scholarly journals Interpolymer Complex Formation Between Linear and Crosslinked Poly(acrylic acid) and Poly(vinyl ether of ethyleneglycol)

2016 ◽  
Vol 2 (2) ◽  
pp. 125
Author(s):  
Z.S. Nurkeeva ◽  
G.A. Mun ◽  
V.V. Khutoryanskiy ◽  
V.A. Kan ◽  
E.M. Shaikhutdinov

<p>The formation of H-bonded interpolymer complexes between linear and cross-linked poly(acrylic acid) and poly(vinyl ether of ethyleneglycol) is considered. The effects of pH and concentrations of polymers solution as well as the nature of the solvent on the complexation processes are discussed. It was found that the complexes are formed in aqueous solutions only below some critical pH value, which depends on the concentration of polymers and ionic strength of the solution. The interaction between gel of poly(acrylic acid) swollen in alcohol with solution of linear poly(vinyl ether of ethyleneglycol) is accompanied by formation of turbid layer of polycomplex and contraction of gel.</p>

Soft Matter ◽  
2017 ◽  
Vol 13 (46) ◽  
pp. 8736-8744 ◽  
Author(s):  
Thomas Swift ◽  
Colin C. Seaton ◽  
Stephen Rimmer

Interpolymer complexation of poly(acrylic acid) with other systems via hydrogen bonding only occurs below a critical pH dependent on solvation effects.


2002 ◽  
Vol 280 (3) ◽  
pp. 282-289 ◽  
Author(s):  
Grigoriy A. Mun ◽  
Zauresh S. Nurkeeva ◽  
Vitaliy V. Khutoryanskiy ◽  
Aibek D. Sergaziyev

Polymers ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 148
Author(s):  
Hirokazu Fukumoto ◽  
Kazuhiko Ishihara ◽  
Shin-Ichi Yusa

A mixed aqueous solution of hydrophilic poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) and poly(acrylic acid) (PAAc) becomes cloudy under acidic conditions at room temperature. The pendant carboxylic acid groups in PAAc form hydrogen bonds with the ester and phosphate groups in PMPC. While the polymers aggregate under acidic conditions, neither one associate under basic conditions because of the deprotonation of the pendant carboxy groups in PAAc. We observed that the interpolymer complex formed from PMPC, and PAAc was dissociated in aqueous solutions with increasing temperature, which is an upper critical solution temperature behavior. With increasing temperature, the molecular motion increased to dissociate the interpolymer complex. The phase transition temperature increased with increasing polymer and salt concentrations, and with decreasing pH.


2003 ◽  
Vol 3 (2) ◽  
pp. 117-122 ◽  
Author(s):  
Vitaliy V. Khutoryanskiy ◽  
Maria Grazia Cascone ◽  
Luigi Lazzeri ◽  
Nicoletta Barbani ◽  
Zauresh S. Nurkeeva ◽  
...  

2001 ◽  
Vol 79 (4) ◽  
pp. 370-376 ◽  
Author(s):  
Catherine Morlay ◽  
Yolande Mouginot ◽  
Monique Cromer ◽  
Olivier Vittori

The possible removal of copper(II), nickel(II), or lead(II) by an insoluble crosslinked poly(acrylic acid) was investigated in dilute aqueous solution. The binding properties of the polymer were examined at pH = 6.0 or 4.0 with an ionic strength of the medium µ = 0.1 or 1.0 M (NaNO3) using differential pulse polarography as an investigation means. The highest complexing capacity of the polyacid was obtained with lead(II) at pH = 6.0 with µ = 0.1 M, 4.8 mmol Pb(II)/g polymer. The conditional stability constants of the complex species formed were determined using the method proposed by Ruzic assuming that only the 1:1 complex species was formed; for lead(II) at pH = 6.0 and µ = 0.1 M, log K' = 5.3 ± 0.2. It appeared that the binding properties of the polymer increased, depending on the metal ion, in the following order: Ni(II) < Cu(II) < Pb(II). The complexing capacity and log K' values decreased with the pH or with an increase of the ionic strength. These results were in agreement with the conclusions of our previous studies of the hydrosoluble linear analogues. Finally, with the insoluble polymer, the log K' values were comparable to those previously obtained with the linear analogue whereas the complexing capacity values expressed in mmol g-1 were slightly lower.Key words: insoluble crosslinked poly(acrylic acid), copper(II), nickel(II), and lead(II) complexation.


2010 ◽  
Vol 12 (1) ◽  
pp. 132-140 ◽  
Author(s):  
Wichan Ketjinda ◽  
Nuttanan Sinchaipanid ◽  
Pichet Limsuwan ◽  
Hans Leuenberger ◽  
Ampol Mitrevej

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