scholarly journals ELECTRORESPONSIE BEHAVIOR OF POLYELECTROLYTE GELS (ACRYLIC ACID-CO-N-N' METHYLENE BISACRYLAMIDE) UNDER THE INFLUENCE OF ELECTRIC FIELD

2017 ◽  
Vol 24 (4) ◽  
pp. 419-426
Author(s):  
Nguyen Phuong Hoai Nam ◽  
Eduado Mendes

Polymer gels which were synthesized from acrylic acid and N-N’ methylene bisacrylamide exhibited electrical sensitive behavior. Their swelling properties and electroresponsive behavior were studied. The results indicated that the water take-up ability of the hydrogel increased with the decreased N-N’ methylene bisacrylamide content within the network. The hydrogel membranes swollen in a neutral NaCl solution, bent toward the cathode under non-contact DC electric fields, and their bending speed and equilibrium strain increased with the increased of applied voltage. In addition, the effect of crosslinker concentration of N-N’ methylene bisacrylamide on bending behavior of the gels have been studied. The equilibrium strain decreased as the crosslinker concentration increased. By changing the direction of the applied potential cyclically, the hydrogel membranes exhibited good reversible bending behavior. The bending of the hydro gel membranes was initially explained by a bending theory of polyelectrolyte hydrogel based on the charge of osmotic pressure due to the ion concentration different between the inside and the outside of the network.

2019 ◽  
Vol 41 (4) ◽  
pp. 668-668
Author(s):  
Saud Hashmi Saud Hashmi ◽  
Saad Nadeem Saad Nadeem ◽  
Zahoor Awan Zahoor Awan ◽  
Adeel ur Rehman Adeel ur Rehman ◽  
Ahsan Abdul Ghani Ahsan Abdul Ghani

Superabsorbent hydrogels constitute a group of polymeric materials with three-dimensional network structure, which can swell to absorb an enormous amount of water or aqueous solutions. This property enables various commercial applications of hydrogels such as water holding capability in agriculture and superabsorbent material for baby diapers. Several novel superabsorbent hydrogels based on acrylic acid-co-acrylamide copolymers were synthesized under variation of copolymer compositions through free radical polymerization. N,N’methylenebisacrylamide (MBA) was used as a water soluble crosslinker and potassium persulphate (KPS) as an initiator. Effect of varying the copolymer composition, change in crosslinker concentration, and effect of environmental parameters (pH, temperature, and ion concentration) on both swelling capacity and swelling rate were examined. These gel shows maximum swelling at neutral pH-7, whereas increasing salt concentration in water decrease the swelling capacity. It was found interesting that an increase in crosslinker concentration from 0.020% to 0.16%, the swelling capacity decreases up to 70% while the swelling rate increases from 0.007g water/g dry hydrogel sec to 0.024g water/g dry hydrogel sec, respectively because there is a compromise exists between entropic spring forces between network connection points and the hydrostatic pressure of the water diffusing into the gels. Dynamic swelling curve obtained were fitted to the three different kinetic models namely Peleg’s kinetic model, pseudo 1st order as proposed by Lagergen and pseudo 2nd order kinetics. All these models provided a good agreement with the experimental data; However on the bases of statistical parameters (RMSE, R2 and X2) the Peleg’s model was selected as the most appropriate model for this study. Analyzing rate constant for Peleg’s models at different swelling temperatures disclosed that increasing temperature could only increase the swelling rate without affecting the swelling capacity of the hydrogels. Experimental values for rate constant k1 of Peleg’s model at different temperature shows a sharp decrease from 0.57545 at 30 oC to 0.1535 at 75 oC that contemplated the rate of swelling at 75 oC was 65% faster than that of 30 oC. The diffusion mechanisms in hydrogels were proven to be tailorable by increasing cross-linker concentration and temperature, leading towards the Fickian type diffusion behavior. The synthesized superabsorbent hydrogels were also tested for water retention applications in agriculture.


2016 ◽  
Author(s):  
LUCAS MILITÃO ◽  
MARCELO GANZAROLLI DE OLIVEIRA ◽  
MATHILDE CHAMPEAU ◽  
CARLOS P. JARA ◽  
ELIANA PEREIRA DE ARAUJO

2000 ◽  
Author(s):  
Rainer W. Guelch ◽  
Jens Holdenried ◽  
Andrea Weible ◽  
Thomas Wallmersperger ◽  
Bernd Kroeplin

2007 ◽  
Vol 336-338 ◽  
pp. 2619-2623
Author(s):  
Yasuhide Shindo ◽  
Fumio Narita

We present numerical and experimental results on the nonlinear bending behavior due to domain wall motion in functionally graded piezoelectric actuator under alternating current (ac) electric fields. A nonlinear finite element method is employed to analyze the dynamic response of functionally graded piezoelectric actuator. A phenomenological model of domain wall motion is used in computation, and the effects of ac electric field amplitude and frequency, number of layers, and property gradation on the deflection of the cantilever actuators are examined. Experimental results, which verify the model, are presented using a functionally graded bimorph. The numerical results agree very well with the experimental values.


2018 ◽  
Vol 96 (1) ◽  
pp. 44-50 ◽  
Author(s):  
Nari Kim ◽  
Calvin C.H. Cheng ◽  
M. Cynthia Goh

A long polyelectrolyte chain collapses into a nano-sized particle upon the addition of counterions under appropriate solution conditions. This phenomenon forms the basis for a simple universal method for aqueous synthesis of ultra-small (<10 nm) metal, metal oxide, and other types of nanoparticles in the following manner: the counterion-collapsed polyelectrolyte chains are made stable by crosslinking, effectively trapping the counterions, which are subsequently chemically modified, to form metal nanoparticles via reduction or metal oxides nanoparticles via oxidation, within the collapsed polymer nanoparticle. This highly versatile platform methodology can be applied to almost any polyelectrolyte–counterion pair, making possible the rapid development of syntheses of different nanoparticles within the same chemical environment. Using poly(acrylic acid) as a model system, a methodology for the optimization of conditions for the polyelectrolyte collapse by various mono- and multi-valent metal cations is developed. The optimal counterion concentration did not correlate with ionic strength and metal ion valency and was highly variable from system to system. By monitoring the polyelectrolyte conformation using viscosity and turbidity measurements, the appropriate metal ion concentration for each nanoparticle system was determined.


2018 ◽  
Vol 42 (11) ◽  
pp. 9151-9158 ◽  
Author(s):  
Huijuan Zhang ◽  
Yuran Cheng ◽  
Xinjuan Hou ◽  
Biao Yang ◽  
Fang Guo

A P(AA/AM)–Fe(NO3)3 double crosslinking gel showed a superior tensile strength of 1471 kPa compared to those of all other metal salts tested, which was demonstrated by molecular simulation to result from the stronger hydrogen bonding in this metal–(COO)n complex.


MRS Advances ◽  
2020 ◽  
Vol 5 (17) ◽  
pp. 907-915 ◽  
Author(s):  
Jessica L. Sargent ◽  
Xunkai Chen ◽  
Mitchell C. Brezina ◽  
Sebastian Aldwin ◽  
John A. Howarter ◽  
...  

ABSTRACTIonic hydrogels are an abundant class of materials with applications ranging from drug delivery devices to high performance concrete to baby diapers. A more thorough understanding of interactions between polyelectrolyte networks and ionic solutes is critical as these materials are further tailored for performance applications in highly targeted ionic environments. In this work, we seek to develop structure-property relationships between polyelectrolyte gels and environments containing high concentrations of multivalent ions. Specifically, this work seeks to elucidate the causes behind differences in hydrogel response to divalent ions of main group metals versus transition metals. PANa-co-PAM hydrogels containing low and high fractions of ionic groups are investigated in solutions of DI water, NaCl, CaCl2, and CuSO4 at concentrations ranging from 5 to 100 mM in order to understand 1) the transient or permanent nature of crosslinks produced in these networks by divalent counter-ions, 2) the role of polymer ionic content in these interactions, and 3) how these interactions scale with salt concentration. Gravimetric swelling and mechanical compression testing are employed to characterize water and salt-swollen hydrogels in order to develop guiding principles to control and manipulate material properties through polymer-counter-ion interactions. The work presented here confirms the formation of permanent crosslinks by transition metal ions, offers explanation for the behavioral discrepancy observed between ionic hydrogels and main group versus transition metal ions, and illustrates how such hydrogel properties scale with counter-ion concentration.


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