Preparation of strontium ferrite from strontium residue   总被引：1，自引：0，他引：1  

Chenglun Liu  Longjun Xu  Xueyan Yang  Tiefeng Peng  Jianjun Ren 《中国地球化学学报》2012,31(1):74-77

Strontium ferrite was prepared from Strontium Waste Residue (SWR) as a material. Strontium chloride was obtained by leaching SWR with ammonia chloride, and then SrCl2 was converted to SrCO3. Strontium ferrite (SrFe12O19) was formed by roasting the mixture of SrCO3 and FeCl3 in a proper proportion. The structure and magnetic susceptibility of strontium ferrite were investi-gated. The results showed that strontium conversion ratio increased with decreasing SWR grain diameter. The largest ratio was pre-sented when n(NH4Cl/Sr) was 3.6. What is more, the conversion process coincided with the kinetic characteristics of fractal reaction. The magnetic susceptibility of strontium ferrite decreased with increasing Fe3+/Sr2+ mole ratio and pH. SrFe12O19 exhibited face-centered and cubic closely-packed hexagonal structures. There were the strong diffraction peaks of Fe2O3 in the X-ray diffracto-gram of strontium ferrite. Strontium recovery ratio was 87.0%.  相似文献   

Surface complexation model for strontium sorption to amorphous silica and goethite     

Susan A Carroll  Sarah K Roberts  Louise J Criscenti  Peggy A O'Day 《Geochemical transactions》2008,9(1):2

Strontium sorption to amorphous silica and goethite was measured as a function of pH and dissolved strontium and carbonate concentrations at 25°C. Strontium sorption gradually increases from 0 to 100% from pH 6 to 10 for both phases and requires multiple outer-sphere surface complexes to fit the data. All data are modeled using the triple layer model and the site-occupancy standard state; unless stated otherwise all strontium complexes are mononuclear. Strontium sorption to amorphous silica in the presence and absence of dissolved carbonate can be fit with tetradentate Sr²⁺ and SrOH⁺ complexes on the β-plane and a monodentate Sr²⁺complex on the diffuse plane to account for strontium sorption at low ionic strength. Strontium sorption to goethite in the absence of dissolved carbonate can be fit with monodentate and tetradentate SrOH⁺ complexes and a tetradentate binuclear Sr²⁺ species on the β-plane. The binuclear complex is needed to account for enhanced sorption at hgh strontium surface loadings. In the presence of dissolved carbonate additional monodentate Sr²⁺ and SrOH⁺ carbonate surface complexes on the β-plane are needed to fit strontium sorption to goethite. Modeling strontium sorption as outer-sphere complexes is consistent with quantitative analysis of extended X-ray absorption fine structure (EXAFS) on selected sorption samples that show a single first shell of oxygen atoms around strontium indicating hydrated surface complexes at the amorphous silica and goethite surfaces.  相似文献   

Full-Sized Pore Structure and Fractal Characteristics of Marine-Continental Transitional Shale: A Case Study in Qinshui Basin,North China     

YIN Liangliang  GUO Shaobin 《《地质学报》英文版》2019,93(3):675-691

Based on 10 shale samples collected from 4 wells in Qinshui Basin,we investigate the full-sized pore structure and fractal characteristics of Marine-Continental transitional shale by performing organic geochemistry,mineralogical composition,Nitrogen gas adsorption(N_2 adsorption)and Nuclear Magnetic Resonance(NMR)measurements and fractal analysis.Results show that the TOC content of the shale samples is relatively high,with an average value of 2.44wt%,and the thermal evolution is during the mature-over mature stage.The NMR T_2 spectrum can be used to characterize the fullsized pore structure characteristics of shale.By combining N_2 adsorption pore structure parameters and NMR T_2 spectrums,the surface relaxivity of samples are calculated to be between 1.7877 um/s and 5.2272 um/s.On this basis,the T_2 spectrums are converted to full-sized pore volume and surface area distribution curves.The statistics show that the pore volume is mainly provided by mesopore,followed by micropore,and the average percentages are 65.04%and 30.83%respectively;the surface area is mainly provided by micropore,followed by mesopore,and the average percentages are 60.8004%and39.137%respectively;macropore contributes little to pore volume and surface area.The pore structure characteristics of shale have no relationship with TOC,but strong relationships with clay minerals content.NMR fractal dimensions D_(micro) and D_(meso) have strong positive relationships with the N_2 adsorption fractal dimensions D_1 and D_2 respectively,indicating that D_(micro) can be used to characterize the fractal characteristics of pore surface,and D_(meso) can be used to characterize the fractal characteristics of pore structure.The shale surface relaxivity is controlled by multiple factors.The increasing of clay mineral content,pore surface area,pore surface fractal dimension and the decreasing of average pore size,will all lead to the decreasing of shale surface relaxivity.  相似文献   

利用SAXS表征不同变质程度煤纳米孔隙特征          下载免费PDF全文

刘阳  姚素平  汤中一 《高校地质学报》2019,25(1):108

文章通过小角X 射线散射（SAXS） 的方法研究了自然演化系列不同煤级煤的纳米孔隙结构和分布特征。结果表明, 随着煤级的增高,孔隙表面分形呈多阶段变化： Ro＜0.89%,壳质组开始逐渐液化,发育大量孔隙,分形维数不断增大; Ro 为0.9%~1.5%,因挥发分生油充填孔隙和原油沥青的芳构化等作用,而使微孔表面平整光滑,分形维数减小;Ro 为1.5% ~3.5%,镜质组裂解生气发育了大量纳米孔隙,分形维数再次增大;随后逐渐石墨化,表面分形再次降低。煤中纳米级孔 隙主要集中在50~100 nm 范围内。其中细介孔（2~10 nm） 体积百分比占0.21%~3.12%,中介孔（10~25 nm） 体积百分比占 5.06%~11.28%,粗介孔（25~50 nm） 体积百分比占21.06%~26.36%,大孔（50~100 nm） 所占体积百分比最大,高达 64.63%~68.36%。随着煤级升高,煤样的最可几孔径不断减小,最可几孔径由80 nm 减小到10 nm,减小的速度由缓到快; 中介孔和细介孔体积百分比不断增大,与成熟度分别呈对数和线性关系;粗介孔和大孔百分比不断减少,与成熟度呈对数 关系。最可几孔径变化也十分明显,在低煤化烟煤阶段时,随煤化程度增高最可几孔径略有下降（峰值处的孔径范围在 75~71 nm 内）,中高煤化烟煤阶段时,随煤化程度的增高最可几孔径呈较明显的下降趋势（峰值处的孔径范围在78~53 nm 内）,到无烟煤阶段时,其孔径则快速下降（峰值处的孔径范围在72~9 nm）。  相似文献   

Hydrologic Dynamics of a Subtropical Estuary Using Geochemical Tracers,Celestún,Yucatan, Mexico     

Jeremy C. Stalker  Rene M. Price  Victor H. Rivera-Monroy  Jorge Herrera-Silveira  Sara Morales  Jorge A. Benitez  David Alonzo-Parra 《Estuaries and Coasts》2014,37(6):1376-1387

Oxygen isotopes and strontium concentrations were used as geochemical tracers to discern the sources of water to Celestún Lagoon, a small subtropical estuary on the western side of the Yucatán Peninsula of Mexico. Celestún Lagoon is underlain by karstified limestone with numerous locations where groundwater is observed discharging directly to the lagoon. In this study, samples of groundwater, lagoon surface water, and seawater (SW) were collected in April 2008 and June 2009 and analyzed for salinity, stable isotopes of oxygen, and strontium (Sr²⁺) concentrations. These geochemical tracers were used in two tertiary mixing models to calculate the relative ratio inputs of fresh groundwater, brackish groundwater, and SW to the lagoon. Two sources of groundwater were found to contribute to the surface water in the lagoon; one fresh and the other brackish with an average salinity of 19 psu. The fresh groundwater had an oxygen isotopic signature (δ¹⁸O) and strontium concentration (Sr²⁺) of δ¹⁸O?=?-3.30‰ and Sr²⁺?=?0.03 mmol/l, respectively. The brackish groundwater observed in the northern end of the lagoon add a dissimilar oxygen isotopic signature and Sr²⁺ concentration of δ¹⁸O?=?3.01‰ and Sr²⁺?=?0.12 mmol/l, respectively. Local SW had an isotopic oxygen signature and Sr²⁺ concentration between the two fresher sources (δ¹⁸O?=?1.40‰, Sr²⁺?=?0.09 mmol/l). The lagoonwide results of the two tracer mixing models (δ¹⁸O and Sr²⁺) agreed well (within 5 %) and indicated a ratio of brackish groundwater–fresh groundwater– SW of 31 %–26 %–43 % (±5 %) for the Sr²⁺ model and 35 %–25 %–40 % (± 5 %) for the δ¹⁸O model. Brackish groundwater is dominant in the northern portion of the lagoon, while SW dominates the southern portion. Fresh groundwater discharge is a significant contributor of water along the entire eastern boundary of the lagoon where mangrove forests are the dominant vegetation.  相似文献   

利用FE-SEM、HIP、N₂吸附实验表征生物气化煤系有机岩储层微观孔隙结构演化          下载免费PDF全文

王超勇  鲍园  琚宜文 《地球科学》2020,45(1):251-262

微生物降解前后的煤系有机岩（煤岩和泥页岩）储层微观孔隙结构的变化对生物成气和成藏过程具有重要的意义.利用场发射扫描电子显微镜、高压压汞仪、孔比表面积孔隙度分析仪以及分形维数理论对厌氧微生物降解前后的煤系有机岩样品储层孔隙结构演化进行分析,根据孔隙结构特征并结合微生物生态学特征,将生物气化煤系有机岩的孔隙结构类型分为3类,即孔隙直径大于5 μm的微米孔,孔隙直径介于5 μm~100 nm的微纳孔,以及孔隙直径小于100 nm大于2 nm的纳米孔.微生物作用后的煤岩与泥页岩的微米孔孔容增加,微纳孔和纳米孔孔容减小,孔隙比表面积降低,平均孔隙直径增大.分形维数对比结果表明受微生物作用的煤岩与泥页岩样品的面分形维数（D₁）和孔隙结构分形维数（D₂）均降低,微生物作用使得有机岩孔隙表面变的光滑,孔隙结构变得简单,有利于游离气的运移和富集.   相似文献   

ZH型重金属螯合纤维对水溶液中Sr²⁺的吸附行为     

周琳  董发勤  张伟  周磊  霍婷婷  聂小琴  周嘉琪  谢陶玲 《岩石矿物学杂志》2018,37(4):679-686

研究了ZH型重金属螯合纤维对水溶液中Sr~(2+)的吸附行为,考察了pH值、纤维加入量、Sr~(2+)初始浓度、作用时间等对吸附行为的影响,并采用SEM、EDS和FTIR等现代分析测试手段探讨了ZH型重金属螯合纤维对Sr~(2+)的吸附机制。结果表明,在pH值为7.0、纤维加入量为2.0 g/L、Sr~(2+)初始质量浓度为50 mg/L的条件下,纤维对Sr~(2+)的吸附在4 h左右基本达到平衡。实验条件下ZH型重金属螯合纤维对Sr~(2+)的最大吸附量可达26.22 mg/g。等温吸附拟合结果表明,ZH型重金属螯合纤维对Sr~(2+)的吸附可能是以单分子层为主的单分子层和多分子层吸附共同作用的结果。纤维对Sr~(2+)的动力学吸附过程符合准二级动力学模型。红外光谱分析表明Sr~(2+)与纤维上—NH_2和—COOH等基团进行配位络合从而吸附在纤维表面,—CH_2—和C=CH_2等基团参与此吸附过程。能谱分析表明Sr~(2+)与纤维上Na~+和Ca~(2+)还存在着离子交换作用。  相似文献   

The morphology of calcite crystals grown in a porous medium doped with divalent cations     

《Chemical Geology》2006,225(3-4):314-321

Calcite crystals were grown in the presence of small concentrations (50, 200, and 600 ppm) of divalent cations (Ba²⁺, Sr²⁺, Co²⁺ and Mn²⁺) in a silica hydrogel medium. The calcite crystals grown in the presence of cations larger than Ca²⁺ (Ba²⁺ or Sr²⁺) developed rhombohedral habits defined by {101¯4} form, similar to the morphology of calcite grown in a pure gel. SEM images show that growth on {101¯4} occurs by lateral advancement of layers bounded by macroscopic dendritic or jagged steps. In the case of calcite crystals grown in a gel doped with cations smaller than Ca²⁺ (Co²⁺ or Mn²⁺), a variety of morphologies was obtained, ranging from blocky crystals (at lower concentrations: 50 and 200 ppm) to peanut-like aggregates, spheres and spherulites (at 600 ppm). The macroscopic morphological characteristics of such doped calcite crystals reflect closely the growth behaviour of calcite {101¯4} surface at a nanoscale, reported by previous AFM studies. Morphological features have been interpreted on the basis of the modification of growing steps characteristics as a consequence of asymmetrical cation incorporation. The use of such morphologies as a criterion of biological activity is, therefore, unreliable.  相似文献   

Adsorption of Sr and Ba at the cleaved mica-water interface: Free energy profiles and interfacial structure     

Artur Meleshyn 《Geochimica et cosmochimica acta》2010,74(5):1485-12976

Monte Carlo simulations show that the adsorption position of the Sr²⁺ or Ba²⁺ ion on the cleaved muscovite surface is determined by the radius of the ion’s first hydration shell, hydrogen bonding of the first shell water molecules with the basal oxygens of muscovite as well as a requirement of minimization of the number of muscovite’s lattice cations in the ion’s first coordination shell. Accordingly, Sr²⁺ or Ba²⁺ adsorbs in ditrigonal cavities at a distance of 1.12 Å or 1.35 Å, respectively, from the basal surface on dehydrated mica and above tetrahedral substitutions at a height of 1.93 ± 0.02 Å or 2.15 ± 0.03 Å, respectively, at the highest simulated water coverage of 28 H₂O per ion. The ion’s displacement from a ditrigonal cavity occurs upon adsorption of 2 H₂O per ion for Sr²⁺ and 3 H₂O per ion for Ba²⁺. At a coverage of 28 H₂O per ion, outer-sphere adsorption of Sr²⁺ or Ba²⁺ at a height of 3.9 ± 0.2 Å or 4.17 ± 0.07 Å, respectively, is possible albeit unfavorable on the free energy scale by 107 ± 7 kJ/mol or 89 ± 13 kJ/mol, respectively, as compared to inner-sphere adsorption. Activation energies for the transformation between inner-sphere and outer-sphere adsorptions are calculated to be 121 ± 3 kJ/mol for Sr²⁺ and 99 ± 10 kJ/mol for Ba²⁺. A comparison of these values with those reported recently for Mg²⁺ and Ca²⁺ results in an adsorption affinity sequence Mg²⁺ > Ca²⁺ > Sr²⁺ > Ba²⁺ in agreement with the sequence predicted recently for low dielectric constant solids (which include mica) (Sverjensky, 2006). A recent resonant anomalous X-ray reflectivity study of Sr²⁺ adsorption on muscovite (Park et al., 2006) has questioned the common assumption (Stumm, 1992), which is supported by the present simulation results, that inner-sphere adsorption is stronger than outer-sphere adsorption. A modification of the cleaved muscovite surface as a result of Sr²⁺ adsorption in muscovite’s ditrigonal cavities and related destabilization of muscovite’s hydroxyl groups is proposed as a possible reason for this controversy.  相似文献   

A study of strontium in core 119K,Discovery deep,Red Sea     

M.O.U. Ikpeama  P.D. Boger  G. Faure 《Chemical Geology》1974,13(1):11-22

The isotopic composition of strontium of pore water and of authigenic minerals leached from the sediment of core 119K with hot aqua regia is similar to that of the brine in the Discovery deep and differs from that of normal seawater. The average ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio of strontium removed by acid leaching is 0.7077 ± 0.0007 (1σ) compared to a value of 0.70904 for the Red Sea. The detrital silicate fraction exhibits an approximate inverse correlation between ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios and strontium concentrations which provides tentative support for a model in which the detrital silicate fraction of deep-sea sediment is considered to be a mixture of terrigenous dust of sialic composition enriched in radiogenic ⁸⁷Sr and of volcanogenic material of basaltic composition and low ⁸⁷Sr abundance. The ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios of the shells of foraminifers and pteropods, expressed as δ ⁸⁷Sr‰ relative to 0.70904 for seawater, decrease from $\text{?0.23 ± 0.17‰}$ at 90 cm to $\text{?0.82 ± 0.17‰}$ at 273 cm and remain constant at this value to a depth of 450 cm. The lowering of the δ ⁸⁷Sr values is attributed both to the presence of aragonite overgrowths on pteropod shells and to possible isotope exchange with strontium in the connate fluid.  相似文献   

陆相页岩热演化过程中孔隙分形特征     

马明  陈国俊  徐勇  胡士骏  吕成福  薛莲花 《煤田地质与勘探》2017,45(5):41-47

分形维数可定量表征储层孔隙结构的复杂性,为页岩储层评价提供思路。以热模拟获得的不同热演化阶段的鄂尔多斯盆地长7段页岩为研究对象,应用场发射扫描电镜观察了各演化阶段孔隙变化特征,并通过低温液氮吸附实验,研究各个演化阶段页岩孔隙分形特征,运用FHH模型计算页岩孔隙分形维数,探讨了分形维数与有机碳、矿物成分、孔隙结构参数的关系。研究结果表明:低成熟阶段页岩中纳米级有机质孔发育有限,随着成熟度的增加,在有机质内部开始逐渐发育孔隙,同时黏土矿物颗粒间的有机质也开始分解,出现纳米级层间孔,主要发育墨水瓶状孔和少部分的平行板状孔;孔径峰值主要在2~4 nm和40~50 nm,随着成熟度增加,上述2个孔径段的孔隙相对数量增加,分形维数依次增大,分形维数为2.592~2.717,孔隙非均质性增强。分形维数随着有机碳含量的减少而增加,而与石英、黏土矿物含量相关性不明显;随着成熟度增加,微孔和中孔比例增加,平均孔径减小,孔隙表面越复杂,比表面积和分形维数增加;分形维数与总孔隙体积、微孔体积、中孔体积具有很好的正相关性,而与大孔体积相关性较差。   相似文献   

高温后花岗岩力学性质及微孔隙结构特征研究   总被引：3，自引：1，他引：2  

徐小丽  高峰  沈晓明  金春花 《岩土力学》2010,31(6):1752-1758

采用MTS815液压伺服试验系统及9310型微孔结构分析仪对花岗岩在温度作用下（常温～1 300 ℃）的宏观力学性质及微孔隙结构特征进行了较为系统的研究。结果表明：①在800 ℃之前,岩样力学性质变化规律不明显;超过800 ℃,岩样强度迅速劣化;达到1 200 ℃,岩样基本失去了承载能力。②岩样孔隙率随温度升高而增大,孔隙率的阀值温度在800 ℃左右,与岩样在该温度点强度突然降低相一致。③岩样孔隙率较小,但连通性好,在阶段进汞曲线上显示为不同宽度微裂隙并存的特征,累计进汞曲线呈台阶状,温度超过800 ℃,超微孔逐渐向微孔隙转化,岩样连通性增强。④岩样孔隙分布分形维数随温度的升高反而降低。在高温作用下,岩样中的热损伤由初始非规则的裂隙结构逐渐向均匀化的孔穴结构转化,非均匀性弱化是导致岩样孔隙分布分形维数降低的根本原因。  相似文献   

Selected geochemical factors influencing diagenesis of eocene carbonate rocks,peninsular Florida,U.S.A.     

Anthony F. Randazzo  Timothy J. Sarver  Deborah B. Metrin 《Sedimentary Geology》1983,36(1):1-14

The geochemical significance of three selected ions (Mg²⁺, Na⁺, and Sr²⁺) supports a model of dolomitization by brackish groundwater. This groundwater zone contains sufficient quantities of Mg²⁺ to facilitate dolomitization ($\text{Mg}\text{Ca}\text{ratios 1}$). Rising and falling of sea level and fluctuations of the phreatic zone related to climatic variations account for the thickness of the dolomite layers and the chemical distributions within these layers. Sodium concentrations in the calcite are 70–185 ppm, indicating formation in brackish water. Dolomite has sodium concentrations between 50–1400 ppm, suggesting formation in waters of similar salinity.Strontium in calcite ranges from 320–600 ppm, suggesting diagenesis in slightly saline waters in an open system. Dolomite contains 241 ppm Sr²⁺ on the average and calcite has 418 ppm Sr²⁺. The Sr²⁺ concentrations of the dolomite are characteristic of diagenesis in water less saline than sea water. Average strontium concentrations in the dolomite occur in two distinct groups, 260 ppm for dolomite with 39–43 mole-% MgCo₃ and 195 ppm for the dolomite with 44–50 mole-% MgCO₃. The difference in the Sr²⁺ concentrations of the two dolomite groups indicates the higher mole-% MgCO₃ dolomite recrystallized in a less saline environment than the lower mole-% MgCO₃ dolomite. These different environments are attributed to a relatively more saline coastal environment and a less saline inland environment.The more nearly stoichiometric dolomite (44–50 mole-% MgCO₃) has less scatter when mole-% MgCO₃ is plotted against Sr²⁺ and Na⁺. This suggests a greater approach to equilibrium with the dolomitizing fluid than the lower mole-% MgCO₃ (39–43) dolomite. The more saline environment has higher Mg/Ca ratios and promotes more calcium-rich dolomite during diagenesis because of the inhibition from competing foreign ions and because it is thermodynamically a more favorable environment which causes more rapid crystallization. The less saline waters allow recrystallization to proceed more slowly, producing better ordering in the dolomites, textural preservation and development of subhedral to euhedral rhombic crystals.  相似文献   

川东南彭水地区五峰组-龙马溪组页岩孔隙结构及差异性          下载免费PDF全文

彭女佳  何生  郝芳  何希鹏  张培先  翟刚毅  包书景  何陈诚  杨锐 《地球科学》2017,42(7):1134-1146

页岩孔隙结构及差异性是页岩含气性和产能评价的基础性问题.针对川东南彭水地区五峰组与龙马溪组页岩的孔隙结构已有若干研究成果,然而在页岩孔隙结构差异性和有机孔定量特征方面还缺乏研究.利用低温低压氮气吸附测定和氩离子抛光-场发射扫描电镜（FE-EM）技术,对页岩样品纳米孔隙进行了二维观察与统计以及分形特征计算,研究了3nm至几百nm页岩孔径范围的孔隙结构及其差异性.研究区五峰组-龙马溪组页岩有机孔十分发育;氮气吸附测定页岩孔隙形状包含开放型圆筒状、层状结构狭缝状和墨水瓶状等;扫描电镜观察有机孔形态主要有近圆形、椭圆形和多角形等.五峰组和龙马溪组页岩孔隙结构具有明显的差异性,主要体现在孔径大小、形态和数量上.氮气吸附测定表明,五峰组页岩孔隙比表面积和总孔容较龙马溪组大,微孔所占总孔的比例也较高;五峰组页岩孔径相对龙马溪组更细窄.扫描电镜二维图像观察与统计结果表明,五峰组有机孔径以小于3nm为主,形态以多角形为主;龙马溪组有机孔径以小于0nm为主,形态多呈近圆形和椭圆形.五峰组页岩的分形维值大于龙马溪组页岩,说明前者孔隙复杂程度较高.   相似文献   

Origin of anhedral Sr-rich calcite in deep-water mixed sediment, north-east Australia     

GEORGE R. DIX 《Sedimentology》1995,42(5):711-724

At burial depths of 800-1000 m, within the epicontinental Queensland Trough of north-east Australia (ODP Site 823), microcrystalline inter- and intraskeletal mosaics of anhedral (loaf-shaped, rounded) calcite have Sr²⁺ values ranging from below microprobe detection limits (<150 ppm) to 8100 ppm. Host rocks are well lithified, fine-grained mixed sediment to clayey wackestone and packstone of Middle and Late Miocene age. Petrography demonstrates that calcite precipitation has spanned shallow to deep burial, overlapping formation of framboidal pyrite in the upper 50 m; shallow-burial dolomitization (<300 m); and dedolomitization during sediment consolidation and incipient chemical compaction at greater (>400–500 m) depths. Petrographic observations illustrate that the calcite microfabric formed through coalescing crystal growth resulting from one or a combination of displacive growth in clay, porphyroid neomorphism of aragonite/vaterite, and clay replacement by calcite. Sr²⁺ mean concentrations in calcite between depths of 800 and 1000 m are similar to an expected equilibrium pore-water concentration, using a D^sr of 0.06, and may indicate active calcite precipitation. However, Sr²⁺ variation (2000–5000 ppm) within and among crystals, and concentrations that range well above predicted equilibrium values for a given depth, illustrate either variable Sr²⁺ retention during recrystallization of shelf-derived aragonite (and authigenic local vaterite) or relative uptake of Sr²⁺ during calcite precipitation with burial. Within the context of calcite formation during burial to 1 km, diagenetic attributes that affect the latter process include increased concentrations of pore-water Sr²⁺ with depth associated with aragonite recrystallization/dissolution; upward migration of Sr-rich pore water; and increased D^Sr related to local variation in precipitation/recrystallization rates, differential crystal sector growth rates and/or microvariation in aragonite distribution.  相似文献   

真空冷冻干燥和烘干对滑带土孔隙特征的影响试验          下载免费PDF全文

崔德山  项伟  陈琼  刘清秉  郎林智  吴益平 《地球科学》2014,39(10):1431-1437

采用水蒸气吸附法和恒速压汞法测定了三峡库区巴东县黄土坡滑坡Ⅰ号支洞滑带土在真空冷冻干燥和烘干状态下的孔隙特征.研究表明,滑带土烘干样中墨水瓶形孔道内水分子发生凝聚、堵塞,导致其比表面积和吸附水蒸气的能力均小于滑带土冻干样.滑带土烘干样失水收缩,团粒结构更紧密,滑带土吸附势减小,在微孔区间其累积孔隙体积和最大孔隙体积均小于滑带土冻干样.在考虑水蒸气表面张力情况下,滑带土冻干样吸附和脱附的孔隙表面分形维数均大于烘干样,说明烘干样失水后在各种化学键引力作用下使孔隙表面更趋于平滑.压汞实验结果表明在微孔和中孔区间,冻干滑带土的孔隙直径和孔隙体积均大于烘干样,但孔隙直径在0.133~129.051 μm区间,烘干样的孔隙体积大于冻干样,且直径大于41.421 μm的颗粒体积比冻干样大.   相似文献   

桂中坳陷环江凹陷上古生界海相页岩储层孔隙结构和分形特征研究   总被引：1，自引：0，他引：1       下载免费PDF全文

毛佩筱  金爱民  楼章华  朱蓉  朱振宏 《地质科学》2019,(1):130-144

通过有机地化分析、全岩X衍射矿物分析、甲烷等温吸附及低压氮气吸附实验,本文对桂中坳陷环江凹陷上古生界页岩样品的孔隙结构及分形特征进行了研究.结果表明:研究区页岩总有机碳含量(TOC)平均为2.40%,热成熟度(Ro)平均为2.65%,处于过成熟演化阶段.页岩主要的矿物组成为石英和黏土.页岩的比表面积平均为5.86 m2/g,孔容平均为0.014 9 mL/g,平均孔径为11.2 nm.页岩中发育大量的中孔,主要呈两端开口的圆筒形孔或四边开放的平行板状孔.页岩中TOC含量和石英含量越多,微-中孔越发育、比表面积和孔容越大,而平均孔径则变小.通过Frenkel-Halsey-Hill (FHH)模型和氮气吸附实验数据计算得到孔隙表面分形维数D1(平均为2.428 4)和孔隙结构分形维数D2(平均为2.622 2),对应的相对压力(P/P0)分别是0~ 0.45和0.45 ~ 0.99.分形维数D1、D2随着比表面积、孔容的增加而增加,而平均孔径随着前者的增加而减小.分形维数D1、D2、TOC含量、石英含量和甲烷吸附量之间呈现较好的正相关性,但随着黏土矿物含量的增多而减小.分形维数D1与Langmuir压力存在弱负相关性,分形维数D2随Langmuir压力增大有变大的趋势.桂中坳陷西北部页岩分形维数越大,孔隙结构越复杂,其对天然气的吸附和存储能力越强.  相似文献   

阳泉新景矿高煤级煤的孔隙结构分形特征     

毛潇潇  赵迪斐  杨玉娟  卢晨刚  王雪莲  郭英海 《煤田地质与勘探》2017,45(3):59-66

分形理论是宏观上定量评价储层非均质性的有效手段。以阳泉新景矿高煤级煤样品压汞数据为基础,建立分形几何模型,定量描述了孔隙结构。实验结果表明:样品孔隙以纳米孔为主,孔径、比表面积及孔容也集中分布在纳米孔段。煤样孔径65 nm以上的孔隙具有显著的分形特征,分维值分布范围为2.89~2.99,体积增量呈现阶段式的变化,孔隙结构复杂;孔径65 nm以下孔隙几乎无分形特征,比表面积增量与孔径在对数坐标中呈线性关系;基于分形特征及分子运动规律,将储层孔隙以孔径65 nm为界划分为扩散孔和渗透孔2个大类6个小类。分维值与体积孔隙中值半径、总孔隙体积呈负相关,与孔径65 nm以上的孔隙体积、比表面积呈正相关,与孔隙度无相关性。分形分维值对储层结构具有较全面的表征能力,可以作为综合指标在煤储层孔隙研究中加以应用。   相似文献   

Competitive adsorption of strontium and fulvic acid at the muscovite-solution interface observed with resonant anomalous X-ray reflectivity     

Sang Soo Lee  Changyong Park  Neil C. Sturchio 《Geochimica et cosmochimica acta》2010,74(6):1762-9581

Molecular-scale distributions of Sr²⁺ and fulvic acid (FA) adsorbed on the muscovite (0 0 1) surface were investigated using in situ specular X-ray reflectivity (XR) and resonant anomalous X-ray reflectivity (RAXR). The total amount of Sr²⁺ adsorbed from a 1 × 10⁻² mol/kg SrCl₂ and 100 mg/kg Elliott Soil Fulvic Acid II (ESFA II) solution at pH 5.5 compensated 81 ± 5% of the muscovite surface charge, less than previously measured (118 ± 5%) in an ESFA II-free solution with the same Sr concentration and pH. Inner-sphere (IS) and outer-sphere (OS) Sr²⁺ constituted 87% of the total adsorbed species in IS:OS proportions of 19:81 compared to 42:58 in the solution without FA, suggesting that adsorbed FA competes with the IS Sr²⁺ for surface sites. The coverage of both IS and OS Sr²⁺ decreased even more in a pH 3.5 solution containing the same concentration of FA and 0.5 × 10⁻² mol/kg Sr(NO₃)₂, whereas a significant amount of Sr²⁺ accumulated farther from the surface in the FA layer. The amount of Sr²⁺ incorporated in the ∼10 Å thick FA layer decreased by 79% with decreasing FA concentration (100 → 1 mg/kg) and increasing Sr²⁺ concentration (0.5 × 10⁻² → 1 × 10⁻² mol/kg) and pH (3.5 → 3.6). These results indicate not only that adsorbed FA molecules (and perhaps also H₃O⁺) displace Sr²⁺ near the muscovite surface, but also that the sorbed FA film provides binding sites for additional Sr²⁺ away from the surface. When a muscovite crystal pre-coated with FA after reaction in a 100 mg/kg ESFA II solution for 50 h was subsequently reacted with a 0.5 × 10⁻² mol/kg Sr(NO₃)₂ and 100 mg/kg ESFA II solution at pH 3.7, a significant fraction of Sr²⁺ was distributed in the outer part of the FA film similar to that observed on fresh muscovite reacted at pH 3.5 with a pre-mixed Sr-FA solution at the same concentrations. However, this Sr²⁺ sorbed in the pre-adsorbed organic film was more widely distributed and had a lower coverage, suggesting that pre-sorbed FA may undergo fractionation and/or conformational changes that diminish its capacity, and that of the muscovite (0 0 1) surface, for adsorbing the aqueous Sr cation.  相似文献   

Strontium behavior in the aragonite-calcite transformation: An experimental study at 40–98°C     

A Katz  E SassA Starinsky 《Geochimica et cosmochimica acta》1972

The behavior of strontium during the replacement of aragonite by calcite, in a closed system between 40°C and 98°C, has been experimentally investigated. The experiments were conducted in CaCl₂ solutions, with and without NaCl. The distribution coefficient of strontium in calcite (λ_Sr^2+C) was found to be affected only slightly by temperature changes, and almost insignificantly by the presence of NaCl. λ_Sr^2+C values at 0.01 m_Ca²⁺ (its concentration in normal sea water) are: 0.055 at 40°C and 0.058 at 98°C. These results indicate that the low (around 500 ppm) concentration of strontium in ancient limestones could have been brought about by aragonite-to-calcite transformation in a system open to sea water, and are not necessarily indicative of replacement in fresh waters.  相似文献