塔里木盆地阿克库勒地区石炭系卡拉沙依组成岩作用

阿克库勒地区卡拉沙依组碎屑岩储层的成分成熟度和结构成熟度均较低．储层的次生溶蚀孔隙所占比例远高了：原生孔隙，次生孔隙是储层的主要储集空间．样品数据统计显示，卡拉沙依组储层属于低孔、低渗储层类型．根据岩石薄片、铸体薄片观察及储层样品的扫描电镜和阴极发光分析结果，本区石炭系储层主要经历的成岩作用有压实（压溶）作用、胶结作用、溶蚀作用和交代作用，其中碳酸盐矿物的沉淀和溶蚀作用是本区卡拉沙依组储层所经历的最重要的成岩作用．成岩作用已达到晚成岩B期，早期方解石交代石英颗粒并发生大量溶蚀，生成大量次生孔隙，晚期方解石没有发生溶蚀．     

一种新的储层孔隙成因类型--石英溶解型次生孔隙

石英作为碎屑岩储层中的一种难溶组分,普遍认为它和次生孔隙的形成关系不十分密切。研究认为泌阳凹陷核桃园组储层中的碎屑石英颗粒存在明显的溶解现象,并形成以石英直接溶解型孔隙为主的储集空间特征。石英颗粒被溶解的部分在薄片中所占的范围为 2 %～ 7%者常见,高者达 8%以上,在总孔隙中所占的相对含量也多数在10 %～ 35 %之间,早成岩B期是其最主要形成期。石英溶解型次生孔隙的大量存在为碎屑岩储层中SiO₂ 胶结物及次生孔隙成因等问题的解释以及储层预测和评价提供了新的可能性。     

25～75℃酸性NaCl溶液中方铅矿的溶解动力学

在25～75℃、pH=0.43～2.45的1mol/LNaCl溶液中进行了方铅矿的溶解动力学实验。发现在远平衡条件下,方铅矿的溶解速率r与氢离子活度犤H+犦呈线性关系,溶解速率方程(速率定律)为:r=k犤H+犦,即对H+而言,溶解反应为一级。其中速率常数k为2.344×10-7mol/m2·s(25℃)、1.380×10-6mol/m2·s(50℃)、7.079×10-6mol/m2·s(75℃)。溶解反应的活化能为43.54kJ/mol,方铅矿的溶解机理为表面化学反应,速率决定步骤为表面配合物的离解。     

Variation in element release rate from different mineral size fractions from the B horizon of a granitic podzol

Far-from-equilibrium batch dissolution experiments were carried out on the 2000–500, 500–250, 250–53 and 53–2 μm size fractions of the mineral component of the B horizon of a granitic iron humus podzol after removal of organic matter and secondary precipitates. The different size fractions were mineralogically and chemically similar, the main minerals present being quartz, alkali and plagioclase feldspar, biotite and chlorite. Specific surface area increased with decreasing grain size. The measured element release rates decreased in the order 53–2>>>2000–500>500–250>250–53 μm. Surface area normalised element release rates from the 2000–500, 500–250 and 250–53 μm size fractions (0.6–77×10⁻¹⁴ mol/m²/s) were intermediate between literature reported surface area normalised dissolution rates for monomineralic powders of feldspar (0.1–0.01×10⁻¹⁴ mol/m²/s) and sheet silicates (100×10⁻¹⁴ mol/m²/s) dissolving under similar conditions. Element release rates from the 53–2 μm fraction (400–3000×10⁻¹⁴ mol/m²/s) were a factor of 4–30 larger than literature reported values for sheet silicates. The large element release rate of the 53–2 μm fraction means that, despite the small mass fraction of 53–2 μm sized particles present in the soil, dissolution of this fraction is the most important for element release into the soil. A theoretical model predicted similar (within a factor of <2) bulk element release rates for all the mineral powders if observed thicknesses of sheet silicate grains were used as input parameters. Decreasing element release rates with decreasing grain size were only predicted if the thickness of sheet silicates in the powders was held constant. A significantly larger release rate for the 53–2 μm fraction relative to the other size fractions was only predicted if either surface roughness was set several orders of magnitude higher for sheet silicates and several orders of magnitude lower for quartz and feldspars in the 53–2 μm fraction compared to the other size fractions or if the sheet silicate thickness input in the 53–2 μm fraction was set unrealistically low. It is therefore hypothesised that the reason for the unpredicted large release rate from the 52–3 μm size fraction is due to one or more of the following reasons: (1) the greater reactivity of the smaller particles due to surface free energy effects, (2) the lack of proportionality between the BET surface area used to normalise the release rates and the actual reactive surface area of the grains and, (3) the presence of traces quantities of reactive minerals which were undetected in the 53–2 μm fraction but were entirely absent in the coarser fractions.     

Phénomènes karstiques fossiles et actuels au sein des formations métamorphiques silico-alumineuses de la nappe pan-africaine de Yaoundé (Sud-Cameroun)Fossil and present-time karstic phenomena in silico-aluminous metamorphic formations of the Pan-African nappe of Yaoundé (South-Cameroon)

Numerous karstic features have been recognised in the non-carbonaceous micaschists and gneisses of the Yaoundé Pan-African nappe, south of Cameroon. It is shown that their formation was controlled by the structural features of the rocks. The wells and the pipes in the bedrock outcrops point out a current karstification process, resulting from the plagioclase dissolution by the acid rain waters. Hill wall alveoli and caves, of pre-Miocene age, are exhumed features that were done by dissolution in the aquiferous underground. To cite this article: J.-P. Vicat et al., C. R. Geoscience 334 (2002) 545–550.     

An EFTEM/HRTEM high-resolution study of the near surface of labradorite feldspar altered at acid pH: evidence for interfacial dissolution-reprecipitation

Using an approach combining high-resolution and energy-filtered transmission electron microscopy (HRTEM and EFTEM), we have studied with Å to nm-spatial resolution the interfacial region that delimits the near-surface altered zone and non-altered labradorite feldspar after dissolution under acid pH conditions. The interface is characterized by extremely sharp and spatially coincident changes in structure and chemistry. The 500-nm-thick altered zone is depleted in interstitial cations (Ca, Na, K) and Al, a framework element, whereas it is enriched in H, O, and Si. Modeling H⁺-alkali interdiffusion within a 500-nm-thick altered zone shows that volume interdiffusion cannot reproduce the sharp chemical interfaces measured by EFTEM. Based on these new data, we propose that the near-surface altered zone is a result of interfacial dissolution-reprecipitation, and not of preferential leaching of cations and interdiffusion with H⁺. This implies an intrinsic dissolution process that is stoichiometric, where the breaking of bonds and release of interstitial cations and framework elements (Al, Si, and O) to solution occur contemporaneously at equal relative rates from the original fluid–mineral interface.     

地球化学样品中硒的循序提取技术

研究开发了一种硒的循序偏提取步骤，将地球化学样品中的硒选择性地循序提取到六个“操作上”定义的相态中：水溶性硒（水提取）；吸附在氧化矿物和粘土矿物上配位可交换的亚硒酸根离子（０．１ｍｏｌ／ＬＫＨ２ＰＯ４提取）；与有机质结合的硒（０．１ｍｏｌ／ＬＮａ４Ｐ２Ｏ７提取）；与铁锰铝氧化物和碳酸盐结合的硒（４．０ｍｏｌ／ＬＨＣｌ提取）；硫化物中的硒（ＫＣｌＯ３＋浓ＨＣｌ提取）；硅酸盐残渣中以副矿物和被硅质包裹的硒微粒存在的硒（ＨＦ＋ＨＮＯ３＋ＨＣｌＯ４强混合酸溶解）。对提取步骤的可行性和实用性作了详细的讨论。     

浅层地下水氟的溶解／沉淀作用的定量研究

以河北邢台山前平原浅层高氟地下水为例，根据氟的化学热力学分析，确定了控制浅层地下水中氟迁移和富集的固相沉淀物，以及不同化学类型的浅层地下水中含氟固相沉淀物的溶解／沉淀条件；利用浅层地下水化学平衡反应模型和ＰＨＲＥＥＱＥ软件，确定了氟化的稳定区域，计算了氟化钙的饱和指数．研究结果表明，在浅层高氟地下水的整个形成过程中，都表现为氟由固相转入水相的趋势，有利于氟的迁移和富集     

塔里木北部地区三叠系储层溶蚀作用机理

塔里木北部地区三叠系储层在成岩演化过程中曾经历两期溶蚀作用，深埋成岩环境的晚期溶蚀较早期近地表－浅埋成岩环境溶蚀要剧烈得多，溶蚀作用的最大特点是铝硅酸盐矿物较碳酸盐矿物剧烈。溶蚀作用发生的机理是由于三叠系储层处于８０～１２０℃热窗、成岩流体富含低分子量羧酸、碱度由低分子量羧酸控制，铝硅酸盐和碳酸盐矿物均处于去稳定状态。溶蚀作用的发育程度受控于储层砂体的沉积和岩石学特征以及早期成岩发育程度。     

Simulations of a coupled hydro-chemo-mechanical system in rocks

A coupled hydro-chemo-mechanical numerical model is developed for these coupled phenomena in many engineering fields. The model has been applied to predicting the response of a stressed rockmass column to an injected reactive fluid (reagent) flow. The response includes evolutions of porosity, permeability, reagent and mineral concentrations during dissolution. In the model, the progress of dissolution is defined by the change in porosity ratio and the porosity increases with dissolution assuming there is no precipitation. The numerical evolutions of porosity, permeability, reagent and mineral concentrations during dissolution are validated against steady state solutions. The model results show that these evolutions are regulated to a certain extent by the applied external loadings: an applied extensional stress enhances the progress of the dissolution process while an applied compression stress slows the progress of the dissolution process. This revised version was published online in July 2006 with corrections to the Cover Date.