The dangers posed by nuclear accidents necessitate developments in techniques for cesium removal. One such is the adsorption of cesium cations in Prussian blue (PB) materials, on which adsorption can be a substation process or pure physisorption. The underlying mechanism of the latter is not well understood, although a Langmuir isotherm is frequently used to model experimental results. In this work, we exploit tight-binding density-functional theory (DFTB) methods to probe the atomic interactions in the physisorption process. The results show that there is a diminishing return for the energy of adsorption as more sites are filled. This means that the adsorption sites are not independent, as stipulated by the ideal Langmuir isotherm. Instead, the results indicate that electrostatic effects need to be considered to explain the theoretical and experimental results. Therefore, an electrostatic Langmuir (EL) model is introduced, which contains an electrostatic ideality correction to the classic Langmuir isotherm. For future materials development, these physical insights indicate that shielding effects as well as the number of independent physical sites must be considered when synthesizing effective Prussian blue analogs (PBA). In conclusion, the study provides insights into the limiting mechanisms in the physisorption of cesium cations on PB.
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http://dx.doi.org/10.1039/d2cp04317c | DOI Listing |
Anal Chem
January 2025
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang 212013, PR China.
Wearable sensors have broad application potential in motion assessment, health monitoring, and medical diagnosis. However, relying on a specialized instrument for power supply and signal reading makes sensors unsuitable for on-site detection. To solve this problem, a reusable self-powered electrochromic sensor patch based on enzymatic biofuel cells were constructed to realize the on-site visualized monitoring.
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Department of Gynecology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, China.
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China Uruguay Bio-Nano Pharmaceutical Joint Laboratory, Institute of Neuroregeneration and Neurorehabilitation, Qingdao University, 308 Ningxia Road, Qingdao, 266071, Shandong, China.
Well-designed artificial scaffolds are urgently needed due to the limited self-repair capacity of bone, which hampers effective regeneration in critical defects. Optimal scaffolds must provide physical guidance to recruit cells and immune regulation to improve the regenerative microenvironment. This study presents a novel scaffold composed of dual-sided centripetal microgrooved poly(D,L-lactide-co-caprolactone) (PLCL) film combined with a dynamic hydrogel containing prednisolone (PLS)-loaded Prussian blue nanoparticles (PB@PLS).
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Key Laboratory of Fermentation Engineering (Ministry of Education), Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Glyn O. Phillips Hydrocolloid Research Centre at HBUT, School of Life and Health Sciences, Hubei University of Technology, Wuhan, 430068, China; Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, College of Health Science and Engineering, School of Materials Science and Engineering, Hubei University, Wuhan 430062, China. Electronic address:
The integration of photothermal therapy (PTT) and gas therapy (GT) on a nanoplatform shows great potential in cancer treatment. In this paper, a tumor-targeted near-infrared/ultraviolet (NIR/UV) triggered PTT/GT synergistic therapeutic nanoplatform, PB-CD-PLL(NF)-FA, was designed based on Prussian blue (PB) nanoparticles, 5-chloro-2-nitrobenzotrifluoro (NF)-grafted polylysine (PLL(NF)), and folic acid (FA). PB serves as a core to load PLL(NF) through host-guest interaction and can further modify FA.
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School of Pharmaceutical Sciences, Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, Sun Yat-Sen University, University Town, Guangzhou 510006, China.
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