Inductively coupled plasma atomic emission spectrometry — Optimization of the operating conditions in the determination of trace of elements in line-rich emission matrices

Radial viewing 40.68 MHz inductively coupled plasma atomic emission spectrometer was used in the determination of Y, Sc and rare earth elements in Eu₂O₃ or Lu₂O₃ as pure rare earth matrices. The Mg II 280.270 nm/Mg I 285.213 nm line intensity ratio was measured to evaluate the robustness of the operating conditions. The operating conditions were affected by varying the incident power and sheathing gas flow rate. The carrier gas flow rate remained a constant value. The relationship between the Mg II 280.270 nm/Mg I 285.213 nm ratio and the excitation temperature was obtained. A dependence of the magnesium ratio in the pure solvent and the corresponding values in the presence of the above matrices was established.     

Trace analysis of volatile polar organics by direct aqueous injection gas chromatography

Summary Procedures for the quantitative analysis of industrial effluents which involve concentration by solvent extraction or the purge-and-trap method are time-consuming, labor-intensive, and prone to error. Direct aqueous injection gas chromatography using an electron-capture detector for the analysis of volatile halocarbons at the ppb level is in routine use in many laboratories. We now discuss the development of a similar protocol for the analysis of volatile polar organics such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and tretrahydrofuran using a flame-ionization detector.     

On the trace problem for Lizorkin–Triebel spaces with mixed norms

The subject is traces of Sobolev spaces with mixed Lebesgue norms on Euclidean space. Specifically, restrictions to the hyperplanes given by x₁ = 0 and x_n = 0 are applied to functions belonging to quasi‐homogeneous, mixed norm Lizorkin–Triebel spaces ; Sobolev spaces are obtained from these as special cases. Spaces admitting traces in the distribution sense are characterised up to the borderline cases; these are also covered in case x₁ = 0. For x₁ the trace spaces are proved to be mixed‐norm Lizorkin–Triebel spaces with a specific sum exponent; for x_n they are similarly defined Besov spaces. The treatment includes continuous right‐inverses and higher order traces. The results rely on a sequence version of Nikol'skij's inequality, Marschall's inequality for pseudodifferential operators (and Fourier multiplier assertions), as well as dyadic ball criteria. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

离子交换树脂相分光光度法测定水中痕量铋

利用离子交换树脂相通过光度法测定痕量铋。铋离子在碱性介质中与邻苯二酚紫形成紫色络合物将其富集在苯乙烯阴离子交换树脂上,通过制作成薄层直接光度法测定。本法操作简便,装皿容易,选择性好,精密度高(测定5μgBi3 5次,RSD=3.8%),铋浓度在0~10μg(50ml)时与吸光度呈线性关系,线性回归方程为A=0.010 0.075C(μg/50ml),相关系数r=0.9997,铋的回收率为98%~99%,检出限为3.2μg/L,用于水中痕量铋的测定,结果满意。     

关于四元数体上自共轭矩阵的行列式和迹的几个定理

本文采用分析和代数的方法得到了四元数体上自共轭矩阵的行列式和迹的几个定理，推广和改进了文［３］，文［５］相类定理的结果。     

On a capacity for modular spaces

The purpose of this article is to define a capacity on certain topological measure spaces X with respect to certain function spaces V consisting of measurable functions. In this general theory we will not fix the space V but we emphasize that V can be the classical Sobolev space W1,p(Ω), the classical Orlicz-Sobolev space W1,Φ(Ω), the Haj?asz-Sobolev space M1,p(Ω), the Musielak-Orlicz-Sobolev space (or generalized Orlicz-Sobolev space) and many other spaces. Of particular interest is the space given as the closure of in W1,p(Ω). In this case every function u∈V (a priori defined only on Ω) has a trace on the boundary ∂Ω which is unique up to a Capp,Ω-polar set.     

A validated method for the determination of traces of UV filters in fish using LC–MS/MS

An analytical method for the determination of UV filter substances in fish tissue has been developed and validated using benzophenone-3, 3-(4-methylbenzylidene)-camphor, 2-ethylhexyl-2-cyano-3,3-diphenyl-2-propenoate and 2-ethylhexyl 3-(methoxyphenyl)-2-propenoate as target analytes. The fish fillets were homogenised and extracted by Soxhlet extraction. The extracts were run through a clean-up process including gel permeation chromatography followed by solid-phase extraction. Quantification of the compounds was performed using liquid chromatography with tandem mass spectrometric detection. Blank fish as well as spiked blank fish were analysed to validate the analytical method. The analytical method developed has the multiple advantages of enabling separation, simultaneous identification and quantification of each of the four selected compounds in a single run. Contamination of blank samples and abnormally high concentrations in spiked samples were avoided by taking extensive precautions during the fish preparation procedure. The method was validated in accordance with internationally accepted criteria, such as specificity, accuracy and repeatability. The combination of LC with tandem mass spectrometry ensures a high level of specificity. The accuracy of the method was reported as the mean recovery rate for the analytes in the sample matrix. Mean recoveries were in the range 86–108%. The precision is expressed as the relative standard deviation, and in all but one of the cases was 20% or below. The accuracy of the method allows residue analyses to be performed on biological matrices at ng/g levels. The determined limit of quantification for each analyte was 8 ng/g fish. For all spiking levels ≥8 ng/g, relative standard deviations were ≤ 20%.     

尿液中痕量铬的化学发光分析法

报道了化学发光分析法测定尿液中痕量铬,研究了适宜鲁米诺－过氧化氢－Ｃｒ（Ⅲ）体系进行化学发光分析测定的条件,讨论了酸度、还原剂用量、测定时间、干扰离子等因素对测定结果的影响。方法操作简便,灵敏度高,具有较好选择性和准确度,便于普普推广。加标回收率在９６．７％￣１０３％之间,结果满意,为尿液中痕量铬的测定提供一个快速、准确的分析方法。     

高效液相色谱-光度法测定金属离子的进展

评述了近年以来柱前衍生高效液相色谱一光度法分析痕量金属离子的进展,并简要介绍了一些新方法（引述文献61篇）。