SO2 scrubbing during percolation through rhyolitic volcanic domes. (15th July 2019)

• Record Type: Journal Article
• Authors: Casas, Ana S.; Wadsworth, Fabian B.; Ayris, Paul M.; Delmelle, Pierre; Vasseur, Jérémie; Cimarelli, Corrado; Dingwell, Donald B.
• Is Part Of: Geochimica et cosmochimica acta. Volume 257(2019)
• Page Start: 150
• Page End: 162
• Publication Date: 2019-07-15
• Subjects: Rhyolitc glass -- SO2 scavenging -- Volcanic dome; Geochemistry -- Periodicals; Meteorites -- Periodicals; Géochimie -- Périodiques; Météorites -- Périodiques; Geochemie; Astrochemie; Electronic journals; 551.905
• DOI: 10.1016/j.gca.2019.04.013
• Languages: English
• ISSNs: 0016-7037

Abstract

Abstract: Accurate estimates of the atmospheric impacts of large eruptions on the environment are complicated by a paucity of models for gas-magma or gas-rock interactions that can occur in the subsurface. It is in these environments that high-temperature scavenging of magmatic gases, released during eruptions, may play a major role, resulting in significant time-dependence of the bulk gas budget of the major erupted volatile species. Recent experimental work has identified the principal mechanisms involved in high-temperature scavenging in SO2 - and HCl-dominated gas environments, but has neglected the effect of humidity and in-dome gas-magma reactions. Here we present scaled experimental results for the scavenging potential in SO2 -H2 O mixtures using rhyolitic glass particles above the acid dew point at 200–800 °C. First, we reproduce previous results for anhydrous SO2 scavenging. Such scavenging is accommodated by the growth of CaSO4 crystals on the surface of glass present on ash and limited by the temperature- and particle size-dependent diffusion of Ca 2+ to the surface of the glass. Subordinate concentrations of Na2 SO4 and potassium-bearing salts also grow on the glass surfaces. Na + and K + diffusion appear to be the limiting mechanisms for the formation of these salts, but once the bulk glass network is relaxed and equilibrates oxidation state above ∼600 °C, the diffusion of these cations is inhibited by charge compensation with Fe 3+ . In SO2 -H2 O mixed-gas atmospheres, the diffusion of Ca 2+ appears unaffected by the activity of H2 O on the ash surface. In contrast, the diffusion of Na + and K + toward the ash surface is enhanced. We speculate that this occurs by alkali exchange with inward diffusing H + . In hydrous atmospheres, the diffusion of Na + and K + is also markedly less at the threshold oxidation temperature. This oxidation temperature is reduced to lower values as the water activity at the surface is increased by increasing the partial pressure of H2 O. Taken together, these results enable the exploration of scenarios for in-dome processes where either open-system or batch outgassing prevails through fractures filled with populations of welding volcanic ash. Such scenarios predict that a large fraction of the SO2 flowing through the ash-filled fracture networks may be scavenged in permeable fractured domes, which act as scrubbing filters, potentially explaining some unexpectedly low SO2 emissions from rhyolitic dome-forming eruptions.