Distillation boundaries originate from saddle azeotropes, dividing the composition space into distillation regions. In heterogeneous mixtures distilled in packed columns, distillation regions overlap. The common area of distillation regions is parametrically sensitive, and it determines the possibilities of crossing (at a finite reflux) the distillation boundaries defined for a total reflux or reboil ratio. This work is an extended research of the paper (Królikowski et al., 2011) conducted to scrutinize whether the distillation regions overlapped in heteroazeotropic systems distilled in staged columns. Presented studies were performed by finding such composition points of the products, for which the rectifying profiles of staged columns were ended in different distillation regions. Calculations were executed for the heterogeneous mixture classified under Serafimov's topological class as 3.1-2: ethanol - benzene - water. Distillation regions for staged columns were found to overlap each other in the heterogeneous systems. As a result, their common part was parametrically sensitive.

In this work the esterification of diethyl tartrate was studied. The research was focused on the enhancement of reversible reaction yield, which is accomplished by dewatering of the reaction mixture. The removal of water shifts the equilibrium towards the main product. Pervaporation was applied for this purpose, and results were compared to distillation. The advantages and limitations of both processes are discussed. The experimental part consists of dewatering of mixture after the reaction had reached the equilibrium, and was subsequently fed to the test rig equipped with a single zeolite membrane purchased from Pervatech B.V. Results show a significant conversion increase as a result of water removal by pervaporation. Compared to distillation no addition of organics is necessary to efficiently remove water above the azeotrope. Nevertheless, some limitations and issues which call for optimisation are pointed out. A simple numerical model is proposed to support design and sizing of the pervaporation system. Various modes of integrated system operation are also briefly discussed.

Numerical values of the NRTL equation parameters for calculation of the vapour - liquid - liquid equilibria (VLLE) at atmospheric pressures have been presented for 5 ternary mixtures. These values were fitted to the experimental VLLE and vapour - liquid equilibrium (VLE) data to describe simultaneously, as accurately as possible, the VLE and the liquid - liquid equilibria (LLE). The coefficients of this model called further NRTL-VLL were used for simulations of n-propanol dehydration via heterogeneous azeotropic distillation. The calculations performed by a ChemCAD simulator were done for 4 mixtures using hydrocarbons, ether and ester as an entrainer. In majority simulations the top streams of the azeotropic column had composition and temperature similar to the corresponding experimental values of ternary azeotropes. The agreement between the concentrations of both liquid phases formed in a decanter and the experimental values of the LLE was good for all four simulations. The energy requirements were the most advantageous for the simulation with di-npropyl ether (DNPE) and isooctane. Simulations were performed also for one mixture using the NRTL equation coefficients taken from the ChemCAD database. In that case the compositions of the liquid organic phases leaving the decanter differed significantly from the experimental LLE data.

Analiza ultraśladowa wymaga stosowania ekstremalnie czystych odczynników, w tym wody. Jakość wody stosowanej w laboratoriach decyduje o wiarygodności uzyskiwanych wyników. W laboratoriach chemicznych i biologicznych, jak również przemysłowych, stosowana jest woda destylowana, redestylowana i dejonizowana. Ważnym parametrem określającymjakość wody jest zawartość nieorganicznych jonów. Jedną znajbardziej odpowiednich metod analitycznych w zakresie oznaczania nieorganicznych anionów i kationów jest chromatografia jonowa. W pracy opisano zastosowanie chromatografii jonowej do oznaczania śladowych ilości nieorganicznych anionów (fluorków, chlorków, azotanów(Y), fosforanów i siarczanów(VI) oraz kationów (litu, sodu, amonu, potasu, magnezu i wapnia) w wodach destylowanych, rcdcstylowanych i dejonizowanych.

The literature on membrane distillation and forward osmosis for treating natural and recovered wastewaters is reviewed. There is renewed interest in these membrane technologies as alternatives to pressure driven processes such as reverse osmosis, which are expensive in both capital and energy, and generally require pre-treatment of the feed water. Membrane distillation with hydrophobic microfiltration membranes can make use of low-grade heat energy, and give higher yields of product water from concentrated feed waters. Forward osmosis uses hydrophilic membranes akin to reveres osmosis, and needs a draw solution that is appropriate in the product water. or must be recovered and reused in large-scale operation. Although they show great promise as simple low energy systems, no large-scale installation of either process exists as yet. Membrane distillation has considerable potential for desalination to produce drinking water, whereas FO is currently confined to small-scale systems, especially as a source of energy drinks in emergency situations.

Liquid Metal Extraction process using molten Mg was carried out to obtain Nd-Mg alloys from Nd based permanent magnets at 900oC for 24 h. with a magnet to magnesium mass ratio of 1:10. Nd was successfully extracted from magnet into Mg resulting in ~4 wt.% Nd-Mg alloy. Nd was recovered from the obtained Nd-Mg alloys based on the difference in their vapor pressures using vacuum distillation. Vacuum distillation experiments were carried out at 800oC under vacuum of 2.67 Pa at various times for the recovery of high purity Nd. Nd having a purity of more than 99% was recovered at distillation time of 120 min and above. The phase transformations of the Nd-Mg alloy during the process, from Mg12Nd to α-Nd, were confirmed as per the phase diagram at different distillation times. Pure Nd was recovered as a result of two step recycling process; Liquid Metal Extraction followed by Vacuum Distillation.

This paper presents the results of thermodynamic analysis of the crude distillation units of two refineries in Nigeria. The analysis was intended to assess the thermodynamic efficiencies of the refineries and proffer methods of improving the efficiencies. Presented results show the atmospheric distillation units of the refineries have 33.3% and 31.6% exergetic efficiencies and 86.5% and 74.6% energetic efficiencies, respectively. Modifications of the operating and feed conditions of the refineries resulted in increased exergetic efficiencies for as much as 62.3% and 38.7% for the refineries. Thermodynamic analysis of the refineries can bring about efficiency improvement and effectiveness of the refineries.

The aim of the study was to determine the effect of adding bio-components in the form of methyl esters of corn oil to the milesPLUS diesel oil on its fractional composition. The corn biofuel was produced in-house by using an own-design GW-200 reactor. The diesel fuel evaporated at temperatures ranging from 162 to 352oC. The addition of 7, 20 and 40% of a bio-component in principle does not affect the deterioration of the starting point distillation temperatures. They affect the temperature at the end of distillation to a greater extent, resulting in temperatures exceeding 360oC.

Easy-to-handle and effective methods of juice clarification and concentration by membrane technologies are still under exploration. The current article presents results of research on the technological development of an alternative natural sweetener of high biological value and improved organoleptic properties. Sorghum saccharatum stem juice is used in research. It is pre-clarified enzymatically with α-amylase and glucoamylase, clarified by ultrafiltration, and concentrated by the direct contact membrane distillation in various temperature ranges. The study shows the efficacy of membrane methods for improving juice purity, total soluble solids ( TSS), and total sugar (TS) content in the syrup obtained. Clarification depends on membrane characteristics at the beginning of the process, as there are no differences at the end of it. Juice concentration at high-temperature differences allows to accelerate the process by approx. 60% comparing to low-temperature differences. A lower temperature difference ( ΔТ = 20–30°С) in the concentration process results in a longer process and syrup acidisation, whereas a higher temperature difference ( ΔТ = 70°С) affects physicochemical properties of syrup due to local overheating and formation of Maillard reaction products. The juice concentration at ΔТ = 50–60°С allows to obtain high values of total soluble solids without significant degradation of physicochemical and organoleptic properties.