New extractive configuration separating azeotropic mixture in semi-batch way

A new variant of batch extractive distillation, the so-called inverse-fed batch extractive distillation is presented. The total amount of the entrainer is pre-loaded to the boiler, and the mixture charge to be separated is continuously fed to the column in this novel configuration. The feasibility study of conventional extractive distillation was extended and a thorough study was performed to separate a maximum boiling azeotrope with intermediate boiling entrainer. The new configuration was found more efficient than the conventional one. The results of the feasibility study was validated and completed with a sensitivity analysis performed with commercial simulator software

Batch Extractive Distillation with Light Entrainer

Use of a light entrainer in batch extractive distillation is justified when the mixture boils at a high temperature, or when an appropriate heavy or intermediate entrainer cannot be found. Feasibility of batch extractive distillation with light entrainer for separating minimum and maximum boiling azeotropes and close boiling mixtures is studied in this article. Our test mixtures are: ethanol/water (minimum boiling azeotrope) with methanol, water/ethylene diamine (maximum boiling azeotrope) with methanol, and chlorobenzene/ethylbenzene (close boiling mixture) with 4-methylheptane. Feasibility, operating steps, limiting entrainer flows, limiting reflux ratios, and limiting number of theoretical stages are determined by parametric study on profiles maps, and verified by rigorous simulation. The effects of reflux ratio, feed ratio, feed stage, number of stages, and thermodynamic state of the entrainer are also examined. It can be established, as a result, that processes separating either minimum or maximum boiling azeotropes, or close boiling mixtures, in batch extractive distillation using a light entrainer are feasible

Feasibility of extractive distillation process variants in batch rectifier column

A systematic comparison is presented about the separation tasks of azeotropic and close-boiling mixtures applying batch extractive distillation (BED) in rectifier. All the eight possible mixture types with at most a single azeotrope (minimum and maximum boiling azeotropes with heavy, light, and intermediate boiling entrainers; and close boiling mixtures with heavy and light entrainers) are compared. The main results of the feasibility studies on the hitherto unpublished cases are presented. All the cases are feasible in batch rectifier, applying BED. The operation steps are determined by the relative position of the azeotropic composition and entrainer in bubble point ranking. The main limiting parameters (F/V, N, Epremix) are also determined by the mentioned relative position; only the existence of maximum number of stages in the rectifying section is determined by the type of the azeotrope. Use of residue curves maps (RCMs) for predicting feasibility is not generally satisfactory, but profiles maps can be used instead. Studying only the total reflux case can be misleading, and should be treated with great care. The theoretical results of separation variants applying intermediate boiling entrainer were proved experimentally

The mitochondrial phosphate carrier: Role in oxidative metabolism, calcium handling and mitochondrial disease

The mitochondrial phosphate carrier (PiC) is a mitochondrial solute carrier protein, which is encoded by SLC25A3 in humans. PiC delivers phosphate, a key substrate of oxidative phosphorylation, across the inner mitochondrial membrane. This transport activity is also relevant for allowing effective mitochondrial calcium handling. Furthermore, PiC has also been described to affect cell survival mechanisms via interactions with cyclophilin D and the viral mitochondrial-localized inhibitor of apoptosis (vMIA). The significance of PiC has been supported by the recent discovery of a fatal human condition associated with PiC mutations. Here, we present first the early studies that lead to the discovery and molecular characterization of the PiC, then discuss the very recently developed mouse models for PiC and pathological mutations in the human SLC25A3 gene. © 2015