The chemical cross-linking of carboxymethyl chitosan (O-CM-chitosan), as a method for its modification, was performed using trimellitic anhydride isothiocyanate to obtain novel cross-linked O-CM-chitosan hydrogel. Its structure was proven using FTIR, XRD and SEM. Its adsorption capacity for the removal of Methylene Blue (MB) dye from aqueous solution was studied. The effects of different factors on the adsorption process, such as the pH, temperature and concentration of the dye, in addition to applications of the kinetic studies of the adsorption process, adsorption isotherm and thermodynamic parameters, were studied. It was found that the amount of adsorbed MB dye increases with increasing temperature. A significant increase was obtained in the adsorption capacities and removal percentage of MB dye with increasing pH values. An increase in the initial dye concentration increases the adsorption capacities, and decreases the removal percentage. It was found that the pseudo-second-order mechanism is predominant, and the overall rate of the dye adsorption process appears to be controlled by more than one step. The Langmuir model showed high applicability for the adsorption of MB dye onto O-CM-chitosan hydrogel. The value of the activation energy (Ea) is 27.15 kJ mol−1 and the thermodynamic parameters were evaluated. The regeneration and reuse of the investigated adsorbent was investigated.

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Novel Cyanoguanidine-modified chitosan (CCs) adsorbent was successfully prepared via a four-step procedure; first by protection of the amino groups of chitosan, second by insertion of epoxide rings, third by opening the latter with cyanoguanidine, and fourth by restoring the amino groups through elimination of the protection. Its structure and morphology were checked using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The adsorption capacity of CCs for Congo Red (CR) dye was studied under various conditions. It decreased significantly with the increase in the solution pH value and dye concentration, while it increased with increasing temperature. The adsorption fitted to the pseudo-second order kinetic model and Elovich model. The intraparticle diffusion model showed that the adsorption involved a multi-step process. The isotherm of CR dye adsorption by CCs conforms to the Langmuir isotherm model, indicating the monolayer nature of adsorption. The maximum monolayer coverage capacity, qmax, was 666.67 mg g−1. Studying the thermodynamic showed that the adsorption was endothermic as illustrated from the positive value of enthalpy (34.49 kJ mol−1). According to the values of ΔG°, the adsorption process was spontaneous at all selected temperatures. The value of ΔS° showed an increase in randomness for the adsorption process. The value of activation energy was 2.47 kJ mol−1. The desorption percentage reached to 58% after 5 cycles. This proved that CCs is an efficient and a promising adsorbent for the removal of CR dye from its aqueous solution.

Novel Uracil-modified chitosan (UCs) adsorbent has successfully been synthesized through a four-step method during which the amino groups of chitosan have been protected, then epoxy nuclei have been incorporated, afterwards the latter have been opened using 6-amino-1,3-dimethyl uracil, and finally the amino groups have been regained via removing the protection. Its structure was checked using FTIR, XRD and SEM techniques. The adsorption capacity of UCs for anionic Congo Red (CR) dye was studied under various conditions. It decreased significantly with increasing the solution pH value and dye concentration, while increased with increasing temperature. The adsorption of UCs for CR dye at different temperatures, solution pH and dye concentrations fitted to the kinetic model of pseudo-second order and Elovich model. The intraparticle diffusion model showed that the adsorption process involves multi-step process. The isotherm of CR dye adsorption by UCs conforms to the Langmuir isotherm model indicating the monolayer nature of adsorption. The maximum monolayer coverage capacity, qmax, was 434.78 mg g−1. Studying the thermodynamic showed that the adsorption of CR dye onto UCs was endothermic as illustrated from the positive value of enthalpy (21.37 kJ mol−1). According to the values of ΔG°, the adsorption process was spontaneous at all selected temperatures. The value of ΔS° showed an increase in randomness for the adsorption of CR dye by UCs. The value of activation energy was 18.40 kJ mol−1.

This review investigates antifouling agents used in the process of membrane separation (MS), in reverse osmosis (RO), ultrafiltration (UF), nanofiltration (NF), microfiltration (MF), membrane distillation (MD), and membrane bioreactors (MBR), and clarifies the fouling mechanism. Membrane fouling is an incomplete substance formed on the membrane surface, which will quickly reduce the permeation flux and damage the membrane. Foulant is colloidal matter: organic matter (humic acid, protein, carbohydrate, nano/microplastics), inorganic matter (clay such as potassium montmorillonite, silica salt, metal oxide, etc.), and biological matter (viruses, bacteria and microorganisms adhering to the surface of the membrane in the case of nutrients) The stability and performance of the tested nanometric membranes, as well as the mitigation of pollution assisted by electricity and the cleaning and repair of membranes, are reported. Physical, chemical, physico-chemical, and biological methods for cleaning membranes. Biologically induced biofilm dispersion effectively controls fouling. Dynamic changes in membrane foulants during long-term operation are critical to the development and implementation of fouling control methods. Membrane fouling control strategies show that improving membrane performance is not only the end goal, but new ideas and new technologies for membrane cleaning and repair need to be explored and developed in order to develop future applications.

Dyes removal from wastewater of industries is considered the prime demand of the environment. Three trimellitic anhydride isothiocyanate-cross-linked chitosan hydrogels, previously reported as novel antimicrobial agents, were investigated for the first time in this work as adsorbents for Basic Red 12 (BR 12) cationic dye. These hydrogels behave as polyanionic materials. Their adsorption capacity for the BR 12 dye increased significantly with increasing both the temperature, the solution pH and their cross-linking content. Their adsorption fitted to the pseudo-second-order kinetic model. Their adsorption isotherms conform to the Langmuir model suggesting that the adsorption nature is a monolayer having an optimum sorption capability of 38.27 mg g−1 and removal efficiency of 97.38%. The results proved that the adsorption process is remarkably proceeded by chemisorption phenomenon. The data of adsorption thermodynamics indicate that the adsorption is an endothermic process. The regeneration and reuse of the hydrogels were possible. Thus, incorporation of the functionality of the cross-linker into chitosan within the same structure efficiently enhanced its features. It is a good manner for achieving appropriate series of efficient adsorbents which are considered as favorable nominees in the field of basic dyes removal.

Due to the impacts of water scarcity, the world is looking at all possible solutions for decreasing the over-exploitation of finite freshwater resources. Wastewater is one of the most reliable and accessible water supplies. As the population expands, so do industrial, agricultural, and household operations in order to meet man’s enormous demands. These operations generate huge amounts of wastewater, which may be recovered and used for a variety of reasons. Conventional wastewater treatment techniques have had some success in treating effluents for discharge throughout the years. However, advances in wastewater treatment techniques are required to make treated wastewater suitable for industrial, agricultural, and household use. Diverse techniques for removing heavy metal ions from various water and wastewater sources have been described. These treatments can be categorized as adsorption, membrane, chemical, or electric. Membrane technology has been developed as a popular alternative for recovering and reusing water from various water and wastewater sources. This study integrates useful membrane technology techniques for water and wastewater treatment containing heavy metals, with the objective of establishing a low-cost, high-efficiency method as well as ideal production conditions: low-cost, high-efficiency selective membranes, and maximum flexibility and selectivity. Future studies should concentrate on eco-friendly, cost-effective, and long-term materials and procedures.