Poly(acrylic acid/acrylamide/sodium humate) superabsorbent hydrogels for metal ion/dye adsorption: Effect of sodium humate concentration

2012 ◽  
Vol 125 (2) ◽  
pp. 1267-1283 ◽  
Author(s):  
Tripti Singh ◽  
Reena Singhal
Keyword(s):  
Acrylic Acid ◽  
Metal Ion ◽  
Dye Adsorption ◽  
Adsorption Effect ◽  
Sodium Humate ◽  
Superabsorbent Hydrogels ◽  
Poly Acrylic Acid

Determination of the complexation properties of a crosslinked poly(acrylic acid) gel with copper(II), nickel(II), and lead(II) in dilute aqueous solution

2001 ◽  
Vol 79 (4) ◽  
pp. 370-376 ◽  
Author(s):  
Catherine Morlay ◽  
Yolande Mouginot ◽  
Monique Cromer ◽  
Olivier Vittori
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Acrylic Acid ◽  
Metal Ion ◽  
Conditional Stability ◽  
Binding Properties ◽  
Complex Species ◽  
Complexing Capacity ◽  
Dilute Aqueous Solution ◽  
Poly Acrylic Acid

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.

Lignin-graft-poly(acrylic acid) for enhancement of heavy metal ion biosorption

2017 ◽  
Vol 52 (24) ◽  
pp. 13689-13699 ◽  
Author(s):  
Li-Qiu Hu ◽  
Lin Dai ◽  
Rui Liu ◽  
Chuan-Ling Si
Keyword(s):  
Heavy Metal ◽  
Acrylic Acid ◽  
Metal Ion ◽  
Heavy Metal Ion ◽  
Poly Acrylic Acid

Trace metal ion retention properties of crosslinked poly(4-vinylpyridine) and poly(acrylic acid)

2004 ◽  
Vol 92 (5) ◽  
pp. 2908-2916 ◽  
Author(s):  
Bernabé L. Rivas ◽  
Benita Quilodrán ◽  
Eduardo Quiroz
Keyword(s):  
Acrylic Acid ◽  
Trace Metal ◽  
Metal Ion ◽  
Trace Metal Ion ◽  
Poly Acrylic Acid

Universal aqueous synthesis of ultra-small polymer-templated nanoparticles: synthesis optimization methodology for counterion-collapsed poly(acrylic acid)

2018 ◽  
Vol 96 (1) ◽  
pp. 44-50 ◽  
Author(s):  
Nari Kim ◽  
Calvin C.H. Cheng ◽  
M. Cynthia Goh
Keyword(s):  
Acrylic Acid ◽  
Metal Ion ◽  
Rapid Development ◽  
Ion Concentration ◽  
Universal Method ◽  
Aqueous Synthesis ◽  
System A ◽  
Metal Metal ◽  
Optimization Methodology ◽  
Poly Acrylic Acid

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.

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