Under the ANDRA Meuse/Haute Marne underground research laboratory scientific programme, two boreholes (EST204 and EST205) were drilled to a depth of 510 m for the purposes of scientific characterization. Twenty-nine core samples were taken in borehole EST205 every 3 m between 422 and 504 m depth. Physical property measurements (water content, porosity, density, specific surface), geochemical analyses (major and trace
AB ST R ACT : The diagenetic evolution of kaolin and illitic minerals in sandstones is described here. The structural characterization of these minerals, the possible reaction pathways leading to their crystallization, and the origin of the fluids involved are discussed specifically.While early precipitation of kaolinite is in general related to flushing by meteoric waters, subsequent diagenetic kaolinite-to-dickite transformation probably results from invasion by acidic fluids of organic origin. Dickite is the stable polytype in most sandstone formations and the kaoliniteto-dickite conversion is kinetically controlled.The conventional model of kaolin illitization, assuming a thermodynamic control in a closed system, is discussed and compared to an alternative model in which illitization of kaolin is not coupled to dissolution of K-feldspar (Berger et al., 1997). In the latter model, illite crystallization at the expense of kaolin implies that an energy barrier is overcome either by an increased K + /H + activity ratio in solution or by a considerable temperature increase.
A B S TRACT: The SEM, XRD, FFIR and DTA analyses of different size-fractions of clay material from sandstone reservoirs which have experienced a large range of burial conditions have been used to examine the different steps of the depth-related kaolinite-dickite reaction. Dickite progressively replaced kaolinite within a range of burial depths estimated between about 2500 m and 5000 m. The kaolinite-to-dickite reaction proceeds by gradual structural changes concomitant to crystal coarsening and change from booklet to blocky morphology. The crystallization of dickite proceeds by two distinct paths: (1) Accretion of new material from either dissolution of smaller unstable kaolinite crystals and/or detrital minerals (chiefly feldspars), on early-formed coarser metastable kaolinite crystals which exert extended morphological control on the growing crystals.(2) Neoformation of ordered dickite which will continue to grow by a dissolution-crystallization process. The kaolinite-todickite reaction is kinetically controlled and anomalies in the kaolinite/dickite ratio observed in certain sandstone reservoirs may be used to assess the timing of invasion by hydrocarbons.
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