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Adsorption of Polycomplexes at Solution/Air Interface

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The effect of complex formation of polyacids (polyacrylic (PAAc) and polymethacrylic (PMAAc)) with polyacrylamide (PAA) on their surface properties at solution/air interface has been studied by surface tension, electric conductivity and potentiometric measurements at 293В±0.2 K. The relaxation time and surface activity of polycomplexes were calculated from kinetic data on the surface tension. It was found that during complex formation the relaxation time of a surface layer has a maximum and the surface activity of macromolecules is increased. Also the standard free energy of adsorption for PAA and polyacid-PAA polycomplexes were calculated. They are equal DadsGВ°293 = - 19.1В±0.1 kJ/base-mol. for PAA, DadsGВ°293 = -21.2В±0.1 kJ/basemol. for PMAAc-PAA polycomplex and DadsGВ°293 = -23.0В±0.1 kJ/base-mol. for PAAc-PAA polycomplex (calculation per base-mole of PAA monomer link). It is shown that the surface activity and ability to decrease of the water surface tension is less for PMAAc-PAA than for PAAc-PAA. Such anomalous behaviour of PMAAc-PAA polycomplex probably is caused by an excessive strengthening of inner- and intermolecular hydrophobic interactions in macromolecules of PMAAc- PAA polycomplexes due to the presence of О±-methyl groups in PMAAc macromolecules. Because of the rebuilding of macromolecule segments of complex by polarity at the interface is becoming a difficult one.
Title: Adsorption of Polycomplexes at Solution/Air Interface
Description:
The effect of complex formation of polyacids (polyacrylic (PAAc) and polymethacrylic (PMAAc)) with polyacrylamide (PAA) on their surface properties at solution/air interface has been studied by surface tension, electric conductivity and potentiometric measurements at 293В±0.
2 K.
The relaxation time and surface activity of polycomplexes were calculated from kinetic data on the surface tension.
It was found that during complex formation the relaxation time of a surface layer has a maximum and the surface activity of macromolecules is increased.
Also the standard free energy of adsorption for PAA and polyacid-PAA polycomplexes were calculated.
They are equal DadsGВ°293 = - 19.
1В±0.
1 kJ/base-mol.
for PAA, DadsGВ°293 = -21.
2В±0.
1 kJ/basemol.
for PMAAc-PAA polycomplex and DadsGВ°293 = -23.
0В±0.
1 kJ/base-mol.
for PAAc-PAA polycomplex (calculation per base-mole of PAA monomer link).
It is shown that the surface activity and ability to decrease of the water surface tension is less for PMAAc-PAA than for PAAc-PAA.
Such anomalous behaviour of PMAAc-PAA polycomplex probably is caused by an excessive strengthening of inner- and intermolecular hydrophobic interactions in macromolecules of PMAAc- PAA polycomplexes due to the presence of О±-methyl groups in PMAAc macromolecules.
Because of the rebuilding of macromolecule segments of complex by polarity at the interface is becoming a difficult one.

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