塔中地区志留系沥青砂岩成岩作用及其对储层性质的影响   总被引：5，自引：0，他引：5  

张金亮  杜桂林 《矿物岩石》2006,26(3):85-93

运用沉积学原理对塔中地区志留系经历复杂成岩演化的沥青砂岩进行研究分析,了解到该岩石主要经过压实作用、胶结作用和溶蚀作用等成岩作用。其胶结物的主要类型有绿泥石、伊利石、高岭石、伊-蒙混层等粘土矿物以及碳酸盐矿物、石英、长石、黄铁矿等。孔隙类型以粒间孔隙、粒内孔、铸模孔、特大孔、裂缝孔隙等为主,其中以粒间孔隙最为发育,低地温梯度有利于在深层形成次生孔隙。志留系沥青砂岩储层物性受沉积和成岩双重因素的影响,成岩演化阶段处于晚成岩A期。根据影响储层物性的储层成岩作用,可将成岩相类型划分为不稳定碎屑溶蚀成岩相、压实-弱溶蚀成岩相、压实充填成岩相、压实压溶成岩相、碳酸盐胶结成岩相等几种主要类型,成岩相类型决定了储层性质,不稳定碎屑溶蚀成岩相和压实-弱溶蚀成岩相是本区较好的油气储层。  相似文献   

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

WU Daqing DIAO Guiyi YUAN Peng PENG Jinlian 《《地质学报》英文版》2006,80(2):192-199

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.  相似文献   

铝土矿粘土研究的回顾(续)          下载免费PDF全文

刘长龄 《地质找矿论丛》2006,21(3):188-190

我国球粘土应成为独立矿种,湖沼球粘土中含“内胶体”的自生高岭石是生物有机质作用造成,水云母、I-M间层粘土矿物及有机质会增加可塑性、粘结性及干燥强度,钾、钠的增加可降低烧结温度。沉积球粘土与残积成因高岭石为无序或较无序,古生代煤系高岭石为有序和高度有序,岩浆热液成因的高岭石常为有序或高度有序;北方古生代软质粘土（紫矸）为规模较大、较为均匀稳定的高度有序高岭石,应积极开发。硬水铝石岩溶铝土矿应属于生物有机质成矿作用的沉积型铝土矿。  相似文献   

叶蜡石、高岭石和迪开石的吸收光谱研究   总被引：3，自引：0，他引：3  

张惠芬  杨振国等 《矿物学报》1990,10(1):23-28

对不同地区叶蜡石、高岭石、迪开石的吸收光谱测量及其高斯谱拟合说明，三各矿物的吸收光谱均由一个吸收边和三个吸收峰叠加而成。主吸收峰在562nm左右，峰高以迪开石为最大，高岭石次之，叶蜡石最低。同一地区不同颜色的叶蜡石，其主吸收峰位置随铁含量的增加向短波方向移动，相对峰高也随之增大。叶蜡石的颜色主要取决于主吸收峰的位置、高度和吸收边位置。可以认为，此吸收边为Fe^3 →O^2-荷移谱的低能拖尾部分，吸收峰则为铁离子的晶场谱带或晶场谱与Fe^2 →Fe^3 荷移的叠加。  相似文献   

高岭石的结晶有序度及其对纸张涂布粘浓度的影响   总被引：5，自引：0，他引：5  

周国平  林毓川 《矿物学报》1991,11(3):267-273

粘浓度是纸张涂布的一项重要指标,测定的变化范围从46.4—72％。用Hinckley方法测定了高岭石的结晶度指数,从0.57变化至1.40。当粘浓度>67％时,结晶度指数>1。粘浓度<67％,结晶度指数<1,有序高岭石有利于粘浓度提高。随着结构无序化,晶粒变小,晶片变薄,比表面增加,晶体边缘和角易破损,使粘浓度降低。结构无序化破坏了颗粒的均匀性,使颗粒长/厚比增加,粘浓度降低。高岭石八面体中Fe~(3+)的存在一定程度上影响了有序度。  相似文献   

Exfoliation of kaolinite by urea-intercalation precursor and microwave irradiation assistance process     

Pi Zhenbang  Liu Zhuoqin  Yang Chao  Tian Xike  Fei Jinbo  Zheng Jianhua 《Frontiers of Earth Science》2007,1(1):26-29

A type of exfoliated kaolinite was produced by urea-intercalation and original microwave irradiation assisted method. The product was investigated by Fourier transformation infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electronic microscopy (SEM), Brunauer-Emmett-Teller (BET) and laser particle analysis techniques. FT-IR spectra show that NHCO molecule exists in the intercalated kaolinite. XRD analyses indicate that the kaolinite sheet-like structure was disordered after microwave irradiation. The urea decomposition process and explosion effect between the sheet-like structures of kaolinite under microwave irradiation were discussed. The SEM and BET analyses reveal that the end product is exfoliated kaolinite with thin particles and increased surface area. Size and zeta potential analyses show that the particle size distribution is between 250 nm and 550 nm with normal distribution and the particle is negatively charged. In comparison with the conventional grind method, the process adopted appears to be economic and the exfoliated kaolinite end product may display a significantly enhanced performance in industrial applications.  相似文献   

蒙脱石、高岭石、伊利石对重金属离子吸附容量的实验研究   总被引：48，自引：4，他引：48       下载免费PDF全文

何宏平郭九皋  朱建喜杨丹 《岩石矿物学杂志》2001,20(4):573-578

在pH=4,t=23℃和微量浓度条件下,不改变离子浓度,通过增加吸附液体积进而增加体系中重金属离子含量的方法进行了蒙脱石、伊利石、高岭石对Cu2+、Pb2+、Zn2+、Cd2+、Cr3+等重金属离子吸附容量的实验研究,结果表明,3种矿物吸附容量大小顺序为蒙脱石>伊利石>高岭石,与其阳离子交换容量密切相关.Cu-蒙脱石和Cr-蒙脱石的X射线衍射结果表明,Cu2+、Cr3+通过离子交换作用进入了蒙脱石的层间.同一矿物对不同重金属离子也有不同的吸附容量蒙脱石Cr3+>Cu2+>Zn2+>Cd2+>Pb2+;高岭石Cr3+>Pb2+>Zn2+>Cu2+>Cd2+;伊利石Cr3+>Zn2+>Cd2+>Cu2+>Pb2+.  相似文献   

重金属离子在胡敏酸-高岭石复合体上的吸附   总被引：6，自引：0，他引：6  

何为红李福春  吴志强代静玉 刘本定 《岩石矿物学杂志》2007,26(4):359-365

本文研究了胡敏酸存在下高岭石对重金属离子的吸附行为。实验结果表明:①胡敏酸和Cu2 溶液按先后顺序或同时加入高岭石中反应,在Cu2 平衡浓度<10mg/L时,3种加入顺序对Cu2 的吸附量基本相同,当Cu2 平衡浓度>10mg/L时,(K Cu) HA和(K Cu HA)两种加入顺序对Cu2 的吸附量比(K HA) Cu的略大。②在pH=5时,胡敏酸-高岭石复合体对Cu2 的吸附量明显大于纯高岭石。这是由于胡敏酸含有大量的羧基和酚羟基等活性基团,吸附在高岭石上的胡敏酸增加了其表面吸附位,在复合体表面形成了S—HA—Cu三元配合物,且Cu2 的吸附量与复合体中胡敏酸的含量在一定范围内成正相关;③溶液pH值在4～7之间变化可调控复合体对Cu2 的吸附机制。④在Cu2 和Cd2 共存时,随着金属离子初始浓度的增大,Cu2 的吸附量呈直线上升,而Cd2 的吸附量增加缓慢,表明复合体对Cu2 的吸附能力比对Cd2 强。  相似文献   

有机酸对高岭石形成影响的模拟试验研究   总被引：2，自引：0，他引：2  

刘钦甫  丁述理 《煤田地质与勘探》1998,26(2):6-9

利用富里酸、胡敏酸和盐酸与天然矿物－长石、蒙脱石和云母在常温常压下进行反应,探讨矿物溶解及高岭石形成机理。实验表明富里酸对这些矿物具有较大的溶解能力,其原因是由于形成了具有较大溶解度和活动性的有机硅和有机铝复合体。在中性－碱性条件下有利于有机硅复合体的形成,酸性条件下有利于有机铝复合体的形成。在富里酸作用下,蒙脱石和云母分别在４个月和８个月有少量转化成高岭石,说明层状硅酸盐矿物比架状硅酸盐矿物更易  相似文献   

Mineralogy and major-element geochemistry of the lower Permian Greta Seam,Sydney Basin,Australia     

L. Zhao  C. R. Ward  D. French  I. T. Graham 《Australian Journal of Earth Sciences》2014,61(3):375-394

The mineralogy of the high-volatile bituminous coals and associated strata from the Greta seam, Sydney Basin, Australia, has been evaluated in this study. Although the seam is not immediately overlain by marine strata, percolation of marine water into the original peat bed is indicated by the petrological, mineralogical and geochemical characteristics, which resemble those of coals with marine roof strata. The upper and lower sections of the seam have contrasting mineralogy. Pyrite typically comprises 40 to 56 wt% of the mineral assemblage in the marine-influenced upper part of the seam section. The lower part contains much less pyrite (typically <5 wt%, organic-free basis), and also relatively abundant dawsonite (up to 14 wt%, organic-free basis). The minerals within most coal plies are largely of authigenic origin. These include pyrite, siderite, clay minerals (mainly kaolinite and Na-rich mixed-layer illite/smectite), and quartz, most of which have a relatively early, syngenetic origin. Minor Ti-bearing minerals, anatase or rutile, and phosphate minerals, fluorapatite and goyazite, were probably also formed during early diagenesis. Other minerals have features that indicate late-stage precipitation. These include abundant cleat- and fracture-filling dawsonite, which may be the result of reactions between earlier-precipitated kaolinite and Na₂CO₃- or NaHCO₃-bearing fluids. Minor albite may also be epigenetic, possibly precipitated from the same Ca–Al bearing fluids that formed the dawsonite. The most abundant detrital minerals in the Greta coals are quartz, poorly ordered kaolinite, illite and mixed-layer illite/smectite (I/S). These occur mainly in the floor, roof and other epiclastic horizons of the seam, reflecting periods of greater clastic influx into those parts of the original peat-forming environment. Detrital minerals are rare in the coals away from the epiclastic horizons, probably owing to almost complete sediment bypassing in the depositional system. Alternatively, any detrital minerals that were originally present may have been leached from the peat bed by diagenetic or post-diagenetic processes.  相似文献