Amino acid adsorption by clay minerals in distilled water

The adsorption of 15 protein amino acids from dilute (~ 10 μM) distilled water solutions onto organic-free kaolinite and montmorillonite clay minerals (1 wt% suspensions) was determined at room temperature over a 48 hour period. The systems came to steady state within 2 hours. Basic (positively charged) amino acids were strongly adsorbed (40–80% removal) by both clay minerals. Neutral (uncharged) amino acids were taken up appreciably (10–15%) by montmorillonite, but little if any (<5%) by kaolinite. Acidic (negatively charged) amino acids were adsorbed (20–35%) only by kaolinite. These adsorption patterns appear to be related in part to electrostatic interactions between the clay mineral surfaces and the different amino acid types. The measured extents and selectivities of adsorption onto these clay minerals are sufficiently great to potentially affect the distributions and reactions of free amino acids in natural environments.     

Adsorption of Pentachlorophenol onto Oxide and Clay Minerals： Surface Reaction Model and Environmental Implications

The adsorption of pentachlorophenol （PCP） onto quartz, kaolinite, illite, montmorillonite and iron oxides has been investigated by batch equilibrium techniques. The pH-dependent isotherms are curves with peak values, the position of which is at about pH = 5-6 depending on the mineral species. Based on distribution of both speciation of surface hydroxyls on minerals and PCP in solution a surface reaction model involving surface complexation and surface electrostatic attraction is presented to fit the pH-dependent isotherms, and both reaction constants are calculated. The results show that on quartz and phyllosilicate minerals the predominant adsorption reaction is surface complexation, meanwhile both of surface electrostatic attraction and surface complexation are involved on the iron oxide minerals. The reaction constants of surface electrostatic adsorption are usually one to three orders in magnitude, larger than that of surface complexation. The concentration-dependent isotherms can be well fitted by Langmnir equation with the correlation coefficient R〉0.93 for kaolinite and iron oxides. The maximum adsorption is found in the order： hematite 〉 lepidocrocite 〉 goethite 〉 kaolinite 〉 quartz 〉 montmorillonite ≈ illite, which can be interpreted by consideration of both reaction mechanism and surface hydroxyl density. The significant adsorption of PCP onto mineral surfaces suggests that clay and iron oxide minerals will play an important role as HIOCs are adsorbed in laterite or latertoid soil, which is widespread in South China.     

Mobilization of aluminium and magnesium by roots of banana (Musa spp.) from kaolinite and smectite clay minerals

Banana plants (Musa spp.) are very sensitive to Al, which is mobilized in acid soil conditions. These plants may, however, contribute to their own intoxication because their roots can excrete protons in large quantities. The authors studied the mobilization of Al by banana roots from clay minerals in experimental designs exacerbating the root–mineral contact. The plants were grown on agarose-gel or sand substrates previously mixed with smectite (montmorillonite) and kaolinite as sole source of Al. The pH and the ion concentrations in the aqueous and exchangeable phases of the substrates were determined as concentrations of Al, Ca, Mg and K in plants. In both agarose and sand substrates, pH significantly decreased in the close vicinity of roots, relative to the bulk substrate. This root-induced acidification involved a preferential mobilization of Al in kaolinite substrates and of Mg in smectite substrates, and thereby a significant plant uptake of Al and Mg from these respective substrates. Root-induced weathering of kaolinite and montmorillonite thus suggests that the mobilization of, respectively, Al and Mg are the limiting steps in the dissolution of these respective minerals, just as demonstrated in previous chemical weathering studies.     

骨架矿物—粘土矿物碱耗协同效应研究

选择了克拉玛依油田二中区Ｔ２ｋ１砂砾岩储层中的六种储层矿物,石英,正长石,微斜长石,Ｃａ－蒙脱石,高岭石,伊利石。在不同的条件下研究了这六种矿物的碱耗量,还研究骨架矿物与粘土矿物按照一定的质量配比而成的复配矿物的碱耗量,探讨了矿物碱耗的协同效应,结果表明单矿物的碱耗序列为,蒙脱石（Ｓ）〉高岭石（Ｋ）〉伊利石（Ｉ）〉微斜长石（Ｍ）〉石英（Ｑ）〉正长石（Ｊ）,复配物的碱耗总体上受粘土矿物控制,尤其是蒙     

粘土沉积物XRD定量分析方法

从理论上推导了无序混合层粘土矿物混层比f与XRD视面网间距d之间的近似函数关系,制定出I/S混层矿物的d-f换算表;通过对济阳拗陷泥质岩石的研究,从一种新的途径求出了粘土矿物的强度因子,提出混层矿物XRD强度因子与混层比的线性关系式。根据不同的制样方法,利用微机运算,可以对粘土沉积物中的6种或10种矿物进行大量快速的定量分析。     

东太平洋水合物海岭沉积物中黏土矿物与水合物饱和度相关性研究

为了探讨水合物储层中不同黏土矿物与水合物饱和度的关系,选取位于东太平洋水合物海岭国际大洋钻探计划204航次中的3个钻孔(1245B孔、1244C孔和1251B),开展储层沉积物黏土矿物的测试和综合分析。结果表明,蒙脱石、伊利石、绿泥石为主要黏土矿物(平均含量分别为40.3%、33.4%、21.4%);高岭石为次要黏土矿物(平均4.9%)。伊利石、绿泥石、高岭石三种矿物含量的垂向变化规律相似,但它们与蒙脱石的垂向变化趋势相反。该区水合物饱和度与蒙脱石含量呈正相关,且正相关程度在“细粒岩性”层段较高(R=0.55~0.97);水合物饱和度与伊利石、绿泥石、高岭石则显示负相关。3个钻孔中水合物储层厚度、水合物饱和度在各钻孔中分布的差异性表明水合物饱和度的受控因素复杂,首先是气源和流体迁移与供给,其次为沉积物岩性;而“细粒岩性”层段较高含量蒙脱石与水合物饱和度正相关关系可能代表了更次一级的沉积影响因素。为检验其它海区是否也存在黏土矿物对水合物饱和度的影响,将上述3个钻孔与印度外海Krishna-Godavari盆地17-07P钻孔记录进行对比。结果显示,17-07P孔的砂含量高,在粗砂层蒙脱石含量与水合物饱和度呈正相关,反映两个海域岩性对水合物饱和度控制机理不同。上述“细粒岩性”层段蒙脱石含量和伊利石、绿泥石、高岭石3种黏土矿物含量与水合物饱和度之间相关性的差异,可能因为蒙脱石具有特殊层状结构和表面化学性质(层间表面带负电荷、具有可交换的层间水合阳离子等),有利于促进水合物的形成和富集,因而表现为正相关;而伊利石、绿泥石、高岭石自身属性与蒙脱石不同(吸水膨胀能力、对甲烷的吸附能力较蒙脱石弱),不利于水合物的聚集,表现为负相关。     

太平洋中部沉积物中粘土矿物的初步研究

笔者对采自太平洋中部170°E至178°W,6°到17°S,即新赫布里底群岛至乌佛阿岛,斐济群岛到埃利斯群岛间海区(见图1)的10个站位,20个海底沉积物样品,进行了分析和研究。 该区的地质构造受西太平洋岛孤活动带的控制,海底地形复杂,水深变化大。火山活动频繁,区内散布许多白垩纪至老第三纪形成的火山岛和水下火山体。第四纪以来,火山活动依然十分频繁[1]。根据海底地形，水深和沉积物的差异，将该区分为三个小区。(1)斐济群岛和霍恩群岛以北海区，水深一般小于2500米，但深度变化大，地形复杂，水下火山体和珊瑚礁星罗棋布，沉积物以钙质生物沉积为主。( 2)北斐济海盆，水深多为3000-400。米，海盆边缘散布着许多水下火山体，沉积物以钙质生物沉积一火山碎屑沉积为主。(3)美拉尼西亚海盆南部，水深5000米左右，海域开阔，水下火山体较少，沉积物以多源性红粘土沉积为主。     

黑龙江金厂金矿床18号矿体围岩蚀变及短波红外光谱特征

金厂金矿18号矿体围岩蚀变发育顺序从早到晚为:钾化、硅化、绿泥石化、绢云母化、碳酸盐化、高蛉土化,从内往外依次发育青磐岩化带、绢英岩化带和钾化带.矿化出现在泥化和绢英岩化叠加处,以及泥化和青磐岩化叠加处.通过短波红外光谱测试技术,识别出本矿区有26种蚀交矿物,其中白云母含量与金矿体呈正相关,说明绢云母化与金矿化关系密切;青磐岩化带蚀变矿物组合为绿泥石+绿帘石+伊利石±埃洛石±蒙脱石±石英;钾化带蚀变矿物组合为钾长石+高岭石+埃洛石±蒙脱石±石英;绢英岩化带蚀变矿物组合为绢云母+埃洛石±蒙脱石±高岭石±石英.     

高岭石和蒙脱石吸附胡敏酸的对比研究

高岭石和蒙脱石分别是暖湿和冷干气候带内典型土壤的代表性矿物,对二者吸附胡敏酸特点的对比研究可以为探索不同地带土壤中重金属的环境行为提供重要的依据。笔者通过一系列实验研究了pH值、离子强度和胡敏酸初始浓度对胡敏酸在高岭石和蒙脱石上吸附量的影响,重点剖析了引起高岭石和蒙脱石在吸附胡敏酸方面表现出的共性和差异的原因。研究结果表明:1)在pH=5条件下,胡敏酸在高岭石和蒙脱石上的吸附量均随着胡敏酸初始浓度和离子强度的升高而逐渐增加;2)胡敏酸在高岭石和蒙脱石上的吸附量均随着pH值的升高而降低;3)pH<6时,高岭石吸附的胡敏酸量多于蒙脱石,pH>6时则相反。这是由高岭石和蒙脱石在不同pH条件下吸附胡敏酸的机制不同造成的。在pH<6时,高岭石与胡敏酸之间的静电引力起主导作用,其次是配位交换作用和氢键作用。此时,蒙脱石以氢键作用为主要吸附机制。在pH>6时,高岭石和蒙脱石的主要吸附机制分别是疏水性作用和阳离子键桥。     

洛川姜石的矿物药材特征

用化学分析、光谱分析、X射线衍射分析、差热分析和扫描电镜等对产于陕西洛川黄土不同层位中的三种成因类型五种结构类型姜石测试表明,姜石是由方解石(为主)、石英、长石和粘土矿物伊利石、蒙脱石、高岭石等构成的多矿物聚集体。 姜石作为矿物药材用于防治疾病,其药理作用主要在于含有具特殊疗效的微量元素和矿物成分。当方解石和具有强吸附性能及离子交换容量大的粘土矿物含量占一定比例时,疗效最佳。产于晚第三系三趾马红粘土层(N_2)和第四系早更新世午城黄土下部(Q_1~1),且具有碎斑状结构及均质结构的姜石药性最佳     

西南喀斯特地区不同石漠化阶段土壤黏土矿物组成及其含量变异研究

为了探索西南喀斯特地区土壤中黏土矿物组成及其含量的变异规律,以贵州省普定县和荔波县不同石漠化阶段典型土壤的黏土矿物为例,采用x-射线衍射仪图谱分析方法,计算得到黏土矿物组成及其含量,探讨不同石漠化阶段黏土矿物组成变化规律及其含量之间的线性关系。结果表明：不同石漠化阶段黏土矿物的组成是相同的,均为高岭石、蒙脱石和伊利石;在未石漠化、轻度石漠化、中度石漠化阶段,蒙脱石在剖面表层的质量分数分别为27．82％、29．34％、58．32％,高岭石分别为21．39％、31．81％、36．93％,伊利石分别为50．79％、38．85％、4．75％;在西南喀斯特地区,各石漠化阶段伊利石与蒙脱石的含量之间以及伊利石和高岭石的含量之间都呈显著的线性相关,相关系数分别为-0．9703、-0．9456;西南喀斯特地区土壤相似的成土作用和成土环境造成了黏土矿物相同的组成,而黏土矿物含量的差异说明各成土作用的程度或阶段是不同的;粉粒中的黏土矿物主要为石英和白云母,而砂砾中的黏土矿物主要为石英。     

粘土矿物碱耗协同效应研究

选择蒙脱石,高岭石,伊利石等三种在储层中最党风的储层粘土矿物,两两分别按２Ｌ：０,１：１,０：２质量配比组成复配物系列;在３０℃、５０℃温度下按１：５,１：８,１：１０（ｇ／ｍｌ）固／液比分别与１．６％的Ｎａ２ＣＯ３深液反应８ｈ,３６０ｈ;监测反应前后碱液浓度的变化;计算了各条件下各自的绝对碱耗量。结果表明三种粘土矿物中蒙脱石耗碱最大,高蛉石的耗碱量与伊利石的接近;随着固／液比减小和温度升高,矿物     

Lime stabilization of clay minerals and soils

Clay soil can be stabilized by the addition of small percentages, by weight, of lime, thereby enhancing many of the engineering properties of the soil and producing an improved construction material. In order to illustrate such improvements, three of the most frequently occurring minerals in clay deposits, namely, kaolinite, montmorillonite and quartz were subjected to a series of tests. As lime stabilization is most often used in relation to road construction, the tests were chosen with this in mind. Till and laminated clay were treated in similar fashion. With the addition of lime, the plasticity of montmorillonite was reduced whilst that of kaolinite and quartz was increased somewhat. However, the addition of lime to the till had little influence on its plasticity but a significant reduction occurred in that of the laminated clay. All materials experienced an increase in their optimum moisture content and a decrease in their maximum dry density, as well as enhanced California bearing ratio, on addition of lime. Some notable increases in strength and Young's Modulus occurred in these materials when they were treated with lime. Length of time curing and temperature at which curing took place had an important influence on the amount of strength developed.     

辽河坳陷古近系碎屑岩储层孔隙演化特征探讨

辽河坳陷古近系的沉积特征是物源多、沉积体系多、砂岩成熟度低及砂体规模小。通过成岩作用和成岩相研究,储层成岩相可划分为4种,即碳酸盐胶结相、自生粘土矿物胶结相、石英胶结相和粘土矿物转化相。这4个相可进一步划分为7个亚相：自生粘土膜胶结亚相、晶粒状碳酸盐胶结亚相、自生高岭石胶结亚相、石英胶结亚相、嵌晶状碳酸盐胶结亚相、伊/蒙混层亚相和伊利石亚相。不同成岩相分布明显受深度控制,具有在垂向相连的展布特征,垂向上可组成6个成岩相带。通过大量的砂岩和泥岩孔渗数据统计分析,建立了6个对应的高孔渗带（ABCDEF）与6个低孔渗带（abcdef）,它们与6个成岩相带在空间分布上具有一一对应关系,即A－a、B－b、C－c、D－d、E－e和F－f分别与晶粒状碳酸盐相带、自生高岭石相带、石英胶结相带、嵌晶状碳酸盐相带、伊／蒙混层粘土矿物相带和伊利石相带相对应。可见,不同成岩相带对应不同孔隙度发育带的孔隙演化,并从有机质演化的角度解释了上述对应关系。应用这一规律在鸳鸯沟地区有利储层孔隙预测中取得了较好效果,验证了该区储层孔隙演化特征及其对油气运聚的影响。     

Parameters controlling the partitioning of tributyltin (TBT) in aquatic systems

In the present study the distribution of TBT between solid and water phase as a function of several parameters was determined. Two types of clay minerals (Na-montmorillonite SWy and kaolinite KGa) and quartz sand were used as sorbents in conventional batch experiments. Sorption coefficients (K_d) followed the order montmorillonite (89 l/kg) > kaolinite (51 l/kg) > quartz (25 l/kg), while for sorption coefficients normalized to the surface area (Kd′) an opposite trend was observed, with the lowest value determined for montmorillonite (2.79 × 10⁻³ l/m²) and the highest for quartz sand (8.04 × 10⁻² l/m²). The results demonstrate that numerous environmental parameters influence the adsorption process of TBT, such as solid/solution ratio, clay content and salinity. Another important factor governing TBT adsorption is pH, because it affects both the TBT species in the water phase as well as the surface properties of the mineral phase. The maximum of TBT adsorption onto clays was always around pH 6–7. According to the data, it is evident that the content of organic matter in the solid phase plays an important role on TBT adsorption, either as particulate organic matter (POM) or organic matter adsorbed to mineral particles (AOM). Experiments were carried out with well characterized organic matter and the results showed a linear increase of K_d from 51 up to 2700 l/kg upon the addition of 5% of particulate organic matter to pure phased kaolinite. TBT adsorption onto mineral surfaces, which were previously enriched with adsorbed organic matter, was investigated at different pH. The present study points to the importance of identifying and characterizing sorbents and envrionmental conditions, in order to predict and model TBT distribution in natural systems.     

台湾海峡西部沉积物中粘土矿物的初步研究

利用X射线衍射,红外光谱,电子显微镜和化学分析等手段,综合分析和研究了台湾海峡西部海域的以水云母为主,高岭石次之的粘土矿物组合特征。结果表明其含量变化和分布特点受物质来源,沉积环境,气候条件,水动条件所制约。高岭石系湿热气候风化型陆源次生矿物,沿闽江和九龙江河口外迅速递减。绿泥石除少量陆源成因外,主要是次生和自生的绿泥石,蒙脱石变以蚀变型自生蒙脱石为主。粘土矿物含量的垂直变化能够为古气候和古沉境环境提供佐证     

利用扫描电镜和X射线衍射仪对滑坡滑带土的研究

利用扫描电子显微镜（SEM）和X射衍射仪（XRD）研究了三峡库区，黄河小浪底等地40个滑坡滑带土的结构及物质组合，指出当滑坡处于滑动阶段时，滑带土表居可见粘土矿物定向排列，普遍可见擦痕（弧型，线型，紊乱型），微裂隙和微空隙发育，微生物较多，当斜坡处于稳定阶段时，岩层软弱带可见粘土矿物无定向排列，表面无擦痕，常见树枝状结构。滑带土的物质组合主要为：蒙脱石，蛭石，伊利石，高岭石，绿泥石，方解石，石英，长石和微生物，而蒙脱石，蛭石和微生物含量是滑坡滑动的一个重要因素。据微结构的变化和物质组合可以分析滑坡的活动次数，活动阶段和形成机理，为滑坡治理和稳定性评价提供依据。     

晋城矿区粘土矿物特征及沉积-成岩响应

在X射线衍射和扫描电镜观测的基础上,结合区域沉积演化分析,探讨了晋城矿区粘土类型、组合特征、微观结构与沉积-成岩作用的关系。结果表明,晋城矿区粘土矿物以高岭石为主,其次为伊利石和伊利石/蒙脱石混层,还有少量的绿泥石和蒙脱石;山西组粘土矿物颗粒排列定向性优于太原组,多呈带状或平叠状产出,而太原组多为蜂巢状、花朵状或凝絮状;由于太原期频繁的海侵海退致使煤层顶底板处于pH值较高的碱性环境,使成岩过程中高岭石向伊利石转化,造成太原组粘土矿物的伊利石含量明显高于山西组,而高岭石含量相对较低。     

不同粘土矿物对赖氨酸的吸附行为对比研究

以皂石、高岭石、绿泥石和伊利石为原材料,分别与赖氨酸进行反应,研究赖氨酸在上述粘土矿物上的吸附行为, 并运用粉末X-射线衍射技术（XRD）、傅里叶变换红外吸收光谱术（FTIR）和热重（TG）等分析方法,表征反应前后粘土 矿物的变化。实验结果表明,不同粘土矿物对赖氨酸的吸附等温线均符合Freundlich等温方程,且不同粘土矿物对赖氨酸的 饱和吸附量大小顺序为：皂石>蒙脱石>绿泥石>高岭石>伊利石;XRD结果表明皂石对赖氨酸的吸附发生在矿物层间,而绿 泥石、高岭石和伊利石对赖氨酸的吸附主要在矿物表面进行;FTIR和TG结果表明赖氨酸主要取代粘土矿物层间吸附水,以 氢键的形式与Si-O-Si(IVAl)键合。实验结果将有助于进一步探明环境中粘土矿物对有机质的吸附机理。     

Characteristics and distribution of clay minerals and their effects on reservoir quality: Huagang Formation in the Xihu Sag,East China Sea Basin

Abstract

The characteristics and distribution of clay minerals and their effects on reservoir quality in the Huagang sandstones in the Xihu Sag, East China Sea Basin were studied by using X-ray diffraction, casting thin-sections, scanning electron microscopy, electron microprobe analysis, fluid inclusion analysis, constant-rate mercury injection and nuclear magnetic resonance. Clay minerals consist of kaolinite, chlorite, illite and illite–smectite mixed layer (I/S); kaolinite forms from dissolved feldspars, chlorite occurs as clay coatings that are transformed from clay precursors owing to the flocculation of suspended detrital clays or the crystallisation of pore fluids, and illite forms from the illitisation of detrital smectite, authigenic kaolinite and K-feldspars. Clay distribution is controlled by sedimentary environments, burial history and lithologies. Typical reservoirs in the western sub-sag are thin and developed in braided river facies at relatively shallow burial depths with clays dominated by kaolinite. However, typical reservoirs in the central inversion tectonic zone are thicker and developed in a braided delta front facies at deeper burial depths with clays mainly consisting of chlorite, illite and I/S. High-quality reservoirs are characterised by coarse granularity, high quartz content and low clay content with widespread development of chlorite coatings that inhibit quartz cements at low temperatures. At higher temperatures, the high-quality reservoirs develop more pores providing growth space for quartz cements and result in the coexistence of chlorite coatings and quartz cements. The high-quality reservoirs are controlled by their lithological characteristics rather than chlorite coatings. Illite and I/S clays create severe damage to reservoirs by reducing the size and connectivity of pore-throats.