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Magnetic separation technology is an efficient and feasible way to achieve rapid recovery of adsorbents, thus, the use of magnetic adsorbents has attracted the attention of many researchers. However, currently reported magnetic adsorbents have limited adsorption capacity due to insufficient adsorption sites and reactive groups. In this work, a novel magnetic chitosan-based amphiphilic adsorbent (PFSC) was synthesized by using UV-light irradiation method to combine with acryloyloxyethyl dimethylbenzyl ammonium chloride (AO), a molecule containing benzyl groups. PFSC and its precursors were carefully characterized, and their adsorption performances for the removal of anionic dyes were explored. The characterization results showed that the magnetic copolymers with a type of microsphere structure were successfully synthesized. Moreover, PFSC exhibited superior adsorption efficiency and pH resistance compared to those of an unmodified chitosan-based magnetic adsorbent (FSC). The maximum adsorption capacities of PFSC towards orange II (OG), acid red 88 (AE) and red amaranth (RM) were 955.0, 1075.8 and 567.5 mg/g at pH 3.0, respectively. The adsorption kinetics and isotherms of PFSC were consistent with that of a pseudo-second order kinetic model and the Langmuir isotherm model. In addition, adsorption-desorption experiments showed that PFSC could be rapidly separated and efficiently recycled even after 4 uses. More importantly, the FTIR and XPS results revealed that electrostatic adsorption and π-π stacking interactions were the main adsorption mechanisms for the PFSC-enhanced removal of anionic dyes. [Display omitted] • The chitosan-based amphiphilic magnetic copolymer was successfully synthesized by the UV-light initiated method. • The novel magnetic copolymer can be easily separated from solution by magnetic force. • The enhanced electrostatic adsorption and π-π stacking effect played an important role in the removal of anionic dyes. • The novel magnetic copolymer can be reused by simple acid-alkali adjustment. [ABSTRACT FROM AUTHOR]

[Display omitted] • Magnetic alginate-based biosorbents are prepared by free radical polymerization. • FSSEB-20 shows excellent adsorption capacities for DS and X-3B, respectively. • FSSEB-20 still shows satisfactory recycling rate after five runs. • The mechanism includes electrostatic action, hydrogen bonding and π-π interaction. In this work, we unveiled a novel magnetic biosorbent, poly (Benzyldimethyl[2-[(2-methyl-1-oxoally) oxy] ethyl] ammonium chloride)-immobilized magnetic sodium alginate composite-20 (FSSEB-20), and studied its adsorption behavior for two groups of toxic anionic organic pollutants, DS and X-3B from simulation wastewater. Results demonstrated that the Langmuir model could well describe the adsorption behavior of DS and X-3B on FSSEB-20, the maximum adsorption capacity of FSSEB-20 towards DS and X-3B are 340.58 mg g−1 and 370.85 mg g−1, respectively; according to kinetic results, the adsorption processes of both DS and X-3B on FSSEB-20 followed the pseudo-second-order kinetic model. To test the reusability of FSSEB-20, five runs of regeneration tests were performed. The removal rates of FSSEB-20 towards DS and X-3B are more than 74%. In addition to these, the surface interactions between FSSEB-20 and DS/X-3B were systematically analyzed based on the characterization results of FT-IR and XPS, which provided significant insights into the interactions between biosorbents and pollutants in wastewater. The mechanism of DS and X-3B adsorption by FSSEB-20 includes electrostatic interaction, hydrogen bonding and π-π interaction. Furthermore, this study also provides a new enlightenment for expanding the treatment of pollutants in wastewater with sodium alginate-based magnetic biosorbent. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel floating-separation adsorbent (APHGS-g-P(AMPS)) was designed and synthesized. • APHGS-g-P(AMPS) showed outstanding self-floating separation ability. • APHGS-g-P(AMPS) with satisfactory adsorption capacity was rich in –OH, –NH 2 and -SO 3 -. • The electrophilic addition strategy facilitated the grafting of P(AMPS) polymerized chains. • The sulfonic acid group exhibited excellent universal adsorption for MB and Pb(II). Inferior solid–liquid separation behavior and inadequate adsorption capacity are the main bottlenecks of current wastewater treatment adsorbents, especially in the purification of wastewater containing dyes and heavy metals. Accordingly, a novel floating separation adsorbent with polymeric chain structure, hollow glass sphere-g-(3-aminopropyl) triethoxysilane-g-poly(2-acrylamide-2-methyl-1-propanesulfonic acid) (APHGS-g-P(AMPS)), was fabricated through an electrophilic addition post-grafting strategy. The obtained APHGS-g-P(AMPS) exhibited satisfactory adsorption for methylene blue (MB) and lead ion (Pb(II)), as well as efficient flotation. Adsorption behavior analysis showed that the Pseudo-second-order kinetic model and Langmuir isotherm model were suitable for describing the adsorption process, and the maximum adsorption capacities for MB and Pb(II) were 249.33 and 345.93 mg·g−1 (313.15 K), respectively. Analysis of the adsorption mechanism indicated that the sulfonic acid group exhibited excellent universal adsorption for MB and Pb(II), which played a crucial role in the adsorption process. Furthermore, the efficient grafting of P(AMPS) polymerized chains onto the adsorbent was the pivotal factor to enhance adsorption. This study provided an efficient electrophilic addition post-grafting strategy for the structural design and functional modification of floating separation adsorbents. The results of this study are expected to have positive implications for the efficient purification of dyes and heavy metals wastewater. [ABSTRACT FROM AUTHOR]