Soil column experiments for iodate and iodide using K-edge XANES and HPLC–ICP-MS     

Yoko S. Shimamoto  Takaaki Itai  Yoshio Takahashi 《Journal of Geochemical Exploration》2010

Radioactive iodine is one of the most problematic radionuclides because of its long half life and high mobility. Mobility of iodine depends on the chemical form to a great extent. This paper reports the results of soil column experiments we conducted to evaluate the mobilities of IO₃⁻ and I⁻. In order to determine the mechanisms of adsorption of IO₃⁻ and I⁻ on soil, adsorption isotherms were obtained by batch experiments. Both adsorption isotherms of IO₃⁻ and I⁻ are well explained by Langmuir model. The adsorption maximum of IO₃⁻ is about five times larger than that of I⁻. In the column experiments, iodine distributions between soil and pore water in the soil column were determined at various depths. Chemical forms of iodine in soil and pore water were determined by X-ray absorption near-edge structure (XANES), and high performance liquid chromatography connected to inductively coupled plasma mass spectrometry (HPLC–ICP-MS), respectively. Vertical profiles of iodine in pore water were simulated using Visual MODFLOW. Our results showed, upon I⁻ infiltration through the column, that a small amount of I⁻ adsorbed on soil, and its mobility is mainly controlled by advection and dispersion. The profile of iodine concentration in pore water was well simulated by assuming equilibrium-controlled Langmuir type adsorption without considering any chemical transformations. For the IO₃⁻ addition system into the column, however, IO₃⁻ adsorbed to soil to a larger degree, which causes a much larger retardation effect than I⁻. In addition, reduction of IO₃⁻ to I⁻ was also confirmed in both soil and pore water by XANES and HPLC–ICP-MS, respectively. The fraction of I⁻ increased toward the deeper end in both phases because of its lower affinity for soil than IO₃⁻, where the reduced I⁻ was released to the pore water and transported by the water flow. In this study, such reduction effect was clearly demonstrated by the speciation analyses of iodine in both soil and water phases, which confirmed that the mobility of I⁻ is a dominant factor that controls the fate of iodine in the surface environment.  相似文献   

A snapshot of environmental iodine and selenium in La Pampa and San Juan provinces of Argentina     

M.J. Watts  J. O'Reilly  A. Maricelli  A. Coleman  E.L. Ander  N.I. Ward 《Journal of Geochemical Exploration》2010

Soil and water samples were collected from farmsteads and provincial towns across the provinces of La Pampa and San Juan in Argentina. Inductively coupled plasma mass spectrometry was used for the determination of iodine in water following addition of TMAH to 1% v/v and soils extracted with 5% TMAH. Iodine in agricultural soils was in the range of 1.3–20.9 mg/kg in La Pampa located in central Argentina and 0.1–10.5 mg/kg in San Juan located in the northwest Andean region of Argentina, compared to a worldwide mean of 2.6 mg/kg. Mean selenium concentrations for soils from both provinces were 0.3 mg/kg, compared to a worldwide mean of 0.4 mg/kg. The majority of soils were slightly alkaline at pH 6.7 to 8.8. The organic content of soils in La Pampa was 2.5–5.9% and in San Juan 0.1–2.3%, whilst, mobile water extractable soil-iodine was 1–18% for La Pampa and 2–42% for San Juan. No simple relationship observed for pH and organic content, but mobile iodine (%) was highest when organic content was low, higher for lower total iodine concentrations and generally highest at pH > 7.5. Water drawn for drinking or irrigation of a variety of crops and pasture was found to range from 52 to 395 µg/L iodine and 0.8 to 21.3 µg/L selenium in La Pampa and 16–95 µg/L iodine and 0.6 to 8.2 µg/L selenium in San Juan. The water samples were all slightly alkaline between pH 8 and 10. Water–iodine concentrations were highest at pH 7.8 to 8.8 and in groundwaters positively correlated with conductivity. Raw water entering water treatment works in La Pampa was reduced in iodine content from approximately 50 µg/L in raw water to 1 µg/L in treated drinking water, similar to levels observed in regions experiencing iodine deficiency.  相似文献   

江西铜坑嶂钼矿和红山铜矿含矿斑岩锆石U-Pb定年及其地质意义   总被引：10，自引：2，他引：8  

苏慧敏  谢桂青  孙嘉  张承帅  程彦博 《岩石学报》2010,26(3):819-829

江西铜坑嶂钼矿和红山铜矿是在武夷山成矿带中最近发现的两个斑岩型矿床。本文利用LA-ICP-MS锆石U-Pb定年方法对铜坑嶂花岗斑岩和红山含矿花岗斑岩分别进行了年代学研究,获得铜坑嶂岩体中花岗斑岩的锆石年龄为138±1Ma,代表斑岩体侵位的年龄;红山矿区含矿斑岩的锆石年龄,分作两期,分别为99Ma和49Ma,两期不同的年龄可能代表了两期热事件。研究表明,铜坑嶂钼矿的成岩成矿时代均发生在白垩纪,其岩浆作用与成矿作用基本吻合。综合前人资料,认为铜坑嶂钼矿区的斑岩和红山铜矿区的斑岩可能分别形成于大陆弧后伸展带和岩石圈伸展环境。  相似文献   

共沉淀富集法测定海水中稀土元素含量方法研究          下载免费PDF全文

林梵宇  曾怡杭  尹希杰  梁毓娜 《应用海洋学学报》2020,39(4):581-589

稀土元素已越来越多地应用于示踪各类地球化学体系的物质来源与岩石矿物形成等演化过程。但在进行海水样品的稀土元素检测时，由于样品的高盐特征和稀土元素的痕量特征又使得分析具有相当的挑战性。本研究旨在从高盐的海水基质中有效分离并富集痕量的稀土元素，同时结合电感耦合等离子体质谱（Inductively Coupled Plasma Mass Spectrometry, ICP-MS）技术对海水中的稀土进行定量分析。通过对海水样品稀土元素的定量限分析、加标回收实验和梯度加标回收实验，验证了方法的准确性，评估方法的分离富集效率。通过共沉淀过程中的pH比较、氢氧化钠与氨水作为共沉淀剂的比较，确定了富集过程中共沉淀剂用量、种类等影响因素。通过稀土元素配分曲线的绘制与类似样品结果进行比对，以及标准海水的检测结果，验证了方法在实际样品中的可行性。本研究探索了共沉淀富集法在分离富集海水中稀土元素的实验条件，实现高盐背景下痕量稀土的准确定量，并将其用于近岸海水与孔隙水的实际检测。  相似文献   

ICP-MS测定海水中溶解态痕量重金属——直接稀释法   总被引：7，自引：0，他引：7       下载免费PDF全文

刘莹  翟世奎  张爱滨  王蓓 《海洋学报》2008,30(5):151-158

海水水质监测是环境监测中的重要一环[1]。海水中痕量重金属元素地球化学研究现今仍面临两大挑战:一是痕量重金属元素有机和无机形态分析,二是海水中痕量重金属元素的含量测定[2]。海水的含盐量为35 g/dm3左右,基体中除了大量的NaCl外,还含有相当量的SO₄2-,Ca2+,Mg2+等离子及有机质。由于海水中溶解态重金属元素的含量基本上都在微克每立方分米量级或更低,在传统的分析方法中这部分元素含量的测定或受到严重的光谱干扰、或低于仪器检测限,定量分析相当困难。  相似文献   

无机多元素现代仪器分析技术   总被引：11，自引：0，他引：11  

李冰  周剑雄  詹秀春 《地质学报》2011,85(11):1878-1916

本文重点介绍地质领域目前广泛应用的无机多元素现代仪器分析技术,包括电感耦合等离子体原子发射光谱(ICP-AES)、电感耦合等离子体质谱(ICP-MS)、X射线荧光光谱(XRF)、原子吸收光谱(AAS)、原子荧光光谱(AFS)、电子探针分析技术和共享平台的建立、激光剥蚀等离子体质谱(LA-ICP-MS)微区原位分析技术以...  相似文献   

High resolution LA-ICP-MS mapping of U and Th isotopes in an early Pleistocene equid tooth from Fuente Nueva-3 (Orce, Andalusia, Spain)     

Mathieu Duval  Maxime Aubert  John Hellstrom  Rainer Grün 《Quaternary Geochronology》2011,6(5):458-467

We have produced detailed maps of U and Th isotopes for three cross-sections of an Early Pleistocene equid tooth from the archaeological site of Fuente Nueva-3 (Orce, Andalusia, Spain). This permits us to visualise, for the first time, U migration processes in 3 dimensions. The tooth shows a concentration gradient from the top to the base, indicating the U profile had not equilibrated after >1 Ma. The spatial pattern of ²³⁰Th/²³⁴U and ²³⁴U/²³⁸U indicates complex U-mobilisation processes over the last 100 ka, dominated by small-scale redistribution of U. Leaching from the tooth through the pulp cavity started at least 93 ka ago with several later phases in various domains of the dentine and cement. This leaching event could have been triggered by changes in the local hydrological regime associated with periods of increased erosion in the Guadix-Baza basin. The results illustrate the difficulty of dating faunal material from Early Pleistocene sites. They also demonstrate that dental tissues can neither be considered as homogeneous media for U-diffusion, nor behave as closed systems for U-series isotopes because diagenetic alterations seem to trigger U-migration. The results do not support the notion that U-uptake into dental tissues is necessarily of short duration. Nevertheless, rapid laser ablation scanning can be used to identify suitable samples for dating as well as domains within the teeth that may have preserved original isotopic signatures, i.e. domains that have not been affected by recent U-mobilisation process.  相似文献   

电感耦合等离子体质谱(ICP-MS)测定盐湖水中铀含量          下载免费PDF全文

闵秀云  许建新  李雷明  马海州  范惠萍  吕亚平 《盐湖研究》2012,20(2):18-23

利用电感耦合等离子体质谱(ICP-MS)技术,对比分析了直接稀释法和基体匹配法测定含盐水样中微量铀的精密度、准确度和回收率。结果表明,两种方法的铀标准曲线线性相关系数均大于0.999 9,精密度、准确度和回收率都满足样品测定要求,二者均可用于盐湖水中微量铀的测定。但基体匹配法稳定性高,重现性好,更适合于盐湖水中微量铀的快速、准确测定。  相似文献   

锍镍试金富集—等离子质谱法测定地质样品中的金铂钯铑铱钌   总被引：1，自引：0，他引：1  

施意华  靳晓珠  熊传信  黄俭惠 《矿产与地质》2009,23(1)

建立了锍镍试金富集—电感耦合等离子质谱法测定地质样品中金铂钯铑铱钌的方法。研究了富集时各种实验因素的影响,样品用琉试金富集,盐酸处理锍镍扣,碲共沉淀富集,过滤,沉淀用王水溶解,ICP-M S测定。方法检出限:A u为0.11、P t为0.050、Pd为0.028、R h为0.018、Ir为0.013、R u为0.02,相对标准偏差(n=12),A u为8.25%、P t为4.76%、P t为4.97%、R h为5.63%、Ir为5.38%、R u为6.81%。经国家一级地球化学标准物质验证,铂族元素和金的测定值与标准质相吻合。  相似文献   

Post-Orogenic Granites in Pingwu Region, Northwest Sichuan: Evidence for North China Block and Yangtze Block Collision during Triassic     

Pei Xianzhi  Li Zuochen  Ding Saping  Feng Jianyun  Li Ruibao  Sun Yu  Zhang Yafeng  Liu Zhanqing 《中国地质大学学报(英文版)》2009,20(2)

The Nanyili (南一里), Laohegou (老河沟), and Shaiziyan (筛子岩) granitic intrusions are located in the southern margin of the Bikou (碧口) block in Pingwu (平武) area, Northwest Sichuan (四川). The petrography and geochemical characteristics of the granitic intrusions as well as their source and tectonic settings are reported and discussed in this article. The Laohegou and Shaiziyan granites are with high SiO2 (69.89 wt.%-73.05 wt.%) and Al2O3 contents, and A/CNK=1.04-1.12. They are typi-cal strongly peraluminous granites, with supersaturation in Al and Si. The abundance of ∑REE varies in the range of (33.13-89.12)×106. The rocks show an LREE enrichment pattern and obvious Eu nega-tive anomaly. The trace element geochemistry is characterized evidently by a negative anomaly of Ta, Nb, Ti, etc. and a positive anomaly of Rb, Ba, Sr, etc.. Zircons of the Nanyili granite have higher Th/U ratios, and their CL images have internal oscillatory zoning, suggesting that the zircons of the samples are igneous in origin. The LA ICP-MS zircon U-Pb isotopic concordia diagram yields an age of 223.1±2.6 Ma (MSWD=1.4), which indicates that the granodiorite intrusions formed in the early Late Triassic. The Nanyili, Laohegou, and Shaiziyan granites have the characteristics of post-eollisional granites and are regarded as post-orogenic granites. Thus, the granite intrusions are interpreted as syn-collisional granites that resulted from the crustal thickening caused by the collisions between the North China plate and the Yangtze plate during the Indosinian. The granitic intrusions formed in a transitional environment from syn- (compres-slonal environment) to post-collision (extensionalenvironment).  相似文献