743阳离子交换快速分离——ICPS-PGS2单道扫描直读光谱仪测定地质样品中15个微量稀土元素

本文采用过氧化钠(Na_2O_2)熔样,743阳离子交换树脂快速分离,0.4mol/L柠檬酸25ml洗脱稀土,无需浓缩,即可用lCPS-PGS2单道扫描直读光谱仪直接测定15个微量稀土元素。在选择的最佳测量条件下,本法测定下限为0.005~g/ml(Eu)-0.50μg/ml(Ce),标准加入回收在88％—110％之间,样品分析精度为3.3％—17％,样品分析结果与参考值相符。本法适用于一般地质样品中微量稀土元素的例行分析。     

郑家-王庄地区沙一段粘土矿物特征及对储层敏感性影响

东营凹陷郑家—王庄地区沙一段砂岩储集层中蕴藏大量稠油油藏,但开发过程中粘土矿物的敏感性严重制约了该油类藏的有效开发。定向X射线衍射分析结果表明,本区沙一段砂岩储层中粘土矿物组成类型为伊/蒙无序间层矿物(S/I)、高岭石、伊利石和绿泥石,其中以伊/蒙无序间层矿物的相对含量居多。这就决定了研究区储层敏感性以水敏性为主,其余敏感性无或较弱。据定向X射线衍射谱图上S/I主峰d值大小,进一步识别出钙型S/I、钠型S/I及钙钠过渡型S/I。扫描电镜观察表明,S/I具有丝状、网状和蜂窝状三种形态,且大都包裹在岩石骨架颗粒的表面作为孔隙衬里而存在。阳离子交换容量和膨胀率研究结果显示,二者与样品中S/I含量和层间阳离子类型相关。膨胀率和阳离子交换量与S/I含量都呈较好的正相关关系。在S/I中蒙皂石层含量相当的情况下,钠型S/I的膨胀率和阳离子交换量值偏大,钙型偏小,钙钠过渡型居中。此外,粘土总量以及S/I产状对储层损害也有较大的影响。     

累托石的阳离子交换性能及其应用研究

累托石是二八面体云母层与蒙脱石层1:1规则间层矿物。本文阐明累托石矿物结晶构造与阳离子交换性能的关系。阳离子交换性能在累托石定量与定性、改型、合成交联累托石和有机累托石等方面的应用。并介绍氧化钛交联累托石和在机累托石的有关特性。     

水电开发移民非农就业研究——以向家坝电站绥江县为例

针对水电开发中移民农业安置的困境,以及社会发展趋势,从农村劳动力转移理论和模型出发,着重对农村剩余劳动力＂开流断源＂的模型进行介绍,以向家坝电站绥江县为案例分析该库区非农就业的必然性和艰巨性。基于＂开流断源＂的模型对非农就业的几个方面进行思考,提出：（1）从人的生产与消费两面性,以及剩余劳动力的角度而言,移民安置需要考虑库区人口规模的控制,以及趋向于增加就业的人口结构调整;（2）特定区域背景和不同移民人群对于非农就业的预期目标不同,区域发展规划和劳务输出设计需要相应地做出反映;（3）政府的移民工作需要将教育和培训方面的服务纳入重点,以提高个体预期目标部门的非农就业概率;（4）从教育、培训、基础设施建设和社会保障制度等方面,政府可以为农村劳动力向非农化转移提供支持,并在移民安置中得到具体体现。     

金属离子对粘土土工性状影响的实验

在正交实验设计的基础上,通过大量的室内实验,对粘土吸附性的影响因素加以分析,为金属离子影响下的粘土土工性状研究奠定基础。在粘土吸附性的基础上,对粘土吸附离子后的基本土工特性进行实验研究,得出了粘土土工特性的变化趋势。结果表明:在单离子体系中粘土对离子的吸附量明显大于混合离子体系中对该离子的吸附量;在多离子体系中,则表现为高价离子具有更强的竞争力;粘土的塑性指数基本是随离子含量的增加而增大;粘土强度随着离子总含量的增高而逐渐降低。     

滨海含水层胶体絮凝导致地层损害的实验研究

滨海含水层地层损害是指淡水驱替咸水过程中,释放后的黏土胶体发生絮凝沉降,导致地层孔隙被堵塞,引起含水介质的渗透性降低的现象。该文通过絮凝沉降实验和定流速砂柱实验,分析不同离子强度和阳离子价态(一价、二价)对胶体絮凝沉降的影响,结果表明:NaCl作为电解质时,絮凝发生的离子强度范围在0.032~0.034 mol/L之间,絮凝时间从82 min减少至39 min;而电解质为CaCl 2,离子强度为0.006 mol/L时,胶体的絮凝时间仅需6 min;钙钠比越高,黏粒絮凝发生的越快。砂柱实验结果显示,含水介质渗透性会随着电解质溶液的离子强度增加和阳离子价态的升高快速降低。当电解质为NaCl,离子强度分别为0.054 mol/L和0.017 mol/L时,含水介质渗透性降低20%所需时间分别为15 min和50 min;当电解质为CaCl2,离子强度为0.011 mol/L时,含水介质渗透性降低20%仅需5 min。因为高离子强度和高价阳离子可以加速胶体絮凝,多孔介质的孔吼更容易发生堵塞,研究成果对降低滨海含水层的地层损害有一定的实际应用价值。     

BOOK REVIEWS

Books reviewed in this article: Boundary Control and Legal Priniciples . Curtis M. Brown , Walter G. Robillard and Donald A. Wilson . Lost Initiatives: Canada's Forest Industries, Forest Policy, and Forest Conservation . R. Peter Gillis and Thomas R. Roach . The Navajo Atlas: Resources, People, and History of the Dine Bikeyah . James M. Goodman . The City and the Sign . M. Gottdiener AND Alexandros Ph . Lagopoulos , EDS. The Comfortable House: North American Suburban Architecture 1890–1930 . Alan Gowans . Arabic-Islamic Cities. Building and Planning Principles . Besim Salim Hakim . Contemporary Climatology . Ann Henderson -Sellers and Peter J. Robinson . A Trace of Desert Waters . Samuel G. Houghton . Geography, Resources and Environment. Vol. 1: Selected Writings of Gilbert F. White. Vol. 2: Themes from the Work of Gilbert F. White . Robert W. Kates AND Ian Burton , ED. Spatial Dimensions of Unemployment and Underemployment (A Case Study of Rural Punjab) . Gopal Krishan . Maps of the Holy Land: Cartobibliography of Printed Maps, 1475–1900 . Compiled by Eran Laor , assisted by Shoshana Klein . The Geography of Third World Cities . Stella Lowder . A Perspective on U.S. Farm Problems and Agricultural Policy . Lance Mc Kinzie , Timothy G. Baker AND Wallace E. Tyner . Soil Erosion and Its Control. R.P.C . Morgan , ED Geopolitics . Patrick O'Sullivan . Landscape, Meanings and Values . Edmund C. Penning -Rowsell AND David Lowenthal , EDS.     

安徽马鞍山市当涂地区地下水水化学特征及演化机制

【研究目的】 了解长江中下游平原地区地下水流系统并深入分析其地下水水化学特征及其演化机制。【研究方法】 综合马鞍山市当涂地区的水文地质条件、水动力场等,基于研究区水化学基本特征,运用多元统计分析、水化学图件、离子比值和反向水文地球化学模拟等方法对该地区浅层地下水水化学演化进行分析。【研究结果】 结果表明：（1）研究区地下水主要为低矿化度偏碱性水,地下水组分中阳离子以Ca²⁺和Mg²⁺为主,阴离子以HCO₃^-和SO₄^2-为主。（2）研究区地下水水化学类型主要可分为7类,其中松散岩类孔隙含水岩组和碎屑岩类孔隙裂隙含水岩组的水化学类型主要为HCO₃^-Ca型、HCO₃^-Ca·Na型、HCO₃·Cl-Ca·Na型以及HCO₃^-Ca·Mg型;基岩类裂隙含水岩组的化学类型主要为HCO₃·SO₄-Ca·Mg型和SO₄·HCO₃^-Ca·Mg型。（3）研究区浅层地下水水样超标率为46%,总体水质较差,超标率较高的组分依次为Mn、高锰酸盐指数（COD_Mn）、硝酸盐（以N计）、Fe、As、氨氮（以N计）等。（4）研究区地下水的化学组分主要受到岩石风化作用的控制;此外,还存在Na-Ca的正向阳离子交替吸附作用。反向水文地球化学模拟结果进一步定量论证了水岩相互作用对本区浅层地下水组分的形成和演化起着主导作用。【结论】 研究区地下水主要为低矿化度偏碱性,主要可分为松散岩类孔隙水、碎屑岩类孔隙裂隙水和基岩类裂隙水。主要离子比例和反向水文地球化学模拟揭示了本区浅层地下水化学组分主要是地下水溶滤方解石、白云石等碳酸盐矿物、石英、长石等硅酸盐矿物,高岭土等黏土矿物以及岩盐、石膏等达到过饱和之后形成的。     

The effect of acid deposition on base cation cycling in a karstic-forested catchment： Evidence from strontium isotopes

Bedrock weathering and atmospheric deposition are the two primary sources of base cations （K^＋, Na^＋, Ca^2＋ and Mg^2＋） to forest ecosystems. Therefore, the key problem is to understand the relative inputs from these two sources and the cycling in the ecosystem. This study focuses on the effects of acid deposition on cation cycling in a small-forested karstic catchment in Guizhou Province. Sr isotope ratios were used as a tracer for understanding the transport process between the different cation pools： rock, soil, surface water, atmospheric deposition and plant. The samples of wet deposition, total deposition, throughfall, surface and ground waters, vegetation, and soil were monthly collected. The exchangeable Sr^2＋ and Ca^2＋ in soil samples were extracted by using 1 M ammonium acetate. The leaf-tissue samples were ashed at 550℃, and the residue was digested in ultrapure HClO4 and HNO3. All water samples were filtrated through 0.45 μm aperture filter paper. Base cation concentrations and Sr isotopic composition were analyzed for all the samples. The results show that acid deposition （average pH 4.9） frequently occurred in the studied region. Cation abundance follows an increasing manner from rainwater, throughfall, to surface water or ground water samples, suggesting that acid deposition at first eiuviates Ca^2＋ , Mg^2＋ and Sr^2＋ from leaf, then the exchangeable cations from soil, and at last cations accumulate in surface water or ground water.     

Iron oxidation state in lower mantle mineral assemblages: II. Inclusions in diamonds from Kankan, Guinea

Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O₃ perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe³⁺/ΣFe. Fe³⁺ concentration in the (Mg,Fe)(Si,Al)O₃ inclusion is consistent with empirical relations relating Fe³⁺/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na_0.5M_0.5³⁺O (M=Fe³⁺, Cr³⁺, Al³⁺). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO₂ equilibrium. Fe²⁺/Mg partition coefficients between (Mg,Fe)(Si,Al)O₃ and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe³⁺ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ¹³C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe³⁺ concentration in (Mg,Fe)(Si,Al)O₃ perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.