Utilization and value-adding of waste: Fabrication of porous material from chitosan for phosphate capture and energy storage.

Efficient removal and recycling of phosphorus from complex water matrices using environmentally friendly and sustainable materials is essential yet challenging. To this end, a novel bio-based adsorbent (DX-FcA-CS) was developed by coupling oxidized dextran-crosslinked chitosan with ferrocene carboxylic acid (FcA). Detailed characterization revealed that the incorporation of FcA reduced the total pore area of DX-FcA-CS to 7.21 m2·g-1, one-third of ferrocene-free DX-CS (21.71 m2·g-1), while enhancing thermal stability and PO43- adsorption performance. Adsorption kinetics and isotherm studies demonstrated that the interaction between DX-FcA-CS and PO43- followed a pseudo-second-order kinetic model and Langmuir model, indicating chemical and monolayered adsorption mechanisms, respectively. Moreover, DX-FcA-CS exhibited excellent anti-interference properties against concentrated co-existing inorganic ions and humic acid, along with high recyclability. The maximum adsorption capacity reached 1285.35 mg·g-1 (∼428.45 mg P g-1), three times that of DX-CS and surpassing many other adsorbents. PO43--loaded DX-FcA-CS could be further carbonized into electrode material due to its rich content of phosphorus and nitrogen, transforming waste into a valuable resource. These outstanding characteristics position DX-FcA-CS as a promising alternative for phosphate capture and recycling. Overall, this study presents a viable approach to designing environmentally friendly, recyclable, and cost-effective biomaterial for wastewater phosphate removal and value-added applications.

Redox-responsive microemulsion: Fabrication and application to curcumin encapsulation.

HYPOTHESIS: Stimulus-responsive microemulsions have aroused significant attention because of their versatile and reversible switchability between stable and unstable states. However, most stimuli-responsive microemulsions are based on stimuli-responsive surfactants. We posit that the change in the hydrophilicity of a selenium-containing alcohol triggered by a mild redox reaction could also influence the stability of microemulsions and provide a new nanoplatform for the delivery of bioactive substances. EXPERIMENTS: A selenium-containing diol (3,3'-selenobis(propan-1-ol), PSeP) was designed and used as a co-surfactant in a microemulsion with ethoxylated hydrogenated castor oil (HCO40), diethylene glycol monohexyl ether (DGME), 2-n-octyl-1-dodecanol (ODD) and water. The redox-induced transition in PSeP was characterized by 1H NMR, 77Se NMR, and MS. The redox-responsiveness of the ODD/HCO40/DGME/PSeP/water microemulsion was investigated through determination of a pseudo-ternary phase diagram, analysis by dynamic light scattering, and electrical conductivity, and its encapsulation performance was evaluated by determination of the solubility, stability, antioxidant activity, and skin penetrability of encapsulated curcumin. FINDINGS: The redox conversion of PSeP enabled efficient switching of ODD/HCO40/DGME/PSeP/water microemulsions. Addition of oxidant (H2O2), oxidized PSeP into more hydrophilic PSeP-Ox (selenoxide), disrupting the emulsifying capacity of the combination of HCO40/DGME/PSeP, markedly reducing the monophasic microemulsion region in the phase diagram, and inducing phase separation in some formulations. Addition of reductant (N2H4·H2O), reduced PSeP-Ox and restored the emulsifying capacity of the combination of HCO40/DGME/PSeP. In addition, PSeP-based microemulsions can significantly enhance the solubility in oil (by 23 times), stability, antioxidant capacity (DPPH∙ radical scavenging by 91.74 %), and skin penetrability of curcumin, showing clear potential for encapsulation and delivery of curcumin and other bioactive substances.

Oxidized dextran-crosslinked ferrocene-chitosan-PEI composite porous material integrating adsorption and degradation to malachite green.

Treating wastewater containing malachite green (MG) using porous materials with both adsorption and degradation functions have become a major challenge in achieving the carbon neutrality goal. Herein by incorporating the ferrocene (Fc) group as a Fenton active center, a novel composite porous material (DFc-CS-PEI) was prepared using chitosan (CS) and polyethyleneimine (PEI) as skeletons and oxidized dextran as a crosslinker. DFc-CS-PEI not only possesses satisfactory adsorption performance to MG but also excellent degradability in the presence of a minor amount of H2O2 (3.5 mmol/L) without any additional assistance, due to high specific surface area and active Fc group. The maximum adsorption capacity is ca. 177.73 ± 3.11 mg/g, outperforming most CS-based adsorbents. The removal efficiency of MG is significantly enhanced from 20 % to 90 % as DFc-CS-PEI and H2O2 coexist, due to ·OH-dominated Fenton reaction, and remained in a wide pH range (2.0-7.0). Cl- exhibits notable suppression on the degradation of MG because of quenching effects. Note that DFc-CS-PEI has a very small iron leaching (0.2 ± 0.015 mg/L), and can be rapidly recycled by simple water-washing, without any harmful chemicals and potential second pollution. Such versatility, high stability, and green recyclability make the as-prepared DFc-CS-PEI a promising porous material for the treatment of organic wastewater.