CALL FOR PROPOSALS:

ORGANIZERS

  • Harvey Thorleifson, Chair
    Minnesota Geological Survey
  • Carrie Jennings, Vice Chair
    Minnesota Geological Survey
  • David Bush, Technical Program Chair
    University of West Georgia
  • Jim Miller, Field Trip Chair
    University of Minnesota Duluth
  • Curtis M. Hudak, Sponsorship Chair
    Foth Infrastructure & Environment, LLC

 

Paper No. 10
Presentation Time: 11:15 AM

EFFECTS OF ACTIVITY OF WATER ON THE DISSOLUTION RATES OF K-JAROSITE


PRITCHETT, Brittany, ConocoPhillips School of Geology and Geophysics, University of Oklahoma, 100 E Boyd, SEC 710, Norman, OK 73019, ELWOOD MADDEN, Megan E., School of Geology and Geophysics, Univ. of Oklahoma, 100 E. Boyd Street, Norman, OK 73072 and MADDEN, Andrew S., School of Geology and Geophysics, University of Oklahoma, 100 East Boyd St. Rm. 710, Norman, OK 73019, brittanyp@ou.edu

Jarosite, ((K, H, Na)Fe3(SO4)3(OH)6), is a ferric sulfate salt that forms both on Earth and on Mars. The presence of jarosite provides evidence of liquid water and can supply valuable information on the geochemistry of formation fluids and environments. Models for Martian jarosite formation are largely based off of terrestrial analogs and vary widely, including acid saline lake environments, where jarosite is known to form on Earth. In order to better understand the conditions necessary for jarosite formation and dissolution, the reactivity of jarosite in solutions with varying ionic strength, and hence activity of water, are reported here.

Mars brines associated with jarosite-bearing sediments have been estimated to contain Fe2(SO4)3, MgSO4, AlCl3, Na2SO4, CaCl2, MnSO4 and KH2PO4 at low pH, based on APEX spectra of outcrops at Meridiani Planum, Mars. Dissolution rates of K-jarosite were measured in 3 different fluids (ultra pure water, NaCl-saturated brine, and CaCl2 –saturated brine) covering a range of water activity (αH2O of 1.0, 0.75, and 0.35 respectively) in batch reactor experiments. 0.1g of K-jarosite was mixed with 100mL of each fluid and10 mL samples were removed at predetermined intervals over several hours and passed through a 0.2 μm filter. The aqueous samples were then diluted 1:8 and K+ concentrations analyzed using matrix-matched Flame Atomic Absorption Spectrophotometry.

Preliminary data show the rate of jarosite dissolution is affected by the αH2O. The average dissolution rate for the pure water experiment was approximately 4.21x10-9 mol/m2/s. The K-jarosite dissolution experiments in NaCl brine (αH2O = 0.75) produced an average rate of 9.27x10-11 mol/m2/s, while CaCl2 had the slowest of the three dissolution rates with an average rate of about 5.51x10-11 mol/m2/s. These results show that the dissolution rates of K-jarosite decrease as the αH2O decreases. Therefore, jarosite lifetimes are extended in high salinity systems, allowing for longer periods of aqueous alteration at Meridiani Planum.

Meeting Home page GSA Home Page