Search results for "Liquid liquid"
showing 9 items of 19 documents
Two-phase flow of liquid–liquid mixture in the range of the water droplet pattern
2002
Abstract Phenomena accompanying flow of water–oil mixture during droplet flow of water in oil have been described. Aims used in the determination of characteristic parameters in two-phase liquid–liquid flow have been presented. The method for calculating the equivalent viscosity and pressure drop during flow of liquid–liquid mixture in the range of the water droplet pattern has been given.
MicroSISAK: continuous liquid–liquid extractions of radionuclides at 0.2 mL/min
2013
Abstract Continuous liquid–liquid extraction of short-lived radionuclides has traditionally been performed with the SISAK system consisting of static mixers and H-centrifuges for phase separation. SISAK operates at flow rates of typically 1 mL/s. Thus, it produces large volumes of radioactive liquid waste that is difficult to dispose of. Therefore, it has been aimed to develop and use a further miniaturised extraction unit based on microtechnology and precision engineering to reduce the flow rate by at least two orders of magnitude. The accordingly developed MicroSISAK device is a micro membrane extractor in which a micromixer element with 2 × 16 feed channels of 30 µm width followed by a 6…
Effect of self-assembled surfactant structures on ion transport across the liquid|liquid interface
1999
In this paper, the effect of a coadsorbed polyanion–cationic surfactant system on the transport of tetraethylammonium ion across the water|1,2-dichloroethane interface is studied. It is shown that the change in double-layer structure due to the presence of adsorbed or coadsorbed surfactant can explain the experimental observations, thus concluding that no other effects on ion transfer (e.g., steric hindrance) are relevant under these experimental conditions. The implications of these results are discussed. Keywords: ITIES, Ion transfer, Self-assembled monolayers, Surfactants, Double-layer effects
The influence of the temperature on the liquid–liquid equlibria of the mixture limonene + ethanol + H2O
2004
Abstract In this work, experimental liquid–liquid equilibria (LLE) of the limonene + ethanol + water system are presented. The LLE of this system has been measured at 293.15, 303.15, 313.15 and 323.15 K. The equilibrium data presented are correlated using NRTL and UNIQUAC equations. Finally, the reliability of these models is tested by comparison with experimental results.
Liquid–liquid equlibria of the system dimethyl carbonate+methanol+water at different temperatures
2006
Abstract In this work, experimental liquid–liquid equilibria (LLE) data of the dimethyl carbonate + methanol + water system are presented. The LLE of this system has been measured from 283 to 333 K. On the other hand, LLE and LVE of the binary system dimethyl carbonate + water have been measured. The equilibrium data presented are correlated using NRTL and UNIQUAC equations. The reliability of these models is tested by comparison with experimental results. Finally, the VLE for the system DMC + water at 101.3 kPa was predicted using the UNIQUAC model, with the adjusted parameters obtained from the LLE data. This prediction was successful when is compared with the experimental VLE data.
Fluorenylmethoxycarbonyl-N-methylamino Acids Synthesized in a Flow Tube-in-Tube Reactor with a Liquid-Liquid Semipermeable Membrane
2013
Both steps of the N-methylation of 9-fluorenylmethoxycarbonyl (Fmoc) amino acids were carried out in a microstructured tube-in-tube reactor equipped with a semipermeable Teflon® AF 2400 membrane as the inner tubing. In the first step, gaseous formaldehyde was passed through the inner membrane to effect the acid-catalyzed conversion of the Fmoc amino acids into the corresponding N-Fmoc oxazolidinones. In the second step, liquid–liquid transfer of trifluoroacetic acid was used for the first time in such a reactor for the reductive opening of these oxazolidinones to give Fmoc N-methylamino acids in high yields.
Determination of χ from liquid-liquid phase data in ternary polymer systems (solvent/polymer/polymer) with hydrogen bonding
2008
Two different models accounting for the dependences of χ and g interaction parameters on both temperature and composition have been applied to different ternary polymer systems (TPS) solvent(1)/polymer(2)/polymer(3). The ana- lyzed TPS have consisted on ten different polymer mixtures in chloroform as common solvent that can specifically interact via hydrogen bond. Experimental ternary phase diagrams determined by liquid chromatography were taken from literature. The application of the two models to the experimental data have served to obtain χij and gij interaction parameters for all the binary ij (ij = 12, 13, 23) interactions established between the three components of the system, with si…
Detection of the liquid ? liquid demixing by differential scanning calorimetry
1983
From theoretical considerations it is concluded that the demixing temperatures of moderately concentrated polymer solutions should manifest themselves in a change of the slope of the corresponding DSC trace; the effects are expected to suffice for detection by means of the commercially available dual furnace instrument DSC-2C from Perkin-Elmer.