Chitosan derived from chitin gas gathered much interest as a biopolymer due to its known and possible broad applications. Chitin is a nitrogen-enriched polymer abundantly present in the exoskeletons of arthropods, cell walls of fungi, green algae, and microorganisms, radulae and beaks of molluscs and cephalopods, etc. Chitosan is a promising candidate for a wide variety of applications due to its macromolecular structure and its unique biological and physiological properties, including solubility, biocompatibility, biodegradability, and reactivity. Chitosan and its derivatives have been known to be applicable in medicine, pharmaceuticals, food, cosmetics, agriculture, the textile and paper industries, the energy industry, and industrial sustainability. More specifically, their use in drug delivery, dentistry, ophthalmology, wound dressing, cell encapsulation, bioimaging, tissue engineering, food packaging, gelling and coating, food additives and preservatives, active biopolymeric nanofilms, nutraceuticals, skin and hair care, preventing abiotic stress in flora, increasing water availability in plants, controlled release fertilizers, dye-sensitised solar cells, wastewater and sludge treatment, and metal extraction. The merits and demerits associated with the use of chitosan derivatives in the above applications are elucidated, and finally, the key challenges and future perspectives are discussed in detail.

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Fabrication of chitosan and ilmenite sand-based novel photocatalysts through the catalytic graphitization of chitosan is reported. Nanocomposites consisted of TiO2, Fe2O3 and Fe nanoparticles dispersed on a nitrogen-doped graphitic carbon framework. The surface area, pore volume and macropore structure of the carbon matrix is disturbed by the heterogeneously distributed nanoparticles. The extent of graphitization expanded with increasing metal loading as indicated by variation in the ID/IG ratio. The nanomaterial’s surface consists of Fe3+ and Ti4+, and graphitic, pyridinic and pyrrolic nitrogen were found in the carbon matrix. The band gap values of the composites varied in the 2.06–2.26 eV range. The photocatalytic activity of the synthesized nanomaterials was determined, and the highest rate constant for the photodegradation of methylene blue under sunlight was 4.4 × 10−3 min−1, which resulted with 10 mg/L MB and 25 mg of the best-performing catalyst. The rate constant rose with increasing concentrations of persulfate added to the medium. The rate constant greatly diminished with the addition of isopropyl alcohol as it scavenged hydroxyl radicals. The presence of co-pollutants including Pb2+, rhodamine B, PO43− and Cl− curtailed the rate of reaction. The activity reduced with an increasing number of uses of the catalyst.

Hierarchically porous nitrogen-enriched carbon materials synthesized by polymerization of sucrose and urea (SU) were activated by KOH and H 3 PO 4 (SU-KOH and SU-H 3 PO 4 , respectively). Characterization was undertaken and the synthesized materials were tested for their ability to adsorb methylene blue (MB). Scanning electron microscopic images along with the Brunauer–Emmett–Teller (BET) surface area analysis revealed the presence of a hierarchically porous system. X-ray photoelectron spectroscopy (XPS) confirms the surface oxidation of SU upon activation with KOH and H 3 PO 4 . The best conditions for removing dyes utilizing both activated adsorbents were determined by varying the pH, contact time, adsorbent dosage, and dye concentration. Adsorption kinetics were evaluated, and the adsorption of MB followed second-order kinetics, suggesting the chemisorption of MB to both SU-KOH and SU-H 3 PO 4 . Times taken to reach the equilibrium by SU-KOH and SU-H 3 PO 4 were 180 and 30 min, respectively. The adsorption isotherm data were fitted to the Langmuir, Freundlich, Temkin, and Dubinin models. Data were best described by the Temkin isotherm model for SU-KOH and the Freundlich isotherm model for SU-H 3 PO 4 . Thermodynamics of the adsorption of MB to the adsorbent was determined by varying the temperature in the range of 25–55 °C. Adsorption of MB increased with increasing temperature, suggesting that the adsorption process is endothermic. The highest adsorption capacities of SU-KOH and SU-H 3 PO 4 (1268 and 897 mg g –1 , respectively) were obtained at 55 °C. Synthesized adsorbents were effective in removing MB for five cycles with some loss in activity. The results of this study show that SU activated by KOH and H 3 PO 4 are environmentally benign, favorable, and effective adsorbents for MB adsorption.