铂饰品中Pt, Pd, Au, Ag, Cu, Ni, Zn, Fe的测定

试验研究建立了同一试料溶液连续、同时测定铂饰品中各成分的分析方法。主体Pt以氯铂酸铵称量法及火焰原子吸收光谱(FAAS)法或电感耦合等离子发射光谱(ICP-AES)法测定滤液中残留Pt进行补差而测定。主成分Pd,Au,Ag,Cu和焊料成分Ni,Zn,Fe以FAAS法或ICP-AES法测定。其方法回收率分别为:Pt99.9%~100%;Pd99.3%~99.7%;Au99.5%~l01.5%;Ag98.0%~100%;Cu97.7%~99.3%;Zn98.0%~99.0%;Ni94.0%~105%;Fe95.0%~99.0%。实际试样分析时,各成分质量分数之和一般在99.12%~l01.2%之间,接近于100%,间接说明方法的可靠性。本法适用于Pt-Pd二元体系和Pt-Pd-Au-Cu多元复杂体系的铂饰品的破坏分析,可用于校正X荧光光谱法无损检测铂饰品的分析结果。     

X射线荧光光谱法测定烧结矿中Fe,Al,Ca,Mg,Si,S,Mn,P

烧结矿是高炉冶炼的重要原料之一 ,准确快速分析烧结矿中主、次量元素 ,对于指导烧结矿及高炉生产具有重要意义。由于烧结矿日常分析元素较多 ,采用化学分析方法 ,分析时间长 ,手续繁琐。本文利用多道同步Ｘ射线荧光光谱仪 ,合理选择分析及制样条件 ,对烧结矿中主、次量元素进行分析。结果表明 :该法分析速度快、准确度高 ,完全满足日常分析的要求。1　实验部分1 1　仪器及工作条件Ｓｉｍｕｌｔｉｘ 1 1型Ｘ射线荧光光谱仪 (日本理学 ) ,盘式振动磨 (ＷＣ材质 ) ,5 0ｔ油压机。工作条件 :Ｘ光管 ( 4 0ｋＶ - 2 5ｍＡ) ,Ｐ1 0气体流量 2 5ｍ…     

FAAS法测定铝合金中Fe,Cu,Zn,Mn,Ni,Ca,Mg和Cr

铝合金的分析一般采用化学法、光谱法[1],部分元素的测定也有采用火焰原子吸收法的报导““,化学法操作繁琐,周期长,技术条件严格,而且所用的试剂量大．本文采用火焰原子吸收法连续测定了铝合金中铁、铜、锌、锰、镍、钙、镁和铬．方法操作简单、准确、稳定．1实验部分1．1主要仪器和试剂PE3030B原子吸收光谱仪．氯化钢溶液（lap／L）：称取259LaP。,溶于80rnL盐酸中,用去离子水稀释至250InL;铁、铜、锌、锰、镍、钙、镁、铬标准溶液：浓度均为IIDg／mL。仪器工作条件见表l．1．2分析步骤称取1．00009样品于250mL烧杯中,加人…     

电感耦合等离子体原子发射光谱法测定铁矿石中Si,Ca,Mg,Mn,Al,P,V,Ti

铁矿石中Si O2,CaO,MgO,MnO,Al2O3,P,V2O5,Ti O2,通常用分光光度法或容量法分别测定,方法繁琐费时。用电感耦合等离子体光谱仪测定铁矿石的主体成分,方便快捷,准确性好,无明显的化学干扰。通过研究对比,选择无明显干扰的两条或一条谱线,使选择的波长符合在同一溶液中能同时测定其它组分的要求;同时采用与试样组分相近的标准样品绘制工作曲线,用标准样品进行对照,ICP-AES法测定铁矿石中上述组分,结果令人满意。1实验部分1·1主要仪器及工作条件IRIS IntrepidⅡ型垂直全谱直读等离子光谱仪(美国Thermo公司):固体检测器(CID),波长…     

FAAS法测定磷矿粉中微量Fe,Co,Ni,Cu,Pb,Zn

用火焰原子吸收光谱法对新疆某地的磷矿粉中Fe ,Co ,Ni,Cu ,Pb ,Zn微量元素进行了分析测定 ,并探讨了酸度、干扰离子等对测定的影响。所拟方法快速、简便 ,分析结果十分满意     

X射线荧光光谱仪测定铝合金中Si,Mn,Fe,Cr,Ni,Ti,Cu

采用改造后的VXQ -15 0AX射线荧光光谱仪和日本岛津公司提供的数据软件 ,合理选择分析条件 ,对铝合金中Si,Mn ,Fe ,Cr,Ni,Ti,Cu元素进行测定 ,结果较为满意。     

ICP-AES法测定钼铁中Mo,Si,Cu,Sb,Sn

以电感耦合等离子体光谱法(ICP-AES)直接同时进行钼铁中基体元素Mo和微量杂质元素Si,Sb,Sn,Cu的测定。试验了元素的干扰情况,优化了仪器工作条件,采用钇内标校正与同步背景校正、K系数校正相结合的方法消除基体及试液进样的物理化学影响干扰。精密度、回收率、检出限、标准样品分析对照均取得了满意的结果。     

纯铜中铋,锑,砷,铁,镍,铅,锡,锌的光谱定量分析

本文介绍了一种光谱定量分析方法。该方法使用ＢＹＧ０１－１氧化铜光谱标准样品，对１－４号纯铜中铋、锑、砷、铁、镍、铅、锡、锌８个杂质元素进行定量分析。分析方法简单，测定结果与化学结果基本相符。方法的测定下限为３×１０￣（０６）。     

火焰原子吸收光谱法测定混合铜矿中Cu,Fe,Ni,Zn,Mg,K

用火焰原子吸收光谱法对新疆某地的混合铜矿进行分析测定,并探讨了酸度、干扰离子对测定结果的影响,取得了满意的结果。     

Luminescent properties of MMgP_2O_7：Eu~（3＋）（M=Ca,Sr,Ba） phosphor

A series of red phosphors Eu3+-doped MMgP2O7(M=Ca,Sr,Ba) were synthesized by solid-state reaction method.X-ray powder diffraction(XRD) analysis confirmed the formation of pure CaMgP2O7,SrMgP2O7 and BaMgP2O7 phase.Photoluminescence spectra of MMgP2O7(M=Ca,Sr,Ba):Eu3+ phosphors showed a strong excitation peak at around 400 nm,which was coupled with the characteristic emission(350-400 nm) from UV light-emitting diode.The CaMgP2O7:Eu3+,SrMgP2O7:Eu3+ and BaMgP2O7:Eu3+ phosphors showed strong emission bands peaking at 612,593 and 587 nm,respectively.Due to the difference of the ion sizes between Ba2+(0.142 nm),Sr2+(0.126 nm),Ca2+(0.112 nm),Mg2+(0.072 nm) and Eu3+(0.107 nm),Eu3+ ions were expected to substitute for different sites in CaMgP2O7,SrMgP2O7 and BaMgP2O7 lattice.     

Synthesis of Long Afterglow Phosphors MAl2O4:Eu2+, Dy3+(M=Ca, Sr, Ba) by Microemulsion Method and Their Luminescent Properties

Long afterglow phosphors MAl2O4:Eu2 , Dy3 (M=Ca, Sr, Ba) were synthesized by microemulsion method, and their crystal structure and luminescent properties were compared and investigated. XRD patterns of samples indicate that phosphors CaAl2O4:Eu2 , Dy3 and SrAl2O4:Eu2 , Dy3 are with monoclinic crystal structure and phosphor BaAl2O4:Eu2 , Dy3 is with hexagonal crystal structure. The wide range of excitation spectrum of phosphors MAl2O4:Eu2 , Dy3 (M=Ca,Sr,Ba) indicates that the luminescent materials can be excited by light from ultraviolet ray to visible light and the maximum emission wavelength of phosphors MAl2O4:Eu2 , Dy3 (M=Ca, Sr, Ba) is found mainly at λem of 440 nm (M=Ca), 520 nm (M=Sr) and 496 nm (M=Ba) respectively, the corresponding colors of emission light are blue, green and cyna-green respectively. The afterglow decay tendency of phosphors can be summarized as three processes: initial rapid decay, intermediate transitional decay and very long slow decay. Afterglow decay curves coincide with formula I=At-n, and the sequence of afterglow intensity and time is Sr＞Ca＞Ba.     

Photoluminescence properties of M2ZnSi2O7:Eu2+（M=Sr,Ba）

The hardystonite phosphors of Eu2+ activated M2ZnSi2O7(M=Sr,Ba) were synthesized by combustion-assisted method.They were systematically characterized by photoluminescence excitation and emission spectra.The emission spectra of these two phosphors showed that the main emission peaks are at 475 and 503 nm due to 4f65d1→4f7 transition of Eu2+.Both phosphors could be efficiently excited in the wavelength range of 250-425 nm where the near ultraviolet light-emitting diode was well matched.The(x,y) color coordinates were determined with the emission values(x,y)=(0.41,0.21) and(0.16,0.45) for the M2ZnSi2O7:Eu2+(M=Sr,Ba) phosphors.     

Ba1-xSrxMgSiO4:Eu2+,Mn2+: A novel tunable single-matrix tricolor phosphor for W-LED

The Ba1-xSrxMgSiO4:Eu2+,Mn2+ phosphors were prepared by solid-state reaction. Their photoluminescence properties were inves-tigated with fluorescence spectrum and CIE chromaticity. The emission color of Eu2+ in Ba0.98-xSrxMgSiO4:0.02Eu2+ could be tuned from green to blue by adjusting the content of Sr2+. The blue emission of Eu2+ overlapped well with the excitation spectra of Mn2+, leading to an ef-ficient energy transfer from Eu2+ to Mn2+ in Ba0.98-xSrxMg1-ySiO4:0.02Eu2+,yMn2+. Ba0.93Sr0.03Mg1-ySiO4:0.02Eu2+,yMn2+ could emit three ef-ficient broad bands at 440, 530 and 640 nm. The emission color of Ba0.93Sr0.03Mg1-ySiO4:0.02Eu2+,yMn2+ could be tuned from greenish blue to yellowish white by increasing the content of Mn2+ from 0 to 0.1. By changing the content of Sr2+/Mn2+, white-light with different hues could be conveniently obtained in the Ba1-xSrxMgSiO4:Eu2+,Mn2+ phosphors. The results showed that Ba1-xSrxMgSiO4:Eu2+,Mn2+ is a promising single-phased tricolor phosphor in the fabrication of W-LED.     

Preparation and luminescence properties of the red-emitting phosphor（Sr1-xCax）2Si5N8：Eu^2＋ with different Sr/Ca ratios

A series of Eu2+-doped ternary nitride phosphors, with a formula of (Sr1-xCax)2Si5N8: Eu2+, were synthesized by high-temperature solid-state method. The structure and luminescence properties were characterized, indicating the potential application as a red phosphor in the phosphor-converted white light-emitting diodes. The X-ray diffraction patterns showed that the Sr2Si5N8 and Ca2Si5N8 phases were generated at each end of (Sr1-xCax)2Si5N8: Eu2+ and coexisted in the range of 0.5≤x≤0.75. The emission spectra showed broad emission bands originating from the 4f65d1→4f7 transition of Eu2+ ions. The emission peak changed with the variations in Ca2+ concentration.     

Enhancement of photoluminescence of Ba2SiO4：Eu^2＋ by co-doping of La^3＋ or Y^3＋

Green light-emitting Ba2SiO4:Eu2+ phosphors co-doped with La or Y were synthesized by conventional solid-state reaction technique in reductive atmosphere (a mixture of 5% H2 and 95% N2). The results showed that the co-doping of La and Y could greatly enhance the fluorescence intensity of Ba2SiO4:Eu2+ phosphors. The optimum doping concentration expressed by the x value in (Ba0.985-1.5xREx)2SiO4: 0.03Eu2+ (RE=La or Y) was determined to be of 0.05. The excitation and emission peaks of all as-synthesized phosphors were wide bands. The excitation bands ranged from 250 to 400 nm, which matched well with the wavelength of near ultraviolet white light-emitting diodes (LED) chip and could be used as a potential candidate for the fabrication of white LED. The emission bands from 450 to 550 nm were typical 5d-4f transition emission of Eu2+ and displayed un-symmetry profiles because of the two substitution sites of Ba2+ with Eu2+.     

Photoluminescent properties of Sr2SiO4:Eu3+ and Sr2SiO4:Eu2+ phosphors prepared by solid-state reaction method

Eu2+ and (or) Eu3+ doped Sr2SiO4 phosphors particles were synthesized by a conventional solid-state reaction technique, and their structural and optical properties were investigated. The X-ray diffraction (XRD) results showed that the obtained phosphors were composed of orthorhombic α'-Sr2SiO4 and monoclinic β-Sr2SiO4 phase. When excited under 256 nm, Sr2SiO4:Eu3+ phosphors showed intense emission in the red region. Sr2SiO4:Eu3+ phosphors exhibited white emissions (x=0.30, y=0.40, TC=6500 K) ranging from 425 to 650 nm when it was excited by near-ultraviolet (near-UV) light, indicating that Sr2SiO4:Eu2+ was a good light-conversion phosphor candidate for near-UV chip.     

Luminescent properties of red phosphors K2Ba（MoO4）2：Eu3＋ for white light emitting diodes

K2Ba(MoO4)2:Eu3+ phosphors were synthesized by solid-state reaction. The emission and excitation spectra of K2 Ba(MoO4)2:Eu3+ phosphors exhibited that the phosphors could be effectively excited by near ultraviolet (394 nm) and blue (465 nm) light, and emitted red light at 616 nm. The influence of Eu3+concentration, sintering temperature and charge compensators (K+, Na+ or Li+ ) on the emission intensity were investigated. The results indicated that concentration quenching of Eu3+ was not observed within 30mol.% Eu 3+, 600 oC was a suitable sintering temperature for preparation of K2 Ba(MoO4)2:Eu3+phosphors, and K+ ions gave the best improvement to enhance the emission intensity. The CIE chromaticity coordinates of K2 Ba(MoO4)2:0.05Eu3+phosphor were calculated to be (0.68, 0.32), and color purity was 97.4%.     

Study on Red Long-Time Luminescent Material Y2O2S:Eu,M (M = Mg,Ca, Sr,Ba)

The red long-time luminescent material Y₂O₂S:Eu³⁺, M (M = Mg, Ca, Sr, Ba) was prepared by high temperature solid-state method. The XRD result of the sample showed that the crystal phase was Y₂O₂S, which belong to hexagonal system, and no new crystal phase were by doping different amount of Mg, Ca, Sr, Ba. The excitation spectrum was a broad band within 200 × 400 nm region, the characteristic peaks of emission spectrum were located at 583, 595, 597, 617, 627, 707 nm. There was no marked change in excitation spectra, emission spectra and maximum of their wavelengths of the luminescent materials by doping with different ions. The luminescent intensity of the phosphors were stronger when the concentration of doping ions was Mg/Y = 6%, Ca/Y = 4%, Sr/Y = 8%, Ba/Y = 2.5%, respectively. Its sequence of luminescent intensity from high to low is Sr > Ba > Mg > Ca.     

Mg~（2＋）,Ca~（2＋）,Ba~（2＋）离子部分取代对SrAl_2O_4：Eu~（2＋）,Dy~（3＋）晶体结构和发光性能的影响

采用高温固相反应法制备了Sr0.9M0.1Al2O4：Eu2＋,Dy3＋（M=Mg,Ca,Ba）长余辉发光材料,并对其晶体结构、光谱性质、余辉特性进行了分析.X射线衍射测试结果表明,Mg2＋,Ca2＋,Ba2＋离子部分取代SrAl2O4基质中的Sr后,基质晶体结构并没有发生改变.光谱测试结果表明,Mg2＋,Ca2＋,Ba2＋取代后发光材料的激发光谱都是一个从250~450 nm范围内的宽激发带,在266nm,320nm,360nm,416 nm处各有一个激发峰.发射光谱中Mg2＋和Ba2＋的取代使波长出现蓝移,而Ca2＋的取代使波长出现红移.余辉测试结果表明,Ca2＋取代后的余辉时间长于Mg2＋和Ba2＋的取代.