Mechanisms and Critical Technologies of Transport Inhibitor Agent (TIA) throughout C-S-H Nano-Channels

The critical issue of the durability of marine concrete lies in the continuous penetration and rapid enrichment of corrosive ions. Here a new ion transfer inhibitor, as TIA, with calcium silicate hydrate (C-S-H) interfacial affinity and hydrophobicity is proposed through insights from molecular dynamics into the percolation behavior of the ion solution in C-S-H nano-channels and combined with molecular design concepts. One side of the TIA can be adsorbed on the surface of the cement matrix and can form clusters of corrosive ions to block the gel pores so as to resist the ion solution percolation process. Its other side is structured as a hydrophobic carbon chain, similar to a door hinge, which can stick to the matrix surface smoothly before the erosion solution is percolated. It can then change into a perpendicular chain shape to reduce the percolation channel’s diameter and thereby inhibit the percolation when ions meet the inhibitor. Therefore, once the erosion solution contacts TIA, it can quickly chelate with calcium ions and erosion ions at the interface to form clusters and compact pores. In addition, the water absorption, chloride migration coefficient, and chloride content of concrete samples decreased significantly after adding TIA, proving that TIA can effectively enhance the durability of cement-based materials. The structure–activity relationship of ion transfer that is proposed can provide new ideas for solving the critical problems of durability of cement-based materials and polymer molecular design.

Annexins Bridging the Gap: Novel Roles in Membrane Contact Site Formation

Membrane contact sites (MCS) are specialized small areas of close apposition between two different organelles that have led researchers to reconsider the dogma of intercellular communication via vesicular trafficking. The latter is now being challenged by the discovery of lipid and ion transfer across MCS connecting adjacent organelles. These findings gave rise to a new concept that implicates cell compartments not to function as individual and isolated entities, but as a dynamic and regulated ensemble facilitating the trafficking of lipids, including cholesterol, and ions. Hence, MCS are now envisaged as metabolic platforms, crucial for cellular homeostasis. In this context, well-known as well as novel proteins were ascribed functions such as tethers, transporters, and scaffolds in MCS, or transient MCS companions with yet unknown functions. Intriguingly, we and others uncovered metabolic alterations in cell-based disease models that perturbed MCS size and numbers between coupled organelles such as endolysosomes, the endoplasmic reticulum, mitochondria, or lipid droplets. On the other hand, overexpression or deficiency of certain proteins in this narrow 10–30 nm membrane contact zone can enable MCS formation to either rescue compromised MCS function, or in certain disease settings trigger undesired metabolite transport. In this “Mini Review” we summarize recent findings regarding a subset of annexins and discuss their multiple roles to regulate MCS dynamics and functioning. Their contribution to novel pathways related to MCS biology will provide new insights relevant for a number of human diseases and offer opportunities to design innovative treatments in the future.

The Advantages of EPR Spectroscopy in Exploring Diamagnetic Metal Ion Binding and Transfer Mechanisms in Biological Systems

Electron paramagnetic resonance (EPR) spectroscopy has emerged as an ideal biophysical tool to study complex biological processes. EPR spectroscopy can follow minor conformational changes in various proteins as a function of ligand or protein binding or interactions with high resolution and sensitivity. Resolving cellular mechanisms, involving small ligand binding or metal ion transfer, is not trivial and cannot be studied using conventional biophysical tools. In recent years, our group has been using EPR spectroscopy to study the mechanism underlying copper ion transfer in eukaryotic and prokaryotic systems. This mini-review focuses on our achievements following copper metal coordination in the diamagnetic oxidation state, Cu(I), between biomolecules. We discuss the conformational changes induced in proteins upon Cu(I) binding, as well as the conformational changes induced in two proteins involved in Cu(I) transfer. We also consider how EPR spectroscopy, together with other biophysical and computational tools, can identify the Cu(I)-binding sites. This work describes the advantages of EPR spectroscopy for studying biological processes that involve small ligand binding and transfer between intracellular proteins.

Study of lithium-conducting ceramics Li1.3Al0.3Ti1.7(PO4)3 with the nasicon structure

NASICON-type Li1.3Al0.3Ti1.7(PO4)3 ceramics with a high-density was obtained from powders synthesized from a liquid-phase precursor. The technological scheme of Li1.3Al0.3Ti1.7(PO4)3 solid electrolyte production is given. It is established that at 800 °C a single-phase well-crystallized Li1.3Al0.3Ti1.7(PO4)3 is formed. The ionic conductivity of the sintered Li1.3Al0.3Ti1.7(PO4)3 tablets (density 88–90 %) was 1,9·10–4 S/cm at room temperature, and the electronic conductivity did not exceed 5·10–10 S/cm. The Li+ ion transfer number, measured by potentiostatic chronoamperometry, was 0.99, indicating that the solid electrolyte Li1.3Al0.3Ti1.7(PO4)3 is a purely ionic conductor.

Preliminary Design of the Support Structure for a Rotating Carbon-ion Transfer Line for Medical Applications

The development of new bent superconducting magnets together with the optimization of the support structure open the way to a considerable reduction in the weight and complexity of rotating gantries for medical applications. The magnets, which define the transfer line to deliver carbon ions to the patients from different angles, are supported by a rotating structure that should be as rigid and as lightweight as possible. Relative displacements of the magnets due to deformations cause incorrect beam position and consequent errors in hitting the target tissues. This paper describes a possible rotating structure which is considerably lighter than the previous designs. A method to compensate part of the deformation by complementary rotations of the driving motor is proposed. The influence of the construction tolerances and deformations of the supports is also analyzed and alignment and adjustment possibilities are discussed.

Mathematical Modeling of the Phenomenon of Space-Charge Breakdown in the Galvanostatic Mode in the Section of the Electromembrane Desalination Channel

One of the ways to increase the efficiency of the desalination process in membrane systems is to use intensive current modes. Recently, the phenomenon of space-charge breakdown was theoretically described for desalination under intensive current modes. The space-charge breakdown is a decrease in the magnitude and size of the extended space charge regions (SCRs) of opposite signs, formed at the cation- and anion-exchange membranes in the desalination channel, when they approach each other. Therefore, this phenomenon negatively affects the intensity of electroconvection and the efficiency of mass transfer in membrane systems. We report the results of the first theoretical analysis of the space-charge breakdown in the galvanostatic electric mode, which is generally used in the research and operation of membrane systems. For this purpose, a one-dimensional model of the ion transfer of the electrolyte solution in the section of the desalination channel at the direct current is developed. The regularities of changes in the extended SCRs in the galvanostatic mode are determined. A relation is obtained for the onset time of the space-charge breakdown, which makes it possible to determine the parameters of the effective operation of the membrane system.