Associations and mobility of uranium in soils near a depleted uranium （DU） weapons testing site, SW Scotland     

Margaret C. Graham John G. Farmer Ian W. Oliver Angus B. MacKenzie Robert M. Ellam 《中国地球化学学报》2006,25(B08):112-112

Natural uranium has three isotopes, ^238U, ^235U and ^234U, with natural abundances of 99.27 atom %, 0.72% and 0.0055%, respectively. Only ^235U is fissile and the production of nuclear fuel and nuclear weapons involves enrichment of uranium in ^235U. This process also results in separation of ^234U from ^238U, leaving depleted uranium （DU）, with typical ^234U/^238U and ^235U/^238U activity ratios of about 0.19 and 0.013, respectively, as a waste product. The high density, high melting and boiling points and chemical stability of uranium and the availability of DU in relatively pure form mean that DU has many uses, including armour-piercing munitions. Such munitions have been developed in the UK since the 1960s and testing has been carried out by the Ministry of Defence （MoD） at firing ranges such as Dundrennan, SW Scotland and Eskmeals, NW England. The firing of DU munitions can result in the dispersion of DU and its combustion products （oxides） as aerosols or as larger fragments, with the potential for human exposure either directly at the site of detonation or via post-depositional migration in the environment. The aim of this work was to investigate the potential environmental mobility of DU by characterizing the associations of U in soil porewaters with increasing distance from a firing site. To this end, several soil cores located down-wind of the firing site at Dundrennan, near Kirkcudbright, SW Scotland, were collected in May 2006. These were sectioned on-site into 1- or 2-cm depth intervals and porewaters were isolated by centfifugation （10 minutes; 8873 g） on return to the laboratory. Following filtration through 0.2-micron cellulose nitrate filters, the porewaters were analyzed by ICP-QMS （U concentration） and ICP-OES （Fe, Al, Ca, Mg, Mn concentrations）. Sub-samples were also subjected to centrifugal ultrafiltration （100, 30, and 3 kD） and to gel electrophoretic fractionation （agarose; 0.045 M Tris-borate; 20 mA, 30 minutes）. Results showed that U was present at up to 4 μg/L in the soil porewater and that the associations of U varied with sample location and soil depth.  相似文献   

Effects of low molecular weight organic acids on sorption and desorption behavior of p-chlorophenol by yellow earth     

Daoyong ZHANG Xiangliang PAN Shuimu LIAO Chenglin HUANG Jingmei ZHANG 《中国地球化学学报》2006,25(B08):133-133

Low molecular weight organic acids （LMWOAs） are important components of root exudates. They play an important role in immobilizing and remobilizing contaminants in rhizospheric soil. Effects of four LMWOAs on the sorption and desorption behavior of p-chlorophenol by yellow earth was studied in batch mode. The results showed that the previous application of LMWOAs to enhanced adsorption capacity of p-chlorophenol of the soil in the order of maleic acid〉malic acid〉oxalic acid〉citric acid. However, when LMWOAs were applied to soil where p-chlorophenol had been previously adsorbed, substantial p-chlorophenol was desorbed from soil by oxalic acid, whereas citric acid, malic acid and maleic acid didn＇t desorb as much p-chlorophenol from soil as deionized water.  相似文献   

Origin and three-dimensional fluorescence spectrum of the chromophoric dissolved organic matter in Yangtze estuary, East China     

Fan YANG Qinghui HUANG Jianhua LI Xiaomin ZHU 《中国地球化学学报》2006,25(B08):262-262

Dissolved organic matter （DOM） is an important chemical component in natural water. Chromophoric dissolved organic matter （CDOM）, a fraction of optical properties, plays art important role in the biogeochemical cycle of nutrients in aquatic environment. People realized that DOM cycle is crucial in the global carbon and nitrogen flux, and also is inherently related to nutrients and trace metal elements. Therefore, CDOM was concerned by scientists in global oceanography and limnology fields. Water samples were collected from three sections （North Channel, South Channel and Zhuyuan） of the Yangtze （Changjiang River） estuary in March 2006 Three-dimensional excitation emission matrix （3-DEEM） fluorescence spectra were analyzed for those filtrates through Whatman GF/F filters. Dissolved organic carbon （DOC） was also measured by TOC analyzer. The tidal variety was also taken into account. The 3-D EEM fluorescence scans suggested the fluorescence characteristics of humic acid （Ex=332-344 nm, Em=439-451 nm） and fulvic acid （Ex=250-254 nm, Em=472-478 nm） were obvious, and the fluorescence group of protein-like and tyrosine （Ex=230 nm, Em=283 nm） was also found. They are mainly composed of CDOM in the Yangtze estuary. Further data analysis, especially the fluorescence index （f 450/500）, showed that terrestrial signal was rather strong （1.41-1.65） in the surface water, however, some terrestrial CDOM signals of bottom water showed excursions （1.28-1.39）. On the other hand, anthropogenic sign was impressed in the waters of Zhuyuan, which is one of the main drain outlets of Shanghai Metropolis. DOC concentrations ranged from 2.2 mg/L to 3.4 mg/L in Zhuyuan and South Channel, and from 2.0 mg/L to 2.4 mg/L in North Channel. The tide effect played a role in the composition of the CDOM measured by 3-D fluorescence scan technology.  相似文献   

紫色丘陵区不同土地利用方式下土壤活性有机碳垂直分布特征     

《山地学报》2006,24(B10):21-26

  相似文献   

Dissolved Trace Metal–Organic Complexes in the Lot–Garonne River System Determined Using the C18 Sep-Pak System     

E. Lemaire  G. Blanc  J. Schäfer  A. Coynel  H. Etcheber 《Aquatic Geochemistry》2006,12(1):21-38

An 11-month observation of dissolved and particulate organic matter, chlorophyll a(Chl a), C18 Sep-Pak extractable hydrophobic dissolved organic matter (hDOM) fraction and associated dissolved trace metals (Cd, Cu, V, Co, Ni, Mo, U) was performed in the Lot–Garonne River system. This system includes the Riou Mort, the Lot River and the downstream reaches of the Garonne River and represents the fluvial transport path of trace metals between the major point source of polymetallic pollution, located in the Riou Mort watershed and the Gironde estuary. Spatial and temporal variations of dissolved and particulate organic carbon and Chl areflect the presence of different types of organic matter and their relation with the hDOM fraction. Maximum Chl a/POC ratios (up to 0.03), indicate intense phytoplankton production from March to May. In the Lot River (Temple), DOC and POC concentrations were clearly higher and mean Chl a concentration (2.8 mg g⁻¹) was about three times higher than those of the other sites. High Chl a/POC ratios suggest high phytoplankton activity with maxima in spring and late summer. In the Riou Mort River, very high POC concentrations of up to 40 (mean: 20) occurred, whereas Chl a concentrations were relatively low indicating low phytoplankton activity. High, strongly variable DOC and POC concentrations suggest important natural (Carboniferous soils, forests) or anthropogenic (e.g., former coal mines, waste areas, agriculture, sewage) carbon sources within the small Riou Mort watershed. Despite high DOC concentrations in the Riou Mort River, hDOM metal fractions were generally lower than those at the other sites. The general order of decreasing binding strength between metals and the organic hydrophobic phase (Cu, U > Co, Ni > V, Mo > Cd) at all four sites was in good agreement with the Irving–William series of transition element affinity towards organic ligands. Accordingly, the role of the hydrophobic phase in dissolved Cd transport appeared to be negligible, whereas the hDOM–Cu fraction strongly contributed to dissolved Cu transport.  相似文献   

中国中新生代咸化湖盆烃源岩沉积的问题及相关进展   总被引：8，自引：0，他引：8  

金强  朱光有 《高校地质学报》2006,12(4):483-492

我国东部断陷湖盆和西部坳陷湖盆第三系均有蒸发岩与烃源岩共生现象。前者水体深、咸化范围小，在氯化盐和碳酸盐沉积环境中形成了优质烃源岩，后者水体浅、咸化范围大，在氯化盐和硫酸盐沉积环境中发育了优质烃源岩，作者认为两种湖盆出现的水体分层是有机质堆积和保存的重要条件。济阳坳陷和柴达木盆地为两类咸化湖盆的典型代表，对它们的研究可以深化蒸发岩-烃源岩共生区油气地质的认识、促进勘探发展。  相似文献   

自生片钠铝石的碳氧同位素特征及其成因意义   总被引：4，自引：0，他引：4  

高玉巧  刘立 《高校地质学报》2006,12(4):522-529

自生片钠铝石的碳氧同位素特征可以为片钠铝石的成因研究提供重要的地球化学依据。以海拉尔盆地乌尔逊凹陷和松辽盆地孤店构造片钠铝石碳氧同位素分析为基础，结合国内外已报道的自生片钠铝石的碳氧同位素数据，对自生片钠铝石的碳氧同位素特征及其成因意义进行了探讨。研究表明，海拉尔盆地乌尔逊凹陷和松辽盆地南部孤店CO2气田砂岩中片钠铝石的δ13C范围分别为–5.3‰～–1.5‰（PDB）、–1.9‰～+0.3‰（PDB），均分布于含无机碳物质δ13C分布区间（－9.0‰～＋2.7‰）内。计算出的海拉尔盆地和松辽盆地与片钠铝石平衡的CO2气碳同位素分布范围分别为－10.7～－7.0‰（PDB）、－8.7～－6.9‰（PDB），表明片钠铝石绝大部分形成于无机CO2背景。实际地质观察中形成片钠铝石的CO2绝大多数为岩浆脱气来源，岩浆成因片钠铝石碳同位素分布范围为－5.5～＋4.5‰（PDB）。海拉尔盆地和松辽盆地的片钠铝石是岩浆成因CO2气运移、聚集的特征矿物。计算出的海拉尔盆地和松辽盆地片钠铝石沉淀时介质水的δ18O值范围为-14.3～-9.4‰（SMOW），表现为轻同位素的特点，表明片钠铝石形成时地层水为大气降水。计算出的海拉尔盆地片钠铝石同位素为52.7～93.6℃，与样品所在深度处的古地温范围（65.4～87.6℃）基本吻合。  相似文献   

吸水剖面综合解释方法及应用     

ZHANG Jian-min ZHAO Yong-zhong XU Jing HUANG Juan The Logging Company  Jilin Petroleum Group Co.  Ltd  Songyuan  Jilin  China 《吉林大学学报(地球科学版)》2006,(Z2)

吉林油田同位素吸水剖面测井采用~(113)In同位素追踪技术,根据同位素追踪过程解释基本可以判断配水层段吸水情况。但是在注水井存在沾污、大孔道以及串槽等影响时,吸水面积确定比较困难。在同位素测井中增加井温、流量参数,通过多参数综合解释,不仅可以对沾污影响进行合理校正,确定准确的小层吸水量,而且能够正确判断各级封隔器、配水器的工作情况,在地层存在大孔道的情况下,确定地层的吸水面积。吸水剖面综合解释方法在吉林油田已普遍应用,见到明显的效果。  相似文献   

旧供水井化学处理方法介绍--以加德满都市旧供水井修复为例   总被引：1，自引：0，他引：1  

章伟民 《水文地质工程地质》2005,32(6):100-101,107

本文以加德满都市旧供水井修复项目为例,针对因滤水管缝隙被化学物质堵塞,导致井出水量逐年减少的旧供水井。通过井下电视摄像系统检查,采用六偏磷酸钠、氨基黄酸等有机酸,结合刷洗、高压喷射等机械方法进行处理,使旧供水井出水量得到明显提高。  相似文献   

马朗凹陷马1井储层长石中有机包裹体研究          下载免费PDF全文

张小青  伊海生  危国亮  张小芹 《沉积与特提斯地质》2005,25(4):83-86

根据对马朗凹陷马1井储层长石中有机包裹体的基本特征、均一温度、荧光及荧光光谱分析，得出有机包裹体均一温度为60～90℃．120～140℃，其对应的荧光颜色分别为黄色和蓝绿色。认为储层的油气运移经历了两期，第一期为烃类的主要运移、聚集期，油气为低成熟油；第二期为少量的烃类聚集，并判断出二叠系条湖组该段储层为油气产层。  相似文献