The energy response of LaBr_(3)(Ce),LaBr_(3)(Ce,Sr),and NaI(Tl)crystals for GECAM

The GECAM series of satellites utilizes LaBr_(3)(Ce),LaBr_(3)(Ce,Sr),and NaI(Tl)crystals as sensitive materials for gamma-ray detectors(GRDs).To investigate the nonlinearity in the detection of low-energy gamma rays and address the errors in the calibration of the E-C relationship,comprehensive tests and comparative studies of the three aforementioned crystals were conducted using Compton electrons,radioactive sources,and mono-energetic X-rays.The nonlinearity test results of the Compton electrons and X-rays demonstrated substantial differences,with all three crystals presenting a higher nonlinearity for X/-rays than for Compton electrons.Despite the LaBr_(3)(Ce)and LaBr_(3)(Ce,Sr)crystals having higher absolute light yields,they exhibited a noticeable nonlinear decrease in the light yield,especially at energies below 400 keV.The NaI(Tl)crystal demonstrated an"excess"light output in the 6-200 keV range,reaching a maximum"excess"of 9.2%at 30 keV in the X-ray testing and up to 15.5%at 14 keV during Compton electron testing,indicating a significant advantage in the detection of low-energy gamma rays.Furthermore,we explored the underlying causes of the observed nonlinearity in these crystals.This study not only elucidates the detector responses of GECAM,but also initiates a comprehensive investigation of the nonlinearity of domestically produced lanthanum bromide and sodium iodide crystals.

Centrifugal extraction of rare earths from wet-process phosphoric acid

Phosphorite ore is a potential resource of rare earths （RE） as well as phosphate; therefore, the recovery of RE from wet-process phosphoric acid （WPA） is promising. This study investigated the influence of rotational speed, extractant concentration, flow ratio and phase contact time on the centrifugal extraction of RE from WPA and the separation of RE from impurities. The results indicate that higher rotational speed, higher extractant concentration and larger flow ratio are beneficial to the extraction of RE and impurities from phosphoric acid. It is found that the phase contact time for efficiently extracting RE and that for iron are of great difference, which provides an effective method for separating RE from iron using the non-equilibrium extraction process in centrifugal contactors. Compared with equilibrium extraction, the separation factor βRE/Fe is enhanced from 0.07 to 17.6.

Synergistic extraction of rare earths by mixture of HDEHP and HEH/EHP in sulfuric acid medium

The extraction of RE（Ⅲ） （RE=La, Nd, Sm, Gd） in sulfuric acid medium using the mixture of HDEHP（H2B2） and HEH/EHP（H2L2） was investigated. The synergistic enhancement coefficient（R） was calculated for La （1.96）, Nd（3.52）, Sm（5.96）, and Gd（5.71）, respectively, at pH=2.0, and it was seen that the R increased with the increase of aqueous quilibrium pH. The configuration of the extracted complexes was considered to be RE（SOa）xH2x（HB2）3 with HDEHP, RE（SOa）xH2x（HL2）3 with HEH/EHP, and RE（HB2）2（HL2） with their mixture as the extractant with the slope method. The equilibrium constants and stability constants were calculated. A cation exchange mechanism was proposed as well.

Occurrence and vertical distribution of aluminum and rare earths in weathered crust elution-deposited rare earth ore:Effect of soil solution pH and clay minerals

Weathered crust elution-deposited rare earth ore is crucial source of medium and heavy rare earths,with in-situ leaching being the most common mining method.The high contents of impurity of aluminum in the leach solution are a significant challenge for the subsequent enrichment process of rare earths.A comprehensive understanding of the occurrences and vertical distribution of aluminum and rare earths within typical vertical profiles can provide valuable insights into entire design of the in-situ leaching.This paper improves a five-step sequential extraction method to analyze the occurrence and vertical distribution of rare earths and aluminum in vertical profiles from Chongzuo and Longyan.Experimental results demonstrate that soil solution pH is the main factor affecting the vertical distribution of ionexchangeable rare earths.Both samples have distinct areas of enrichment for ion-exchangeable rare earths or aluminum.Ion-exchangeable rare earths are primary concentrated in the middle and lower parts of the ore layer(4-13 m in Chongzuo,14-22 m in Longyan),while the ion-exchangeable aluminum is mainly enriched in the upper part of the ore layer(1-5 m in Chongzuo,and 2-14 m in Longyan).The vertical distribution of inorganic hydroxy aluminum is likely influenced by the micromorphology and particle size of the clay minerals.The inorganic hydroxy aluminum concentration in Chongzuo samples decreases continuously from 415.65 to 120.95 mg/kg with increasing sampling depth,whereas the concentration in Longyan samples(110.55-171.27 mg/kg)is almost independence with sampling depth.These results provide direct guidance for the entire design of the injection well depth and the leaching parameters,thereby inhibiting the leaching of impurity of aluminum and lower the consumption of leaching agent.

Effect of phase transition during roasting of Mountain Pass rare earth concentrate on leaching efficiency of rare earths

To find a greener and more economical approach for treating the Mountain Pass rare earth concentrate(MPREC),a novel "Combination Method",including the processes of oxidizing roasting,HCI leaching and sulfuric acid roasting,is proposed in this research.In this paper,the effect of phase transition behavior in hydrochloric acid leaching during oxidative roasting at 450-600℃ was studied.During roasting,the bastnasite in MPREC is decomposed into CeLa_(2)O_(3)F_(3) and(Ce_(0.33),La_(0.33),Ca_(0.33))O_(1.5).As the CeLa_(2)O_(3)F_(3) phase has the fluorine-fixation effect,the generated CeLa_(2)O_(3)F_(3) phase can not be dissolved by HCI after roasting at 500 and 550℃,but it can be decomposed by HCI after roasting at over 600℃,resulting in the improvement of the leaching rate of total F element.The maximum leaching efficiency of rare earth elements(REEs) can reach 70.32 wt% at the roasting temperature of 550℃.After roasting at over 600℃,some F^-ions in the solution combined with RE^(3+) to form REF_(3) precipitate and enter the leaching residue,and the others are in the form of [CeF_(3)]^+ in the leaching solution during leaching,therefore,the leaching efficiency of non-ce rium REEs decreases while that of cerium element increases.This work provides basic research for optimizing the actual production process of MPREC.

Efficient removal of Al(Ⅲ)and P507 from high concentration MgCl_(2)solution based on in-situ reaction strategy

For a highly efficient recycling of a wastewater containing a high concentration of MgCl_(2),Al(Ⅲ)and P507 were scheduled to be removed in advance.In this study,the in-situ removal of Al(Ⅲ)and P507 from a high concentration MgCl_(2)solution at different pH values and Al/P molar ratios was investigated.The results showed that P507 formed organic complexes of Al_(x)(OH)_y^(Z+)-P507 at pH of 2.0-4.0.At pH of 4.0-5.0,Al(Ⅲ)precipitated and transferred into Al(OH)_(3)with a flocculent amorphous morphology.Active sites on the Al(OH)_(3)surface enhanced the removal efficiency of P507.At pH of 6.0-6.5,Al(Ⅲ)and Mg(Ⅱ)formed layered crystalline Al(OH)_(3)and MgAl_(2)(OH)_(8with)small pore channels and fewer active sites,resulting in a reduced removal efficiency of P507.When the Al/P molar ratio exceeded 13 and the pH was between 4.0 and 5.0,the removal rates of both Al(Ⅲ)and P507 were higher than98%,while the concentration loss of Mg(Ⅱ)was only 0.2%-0.9%.

Synthesis of Nano-sized Yttria via a Sol-Gel Process Based on Hydrated Yttrium Nitrate and Ethylene Glycol and Its Catalytic Performance for Thermal Decomposition of NH_4ClO_4

Nano-sized yttria particles were synthesized via a non-aqueous sol-gel process based on hydrated yttrium nitrate and ethylene glycol. The effects of the molar ratio of ethylene glycol to yttrium ion and calcination temperature on crystallite size of the products were studied. The catalytic performance of the as-prepared yttria for the ammonium perchlorate （AP） decomposition was investigated by differential scanning calorimetry （DSC）. The results indicate that the nano-sized cubic yttria particles with less than 20 nm in average crystallite size can be obtained after 2 h reflux at 70℃, dried at 90 ℃, forming xerogel, and followed by annealing of xerogel for 2 h, and that the addition of the nano-sized yttria to AP incorporates two small exothermic peaks of AP in the temperature ranges of 310 - 350 ℃ and 400 - 470 ℃ into a strong exothermic peak of AP and increases the apparent decomposition heat from 515 to over 1110 J·g^- 1. It is also clear that the temperature of AP decomposition exothermic peak decreases and the apparent decomposition heat of AP increases with the increase of the amount of nano-sized yttria. The fact that the addition of the 5 % nano-sized yttria to AP decreases the temperature of AP exothermic peak to 337.7℃ by reduction of 114.6℃ and increases the apparent decomposition heat from 515 to 1240 J·g^-1, reveals that nano-sized yttria shows strong catalytic property for AP thermal decomposition.

Synergistic extraction of rare earth by mixtures of 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester and di-(2-ethylhexyl) phosphoric acid from sulfuric acid medium

The extraction of Nd^3＋ and Sm^3＋, including the extraction and stripping capability as well as the separation effect of Nd^3＋ or Sm^3＋, from a sulfuric acid medium, by mixtures of di-（2-ethylhexyl） phosphoric acid （HDEHP, H2A2（0）） and 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester （HEH/EHP, H2L2（0）） were studied. The distribution ratios and synergistic coefficients of Nd^3＋ and Sm^3＋ in different acidities were also determined. A synergistic extractive effect was found when HDEHP and HEH/EHP were used as mixed extractants for Sm^3＋ or Nd^3＋. The chemical compositions of the extracted complex were determined as Nd.（HA2）2-HL2 and Sm.（HA2）2-HL2. The extraction equilibrium constants, enthalpy change, and entropy change of the extraction reaction were also determined.

Leaching behaviors of calcium and magnesium in ion-adsorption rare earth tailings with magnesium sulfate

The leaching behaviors of calcium and magnesium in the rare earth tailings leached with magnesium sulfate using deionized water,CaCl2 solution and lime water were investigated.Experimental data indicated that magnesium in the tailings was easy to be leached out since most of the magnesium was in the form of water-soluble phase.Most of calcium in the lime water was electrostatically adsorbed on the clay mineral of the tailings,and the water-soluble magnesium was also gradually converted into exchangeable phase because of back-adsorption of Mg2+on the clay mineral with increasing the pH values.When the liquid-to-solid ratio was 0.80,the contents of readily-available magnesium and calcium were 104.4−207.6 and 201.7−1426.3 mg/kg,respectively,which could meet the requirements for plants.These results suggest a promising route for the environmental remediation of ion-adsorption rare earth ore after in-situ leaching.

Luminescent Properties of Green Phosphor Ca_8Mg(SiO_4)_4Cl_2:Eu^(2+), Dy^(3+) for LED Applications

The new phosphor calcium magnesium chlorosilicate, codoped with Eu^2＋ and Dy^3＋, was synthesized with the help of the high temperature solid state reaction in reducing atmosphere. The excitation and emission spectra were very similar to that of Ca8Mg（SiO4）4Cl2 ：Eu^2＋, and the Dy^3＋ concentration influenced the emission intensity of this phosphor. The intensity of Eu^2＋ and Dy^3＋ codoped CMSC was stronger than that of Eu^2＋ singly doped CMSC. The emission spectrum of the Dy^3＋ ion overlapped the absorption band of the Eu^2＋ ion, indicating that an energy transfer from Dy^3＋ to Eu^2＋ took place in CMSC：Eu^2＋, Dy^3＋ phosphor. The mechanism of the energy transfer from Dy^3＋ tO Eu^2＋, in this phosphor, might be resonant energy transfer.

A novel method for the synthesis of YAG:Ce phosphor

YAG:Ce phosphor was synthesized by a novel simple method,wherein the admixture of three raw materials(Y2O3,α-Al2O3 and CeO2) were first acidified by diluted nitric acid to prepare a precursor,followed by a high temperature heating treatment of the obtained precursor under reductive atmosphere.Through XRD measurement and SEM observation,it was found that Y2O3,one of the raw material,was firstly dissolved into the diluted nitric acid,and then recrystallized on the surface of both α-Al2O3 and CeO2 to form a no...

Synthesis of YAG∶Ce^(3+) Phosphor by Polyacrylamide Gel Method and Promoting Action of α-Al_2O_3 Seed Crystal on Phase Formation

YAG： Ce^3 ＋ phosphor particles were prepared using polyacrylamide gel method. The structure evolution of powders during annealing process was followed by X-ray diffraction determination. It is found that some intermediate phases, including θ-Al2O3, YAM and YAP, are formed when calcining polyacrylamide gel, however, the pure YAG phase can be formed directly when calcining polyacrylamide gel with α-Al2O3 as seed crystal. These facts show that the existence of α- Al2O3 seed crystal can block the formation of θ-Al2O3, YAM and YAP, and accelerate its reaction with Y2O3 to form YAG phase directly at lower temperature. The emission peak of prepared YAG ： Ce^3 ＋ phosphor is wide with maximum at 550 nm and the exitation band has two peaks, the major one is around at 460 nm, which matches the blue emission of GaN LED and is suitable for the assemble of white LED. Some fluxes can enhance the photoluminescence intensity of phosphor particles, that can be attributed both to the improvement of crystallization processes of YAG and to the stabilization of trivalence cerium ion in YAG：Ce^3 ＋.

Luminescence properties of nitride red phosphor for LED

Eu^2＋-doped ternary nitride phosphor, Sr2Si5N8：Eu^2＋, was synthesized using the high temperature solid-state method. The X-ray diffraction （XRD） pattern showed that Sr2Si5N8 single phase was obtained. The lattice parameters shrank because the radius of Eu^2＋ was smaller than that of Sr^2＋. The emission spectra showed a broad emission band. With an increase in Eu^2＋ concentration, the emission peak position was redshifted. The excitation spectra showed two excitation bands originating from the host and the 4f^7→4f^6 5d^1 transition of Eu^2＋ ions Compared with the luminescent characteristic of Sr2Si5N8：Eu^2＋ and CaS：Eu^2＋ phosphors, at different temperatures, it was noted that the intensity of the two phosphors reduced gradually with an increase in temperature. The intensity of Sr2Si5N8：Eu^2＋ phosphor was stronger than that of CaS：Eu^2＋, which indicated that the luminescent characteristic of the former was better than that of the latter.

Preparation and Luminescent Properties of BAM Blue Phosphor for PDP and CCFL

The Ba x-0.05MgAl 10O 16+x∶Eu 2+ 0.05 (0.88≤x ≤1.02) phosphors with different Ba 2+ content and the Ba 0.85MgAl 10O 16.94∶Eu 2+ 0.09 phosphors with different fluxes (BaF 2, MgF 2, AlF 3, BaCl 2, MgCl 2, AlCl 3, H 3BO 3) were prepared by high temperature solid-state reaction method and their luminescence characteristics were studied under 254 nm excitation and vacuum ultraviolet (VUV) excitation. With the increase of the Ba 2+ content, there is an increase in the emission intensity, and when x=0.94, it reaches a maximum. Then, as the Ba 2+ content increases, the emission intensity slowly falls. The fluorides have better flux-effects than chlorides and H 3BO 3. The possible mechanism in the process of particle growth was discussed when fluorides were used as fluxes. The effect of the activator concentration on this system was also investigated. The quenching concentration is 0.13 mol in per mole host.

Red Emitting Phosphor (Y,Gd)BO_3:Eu^(3+) for PDP Prepared by Complex Method

Red phosphor (Y, Gd)BO3:Eu3+ with grain shape, small size, non-agglomerate, high crystallinity and good photoluminescence (PL) intensity was prepared by a complex method that the precursor of the phosphor was prepared by co-precipitation method and the phosphor was prepared by combustion method. The SEM photos and the photoluminescence spectrum excited under VUV show that the morphology and luminescent properties of this phosphor are satisfied when an appropriate amount of urea was adopted as the combustion agent in the preparation procedure.

Dissolution behaviors of rare earth elements in phosphoric acid solutions

In order to provide practical fundamental data for rare-earth elements （REEs） recovery from phosphoric acid and to betterunderstand REEs behavior during the phosphoric acid evaporation process, the solubilities of REEs in phosphoric acid with variousconcentrations of phosphorus at different temperatures were measured. A simple linear model between REEs solubility andphosphoric acid concentration is built and the experimental data are found to fit it very well （R2〉0.94）. Hydrogen-ion concentration isfound to be the predominant factor controlling the solubility of REEs in phosphoric acid. In addition, the solubility of REEs inphosphoric acid is found to sharply decrease with increasing temperature, which can be attributed to the increase of the Gibbs energyof the REEPO4 dissolution reaction or the restraint of the disassociation of phosphoric acid molecules owing to the elevatedtemperature.

Optimization Design of High-speed Interior Permanent Magnet Motor with High Torque Performance Based on Multiple Surrogate Models

In order to obtain better torque performance of high-speed interior permanent magnet motor(HSIPMM) and solve the problem that electromagnetic optimization design is seriously limited by its mechanical strength, a complete optimization design method is proposed in this paper. The object of optimization design is a 15 kW、20000 r/min HSIPMM whose permanent magnets in rotor is segmented. Eight structural dimensions are selected as its optimization variables. After design of experiment(DOE), multiple surrogate models are fitted, a set of surrogate models with minimum error is selected by using error evaluation indexes to optimize, the NSGA-II algorithm is used to get the optimal solution. The optimal solution is verified by load test on a 15 kW, 20000 r/min HSIPMM prototype. This paper can be used as a reference for the optimization design of HSIPMM.

Research on Y_2O_3:Eu Phosphor Coated with In_2O_3

Y2O3：Eu red phosphor for FED application was prepared by high temperature solid-state reaction. The In2O3 coating by precipitation method to the phosphor was applied and the analyses of XRD, Zeta potential, SEM, EDS and low voltage cathodoluminescence （CL） were conducted for investigating the coating effect. The results showed that In2O3 coating promoted the low voltage CL of the phosphor efficiently. The promotion was possibly due to the enhancement of the surface conductivity of the phosphor grains.

Synthesis of La-hexaaluminate catalyst for methane combustion by a reverse SDS microemulsion

La-hexaaluminate catalyst for methane catalytic combustion was synthesized by a reverse microemulsion. Pseudo-temary phase diagrams of a quaternary microemulsion system of sodium dodecyl sulfate （SDS）, n-pentanol, n-octane, and water （or Al（NO3）3 solution） were presented. The effects of alcohol chain length, cosurfactant-to-surfaqtant rat!0, and salt concentration on the formation and stability of the microemul- sion system were studied. The phenomenon that the conductivity changed with water supported the phase behavior of the microemulsion system. La（MnffFex）Al12_xO19_a catalysts, applied in methane combustion and with high-temperature stability, were synthesized within the stable areas of the phase diagram of the microemulsion system, when SDS was chosen as surfactant, n-pentanol as cosurfactant, and n-octane as oil phase. The physical properties and structure of the catalysts were characterized by BET method, transmission electron microscope （TEM）, and X-ray diffraction （XRD）. A micro-fixed-bed reactor was used to measure the catalytic activity of hexaaluminates in methane combustion. The results show that the reverse microemulsions can be used to produce discrete La-hexaaluminate nanoparticles that display excellent methane combustion activity owing to their high surface area and high thermal stability.

Study on Thermal Expansion Coefficient of Sealing Materials for Ceramic Metal Halide Lamps

With Al2O3, Dy2O3, and SiO2 as starting materials, the basic glass of Al2O3-Dy2O3-SiO2 system was prepared by conventional melting technology, and their thermal expansion coefficients （TECs） at different anneal time were investigated. TECs of the basic glass, which were heat-treated under different temperature, were also investigated. The result showed that TECs of the basic glass gradually approached a fixed value as the anneal time was extended, which suggested that most of the inner stress had been eliminated. After heat treatment, the contents of Dy2O3, Dy2Si2O7, and a new crystal increased up to 1200 ℃ and decreased below 1250 ℃, which was consistent with the TEC change of crystallized samples. This suggests that the crystal has a direct effect on TECs of the crystallized samples.