Reentrant swelling behavior of poly(4-vinyl phenol) gel in aqueous organic solvent mixtures

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Michiko Sakurai ◽  
Mitsuru Satoh

AbstractSwelling behaviours of poly(4-vinyl phenol) (P4VPh) hydrogel in various kinds of mixed solvents (methanol, ethanol, 2-propyl alcohol, t-butyl alcohol, acetone, acetonitrile, dioxane, THF and DMSO) have been investigated. With increasing the organic solvent content, the gel first significantly deswelled and then reswelled via lowest swelling points (10-60 vol.% depending the solvent species), and finally showed a second deswelling in the highest content region (typically ≧ 80 vol.%). The rather unique swelling-deswelling sequence was not reproduced when the solvent content was decreased; namely, the backward swelling curves obtained with increasing water composition in the mixed solvents first followed the forward one until the lowest swelling points, then, however, continued the deswelling trend without recovering the initial swelling state in water. This remarkable hysteresis as well as the reentrant swelling with the extra second deswelling has been interpreted in terms of the intermolecular interactions, i.e., hydrogen bonding between the phenol OH groups and the π- π stacking of the phenol rings, by referring to the corresponding results of poly(vinyl alcohol) (PVA) gel system.

1982 ◽  
Vol 37 (5-6) ◽  
pp. 527-531 ◽  
Author(s):  
Angela de Souza Otero ◽  
Leopoldo de Meis

Abstract The effect of organic solvents on the phosphorylation of the Ca2+-dependent ATPase of sarcoplasmic reticulum by inorganic phosphate in the absence of a calcium gradient was investigated. Kinetic analysis of the reaction in water and water-organic solvent media according to a bireactant scheme shows no correlation between changes in kinetic parameters and the dieletric constant of the mixed solvents. The pronounced increase in equilibrium levels of phosphoenzyme in water-solvent mixtures is attributed to changes in the water activity of the medium.


1976 ◽  
Vol 54 (11) ◽  
pp. 1687-1691 ◽  
Author(s):  
El-Hussieny M. Diefallah

The temperature dependence of the rate of alkaline solvolysis of monochloroacetate ion in water – tert-bulyl alcohol solutions has been determined. The rates of reaction were first order with respect to both the chloroacetate ion and to the total solvoxide ion concentrations. The reactivity is enhanced, first slowly, and then more rapidly, by increasing the concentration of tert-bulyl alcohol in the solvent mixtures. The rate of reaction increases with the reciprocal of the dielectric constant of the medium and the plot of log kvs. 1/D can best be represented by two lines intersecting at a point corresponding to 0.9 water mole fraction. The activation parameters ΔH*and ΔS* for the solvolysis reaction showed a minimum at about 0.9 water mole fraction. The significance of these results from the viewpoint of the electrostatic theory and the changing of solvent structure in such mixtures is discussed.


Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 71
Author(s):  
Takuro Taniguchi ◽  
Kenji Urayama

We investigated the linear dynamic viscoelasticity of dual cross-link (DC) poly(vinyl alcohol) (PVA) (DC-PVA) hydrogels with permanent and transient cross-links. The concentrations of incorporated borate ions to form transient cross-links in the DC-PVA hydrogels (CBIN) were determined by the azomethine-H method. The dynamic viscoelasticity of the DC-PVA hydrogel cannot be described by a simple sum of the dynamic viscoelasticity of the PVA gel with the same permanent cross-link concentration and the PVA aqueous solution with the same borate ion concentration (CB = CBIN) as in the DC-PVA gel. The DC-PVA hydrogel exhibited a considerably higher relaxation strength, indicating that the introduction of permanent cross-links into temporary networks increases the number of viscoelastic chains with finite relaxation times. In contrast, the relaxation frequency (ωc) (given by the frequency at the maximum of loss modulus) for the DC-PVA hydrogel was slightly lower but comparable to that for a dilute PVA solution with the same CB. This signifies that the relaxation dynamics of the DC-PVA hydrogels is essentially governed by the lifetime of an interchain transient cross-link (di-diol complex of boron). The effect of permanent cross-linking on the relaxation dynamics was observed in the finite broadening of the relaxation-time distribution in the long time region.


2003 ◽  
Vol 403 (2) ◽  
pp. 223-229 ◽  
Author(s):  
F.J. Carmona ◽  
J.Antonio González ◽  
Isaı́as Garcı́a de la Fuente ◽  
J.Carlos Cobos

1997 ◽  
Vol 433 (1-2) ◽  
pp. 77-83 ◽  
Author(s):  
Clara Ràfols ◽  
Koit Herodes ◽  
JoséLuis Beltrán ◽  
Elisabeth Bosch ◽  
Martí Rosés

RSC Advances ◽  
2016 ◽  
Vol 6 (105) ◽  
pp. 102947-102955 ◽  
Author(s):  
Deepika Gupta ◽  
Manjeet Jassal ◽  
Ashwini K. Agrawal

The fiber diameters obtained from PVA–DMSO–water ternary system are the result of the interplay between the solvent–solvent and solvent–polymer interactions.


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