RESUMEN
This study introduces a chitosan/boehmite biocomposite as an efficient adsorbent for removing anionic Congo Red (CR) and non-ionic Bromothymol Blue (BTB) from water. Boehmite nanoparticles were synthesized using the Sol-gel method and then attached to chitosan particles using sodium tripolyphosphate through co-precipitation method. Characterized through FTIR, FE-SEM, BET, and XRD, the biosorbent displayed structural integrity with optimized pH conditions of 3 for CR and 4 for BTB, achieving over 90 % adsorption within 30 min. Pseudo second order kinetics model and Langmuir isotherm revealed monolayer sorption with capacities of 64.93 mg/g for CR and 90.90 mg/g for BTB. Thermodynamics indicated a spontaneous and exothermic process, with physisorption as the primary mechanism. The biosorbent demonstrated excellent performance and recyclability over five cycles, highlighting its potential for eco-friendly dye removal in contaminated waters.
Asunto(s)
Hidróxido de Aluminio , Óxido de Aluminio , Quitosano , Contaminantes Químicos del Agua , Colorantes/química , Quitosano/química , Adsorción , Contaminantes Químicos del Agua/química , Termodinámica , Rojo Congo , Agua , Cinética , Concentración de Iones de HidrógenoRESUMEN
Recent studies have suggested that platelets have a crucial role in enhancing the survival of circulating tumor cells in the bloodstream and aggravating cancer metastasis. The main function of platelets is to bind to the sites of the damaged vessels to stop bleeding. However, in cancer patients, activated platelets adhere to circulating tumor cells and exacerbate metastatic spreading. Several hypotheses have been proposed about the platelet-cancer cell interactions, but the underlying mechanisms of these interactions are not completely understood yet. In this work, we quantitatively investigated the interactions between circulating tumor cells, red blood cells, platelets, plasma flow and microvessel walls via computational modelling at the cellular scale. Our highly detailed computational model allowed us to understand and quantitatively explain the role of platelets in deformation, adhesion and survival of tumor cells in their active arrest to the endothelium.