Study of Ion-Solvent Interaction during Acidic Dissociation of Glycine in 10, 20 And 30% Dioxane in Dioxane-Water System At 318.15K by Potentiometric Method
DOI:
https://doi.org/10.32628/IJSRST52310398Keywords:
Ion solvent interaction, Free energy transfer, acidic dissociation constant, modified Davies equation.Abstract
Ion solvent interaction was studied by free energy transfer during acidic dissociation of Glycine in 10,20 and 30% dioxane in dioxane-water system at 318.15K and free energy was given by the thermodynamic relation
ΔGt = 2.303RTΔpK1
where ΔGt = free energy transfer when solvent change from water to dioxane-water.
ΔpK1 = pKs1-pKw1
where pKw1 = -log Kw1 negative logarithmic of dissociation constant of glycine in water.
pKs1 = -log Ks1negative logarithmic of acid dissociation constant of glycine in dioxane-water.
For this purpose acidic dissociatio constant of glycine was determined potentiometrically by setting up the cell:
H2(Pt) | Glycine, HCl, X% Dioxane, Hg2Cl2 | Hg …(C-1)
m1 m2 (100-x)% water
and e.m.f. of the cell was given by the formula:
E = E0- 2.303RT/F (log mH+ mcl- + log ƔH+ ƔCl_) …(1)
In the equation (1) activity coefficient of the solution has been taken into consideration to understand ion solvent interaction and activity coefficient is given by the relation:
log ƔH+ ƔCl_ = -2A¢√μ/(1+ √μ) +ꞵ1μ …(2)
Equation (2) is modified Davies equation given by B. Prasad and hence acidic dissociation constant of glycine can be calculated by calculating mH+ as: log mH+ = (E0 - E)/K - log mCl_ + (2A¢√μ/(1+ √μ)) - ꞵ1μ …(3)
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