Polym. Bull. https://doi.org/10.1007/s00289-018-2379-x ORIGINAL PAPER Gamma radiation‑induced preparation of poly(1‑vinyl‑2‑pyrrolidone‑co‑sodium acrylate) for effective removal of Co(II), Ni(II), and Cu(II) 1 2 Ahmed Galal Ibrahim · Alaaeldine Shaker Saleh · 2 2 2 Emad Mohamed Elsharma · Essam Metwally · Tharwat Siyam Received: 26 October 2017 / Revised: 10 April 2018 / Accepted: 21 May 2018 © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Clearing the water and wastewater from toxic heavy metals has received attentions from many researchers and scientists. In this study, poly(1-vinyl-2-pyrro- lidone-co-sodium acrylate), P(VP-SA), was prepared by gamma radiation-induced copolymerization of VP and SA and utilized for the effective removal of cobalt(II), nickel(II), and copper(II) from their aqueous solutions. Effect of comonomer com - position and concentration besides the adsorbed dose on the conversion percentage and the reduced viscosity was studied. The formed copolymer was characterized using Fourier transform infrared and gel permeation chromatography analysis, and the thermal stability was examined using thermogravimetric analysis. The influence of the adsorption conditions such as contact time, pH, copolymer concentration, and initial metal ion concentration on the metal ion binding capacity was tested. Pseudo- first-order, pseudo-second-order, and intraparticle diffusion adsorption models were used to explain the adsorption kinetics. Finally, the equilibrium adsorption data fitted well with Langmuir isotherm model,
Polymer Bulletin – Springer Journals
Published: May 30, 2018
It’s your single place to instantly
discover and read the research
that matters to you.
Enjoy affordable access to
over 18 million articles from more than
15,000 peer-reviewed journals.
All for just $49/month
Query the DeepDyve database, plus search all of PubMed and Google Scholar seamlessly
Save any article or search result from DeepDyve, PubMed, and Google Scholar... all in one place.
All the latest content is available, no embargo periods.
“Whoa! It’s like Spotify but for academic articles.”@Phil_Robichaud