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1.
大气降尘矿物学特征研究具有重要的环境学意义。文章以华北理工大学校区采集样品为例,应用激光粒度分析仪、扫描电镜、X射线粉末衍射、电感耦合等离子体质谱等对河北省唐山市曹妃甸地区大气降尘矿物学特征进行了初步分析研究。结果表明,曹妃甸地区大气降尘粒径较粗,颗粒物包括块状、柱状、片状、球状及不规则粒状集合体,主要由石英、长石、石膏、云母、绿泥石、角闪石、白云石、方解石和赤铁矿等矿物组成;降尘样品中Cr、Cu、Zn、As、Cd、Pb等重金属元素含量均较高。研究分析表明,降尘样品中硅酸盐矿物主要源自地面扬尘,而石膏、方解石等碳酸盐矿物可能为环境中的次生矿物,样品中重金属污染主要来源于燃煤、工矿企业生产排放和少部分汽车尾气排放。  相似文献   

2.
Detailed chemical and mineralogical data are presented for 37 samples of surface sediments collected from the Kalloni gulf, (eastern half), Lesvos island, northern Greece. The sediments are largely carbonate-rich muds, though near the eastern and northern coast of the gulf higher proportions of biogenic and lithogenic sands and gravels occur. The main minerals are quartz, feldspar (andesine), clay minerals (montmorillonite, illite, Kaolinite) and the carbonate minerals (calcite, Mg-calcite, aragonite). The mathematical method of factor analysis was applied in order to explain the mineralogical and geochemical variations. These variations can be interpreted in terms of variations in provenance and depositional environment. Six factors were produced accounting for 83.6 % of the total data variance: (a) a Si-Al-Na-K-Ti-Rb-Ba-Y-Zr factor controlled by clays and detrital minerals such as feldspars and zircon opposed by a CaCO2-Cu-Sc-Sr-La association (carbonate, minerals), (b) an organic carbon factor (C-Fe-Ce-Zn-Rb-Ni-Y-Nb), (c) a Fe-Mg-Cr-Ni factor representing control by peridotite, (d) a Ce-Nd-Fe-Ni-Zn-La factor controlled by silicate minerals, (e) a Al-Fe-Ti-P-V factor controlled by chlorite amphiboles or pyroxenes of volcanic or basaltic intrusions, (f) a Mn-Fe-Zn-factor controlled by iron-manganese oxides. Similarities in trace element composition among Kalloni gulf bottom sediments, and source lithologies indicate that the trace elements are derived from the adjacent landmasses. The AI/Ti ratio of the sediments is consistent with the terrigenous nature of sendimentation in the Kalloni gulf.  相似文献   

3.
Limestone beds of the Late Cretaceous Abiod formation (Campanian-Maastrichtian system) are fundamentally important for the economic growth of the raw material sector in Tunisia. However, little attention has been paid to the detailed physical and chemical properties of the Abiod limestone. Nine limestone samples collected from the Abiod formation outcropping in the areas of Bizerte, Gafsa and Gabes, Tunisia, as well as their separated clay fractions, were characterized using different techniques, such as XRF, XRD, FTIR and TG/DTA. XRF showed the chemical composition of the limestone in which calcium carbonate was the main constituent, and silica, iron and magnesium were the impurities. XRD also confirmed the presence of small amounts of clay minerals and quartz along with sharp peaks of calcite. FTIR spectra indicated that the limestone was mainly composed of CaCO3 in the form of calcite, as identified by its main characteristic absorption bands. These data were in agreement with XRD and XRF analysis data. The TG/DTA curves of the limestone samples, showing a close similarity to that of pure calcium carbonate, exhibited an endothermic peak between 600 and 760°C, with the maximum near 750°C. Moreover, FTIR spectra of clay fraction samples indicated high silica content in some samples. Especially the samples SD1 and SD2 collected in the northern area showed higher amounts of silica compared with those of AS1, AS2, CHB, ZNC, SND, MKM and GBS collected from southern districts. However, among the latter seven samples, one could recognize two groups based on the clay mineral investigations: (1) limestone with minor amounts of smectite and mixed layer minerals of smectite/illite (AS1 and 2, CHB, ZNC, SND and GBS) and (2) limestone with smectite, kaolinite and apatite (SND and MKM). Differences in these mineralogical and chemical characteristics should be considered when limestone from the Abiod formation is utilized as a medium for heavy metal removal from wastewater.  相似文献   

4.
重质碳酸钙的白度和色相值(Lab)是最重要的工业指标,但影响因素尚不清楚。本文通过扫描电镜、粉晶X射线衍射(XRD)和电感耦合等离子体发射光谱(ICP-OES)等分析手段,对浙江衢州上方镇的重钙方解矿石进行了研究,以期阐明重质碳酸钙白度和色相的影响因素。结果表明,矿石随研磨粒度的减小白度逐渐增加,在100~400目,白度呈快速上升趋势,超过400目,白度的上升趋势减缓,直至几乎不变。相较于青相矿石,红相矿石的方解石结晶程度高、颗粒大且均匀,杂质较少,化学成分较纯。而Fe3+含量与重钙产品白度和L值呈负相关,与a、b值呈正相关关系。综合研究认为,致色元素(Fe)含量的高低和原矿石的杂质含量、结晶程度均可能为重钙色相差异的主要原因,建议在方解石矿工业勘查中将白度指标测试的粒径统一为400目(38μm)。  相似文献   

5.
This study deals with the effect of mechanical treatment, using vibrating mill, on the mineralogy and structure of apatite and associated gangue minerals (dolomite, calcite, quartz, pyrite and gypsum) in Abu-Tartour phosphate ore, Egypt. The evolution of mineralogy, crystallinity and deformation mechanism were evaluated with different techniques (XRD, DTA, TGA and FT-IR). Data obtained using these techniques give a good picture about the mechanochemical behavior of the different components in the ore. X-ray diffraction (XRD) indicated that the mineralogy has been changed quantitatively at short time grinding (30 min). After 45 min of grinding, the sample contained mainly carbonate apatite, quartz and pyrite. On the other hand, dolomite mineral disappeared, while calcite was partially transformed into aragonite. This transformation increased with increasing grinding time. Both Fourier Transform Infrared (FT-IR) and differential thermal analysis (DTA) analyses revealed that remarkable changes in the structural groups have occurred after 45 min of grinding. After 75 min of grinding, the carbonate in the apatite mineral partially decomposed and tricalcium phosphate formed instead. The formation of that simple form (tricalcium phosphate) may be another reason, besides surface area, for increasing the reactivity of phosphate ore by grinding. Scanning electron micrographs (SEM) revealed some idea about the grinding mechanisms of Abu-Tartour phosphate using vibrating mill. They indicate that the different minerals are ground differently. The apatite minerals are ground mostly by abrasion mechanism, while the carbonate minerals are ground mostly by compression. Also, these minerals are ground with different rates, where dolomite is ground faster than calcite, which are referred to the crystal lattice.  相似文献   

6.
《Quaternary Science Reviews》2007,26(19-21):2674-2683
To improve our understanding of the Late Pleistocene and Holocene carbonate system of the western Arabian Sea a high-resolution sedimentary record off Somalia has been analysed. The 15.26-m-long piston core 905 comprises a complete record of the last 90,000 years. We have measured concentrations of carbonate minerals, i.e., aragonite, calcite, Mg-calcite, and element ratios (Sr/Ca) together with pteropod counts and an estimation of the preservation state of pteropod shells to trace temporal changes in carbonate production and preservation.The Sr/Ca ratio shows strong similarities to the aragonite percentage and the δ18O record of the planktic foraminifer Neogloboquadrina dutertrei. High Sr/Ca ratios together with fragments of corals found in the coarse fraction indicate that most of the aragonite is of shallow water origin (high-Sr aragonite) and pteropods contribute much less than expected. High resuspensional input of shallow-marine aragonite occurs during sea-level highstands (interglacials) and low input during lowstands (glacials).The Mg-calcite concentration record resembles the whole pteropod abundance and pteropod shell preservation records confirming the use of Mg-calcite in combination with pteropod preservation proxies to reconstruct past fluctuations in carbonate dissolution. Preservation of aragonite and Mg-calcite increases during stadials, H-equivalents, YD and late Marine Isotope Stage (MIS) 3. During late MIS 5/early MIS 4 and in the Late Holocene absence of few pteropods as well as low Mg-calcite weight percentages point to strong dissolution of aragonite and Mg-calcite.  相似文献   

7.
A 3 km long lateral facies transition from Oligo-Miocene skeletal grainstones into packstones and mudstones displays systematic variation in carbonate skeletal fragment alteration and secondary carbonate mineral composition. Within the skeletal grainstone end-member all aragonitic grains have dissolved, all Mg-calcite skeletal fragments have altered to calcite, and calcite has been precipitated as both void-filling spar and as syntaxial overgrowths on echinoid fragments. Within the transitional grainstone-packstone lithologies some skeletal fragments show preservation of their original mineralogy, while calcite, ferroan calcite spar and dolomite have precipitated in void spaces. Within the packstone-mudstone end-member of the transition, aragonitic grains have been preserved and Mg-calcite skeletal fragments have retained most of their magnesium. Thin, originally porous grainstone layers within the pack-stone-mudstones contain sideroplesite and ferroan calcite spar in void spaces, and iron has been incorporated in skeletal fragments which were originally Mg-calcite. In these grains iron has been incorporated at the expense of magnesium until the grains approach the composition of the surrounding ferroan calcite cement. The lateral variation in diagenetic alteration across this facies transition is a function of differing groundwater movement and composition, controlled ultimately by the composition, porosity and permeability of the host lithologies.  相似文献   

8.
The geochemical processes and thermodynamic behavior of dissolved and precipitated carbonate minerals controlling the hydrochemistry of an aquifer in the seawater/freshwater mixing zone of a small island are identified. Field and laboratory analyses, geochemical modeling (PHREEQC) and multivariate statistical analysis (MSA) provide a quantitative interpretation for the geochemistry of the carbonate-dominated aquifer. Geochemical analyses and modeling results show that dissolution and re-precipitation of CaCO3 are the prevalent processes governing geochemical reactions in the mixing zone. Furthermore, this was confirmed by coherent statistical output that incorporates Principle Component Analysis (PCA) and k-means Cluster Analysis (k-CA). Generally, the composition of the lowland sandy soil was rather homogeneous and was primarily composed of quartz, aragonite, calcite and Mg-calcite. Thermodynamic model calculations indicate that the carbonate minerals calcite, aragonite and dolomite are supersaturated in the mixing zone. Nevertheless, Powder X-ray Diffraction (PXRD) and Scanning Electron Microscope (SEM) examination verified the occurrence of low-Mg-calcite (LMC) and the absence of dolomite, attributed to thermodynamic/kinetic hindrance, cation disorder and the presence of dolomite crystal growth rate inhibitors (such as SO4). The results suggest that dissolution of aragonite and precipitation of LMC drives the solid phase geochemistry in the small tropical island aquifer.  相似文献   

9.
A preliminary mineralogical/geochemical investigation of low-rank coals from Leicestershire, England, has been carried out with a view to their future beneficiation. Analytical scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) have been used to identify and assess the distribution of mineral phases likely to give corrosion-producing or slag-forming materials during combustion, and those minerals which would be potentially valuable by-products of beneficiation processes. Differences in the mineral petrography of borehole samples from the Vale of Belvoir Prospect and coal from Bagworth Colliery are compared. Samples from both areas contain substantial amounts of epigenetic minerals: calcite, dolomite, kaolinite and fluor-apatite are important phases in the Bagworth sample, whilst gypsum, illite, quartz, kaolinite, barytocelestine, pyrite, chalcopyrite, anatase, galena and sphalerite occur in the Vale of Belvoir samples. Whereas the presence of halides in the Bagworth coal would seem to be a possible source of boiler-corrosion problems, the major undesirable characteristic of the Vale of Belvoir coal is the presence of significant amounts of metal sulphides. However, extraction of sulphides from this coal prior to combustion could provide a valuable source of metals as a by-product. Certain trace element concentrations in the Vale of Belvoir samples have also been determined by instrumental neutron activation analysis (INAA) and higher levels of lanthanide elements are present in the whole coal relative to mineral veins (mainly gypsum). Trace-element signatures may provide a useful distinction between syngenetic and epigenetic mineral formation.  相似文献   

10.
Sedimentary phosphates contain-besides the phosphate minerals-, various associated gangue minerals such as: clays, silica, calcareous minerals (mainly calcite and dolomite), carbonaceous matter, iron oxides and/or pyrite. The common practiced flow-sheets for concentrating these types of phosphate ores consist of a combination of various mineral processing units such as: crushing and screening, attrition, washing, magnetic separation, and/or flotation. However, none of these combinations was successfully efficient to upgrade the calcareous ores because of the close similarity of the physical properties (density, particle size, particle shape, etc.) as well as the surface physico-chemical properties of the carbonate and phosphate minerals. For the last five decades extensive efforts have been spent to adopt flotation for separating carbonates from phosphate ores. These efforts include thermodynamic analysis, modification of the technique, controlling the pulp environment, and finding new reagents that can specifically differentiate between carbonates and phosphates.This paper reviews some of the published work on the separation of carbonates from phosphate ores by flotation and presents the flotation results of phosphate ore samples different in their physical properties and mineralogical composition. The results obtained reflect the effect of ore nature on the flotation performance and the reagents consumption.  相似文献   

11.
Comparison of Upper Guadalupian fore-reef, reef and back-reef strata from outcrops in the Guadalupe Mountains with equivalent subsurface cores from the northern and eastern margins of the Delaware Basin indicates that extensive evaporite diagenesis has occurred in both areas. In both surface and subsurface sections, the original sediments were extensively dolomitized and most primary and secondary porosity was filled with anhydrite. These evaporites were emplaced by reflux of evaporitic fluids from shelf settings through solution-enlarged fractures and karstic sink holes into the underlying strata. Outcrop areas today, however, contain no preserved evaporites in reef and fore-reef sections and only partial remnants of evaporites are retained in back-reef settings. In their place, these rocks contain minor silica, very large volumes of coarse sparry calcite and some secondary porosity. The replacement minerals locally form pseudomorphs of their evaporite precursors and, less commonly, contain solid anhydrite inclusions. Some silicification, dissolution of anhydrite and conversion of anhydrite to gypsum have occurred in these strata where they are still buried at depths in excess of 1 km; however, no calcite replacements were noted from any subsurface core samples. Subsurface alteration has also led to the widespread, late-stage development of large- and small-scale dissolution breccias. The restriction of calcite cements to very near-surface sections, petrographic evidence that the calcites post-date hydrocarbon emplacement, and the highly variable but generally ‘light’carbon and oxygen isotopic signatures of the spars all indicate that calcite precipitation is a very late diagenetic (telogenetic) phenomenon. Evaporite dissolution and calcitization reactions have only taken place where Permian strata were flushed with meteoric fluids as a consequence of Tertiary uplift, tilting and breaching of regional hydrological seals. A typical sequence of alteration involves initial corrosion of anhydrite, one or more stages of hydration/dehydration during conversion to gypsum, dissolution of gypsum and precipitation of sparry calcite. Such evaporite dissolution and replacement processes are probably continuing today in near-outcrop as well as deeper settings. This study emphasizes the potential importance of telogenetic processes in evaporite diagenesis and in the precipitation of carbonate cements. The extensive mineralogical and petrophysical transformations which these strata have undergone during their uplift indicates that considerable caution must be exercised in using surface exposures to interpret subsurface reservoir parameters in evaporitic carbonate rocks.  相似文献   

12.
X射线粉晶衍射仪在大理岩鉴定与分类中的应用   总被引：2，自引：2，他引：0  
大理岩主要有方解石大理岩、白云石大理岩和菱镁矿大理岩三种。以往大理岩是依据偏光显微镜下观察岩石结构构造及矿物成分进行分类定名,由于方解石、白云石、菱镁矿都属于三方晶系,具有闪突起、高级白干涉色、一轴晶负光性和菱形解理等相同晶体光学特征,偏光显微镜下区分十分困难。为了准确鉴定大理岩中碳酸盐矿物种类及其相对含量,本文利用岩石薄片偏光显微镜和X射线粉晶衍射技术对32件大理岩岩石样品进行分析测试。岩石薄片鉴定结果表明:大理岩造岩矿物主要有方解石、白云石、菱镁矿、石英、斜长石、白云母、黑云母、绿泥石、黏土和金属矿物。根据岩石结构构造及矿物组分特征,可把32件大理岩样品划分为方解石大理岩、长英质方解石大理岩、石英绿泥白云石大理岩、白云石大理岩、云英质白云石大理岩和菱镁矿大理岩等15个类型。X射线粉晶衍射分析表明:大理岩造岩矿物主要有方解石、白云石、菱镁矿、石英、斜长石、钾长石、云母、绿泥石、滑石和蒙脱石。综合分析认为:岩石薄片偏光显微镜鉴定技术很难区分方解石、白云石和菱镁矿等碳酸盐矿物,以及细小的石英、钾长石和斜长石、滑石和白云母等鳞片状硅酸盐矿物;X射线粉晶衍射分析技术不仅能准确检测出大理岩中方解石、白云石和菱镁矿等碳酸盐矿物种类及相对含量(方解石、白云石和菱镁矿的X射线衍射主峰有明显差异,d值分别为0.303 nm、0.288 nm和0.274 nm),而且能够有效鉴别岩石中粉砂级斜长石、钾长石与石英(三种矿物的X射线衍射主峰d值分别为0.319 nm、0.324 nm、0.334 nm);且能区分蒙脱石、绿泥石、云母和滑石等层状硅酸盐矿物(四种硅酸盐矿物的X射线衍射主峰d值分别为1.400 nm、0.705 nm、0.989 nm、0.938 nm)。综合岩石薄片偏光显微镜鉴定和X射线粉晶衍射分析结果,最终确定32件大理岩样品划分为22个岩石类型。研究认为:仅根据岩石薄片偏光显微镜鉴定或X射线粉晶衍射技术其中一种方法不能准确鉴定大理岩岩石,应将大理岩岩石野外观察、岩石薄片鉴定和X射线粉晶衍射技术结合起来,才能准确确定大理岩岩石类型。  相似文献   

13.
西沙群岛琛航岛碳酸盐沉积物X射线定量分析方法研究   总被引：1，自引：0，他引：1  
曲高生 《矿物学报》1990,10(4):360-369
利用X射线衍射分析技术测定碳酸盐沉积物中的矿物成分及其含量是目前研究碳酸盐最有效的方法。本文根据西沙琛航岛碳酸盐矿物组成的具体情况采用了“自清洗法”,用峰值强度测定方解石、白云石、文石和石英的含量,用方解石特征峰所在位置确定其MgCO_3含量,对西沙琛航岛碳酸盐沉积物进行了比较全面的定量分析测定,取得了较好的效果,从而对西沙群岛第四纪礁相沉积作用、白云岩化作用、地球化学、年代学、地层学等问题的解决提供了有价值的资料。  相似文献   

14.
兰州市取暖期可吸入颗粒物中单颗粒矿物组成特征   总被引：1，自引：1，他引：1  
为研究兰州市2005年冬季大气可吸入颗粒物(PM10)中单颗粒的矿物组成,用能谱扫描电镜识别和统计了兰州市区(东方红广场)和郊区(榆中县)两个采样点的单矿物颗粒。结果在市区样品中识别出方解石、伊/蒙混层、石英、斜长石、伊利石、石膏、绿泥石、高岭石、浊沸石和钾长石等21种矿物,前7种占统计总量的75%以上;郊区样品中识别出20种矿物,以方解石、石英、伊利石、绿泥石、斜长石和伊/蒙混层为主(占70%以上),与市区相比缺少钾石膏、金红石和水铝酸钙而增加了硫酸镁和磷灰石。总体来看,大气PM10中的矿物颗粒可分为粘土类、长石类、碳酸盐类、硫酸盐类、氧化物类和其他六类,以粘土类和碳酸盐类矿物为主(约占60%);冬季市区颗粒物表面的“硫化”现象较郊区严重;这些矿物颗粒主要来自地表土,人为排放和大气中二次化学反应生成的矿物的贡献较小。  相似文献   

15.
海南岛全新世海滩岩   总被引：16，自引：0，他引：16       下载免费PDF全文
在海南岛及邻近小岛沿岸,往往可以发现现代潮间带海滩上的砂砾石沉积物已被胶结成岩的现象。同样,全新世中、晚期形成的各种类型的滨海相沉积物,也经常程度不同地胶结起来了。  相似文献   

16.
The most ubiquitous syn-sedimentary cements affecting Mururoa atoll are composed of magnesian calcite. Three main types are distinguished: fibrous, bladed and sparitic on the basis of petrography, morphology and MgCO3 concentration of the constituting crystals, while peloid infills, a particular form of HMC chemical precipitation, also exist. Petrographic evidence and isotopic signatures are compatible with marine precipitation. Mururoa atoll was exposed several times to meteoric diagenesis resulting in varied diagenetic alterations including selective dissolution and partial dolomitization of Mg-calcite cements. These alterations are responsible for substantial modifications of the initial cement fabrics and may introduce unconformities in the diagenetic chronology. The first stage of the partial dissolution of Mg-calcite induces the development of chalky, white friable zones within the initially crystalline, hard cement layers. At ultrascale, this is due to the creation of micro-voids along the elongate cement fibres. Advanced dissolution includes total disappearance of cement portions as attested to by large voids within the cement crust and/or between superposed cement layers. Mg-calcite dissolution is related to meteoric diagenesis during periods of Quaternary exposure. The creation of voids within Mg-calcite layers is due to the mechanical removal of previously altered calcium carbonate, a process suggesting marine or non-marine water flow, probably in the vadose environment. Selective dolomitization of Mururoa cements involves alternations of calcite and dolomite which form successive cement-like rinds within primary cavities. At Mururoa, these alternations are the result of selective dolomitization of the pre-existing Mg-calcite cements rather than successive precipitation of calcite and dolomite. Selective dolomitization of Mg-calcite cements at Mururoa indicates that a given cement succession is not necessarily a simple chronological sequence. Oxygen isotope values of dolomites are enriched in δ186 by about 3‰ PDB within calcite-dolomite pseudo-alternations. The dolomitizing fluid at Mururoa seems similar to present marine water although some mixture with meteoric water is probable to favour dissolution associated with dolomitization.  相似文献   

17.
Visible to infrared reflectance spectroscopic analyses (0.3-25 micromoles) have been performed on sediments from the Dry Valleys region of Antarctica. Sample characterization for these sediments includes extensive geochemical analyses and X-ray diffraction (XRD). The reflectance spectra and XRD indicate major amounts of quartz, feldspar, and pyroxene in these samples and lesser amounts of carbonate, mica, chlorite, amphibole, illite, smectite, and organic matter. Calcite is the primary form of carbonate present in these Lake Hoare sediments based on the elemental abundances and spectroscopic features. The particle size distribution of the major and secondary components influences their detection in mixtures and this sensitivity to particle size is manifested differently in the "volume scattering" and "surface scattering" infrared regions. The Christiansen feature lies between these two spectral regimes and is influenced by the spectral properties of both regions. For these mixtures the Christiansen feature was found to be dependent on physical parameters, such as particle size and sample texture, as well as the mineralogy. Semiquantitative spectroscopic detection of calcite and organic material has been tested in these quartz- and feldspar-rich sediments. The relative spectral band depths due to organics and calcite correlate in general with the wt% C from organic matter and carbonate. The amounts of organic matter and carbonate present correlate with high Br and U abundances and high Ca and Sr abundances, respectively. Variation in the elemental abundances was overall minimal, which is consistent with a common sedimentary origin for the forty-two samples studied here from Lake Hoare.  相似文献   

18.
The aim of this study is to characterize the pedogenic clay minerals by using simple approach: mixing mineralogical and geochemical findings.The fine clay fractions (< 0.1 μm) of a Vertic Cambisol profile were studied by means of X-ray diffraction (XRD), infrared spectroscopy (FTIR) and cation exchange capacity (CEC).Qualitative and quantitative mineralogical compositions of the clay mixture were determined.Moreover, chemical equilibria and thermodynamic stabilities of minerals (calcite, gypsum, kaolinite, smectites and illites) were studied using results of ionic activities obtained from total concentration of various aqueous species in water extracts from soil-saturated pastes.XRD analysis shows a good homogeneity in the mineralogical composition of the soil material, with depth of soil profiles. The identified clay minerals are mainly illite–smectite mixed layers (I/S) and kaolinite. The chemical analysis of saturated paste extracts with clay minerals shows a slight undersaturation of the illitic phase while smectites and also calcite and gypsum reach the thermodynamic equilibrium along the soil profile.  相似文献   

19.
为了查明火山碎屑岩中自生碳酸盐矿物的分布特征及对储层物性的影响,以海拉尔盆地贝尔凹陷火山碎屑岩为研究对象,调查火山碎屑岩中自生碳酸盐矿物的类型,并通过统计50余口探井的碳酸盐含量及储层物性数据,探讨其分布特征及对储层物性的影响。结果表明：海拉尔盆地贝尔凹陷火山碎屑岩中自生碳酸盐矿物主要为方解石和白云石,其次为菱铁矿、片钠铝石和铁白云石;纵向上随着埋藏深度增加出现两个碳酸盐含量高值带,分别出现在1 500～1 900m和2 200～2 700m深度,前者主要为以胶结作用为主的连生方解石和显晶方解石及菱铁矿,后者主要为以交代作用为主的晚期方解石、白云石、铁白云石和片钠铝石;湖底扇等分选较差的沉积相为碳酸盐矿物发育的有利相带,扇-辫状河三角洲相为次有利相带;靠近德尔布干深大断裂的井碳酸盐含量要高于远离该断裂的井,且在该断裂附近的德2、德6和德8等井中见片钠铝石自生矿物,这主要因为断层是CO2逸散的通道,断层处的富CO2流体能够与围岩反应生成碳酸盐矿物;熔结凝灰岩和凝灰岩中的碳酸盐矿物含量要高于沉凝灰岩、凝灰质砂岩及普通砂岩,这主要因为火山岩及火山碎屑物质中金属离子含量高,易于释放,从而结合CO23-形成碳酸盐矿物;贝尔凹陷内储层孔隙度和渗透率等参数与碳酸盐含量呈负相关关系,说明碳酸盐含量对储层物性主要起破坏作用。  相似文献   

20.
Constructed wetlands can be a low-cost, ecologically based technology to locally treat domestic wastewater prior to discharge. Wetland systems implemented in the resort village of Akumal in the state of Quintana Roo, in the Yucatan Peninsula of Mexico have been considered moderately successful over approximately 10 years of operation. Yet the wide-scale implementation of constructed wetlands has not occurred in the region nor throughout Mexico due largely to the cost of the crushed aggregate used in these systems. Variation in the geotechnical and mineralogical properties of 29 samples of local calcareous beach sands collected from the tourist areas of Akumal and Tulum in the Yucatan, Mexico were analyzed and compared to those of crushed aggregate currently used in constructed wetland systems in Akumal. Powder X-ray diffraction on beach sand samples from Akumal and Tulum indicates that the proportion of aragonite varies from 24 to 84%, calcite varies from 7 to 38% and Mg-calcite varied from 8 to 57% compared to crushed aggregate which consists of 0–25% aragonite and 75–100% calcite. Compared to crushed aggregate beach sands are unimodal and have better uniformity coefficients, making them a better geotechnical choice than crushed sands with respect to these properties. Grain-size of the beach sands is much smaller compared to that of the crushed aggregate currently used in the constructed wetland systems in Akumal which should enhance the efficiency of the filtration of organic matter and bacteria. The average hydraulic conductivity measurements of 0.010 and 0.016 cm/s for beach sands from Akumal and Tulum, respectively are comparable or less than the average of 0.016 cm/s for crushed aggregate currently used in engineered wetland systems. Yet a combination of high bulk porosity, intragranular pores, and the presence of Mg-calcite observed in beach sands may likely result in higher dissolution rates versus the crushed aggregate. Preliminary assessment suggests that the use of local sand may be a technical, economic, and perceptual enhancement to the systems. Still a careful and thorough analysis of the potential environmental and aesthetic impacts of mining beach sands is necessary.  相似文献   

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