软阳离子钾改性蒙脱石矿物对硝基苯的强化吸附实验研究

考察软阳离子钾改性蒙脱石在K+存在的条件下对硝基苯的强化吸附行为,详细分析比较了Henry和Fre-undlich方程对硝基苯吸附等温线的拟合结果,同时还进行了吸附热力学研究。实验结果表明,软阳离子钾对蒙脱石吸附硝基苯具有强化作用;硝基苯在蒙脱石上的吸附符合Freundlich和Henry方程,两模型方程线性拟合结果的相关系数均在0.96以上。热力学分析结果表明,硝基苯在蒙脱石上的吸附过程是一个自发的放热过程,说明蒙脱石对硝基苯的吸附主要由分配与EDA作用机制所控制。钾离子存在可为硝基苯吸附营造有利场所,不仅改善准入条件,同时增加某些吸附点位,从而促进并强化蒙脱石对硝基苯的吸附。     

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。     

Octahedral cation ordering in olivine at high temperature. I: in situ neutron single-crystal diffraction studies on natural mantle olivines (Fa12 and Fa10)

Crystallographic determinations on natural olivine single crystals of mantle composition and origin, carried out by in situ neutron diffraction at high temperature, show that the octahedrally co-ordinated Fe²⁺ and Mg cations undergo two successive trends of cation ordering with increasing temperature. An initial slight preference of Fe²⁺ for site M1, up to a temperature of about 850?°C, is followed by a reverse-ordering reaction with a site preference exchange between the two cations. The cross-over between the two regimes of ordering, corresponding to a situation of complete disorder, occurs at about 900?°C. Above this temperature Fe²⁺ progressively and strongly segregates into site M2 up to 1300?°C, the practical limit of the experimental setup utilized in the experiments. Care was taken to ensure that no chemical changes occurred in the crystals (i.e. oxidation), as testified by Mössbauer spectroscopy determinations carried out before and after the heat treatment. The cation-ordering behaviour is reflected in temperature-dependent changes of geometrical and atomic displacement parameters occurring in the octahedral sites M1 and M2. A thermodynamical explanation of this behaviour is proposed in terms of a prevailing vibrational contribution to entropy.     

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。     

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。     

中国二八面体含铝蒙皂石矿物化学和晶体化学的特征

通过对我国６４个二八面体含铝蒙皂石矿物化学及晶体化学数据的统计分析，研究了它们的矿物化学及晶体化学的基本特征，并得出八面体组分是影响蒙皂石矿物学及物理化学性质的主要因素，在此基础上，利用ＡｌＡｌ－ＡｌＦｅ－ＡｌＭｇ三角图划分了我国二八面体含铝蒙皂石的晶体化学类型，并对原分类图进行了模式化处理，使ＡｌＡｌ－ＡｌＦｅ－ＡｌＭｇ图更具实际意义，蒙皂石的阳离子交换容量与晶体化学模型有对应性，并受八面体三价     

碱金属离子及碱溶液对膨润土性能影响的研究进展

基于前人有关膨润土在碱性环境下的室内试验和数值模拟的研究结果 ,重点阐述了碱金属离子及碱溶液对膨润土矿物成分、微观结构、膨胀性和渗透性等方面的影响,讨论了温度、pH值与溶液浓度等对上述过程的影响。碱金属离子及碱性溶液不仅可交换膨润土中蒙脱石层间阳离子,而且可溶解膨润土中的蒙脱石,生成非膨胀性矿物,并随着温度和pH值升高,蒙脱石被溶解程度增加,从而导致了膨润土膨胀力减小,且随着温度、溶液浓度及pH值的增加,膨胀力削弱程度加强;同时,膨润土与碱金属离子及碱溶液接触时孔隙增多,进而渗透性增强,随着温度和溶液浓度增加,渗透性也明显增强。数值模拟可实现膨润土与碱性溶液长期接触时发生的矿物成分及渗透性变化的预测。高温、不同pH值的低碱性溶液及其耦合作用对膨润土的矿物化学成分、微观结构、膨胀力和渗透性的影响及机理研究应该是今后研究的重点。     

天然膨润土中蒙脱石丰度的定量方法研究

基于膨润土中蒙脱石的基本结构单元在X射线衍射空间的相干散射的分布和总量是一不变量,同一膨润土矿中单位质量蒙脱石的阳离子交换容量和层电荷密度专一性的特点,本研究提出了阳离子交换容量／层电荷密度、阳离子交换容量和X射线衍射多相Rietveld分析三种蒙脱石丰度的定量方法,并测定了我国不同产地、矿物组成和物化性质各异的10种天然膨润土中蒙脱石丰度,分析了可能的干扰因素。结果表明,三种方法测得的蒙脱石丰度值在3％范围内吻合良好,且具有一致的自相关性。     

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.     

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。