Direct osmotic pressure measurements on partially neutralized poly(acrylic acid) gels

1993 ◽  
Vol 3 (6) ◽  
pp. 927-936
Author(s):  
C. Weill ◽  
T. Lachhab ◽  
P. Moucheront

We present a new experimental device to measure the osmotic pressure in gels. The system has been tested on partially neutralized poly(acrylic acid) gels. The variation of the osmotic pressure with polymer concentration, Φ, and ionization degree, α, is linear, provided that α is not too high (I.e. the counterions do not condense on the chains). These results are in good agreement with theoretical models and with compressibility measurements obtained by light scattering experiments. The very charged gels are also studied, and the results are discussed in the frame of existing theories and experiments.

1991 ◽  
Vol 1 (6) ◽  
pp. 637-650 ◽  
Author(s):  
A. Moussaid ◽  
J. P. Munch ◽  
F. Schosseler ◽  
S. J. Candau

1949 ◽  
Vol 22 (3) ◽  
pp. 680-689
Author(s):  
W. E. Mochel ◽  
J. B. Nichols ◽  
C. J. Mighton

Abstract Polychloroprene rubber (Neoprene Type GN) was fractionated by partial precipitation from dilute solution in benzene and the fractions were examined both osmotically and viscometrically in benzene solutions. The molecular-weight distribution curve for Neoprene Type GN based on osmotic pressure measurements shows a pronounced maximum at 100,000, but has a long extension to molecular weights of over one million, indicating the presence of branched or cross-linked material which is still soluble. The uniformity is somewhat less than that of sol natural rubber, while in shape the Neoprene distribution curve resembles more closely that of peptized natural rubber than fresh sol rubber. Observed variations in the slopes of the π/c vs. c and the ηsp/c vs. c curves also indicate the presence in solution of complex, branched and (or) cross-linked molecules. Calibration of the intrinsic viscosity-molecular weight relationship by osmotic pressure measurements gave good agreement with the equation: [η]=KMa, where K=1.46×10−4 and a=0.73.


2021 ◽  
Vol 11 (21) ◽  
pp. 10142
Author(s):  
Małgorzata Matusiak ◽  
Sławomir Kadłubowski ◽  
Piotr Ulański

Carbon-centered radicals have been randomly generated on the chains of poly(acrylic acid), PAA, the simplest synthetic anionic polyelectrolyte, by pulse-irradiating its dilute, oxygen-free aqueous solutions by 6 MeV electron beam. In some experiments, oligo(acrylic acid), OAA, and propionic acid, PA, were used as PAA models. Recombination kinetics of PAA radicals has been followed by fast spectrophotometry. A strong pH dependence of radical lifetime on pH, and thus on the linear charge density due to deprotonated carboxylate groups, has been confirmed, while a weaker amplitude of pH dependence was observed for OAA and PA. Decay kinetics of PAA radicals in the protonated state, at pH 2, have been studied in some detail. At moderate doses of ionizing radiation, resulting in a moderate average initial number of radicals per chain, ZR0, the decay can be satisfactorily described by a second-order kinetic model, but a somewhat better fit is obtained by using a dispersive kinetics approach. While for a constant polymer concentration the reciprocal half-lives are proportional to the initial radical concentrations, such a data series for different PAA concentrations do not overlap, indicating that the overall radical concentration is not the decisive factor controlling the kinetics. Arranging all data, in the form of second-order rate constants, as a function of the average initial number of radicals per chain allows one to obtain a common dependence. The latter seems to consist of two parts: a horizontal one at low ZR0 and another one of positive slope at higher ZR0. This is interpreted as two kinetic regimes where two distinct reactions dominate, intermolecular and intramolecular recombination, respectively. Comparison of the low ZR0 data with calculations based on the translational diffusion model indicate that the latter is not the rate-controlling process in intermolecular recombination of polymer radicals; segmental diffusion is the more likely candidate.


1994 ◽  
Vol 83 (1) ◽  
pp. 183-192
Author(s):  
Sauveur J. Candau ◽  
Rachid Skouri ◽  
François Schosseler ◽  
Jean-Pierre Munch

2009 ◽  
Vol 79-82 ◽  
pp. 1595-1598 ◽  
Author(s):  
Wei Wei Cui ◽  
Li Zhu Liu ◽  
Xing Song Zhu

Semi-Interpenetrating networks (SIPN) hydrogel composed of poly (acrylic acid) (PAA) and poly (vinyl alcohol) (PVA) was prepared by free radical solution polymerization. The SIPN was characterized by Fourier transform infrared spectroscopy (FTIR). The electric stimuli responsive characteristics were investigated. The hydrogel bent toward the anode initially, altered the bending direction for two times and bent toward the anode ultimately when it was placed in a 0.1 M NaCl aqueous solution under non-contact DC field. For interpreting the special deformation the osmotic pressure curves according to Shiga’ osmotic pressure model were simulated and the pH gradient theory was applied to explain the final direction.


2017 ◽  
Vol 4 (9) ◽  
Author(s):  
Lukas Arens ◽  
Felix Weißenfeld ◽  
Christopher O. Klein ◽  
Karin Schlag ◽  
Manfred Wilhelm

2001 ◽  
Vol 1 (4) ◽  
pp. 157-163 ◽  
Author(s):  
Sergey V. Kazakov ◽  
Vladimir I. Muronetz ◽  
Maria B. Dainiak ◽  
Vladimir A. Izumrudov ◽  
Igor Yu. Galaev ◽  
...  

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