X射线荧光光谱法测定球团矿的成分

采用粉末压片法制样，使用ARL9800XP型XRF—XRD结合型荧光光谱仪分析球团矿中TFe、FeO、SiO2、CaO、S、MgO、A12O3及P的含量。建立的工作曲线线性较好，且该方法简便、快速，精密度和准确度能够满足生产需要。     

X射线荧光光谱法测定生铁块中杂质元素

应用荧光光谱仪分析生铁块中Si、Mn、P、S、As、Ti。该分析方法简便、快速,结果较为满意,适用于炼钢生产过程中的在线分析和质量控制。     

X射线荧光光谱法分析锰铁

本文通过对X荧光光谱法测定锰铁中元素进行研究,试样采用粉末压片法制成,用国家标样和自制标样绘制工作曲线,取得了较好的效果.     

X射线荧光光谱法测定高炉渣中的Al2O3

介绍X射线荧光光谱法采用粉末压片的制样方式测定高炉渣中的Al2O3的分析方法．该方法简便、快速、准确、可靠．     

粉末压片X射线荧光光谱法测定氧化铝中杂质元素

介绍了X射线荧光光谱法测定氧化铝中杂质元素的方法。研究了粉末压片法中助研剂丙二醇的选择和用量,考察了氧化铝粒度对X射线荧光强度的影响。试验表明,样品的粒度达到40 μm以下,粒度效应减弱;对于10.0 g氧化铝样品,加2滴丙二醇,研磨40 s,并用硼酸镶边垫底,制备的测量样片效果较好。用系列氧化铝标准样品作校准曲线,对样品中11个元素进行测定,其SiO₂、Fe₂O₃、Na₂O、K₂O、CaO、Ga₂O₃、ZnO测得结果的相对标准偏差（RSD）均小于8.0%,P₂O₅、TiO₂、V₂O₅、Cr₂O₃的含量在3倍检出限以上,RSD小于10%,含量在3倍检出限以下的RSD小于17%。用氧化铝标准样品验证,测量结果与标准样品的认定值基本一致。     

X射线荧光光谱法测定冶炼锡烟尘中10个组分

采用硼酸衬底直接压片法制取锡冶炼烟尘粉末的片状试样,然后用X射线荧光光谱法测定烟尘试样中Al_2O_3,As,SiO_2,Fe_2O_3,CaO,MgO,Pb,S,Sn,Zn含量。元素之间谱线干扰采用ARL9400WinXPF 2.0软件中的Trail-Lachance模型进行校正。对一样品的各组分进行11次测定,得到相对标准偏差在0.09%～3.66%之间,测定结果与滴定法和原子吸收光谱法吻合较好。方法快速、准确,可满足生产快速分析的要求。     

X射线荧光光谱法测定氧化铝中杂质含量

对X射线荧光光谱测定氧化铝中杂质元素的方法进行了研究。利用系列标准样品制作工作曲线,采用混合熔剂四硼酸锂加偏硼酸锂(12+22)熔融制样法分析了SiO2,Fe2O3,Na2O,制备熔片的稀释比为1∶3;直接压片制样法分析了TiO2,V2O5,P2O5,ZnO。SiO2,Fe2O3,Na2O,TiO2,V2O5,P2O5,ZnO测定结果的RSD分别为2.61%,2.61%,2.33%,4.62%,8.24%,8.00%和1.79%。该方法用于氧化铝生产控制及产品分析,数据准确、可靠,结果令人满意。     

粉末压片X射线荧光光谱法测定球团矿中各主次成分

采用粉末压片X射线荧光光谱法测定球团矿中的各主次成分,结合本公司的实际生产工艺和要求,通过优化制样过程中的各项参数,确定最佳的制样条件,选用具有一定梯度含量的自产球团矿样品用化学分析进行定值,而后绘制工作曲线对生产样品进行分析。经实际使用表明,本法测量准确度、精密度较好,所得分析结果与化学分析结果一致。     

X射线荧光光谱法测定钢水净化剂

采用粉末压片法制样，X荧光光谱法分析钢水净化剂（硅铝合金、硅铝钙钡、硅铝钡、硅钙线等）中的si、AL、ca、Ba、S、P，建立了较准曲线，使之测定方法简单、快速、准确。     

SrAl2O4:Eu, Dy Nanometer Phosphors Synthesized by Combustion Method

SrAl2 O4: Eu, Dy nanometer phosphors were synthesized by combustion method at 500 ～ 900℃, followed by heating the combustion sample at 1150℃ at a weak reductive atmosphere and nanometer phosphor with much better luminescent properties was obtained. The influences of the initiating combustion temperature, H3BO3 quantity, the mass ratio of urea and nitrate on the luminescent intensity of nanometer phosphors were studied. The optimum synthetic conditions were determined. The analysis results by transmission electron microscopy (TEM) indicate that the particle size of the synthetic product is less than 75 nm. The luminescent materials do not need to be ground. Their coating can be refined. It supplies a new approach to the rapid preparation of the luminescent materials at low temperature. The excitation and emission spectra indicate that the main peaks in the excitation and emission spectrum of nanometer phosphor synthesized by combustion method shifted to the short wavelength compared with the phosphor obtained by the solidstate reaction synthesis method. The reason of blue shift was explained. The afterglow decay results indicate that the decay speed of the afterglow for nanometer phosphor is faster than that obtained by the solid-state reaction method.     

Preparation and Luminescence of SrAi2O4:Eu2+, Dy3+ Nano-Particle

SrAl2O4: Eu2 , Dy3 nano-particle luminescence material was prepared by sol-gel method. Influences of synthesis conditions on the particle size and luminescence properties of SrAl2O4: Eu2 , Dy3 were studied. The synthesis process and the properties of the samples were analyzed by DTA, TGA, XRD, SEM. The result suggested that the formation of SrAl2O4: Eu2 , Dy3 sol is a slow heat release process beginning at 500 ℃ and peaking at 759 ℃.SrAl2O4: Eu2 ,Dy3 crystalline was formed at 1100 ℃. The luminescence properties of the SrAl2O4: Eu2 , Dy3 nanoparticle were compared with the conventional SrAl2O4: Eu2 , Dy3 particles. The average particle size of the product is about 30 nm. The excitation spectrum of the sample shows a broad band with peaks at 240, 330, 378 and 425 nm. The emission spectrum is a broadband spectrum with a peak at 523 nm.     

蓝色发光材料Sr_2MgSi_2O_7∶Eu~(2+),Dy~(3+)的微波合成及性能

采用微波辐射法合成了Sr2MgSi2O7∶Eu2+,Dy3+粉末,研究了微波辐射功率和加热时间对制备Sr2Mg-Si2O7∶Eu2+,Dy3+的影响,确定了微波法合成Sr2MgSi2O7∶Eu2+,Dy3+的最佳条件,并用x射线衍射(XRD)、荧光光谱等测试手段对其进行了表征。XRD结果表明,合成的Sr2MgSi2O7∶Eu2+,Dy3+属于四方晶系。荧光光谱测试表明,用lem=467nm作为监控波长,在200nm~450nm之间有宽的激发光谱,峰值位于398nm。用lex=398nm激发样品,其发射光谱为一宽带,峰值位于467nm。Sr2MgSi2O7∶Eu2+,Dy3+的荧光强度和余辉性能随辐射功率和时间的不同而发生变化,其中以辐射功率720W,反应时间25min时荧光强度最强,余辉时间可达8h。     

Synthesis of Long Afterglow Phosphors Doped B SrAl2O4:Eu2+, Dy3+ and Its Luminescent Properties

The long afterglow luminescent material SrAl₂O₄: Eu²⁺, Dy³⁺ was prepared by high temperature solid-state method. Effects of doped B on the luminescent properties of phosphors SrAl₂O₄: Eu²⁺, Dy³⁺ were investigated by means of excitation spectra, emission spectra and X-ray diffraction analysis. As the result, the addition of H₃BO₃ as flux promotes the growth of crystalline and reduces the synthesizing temperature, but the wavelength of emission peak of photoluminescent material did not change with the variation of H₃BO₃ content. The effect of Dy³⁺ concentration on the luminescent properties of material was investigated. It was found that the luminescence of phosphors prepared under the condition of the amount of H₃BO₃ 5% and the mole ratio of Eu/Dy = 1/7(Eu = 0.02 mole) had better luminescent property and longer afterglow time.     

Preparation and characterization of flower-like SrAl2O4:Eu2+,Dy3+ phosphors by sol-gel process

A flower-like Eu2+ and Dy3+ co-doped SrAl2O4 long-lasting phosphorescent (LLP) phosphor was synthesized via the inorganic- salt-based sol-gel method.The crystal structure,morphology and optical properties of the composite were characterized.X-ray diffraction diffu-sion (XRD) data and DSC-TG curves of the phosphor revealed that the SrAl2O4 crystallites have been formed after the precursor was calcined at 900 °C and to be single-phase SrAl2O4 at 1100 °C.The SEM photographs indicated that the sample exhibited ...     

Synthesis of Long Afterglow SrAl2O4 :Eu2+, Dy3+ Phosphor by Microemulsion Method

Long afterglow SrAl2 O4: Eu2 , Dy3 phosphor was synthesized by microemulsion method. The synthesized phosphor was characterized by XRD. XRD pattern indicates that the phosphor has monoclinic SrAl2 O4 crystal structre.The microstructure of the phosphor was investigated by SEM and TEM. The excitation spectrum, emission spectrum and afterglow decay curve were measured, the wide range of excitation wavelength indicated that the luminescent material could be excited by the light from ultraviolet ray to visible light, and the emission maximum was found to peak mainly at λem of 525 nm. The sample excited by ultraviolet visible light could emit bright green light.     

A white long-lasting phosphor Y2O2S:Tb3+, Sm3+: an improvement of Y2O2S:Tb3+

As an improvement of reported Y202S:Tb3 , a white-light long-lasting phosphor: Y2O2S:Tb3 , Sm3 was prepared by the solid-state reaction. The photo-luminescence spectra showed that the position and shape of Th3 and Sm3 emissions under UV excitation were similar in this host, which ensured a stable white emission color (daylight standard of IEC) under different excitations. The decay curves of co-doped samples indicated that the decay times of emissions of the two ions were close. The thermo-luminescence measurement suggested that the traps created by the doped Sm3 ions were helpful to postpone the white afterglow of co-doped samples. Therefore, thefunction of co-doped Sm3 ions was confirmned as improving the white emission colors of samples and acting as new trap centers.     

Adjustable Luminescence of SrAl2O4：Eu^2＋ , Dy^3＋ Assembled in Zeolite

Capsulating guest into the nanometer yoids of zeolites is a effective way to form novel host-guest material. In our work, stoichiometric SrAl2O4: Eu^2 , Dy^3 sol guest was prepared by sol-gel method and assembled into the nanometer channels of zeolite ZSM-5 host through mechanical mixing, hydrothermal reaction and microwave heating reaction, respectively. After being reduced and diffused in a microwave muffle, the fluorescence spectra of the host-guest materials exhibit remarkable blue shifts in comparison of that of SrAl2O4 : Eu^2 , Dy^3 . Some interesting phenomena in the assembled hostguest materials are that the after-glow emission spectra exist two bands at about 400 nm and 517 nm and the relative strengths of these two bands can be adjusted by changing the assembly methods and the assembly concentration. These are attributed to the fact that the phosphor was capsulated into the voids of zeolite ZSM-5 and generated the quantum size effect and the host-guest effect.     

SrAl2O4 :Eu2+, Dy3+ Long Afterglow Phosphors Prepared by Chemical Coprecipitation Method

SrAl2 O4: Eu2 , Dy3 long afterglow phosphors were prepared by chemical coprecipitation method. Ammonium carbonate and ammonium hydrogen carbonate were used as the precipitants. The preparation of the SrAl2 O4: Eu2 ,Dy3 precursor was completed at room temperature by controlling the concentration of the metal-salt solution, pH value of the system, etc. The phosphors were prepared by sintering the precursor at 1000 ～ 1200 ℃ in a weak reducing atmosphere for 2 h. The XRD, SEM, excitation spectra, emission spectra and afterglow decay of the samples were tested and the optimal synthesis conditions of the SrAl2O4: Eu2 , Dy3 long afterglow phosphors prepared by precipitation method were determined. The phosphor which had good luminescent properties is prepared and its persistent time can reach more than 1600 min. In the coprecipitation process, a small amount of glucose operates to refe the luminescent powders. The particle size of the phosphor can be less than 1 μm. The sintering temperature of the sample prepared by the coprecipitation method is much lower than that of the one prepared by the high temperature solid state method.Compared with the high temperature solid state method, a clear blue shift occurs in the excitation and emission spectra of the samples.