Abstract
Salt precipitation as subflorescence or efflorescence crust occurs
during saline solutions evaporation from porous media. Non-linear
synergy between evaporation and salt precipitation processes results in
a complex mechanism that has yet to be quantitatively understood.
Presented here is a series of experiments and a mathematical model that
shed light on these processes. Experiments include: (1) long-term column
evaporation experiments to quantify changes in evaporation rates due to
salt precipitation; (2) long-term Hele-Shaw evaporation experiments to
visualize salt precipitation at the macro scale; and (3) CT scans of
evaporated porous media pre-saturated with NaI solutions to observe salt
precipitation at the pore scale. Experiments were conducted for
homogeneous and heterogeneous media using a number of saline solutions
(NaCl, CaSO4, KCl, CuSO4 and NaI). A mathematical model was developed to
explore quantitatively the physical and chemical mechanisms involved in
the evaporation-salt precipitation process. The model simulated salt
precipitation and it affect on evaporation. Three new stages of
evaporation are introduced and defined for saline solutions: SS1, SS2
and SS3. SS1 exhibits a low and gradual decrease in evaporation rate
caused by a changing osmotic potential. During SS2, evaporation rate
falls precipitously a salt precipitates. SS3 is characterized by a
constant, low evaporation rate. The phenomenological similarity to the
classical evaporation stages of pure water, S1, S2 and S3, are only
coincidental, the three saline stages correspond to entirely different
mechanisms. The mathematical model was used to also quantify the
diffusion coefficient through a salt crust. Heterogeneity during saline
evaporation was found to strongly control the location of salt
precipitation: salt precipitation occurred mainly within the fine-pore
regions which act as a wick transporting water from the coarser media.
Heterogeneity also permits greater saline evaporation by concentrating
salt over the fine-pore regions: coarse-pore regions remain relatively
free of salt crystals enabling vapor to flow towards the atmosphere.
Original language | English |
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Title of host publication | American Geophysical Union, Fall Meeting 2010 |
State | Published - 1 Dec 2010 |
Event | American Geophysical Union, Fall Meeting 2010 - Duration: 13 Dec 2010 → 17 Dec 2010 |
Conference
Conference | American Geophysical Union, Fall Meeting 2010 |
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Period | 13/12/10 → 17/12/10 |
Keywords
- 1042 GEOCHEMISTRY / Mineral and crystal chemistry
- 1818 HYDROLOGY / Evapotranspiration
- 1843 HYDROLOGY / Land/atmosphere interactions
- 1875 HYDROLOGY / Vadose zone