Sorption Characteristics of Rare Earth Element Eu^3＋ onto Silica-Water Interfaces Studied by Fluorescence Spectroscopy     

Yin Xiulan China Institute of Geo-environmental Monitoring  Beijing  China Hu Ping Faculty of Earth Sciences  China University of Geosciences  Wuhan  China  Northeastern Illinois University  Chicago  IL  USA Li Dien Division of Earth  Environmental Sciences  Los Alamos National Laboratory  Los Alamos  NM  USA 《中国地质大学学报(英文版)》2004,15(4):355-360

The sorption of Eu species onto nano-size silica-water interfaces was investigated using fluorescence spectroscopy for Ph ranges of 1-8.5 and an initial Eu concentration (Ceu) of 2×10-4 M. The sorption rate of Eu was initially low, but significantly increased at Ph>4. The sorption density of Eu species on a silica surface was ～1.58×10-7 mol/m2 when the dissolved Eu species were completely sorbed onto silica-water interfaces at Ph=～5.8. The sorbed Eu species at Ph<6 is aquo Eu3 , which is sorbed onto silica-water interfaces as an outer-sphere complex at Ph<5, but may be sorbed as an inner-sphere bidentate complex at 5相似文献   

Ruthenium-ion-catalyzed oxidation of asphaltenes and oil-source correlation of heavy oils from the Lunnan and Tahe oilfields in the Tarim Basin, NW China     

马安来张水昌  张大江金之钧马晓娟  陈清棠 《中国地球化学学报》2005,24(1):28-36

The identification of marine source rocks in the Tarim Basin is debated vigorously. The intention of this paper is to investigate the asphahenes in heavy oils from the Lunnan and Tabe oilfields and Well TD2 with ruthenium-ions-catalyzed oxidation technique (RICO), in order to explore its role in oil-oil and oil-source correlations, The RICO products included n-alkanoic acids, α,ω-di-n-alkanoic acids, branched alkanoic acids, tricyclic terpanoic acids, hopanoic acids, gammacerane carboxylic acid , regular sterane carboxylic acids and 4-methylsterane carboxylic acids. The n-alkyl chains and biomarkers bounded on the asphaltenes were of unsusceptibility to biodegradation. The distribution and absolute concentrations of n-alkanoic acids in the RICO products of heavy oils from the Lunnan and Tabe oilfields are different from those of Well TD2. The biomarkers bounded on the asphahenes, especially steranes, have a distribution trend similar to that of the counterparts in saturates. The sterane carboxylic acids and 4-methylsterane carboxylic acids in the RICO products of heavy oils from the Lunnan and Tahe oilfields, dominated by C30 sterane and C31 4-methylsterane carboxylic acids, respectively, are significantly different from those of the heavy oils of Well TD2, whose dominating sterane and 4-methylsterane carboxylic acids are C28 sterane and C29 4-methylsterane acids, respectively. The RICO products of the asphaltenes further indicate that the Middle-Upper Ordovician may be the main source rocks for heavy oils from the Lunnan and Tabe oilfields.  相似文献   

Water soluble components of PM10 Chongqing, China   总被引：1，自引：0，他引：1  

Luo Qingquan  Xian Xuefu  Chen Gangcai  Yang Qinglin 《中国地球化学学报》2005,24(2):155-157

The concentrations of water soluble ions (Na⁺, NH₄ ⁺, K⁺, Mg²⁺, Ca²⁺, NO₃ ^-, Cl^-, and SO ₄ ^2- ) in PM₁₀ samples collected on cellulose filters by a medium-volume cascade impactor were determined, which were obtained from three kinds of areas in Chongqing: industrial area (Jiulongpo district), commercial and residential area (Jiangbei district) and background area (Jinyun Mountain in the Beibei district). The results showed that except for the background site, the annual average values of PM₁₀ are 23% – 61% higher than the national air quality standard (GradeII) (0.1 mg/m³), even that the value of the control site is still 20% higher than American standard (0.05 mg/m³). This implied that serious pollution of fine particles occurred in Chongqing. Nine kinds of soluble ions in water of PM₁₀ were analyzed by ion chromatography (IC) and the annual average concentrations follow the order of [SO ₄ ^2- ] > [NO³ _-] > [Cl^-] > [F^-], and [Ca²⁺] > [NH₄ ⁺] > [K⁺] > [Na⁺] > [Mg²⁺]. Their values were different in these areas: the industrial area > the commercial and living area > the control area. As for NH_{4 +}, K⁺, Ca²⁺, NO₃ ^- and SO ₄ ^2- , their seasonal average concentrations show a similar variation trend: the values in spring and fall were higher than those in summer and winter. The seasonal average concentrations of [Cl^-], [F^-], [Na⁺] and [Mg²⁺] are much lower than those of other ions. However, the concentrations of [Na⁺] changed more greatly in different seasons than those of the other three ions. Correlation coefficients showed that the three areas have been polluted by coal smoke and dust to different extents, while some local resources of pollution should be taken into consideration as well.  相似文献   

浓硫酸钠水溶液中的离子对          下载免费PDF全文

刘元会  房春晖 《盐湖研究》2005,13(4):42-46

不同浓度的Na2SO4水溶液的拉曼光谱显示了SO42-的四个拉曼活性带:980 cm-1处的SO42-的对称伸缩振动模式v1带,1 106 cm-1处的反对称伸缩振动模式v3带,448 cm-1处的变形振动模式v2带和617 cm-1处的变形振动模式v4带。482 cm-1处的肩膀峰是由于NaSO4-离子对的形成对448 cm-1的v2带的影响而形成的SO42-的一个新的振动峰。浓Na2SO4水溶液中,水共享离子对[Na+.H2O.SO42-]-是主要的离子对物种。随着Na2SO4水溶液浓度的增加,Na+和SO42-的相互作用增强,NaSO4-离子对所占的摩尔分数增加。  相似文献   

不同GPS掩星电离层剖面产品相关性分析     

周荣  侯威震  曾晨曦  张绍成  柴炳阳 《测绘通报》2019,(11):31-38,73

将在一定时空限定范围内的不同低轨卫星COSMIC、GRACE、CHAMP、FY3C的电离层掩星电子密度剖面定义为一个掩星对来对比分析不同类型掩星电离层产品。结果表明：COSMIC掩星对之间的电子密度剖面整体轮廓符合得很好，电子密度剖面主要在250 km以下和500 km以上存在较大的偏差，250~500 km的电子密度整体偏差较小，统计得到的COSMIC掩星对的电子密度参量NmF2和hmF2的相关系数能分别达到0.99和0.97，具有高度相关性，不同COSMIC卫星之间没有明显的系统误差；COSMIC、GRACE、CHAMP和FY3C不同低轨卫星间的电子密度剖面略有差异，通过统计电子密度参量NmF2和hmF2之间的相关系数，COSMIC和CHAMP的相关系数分别为0.95和0.86，COSMIC和GRACE的相关系数分别为0.98和0.94，COSMIC和FY3C的相关系数分别为0.96和0.92，不同掩星类型之间的电子密度参量之间也具有高度相关性，验证了不同卫星任务GPS掩星电离层剖面的一致性。  相似文献   

STPIR和MW组合的北斗三频周跳探测与修复          下载免费PDF全文

李迪  柴洪洲  潘宗鹏 《海洋测绘》2018,(1):31-34

针对载波相位观测值中出现周跳的问题及北斗卫星导航系统全星座播发三频信号的现状,提出一种三频相位电离层残差二阶历元差分(STPIR)的算法,克服了传统电离层残差法受观测数据采样间隔影响较大的问题,联合MW组合观测量进行周跳探测又可避免各自的探测盲区。两种组合观测量均很好地削弱了电离层延迟项的影响,联立方程组进行周跳求解时,直接取整即可得到周跳值。通过北斗三频实测数据验证,提出的组合方法在观测数据采样间隔较大时,可以准确探测出所有周跳,并有效修复。  相似文献   

Jason-2高度计电离层GIM误差分析及修正研究     

黄霞凤  苗洪利  苗翔鹰  薛文文 《海洋学报》2019,41(7):143-148

基于Jason-2高度计2015年地球物理数据集(GDR)38个周期太平洋海域的全球电离层图(GIM)电离层校正值和双频校正值的数据，分不同季度和不同纬度区域比较二者的差异，结果表明:GIM值与双频校正值之间存在明显的差异，GIM校正值普遍高于双频校正值，说明GIM高估了电离层路径延迟，GIM校正值与双频校正值的差异与季节和纬度区间有关。用梯度下降法得到GIM值的修正方程，将修正方程应用于2016年Jason-2的全年数据，修正后的GIM值与双频校正值十分接近，在各年份中均具有良好的适用性。在单频高度计不能使用电离层双频校正算法的情况下，可以利用不同季度和不同纬度区域的修正方程对同等高度的高度计GIM值进行修正以达到双频校正值的精度水平。  相似文献   

GPS精密卫星钟差估计研究     

孟范伟 《测绘与空间地理信息》2016,(9):77-79

随着精密单点定位技术的发展,对于精确的卫星坐标以及卫星钟差改正精度的要求越来越高,精密卫星星历以及精密卫星钟差的求解成为制约精密单点定位技术发展的瓶颈。本文基于修复周跳的载波相位观测值与相位平滑伪距观测值,采用无电离层延迟星间单差精密卫星钟差估计模型,在先估计出整周模糊度后,进行了精密卫星钟差的估计,并采用与IGS事后精密钟差作二次差的方法进行精度分析,这对于提高精密单点定位精度具有一定的意义。  相似文献   

电感耦合等离子体质谱法测定铅合金中的微量杂质元素镉和锡   总被引：1，自引：1，他引：0  

郝原芳  刘新  宋丽华  李丽君  徐英奎 《岩矿测试》2016,35(4):378-383

铅合金中的镉和锡由于含量较低,国家标准方法均为单一元素分析,步骤繁琐,检出限高,难以达到理想的检出要求。本文建立了应用电感耦合等离子体质谱法(ICP-MS)测定铅合金中微量级(μg/g级)杂质元素镉和锡的分析方法。采用单一的低浓度硝酸溶解铅合金,用低温慢溶的方式使样品溶解更加完全,减少了多离子对仪器的干扰;通过铅基体匹配和加入酒石酸保证了标准与样品介质的一致性,同时避免了锡的水解;以~(103)Rh作为内标元素,~(111)Cd和~(118)Sn作为测量同位素克服了质谱干扰。方法检出限为镉0.05 ng/g、锡0.04 ng/g,比国家标准方法的检出限(1~6μg/g)低,精密度小于4%。该方法试剂用量少,减少了处理样品的复杂性,实现了合金中微量级元素的准确测定。  相似文献   

广西大容山离子吸附型高铕高钇重稀土矿的发现及勘探意义     

李学彪 《地质论评》2016,62(S1):393-394

近年在广西境内发现众多离子吸附型稀土矿床,离子吸附型稀土矿矿床类型与其成矿母岩岩浆岩演化历程息息相关。新类型的发现不仅丰富了研究该地区稀土矿成矿理论,还延伸了这类矿床的找矿意义。本文首先介绍了新发现的高铕高钇重稀土矿的特征,结合这类矿床的配分类型,探讨了这类矿床的勘探意义。  相似文献