lecture 4 Flashcards
Why are H-bonds in the 1:1 interspace of Kaolinite stronger than the K-bonds in the 2:1 interspace of Micas?
Hydroxides in octahedral layer face apical O atoms of tetrahedral layer forming H-bonds
The relative charge of the H ion is much higher than K due to smaller size = stronger bonding strength
What are the characteristics of Fe and Al oxides and hydroxides / non silicates (sesquioxides)?
- Weathering products of clay minerals that have lost all Si4+ and most other cations except Fe3+ and Al3+
- Consist of modified octahedral sheets with Fe3+ and Al3+
- Have no silicon tetrahedral sheets
- Little or no isomorphous substitution - there are no more cations available
- Little cation exchange capacity
- Posses covalently bound OH-ions which may cause strong adsorption of certain anions like phosphate
What are the characteristics of soil colour?
- Dark colours are usually indicative of high organic carbon contents
- Red colours are characteristic of soil rich in iron oxides
- Blue-grey colours indicate the presence of iron in its reduced form, the gibbsite is dominating- the hematite and goethite have been dissolved and transported away
What chart allows us to identity types of soils?
The Munsell soil colour chart
What is the importance of sesquioxides in soils?
- They dominate in soil colour where there is low organic matter content
- Form cementation in soil when large oxide or hydroxide content (e.g. laterite in Tropics)
- Provide anion exchange capacity!!
What is cation exchange capacity? Where does it occur?
The ability to exchange cations between particle surface and soil solution. It occurs at the negative surfaces of clay minerals and humus.
What are the sources of charge for the cation exchange capacity?
- Isomorphic substitution within clay minerals
- Broken bonds at the edge of clay minerals
- Dissociation of bonds at the edge of the humus
What is the process of cation exchange between soil particles and the soil solution? How does the reverse reaction occur?
Replacement of base cations with H+, e.g. from acid rain or organic matter
This process can be reversed with proper soil management. The displacement of H+ from the exchange complex by base cations can occur through fertilization or nutrient release from decomposing tissues. Fertilization increases the soil pH and recharges the base cations.
What are the mechanisms of neutralization?
- Reaction with carbonates
- H2SO4 + CaCO3 –> CaSO4 + H2CO3 - Reaction with exchangeable cations or weatherable minerals such as feldspars
- Anion adsorption of SO4
What are the characteristics of cation exchange capacity?
- Exchange reactions are not always reversible
- Released cation can either precipitate, volatilize, or strongly associate with an anion
- The relative strengths of adsorption order may be altered on certain clay minerals (influenced by how strongly its neighboring cations are adsorbed)
Under what conditions do cations bind more tightly on the surface of colloids? Which cation has the strongest adsorption capacity?
The higher the charge and the smaller the hydrated radius of the cation, the more strongly it will adsorb to the colloid.
Al has the strongest adsorption capacity - this is why it is left behind even when the soil no longer has any buffering capacity
What is the effect of soil organic carbon and pH and the cation exchange capacity?
The higher the SOC or pH, the higher the cation exchange capacity.
In acidic soils (low pH), there are more hydrogen ions (H⁺), which can occupy the negatively charged sites, reducing the overall CEC.
What is the influence of soil pH on soil charge in clay minerals and how does that impact their preference for anion/cation exchange capacity?
Acid conditions = Positive charge –> prone to anion exchange capacity
Alkaline conditions = Negative charge –> prone to cation exchange capacity
Soils will always have the capacity to do anion and cation exchange capacity but it is dependent on the pH of the soil
What are the base and acidic cations?
Base: Ca, Mg, Na, K
Acidic: H, Al, NH4
Why are Al and Fe the last to mobilize during cation exchanges?
Due to their size and charge