Wastelands and weeds

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    Cation Exchange Sites

    Cations attached to clay particles/OM or free

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    Charge Development

    A. pH dependent charge

    Deprotonation of surface functional groups (organic

    matter)

    COOH + OH-

    = COO-

    + H2O 'Broken-edge charges': These occur at the broken

    edges of clay mineral crystal sheets----- (Edges of layer

    silicates; oxides of Fe and Al) ------the hydrogen of

    hydroxyl groups dissociates slightly and the broken edge

    is left with a negative charge carried by the oxygen.

    pH dependent charge as pH

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    Charge Development

    B. Isomorphic substitution

    replacement of one atom by another of

    similar size in a crystal lattice withoutdisrupting or changing the crystal structure

    of the mineral

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    Isomorphic substitution of Mg2+ for Al3+ in the

    octahedral layer of a 2:1 clay mineral.

    Al2O2OH2 (no charge)

    Al has a +3 charge, O has a -2 charge

    AlMgO2OH2 (minus 1 charge)Mg has a +2 charge

    http://www.soils1.cses.vt.edu/MJE/shockwave/cec_demo/version1.1/cec.shtml

    http://www.soils1.cses.vt.edu/MJE/shockwave/cec_demo/version1.1/cec.shtmlhttp://www.soils1.cses.vt.edu/MJE/shockwave/cec_demo/version1.1/cec.shtmlhttp://www.soils1.cses.vt.edu/MJE/shockwave/cec_demo/version1.1/cec.shtmlhttp://www.soils1.cses.vt.edu/MJE/shockwave/cec_demo/version1.1/cec.shtml
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    CATION EXCHANGE

    Plant roots Vs Surface of Clay and Humus

    Between

    Two Clay Particle

    Two Humus particlesClay and Humus particle

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    CATION EXCHANGE

    The exchange reaction is rapid

    The exchange reaction is diffusion

    controlled

    The exchange reaction is reversible

    The exchange reaction is

    stoichiometric

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    stoichiometric CATION EXCHANGE

    1. Soil solution Vs Surface of Clay or Humus

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    Selectivity of one ion over another

    Some cations have a preference over others for the

    negative surface charge of a soil colloid.

    In general this is related to the charge of the cation andits hydrated radii.

    Higher the charge, more strong is the adsorption

    (exchangeable cation of aluminum, calcium or magnesium

    stays close to the clay particle and initiate soil

    aggregation)

    When the valence of the cations are equal, the cation

    with the smallest hydrated radius is more strongly

    adsorbed.

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    Radius Unit Na+ K+ Mg2+ Ca2+ Al3+

    Hydrated nm 0.360 0.330 0.430 0.410 0.480

    Order of preference for cations with a different valence (mixed series):

    Al3+ > Ca2+ > Mg2+ > K+ = NH4+ > Na+ > H +

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    Cation Concentration

    Concentration of cations in the soil

    solution: If the concentration of a cation in

    soil solution is high, there is an increased

    chance or tendency for that cation to beadsorbed.

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    Cation Exchange Capacity

    -vly charged sites: cation exchangesites.

    Total number of sites = CEC

    No. of cation adsorption sites/unit

    weight of soilor

    Sum total of exchangeable cations thata soil can adsorb

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    Cation Exchange Capacity

    -* Unit: milliequivalents (meq) per 100 g of oven dry soil

    K+, AW: 39; eq wt=39

    Ca++, AW: 40; eq wt =20

    PO4-3 , AW: 95; eq wt =31.6

    1 meq = 10-3 eq

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    Predicting CEC

    1) sum of cations : remove all cations andtotal the amount

    2) NH4+ saturation: soil saturated withNH4+ NH4+ replaced by Ca++ Measure NH4+ removed3) CEC varies with texture:Sandy = 0-3 meq/100 g

    Loamy = 10

    15, Clay Loam = 10-30Clayey = > 30 (depends on kind of clay; 60-100)

    Humus=400 meq/100 g

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    High CEC value (>25) soil rich in clayand/OM

    Low CEC value (

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    % Base Saturation

    (meq Ca+2 + meq Mg+2 + meq K+ + meq Na+)/CEC x 100

    Base Cations

    Calcium

    Magnesium

    PotassiumSodium

    Acid Cations

    Aluminum

    Hydrogen