海洋大气气溶胶的离子色谱分析

对分析方法如采样滤膜的均匀性，滤膜上阴，阳离子的萑萃取率，方法的精密度和检出限等进行了基础性研究，并采用该方法测定了厦门海域大气中的Ｃｌ＾－，Ｆ＾－，ＳＯ＾２－４，ＮＯ＾－３，ＮＨ＾＋４和Ｎａ＾＋。本文法有较高的灵敏度，重现性好，可同时测定多种无机离子，适用于海洋大气气溶胶分析。     

海黍子吸附重金属镉离子的研究

采用廉价的多细胞褐藻海黍子对重金属镉离子进行吸附，研究海黍子不同的预处理方法、溶液的pH值、初始Cd^3 浓度、外加盐等因素对Cd^3 的吸附特性的影响。并对吸附机理进行了初步的探讨，发现镉离子与海黍子中的钙离子发生离子交换作用，交换率占总吸附量的38％～50％。适宜的pH范围为3～6，海黍子的最大吸附量高达181mg/g，得出了适宜的吸附等温线方程，并进行了简单的洗脱研究。     

High‐resolution geochemical record of fluid–rock interaction in a mid‐crustal shear zone: a comparative study of major element and oxygen isotope transport in garnet

Garnet grains from an intensely metasomatized mid‐crustal shear zone in the Reynolds Range, central Australia, exhibit a diverse assortment of textural and compositional characteristics that provide important insights into the geochemical effects of fluid–rock interaction. Electron microprobe X‐ray maps and major element profiles, in situ secondary ion mass spectrometry oxygen isotope analyses, and U–Pb and Sm–Nd geochronology are used to reconstruct their thermal, temporal and fluid evolution. These techniques reveal a detailed sequence of garnet growth, re‐equilibration and dissolution during intracontinental reworking associated with the Ordovician–Carboniferous (450–300 Ma) Alice Springs Orogeny. A euhedral garnet porphyroblast displays bell‐shaped major element profiles diagnostic of prograde growth zoning during shear zone burial. Coexisting granulitic garnet porphyroclasts inherited from precursor wall rocks show extensive cation re‐equilibration assisted by fracturing and fragmentation. Oxygen isotope variations in the former are inversely correlated with the molar proportion of grossular, suggesting that isotopic fractionation is linked to Ca substitution. The latter generally show close correspondence to the isotopic composition of their precursor, indicating slow intergranular diffusion of O relative to Fe²⁺, Mg and Mn. Peak metamorphism associated with shearing (～550 °C; 5.0–6.5 kbar) occurred at c. 360 Ma, followed by rapid exhumation and cooling. Progressive Mn enrichment in rim domains indicates that the retrograde evolution caused partial garnet dissolution. Accompanying intra‐mineral porosity production then stimulated limited oxygen isotope exchange between relict granulitic garnet grains and adjacent metasomatic biotite, resulting in increased garnet δ¹⁸O values over length scales <200 μm. Spatially restricted oxygen interdiffusion was thus facilitated by increased fluid access to reaction interfaces. The concentration of Ca in channelled fracture networks suggests that its mobility was enhanced by a similar mechanism. In contrast, the intergranular diffusion of Fe²⁺, Mg and Mn was rock‐wide under the same P–T regime, as demonstrated by a lack of local spatial variations in the re‐equilibration of these components. The extraction of detailed reaction histories from garnet must therefore take into account the variable length‐ and time‐scales of elemental and isotopic exchange, particularly where the involvement of a fluid phase enhances the possibility of measureable resetting profiles being generated for slowly diffusing components such as Ca and O, even at low ambient temperatures and relatively fast cooling rates.     

重金属离子废水的处理技术进展

重金属离子废水的排放是造成水污染的主要来源,对经济社会已经造成了很大的危害。综述了重金属离子废水处理的研究现状,对目前重金属离子废水常用的处理方法包括沉淀法、生物法、吸附法、絮凝法、离子交换法等技术进行了介绍和评述,同时展望了重金属离子废水处理的未来发展趋势。     

薄层色谱-光密度法分离分析原油族组成

以微型柱色谱为基础,分离原油样的族组成。用薄层色谱扫描仪测定各组分的光密度,建立与柱色谱之间映射关系,计算出各组分的含量和原油的族组成。通过比较发现,薄层色谱测定结果与微型柱色谱吻合较好,且具有分离效果好、灵敏度高、操作简便、快速等优点。对于含蜡量较高的样品,薄层色谱一光密度法测定的原油族组成更精确。     

离子色谱法同时测定铀矿浸出液中的阳离子

对铬铁矿中亚铁的测定方法进行了探讨。首先对已有方法进行了验证和筛选,然后对Li2SO4助熔剂的助溶作用及其反应机理进行了研究,从而推荐了H2SO4-H3PO4-V2O5-V(Ⅳ)-Li2SO4和H2SO4-H3PO4-Ce(SO4)2-Li2SO4两种改进型的溶剂体系用于铬铁矿试样中亚铁的测定,所得结果具有良好的重现性。     

咸淡水过渡带的多组分离子交换行为研究

以大沽河下游海水入侵砂质含水层为研究对象,采集地下淡水、海水和含水介质样品,并测定其组成和性质。通过渗流装置模拟咸淡水驱替过程,测定驱替过程中含水介质的渗透性参数和主要离子的变化规律,并尝试用数值模拟方法定量研究水敏感性影响下的多组分离子交换过程。研究结果表明,海水驱替淡水情况下,Na+能将砂土吸附的Ca2+、Mg2+、K+交换出来,Na+-Ca2+、Na+-K+交换速度很快,而Na+-Mg2+交换反应持续时间较长;在淡水驱替海水的过程中,溶液中的Ca2+、Mg2+将介质吸附的Na+、K+交换出来,但Ca2+-Na+交换起主导作用。含水介质的动力学参数和突破曲线的拐点变化均进一步验证了咸淡过渡带的水敏感性现象,多组分离子的交换行为导致了水敏感现象的发生。     

离子晶体晶形与介质环境关系讨论

为了探讨离子晶体晶形与介质环境的关系,文章引入两个重要概念——离子生长机制与分子生长机制,并以黄铁矿和萤石为例,探讨了在不同介质条件下,两种生长机制对晶体形态的影响。     

GGR Biennial Review: Key Advances in Secondary Ion Mass Spectrometry in the Geological Sciences during the Period 2008–2009

Secondary ion mass spectrometry (SIMS or ion microprobe) remains one of the most powerful techniques in the analytical geochemist’s toolkit. The key strength of SIMS is its capacity to provide trace element and isotope data at sampling sizes which are not approached by other methods. As compared with the main competing technique of laser ablation-ICP-MS, SIMS commonly provides a total sampling mass some 10 to 500 times smaller; this feature can be the deciding factor as to whether an analytical objective is technically achievable. Additional strengths of SIMS lie in the areas of depth profiling and trace element imaging. Though perhaps not as commonly used in the geosciences, these two operational modes represent unique capabilities of SIMS.     

Determination of Fluorine and Chlorine by Pyrohydrolysis and Ion Chromatography: Comparison with Alkaline Fusion Digestion and Ion Chromatography

A method to determine F and Cl in silicate materials by employing pyrohydrolysis and ion chromatography (IC) is described. Pyrohydrolysis involved mixing a pulverised sample (∼ 40 mg) with V₂O₅ (∼ 160 mg) and heating to 1100 °C under a wet oxygen flow in a quartz tube. Recovery yields of F and Cl were ∼ 97% using a NaF + NaCl standard solution. Detection limits of the pyrohydrolysis-IC method for silicate samples were 0.36 and 0.69 μg g^-1 for F and Cl, respectively. Fluorine and Cl concentrations were determined in the reference materials JB-2, JB-3 and JA-1 from the GSJ; BCR-2, BHVO-1, BHVO-2, AGV-1 and AGV-2 from the USGS; and NIST SRM 610, 612 and 614 glasses. Precisions (RSD) for determinations of F were 1–13% (except NIST SRM 614) and 2–19% for Cl, and were dependent on the concentration and blank correction. Most results obtained in this study were in good agreement with those of previous studies. In comparison, the Na₂CO₃ + ZnO fusion method at 900 °C showed that the yields of F and Cl by alkaline fusion systematically decreased with fusion duration time. The yields were 84% and 83% for JB-3, inferring that F and Cl were lost in this alkaline fusion.