Innovative biopolyelectrolytes-based technologies for wastewater treatment.

Developing eco-friendly, cost-effective, and efficient methods for treating water pollutants has become paramount in recent years. Biopolyelectrolytes (BPEs), comprising natural polymers like chitosan, alginate, and cellulose, have emerged as versatile tools in this pursuit. This review offers a comprehensive exploration of the diverse roles of BPEs in combating water contamination, spanning coagulation-flocculation, adsorption, and filtration membrane techniques. With ionizable functional groups, BPEs exhibit promise in removing heavy metals, dyes, and various pollutants. Studies showcase the efficacy of chitosan, alginate, and pectin in achieving notable removal rates. BPEs efficiently adsorb heavy metal ions, dyes, and pesticides, leveraging robust adsorption capacity and exceptional mechanical properties. Furthermore, BPEs play a pivotal role in filtration membrane techniques, offering efficient separation systems with high removal rates and low energy consumption. Despite challenges related to production costs and property variability, their environmentally friendly, biodegradable, renewable, and recyclable nature positions BPEs as compelling candidates for sustainable water treatment technologies. This review delves deeper into BPEs' modification and integration with other materials; these natural polymers hold substantial promise in revolutionizing the landscape of water treatment technologies, offering eco-conscious solutions to address the pressing global issue of water pollution.

Bending of a lipid membrane edge by annexin A5 trimers.

Plasma membrane damage occurs in healthy cells and more frequently in cancer cells where high growth rates and metastasis result in frequent membrane damage. The annexin family of proteins plays a key role in membrane repair. Annexins are recruited at the membrane injury site by Ca+2 and repair the damaged membrane in concert with several other proteins. Annexin A4 (ANXA4) and ANXA5 form trimers at the bilayer surface, and previous simulations show that the trimers induce high local negative membrane curvature on a flat bilayer. The membrane-curvature-inducing property of ANXA5 is presumed to be vital to the membrane repair mechanism. A previously proposed descriptive model hypothesizes that ANXA5-mediated curvature force is utilized at the free edge of the membrane at a wound site to pull the wound edges together, resulting in the formation of a "neck"-shaped structure, which, when combined with a constriction force exerted by ANXA6, leads to membrane repair. The molecular details and mechanisms of repair remain unknown, in part because the membrane edge is a transient structure that is difficult to investigate both experimentally and computationally. For the first time, we investigate the impact of ANXA5 near a membrane edge, which is modeled by a bicelle under periodic boundary conditions. ANXA5 trimers induce local curvature on the membrane leading to global bending of the bicelle. The global curvature depends on the density of annexins on the bicelle, and the curvature increases with the ANXA5 concentration until it reaches a plateau. The simulations suggest that not only do annexins induce local membrane curvature, but they can change the overall shape of a free-standing membrane. We also demonstrate that ANXA5 trimers reduce the rate of phosphatidylserine lipid diffusion from the cytoplasmic to the exoplasmic leaflet along the edge of the bicelle. In this way, membrane-bound annexins can potentially delay the apoptotic signal triggered by the presence of phosphatidylserine lipids in the outer leaflet, thus biding time for repair of the membrane hole. Our findings provide new insights into the role of ANXA5 at the edges of the membrane (the injury site) and support the curvature-constriction model of membrane repair.

Influence of Nano-CeO2 and Graphene Nanoplatelets on the Conductivity and Dielectric Properties of Poly(vinylidene fluoride) Nanocomposite Films.

Novel three-phase polymer nanocomposites (PNCs) based on cerium oxide (CeO2) nanoparticles (NPs) and graphene nanoplatelets (GNPs) incorporated in a poly(vinylidene fluoride) (PVDF) matrix were formulated using a solution-casting approach. To understand the structural and morphological features of PVDF/CeO2/GNP nanocomposites (NCs), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) analyses were accomplished. The PVDF/CeO2/GNP NCs displayed improved thermal stability which resulted from strong bonding between GNPs and CeO2 NPs and restriction of the polymer chain movement. The introduction of CeO2 NPs and GNPs within the PVDF matrix and good synergy between CeO2 NPs and GNPs led to variable mechanical properties of the prepared NCs. The PVDF/CeO2/GNP NCs portrayed reduced thermal stability, which could be due to the increased mobility of PVDF chains imposed by GNPs leading to the formation of volatile degradation products. Moreover, PVDF/CeO2/GNP NCs exhibited good electrical conductivity and high dielectric permittivity. The obtained dielectric permittivity value for the PVDF/CeO2/GNP NCs was 3-fold greater than PVDF/CeO2 NCs, making these novel tertiary composite materials a probable candidate for energy-storage applications.