Acid‐Induced Dissolution of Andesite: Evolution of Permeability and Strength

Volcanic systems often host crater lakes, flank aquifers, or fumarole fields that are strongly acidic. In order to explore the evolution of the physical and mechanical properties of an andesite under these reactive chemical conditions, we performed batch reaction experiments over timescales from 1 day to 4 months. The experiments involved immersion of a suite of samples in a solution of 0.125 M sulfuric acid (pH ∼0.6). Periodically, samples were removed and their physical and mechanical properties measured. We observe a progressive decrease in mass, coincident with a general increase in porosity, which we attribute to plagioclase dissolution accompanied by the generation of a microporous diktytaxitic groundmass due to glass dissolution. Plagioclase phenocrysts are seen to undergo progressive pseudomorphic replacement by an amorphous phase enriched in silica and depleted in other cations (Na, Ca, and Al). In the first phase of dissolution ( t = 24–240 hr), this process appears to be confined to preexisting fractures within the plagioclase phenocrysts. However, ultimately these phenocrysts tend toward entire replacement by amorphous silica. We propose that the dissolution process results in the widening of pore throats and the improvement of pore connectivity, with the effect of increasing permeability by over an order of magnitude relative to the initial measurements. Compressive strength of our samples was also modified, insofar as porosity tends to increase (associated with a weakening effect). We outline broader implications of the observed permeability increase and strength reduction for volcanic systems including induced flank failure and related hazards, improved efficiency of volatile migration, and attendant eruption implications.