Chemomechanical evolution of pore space in carbonate microstructures upon dissolution: Linking pore geometry to bulk elasticity
Chemomechanical evolution of pore space in carbonate microstructures upon dissolution: Linking pore geometry to bulk elasticity
复制标题
溶解时碳酸盐微观结构中孔隙空间的化学机械演化:将孔隙几何形状与体弹性联系起来
DOI:
10.1002/2015jb012087
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
T. Vanorio
中科院分区:
文献类型:
--
作者:
C. Arson;T. Vanorio
One of the challenges faced today in a variety of geophysical applications is the need to understand the changes of elastic properties due to time‐variant chemomechanical processes. The objective of this work is to model carbonate rock elastic properties as functions of pore geometry changes that occur when the solid matrix is dissolved by carbon dioxide. We compared two carbonate microstructures: porous micrite (“mudstone”) and grain‐supported carbonate (“packstone”). We formulated a mathematical model that distinguishes the effects of microporosity and macroporosity on stiffness changes. We used measures of mechanical and chemical porosity changes recorded during injection tests to compute elastic moduli and compare them to moduli obtained from wave velocity measurements. In mudstones, both experimental and numerical results indicate that bulk moduli change by less than 5%. The evolution of elastic moduli is controlled by macropore enlargement. In packstones, model predictions underestimate changes of elastic moduli with total porosity by 10% to 80%. The total porosity variation is 60% to 75% smaller than the chemical porosity variation, which indicates that pore expansion due to dissolution is counterbalanced by pore shrinkage due to compaction. Packstone elastic properties are controlled by grain sliding. The methodology presented in this paper can be generalized to other chemomechanical processes studied in rocks, such as dislocations, glide, diffusive mass transfer, recrystallization, and precipitation.