Organic or inorganic matter with particles less than0.001mm in size and a correspondingly large surface area per unit of mass
Soil colloids
The most active constituent of the soil
Determine the physical and chemical properties of the soil
Important properties of soil colloids
Large specific surface area (area per unit amount of colloid)
Extremely small particle size
Presence of electric charges, (positive and negative)
Exchangeable ions
Weakly held, in contact with soil solution, ready for quick replacement, available for plants
Nonexchangeable ions
Adsorbed by strong bonds or held in inaccessible places (e.g., the K+ between layers of illite)
Classification of soil colloids
Inorganic (clay) colloids
Organic colloids
Inorganic colloids
Made up of Si, Al, O
Inorganic and crystalline/ amorphous
Relatively stable
Have definite and well-known structure
Organic colloids
Made up of C, H, O
Complex amorphous organic colloid
More dynamic
Complex structure
Inorganic soil colloids
Crystalline silicates
Non-silicates or Fe/Al oxides
Amorphous silicates
Non-silicates or Fe/Al oxides
Crystalline silicate clay minerals
Kaolinite
Montmorillonite
Vermiculite
Illite
Chlorite
Isomorphous substitution
Replacing one structural cation for another of similar size
Kaolinite
1:1 type - one Tetrahedral (Th) sheet linked to an Octahedral (Oh) sheet
Adjacent layers are tightly bound together by H-bond
Non-expanding mineral, unable to absorb water into the interlayer position
Failure of soils to swell or shrink much on wetting and drying
Basal spacing fixed at 0.72nm (7 Å)
Lacks significant isomorphous substitution - small capacity to adsorb exchangeable cations
Montmorillonite
High (-) charges from isomorphous substitution (Mg2+ replaces Al3+ in Oh layer; Al3+ replaces Si4+ in Th layer)
High CEC (80-100meq/100g)
Specific surface (m2/g)= 700-800
Adjacent layers are loosely bound by weak O-O linkage & cation-O linkage
High water holding capacity (ultramicropores)
High shrink-swell potential
Vermiculite
High CEC (100-150meq/100g)
Limited expansion compared with smectite (interlayer constituents)
Variable d-spacing (14 Å expanded, 10 Å collapsed)
Larger crystal than smectite
2:1 type of structure
Hydrous Mica (Illite)
2:1 type minerals containing interlayer K+ resulting to no expansion on wetting
Replacement of Si4+ with Al3+, each substitution leaves 1 (-) charge
K+ ions are a bridge between layers and hold them tightly together
The K+ content of hydrous mica is less than that of micas
Chlorite
Non-expanding, contains two octahedral sheets, thus a 2:1:1 layer mineral
Chlorites differ from other 2:1 layer minerals in that they contain a stable, positively charged Oh sheet rather than adsorbed cations in the interlayer space
By virtue of its positive charge, the interlayer sheet neutralize the negative charge of the 2:1 sheets
Mineral colloids other than silicates
Hydrous oxide clays of iron and aluminum
Allophane and other amorphous minerals
Hydrous oxide clays of iron and aluminum
They are in the advance stage of weathering usually found in humid tropics
Gibbsite – Al(OH)3 or [Al2O3.XH2O]
Goethite – Fe(OH)3 or[Fe2O3.XH2O]
Limonite - Fe2O3.XH2O
Amorphous clay minerals
High specific areas, such as allophane, imogolite, and other non-crystalline soil colloids
Have high variable charge, high water retention capacity (thixotropic), high water permeability and low bulk density (<0.9 Mg/m3)
Allophane - chemical combination of Aluminum and silicon (Al2O3.2SiO2.H2O)
CEC varies from 20-150 meq/100g - large amount of negative charges are pH dependent