- Title
- Magnetic responsive mesoporous alginate/β-cyclodextrin polymer beads enhance selectivity and adsorption of heavy metal ions
- Creator
- Hassan, Masud; Naidu, Ravi; Du, Jianhua; Qi, Fangjie; Ahsan, Md Ariful; Liu, Yanju
- Relation
- International Journal of Biological Macromolecules Vol. 207, p. 826-840
- Publisher Link
- http://dx.doi.org/10.1016/j.ijbiomac.2022.03.159
- Publisher
- Elsevier
- Resource Type
- journal article
- Date
- 2022
- Description
- Mesoporous (~7–8 nm) biopolymer hydrogel beads (HNTs-FeNPs@Alg/β-CD) were synthesised via ionic polymerisation route to separate heavy metal ions. The adsorption capacity of HNTs-FeNPs@Alg/β-CD was higher than that of raw halloysite nano tubes (HNTs), iron nanoparticles (FeNPs), and bare alginate beads. FeNPs induce the magnetic properties of adsorbent and metal-based functional groups in and around the hydrogel beads. The mesoporous surface of the adsorbent permits access of heavy metal ions onto the polymer beads to interact with internal active sites and the mesoporous polymer network. Maximum adsorption capacities of lead (Pb), copper (Cu), cadmium (Cd), and nickel (Ni) were 21.09 mg/g, 15.54 mg/g, 2.47 mg/g, and 2.68 mg/g, respectively. HNTs-FeNPs@Alg/β-CD was able to adsorb heavy metals efficiently (75–99%) under environment-relevant concentrations (200 μg/L) from mixed metal contaminants. The adsorption and selectivity trends of heavy metals were Pb > Cu > Cd > Ni, despite electrostatic binding strength of Cd > Cu > Pb > Ni and covalent binding strength of Pb > Ni > Cu > Cd. It demonstrated that not only chemosorption but also physisorption acts as the sorption mechanism. The reduction in surface area, porosity, and pore volume of the expended adsorbent, along with sorption study results, confirmed that pore filling and intra-particle diffusion played a considerable role in removing heavy metals.
- Subject
- hydrogel; nanoparticle; adsorption; heavy metal ions
- Identifier
- http://hdl.handle.net/1959.13/1464426
- Identifier
- uon:46993
- Identifier
- ISSN:0141-8130
- Language
- eng
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