Biodegradable cellulose nanocrystals hydrogels (CNCsH) were synthesized from cellulose nanocrystals (CNCs) which were prepared from office wastepaper (OWP) by a chemical crosslinking method using epicholorohydrin (ECH) as a cross-linker. CNCsH were tested for their swelling behavior and biodegradability and the point of zero charge had been determined. The ability of CNCsH for removing the Acid Red 8 (AR8) anionic dye from its aqueous solution was evaluated. The different parameters affecting removal of the dye, such as pH, initial concentration of dye, content of CNCs, temperature and adsorbent dosage were investigated. The optimum conditions for 68% removal efficiency were pH = 1, initial concentration of dye = 10 ppm, contact time = 105 min, CNCs content = 5% and CNCsH dosage = 0.5 g at 30 °C. The adsorption isotherms, kinetics, and thermodynamic parameters have been studied. The results showed an appropriate fit for Langmuir adsorption isotherm and pseudo-second order kinetics model with an adsorption capacity of 17.12 mg/g. According to the obtained values of thermodynamic parameters, the removal of Acid red 8 by CNCs hydrogels was exothermic spontaneous process.

The necessity to resolve the issue of rapid charge carrier recombination for boosting photocatalytic performance is a vigorous and challenging research field. To address this, the construction of a binary system of step-scheme (S-scheme) CuO@TiO2 heterostructure composite has been demonstrated through a facile solid-state route. The remarkably enhanced photocatalytic performance of CuO@TiO2, compared with single TiO2, which can consequence in the more efficient separation of photoinduced charge carriers, reduced the band gap of TiO2, improved the electrical transport performance, and improved the lifetimes, thus donating it with the much more powerful oxidation and reduction capability. A photocatalytic mechanism was proposed to explain the boosted photocatalytic performance of CuO@TiO2 on a complete analysis of physicochemical, DFT calculations, and electrochemical properties. In addition, this work focused on the investigation of the stability and recyclability of CuO@TiO2 in terms of efficiency and its physical origin using XRD, BET, and XPS. It is found that the removal efficiency diminishes 4.5% upon five recycling runs. The current study not only promoted our knowledge of the binary system of S-scheme CuO@TiO2 heterojunction composite photocatalyst but also shed new light on the design of heterostructure photocatalysts with high-performance and high stability.

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