In this study, the synthesis of iron oxide stabilized by chitosan was carried out for the application and optimization in the removal process of aqueous Cr(VI) by central composite design (CCD). The calculation of these effects allowed to know, quantitatively, the variables and the interaction between them that could affect the Cr(VI) removal process. It was also verified that the most favorable conditions for chromium removal were the following: pH 5.0, Cr(VI) concentration of 130 mg L⁻¹, adsorbent mass of 5 mg, and Fe(II) content of 45% (w/w) in the CT-Fe beads. The adsorption kinetics performed under these conditions showed that the chitosan/iron hybrid composite is an adsorbent material with high chromium removal capacity (46.12 mg g⁻¹). It was found that all variables were statistically significant. However, it was observed that the variable that most affected Cr(VI) removal was the pH of the solution, followed by the concentration of chromium ions in solution and the interaction between them. Therefore, the studied experimental conditions are efficient in chromium adsorption, besides the operational simplicity coming from statistical design. Theoretical calculations showed that the most stable chitosan was that with Fe(II) in the structure, that is, in the reaction mechanism, there is no competition of Fe(II) with Cr(III, VI) in the available sites of chitosan. Thus, the theoretical calculations show that the proposed Cr(VI) removal is effective.

This study aims to produce and apply a biosurfactant from Gordonia westfalica GY40 for enhancing fuel oil solubilization and degradation in seawater. The immobilization of G. westfalica GY40 cells on chitosan flakes increased biosurfactant yield, and we achieved a biosurfactant concentration as high as 1.85 g L⁻¹ when using 2 % soybean oil as the carbon source. The critical micelle dilution (CMD) value of cell-free broth was 25 % and the lowest surface tension was 35 mN m⁻¹. The cell-free broth was able to solubilize and disperse fuel oil, at efficiencies corresponding to biosurfactant concentrations and CMD values. The surface activity of cell-free broth was stable under wide ranges of salinity, temperature, and pH. For the oil degradation test, cell-free broth at 0.5× CMD was added along with polyurethane foam-immobilized Gordonia sp. JC11, an efficient oil-degrading bacterial inoculum, to fuel oil spiked seawater. The system removed 81 % of 1 g L⁻¹ fuel oil in nutrient seawater medium within 6 days. When tested with three seawater samples collected along the Thai coastal area, the addition of both biosurfactant and immobilized Gordonia sp. JC11 was able to remove 60–70 % of 1 g L⁻¹ fuel oil, while the natural attenuation (control) removed only 26–35 % of fuel oil. The application of cell-free broth reduced the extraction and purification steps. In addition, the simple production of G. westfalica GY40 biosurfactant and Gordonia sp. JC11 inoculum suggested that they are suitable for cleaning-up oil spills in seawater.

A granular hydrogel of chitosan-g-poly(vinylimidazole-co-2-acrylamido-2-methyl propane sulfonic acid) was successfully synthesized by one-step free radical polymerization based on the grafting backbone of chitosan and the monomers of vinylimidazole and 2-acrylamido-2-methyl propane sulfonic acid. The resulting hydrogel could be used as the adsorbent for the efficient and selective removal of Hg²⁺ ions from the aqueous solution. The adsorption results could be well described by the pseudo-second-order kinetic mode and the Langmuir isotherm model with a maximum adsorption capacity of 363.55 mg/g for Hg²⁺. Furthermore, the as-prepared granular hydrogel exhibited an excellent cycling stability for the adsorption of Hg²⁺ after multiple repeated adsorption-desorption process. It suggested that the obtained granular hydrogel has potential application for Hg²⁺ removal and recovery from wastewater. Graphical Abstract A kind of granular hydrogel with excellent selectivity adsorption of Hg2+ ions was successfully synthesized by grafting polymerization of VIM and AMPS onto the CTS backbone via a facile free radical polymerization.

This paper aims to demonstrate the benefits of using a natural coagulant to enhance gravitational sedimentation of pig slurry. The separation process would lead to a liquid fraction, more biodegradable and with lower nutrient content, and a solid fraction highly concentrated in organic matter. Experimental trials were conducted in order to achieve the following objectives: (i) compare the effect of gravitational sedimentation with coagulation–flocculation process, (ii) compare the efficiency of conventional coagulants (such as aluminium sulphate or ferric chloride) with chitosan biopolymer and (iii) test the optimum coagulation–flocculation operational conditions to slurry sample. Assessment criteria included removal efficiencies but also took into consideration the advantages/disadvantages regarding sludge management. Results showed that gravitational sedimentation process can be improved by addition of coagulants; turbidity and COD removal increased around 2 and 3 times, respectively.

A novel sorbent, chitosan-immobilized pumice, has been prepared for the sorption of As(V) from waters prior to its determination by hydride generation atomic absorption spectrometry. The success of the immobilization has been checked with such characterization techniques as scanning electron microscopy, thermal gravimetric analysis, and elemental analysis. Points of zero charge of the sorbents were determined with potentiometric mass titration. Batch-type equilibration studies have shown that the novel sorbent can be employed at a wide pH range resulting in quantitative sorption (>90 %) at pH 3.0–7.0 and greater than 70 % sorption at pH >8.0. These results demonstrate the advantage of immobilizing chitosan onto pumice, because, under the same conditions, pumice displays <20 % sorption toward As(V), whereas chitosan gives approximately 90 % sorption only at pH 3.0. The validity of the method was verified through the analysis of ultrapure, bottled drinking, and tap water samples spiked with arsenate; the respective sorption percentages of 93.2 (±0.7), 89.0 (±1.0), and 80.9 (±1.3) were obtained by batch-type equilibration. Arsenic sorption was also examined in the presence of common interfering ions resulting in competing effects of PO₄ ³⁻ and NO₃ ⁻ on As(V) adsorption.

Carbonic anhydrase (CA) has been immobilized on chitosan stabilized iron nanoparticles (CSIN) for the biomimetic carbonation reaction. CSIN was characterized using scanning electron microscope, energy dispersive X-ray, X-ray diffraction spectroscopy, and Fourier transform infrared analysis. The effect of various parameters such as pH, temperature and storage stability, on immobilized CA was investigated using a p-NPA assay. Kinetic parameters of immobilized and free CA (K ₘ and V ₘₐₓ values) were also evaluated. The K ₘ and V ₘₐₓ for immobilized CA was 1.727 mM and 1.189 μmol min⁻¹ ml⁻¹, respectively, whereas for free enzyme the K ₘ and V ₘₐₓ was 1.594 mM and 1.307 μmol min⁻¹ ml⁻¹, respectively. It was observed that the immobilized enzyme had longer storage stability and retained 50 % of its initial activity upto 30 days at room temperature. CA immobilized on CSIN has been used for hydration of CO₂, and the results were validated by using a gas chromatographic method. Proof of concept has been established for the biomimetic carbonation reaction. Immobilized CA show reasonably good CO₂ sequestration capacity of 21.55 mg of CaCO₃/mg of CA as compared to CO₂ sequestration capacity of 34.92 mg of CaCO₃/mg of CA for free CA respectively, under a limiting concentration of CO₂ (14.5 mg of CO₂/10 ml).

The use of membranes prepared with alginate and chitosan to adsorb paraquat aqueous solution was evaluated as a potential alternative technique for remediation of contaminated water. Production of bilayer membranes was based on the electrostatic interaction between alginate (a polyanion) and chitosan (a polycation). Herbicide adsorption experiments were performed using three different membranes, consisting of pure alginate, pure chitosan, and a chitosan/alginate bilayer. Adsorption was characterized using the Langmuir and Freundlich isotherm models, as well as by applying pseudo-first order and pseudo-second order kinetic models. The potential use of the membranes in environmental applications was evaluated using water collected from the Sorocabinha River in São Paulo State, Brazil. The results indicated that interactions between the membranes and the herbicide were strongly related to the type of biopolymer and the physical–chemical characteristics of the herbicide.

The preparation, characterization, and environmental application of crosslinked chitosan-coated bentonite (CCB) beads for tartrazine adsorption have been investigated. CCB beads were characterized by using Fourier transform infrared spectrophotometer (FTIR), scanning electron microscope (SEM), and Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) pore size distribution analyses were also determined. The values of pH of the aqueous slurry and pH of zero point charge (pHZPC) were almost equal. The adsorption at equilibrium of tartrazine was found to be a function of pH of the solution, stirring rate, contact time, and tartrazine concentration. The optimum conditions for tartrazine adsorption were pH 2.5, stirring rate of 400 rpm and contact time of 80 min. Pseudo-first-order and pseudo-second-order models were used to analyze the kinetics of adsorption with the latter found to agree well with the kinetics data, suggesting that the rate determining step may be chemisorption. The two most common isotherm models, Langmuir and Freundlich, were used to describe the adsorption equilibrium data. On the basis of Langmuir isotherm model, the maximum adsorption capacities were determined to be 250.0, 277.8, and 294.1 mg g⁻¹ at 300, 310, and 320 K, respectively. Desorption studies were carried out at different concentrations of EDTA, H₂SO₄, and NaOH. All desorbing solutions showed poor recovery of tartrazine.

This paper presents a new material easily synthesized and with low cost, with the possibility of remove arsenic and the potential capability for the remediate water bodies. In this work, the efficiency in removing arsenic of the chitosan, supported onto modified polypropylene membrane, was studied using an aqueous As(V) solution of 0.4 mg/L, achieving a removal efficiency of 75%, which corresponds to an adsorption capacity of 0.031 mg/g. The As(V) adsorption depends on pH and the degree of chitosan grafting on the polypropylene membrane. A pseudo-second-order equation describes the adsorption of the membrane, classifying it as a chemisorption process. The chitosan supported on the membrane was characterized by the analysis of wettability, FT-IR-ATR, SEM-EDS, XRD powder, and surface charge. The As ions coordinate to the chitosan polar groups, allowing their removal from the aqueous solution.

Petroleum oil leakage and industrial oily waste on the water surface are sustainable pollutions. The removal process by eco-friendly adsorbents is a critical challenge. It also requires sustainable treatment. The natural hydrophobic material such as abietic acid, boswellic acid, and chitosan was added to magnetite nanoparticles with different concentrations of 10, 15, and 20% on its surface. The magnetite acquires partially hydrophobic properties. The prepared natural adsorbents were analyzed by employing wide-angle X-ray diffraction (WAXD), vibrating sample magnetometer (VSM), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), particle size and zeta potential, and contact angle measurements. Chitosan adsorbs at the outer surface of magnetite nanoparticles while boswellic and abietic absorb in bulk. All prepared adsorbents are effective in adsorbing waste oil from the water surface. The contact angle of MB20 (magnetite/20 percent boswellic) is greater than that of MA20 and MC20 (magnetite/20% abietic or chitosan, respectively), indicating that it has more hydrophobic characteristics. The oil removal efficiency and adsorption capacity of MB20 are the highest values 57.6%, and 24 g/g, respectively. All eco-friendly adsorbents are nontoxic with low-cost production and are used many times.