-prepared glasses were determined and used to calculate the spontaneous emission probabilities and the radiative lifetime for the 4f-4f transitions of the Tm3＋ ions.Stimulated emission cross sections in the 1470 nm region（σse） were evaluated by Füchtbauer-Ladenburg formula.The results showed that KF substitution of Te O2 was beneficial to improving the thermal stability, decreasing glass density and reducing the content of OH related groups for the investigated fluorotellurite glasses.The glass with composition of 66 Te O2-25KF-9La2O3（named TKL25） had the longest radiative lifetime of the 3H4（361 μs） and the largest FWHM×σse value（420.07×10–28 cm3）, which made it a promising material for S-band fiber amplifiers.

Effect of fluxes on synthesis and luminescence properties of BaSi_2O_2N_2:Eu^(2+) oxynitride phosphors

Eu^2＋ activated BaSi2 O2 N2 oxynitride bluish-green phosphor was synthesized adopting conventional high-temperature solid-state reaction method, in which BaF2, Na2 CO3 and NH4 Cl were used as the fluxes.The phase formation, size distribution and microscopic morphology were characterized to investigate the influence of adding fluxes on photo luminescence properties. The results indicate that with the addition of BaF2 flux, the particle morphology becomes regular and size distribution narrows and the phase purity of BaSi2 O2 N2：Eu^2＋ phosphor can be improved effectively. The photoluminescence intensity of BaSi2 O2 N2：Eu^2＋ phosphor with BaF2 as flux gets enhanced obviously, which is much higher than that of Na2 CO3, NH4 Cl and without flux. The optimum content of BaF2 flux is 4 wt%, and the maximum photoluminescence intensity of the BaSi2 O2 N2：Eu^2＋ phosphor prepared with BaF2 flux rises to 141%,meanwhile, the phosphors with BaF2 flux exhibits low thermal quenching. The results indicate that the BaSi2 O2 N2：Eu^2＋ is sort of promising bluish-green phosphor for application in full-spectra LED.

Magnetic Properties and Thermal Stability of Sintered Nd-Fe-B Magnet with Dy-Ni Additive

A sintered（Nd_（0.8）Pr_（0.2））_（30.7）FebalB_（0.98）Cu_（0.2） magnet with 3% intergranular Dy_（85）Ni_（15） additive is prepared to study the magnetic properties and thermal stability of the Nd-Fe-B magnet. The results show that the magnet with or without additive obtains its optimum comprehensive magnetic properties at the sintering temperature of 1 030 ℃ and 1 040 ℃, respectively. The maximum coercivity of the magnet with additive reaches 15.16 k Oe, while that of the magnet without additive is just 11.88 k Oe. Further investigation on microstructure indicates that the grains of the magnet with additive form a modified ＂core shell＂ structure. Adding Dy_（85）Ni_（15） can significantly enhance the coercivity of Nd-Fe-B magnet and thus decrease its coercivity temperature coefficient.

Effect of niobium substitution on microstructures and thermal stability of TbCu7-type Sm-Fe-N magnets

This paper reports crystal structures, magnetic properties and thermal stability of TbCu7-type Sm（8.5）Fe（（85.8-x）Co（4.5）Zr（1.2）Nbx（x = 0-1.8） melt-spun compounds and their nitrides, investigated by means of X-ray diffraction, vibrating sample magnetometer, flux meter and transmission electron microscope. It is found that the lattice parameter ratio c/a of TbCu7-type crystal structure increases with Nb substitution, which indicates that the Nb can increase the stability of the metastable phase in the Sm-Fe ribbons. Nb substitution impedes the formation of magnetic soft phase a-Fe in which reversed domains initially form during the magnetization reversal process. Meanwhile, Nb substitution refines grains and leads to homogeneous micro structure with augmented grain boundaries. Thus the exchange coupling pining field is enhanced and irreversible domain wall propagation gets suppressed. As a result, the magnetic properties are improved and the irreversible flux loss of magnets is notably decreased. A maximum value 771.7 kA/m of the intrinsic coercivity H（cj） is achieved in the 1.2 at% substituted samples.The irreversible flux loss for 2 h exposure at 120 ℃ declines from 8.26% for Nb-free magnets to 6.32% for magnets with 1.2 at% Nb substitution.

Study on electrochemical property of La_(0.75)Mg_(0.25)Ni_(2.85)Co_(0.45–x)(AlSn)_x (x=0.0,0.1,0.2,0.3) alloys

La_（0.75）Mg_（0.25）Ni_（2.85）Co_（0.45–x）（AlSn）_x（AlSn）_x（x=0.0,0.1,0.2,0.3） alloys were prepared by magnetic induction melting method, and the phase composition and electrochemical properties were investigated systematically. The alloys were mainly composed of LaNi5, La2Ni7 and LaNi3 phase, and the cell volume of LaNi5 increased with the Al and Sn contents. For the alloy corresponding to x=0.0, the Cmax and C150 were 348.9 and 185 mA h/g, respectively, then for the alloy electrode with x=0.2, even though the Cmax was only 309.0 mA h/g less than 348.9 mA h/g, the C150 of 231 mA h/g was much higher than 185 mA h/g. And the values of the limit current density, anodic peak current density and hydrogen diffusion coefficient of the La0.75Mg0.25Ni2.85Co0.35（AlS n）0.1（x=0.1） alloy were 1079.5, 1023.8 mA /g and 5.71×10–10 cm2/s, respectively. Which were the highest than that of any other electrodes. These results suggested that the kinetic property of the La_（0.75）Mg_（0.25）Ni_（2.85）Co_（0.45–x）（AlSn）_x（AlSn）_x（x=0.0, 0.1, 0.2, 0.3） electrodes could be improved effectively by adding moderate contents of Al and Sn.

Temperature stability of magnetic field for periodic permanent-magnet focusing system

In this study, finite element analysis based on an Ansoft Maxwell software was used to reveal the temperature stability of a magnet ring and the equivalent structural periodic permanent-magnet（PPM） focusing system. It is found that with the temperature increasing, the decrease rate of magnetic induction peak（Bz）maxof single magnet ring is greater than that of remanence Brof magnet in the range from room temperature to 200 °C, however,the PPM focusing system do have the same temperature characteristics of permanent-magnet materials. It indicates that the magnetic temperature properties of the PPM system can be effectively controlled by adjusting the temperature properties of the magnets. Moreover, the higher permeability of the magnets indicates the less Hcb, giving rise to lower magnetic induction peak （Bz）′max： Finally, it should be noted that the magnetic orientation deviation angle θ（／15°） of permanent magnets has little effect on the focusing magnetic field of the PPM system at different temperatures and the temperature stability. The obtained results are beneficial to the design and selection of permanent magnets for PPM focusing system.

Effect of Tb(Ⅲ) on the unfolding of ciliate Euplotes octocarinatus centrin induced by guanidine hydrochloride

To understand the unfolding of ciliate Euplotes octocarinatus centrin（EoCen）, the glycine positioned at 115, the sixth residue of the loop of the protein＇s third EF-hand, was mutated into tryptophan（Trp）.Intrinsic fluorescence and Tb（Ⅲ） binding properties of wild type EoCen and G115W mutant were monitored by fluorescence spectra in 10 mmol/L Hepes. The emission maximum of EoCen was 306 nm and mutation had no impact on the Tb（Ⅲ） binding properties. The properties of G115W were investigated by fluorescence, far-UV circular dichroism（CD） spectra and fluorescence decays in the absence or in the presence of 6 mol/L guanidine hydrochloride（GdnHCl）. For the increase in polarity of microenvironment around Trp residue, the emission maximum of apoG115 W at 343 nm is shifted to 359 nm in 6 mol/L GdnHCI. Also the secondary structure is lost nearly and fluorescence lifetime decreases in 6 mol/L GdnHCI. The unfolding of G115W induced by GdnHCI was assessed by using the model of structural element The unfolding of proteins is a sequential reaction, namely two-transition. three-state process. The first transition belongs to the unfolding of the C-terminal domain, and the second transition is assigned to the unfolding of the N-terminal domain. The ⊿〈△G_（total）~0（H_2O）〉 was used to determine the effect of Tb（Ⅲ） on the stability of apoprotein. The 〈△G_（total）~0（H_2 O）〉for Tb_2-G115 W has a less increase of0.68 kJ/mol compared with apoG115W, proving Tb（Ⅲ） situated at C-terminal has negligible impact on the stability of protein. Whereas the 〈△G_（total）~0（H_2 O）〉 for Tb_4-G115W has a rise of 1.29 kJ/mol compared with Tb_2-G115W, manifesting Tb（Ⅲ） lcocated at low affinity sites has considerable influence on protein stability. mainly stabilizing the N-terminal domain.

Chemical stability of simulated waste forms Zr1–xNdxSiO4–x/2： Influence of temperature, pH and their combined effects

The chemical stability of simulated waste forms Zr_（1–x）Nd_xSiO_（4–x/2） was investigated using the static leach test（MCC-1） with lixiviants of three pH values（pH=4, 6.7 and 10） at three temperature points（40, 90 and 150 oC） for periods ranging from 1 to 42 d, and the influence of temperature, pH, as well as their combined effects were explored in detail. The results showed that all the normalized release rate of Nd firstly decreased with leaching time and closed to equilibrium after 14 d. As the temperature increased, the normalized release rate of Nd also increased, but it was no more than 3×10^（–5） g/（m^2·d）. And, the normalized release rate of Nd reached the highest values（~5×10^（–5） g/（m^2·d）） when pH=4, whilst the normalized release rate of Nd remained the lowest value（~1×10^（–5） g/（m^2·d）） near neutral environment（pH=6.7）.