TY - JOUR
T1 - Impact and recovery of pH in marine sediments subject to a temporary carbon dioxide leak
AU - Taylor, Peter
AU - Lichtschlag, Anna
AU - Toberman, Matthew
AU - Sayer, Martin D. J.
AU - Reynolds, Andy
AU - Sato, Toru
AU - Stahl, Henrik
PY - 2015/7
Y1 - 2015/7
N2 - A possible effect of a carbon dioxide leak from an industrial sub-sea floor storage facility, utilised for Carbon Capture and Storage, is that escaping carbon dioxide gas will dissolve in sediment pore waters and reduce their pH. To quantify the scale and duration of such an impact, a novel, field scale experiment
was conducted, whereby carbon dioxide gas was injected into unconsolidated sub-sea floor sediments for a sustained period of 37 days. During this time pore water pH in shallow sediment (5mm depth) above the leak dropped >0.8unit, relative to a reference zone that was unaffected by the carbon dioxide. After the gas release was stopped, the pore water pH returned to normal background values within a three-week recovery period. Further, the total mass of carbon dioxide dissolved within the sediment pore fluids above the release zone was modelled by the difference in DIC between the reference and release zones. Results showed that between 14 and 63% of the carbon dioxide released during the experiment could remain in the dissolved phase within the sediment pore water.
AB - A possible effect of a carbon dioxide leak from an industrial sub-sea floor storage facility, utilised for Carbon Capture and Storage, is that escaping carbon dioxide gas will dissolve in sediment pore waters and reduce their pH. To quantify the scale and duration of such an impact, a novel, field scale experiment
was conducted, whereby carbon dioxide gas was injected into unconsolidated sub-sea floor sediments for a sustained period of 37 days. During this time pore water pH in shallow sediment (5mm depth) above the leak dropped >0.8unit, relative to a reference zone that was unaffected by the carbon dioxide. After the gas release was stopped, the pore water pH returned to normal background values within a three-week recovery period. Further, the total mass of carbon dioxide dissolved within the sediment pore fluids above the release zone was modelled by the difference in DIC between the reference and release zones. Results showed that between 14 and 63% of the carbon dioxide released during the experiment could remain in the dissolved phase within the sediment pore water.
KW - Carbon capture and storage
KW - Sediment pore water
KW - pH
KW - CO2
U2 - 10.1016/j.ijggc.2014.09.006
DO - 10.1016/j.ijggc.2014.09.006
M3 - Article
SN - 1750-5836
VL - 38
SP - 93
EP - 101
JO - INTERNATIONAL JOURNAL OF GREENHOUSE GAS CONTROL
JF - INTERNATIONAL JOURNAL OF GREENHOUSE GAS CONTROL
ER -