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Dye released by industrial is one of the main known pollutants in wastewater, which is harmfully affected to the human health. Adsorptive method by absorbents and photocatalytic degradation technique are advanced technologies to remove dyes from wastewater. However, the single technique mentioned above has imperfections limiting its application. Herein, in order to integrate the two techniques and take both advantages, bacterial cellulose (BC) based titanium dioxide (TiO 2 )‑cadmium sulfide (CdS) nanocomposite gel was prepared by microwave-assisted solvothermal synthesis. The BC@TiO 2 -CdS nanocomposite gel was characterized by SEM, EDS, XRD, XPS, Raman spectral and TG, its photocatalytic mechanism was proved by PL. The results showed the TiO 2 -CdS nanophotocatalyst exhibited binary hierarchical structure and followed the Z-scheme type photocatalytic system. The Z-scheme heterojunction is advantageous for photo-generated charge separation and migration. The photocatalytic performance of BC@TiO 2 -CdS nanocomposite gel was evaluated by MB degradation under visible light irradiation. Due to synergistic effect of BC matrix and TiO 2 -CdS, the as-prepared BC@TiO 2 -CdS nanocomposite gel possesses enhanced photocatalytic activity with 94.47 % removal of methylene blue (MB) after 180 min visible light irradiation. Therefore, this work provides a facile route to fabricate bio-mass based efficient nanophotocatalytic material for pretreating the water pollution., 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. Published by Elsevier B.V.)

A fast and sensitive method based on fluorescent carboxymethyl chitosan/CdS quantum dots (CMCS-CdS QDs) composites was developed for specific detection of Staphylococcus aureus in food and the environment. Fluorescent CMCS-CdS QDs were prepared in aqueous solution through a green method. A human immunoglobulin (IgG) antibody was then bioconjugated to the QDs in the presence of 1-ethyl-3-(3)-dimethylaminopropyl carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) to make a novel type of mono-dispersed water-soluble fluorescent bioprobes. The fluorescent bioprobes were employed to identify S. aureus by incubating them with the bacteria for a certain time and observing the marked cells under fluorescence microscopy after removing free fluorescent QDs. Fluorescence microscopy images showed the S. aureus cells were successfully recognized by the bioprobes. Several other bacteria commonly found in environment such as Escherichia coli and Bacillus subtilis were also incubated with the bioprobes to test their specificity. It was found that the novel QDs-CMCS-IgG bioprobes had specific identification to S. aureus cells. Fluorescence measurement using a luminescence spectrometer could be applied to quantify S. aureus cells. The fluorescence intensity of the samples at 600 nm was proportional to the cell concentration in the range of 10(3)-10(7) cfu/ml, and the detection limit was as low as 900 cfu/ml. Considering the simplicity and cost-efficiency of this method, its application in the identification and quantification of bacteria in clinical, food and environmental samples is anticipated., (© Koninklijke Brill NV, Leiden, 2011)