HR: 0830h
AN: V51H-0383 [PDF]
TI: Formation of Quartz-Carbonate Veins: Evidence From Experimental Supercritical Carbon
Dioxide-Brine-Rock System
AU: * Janecky, D R
EM: janecky@lanl.gov
AF: Los Alamos National Laboratory, RRES/EA MS-J591, Los Alamos, NM 87545 United States
AU: Kaszuba, J P
EM: jkaszuba@lanl.gov
AF: Los Alamos National Laboratory, C-INC MS-J514, Los Alamos, NM 87545 United States
AB:
Quartz-carbonate veins are common in a variety of moderate temperature hydrothermal systems and ore deposits. Associated
fluid inclusions have a wide range of compositions, including liquid carbon dioxide fillings. Examination of chemical and
physical conditions which result precipitation of quartz and carbonate in veins raises several key questions about multiphase
fluid processes and reaction rates.
We have been experimentally investigating physical-chemical reaction processes of mixed brine-carbon dioxide fluids for the
shallow crust. Synthetic arkose (microcline + oligoclase + quartz + biotite) plus argillaceous shale were reacted with 5.5
molal NaCl brine. The system was held at 200 C and 200 bars for 32 days to approach steady state, then injected with carbon
dioxide and allowed to react for an additional 45 days. In a parallel experiment, the system was allowed to react for 77
days without injection of carbon dioxide. Trace ions initially absent from NaCl brine appeared in solution at mM (K, Ca, and
silica) to uM (Mg, Al, Fe and Mn) quantities, reflecting reaction of brine with rock. Without carbon dioxide injection, the
silica concentration (2.4 mM) was stable below calculated quartz solubility (3.9 mM). Injection of carbon dioxide resulted
in decreased pH and increased silica concentration to a level near calculated chalcedony solubility (5.4 mM). Dissolution of
silicate minerals is apparently coupled to the acidity, and concomitant inhibition of the precipitation of quartz (and other
silicates). A significant increase in concentration of trace metals is consistent with in-situ pH decrease and increased
carbon dioxide dissolved in brine.
Multi-phase fluid reaction relationships between supercritical carbon dioxide and brine-rock systems allow formation of
carbonate vein precipitates in substantial quantities. Brine and continued rock reactions provide a substantial reservoir
for Ca, Mg and Fe components. A separate carbon dioxide liquid allows precipitation from relatively small volumes of total
fluid, with coupled increases in pH and mineral stability. The doubling of silica concentration in the experimental system
containing acidic brine and supercritical carbon dioxide indicates that precipitation of silica can occur in parallel to
carbonate minerals when pH increases. Emplacement of silica super-saturated brine into a rock-dominated reaction system
buffered to more neutral pH conditions may enhance precipitation of quartz, chalcedony, or amorphous silica as veins or
cements, depending on the permeability structure of the host rock. Phase separation or loss of carbon dioxide with
decreasing pressure can substantially shift pH upwards, with potential for creating massive vein or scale formation.
DE: 1000 GEOCHEMISTRY (New field, replaces Rock Chemistry)
DE: 3015 Heat flow (benthic) and hydrothermal processes
DE: 3630 Experimental mineralogy and petrology
DE: 3660 Metamorphic petrology
SC: Volcanology, Geochemistry, Petrology [V]
MN: 2003 Fall Meeting