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1.
The Al-Batin alluvial fan covers a broad area of southern Iraq. It was the main battlefield of two devastating wars in 1991 and 2003, during which huge amounts of depleted uranium (DU) were used. This study aims to assess the geochemistry of this fan sediment including the potential effects of the DU used. Sixty-three samples were collected from sediments including three samples from sediments under tanks attacked by DU ammunition. Major elements were measured by XRF (fusion bead method), whereas ICP-MS was used to measure the trace elements. The results suggest that the most dominant major minerals are in the order of: quartz?>?secondary gypsum?>?calcite?>?feldspar, clay minerals?>?iron oxide, and show abnormal concentrations of Sr, Cr, Ni, and V. This study also determined an area with high concentration of U in the north east part of the fan. Statistical analysis and spatial distribution of important elements suggests that two major factors affect mineral formation. The first factor reflects the influence of minerals in the source area of the sediments (Arabian Shield): quartz, carbonate, clay minerals, feldspars, as well as iron oxides and elevated concentrations of V, Ni, and Cr. The second factor points at authigenic formation of secondary gypsum and celestite and elevated U concentration under the control of a hot arid climate and the specific groundwater situation. However, the origin of the sediments is geogenic, while the anthropogenic impact seems to be minor. Spatial distribution of U and the 235/238U ratio did not show any peaks in the places where tanks have been destroyed. This is contrary to media speculations and some scientific reports about the permanent risks of DU in the area, which creates public concern about the potential risk of living in this area. 相似文献
2.
Adsorption, desorption and oxidation of arsenic affected by clay minerals and aging process 总被引：20，自引：0，他引：20
Adsorption/desorption and oxidation/reduction of arsenic at clay surfaces are very important to the natural attenuation of
arsenic in the subsurface environment. Although numerous studies have concluded that iron oxides have high affinities for
the adsorption of As(V), very little experimental work has addressed the arsenic attenuation capacities of different clay
minerals and aging process affecting the transformation of arsenic. The abundance of clay minerals in a variety of geochemical
environments and their influence on adsorption of contaminants suggests a need for more experimental work to characterize
the adsorption desorption, and oxidation of arsenic on clay minerals. In this investigation three types of clay mineral were
studied: the 1 : 1 layer clays [halloysite (IN), sedimentary M-kaolinite, and weathered EPK-kaolinite]; the 2 : 1 layer clays
[illite (MT) and illite/montmorillonite (MT)]; the 2 :>: 1 layer clay [chlorite (CA)]. The halloysite and the chlorite had
much greater As(V) adsorption (25–35 folds) than the other clay minerals. The clay minerals had lower As(III) adsorption than
As(V) adsorption, and the adsorption was affected by pH. Desorption of arsenic from the clay minerals was significantly influenced
by the aging process. The quantities of extractable As(III) and As(V) decreased with increasing aging time. The results demonstrated
that oxidation of As(III) to As(V) occurred on the clay surfaces, whereas reduction of As(V) to As(III) was not found in any
of the clay minerals studied. The oxidation of As(III) was affected by the types of clay and aging time.
Received: 22 March 1999 · Accepted: 15 April 1999 相似文献
3.
Microbial reduction of Fe(III) in clay minerals is an important process that affects properties of clay-rich materials and iron biogeochemical cycling in natural environments. Microbial reduction often ceases before all Fe(III) in clay minerals is exhausted. The factors causing the cessation are, however, not well understood. The objective of this study was to assess the role of biogenic Fe(II) in microbial reduction of Fe(III) in clay minerals nontronite, illite, and chlorite. Bioreduction experiments were performed in batch systems, where lactate was used as the sole electron donor, Fe(III) in clay minerals as the sole electron acceptor, and Shewanella putrefaciens CN32 as the mediator with and without an electron shuttle (AQDS). Our results showed that bioreduction activity ceased within two weeks with variable extents of bioreduction of structural Fe(III) in clay minerals. When fresh CN32 cells were added to old cultures (6 months), bioreduction resumed, and extents increased. Thus, cessation of Fe(III) bioreduction was not necessarily due to exhaustion of bioavailable Fe(III) in the mineral structure, but changes in cell physiology or solution chemistry, such as Fe(II) production during microbial reduction, may have inhibited the extent of bioreduction. To investigate the effect of Fe(II) inhibition on CN 32 reduction activity, a typical bioreduction process (consisting of lactate, clay, cells, and AQDS in a single tube) was separated into two steps: (1) AQDS was reduced by cells in the absence of clay; (2) Fe(III) in clays was reduced by biogenic AH2DS in the absence of cells. With this method, the extent of Fe(III) reduction increased by 45-233%, depending on the clay mineral involved. Transmission electron microscopy observation revealed a thick halo surrounding cell surfaces that most likely resulted from Fe(II) sorption/precipitation. Similarly, the inhibitory effect of Fe(II) sorbed onto clay surfaces was assessed by presorbing a certain amount of Fe(II) onto clay surfaces followed by AH2DS reduction of Fe(III). The reduction extent consistently decreased with an increasing amount of presorbed Fe(II). The relative reduction extent [i.e., the reduction extent normalized to that when the amount of presorbed Fe(II) was zero] was similar for all clay minerals studied and showed a systematic decrease with an increasing clay-presorbed Fe(II) concentration. These results suggest a similar inhibitory effect of clay-sorbed Fe(II) for different clay minerals. An equilibrium thermodynamic model was constructed with independently estimated parameters to evaluate whether the observed cessation of Fe(III) reduction by AH2DS was due to exhaustion of reaction free energy. Model-calculated reduction extents were, however, over 50% higher than experimentally measured, indicating that other factors, such as blockage of the electron transfer chain and mineralogy, restricted the reduction extent. Another important result of this study was the relative reducibility of Fe(III) in different clays: nontronite > chlorite > illite. This order was qualitatively consistent with the differences in the crystal structure and layer charge of these minerals. 相似文献
4.
5.
In this study a series of CH4 adsorption experiments on clay-rich rocks were conducted at 35 °C, 50 °C and 65 °C and at CH4 pressure up to 15 MPa under dry conditions. The clay-dominated rock samples used are fresh samples from quarries and mines. Samples are individually dominated by montmorillonite, kaolinite, illite, chlorite, and interstratified illite/smectite. The experimental results show that clay mineral type greatly affects CH4 sorption capacity under the experimental conditions. In terms of relative CH4 sorption capacity: montmorillonite ? illite/smectite mixed layer > kaolinite > chlorite > illite. Physisorption is the dominant process for CH4 absorption on clay minerals, as a result, there is a linear correlation between CH4 sorption capacity and BET surface area in these clay-mineral dominated rocks. The abundance of micro-mesopores in the size range of a few to a few 10 s of nanometers in montmorillonite clay and illite–smectite interstratified clay results in large BET surface area values for these mineral species. 相似文献
6.
Ni Shijun Luo Yutian Liu Lihua Wang Xuben Li Sue Luo Yangdi Han Dingrong 《中国地球化学学报》1994,13(3):193-201
This study focuses on the thermodynamics of diagenetic fluid from the Eogene Xingouzui Formation which represents the most
important reservoir in Field Oil T in the Jianghan Basin. The measured homogenization temperatures (110–139 °C) of fluid inclusions
in diagenetic minerals fell within the range of 67 –155 °C at the middle diagenetic stage. The pressure of diagenetic fluid
is estimated at 10.2 –56 MPa. The activity of ions in the fluid shows a tendency of Ca2+ > Mg2+ > Na+ > K+ > Fe3+ > Fe2+ for cations, and HCO
3
−
> SO
4
2−
> F− > Cl− > CO
3
2−
for anions. For the gaseous facies, there is a tendency of CO2> CO> H2S> CH4> H2. According to the thermodynamic calculations, the pH and Eh of the fluid are 5.86–6.47 and −0.73–−0.64V, respectively. As
a result of the interaction between such a diagenetic fluid and minerals in the sediments, feldspars were dissolved or alterated
by other minerals. The clay mineral kaolinite was instable and hence was replaced by illite and chloritoid.
This project was jointly funded by the National Natural Science Foundation of China (49133080) and the Open Laboratory of
Ore Deposit Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences. 相似文献
7.
Susana Serrano Peggy A. O’Day Maria Teresa García-González 《Geochimica et cosmochimica acta》2009,73(3):543-558
The bioavailability and fate of heavy metals in the environment are often controlled by sorption reactions on the reactive surfaces of soil minerals. We have developed a non-electrostatic equilibrium model (NEM) with both surface complexation and ion exchange reactions to describe the sorption of Pb and Cd in single- and binary-metal systems over a range of pH and metal concentration. Mineralogical and exchange properties of three different acidic soils were used to constrain surface reactions in the model and to estimate surface densities for sorption sites, rather than treating them as adjustable parameters. Soil heterogeneity was modeled with >FeOH and >SOH functional groups, representing Fe- and Al-oxyhydroxide minerals and phyllosilicate clay mineral edge sites, and two ion exchange sites (X− and Y−), representing clay mineral exchange. An optimization process was carried out using the entire experimental sorption data set to determine the binding constants for Pb and Cd surface complexation and ion exchange reactions.Modeling results showed that the adsorption of Pb and Cd was distributed between ion exchange sites at low pH values and specific adsorption sites at higher pH values, mainly associated with >FeOH sites. Modeling results confirmed the greater tendency of Cd to be retained on exchange sites compared to Pb, which had a higher affinity than Cd for specific adsorption on >FeOH sites. Lead retention on >FeOH occurred at lower pH than for Cd, suggesting that Pb sorbs to surface hydroxyl groups at pH values at which Cd interacts only with exchange sites. The results from the binary system (both Pb and Cd present) showed that Cd retained in >FeOH sites decreased significantly in the presence of Pb, while the occupancy of Pb in these sites did not change in the presence of Cd. As a consequence of this competition, Cd was shifted to ion exchange sites, where it competes with Pb and possibly Ca (from the background electrolyte). Sorption on >SOH functional groups increased with increasing pH but was small compared to >FeOH sites, with little difference between single- and binary-metal systems. Model reactions and conditional sorption constants for Pb and Cd sorption were tested on a fourth soil that was not used for model optimization. The same reactions and constants were used successfully without adjustment by estimating surface site concentrations from soil mineralogy. The model formulation developed in this study is applicable to acidic mineral soils with low organic matter content. Extension of the model to soils of different composition may require selection of surface reactions that account for differences in clay and oxide mineral composition and organic matter content. 相似文献
8.
《Applied Geochemistry》2004,19(11):1699-1709
One of the French options for the final disposal of high-level radioactive waste is a deep geological repository. The Callovo-Oxfordian formation in the Meuse and Haute-Marne (France) was proposed, by the French agency for the management of radioactive wastes (ANDRA), to be the site of a research laboratory in order to evaluate in situ the interaction between the host formation and the engineered barriers.In the previous experimental part, secondary minerals such as zeolites, tobermorite and katoite have been observed after the alteration of the Callovo-Oxfordian clay under alkaline conditions. Three different reactions of phyllosilicates alteration have been proposed as a function of both pH and chemical composition of the reacting solutions. The aim of this work was to simulate the reaction between the Callovo-Oxfordian clay and high-pH solutions in order to validate the proposed alteration reactions from experimental data.The thermodynamic modelling of stability relationships among minerals in the Callovo-Oxfordian clay was performed using the solution speciation solubility modelling code KINDIS at 120 °C for different chemical media (NaOH, KOH and Ca(OH)2). Input data were the mineralogical composition of the <2 μm fraction of Callovo-Oxfordian clay at nearly the same burial depth of the underground laboratory construction as well as the neoformed minerals observed after the experimental alteration of this clay (zeolites and cement phases). In the NaOH and KOH runs, anacime, phillipsite and chabazite, respectively were the first stable minerals which appeared at the beginning of modelling. In the Ca(OH)2 runs, oversaturated with respect to portlandite, katoite and then tobermorite were the first minerals occurring at the beginning of the alteration. Smectites and illites were undersaturated whatever the chemical composition. Both minerals and the interstratified illite-smectite were less stable in Ca(OH)2 than in NaOH and KOH solutions. Concerning the secondary minerals, a discussion is developed in order to improve modelling and to predict the long term reactions between clays and alkaline solutions. 相似文献
9.
Certain factors influencing the incorporation, transport and release of fatty acids by clay minerals, calcite and marine sediments have been investigated.Salinity was found to be an important factor. The adsorption of heptadecanoic acid by bentonite clay at 4%. was nearly triple that at 0%.. However, from 4%. to 35%., only a minor adsorption increase occurred. This behavior is believed to be related to flocculation of the clay at the lower salinity range. The pH over the range of 6.0–8.5 has a small influence on fatty acid-clay association, depressing it somewhat as the basicity increases.When the temperature of the fatty acid solution was increased from 0°C to 50°C, a decrease in adsorption on to clay was found. This effect may be due to increased water solubility of the acid at higher temperatures, since solubility is very important in controlling the degree of fatty acid-mineral interaction. Furthermore, apparent solubilization of fatty acids by indigenous dissolved organic matter in sea water reduces adsorption on to clay minerals.Based upon the heat of adsorption of ?14.6 kcal/mole, fatty acids are physically bound to clay minerals by weak van der Waals forces and hydrogen bonds.Bentonite and kaolinite were found to be the most adsorptive minerals investigated, followed in order by illite, montmorillonite and calcite. Sediments from Narragansett Bay were found to lie between illite and montmorillonite in adsorptive capacity after indigenous sediment organic matter had been removed. Sediment organic matter reduced fatty acid uptake by a factor of 1.6. 相似文献
10.
B. Gururaj J.P. Sharma A. Baldawa S.C.D. Arora N. Prasad A.K. Biswas 《International Journal of Mineral Processing》1983,11(4):285-302
Studies have been made on the separability of clay minerals such as kaolinite, illite and montmorillonite from hematite in dispersant-starch flocculant systems. The grossly different dispersibility of hematite from that of clay minerals aided separation by selective dispersion and flocculation. Moderate success has been achieved with a selectivity index nearing 4.0 (average recovery values around 80%).The studies have been extended to hematite recovery and clay rejection from the slimes of the Barsua iron ore washing plant owned by Rourkela Steel Plant, India. Limited success achieved in the starch selective flocculation method has been attributed to the difficulties associated with fine grain size, clay mineraloty and liberation.The ore exhibits the phenomenon of differential grinding. Hematite-rich coarser particles in the slime can be separated by differential settling in dispersant systems followed by selective flocculation in low-starch systems. 相似文献
11.
土体固化的核心问题之一就是使用适宜的固化剂固化黏土矿物。通过扫描电镜(SEM)、傅里叶红外光谱(FTIR)、X射线衍射(XRD)以及X射线光电子能谱(XPS)等试验方法,研究不同碱含量下碱激发地聚物固化的蒙脱石、伊利石和高岭土的微观结构、物质组成及物理化学反应过程,探究碱激发地聚物与黏土矿物之间的相互作用机理。研究结果表明:黏土矿物经碱激发地聚物固化后,由松散颗粒转变为块状致密结构;随着地聚物中碱含量的增加,Si、Al及Ca元素电子结合能下降;蒙脱石在衍射角为5°左右(001)峰形右移,层间距减小;蒙脱石吸附水含量减小,亲水能力下降,矿物活性被限制。 相似文献
12.
Neha Singh Ravi Prakash Singh Saumitra Mukherjee Kyle McDonald K. J. Reddy 《Environmental Earth Sciences》2014,72(1):111-118
A study was conducted to understand the hydrogeological processes dominating in the North 24 Parganas and South 24 Parganas based on representative 39 groundwater samples collected from selected area. The abundance of major ions was in the order of Ca2+ > Na+ > Mg2+ > K+ > Fe2+ for cations and HCO3 ? > PO4 3? > Cl? > SO4 2? > NO3 ? for anions. Piper trilinear diagram was plotted to understand the hydrochemical facies. Most of the samples are of Ca-HCO3 type. Based on conventional graphical plots for (Ca + Mg) vs. (SO4 + HCO3) and (Na + K) vs. Cl, it is interpreted that silicate weathering and ion exchange are the dominant processes within the study area. Previous studies have reported quartz, feldspar, illite, and chlorite clay minerals as the major mineral components obtained by the XRD analysis of sediments. Mineralogical investigations by SEM and EDX of aquifer materials have shown the occurrence of arsenic as coating on mineral grains in the silty clay as well as in the sandy layers. Excessive withdrawal of groundwater for irrigation and drinking purposes is responsible for fluctuation of the water table in the West Bengal. Aeration beneath the ground surface caused by fluctuation of the water table may lead to the formation of carbonic acid. Carbonic acid is responsible for the weathering of silicate minerals, and due to the formation of clay as a product of weathering, ion exchange also dominates in the area. These hydrogeological processes may be responsible for the release of arsenic into the groundwater of the study area, which is a part of North 24 Parganas and South 24 Parganas. 相似文献
13.
Michel Cathelineau Serge Fourcade Stephane Buschaert Davy Rousset Alain Meunier Marc Javoy 《Geochimica et cosmochimica acta》2004,68(11):2529-2542
Isotopic age determination of fluid events in basement fractures is of prime importance for the reconstruction of paleo-hydraulic regimes. However, material from fracture or wall-rock is not generally easily dated. In the case of fractures filled by minerals such as phyllosilicates, it can be expected that subsequent fluid circulation may cause partial alteration or recrystallization of the previous phyllosilicates, disturbing the isotope signature. Using a specific methodology, including the extraction process without contamination of the finest (<0.2 μm) authigenic fractions, identification of clay fractions by X-ray diffraction (XRD), scanning electron microscopy, and electron microprobe, analysis of stable isotope composition (D/H, δ18O) and K-Ar dating, fluid event ages can be estimated. This methodology was applied to the northwestern margin of the French Massif Central, where basinal brines have interacted with the sedimentary cover (infra-Toarcian formations) and the fractured Hercynian crystalline basement. During periods of unknown age, precipitates from brines sealed most basement fractures as carbonates, and a recrystallization of early Hercynian phengite (+chlorite) into illite and illite/smectite minerals occurred in the earlier fractures.XRD patterns show that the clay fraction is dominated by illite and ordered mixed-layer minerals having a relatively high amount of illite (I-S R3). In the shallowest samples beneath the paleo-surface, a late assemblage is identified as a mixture of I-S minerals, a part of them being characterized by significant amounts of swelling layers (I-S R0).The δD values of the clay fractions are fairly constant around −50 ± 10‰, but δ18O values of the same clay fractions display a wide range from 8‰ to 18‰ (SMOW). The study of the size fractions between 2 and 0.2 μm reveals a correlation between K-Ar ages and δ18O values, which cannot be related to a change in the relative amounts of clay minerals. Deep fractures (at depths of 570 and 923 m) are characterized by δ18O values around 10.3 ± 0.4‰ SMOW and old ages ranging from 253 to 272 Ma. The finest fractions (<0.2 μm) of clays located at shallow level (<300 m) beneath the paleo-surface yield the highest δ18O values (15.7-18.2‰) and the youngest K-Ar dates (188 to 198 Ma). These dates are likely to record the extensional episode and thermal anomaly related to the rifting of central Atlantic Ocean (c. 190 Ma). The other important thermal/extensional episode which affected the Aquitaine Basin, namely the opening of the Gascogne gulf at c. 120 Ma, is not detected by the K-Ar method on the clay fractions. We believe that resetting of clay-type K-Ar ages linked to recrystallization was favoured in the upper part of the basement where the ancient (Hercynian) clay minerals were destabilized by subaerial low-temperature alteration during Permo-Triassic times.From a methodologic point of view, the analytical characterization of several size fractions of clays from reactivated fractures, using both stable isotope geochemistry and K-Ar isotope geochemistry, can be considered as a powerful tool for dating fluid events when no suitable material for conventional methods is available. 相似文献
14.
Long-term behavior of lime-stabilized kaolinite clay 总被引：1，自引：1，他引：0
Clay soils create many problems for highway construction and they have to be replaced or improved by stabilization for satisfactory performance. Lime stabilization is a well-established technique to improve the performance of clays. Cementitious minerals form upon mixing of clay with lime causing an improvement in strength and durability. In the study, the changes in the microfabric of long-term cured lime-stabilized kaolinite clay using X-ray diffraction pattern, scanning electron microscope and unconfined compressive strength (UCS) is presented. Unconfined compression test samples at two different lime contents (4 and 12% by weight) were prepared and cured in a humidity room for long time curing. The UCS of pure kaolinite was originally 125 kPa, which increased to 1,015 kPa after 1 month and to 2,640 kPa (21 times the initial value) after 10 years for cured lime-stabilized kaolinite samples. Similar long-term strength increases were also observed for stabilized kaolinite with 12% lime. Calcium aluminate silicate hydrate minerals were detected in the structure of the kaolinite. This suggests pozzolanic reactions with lime stabilization may continue in the long-term for up to 10 years. 相似文献
15.
Kerogen has been artificially matured under “hydrous pyrolysis” conditions in the presence of various minerals in order to investigate the influence of the latter on the organic products. In addition to three clay minerals (montmorillonite, illite, kaolinite), calcium carbonate and limonite were also employed as inorganic substrates. Kerogen (Type II) isolated from the Kimmeridge Blackstone band was heated in the presence of water and a 20-fold excess of mineral phase at two different temperatures (280 and 330°C) for 72 hr. Control experiments were also carried out using kerogen and water only and kerogen under anhydrous conditions. This preliminary study describes the bulk composition of the pyrolysates with detailed analyses of the aliphatic hydrocarbon distributions being provided by gas chromatography and combined gas chromatography-mass spectrometry.In the 280°C experiments, considerably more organic-soluble pyrolysate (15% by weight of original kerogen) was produced when calcium carbonate was the inorganic phase. At 330°C, all samples generated much greater amounts of organic-soluble products with calcium carbonate again producing a large yield (40% wt/wt). Biomarker epimerisation reactions have also proceeded further in the 330°C pyrolysate formed in the presence of calcium carbonate than with other inorganic phases. Implications of these and other observations are discussed. 相似文献
16.
A centrifugal mill is a high-power intensity media mill that can be used for ultra-fine grinding, employing centrifugal forces generated by gyration of the axis of the mill tube in a circle. The mill charge motion is quite different depending on the ratio of the gyration diameter to the mill diameter (G / D ratio), varying from a motion similar to that of a conventional tumbling media mill to that of a vibration mill. In this study, a centrifugal mill was constructed with an arrangement where the gyration diameter could be readily adjusted. The batch grinding characteristics of three different minerals (limestone, talc and illite) in water with dispersing agent were investigated at various G / D ratios. It was found that the optimum G / D ratio in terms of the specific energy consumption to give a desired fineness of product was different for the three minerals. This was due to their different reactions to the breakage mechanisms provided by the mill charge motion at varying G / D ratios. The size distributions became progressively narrower at increased grinding times, and particles finer than about 0.1 μm were not detected even for prolonged grinding times. Measurement of specific surface areas indicated that this was not due to an artifact of the size measurements by laser diffractometry. This implies that there is a limitation in which particles finer than 0.1 μm are not produced under the conditions tested in this type of mill, but further investigation is needed for experimental verification of this limit of comminution. 相似文献
17.
《International Journal of Mineral Processing》2005,75(1-2):101-112
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
18.
从实际资料入手,深入分析煤层气水平井煤粉形成原因、煤粉产出规律及防治煤粉措施。分析结果表明:井壁原始应力状态改变、煤岩物质成分及组成、钻具的碾磨作用和钻遇煤层段井眼轨迹弯曲大煤层局部受到钻具挤压以及排采工作制度改变使降液速率变化大等是影响煤层气水平井煤粉形成的主要原因;黏土矿物是煤粉的主要来源,且黏土矿物含量越高,煤层出粉的可能性越大;排采早期产出的煤粉颗粒直径在几十微米到几百微米之间,粒径变化明显,表明排采早期产生的煤粉以钻具碾磨和井壁原始应力状态改变形成为主,排采后期产出的煤粉颗粒直径主要在几十微米左右,粒径分布相对均匀,表明排采后期产生的煤粉以煤层煤岩物质成分组成和排采工作制度变化影响形成为主;加强水平段循环清洗工作,优化合理的筛管缝隙尺寸、筛管直径、筛管长度等综合工艺技术,优选合适的排煤粉设备、制定合理的控煤粉排采制度等是煤层气水平井煤粉防治的主要措施。 相似文献
19.
骨架矿物—粘土矿物碱耗协同效应研究 总被引：2，自引：0，他引：2
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 相似文献
20.
Michael E. Bishop Ravi K. Kukkadapu Richard E. Edelmann 《Geochimica et cosmochimica acta》2011,75(18):5229-5246
99Technetium (99Tc) is a fission product of uranium-235 and plutonium-239 and poses a high environmental hazard due to its long half-life (t1/2 = 2.13 × 105 y), abundance in nuclear wastes, and environmental mobility under oxidizing conditions [i.e., Tc(VII)]. Under reducing conditions, Tc(VII) can be reduced to insoluble Tc(IV). Ferrous iron, either in aqueous form (Fe2+) or in mineral form [Fe(II)], has been used to reduce Tc(VII) to Tc(IV). However, the reactivity of Fe(II) from clay minerals, other than nontronite, toward immobilization of Tc(VII) and its role in retention of reduced Tc(IV) has not been investigated. In this study the reactivity of a suite of clay minerals toward Tc(VII) reduction and immobilization was evaluated. The clay minerals chosen for this study included five members in the smectite-illite (S-I) series, (montmorillonite, nontronite, rectorite, mixed layered I-S, and illite), chlorite, and palygorskite. Surface Fe-oxides were removed from these minerals with a modified dithionite-citrate-bicarbonate (DCB) procedure. The total structural Fe content of these clay minerals, after surface Fe-oxide removal, ranged from 0.7% to 30.4% by weight, and the structural Fe(III)/Fe(total) ratio ranged from 45% to 98%. X-ray diffraction (XRD) and Mössbauer spectroscopy results showed that after Fe oxide removal the clay minerals were free of Fe-oxides. Scanning electron microscopy (SEM) revealed that little dissolution occurred during the DCB treatment. Bioreduction experiments were performed in bicarbonate buffer (pH-7) with structural Fe(III) in the clay minerals as the sole electron acceptor, lactate as the sole electron donor, and Shewanella putrefaciens CN32 cells as a mediator. In select tubes, anthraquinone-2,6-disulfate (AQDS) was added as electron shuttle to facilitate electron transfer. In the S-I series, smectite (montmorillonite) was the most reducible (18% and 41% without and with AQDS, respectively) and illite the least (1% for both without and with AQDS). The extent and initial rate of bioreduction were positively correlated with the percent smectite in the S-I series (i.e., layer expandability). Fe(II) in the bioreduced clay minerals subsequently was used to reduce Tc(VII) to Tc(IV) in PIPES buffer. Similar to the trend of bioreduction, in the S-I series, reduced NAu-2 showed the highest reactivity toward Tc(VII), and reduced illite exhibited the least. The initial rate of Tc(VII) reduction, after normalization to clay and Fe(II) concentrations, was positively correlated with the percent smectite in the S-I series. Fe(II) in chlorite and palygorskite was also reactive toward Tc(VII) reduction. These data demonstrate that crystal chemical parameters (layer expandability, Fe and Fe(II) contents, and surface area, etc.) play important roles in controlling the extent and rate of bioreduction and the reactivity toward Tc(VII) reduction. Reduced Tc(IV) resides within clay mineral matrix, and this association could minimize any potential of reoxidation over long term. 相似文献