4.7 Article

Removal of fluoroquinolone antibiotics using actinia-shaped lignin-based adsorbents: Role of the length and distribution of branched-chains

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 403, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2020.123603

Keywords

Actinia-shaped lignin-based adsorbents; Fluoroquinolone antibiotics; Modeling of structural factors; Adsorption mechanisms; Structure-activity relationship

Funding

  1. National Natural Science Foundation of China [51778279, 51978325]

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A series of actinia-shaped lignin-based adsorbents were designed and fabricated for the removal of ofloxacin and ciprofloxacin from water. Experimental and calculation results indicated that hydrogen bonding contributes more than electrostatic attraction to adsorption. The distribution density of the branched chains was more efficient in promoting adsorption than the chain length.
A series of actinia-shaped lignin-based adsorbents (LNAEs) featuring lignin(LN) as the core and grafted poly (acrylic acid) (PAA) as the tentacle were designed and fabricated. LNAEs were applied to remove ofloxacin and ciprofloxacin from water, and their maximum adsorption capacities were 0.835 and 0.965 mmol/g at pH 6.0, respectively. However, their adsorption capacities were up to about 20 % and 31 % reductions in the present of NaCl and humic acid, respectively. Electrostatic attraction (EA) and hydrogen bonding (HB), including ordinary HB and negative charged auxiliary HB, were mainly involved in adsorption. Experimental and calculation results indicated HB contributes more than EA. The effects of two structural factors of LNAEs, namely, PAA branched chain length(L) and distribution density(D), on the adsorption performance associated with HB and EA, were quantitatively discussed using a binary nonlinear model based on phenomenological theory. The fitting results were completely consistent with the experimental findings. D was more efficient than L in promoting HB and EA in adsorption due to the cooperative effects of adjacent branched-chains and enhanced activity of terminal groups. This study provides a better understanding of the structure-activity relationship of surface grafting modified adsorbents and fundamental guidance for the exploitation and design of novel and efficient adsorbents.

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