Measurement of X-ray production cross-sections of Ti,V, Cr,Mn, Fe,Co, Ni and Cu molecules

K shell X-ray production cross-sections in the Ti, V, Cr, Mn, Fe, Co, Ni, and Cu in the molecules were studied at 59.5 keV excitation energy by using a Si(Li) detector ( FWHM = 155 eV at 5.96 keV). The present results are compared with other theoretical values.     

Determination of trace elements in natural water using X‐ray fluorescence spectrometry after preconcentration with powdered silica gel

A simple and cheap method is described for simultaneous determination of V, Cr, Mn, Fe, Co, Ni, Cu and Zn contents in water by means of wavelength‐dispersive X‐ray fluorescence (WDXRF) spectrometry after preconcentration. The method of preconcentration is based on sorbing analytes onto silica gel powder. 1‐(2‐pyridylazo)‐2‐naphthol (PAN) is used as a chelating agent. The effect of some parameters such as pH, temperature, stirring time, amount of ligand, breakthrough volume and the limit of detection has been studied. The detection limits 0.120, 9.75 × 10^?4, 0.075, 0.070, 0.061, 0.089, 0.029 and 0.044 mg l^?1 were achieved for V, Cr, Mn, Fe, Co, Ni, Cu and Zn, respectively. Copyright © 2009 John Wiley & Sons, Ltd.     

Measurement of mass attenuation coefficients in some Cr,Co and Fe compounds around the absorption edge and the validity of the mixture rule

The total mass attenuation coefficients for elements Cr, Co and Fe and compounds CrCl₂, CrCl₃, Cr₂(SO₄)₃K₂SO₄·24H₂O, CoO, CoCl₂, Co(CH₃COO)₂, FePO₄, FeCl₃·6H₂O, Fe(SO₄)₂NH₄·12H₂O were measured at different energies between 4.508 and 14.142 keV using secondary excitation method. Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Rb, Sr were chosen as secondary exciters. 59.5 keV γ-rays emitted from a ²⁴¹Am annular source were used to excite a secondary exciter and K_α(K-L₃, L₂) lines emitted by the secondary exciter were counted by a Si(Li) detector with a resolution of 160 eV at 5.9 keV. It was observed that mixture rule method is not a suitable method for determination of the mass attenuation coefficients of compounds, especially at an energy that is near the absorption edge. The obtained values were compared with theoretical values.      

NMR study of some heusler alloys containing Co and Mn

The⁵⁹Co and⁵⁵Mn NMR were measured at 4.2 K by spin echo technique. The hyperfine fields in Co₂ MnAl and Co₂MnSb were determined, and it was suggested that in the Co₂MnZ compounds the Co hyperfine field depends on Z. The magnitude of the hyperfine field at Mn dilutely dissolved in Co₂TZ by replacing T (T=Ti, V, Cr, Fe) was found to be larger by 30–80 kOe than that in Co₂MnZ with the same Z. The hyperfine field at Co dilutely dissolved in X₂ MnZ (X=Ni, Cu) by replacing X had a value quite near to that in Co₂MnZ.     

Determination of probabilities of vacancy transfer from K to L shell using K X-ray intensity ratios

K to L shell vacancy transfer probabilities (η_KL) for 26 elements in the atomic region 23≤Z≤57 were determined by measuring the I_Kβ/I_Kα intensity ratios. The targets were irradiated with γ-photons at 59.543 keV from ²⁴¹Am annular source. The K X-rays from different targets were detected with a high resolution Si(Li) detector. Theoretical values were calculated using the radiative and radiationless transition rates of these elements. The measured values of η_KL are compared with the theoretical values and data of others. The measurement vacancy transfer probabilities are least-square fitted to third-order polynomials to obtain analytical relations that represent these probabilities as a function of atomic number. The measured values of η_KL for V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se and Br are being reported here for the first time.     

Structural features of triple equilibrium diagrams of the systems based on Ni-Al

We present the results from our search for common regularities between the number of compounds on the diagrams of state in the Ni-Al-Me triple systems (Me = Ti, V, Cr, Mn, Fe, Co, Cu, Zr, Nb, Mo, Ru, Hf, Ta, Re) in dependence on the thermodynamic and dimensional parameters of the third component in compounds based on Ni-Al. We determine the correlation between the number of electrons outside the shell of the inert gas of the third element in the Ni-Al-Me system and the number of compounds in the corresponding triple diagrams.     

K Shell Fluorescence Parameters by Impact of 5.96 keV Photons on Ti and Its Compounds

K shell fluorescence parameters of pure Ti and some of its compounds have been determined experimentally using an Ultra-LEGe detector with resolution 150 eV at 5.9 keV. The samples were excited 5.96 keV photons emitted from a 55Fe radioisotope source with 50 mCi activity. The experimental values of the K shell fluorescence parameters have been compared with the experimental and theoretical values available in the literature for pure Ti.     

Chemical effects on the K<Subscript>β</Subscript>/K<Subscript>α</Subscript> X-ray intensity ratios of Mn,Ni and Cu complexes

Chemical effects on the K_β/K_α X-ray intensity ratios for some Mn, Ni, and Cu complexes of a new schiff-base with salen N₂H₂ type were investigated. The samples were excited by 59.543 keV γ-rays from a ²⁴¹Am annular radioactive source. K X-rays emitted by samples were counted by a Si(Li) detector with resolution 157 eV at 5.9 keV. We observed the chemical effect on the K_β/K_α X-ray intensity ratios for Mn, Ni and Cu complexes. The experimental results showed that the K_β/K_α X-ray intensity ratios for compounds with complexes are generally larger than those with salt form. The experimental values have been compared with the other experimental and the theoretically calculated values of pure elements. The results are in very good agreement with the others.     

Determination of experimental K-shell fluorescence yield for potassium and calcium compounds

K-shell fluorescence yields were experimentally determined for potassium and calcium compounds using a Si(Li) X-ray detector system (FWHM=5.96 keV at 160 eV). The samples were excited by 5.96 keV photons produced by a ⁵⁵Fe radioisotope source. The experimental values are systematically lower than the theoretical values.      

The magnetic hyperfine field at Cu in Fe,Co and Ni and the magnetic moment of the 41 keV, 2+ state of62Cu

The magnetic hyperfine interaction of Cu in Fe, Co and Ni was studied by means of the γ-γ perturbed angular correlation method using⁶²Zn(⁶²Cu) as a probe. With the publishedg-factor (g=+0.661(12)) of the 41 keV, 2⁺ state hyperfine fields ofB _HF=16.95(51) T,B _HF=13.15(41) T andB _HF=4.05(30) T atT=0 K for Cu in Fe, Co and Ni are derived, respectively. The systematic discrepancy of these values with several independent measurements of these hyperfine fields is removed by deriving a new value ofg=0.55(5) for the 41 keV, 2⁺ state of⁶²Cu.     

FAAS法测定不同消化方法栽培桔梗中12种金属元素含量的研究

分别采用湿法、干法和先灰化再用硝酸-高氯酸(φ,4∶1)常压微沸条件下消解桔梗样品,用火焰原子吸收法测定栽培桔梗中的金属元素K,Mg,Ca,Cu,Zn,Mn,Fe,Co,Ni,Cd,Cr和Pb含量。研究了不同消化方法对测定栽培桔梗中的金属元素含量的影响以及测定不同元素的仪器最佳工作条件,并做了方法的准确度和精密度考察。结果表明,不同消化方法对测定Mg和Ca有显著影响,不同消化方法测定的栽培桔梗中K, Mg, Ca, Mn, Fe, Cu, Zn的平均含量分别为13 226.32, 922.57, 1 710.72, 9.23, 336.66, 8.75, 19.62 μg·g-1;Ni,Co,Cd,Cr和Pb未检出。方法的加标回收率为95.45%～105.50%, 相对标准偏差(n=9)为0.34%～5.78%。选择先灰化再用混酸消化测定栽培中药材金属元素含量,方法简单易行,结果令人满意。     

A theoretical study of the structure and stability of borohydride on 3d transition metals

The adsorption of borohydride on 3d transition metals (Cr, Mn, Fe, Co, Ni and Cu) was studied using first principles calculations within spin-polarized density functional theory. Magnetic effect on the stability of borohydride is noted. Molecular adsorption is favorable on Co, Ni and Cu, which is characterized by the strong s–d_zz hybridization of the adsorbate-substrate states. Dissociated adsorption structure yielding one or two H adatom fragments on the surface is observed for Cr, Mn and Fe.     

土壤重金属沿山地森林海拔梯度的分布特征

采用电感耦合等离子体发射光谱法与石墨炉原子吸收光谱法,研究了14种重金属(Fe,Al,Ti,Cu,Cr,Mn,V,Zn,Ni,Co,Pb,Se,Cd,As)沿山地森林海拔梯度的分布特征.结果表明海拔梯度对14种重金属中的6种重金属浓度(Fe,A1,Ti,V,Pb与As)有显著的影响,对其他八种重金属浓度(Cu,Cr,M...     

火焰原子吸收法测定栽培小茴香中13种金属元素含量

采用先灰化、再用硝酸-高氯酸(φ 4∶1)常压微沸条件下消解小茴香样品,应用火焰原子吸收法测定栽培小茴香中的金属元素Na,K,Mg,Ca,Cu,Zn,Mn,Fe,Co,Ni,Cd,Cr和Pb含量,研究了测定不同元素的仪器最佳工作条件,并作了方法的准确性和精密度考察。结果表明,栽培小茴香中Na,K,Mg,Ca,Mn,Fe,Cu,Zn和Pb含量分别为1 508.7,27 653.0,2 036.0,4 848.1,24.8,323.5,15.2,23.7和10.8 μg·g-1;Ni,Co,Cd和Cr未检出。方法的加标回收率为97.45%～102.50%, 相对标准偏差(n=9)为0.34%～2.77%。测定方法简单易行,方便快捷,结果令人满意。     

Energy‐dispersive x‐ray fluorescence analysis of modern coloured glasses from Marinha Grande (Portugal)

The elemental composition (K, Ca, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Ba, Nd and Pb) of modern coloured glasses was obtained by energy‐dispersive x‐ray fluorescence (EDXRF) spectrometry. This non‐destructive technique is frequently used in the analysis of historical glass objects. Two reference glasses were also measured to assess the overall accuracy of the EDXRF method. Reference and unknown glasses were analysed without any preparation. The coloured glass samples studied belong to the Glass Museum of Marinha Grande and were chosen from two distinct collections, which were characterized by the different concentrations of some elements (K, Ti, Cr, Mn, Fe, Ba and Pb). The determined major elements allowed the identification of two raw materials used in glass manufacture, sand and lime. Multivariate statistical analysis, namely principal component extraction, simplified the identification of some of the colouring chemical elements, associating them with the different colours of the glass objects. Copyright © 2003 John Wiley & Sons, Ltd.     

同步辐射X射线荧光微探针技术测定熔融包裹体中的微量元素

采用同步辐射X射线荧光微探针无损分析技术,对吉林龙岗火山群地幔捕掳体中的斜方辉石矿物及其熔融包裹体进行了测试,并用美国玻璃标样(NIST 612)标定出K,Sc,Ti,Cr,Mn,Fe,Co,Ni,Cu,Zn,Ga,Sr,Y等13种元素的含量.其中,斜方辉石中的Cr?,Mn?,Fe?,Ni等元素含量与波长色散电子探针分析结果相对误差分别为15%,5%,7%,8%.包裹体中过渡族元素球粒陨石标准化曲线型式与中子活化全岩分析结果相似,反映原始岩浆在上升过程中经历了部分熔融或分离作用     

Mössbauer and magnetization studies of the NpM2Ge2(M=Cr,Fe, Co,Ni, Cu) intermetallic compounds

Magnetization and ²³⁷Np Mössbauer studies were performed on tetragonal NpM₂Ge₂ intermetallic compounds. All the compounds order antiferromagnetically. The Néel points and the magnetic hyperfine interactions of the NpM₂Ge₂ compounds are 62(3), 28(3), 36(5), 27(3), 34(3) K and 2860(40), 1800(40), 3040(40), 2600(40), 2330(90) Mc/sec for M=Cr, Fe, Co, Ni and Cu respectively.     

高压密封微波消解-ICP-AES法测定五种蒙药中无机元素

采用HNO3-HClO4消解体系分别对额日敦-乌日勒、德都红花七味丸、通拉嘎-5、乌珠目-7、给旺-9等五种蒙药样品进行高压微波消解制样,利用电感耦合等离子体原子发射光谱法(ICP-AES)同时测定了镁、铝、钙、铬、锰、铁、钴、镍、铜、锌、砷、硒、锶、钼、银、镉和铅等17种无机元素的含量。通过添加标准回收实验,回收率均在97.25%~106.35%之间,验证了分析数据的可靠性。所有元素测定结果的相对标准偏差均小于3.3%,具有良好的准确度和精密度。实验结果表明,其中常量元素Ca,Mg和Fe,Mn,Zn,Cu的含量较高,测定结果可为开发研制蒙药新制剂、研制蒙药的质量控制标准和提高蒙药药效提供理论依据。     

偏振能量色散X射线荧光光谱法在土壤环境监测中的应用

以土壤和水系沉积物标准物质为校准样品,采用粉末样品压片制样.建立了偏振能量色散X射线荧光光谱仪测定土壤中As、Ba、Cu、Co、Cd、Cr、Mo、Mn、Ni、Pb、Sr、Ti、V、Zn、Rb、Sc、Bi、Si、Al、Fe、Ca、Mg、Na、K 24种元素的方法.该方法采用Al、CaF2、Fe、Zn、KBr、Al2O3、...