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Figure 3.18 pH at iso-electric point vs. von Post degree of peat humification ( after Asadi et al. , 2009d).
Table 3.8 Zeta potential of very slightly decomposed peat ( after Asadi, 2010).
Hydrated
Cation
Concentration
Zeta potential
Cation
radius (nm)
valence
(mol L 1 )
pH
(mV)
Na
0.36
1
1.00E-02
3.04
7.1
1.00E-02
9.1
19.9
1.00E-02
10.46
25.23
1.00E-04
3.04
6.7
1.00E-04
10.2
24.2
Ca
0.41
2
1.00E-02
3.42
2
1.00E-02
7.42
9.3
1.00E-03
3.5
3.7
1.00E-04
9.65
11.3
1.00E-04
11.2
14.4
Al
0.48
3
1.00E-03
7.54
3.1
1.00E-03
11.63
17.2
1.00E-04
11.77
22.8
the pH effects can possibly be ascribed to dissociation of H + from the functional
groups. Many carboxylic groups are sufficiently acid to dissociate below pH 6 leaving
a negative charge on the functional group:
COO +
H +
R
COOH
=
R
(3.10)
R represents organic species whose differing electronegativities change the tendency for
H + to dissociate. Thus the various R-COOH units dissociate at different pH values.
As the pH of the system increases, still weaker carboxylic groups and other very weak
acids dissociate (Stevenson, 1994).
 
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