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The metal organic frameworks (MOFs) are considered as the effective adsorbents for phosphate removal, while their ultrafine powders limit their practical application. In this study, we fabricate two chitosan (CS) gel beads added with different cerium-based MOFs and coated with PDA for phosphate adsorption. The MOFs doped in beads are CM1 and CM2, in which the Ce(III)/Ce(IV) ratio is 0.36 and 1.46, indicating CM2 is Ce(III) dominated and more suitable for phosphate removal. However, during the process of preparing gel beads, the mixture of chitosan and CM1/CM2 are added drop-by-drop to NaOH solution, leading to the decrease of Ce(III) contents in both of the two beads on account of oxidization. On this basis, in order to improve the phosphate uptake performance and enhance the mechanical strength, polydopamine (PDA) is applied to be coated on the outside. The adsorption capacities of CS-CM1 and CS-CM2 are no more than 20 mg/g higher than that of pure CS, which is also quite equal with the phosphate uptake of CS@PDA (63 mg/g). Due to the reduction of PDA, the content of Ce(III) increasing evidently in the two adsorbents. The maximum phosphate adsorption capacities are 146.8 mg/g and 114.8 mg/g for CS-CM1@PDA and CS-CM2@PDA, respectively. CS-CM2@PDA exhibits the largest treatment volume of ∼1166 BV in the fix-bed column study, much higher than that of CS-CM1@PDA (976 BV). The main reason is that Ce(III) could form binding with phosphate through ligand exchange and precipitation. Those inner-sphere interactions are much stronger than the electrostatic attraction between Ce(IV) and phosphate. Thus, due to this strong affinity, CS-CM2@PDA possessing a higher content of Ce(III) can capture phosphate more easier at low concentration. In summary, owing to reduction of PDA, the Cerium-based MOFs are successfully introduced in CS to realize excellent phosphate removal and exhibit a great prospect in application., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

An easily separation composite, magnetic chitosan@bismuth tungstate coated by silver (MCTS-Ag/Bi 2 WO 6 ), was successfully synthesized by the simple hydrothermal method. Moreover, the MCTS-Ag/Bi 2 WO 6 demonstrated excellent adsorption/photocatalytic removal of Cu(II) in aqueous solution. Adsorption played a leading role in the synergistic reaction. The catalysts were characterized by fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The effects on adsorption of Cu(II) were investigated, which included illumination, pH, and initial concentration. The experimental results showed that the theoretical maximum adsorption capacity of Cu(II) (181.8 mg/g) was achieved under simulated solar light irradiation with the optimal pH value of 6.0, indicating that illumination could enhance the adsorption of Cu(II) by MCTS-Ag/Bi 2 WO 6 . Meanwhile, the composite exhibited desirable adsorption ability of Cu(II) after 5 cycles. The copper ion adsorption fitted well with pseudo-second-order kinetic model and its isotherm followed Freundlich model., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Wastewater containing highly toxic and non-biodegradable heavy metals and organic dyes poses a serious threat to ecological environment and human health. Adsorption has been regarded as a promising technology to purify this kind of wastewater. Therefore, it is of great importance to develop efficient adsorbents. Herein, a magnetically recyclable adsorbent Fe 3 O 4 -CS/PDAC was facilely fabricated by coating poly(acryloyloxyethyltrimethyl ammonium chloride)-modified chitosan on the surface of Fe 3 O 4 nanoparticles. The morphology, physical-chemical and magnetic properties of as-prepared Fe 3 O 4 -CS/PDAC was fully characterized by various techniques. Its adsorption behaviors towards heavy metal Cr(VI) and organic dye sunset yellow (SY) were systematically investigated. Evidently, Fe 3 O 4 -CS/PDAC exhibited adsorption capacities of 163.93 and 769.23 mg/g for Cr(VI) and SY respectively, much higher than other reported adsorbents. Besides, batch experiment results showed that adsorption capacities decreased slightly with pH increasing from 2.0 to 10.0. Furthermore, Fe 3 O 4 -CS/PDAC could be easily separated and effectively regenerated after adsorption. The superior adsorption performance of Fe 3 O 4 -CS/PDAC could be attributed to the electrostatic interaction and ion exchange between target pollutants and the grafted cationic polymer. Owing to its high adsorption capacity over a wide pH range, rapid separation, easy regeneration and good reusability, Fe 3 O 4 -CS/PDAC has great potential for practical application in water treatment., Competing Interests: Declaration of competing interest None., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Due to the complexity of contaminants, the effectiveness of traditional flocculants toward water purification is insufficient. To break the limitation, a novel polymer flocculant [chitosan grafted poly (acrylamide-itaconic acid), CS-g-P(AM-IA)] was synthesized via ultraviolet-initiated graft copolymerization reaction. Characterization results revealed that the graft copolymers were successfully synthesized and with rougher surface structure. The solubility of CS-g-P(AM-IA) and chitosan grafted polyacrylamide (CS-g-PAM) were greatly improved and they can dissolve in the wide pH range of 2.0–12.0. CaCl 2 was used as a source of cation bridge to enhance the flocculation of kaolin particles, and its optimum dosage was 150 mg·L −1 . At dosage of 30 mg·L −1 and pH of 5.0, the turbidity removal efficiency of CS-g-P(AM-IA) reached the maximum of 93.8%, whereas those of CS-g-PAM and CS were 96.7% and 76.9%, respectively. The patchwise adsorption of ionic groups embedded in the molecular chain on Ca 2+ -clay complexes took effect to generate flocs with larger particle size. Besides, the decolorization ability of cationic dyes by CS-g-P(AM-IA) was greatly enhanced due to the role of abundant carboxyl groups. In the crystal violet (CV) adsorption experiment, the maximum CV dye removal efficiency for CS-g-P(AM-IA) reached the maximum of 81.6% at dosage of 0.7 mg·mL −1 and pH of 9.0, while those for CS-g-PAM and CS were 51.7% and 36.5%, respectively. [ABSTRACT FROM AUTHOR]

Modified natural polymer flocculants has been the focus of research in environmental engineering field. Natural large molecular compound, chitosan (CTS) with many functional amino and hydroxyl groups can be easily modified to enhance its original functions. This work presents an environmentally friendly chitosan-based cationic polyacrylamide flocculants (CTS-g-PAMA) with enhanced function of sterilization and flocculation. CTS-g-PAMA was synthesized through Ultraviolet (UV)-initiated copolymerization. Structure characterization of FTIR, 1 H NMR, XRD and UV spectrum confirmed the successful grafting of AM and MAPTAC. Scanning electron microscopy (SEM) analysis results showed that CTS-g-PAMA exhibited a porous structure with a prodigious surface area. CTS-g-PAMA was then applied to treat a series of simulated waste water containing kaolin or Escherichia coli . Flocculation tests indicated that CTS-g-PAMA not only showed excellent flocculation effect but also showed high sterilization capability. A series of ONP concentration measurement tests through UV spectra analysis and 3D EEM analysis of suspension before and after flocculation were conducted to study sterilization mechanism, and results revealed the sterilization effect of CTS-g-PAMA was essentially bactericidal, not just antibacterial. [ABSTRACT FROM AUTHOR]