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Although widely used in the textile industry, methyl orange is considered one of the most toxic dyes, which have negative impacts on the aquatic environment and needs to be removed from water bodies. Hence, the present paper reports the synthesis of new floating photo-Fenton catalysts based on the immobilization of Fe2O3 nanoparticles on the surface of Luffa sponges for the oxalate-induced-degradation of methyl orange. The floating catalytic sponges were prepared through a simple precipitation method followed by a reflux heating process and then characterized by field emission scanning electron microscopy, X-ray diffraction, atomic absorption spectrometry, and nitrogen adsorption-desorption experiments. According to the experimental results, methyl orange was effectively degraded over our floating catalytic sponges under light illumination at near neutral pH. The catalytic activity was also found to be enhanced with the increase in crystallinity of Fe2O3 nanoparticles, which can be achieved by the reflux heating. Besides, owing to the floating feature, these sponges are easily separated from the solution, thereby not forming a secondary source of pollution for water

Cisplatin-complexed gold nanoparticles (PtII-AuNP) provide a promising strategy for chemo-radiation-based anticancer drugs. Effective design of such platforms necessitates reliable assessment of surface engineering on a quantitative basis and its influence on drug payload, stability, and release. In this paper, poly(ethylene glycol) (PEG)-stabilized PtII-AuNP was synthesized as a model antitumor drug platform, where PtII is attached via a carboxyl-terminated dendron ligand. Surface modification by PEG and its influence on drug loading, colloidal stability, and drug release were assessed. Complexation with PtII significantly degrades colloidal stability of the conjugate; however, PEGylation provides substantial improvement of stability in conjunction with an insignificant trade-off in drug loading capacity compared with the non-PEGylated control (

Metal–organic frameworks (MOFs) and their composites have garnered significant attention in recent years due to their exceptional properties and diverse applications across various fields. The conventional batch synthesis methods for MOFs and their composites often suffer from challenges such as long reaction times, poor reproducibility, and limited scalability. Continuous flow synthesis has emerged as a promising alternative for overcoming these limitations. In this short review, we discuss the recent advancements, challenges, and future perspectives of continuous flow synthesis in the context of MOFs and their composites. The review delves into a brief overview of the fundamental principles of flow synthesis, highlighting its advantages over batch methods. Key benefits, including precise control over reaction parameters, improved scalability and efficiency, rapid optimization capabilities, enhanced reaction kinetics and mass transfer, and increased safety and environmental sustainability, are addressed. Additionally, the versatility and flexibility of flow synthesis techniques are discussed. The article then explores various flow synthesis methods applicable to MOF and MOF composite production. The techniques covered include continuous flow solvothermal synthesis, mechanochemical synthesis, microwave and ultrasound-assisted flow synthesis, microfluidic droplet synthesis, and aerosol synthesis. Notably, the combination of flow chemistry and aerosol synthesis with real-time characterization is also addressed. Furthermore, the impact of flow synthesis on the properties and performance of MOFs is explored. Finally, the review discusses current challenges and future perspectives in the field of continuous flow MOF synthesis, paving the way for further development and broader application of this promising technique. [ABSTRACT FROM AUTHOR]

A new and efficient technique is developed by combining the hyphenated microfluidic‐ and aerosol‐based synthesis with the coupled differential mobility analysis for the effective and continuous synthesis and simultaneous analysis of metal–organic frameworks (MOFs)‐derived hybrid nanostructured products. HKUST‐1, a copper‐based MOF, is chosen as the representative to fabricate Cu‐based hybrid catalysts for reverse water‐gas shift (RWGS) reaction, an effective route for CO2 utilization. The effect of precursor concentration and carrier selection on the properties of the resulting products, including mobility size distribution, crystallization degree, surface area, and metal dispersion are investigated, as well as the correlation between the material properties of the synthesized catalysts and their catalytic performance in RWGS reaction in terms of conversion ratio/rate, selectivity, and operational stability. The results indicate that the continuous microfluidic droplet system can successfully synthesize MOF colloids, followed by the continuous production of MOF‐derived hybrid materials through the tandem aerosol spray‐drying‐reaction system. High catalytic activity and low initiate temperature toward RWGS (turnover frequency = 0.0074 s−1; 450 °C) are achievable. The work facilitates the production and the designed concept of relevant MOF‐derived hybrid nanostructured catalysts in the continuous synthesis system and the enhancement of applications in CO2 capture and utilization. [ABSTRACT FROM AUTHOR]