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Metal scavenging by calcium carbonate at the Eyjafjallajökull volcano:A carbon capture and storage analogue

Authors :
Olsson, J.
Stipp, S. L S
Makovicky, E.
Gislason, S. R.
Olsson, J.
Stipp, S. L S
Makovicky, E.
Gislason, S. R.
Source :
Olsson , J , Stipp , S L S , Makovicky , E & Gislason , S R 2014 , ' Metal scavenging by calcium carbonate at the Eyjafjallajökull volcano : A carbon capture and storage analogue ' , Chemical Geology , vol. 384 , pp. 135-148 .
Publication Year :
2014

Abstract

The reaction of CO2 and water with basaltic rock can release trace heavy metals, which pose a serious threat to the quality of surface waters. The pH of the carbonated water increases during dissolution of the host rock or dilution by pore fluids. This leads to precipitation of carbonate and other secondary minerals that often scavenge the released heavy metals. However, very little is known about uptake capacity of the precipitates in natural systems or how much divergence there could be, compared with behavior in laboratory experiments. The spring 2010 eruption of the Eyjafjallajökull volcano, Iceland, provides a unique opportunity to study the mobility of heavy metals that are released during CO2 injection into shallow basaltic aquifers and the ensuing precipitation of carbonate minerals. Following the Eyjafjallajökull eruption, rapid and constant travertine formation was discovered in the Icelandic river, Hvanná, in the vicinity of the volcano. The river water emerged from under the lava flow and was heavily charged with cations and dissolved CO2. The concentration of the major dissolved constituents was: dissolved inorganic carbon (DIC), 33.08mM; calcium, 6.17mM; magnesium, 4.27mM; sodium, 2.78mM and sulfur, 1.92mM. Carbon dioxide degassing of the river water increased pH from 6.6 to 8.5 and travertine precipitated for hundreds of meters downstream, rendering the stream bed white with calcite. Rapid crystallization rate produced dendritic structures or sometimes very porous material. Boxwork textures were observed within the porous calcite that probably originated from transformation of a metastable phase such as ikaite (CaCO3·6 H2O). A gradual decrease of conductivity from 1.8mS/cm at the river water outlet to 1.1mS/cm downstream and a clear drop in dissolved metal concentration strongly correlated with the precipitated calcite. Considering the complexity of the natural system, the estimated partition c

Details

Database :
OAIster
Journal :
Olsson , J , Stipp , S L S , Makovicky , E & Gislason , S R 2014 , ' Metal scavenging by calcium carbonate at the Eyjafjallajökull volcano : A carbon capture and storage analogue ' , Chemical Geology , vol. 384 , pp. 135-148 .
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1322657668
Document Type :
Electronic Resource