We have located links that may give you full text access.
Free radical synthesis of nanosilver/gelatin-poly (acrylic acid) nanocomposite hydrogels employed for antibacterial activity and removal of Cu(II) metal ions.
Journal of Hazardous Materials 2018 June 6
The present work involves the synthesis of porous gelatin/AcA (PGE-AcA) hydrogel and novel porous gelatin-silver/AcA (NPGESNC-AcA) nanocomposite hydrogel, and their ability as effective biosorbents for the removal of Cu2+ ions from contaminated water. The formation of the samples was confirmed by UV-Vis, TEM, SEM, EDX, DLS, AFM, XRD, TGA/DTG and FTIR techniques. The adsorption studies results showed that maximum monolayer adsorption capacity of copper ions for PGE-AcA was achieved about 130.50 mg g-1 in pH 6.0 for 50 min, and adsorption capacity for the NPGESNC-AcA was nearly 147.10 mg g-1 in pH 5.5 for 40 min by atomic absorption spectroscopy technique. The Cu2+ ions loaded on the PGE-AcA and NPGESNC-AcA could be recovered by HCl above 65.8% and 78.7% after five consecutive cycles of adsorption/desorption, respectively. The results showed that the both of biosorbents loaded by Cu2+ ions could be easily regenerated and reusable. On the other hand, the results of adsorption kinetics and equilibrium isotherms were indicated high correlation coefficient (closer to a unit) for the pseudo-second-order and excellent fitted the adsorption data with the Langmuir isotherm model. Furthermore, the antimicrobial efficiency of the synthesized samples were tested on the Staphylococcus aureus and the Escherichia coli.
Full text links
Related Resources
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app