共查询到20条相似文献，搜索用时 15 毫秒
1.
Multi-component mineral precipitation in porous, subsurface environments is challenging to simulate or engineer when in situ reactant mixing is controlled by diffusion. In contrast to well-mixed systems, the conditions that favor mineral precipitation in porous media are distributed along chemical gradients, which evolve spatially due to concurrent mineral precipitation and modification of solute transport in the media. The resulting physical and chemical characteristics of a mixing/precipitation zone are a consequence of coupling between transport and chemical processes, and the distinctive properties of individual chemical systems. We examined the spatial distribution of precipitates formed in “double diffusion” columns for two chemical systems, calcium carbonate and calcium phosphate. Polyacrylamide hydrogel was used as a low permeability, high porosity medium to maximize diffusive mixing and minimize pressure- and density-driven flow between reactant solutions. In the calcium phosphate system, multiple, visually dense and narrow bands of precipitates were observed that were reminiscent of previously reported Liesegang patterns. In the calcium carbonate system, wider precipitation zones characterized by more sparse distributions of precipitates and a more open channel structure were observed. In both cases, formation of precipitates inhibited, but did not necessarily eliminate, continued transport and mixing of the reactants. A reactive transport model with fully implicit coupling between diffusion, chemical speciation and precipitation kinetics, but where explicit details of nucleation processes were neglected, was able to qualitatively simulate properties of the precipitation zones. The results help to illustrate how changes in the physical properties of a precipitation zone depend on coupling between diffusion-controlled reactant mixing and chemistry-specific details of precipitation kinetics. 相似文献
2.
Effect of the addition of granitic powder to an acidic soil from Galicia (NW Spain) in comparison with lime 总被引：1，自引：1，他引：0
The impact of diffuse pollution, agricultural land use and climate change on the long-term response of subsurface–surface water quality is not well understood, but is a prerequisite for evaluation of water management options. The goal of this study is to model geochemical evolution of water chemistry from the infiltration through soil into the unsaturated zone, transport through bedrocks and granular aquifers to a river in order to identify zones of steep concentration gradients and high dynamics under transient flow conditions. A numerical model was constructed comprising a 2-D 1,500 m × 150 m vertical cross-section of typical sedimentary rock formations, a glacio-fluvial quaternary gravel aquifer in the valley and soil layers. The model coupled saturated/un-saturated flow and reactive transport under steady state and transient conditions. Geochemical interactions, include intra-aqueous kinetic reactions of oxygen with dissolved organic matter, as well as kinetics of carbonate dissolution/precipitation. This model section was chosen to provide insight in to the principal processes and time scales affecting water chemistry along different flow paths. The numerical simulator MIN3P was used, a finite volume program for variably saturated subsurface flow and multi-component reactive transport. The results show that subsurface water residence times range from approximately 2 to 2,000 years. Different zones are to be expected with respect to the development of mineral equilibria; namely, purely atmospherically influenced, as well as open and closed system carbonate dissolution. Short-term responses to daily averaged changes in precipitation, however, are only visible to some extent in the shallower and near-river parts of flow system and solute loads. This can most likely be explained by directional changes in flow paths, indicating that equilibrium geochemical condition predominate at the hillslope scale, i.e. water quality depends on transport pathways rather than on kinetic effects. The extent of reducing conditions is controlled by the presence of organic-rich layers (i.e. peat deposits), the dissolution kinetics of aquifer organic matter and the subsequent mixing with oxygenated water by hydrodynamic dispersion. 相似文献
3.
Enzyme induced carbonate precipitation (EICP) is an emerging soil improvement method using free urease enzyme for urea hydrolysis. This method has advantages over the commonly used microbially induced carbonate precipitation (MICP) process as it does not involve issues related to bio-safety. However, in terms of efficiency of calcium carbonate production, EICP is considered lower than that of MICP. In this paper, a high efficiency EICP method is proposed. The key of this new method is to adopt a one-phase injection of low pH solution strategy. In this so-called one-phase-low-pH method, EICP solution consisting of a mixture of urease solution of pH?=?6.5, urea and calcium chloride is injected into soil. The test results have shown that the one-phase-low-pH method can improve significantly the calcium conversion efficiency and the uniformity of calcium carbonate distribution in the sand samples as compared with the conventional two-phase EICP method. Furthermore, the unconfined compressive strength of sand treated using the one-phase-low-pH method is much higher than that using the two-phase method and the one-phase-low-pH method is also simpler and more efficient as it involves less number of injections.
相似文献4.
Microbial induced calcite precipitation (MICP) has been well studied to date in the laboratory as a viable alternative soil improvement technique that harnesses a natural bacterial process to induce cementation. Specifically, MICP utilizes the microbial process of hydrolysis of urea to induce pH increase leading to calcite precipitation. The study presented herein demonstrates the utility of a simple bio-geochemical reactive transport model to predict MICP in one-dimensional column experiments. The mathematical model was originally developed in the framework of the TOUGHREACT code to include kinetically controlled reaction rates for urea hydrolysis and calcite precipitation. Inverse modeling, via UCODE-2005, is utilized to calibrate and verify the model to experimental data including aqueous and mineral chemistry. Results indicate good agreement between data and simulated results for capturing the trends and magnitudes of a variety of MICP treatment schemes in half meter, one-dimensional flow columns. A design procedure is presented for predicting MICP in one-dimensional flow by sequentially coupling UCODE-2005 with TOUGHREACT. 相似文献
5.
植物源脲酶诱导碳酸钙沉淀（enzyme induced carbonate precipitation,简称EICP）可以显著改善砂土的工程力学特性,但在具体操作时,参数取值无对应规范,固化效果有待提升。基于黄豆脲酶,研究了温度、脲酶浓度、尿素浓度、钙浓度、pH值、钙源种类等变量对脲酶活性与碳酸钙沉淀的影响,并进行了沉淀物（碳酸钙晶体）的扫描式电子显微镜（scanning electron microscope,简称SEM）与X射线衍射（X-ray diffraction,简称XRD）测试,在此基础上开展了黄豆脲酶固化砂的无侧限抗压强度与固化效果试验研究。结果表明：脲酶活性随脲酶浓度的增加而线性增长,但存在温度阈值,温度超过阈值后,脲酶将完全失活,且阈值随脲酶浓度的增大而降低;尿素浓度与pH值共同影响脲酶活性,二者存在一个最优组合,当尿素浓度在0.1～1.0 mol/L时最优pH值为7,当尿素浓度在1.0～1.5 mol/L时最优pH值为8。脲酶是沉淀反应的催化剂,脲酶浓度越高,反应越完全,碳酸钙沉淀率越高;尿素与钙溶液则主要通过掺入量影响碳酸钙沉淀量,掺量比例宜为1:1,且二者浓度与pH值可通过影响脲酶活性来影响碳酸钙的沉淀情况;不同钙源对碳酸钙沉淀量的影响幅度不大。不同钙源沉淀碳酸钙晶体的成分与密度基本相同,但晶体结构差异较大,氯化钙沉淀碳酸钙晶体以块状为主,表面分布球状、类球状晶体,胶结面大,可作为EICP技术中较为理想的钙源。基于黄豆脲酶和氯化钙钙源固化砂的无侧限抗压强度约为掺粉煤灰砂样的6倍,通过SEM图像可发现,沉淀碳酸钙晶体包裹并黏结砂粒成为整体,固化效果非常理想。 相似文献
6.
Among the processes leading to a decrease in productivity, chemical clogging is often mentioned as one of the major features.
De-watering of a confined aquifer caused by an unsuitable pumping scheme produces a phenomenon involving the diffusion of
oxygen in the aquifer which disturbs the geochemical conditions in the initial system. Coupled chemical and transport processes
are proposed in an assessment of the impact of de-watering on the precipitation of carbonate and iron oxide. The reactions
are studied for waters showing low dissolved iron concentrations such as commonly observed in drinking water supplies. The
quantity and distribution of precipitated iron oxide and calcium carbonate are used in a permeability model to calculate the
productivity loss. For the conditions used in the simulations, the carbonate precipitate can be neglected compared to iron
deposits which remain weak. The spatial distribution is heterogeneous and quite similar to the patterns observed in the field.
This shape is mainly caused by a competition between the diffusion of oxygen due to the de-watering process and the rate of
precipitation of iron oxide. However, the loss of well productivity remains moderate. It is clearly shown that de-watering
of the well and the associated chemical incrustations that this induces cannot alone explain field data. More complex processes
involving biological clogging and accurate hydrodynamic behaviour in the closest part of the well remain to be included in
the modelling approach in order to provide valuable insights into the problem of well ageing. 相似文献
7.
In recent years, a series of important progresses have been made in the aspect of magnesium isotopes behavior in weathering processes. These progresses are not only favorable to understand the change of the magnesium isotopic compositions in rivers, but also establish the foundation to further reveal the magnesium isotope geochemical cycle. The magnesium in rivers is both magnesium sink for weathering and magnesium source for the ocean. The Mg isotopic compositions in rivers are dominated by the magnesium sources and Mg isotope fractionations processes. The sources of magnesium in rivers originate mainly from draining rocks, as well as less contribution from the eolian deposition, groundwater, plant debris, and precipitation. The Mg isotope fractionations in rivers are mainly related to precipitation and dissolution of carbonate minerals, silicate mineral hydrolysis, adsorption on mineral or colloidal matter surface, and plant uptake. Generally, the contribution of carbonate minerals dissolution or precipitation is equal to add or reduce magnesium from carbonate endmember, which has a remarkably negative δ26Mg value. Based on the fact that most clay minerals are rich in 26Mg during nature silicate mineral hydrolysis, then it is possible to infer that residual weathering products enrich in 26Mg. However, there is no significant Mg isotope fractionation causing by the adsorption on mineral or colloidal matter surface during river water migration. For the plant uptake, the root prefers to have 26Mg, leading the plant itself rich in heavier Mg isotopic composition. In addition, formation of secondary minerals in rivers could also reflect the changes of chemical parameters in rivers (such as major elements, CO2 solubility, pH, etc.). Hence, Mg isotopic composition in rivers and associated isotope fractionations are not only the basis for the application of magnesium isotope to trace surface material cycle, but also have important significance for the further understanding the geochemical cycle of magnesium isotopes. 相似文献
8.
微生物诱导碳酸钙沉淀(microbially induced calcium carbonate precipitation, MICP)是一种在自然界中广泛存在的生物矿化过程。由于MICP具有反应速度快、环境条件要求低、应用范围广、温室气体减排效应显著等特点,在地质、土木、水利、环境多个领域中广泛推广应用。文章在分析国内外相关研究成果的基础上,归纳整理出反硝化过程、硫酸盐还原作用、尿素分解作用等多种微生物诱导下碳酸钙矿化途径和作用机制。以尿素分解菌为代表,重点讨论微生物诱导碳酸盐沉淀过程中pH、温度、离子浓度等环境因素对生成矿物晶型晶貌等方面的影响,总结了MICP的环境应用机制,即环境中的重金属元素通过替换作用替换矿化矿物中的Ca2+或CO32?从而被固定。MICP作为一种简单高效的地质环境过程,在生态环境修复领域具有广阔的应用前景。 相似文献
9.
《Applied Geochemistry》2004,19(6):917-936
Carbon dioxide disposal into deep aquifers is a potential means whereby atmospheric emissions of greenhouse gases may be reduced. However, our knowledge of the geohydrology, geochemistry, geophysics, and geomechanics of CO2 disposal must be refined if this technology is to be implemented safely, efficiently, and predictably. As a prelude to a fully coupled treatment of physical and chemical effects of CO2 injection, the authors have analyzed the impact of CO2 immobilization through carbonate mineral precipitation. Batch reaction modeling of the geochemical evolution of 3 different aquifer mineral compositions in the presence of CO2 at high pressure were performed. The modeling considered the following important factors affecting CO2 sequestration: (1) the kinetics of chemical interactions between the host rock minerals and the aqueous phase, (2) CO2 solubility dependence on pressure, temperature and salinity of the system, and (3) redox processes that could be important in deep subsurface environments. The geochemical evolution under CO2 injection conditions was evaluated. In addition, changes in porosity were monitored during the simulations. Results indicate that CO2 sequestration by matrix minerals varies considerably with rock type. Under favorable conditions the amount of CO2 that may be sequestered by precipitation of secondary carbonates is comparable with and can be larger than the effect of CO2 dissolution in pore waters. The precipitation of ankerite and siderite is sensitive to the rate of reduction of Fe(III) mineral precursors such as goethite or glauconite. The accumulation of carbonates in the rock matrix leads to a considerable decrease in porosity. This in turn adversely affects permeability and fluid flow in the aquifer. The numerical experiments described here provide useful insight into sequestration mechanisms, and their controlling geochemical conditions and parameters. 相似文献
10.
地下孔隙率和渗透率在空间和时间上的变化及影响因素 总被引：18，自引：5，他引：18
地下岩石孔隙率和渗透率在空间和时间上的变化受众多因素控制,总的说来,包括沉积与成岩两个最为主要的因素。沉积盆地的性质和沉积环境控制了沉积物的组成、岩石的结构和原生孔隙。沉积作用所经历的时间相对较短而进程较快;成岩作用所经历的时间相对较长而进程较慢。从对孔隙率和渗透率的控制作用来说,成岩作用的研究难度相对较大。近年来,一些传统的形成地下岩石次生孔隙的机制受到挑战,这些传统机制中最为主要的是有机酸对铝硅酸溶解形成次生孔隙,但这会造成介质pH值的升高,碳酸盐矿物和高岭石的沉淀。地下岩石中碳酸水溶解产生的次生孔隙也是有限的。新的机制如大气淡水的溶解作用,深部冷却地下水的溶解作用,硅酸盐的水解都得到了人们的普遍接受,这对于次生孔隙成因的解释及地下岩石孔隙率和渗透率的预测十分重要。对于碳酸盐岩来说,与不整合面附近的古喀斯特有关的油气藏得到了更多的关注。深埋藏过程中碳酸盐岩成岩作用的研究中,温度和压力的影响对不同碳酸盐矿物溶解及沉淀作用的差异性控制了地下碳酸盐岩孔隙率和渗透率分布. 相似文献
11.
《Journal of Asian Earth Sciences》2011,40(6):713-723
Bleaching related to seepage of petroleum fluids and subsurface migration of crude oil and natural gas can alter the chemical and mineralogical properties of rocks, while concurrently depleting hydrocarbon reservoirs. Mud volcanoes constitute one type of petroleum seepage present in several areas on the southern margin of the Junggar Basin in the Xinjiang Uygur Autonomous Region, NW China. The results of XRD, XRF, XANES, and Mössbauer spectroscopy on rock samples collected from areas affected by these mud volcanoes revealed an enrichment of certain minerals and elements, as well changes in mineralogical, molecular, or ionic carrier (“species”). After bleaching, reddish sedimentary rocks showed depletion in silica and enrichment of calcium, magnesium, manganese, and iron. Other elements, including aluminum, potassium, sodium, and titanium, were largely unchanged. Reduced iron and sulfur compounds predominated in the bleached rocks, producing changes in color from the original reddish into green, deep gray, and black. Iron and calcium were associated with carbonates, indicating carbonation of these elements during the bleaching processes. Manganese also appeared to be associated with carbonate, though not with sulfate even though sulfate was present in the bleached rocks. Alkaline conditions were apparently the dominant because reduced manganese would have been absent under acidic condition. The alteration of certain minerals, clay minerals in particular, was also observed in bleached rocks, the alteration of smectite-group minerals to chlorite and muscovite, for example. Mineralogical and geochemical changes in rocks bleached by hydrocarbon fluids could provide a better overall understanding of bleaching processes, and may have applications in surface geochemical exploitation and remote imaging. 相似文献
12.
Changes in water quality in the North Fork of the Humboldt River, Nevada are caused by weathering of waste rock from an inactive Carlin-type gold mine. Review of historical water-quality data, monthly water sampling, and continuous monitoring of water-quality parameters were used to quantify these impacts. River water pH, which ranged between 7 and 8, did not show statistically significant variation from upstream of the mine to downstream. Several constituents, most notably sulfate, calcium, and magnesium, showed statistically significant increases in dissolved-ion concentrations. These data, along with geochemical modeling, suggest that oxidation of sulfide minerals and in situ acid neutralization by carbonate host rocks are occurring. Large increases in dissolved-ion concentrations were observed twice a year—during spring snow melt and the onset of the winter precipitation season. These spikes are likely caused by flushing of pore waters that have reacted with waste rock during months-long periods when shallow groundwater recharge is not occurring. 相似文献
13.
地球化学模式程序的原理,分类与功能 总被引：15，自引：0，他引：15
地球化学模式是用化学反应式和数学公式来描述地球化学作用的一种概念化的模式，在这种概念化的模式基础上利用数学方法和计算机语言编制的软件便是地球化学模式程序。按照原理和复杂程度可把地球化学模式程序分为３大类，即质量平衡程序、物质转化程序和溶质迁移程序。地球化学模式程序的主要功能包括计算元素在水溶液中的存在形式，预测各类地球化学反应进行的方向，物质的溶解与沉淀，溶液的Ｅｈ、ｐＨ值，计算地球化学作用的反应速度和反应途径等。 相似文献
14.
The systematic sampling of the chemical composition of the groundwater from five karst springs (including an overflow spring) and one outflowing borehole have permitted to determine distinctive chemical changes in the waters that reflect the geochemical processes occurring in a carbonate aquifer system from southern Spain. The analysis of the dissolution parameters revealed that geochemical evolution of the karst waters basically depends on the availability of the minerals forming aquifer rocks and the residence time within the aquifers. In the three proposed scenarios in the aquifers, which include the preferential flow routines, the more important geochemical processes taking place during the groundwater flow from the recharge to the discharge zones are: CO2 dissolution and exsolution (outgassing), calcite net dissolution, calcite and dolomite sequential dissolution, gypsum/anhydrite and halite dissolution, de-dolomitization and calcite precipitation. A detailed analysis of the hydrochemical data set, saturation indices of the minerals and partial pressure of CO2 in the waters joined to the application of geochemical modelling methods allowed the elaboration of a hydrogeochemical model of the studied aquifers. The developed approach contributes to a better understanding of the karstification processes and the hydrogeological functioning of carbonate aquifers, the latter being a crucial aspect for the suitable management of the water resources. 相似文献
15.
在三维空间中综合已揭露浅部地质和深部地球物理资料进行深部预测,既能深化浅部认识,还能减少地球物理多解性带来的困扰,成为深部成矿预测的新趋势和重要手段.以北衙金矿床万硐山矿段为例,通过收集钻孔、勘探线剖面、化探和地球物理等资料,在三维建模平台中建立了万硐山矿段三维地质模型;基于建模结果,综合地表、浅部和深部重力资料,对成矿地质条件和深部成矿潜力进行了研究和分析,筛选出隐伏断裂、斑岩体和青天堡组砂岩3种成矿有利要素,对应建立了成矿有利区三维体模型（sgrid）.在此基础上,采取多源信息综合方法,对3种成矿控制要素的有利成矿区域取交集,圈定了万硐山矿段海拔1 100~900 m内深部靶区,为周边同类型矿段深部靶区预测提供了参考. 相似文献
16.
Kitchen waste and wind erosion are two worldwide environmental concerns. This study investigated the feasibility of using kitchen waste for Sporosarcina pasteurii cultivation and its application in wind erosion control of desert soil via microbially induced carbonate precipitation (MICP). Enzymatic hydrolysis was adopted to improve the release and recovery of protein in kitchen waste for subsequent microorganism production. After conditions optimized, the maximum biomass concentration (OD600) and urease activity of Sporosarcina pasteurii in the kitchen waste-based medium reached 4.19, and 14.32 mM urea min?1, respectively, which were comparable to those obtained in conventional standard media. The harvested Sporosarcina pasteurii was then used to catalyze the precipitation of calcium carbonate in the desert soil, and its performance in wind erosion control was evaluated through wind tunnel tests. The microbially mediated calcium carbonate could significantly decrease wind erosion loss of the desert soil even after 12 wet–dry or freeze–thaw cycles. Scanning electron microscopy (SEM) with energy-dispersive X-ray (EDX) confirmed the bridge effect of calcium carbonate crystals in the soil matrix. The kitchen waste, as a cost-effective alternative nutrient for bacterial cultivation and carbonate precipitation, showed great potential for large-scale applications in wind erosion control of desert soils.
相似文献17.
18.
Yu-Shu Wu Guoping Lu Keni Zhang Lehua Pan Gudmundur S. Bodvarsson 《Hydrogeology Journal》2007,15(3):553-572
Characterizing percolation patterns in unsaturated fractured rock has posed a greater challenge to modeling investigations than comparable saturated zone studies due to the heterogeneous nature of unsaturated media and the great number of variables impacting unsaturated flow. An integrated modeling methodology has been developed for quantitatively characterizing percolation patterns in the unsaturated zone of Yucca Mountain, Nevada (USA), a proposed underground repository site for storing high-level radioactive waste. The approach integrates moisture, pneumatic, thermal, and isotopic geochemical field data into a comprehensive three-dimensional numerical model for analyses. It takes into account the coupled processes of fluid and heat flow and chemical isotopic transport in Yucca Mountain’s highly heterogeneous, unsaturated fractured tuffs. Modeling results are examined against different types of field-measured data and then used to evaluate different hydrogeological conceptualizations through analyzing flow patterns in the unsaturated zone. In particular, this model provides clearer understanding of percolation patterns and flow behavior through the unsaturated zone, both crucial issues in assessing repository performance. The integrated approach for quantifying Yucca Mountain’s flow system is demonstrated to provide a practical modeling tool for characterizing flow and transport processes in complex subsurface systems. 相似文献
19.
自生泥晶,也称作原地微晶碳酸钙或原地灰泥以区分他生泥晶或异地泥晶,指的是通过无机和/或有机媒介过程作用在原地形成的泥晶碳酸钙。在前人的基础上,对自生泥晶概念的提出和发展进行了概括;对自生泥晶的矿物组成、显微结构、荧光和阴极发光特征进行了总结;对自生泥晶的形成过程和来源（包括生物矿化作用、有机矿化作用和无机沉淀三种方式）进行了探讨;对自生泥晶在不同沉积环境碳酸盐岩中的贡献及其地球化学指示进行了论述;对自生泥晶在地质历史时期的分布做了归纳;最后对自生泥晶的后续研究提出了一些展望。认为正确认识自生泥晶的性质,其形成过程和来源对碳酸盐岩的结构成因分类、地质历史时期生物礁丘的演化和地球化学指示、建筑工程和环境修复、探寻地外生命和油气地质等方面都将产生深远的影响。 相似文献
20.
New insights into geochemical behaviour in ancient marine carbonates (Upper Jurassic Ammonitico Rosso): Novel proxies for interpreting sea‐level dynamics and palaeoceanography 
下载免费PDF全文
下载免费PDF全文 Rute Coimbra Adrian Immenhauser Federico Olóriz Víctor Rodríguez‐Galiano Mario Chica‐Olmo 《Sedimentology》2015,62(1):266-302
Elemental concentrations in Phanerozoic sea water are known to fluctuate both in time and space. With regard to carbonates precipitated from marine fluids, elemental concentrations in the carbonate crystal lattice are affected by a complex array of equilibrium and non‐equilibrium as well as post‐depositional alteration processes. To assess the potential of carbonate elemental chemostratigraphy, seven Upper Jurassic sections were investigated along a proximal to distal transect across the south‐east Iberian palaeomargin. The aim was to explore stratigraphic and spatial variations in calcium, strontium, magnesium, iron and manganese elemental abundances. The epicontinental geochemical record is influenced by the combination of continental runoff and a significant diagenetic overprint. In contrast, the epioceanic geochemical record agrees with reconstructed open marine sea water values, reflecting a moderate degree of syn‐depositional to early marine pore water diagenesis. Establishing a fair degree of preservation of matrix micrite, a thorough statistical approach was applied and elemental associations tested for their environmental significance. Principal component and hierarchical cluster analyses revealed a persistent relation between carbonate magnesium, iron and strontium abundances. Processes related to early diagenetic nodulation in Ammonitico Rosso facies most probably account for the incorporation of these elements in the calcium carbonate lattice. The clear decoupling of carbonate manganese abundance with respect to the remaining elements is documented and related to high sea floor spreading rates and hydrothermal activity during the Late Jurassic. The investigation of potential time‐fluctuation of geochemical patterns was approached through variogram computation. The observed temporal behaviour is most likely to be forced by relative sea‐level dynamics, reflecting Late Jurassic palaeoceanographic conditions and potential planetary interactions. The data obtained in this study highlight the utility of elemental data from carbonate matrix micrites as geochemical proxies for studying the influence of remote trigger factors. 相似文献