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1.
桂西堆积型铝土矿中三水铝石成因矿物学研究   总被引：1，自引：0，他引：1       下载免费PDF全文
桂西堆积型铝土矿中三水铝石的矿物共生组合、矿物空间分布规律、产出特征、矿物的形成世代、化学成分、稀土元素和矿体内外的水质成分等成因矿物学特征研究结果表明，红土中的三水铝石是由硬水铝石水解形成的，三水铝石形成于本区特殊的气候和地质条件，特别是地下水溶液中Al^ 3、[SiO4]^-2浓度及pH值等多种因素的制约，经历了Al(OH)3的沉淀、老化、脱玻化、结晶几个阶段。在淋滤作用的早期，形成了高岭石；在淋滤作用较弱的位置，形成了次生石英。不仅是新类型矿床，而且其成因也是独特的，是正处于退化中的铝土矿。  相似文献   

2.
In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation, and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka Marine Terrace Chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized [White A. F., Schulz M. S., Vivit D. V., Blum A., Stonestrom D. A. and Anderson S. P. (2008) Chemical weathering of a Marine Terrace Chronosequence, Santa Cruz, California. I: interpreting the long-term controls on chemical weathering based on spatial and temporal element and mineral distributions. Geochim. Cosmochim. Acta72 (1), 36-68] and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisserand [Hellmann R. and Tisserand D. (2006) Dissolution kinetics as a function of the Gibbs free energy of reaction: An experimental study based on albite feldspar. Geochim. Cosmochim. Acta70 (2), 364-383] or the aluminum inhibition model proposed by Oelkers et al. [Oelkers E. H., Schott J. and Devidal J. L. (1994) The effect of aluminum, pH, and chemical affinity on the rates of aluminosilicate dissolution reactions. Geochim. Cosmochim. Acta58 (9), 2011-2024], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site.Additionally, observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO2(aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total mass removed from the weathering profile. Our analysis suggests that secondary clay precipitation is as important as aqueous transport in governing the amount of dissolution that occurs within a profile because clay minerals exert a strong control over the reaction affinity of the dissolving primary minerals. The modeling also indicates that the weathering advance rate and the total mass of mineral dissolved is controlled by the thermodynamic saturation of the primary dissolving phases plagioclase and K-feldspar, as is evident from the difference in propagation rates of the reaction fronts for the two minerals despite their very similar kinetic rate laws.  相似文献   

3.
Batch reactor experiments were conducted to assess perthitic alkali-feldspar dissolution and secondary mineral formation in an initially acidic fluid (pH = 3.1) at 200 °C and 300 bars. Temporal evolution of fluid chemistry was monitored by major element analysis of in situ fluid samples. Solid reaction products were retrieved from two identical experiments terminated after 5 and 78 days. Scanning electron microscopy revealed dissolution features and significant secondary mineral coverage on feldspar surfaces. Boehmite and kaolinite were identified as secondary minerals by X-ray diffraction and transmission electron microscopy. X-ray photoelectron spectroscopy analysis of alkali-feldspar surfaces before and after reaction showed a trend of increasing Al/Si ratios and decreasing K/Al ratios with reaction progress, consistent with the formation of boehmite and kaolinite.Saturation indices of feldspars and secondary minerals suggest that albite dissolution occurred throughout the experiments, while K-feldspar exceeded saturation after 216 h of reaction. Reactions proceeded slowly and full equilibrium was not achieved, the relatively high temperature of the experiments notwithstanding. Thus, time series observations indicate continuous supersaturation with respect to boehmite and kaolinite, although the extent of this decreased with reaction progress as the driving force for albite dissolution decreased. The first experimental evidence of metastable co-existence of boehmite, kaolinite and alkali feldspar in the feldspar hydrolysis system is consistent with theoretical models of mineral dissolution/precipitation kinetics where the ratio of the secondary mineral precipitation rate constant to the rate constant of feldspar dissolution is well below unity. This has important implications for modeling the time-dependent evolution of feldspar dissolution and secondary mineral formation in natural systems.  相似文献   

4.
http://www.sciencedirect.com/science/article/pii/S1674987110000095   总被引：1，自引：0，他引：1  
<正>Bauxite deposits are studied because of their economic value and because they play an important role in the study of paleoclimate and paleogeography of continents.They provide a rare record of the weathering and evolution of continental surfaces.Geomicrobiological analysis makes it possible to verify that microorganisms have played a critical role during the formation of bauxite with the possibility already intimated in previous studies.Ambient temperature,abundance of water,organic carbon and bioavailable iron and other metal substrates provide a suitable environment for microbes to inhabit.Thio-bacillus, Leptospirilum,Thermophilic bacteria and Heterotrophs have been shown to be able to oxidize ferrous iron and to reduce sulfate-generating sulfuric acid,which can accelerate the weathering of alumi-nosilicates and precipitation of iron oxyhydroxides.Microorganisms referred to the genus Bacillus can mediate the release of alkaline metals.Although the dissimilatory iron-reducing and sulfate-reducing bacteria in bauxites have not yet been identified,some recorded authigenic carbonates and "bacteriopyrites" that appear to be unique in morphology and grain size might record microbial activity.Typical bauxite minerals such as gibbsite,kaolinite,covellite,galena,pyrite,zircon,calcium plagioclase,orthoclase, and albite have been investigated as part of an analysis of microbial mediation.The paleoecology of such bauxitic microorganisms inhabiting continental(sub) surfaces,revealed through geomicrobiolo-gical analysis,will add a further dimension to paleoclimatic and paleoenvironmental studies.  相似文献   

5.
堆积铝土矿中三水铝石成因探讨   总被引：2，自引：0，他引：2  
堆积铝土矿中三水铝石成因探讨谌建国，刘云华（中国地质科学院宜昌地质矿产研究所，宜昌４４３００３）关键词堆积铝土矿，三水铝石－硬水铝石矿床，三水铝石成因，大气降水淋滤我国桂西至滇东广泛发育堆积型铝土矿，资源量很大。矿体是杂基支撑的角砾堆积物，砾石和基质...  相似文献   

6.
We present a numerical approach which accounts for nucleation, growth and/or resorption of particles of fixed composition in aqueous solutions, and which involves functionalities suited to the formation of simple clay minerals in weathering processes, such as: formation of non-spherical particles, heterogeneous/homogeneous nucleation, several growth laws, precipitation resulting from the dissolution of primary minerals. The overall model is now embedded into a new numerical code called NANOKIN, in which several optimization procedures have been introduced in order to allow long dynamics to be followed. NANOKIN was applied to the precipitation of Al- bearing minerals from aqueous solutions: halloysite, kaolinite and Ca-montmorillonite. It allowed us to propose a stable scheme for the competitive precipitation of halloysite and kaolinite under two different types of initial conditions: (1) a given initial super-saturation state of the aqueous solution; (2) progressive super-saturation resulting from the kinetic dissolution of the minerals from a granitic rock under weathering conditions. Both yield particle sizes in the micron range, but with distinct crystal size distribution functions. The interplay between kinetic and thermodynamic effects is discussed.  相似文献   

7.
Bauxite deposits of the Fria district, Guinea, have been exploited since 1960. These lateritic bauxites, located on the upper parts of plateaus, result from weathering of paleozoic schists. The ores are composed of gibbsite associated with pyrophyllite, Al-substituted gœthite, and kaolinite. Pyrophyllite and Al-substituted gœthite may contain up to 9% of the total Al2O3 content of the bauxite; this cannot be recovered through the Bayer process because these phases are insoluble in the leaching solutions. Kaolinite is soluble under Bayer leaching but this dissolution induces precipitation of sodium aluminosilicates, which apart from loss of further alumina results in decreasing efficiency of the process through scale formation. Detailed knowledge of the distribution of the different ore types and their mineralogical composition is necessary for efficient processing.  相似文献   

8.
广汉市平原区浅层地下水化学演化及其控制因素   总被引：4，自引：0，他引：4  
为在广汉市城乡规划过程中提供地下水资源开发利用的基础信息,采用矿物风化系统分析、相关性分析、主成分分析和PhreeQC反向水文地球化学模拟等方法对广汉市平原区的浅层地下水的地下水水化学组分进行分析,确定了浅层地下水的水化学演化及控制因素,完成了地下水资源的质量及时空分布特征分析。分析表明：Gibbs图显示岩石风化主导该区地下水水化学特征,风化过程产生离子和次生矿物又经历水解作用,在矿物风化系统稳定场图中显示水样中铝硅酸盐矿物逐渐趋于溶解,碳酸盐矿物处于饱和状态;PhreeQC反向水文地球化学模拟结果显示在水流模拟路径上主要发生了钙蒙脱石、钾长石溶解和高岭石、石英、钠长石的沉淀,以及Ca-Na2之间的阳离子交换吸附作用;离子相关性和主成分分析进一步的验证了溶滤作用、蒸发浓缩作用和阳离子交换吸附作用是引起浅层地下水水化学过程和矿物组成改变的主要原因。研究区地下水水质总体不会对人体健康造成不良影响。  相似文献   

9.
Chemical, mineralogical, and petrographic data from the Los Pijiguaos bauxite deposit, together with the water chemistry of the streams draining the area, were used to study the problem of lateritic bauxite formation at this location. The Los Pijiguaos bauxite, located at the northwestern edge of the Guayana Shield in Venezuela, is a lateritic bauxite developed on a Precambrian Rapakivi Granite Batholith, the Parguaza Granite. This deposit is situated on a planation surface at elevations between 600 and 700 m; it is believed to have originated during an erosional event that took place during Late Cretaceous-early Tertiary times.The weathering profile is composed of an upper bauxite zone, followed by a saprolite, and merging gradually to the fresh granite. The upper bauxitic zone contains gibbsite, quartz, hematite, and goethite. The saprolite contains kaolinite, quartz, and goethite and is characterized by a relict granitic texture that indicates little bulk volume change associated with the weathering process. The upper bauxitic zone has lost any textural resemblance with the parent granite, consistent with extensive volume loss.Bauxite and saprolite are separated by a transition zone where gibbsite and kaolinite coexist. Textures indicating the replacement of kaolinite by gibbsite point to the dynamic nature of the weathering profile, characterized by advancing reaction fronts.The chemical composition of the deposit defines trends that can be traced back to the composition of the parent granite and shows enrichment of Al2O3, Fe2O3, and TiO2, and depletion of SiO2, relative to the parent granite. The uppermost part of the profile is characterized by a further enrichment of Fe2O3 with respect to the other components of the bauxite. Important volume and mass losses in the bauxite have also been calculated, based on chemical composition and density measurements. The calculated losses are consistent with the textural observations in the bauxite.The chemical composition of the waters of streams draining the area shows strong seasonal patterns, consistent with the seasonal nature of the local climate (one dry and one rainy season per year, both about six months long). The balance between dissolved and suspended loads in these streams indicates that the magnitudes of chemical and physical denudation are similar, leading to approximately constant thicknesses of the weathering profiles. These observations are consistent with model calculations based on current climatic conditions and suggest that the bauxitization process is still active.  相似文献   

10.
This study reports the kinetic experimental results of albite in water and in KCI solution at 22 MPa in the temperature range of 25 to 400℃. Kinetic experiments have been carried out in an open flow-through reaction system (packed bed reactor). Albite dissolution is always incongruent in water at most temperatures, but becomes congruent at 300℃ (close to the critical point 374℃). At temperatures from 25 to 300℃, the incongruent dissolution of albite is reflected by the fact that sodium and aluminum are easily dissolved into water; from 300 to 400℃ it is reflected by silicon being more easily dissolved in water than Al and Na. Maximum albite dissolution rates in the flow hydrothermal systems have been repeatedly observed at 300℃, independent of flow rates.The kinetic experiments of albite dissolution in a KCl aqueous solution (0.1 mol KCl) indicate that the dissolution rate of albite increases with increasing temperature. Maximum silicon release rates of albite have been observed at 400℃, while ma  相似文献   

11.
贵州碳酸盐岩红土中的粘土矿物及其形成机理   总被引：13，自引：2，他引：13  
朱立军  傅平秋 《矿物学报》1996,16(3):290-297,T001
本文运用Ｘ射线衍射、红外光谱、差热、透射电镜和扫描电镜等方法对贵州碳酸盐岩红土中的粘土矿物进行了系统研究。高岭石和０．７ｎｍ埃洛石是碳酸盐岩红土中的主要粘土矿物，其次为伊利石、蛭石、绿泥石、绿泥石／蛭石混层矿物，水铝英石和三水铝石等。  相似文献   

12.
广西靖西县新圩铝土矿Ⅶ号矿体矿石热分析   总被引：1，自引：0，他引：1  
广西靖西新圩堆积型铝土矿为我国典型的一水铝型铝土矿。以新圩堆积型铝土矿的典型样品为研究对象,通过X衍射分析确定其矿物组成,进一步借助差热(DTA)与热重(TG/DTG)分析,探索铝土矿石加热过程。X衍射分析显示5个铝土矿样品矿物组成主要为硬水铝石、赤铁矿、绿泥石、三水铝石、锐钛矿、金红石、针铁矿以及少量的高岭石。差热(DTA)分析显示铝土矿样品有2个明显的吸热峰,分别为三水铝石和硬水铝石吸热峰;热重(TG/DTG)曲线显示样品分解分为4个阶段,分别为吸附水失去阶段和三水铝石、针铁矿、硬水铝石脱羟基作用阶段。利用热重(TG/DTG)数据分别计算了硬水铝石、三水铝石、针铁矿矿物相对百分含量,与国内外同类型铝土矿矿石热分析特征对比显示具有大体一致的热分析特征。  相似文献   

13.
Mineral dissolution and precipitation reactions actively participate to control fluid chemistry during water-rock interaction. However, it is difficult to estimate and normalize bulk reaction rates if the mineral surface area effectively participating in the reactions is unknown. In this study, we evaluated the changing of the reactive mineral surface area during the interaction between CO2-rich fluids and albitite rock reacting under flow-through conditions. Our methodology, adopting an inverse modelling approach, is based on the measured chemical fluid composition as raw data. We estimated the rates of dissolution and the reactive surface areas of the different minerals by reconstructing the chemical evolution of the interacting fluids. This was done by a reaction process schema that was defined by a fractional degree of advance of the irreversible mass-transfer process and by attaining the continuum limit during the water-rock interaction. Calculations were carried out for albite, microcline, biotite and calcite assuming that the ion activity of dissolved silica and aluminium ions was limited by the equilibrium with quartz and kaolinite.We found that the absolute dissolution rate of albite, microcline, biotite and calcite remains essentially constant as a function of time, and the calcite dissolution rate is orders of magnitude higher than silicate minerals. On the contrary, the reactive surface area of the parent minerals varied by more than two orders of magnitude during the observed reaction time, especially for albite. We propose that the reactive surface area depends mainly on the stability of the secondary mineral coating that may passivate the effective reactive surface area of the parent minerals.  相似文献   

14.
重庆南川-武隆铝土矿属于渝南-黔北铝土矿成矿带,为喀斯特型铝土矿床。经显微镜、X射线粉晶衍射、矿物自动分析仪（MLA）、扫面电子显微镜等方法对该矿床矿物学的研究,发现组成铝土矿的主要矿物为一水硬铝石、高岭石、绿泥石,次要矿物为伊利石、一水软铝石、三水铝石、鲕绿泥石、菱铁矿、赤铁矿、针铁矿、黄铁矿、锐钛矿、金红石、磷灰石、石英、锆石、方解石、长石及稀土矿物等。矿石组构及矿物组合表明形成铝土矿的沉积/成岩环境为接近于潜流的环境。矿石结构和锆石形态指示成矿物质经过了短距离的搬运。地球化学研究结果显示,组成铝土矿的主要化学成分为Al2O3、TFeO、SiO2和TiO2,铝土矿化过程中REE、Zr、Hf、Nb、Ta、Th、Sc、Li和Ga发生富集。形成铝土矿的母岩物质主要来自下伏页岩的风化作用,灰岩和酸性火山岩对铝土矿的形成也有一定的贡献。结合稳定同位素资料,认为铝土矿的形成可能与生物作用有关。  相似文献   

15.
Bauxite occurring as a blanket over volcanics of Precambrian Iron Ore Group in Kusumdih and Jaldih of Sundergarh district, Odisha, Eastern India exhibits four types of morphology viz. pisolitic, disseminated, spotted and massive. The volcanics/tuffs are altered to shale and is predominantly constituted of kaolinite. Microstructures documented in different morphologies of bauxite are collomorphous, framework, chain, stalactitic, reticulate, vesicle filled and foliated-platy types. Gibbsite, diaspore and kaolinite exhibit the abovementioned morphological and microstructural features. The morphological and microstructural characteristics are interpreted in terms of genetic evolution of aluminous minerals of bauxite in such a setup. Gibbsite and diaspore are formed through solution and precipitation/recrystallisation from kaolinite booklets present in parent tuffaceous shales. Some diaspores were formed at the expense of gibbsites. Small well-ordered kaolinites are of authigenic nature. Kaolinite formed inside a localized closed system containing supersaturated solution exhibits growth spirals. The textural and morphological diversities of the bauxite, abundance of well-ordered bauxite minerals and the absence of any iron/silica phase along with limited occurrence of primary kaolinite together suggest that the deposit has attained a high degree of bauxitisation in weathering environment at surface temperature.  相似文献   

16.
Bauxite deposits of Mainpat Plateau Surguja District, India, are composed of kaolinite, gibbsite, goethite, anatase, and bohemite. Quartz and micas are absent in the samples. The presence of boehmite and goethite are evidences of intense weathering during the formation of the bauxite deposits. The Mainpat Plateau is a mesa landform, at an elevation of around 1,060 m from msl in comparison to the general elevation of 580, consisting of Archaeans (granite?gneisses, phyllite, etc.) at the base, Gondwanas and Deccan basalt, and at the top having a cover of laterite and bauxite. The extremely high values of the chemical index of alteration, and the low values of the alkali metals and alkali earth metals, support an intense weathering origin for the bauxite deposit. There is evidence of deposition in the deposits based on the presence of pisoids in the bauxite samples and the composition of the parent rock. Kaolin minerals were first produced by the hydrolytic weathering of aluminous sediments and then gibbsite was formed as early kaolin was desilicated. The bauxite is having high TiO2 up to 17 %. The Mainpat laterite/bauxite deposits are characterized by having 50?58 % average Al2O3 and 10?30 % Fe2O3.  相似文献   

17.
This study focused on typical injection layers of deep saline aquifers in the Shiqianfeng Formation used in the Carbon Capture and Sequestration Demonstration Projects in the Ordos Basin, Northwest China. The study employed experiments and numerical simulations to investigate the mechanism of CO2 mineral sequestration in these deep saline aquifers. The experimental results showed that the dissolved minerals are plagioclase, hematite, illite–smectite mixed layer clay and illite, whereas the precipitated minerals are quartz (at 55, and 70 °C) and kaolinite (at 70 °C). There are rare carbonate mineral precipitations at the experimental time scale, while the precipitation of quartz as a product of the dissolution of silicate minerals and some intermediate minerals rich in K and Mg that transform to clay minerals, reveals the possibility of carbonate precipitation at the longer time scale. These results are consistent with some results previously reported in the literature. We calibrated the kinetic parameters of mineral dissolution and precipitation by these experimental results and then simulated the CO2 mineral sequestration under deep saline aquifer conditions. The simulation results showed that the dissolved minerals are albite, anorthite and minor hematite, whereas the precipitated minerals are calcite, kaolinite and smectite at 55 and 70 °C. The geochemical reaction of illite is more complex. At 55 °C, illite is dissolved at the relatively lag time and transformed to dawsonite; at 70 °C, illite is precipitated in the early reaction period and then transformed to kaolinite. Based on this research, sequestrated CO2 minerals, which are mainly related to the temperature of deep saline aquifers in Shiqianfeng Fm., are calcite and dawsonite at lower temperature, and calcite at higher temperature. The simulation results also establish that calcite could precipitate over a time scale of thousands of years, and the higher the temperature the sooner such a process would occur due to increased reaction rates. These characteristics are conducive, not only to the earlier occurrence of mineral sequestration, but also increase the sequestration capacity of the same mineral components. For a sequestration period of 10,000 years, we determined that the mineral sequestration capacity is 0.786 kg/m3 at 55 °C, and 2.180 kg/m3 at 70 °C. Furthermore, the occurrence of mineral sequestration indirectly increases the solubility of CO2 in the early reaction period, but this decreases with the increase in temperature.  相似文献   

18.
河南铝土矿矿物成因及其演化序列   总被引：2，自引：0，他引：2  
刘学飞 《地质与勘探》2012,48(3):449-459
[摘 要]豫西铝土矿是我国喀斯特型铝土矿的典型代表。本文选取豫西典型的喀斯特型铝土矿为研究对象,通过XRD 分析、扫描电镜-能谱分析、电子探针分析和差热分析多种手段,探测铝土矿的物质组成及其赋存状态,并且分析其矿物成因,总结矿物演化序列。研究显示,豫西铝土矿的主要矿物成分包括硬水铝石、伊利石、锐钛矿、高岭石、针铁矿、赤铁矿、金红石等。硬水铝石主体为简单结晶成因。伊利石主体为风化过程中产物,部分为后期硬水铝石硅质交代的结果。锐钛矿和硬水铝石同期结晶形成于还原环境下。大部分高岭石形成于陆源期风化阶段,少部分为后期硬水铝石硅化转变形成。针铁矿和赤铁矿形成于两个阶段,第一阶段为成矿前风化作用形成的铁质风化壳;第二阶段为铝土矿成岩晚期出现了一期铁质流体活动形成了大量的赤铁矿和针铁矿。重砂矿物金红石和锆石等主要是母岩风化作用的残留物。豫西铝土矿中矿物形成演化可归纳为如下五个阶段:陆源期、同生期、成矿期、成矿后期和表生期。  相似文献   

19.
The peculiarities of weathering processes involving duration, slow change of ambient conditions, isothermality as well as proceeding in open systems permit to study these processes in a steady-state approach (dCi/dt = 0, where Ci is concentration of intermediates; and t is time). The most typical quasi-stationary processes for a water-rock system are: (1) non-equilibrium step - surface reaction of primary-mineral dissolution; and (2) non-equilibrium step - secondary-mineral precipitation. These respectively determine two extreme mechanisms of mineral formation: (1) pseudomorphous replacement; and (2) dissolution-transfer-crystallization. Besides non-stationary weathering processes are known. It is the case when a process is controlled by diffusion through a layer of secondary minerals which have been deposited on the surface of the primary mineral. A mathematical model of weathering dynamics of feldspar with its metasomatic replacement by clay minerals is presented. Numerical simulation led to the prediction of mineral zonality development along the weathering profile at any time.  相似文献   

20.
Weathering rates of silicate minerals observed in the laboratory are in general up to five orders of magnitude higher than those inferred from field studies. Simple calculations show that even if the field conditions were fully simulated in standard laboratory experiments, it would be impossible to measure the slow rates of mineral dissolution that are observed in the field. As it is not possible to measure the dissolution rates under typical field conditions, one should extrapolate the available data to the field conditions. To do this, a rate law for the dissolution of plagioclase in the field was formulated by combining the far from equilibrium dissolution rate of weathered natural oligoclase at 25°C with the effect of deviation from equilibrium on dissolution rate of fresh albite at 80°C. In contrast to the common view that laboratory experiments predict dissolution rates that are faster than those in the field, the simulation based on this rate law indicates that laboratory dissolution experiments actually predict slower rates than those observed in the field. This discrepancy is explained by the effect of precipitation of secondary minerals on the degree of saturation of the primary minerals and therefore on their dissolution rate. Indeed, adding kaolinite precipitation to the simulation significantly enhances the dissolution rate of the plagioclase. Moreover, a strong coupling between oligoclase dissolution and kaolinite precipitation was observed in the simulation. We suggest that such a coupling must exist in the field as well. Therefore, any attempt to predict the dissolution rate in the field requires knowledge of the rate of the secondary mineral precipitation.  相似文献   

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