The Crystal Structure of Pb8FeIIFeF24: an ordered Fluorite-like Compound

Pb₈Fe^IIFeF₂₄ is triclinic: a = 20.118(3) Å, b = 5.597(1) Å, c = 9.440(2) Å, α = 89.75(2)°, β = 105.79(2)°, α = 89.38(2)°, Z = 2. The structure is solved in the unconventional space group C1 , from X-ray single crystal data using 1 641 independent reflections (R = 0.048, R_w = 0.051). It is built up from the stacking of two subnetworks along the a axis: fluorite-like [Pb₈F₁₀]_n⁶ⁿ⁺ layers and infinite dimetallic [Fe^IIFeF₁₄]_n^6n? double-chains of corner-sharing octahedra running along the b axis.     

The neodymium isotopic characteristic and geological significance of Kuokesu plagioclase amphibolites from the Kuruktag, Xinjiang, China

The plagioclase amphibolites from Kuokesu area, Kuruktag, Xinjiang occur as enclaves embedded in the granodioritic gneiss. In the light of major elements and REE data, the parent rocks of the plagioclase amphibolites belong to weak_alkaline basalts. Their Nd model ages mainly range from 2 832 to 3 075 Ma. The seven plagioclase amphibolites yield a reasonable good isochron age of (828±86) Ma(2σ) with I Nd =0.510 981±82, ε Nd ( t )=-11.5±1.6. Such a case shows the existence of great proportion of the Archaean mafic crustal basement on the Kuokesu area. The strong tectonic_thermal event at about 820 Ma made the Sm_Nd isotope of the metamorphic rocks homogenization. This event would be associated with the Tarim Movement.     

石英的粒度对其前剂量热释光效应的影响

本文介绍了用石英粉末进行前剂量热释光效应的测量方法,并就不同粒度的石英样品对其１１０℃峰的ＴＬ响应的影响进行了专门研究。     

Rapid dissolution procedure for base-metals-bearing complex materials for quality control assessment

A less labour-intensive method, involving a mixture of 1.0 g MnO₂ + 20 mL HCl (11), is proposed for decomposing seven ores and six metallurgical products for accurate and precise estimation of copper, lead, zinc, cobalt and nickel for quality control assessment. Twentyone international reference materials were also analysed. Results of regression analyses are presented and intermethod comparison studies reveal that the probability of results being different compared with a reference method was less than 1%. Sample decomposition is straightforward and the method has been found to be very simple, rapid and easily adaptable, as it involves no separation of the analyte from the matrix elements.     

阳极溶出伏安法测定塑料制品中的铜和铅

铅等重金属的化合物常用作塑料的稳定剂。由于铅等重金属对人体有害,因此研究塑料制品中铅、铜含量对人体健康的影响是环境卫生学急待解决的问题。本文介绍的方法中,0.5M HCl既作为干法灰化塑料残渣的溶解液,同时又是测定铜、     

流动注射在线共沉淀HG-AFS测定痕量铅

建立了流动注射在线共沉淀HG-AFS测定痕量铅的分析方法。方法基于铅在碱性介质中与氢氧化镁共沉淀，沉淀收集在锥形沉淀腔中，用HCl溶洗沉淀和NaBH4反应，产生的氢化物被载气引入原子化器中进行测定。测定铅的RSD为3％(5ng/mL，n=10)，检出限为0．01ng。检出限较直接进样降低了11倍。对国家标准物质中铅的测定结果与标准值相符。     

铅影响儿童健康

对１９９３年６月至１９９６年６月因体弱多病，生长发育矮小等来诊的３５１例儿童作了血铅测查和临床全征分析，以期引起儿科临床医师重视。     

Simplified method for the Re-Os dating of molybdenite using acid digestion and isotope dilution ICP-MS

An analytical method was developed for Os-Re dating of molybdenite. The method is based on determination of Os and Re concentrations in molybdenite by isotope dilution inductively-coupled plasma mass spectrometry (ID-ICP-MS). Sample digestion and sample/spike equilibration were achieved by a two-stage autoclave-based procedure using a mixture of nitric and sulphuric acids. Os was separated from the sample digest by modified single-stage distillation of osmium tetraoxide (OsO₄) using elevated temperature and on-line addition of hydrogen peroxide. OsO₄(g) was trapped in a mixture of 0.05% thiourea in 0.05 M sodium hydroxide. An anion-exchange column was used to separate Re from excess Mo in the solution remaining after distillation. Os and Re isotope ratio measurements were performed by single-collector, double focusing inductively-coupled plasma mass spectrometry (ICP-MS) with on-line mass-bias correction. Typical instrumental precision was in the range 0.02-0.2% relative standard deviation (R.S.D.) depending on the analyte concentrations. Notorious Os memory effects in the ICP-MS introduction system were eliminated using 5% ammonia solution, both as matrix for final dilution of the trap mixture as well as for washing between the samples. The reproducibility of the entire analytical procedure was accessed by replicate dating of two molybdenite standards and three molybdenite separates, and was found to be in the range 0.87-1.52% R.S.D. Though accuracy of the method is limited by difficulties in evaluating exact concentration of Os in spike solution, ages obtained in the course of these work agrees well with previously published data.     

铅中毒——消化系统的表现

分析了铅中毒引起的消化系统改变及临床特点。     

Evaluation of dithiocarbamates and beta-diketones as chelating agents in supercritical fluid extraction of Cd, Pb, and Hg from solid samples

The use of four dithiocarbamates and three fluorinated β-diketones as potential chelating agents for three transition metal ions (Cd²⁺, Pb²⁺, and Hg²⁺) extracted from spiked sand and filter paper samples by supercritical fluid extraction (SFE) was investigated. The extractions were performed at 45°C and 250 atm for spiked sand samples and at 60°C and 200 atm for filter paper samples using supercritical carbon dioxide modified with 5% methanol. At 250 atm and using carbon dioxide modified with 5% methanol, the recoveries of Cd²⁺, Pb²⁺, and Hg²⁺ ions from spiked sand samples were 95% with lithium bis(trifluoroethyl)dithiocarbamate (LiFDDC) as the chelating agent; they ranged from 83–97% with diethylammonium diethyldithiocarbamate and from 87–97% with sodium di-ethyldithiocarbamate as chelating agents, and from 68–96% with trifluoracetylacetone, hexafluoroacetylacetone, and thenoylfluoroacetone as chelating agents. Ammonium pyrrolidinedithiocarbamate was not effective in the chelation SFE of Cd²⁺, Pb²⁺, and Hg²⁺ ions from either spiked sand or spiked filter paper samples under the extraction conditions used. Supercritical carbon dioxide alone gave consistently lower analyte recoveries than supercritical carbon dioxide modified with 5% methanol. The results suggest that the solubility of the metal chelate in the supercritical fluid plays a more important role than the solubility of the chelating agent in the supercritical fluid, as long as sufficient chelating agent is present in the fluid phase. Fluorination of the chelating agent, as in the case of LiFDDC, increases the solubility of the metal chelate, and subsequently enhances the extraction efficiency for the metal ions.