碘酸钡置换碘-四氯化碳萃取光度法测定矿物气液包裹体中微量SO_4~(2-)

本文根据碘酸钡与矿物气液包裹体中ＳＯ２－４交换反应析出的碘酸根与碘化镉反应析出碘,采用碘－四氯化碳萃取光度法间接测定ＳＯ２－４,取得了较为满意的结果。     

The UV-Visible Absorption Cross-Sections and Atmospheric Photolysis Rate of HOI

The UV-visible absorption cross-sections of HOI have been recorded over the wavelength range 278-494 nm and at 298 K following generation of HOI in the gas phase using laser flash photolysis. The gas phase reaction of OH with I₂ was used to produce HOI, and the absorption spectrum of HOI was calibrated relative to the consumption of I₂. The HOI spectrum recorded exhibits 2 broad absorption maxima of = 3.99 × 10^-19 cm² and = 2.85 × 10^-19 cm², centred at 338.4 nm and 404.8 nm respectively. The spectrum is adequately described by a parameterisation consisting of two semi-logarithmic Gaussian distribution functions. The HOI spectrum is more intense than that recorded in previous work of Jenkin, but is in good agreement with more recent work by Bauer et al. The parameterised HOI absorption spectrum recorded in this work was used in a radiative model to calculate the atmospheric photolysis rate (J-value) of HOI. These results indicate that, under most sunlit conditions, HOI has a lifetime with respect to solar photolysis of the order of minutes. Experiments attempting to generate HOI by the reaction of O atoms with C₂H₅I led to complex absorption spectra containing a negative contribution to the absorption from the photolytic removal of an unidentified species. In addition, evidence was found for adsorption and desorption of an iodine-containing species in the reaction vessel. This behaviour is rationalised in terms of the disproportionation of HOI to I₂O, and an uncalibrated spectrum tentatively attributed to I₂O has been recorded.     

Photochemical aspects of tropospheric iodine behaviour

The I-atom sensitised decomposition of ozone in air at 1 atm pressure and ambient temperature has been investigated. Iodine atoms were produced by photolysis of I₂ using visible light or of CH₃I using ultraviolet light. In both cases, the quantum yield for O₃ decomposition was 1.25 (±0.11) per I atom. An important role is proposed for the self-reaction of IO radicals leading to higher oxides of iodine, IO+IO(+M)I₂O₂(+M)higher oxides, which predominated over the bimolecular reaction leading to regeneration of I atoms, IO+IO2I+O₂, with k _2a/k _2b4. Simple computer modelling calculations indicate that reaction (2a) may be important in determining the fate of photolabile iodine species in the atmosphere. The consequences for the behaviour of radioiodine releases are also discussed.     

碘分析方法研究进展

对国内外碘测定的样品前处理方法作了简要回顾,重点介绍了近10年来有关碘的测定方法及碘形态分析的最新研究进展。碘测定方法主要包括容量法、光度法、电化学法、中子活化法、色谱法、原子光谱法以及质谱法等。对测定碘形态的联用技术进行了简要介绍。引用文献113篇。     

积分安培检测-离子色谱法同时测定地下水中的溴离子和碘离子

采用积分安培-离子色谱法同时测定地下水中的溴离子和碘离子,该方法的相关性好（ r＞0．999）,精密度高（RSD％＜4．0）,样品加标回收率为90～110％,溴离子检出限为5．6μg/L ,碘离子检出限为2．1μg/L。本法简便、快速、准确且选择性好,可用于分析地下水中的溴离子和碘离子。     

封闭酸溶-盐酸羟胺还原ICP-MS法测定土壤沉积物岩石中的痕量碘

碘是活跃元素,价态多,各价态间易相互转化,化学性质不稳定,使用ICP-MS测定土壤、沉积物和岩石样品中的痕量碘,样品前处理和测定结果的稳定性是主要问题。本文采用磷酸-高氯酸高压密闭消解处理样品,提高了样品分解效率,也避免了碘的挥发损失,通过加入0.5mL 20g/L盐酸羟胺溶液将碘还原为I~-,提高了碘的稳定性,再于100℃烘箱中保温至少20min,以稀氨水作介质,降低了ICP-MS测定过程中的记忆效应。方法相对标准偏差(RSD)为4.88%～9.19%,相对误差为-6.90%～8.33%,回收率为92.5%～109.6%,检出限(3s)为0.012μg/g。本方法的测定数据与半熔法一致,解决了当前方法存在的分析流程长、空白高、岩石样品提取不完全、提取装置繁多等问题,可以作为土壤、沉积物、岩石中痕量碘测定方法的一种补充,适合批量样品分析。     

热解——动力学法测定岩石和化探样品中痕量碘

以五氧化二钒和三氧化二铋为熔剂,研究了分离富集痕量碘的最佳条性,以及影响催化反应速度的因素。用改变温度和时间的方法提高测定方法的灵敏度和扩大碘的测定范围。本方法具有灵敏度高、选择性好、操作简便、快速和经济的特点,最低检出限为0.033ppm碘,标准偏差为4.45％。     

Anthropogenic 129I in seawaters along the north-central part of the English Channel: Levels and tracer applications

The English Channel (the Channel) represents a major sink and transport pathway of anthropogenic radioactive 129I. Despite this important role, data concerning the distribution of 129I in seawater of the Channel are scarce, and most of existing data are restricted to the eastern part of the Channel. The advection and dispersion of 129I from the French coast toward the central and further the English coast, especially in the Channel west of Cap de La Hague, are not fully investigated. We present results of iodine isotopes (127I and 129I) analyses of surface water samples collected along the central English Channel in October, 2010. The data show high 129I concentrations between Dover Strait and La Hague, followed by a dramatic drop towards the Celtic Sea and reveal the dispersal of 129I towards central and northern part of the Channel. Our observation also implies that the entire British coast is contaminated by 129I. 129I levels in the westernmost English Channel, close to the English coast, may reflect combined influences from La Hague and Sellafield. Evolution of 129I between 2005 and 2010 suggests a strong link to temporal marine discharges from La Hague plant. The discharges from the nuclear reprocessing facility have continued since 2010 and thus an ecological evaluation of 129I radioactive hazards in the environment of the Channel may be needed.     

沉积盆地卤水来源的非传统同位素示踪研究进展

世界上大多数的沉积盆地内,在结晶基底或者沉积地层内都有矿化度较高的卤水,由于这些卤水通常携带或富含有钾、硼、锂、溴、碘、铷、铯、稀有气体及重金属元素,因此,它们是地学界的研究热点之一。随着测试技术的不断进步,非传统同位素的应用也日益广泛,但在沉积盆地卤水来源和演化方面的研究还十分薄弱,对卤水的来源和演化也还存在争议。文章回顾了硼、锂、碘和惰性气体氦、氩同位素在卤水来源研究方面的进展,并指出由于单一同位素在解释上的片面性,多种同位素相结合的示踪方法研究沉积盆地卤水的来源是国际趋势。     

Soil and landscape geochemical factors which contribute to iodine spatial distribution in the main environmental components and food chain in the central Russian plain

The distribution of iodine (Ι) has been studied in the main environmental components (soils and soil microorganisms, ground water and dominating plant species) and in the food chain (drinking water, forage and cow's milk) in the geochemically different areas of the non-chernozem zone of the Russian plain.