Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/9203
Title: Adsorption of Cr6+ ion using activated Pisum sativum peels‑triethylenetetramine
Authors: El‑Nemr, Mohamed A. 
Aigbe, Uyiosa Osagie 
Ukhurebor, Kingsley E. 
Onyancha, Robert B. 
El Nemr, Ahmed 
Ragab, Safaa 
Osibote, Otolorin Adelaja 
Hassaan, Mohamed A. 
Keywords: Aquatic environment;Cr6+ removal;Water treatment;Pea peels;Pollution
Issue Date: 2022
Publisher: Springer
Source: El‑Nemr, M. A., Aigbe, U. O., Ukhurebor, K. E. et al. 2022. Adsorption of Cr6+ ion using activated Pisum sativum peels‑triethylenetetramine. Environmental Science and Pollution Research, 29: 91036–91060. [https://doi.org/10.1007/s11356-022-21957-6]
Journal: Environmental Science and Pollution Research 
Abstract: The adsorption of Cr6+ ions from water-soluble solution onto activated pea peels (PPs) embellished with triethylenetetramine (TETA) was studied. The synthesized activated TETA-PP biosorbent was further characterized by SEM together with EDX, FTIR and BET to determine the morphology and elementary composition, functional groups (FGs) present and the biosorbent surface area. The confscation of Cr6+ ions to activated TETA-PP biosorbent was observed to be pH-reliant, with optimum removal noticed at pH 1.6 (99%). Cr6+ ion adsorption to activated TETA-PP biosorbent was well defned using the Langmuir (LNR) and the pseudo-second-order (PSO) models, with a determined biosorption capacity of 312.50 mg/g. Also, it was found that the activated TETA-PP biosorbent can be restored up to six regeneration cycles for the sequestration of Cr6+ ions in this study. In comparison with other biosorbents, it was found that this biosorbent was a cost-efective and resourceful agro-waste for the Cr6+ ion confscation. The possible mechanism of Cr6+ to the biosorbent was by electrostatic attraction following the surface protonation of the activated TETA-PP biosorbent sites.
Description: Article
URI: http://hdl.handle.net/11189/9203
ISSN: 1614-7499
DOI: https://doi.org/10.1007/s11356-022-21957-6
Appears in Collections:Appsc - Journal Articles (DHET subsidised)

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