1. Resistance to weathering depends on:
internal resistance of material
magnitude of external forces
2. Growth in voids
a. freeze-thaw
b. crystal growth; salt weathering
3. Wetting & drying
a. hydration: addition of water to mineral structure causes structure to expand
chemical reaction with physical results
b. susceptible soils & rocks:
soils with 2:1 layered clays (e.g. montmorillonite)
shale, clayey siltstones and sandstones, granite
c. result:
4. Thermal expansion
different minerals have different coefficients of thermal expansion
e.g. quartz is about 3 times that of feldspar
5. Unloading
1. Introduction
progression from less stable minerals to more stable minerals
primary minerals - secondary minerals - new secondary minerals
water is critical
geochemical weathering: driven by inorganic processes; produces "rotten" rocks or saprolites
pedochemical weathering: controlled by biologic processes; leads to formation of soil from saprolites
2. Solution
a. virtually all chemical weathering involves some solution
b. most common minerals are soluble to some degree in normal waters
except:
silica when contained in quartz
aluminum oxides - virtually insoluble under normal conditions
ferric iron - requires very acidic fluids
3. Oxidation & reduction
a. an element in a mineral structure loses electrons to an oxygen ion; forms oxides and hydroxides
e.g. ferrous iron (Fe+2) oxidizes to ferric iron (Fe+3)
4Fe+2 + 3O2 = 2Fe2O3
iron + oxygen = iron oxide
b. most elements at earth's surface exist in an oxidized state
c. reduced form of elements are more mobile than oxidized because they're more soluble
4. Hydrolysis
a. water dissociates into H+ and OH-
b. H+ displaces other cations in mineral structure
c. important mechanism for breaking apart silicate minerals
5. Ion exchange
a. substitution of ions in minerals (usually cations) by ions in solution without rearrangement of mineral structure
b. most effective in clays
cations held to clay surface by adsorption; not held too tightly
H+ and Ca+2 are most readily adsorbed; Na+2 is most readily released
c. cation exchange capacity: propensity for adsorbing cations
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©
K.A. Lemke (klemke@uwsp.edu)
Last modified November 7, 2006 |