Poly(acrylic acid)/SiO2 composite nanofiber membranes functionalized with mercapto groups for removal of humic acid from aqueous solution

2019 ◽  
Vol 141 ◽  
pp. 115-123
Author(s):  
M.A. Zulfikar ◽  
D. Maulina ◽  
M. Nasir ◽  
A. Alni ◽  
M. Zunita ◽  
...  
2011 ◽  
Vol 356-360 ◽  
pp. 488-492
Author(s):  
Ran Xu ◽  
Min Jia ◽  
Feng Ting Li

Thiol-functionalized poly (acrylic acid)/SiO2 (PAA/SiO2) composite nanofiber membranes have been fabricated by a sol-gel electrospinning method and their adsorption capacity for Ag+, Cu2+ was investigated. Results showed the PAA/SiO2 fibers had a diameter between 300 nm-700 nm. FTIR results demonstrated that the mercapto groups have been introduced into the silica skeleton. The adsorption of Ag+, Cu2+ on the membranes fit the Redlich-Peterson isotherm model best. The equilibrium adsorption capacity of Ag+ (575.64 mg/g) on PAA/SiO2 nanofiber membranes is higher than Cu2+ (331.52 mg/g). The desorption rate reached 98% in 30 min. The removal rate of Ag+, Cu2+ still maintained above 75% after six regeneration cycles. Adsorption kinetics of Ag+, Cu2+ followed a pseudo-second-order model.


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.


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.


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