Carboxymethylcellulose-chitosan film modified magnetic alkaline Ca-bentonite for the efficient removal of Pb(II) and Cd(II) from aqueous solution

In order to endow alkaline Ca-bentonite (ACB) with magnetic separation ability, simultaneously obtain better magnetic stability and stronger removal capacity of heavy metal cations; magnetic alkaline Ca-bentonite/carboxymethylcellulose-chitosan film (MACB/C-C) was prepared by organic modification of...

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Veröffentlicht in:Environmental science and pollution research international 2021-06, Vol.28 (23), p.30312-30322
Hauptverfasser: Wang, Yingya, Zhang, Hanbing, Yaseen, Muhammad, Tong, Zhangfa, Chen, Ninghua, Shi, Huazhen
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Sprache:eng
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Zusammenfassung:In order to endow alkaline Ca-bentonite (ACB) with magnetic separation ability, simultaneously obtain better magnetic stability and stronger removal capacity of heavy metal cations; magnetic alkaline Ca-bentonite/carboxymethylcellulose-chitosan film (MACB/C-C) was prepared by organic modification of magnetic alkaline Ca-bentonite (MACB) using non-toxic carboxymethylcellulose and chitosan. Textural characterization results revealed that magnetic Fe 3 O 4 nanoparticles were successfully immobilized on ACB and modified with C-C. The functionalized layer of C-C concurrently enhanced the stability of Fe 3 O 4 and removal performances of heavy metal cations. Adsorption results indicated that MACB/C-C exhibited thorough separation from aqueous solution and greater uptake ability for Pb(II) and Cd(II) (483 mg·g −1 and 123 mg·g −1 ) than the nascent MACB (335 mg·g −1 and 76 mg·g −1 ), respectively, at pH 5 and 25 °C temperature. The adsorption of Pb(II) and Cd(II) on MACB/C-C mainly occurred via surface precipitation and complexation when pH > 2. MACB/C-C could be efficiently recycled with marginal decrease in adsorption capacity. The current approach credited to the convenient operation, simplified synthesis, and high efficiency of MACB/C-C could be deemed as a promising alternative for the removal of heavy metal cations from wastewater.
ISSN:0944-1344
1614-7499
DOI:10.1007/s11356-020-12156-2